Mixed Plastics Waste To Ethylene and Propylene Feedstocks
Mixed Plastics Waste To Ethylene and Propylene Feedstocks
ScholarlyCommons
4-21-2020
Sarah M. Engelhardt
Matthew C. Larson
Abstract
Circular recycle of waste plastic holds significant environmental benefit in reducing the need for crude oil
feed to produce plastic monomers and in addressing massive global accumulation of plastic waste. A
two-stage cracking process is here explored for the reduction of long-chain polyethylene (PE),
polypropylene (PP), and polystyrene (PS) to ethylene and propylene. The reaction yields useful
byproducts, such as liquid fuel used to sustain the high energy demands of the process, and pressurized
steam. A feed of 70 MT/day of PE, PP, and PS is assumed to be treated first in a rotary kiln pyrolysis
reactor and secondly in a steam-cracking unit for the formation of short-chain unsaturated hydrocarbons.
41% of the feedstock by weight is converted to either ethylene or propylene. Due to the random nature of
cracking, a pilot plant is deemed necessary to better understand this conversion. Heat integration is
explored extensively throughout the cracking to employ other process products as fuel sources. A novel
separation train and refrigeration cycle are then designed to isolate the two products of interest. The
process is found not to be profitable, with an Internal Rate of Return of -4.74%, Net Present Value of -
$18.8MM, and Return on Investment (ROI) in the third year of operation of -2.12%. However, a circular
monomers facility holds significant value environmentally, and options are thus explored to potentially
reduce the cost or make the process profitable.
Disciplines
Biochemical and Biomolecular Engineering | Chemical Engineering | Engineering
University of Pennsylvania, School of Engineering and Applied Science
Department of Chemical and Biomolecular Engineering
220 South 33rd Street
Philadelphia, PA 19104
The enclosed report contains a process design for converting consumer and industrial
waste plastic into ethylene and propylene monomers. The process is fed 68.9 imperial tons of a
mix of low-density polyethylene, high-density polyethylene, polypropylene, and polystyrene. We
initially aimed to follow a patent issued to Plastics Energy, but eventually decided to follow
another pathway. In our design, the plastics are washed, dried, extruded, and are then pyrolyzed
in two successive rotary kilns. Light gas product is then cracked in a steam cracker and is rapidly
quenched to prevent further reactions. The resulting stream is then compressed and finally
separated to in order to recover ethylene and propylene.
From an economic standpoint, this process is not profitable. The plant requires a total
capital investment of $27.5 MM dollars to achieve the desired conversion of 68.9 tons of plastic
waste per day. The Internal Rate of Return (IRR) is -4.47%. While we do not recommend
investing in this particular process, we believe that the chemical recycling of plastic waste is a
worthy area of research and development, and we offer some modifications and alternatives to
our proposed process that may result in a profitable process.
Sincerely,
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Mixed Plastics Waste to Ethylene and Propylene Feedstocks
Promise Adebayo-Ige | Sarah Engelhardt | Matthew Larson
Project submitted to Dr. Sean Patrick Holleran and Prof. Bruce Vrana
Project proposed by Stephen Tieri
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Table of Contents
Section 1. Abstract ............................................................................................................... 7
Section 2. Introduction and Objective-Time Chart ................................................................ 8
i. Introduction: Motivation and Goals ............................................................................... 10
ii. Introduction: Objective-Time Chart ............................................................................... 13
Section 3. Market and Competitive Analysis ...................................................................... 14
Section 4. Customer Requirements ..................................................................................... 15
Section 5. Preliminary Process Synthesis ............................................................................ 15
i. Pyrolysis Process and Alternatives................................................................................. 15
ii. Secondary Cracking Operation ...................................................................................... 22
iii. Self-Sustaining Fuel Considerations .......................................................................... 23
iv. Separation Process and Alternatives........................................................................... 23
v. Material Balances .......................................................................................................... 28
vi. Feed Assumptions ..................................................................................................... 32
Section 6. Process Flow Diagrams and Stream Tables ........................................................ 34
i. Block Flow Diagram ..................................................................................................... 34
ii. Section 000: Upstream Processing ................................................................................. 35
iii. Section 100: Rotary Kiln Pyrolysis ............................................................................ 36
iv. Section 200: Steam Cracking, Quen ching, and Compression..................................... 38
v. Section 300: Separations................................................................................................ 40
vi. Section 400: Refrigeration System ............................................................................. 42
Section 7. Assembly of Database ........................................................................................ 44
i. Thermophysical Properties ............................................................................................ 44
ii. Raw Materials ............................................................................................................... 44
Section 8. Process Description ............................................................................................ 45
i. Process Description: Overall Process ............................................................................. 45
ii. Section 000: Upstream Processing ................................................................................. 45
iii. Section 100: Rotary Kiln Pyrolysis ............................................................................ 46
iv. Section 200: Steam Cracking, Quenching, and Compression ..................................... 48
v. Section 300: Separations................................................................................................ 53
vi. Section 400: Refrigeration System ............................................................................. 57
Section 9. Energy Balance and Utility Requirements .......................................................... 59
i. Section 100: Rotary Kiln Pyrolysis ................................................................................ 59
ii. Section 200: Steam Cracking, Quenching, and Compression ......................................... 59
iii. Section 300: Separations ............................................................................................ 61
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iv. Section 400: Refrigeration System ............................................................................. 63
Section 10. Equipment List and Unit Descriptions ................................................................ 65
i. Section 000: Upstream Processing ................................................................................. 65
ii. Section 100: Rotary Kiln Pyrolysis ................................................................................ 66
iii. Section 200: Steam Cracking, Quenching, and Compression ..................................... 71
iv. Section 300: Separations ............................................................................................ 75
v. Section 400: Refrigeration System ................................................................................. 85
Section 11. Specification Sheets ........................................................................................... 89
i. Section 100: Rotary Kiln Pyrolysis ................................................................................ 89
ii. Section 200: Steam Cracking, Quenching, and Compression ......................................... 95
iii. Section 300: Separations .......................................................................................... 111
iv. Section 400: Refrigeration System ........................................................................... 123
Section 12. Equipment Cost Summary................................................................................ 127
Section 13. Fixed Capital Investment Summary.................................................................. 130
Section 14. Operating Cost-Cost of Manufacture ................................................................ 133
Section 15. Other Important Considerations ....................................................................... 137
i. Environmental Factors ................................................................................................. 137
ii. Safety Factors .............................................................................................................. 138
iii. Global factors .......................................................................................................... 139
iv. Robustness of feedstock........................................................................................... 140
Section 16. Profitability Analysis ....................................................................................... 141
i. Profitability Metrics..................................................................................................... 141
ii. Sensitivity Analyses .................................................................................................... 146
iii. Potential Adjustments for Increased Profitability ..................................................... 148
iv. Summary ................................................................................................................. 150
Section 17. Conclusions and Recommendation ................................................................... 151
Section 18. Acknowledgments ........................................................................................... 153
Section 19. Works Cited ..................................................................................................... 154
Section 20. Appendix ......................................................................................................... 160
Appendix A: Calculations ................................................................................................... 160
Rotary Kiln Pyrolysis Unit .............................................................................................. 160
Solid/Liquid Splitter ........................................................................................................ 163
Plastic Extrusion Screw ................................................................................................... 163
Bucket Elevators ............................................................................................................. 165
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Screw Feeder................................................................................................................... 166
Feed Silo ......................................................................................................................... 166
Blower ............................................................................................................................ 167
Steam Cracker ................................................................................................................. 167
Quench Tower ................................................................................................................. 168
Transfer Line Exchanger ................................................................................................. 170
Distillation Columns........................................................................................................ 171
Pumps ............................................................................................................................. 173
Heat Exchangers.............................................................................................................. 173
Storage Tanks.................................................................................................................. 174
Compressors .................................................................................................................... 175
Flash Vessels ................................................................................................................... 176
Appendix B: MSDS Sheets ................................................................................................. 177
Appendix C: ASPEN Report ............................................................................................... 194
Section 200: Compressor Blocks and Streams ................................................................. 194
Section 200: Intercooler blocks and streams .................................................................... 209
Section 200: Pump blocks and streams ............................................................................ 238
Section 200: Blower block and streams ........................................................................... 244
Section 300: Separations Blocks and Streams .................................................................. 248
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Section 1. Abstract
Circular recycle of waste plastic holds significant environmental benefit in reducing the
need for crude oil feed to produce plastic monomers and in addressing massive global
accumulation of plastic waste. A two-stage cracking process is here explored for the reduction of
long-chain polyethylene (PE), polypropylene (PP), and polystyrene (PS) to ethylene and
propylene. The reaction yields useful byproducts, such as liquid fuel used to sustain the high
energy demands of the process, and pressurized steam. A feed of 70 MT/day of PE, PP, and PS is
assumed to be treated first in a rotary kiln pyrolysis reactor and secondly in a steam-cracking unit
for the formation of short-chain unsaturated hydrocarbons. 41% of the feedstock by weight is
converted to either ethylene or propylene. Due to the random nature of cracking, a pilot plant is
deemed necessary to better understand this conversion. Heat integration is explored extensively
throughout the cracking to employ other process products as fuel sources. A novel separation train
and refrigeration cycle are then designed to isolate the two products of interest. The process is
found not to be profitable, with an Internal Rate of Return of -4.74%, Net Present Value of -
$18.8MM, and Return on Investment (ROI) in the third year of operation of -2.12%. However, a
circular monomers facility holds significant value environmentally, and options are thus explored
7
Section 2. Introduction and Objective-Time Chart
Plastic has become an essential part of life for people across the globe. With a diverse set
of properties that allow it to perform myriad functions, it has become an indispensable material in
a number of industries, from medicine to consumer-packaged goods. Unfortunately, with the surge
of plastic use over the past few decades, plastic waste has become a huge threat to the environment.
It is therefore imperative that a safe, effective, sustainable solution is developed to handle the
More than eight million metric tons of plastic waste are dumped into the ocean every year,
which can harm marine organisms [2.1]. Plastic waste is equally harmful in an above-water setting.
Only a small percent of plastic waste makes it to a recycling bin, let alone to a recycling plant.
Countries like China that are equipped with recycling plants have stopped accepting plastic waste,
and countries such as Malaysia, Vietnam, and Thailand have become the primary collectors,
despite their waste management systems already nearing capacity [2.2]. Burdened with an
overwhelming amount of plastic waste, these countries turn to dangerous methods of disposal,
including dumping and incinerating waste near residents who are then harmed by these toxic
fumes.
Currently, recycling is the most sustainable option for plastic waste disposal, although it is
estimated that less than 10% of plastic globally gets recycled [2.3]. There are two main recycling
processes for plastic waste: mechanical recycling and chemical recycling. In mechanical recycling,
plastic goods are broken down mechanically (i.e. through cutting or shredding) and turned into
new products. The chemical structure of the plastic material stays the same, but the function of the
material itself changes; for example, polyethylene terephthalate, or PET, which is the material that
most plastic bottles are made from, can be mechanically recycled into polyester thread, which can
be used to make clothing. While this does reduce the number of plastic bottles being thrown into
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the ocean, there is a limit to how helpful such a process is; the world only needs so many polyester
shirts, and the need for plastic bottles will remain. The production of plastic bottles will continue,
and it will outpace the rate of production for polyester shirts. Inevitably, many of those plastic
In chemical recycling, plastic goods are broken down using chemical processes. The
chemical structure of the plastic material is altered into a new material. For example, polyethylene
plastic, which is one of the most prevalent types of plastic, is a polymer. It can be treated
chemically so that it breaks down into hydrocarbons of varying lengths. There have been several
studies in which plastic waste was converted to natural gas and oil using processes like pyrolysis
and supercritical hydrothermal liquefaction on a lab scale [2.5, 2.6]. Natural gas and oil have
several important uses, from making fuels to being refined into monomers that can be used as
feedstock for plastic production. On an industrial scale, these processes could be used to create a
direct path for plastic waste to be returned to new plastic products. As a result, less plastic waste
Chemical recycling is not a well-established industry practice. There are strict limitations
on what can be recycled. Current processes require plastic to be sorted into the different types
before being recycled, which is a time- and energy-consuming endeavor. Plastic waste must also
be clean before being processed. These constraints make chemical recycling financially,
energetically, and feasibly unattainable; because of this, mechanical recycling and the dangerous
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i. Introduction: Motivation and Goals
In completing this project, we set out to design a robust method to chemically recycle
plastic waste in an affordable and efficient manner. The goal of our project was to convert 70
metric tons of plastic waste per day into clean plastic feedstock monomers—ethylene and
propylene—which could then be sold to other facilities producing plastic. The feed would be a
and Polyvinyl Chloride) are not included in the feed because they contain non-hydrocarbon
compounds, which could produce harmful byproducts (for example, chloride from the PVC) and
would require extra processing beyond what is required for the specified types. Plastic type 7,
which consists of any plastics that do not fall into categories 1-6, is also not included, because it
is so ill-defined and would be impossible to predict how it would behave in our process.
We initially modeled our design for this process after a chemical recycling plant created
by Plastic Energy, LLC, an English company that develops solutions for recycling plastic waste
[5.7]. The process set forth by Plastic Energy, LLC boasted an ability to produce high-quality
hydrocarbon fuels including naphtha, kerosene, and diesel from a mix of all plastic types through
pyrolysis. From this point, further processing would be required to obtain the plastic feedstock
monomers desired for the purposes of this project. Light hydrocarbon oils like naphtha are
frequently used as feedstock in the production of short-chain hydrocarbons such as ethylene and
propylene monomers, and methods to do so like steam cracking are well-established industrial
processes. To successfully complete this project, we would need to unite these two processes
within one chemical recycling plant, where a feedstock of plastic waste could be converted to light
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Over the course of completing this project, we determined that Plastic Energy, LLC’s
technology was not suited to our goal in producing ethylene and propylene monomers. However,
the overall objective remained the same: to convert plastic waste into material that could then be
used to produce ethylene and propylene. Because ethylene and propylene are very short
hydrocarbon chains, it would be most desirable for the products from the initial pyrolysis to be as
short in length as possible. The products of Plastic Energy, LLC’s pyrolysis process were quite
long hydrocarbon chains, ranging in length from four to more than twenty carbons. When it
became clear that an alternative method of plastic degradation would be required, we turned to
existing chemical recycling research and identified that pyrolysis of our plastic waste feedstock in
a rotary kiln would provide us with a gas product that was well-suited for further processing into
From an economic perspective, our initial goal was to make this a profitable endeavor.
Because our process uses plastic waste as its feed, we assumed that cities or other entities would
pay us to collect their plastic waste. An additional goal was to determine the ideal location to build
our plant; our choices were California, the Netherlands, and Indonesia. Ultimately, we chose
Indonesia as the plant location, and found that the process would not breakeven after fifteen years
of operation. The IRR for the plant is -4.47%, and the ROI in the third year of production is -
2.01%.
In this report, we present our design of a chemical recycling plant that produces 33,600
pounds of 99.0 wt% ethylene and 30,000 pounds of 95.7 wt% propylene per day. This corresponds
to a 20.67% yield of ethylene and a 19.48% yield of propylene, which is a 40.14% overall yield.
The remaining products from the process include hydrogen and various hydrocarbons ranging in
11
length from 1 to 4 carbons, which can be used as fuel for several of the process units. We also
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ii. Introduction: Objective-Time Chart
Figure 5.1 shows the objective-time chart for the completion of this project.
Figure 2.1: Objective-Time Chart for the Completion of Mixed Plastic Waste to Ethylene and
Propylene Feedstock.
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Section 3. Market and Competitive Analysis
Ethylene, a volatile organic compound, is the most widely used hydrocarbon in the
ethylene glycol, and vinyl chloride. It is also the building blocks of #2 and #4 plastics, HDPE and
LDPE. Like ethylene, propylene is a very important product in the petrochemical industry because
it is also a feedstock to many B2B and B2C products such as, film fibers, polypropylene, cumene,
and butyraldehyde. In 2019 the global ethylene production capacity was 207.58 million tons per
annum (mtpa), with North America and Asia being highest producing regions [3.1], and in 2018
the global production capacity of propylene was 120 mtpa [3.2]. The main conventional techniques
for ethylene and propylene production are steam cracking and catalytic cracking. In steam
cracking, gaseous or liquid hydrocarbons, such as naphtha and liquefied petroleum gas, are diluted
with steam and are cracked in a pyrolysis furnace. In catalytic cracking, longer hydrocarbons are
cracked in the presence of catalysts at moderate temperatures. Still, both processes produce
significant amounts of CO2 emissions, with steam cracking alone contributing to 180 – 200 mtpa
shifting to unconventional methods to become more sustainable. This entails the use of biomass
polyethylene, is made from ethanol after undergoing a dehydration process and also from
bioethanol that originates from sugar cane, sugar beet, and wheat grain. The Coca-Cola Company
uses this in their PlantBottle™ product, which is a polyethylene terephthalate (PET) bottle made
from plants. The paraxylene used to create their PET bottles are sourced from bio-based iso-
butanol [3.4]. Dow Chemical Company has also produced AGILITY™ CE, which is a resin made
with 70% recycled LDPE. Fuenix Ecogy Group in the Netherlands also has patent to similar to
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that of Plastics Energy; in their process mixed plastic waste is burned in two successive pyrolysis
In this report we propose an unconventional process that uses a rotary kiln to pyrolyze
2,4,5,6 plastics. Our downstream process is the same of that in chemical plants that have a steam
crackers. Though our ethylene and propylene output is not as large as conventional ethylene
production plants, our process is unique because it establishes a circular plastic economy, with the
potential for scale up. Currently, there are no industrial-scale chemical plants that process post-
consumer and post-industrial plastic waste in a circular process. The unconventional methods
mentioned work for specific uses, but they do not convert feedstock to ethylene and propylene. In
addition, rather than drilling for feedstock, federal and local governments would pay for us to
which recycling means, “any recovery operation by which materials are reprocessed into products,
materials or substances whether for the original or other purposes.” Any diesel or fuel coproduct
must comply with ASTM D975 or EN590 standards, and the minimum purity for polymer grade
ethylene and propylene are both 99.5%. For propylene, the minimum purity for chemical grade is
95.0%.
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Existing research and operations regarding treatment of mixed plastic waste focus on the
capacity to convert solid feed into liquid fuel, comparable to gasoline, kerosene, or diesel. Limited
operations are used for the conversion of plastic waste to short-chain hydrocarbon gas product,
and most gas produced is used a natural gas substitute to make cracking operations self-sustaining
[5.1]. At present, industrial production of ethylene and propylene employs steam cracking to break
hydrocarbons to C2 and C3. Common feeds for this process are ethane, propane, and naphtha, a
light oil ranging from C5-C10 hydrocarbons [5.2]. Steam cracking using ethane or propane as
feedstock runs the advantage of cheaper, less complex plants with high ethylene and propylene
yield [5.1,3]. Additionally, it is well established that cracking of plastic waste produces a gas in
the range of C1-C6, and an oil product in the range of C6-C24 [5.1]. The exact compositions of
the oil and gas products will be discussed in greater detail in section 15. In the interest of achieving
higher product yield and greater plant simplicity, the initial cracking reaction will thus focus on
Multiple vessels were considered for the primary cracking reaction in this process. As the
initial treatment of plastic waste poses perhaps the greatest barrier to circular recovery of
monomers, this stage in the process was explored extensively. The options considered as discussed
below, and ultimately a decision matrix is used to justify the choice of a rotary kiln.
As originally proposed, the project was to make use of a patent for “Conversion of Waste
Plastics Material to Fuel” by David McNamara and Michael Murray. Their system employs a novel
pyrolysis and contactor system, modeled as a CSTR, to convert dirty plastic feedstock to
16
hydrocarbons ranging from C1-C21 [5.4]. However, due to an absence of available data and
conflicting operating conditions, use of this technology was not possible [5.4,5].
Simple pyrolysis was considered as an alternative to the novel pyrolysis in the patent due
to the abundance of data on the subject. Pyrolysis is the thermal degradation of long-chain
polymers to small and less complex molecules through heating to temperatures in the range of 752
– 1472 ⁰F, and is used primarily for the treatment of PE, PP, and PS [5.1]. Pyrolysis produces a
gas product, liquid oil product, and solid char product. In practice, the production of liquid oil is
often favored for use as a fuel oil due to its high calorific value, and the gaseous product is often
used as a fuel source to make the pyrolysis unit self-sustaining [5.6]. Data exist to aid in prediction
of products, and the unit is robust in ability to pyrolyze dirty plastic [5.1,6]. Pyrolysis is flexible
in manipulation of operating variables to produce desired product, does not require extensive feed
sorting, and may not require feed cleaning [5.7]. Notably, pyrolysis data is lacking in study of
mixed plastic feed and is susceptible to the random nature of the cracking reaction [5.8].
The batch pyrolysis reactor is most commonly studied in literature. Batch pyrolysis is
useful in manipulation of residence time and simplicity of unit design. However, batch pyrolysis
suffers from variable product composition, and on the scale of this project, the size of a batch
pyrolysis reactor is not realistic (estimated at slightly over 1,000 ft3) [5.9]. In contrast, when
increases significantly [10]. Both units require a residence time of 15-60 minutes, which presents
Pyrolysis runs the major disadvantages of heat transfer and ease of operation. Heat transfer
is most commonly achieved via passage of an inert gas on an industrial pilot scale [5.11].
17
However, this process is to focus on the product of gaseous product, and oxygen-rich gas may not
be used due to the favorable formation of CO and CO2, nitrogen gas proposes a complex
separations problem, and other carrier gases are too expensive on the required scale [5.1].
Additionally, both types of pyrolysis require high operation cost due to oil and char accumulation,
Liquefaction
hydrogenated biomass into oil-like product, often in the presence of a catalyst [5.13]. Liquefaction
is used for treatment of plastic waste due to the lower heat requirement (waste need be heated in
the range of 300-500 OC), robustness of the process to handle multiple types of plastic, and ability
to process wet and dirty feedstock [5.12,13]. Liquefaction has been shown to give high yield of oil
product (around 90% by weight of feed) and with residence times of 30-60 minutes, which is
However, liquefaction requires high pressures, on the order of 30 atm, which are difficult
to achieve in large vessels prior to the production of gaseous product [5.12]. Additionally, the
liquefaction process is used primarily to generate oil product, and in the studies here considered
gives a maximum gas yield of less than 20% by weight of feedstock [5.12,13,14]. Finally,
liquefaction often requires a catalyst for high conversion rates of the feedstock to oil product,
Fluidized Bed
The fluidized bed has the major advantages of efficient heat transfer and short residence
time [1]. Additionally, a fluidized bed has been used in previous pilot-scale work termed the
Hamburg Process for conversion of plastic waste to fuel gas [5.15]. It has the advantages of
18
moderate maintenance cost, ease of catalyst introduction, and formation of gaseous product (which
is favored in our process) [5.1,16]. However, the operation of a fluidized bed for treatment of
viscous liquid is complex and requires the bed to be filled often with expensive material [5.17].
Issues arise with plastic melt sticking to the surface of the bed material and the unit and scale up
becomes complex [5.18]. Additionally, massive amounts of nitrogen effluent are required,
purity. Finally, the fluidized bed is primarily used to form methane gas for use as a natural gas
substitute, and conversion of methane to ethene and propene on an industrial scale is unfeasible
Rotary Kiln
The rotary kiln has little data available and has rarely been used to treat plastic waste.
However, under the assumption that the rotary kiln behaves much like a continuous pyrolysis unit,
the expected product and composition may be estimated. The rotary kiln may handle large amounts
of plastic waste and offers significant control over the residence time as a function of angle. Heat
transfer in the kiln is difficult but may occur without introducing an effluent gas and thus reduce
the need for complex separation. Additionally, through a cleverly designed indirect fired kiln, the
necessary heat transfer may be achieved due to the nature of a moving liquid in the reactor. The
rotary kiln is also expected to require minimal maintenance, as the angular nature aids in removal
Evaporator
An evaporator was explored as an alternative due to the desire of forming gaseous product,
and their efficient heat transfer. Evaporators are already used in the handling of hydrocarbons,
predominately in the fuel industry for removal of water from crude oil. However, the evaporator
19
is not used at the temperatures required for the pyrolysis of plastic waste, is not used in practice
Spouted Bed
The sprouted bed reactor has been explored for treatment of plastic waste as a theoretically
sound option for treatment of plastic waste to address the defluidization and bed segregation issues
accompanying a fluidized bed [5.20]. It is able additionally to handle the viscous molten plastic
without need for significant operating cost associated with cleaning [5.21]. However, the spouted
bed reactor is most suitable for producing gasoline-range hydrocarbons in oil form and has a
complex design with high pumping requirements [5.22,23]. Additionally, the design requires a
Use of a Catalyst
Catalysts are commonly used in plastic waste pyrolysis for enhancing yield and promoting
gasoline-range hydrocarbons. Little work has been done to encourage the formation of gaseous
product, but H-ZSM-5 and red mud have emerged as potential catalysts to promote gas formation.
The greatest challenge with catalyst uses on the scale of this project is recycle, due to the viscous
nature of the plastic and oil product [5.25]. In the case of a fluidized bed, catalyst recycle is
feasible, but beyond this system recycle becomes complex and energy consuming.
c. Decision Matrix
Many characteristics of the mentioned systems were considered and synthesized into a
decision matrix (Table 13.1). The rotary kiln option was found to be the only option with no
apparent major design challenges and was thus selected for the process.
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Table 5.1 Decision Matrix
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ii. Secondary Cracking Operation
The gaseous product of the rotary kiln does not contain enough ethylene and propylene to
separate and sell, thus further cracking is required to obtain desired products. As it is well
established in industry and is the traditional method of ethylene and propylene production, steam
cracking was selected for the secondary cracking operation. The subsequent operations on the
steam cracking product, involving transfer line exchange, quench, and purification were
implemented. In practice, this process often uses a caustic tower for the removal of acidic gas (such
as sulfur contamination and CO), and a molecular sieve dryer for removal of steam from the
product stream. However, given the assumptions of this project, these two units are not necessary.
The chemistry of steam cracking is thankfully well known. The cracking yields were
approximated using the distribution provided by Akah [5.41] and given in Table 5.2.
To determine the distribution, hydrogen, methane, ethene, and propene were assumed inert
in the steam cracker. Ethane, propane, and butane were assumed to crack according to the
distribution of table 5.2. Butane was used to represent butane, butadiene, and all C5+ compounds
for energy balances and separations. The product composition, given as weight percent from the
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Species % Weight
Ethane 4.2
Ethene 38.3
Propane 1
Propene 24.9
C4+ 8.0
and product distribution are estimated in section 15. Due to the partly unknown nature of the
compounds in the oil and the major heat requirements of the rotary kiln and steam cracker, all the
pyrolytic oil produced is used as fuel. Additionally, due to the small amount of oil produced (1181
lb/hr), a separation train to provide on-specification commercial fuel product is not economically
viable.
a. Separations Goal
The goal of the separation process was to achieve a split between our final monomer
products, ethylene and propylene, and the rest of the hydrocarbons produced in the steam-cracking
unit that were to be used as fuel. Additional separation processes were also considered in
conjunction with some of the alternative pyrolysis methods that were considered.
b. Extractive Distillation
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In certain studies, it was found that a significant amount of aromatic species would be
produced in the pyrolytic oil. The aromatic species estimated to be in the pyrolytic oil were
benzene, toluene, xylene (BTX), naphthalene, and styrene. We considered using extractive
distillation to remove BTX and the other aromatics from the pyrolytic oil, to sell them together or
separately. To do this, all products from the rotary kiln will be sent to an extractive distillation
column where a solvent would be feed from the top of the column. The aliphatic species would
exit in the column overhead, while the aromatic species and solvent would leave in the bottoms
and be fed to another tower where they would be separated. The solvent would leave in the
overhead of the second column and would be recycled back to the first column. The solvent we
considered using was Tetrahexly ammonium-bromide. We decided against this process given that
capital costs of trying to separate the aromatics further, and the hazards of having solvent in the
One method that was considered for the separation process was to include a one-stage flash
vessel as the first separation event, to remove the lightest components, hydrogen and methane.
However, because all of the components being separated are quire light and have low boiling
points, achieving this separation in a flash vessel would require either extreme pressures (on the
order of 10,000 psia) or extreme temperatures (nearing -425°F). Only at these conditions will the
desired products, hydrogen and methane, exist in the vapor phase while the rest of the products
stayed in the liquid phase. This approach was also tested using ASPEN, and the simulation
confirmed the predicted outcome. It was clear that tray towers would need to be used, which are
what is used in industrial petrochemical plants that process similar product streams.
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Demethanizer Column Design
The separation train configuration was modeled after standard industrial separation
processes in ethylene and propylene plants. In the industry, feeds of refined hydrocarbons with
hydrogen are sent into a demethanizer column, a type of distillation column that separates the
lightest gasses (methane and hydrogen) from heavier hydrocarbons. Demethanizer columns
require extremely low temperatures, and designing these columns is much less straightforward
than a standard distillation column that can be run at more typical operating conditions.
The separation would occur between the light key, ethylene, and the heavy key, methane;
we wanted to recover our hydrogen and methane in our distillate, and all of our hydrocarbons
heavier than methane in our bottoms product. We knew that a total condenser would be
implausible. The critical temperature of hydrogen is -400ºF, which is less than 100ºF above
absolute zero temperature. Clearly, the distillate exiting the demethanizer would be a vapor. So,
for our first pass at the design using ASPEN, we initially selected a partial condenser with all vapor
distillate and set the column pressure to 450 psia (a reasonable guess for a distillation column with
Using DSTWU in ASPEN as a first attempt for column design, we found that the required
condenser temperature to achieve a successful split between the components (i.e., removing 99%
of the light key) was -230ºF. While condensers for demethanizer columns do operate at extremely
low temperatures, they usually hover around -130ºF; any colder and the energy requirements
become too great to be feasible. So, we increased the pressure of the column to bring the
temperature of the distillate up to a more reasonable value. Even at an unrealistically high pressure
of 1000 psia, the distillate was still coming out of the column around -220ºF; it was clear that
25
increasing the pressure of the column would not be sufficient in increasing the distillate
temperature.
One reason that the distillate would need to be at such a low temperature was that the other
components being separated from the hydrogen and methane were also very light. Ethylene’s
normal boiling point is -154.7ºF, and that is the lightest of the heavy hydrocarbons. To obtain a
split between methane and ethylene, an extremely low temperature would be needed. Rather than
increase the pressure to an extremely high number, it would be more sensible to allow some of the
ethylene to exit the column from the top of the column, which would increase the temperature
required in the condenser. This would also allow us to operate the condenser at a more reasonable
pressure of 550 psia. The downside of this is that some of the ethylene product is lost and cannot
be recovered (for the same reason that it could not be recovered in this column), but we did not
consider this to be a total loss—the ethylene that exits through the top of the demethanizer column
could be used as fuel elsewhere in the process and would be valuable to the process in that regard.
To implement this into the design, the demethanizer column was modeled in ASPEN as a
RadFrac column using a partial-condenser with vapor and liquid distillate. After some trial-and-
error to determine what amount of ethylene would allow the demethanizer condenser temperature
to reach a more reasonable value, a distillate flowrate of 1,702 lbs/hr and a vapor fraction of 0.448
was chosen. The vapor distillate also contained 539 lbs/hr of ethylene, though, to increase the
temperature of the condenser, as discussed above. Most of our ethylene product (1,437 lbs/hr)
exited the column in the liquid distillate stream, meaning that we were recovering a significant
portion of the ethylene product in our first distillation event. However, the ethylene recovery
26
Deethanizer
The deethanizer column would need to perform a similar function to the demethanizer
column—removing the remaining methane from the ethylene recovery stream. The same
challenges related to the demethanizer column also held true for the deethanizer column; the
condenser would need to operate at a very low temperature to allow for separation between the
very light components. Originally, a partial-condenser with vapor and liquid distillate was tested,
but upon closer examination, it appeared that the concentration of ethylene became greater lower
in the column, so a side-stream was taken off the column instead. This meant that a partial-
condenser with all vapor distillate would need to be used. Again, some ethylene was permitted to
exit the top of the column to allow for a more reasonable condenser temperature.
Depropanizer
The bottoms products from both the demethanizer and deethanizer column are sent to the
depropanizer for separations. The remaining components in the separations process were heavy
enough that a higher condenser temperature of -29.06ºF could be used. A partial-condenser with
vapor and liquid distillate was considered, but, similar to the deethanizer, taking off a side stream
One modification to the process that could result in better propylene product yield would
be to add the two feed streams to the depropanizer column at different stages based on their
composition. In the stream from the demethanizer, there is a higher mass fraction of butane, which
is the heaviest component; it would be worth trying to feed this stream at a lower stage than the
stream from the deethanizer, which has a higher mass fraction of lighter components. Doing so
could potentially reduce the amount of energy required in the separations. Throughout the column,
the composition of heavy components increases toward the bottom of the column, and the
27
composition of light components increases toward the top of the column. A feed with more heavy
components that is fed to the top of the column will require more energy for separations than if
that same feed is fed closer to the bottom of the column, since the upper stages have to do less
work separating those heavy components. This logic also applies to feed streams that have more
v. Material Balances
Central to understanding the operation of the rotary kiln is determining amount and
composition of each of the products exiting the rotary kiln. As the rotary kiln model is new in the
treatment of plastic waste, data from batch pyrolysis units will be used to determine the products
of the kiln reactor. The following analysis is best considered as a theoretical template exclusively.
In practice, the cracking reactions of interest are random in product distribution, and subsequently
published data lacks consensus on product distribution. A pilot plant would be necessary to
The percent of feed converted to gas is of primary interest. The production of gas in the
kiln is dependent on pressure, temperature, feedstock, and residence time. High temperature and
long residence time are most important for maximizing raw production of gas [5.27]. However,
residence time beyond a threshold has minimal impact on gas yield [5.28], and temperatures above
700oC favor the production of hydrogen and methane, which are not useful in forming ethylene
and propylene [5.29]. Additionally, pyrolysis is not well studied above temperatures of 650oC is
not well studied [5.27]. and cracking performed at temperatures above this often use fluidized bed
reactors.
28
We adopt the gas conversion value found by Lopez et. Al. that at 600 0C, 56.2% of the feed
is converted to a gaseous phase, as this study most reflects the pressures we intend to use and the
The residence time is also of interest and expected to play a significant role in the
production of gaseous product in the rotary kiln. Again, studies focusing on the residence time are
inconclusive, and unfortunately only two studies have analyzed the impact of residence time on
non-homogeneous plastic waste samples and gave conflicting results. Adopting the findings of one
study and assume that being held at high temperature for up to 30 minutes continues to aid in the
formation of gaseous product, but a pilot scale plant would be required to determine the true impact
An additional impacting factor is the heating rate of the plastic feed. In most experiments,
a 20⁰ C/min heating rate is used. Therefore, the rotary kiln is designed such that the heating rate is
at minimum 20⁰ C/min, but it is recognized that a heating rate higher than this is achievable and
To determine the ultimate amount of gas produced in the rotary kiln, the following
assumptions are made. First, the Lopez et. Al. value of 56.2% is used to determine that in heating
to 6000 C, 56.2% of the inlet is converted to a gaseous state. Extrapolating one data set of residence
time dependence, it may be expected that after reaching the reaction temperature, maintaining the
temperature for 30 minutes will give an overall gaseous yield of 65.9% by weight [5.28]. However,
in an optimistic approach, we assume that those reactions which produce gas in the initial 30-
minute heating period of the Lopez study repeat in a second 30-minute heating period, and thus
56.2% of the oil produced after 30 minutes is again converted to gaseous phase. This gives an
ultimate conversion of 80.3 % weight of the inlet molten plastic to a gaseous state.
29
The rotary kiln is designed according to the parameters hereby assumed. Ultimately, the
assumed conversion is relatively arbitrary, but we expect that in a pilot plant, by controlling
residence time, temperature, pressure, and heating rate, that 80.3% conversion to gas is feasible.
Thus, the downstream operations need not necessarily be scaled to drastic changes in the outlet of
The gas product exiting the rotary kiln is known to be exclusively short chain (C1-C6)
hydrocarbons and hydrogen gas. The exact composition is known to be a function of temperature
and residence time (both to a threshold) and is likely dependent on pressure and heating rate as
well. The composition used henceforth in this process design is that presented by Lopez. Et. Al.
for a reactor temperature of 6000C and residence time of 0 minutes once said temperature is
achieved (table 15.1). Several changes are made to the published distribution. As the Lopez study
includes PET in the feed, CO and CO2 are formed. As this is impossible in an oxygen-free rotary
kiln, these products are scaled out of the ultimate distribution. Additionally, the Lopez distribution
9.5% by weight of C5 and C6, which is semi-consistent with other published distributions. Due to
the availability of steam cracking data, C4-C6 are lumped together as butane for downstream mass
balances. Thus, by weight, the gas product distribution is presented in table 5.4.
0.72 Hydrogen
13.36 Methane
10.59 Ethane
19.84 Ethene
10.09 Propane
18.90 Propene
26.52 Butane
Table 5.4 Pyrolytic Gas Composition
30
Liquid product composition:
The distribution of liquid products is less understood than that of gaseous, due to greater
variation in larger carbon chains. For consistency, the Lopez distribution is again used, although
this distribution is arbitrary and only important for understand the thermodynamic value of the oil
outlet. The distribution accounts for only 78.5% of the oil outlet, and is thus scaled both for the
absence of oxygenated compounds and to account for those molecules not otherwise recorded in
the study:
Toluene 22.29
ethylbenzene 10.32
xylene 5.73
styrene 41.27
α-methyl-styrene 5.61
naphthalene 8.28
methylnaphthalene 6.50
Table 5.5 Pyrolytic Oil Composition
Using this distribution, the properties of the oil are estimated. Notably, the heat of
31
vi. Feed Assumptions
The availability of waste plastic is complex insofar as most plastic is sent to landfills and
is not sorted or recycled. For example, an estimated 10% of plastic waste in the United States is
recycled, meaning that nearly 27 million tons is annually sent to landfill [5.31]. This plastic is not
sustainable as a feedstock. However, there exist Materials Recovery Facilities and private
companies which specialize in treatment and recovery of plastic waste. Plastic waste is solid in a
variety of forms, potentially as curbside, contaminated waste, processed and cleaned bales, or
sorted and shredded shards. Additionally, HDPE, LDPE, PP, and PS are all available in varying
amounts. Therefore, a consistent homogenous feedstock is unlikely for this process, and the
The composition of the plastic feed is approximated by scaling production data since 1950
to account for just the four types of interest [5.32]. The feedstock is hereby assumed to be
composed by weight of the values in Table 5.4, and properties of the feedstock are estimated as a
V Polypropylene 37.2
VI Polystyrene 11.6
Plastic waste contains an average of 7% by weight of additives, such as dyes and structural
enhancers, which are assumed to remain in the feedstock. The plastic shards are estimated to be
32
100mm flakes, as is standard for recycled waste [5.33]. The feedstock is likely to arrive in varying
amounts of each type of plastic, but this does not impact the process design or operating conditions.
As priced from a weighted average of multiple online sources, this feedstock costs an estimated
$0.19/lb [5.34-5.40]. This cost is attributed to the transport, cleaning, sorting, and shredding of the
plastic waste. The feed stock is additionally assumed to have density of 58.9 lb/ft3 and heat capacity
Plastic washing, cleaning, drying, sorting, and shredding are well-established processes for
which the required units may be purchased as needed to account for different feeds. Companies
such as Herbold Meckesheim and MG Machinery offer entire plastic treatment lines which handle
all the aforementioned waste treatment steps for industrial purchase, as well as individual line
components. Therefore, although this design assumes a shard feedstock, other units may be
33
Section 6. Process Flow Diagrams and Stream Tables
34
ii. Section 000: Upstream Processing
35
iii. Section 100: Rotary Kiln Pyrolysis
36
Stream Feed Waste Molten Waste Air Pdt Dirty Oil Oil Pdt Oil Feed 1 Oil Feed 2 Excess Oil Wet Char Air 1 Air 2 Hot Air 1 Hot Air 2
Phase solid liquid gas liquid/solid liquid liquid liquid liquid liquid/solid gas gas gas gas
Temperature (F) 77 482 1112 1112 1112 1112 1112 1112 1112 77 77 1292 1292
Pressure (psia) 14.7 73.5 73.5 73.5 73.5 73.5 73.5 73.5 14.7 14.7 36.8 36.8
Flow Rate (lb/hr) 6429 6429 5163 1265 1003 306 20 675 262 7045 459 7594 692
Component Flow Rates (lb/hr)
Polyethylene 3291 3291
Polypropylene 2392 2392
Polystyrene 746 746
Hydrogen 37
Methane 690
Ethane 547
Ethene 1024
Propane 521
Propene 975
Butane 1369
Toluene 263 224 68 4 150 39
ethylbenzene 122 104 32 2 70 18
xylene 68 57 18 1 39 10
styrene 487 414 126 8 279 72
a-methyl-styrene 66 56 17 1 38 10
naphthalene 98 83 25 2 56 14
methylnaphthalene 77 65 20 1 44 11
water vapor 437 216
Carbon Dioxide 112 17
air 7045 459 7045 459
Carbon 84 84
37
iv. Section 200: Steam Cracking, Quen ching, and Compression
38
39
v. Section 300: Separations
40
41
vi. Section 400: Refrigeration System
42
43
Section 7. Assembly of Database
i. Thermophysical Properties
The primary chemicals in this process are ethylene, propylene, hydrogen, methane, butane,
styrene, and ethylbenzene. Styrene and ethylbenzene are heavily present in the pyrolytic oil, while
the rest are present in the process streams. Note that the C4+ species in the process streams were
properties of all chemicals were found from the NIST Chemistry WebBook and Engineering
Toolbox. Wherever exact figures were not available, approximate figure were interpolated or
extrapolated. Data from these sources were used to approximate heats of combustion, average
The raw materials in this process are the plastic shards that purchased. The price of the raw
materials is $261/MT, where 70MT/day is being fed to the process. The safety information for 2,
44
Section 8. Process Description
The process is comprised of four major processing events: upstream processing of the
plastic waste, pyrolysis of the clean plastic waste, steam cracking of the pyrolysis gas product, and
a separation train to isolate the desired products and hydrocarbon byproducts that can be used as
fuel within the process. Assuming a daily feed of 70 MT, the feed to the process is 6,417 lbs/hr of
mixed plastic waste, which is 12% polystyrene, 23% high-density polyethylene, 28% low-density
polyethylene, and 37% polypropylene. Upstream processing includes shredding, washing, and
drying the plastic waste, then feeding the clean, shredded plastic into an extrusion screw to melt
the plastic into liquid. Pyrolysis takes place in a rotary kiln, and produces solid char, liquid oil, and
a gas product. The pyrolysis gas is refined in a steam cracker unit, then processed to be sent through
a separation train. The separation train involves four distillation columns and yields seven product
streams, two of which are the desired ethylene and propylene monomer feedstock products.
The feed to the process is a mixture of HDPE, LDPE, PP, and PS flakes which arrive in
section 5.6 Feed Assumptions, as is the variability of units in this section. The plastic shards are
loaded via a 55 ft bucket elevator into two storage silos, each with a capacity of 10500 ft3 to account
for 3 days’ worth of feedstock. The silos are kept at standard temperature and pressure. The silos
are designed to hold a combined 6 days’ worth of feedstock due to variability in waste availability,
and the likelihood that the feed comes from multiple sources. This is enough to prevent a halt in
downstream production should waste availability become a bottleneck. A screw conveyor is used
to transport the plastic shards to a second bucket elevator of 16ft, from which the shards are
45
emptied into the hopper of the extrusion screw in section 100. The feed rate is assumed a constant
6430 lb/hr through the conveyor and second bucket elevator, as the subsequent sections operate
continuously.
The clean and pelletized plastic waste is fed into a standard polymer processing extrusion
screw. The screw is used simply as an efficient way to melt the plastic, making use of the friction
generated by the screw to reduce heating requirements. The screw relies on an 820 hp motor, as
well as scattered heaters, to melt the plastic shards primarily due to friction and pressure created
by the screw. The plastic leaves the screw at 482 ⁰F, at which point it should be entirely liquid.
Although the rotary kiln is capable of processing solid plastic waste, the screw is used to ensure
efficient heat transfer throughout the kiln. The melted plastic is fed immediately to the rotary kiln,
where it is heated inside an inner pressurized chamber of the rotary kiln which is 42 feet long and
2.8 feet in diameter. The plastic waste remains in the kiln for 47.5 minutes, as determined by the
angle of the kiln. The plastic is expected to be heated at a rate of 68⁰ F/min to 1112⁰ F for 17.5
minutes, and then maintained at that temperature for 30 minutes. A screw conveyor moves the
plastic and liquid waste through the kiln at a constant speed of 0.0147 ft/sec. The gas buildup in
the container ultimately reaches a pressure of 5 bar, in which case a pressure cap allows the gas to
pass downstream. This pressure is expected to carry the gas product to the steam cracker at a
At the far end of the kiln, 1265 lb/hr of a char and oil mix is sent to a small cylindrical
vessel where the liquid oil and solid char are separated. This vessel is designed to be 60% full,
with a carbon steel grating designed as a baffle positioned in the center. There is one outlet on each
side of the baffle, one which removes pure liquid oil at a rate of 1003 lb/hr, and another which
46
removes an oil and char slurry at a rate of 262 lb/hr, assuming that 15% of the oil product remains
in the slurry. Two small MOYNO pumps made of temperature may be necessary to continue to
drive the wet char and liquid products from the pressure vessel. However, in this process, it is
assumed that the pressure of the liquid is enough to force both streams to flow. Regular cleaning
of the grating may be necessary. A pilot plant will be used to determine the need for pumps,
cleaning, and the flow rates of both streams. The slurry is sent to a storage tank where it is sold for
its heating value and for potential applications in road covering for a price equal to that of
transporting it. The pure liquid product is split three ways, with 306 lb/hr sent to the heating section
of the rotary kiln, 19.9 lb/hr sent to the constant temperature section of the kiln, and 674 lb/hr sent
to a storage tank for sale as a fuel oil. The pyrolytic oil is sold for half the price of NAPTHA oil,
To the heating section of the rotary kiln, a blower pumps in 2474 lb/hr of air at 77 ⁰F and
14.7 psia, while a second blower pumps 161 lb/hr of air to the heating section. In both combustion
chambers surrounding the rotary kiln, complete combustion is assumed due to the excess air added.
The pressures in each chamber are maintained at 36.8 psia, at which point a pressure cap permits
the gas to exit. The combustion gases exit the combustion chambers at 36.8 psia and 1292 ⁰F where
there are sold for their heating value at a price assumed equal to that of pumping the gas.
47
iv. Section 200: Steam Cracking, Quenching, and Compression
The steam cracker pyrolyzes gas feed into smaller carbon chains with a dominant
selectivity of propylene and ethylene. Typical feedstocks are naphtha, liquefied petroleum gas, or
ethane; though in this design, a mixture of light gases ranging from hydrogen to C4+ species are
the feed. Note that the C4+ species are estimated as butane for calculation purposes and the feed
was not burned in the presence of oxygen. A stream of 5,163 lb/hr of light gases flows from the
rotary kiln to the steam cracker at a pressure of 75 psia and a temperature of 1,112°F. This stream
is also diluted with low pressure steam upon entering the cracker. Steam to hydrocarbon ratios
depends on the feedstock. For ethane cracking the ratio ranges from 0.25 – 0.35 and for naphtha
cracking they range from 0.4-0.5. A ratio 0.4 was chosen and the flowrate of steam for the process
48
Note that steam crackers are split into three sections: convection, radiant, and the transfer
line exchanger (TLE). Though the convection section traditionally performs the functions shown
in figure 8.1, for the design in this report, only the heating of the process steam will occur. It is
intended that the light gas feed enters the furnace close to the radiant section. Note that the process
steam is a recycled stream from the split water stream exiting the Quench Tower (QT-201). The
process steam will be preheated from 120°F to 1,112°F, the crossover temperature with the light
gas feed.
The cracking of the light gases occurs in the radiant section. The fuel requirement for the
radiant section is determined from heat needed to preheat the process steam, the sensible heat
needed to raise the temperature of the light gas and steam mixture, and the heat needed to crack
the gas into the products. Fuel for the radiant section is drawn from the storage tanks used to store
recovered hydrocarbons and from pyrolytic oil product from the rotary kiln. 10% excess air was
assumed for complete combustion and hot flue gases will flow up into through the convection
Highly reactive cracked gas must be rapidly quenched below critical temperature within
very short amounts of time. TLEs can have residence times as short as milliseconds [8.3]. After
passing through the furnace the cracked gas flows in a co-current tube in tube TLE with bfw as a
coolant. 4,163 lb/hr of bfw is pumped to 470 psi upon before entering the TLE. The bfw undergoes
a phase change, reaches its saturation temperature of 460°F, is then superheated to 600°F, and is
49
b. Transfer Line Exchanger
A consideration that was not implemented was that the convection section of the steam
cracker could be used to reheat low pressure steam used in the reboilers of distillation columns
and elsewhere in the plant. At current capacity, there is still an abundance of fuel recovered from
separation processes that can be burned. Just as seen in figure 8.2, systems that incorporate TLEs
often have steam drums and economizers to regulate the production of steam. An economizer and
steam drum are not needed in this design because heat integration will not be conducted with the
steam, and because we assumed that all of the bfw fed to the TLE will undergo a phase change to
50
become steam. The bfw stream would also need to be tested for alkalinity levels, else it will
increase fouling in the TLE. Finally more accurate fuel requirements could have been made if
calculations incorporated the rate of heat transfer through the Inconel™ tubes in the cracker
furnace. Given the time constraints and peculiarity of the semester, we elected to not proceed with
these options.
The quench tower is the second stage of rapid cooling of the cracked gas stream. Cracked
gas and process steam will exit the TLE at 752°F and at pressure of 78 psia. 185,480 lb/hr of 90°F
cooling water will be used to cool the cracked gas to 100°F. It is assumed that the cracked gases
will not contaminate the contacting water because the gases will not condense in the tower
conditions. Given the outlet temperature of the gas is below the critical point of water, we assume
perfect mixing which results in all of the process steam mixed in with the cracked gas condensing
out. Thus the cracked gas exiting the quench tower (CG-1) will have no water in it. We recognize
that is not the case in a real tower, but we did not have enough information to carry out necessary
calculations.
187,546 lb/hr of water flows through the bottom of the tower and 2066 lb/hr, an amount
equivalent to the process steam originally fed, is split and is recycled to steam cracker to be
reheated. The rest of the water is then cooled in a heat exchanger, and finally is recycled to the
quench tower to be reused for cooling the cracked gas stream. Note that an inventory of water
would be supplied to the tower upon startup and the stream will then recycle through.
Most ethylene plants will have a caustic tower to remove acidic and sulfuric wastes from
the gases. Since we are not recycling PET, PVC, or #7 plastics, we assume that no halides, acids,
51
or sulfur derivatives will enter the process. A molecular sieve dryer would be used to remove water
from the cracked gas stream, but it is not needed given the perfect mixing assumption. If molecular
sieves were required, two or more sieves would need to be operating parallel. By placing the
molecular sieves in parallel, one or more will be operating at regular capacity, while the other units
are being cleaned. It should be noted that the dehydration rates of the sieves will not be linear
because the mass transfer driving force weakens as more water is absorbed. That being said,
Before they can be separated, the cracked gases must be compressed significantly so that
their boiling points can increase to feasible temperature for separations purposes. Based on the
Section 200 PFD, stream CG-1 enters at 60 psia and stream CG-9 exits at 559.5 psia. Between
each compressor there is a cooler unit because the temperature of streams increases after
compression, and it takes less work to compress a cooler gas than a hotter one. Four compressors
were chosen due to its frequency in the models that we studied, but it would be reasonable to
optimize this since the output of this plant is much less than any large ethylene plant.
52
v. Section 300: Separations
After the cracked gas is quenched and compressed, it is sent to the separations section to
isolate the two desired products, ethylene and propylene, as well as the waste hydrocarbons that
will be used as fuel for the pyrolysis and steam cracking units. A vapor stream consisting of
hydrogen, ethylene, propylene, and other light hydrocarbons is sent into this section at a rate of
5,164 lbs/hr at 142.5°F and 555 psia. Our project goal was to produce ethylene and propylene
monomer feedstock. We were able to produce 99.0% pure ethylene product, which qualifies as
polymer grade, and 95.7% pure propylene, which qualifies as chemical grade. Each of the four
separation processes includes a column, condenser, reflux drum, and kettle-reboiler, as well as
The first distillation column, referred to as the demethanizer, is a tray tower that has vapor
and liquid distillates and a liquid bottoms product. The vaporous stream from the steam cracking
section is fed above stage six at a rate of 5,164 lbs/hr, a temperature of 142.5°F, and pressure of
555 psia. A partial condenser with a vapor/liquid split of 0.448 is used to obtain two distillate
products, and a kettle-reboiler is used for the bottoms product. The tray tower has a total of 17
stages, including the partial condenser with a reflux ratio of 5, 15 sieve-trays, and a kettle-reboiler.
The vapor distillate from the demethanizer is a mix of mainly hydrogen, methane, and
ethylene at -131.2°F and 550 psia. These extreme operating conditions are necessary to achieve
the desired split, because all of the components fed to the column are quite light and volatile.
Ideally, only the most volatile components, hydrogen and methane, should come off the top of this
column. Unfortunately, this would require an even lower temperature of about -230°F. The amount
of energy and refrigerant required to obtain this temperature in the condenser would be an
53
enormous expense and was not a feasible option for the purpose of this project. Instead, we allowed
539 lbs/hr of ethylene to exit the condenser with the vapor distillate, which brought the temperature
up to a more reasonable -131.2°F. This means that a significant portion of our ethylene product
could not be recovered, but we do not count this as a total loss; the vapor distillate from the
demethanizer is fed to the refrigeration system, then used as fuel for other process units in the
process. A pressure of 550 psia was selected to increase the temperature of the vapor distillate as
well.
The liquid distillate from the demethanizer, referred to as the ethylene recovery stream,
exits as a liquid at a rate of 2,098 lbs/hr and is composed mostly of methane, ethylene, ethane, and
propylene. It has a temperature of -131.2°F and a pressure of 550 psia. This stream contains all of
the ethylene that will be eventually recovered as product, but it also has residual methane that was
not removed in the demethanizer column. This stream is fed directly to a second tray column,
which we refer to as the deethanizer column. It also has propylene, which must be removed and
sent to the depropanizer so that it can be recovered as product. The liquid bottoms product exits at
a rate of 1,364 lbs/hr and is composed mostly of propylene, propane, and butane.
The deethanizer column has a total of 45 stages, including a partial condenser with all-
vapor distillate, and a reflux ratio of 25; 43 sieve-trays; and a kettle reboiler. The ethylene recovery
stream from the demethanizer is fed above stage 29 of the tray tower at 2,098 lbs/hr, and there are
three streams that exit the tower: the all-vapor distillate at 120 lbs/hr, which is composed mostly
of methane and ethylene; a liquid C2 side-stream that exits from stage 9 at 1,500 lbs/hr and is
composed mostly of ethylene and ethane; and a bottoms product at 475 lbs/hr that is composed
mostly of ethane, propylene, propane, and butane. The vapor distillate, which leaves the condenser
54
at -129.8°F and 200 psia, is sent to the refrigeration system before being used as fuel for the steam
cracking unit. The C2 side-stream exits at -44.2 °F and 203.56 psia, and is fed to the third column,
which we refer to as the C2-Splitter. Finally, the bottoms product exits at 57.5°F and 207.2 psia
and is fed with the demethanizer bottoms product to the final column, the depropanizer.
A reflux ratio of 25 might sound alarmingly high, but it only corresponds to a reflux rate
of 3,000 lbs/hr. This is because the vapor distillate flowrate is quite small compared to the other
streams in the process (120 lbs/hr compared to thousands of lbs/hr). If the flowrate of the vapor
distillate was on that order, the condenser duty would be unreasonably high at that reflux ratio and
temperature, but because the distillate flowrate is low, it is feasible for the purposes of this project.
For a higher flowrate on the order of 1,200 lbs, the reflux rate would have been 30,000 lbs/hr and
would have over-burdened the condenser. In addition, the original design called for a reflux ratio
Because the deethanizer condenser must also operate at an extremely low temperature, it
was necessary to allow some ethylene to exit the tower with the vapor distillate. This allowed for
a more reasonable condenser temperature. A liquid side-stream was selected rather than using a
partial-vapor condenser because it yielded better results. Stage 9 was selected to remove the side-
stream because this was determined to be the stage at which the ethylene composition was highest;
since the side stream is the stream from which the ultimate ethylene product is removed, it is
preferable to have the highest ethylene content possible so that the most ethylene possible is
recovered overall.
The liquid side-stream from the deethanizer is fed above stage 12 of the C2-Splitter, the
third tray tower. This feed has a flowrate of 1,500 lbs/hr, a temperature of -44.2°F, and a pressure
55
of 300 psia. A feed pump is used to bring the feed stream to an appropriate pressure; the feed
stream exits the deethanizer at 204 psia but needs to be increased to 300 psia to be fed to the C2-
Splitter, which operated at 290 psia. The C2-Splitter has 25 stages, including a partial condenser
with all vapor distillate and a reflux ratio of 10, 23 sieve-trays, and a kettle reboiler. A vapor
distillate of 99.0% pure ethylene product exits the condenser and is sent to be used as feedstock
via gas pipelines at a flowrate of 1,410 lbs/hr, a temperature of -20.6°F, and a pressure of 290 psia.
A liquid bottoms product that is 94.5% ethane exits the reboiler and is sent to a tank to be stored
and used as fuel for other units in the process at a flowrate of 90 lbs/hr, a temperature of 17.3°F,
The bottoms products from both the demethanizer and deethanizer are sent to the final tray
tower, which we refer to as the depropanizer. The depropanizer has 42 stages, including a partial
condenser with all vapor distillate and a reflux ratio of 42, 40 sieve-trays, and a kettle-reboiler.
Both feed streams are fed above stage 23. Three streams exit the C2 splitter: a vapor distillate of
96 lbs/hr at -11.3°F and 150 psia, a liquid propylene side stream or 1250 lbs/hr at 69.2°F and 154
psia exiting at stage 15, and a liquid bottoms product of 495 lbs/hr at 149.1°F and 157 psia.
Similar to the deethanizer, the reflux ratio may seem alarming at first glance. However, the
same logic that applies to the deethanizer applies here, too: the reflux rate is 4,032 lbs/hr, which
does not cause the condenser duty to be too high. For a larger distillate rate of, say, 1,000 lbs/hr, a
reflux ratio on the order of 1 might be selected instead (say, for example, 3); this would correspond
to a reflux rate of 3,000 lbs/hr. So, while the reflux ratio does seem quite high, when considering
the reflux rate (which is what dictates the condenser duty), it makes sense how such a large reflux
56
vi. Section 400: Refrigeration System
The condensers of the columns in the separation section of this process operate at extremely
low temperatures. To achieve these low temperatures, a refrigeration system is used. Since the
vapor distillates of each column come off at very cold temperatures, too, a plate-fin heat exchanger
is used in the refrigeration system to “recover” this cold. Apart from the cold distillates that pass
through the plate-fin exchanger, the refrigeration system is a closed loop. Ethylene refrigerant
enters the refrigeration system at a flowrate of 66,000 lbs/hr, a temperature of 85°F, and a pressure
of 30 psia. The refrigerant passes through a condenser, where it reaches 2000 psia, before being
fed to the plate-fin exchanger. The refrigerant is then flashed in a flash drum, and vapor product is
sent immediately back to the plate-fin exchanger. The liquid product is split into two streams. The
first stream, which has a flowrate of 19,000 lbs/hr, a temperature of -29°F, and a pressure of 252
psia, is sent to the condensers of the C2-Splitter and the depropanizer column, whose operating
temperatures are -30°F and -10°F, respectively. The second stream is sent to a second flash drum,
and the vapor product is sent immediately back to the plate-fin exchanger. The liquid product flows
The condenser duties for the demethanizer and deethanizer columns are -5MM BTU/hr and
-605,000 BTU/hr, respectively. A refrigerant flowrate of 24,925 lbs/hr at the given conditions
satisfies the condenser duties of both columns. Then, because the vapor distillates of these columns
are so cold (-131°F and -129°F, respectively), they are sent back to the plate-fin exchanger to help
cool the refrigerant coming from the condenser. The condenser duties for the C2-Splitter and
depropanizer columns are -1.97MM BTU/hr and -702,000 BTU/hr, respectively. A refrigerant
flowrate of 19,000 lbs/hr at the given conditions satisfies the condenser duties of both columns.
57
A plate-fin exchanger was selected as the heat exchanger for this process because it is
capable of handling many streams at a given time. As the name implies, a plate-fin exchanger is
made of several plates with fins to facilitate heat transfer. In this plate-fin exchanger, several
corrugated stainless-steel plates, which serve as the fins, are stacked between flat stainless-steel
plates that separate the different streams passing through the exchanger. This plate-fin exchanger
handles fourteen streams in total: seven inlet streams, and seven outlet streams. The duty of the
For startup, since there would not be cold streams from the column condensers to cool the
ethylene after compression, refrigerant is required to supply this duty. This refrigerant can be used
to supply the initial -5.2MM BTU/hr of cooling duty in the plate-fin exchanger. Refrigerant at -
30°F can be purchased for $4/ton-day. One ton-day is equivalent to 12,000 BTU, so 433 ton-days
are required. This corresponds to $1,732/hr worth of -30°F refrigerant for startup. Startup is
58
Section 9. Energy Balance and Utility Requirements
The rotary kiln unit is self-sustaining in energy requirement and does not need fuel oil for
the heating requirement of the plastic waste. The extrusion screw demands significant energy input
with an 820 hp motor. Use of extra pyrolytic oil or steam from downstream in the process was
considered, but polymer extrusion screws are not designed for this type of heating. Alternatives to
make use of the oil and steam for melting were considered, but due to the nature of solid processing
and need for a continuous feed, the extrusion screw is most appealing.
Utilities required in the overall process are cooling water, low pressure steam, boiler feed
water, refrigerant, and electricity. In the steam cracking portion, boiler feed water and cooling
water are used to rapidly quench hot gases, as well as other streams in that section. In the separation
train, low pressure steam will be used to heat the reboilers and refrigerant will be used in the
refrigeration cycle. Electricity will be needed for pumps, compressors, and blowers throughout the
plant. The following tables will provide information on the quantity of utilities being used in the
plant.
a. Fuel Requirements
Fuel to fire the steam cracker furnace will come from recovered fuel from the separation
processes and from the pyrolytic oil product from the rotary kiln. The fuel requirement of the steam
cracker was completely satisfied with the recycled fuel streams. The fuel that was burned in the
steam cracker consists of hydrogen, methane, ethane, ethylene, propane, propylene, butane, and
pyrolytic oil which is mostly styrene. The duty of the steam cracker is 34.24 MM BTU/hr.
59
Table 9.2 Fuel Specifications
Compound Amount (lb/hr) % of Furnace Duty LHV (BTU/lb)
Hydrogen 607 27.6 51,628
Methane 599 47.7 21,433
Ethene 582 32.3 20,525
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iii. Section 300: Separations
a. Energy Balance
In the separations part of the process, there are four distillation columns, which each have a
condenser with cooling duty. The cooling for each condenser is achieved by streams from the
refrigeration cycle. The following table shows the energy balance on each condenser:
Each column in the separation part of the process also has a reboiler with a heating duty.
Low-pressure steam provides heat to the demethanizer, deethanizer, and depropanizer reboilers,
while 60°F cooling water provides heat to the C2-Splitter reboiler. The following table shows the
Calculations to determine the required flowrate of heat source are found in the following
section.
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b. Utilities
The reboilers of the tray towers each require a utility to provide heat. For the demethanizer,
deethanizer, and depropanizer, low-pressure steam is used to provide heating. For the C2-Splitter,
cooling water is used to provide heat, because the temperature of the bottoms product is very low
at 17°F. The following table summarizes the steam requirements for each column based on the
Table 9.5: Low-pressure steam requirements for the reboilers of the demethanizer,
deethanizer, and depropanizer columns
Demethanizer Deethanizer Depropanizer
Reboiler Heat Duty (BTU/hr) 3,599,122 749,516 597,034
Reboiler Temp (°F) 205.2 57.5 149.1
Steam Pressure required 50 50 50
(psig):
Latent Heat (BTU/hr): 912 912 912
Required Flowrate (lbs/hr): 3,946.4 821.84 654.64
Because the reboiler temperatures are all relatively low, low-pressure steam is required to
provide heating.
Interestingly, the reboiler of the C2-Splitter requires cooling water to provide heating. This
is because the bottoms product of the C2-Splitter is 17°F. A stream in the range of 60-70°F would
be ideal to provide heating, but something hotter would run the risk of causing film boiling. Thus,
cooling water was selected as the utility, since it is in that temperature range. The reboiler heat
duty is 2,2MM BTU/hr. Since the specific heat capacity of water at that temperature is 1 BTU/lb-
Whence the cooling water has passed through the reboiler, it will be at a temperature of
40°F, qualifying it as chilled water. Some of this chilled water will be sent to the quench tower at
a rate of 80,200 lbs/hr, and the remaining 29,600 lbs/hr will be sold as chilled water.
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In addition to the condensers and reboilers in the separations part of the process, there are
five pumps that are powered by electricity—four pumps that are used for the reflux streams for
each column, and one pump that is used for the feed to the C2-Splitter. The following table
Table 9.6: Utilities requirements for pumps in the separations part of the process
Demethanizer Deethanizer C2-Splitter Depropanizer C2 Feed
Reflux Reflux Reflux Reflux
Net Work 0.297 hp 0.5194 hp 0.3695 hp 0.5079 hp 1.22 hp
Electricity 0.2215 kW 0.3876 kW 0.2731 kW 0.3791 kW 0.914 kW
Requirement
a. Energy Balance
The refrigeration cycle consists of a compressor, plate-fin exchanger, and two flash vessels,
each of which has an associated cooling or heat duty with it. This part of the process has immense
energy and utility requirements, and contributes significantly to the annual cost
The compressor compresses 66,000 lbs/hr of ethylene refrigerant from 85 psia to 2,000
psia. Electricity is used to achieve this pressure change; 4,333 kW are needed to power this unit.
The plate-fin exchanger involves 14 streams. It recovers the cold from the vapor distillates
from the demethanizer and deethanizer columns, as well as the vapor streams from both flash
vessels, and cools the ethylene refrigerant before it goes to the flash vessels. The plate-fin
The first flash vessel reduces the temperature of the refrigerant from -1.2°F to -29.06°F by
dropping the pressure 2000 psia to 252 psia. The Joule-Thompson effect is responsible for this
temperature drop. The gas is allowed to expand through a throttle. During this expansion, there is
no change in energy, which means that the duty of the flash vessel is zero. This is because for all
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non-ideal gasses (i.e. gasses other than hydrogen or helium), enthalpy is a function of temperature,
so if the enthalpy remains constant, the temperature will, too. Since the gas in the process is not an
ideal gas (especially since it is at an extremely high pressure), constant enthalpy does not equal
constant temperature, so the temperature of the gas drops significantly when the gas is throttled.
The second flash vessel reduces the temperature of the refrigerant from -29.06°F to
-143.7°F by dropping the pressure from 252 psia to 21 psia. Similar to the first flash vessel, the
Joule-Thompson effect is responsible for the temperature drop. There is no change in energy
b. Utilities:
In the refrigeration cycle, the compressor uses 5,810 hp of work and requires 4,333 kW of
electricity for power. This amount of electricity is one of the costliest utilities in the entire process,
with over $2.5MM being spent annually. For comparison, the second costliest compressor is in the
compression cascade of the steam cracking process, and costs $162,000 per year.
For startup, 433 ton-day, or $8,660 worth, of -30°F refrigerant are needed for the plate-fin
exchanger; afterwards, the cold streams from the demethanizer and deethanizer condensers are
64
Section 10. Equipment List and Unit Descriptions
Storage Silos
The function of T-001 and T-002 is to store three days’ worth of feed shard each to prevent
production halt. The temperature and pressure are not regulated and are therefore said to be
atmospheric. The volume of each silo is 10500 ft3, found using an assumed shard density of 58.9
lb/ft3 and a 25% void fraction due to packing. An aspect ratio of 3, common for storage vessels, is
used. Each silo has an upper cylindrical section and lower conical section. The purchase cost of
Bucket Elevators
The function of the bucket elevators is to move plastic shard from the transport units to
storage silos, and again from the screw conveyor to the extrusion screw. The units consist of chains
of buckets, 12 inches in width and 1.5 feet apart, which move the plastic shard vertically. Due to
the nature of the plastic shards, there is no concern that waste sticks to the bucket, and high speeds
are usable, but 150 ft/sec is estimated. The speed and bucket volume more importantly depend on
unit availability for purchase. The 55-foot bucket elevator has a power requirement of .626 hp, and
the 16-foot elevator 0.206 hp, which account for both the mass flow rate and vertical distance
65
travelled. The purchase cost of the 55-foot elevator is $23,534, and that of the 16-foot elevator is
Screw Conveyor
The screw conveyor is selected for transport of shards due to its ability to regulate volumetric
flow capacity and handle particles of small size. The feed rate of the screw is 81.9 ft3/hr, which
roughly correlates to a 6-inch diameter 50 rpm conveyor. The length of transport is estimated as
40 feet, which is to account for the space occupied by the silos. The power requirement is 0.958
hp, which assumes no elevation change. The purchase cost of the feeder is $2,883. No specification
sheet is included.
The rotary kiln is the first of two cracking units in the process. It degrades the molten plastic
waste to a short-chain hydrocarbon gas and a pyrolytic oil product, with the presence of some char.
The rotary kiln is considered as two concentric pressure vessels. The inner vessel is 2.8 ft diameter,
and feed molten plastic continuously at 6430 lb/hr. The plastic is moved through the inner chamber
at a constant rate of 0.0147 ft/s as governed by a carbon steel screw conveyor. The inner chamber
is maintained at 73.5 psia, at which point a pressure cap, fitted to not rotate with the kiln, permits
66
gaseous product to exit from the highest point in the kiln. The molten plastic is heated first in the
kiln over a length of 15.5 ft a rate of 68⁰F/min to reach 1112⁰F. The plastic is then held at a that
temperature for the remaining 26.5 ft. The gaseous product is said to form at a constant rate in the
kiln. Over the entire length of the chamber, the energy demand to heat and maintain the plastic
temperature is 3.66 x 106 BTU/hr. The inner chamber is made from a 0.25-inch-thick layer of
Carbon Steel, which is the thickness as estimated for the pressure vessel, surrounded by 8.4 inches
of alumina oxide refractory, which is selected due to its high thermal conductivity, strength, and
is used to estimate the wall thickness to achieve a desired ∆T. Due to the thickness of the refractory
layer, the temperatures which carbon steel is exposed to should not cause any deformation of the
shell.
There are two chambers outside the alumina oxide refractory, which are separated by a
refractory wall, which are used for combustion. Both chambers are operated at 36.8 psia and 2732
⁰F. The feed rate to each chamber of pyrolytic oil and air is dependent on the energy demands of
specific section, assuming 40% thermal efficiency. Not-rotating pressure caps are again used to
remove the gaseous product. The combustion chamber is 6 inches, with burners located primarily
beneath the inner shell to concentrate heat near the molten plastic.
The outermost layer of the rotary kiln is 14.4 inches of alumina oxide refractory covered
with 0.25 inches of carbon steel for structural support. This layer should prevent the exposed
surface from exceeding 200 ⁰F for safety concerns. The reactor is set up at a 1.1⁰ incline from the
horizontal. Due to the complex nature of cracking reactions and unknown intermediates, the
reactor was not modeled in Aspen except for energy balance purposes.
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The electricity demands are estimated as 80 kW to power the rotary kiln, per online
estimates, accounting for both the rotation of the vessel at nearly 2 rpm and the screw conveyor.
The costing is roughly estimated as summing two horizontal pressure vessels, giving a purchase
cost of $167,171.
Extrusion Screw
The extrusion screw is purchased directly from a third-party seller. A twin-screw extruder
is likely necessary due to the high mass flow rate. The molten plastic is said to be heated from
room temperature to 482⁰F, which is 50⁰F greater than the melting point of polystyrene (which
has the highest melting point of all three types of plastic involved). The work required is 820 hp,
and per online estimate the purchase cost is $500,000. No specification sheet is included, but a
Blower 1
The blower adds air to the first combustion chamber which supplies heat to raise the
temperature of the plastic waste in the rotary kiln. It raises incoming pressure from atmospheric to
36.8 psia. The temperature is said to be atmospheric at both the inlet and outlet of the blower, and
thus the blower is made from aluminum. It requires a net work of 26.1 hp due to 88% efficiency.
The flow rate through the blower is 539 ft3/min, and the purchase cost is an estimated $8,820.
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Blower 2
Nearly identical to B 101, except a lesser volumetric flow rate of 35.1 ft3/min is used,
creating a work requirement of 3.8 hp and efficiency of 83%. The purchase cost is an estimated
$8,820.
This unit is largely hypothetical, and a pilot plant would be necessary to determine the
feasibility. To remove the char from the liquid oil as best as possible, the solid/liquid slurry flows
into the vessel at 1265 lb/hr, driven by the pressure in the rotary kiln. The size is approximated
considering how much oil/char mixture enters the unit over the course of one residence time (47.5
minutes), and an assumed aspect ratio of 5. The splitter is said to be 60% full, and still at a pressure
of 73.5 psia. There is a fine carbon steel mesh, which is oriented as a baffle, near the center of the
vessel. There are two outlets, which have volumetric flow rates of 1003 lb/hr (oil product), and
262 lb/hr (slurry). The ratio of outlet sizes of the tank reflects the ratio of flow rates. The pressure
is assumed to be sufficient to drive the operation of this unit. It is possible that MOYNO pumps,
capable of low flow rates and sustaining very high temperatures, would be required to drive the
69
Oil Storage Tank
Given a flow rate of oil for sale of 674 lb/hr, an assumed density of 58.3 lb/ft3, and a desired
capacity to store 6 days of product, a total storage volume of 925 ft3 is required. Using an assumed
aspect ratio of 3, the dimensions of this unit are 7.3 ft diameter and 21.9 ft height. The oil product
enters the storage tank at high temperature of 1112 ⁰F and pressure of 73.5 psia, but no effort is
made to maintain these conditions. The tank is designed as a conical roof storage vessel, and a
nitrogen blanket is used to maintain safe oxygen concentration. The purchase cost is an estimated
$24,728.
The same approach is taken here to modeling the tank as the pyrolytic oil storage tank,
although the inlet flow is now 262 lb/hr. The purchase cost is an estimated $3404.
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iii. Section 200: Steam Cracking, Quenching, and Compression
Steam Cracker
The steam cracker takes paraffinic light gas mixed with steam and dehydrates, or cracks,
the compounds into ethylene and propylene. The steam cracker also preheats 242,480 lb/hr of
boiler water and 2,066 lb/hr of water to be used as process steam. Fuel to fire the steam cracker
comes from oil product from the rotary kiln, and recovered fuel from separation processes. The
steam cracker has severity of 0.66, which corresponds to a 1 second residence time in the
furnace. The steam cracker has a convective section and radiation section. The exact dimensions
of the steam cracker were not calculated, but a private consultant provided costing data based on
The transfer line heat exchanger rapidly quenches the cracked gas to prevent more
propagation reactions from occurring. The transfer line exchanger is modeled after a BORSIG
tunnelflow exchanger. Hot gases will flow through the tubes and boiler water will flow
71
concurrently in the annulus of the tubes. Within the TLE, the boiler water will undergo a phase
The heat exchanger in the quench tower recycle system is a shell and tube heat exchanger, and
it cools the recycle spray water stream from 120°F back down to 90°F. The chiled water
experiences a temperature change from 40°F to 105°F. Flow in the heat exchanger is
countercurrent.
Intercooler 1
The intercooler is modeled as a shell and tube heat exchanger on ASPEN. It cools the stream
after COMP-1 from 324°F to 224°F. The gas stream experiences a temperature drop of 100°F in
all four intercoolers. The temperature change in the cooling water is 80°F to 120°F, which is the
same for all four units. Inter-stage coolers are needed because it takes less work to compress a
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Intercooler 2
Intercooler 3
Intercooler 4
Compressor 1
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Compressor 1 is a centrifugal compressor used to increase the pressure of the cracked gas
before it undergoes separation. The gas enters the series of compressors at 60 psia and leaves
at 559.5 psia. The pressure of this stream needs to be increased so that the boiling point of
certain compounds will shift to temperature to a more feasible one for separation. All
compressors in Section 200 were modeled on ASPEN. The isentropic efficiency was assumed
to be 0.81.
Compressor 2
Compressor 3
Compressor 4
74
Blower 1
Blower 1 is used to move fuel gases from the storage tanks to the steam cracker furnace. It
was modeled as an isentropic compressor on ASPEN. It is sized to move 606 lb/hr of hydrogen,
Tray Towers
Demethanizer Column
The demethanizer separates a significant portion of the hydrogen and methane gas produced
in the steam cracking of the pyrolysis gas from the light hydrocarbons and the heavy hydrocarbons.
The feed to the demethanizer is 5,164 lbs/hr of cracked gas, which enters the column at 142.5°F
According to an ASPEN simulation, 12 theoretical stages are needed to achieve the desired
separation, with the feed stream entering above stage 4. Assuming a tray efficiency of 0.7, this
means that fifteen real stages are needed, with the feed stream entering above the sixth stage. Given
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eighteen-inch spacing between each tray, a height of 22.5 ft is obtained. One 3-foot manhole at the
feed stage and an additional 3-foot manhole every ten trays are included, as well as a 10-foot sump
and 4-ft of height at the top of the column, resulting in a functional height of 42.5 ft. Including a
skirt height of 15 ft, the total demethanizer height is 57.5 ft. An L/D aspect ratio of 8 was chosen,
A reflux ratio of 5 is required. The vapor distillate rate is 1,702 lbs/hr, the liquid distillate rate
is 2,098 lbs/hr, and the bottoms rate is 1,364 lbs/hr. The selected material of construction is carbon
steel. The temperatures of the columns are extremely cold. Carbon steel is the material of
construction for many cryogenic units, including cold boxes, which operate at temperatures similar
to those in this process. So, carbon steel is an appropriate choice of material for the columns.
The reflux drum for the demethanizer condenser was sized so that fifteen minutes of
accumulation would result in the drum being half-full. Given a volumetric reflux rate of 682
cuft/hr, the reflux drum would need to have a volume of 341 cubic feet for fifteen minutes’ worth
of accumulation to fill half of the drum. Using an L/D aspect ratio of 4 for a horizontal vessel, a
The kettle reboiler for the demethanizer column has a heat duty of 3.6MM BTU/hr, as
Deethanizer Column
76
The deethanizer results in three outlet streams: a vapor distillate, which contains the remaining
hydrogen and methane, as well as some of the ethylene product; a liquid side stream, which
contains both ethylene and ethane hydrocarbons; and the bottoms product, which contains all the
hydrocarbons heavier than ethane. The feed to the deethanizer is the 2,098 lbs/hr ethylene recovery
stream from the demethanizer, which enters the deethanizer at -131.2°F and 550 psia.
According to an ASPEN simulation, 30 theoretical trays are needed to achieve the desired
separation, with the feed stream entering above the twentieth stage. Assuming a tray efficiency of
0.7, this means that 43 real stages are needed, with the feed stream entering above the twenty-ninth
stage. Given eighteen-inch spacing between each tray, a height of 64.5 ft is obtained. One 3-foot
manhole at the feed stage and an additional 3-foot manhole every ten trays are included, as well as
a 10-foot sump and 4-ft of height at the top of the column, resulting in a functional height of 84.5
ft. Including a skirt height of 15 ft, the total demethanizer height is 99.5 ft. An L/D aspect ratio of
A reflux ratio of 25 is required. The distillate rate is 120 lbs/hr, the side stream flow rate is
1,500 lbs/hr, and the bottoms rate is 475 lbs/hr. The selected material of construction is carbon
steel. The temperatures of the columns are extremely cold. Carbon steel is the material of
construction for many cryogenic units, including cold boxes, which operate at temperatures similar
to those in this process. So, carbon steel is an appropriate choice of material for the columns.
The reflux drum for the deethanizer condenser was sized so that fifteen minutes of
accumulation would result in the drum being half-full. Given a volumetric reflux rate of 107
cuft/hr, the reflux drum would need to have a volume of 53.5 cubic feet for fifteen minutes’ worth
of accumulation to fill half of the drum. Using an L/D aspect ratio of 3 for a horizontal vessel, a
77
The kettle reboiler for the deethanizer column has a heat duty of 750,000 BTU/hr, as calculated
As discussed in the process description in Section 8, a reflux ratio of 25 for the deethanizer
column might seem alarmingly high at first. The distillate rate of the deethanizer column is only
120 lbs/hr, and the reflux rate is 3,000 lbs/hr. This corresponds to a cooling duty of -604,000
BTU/hr. This duty is far less than that of either the demethanizer or C2-Splitter condensers, whose
reflux ratios are much smaller (5 and 10, respectively) but who have much higher cooling duties
on the order of MM BTU/hr because their distillate flowrates (and, thus, their reflux rates) are
much higher, even at a relatively low reflux ratio. Clearly, the value of the reflux ratio is not the
best indicator of condenser duty, but rather the reflux flowrate is.
C2 Feed Pump
The side stream that exits the deethanizer to enter the C2-Splitter has a pressure of 204
psia. This is below the operating pressure of the C2-Splitter (290 psia), so the stream must be sent
to a pump to increase the pressure. A head of 477.0 ft and net work of 1.22 hp were calculated
using ASPEN.
78
C2-Splitter
The C2-Splitter separates the recovered ethylene from the other components that exit the
deethanizer column in the side-stream. The feed to the C2-Splitter is 1,500 lbs/hr, which enters the
column at -44.2°F and 300 psia after passing through the C2 feed pump.
According to an ASPEN simulation, 23 theoretical trays are needed to achieve the desired
separation, with the feed stream entering above the twelfth stage. In the industry, C2-Splitters
typically have an efficiency of 1.0 or even greater than 1. Assuming a tray efficiency of 1, this
means that 23 real stages are needed, with the feed stream entering above the twelfth stage. Given
eighteen-inch spacing between each tray, a height of 34.5 ft is obtained. One 3-foot manhole at the
feed stage and an additional 3-foot manhole every ten trays are included, as well as a 10-foot sump
and 4-ft of height at the top of the column, resulting in a functional height of 54.5 ft. Including a
skirt height of 15 ft, the total demethanizer height is 69.5 ft. An L/D aspect ratio of 10 was chosen,
A reflux ratio of 10 is required. The distillate rate is 1,410 lbs/hr, and the bottoms rate is 90
lbs/hr. The selected material of construction is carbon steel. The temperatures of the columns are
extremely cold. Carbon steel is the material of construction for many cryogenic units, including
cold boxes, which operate at temperatures similar to those in this process. So, carbon steel is an
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The reflux drum for the C2-Splitter condenser was sized so that fifteen minutes of
accumulation would result in the drum being half-full. Given a volumetric reflux rate of 567
cuft/hr, the reflux drum would need to have a volume of 283 cubic feet for fifteen minutes’ worth
of accumulation to fill half of the drum. Using an L/D aspect ratio of 3 for a horizontal vessel, a
The kettle reboiler for the C2-Splitter column has a heat duty of 2.2MM BTU/hr, as calculated
by ASPEN. The bottoms product of the C2-Splitter exits at 17°F, meaning that a heat source
around 60°F would be ideal. Cooling water at a temperature of 60°F must be supplied at a flowrate
of 110,000 lbs/hr. This cooling water exits the reboiler at a temperature of 40°F, meaning that it
can be used as chilled water in other parts of the plant, and the remaining water can be sold as
chilled water (which is worth more than the cooling water that would need to be purchased to
Depropanizer
The depropanizer separates the bottoms products from both the demethanizer and deethanizer
into three products: a C2-fuel, the 95.7% pure propylene product, and impure butane to be used as
fuel. The feed to the depropanizer is 1,839 lbs/hr, which enters the column at -103.3°F and a
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According to an ASPEN simulation, 28 theoretical trays are needed to achieve the desired
separation, with the feed stream entering above stage 16. Assuming a tray efficiency of 0.7, this
means that 40 real stages are needed, with the feed stream entering above stage 23. Given eighteen-
inch spacing between each tray, a height of 60.0 ft is obtained. One 3-foot manhole at the feed
stage and an additional 3-foot manhole every ten trays are included, as well as a 10-foot sump and
4-ft of height at the top of the column, resulting in a functional height of 80.0 ft. Including a skirt
height of 15 ft, the total demethanizer height is 95.0 ft. An L/D aspect ratio of 10 was chosen,
A reflux ratio of 42 is required. The distillate rate is 96 lbs/hr, the propylene-product side
stream flowrate is 1,250 lbs/hr, and the bottoms rate is 90 lbs/hr. The selected material of
construction is carbon steel. The temperatures of the columns are extremely cold. Carbon steel is
the material of construction for many cryogenic units, including cold boxes, which operate at
temperatures similar to those in this process. So, carbon steel is an appropriate choice of material
The reflux drum for the depropanizer condenser was sized so that fifteen minutes of
accumulation would result in the drum being half-full. Given a volumetric reflux rate of 145.5
cuft/hr, the reflux drum would need to have a volume of 72.7 cubic feet for fifteen minutes’ worth
of accumulation to fill half of the drum. Using an L/D aspect ratio of 3 for a horizontal vessel, a
The kettle reboiler for the depropanizer column has a heat duty of 600,000 BTU/hr, as
As discussed in the process description in Section 8, a reflux ratio of 42 for the depropanizer
column might seem alarmingly high at first. However, the same reasoning that is applied to the
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deethanizer column condenser is relevant here. The distillate rate for the depropanizer column is
only 96 lbs/hr, and the reflux rate is only 4,032 lbs/hr. This corresponds to a condenser cooling
duty of -597,000 BTU/hr. This duty is far less than that of either the demethanizer or C2-Splitter
condensers, whose reflux ratios are much smaller (5 and 10, respectively) but who have much
higher cooling duties on the order of MM BTU/hr because their distillate flowrates (and, thus, their
reflux rates) are much higher, even at a relatively low reflux ratio. Clearly, the value of the reflux
ratio is not the best indicator of condenser duty, but rather the reflux flowrate is.
Reflux Pumps
The reflux stream that exits the condenser of each column must be pumped back to the top
of the demethanizer tower. The pump is not at the same elevation as the condenser; in chemical
plants, pumps are placed on the ground to allow for easy access for maintenance. As the reflux
stream flows downward to the pump, it gains some pressure. Then, the pump increases the pressure
of the stream further to allow it to travel back up to the top of the condenser for reflux. The head
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Deethanizer Reflux Pump
Storage Tanks
Storage tanks are needed for both monomer products, ethylene and propylene, and the
hydrocarbon streams that will be stored and used as fuel. Since the products of the steam cracking
process are all light hydrocarbons that are gasses as atmospheric pressure, each tank is designed
to hold one hour’s worth of product. For the ethylene and propylene products, the streams will
then be sold and transported to plants via pipeline to be used as monomer feedstock. One hour of
storage is needed in case the purchasing plant needs to shut down; in that case, there would be a
buffer to allow for gas to stop flowing to the shut-down plant while still being produced until our
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plant could be properly shut down, too. In such an event, the rotary kiln would be shut off upstream,
and the product would accumulate in the storage vessel; one hour is sufficient time for the
remaining material in the process to reach the storage vessel, so one hour’s worth of storage is
The 99.0% pure ethylene product exits the C2-Splitter at a flowrate of 1410 lbs/hr at
-20.6°F and 290 psia. At the conditions in the tank, ethylene has a density of 0.079 lbs/cuft, and
134,193 gallons of storage are needed for one hour’s worth of product. This gas is then transported
The 95.7% pure propylene product exits the depropanizer at a flowrate of 1250 lbs/hr at
70°F and 154 psia. At these conditions, propylene is a liquid. However, at the conditions in the
tank, it will be a vapor whose density is 0.118 lb/cuft. This means that 85,704 gallons of storage
are needed to hold one hour’s worth of propylene product. This propylene is then transported to
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Fuel Storage Tank
Five streams are sent to the fuel storage tank to be stored and used as fuel. One hour’s
worth of fuel is stored in this tank. Because a mix of several different hydrocarbons are stored,
each with a different density at these conditions, a weighted average was calculated to determine
the density of the gas in the fuel storage tank (which was 0.0645 lbs/cuft). Any streams that exit
The compressor in the refrigeration system must compress 66,000 lbs/hr of ethylene
refrigerant. The ethylene refrigerant comes into the compressor at a temperature of 85°F and a
pressure of 30 psia. The compressor uses electricity as its utility and does 5,810 hp of work. The
refrigeration system is a closed cycle; the ethylene is compressed, cooled and flashed, and then it
is sent to the appropriate compressors to provide cooling, after which it is sent back through the
85
Flash Vessel 1
Flash Vessel 1 is used in the refrigeration cycle to lower the refrigerant temperature so that
it can be used in the condensers of the columns in the separation section of the process. 66,000
lbs/hr of refrigerant are fed into Flash Vessel 1 at 4.6°F and 2000 psia. 8,3971 lbs/hr exit the vessel
as vapor and are sent back to the plate-fin exchanger. 57,603 lbs/hr of refrigerant exit the vessel as
liquid and are split into two streams: the first stream goes directly to the condensers of the C2-
Splitter and the depropanizer, and the second stream is sent to the second flash vessel to lower the
temperature further.
The Jules-Thompson effect is responsible for the temperature and pressure change
experienced by the ethylene refrigerant. For all gases other than hydrogen and helium, a decrease
The vessel was modeled as a vertical pressure vessel. Assuming a residence time of 5
minutes, which is a standard residence time for flash vessels, and given a volumetric flowrate of
2,631 cuft/hr through the vessel, this corresponds to a volume of 1,640 gallons. Using an L/D
aspect ratio of 3, this also gives a height of 13.6 ft and a diameter of 4.5 ft.
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Flash Vessel 2
Flash Vessel 2 is used in the refrigeration cycle to further lower the temperature of some
of the liquid outlet of the first flash vessel so that it can be used in the condensers of the columns
in the separation section of the process. 38,603 lbs/hr of refrigerant are fed into Flash Vessel 2 at
-29.06°F and 252 psia. 13,677 lbs/hr exit the vessel as vapor and are sent back to the plate-fin
exchanger. 24,926 lbs/hr of refrigerant exit the vessel as liquid and this stream is sent to the
separation section of the process to be used in the condensers of the demethanizer and deethanizer
columns.
The Jules-Thompson effect is responsible for the temperature and pressure change
experienced by the ethylene refrigerant. For all gases other than hydrogen and helium, a decrease
The vessel was modeled as a vertical pressure vessel. Assuming a residence time of 5
minutes and given a volumetric flowrate of 1,380 cubic feet per hour through the vessel, this
corresponds to a volume of 860 gallons. Using an L/D aspect ratio of 3, this also gives a height of
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Plate-Fin Exchanger
exchanger. Several corrugated stainless-steel sheets are layered between flat stainless-steel sheets.
Seven inlet streams and seven outlet streams flow through this heat exchanger, allowing for the
refrigerant to be cooled by the cold distillate streams from the separation section of the process.
This model of heat exchanger is very efficient at transferring heat, because there are many
opportunities for heat transfer among the various inlet and outlet streams. The refrigerant is then
sent to the separation process to be used in the condensers of the separation columns. The duty of
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Section 11. Specification Sheets
89
90
91
92
93
94
ii. Section 200: Steam Cracking, Quenching, and Compression
95
96
97
98
99
100
101
102
103
104
105
106
107
108
109
110
iii. Section 300: Separations
111
112
113
114
115
116
117
118
119
120
121
122
iv. Section 400: Refrigeration System
123
124
125
126
Section 12. Equipment Cost Summary
The following table highlights the purchase costs and bare module costs of all equipment
in this process. Design specifications of equipment were determined from ASPEN simulations and
hand calculations. Equipment costs were calculated using equations presented in Chapter 16 of
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HX-204 Fabricated Equipment $12,370 3.17 $39,213
HX-205 Fabricated Equipment $12,459 3.17 $39,495
HX-206 Fabricated Equipment $12,613 3.17 $39,983
HX-201 Fabricated Equipment $16,302 3.17 $51,677
F-401 Fabricated Equipment $136,099 4.16 $566,172
F-402 Fabricated Equipment $36,129 4.16 $150,297
R-301 Fabricated Equipment $152,261 4.16 $633,406
R-302 Fabricated Equipment $14,068 4.16 $58,523
R-303 Fabricated Equipment $82,433 4.16 $342,921
R-304 Fabricated Equipment $18,686 4.16 $77,734
R-101 Fabricated Equipment $167,171 4.16 $695,431
QT-201 Fabricated Equipment $20,329 4.16 $84,569
E-102 Fabricated Equipment $11,246 4.16 $46,783
D-301 Fabricated Equipment $227,850 4.16 $947,856
D-302 Fabricated Equipment $385,971 4.16 $1,605,639
D-303 Fabricated Equipment $183,872 4.16 $764,908
D-304 Fabricated Equipment $307,482 4.16 $1,279,125
T-301 Storage $199,996 4.00 $799,984
T-303 Storage $159,328 4.00 $637,312
T-302 Storage $295,879 4.00 $1,183,516
T-101 Storage $83,332 4.00 $333,328
T-102 Storage 4.00
T-001 Storage $45,707 3.21 $146,719
T-002 Storage $45,707 3.21 $146,719
E-002 Fabricated Equipment $2,883 3.21 $9,254
E-001 Fabricated Equipment $23,534 3.21 $75,544
E-003 Fabricated Equipment $11,642 3.21 $37,371
E-101 Fabricated Equipment $500,000 3.21 $1,605,000
HX-SPARE Spares $16,302 3.17 $51,677
P-SPARE1 Spares $4,770 3.30 $15,741
P-SPARE2 Spares $4,581 3.30 $15,117
P-SPARE3 Spares $11,393 3.30 $37,597
B-SPARE Spares $14,604 2.15 $31,399
TOTAL $21,349,818
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A breakdown of costs is shown in the figure below:
13%
33% 7%
Section 100
Section 200
Section 300
45% Section 400
Other
58 units were accounted for in Table 20.1, nine from Section 000-100, 15 from Section
200, 25 from Section 300, four from Section 400, and five units in other. Section 400, the
refrigeration cycle, has the least number of units but accounts for 33% of total equipment costs.
The compressor (C-401) in the refrigeration cycle is the most expensive unit in the plant and its
bare module cost is $4.79MM. The compressor is that expensive because it compresses 66,000
lb/hr of ethylene gas from 30 psia to 2000 psia. Even though temperature only increases from 85°F
to 100°F, ethylene will still be a gas. Section 300, separation processes, accounts for almost half
of the total equipment costs. The most expensive units in Section 300 are distillation columns and
the storage tanks. All the columns are made of carbon steel, the cheapest material, and they can
withstand pressures of up to 15,000 psia. We considered having more storage tanks in a previous
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Section 13. Fixed Capital Investment Summary
The total capital investment for the project was determined to be $27.5 MM. This value
was calculated using the method from Chapter 16 of Seider et al. The calculation sequence can be
The costs of certain factors such as site preparations and service facilities were not as clear as
others. The table below shows the assumptions that were made in calculating the total capital
investment.
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Table 13.2: Assumptions made to calculate require fees in the total capital investment.
Cost of site preparations 5% of Total bare-module costs
Cost of service facilities 5% of Total bare-module costs
Cost of contingencies and contractor fees 18% of Direct permanent investment
Cost of land 2% of Total depreciable capital
Cost of plant start-up 10% of Total depreciable capital
Table 13.3: Further analysis on total capital investment and working capital.
Investment Summary
131
Cost of Royalties: $ -
Cost of Plant Start-Up: $ 2,771,206
Working Capital
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Section 14. Operating Cost-Cost of Manufacture
i. Variable Costs
Annual variable operating costs were calculated to be $5MM and this includes the costs of
raw material, general expenses, utilities, and revenue generated from byproducts. The following
General Expenses
Total General
Expenses $ 1,780,705
The raw materials in this process are LDPE, HDPE, PP, and PS plastic shards. The total
feed rate is 70 MT/day or 6,430 lb/hr. Unlike the other monomers that are produced in the rotary
kiln, styrene does not proceed through the process as it is the primary component of the pyrolytic
oil. Ethylene was also purchased as a raw material for the start-up of the refrigeration cycle.
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The byproducts from the process are 450 psig steam, chilled water, and pyrolytic oil. High
pressure steam is generated when boiler water undergoes a phase change while quenching cracked
gases in the transfer line exchanger. Chilled water is generated in the reboiler of the C2 splitter
column (D-303) as cooling water is used to heat the boil-up stream Some of the chilled water is
sent to HX-202, while the rest is sold as a byproduct. Pyrolytic oil that was not burned in the rotary
Utilities used in the process are boiler feed water, cooling water, low pressure steam,
refrigerant, and electricity. Boiler feed water was used for quenching the cracked gases in the
transfer line exchanger, cooling water was used as a coolant in heat exchangers and in the quench
tower, refrigerant was bought for start-up purposes in the plate-fin exchanger in the refrigeration
cycle, and low pressure steam was used to heat reboilers in the demethanizer (D-301), deethanizer
(D-302), and depropanizer (D-304) columns. Electricity is the most expensive utility in the process
Table 15.2: Summary of Raw Materials, Byproducts, and Utilities in the process
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ii. Fixed Costs
Fixed costs were calculated to be $8.03MM per year. This includes the costs for operations,
maintenance, and operating overhead as well as property taxes and insurance. We assumed that
we would need four working shifts with five operators per shift. There will be four teams, one
working a 12-hr day shift and another working a 12-hr night shift, while two teams are off over a
four day period. The rotating work schedule will be 4 days on and 4 days off. At the plant there
will be two consoles, each with one operator, and there will be three process technicians in the
field. The technical assistance to manufacturing costs account for two process engineers and two
process control engineers that work regular 40-hr weeks. This work schedule was recommended
by an industrial consultant. The following table presents a summary of our fixed costs.
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Table 15.3: Summary of fixed costs estimated for the project on an annual basis.
Operations
Direct Wages and Benefits $ 1,664,000
Direct Salaries and Benefits $ 249,600
Operating Supplies and Services $ 99,840
Technical Assistance to Manufacturing $ 1,800,000
Control Laboratory $ -
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Section 15. Other Important Considerations
i. Environmental Factors
The main motivation of this project is to reduce the amount of plastic waste that gets disposed
of in harmful ways, such as being dumped into the ocean or being incinerated dangerously close
to habitation. One obvious way in which our project meets this goal is that it takes plastic waste in
as its feed and prevents that plastic waste from reaching the ocean or incineration facilities. Given
a feed of 68.9 tons of plastic each day, this corresponds to an annual 25,150 tons of plastic waste
that are saved from dangerous disposal. This is only 0.3% of the 8 million tons of plastic waste
that get dumped into the ocean each year— one plant will not be enough to eliminate the world’s
plastic waste problem. However, if similar plants were built around the world, it is conceivable
that a significant portion of the world’s plastic waste could be dealt with in a more sustainable
manner.
Another important metric of success for our project is how well it can reduce the need for
additional plastic to be created. Of the 68.9 tons of plastic waste entering the system each day,
40.14% is converted into ethylene and propylene by mass. These monomers can be used to create
can be polymerized to polypropylene. These resins can then be used to make plastic products. How
much of our plastic waste feed gets converted into these products relies in part on the efficiency
of these processes, in addition to our own. Given that an estimated 300MM tons of plastic are
produced each year, our annual ethylene and propylene output of 7,980 tons seems woefully small,
but, again, if several such plants were built around the world, it is possible that we could
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The process itself could also be modified to increase the ethylene and propylene yield—
but as of now, that is an expensive proposition. The catalysts that we considered for our process
each had their own problems, but some of them had higher yields of light hydrocarbons, meaning
that a greater amount of pyrolytic product could be cracked in the steam cracker to produce the
desired products.
Plastic waste is not the only problem that currently threatens the environment. Greenhouse
gas emission is a huge contributor to global climate change, which poses a huge threat to humanity
and all organisms. Industrial processes are one of the most significant sources of greenhouse gas
emission. It is important for our project not to offset the good done for the environment by emitting
a large amount of CO2 into the atmosphere. A chemical plant is considered to be a very significant
greenhouse gas emitter if it produces a high-digit six-figure number of tons of greenhouse gas
annually, a significant greenhouse gas emitter if it produces a low-digit six-figure number of tons
of greenhouse gas annually, and a moderate greenhouse gas emitter if it produces 100,000 tons or
less of greenhouse gas annually. Our process produces 3,706 tons of CO2 annually, meaning that
we produce far less than even a moderate greenhouse gas emitter. So, our goal to create an
environmentally beneficial process without offsetting these benefits with greenhouse gas
The rotary kiln operates at high temperatures and poses a risk to plant operators if they get
too close. To prevent any dangerous accidents, it is important to monitor the temperature of the
kiln to ensure that it does not reach extreme temperatures. Devices such as UV detectors can be
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The storage tanks all contain flammable hydrocarbon gas. To prevent explosions, the
pressure of the storage tanks is maintained at 30 psia, so that in the case of a puncture, gas would
flow out to the atmosphere rather than air flowing in. It is dangerous for oxygen to enter the tanks
Plastic waste is a threat across the globe. As discussed in the introduction, big plastic
buyers like China have stopped purchasing plastic waste, and now other countries, mainly in
Southeast Asia, have stepped in to become the primary purchasers. However, much of this plastic
waste is disposed of in ways that are harmful to the environment and the people who live near the
disposal plants. Incineration plants emit harmful compounds into the atmosphere that nearby
habitants may breathe in, resulting in health problems. The fumes are also unpleasant and affect
the quality of life for habitants living near the plant. Implementing recycling processes like the one
proposed in this project could benefit communities throughout the world that suffer as a result of
dangerous plastic waste disposal. For this reason, countries that are being overwhelmed with
plastic waste stand to benefit the most from chemical recycling facilities.
This was one reason that Indonesia was selected for the plant location. Indonesia is believed
to be the second-largest contributor to plastic waste ocean pollution, behind China [1]. While
Indonesia is not a major plastic purchaser like many of its neighbors in Southeast Asia, its
waterways are among the most polluted in the world, because the Indonesian population generates
tons of plastic waste annually. Building a chemical recycling plant here would allow for convenient
sourcing of plastic waste; because there is already so much plastic waste in Indonesia,
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iv. Robustness of feedstock
It is interesting to consider the feedstock as proposed by the project author. The feed to the
process is PE, PP, and PS, which are selected as they are entirely composed of carbon and
hydrogen. Introducing other types of plastic, notably PVC and PET, presents hazards due to
oxygen and chlorine content, and thus other methods of recycling need be considered for those
plastics. Due to the stability of the aromatic rings of polystyrene, polystyrene is converted to other
aromatic compounds, namely styrene, toluene, and ethylbenzene. In this sense, polystyrene is
primarily useful in the production of fuel oils from plastic waste, or in the production of styrene
itself. Additionally, polystyrene has a significantly higher melting point than polypropylene and
polyethylene, which increases electricity demands on the plastic extruder. It follows that in a pilot
scale plant, excluding polystyrene from a feedstock should be considered, as its utility for making
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Section 16. Profitability Analysis
i. Profitability Metrics
The proposed process for chemical recycling of mixed plastic waste is not a profitable
venture. The Net Present Value of the recycling plant in 2022 is -$18.8MM, and the Internal
Rate of Return (IRR) is -4.72%. In the third year of production, a -2.12% Return on Investment
(ROI) is obtained. The table below summarizes key profitability insights at a nominal interest
rate of 15%:
Table 16.1: Profitability Measures for the proposed process of chemical recycling.
Profitability Measures
This financial assessment is based on the following timeline: the plant is designed in one
year (2022), constructed in the next year (2023), and operated for the following fifteen years (2024-
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Table 16.2: Chronology of the proposed plant. One year will be used for design, one year for construction, and
fifteen for production of ethylene and propylene product.
Chronology
Distribution of Production Depreciation Product Price
Year Action Permanent Investment Capacity 5 year MACRS
2022 Design 0.0%
2023 Construction 100% 0.0%
2024 Production 0% 45.0% 20.00% $0.69
2025 Production 0% 67.5% 32.00% $0.69
2026 Production 0% 90.0% 19.20% $0.69
2027 Production 90.0% 11.52% $0.69
2028 Production 90.0% 11.52% $0.69
2029 Production 90.0% 5.76% $0.69
2030 Production 90.0% $0.69
2031 Production 90.0% $0.69
2032 Production 90.0% $0.69
2033 Production 90.0% $0.69
2034 Production 90.0% $0.69
2035 Production 90.0% $0.69
2036 Production 90.0% $0.69
2037 Production 90.0% $0.69
2038 Production 90.0% $0.69
This process has a negative IRR and a negative NPV, meaning that it does not produce
value. A large contributor to these negative values is the large annual cost associated with running
this plant. At 90% capacity, variable costs for the process are $4.5MM, and fixed costs are $8MM,
equaling $12.5MM in total annual cost. Annual sales are $13.9MM, just $1.4MM more than annual
cost. With depreciation and taxes, this leads to net earnings of -$560,000 in the third year of
production. The plant earns negative dollars until 2030, when it finally begins to generate positive
net earnings.
If this plant were built, it would require one year for design (2022) and one year for
construction (2023), followed by a lifespan of fifteen years (2024-2038) of ethylene and propylene
production. During the first year of production, 45% of plant capacity is reached. During the
second year of operation, 68% of plant capacity is reached. For the remaining thirteen years of
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operation, 90% of plant capacity is reached, where 100% capacity is 70 MT per day feed of plastic
waste. The following table summarizes the cashflow of the plant for the entire fifteen-year lifespan:
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Table 16.2: Cashflow Spreadsheet for fifteen years of operation of chemical plant
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The following figure summarizes the cumulative NPV at 15% for the two years prior to
Figure 16.1: Cumulative discounted cash flow for the proposed chemical recycling process. The plant has an NPV
of -$18.8MM. The process does not break even after 15 years of operation.
The following figure summarizes net earnings for the two years prior to operation and for
Figure 16.2: Annual net earnings ($) for the proposed process of chemical recycling. The plant has an NPV of
-$18.8MM. The process does not break even after 15 years of operation.
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In 2030, the plant begins to generate positive annual earnings. To breakeven, the plant
would need to operate for an additional seventeen years, after which point it could begin turning a
profit. This means that a total of thirty-two years of operation are required to even reach the
The profitability analysis was performed using a product price of $0.69 and an annual
variable cost of $4.5MM. It would be beneficial to examine how product price point and annual
variable costs affect the profitability of the plant. Given our current annual variable costs, a product
price of $0.76 per pound would result in a positive IRR. It would be worth investigating the
possibility of pricing our product slightly above market value. Typically, ethylene and propylene
sell for roughly $0.70 per pound. However, some companies might be willing to pay a slightly
higher price for our product since it is generated using a green process; it is possible that companies
that source their plastic feedstock from a green facility rather than the typical petrol plant could
receive tax credit or a government subsidy for being more sustainable. Depending on the size of
the credit, this could serve as incentive to choose our product over other, cheaper feedstock options.
The table on the following page shows a sensitivity analysis for the Internal Rate of Return
in several different scenarios of product price and variable costs, with the current IRR scenario
highlighted in red, and acceptable-IRR scenarios (those above an IRR of 12%) highlighted in
green:
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Table 16.3: Sensitivity analysis for different product price points and annual variable
costs.
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According to this sensitivity analysis table, when annual variable costs are $5MM at 100%
(and $4.5MM at 90% capacity, which is our case), a product price of $0.76 per pound is necessary
to obtain a positive, albeit small, IRR of 2.11%. However, to reach a more acceptable IRR of at
least 12%, a product price of $0.97 is necessary. At our current product price, annual variable costs
would need to be reduced to $3.99MM to have a (barely) positive IRR. At the current product
price, not even a 50% reduction in annual variable cost would yield a suitable IRR. This project
has very high annual costs. Refer to Section 13 for the tables summarizing fixed and variable cost.
A simple balance on the ethylene and propylene sales, byproduct sales, cost of raw
materials, and cost of utilities can be performed on a per-pound of ethylene and propylene basis to
The cost of raw material and utilities equal 66.7% of the value of the ethylene and
propylene product, and the byproducts generated in the process equal 44.9% of the value of the
ethylene and propylene product. One way to increase the value of the process overall would be to
reduce the amount of raw materials and utilities required in the process, as shown in the sensitivity
of plastic waste may still be a worthy process for investors to consider. There are several parts of
our process that could be modified to reduce costs and make the process more economically viable.
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In this process, there are several streams that have some valuable property that are not
currently being exploited. These alternatives were not considered for the purposes of this project
due to time constraints, but it would be worthwhile to investigate further if this plant were to be
designed. The distillate from the C2-Splitter and depropanizer columns exit the condenser at
roughly -30°F. These streams could be used to cool water so that it could be sold as a chilled water
byproduct. Further, all of the streams that exit the separations process are sent to be stored in
storage tanks at 30 psia. They each exit the column at fairly high pressure (ranging from 150 psia
to 300 psia). As these gases move from high pressure to low pressure, they will expand. When a
gas expands, it can be used to perform work. Gas expansion in a turbine can generate electricity.
That would be an idea worth investigating for future development of this process.
There are also opportunities to reduce the amount of utilities used in the process. For
example, in the depropanizer column, the two feed streams are fed at the same tray location. As
discussed in Section 10, these feeds could be fed into the column at different locations to reduce
the amount of cooling and heating duty needed in the condenser and reboiler of the column (see
Section 10 for a detailed explanation of this reasoning). This would lower the amount of utilities
required for the depropanizer column. However, this is only a small contribution to the utilities
cost; the compressor in the refrigeration cycle requires $2MM worth of electricity annually, which
One drastic modification that could potentially turn this endeavor into a profitable one
would be to do away with the separations and refrigeration processes and sell the steam-cracked
product to a plant that is equipped to handle these costly separations. Petroleum and ethylene plants
use similar separations processes to produce ethylene and propylene from naphtha and other
hydrocarbon oils, but because they sell a greater amount of product, they are able to turn a profit.
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The steam-cracked product from our process, which is comprised of the same light hydrocarbons
found in natural gas, could be used as supplemental feedstock in plants that already produce
ethylene and propylene. The utilities associated with the separations process in our project are
extremely costly; the electricity for the compressor in the refrigeration cycle costs over $2MM per
year, and accounts for almost half of the total variable cost. Eliminating these costs would save a
With this modification, ethylene and propylene would no longer be the products; rather, a
light hydrocarbon oil would be the product. Price information for this light hydrocarbon oil would
need to be determined to analyze the profitability of the process with this modification. Another
consequence of this modification would be that some of the byproducts would no longer be
Removing the separations and refrigeration sections would also significantly reduce the
total capital investment. The equipment cost for the separations and refrigeration process units is
$10MM. This represents 78% of the total equipment cost. Getting rid of this equipment, would
significantly reduce the total capital investment from $27.5MM to $17.5MM (and that’s only
considering the equipment itself—removing this section would also reduce the amount of land
required for the plant, the cost of plant start-up, and other components of capital investment that
depend on the bare module cost). With a lower total capital investment, it would be easier to
iv. Summary
While the proposed process for chemical recycling of mixed plastic waste is not a profitable
endeavor, the concept is still a worthy pursuit, as there are several possible modifications and
alternatives to the existing process that could make the process a profitable one.
150
Section 17. Conclusions and Recommendation
The process described offers insight into a circular monomers’ economy. 70 MT/day of
converted to 33,840 lb/day of 99% purity ethylene and 30,000 lb/day of 95.7% purity propylene.
Pyrolytic oil, chilled water, and high-pressure steam are additionally produced for sale. The overall
The innovative design combines plastic waste processing technology with established
byproducts of the cracking reactions provide a sufficient fuel source to meet the high energy
demands of cracking chemistry, which has both economic and environmental benefits.
Economically, the process is not profitable, and we do not recommend investing in the
process as it is currently modeled. The Internal Rate of Return (IRR) is -4.74%, the Net Present
Value (NPV) is -$18.8MM, and the Return on Investment (ROI) in the third year of operation is -
2.12%; it would not be worth investing in this project unless the IRR and ROI were much higher,
recycling option; there are ways to make the process more profitable, and the environmental
benefits of the process are important enough to warrant further development and consideration.
Additionally, exploration into government subsidy for the environmental merits of the process may
the process, especially the rotary kiln. The true product distribution and function of the kiln, as
well as the proposed method for purifying the fuel oil product, are It is recommended that a pilot-
scale facility is constructed to better understand and optimize the process, especially the rotary
kiln. The true product distribution and function of the kiln, as well as the proposed method for
151
purifying the fuel oil product, are at this time theoretical. In scale-up, challenges will arise
surrounding heat transfer in all stages of the process, given the high temperatures of the cracking
152
Section 18. Acknowledgments
Our team would like to thank Professor Our team would like to thank Professor Bruce
Vrana and Dr. Sean Holleran for their support throughout the completion of this project. Their
guidance—in our weekly meetings, in office hours, and in numerous email exchanges—was
invaluable, and we could not have accomplished this feat without them. We would also like to
thank Mr. Stephen Tieri for writing a problem statement that was at once challenging and
interesting; each moment of frustration was matched with many moments of excitement, and we
appreciate the chance to work on a project that reminded us why we chose our major in the first
place. We would like to thank each of the other industry consultants who offered their Tuesday
afternoons to us, even in the midst of a global pandemic. We would especially like to thank
engineering practices, teaching us about refractory materials and rotary kilns, and for his
willingness to spend multiple hours on Skype walking us through ASPEN simulations. The stories
he shared about his years in process engineering were an added bonus. Finally, we would like to
thank the entire CBE faculty and administration for making our education possible, and for
preparing us to complete what once felt like a Herculean task with confidence.
153
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159
Section 20. Appendix
Appendix A: Calculations
v = 0.0147 ft/s
Area for flow = 0.738 ft2
Wetted perimeter = 2.04 ft
Rh = 0.738/2.04 = 0.362 ft
K = 1.49 (English Units)
n = 0.019 (Gauckler-Manning Coefficient for rough steel due to presence of char)
S = 0.0192 ft/ft (rotary kiln standard is 0.02-0.04 ft/ft)
ϴ = 1.10
Gas generated = 5161 lb/hr = 4086 lb/47.5 min
Vgas = 259-51.8 = 207.2 ft3
T = 1112 ⁰F
Approximate molar mass of gas as 38.6 g/mol
Ngen = 48015 mol/47.5 min
P = nRT/V
Pclosed = 8610 psia (!)
160
Thus, will use a pressure cap to operate at 73.5 psia
Cp = f(t). Values of Cp for PE, PP, PS established as functions of temperature on a per-mol basis.
Not per kg. Conversion is complex, thus approximate with:
Cp (polystyrene) = 1400 J / kg K
Cp(polyethylene) = 1900 J / kg K
Cp(polypropylene) = 1920 J / kg K
Average = 0.442 BTU/lb ⁰F
Q = Hin – Hout
T2 = 8852⁰F
Too high, thus will need to dilute with air. Assume that the pyrolysis temperature chamber is
2732 ⁰F (1500⁰C). This temperature is non-trivially selected due to the nature of insulating
refractories.
nair = 28 mol
Thus 1 mol of pyrolysis oil combusts to 8 mol CO2, 5 mol H2O, and 28 mol air at 2732 ⁰F.
161
∆H (using above with nair = 28 and T1 = 700⁰C) = 2501 BTU gas available/mol combusted
Fuel requirement is therefore (using 100.8 g/mol mass of fuel oil): 306 lb/hr
-this is for the first 15.5 ft of the kiln, during which the heating is said to occur-
-consider the second 26.5 ft, during which the temperature need be maintained at 1112⁰F-
With the same combustion temperature, oil demand is therefore: 19.9 lb/hr
Castable thickness:
The heat flux in the heating region is: (1.39 x 106 BTU/hr)/(π*2.8 ft*15.5ft)
k = 10.4 BTU/h ft ⁰F
Suppose ∆Trefractory should be 1000⁰F to prevent overheating in the reaction chamber and to
protect the inner carbon steel
Thus, the inner wall has a thickness of 0.25 in of Carbon Steel and 8.4 in of alumina oxide
refractory.
Now, ∆T (combustion chamber to outside) = 2532 (if kiln exterior is no more than 200⁰F)
∆Trefractory = 1500 ⁰F
L = 1.2 ft = 14.4 in
162
The outer wall of the kiln will be 14.4 inches of alumina oxide refractory with 0.25 in of carbon
steel exterior for support.
Solid/Liquid Splitter
The vessel needs to handle 1181 lb/hr of oil and 84 lb/hr of char. The density of the oil is an
estimated 46.2 lb/ft3. The vessel is assumed to be 60% full, and it is desired that it can contain up
to 1 residence time cycle of kiln product (1000 lb). The volume required is thus 36.1 ft3. Using
an assumed aspect ratio of 5, the dimensions of the unit are found. 36.1 ft3 = (π/4)*(D2)*(5D),
which gives dimensions of 2.09 ft diameter and 10.5 ft length.
There are two outlets of this vessel, one with liquid product and one with a slurry. The slurry is
assumed to be the char and to have 15% of liquid in it. Thus, the liquid outlet flow rate is 1003
lb/hr, and the slurry is 262 lb/hr.
Costing:
CP = FMCV + CPL
FM = 1(Carbon Steel)
CPL = 2275D0.2094
CPL = $2655
CV = $7973
CP = $10,628
The extrusion screw is simply a unit purchased from manufacturers. The desired capacity used
for search is 3000 kg/hr. The full details on what is found are included in Appendix II. The cost,
estimated from online, is $500,000.
The power requirement is estimated: It should be noted that in an extrusion screw, much of the
heat generated is as a result from the friction between the plastic and the wall and viscous
heating effects. A detailed analysis on the temperature profile and heating zones of the screw are
not included.
163
Heat requirement = (1490 kg/hr)*((287.6 kJ/kg)+(1.9 kJ/kg K)(225 K)) = 1065499 kJ/hr = 295
kW
PP: heat of melting = 103.8 kJ/kg, Cp = 1920 J / kg K, melting point = 158⁰C.
Assume PP flow is 2916 kg/hr * (.372) = 1084 kg/hr
Heat Requirement = (1084 kg/hr) * ((103.8 kJ/kg) + (1.92 kJ/ kg K)(225 K)) = 161 kW
Heat required for melting = 490 kW. This is primarily supplied by the drive force to the motor.
80% efficiency is assumed, and the demand is thus 612.5 kW = 821 hp.
The two models below are used to inform power requirement and economics:
164
Bucket Elevators
The height of the bucket elevators estimated as 5 feet above the required height. For the elevator
to the silos, this means that the height is 55 feet. For the elevator to section 001 and the extrusion
screw, the height is estimated from summing the rotary kiln diameter and slant height and adding
10 feet for machinery and equipment beneath the kiln. This height is 16 feet.
Costing:
Power Requirement:
165
P = 0.02 m (L0.63) + 0.00182 mL
Screw Feeder
Assuming a 75% empty space due to packing, density is approximate as 78.5 lb/ ft3:
Costing:
Power Requirement:
P = 0.0146 L (m)0.85
Feed Silo
Daily processing capacity = 70 MT = 154324 lb; space demand is 2620 ft3 for one day of plastic
Assume, due to packing, 75% empty space thus space demand is 3490 ft3 per day.
166
Blower
k = 1.4; nB = 0.75; PB = 23 hp
ηm = 0.8 + 0.0319 ln(PB) – 0.00182(ln(PB))2
ηm = 0.882
PC = PB / ηm = 26.1 hp
Costing:
CP = CBFM
FM = 0.6 (aluminum)
CB = exp(7.0187 + 0.79 ln(PC))
CB = $14,700
CP = $8,820
Steam Cracker
Calculating heat required
The heat required for the radiative section of the furnace is found by adding the heat required of
the cracking reaction and the sensible heat required to heat the feed stream to the coil outlet
temperature (COT).
where i represents all the product components, j represents the reactant components, and is the
mass flow rate. Using this equation, the heat of cracking was calculated to be 10.4 MM BTU/hr.
The temperature dependent specific enthalpies of formation of components was acquired from
NIST.
The sensible heat required to increase the temperature of the cracked gas (diluent steam and light
gas) from the crossover temperature (XOT) to the COT is:
where is the mass flow rate of steam, , is the specific enthalpy of steam at the COT, is the
specific enthalpy of steam at the XOT, is the mass flow rate of light gas, and is the average
specific heat. The sensible heat was calculated to be 2.65 MM BTU/hr.
167
The heat needed to preheat the process steam to XOT is found from:
where is the latent heat of vaporization of water and is the temperature of the water leaving the
purge stream, and is the saturation temperature of water at atmospheric pressure. The heat
needed to preheat the process steam is 3.04 MM BTU/hr.
The heat needed to preheat the boiler feed water is 13.09 MM BTU/hr and is found from:
The total heat requirement from the radiation section of the steam cracker is found from:
The following equations show the general method of calculating the flue gas and fuel
requirements to satisfy .
Where is a fraction of radiation section duty that a specific fuel, k, will satisfy, is the specific
enthalpy of flue gas leaving the firebox into the convection section, and is the specific enthalpy
of the flue gas in the firebox. was determined from the following combustion reaction:
where k is methane, 10% excess air was assumed, and the lower heating value (LHV) is 21,433
BTU/lb. Through this combustion reaction, can be calculated:
A mass balance can be done to calculate the amount of fuel needed to supply amount of heat:
where b is 0.477.
Quench Tower
A tower diameter and height of 3.5 and 8 feet respectively is assumed. The tower would be made
from carbon steel, which has a density of 490 lb/ft3.
168
169
Transfer Line Exchanger
The heat duty of the TLE, or any heat exchanger, is determined from the desired sensible heat
changer of the stream of interest. The heat duty can be calculated from the following equation:
where is the mass low rate of the stream, is the average specific heat capacity of the stream, and
is the inlet and outlet temperature difference.
The calculated heat duty is then equated to an identical equation of the alternate stream passing
through the heat exchanger. In the second case, either or is unknown and it must be solved for.
Once specified, the area of the heat exchanger can be calculated from its overall heat transfer
coefficient U [BTU/ft2-lb-hr], heat duty Q [BTU/hr], and log-mean temperature difference.
The velocity of the stream can calculated, or one can assume a value from 1-10ft/s, the cross-
sectional area of the heat exchanger can be calculated from:
where is the density of the stream and is the velocity. A pipe inner diameter can be assumed and
the number of tubes per pass in the HX can be found from:
Assume a tube length of 8ft, 12ft, 16ft, or 20ft and calculate the surface area of one tube and
then the number of tube passes can be calculated.
170
Distillation Columns
Costing
Cp=FMCV+CPL
FM = 1
CP = 190,083 + 25,236
CP = $215,318 at CE = 567
CP = $227,850 at CE = 600
CV = exp{10.5449-0.4672 [ln(W)]+0.0.05482[ln(W)]2}
W = 69,955 lbs
CV = $190,083
CPL = 341*(D)0.63316(L)0.80161
D = 5.4 ft
L = 57.5 ft
CPL = $25,236
Pd = exp{0.60608+0.91615[ln(Po)]+0.0015655[ln(Po)]2}
Po = 535.3 psig
Pd = 616 psig
171
CT=NTFNTFTTFTMCBT
NT = 15
FTT = 1
FTM = 1
CT = $18,853 at CE = 567
CT = $19,950 at CE = 600
FNT = 2.251/0414NT
FNT = 1.22
CBT = 468exp(0.1482Di)
CBT = 1,027
CTOT = CT + CP
CTOT = 19,950 + 227,850 = $247,800
172
Pumps
Sizing
S = Q(H)0.5
S = (7.06 gal/min)*(477ft)0.5
S = 916 (gpm)(ft)0.5
Costing
CP = FTFMCB
FM = 1 for cast iron
FT = 1
CP = (1)(1)(4305) = $4296 for CE = 567
CP = $4,546 FOR CE = 600
Costing
Example: Demethanizer Condenser
CP = FPFMFLCB
CP = 1.13*1*1*19,085
CP = $21,579 for CE = 567
CP = $22,835 for CE = 600
FM = a + (A/100)b
173
a=0
b=0
FM = 1 for carbon steel/carbon steel
FL = 1 for 20 ft tube
Storage Tanks
Sizing
Storage tanks were designed to allow for one hour’s worth of storage of gas product. To
determine the volume needed for one hour’s worth of storage, the volumetric flowrate was
determined and multiplied by the amount of time for storage (one hour). The storage tanks are
kept at 70°F and 14.7 psia, and properties of the components were calculated at these conditions.
Example: Ethylene Product Storage Tank
Volume:
ρethylene = 0.073 lbs/cuft at 70°F, 14.7 psia
methylene = 1410 lbs/hr
vethylene = methylene / ρethylene = 19,316 cuft/hr
Length and Diameter:
L = 59.0 ft
L/D = 3
D = L/3
D = 19.7 ft
174
Costing
Storage tanks were modeled as floating roof storage tanks because the contents of the tanks are
all in gas form.
Example: Ethylene Storage Tank
Cp = 475*V0.507
V = 144,494 gallons
Cp = $188,996 at CE = 567
Cp = $199,996 at CE = 600
Compressors
Sizing
ASPEN provided sizing information for the compressor. See section 11 specification sheet for
sizing information.
Costing
Cp = FDFMCB
FD = 1
FM = 1
CB = $2,226,011
CP = $2,226,011 at CE = 567
CP = $2,355,567 at CE = 600
CB = exp{9.1553+0.63[ln(PC)]}
PC = 5810 hp
CB = $2,226,011
175
Flash Vessels
Sizing
Flash Vessels were modeled as vertical pressure vessels and sized assuming a 5-minute residence
time. The volume needed for 5 minutes’ worth of accumulation was calculated and an L/D aspect
ratio of 3 was assumed to determine the dimensions of the vessels.
Example: Flash Vessel 1
L = 13.6 ft
D = 4.53 ft
Costing
Example: Flash Vessel 1
CP = FMCV + CPL
FM = 1 for carbon steel
Cv = 120,685
CPL = 410(Di)0.73960(L)0.70864
CP = $128,614 for CE = 567
CP = 136,099 for CE = 600
CV = exp{7.1390 + 0.18255[ln(W)] + 0.2297 [ln(W)]2}
CV = $120,685
176
Appendix B: MSDS Sheets
177
178
179
180
181
182
183
184
185
186
187
188
189
190
191
192
193
Appendix C: ASPEN Report
Section 200: Compressor Blocks and Streams
LOCK: C-201 MODEL: COMPR
-----------------------------
INLET STREAM: CG-1
OUTLET STREAM: CG-2
PROPERTY OPTION SET: RK-SOAVE STANDARD RKS EQUATION OF
STATE
194
*** RESULTS ***
195
PROPERTY OPTION SET: RK-SOAVE STANDARD RKS EQUATION OF
STATE
196
ISENTROPIC HORSEPOWER REQUIREMENT HP 141.407
CALCULATED OUTLET PRES PSIA 273.500
CALCULATED OUTLET TEMP F 326.707
ISENTROPIC TEMPERATURE F 307.839
EFFICIENCY (POLYTR/ISENTR) USED 0.81000
OUTLET VAPOR FRACTION 1.00000
HEAD DEVELOPED, FT-LBF/LB 54,229.4
MECHANICAL EFFICIENCY USED 1.00000
INLET HEAT CAPACITY RATIO 1.28050
INLET VOLUMETRIC FLOW RATE , CUFT/HR 21,167.5
OUTLET VOLUMETRIC FLOW RATE, CUFT/HR 14,162.9
INLET COMPRESSIBILITY FACTOR 1.00308
OUTLET COMPRESSIBILITY FACTOR 1.00731
AV. ISENT. VOL. EXPONENT 1.27956
AV. ISENT. TEMP EXPONENT 1.26772
AV. ACTUAL VOL. EXPONENT 1.35763
AV. ACTUAL TEMP EXPONENT 1.34354
197
ENTHALPY(BTU/HR ) 539151. 820758. -0.343106
198
INLET HEAT CAPACITY RATIO 1.28483
INLET VOLUMETRIC FLOW RATE , CUFT/HR 12,339.8
OUTLET VOLUMETRIC FLOW RATE, CUFT/HR 9,556.64
INLET COMPRESSIBILITY FACTOR 1.00552
OUTLET COMPRESSIBILITY FACTOR 1.00987
AV. ISENT. VOL. EXPONENT 1.29011
AV. ISENT. TEMP EXPONENT 1.27116
AV. ACTUAL VOL. EXPONENT 1.37322
AV. ACTUAL TEMP EXPONENT 1.35039
199
*** INPUT DATA ***
200
AV. ACTUAL TEMP EXPONENT 1.36058
201
CG-1 SFRAC 0.0
---- ENTHALPY:
BTU/LBMOL 68.5900
STREAM ID CG-1 BTU/LB 6.0537
FROM : ---- BTU/HR 3.1255+04
TO : C-201 ENTROPY:
BTU/LBMOL-R -7.6582
SUBSTREAM: MIXED BTU/LB-R -0.6759
PHASE: VAPOR DENSITY:
COMPONENTS: LBMOL/HR LBMOL/CUFT 7.2437-03
HYDROGEN 301.1092 LB/CUFT 8.2074-02
METHANE 37.8364 AVG MW 11.3303
MONOXIDE 0.1071
ETHANE 7.2831 CG-2
ETHENE 70.5431 ----
PROPANE 1.1792
PROPENE 30.5841 STREAM ID CG-2
BUTANE 7.0368 FROM : C-201
WATER 0.0 TO : HX-203
TOTAL FLOW:
LBMOL/HR 455.6790 SUBSTREAM: MIXED
LB/HR 5163.0000 PHASE: VAPOR
CUFT/HR 6.2907+04 COMPONENTS: LBMOL/HR
STATE VARIABLES: HYDROGEN 301.1092
TEMP F 100.0000 METHANE 37.8364
PRES PSIA 43.5000 MONOXIDE 0.1071
VFRAC 1.0000 ETHANE 7.2831
LFRAC 0.0 ETHENE 70.5431
202
PROPANE 1.1792 FROM : HX-203
PROPENE 30.5841 TO : C-202
BUTANE 7.0368
WATER 0.0 SUBSTREAM: MIXED
TOTAL FLOW: PHASE: VAPOR
LBMOL/HR 455.6790 COMPONENTS: LBMOL/HR
LB/HR 5163.0000 HYDROGEN 301.1092
CUFT/HR 2.4289+04 METHANE 37.8364
STATE VARIABLES: MONOXIDE 0.1071
TEMP F 324.3175 ETHANE 7.2831
PRES PSIA 158.5000 ETHENE 70.5431
VFRAC 1.0000 PROPANE 1.1792
LFRAC 0.0 PROPENE 30.5841
SFRAC 0.0 BUTANE 7.0368
ENTHALPY: WATER 0.0
BTU/LBMOL 2128.7462 TOTAL FLOW:
BTU/LB 187.8801 LBMOL/HR 455.6790
BTU/HR 9.7002+05 LB/HR 5163.0000
ENTROPY: CUFT/HR 2.1168+04
BTU/LBMOL-R -7.1457 STATE VARIABLES:
BTU/LB-R -0.6307 TEMP F 224.3176
DENSITY: PRES PSIA 158.5000
LBMOL/CUFT 1.8761-02 VFRAC 1.0000
LB/CUFT 0.2126 LFRAC 0.0
AVG MW 11.3303 SFRAC 0.0
ENTHALPY:
CG-3 BTU/LBMOL 1171.4576
---- BTU/LB 103.3912
BTU/HR 5.3381+05
STREAM ID CG-3 ENTROPY:
203
BTU/LBMOL-R -8.4512 STATE VARIABLES:
BTU/LB-R -0.7459 TEMP F 326.7066
DENSITY: PRES PSIA 273.5000
LBMOL/CUFT 2.1527-02 VFRAC 1.0000
LB/CUFT 0.2439 LFRAC 0.0
AVG MW 11.3303 SFRAC 0.0
ENTHALPY:
CG-4 BTU/LBMOL 2146.2655
---- BTU/LB 189.4263
BTU/HR 9.7801+05
STREAM ID CG-4 ENTROPY:
FROM : C-202 BTU/LBMOL-R -8.2128
TO : HX-204 BTU/LB-R -0.7249
DENSITY:
SUBSTREAM: MIXED LBMOL/CUFT 3.2174-02
PHASE: VAPOR LB/CUFT 0.3645
COMPONENTS: LBMOL/HR AVG MW 11.3303
HYDROGEN 301.1092
METHANE 37.8364 CG-5
MONOXIDE 0.1071 ----
ETHANE 7.2831
ETHENE 70.5431 STREAM ID CG-5
PROPANE 1.1792 FROM : HX-204
PROPENE 30.5841 TO : C-203
BUTANE 7.0368
WATER 0.0 SUBSTREAM: MIXED
TOTAL FLOW: PHASE: VAPOR
LBMOL/HR 455.6790 COMPONENTS: LBMOL/HR
LB/HR 5163.0000 HYDROGEN 301.1092
CUFT/HR 1.4163+04 METHANE 37.8364
204
MONOXIDE 0.1071 ----
ETHANE 7.2831
ETHENE 70.5431 STREAM ID CG-6
PROPANE 1.1792 FROM : C-203
PROPENE 30.5841 TO : HX-205
BUTANE 7.0368
WATER 0.0 SUBSTREAM: MIXED
TOTAL FLOW: PHASE: VAPOR
LBMOL/HR 455.6790 COMPONENTS: LBMOL/HR
LB/HR 5163.0000 HYDROGEN 301.1092
CUFT/HR 1.2340+04 METHANE 37.8364
STATE VARIABLES: MONOXIDE 0.1071
TEMP F 226.7066 ETHANE 7.2831
PRES PSIA 273.5000 ETHENE 70.5431
VFRAC 1.0000 PROPANE 1.1792
LFRAC 0.0 PROPENE 30.5841
SFRAC 0.0 BUTANE 7.0368
ENTHALPY: WATER 0.0
BTU/LBMOL 1183.1812 TOTAL FLOW:
BTU/LB 104.4259 LBMOL/HR 455.6790
BTU/HR 5.3915+05 LB/HR 5163.0000
ENTROPY: CUFT/HR 9556.6392
BTU/LBMOL-R -9.5220 STATE VARIABLES:
BTU/LB-R -0.8404 TEMP F 292.1519
DENSITY: PRES PSIA 388.5000
LBMOL/CUFT 3.6927-02 VFRAC 1.0000
LB/CUFT 0.4184 LFRAC 0.0
AVG MW 11.3303 SFRAC 0.0
ENTHALPY:
CG-6 BTU/LBMOL 1801.1761
205
BTU/LB 158.9692 LBMOL/HR 455.6790
BTU/HR 8.2076+05 LB/HR 5163.0000
ENTROPY: CUFT/HR 8258.4021
BTU/LBMOL-R -9.3646 STATE VARIABLES:
BTU/LB-R -0.8265 TEMP F 192.1519
DENSITY: PRES PSIA 388.5000
LBMOL/CUFT 4.7682-02 VFRAC 1.0000
LB/CUFT 0.5403 LFRAC 0.0
AVG MW 11.3303 SFRAC 0.0
ENTHALPY:
CG-7 BTU/LBMOL 848.8522
---- BTU/LB 74.9185
BTU/HR 3.8680+05
STREAM ID CG-7 ENTROPY:
FROM : HX-205 BTU/LBMOL-R -10.7230
TO : C-204 BTU/LB-R -0.9464
DENSITY:
SUBSTREAM: MIXED LBMOL/CUFT 5.5178-02
PHASE: VAPOR LB/CUFT 0.6252
COMPONENTS: LBMOL/HR AVG MW 11.3303
HYDROGEN 301.1092
METHANE 37.8364 CG-8
MONOXIDE 0.1071 ----
ETHANE 7.2831
ETHENE 70.5431 STREAM ID CG-8
PROPANE 1.1792 FROM : C-204
PROPENE 30.5841 TO : HX-206
BUTANE 7.0368
WATER 0.0 SUBSTREAM: MIXED
TOTAL FLOW: PHASE: VAPOR
206
COMPONENTS: LBMOL/HR AVG MW 11.3303
HYDROGEN 301.1092
METHANE 37.8364 CG-9
MONOXIDE 0.1071 ----
ETHANE 7.2831
ETHENE 70.5431 STREAM ID CG-9
PROPANE 1.1792 FROM : HX-206
PROPENE 30.5841 TO : ----
BUTANE 7.0368
WATER 0.0 SUBSTREAM: MIXED
TOTAL FLOW: PHASE: VAPOR
LBMOL/HR 455.6790 COMPONENTS: LBMOL/HR
LB/HR 5163.0000 HYDROGEN 301.1092
CUFT/HR 6359.0251 METHANE 37.8364
STATE VARIABLES: MONOXIDE 0.1071
TEMP F 258.3075 ETHANE 7.2831
PRES PSIA 559.5000 ETHENE 70.5431
VFRAC 1.0000 PROPANE 1.1792
LFRAC 0.0 PROPENE 30.5841
SFRAC 0.0 BUTANE 7.0368
ENTHALPY: WATER 0.0
BTU/LBMOL 1461.5228 TOTAL FLOW:
BTU/LB 128.9919 LBMOL/HR 455.6790
BTU/HR 6.6599+05 LB/HR 5163.0000
ENTROPY: CUFT/HR 5292.0409
BTU/LBMOL-R -10.5595 STATE VARIABLES:
BTU/LB-R -0.9320 TEMP F 142.3075
DENSITY: PRES PSIA 559.5000
LBMOL/CUFT 7.1659-02 VFRAC 1.0000
LB/CUFT 0.8119 LFRAC 0.0
207
SFRAC 0.0 BTU/LBMOL-R -12.2194
ENTHALPY: BTU/LB-R -1.0785
BTU/LBMOL 368.0489 DENSITY:
BTU/LB 32.4835 LBMOL/CUFT 8.6106-02
BTU/HR 1.6771+05 LB/CUFT 0.9756
ENTROPY: AVG MW 11.3303
208
Section 200: Intercooler blocks and streams
BLOCK: HX-203 MODEL: HEATX
-----------------------------
HOT SIDE:
---------
INLET STREAM: CG-2
OUTLET STREAM: CG-3
PROPERTY OPTION SET: RK-SOAVE STANDARD RKS EQUATION OF STATE
COLD SIDE:
----------
INLET STREAM: CW-IN3
OUTLET STREAM: CW-OUT3
PROPERTY OPTION SET: RK-SOAVE STANDARD RKS EQUATION OF STATE
209
FLASH SPECS FOR HOT SIDE:
TWO PHASE FLASH
MAXIMUM NO. ITERATIONS 30
CONVERGENCE TOLERANCE 0.000100000
PRESSURE SPECIFICATION:
HOT SIDE PRESSURE DROP PSI 0.0000
COLD SIDE PRESSURE DROP PSI 0.0000
STREAMS:
--------------------------------------
| |
CG-2 ----->| HOT |-----> CG-3
T= 3.2432D+02 | | T= 2.2432D+02
210
P= 1.5850D+02 | | P= 1.5850D+02
V= 1.0000D+00 | | V= 1.0000D+00
| |
CW-OUT3 <-----| COLD |<----- CW-IN3
T= 1.1981D+02 | | T= 8.0000D+01
P= 1.4696D+01 | | P= 1.4696D+01
V= 0.0000D+00 | | V= 0.0000D+00
--------------------------------------
PRESSURE DROP:
HOTSIDE, TOTAL PSI 0.0000
COLDSIDE, TOTAL PSI 0.0000
211
PRESSURE PROFILE: CONSTANT2
PRESSURE DROP: 0.0 PSI
PROPERTY OPTION SET: RK-SOAVE STANDARD RKS EQUATION OF STATE
-----------------------------------------------------
! DUTY ! PRES ! TEMP ! VFRAC !
! ! ! ! !
! ! ! ! !
! ! ! ! !
! BTU/HR ! PSIA ! F ! !
! ! ! ! !
!============!============!============!============!
! 0.0 ! 14.6959 ! 119.8091 ! 0.0 !
! 2.0772+04 ! 14.6959 ! 117.9127 ! 0.0 !
! 4.1544+04 ! 14.6959 ! 116.0163 ! 0.0 !
! 6.2317+04 ! 14.6959 ! 114.1199 ! 0.0 !
! 8.3089+04 ! 14.6959 ! 112.2234 ! 0.0 !
!------------+------------+------------+------------!
! 1.0386+05 ! 14.6959 ! 110.3270 ! 0.0 !
! 1.2463+05 ! 14.6959 ! 108.4307 ! 0.0 !
! 1.4541+05 ! 14.6959 ! 106.5343 ! 0.0 !
! 1.6618+05 ! 14.6959 ! 104.6381 ! 0.0 !
! 1.8695+05 ! 14.6959 ! 102.7419 ! 0.0 !
!------------+------------+------------+------------!
! 2.0772+05 ! 14.6959 ! 100.8458 ! 0.0 !
! 2.2849+05 ! 14.6959 ! 98.9499 ! 0.0 !
! 2.4927+05 ! 14.6959 ! 97.0540 ! 0.0 !
! 2.7004+05 ! 14.6959 ! 95.1583 ! 0.0 !
! 2.9081+05 ! 14.6959 ! 93.2628 ! 0.0 !
!------------+------------+------------+------------!
212
! 3.1158+05 ! 14.6959 ! 91.3675 ! 0.0 !
! 3.3236+05 ! 14.6959 ! 89.4723 ! 0.0 !
! 3.5313+05 ! 14.6959 ! 87.5774 ! 0.0 !
! 3.7390+05 ! 14.6959 ! 85.6826 ! 0.0 !
! 3.9467+05 ! 14.6959 ! 83.7882 ! 0.0 !
!------------+------------+------------+------------!
! 4.1544+05 ! 14.6959 ! 81.8939 ! 0.0 !
! 4.3622+05 ! 14.6959 ! 80.0000 ! 0.0 !
-----------------------------------------------------
-----------------------------------------------------
! DUTY ! PRES ! TEMP ! VFRAC !
! ! ! ! !
! ! ! ! !
! ! ! ! !
! BTU/HR ! PSIA ! F ! !
! ! ! ! !
!============!============!============!============!
! 0.0 ! 158.5000 ! 324.3175 ! 1.0000 !
! 2.0772+04 ! 158.5000 ! 319.6650 ! 1.0000 !
! 4.1544+04 ! 158.5000 ! 315.0022 ! 1.0000 !
! 6.2317+04 ! 158.5000 ! 310.3290 ! 1.0000 !
! 8.3089+04 ! 158.5000 ! 305.6452 ! 1.0000 !
!------------+------------+------------+------------!
213
! 1.0386+05 ! 158.5000 ! 300.9509 ! 1.0000 !
! 1.2463+05 ! 158.5000 ! 296.2459 ! 1.0000 !
! 1.4541+05 ! 158.5000 ! 291.5300 ! 1.0000 !
! 1.6618+05 ! 158.5000 ! 286.8033 ! 1.0000 !
! 1.8695+05 ! 158.5000 ! 282.0656 ! 1.0000 !
!------------+------------+------------+------------!
! 2.0772+05 ! 158.5000 ! 277.3167 ! 1.0000 !
! 2.2849+05 ! 158.5000 ! 272.5567 ! 1.0000 !
! 2.4927+05 ! 158.5000 ! 267.7854 ! 1.0000 !
! 2.7004+05 ! 158.5000 ! 263.0027 ! 1.0000 !
! 2.9081+05 ! 158.5000 ! 258.2084 ! 1.0000 !
!------------+------------+------------+------------!
! 3.1158+05 ! 158.5000 ! 253.4026 ! 1.0000 !
! 3.3236+05 ! 158.5000 ! 248.5850 ! 1.0000 !
! 3.5313+05 ! 158.5000 ! 243.7556 ! 1.0000 !
! 3.7390+05 ! 158.5000 ! 238.9143 ! 1.0000 !
! 3.9467+05 ! 158.5000 ! 234.0609 ! 1.0000 !
!------------+------------+------------+------------!
! 4.1544+05 ! 158.5000 ! 229.1953 ! 1.0000 !
! 4.3622+05 ! 158.5000 ! 224.3176 ! 1.0000 !
-----------------------------------------------------
214
----------
INLET STREAM: CW-IN4
OUTLET STREAM: CW-OUT4
PROPERTY OPTION SET: RK-SOAVE STANDARD RKS EQUATION OF STATE
215
FLOW DIRECTION AND SPECIFICATION:
COUNTERCURRENT HEAT EXCHANGER
SPECIFIED HOT TEMP CHANGE
SPECIFIED VALUE F 100.0000
LMTD CORRECTION FACTOR 1.00000
PRESSURE SPECIFICATION:
HOT SIDE PRESSURE DROP PSI 0.0000
COLD SIDE PRESSURE DROP PSI 0.0000
STREAMS:
--------------------------------------
| |
CG-4 ----->| HOT |-----> CG-5
T= 3.2671D+02 | | T= 2.2671D+02
P= 2.7350D+02 | | P= 2.7350D+02
V= 1.0000D+00 | | V= 1.0000D+00
| |
CW-OUT4 <-----| COLD |<----- CW-IN4
T= 1.1983D+02 | | T= 8.0000D+01
P= 1.4696D+01 | | P= 1.4696D+01
V= 0.0000D+00 | | V= 0.0000D+00
--------------------------------------
216
DUTY AND AREA:
CALCULATED HEAT DUTY BTU/HR 438857.3039
CALCULATED (REQUIRED) AREA SQFT 31.3343
ACTUAL EXCHANGER AREA SQFT 231.4625
PER CENT OVER-DESIGN 638.6875
PRESSURE DROP:
HOTSIDE, TOTAL PSI 0.0000
COLDSIDE, TOTAL PSI 0.0000
-----------------------------------------------------
! DUTY ! PRES ! TEMP ! VFRAC !
! ! ! ! !
! ! ! ! !
! ! ! ! !
217
! BTU/HR ! PSIA ! F ! !
! ! ! ! !
!============!============!============!============!
! 0.0 ! 14.6959 ! 119.8321 ! 0.0 !
! 2.0898+04 ! 14.6959 ! 117.9346 ! 0.0 !
! 4.1796+04 ! 14.6959 ! 116.0371 ! 0.0 !
! 6.2694+04 ! 14.6959 ! 114.1396 ! 0.0 !
! 8.3592+04 ! 14.6959 ! 112.2421 ! 0.0 !
!------------+------------+------------+------------!
! 1.0449+05 ! 14.6959 ! 110.3446 ! 0.0 !
! 1.2539+05 ! 14.6959 ! 108.4471 ! 0.0 !
! 1.4629+05 ! 14.6959 ! 106.5497 ! 0.0 !
! 1.6718+05 ! 14.6959 ! 104.6523 ! 0.0 !
! 1.8808+05 ! 14.6959 ! 102.7550 ! 0.0 !
!------------+------------+------------+------------!
! 2.0898+05 ! 14.6959 ! 100.8579 ! 0.0 !
! 2.2988+05 ! 14.6959 ! 98.9608 ! 0.0 !
! 2.5078+05 ! 14.6959 ! 97.0639 ! 0.0 !
! 2.7167+05 ! 14.6959 ! 95.1671 ! 0.0 !
! 2.9257+05 ! 14.6959 ! 93.2705 ! 0.0 !
!------------+------------+------------+------------!
! 3.1347+05 ! 14.6959 ! 91.3740 ! 0.0 !
! 3.3437+05 ! 14.6959 ! 89.4778 ! 0.0 !
! 3.5527+05 ! 14.6959 ! 87.5817 ! 0.0 !
! 3.7616+05 ! 14.6959 ! 85.6859 ! 0.0 !
! 3.9706+05 ! 14.6959 ! 83.7904 ! 0.0 !
!------------+------------+------------+------------!
! 4.1796+05 ! 14.6959 ! 81.8950 ! 0.0 !
! 4.3886+05 ! 14.6959 ! 80.0000 ! 0.0 !
-----------------------------------------------------
218
HEATX HOT-TQCUR HX-204 TQCURV INLET
-------------------------------------
PRESSURE PROFILE: CONSTANT2
PRESSURE DROP: 0.0 PSI
PROPERTY OPTION SET: RK-SOAVE STANDARD RKS EQUATION OF STATE
-----------------------------------------------------
! DUTY ! PRES ! TEMP ! VFRAC !
! ! ! ! !
! ! ! ! !
! ! ! ! !
! BTU/HR ! PSIA ! F ! !
! ! ! ! !
!============!============!============!============!
! 0.0 ! 273.5000 ! 326.7066 ! 1.0000 !
! 2.0898+04 ! 273.5000 ! 322.0500 ! 1.0000 !
! 4.1796+04 ! 273.5000 ! 317.3835 ! 1.0000 !
! 6.2694+04 ! 273.5000 ! 312.7068 ! 1.0000 !
! 8.3592+04 ! 273.5000 ! 308.0201 ! 1.0000 !
!------------+------------+------------+------------!
! 1.0449+05 ! 273.5000 ! 303.3230 ! 1.0000 !
! 1.2539+05 ! 273.5000 ! 298.6157 ! 1.0000 !
! 1.4629+05 ! 273.5000 ! 293.8979 ! 1.0000 !
! 1.6718+05 ! 273.5000 ! 289.1697 ! 1.0000 !
! 1.8808+05 ! 273.5000 ! 284.4308 ! 1.0000 !
!------------+------------+------------+------------!
! 2.0898+05 ! 273.5000 ! 279.6813 ! 1.0000 !
! 2.2988+05 ! 273.5000 ! 274.9210 ! 1.0000 !
! 2.5078+05 ! 273.5000 ! 270.1499 ! 1.0000 !
219
! 2.7167+05 ! 273.5000 ! 265.3678 ! 1.0000 !
! 2.9257+05 ! 273.5000 ! 260.5747 ! 1.0000 !
!------------+------------+------------+------------!
! 3.1347+05 ! 273.5000 ! 255.7705 ! 1.0000 !
! 3.3437+05 ! 273.5000 ! 250.9551 ! 1.0000 !
! 3.5527+05 ! 273.5000 ! 246.1283 ! 1.0000 !
! 3.7616+05 ! 273.5000 ! 241.2902 ! 1.0000 !
! 3.9706+05 ! 273.5000 ! 236.4406 ! 1.0000 !
!------------+------------+------------+------------!
! 4.1796+05 ! 273.5000 ! 231.5794 ! 1.0000 !
! 4.3886+05 ! 273.5000 ! 226.7066 ! 1.0000 !
-----------------------------------------------------
220
MASS(LB/HR ) 14388.0 14388.0 0.00000
ENTHALPY(BTU/HR ) -0.627804E+08 -0.627804E+08 0.00000
PRESSURE SPECIFICATION:
HOT SIDE PRESSURE DROP PSI 0.0000
221
COLD SIDE PRESSURE DROP PSI 0.0000
STREAMS:
--------------------------------------
| |
CG-6 ----->| HOT |-----> CG-7
T= 2.9215D+02 | | T= 1.9215D+02
P= 3.8850D+02 | | P= 3.8850D+02
V= 1.0000D+00 | | V= 1.0000D+00
| |
CW-OUT5 <-----| COLD |<----- CW-IN5
T= 1.2078D+02 | | T= 8.0000D+01
P= 1.4696D+01 | | P= 1.4696D+01
V= 0.0000D+00 | | V= 0.0000D+00
--------------------------------------
222
LOG-MEAN TEMPERATURE DIFFERENCE:
LMTD CORRECTION FACTOR 1.0000
LMTD (CORRECTED) F 139.6743
NUMBER OF SHELLS IN SERIES 1
PRESSURE DROP:
HOTSIDE, TOTAL PSI 0.0000
COLDSIDE, TOTAL PSI 0.0000
-----------------------------------------------------
! DUTY ! PRES ! TEMP ! VFRAC !
! ! ! ! !
! ! ! ! !
! ! ! ! !
! BTU/HR ! PSIA ! F ! !
! ! ! ! !
!============!============!============!============!
! 0.0 ! 14.6959 ! 120.7836 ! 0.0 !
! 2.0664+04 ! 14.6959 ! 118.8408 ! 0.0 !
! 4.1329+04 ! 14.6959 ! 116.8980 ! 0.0 !
! 6.1993+04 ! 14.6959 ! 114.9552 ! 0.0 !
! 8.2658+04 ! 14.6959 ! 113.0123 ! 0.0 !
!------------+------------+------------+------------!
223
! 1.0332+05 ! 14.6959 ! 111.0695 ! 0.0 !
! 1.2399+05 ! 14.6959 ! 109.1267 ! 0.0 !
! 1.4465+05 ! 14.6959 ! 107.1840 ! 0.0 !
! 1.6532+05 ! 14.6959 ! 105.2413 ! 0.0 !
! 1.8598+05 ! 14.6959 ! 103.2987 ! 0.0 !
!------------+------------+------------+------------!
! 2.0664+05 ! 14.6959 ! 101.3562 ! 0.0 !
! 2.2731+05 ! 14.6959 ! 99.4138 ! 0.0 !
! 2.4797+05 ! 14.6959 ! 97.4715 ! 0.0 !
! 2.6864+05 ! 14.6959 ! 95.5294 ! 0.0 !
! 2.8930+05 ! 14.6959 ! 93.5875 ! 0.0 !
!------------+------------+------------+------------!
! 3.0997+05 ! 14.6959 ! 91.6457 ! 0.0 !
! 3.3063+05 ! 14.6959 ! 89.7042 ! 0.0 !
! 3.5130+05 ! 14.6959 ! 87.7628 ! 0.0 !
! 3.7196+05 ! 14.6959 ! 85.8217 ! 0.0 !
! 3.9263+05 ! 14.6959 ! 83.8809 ! 0.0 !
!------------+------------+------------+------------!
! 4.1329+05 ! 14.6959 ! 81.9403 ! 0.0 !
! 4.3395+05 ! 14.6959 ! 80.0000 ! 0.0 !
-----------------------------------------------------
-----------------------------------------------------
! DUTY ! PRES ! TEMP ! VFRAC !
224
! ! ! ! !
! ! ! ! !
! ! ! ! !
! BTU/HR ! PSIA ! F ! !
! ! ! ! !
!============!============!============!============!
! 0.0 ! 388.5000 ! 292.1519 ! 1.0000 !
! 2.0664+04 ! 388.5000 ! 287.4937 ! 1.0000 !
! 4.1329+04 ! 388.5000 ! 282.8255 ! 1.0000 !
! 6.1993+04 ! 388.5000 ! 278.1473 ! 1.0000 !
! 8.2658+04 ! 388.5000 ! 273.4590 ! 1.0000 !
!------------+------------+------------+------------!
! 1.0332+05 ! 388.5000 ! 268.7606 ! 1.0000 !
! 1.2399+05 ! 388.5000 ! 264.0521 ! 1.0000 !
! 1.4465+05 ! 388.5000 ! 259.3332 ! 1.0000 !
! 1.6532+05 ! 388.5000 ! 254.6040 ! 1.0000 !
! 1.8598+05 ! 388.5000 ! 249.8644 ! 1.0000 !
!------------+------------+------------+------------!
! 2.0664+05 ! 388.5000 ! 245.1143 ! 1.0000 !
! 2.2731+05 ! 388.5000 ! 240.3536 ! 1.0000 !
! 2.4797+05 ! 388.5000 ! 235.5823 ! 1.0000 !
! 2.6864+05 ! 388.5000 ! 230.8003 ! 1.0000 !
! 2.8930+05 ! 388.5000 ! 226.0076 ! 1.0000 !
!------------+------------+------------+------------!
! 3.0997+05 ! 388.5000 ! 221.2040 ! 1.0000 !
! 3.3063+05 ! 388.5000 ! 216.3896 ! 1.0000 !
! 3.5130+05 ! 388.5000 ! 211.5642 ! 1.0000 !
! 3.7196+05 ! 388.5000 ! 206.7278 ! 1.0000 !
! 3.9263+05 ! 388.5000 ! 201.8803 ! 1.0000 !
!------------+------------+------------+------------!
225
! 4.1329+05 ! 388.5000 ! 197.0217 ! 1.0000 !
! 4.3395+05 ! 388.5000 ! 192.1519 ! 1.0000 !
-----------------------------------------------------
226
*** INPUT DATA ***
PRESSURE SPECIFICATION:
HOT SIDE PRESSURE DROP PSI 0.0000
COLD SIDE PRESSURE DROP PSI 0.0000
STREAMS:
--------------------------------------
227
| |
CG-8 ----->| HOT |-----> CG-9
T= 2.5831D+02 | | T= 1.4231D+02
P= 5.5950D+02 | | P= 5.5950D+02
V= 1.0000D+00 | | V= 1.0000D+00
| |
CW-OUT6 <-----| COLD |<----- CW-IN6
T= 1.2075D+02 | | T= 8.0000D+01
P= 1.4696D+01 | | P= 1.4696D+01
V= 0.0000D+00 | | V= 0.0000D+00
--------------------------------------
PRESSURE DROP:
HOTSIDE, TOTAL PSI 0.0000
COLDSIDE, TOTAL PSI 0.0000
228
HEATX COLD-TQCU HX-206 TQCURV INLET
-------------------------------------
PRESSURE PROFILE: CONSTANT2
PRESSURE DROP: 0.0 PSI
PROPERTY OPTION SET: RK-SOAVE STANDARD RKS EQUATION OF STATE
-----------------------------------------------------
! DUTY ! PRES ! TEMP ! VFRAC !
! ! ! ! !
! ! ! ! !
! ! ! ! !
! BTU/HR ! PSIA ! F ! !
! ! ! ! !
!============!============!============!============!
! 0.0 ! 14.6959 ! 120.7539 ! 0.0 !
! 2.3727+04 ! 14.6959 ! 118.8126 ! 0.0 !
! 4.7455+04 ! 14.6959 ! 116.8712 ! 0.0 !
! 7.1182+04 ! 14.6959 ! 114.9297 ! 0.0 !
! 9.4909+04 ! 14.6959 ! 112.9883 ! 0.0 !
!------------+------------+------------+------------!
! 1.1864+05 ! 14.6959 ! 111.0469 ! 0.0 !
! 1.4236+05 ! 14.6959 ! 109.1055 ! 0.0 !
! 1.6609+05 ! 14.6959 ! 107.1642 ! 0.0 !
! 1.8982+05 ! 14.6959 ! 105.2229 ! 0.0 !
! 2.1355+05 ! 14.6959 ! 103.2817 ! 0.0 !
!------------+------------+------------+------------!
! 2.3727+05 ! 14.6959 ! 101.3406 ! 0.0 !
! 2.6100+05 ! 14.6959 ! 99.3997 ! 0.0 !
! 2.8473+05 ! 14.6959 ! 97.4588 ! 0.0 !
229
! 3.0845+05 ! 14.6959 ! 95.5181 ! 0.0 !
! 3.3218+05 ! 14.6959 ! 93.5776 ! 0.0 !
!------------+------------+------------+------------!
! 3.5591+05 ! 14.6959 ! 91.6372 ! 0.0 !
! 3.7964+05 ! 14.6959 ! 89.6971 ! 0.0 !
! 4.0336+05 ! 14.6959 ! 87.7572 ! 0.0 !
! 4.2709+05 ! 14.6959 ! 85.8175 ! 0.0 !
! 4.5082+05 ! 14.6959 ! 83.8781 ! 0.0 !
!------------+------------+------------+------------!
! 4.7455+05 ! 14.6959 ! 81.9389 ! 0.0 !
! 4.9827+05 ! 14.6959 ! 80.0000 ! 0.0 !
-----------------------------------------------------
-----------------------------------------------------
! DUTY ! PRES ! TEMP ! VFRAC !
! ! ! ! !
! ! ! ! !
! ! ! ! !
! BTU/HR ! PSIA ! F ! !
! ! ! ! !
!============!============!============!============!
! 0.0 ! 559.5000 ! 258.3075 ! 1.0000 !
! 2.3727+04 ! 559.5000 ! 252.9138 ! 1.0000 !
! 4.7455+04 ! 559.5000 ! 247.5075 ! 1.0000 !
230
! 7.1182+04 ! 559.5000 ! 242.0884 ! 1.0000 !
! 9.4909+04 ! 559.5000 ! 236.6565 ! 1.0000 !
!------------+------------+------------+------------!
! 1.1864+05 ! 559.5000 ! 231.2117 ! 1.0000 !
! 1.4236+05 ! 559.5000 ! 225.7539 ! 1.0000 !
! 1.6609+05 ! 559.5000 ! 220.2831 ! 1.0000 !
! 1.8982+05 ! 559.5000 ! 214.7993 ! 1.0000 !
! 2.1355+05 ! 559.5000 ! 209.3023 ! 1.0000 !
!------------+------------+------------+------------!
! 2.3727+05 ! 559.5000 ! 203.7921 ! 1.0000 !
! 2.6100+05 ! 559.5000 ! 198.2688 ! 1.0000 !
! 2.8473+05 ! 559.5000 ! 192.7323 ! 1.0000 !
! 3.0845+05 ! 559.5000 ! 187.1825 ! 1.0000 !
! 3.3218+05 ! 559.5000 ! 181.6194 ! 1.0000 !
!------------+------------+------------+------------!
! 3.5591+05 ! 559.5000 ! 176.0431 ! 1.0000 !
! 3.7964+05 ! 559.5000 ! 170.4535 ! 1.0000 !
! 4.0336+05 ! 559.5000 ! 164.8507 ! 1.0000 !
! 4.2709+05 ! 559.5000 ! 159.2346 ! 1.0000 !
! 4.5082+05 ! 559.5000 ! 153.6054 ! 1.0000 !
!------------+------------+------------+------------!
! 4.7455+05 ! 559.5000 ! 147.9630 ! 1.0000 !
! 4.9827+05 ! 559.5000 ! 142.3075 ! 1.0000 !
-----------------------------------------------------
231
CW-IN3 ENTHALPY:
------ BTU/LBMOL -1.2421+05
BTU/LB -6894.4368
STREAM ID CW-IN3 BTU/HR -6.5497+07
FROM : ---- ENTROPY:
TO : HX-203 BTU/LBMOL-R -40.7945
BTU/LB-R -2.2644
SUBSTREAM: MIXED DENSITY:
PHASE: LIQUID LBMOL/CUFT 3.4388
COMPONENTS: LBMOL/HR LB/CUFT 61.9503
HYDROGEN 0.0 AVG MW 18.0153
METHANE 0.0
MONOXIDE 0.0 CW-OUT3
ETHANE 0.0 -------
ETHENE 0.0
PROPANE 0.0 STREAM ID CW-OUT3
PROPENE 0.0 FROM : HX-203
BUTANE 0.0 TO : ----
WATER 527.3301
TOTAL FLOW: SUBSTREAM: MIXED
LBMOL/HR 527.3301 PHASE: LIQUID
LB/HR 9500.0000 COMPONENTS: LBMOL/HR
CUFT/HR 153.3488 HYDROGEN 0.0
STATE VARIABLES: METHANE 0.0
TEMP F 80.0000 MONOXIDE 0.0
PRES PSIA 14.6959 ETHANE 0.0
VFRAC 0.0 ETHENE 0.0
LFRAC 1.0000 PROPANE 0.0
SFRAC 0.0 PROPENE 0.0
232
BUTANE 0.0
WATER 527.3301 SUBSTREAM: MIXED
TOTAL FLOW: PHASE: LIQUID
LBMOL/HR 527.3301 COMPONENTS: LBMOL/HR
LB/HR 9500.0000 HYDROGEN 0.0
CUFT/HR 156.7670 METHANE 0.0
STATE VARIABLES: MONOXIDE 0.0
TEMP F 119.8091 ETHANE 0.0
PRES PSIA 14.6959 ETHENE 0.0
VFRAC 0.0 PROPANE 0.0
LFRAC 1.0000 PROPENE 0.0
SFRAC 0.0 BUTANE 0.0
ENTHALPY: WATER 530.2166
BTU/LBMOL -1.2338+05 TOTAL FLOW:
BTU/LB -6848.5193 LBMOL/HR 530.2166
BTU/HR -6.5061+07 LB/HR 9552.0000
ENTROPY: CUFT/HR 154.1882
BTU/LBMOL-R -39.3155 STATE VARIABLES:
BTU/LB-R -2.1823 TEMP F 80.0000
DENSITY: PRES PSIA 14.6959
LBMOL/CUFT 3.3638 VFRAC 0.0
LB/CUFT 60.5995 LFRAC 1.0000
AVG MW 18.0153 SFRAC 0.0
ENTHALPY:
CW-IN4 BTU/LBMOL -1.2421+05
------ BTU/LB -6894.4368
BTU/HR -6.5856+07
STREAM ID CW-IN4 ENTROPY:
FROM : ---- BTU/LBMOL-R -40.7945
TO : HX-204 BTU/LB-R -2.2644
233
DENSITY: PRES PSIA 14.6959
LBMOL/CUFT 3.4388 VFRAC 0.0
LB/CUFT 61.9503 LFRAC 1.0000
AVG MW 18.0153 SFRAC 0.0
ENTHALPY:
CW-OUT4 BTU/LBMOL -1.2338+05
------- BTU/LB -6848.4927
BTU/HR -6.5417+07
STREAM ID CW-OUT4 ENTROPY:
FROM : HX-204 BTU/LBMOL-R -39.3147
TO : ---- BTU/LB-R -2.1823
DENSITY:
SUBSTREAM: MIXED LBMOL/CUFT 3.3637
PHASE: LIQUID LB/CUFT 60.5987
COMPONENTS: LBMOL/HR AVG MW 18.0153
HYDROGEN 0.0
METHANE 0.0 CW-IN5
MONOXIDE 0.0 ------
ETHANE 0.0
ETHENE 0.0 STREAM ID CW-IN5
PROPANE 0.0 FROM : ----
PROPENE 0.0 TO : HX-205
BUTANE 0.0
WATER 530.2166 SUBSTREAM: MIXED
TOTAL FLOW: PHASE: LIQUID
LBMOL/HR 530.2166 COMPONENTS: LBMOL/HR
LB/HR 9552.0000 HYDROGEN 0.0
CUFT/HR 157.6272 METHANE 0.0
STATE VARIABLES: MONOXIDE 0.0
TEMP F 119.8321 ETHANE 0.0
234
ETHENE 0.0 STREAM ID CW-OUT5
PROPANE 0.0 FROM : HX-205
PROPENE 0.0 TO : ----
BUTANE 0.0
WATER 512.0653 SUBSTREAM: MIXED
TOTAL FLOW: PHASE: LIQUID
LBMOL/HR 512.0653 COMPONENTS: LBMOL/HR
LB/HR 9225.0000 HYDROGEN 0.0
CUFT/HR 148.9098 METHANE 0.0
STATE VARIABLES: MONOXIDE 0.0
TEMP F 80.0000 ETHANE 0.0
PRES PSIA 14.6959 ETHENE 0.0
VFRAC 0.0 PROPANE 0.0
LFRAC 1.0000 PROPENE 0.0
SFRAC 0.0 BUTANE 0.0
ENTHALPY: WATER 512.0653
BTU/LBMOL -1.2421+05 TOTAL FLOW:
BTU/LB -6894.4368 LBMOL/HR 512.0653
BTU/HR -6.3601+07 LB/HR 9225.0000
ENTROPY: CUFT/HR 152.3132
BTU/LBMOL-R -40.7945 STATE VARIABLES:
BTU/LB-R -2.2644 TEMP F 120.7836
DENSITY: PRES PSIA 14.6959
LBMOL/CUFT 3.4388 VFRAC 0.0
LB/CUFT 61.9503 LFRAC 1.0000
AVG MW 18.0153 SFRAC 0.0
ENTHALPY:
CW-OUT5 BTU/LBMOL -1.2336+05
------- BTU/LB -6847.3957
BTU/HR -6.3167+07
235
ENTROPY: CUFT/HR 171.1050
BTU/LBMOL-R -39.2806 STATE VARIABLES:
BTU/LB-R -2.1804 TEMP F 80.0000
DENSITY: PRES PSIA 14.6959
LBMOL/CUFT 3.3619 VFRAC 0.0
LB/CUFT 60.5660 LFRAC 1.0000
AVG MW 18.0153 SFRAC 0.0
ENTHALPY:
CW-IN6 BTU/LBMOL -1.2421+05
------ BTU/LB -6894.4368
BTU/HR -7.3081+07
STREAM ID CW-IN6 ENTROPY:
FROM : ---- BTU/LBMOL-R -40.7945
TO : HX-206 BTU/LB-R -2.2644
DENSITY:
SUBSTREAM: MIXED LBMOL/CUFT 3.4388
PHASE: LIQUID LB/CUFT 61.9503
COMPONENTS: LBMOL/HR AVG MW 18.0153
HYDROGEN 0.0
METHANE 0.0 CW-OUT6
MONOXIDE 0.0 -------
ETHANE 0.0
ETHENE 0.0 STREAM ID CW-OUT6
PROPANE 0.0 FROM : HX-206
PROPENE 0.0 TO : ----
BUTANE 0.0
WATER 588.3894 SUBSTREAM: MIXED
TOTAL FLOW: PHASE: LIQUID
LBMOL/HR 588.3894 COMPONENTS: LBMOL/HR
LB/HR 1.0600+04 HYDROGEN 0.0
236
METHANE 0.0 VFRAC 0.0
MONOXIDE 0.0 LFRAC 1.0000
ETHANE 0.0 SFRAC 0.0
ETHENE 0.0 ENTHALPY:
PROPANE 0.0 BTU/LBMOL -1.2336+05
PROPENE 0.0 BTU/LB -6847.4299
BUTANE 0.0 BTU/HR -7.2583+07
WATER 588.3894 ENTROPY:
TOTAL FLOW: BTU/LBMOL-R -39.2817
LBMOL/HR 588.3894 BTU/LB-R -2.1805
LB/HR 1.0600+04 DENSITY:
CUFT/HR 175.0128 LBMOL/CUFT 3.3620
STATE VARIABLES: LB/CUFT 60.5670
TEMP F 120.7539 AVG MW 18.0153
PRES PSIA 14.6959
237
Section 200: Pump blocks and streams
BLOCK: P-201 MODEL: PUMP
----------------------------
INLET STREAM: BW-1
OUTLET STREAM: BW-2
PROPERTY OPTION SET: STEAM-TA ASME STEAM TABLE EQUATION OF STATE
FLASH SPECIFICATIONS:
LIQUID PHASE CALCULATION
NO FLASH PERFORMED
MAXIMUM NUMBER OF ITERATIONS 30
238
TOLERANCE 0.000100000
239
UTILITIES CO2E PRODUCTION 0.00000 LB/HR
TOTAL CO2E PRODUCTION 0.00000 LB/HR
FLASH SPECIFICATIONS:
LIQUID PHASE CALCULATION
NO FLASH PERFORMED
MAXIMUM NUMBER OF ITERATIONS 30
TOLERANCE 0.000100000
240
PROPERTY OPTION SET: STEAM-TA ASME STEAM TABLE EQUATION OF STATE
FLASH SPECIFICATIONS:
LIQUID PHASE CALCULATION
NO FLASH PERFORMED
MAXIMUM NUMBER OF ITERATIONS 30
TOLERANCE 0.000100000
241
NPSH AVAILABLE FT-LBF/LB 59.0516
FLUID POWER HP 0.12660
BRAKE POWER HP 0.15629
ELECTRICITY KW 0.14389
PUMP EFFICIENCY USED 0.81000
NET WORK REQUIRED HP 0.19295
HEAD DEVELOPED FT-LBF/LB 121.327
SUBSTREAM: MIXED
PHASE: LIQUID LIQUID LIQUID LIQUID LIQUID
COMPONENTS: LBMOL/HR
WATER 1.3443+04 1.3443+04 114.6804 114.6804 1.0296+04
TOTAL FLOW:
LBMOL/HR 1.3443+04 1.3443+04 114.6804 114.6804 1.0296+04
LB/HR 2.4218+05 2.4218+05 2066.0000 2066.0000 1.8548+05
CUFT/HR 4048.1762 4043.4331 33.4703 33.4752 2985.6609
STATE VARIABLES:
TEMP F 212.0000 212.6674 120.0596 120.0000 90.0000
PRES PSIA 64.6959 484.6959 79.0000 27.0000 35.0000
VFRAC 0.0 0.0 0.0 0.0 0.0
LFRAC 1.0000 1.0000 1.0000 1.0000 1.0000
SFRAC 0.0 0.0 0.0 0.0 0.0
242
ENTHALPY:
BTU/LBMOL -1.2045+05 -1.2042+05 -1.2211+05 -1.2211+05 -1.2265+05
BTU/LB -6686.0829 -6684.4790 -6777.9843 -6778.1768 -6808.0526
BTU/HR -1.6192+09 -1.6188+09 -1.4003+07 -1.4004+07 -1.2628+09
ENTROPY:
BTU/LBMOL-R -34.9473 -34.9399 -37.5992 -37.5999 -38.5541
BTU/LB-R -1.9399 -1.9395 -2.0871 -2.0871 -2.1401
DENSITY:
LBMOL/CUFT 3.3208 3.3247 3.4263 3.4258 3.4484
LB/CUFT 59.8245 59.8946 61.7263 61.7174 62.1236
AVG MW 18.0153 18.0153 18.0153 18.0153 18.0153
243
Section 200: Blower block and streams
244
*** RESULTS ***
245
FU-1 SFRAC 0.0
---- ENTHALPY:
BTU/LBMOL -2080.0146
STREAM ID FU-1 BTU/LB -417.5123
FROM : ---- BTU/HR -7.4609+05
TO : B-201 ENTROPY:
BTU/LBMOL-R -1.7497
SUBSTREAM: MIXED BTU/LB-R -0.3512
PHASE: VAPOR DENSITY:
COMPONENTS: LBMOL/HR LBMOL/CUFT 2.5848-03
HYDROGEN 300.6131 LB/CUFT 1.2877-02
METHANE 37.3377 AVG MW 4.9819
ETHANE 0.0
ETHENE 20.7459 FU-2
PROPANE 0.0 ----
PROPENE 0.0
BUTANE 0.0 STREAM ID FU-2
WATER 0.0 FROM : B-201
TOTAL FLOW: TO : ----
LBMOL/HR 358.6967
LB/HR 1787.0000 SUBSTREAM: MIXED
CUFT/HR 1.3877+05 PHASE: VAPOR
STATE VARIABLES: COMPONENTS: LBMOL/HR
TEMP F 70.0000 HYDROGEN 300.6131
PRES PSIA 14.7000 METHANE 37.3377
VFRAC 1.0000 ETHANE 0.0
LFRAC 0.0 ETHENE 20.7459
246
PROPANE 0.0 SFRAC 0.0
PROPENE 0.0 ENTHALPY:
BUTANE 0.0 BTU/LBMOL -419.4368
WATER 0.0 BTU/LB -84.1917
TOTAL FLOW: BTU/HR -1.5045+05
LBMOL/HR 358.6967 ENTROPY:
LB/HR 1787.0000 BTU/LBMOL-R -1.7497
CUFT/HR 5.3056+04 BTU/LB-R -0.3512
STATE VARIABLES: DENSITY:
TEMP F 292.8926 LBMOL/CUFT 6.7607-03
PRES PSIA 54.7000 LB/CUFT 3.3681-02
VFRAC 1.0000 AVG MW 4.9819
LFRAC 0.0
247
Section 300: Separations Blocks and Streams
**********************
**** INPUT DATA ****
**********************
NUMBER OF STAGES 25
ALGORITHM OPTION STANDARD
ABSORBER OPTION NO
INITIALIZATION OPTION STANDARD
HYDRAULIC PARAMETER CALCULATIONS NO
INSIDE LOOP CONVERGENCE METHOD BROYDEN
DESIGN SPECIFICATION METHOD NESTED
MAXIMUM NO. OF OUTSIDE LOOP ITERATIONS 70
MAXIMUM NO. OF INSIDE LOOP ITERATIONS 10
MAXIMUM NUMBER OF FLASH ITERATIONS 30
FLASH TOLERANCE 0.000100000
OUTSIDE LOOP CONVERGENCE TOLERANCE 0.000100000
248
**** COL-SPECS ****
*******************
**** RESULTS ****
*******************
OUTLET STREAMS
--------------
ETHYLENE ETHANE
COMPONENT:
HYDROGEN 1.0000 0.0000
METHANE 1.0000 .12196E-10
ETHENE .99649 .35118E-02
ETHANE .73807E-01 .92619
PROPENE .51892E-08 1.0000
PROPANE .51391E-09 1.0000
249
COMPONENT MASS BALANCE 0.18410E-04 STAGE= 12 COMP=HYDROGEN
ENERGY BALANCE 0.10868E-04 STAGE= 18
**NOTE** REPORTED VALUES FOR STAGE LIQUID AND VAPOR RATES ARE THE
FLOWS
FROM THE STAGE INCLUDING ANY SIDE PRODUCT.
ENTHALPY
STAGE TEMPERATURE PRESSURE BTU/LBMOL HEAT DUTY
F PSIA LIQUID VAPOR BTU/HR
250
24 0.1577E+05 0.1565E+05
25 90.00 0.1568E+05 89.9994
251
**** K-VALUES ****
STAGE HYDROGEN METHANE ETHENE ETHANE PROPENE
1 31.155 4.0983 0.99497 0.69961 0.21581
2 30.421 4.0692 1.0005 0.70541 0.21982
11 29.994 4.0719 1.0287 0.72073 0.22991
12 29.927 4.0759 1.0368 0.72501 0.23266
13 29.827 4.0842 1.0502 0.73237 0.23724
14 29.722 4.0965 1.0677 0.74192 0.24318
24 27.785 4.4294 1.4210 0.96152 0.37673
25 27.650 4.4433 1.4376 0.97288 0.38392
252
STAGE HYDROGEN METHANE ETHENE ETHANE PROPENE
1 0.11705E-04 0.51276E-02 0.99005 0.48084E-02 0.10983E-16
2 0.14045E-05 0.15999E-02 0.99173 0.66655E-02 0.47119E-16
11 0.10924E-05 0.59733E-03 0.92580 0.73603E-01 0.14651E-10
12 0.10931E-05 0.59752E-03 0.90629 0.93107E-01 0.57818E-10
13 0.36649E-07 0.14708E-03 0.87644 0.12341 0.59611E-10
14 0.12326E-08 0.36119E-04 0.83641 0.16355 0.62042E-10
24 0.30709E-23 0.19271E-10 0.11193 0.88807 0.48607E-08
25 0.11091E-24 0.43603E-11 0.78717E-01 0.92128 0.12754E-07
********************************
***** HYDRAULIC PARAMETERS *****
********************************
TEMPERATURE
253
F
STAGE LIQUID FROM VAPOR TO
1 -20.572 -19.359
2 -19.359 -19.135
11 -16.354 -15.563
12 -15.563 -14.288
13 -14.288 -12.667
14 -12.667 -10.589
24 15.980 17.281
25 17.281 17.281
254
14 -.14864 0.29971 2032.8 10109.
24 -.70344E-01 0.30615 2071.8 10083.
25 -.52559E-01 0.0000 0.0000
************************************
***** TRAY SIZING CALCULATIONS *****
************************************
*******************
*** SECTION 1 ***
*******************
DESIGN PARAMETERS
-----------------
PEAK CAPACITY FACTOR 1.00000
SYSTEM FOAMING FACTOR 1.00000
FLOODING FACTOR 0.80000
MINIMUM COLUMN DIAMETER FT 1.00000
MINIMUM DC AREA/COLUMN AREA 0.100000
HOLE AREA/ACTIVE AREA 0.100000
DOWNCOMER DESIGN BASIS EQUAL FLOW PATH LENGTH
TRAY SPECIFICATIONS
-------------------
TRAY TYPE SIEVE
NUMBER OF PASSES 1
TRAY SPACING FT 1.50000
255
CENTER DOWNCOMER WIDTH FT 0.0
CENTER WEIR LENGTH FT MISSING
OFF-CENTER DOWNCOMER WIDTH FT 0.0
OFF-CENTER SHORT WEIR LENGTH FT MISSING
OFF-CENTER LONG WEIR LENGTH FT MISSING
TRAY CENTER TO OCDC CENTER FT 0.0
FLOODING DC BACKUP/
STAGE FACTOR PRES. DROP DC BACKUP (TSPC+WHT)
PSI FT
2 76.71 0.7567E-01 0.7804 48.03
3 76.74 0.7569E-01 0.7809 48.06
4 76.74 0.7569E-01 0.7811 48.07
5 76.74 0.7569E-01 0.7812 48.07
256
6 76.74 0.7568E-01 0.7813 48.08
7 76.73 0.7566E-01 0.7814 48.08
8 76.71 0.7564E-01 0.7814 48.09
9 76.70 0.7561E-01 0.7815 48.09
10 76.68 0.7557E-01 0.7815 48.09
11 76.65 0.7551E-01 0.7815 48.09
12 78.38 0.7674E-01 0.8249 50.77
13 78.35 0.7665E-01 0.8253 50.79
14 78.30 0.7649E-01 0.8254 50.79
15 78.25 0.7631E-01 0.8260 50.83
16 78.22 0.7611E-01 0.8273 50.91
17 78.24 0.7590E-01 0.8297 51.06
18 78.33 0.7572E-01 0.8335 51.30
19 78.52 0.7559E-01 0.8389 51.62
20 78.79 0.7552E-01 0.8454 52.03
21 79.12 0.7550E-01 0.8524 52.46
22 79.44 0.7553E-01 0.8593 52.88
23 79.75 0.7558E-01 0.8653 53.25
24 80.00 0.7563E-01 0.8704 53.56
257
BLOCK: DEETH MODEL: RADFRAC
-------------------------------
CONFIGURATION NOTES
INLETS - C2H4-REC STAGE 20
OUTLETS - H2-CH4-2 STAGE 1
DE-BOT STAGE 32
C2-OUT STAGE 6
PROPERTY OPTION SET: PENG-ROB STANDARD PR EQUATION OF STATE
**********************
**** INPUT DATA ****
**********************
NUMBER OF STAGES 32
ALGORITHM OPTION STANDARD
ABSORBER OPTION NO
INITIALIZATION OPTION STANDARD
HYDRAULIC PARAMETER CALCULATIONS NO
INSIDE LOOP CONVERGENCE METHOD BROYDEN
DESIGN SPECIFICATION METHOD NESTED
MAXIMUM NO. OF OUTSIDE LOOP ITERATIONS 70
MAXIMUM NO. OF INSIDE LOOP ITERATIONS 10
MAXIMUM NUMBER OF FLASH ITERATIONS 30
FLASH TOLERANCE 0.000100000
OUTSIDE LOOP CONVERGENCE TOLERANCE 0.000100000
258
MOLAR VAPOR DIST / TOTAL DIST 1.00000
MASS REFLUX RATIO 25.0000
MASS DISTILLATE RATE LB/HR 120.000
*******************
**** RESULTS ****
*******************
OUTLET STREAMS
--------------
H2-CH4-2 DE-BOT C2-OUT
COMPONENT:
HYDROGEN .99372 0.0000 .62819E-02
METHANE .92076 .67575E-11 .79235E-01
ETHENE .23133E-01 .20315E-02 .97484
ETHANE .72976E-03 .49190 .50737
PROPENE .11939E-14 1.0000 .79918E-08
PROPANE 0.0000 1.0000 .30339E-09
BUTANE 0.0000 1.0000 .46527E-13
259
COMPONENT MASS BALANCE 0.33906E-04 STAGE= 1 COMP=HYDROGEN
ENERGY BALANCE 0.17310E-03 STAGE= 1
**NOTE** REPORTED VALUES FOR STAGE LIQUID AND VAPOR RATES ARE THE
FLOWS
FROM THE STAGE INCLUDING ANY SIDE PRODUCT.
ENTHALPY
STAGE TEMPERATURE PRESSURE BTU/LBMOL HEAT DUTY
F PSIA LIQUID VAPOR BTU/HR
260
STAGE FLOW RATE FEED RATE PRODUCT RATE
LB/HR LB/HR LB/HR
LIQUID VAPOR LIQUID VAPOR MIXED LIQUID VAPOR
1 3000. 120.0 120.0022
2 3597. 3120.
5 3801. 3916.
6 3799. 3921. 1499.9994
7 2297. 3919.
18 2277. 3904.
19 2256. 3897. 12.0557
20 5063. 3864. 2085.5432
21 5104. 4586.
22 5105. 4626.
23 5101. 4628.
31 5156. 4582.
32 477.6 4679. 477.5973
261
23 0.15945E-02 0.26162E-03
31 0.11718E-01 0.89081E-03
32 0.18167E-01 0.34148E-02
262
21 58.582 5.7135 1.1602 0.75292 0.20306
22 58.012 5.7697 1.2054 0.77914 0.21526
23 57.523 5.8349 1.2565 0.80823 0.22916
31 57.427 8.3057 2.2035 1.5225 0.51926
32 55.570 9.3084 2.6546 1.9098 0.69044
263
19 0.60796E-03 0.65829E-04
20 0.22789E-02 0.51391E-03
21 0.22879E-02 0.50968E-03
22 0.23167E-02 0.50901E-03
23 0.23538E-02 0.50905E-03
31 0.14165E-01 0.14193E-02
32 0.20469E-01 0.50714E-02
********************************
***** HYDRAULIC PARAMETERS *****
********************************
264
*** DEFINITIONS ***
TEMPERATURE
F
STAGE LIQUID FROM VAPOR TO
1 -129.79 -63.032
2 -63.032 -48.675
5 -44.805 -44.162
6 -44.162 -43.356
7 -43.356 -42.655
18 -38.984 -37.940
19 -37.940 -35.319
20 -34.323 -29.695
21 -29.695 -26.598
22 -26.598 -23.249
23 -23.249 -19.471
31 33.509 57.475
32 57.475 57.475
265
19 2256.4 3876.4 77.431 2483.3 28.661 27.709
20 5063.4 4585.8 171.84 2861.1 29.274 28.526
21 5103.8 4626.2 174.10 2879.1 29.485 28.753
22 5105.1 4627.5 174.73 2879.7 29.669 28.946
23 5101.5 4623.8 175.27 2877.6 29.872 29.159
31 5156.3 4678.7 169.37 2747.3 36.480 36.229
32 477.60 0.0000 15.496 0.0000 39.137
266
************************************
***** TRAY SIZING CALCULATIONS *****
************************************
*******************
*** SECTION 1 ***
*******************
DESIGN PARAMETERS
-----------------
PEAK CAPACITY FACTOR 1.00000
SYSTEM FOAMING FACTOR 1.00000
FLOODING FACTOR 0.80000
MINIMUM COLUMN DIAMETER FT 1.00000
MINIMUM DC AREA/COLUMN AREA 0.100000
HOLE AREA/ACTIVE AREA 0.100000
DOWNCOMER DESIGN BASIS EQUAL FLOW PATH LENGTH
TRAY SPECIFICATIONS
-------------------
TRAY TYPE SIEVE
NUMBER OF PASSES 1
TRAY SPACING FT 1.50000
267
**** SIZING PROFILES ****
FLOODING DC BACKUP/
STAGE FACTOR PRES. DROP DC BACKUP (TSPC+WHT)
PSI FT
2 63.72 0.6280E-01 0.5562 34.23
3 66.58 0.6483E-01 0.5823 35.83
4 67.17 0.6523E-01 0.5879 36.18
5 67.26 0.6528E-01 0.5890 36.24
268
6 67.26 0.6524E-01 0.5891 36.25
7 65.82 0.6369E-01 0.5491 33.79
8 65.80 0.6364E-01 0.5491 33.79
9 65.79 0.6359E-01 0.5492 33.79
10 65.77 0.6355E-01 0.5492 33.80
11 65.76 0.6352E-01 0.5492 33.80
12 65.75 0.6349E-01 0.5493 33.80
13 65.73 0.6347E-01 0.5493 33.80
14 65.72 0.6344E-01 0.5493 33.80
15 65.71 0.6343E-01 0.5492 33.80
16 65.69 0.6340E-01 0.5491 33.79
17 65.64 0.6337E-01 0.5486 33.76
18 65.51 0.6328E-01 0.5471 33.67
19 65.15 0.6309E-01 0.5429 33.41
20 78.02 0.7683E-01 0.6921 42.59
21 78.85 0.7741E-01 0.7024 43.22
22 79.02 0.7736E-01 0.7055 43.41
23 79.13 0.7722E-01 0.7082 43.58
24 79.30 0.7711E-01 0.7118 43.80
25 79.55 0.7706E-01 0.7164 44.09
26 79.83 0.7706E-01 0.7213 44.39
27 80.00 0.7706E-01 0.7243 44.57
28 79.81 0.7692E-01 0.7216 44.40
29 78.85 0.7652E-01 0.7069 43.50
30 77.12 0.7623E-01 0.6795 41.81
31 76.31 0.7744E-01 0.6606 40.65
269
18 0.1080 0.5355 0.2475 42.61
19 0.1066 0.5370 0.2479 42.39
20 0.2515 0.5401 0.2223 49.82
21 0.2546 0.5384 0.2212 50.59
22 0.2552 0.5373 0.2211 50.83
23 0.2556 0.5361 0.2212 51.04
24 0.2563 0.5346 0.2213 51.33
25 0.2573 0.5330 0.2213 51.67
26 0.2584 0.5314 0.2211 52.03
27 0.2591 0.5305 0.2211 52.31
28 0.2584 0.5309 0.2213 52.34
29 0.2549 0.5343 0.2223 51.85
30 0.2492 0.5416 0.2239 50.90
31 0.2479 0.5492 0.2239 50.71
**********************
**** INPUT DATA ****
**********************
NUMBER OF STAGES 12
270
ALGORITHM OPTION STANDARD
ABSORBER OPTION NO
INITIALIZATION OPTION STANDARD
HYDRAULIC PARAMETER CALCULATIONS NO
INSIDE LOOP CONVERGENCE METHOD BROYDEN
DESIGN SPECIFICATION METHOD NESTED
MAXIMUM NO. OF OUTSIDE LOOP ITERATIONS 70
MAXIMUM NO. OF INSIDE LOOP ITERATIONS 10
MAXIMUM NUMBER OF FLASH ITERATIONS 30
FLASH TOLERANCE 0.000100000
OUTSIDE LOOP CONVERGENCE TOLERANCE 0.000100000
*******************
**** RESULTS ****
*******************
OUTLET STREAMS
--------------
H2-CH4-1 C2H4-REC DM-BOT
COMPONENT:
HYDROGEN .99567 .43312E-02 .39198E-09
METHANE .84957 .15043 .16161E-05
ETHENE .27236 .72617 .14681E-02
ETHANE .16177 .82800 .10235E-01
PROPENE .66451E-02 .29018 .70318
PROPANE .31042E-02 .18771 .80918
BUTANE .37777E-04 .58465E-02 .99412
271
TOP STAGE LIQUID FLOW LBMOL/HR 664.623
BOTTOM STAGE LIQUID FLOW LBMOL/HR 29.7236
TOP STAGE VAPOR FLOW LBMOL/HR 352.323
BOILUP VAPOR FLOW LBMOL/HR 1,185.29
MOLAR REFLUX RATIO 1.56126
MOLAR BOILUP RATIO 39.8771
CONDENSER DUTY (W/O SUBCOOL) BTU/HR -5,002,050.
REBOILER DUTY BTU/HR 3,602,910.
**NOTE** REPORTED VALUES FOR STAGE LIQUID AND VAPOR RATES ARE THE
FLOWS
FROM THE STAGE INCLUDING ANY SIDE PRODUCT.
ENTHALPY
STAGE TEMPERATURE PRESSURE BTU/LBMOL HEAT DUTY
F PSIA LIQUID VAPOR BTU/HR
272
10 1235. 1219.
11 1215. 1205.
12 29.72 1185. 29.7236
273
2 0.28681 0.81930E-01 0.49016 0.56622E-01 0.82048E-01
3 0.24802 0.46470E-01 0.40389 0.61052E-01 0.23130
4 0.14753E-01 0.12746E-01 0.32312 0.64525E-01 0.55996
8 0.10145E-04 0.21713E-03 0.48772E-01 0.17561E-01 0.86637
9 0.20286E-05 0.85117E-04 0.29869E-01 0.12243E-01 0.87201
10 0.41785E-06 0.33681E-04 0.18084E-01 0.84496E-02 0.86095
11 0.87693E-07 0.13354E-04 0.10750E-01 0.57509E-02 0.83312
12 0.18640E-07 0.52725E-05 0.62255E-02 0.38410E-02 0.78742
274
STAGE HYDROGEN METHANE ETHENE ETHANE PROPENE
1 0.12525E-02 0.43501E-01 0.68509 0.86314E-01 0.17803
2 0.90301E-03 0.12280E-01 0.45249 0.77120E-01 0.43698
3 0.78404E-03 0.53907E-02 0.23908 0.51233E-01 0.65487
4 0.95697E-04 0.16962E-02 0.14411 0.36677E-01 0.76419
8 0.93919E-07 0.31379E-04 0.19299E-01 0.84968E-02 0.85981
9 0.19075E-07 0.12251E-04 0.11540E-01 0.57938E-02 0.83703
10 0.39395E-08 0.47869E-05 0.67668E-02 0.38907E-02 0.79711
11 0.82350E-09 0.18619E-05 0.38606E-02 0.25588E-02 0.73894
12 0.17431E-09 0.71868E-06 0.21299E-02 0.16407E-02 0.66340
275
********************************
***** HYDRAULIC PARAMETERS *****
********************************
TEMPERATURE
F
STAGE LIQUID FROM VAPOR TO
1 -131.22 19.170
2 19.170 63.974
3 63.974 109.59
4 131.01 151.69
8 177.91 183.46
9 183.46 189.39
10 189.39 196.50
11 196.50 205.24
12 205.24 205.24
276
4 39449. 38085. 1574.9 6470.5 38.866 38.654
8 52992. 51628. 2274.3 7708.9 42.505 42.422
9 53837. 52473. 2319.0 7766.3 43.118 43.051
10 54152. 52788. 2336.0 7763.0 43.842 43.792
11 54375. 53011. 2347.5 7729.5 44.752 44.724
12 1364.0 0.0000 58.989 0.0000 45.891
************************************
***** TRAY SIZING CALCULATIONS *****
************************************
*******************
*** SECTION 1 ***
*******************
277
STARTING STAGE NUMBER 2
ENDING STAGE NUMBER 10
FLOODING CALCULATION METHOD GLITSCH6
DESIGN PARAMETERS
-----------------
PEAK CAPACITY FACTOR 1.00000
SYSTEM FOAMING FACTOR 1.00000
FLOODING FACTOR 0.80000
MINIMUM COLUMN DIAMETER FT 1.00000
MINIMUM DC AREA/COLUMN AREA 0.100000
HOLE AREA/ACTIVE AREA 0.100000
DOWNCOMER DESIGN BASIS EQUAL FLOW PATH LENGTH
TRAY SPECIFICATIONS
-------------------
TRAY TYPE SIEVE
NUMBER OF PASSES 1
TRAY SPACING FT 1.50000
278
6 4.1247 13.362 7.7086 2.8267
7 4.1247 13.362 7.7086 2.8267
8 4.1247 13.362 7.7086 2.8267
9 4.1247 13.362 7.7086 2.8267
10 4.1247 13.362 7.7086 2.8267
FLOODING DC BACKUP/
STAGE FACTOR PRES. DROP DC BACKUP (TSPC+WHT)
PSI FT
2 41.32 0.6385E-01 0.6124 37.68
3 41.40 0.6219E-01 0.6065 37.32
4 51.12 0.9134E-01 0.9453 58.18
5 59.92 0.9561E-01 1.094 67.32
6 67.72 0.9858E-01 1.206 74.22
7 73.27 0.1005 1.287 79.18
8 76.92 0.1018 1.340 82.47
9 78.99 0.1026 1.369 84.26
10 80.00 0.1031 1.381 84.97
279
MOLE(LBMOL/HR) 41.9268 41.9268 0.169472E-15
MASS(LB/HR ) 1841.64 1841.64 0.628359E-06
ENTHALPY(BTU/HR ) -438973. -544581. 0.193925
**********************
**** INPUT DATA ****
**********************
NUMBER OF STAGES 30
ALGORITHM OPTION STANDARD
ABSORBER OPTION NO
INITIALIZATION OPTION STANDARD
HYDRAULIC PARAMETER CALCULATIONS NO
INSIDE LOOP CONVERGENCE METHOD BROYDEN
DESIGN SPECIFICATION METHOD NESTED
MAXIMUM NO. OF OUTSIDE LOOP ITERATIONS 70
MAXIMUM NO. OF INSIDE LOOP ITERATIONS 10
MAXIMUM NUMBER OF FLASH ITERATIONS 30
FLASH TOLERANCE 0.000100000
OUTSIDE LOOP CONVERGENCE TOLERANCE 0.000100000
*******************
**** RESULTS ****
*******************
280
*** COMPONENT SPLIT FRACTIONS ***
OUTLET STREAMS
--------------
C2-WASTE BUTANE PROPENE
COMPONENT:
HYDROGEN .99680 0.0000 .31966E-02
METHANE .98015 0.0000 .19847E-01
ETHENE .91591 .12254E-10 .84086E-01
ETHANE .87267 .65823E-08 .12733
PROPENE .85133E-02 .55470E-01 .93602
PROPANE .20561E-02 .21106 .78688
BUTANE .11597E-10 .99880 .11986E-02
**NOTE** REPORTED VALUES FOR STAGE LIQUID AND VAPOR RATES ARE THE
FLOWS
FROM THE STAGE INCLUDING ANY SIDE PRODUCT.
ENTHALPY
STAGE TEMPERATURE PRESSURE BTU/LBMOL HEAT DUTY
F PSIA LIQUID VAPOR BTU/HR
281
1 -11.317 150.00 -30174. -30181. -.70235+06
2 11.548 153.00 -19319. -24570.
3 37.506 153.14 -9140.1 -13583.
9 69.004 153.98 -275.34 5092.4
10 69.163 154.12 -426.14 4994.3
11 69.323 154.26 -636.44 4846.9
14 70.935 154.68 -2246.9 4223.3
15 73.234 154.82 -4350.7 3606.8
16 77.314 154.96 -6755.2 3438.2
17 78.159 155.10 -6699.2 3802.5
29 125.06 156.78 -38007. -15738.
30 149.11 156.92 -48418. -29157. .59674+06
282
30 495.6 4013. 495.6388
283
**** MOLE-Y-PROFILE ****
STAGE PROPANE BUTANE
1 0.78067E-03 0.26655E-10
2 0.28366E-02 0.39399E-09
3 0.70400E-02 0.38563E-08
9 0.24903E-01 0.21169E-04
10 0.27483E-01 0.76956E-04
11 0.30304E-01 0.27924E-03
14 0.35703E-01 0.59971E-02
15 0.36478E-01 0.15637E-01
16 0.38151E-01 0.29286E-01
17 0.40918E-01 0.29655E-01
29 0.72061E-01 0.33262
30 0.50188E-01 0.57400
284
**** MASS-X-PROFILE ****
STAGE HYDROGEN METHANE ETHENE ETHANE PROPENE
1 0.24875E-10 0.10460E-05 0.27261E-01 0.65541 0.31346
2 0.80122E-12 0.10727E-06 0.10668E-01 0.38193 0.59866
3 0.58257E-12 0.24799E-07 0.35857E-02 0.17293 0.81001
9 0.60713E-12 0.15558E-07 0.39319E-03 0.95498E-02 0.96030
10 0.60807E-12 0.15565E-07 0.39183E-03 0.92999E-02 0.95723
11 0.60904E-12 0.15575E-07 0.39110E-03 0.92069E-02 0.95297
14 0.61157E-12 0.15492E-07 0.38003E-03 0.90217E-02 0.91920
15 0.61219E-12 0.15305E-07 0.36289E-03 0.87683E-02 0.87540
16 0.16364E-13 0.21266E-08 0.13395E-03 0.44762E-02 0.82570
17 0.22879E-15 0.16772E-09 0.34675E-04 0.16616E-02 0.82624
29 0.16576E-37 0.77429E-23 0.10759E-11 0.53991E-08 0.28963
30 0.28237E-39 0.52934E-24 0.14401E-12 0.12125E-08 0.14307
285
STAGE PROPANE BUTANE
1 0.11120E-02 0.50044E-10
2 0.37965E-02 0.69505E-09
3 0.85730E-02 0.61897E-08
9 0.26361E-01 0.29536E-04
10 0.29080E-01 0.10733E-03
11 0.32054E-01 0.38932E-03
14 0.37672E-01 0.83408E-02
15 0.38348E-01 0.21668E-01
16 0.39690E-01 0.40160E-01
17 0.42405E-01 0.40509E-01
29 0.66811E-01 0.40648
30 0.43065E-01 0.64921
********************************
***** HYDRAULIC PARAMETERS *****
********************************
TEMPERATURE
F
STAGE LIQUID FROM VAPOR TO
1 -11.317 11.548
2 11.548 37.506
3 37.506 55.248
9 69.004 69.163
10 69.163 69.323
286
11 69.323 69.544
14 70.935 73.234
15 73.234 78.327
16 77.314 78.159
17 78.159 78.529
29 125.06 149.11
30 149.11 149.11
287
1 0.19295 699.27 3784.7
2 0.68568E-01 0.19388 686.97 3785.2
3 -.26063 0.19758 698.70 3877.2
9 -.10059E-01 0.20396 741.85 4100.1
10 -.68579E-02 0.20410 741.88 4099.6
11 -.65952E-02 0.15022 741.68 4098.0
14 -.28101E-01 0.14988 737.74 4078.3
15 -.65037E-01 0.14907 732.82 4056.1
16 -.62188E-01 0.23498 599.69 3321.9
17 -.29329E-01 0.23523 601.12 3328.5
29 -.62463 0.24458 588.44 3253.7
30 -.61015 0.0000 0.0000
************************************
***** TRAY SIZING CALCULATIONS *****
************************************
*******************
*** SECTION 1 ***
*******************
DESIGN PARAMETERS
-----------------
PEAK CAPACITY FACTOR 1.00000
SYSTEM FOAMING FACTOR 1.00000
FLOODING FACTOR 0.80000
MINIMUM COLUMN DIAMETER FT 1.00000
MINIMUM DC AREA/COLUMN AREA 0.100000
HOLE AREA/ACTIVE AREA 0.100000
DOWNCOMER DESIGN BASIS EQUAL FLOW PATH LENGTH
TRAY SPECIFICATIONS
-------------------
TRAY TYPE SIEVE
NUMBER OF PASSES 1
TRAY SPACING FT 1.50000
288
***** SIZING RESULTS @ STAGE WITH MAXIMUM DIAMETER *****
289
27 1.1018 0.95351 0.69099 0.13126
28 1.1018 0.95351 0.69099 0.13126
29 1.1018 0.95351 0.69099 0.13126
FLOODING DC BACKUP/
STAGE FACTOR PRES. DROP DC BACKUP (TSPC+WHT)
PSI FT
2 73.59 0.7423E-01 0.6231 38.34
3 75.06 0.7730E-01 0.6318 38.88
4 77.49 0.8039E-01 0.6547 40.29
5 78.98 0.8211E-01 0.6694 41.20
6 79.62 0.8285E-01 0.6762 41.61
7 79.87 0.8312E-01 0.6788 41.77
8 79.96 0.8322E-01 0.6798 41.84
9 79.99 0.8325E-01 0.6802 41.86
10 80.00 0.8325E-01 0.6804 41.87
11 78.87 0.8209E-01 0.6492 39.95
12 78.83 0.8203E-01 0.6487 39.92
13 78.71 0.8190E-01 0.6475 39.85
14 78.45 0.8161E-01 0.6445 39.66
15 77.90 0.8103E-01 0.6384 39.28
16 65.21 0.6699E-01 0.5596 34.43
17 65.37 0.6714E-01 0.5610 34.52
18 65.44 0.6720E-01 0.5616 34.56
19 65.46 0.6722E-01 0.5619 34.58
20 65.48 0.6723E-01 0.5621 34.59
21 65.49 0.6724E-01 0.5623 34.60
22 65.50 0.6724E-01 0.5624 34.61
23 65.50 0.6724E-01 0.5625 34.62
24 65.46 0.6721E-01 0.5624 34.61
25 65.31 0.6708E-01 0.5613 34.54
26 64.90 0.6675E-01 0.5579 34.33
27 64.05 0.6614E-01 0.5510 33.91
28 63.30 0.6581E-01 0.5450 33.54
29 64.36 0.6705E-01 0.5537 34.07
290
6 0.2491 0.5656 0.2105 56.21
7 0.2501 0.5654 0.2102 56.46
8 0.2506 0.5653 0.2101 56.55
9 0.2507 0.5652 0.2100 56.59
10 0.2508 0.5651 0.2101 56.61
11 0.2044 0.5650 0.2101 56.37
12 0.2043 0.5650 0.2102 56.35
13 0.2039 0.5651 0.2104 56.30
14 0.2030 0.5653 0.2108 56.17
15 0.2009 0.5659 0.2115 55.92
16 0.2172 0.5662 0.2426 45.92
17 0.2179 0.5661 0.2423 46.07
18 0.2182 0.5660 0.2421 46.13
19 0.2184 0.5659 0.2421 46.16
20 0.2185 0.5658 0.2421 46.17
21 0.2186 0.5657 0.2421 46.18
22 0.2187 0.5656 0.2422 46.18
23 0.2187 0.5655 0.2422 46.17
24 0.2186 0.5655 0.2423 46.05
25 0.2181 0.5655 0.2427 45.93
26 0.2166 0.5658 0.2437 45.57
27 0.2136 0.5665 0.2458 44.89
28 0.2118 0.5670 0.2480 44.54
29 0.2178 0.5654 0.2463 46.24
291
BUTANE C2-FEED C2-OUT C2-WASTE C2H4-REC
---------------------------------------
SUBSTREAM: MIXED
PHASE: LIQUID LIQUID LIQUID VAPOR LIQUID
COMPONENTS: LBMOL/HR
HYDROGEN 0.0 8.1869-03 8.1869-03 1.1758-07 1.3033
METHANE 1.6354-23 0.4507 0.4507 5.9895-05 5.6878
ETHENE 2.5443-12 49.9360 49.9360 0.1902 51.2248
ETHANE 1.9986-08 3.0549 3.0549 2.6497 6.0211
PROPENE 1.6851 7.0919-08 7.0919-08 0.2586 8.8741
PROPANE 0.2485 6.7261-11 6.7261-11 2.4208-03 0.2217
BUTANE 7.1189 1.9388-15 1.9388-15 8.2655-11 4.1672-02
TOTAL FLOW:
LBMOL/HR 9.0524 53.4498 53.4498 3.1009 73.3744
LB/HR 495.6388 1499.9994 1499.9994 96.0001 2097.5991
CUFT/HR 15.6363 51.9239 51.5214 83.1029 61.6375
STATE VARIABLES:
TEMP F 149.1145 -40.9305 -44.1624 -11.3169 -131.2174
PRES PSIA 156.9200 300.0000 203.5600 150.0000 550.0000
VFRAC 0.0 0.0 0.0 1.0000 0.0
LFRAC 1.0000 1.0000 1.0000 0.0 1.0000
SFRAC 0.0 0.0 0.0 0.0 0.0
ENTHALPY:
BTU/LBMOL -4.8418+04 1.2767+04 1.2709+04 -3.0181+04 3517.1063
BTU/LB -884.3223 454.9390 452.8657 -974.8802 123.0289
BTU/HR -4.3830+05 6.8241+05 6.7930+05 -9.3589+04 2.5807+05
ENTROPY:
BTU/LBMOL-R -89.8621 -32.7966 -32.8967 -45.5229 -39.5110
BTU/LB-R -1.6413 -1.1686 -1.1722 -1.4705 -1.3821
DENSITY:
LBMOL/CUFT 0.5789 1.0294 1.0374 3.7314-02 1.1904
LB/CUFT 31.6980 28.8884 29.1141 1.1552 34.0312
AVG MW 54.7520 28.0637 28.0637 30.9584 28.5876
292
SUBSTREAM: MIXED
PHASE: LIQUID LIQUID MIXED LIQUID VAPOR
COMPONENTS: LBMOL/HR
HYDROGEN 1.3272-24 1.1795-07 1.1795-07 1.7883-25 8.1869-03
METHANE 3.8434-11 6.1106-05 6.1106-05 5.4964-12 0.4507
ETHENE 0.1041 0.1036 0.2076 0.1754 49.7607
ETHANE 2.9617 7.4427-02 3.0362 2.8294 0.2255
PROPENE 8.8739 21.5042 30.3781 7.0919-08 3.6801-16
PROPANE 0.2217 0.9557 1.1774 6.7261-11 3.4566-20
BUTANE 4.1671-02 7.0857 7.1274 0.0 0.0
TOTAL FLOW:
LBMOL/HR 12.2031 29.7236 41.9268 3.0048 50.4450
LB/HR 477.5974 1364.0427 1841.6401 89.9994 1410.0000
CUFT/HR 15.4960 58.9891 443.0044 3.4553 595.3505
STATE VARIABLES:
TEMP F 57.4754 205.2431 103.2282 17.2805 -20.5717
PRES PSIA 207.2000 554.4000 207.2000 296.2200 290.0000
VFRAC 0.0 0.0 0.4240 0.0 1.0000
LFRAC 1.0000 1.0000 0.5760 1.0000 0.0
SFRAC 0.0 0.0 0.0 0.0 0.0
ENTHALPY:
BTU/LBMOL -9828.5061 -1.0733+04 -1.0470+04 -3.8271+04 2.0210+04
BTU/LB -251.1288 -233.8889 -238.3598 -1277.7355 723.0350
BTU/HR -1.1994+05 -3.1903+05 -4.3897+05 -1.1500+05 1.0195+06
ENTROPY:
BTU/LBMOL-R -52.2978 -56.1697 -54.1629 -56.6729 -21.6822
BTU/LB-R -1.3363 -1.2240 -1.2331 -1.8921 -0.7757
DENSITY:
LBMOL/CUFT 0.7875 0.5039 9.4642-02 0.8696 8.4732-02
LB/CUFT 30.8207 23.1236 4.1572 26.0470 2.3684
AVG MW 39.1373 45.8908 43.9252 29.9520 27.9512
SUBSTREAM: MIXED
PHASE: VAPOR VAPOR LIQUID VAPOR
COMPONENTS: LBMOL/HR
HYDROGEN 299.6040 1.2951 3.7705-10 300.9073
METHANE 32.1232 5.2370 1.2128-06 37.8110
ETHENE 19.2126 1.1850 1.7459-02 70.5410
ETHANE 1.1764 4.3939-03 0.3866 7.2719
293
PROPENE 0.2032 1.0595-14 28.4343 30.5815
PROPANE 3.6662-03 2.1741-18 0.9265 1.1810
BUTANE 2.6926-04 2.5603-24 8.5428-03 7.1277
TOTAL FLOW:
LBMOL/HR 352.3234 7.7215 29.7734 455.4214
LB/HR 1702.3991 120.0022 1250.0000 5164.0430
CUFT/HR 2242.3848 120.6316 39.1603 5275.4676
STATE VARIABLES:
TEMP F -131.2174 -129.7919 69.1628 142.5000
PRES PSIA 550.0000 200.0000 154.1200 555.0000
VFRAC 1.0000 1.0000 0.0 1.0000
LFRAC 0.0 0.0 1.0000 0.0
SFRAC 0.0 0.0 0.0 0.0
ENTHALPY:
BTU/LBMOL -3337.9202 -2.0170+04 -426.1427 355.9486
BTU/LB -690.8059 -1297.8502 -10.1502 31.3914
BTU/HR -1.1760+06 -1.5574+05 -1.2688+04 1.6211+05
ENTROPY:
BTU/LBMOL-R -12.3661 -22.8672 -51.8721 -12.2323
BTU/LB-R -2.5593 -1.4714 -1.2355 -1.0788
DENSITY:
LBMOL/CUFT 0.1571 6.4009-02 0.7603 8.6328-02
LB/CUFT 0.7592 0.9948 31.9201 0.9789
AVG MW 4.8319 15.5414 41.9838 11.3390
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