Fire Heat
Fire Heat
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FIRED HEATERS
TABLE OF CONTENTS
1.0
1.0
INTRODUCTION
1.1
GENERAL
1.2
CHARACTERISTICS AND USE OF FIRED HEATERS
1.3
SPECIFICATION SHEETS
1.4
DATA SOURCES
1.5
TERMS AND DEFINITIONS
2.0
3.0
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3.3
3.4
3.5
3.6
SPECIFICATION SHEETS
3.3.1 Average (Radiant) Flux Density
3.3.2 Process Tube Design Temperature and Pressure
3.3.3 Decoking Pressure and Temperature
3.3.4 Items Included in Scope of Each Heater
3.3.5 Site and Utility Data
3.3.6 Fuel Data
3.3.7 Materials of Construction and Corrosion Allowance
AUXILIARY EQUIPMENT
3.4.1 Reboiler Circulation System and Control
3.4.2 Decoking Effluent Quench Drum
3.4.3 Emergency Shutdown System
EXAMPLE SPECIFICATION SHEETS
ADVANTAGES AND DISADVANTAGES
4.0
5.0
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5.5
6.0
MATERIALS OF CONSTRUCTION
6.1
TUBE MATERIALS
7.0
UTILITY REQUIREMENTS
8.0
9.0
REFERENCE ARTICLES
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1.0
INTRODUCTION
1.1
GENERAL
Fired heaters or furnaces are used extensively in the process industry. Some familiar
examples are open hearth blast furnaces, cement kilns, refinery crude oil heaters and
glass furnaces. We will limit our discussion here, however, to fired heaters commonly
used in the chemical process industry, i.e., direct fired tubular heaters. We will use the
words "fired heater" and "furnace" in this context even though they do not fully define the
normal process-type heater.
You, as a Process Engineer, are responsible for specifying required process parameters
such as heat duty, flow, and fuel composition as well as basic furnace configuration. The
task force Mechanical Engineer assigned to fired heaters can assist in formulating a
basic configuration for the furnace. Using all this information the vendor does the
mechanical design, specifying the number of tubes, tube length, and other detailed
information. In short, FDI specifies the performance requirements for a fired heater while
the vendor actual designs it.
This section provides some examples of calculations and specification data sheets for
several types of fired heaters. All are widely used throughout the refining and
petrochemical industries. You should note that the examples presented here are taken
from actual FDI projects.
1.2
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Figure 1-1
BOX HEATER COMPONENTS
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Figure 1-2
VERTICAL HEATER COMPONENTS
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Incinerators are used to burn waste gases. These gases usually have low heating values
and are often toxic. Incinerators ensure essentially complete combustion of such
material. Usually as much heat of combustion as possible is recovered and, hence, the
incinerator is used to heat some process material. A reactor heater also transfers heat to
the process material, but in addition to producing a physical change, the heat initiates
and drives a chemical reaction. A catalyst may be present in the heater tubes to
promote the reaction. Such is the case for a reformer and a fired catalytic cracker.
Other types of reactor heaters such as thermal crackers or fired hydrodealkylation
reactors require no catalyst. Examples of calculations and equipment specification
sheets for both simple and reactor heaters are presented in this section.
At this point you might ask why there is a need for simple or reactor-type fired heaters.
Why not just use conventional shell and tube heat exchangers or reactors with heating
jackets? Generally, a fired heater is used when the required heat duty is unusually large
or when the process temperature is too high for steam or a heat transfer medium such as
Dow-therm or hot oil. Very large heat duties require very large shell and tube heat
exchangers. The practical size of such exchangers is limited by required fluid velocities,
fouling tendencies, etc. Such considerations may warrant the use of a fired heater.
Steam pressures required to give a saturation temperature above 400 oF (204 oC) are not
always available in a process plant. And, above the critical temperature of 703 oF
(373 oC), the latent heat of steam ceases to exist. Dowtherm A generally cannot be used
at temperatures above 750 oF (399 oC). The upper limit for hot oil is around 600 oF
(316 oC). Molten salts can be used at temperatures up to 1,100 oF (529 oC), but these
have very limited application. Invariably, there may be circumstances where either a
fired heater or a shell and tube exchanger will work. In that case, economics and space
requirements may dictate the choice. Note that a fired heater cannot be used if the
process fluid is heat sensitive or if plant or area safety requirements prohibit the use of
an open flame. We have now highlighted some of the major considerations in the
application of fired heaters. You, the Process Engineer, should recognize that client
preferences, site-specific concerns and other matters pertaining to a given project also
influence the selection of process equipment. These will vary in nature and importance
depending upon the project, but still must be considered.
Before concluding our discussion, we want to give you some idea of the variety of
applications of fired heaters in the process industry along with typical operating
temperatures. These are presented in Table 1-1.
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Table 1-1
TYPICAL FIRED HEATER APPLICATIONS
Typical Process Outlet
Temperature, o F (oC)
Service
1.3
400 - 750
(204 - 399)
Reboiler
350 - 650
(177 - 343)
Thermal Cracker
850 - 1,000
(454 - 538)
Visbreaker (Soaker)
900
(482)
1,000 - 1,025
(538 - 554)
Cat Reformer
900 - 1,050
(482 - 566)
Hydrogenation Preheater
400 - 700
(204 - 371)
Hydrocracking
700 - 850
(371 - 454)
1,500 +
(815 + )
Dealkylation (Thermal)
1,400 +
(760 + )
Waste Incinerator
2,500 - 3,500
(1,371 - 1,927)
300 - 700
(149 - 371)
Steam-Methane Reformer
1,450 - 1,500 +
(788 - 815 +)
SPECIFICATION SHEETS
The Process Engineer is responsible for completing all necessary process calculations
prior to initiating the fired heater specification sheets. The Process Engineer and
Mechanical Engineer are jointly responsible for completing the fired heater specification
sheets, such as forms E-0522A-I, the Steam-HC Reformer Specification Sheets, and
forms E-553A-H, the Fired Heater Specification Sheets. This section contains completed
examples of these specification sheets and the calculations pertaining to each.
The following FDI specification forms for fired heaters are routinely used:
Description
Form
Incinerator
Steam-HC Reformer
Fired Heater
E-460A-F
E-522A-I
E-553A-H
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1.4
DATA SOURCES
The Process Engineer should complete the following items before starting fired heater
calculations:
Process Flow Diagram
Heat and Material Balance
Pressure-Temperature-Metallurgical Survey
General specifications for fired heaters are written by the Mechanical Engineers. A copy
should be obtained as soon as it is available. In some cases the client's specifications
are used. These should be read prior to starting calculations, otherwise you may have to
start over. Process guidelines may be issued in the form of job bulletins or they may
have been developed in book form. Other books such as Process Design Guidelines for
Gas Plants, Design Manuals, etc. should be read when applicable.
A preliminary plot plan is usually available in the early stages of a job.
available, you can make your own sketches and refer to previous similar
case, you must update your pressure and temperature survey and
calculations as information is developed or received throughout the job. It
necessary to revise the fired heater specification.
If one is not
jobs. In any
revise your
may become
Physical properties may be obtained from computer runs, Vol. II General Data, or other
sources. Your lead engineer should give you some guidelines in order to maintain
uniformity on the job. In addition, refer to Section III, References for Physical Properties.
1.5
Arch
Atomizer
Anchor
Balanced
Draft Heater
Breeching
Bridgewall
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Bridgewall
Temperature
Burner
Casing
Coking
Allowance
Convection
Section
Corbel
Corrosion
Allowance
Crossover
Damper
Draft
Duct
Efficiency,
Fuel
Efficiency,
Thermal
Excess Air
Explosion Door
Extended Surface
Flux
Density
(Average)
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Flux
Density
(Maximum)
Forced
Draft
Heater
Fouling
Resistance
Header
Header Box
Heat
Absorption
Heat Release
The total heat liberated from the specified fuel, using the
lower heating value of the fuel.
Heating Value,
Higher (HHV)
Heating Value,
Lower (LHV)
Induced Draft
Heater
Natural Draft
Heater
Pilot
Plenum
Primary Air
The portion of the total combustion air which first mixes with
the fuel.
Radiant Section
Secondary Air
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Shield Section
Sootblower
Stack
Strakes
Tube Guide
Tube Pass
Volumetric Heat
Release
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2.0
GENERAL
Before discussing the examples presented in this section, we want to give you some
process design guidelines for fired heaters. Unless otherwise noted, what we present
here will apply to process heaters in general. Details that are specific to a particular type
of fired heaters are discussed either in the corresponding example (presented later in this
section) or in the appropriate FDI design manual or other reference. You should refer to
these as needed.
Our discussion here will provide you with some of the fundamental means needed for
calculating and specifying process heaters. You should note that the numerical values of
certain parameters given in our discussion, e.g., furnace efficiencies and radiant heat
fluxes, are based on experience and "generally accepted practice" in the process
industry. As such, they should not be construed as "hard and fast" rules but rather as
guidelines. With this in mind, let's now proceed with our discussion.
2.2
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Table 2-1
TYPICAL AVERAGE DESIGN PARAMETERS FOR VARIOUS HEATERS
Average Radiant
Flux (2)(3)
Minimum Coil
Pressure Drop
Mass
Velocity
Btu/hr ft2
psi
lb/ft2 sec
Single
Fired
Double
Fired
Single
Fired
Double
Fired
H2 Reformers (1)
14,000
20,000
20
25
150
Naphtha/Kerosene
Light Gas Oil
12,000
15,000
25
30
175
10,000
12,500
30
35
200
Crude
10,000
12,500
100
150
225
Atmos./Vacuum Resid
9,000
11,000
100
150
250
kg/m2 sec
MPa
kW/m
H2 Reformers (1)
44.2
63.1
0.138
0.172
732
Naphtha/Kerosene
Light Gas Oil
37.9
47.3
0.172
0.207
854
31.5
39.4
0.207
0.241
976
Crude
31.5
39.4
0.689
1.034
1,098
Atmos./Vacuum Resid
28.4
34.7
0.689
1.034
1,220
Notes:
(1)
I.D. Basis
(2)
The maximum average heat flux to any tube in the convection section, based on bare outside
diameter surface, shall not exceed the maximum average flux allowable in the radiant section.
Steam generation coils may have up to 40,000 Btu/hr ft2 (126.2 kW/m2) maximum average flux.
Source: Fluor Daniel Process Design Criteria Manual.
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Table 2-2
HEATER SELECTION GUIDE (1)
Service
Horizontal
Individual
Pass
Control
Vertical
Multi
Pass
Control
Individual
Pass
Control
Helical
Multi
Pass
Control
Noncoking
Below 30 MM Btu/hr (8.8 MW)
Single Phase
Vaporizing (below 600 oF) (316 oC)
o
Hydrogen Reformer
Hydrogen
Coking
Single Phase
Vaporizing
Hydrotreater (2)
Coker
Visbreaker
Crude/Vacuum
Notes:
(1)
If required to meet low pressure drop requirements, heaters handling 100 % vapor at inlet and
outlet conditions may be designed with arbor type coils.
(2)
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You can obtain the radiant duty from the process heat and material balance if the
process fluid only goes through the radiant section. Otherwise you will have to split the
process duty between the radiant and convection sections.
In the early stages of a job, vendor data for your particular heater will not be available, so
you will have to estimate the radiant and overall efficiencies. And, as we mentioned
above, you may also have to estimate the split in process duty between the radiant and
convection sections. For guidance, you should refer to the design data for similar
heaters on past jobs and to the appropriate FDI design manual. Also, you should consult
with a heater specialist to the Mechanical Engineering Department.
Instead of using the above equation, you can calculate the amount of flue gas heat
available for recovery using a computer program (consult with a computer specialist).
The output for this program should include temperature-enthalpy data for the stack gas.
Using this data, you can plot a cooling curve and find the amount of available heat. Use
of this method is discussed in detail in Section 5.2 of this manual, Reformer Calculations.
Even though the example presented there is a steam-hydrocarbon reformer, the
discussion of the Furnace Calculation Program applies to fired heaters in general. You
should refer to that part of our discussion for further information.
The second major step in specifying convection section heat recovery is to decide what
to do with the available heat. There are three options generally available. First, you can
heat the process fluid before it goes to the radiant section. This reduces the furnace
radiant duty and size and thus can significantly reduce the initial cost of the heater.
Second, you can use the stack gases to generate steam in either a waste heat boiler or
in steam coils fitted into the flue stack. This is often the preferred choice if the steam can
be used in the plant. Third, you can preheat the incoming combustion air. This is often
done as it does the most to improve furnace efficiency. We should point out that the use
of air preheat requires mechanical draft operation. The relatively high friction losses in
the air preheater and associated duct work make natural draft operation infeasible.
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The expected overall thermal efficiencies for mechanical draft fired heaters range up to
91 % with air preheat and up to 89 % using only a waste heat boiler. For natural draft
heaters, the maximum expected efficiencies range from 84 to 88 %. Most convection
heat recovery schemes usually employ air preheat and one of the other two types of
recovery we have discussed. We will now present a few examples of such schemes
along with some further discussion.
Figure 2-1 shows a typical fired reboiler flow scheme. Material from the column sump is
first heated in the convection section and then in the radiant section. Heating the
process fluid in the convection section reduces the radiant duty and overall size of the
furnace. An induced draft fan pulls flue gas out of the stack and through the air
preheater, while the combustion air is pressured through the air preheater by a forced
draft fan. Here the flue gas heats the incoming combustion air on its way to the
burners.With air preheat included, overall thermal efficiencies as high as 91 % can be
achieved. See the article entitled Fired Heaters - IV ... located at the end of this manual
for a discussion on the types of air preheaters available.
Figure 2-2 shows another typical convection heat recovery scheme for a fired heater.
For heaters with fired duties on the order of one to several hundred million Btu per hour,
and with radiant efficiencies of around 50 %, there is considerable heat that can be
recovered from the flue gas. Generally, the convection heat recovery schemes for such
heaters are an integral part of the plant steam balance. For the case shown in Figure
2-2, we are preheating the feed and generating steam in the convection section. The
steam drum operates at saturated conditions. It is really a surge drum for both water and
heat. Use of it allows better control of steam generation and superheating in the
convection coils. Without the upper three "economizer" coils, this type of heater would
have an overall thermal efficiency of about 58 %. With them, its overall efficiency is
around 85 %.
Before concluding our remarks here, we should tell you about the limitations in flue gas
heat recovery. First, the maximum average heat flux rate to any tube in the convection
section, based on bare outside diameter surface, shall not exceed the maximum average
flux rate allowable in the radiant section. Steam generation coils, however, may have up
to a 40,000 Btu/hr ft2 (126.2 kW/m2) maximum average flux rate. Second, for steam
generation coils, the limiting approach temperature is 50 oF (28 oC). The controlling
resistance to heat transfer is obviously on the flue gas side of the coil. The film
coefficients on this side are on the order of 0.2-20 Btu/hr ft2 oF (1.14-114 W/m2 oC) versus
1,000 - 3,000 Btu/hr ft2 oF (5,680-17,030 W/m2 oC) on the vaporizing side. Extended heat
transfer surface, e.g., fin tubes, and relatively high approach temperatures are used to
compensate for this. Experience has shown that for stable operation, 50 oF (28 oC)
should be the lowest approach temperature for this service. Third, the amount of heat
that you can ultimately extract from the flue gas is often limited by the SO3 content of the
gas. Sulfur in furnace fuels partially ends up as SO3 in the stack gas. If the stack
temperature gets low enough, this will combine with condensing moisture to produce
sulfuric acid. The obvious result is severe corrosion problems in the convection section.
The acid dew point in flue gases is normally in the range of 300-350 oF (149 -177 oC).
We will say more about this in Section 2.6 of this section dealing with combustion.
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Figure 2-1
TYPICAL FIRED REBOILER FLOW SCHEME WITH AIR PREHEAT
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Figure 2-2
FIRED HEATER WITH STEAM GENERATION
FOR WASTE HEAT RECOVERY
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Gaseous Fuels
Pure component heats of combustion (Btu/SCF or kJ/Nm3) for organic
gases are given in such references as Perry's Chemical Engineers
Handbook and the GPSA Engineering Data Book. If the fuel gas has
two or more components, you should calculate a more average heating
value. To do this, multiply the mole fraction of each component times its
respective heating value and take the sum. The lower heating value
(LHV) is used in these calculations.
Often, the principle furnace fuel is a refinery or plant fuel gas. Such fuel
gas is usually a mixture of by-product and waste gases from various
units at the site. Its composition can change considerably as the various
contributing units are taken on or off line or operated at varying rates.
For such fuels, you should determine the range of compositions the gas
could logically have and calculate the LHV and HHV (higher heating
value) for each of these compositions. Alternately, you could estimate
the heating values according to the following equations:
HHV
LHV
=
=
215 + 51.7 M
155 + 49.1 M
where:
M
You should note that the LHV equation also correlates saturated
hydrocarbons with hydrogen to within 35 Btu/SCF (1,380 kJ/Nm3) up to
44 molecular weight. Based on the results of these calculations, you
need to report the range of heating values, compositions and molecular
weights for the fuel gas.
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b.
Liquid Fuels
A chart for determining the net and gross heats of combustion of fuel oils
and petroleum fractions is given in Figure 2-3. Alternately, you can
estimate the heating values of liquid fuels using the following equations:
HHV (Btu/lb)
LHV (Btu/lb)
Solid Fuels
For combustion data on coal, you should refer to Perry's Chemical
Engineers Handbook. The data contained in Perry's is limited; however,
methods for estimating coal heating values are given. Also, there are
various references in the Fluor-Houston Library that contain data on
coal. But, the best approach is to obtain combustion data on the specific
coal to be used on the project in question.
2.5.2
2.5.3
2.5.4
Sulfur Content
As mentioned earlier, the sulfur in fuel burns to SO2 and SO3. The SO2, of
course, is an air pollutant regulated by the Federal EPA. The SO3 combines with
any condensing moisture in the stack gas to make highly corrosive H2SO4. We
will say more about this in the next part of our discussion, Section 2.6 dealing
with combustion.
2.5.5
Other Considerations
a.
Heat Release
Heat release for process heaters shall be based on the LHV (lower
heating value) of the fuel. Fuel oil and/or gas composition analysis shall
be supplied with the heater specification. Vanadium, sodium and sulfur
should be included in the fuel analysis.
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Figure 2-3
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b.
Fuel Gas
Fuel gas should normally be supplied upstream of the fuel control valve
at 35 psig (0.241 MPag), and at 20 psig (0.138 MPag) to the burner.
Provisions must be made to ensure that no condensation occurs in the
fuel lines. Together, these measures will allow adequate flow control of
the furnace fuel gas.
Consult with the heater representative of
Mechanical Engineering regarding burning of low pressure or low heating
valve gases.
c.
Fuel Oil
To ensure stable and complete combustion, fuel oil must be atomized at
the burners. This can be done by using either mechanically atomized
burners or steam atomized burners. Mechanically atomized burners
require fuel oil supplied at 500 psig (3.447 MPag). The high pressure oil
forces its way into the combustion chamber through tiny openings in the
burner nozzle. In the process, it disperses into a mist of tiny droplets. In
steam atomizing burners, on the other hand, steam is injected into the
fuel oil are a ratio of 0.5 lb (kg) steam to 1.0 pound (kg) of oil. The oil is
normally supplied at 150 psig (1.034 MPag). The steam should be at
least 30 psi (0.207 MPa) above the fuel oil pressure and should have at
least 50 oF (28 oC) superheat.
Note that heavy fuel oil systems should be recirculating loop type. One
barrel of oil should be circulated through the system for each barrel
consumed at the design heat release of the burners. Light fuel oil
systems, on the other hand, may be dead end types. Regardless of
configuration, the system should deliver fuel oil to the burners at a
viscosity of 30 centistokes.
d.
Pilot Burners
Pilot burners are supplied as an integral part of the main burner. They
are most often installed where it is desired to simplify burner ignition
procedures (particularly with oil firing), where an extreme turndown to a
fixed, minimum load is required, where intermittent on-off operation is
required or where extreme modulation of firing rate is needed.
The primary disadvantage of pilot burners is that they constitute a
potential source of gas leakage into the firebox. The possibility always
exists of a pilot being accidentally extinguished, permitting gas to be
admitted to the heater during a shutdown. Also, because of their small
port drillings, pilot burners clog easily and should be routinely inspected
and cleaned.
Pilot burners are almost always gas-fired and are usually fueled from an
independent source such as a propane or LPG drum or a natural gas
leader which is not part of the regular refinery fuel gas system. If the
pilots are fueled from the main burner supply line, the gas offtake to the
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piles must be upstream of the control and block valves for the main
burner supply.
A typical heat release from a pilot is 50,000 to 100,000 Btu/hr
(15 to 30 kW).
e.
Soot Blowers
Soot removal is often required on heaters fired with fuel oil. It is not
needed if the heater is only fired with fuel gas. The main cause of
outside tube deposits is high vanadium, sulfur, sodium and ash content
in the fuel oil. They must be provided on heaters with convection tubes
and primary fuel oil firing if fuel contains:
1.
2.
3.
4.
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cool. The rate of travel is about 6 ft/min (1.83 m/min) and rotation about
once per inch of travel length. This type may also be used in a vertical
position if clearance is a problem. Maximum travel length is about
40 feet (12.2 m).
Steam is usually 150 to 200 psig (1.034 to 1.379 MPag) but 400 to 600
psig (2.758 to 4.137 MPag) is more effective and should be considered if
it is available. Steam consumption of the lance type is about 8,000 to
12,000 lbs/hr (3,630 to 5,440 kg/hr) per blower. The blower operates
about 2.5 minutes once each eight hours. The nonretractable type uses
about 10,000 to 14,000 lbs/hr (4,540-6,350 kg/hr) for about 40 seconds.
Total steam consumption is about the same for the two types.
Controls may be provided to operate the blowers on a predetermined
cycle. Otherwise, an increase in stack temperature or fuel flow can be
used to indicate that blowing is needed.
Soot blowing may all 10 % to the cost of a heater installation. If there is
uncertainty about the need for soot blowers, provision may be made for
future installation by allowing space between tube banks and access
doors in heater walls.
Drive motors for soot blowers can be either electric or air, although
electric drive is most common.
2.6
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the convection section. Figure 2-4 will enable you to do this once you know the SO3
content of the flue gas.
How does one determine the SO3 content of the furnace stack gas? To answer this, let's
look at an example calculation. Consider a furnace fuel oil of the composition given in
the example calculations in Section 2.12.2. First, we must calculate the number of moles
of each fuel component in some given amount of fuel. here we chose 100 lb of fuel as
our basis. Now, most of the sulfur in the fuel will form SO2 in the flue gas and some will
form SO3. In practice, the maximum SO3 level in furnace flue gases is found to be 5 % of
the SO2 concentration. This is higher than that predicted by equilibrium considerations,
but closely agrees with actual measurements. Using this along with the total moles of
sulfur in our 100 lb (basis) sample, we can calculate the relative number of moles of SO2
and SO3 in the flue gas. From here the stoichiometry calculations required to find the
complete stack gas composition and the subsequent use of Figure 2-4 are rather
straightforward. Therefore, we leave it to you to follow our example calculations at the
end of this subsection on your own. Before we move on, however, we should mention
one more thing. Once you have found the acid gas dew point for a particular heater, you
should add a safety factor to that temperature. In the absence of client specifications or
other guidelines, the lower flue gas temperature limit should 50 oF (28 oC) above the acid
dew point. This will cover operating conditions different from design. Watch out for
turndown operations. You may have to provide bypasses for the process fluid controlled
according to the stack temperature. We will say more about turndown in Section 2.8.
Nitrogen oxides are a by-product from most combustion operations. They form by
thermal fixation of molecular nitrogen in the combustion air. NOx also forms from
nitrogen compounds in the fuel. The Federal EPA regulations, made effective in
December 1971, impose a national limit on NOx emissions from new boilers of over
250 MM Btu/hr (73.3 MW) heat release. Various states and municipalities have also
passed laws limiting the emission of NOx from combustion units. Reference tot he legal
restrictions of various locations is required to determine limits imposed on process fired
heaters. Consult with an environmental engineer.
Tests show that certain restrictions can be met on fired heaters without modification or
special designs because of their smaller size and design characteristics. Relatively low
flame burst temperature due to low heat flux and distributed of burner arrangement is
credited. However, problems may arise with large forced draft burners and from fuel
nitrogen content greater than 0.3 % wt. Your responsibility is to inform the vendor of NOx
regulation requirements so he can design for them.
2.7
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Figure 2-4
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2.7.1
SECTION
FIRED HEATERS
b.
Firing Rate
The firing rate is usually controlled by adjusting the fuel flow according to
the heater process outlet temperature. This is depicted in Figure 2-5.
Note, however, that vaporizing streams may have little outlet
temperature variation with heat input. In that case, another control
variable must be chosen. Most heaters shut down automatically for low
fuel pressure or flow.
c.
Air Supply
This is normally controlled by adjustable dampers either in the flue stack
or inlet air duct. Manual control is common for natural draft heaters, but
automation will improve the thermal efficiency of the heater.
If forced or induced draft fans are used, the air flow can be controlled
either by fan plenum dampers or fan (driver) speed control. (The plenum
is a chamber surrounding the burners. It is used to distribute air to the
burners and reduce combustion noise.) The air flow control is usually
set automatically according to the fuel flow rate as shown in Figure 2-6.
In this way a constant air to fuel ratio can be maintained.
At this point we should mention that the control scheme shown in
Figure 2-6 is for heaters fired with fuels of fixed composition. Often, the
principle furnace fuel is a refinery or plant fuel gas. As we mentioned
earlier, the composition of such gas can vary considerably. This requires
a more complicated control scheme than the one we have shown here.
Such a scheme might include an automatic chromatograph to monitor
fuel gas composition. This information, along with heater process outlet
temperature, can be fed to a process control computer. The computer
then can be programmed to calculate the required fuel and air flowrates
and reset the respective flow controllers. The exact control requirements
for any given heater will vary depending on the service it is in, the
magnitude of changes in fuel gas composition, etc. You should consult
your Lead Engineer and the Control System Engineer assigned to
process heaters for help in setting up such a control scheme.
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Figure 2-5
TYPICAL CONTROL SYSTEM FOR A NATURAL (DRAFT) HEATER
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Figure 2-6
TYPICAL HEATER CONTROL SCHEME WITH FORCED (DRAFT)
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2.7.2
SECTION
FIRED HEATERS
Secondary Instrumentation
a.
b.
c.
d.
Tubeskin Thermocouples
These warn of excessive temperatures where metal strength might be
dangerously reduced. Using the reading from them, operators can
estimate tube life. And these thermocouples provide yet another way of
monitoring the firing of the furnace.
e.
Draft Gauges
These are usually inclined manometers. They provide air and flue gas
pressure drop and flow data. They are used when adjusting burners and
to indicate limiting operating conditions.
f.
Individual Control
Combination heaters handling multiple services are acceptable providing
the overall heater design permits individual control of each service
without affecting other process services.
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2.7.3
SECTION
FIRED HEATERS
2.7.4
Safety Devices
a.
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b.
Peep Doors
These allow operators to see the internals of the radiant section. They
can thus visually check for tube or burner damage or monitor the tubes
during decoking.
2.8
Turndown Operation
Often, plant personnel will operate a fired heater at lower than design throughput.
This is called turndown operation. If you are aware of special turndown
conditions at which the client wishes to be able to operate, you should indicate
this under "Remarks" on the specification data sheets. The vendor will take this
into account in the mechanical design of the heater. Generally, the minimum
operating range of the burners is 25-35 % of the normal design duty.
Satisfactory turndown operation may require special instrumentation or one or
more auxiliary burners. To illustrate why, let's look at an example.
Consider the fired heater shown in Figure 2-2. Assume that we are operating the
heater at 75 % throughput. Now consider the convection section where we
generate and export steam to the other parts of the plant. Let's say that the
plant does not have enough boiler capacity to make up for any cutback in steam
production here. At 75 % of design throughput, fired duty is about 75 % of its
design value. And, it follows that there is about three-fourths as much flue gas
going up the stack relative to the design case. Now, if we keep the water flow
through the convection coils at design rates, we might still be able to extract
enough heat to maintain design steam production. But, in the process, we will
most likely cool the flue gas below its acid dew point. From our earlier
discussion, this is clearly an untenable situation. In this case, one or more
auxiliary burners are needed in the stack. During turndown operation, the
operators can fire these burners to put sufficient heat into the flue gas to
maintain the desired level of steam production and keep the flue gas above its
acid dew point. Alternately, stainless steel tubes may be used in the uppermost
convection coil along with a stainless steel liner in the stack itself. Stainless steel
will not corrode in an acid environment; however, this material is very expensive
relative to carbon steel.
Now, if it is not critical to maintain design steam production at all times, then we
might choose to limit steam production at reduced furnace firing rates. To do
this, we could provide a bypass for the boiler feedwater around the preheat coil.
Flow through the bypass could be controlled to maintain stack exit temperature
safely above the acid dewpoint. During turndown operation, the bypass will open
allowing colder boiler feedwater to enter the steam drum. This changes the
system heat balance, lowering the overall steam production. As you can see,
client preferences and site specific considerations can dictate what
accommodations are needed for turndown operation.
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Before leaving this subject, let's look at one more example. Consider the fired
reboiler shown in Figure 2-1. In this case, the convection section is used to heat
the process fluid and the incoming combustion air. For a reduced process
throughput, the fired duty and air flow are proportionally lower. Since no
significant imbalance in the various heat duties should result, special burners or
instruments are probably not needed. Note that in this case, turndown operation
of the system as a whole is likely to be limited by the design of the associated
distillation column.
2.8.2
Overdesign
Fired heaters are often capable of satisfactory operation at nominally higher than
design duties and process throughputs. Such "overdesign" is inherent in most
process equipment. As you are probably aware, the heat transfer and pressure
drop correlations used in the design of fired heaters all have varying degrees of
uncertainty. To compensate for this, the vendor allows for more heat transfer
surface, a greater number of tubes, extra firing, etc. The vendor can then
confidently guarantee the required performance of the heater. Sometimes the
client specifies the amount of overdesign for various parts of the furnace. If,
however, this is left up to you (and the vendor), the following two general
guidelines may be used. First, burners and flues should be specified to permit
operation at 125 % of design heat release and 30 % excess air for fuel gas or
40 % excess for fuel oil. Second, fired heater duty should generally be designed
for continuous service at 10 % above the normally expected process operating
duty. This should be defined as normal flow at a lower inlet temperature. These
guidelines also compensate for variations in operations elsewhere in the unit,
e.g., fouling in an exchanger that preheats the furnace feed.
2.9
MISCELLANEOUS GUIDELINES
2.9.1
Heater Selection
Heater type selection is the joint responsibility of the Process and mechanical
Engineers. You can refer to Table 2-2 for general guidance. You should first
review the article entitled "Fired Heaters -1" taken from the July 19, 1978 issue of
Chemical Engineering. A copy of this article, included at the end of this article,
discusses the various types of fired heaters listed in Table 2-2.
Occasionally, several different services ("coils") may be placed in a single heater
with a cost saving. This is possible if the services are closely tied to each other
in the process. Catalytic reforming preheater and reheaters in one casing is an
example. Desulfurizer reactor heater and stripper reboiler in one casing is
another example. This arrangement is made possible by using a refractory
partition wall to separate the radiant coils. The separate radiant coils may be
controlled separately over a wide range of conditions by means of their own
controls and burners. If a convection section is used, it is usually common to the
several services. If maintenance on one coil is required, the entire heater must
be shut down. Also, the range of controllability is less than with separate
heaters.
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Each of these heater types may be shop fabricated if size permits. Shop
fabrication reduces costs. However, shop fabrication should not be forced to the
extent of getting an improperly proportioned heater.
2.9.2
Design Temperature
Tube design fluid temperature shall be set according to the following:
Outlet Temperature
Design Fluid Temperature
Up to 750 oF (399 oC)
750 oF (400 oC) or over
Outlet temperature + 10 %
Outlet temperature + 75 oF (42 oC)
For vacuum or coking services, maximum oil film temperature should not
be more than 50 oF (28 oC) above the maximum bulk oil temperature.
b.
Design Pressure
Design pressure shall be set according to the following:
Maximum Operating Pressure
(Under Fouled Conditions)
-
Design Pressure
operating + 10 %
operating + 100 psi
(6.895 MPa)
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Material
Carbon Steel & Low Chrome
(up to 4 %)
Alloy (above 4 % chrome)
2.9.4
SECTION
FIRED HEATERS
Corrosion Allowance
1/8"
1/16"
Pressure Drop
The process engineer must specify allowable pressure drop. Pressure drop is
the main factor in determining tube size and number of parallel passes.
Heater designers like to see high allowable pressure drop because this reduces
the number of parallel passes and tube size, hence, cost. It also reduces the
process piping, valving and controls required. If a maximum skin temperature or
film temperature is specified, higher pressure drop permits these criteria to be
met with less heater surface. These savings, however, are balanced by the
higher pumping cost.
Large heaters justify more pressure drop than small heaters because the larger
flow rates require more parallel passes at the usual diameters and lengths of
heater tubes.
When the process fluid is heated in both the radiant and convection sections of
the heater, consider providing a combined allowable pressure drop. This lets the
heater designer utilize the available pressure drop in an optimum design.
Manifolds are the piping outside the heater box which connect the passes to
process piping. Sometimes they are furnished by the heater manufacturer when
the thermal expansion of the manifold and the heater tubes can be handled best
by one designer, or whenever it is economical to use extruded header openings.
Sometimes they are furnished by Fluor Daniel as part of the process piping.
Unless it is certain that the heater vendor will furnish the manifolds and include
the manifold pressure drop in the allowed pressure droop for the heater, then the
process engineer should allow for it in the process piping pressure drop.
See Table 2-1 for a listing of typical pressure drops for various types of heater
services.
2.9.5
Piping Considerations
a.
Multipass Heaters
Process engineers often specify that piping to multipass heaters must be
symmetrical. Piping designers will interpret this instruction literally, and a
very expensive manifold can result. If the heater has an odd number of
passes, it is impossible to have symmetrical piping. It may be more
economical to allow a few extra psi in the pumps and achieve equal flow
resistance by means of a globe valve on each pass. However,
symmetrical piping is very important on heaters which cannot
have
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individually controlled passes and which have low pressure drops, i.e.,
catalytic reformer heaters. Also, keep in mind that similar equivalent
lengths and head are required and not absolute symmetry.
Multipass heaters in vaporizing service should have flow control on each
pass if practical. This usually means flow indicators and hand operated
globe valves, but occasionally automatic flow control is used. Do not
forget to allow pressure drop for this control.
b.
Two-Phase Flow
Certain processes (desulfurizers, hydrocrackers) have heat exchange
trains which preheat the feed to the furnace. Hydrogen recycle may also
be mixed with the feed. This situation causes a two-phase feed to the
heater. It is very desirable to flow control each pass to a multipass
heater and this cannot be done with two-phase flow. The use of single
pass heaters is one solution, but the tubes may become very large.
Some other solutions to the problem which may be considered are:
Heat Hydrogen recycle in a separate heater.
Separate the two-phase mixture in a vessel and flow control
each phase separately.
Use parallel trains with single pass heaters.
Slugging and vibration has been encountered in heater outlet lines with
two-phase flow when the velocity is too low.
The following
recommendations should help prevent these problems from occurring in
these situations.
1.
Calculate the velocity and mix density at the highest and lowest
pressure of the line. A large pressure drop in the line may
require intermediate velocity and density calculations and line
size changes. Pressure drop is to be calculated in the usual way
for two-phase flow.
2.
If the velocity is too low, either the line size must be decreased and
higher pressure drop allowed, or the mixture density must be varied by
changing the vapor/liquid ratio; or a piping design must be used as
described in the following paragraph.
Piping design has a significant effect on slugging. If slugging will occur
according to the limiting velocity chart and the line may not be
reduced
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due to pressure drop limitations, then the larger line may be used
provided the horizontal portions are sloped downward and a P-trap is
added to the vertical portion. Two methods of sloping the line are shown
in Figure 2-8.
In all cases, even if slugging is not indicated on the limiting velocity chart,
all upward changes in direction should be vertical and not sloped. This
will prevent a liquid pocket from forming at the bend which would
ultimately lead to slugging as shown in Figure 2-8.
c.
Burner Piping
Burner valves are usually special globe or needle valves with position
indicators. Gas burner valves are located close to the burners, but far
enough away to protect the operator from flashback. Oil burner valves
are located close to the peepholes. When atomizing steam is required, a
check valve is provided in the steam line to prevent oil from backing into
the steam system.
2.9.6
Heater Grid
You should prepare a heater grid as part of the specification for any heater in
vaporizing service where the pressure drop through the tubes is 50 psi
(0.345 MPa) or greater and where the process material is a mixture of
components, e.g., crude oil or naphtha. Typically, crude and vacuum heaters
and fired reboilers fall into this category. A heater grid graphically shows the
equilibrium relationships between temperature, pressure, enthalpy and
vapor-liquid distribution for the process material. Figure 2-9 shows an example
heater grid. The exact temperature-pressure equilibrium path through the heater
cannot normally be predicted in advance and varies with vendor design. The
heater grid enables the vendor to extrapolate the equilibrium data as needed in
the design.
To prepare a heater grid, you must first estimate the pressure profile for the
process flowpath. You can refer to Table 2-1 for guidelines for minimum
pressure drop through the heater. From the column or crude tower computer
simulation, you know the pressure and temperature of the process material at
the tower inlet and the required duty of heater. You must decide on the percent
vaporization in the heater. This is usually on the order of 40-50 % for reboilers
and 50-75 % for crude and vacuum heaters. When dealing with a crude or
vacuum heater, you know the pseudo-composition of the process material, i.e.,
ASTM distillation data, characterization factors, etc., and its flowrate from the
process heat and material balance. In the case of a reboiler, however, you must
estimate the process stream composition based on the composition and
flowrates of both the bottoms liquid and the liquid leaving the bottom tray. Once
you determine the process material composition for the reboiler loop, and set the
percent vaporization, then the process flowrate is fixed. you can then run
computer flash calculations on the material for various temperatures, over the
range of system pressures. Using the results, you can construct a heater grid as
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shown in Figure 2-9. For vacuum column heaters, the procedure we have
outlined here is further complicated by
Figure 2-7
LIMITING VELOCITY - 2 PHASE FLOW IN VERTICAL LINES
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Figure 2-8
PIPING DESIGN FOR TWO-PHASE FLOW
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Figure 2-9
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the need for a trial and error calculation to optimize the size of the line between
the heater and the column. Refer to the Fluor Daniel Crude and Vacuum Unit
Design Manual for more details.
2.10
DECOKING
Coke is a residue of heavy aromatic compounds often formed on heat transfer surfaces
from which hydrocarbons are evaporated. In general, coke deposits can be expected on
the insides of fired heater tubes in hydrocarbon service above 600 oF (316 oC). The
heavier the hydrocarbons, the greater their coking tendency is. The presence of
hydrogen and/or steam tends to retard coke formation. Some coking and noncoking
furnace applications are listed below.
Coking Services
Atmospheric and vacuum pipe stills
H2 treater preheaters and interheaters
Thermal reforming
Visbreaking
Steam cracking
Crude
Noncoking Services
Hydrocarbon operations below 600 oF (316 oC)
Reforming furnaces (high H2)
For a process heater in coking service, you must specify tube temperature and pressure
during decoking. Usually, pressures are in the range of 10-50 psig (0.069-0.345 MPag).
Tube temperatures must be kept below 1300 oF (704 oC). You must also specify the
necessary auxiliary equipment such as the decoking quench drum, steam and air flow
meters, etc.
Decoking of furnace tubes is, in general, carried out as follows. The operators first shut
the heater down and remove any process material remaining in the tubes. next, they put
steam through the tubes at rates of 15-20 lb/sec ft2 (73.2-97.6 kg/m2 sec) and fire the
heater to yield a flue gas temperature of 1,350 oF (732 oC). This cracks about 90 % of
the coke off the tubes. next, the operators reduce the steam rates to around 5-7 lb/sec
ft2 (24.4-34.2 kg/m2 sec) and cut back on firing to lower the flue gas temperature to
1,200 oF (649 oC). Next, they gradually admit air in with the steam to burn off the
remaining coke. The burning process is monitored by watching tube temperature and
CO2 levels in the furnace effluent. Tubes must be kept below 1,300 oF (704 oC) and CO2
should stay below 19 % in the effluent gas. Visual monitoring of the tubes to watch for
hot spots is a must. Sometimes the operators choose to decoke at night when hot spots
are easier to see.
For a heater in coking service, you should specify a permanent steam-air decoking
system. One such system having two-directional manifolds appears in Figure
2-10.
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These are called "two directional" since steam and air can flow in either direction through
the furnace tubes. Using this type of system, only one tube pass can be decoked at a
time. Water is injected into the decoke effluent from each pass to stop the cracking and
combustion processes and to cool the material off. A knockout drum is needed to catch
the quench effluent. The drum should drain or be pumped out to an API separator where
oil, water and coke solids can be separated.
Figure 2-11 shows an alternate decoking system. In this system, all furnace tubes are
decoked at the same time. This saves considerable time and, hence, results in greater
on-stream time for both the heater and the unit in general. Steam and air injection is in
one direction only and this simplifies the manifolding at the heater. Here the decoking
effluent is quenched to 1,000 oF (538 oC) upstream of the knockout drum. Water is then
injected into the drum to further cool the effluent. There are, however, several
disadvantages to this type of system compared to the two-directional type. Since the
decoking steam is not condensed by the initial water injection, the knockout drum must
be bigger and must operate at a higher temperature. The venting rate from the drum is
higher since the incoming steam is not condensed. In practice, the cracking step in the
decoking process is not as effective as for a two-directional system.
2.11
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DATE
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FIRED HEATERS
PROCESS DESIGN CRITERIA
PROCESS MANUAL
1.0
Figure 2-10
TWO-DIRECTIONAL STEAM-AIR DECOKING SYSTEM
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1.0
Figure 2-11
ALTERNATE STEAM-AIR DECOKING SYSTEM
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DATE
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FIRED HEATERS
PROCESS DESIGN CRITERIA
PROCESS MANUAL
1.0
2.12
EXAMPLE CALCULATIONS
2.12.1 Boiler Efficiency Calculation
a.
Basic Data
1.
2.
Diesel one barrel = 5.4 x 106 Btu LHV or 5.8 x 106 Btu HHV
FX-B, 2/12/79.
Assume diesel data based on attached charts
38 o API S.G. = 0.835
1 BBL = 292.1 lb
LHV
Gal
= 5.4 x 106 Btu BBL
= 18.484 Btu/lb
BBL
42 gal 8.33 x 0.835 lb
C:
H:
MW
1BBL
wt %
86
14
100
wt
6
1
7
lbs/BBL
251
41
292
= 205
= 1.43 MOLES
Heat Balance
Base firing on 100 MOL/hr gas
Oil fired duty
Total fired duty
Diesel Required
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= 2.76 - 2.76
0.9
6
Btu/hr = 0.057 BBL/hr
= 0.31 x 10
6
5.4 x 10 Btu/BBL
MOL/BBL
20.92 C
20.50 H2
` FLUOR DANIEL
MW
(a)
MOL/hr(b)
2.02
H2
2.0
PAGE
36
DATE
10-94
PROCESS MANUAL
COMP
SECTION
FIRED HEATERS
O2
X
O2 REQ
MOL/hr
SO2
CO2
H2 O
O2
N2
COMBUSTION CALCULATIONS
CO
0.5
51,623
4,347
CO
28.01
0.5
CO2
44.01
21,495
20,418
CH4
16.04
2.0
C 2 H6
30.07
3.5
20,275
19,937
C 2 H4
28.05
3.0
C 3 H8
44.10
5.0
19,687
19,678
C 3 H6
42.08
4.5
C4H10
58.12
6.5
C 4 H6
56.11
6.0
N2 + A
28.01
1.5
6,537
4,149
H2 S
34.08
COS
60.08
1.5
S02
64.06
H2 O
DIESEL
205
Total MOL/hr
1.43
1.43
11.8
31.17
20.92 -
20.50
31.17
20.92
20.50
18,484
Assume None
178.04
3.77
140.64
3.77
181.81
FLUE GAS
COMPONENTS, MOL/hr
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6.23
37.40
6.23
140.64
19,493
1
31.17
(a)(b)(c) Heat
Released Btu/hr
20.92
24.27
6.23
140.64
5,4 X 106
` FLUOR DANIEL
H2
2.0
PAGE
37
DATE
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PROCESS MANUAL
COMP
SECTION
FIRED HEATERS
MW
(a)
MOL/hr(b)
2.02
7.83
O2
X
0.5
CO
28.01
1.91
0.5
CO2
44.01
27.18
O2 REQ
MOL/hr
3.92
1
0.96
-
CO2
SO2
H2 O
1
COMBUSTION CALCULATIONS
CO
(c)LHV Btu/lb
(a)(b)(c) Heat
Released Btu/hr
O2
N2
7.83
51,623
816,500
1.91
4,347
232,561
27.18
CH4
16.04
1.25
2.0
2.50
1.25
C 2 H6
30.07
0.46
3.5
1.61
2.50
21,495
430,975
0.92
1.38
20,418
0.56
232,426
0.56
20,275
159,240
0.66
0.88
19,937
193,429
0.63
19,687
173,970
0.65
19,678
148,679
19,493
C 2 H4
28.05
0.28
3.0
0.84
C 3 H8
44.10
0.22
5.0
1.10
0.63
0.52
C 3 H6
42.08
0.21
4.5
0.95
C4H10
58.12
0.13
6.5
0.85
C 4 H6
56.11
NH3
17.03
0.08
N2 + A
28.01
55.27
6.0
H2 S
34.08
0.002
1.5
60.08
1.5
64.06
H2 O
C5 +
86.17
Total MOL/hr
COS
S02
0.003
0.002
0.08
55.27
446
0.002
6,537
4,149
5.01
5.01
0.19
7.5
1.14
1.33
19,415
317,868
100.02
1.81
14.54
17.45
65.61
83.06
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55.35
2.91
20.77
Assume None
14.54
2.91
1.76
65.61
1.76
84.82
34.77
0.002
22.53
2.91
120.96
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38
DATE
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FIRED HEATERS
PROCESS DESIGN CRITERIA
BOILER FREQUENCY
STACK LOSSES
CO2
MOLS F.G. from 100 MOL/hr Gas
34.77
O2
TOTAL
N2
2.91
120.96
1.38
0.36
8.02
35.96
23.91
3.27
128.98
10.1
8.2
7.25
7.05
1.19
0.002
H2 O
22.53
SO2
N/L
152,542
82,346
Atomizing Steam
9,957
381,910
626,755
Neglect
626,755
10
8.2
133,052
7.25
75,543
Atomizing Steam
8,772
7.05
336,444
553,811
Neglect
o
553,811
Note:
Assume 80 oF Base Temperature
BOILER HEAT BALANCE
OUT @ 500 oF
IN
Air @ 80 oF
o
Fuel Gas @ 95 F
Fuel Oil @ ? oF
Atomizing Steam
Total Fuel LHV Btu/hr
10,500
Neglect
Neglect
3,070,000
2,376,732
OUT @ 450 oF
3,080,500
o
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2,439,176
626,755
553,811
77,013
77,013
3,080,500
3,080,500
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39
DATE
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FIRED HEATERS
PROCESS DESIGN CRITERIA
PROCESS MANUAL
MW
MOLES
Carbon
87.26
87.26
12
7.27
Hydrogen
10.49
10.49
10.49
Oxygen
0.64
0.64
16
0.04
Nitrogen
0.28
0.28
14
0.02
Sulfur
0.84
0.84
32.06
0.26
Ash
0.04
0.04
100
b.
Lb
100
18.08
0.26
= 20
0.26 = 21
0.0124 = = MOLES SO3, and
0.26 - 0.0124 = 0.2476 MOLES SO2
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FIRED HEATERS
PROCESS DESIGN CRITERIA
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c.
d.
7.27 C
(1/1) 7.27 O2
7.27 CO2
7.27
10.49 H
(1/4) 10.49 O2
5.245 H2O
2.62
0.04 O
(1/2) 0.04 O2
0.04 O2
0.02
0.02 N
(1/1) 0.02 O2
0.02 NO2
0.02
0.2476 S
(1/1) 0.02476 O2
0.2476 SO2
0.25
0.0124 S
(3/2) 0.0124 O2
0.0124 SO3
0.0186
10.1992
Air Required
= 46.04 MOLES
= 12.239 - 10.1992
= 2.0398 MOLES O2
Note that we have implicitly assumed that none of the N2 from the air
reacts to form NOx. Strictly speaking, this is not true, but is a good
approximation.
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FIRED HEATERS
PROCESS DESIGN CRITERIA
PROCESS MANUAL
MOLES
MW
MOLE
FRACTION
CO2
7.27
44
0.1194
319.88
H2O
5.250
19
0.0862
94.41
O2
2.040
32
0.0335
65.28
46.04
28
0.7563
1,289.12
NO2
0.02
46
0.0003
0.92
SO2
0.2476
64
0.0041
15.81
SO3
0.0124
80
0.0002
1.04
1.0000
1,786.46
N2
60.875
e.
LB
Calculate PPM SO3 (Dry Basis) and partial pressure of H2O vapor, then
find SO3 dew point from Figure 2-4.
SO3 PPM Dry = [ 0.0124 / (60.875 - 5.245) ] 106 = 223 PPM
H2O Partial Press
Pressure leaving radiant zone is slightly negative.
Assume P = 750 mm Hg
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DATE
03-96
FIRED HEATERS
FIRED HEATER REBOILER
PROCESS MANUAL
1.0
1.0
2.0
3.0
GENERAL
We now discuss heater process calculations and how to specify a fired heater reboiler.
This is one of the most common kinds of fired heaters used in the oil and petrochemical
industries. The principle uses for fired heater reboilers are large duty, high temperature
services such as crude towers, large debutanizers, and large desulfurizer fractionators
(the case for out example reboiler). At appropriate points in our presentation, we refer to
the Fired Heater Specification Sheets at the end of this subsection to point out where the
results of our calculations should be filled in. Before beginning, however, we want to give
you some background information about our example heater.
The example is for a fired reboiler on a stripping column in a naphtha
hydrodesulfurization (HDS) unit. The naphtha is hydrotreated in a fixed bed catalytic
reactor to convert the sulfur, which is present in various compounds, to H2S. The
naphtha and unreacted hydrogen are separated in a vessel before the naphtha is fed to
the stripping column where H2S is removed. In the stripper, the C5 and lighter
hydrocarbons are also taken overhead since they are not desirable in the downstream
reformer which converts the naphtha to a high octane gasoline blending stock.
3.2
CALCULATIONS
The first step in the calculations is to establish the heat and material balance for the unit
in which the reboiler functions. This is usually done on the computer. Figures 3-1A and
3-1B show an example of what the output looks like. (Computer output is from a different
example.) At this point we know only the reboiler duty and some of the properties of the
liquid to the reboiler. For our example heater, the required duty is 55.56 MM Btu/hr
(16.3 MW). The fluid conditions at the column inlet are 498 oF (259 oC) and 140 psig
(0.965 MPag). The computer calculations are based on a once-through thermosyphon
reboiler with liquid from the last tray as feed. For a fired reboiler, the Process Engineer
sets the percent vaporization and performs additional calculations, either by hand or
computer, to characterize the process conditions for the fired heater. The calculations
should proceed as follows:
3.2.1
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FIRED HEATERS
FIRED HEATER REBOILER
1.0
Figure 3-1A
STRIPPER MATERIAL AND HEAT BALANCE
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FIRED HEATERS
FIRED HEATER REBOILER
1.0
Figure 3-1B
STRIPPER
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FIRED HEATERS
FIRED HEATER REBOILER
1.0
Figure 3-2
REBOILER CIRCULATION LOOP SKETCH
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FIRED HEATERS
FIRED HEATER REBOILER
1.0
3.2.2
Pressure Profile
You must estimate the pressure profile for the reboiler circulation loop. We have
done this in Figure 3-2 for our example reboiler. From the computer stripper
calculation we know that the fluid conditions at the column inlet are 140 psig
(0.965 MPag) and 498 oF (259 oC). Based on experience with similar heaters,
we assumed a total pressure drop through the radiant and convection sections of
45 psi (0.31 MPa). We have allowed 20 psi (0.138 MPa) drop across the heater
inlet control valve. The static head loss between the pump centerline and the
heater inlet is approximately 7 psi (0.048 MPa) (20' (6.1 m) of liquid with 0.7531
specific gravity). And, we have assumed the following line friction losses:
10 psi (0.069 MPa) from the pump to the heater inlet control valve.
3 psi (0.021 MPa) from the control valve to the heater inlet.
15 psi (0.103 MPa) from the heater outlet to the tower inlet.
3.2.3
Fluid Composition
As we mentioned earlier, the composition of the reboiler liquid as given by the
computer stripper simulation is incorrect. For our example stripper, the
composition and conditions of the bottoms product and the reboiler inlet liquid are
the same. The liquid at the heater inlet has an API gravity of 56.4 and a
temperature of 484 oF (251 oC).
3.2.4
Percent Vaporization
This usually ranges from 40-50 % for fixed reboilers. In this case we have
chosen 42 %. Vaporization of more than 50 % of the heater throughput often
leads to increased coking, poor fluid hydraulics, reduced internal heat transfer,
and tube overheating. Now, we know the reboiler duty and we have set the
composition of the reboiler feed and the percent vaporization. This fixes the
circulation rate through the reboiler. To calculate this number, we must now run
flash calculations on the system.
3.2.5
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54.5o at the heater outlet. The heater outlet temperature is 507 oF (264 oC) at a
pressure of 155 psig (1.069 MPag).
We plotted the results of the flash calculations on a heater grid as shown with the
heater specification sheets at the end of this subsection. Note that we split the
data between two separate graphs instead of putting it all on one chart as shown
in the design criteria part of this section.
3.3
SPECIFICATION SHEETS
After completing the above calculations you can fill in the following general information
and material balance data on "Revision A" of the Fired Heater Specification Sheets
(Form E-533A):
Line Number
1
2
3
4
5
6
7
8
9
10
15-24
25-35
Description
Client Name
Heater Service
Unit
Heater Type
Heater Section
Service
Heat Absorption
Fluid Type
Process Fluid Flowrate
Allowable Pressure Drop Through Heater Tubes
Fluid Conditions at Heater Inlet
Fluid Conditions at Heater Outlet
Note that we have left the vendor to decide the split of heat absorption between the
radiant and convection sections. Furnace designers have developed many proprietary
designs for tubular heaters to make efficient use of fuel and provide satisfactory and
economic mechanical design. Unless you encounter a special situation, you should give
the vendor a free hand in this phase of the design.
As a continuation of our discussion we will complete filling out "Revision A" of the Fired
Heater Specification Sheets and we will present these along with the final "Approved for
Construction" version of these data sheets for our example in Section 3.5. You should
note that other than specifying materials of construction and corrosion allowance, the
Mechanical Engineer assigned to fired heaters made no changes to the "Revision A"
data sheets. There are probably two reasons for this. First, as mentioned in the
introduction to this section, Fluor Daniel specifies the performance of a fired heater while
the furnace vendor actually does the mechanical design. The Mechanical Engineer
monitors and checks the vendor's work throughout the design on behalf of both Fluor
Daniel and the client. He or she will keep the Process Engineer abreast of any changes
recommended by the vendor and will assist in revising the specification sheets as
needed. Second, the Process Engineer consulted with his counterpart in the Mechanical
Engineering Department during the initial specifications of the heater. Such matters as
basic furnace configuration, convection heat recovery, equipment items included in the
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FIRED HEATERS
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scope, etc., were discussed. This should be a standard practice in all such cases. In
this way, much unnecessary recycle of information can be avoided.
The following items must also be filled in by the Process Engineer for the initial issue of
the specification sheets. These are listed below and discussed according to subject and
location on the data sheets.
3.3.1
3.3.2
3.3.3
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FIRED HEATERS
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3.3.4
3.3.5
3.3.6
Fuel Data
(Form E-553-B, Line 18-34)
The client may supply information on fuel types, composition and available
temperature and pressure. Otherwise, the Utilities Engineers develop this
information. For our example, we have specified three fuels, two for the furnace
burners and one for the pilots. Refinery fuel gas is the normal heater fuel. The
composition of this gas varies and the supply of it is subject to interruption.
Pipeline natural gas, on the other hand, is the fuel for the pilots. This is not
unusual since for stable operation the pilots require a reliable supply of gaseous
fuel having constant composition. For future operation, we have specified No. 6
Fuel Oil.
The heating value of the fuel gas ranges from 600 - 1,034 Btu/SCF
(23,620 - 41,010 kJ/Nm3) and its specific gravity ranges from 0.567 to 0.704.
These numbers reflect wide variations in composition. We have provided the
composition of the fuel gas corresponding to its lowest heating value. Under
these conditions, the gas contains 40.8 % H2 and 8.0 % N2, both on a molar
basis. The gas also contains 0.2 grains of sulfur per standard cubic foot (SCF)
(0.48 g/Nm3). Paraffin hydrocarbons ranging from methane through butane
comprise the balance of the fuel gas.
Our client wants the capability to fire the heater with No. 6 Fuel Oil. This oil has
a LHV of 18,000 Btu/lb (41,870 kJ/kg) and a HHV of 19,000 Btu/lb
(44,200 kJ/kg). Its carbon to hydrogen ratio is 8.7/1 on a weight bases and it has
a flash point of 150 oF (66 oC). The oil contains 0.30 % bound nitrogen, 0.74 %
sulfur, and 0.05 % ash, all on a weight basis. The levels of sodium and
vanadium are 40 ppm and 20 ppm, respectively.
The pilot gas is pipeline natural gas containing 97 % methane, 1.6 % CO2, and
1.4 % N2, all on a molar basis. Its molecular weight is 16.6 and its specific
gravity is 0.575. The gas has a LHV of 882 Btu/SCF (34,720 kJ/Nm3) and a
HHV of 975 Btu/SCF (38,380 kJ/Nm3), and we will deliver it to the pilots at
150 psig.
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FIRED HEATERS
FIRED HEATER REBOILER
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3.3.7
3.4
AUXILIARY EQUIPMENT
A fired reboiler is a simple-type direct fired tubular heater as defined in the introduction to
this section. From our discussion so far, you probably realize that a fired reboiler
basically consists of a radiant and a convection section, a flue stack, burners, internal
piping and ducts, and numerous related controllers and indicators. Other related
equipment items, e.g., combustion air fans, are not part of the heater itself even though
they may be supplied by the vendor and their functions may be directly linked to that of
the heater. The auxiliary equipment is basically descried in the first section on Page 2 of
the specification. In addition, the following items may also be considered auxiliaries.
3.4.1
3.4.2
3.4.3
3.5
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FIRED HEATER REBOILER
1.0
Pages 3-8 of the Revision A specification sheets (Forms E533C-H) are not shown since
the Process Engineer did not add any information to them in this example. In practice,
however, you should include these blank data sheets with your original specification.
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3.6
These considerable disadvantages have limited the application of fired heater reboilers in
recent years. Principal uses are now large duty, high temperature services such as
crude
towers,
large
debutanizers/naphtha
stabilizers,
large
desulfurizer
stabilizers/fractionators.
An early decision on fired heater usage is required to improve plot plan layout, to ensure
proper cost estimation, sufficient allocation of plot space, and design/construction
manpower.
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FIRED HEATERS
CRUDE OIL HEATER
PROCESS MANUAL
1.0
1.0
2.0
3.0
4.0
GENERAL
We now discuss heater process calculations and how to specify a crude oil heater. This
type of heater is found exclusively in oil refineries. It is used to partially vaporize the oil
feed to an atmospheric crude tower in a crude unit. At appropriate points in our
presentation, we refer to the Fired Heater Specification Sheets at the end of this
subsection to point out where the results of our calculations should be filled in. Before
beginning, however, we want to give you some background information about our
example heater.
Our example is a crude heater on an atmospheric crude column in an oil refinery. The
atmospheric column is part of a crude unit. Such a unit separates virgin crude oil into
several fractions which have characteristic boiling ranges. The refiner can either market
these directly or process the further into saleable products. In a typical crude unit, the
virgin oil is first treated to remove chlorides and other ionic species. This is called
desalting. The oil is then heated and partially vaporized in a fired heater, the crude
heater. From here, the crude goes to the atmospheric tower where the vapor is
fractionated into an overhead product and several sidedraw products. These are sent to
other units for further separation and processing. Refer to the flowsketch shown in
Figure 4-1. The higher boiling crude fractions, taken out the bottom of the column,
undergo further separation in a vacuum stripping tower.
4.2
CALCULATIONS
Establishing the heat and material balance is the first step in calculating a crude unit.
This is usually done on the computer. Figure 4-2 shows the computer printout for the
crude oil feed to the heater. At the heater inlet the oil conditions are 148.7 psia
(1,025 MPaa) and 517 oF (269 oC). The total flow is 765,600 lb/hr (347,270 kg/hr).
Figure 4-3A and 4-3B shows the feed compositions and conditions at inlet to the crude
column. At a pressure of 44.7 psia (0.308 MPaa) and a temperature of 710 oF, (377 oC)
there are 609,631 lb/hr (276,530 kg/hr) of liquid and 155,963 lb/hr (70,744 kg/hr) of
vapor.
The heat required to vaporize slightly over 20 % of the crude oil feed and deliver it to the
tower at these conditions equals 113.69 MM Btu/hr (33.31 MW). This is the duty of the
crude heater. At this point you do not know the process conditions at the heater outlet.
You must calculate these as follows:
4.2.1
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Figure 4-1
BASIC CRUDE UNIT FLOW SKETCH AND CONTROL SCHEME
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Figure 4-2
DATA FOR FEED TO CRUDE HEATER
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Figure 4-3A
DATA FOR CRUDE TOWER FEED AT TOWER INLET
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Figure 4-3B
DATA FOR CRUDE TOWER FEED AT TOWER INLET
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process equipment and 100 ft (30.48 m) away from building, boilers, motor
control centers, etc. These minimum distances are favored by the Oil Insurance
Association (O.I.A.) and Factory Mutual Insurance and should be followed if
client standards are not given. Remember, that in addition to the safety
problems posed by an open flame, you must consider accessibility for
maintenance in locating a heater. Taken together, these considerations ensure
that a crude heater will be located some finite distance (on the order of 50 ft)
(15.24 m) away from the column it serves.
4.2.2
Pressure Profile
You must estimate the pressure drop through the heater and from the heater to
the column. The heater pressure drop is usually in the range of 70-100 psi
(0.482-0.689 MPa); however, the drop can be as high as 150-200 psi
(1.034-1.379 MPa). For our example, we chose 100 psi (0.689 MPa) pressure
loss through the crude heater. For the line running from the heater to the column
there is no static head loss. We have allowed 4 psi (0.028 MPa) friction loss in
this line.
4.2.3
Flash Calculations
You should now do flash calculations on the crude oil for ranges of temperature
and pressure that overlap those you expect the system to operate at. Base
these conditions on your heat and material balance and pressure profile. The
flash calculations are most often done on the computer. The preferred models
are a heat exchanger or a series of flashes.
For our example, we ran computer flash calculations for pressures of 1.0, 34, 60,
100 and 140 psig (0.007,0.234, 0.414, 0.689 and 0.965 MPag) at temperatures
ranging from 500 oF (260 oC) to 750 oF (399 oC). At the heater outlet we found
that out of a total flowrate of 765,600 lb/hr (347,270 kg/hr), we have 601,425
lb/hr (272,800 kg/hr of liquid having an API gravity of 11 o at 60 oF (16 oC) and
164,175 lb/hr (74,470 kg/hr) of vapor having a molecular weight of 159.8. This
represents 21.4 % vaporization by weight in the heater. The outlet temperature
is 718 oF (381 oC) at a pressure of 34 psig (0.234 MPag).
We plotted the results of the flash calculations as shown on pages 9-12 of the
"Revision A" heater specification sheets (see Section 4.5). Note that we present
the data on four separate plots instead of putting it all on one chart as shown in
the design criteria part of this section. Note also that we have not included
enthalpy data in our plots. This is acceptable since the vendor uses our flash
data to calculate the two phase pressure drop throughout the heater. The
necessary parameters include temperature, pressure, vapor-liquid distribution,
liquid gravity, and vapor molecular weight. The vendor designs the burners and
other pieces of the furnace based on the duty we calculate.
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4.2.4
1
Convection Duty = Radiant Duty
Radiant Efficiency
And we find that the available convection heat is 49.55 MM Btu/hr (14.53 MW).
The process fluid absorbs 34.10 MM Btu/hr (10.0 MW) of this heat (30 % of the
absorbed duty), and, hence there are 15.44 MM Btu/hr (4.53 MW) left over.
How should we recover the remaining stack gas heat? We could only generate
approximately 15,000 lb/hr (6,804 kg/hr) of steam with it. This is insignificantly in
terms of the overall needs of the refinery and probably wouldn't yield a sufficient
return on the investment in the necessary equipment such as a stream drum and
boiler feed pumps. And, besides, there isn't room for such auxiliary equipment in
our example since plot space is limited. We could use the flue gas heat to
preheat the incoming combustion air. This would raise the overall thermal
efficiency of the heater to around 90 % but would require a capital investment in
the preheater, air ducts, etc. This is often what is done but in our case there is
still a better alternative. Upon examining the heat and material balance for the
crude unit we notice that the required reboiler duty for a column called the
prefractionator is 12.8 MM Btu/hr (3.75 MW). This column separates the crude
column overhead product into an overhead off gas stream and a light naphtha
bottoms product. To reboil this column using heat from crude heater flue gas
eliminates the need for a separate reboiler. Also, the capital investment in the
required flue stack coils for the crude heater is minimal. Hence, this is our
choice.
Note that according to our estimates we still have 2.64 MM Btu/hr (0.77 MW) of
recoverable flue gas heat. Remember, though, we made a number of
assumptions in our calculations and used a "rule of thumb" correlation. Based
on the results we are confident that there is sufficient heat in the flue gas to heat
the incoming crude oil and to reboil the prefractionator. To go beyond this
requires an accurate determination of the split in absorbed duty between the
radiant and convection sections and a more rigorous calculation of the
recoverable heat. We did this is the case of the steam-hydrocarbon reformer
example presented in Section 5.0. We refer you there for details. In the case of
our crude heater example, however, the project schedule didn't allow sufficient
time for an in-depth look at convection heat recovery. The vendor will ultimately
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decide on the split of absorbed duty between the radiant and convection sections
and will rigorously calculate the convection heat recovery. The vendor will inform
FDI of any necessary changes and will recommend if any additional heat
recovery is feasible.
To adequately specify the convection reboiler section, you must calculate the
process conditions for the reboiler circulation loop. This is discussed in detail in
Section 3.2 entitled Fired Heater Reboiler. For our example here, we present the
final results of the required calculations and leave it to you to research the
details. The results appear on the specification sheets in Section 4.5.
4.3
SPECIFICATION SHEETS
After completing the above calculations you can fill in the following general information
and material balance data on "Revision A" of the Fired Heater Specification Sheets
(Form E-533A):
Line Number
Description
Client Name
Heater Service
Unit
Heater Type
Heater Section
Service
Heat Absorption
Fluid Type
10
15-24
25-35
As a continuation of our discussion we will complete filling out "Revision A" of the Fired
Heater Specification Sheets and we will present these along with the final "Approved for
Construction" version of these data sheets for our example in Section 4.5. You should
note that other than specifying materials of construction and corrosion allowance, the
Mechanical Engineer assigned to fired heaters made no changes to the "Revision A"
data sheets. There are probably two reasons for this. First, as mentioned in the
introduction to this section, Fluor Daniel specifies the performance of a fired heater while
the furnace vendor actually does the mechanical design. The Mechanical Engineer
monitors and
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checks the vendor's work throughout the design on behalf of both Fluor Daniel and the
client. He or she will keep the Process Engineer abreast of any changes recommended
by the vendor and will assist in revising the specification sheets as needed. Second, the
Process Engineer consulted with his counterpart in the Mechanical Engineering
Department during the initial specifications of the heater. Such matters as basic furnace
configuration, convection heat recovery, equipment items included in the scope, etc.,
were discussed. This should be a standard practice in all such cases. In this way, much
unnecessary recycle of information can be avoided.
The following items must also be filled in by the Process Engineer for the initial issue of
the specification sheets. These are listed below and discussed according to subject and
location on the data sheets.
4.3.1
4.3.2
4.3.3
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4.3.4
4.3.5
4.3.6
Fuel Data
(Form E-553-B, Line 18-34)
The client may supply information on fuel types, composition and available
temperature and pressure. Otherwise, the Utilities Engineers develop this
information. For our example, the client specified three fuels, two for the furnace
burners and one for the pilots. No. 2 Fuel Oil is the normal heater fuel. No. 6
Fuel Oil is an alternate fuel. Pipeline natural gas, on the other hand, is the fuel
for the pilots. This is not unusual since for stable operation, the pilots require a
reliable supply of gaseous fuel having constant composition. Table 4-1 gives the
composition and properties of each of these fuels.
4.3.7
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4.4
AUXILIARY EQUIPMENT
A crude heater is a simple-type direct fired tubular heater as defined in the introduction to
this section. From our discussion so far, you probably realize that a crude heater
basically consists of a radiant and a convection section, a flue stack, burners, internal
piping ducts, and numerous related controllers and indicators. Other related equipment
items, e.g., combustion air fans, are not part of the heater itself even though they may be
supplied by the vendor and their functions may be directly linked to that of the heater.
The auxiliary equipment is basically described in the first section of page 2 of the
specification. In addition, the following items may also be considered auxiliaries.
4.4.1
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Table 4-1
FURNACE FUEL DATA TRANSMITTED FROM CLIENT
TYPE
OIL
DESCRIPTION
FUEL OIL
No. 2
API
37
o
NATURAL GAS
(PILOTS ONLY)
35
325
AMB
FUEL OIL
No. 6
14
GAS
18,400
(42,790)
150
(66)
17,500
(40,700)
75
(24)
55
(0.379)
Hydrogen, Wt. %
Sulfur, Wt. %
0.65
0.7
50
Ash. Wt. %
0.15
NIL
100
(0.689)
100
(0.689)
60
(0.414)
60
(0.414)
Composition - mole %
CH4
97
C2H6
C3H8+
N2
1.4
CO2
1.6
3
15
(36)
16.6
882
(34,720)
995
(39,170)
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4.4.2
4.5
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Pages 3 - 8 of the Revision A Specification Sheets are not shown since the only
information the Process Engineer added to them for this example was process
tube metallurgy. In practice, however, you should include these blank data
sheets with your original specification.
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FIRED HEATERS
STEAM - HYDROCARBON REFORMER
PROCESS MANUAL
1.0
2.0
3.0
4.0
5.0
GENERAL
As we said earlier, the steam-hydrocarbon reformer is a reactor-type fired heater used
primarily to produce synthesis gas (H2 + CO) which in turn is used to produce a variety of
products. In our example, the final product is hydrogen. In this process, methane and/or
heavier paraffin hydrocarbons in the vapor state are mixed with steam and fed to the
reformer tubes (fired heater) containing a nickel catalyst. The process starts with all
heavier hydrocarbons cracking to form methane. The methane then reacts with the
steam to produce hydrogen, CO, and CO2. The main reactions are as follows:
CH4
CH4
CO
CH4
+
+
+
+
H2O
2H2O
H2O
CO2
3H2
4H2
CO2
2CO
+
+
+
+
CO
CO2
H2
2H2
(1)
(2)
(3)
(4)
REFORMER CALCULATIONS
5.2.1
Background
The example presented here was a major equipment item in a 50 MMSCFD
(1.34 x 106 Nm3/d) hydrogen plant. The plant was part of a large refinery
modernization designed and built by Fluor Daniel. There are six material balance
cases for the hydrogen plant. Reformer throughput and feed composition
change with each case. The example presented here covers the case for
naphtha feed, the case that sized the reformer, its auxiliaries such as the waste
heat boiler, and most of the other equipment in the Hydrogen Plant.
The naphtha feed in our example has an API gravity of 68 o and a molecular
weight of 73.67. ASTM (D-86) distillation data for the material is given on page 4
of the "Revision A" Specification sheets.
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STEAM - HYDROCARBON REFORMER
Figure 5-1
HYDROGEN PLANT
SIMPLIFIED PROCESS FLOW DIAGRAM
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5.2.2
SECTION
FIRED HEATERS
Calculations
a.
General
We will present and discuss calculations for the example reformer in the
order in which you should perform them. At appropriate points we will
refer to the reformer specification to show where the results of the
calculations should be filled in.
The example calculations and
appropriate tables and graphs follow this narrative in Section 5.5. You
should refer to these throughout this discussion.
b.
Value
4/1
1,550 OF
50 OF
(848 OC)
(10 OC)
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STEAM - HYDROCARBON REFORMER
Figure 5-2
RESULTS FROM COMPUTER MATERIAL BALANCE REFORMER CALCULATION
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1
Convection Duty = (Radiant Duty)
Radiant Efficiency
Alternately, you could use a computer program. The program should calculate
the fired duty, combustion air flow, fuel usage, and radiant efficiency for given
conditions of radiant duty, and preheat air temperature. It is especially useful if
the reformer convection heat balance requires a trial and error solution as is the
case in our example.
Before we discuss this calculation any further, let's look at the heat recovery
scheme we devised for our example. This is shown in Figure 5-3.
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Figure 5-3
HYDROGEN PLANT STEAM BALANCE/HEAT RECOVERY SCHEME
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Reformer effluent gas is used to make steam in the waste heat boiler and is then
sent on to the High Temperature Shift Reactor (HTS). From here the process
gas goes to the Low Temperature Shift Reactor (LTS) where it is cooled against
boiler feed water both as it enters and leaves this reactor. This heated boiler
feed water goes to a vessel called a steam drum. The steam drum operates at
650 psig (4.482 MPag) and 498 oF (259 oC) (saturation conditions). There are
two water circulation loops in operation here. Saturated water from the steam
drum passes through the waste heat boiler and a steam/water mixture returns to
the drum via natural circulation. Circulation pumps send another stream of
saturated water through furnace convection coil No. 3 and a saturated mixture is
then returned to the drum. Steam from the drum is superheated in convection
coils Number 1 and 2. From coil No. 2, steam at 750 oF (399 oC) is sent to the
plant 600 psig (4.137 MPag) steam system. From coil No. 1 superheated steam
at 817 oF (436 oC) is mixed with naphtha vapor in the feed to the reformer. The
molar steam to carbon ratio of the mixture is 4/1 as discussed in Section 5.2.2b,
Process Heat and Material Balance. The heat from the steam raises the
temperature of the combined feed to 800 oF (427 oC). Now that we understand
the flow paths of the Hydrogen Plant steam balance, let's proceed with the
calculations.
5.2.4
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Let's go through the calculation scheme and look at the results for the 400 oF
(204 oC) air preheat case:
Program the computer to perform the Furnace Calculation. Fix the
radiant duty (229.64 MM Btu/hr) (67.35 MW), the percent excess air
(10 %), the fuel gas properties and the flue gas temperature leaving the
radiant section (1,900 oF (1,038 oC), a reasonable estimate). Increment
the air preheat temperature and allow the air flow and fuel flow to vary.
The output for our example is shown in Figure 5-4 A&B.
Using the computer output (Figure 5-4 A&B), plot the flue gas cooling
curve for each case, as shown in Figure 5-5.
Calculate the Hydrogen Plant steam balance for each case as shown in
the example hand calculations at the end of this subsection. The results
for our example are summarized below.
Coil
#1 - Steam to Process
176,500 (80,060)
39.38 (11.54)
#2 - Steam Superheat
169,900 (77,070)
29.78 ( 8.73)
#3 - Steam Generation
213,800 (96,980)
153.27 (44.91)
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Using the information from the foregoing calculations, we can fill in the following
items on page 2 of "Revision A" of the Steam-HC Reformer Specification Sheets
(Form E-522-B):
Line Number
1-3
Description
Description of coils in Convection
Section
Coil Duties
13-21
23-31
Note that we are instructing the vendor to specify various parameters for the air
preheat coil even though we have calculated some of these already. Thermal
and Mechanical design of this part of the reformer (or any furnace for that
matter) is the responsibility of the vendor. Although we are reasonably confident
of our results, we can, in this way, use the vendor's numbers as a check. Note
also that we specifically gave the vendor permission to vary our steam flows and
duties if greater furnace efficiency will result. Furnace designers have developed
numerous proprietary designs for tubular heaters to make efficient use of fuel
and provide satisfactory and economic mechanical design. In short, we wish to
take advantage of the vendor's greater knowledge of heater design.
There are still some items on the reformer specification sheets that we have not
yet filled in. These are covered in the next part of this section entitled
Specification Sheets.
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Figure 5-4A
RESULTS FORM COMPUTER FURNACE (STACK GAS) CALCULATION
400 oF AIR PREHEAT CASE 2
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Figure 5-4B
RESULTS FROM COMPUTER FURNACE (STACK GAS) CALCULATION
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Figure 5-5
STACK GAS COOING CURVE/CONVECTION HEAT DUTIES
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5.3
SECTION
FIRED HEATERS
SPECIFICATION SHEETS
Using the information from the computer calculations, we can fill in the following items on
the first page of "Revision A" the Steam-HC Reformer Specification Sheets (Form
E-522-A): Note that specification sheets must be filled out for each of the six cases of
the material balance (refer to the "background" part of this subsection).
Line Number
Description
Client Name
2&7
Radiant Duty
13
14
15
Inlet/Outlet Temperatures
16
Inlet/Outlet Pressures
18-30
In this part of our discussion, we will complete filling out "Revision A" of the reformer
specification sheets and will present these along with the final "Approved for
Construction" version of these data sheets for our example in Section 5.5. You should
note that in this case the Mechanical Engineer assigned to fired heaters made no
changes to the "Revision A" data sheets. There are probably two reasons for this. First,
as mentioned in the introduction to this section, Fluor Daniel specifies the performance of
a fired heater while the furnace vendor actually does the mechanical design. Further, a
steam-hydrocarbon reformer is a highly specialized piece of equipment. Even such
details as tube and fitting metallurgy, normally specified by the Mechanical Engineer, are
usually left up to the vendor. The Mechanical Engineer monitors and checks the
vendor's work throughout the design on behalf of both Fluor Daniel and the client. He or
she will keep the Process engineer abreast of any changes recommended by the vendor
and will assist in revising the specification sheets as needed. Second, the Process
Engineer consulted with his counterpart in the Mechanical Department during the initial
specifications of the heater. Such matters as basic furnace configuration, convection
heat recovery, equipment items included in the scope, etc., were discussed. This should
be a standard practice in all such cases. In this way much unnecessary recycle of
information can be avoided.
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The following items must also be filled in by the Process Engineer for the initial issue of
the specification sheets. These are listed below and discussed according to subject and
location on the data sheets.
5.3.1
5.3.2
5.3.3
5.3.4
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5.3.5
SECTION
FIRED HEATERS
5.3.6
Fuel Data
(Form E-522-C, Line No. 25-41)
The client may supply information on fuel types, composition, and available
temperature and pressure. Otherwise, the Utilities Engineer will have to develop
this information. For our example, we have specified three fuels: purge gas
natural gas, fuel oil. Each of these is discussed below.
a.
Purge Gas
Purge gas is a waste gas stream from the H2 product purification step.
As per client preference, we indicated to the vendor that all available
purge gas will always be fired. Natural gas or fuel oil will supplement the
purge gas.
On a molar basis, purge gas contains 63.55 % CO2, 26.89 % H2, 7.58 %
CH4, 1.2 % CO, 0.78 % H2O. It has a molecular weight of 30.20, an
HHV of 168 Btu/SCF (6,610 kJ/Nm3), and an LHV of 146 Btu/SCF
(5,750 kJ/Nm3). We will deliver the purge gas to the burners at 2 psig
(0.014 MPag) and 100 oF (38 oC). Its design flowrate is 30.84 MMSCFD
(826 x 103 Nm3/d).
b.
Natural Gas
This is pipeline natural gas containing 92.55 % methane, 1.31 % C2H4
and 5.81 % nitrogen, all on a molar basis. Other components, present in
small amounts, include He, CO2, and C3H8. The total sulfur content
including H2S and organically bonded sulfur is 20 ppm. The gas has a
molecular weight of 16.9, and HHV of 963 Btu/SCF (37,900 kJ/Nm3), and
an LHV of 865 Btu/SCF (34,000 kJ/Nm3). We will deliver it to the
burners at 20 psig (0.138 MPag) and at temperatures ranging from 40 oF
(4.4 oC) to 100 oF (38 oC), depending on the season of the year.
c.
Fuel Oil
The fuel oil for our example has an API gravity of 27 o and lower and
higher heating values of 18,100 Btu/lb (42,100 kJ/kg) and 19,240 Btu/lb,
(44,750 kJ/kg) respectively. It contains 0.3 % sulfur by weight, but has
negligible amounts of vanadium, sodium and ash. We will deliver it to
the burners at 60 oF (16 oC) and provide atomizing steam at 250 psig
(1.724 MPag) and 450 oF (232 oC). ASTM (D-86) distillation data for the
oil is given on page 4 of the specification sheets.
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AUXILIARY EQUIPMENT
Early in our discussion, we defined a reformer as a reactor-type direct fired tubular
heater. We went on to talk about the reforming process and how our example reformer
fits into the overall process scheme of a hydrogen plant. From the context of our
discussion, you should have realized that a reformer consists of a radiant and a
convection section, a flue stack, burners, internal piping and ducts, and numerous related
controllers and indicators. Other related equipment items, e.g., the combustion air fans,
are not part of the reformer itself even though they may be supplied by the reformer
vendor and their functions may be directly linked top that of the reformer. The auxiliary
equipment is basically described in the first section on page 3 of the Specification
Sheets. In addition, the emergency shutdown system may be considered an auxiliary.
Fluor Daniel usually designs the emergency shutdown system for fired heaters. Some
elements, however, such as the flame detector may be supplied by the vendor.
5.5
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Heat Available
Heat In
1.
2.
3.
4.
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5.
Coil #3
Total Duty = 183.12 x 106 Btu/hr
Coils 2&3
Duty Coil #2 = ( - 0.01 - 176,500) 1,377.8
lb/hr
Btu/lb
Duty Coil #3
Steam to Coil #1
176,500 lb/hr
H = 1,202.5 Btu/hr
2.
Blowdown
O.01 lb/hr
H = 485.6 Btu/lb
2.
Coil #3 Steam
lb/hr
H = 1,202.5 Btu/lb
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3.
Flow
= 1,202.5 Btu/lb
Heat Out
1.
Blowdown
3,490 lb/hr
H = 485.6 Btu/lb
2.
H2OL to WHB
155,935 lb/hr
H = 485.6 Btu/lb
3.
H2OL to Coil #3
lb/hr
4.
Coil #3 Duty
Duty = (213,800) (1,202.5 - 485.6) = 153.27 x 106 Btu/hr
lb/hr
Btu/lb
Coil #2 Flow/Duty
Flow = 349,900 - 3,490 - 176,500 = 169,910 lb/hr
Use
169,900 lb/hr
Duty = 169,900 (1,377.8 - 1,202.5) = 29.78 x 106 Btu/hr
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6.0
MATERIALS OF CONSTRUCTION
6.1
TUBE MATERIALS
The Mechanical Engineer generally chooses the heater tube material. You should review
his or her choice to be sure you agree with it. The Mechanical Engineer selects a given
material based on its ability to withstand the temperature and pressure of the particular
service. Temperature, however, is of primary consideration in choosing the right tube
material. Some typical applications are summarized below:
Maximum Tube Wall Temperature
o
700 - 850 F
o
900 - 1,200 F
o
Material
Carbon steel
(371 - 454 C)
(482 - 649 C)
1,200 - 1,350 F
(649 - 732 C)
1,500 - 1,800 oF
Choosing a material for furnace tube application must balance tube cost against tube life.
Often, shorter tube life may be more economical than expensive alloy tubes. Sometimes
it is economical to use different tube materials in the radiant and convection sections;
however, welding problems may occur with dissimilar alloys. The desired tube life is
generally 100,000 hours. This equals 11.4 years at 8,760 hours per year. Figure 6-1
gives data for furnace tube design stress for different steels over some commonly
encountered operating temperature ranges. Information on the relative cost of these
steels is included.
Sometimes process considerations require special tube metallurgy. In that case, the
Process Engineer should select the tube material. The following important items related
to corrosion or service problems come up frequently in process furnaces. They influence
material selection and the Process Engineer should always consider them.
Hydrogen service
Sulfur/H2S service
Vanadium and sodium
Carbon deposits
Carbide precipitation
Graphitization
Carburization
Oxidation
Stress corrosion cracking
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PAGE
DATE
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FIRED HEATERS
MATERIALS OF CONSTRUCTION
1.0
Figure 6-1
FURNACE TUBE DESIGN STRESSES AND RELATIVE COSTS
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FIRED HEATERS
UTILITY REQUIREMENTS
1.0
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2.0
3.0
4.0
5.0
6.0
7.0
UTILITY REQUIREMENTS
In the early stages of a project you must estimate the utilities required for the fired heater you are
specifying. The estimates are a necessary part of both the furnace calculations and the plant
utility balance. The utilities you must consider include fuel, steam or electricity and boiler feed
water. Fuel consumption is estimated through stoichiometry calculations. These can be done by
hand or by using the Furnace Calculation Program on the computer. Refer to Section 2.6 and
Section 5.2 for further discussion of this program. For mechanical draft furnaces, you must
estimate the steam or electric consumption of the drivers for the forced and induced draft fans.
Hydraulic horsepower and efficiencies for the drivers are needed. Refer to the section in this
manual on motors and drivers for guidance. For those heaters where steam is generated in the
convection section, you must estimate the boiler feedwater requirements and the power or steam
consumption of the accompanying pumps. Note that the amount of boiler feed water required is
influenced by both the amount of recoverable heat in the flue gas and by the demand for the
steam to be produced.
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FIRED HEATERS
REFERENCES, CODES AND STANDARDS
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1.0
2.0
3.0
4.0
5.0
6.0
7.0
8.0
REFERENCES
1.
*Berman, Herbert L., Fired Heaters-I, Finding the basic design for your
application; Chemical Engineering, June 19, 1978.
2.
3.
4.
*Berman, Herbert L., Fired Heaters-IV, How to Reduced your Fuel Bill, Chemical
Engineering, September 11, 1978.
5.
6.
* Neal, James E. and Clark, Roger S., Saving Heat Energy in Refractory-Lined
Equipment; Chemical Engineering, May 4, 1981.
7.
* Frankel, Irwin, Shortcut Calculation for Flue Gas Volume, Chemical Engineering,
June 1, 1981.
8.
9.
Krebs; T.M.' Hydrocarbon Processing and Petroleum Refiner, Volume 41; page
135, 1962.
10.
11.
12.
Rickerman, J. H., Heater Designs for the Petroleum Industry, Transactions of the
A.S.M.E., October, 1945.
13.
Maker, F.L., Flashflow Pressure Drop in Heaters; Petroleum Refiner, Volume 34,
No. 11; November, 1955, p.140.
14.
Gallagher, J.T., Cost of Direct Fired Heaters, Chemical Engineering, July 17,
1967, p.232
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FIRED HEATERS
REFERENCES, CODES AND STANDARDS
1.0
8.2
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REFERENCE ARTICLES
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3.0
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5.0
6.0
7.0
8.0
9.0
REFERENCE ARTICLES
Included in this section are copies of articles identified in Section 8.1 from 1. through 7.
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