Continous Distllation 3
Continous Distllation 3
DCA/EV)
(mod. DCA/EV)
November 2023
Automated Distillation Pilot Plant (mod. DCA/EV)
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Automated Distillation Pilot Plant (mod. DCA/EV)
1. Introduction
The multi-stage distillation is a basic unitary operation of chemical industry. The liquid-vapor separation
(L-V) is a process which has been used for many years and many are the methods and devices developed
in the meantime to obtain the balance between the phases in contact. The mass transfer increases in
proportion with the contact area between the phases and this is the reason why the devices have been
planned to obtain a maximum interface area. With constant liquid and vapor flows, the contact time
between the two phases is constant so when the contact area increases, so does the mass transfer and with
it the possibility to reach the balance of the system, which represent the 100% of efficiency. The
combination of factors as the production of contact devices, the operative conditions, the characteristics
of the system rarely take to an efficiency of the 100%. The separation process is usually carried out in
columns which consist in devices enabling the continuous or discontinuous liquid-vapor contact.
The contact can be made either using a packed column or plate column. Plate towers exhibit
larger pressure drops and liquid holdup at higher gas flow rate. While, packed towers are not appropriate
for very low liquid flow rates. Packed column is the preferred choice than a plate column to handle toxic
and flammable liquids due to lower liquid holdup to keep the unit as small as possible for the sake of
safety. Plate columns are normally suitable for fouling liquids or laden with solids. They are easier to
clean and could handle substantial temperature variation during operation. Packed towers are more
suitable for foaming and corrosive services. It is easier to make the provision for the installation of
internal cooling coils or withdrawal of side streams from a plate column.
In a continuous distillation, the system is kept in a steady state or approximate steady state.
Steady state means that quantities related to the process do not change as time passes during operation.
Such constant quantities include feed input rate, output stream rates, heating and cooling rates, reflux
ratio, and temperatures, pressures, and compositions at every point (location). Unless the process is
disturbed due to changes in feed, heating, ambient temperature, or condensing, steady state is normally
maintained. For a distillation process using a distillation column, at steady state, if the feed rate and feed
composition are kept constant, product rate and quality are also constant. However if there is change
(disturbance) to one of the variables such as, feed pre-heating temperature, reflux ratio, feeding flow rate,
reboiler heating power, feeding composition, and residual pressure the quality of the product will be
changed. For a set of variables a desired product quality can be obtained by appropriate design of a
distillation column (for example by determining the required number of plates). The desired production
rate and quality determines the amount of energy required during a distillation process.
In this laboratory work the effect of the stated variables on the top and bottom product quality
will be investigated. The theoretical number of plates will be calculated for a set of operating variables.
Energy and material will also be performed. For this study a continuous distillation pilot plant (mod.
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Automated Distillation Pilot Plant (mod. DCA/EV)
DCA/EV) (Fig. 1) will be employed. The distillation column is completely made of glass and it consists
of a reboiler, of a column with packing of steel mesh and of a condenser with reflux valve and head. The
bottom product and the distillate are collected into two glass tanks after being cooled by two heat
exchangers. The pilot plant is equipped with two PID controllers being able to control the flow rate of
cooling water crossing the condenser, the vacuum degree of the plant and the feeding pre-heating
temperature, automatically.
3. Theory
3.1. Components of a distillation column
A typical Continuous Distillation Column has several components to facilitate the overall process. These
four main components are:
Column (incorporating the enriching and stripping sections), where the liquid/gas phase
separation takes place.
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Automated Distillation Pilot Plant (mod. DCA/EV)
Reboiler (heat exchanger), which provides the heat energy to partially vaporize the columns input
feed (liquid) for the separation (distillation) process to take place. The input feed flows into the
center of the column and down through the stripping section to the base, before entering the
reboiler where the feed liquid is heated to generate the feed vapor (through evaporation). This
feed vapour travels up through the column by convection, to continue the feed components
separation process.
Condenser, which cools and condenses the separated and enriched feed vapour at the top of the
column before it enters the reflux drum.
Reflux drum, which collects the condensed feed vapour (as a liquid), and splits it into two
streams, 1. the distillation process output (distillate) and 2. the reflux drums recycled liquid
(reflux), which is fed back into the top of the column, to further enrich and purify the distillate.
Enriching
column
Depletion
column
Each stage of the column corresponds to an ideal stage of the process: the liquid and the vapor
leaving each stage are in thermodynamic equilibrium.
The column is adiabatic (there is no heat exchange with the outside).
Reflux occurs at the boiling point.
The molar flow rates of liquid and vapor are constant along the column.
Molar specific heat and molar heat of vaporization do not depend on the composition.
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(1)
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Automated Distillation Pilot Plant (mod. DCA/EV)
(3)
If the indices of the equation (3) are omitted, the result is:
(4)
Eq.3 can be rearranged as
(5)
Then substitute the Eq.2 in the formula Eq. 5 and divide by D: the result is:
(6)
L/D is the reflux ratio (r) and Eq. 6 can be written as
Fig. 4: (a) system boundaries of material balance for enriching and depletion columns, and (b)
theoretical number of stages for enriching section using Mc-Cabe-Thiele diagram for feed at
boiling point.
3.4.2. Depletion column
Similar to the enriching column, from material balance for the depleting column (Fig 4 a) an
operating line for depleting column (Eq. 8) can be derived.
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Automated Distillation Pilot Plant (mod. DCA/EV)
(8)
This is the operating line of the depletion column intersecting the point (yR = xR, xR)
If the slope for the operating line of the depletion column (L’/V’) is known the number of plates can
be determined graphically (Fig. 5).
Fig.5: Mc Cabe-Thiele diagram for calculating the number of theoretical plates in the depletion
column feed at the boiling point
However, if these data are not known, the operating line of the depletion column can also be drawn
through the method of the feed line and the known degree of vaporization.
(9)
Where; A = weight flow rate of feed, = fraction of feed in vapor phase, and = liquid phase feed
fraction.
The flow rates of liquid and vapor in the two operating sections of the column can be expressed as follows (Eq.
10-11):
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Automated Distillation Pilot Plant (mod. DCA/EV)
(10)
(11)
The Fig. 6 shows how feed is distributed in the two sections. Therefore, the degree of vaporization ϕ can be
calculated through the following formula (Eq. 12-13):
(12)
(13)
Fig. 6: Displaying how the feed is distributed in liquid and vapor phases
(14)
where: ZA is generical composition of feed; and is the slope of the feed line.
The fig. 7 (a, b, c,) shows the three main thermal conditions of feed, that is:
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Automated Distillation Pilot Plant (mod. DCA/EV)
Fig. 7: Drawing the feed line vs. the variation of thermal conditions
Now what explained above makes drawing the operating line of the depletion column easier. In fact this
line meets the point I of intersection of the operating line of the enriching column with the feed line:
both these lines can be determined when the following parameters: feed titer, distillate titer, residue
titer, reflux ratio, thermal condition of feed (degree of vaporization), are known the Fig. 8 shows how
these three lines can be drawn according to these parameters.
xD
1 r
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Automated Distillation Pilot Plant (mod. DCA/EV)
point 2 = (y2, x2) is determined on the equilibrium curve. Then it is possible to fix the point (y3, x2) on
the operating line and so on. The number of steps between operating lines and equilibrium curve
corresponds to the number of theoretical (or ideal) stages required to obtain a distillate of
composition xD and a residue of composition xR starting from a mixture of composition Z A with a
degree of vaporization and a reflux ratio r.
ZA = feed composition
xD = composition of distillate
= degree of vaporization
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Automated Distillation Pilot Plant (mod. DCA/EV)
The formulae (15) and (16) are two simultaneous equations with two unknown quantities (R and χR): the solution
is easy. Furthermore, from a material balance of the condenser it is possible to get:
(17)
that is:
(18)
When V, L and the degree of vaporization are known, the flow rates V' and L' can be calculated through
the equations (12) and (13):
(19)
(20)
The fig. 10 is a symbolic representation of the heats involved in the continuous distillation. The balance
equation states that the sum of the heat flows in inlet must be equal to the sum of the heat flows in outlet,
that is:
(21)
where:
JA = specific enthalpy of feed (cal/mol)
A = flow rate of feed (mole/h)
Qr = heat delivered by the reboiler (cal/h)
Qc = heat subtracted from the condenser (cal/h)
JD = specific enthalpy of the distillate (cal/mol)
D = flow rate of the distillate (mol/h)
JR = specific enthalpy of residue (cal/mol)
R = flow rate of residue (mol/h)
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Automated Distillation Pilot Plant (mod. DCA/EV)
(22)
where:
CPA,l = molar specific heat of feed (cal/mol)
TbA = boiling point of feed (°C)
CPD,l = specific heat of the distillate (cal/mol)
CPR,l = specific heat of residue (cal/mol)
TD = temperature of distillate (°C)
TR = temperature of residue (°C)
The value of can easily be calculated from the diagram (x,y) vs. (T), through the lever method (Fig.
12):
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1
2
Composition of distillate (%) 3
4
5
_
N
Average value of composition of distillate (%)
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Automated Distillation Pilot Plant (mod. DCA/EV)
Analyze the purity of the top product as well as the concentration of ethanol/methanol at the
bottom
Analyze mass and energy balance and determine the losses for each reflux ratio
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