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Effect Pulse
Effect Pulse
ABSTRACT
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_______________________________________ CONTINUOUS STIRRED TANK REACTOR in SERIES
INTRODUCTION
A stirred tank is the most fundamental of mixers and many common mixers from
the Brabender mixer used in lab to a cup of coffee with a spoon can be
considered a stirred tank under some set of approximation. Mixing in a stirred
tank is complicated and not well described (Middleman p. 340-348) although the
use of dimensionless numbers and comparison with literature accounts can lead
to some predictive capabilities. Often stirred tanks are used as industrial reactors
where a chemical component of a flow stream resides for some time in the tank
and then proceeds on to other steps in a chemical process. The residence time
distribution becomes a measure of the extent of a chemical reaction in this
situation. For mixing one can sometimes assume a constant rate of strain in the
stirred tank, Middleman p. 340-348, and the residence time distribution can then
be used under this approximation, as a measure of the extent of mixing. Dead
zones in a stirred tank for high viscosity fluids should be very familiar to anyone
who has worked in a kitchen mixing dough with a hand mixer.
Fluid motion in a stirred tank is confined to the immediate region of the
mixer blades for high viscosity fluids. In the simplest approximation that a uniform
extent of mixing occurs in the stirred tank, Middleman p. 301-306, this is called
the "perfect mixer". Consider a stream of butene in cyclohexane that is converted
to butene epoxide by reaction with a peroxide in a CSTR. The flow rate through
the tank is Q and the concentration of heptene is C 0. The tank is at steady state
meaning the volumetric in-flow equals the volumetric out-flow. The tank volume is
V. The ratio of butene epoxide to butene is governed by the temperature, catalyst
concentration, effectiveness of the catalyst and the residence time in the reactor.
A master curve in terms of conversion at constant conditions as a function of
reaction time can easily be made in the lab.
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_______________________________________ CONTINUOUS STIRRED TANK REACTOR in SERIES
so
Then F(t) is the response, efflux, of the system to a pulse of concentration in the
influx.A material balance for the CSTR under the assumption of perfect mixing
yields,
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_______________________________________ CONTINUOUS STIRRED TANK REACTOR in SERIES
with the starting condition that the concentration of the tagged component in the
effluent is 0 at t = 0, C(t=0) = 0. The solution to this differential equation is, where
V/Q = t is a kind of time constant for the system. Under the assumption of perfect
mixing, this time constant is the mean residence time for the CSTR, t = V/Q. The
residence time distribution function is the derivative of the cumulative residence
time distribution function,
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_______________________________________ CONTINUOUS STIRRED TANK REACTOR in SERIES
THEORY
Figure 1
Continuously Stirred Run at steady state with continuous flow of reactants and
Tank Reactor (CSTR) products; the feed assumes a uniform composition throughout
the reactor, exit stream has the same composition as in the
tank
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_______________________________________ CONTINUOUS STIRRED TANK REACTOR in SERIES
7.Easy to clean
Figure 2
Assumptions
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_______________________________________ CONTINUOUS STIRRED TANK REACTOR in SERIES
In terms of conversion
Reactor Sizing
Given rA as a function of conversion, rA = f(X), one can size any type of reactor.
The volume of a CSTR can be represented as the shaded areas in the
Levenspiel Plot shown below:
Figure 3
Reactors in Series
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Figure 4
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Given rA = f(X) the Levenspiel Plot can be used to find the reactor volume
Figure 5
Figure 6
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Given -rA = f (x), the Levenspiel Plot can be used to find the reactor volume
Figure 7
CO
C1 C2 C3
Figure 8
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_______________________________________ CONTINUOUS STIRRED TANK REACTOR in SERIES
Where, I = /n
tm = = nI
In dimensionless from
= t / = t/I
n = t / I
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_______________________________________ CONTINUOUS STIRRED TANK REACTOR in SERIES
2 = 2 = 0 ( t )2 E (t) d
2 2
2 = 2 = 0 ( - 1 )2 E ( ) d
2
2 = 2 = 1
2 n
n= 2
2
X = 1- 1 i =
( 1 + i k ) n n
For reactions other than first order and for multiple reactions, the sequential
equations must be solved.
Vi = V / n
Vi = vo ( CAo CA1)
-rA1
Vi = vo ( CA1 CA2)
-rA2
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_______________________________________ CONTINUOUS STIRRED TANK REACTOR in SERIES
Vi = vo ( CA(n 1) CAn )
-rAn
Example
V3 = ( CAo CA ) vo
kCA2
( 1 = 2 = 3 )
3 = kCA2 + CA - CA = 0
CA1 = -1 + 1+ 4 3 k C Ao
2 3 k
Similarly,
CA2 = -1 + 1+ 4 3 k C A1
2 3 k
CA3 = -1 + 1+ 4 3 k C A2
2 3 k
X = 1 - (CA3 / CA0) , 3 = / 3
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OBJECTIVE
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To determine;
The effect of step changes in input concentration of solute.
The effect of pulse or residence time in input concentration of solute
curve.
APPARATUS
1. Distillation water
2. Sodium Chloride
3. Continuous reactor in series
4. Stirrer system
5. Feed tanks
6. Waste tank
7. Dead time coil
8. Computerize system
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_______________________________________ CONTINUOUS STIRRED TANK REACTOR in SERIES
APPARATUS DISCRIPTION
Figure 11
Before operating the unit, we must familiarize ourselves with the unit. Please
refer to figure 1 to understand the process. The unit consists of the followings:
Reactors
Three reactors made of borosilicate glass, each having approximately 2 liters
capacity. Each reactor is fitted with variable speed stirred mounted on the top
plate. Temperature and conductivity sensors are provided for each reactor. Flows
between vessels are by gravity. Overflow tubes are provided for the 2 nd and 3rd
reactor.
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_______________________________________ CONTINUOUS STIRRED TANK REACTOR in SERIES
Stirred System
Variable speed stirred system with digital display consisting of a motor and a
shaft with impellers made of stainless steel. Speed adjustment by means of a
speed controller knob on each stirrer.
Feed Tanks
Two 15-L cylindrical tanks made of stainless steels are provided with the unit.
Each tank has a feed pump to transfer the liquid from feed tank to the reactors.
Each tank is fitted with a level switch to protect the pumps from dry on.
Waste Tank
A rectangular 50-L waste tank made of stainless steel is provided at the bottom of
the equipment.
2) Conductivity Meter
Sensor Range: 0 to 200 mS/cm
No. of sensors: 4 (CT1, CT2, CT3, CT4)
Output: 4 to 20 mA
Display: conductivity controller with digital display for each sensor
mounted on the control panel.
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3) Temperature Sensor
No. Of sensors: 3 (TT1, TT2, TT3)
Sensor type: RTD
Equipment Description
The system consists of three agitated, glass reactor vessels connected in series,
two feed tanks, two variable through put feed pumps, variable speed
agitators, fixed height overflow, and an electrical conductivity meter. Two
feed systems are provided. Each feed system consists of a feed tank, a
variable speed pump, and a mixer (tee-type) at the first tank inlet. The feeds
flow through each tank where a constant liquid holdup (steady-state
operation).
Chemicals
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EXPERIMENTAL PROCEDURES
Experiment A: The effect of Step Change
In this experiment a step change input would be introduced and the
progression of the tracer will be monitored via the conductivity measurement in
all the three reactors.
1. The two of three tanks (tank 1 and tank 2) was filled up with 20L feeds
deionized water.
2. 300 g of sodium chloride in tank 1 was dissolved. Make sure the salts
dissolve entirely and the solution is homogenous.
3. The three way valve (V3) was setting to position 2 so that the deionized
water from tank 2 will flow into reactor 1.
4. The pump 2 is switch on to fill up all three reactors with deionized water.
5. The flow rate (Fl1) was set to 150 ml/min by adjusting the needles valve
(V4). Do not use too high flow rate to avoid the over flow. Make sure no air
bubbles trapped in the piping. The stirrers 1, 2 and 3 were switch on.
6. The deionized water was continued pumped for about 10 minute until the
conductivity readings for all three reactors are stable at low values.
7. The values of conductivity were recorded at t 0.
8. T he pump 2 was switch off after 5 minutes. The valve (V3) was switch to
position 1 and the pump 1 was switch on. The timer was started.
9. The conductivity values for each reactor were recorded every three
minutes.
10. Record the conductivity values were continued until reading for the three
reactors were closed to the starting value recorded.
11. Pump 2 was switch off and the valve (V4) was closed.
12. All liquids in reactors were drained by opening valves V5 and V6.
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_______________________________________ CONTINUOUS STIRRED TANK REACTOR in SERIES
1. The two of three tanks (tank 1 and tank 2) was filled up with 20L feeds
deionized water.
2. 300 g of sodium chloride in tank 1 was dissolved. Make sure the salts
dissolve entirely and the solution is homogenous.
3. The three way valve (V3) was setting to position 2 so that the deionized
water from tank 2 will flow into reactor 1.
4. The pump 2 is switch on to fill up all three reactors with deionized water.
5. The flow rate (Fl1) was set to 150 ml/min by adjusting the needles valve
(V4). Do not use too high flow rate to avoid the over flow. Make sure no air
bubbles trapped in the piping. The stirrers 1, 2 and 3 were switch on.
6. The deionized water was continued pumped for about 10 minute until the
conductivity readings for all three reactors are stable at low values.
7. The values of conductivity were recorded at t 0.
8. Switch off pump 2 after 5 minutes. The valve (V3) was switch to position 1
and switch on pump 1. The timer was started.
9. Let the pump 1 to operate for 5 minute, and then switch off pump 1.
Switch the three ways valve (V3) back to position 2. The pump 2 was
switch on.
10. The conductivity values for each reactor were recorded every three
minutes.
11. Record the conductivity values were continued until reading for the three
reactors were closed to the starting value recorded.
12. Pump 2 was switch off and the valve (V4) was closed.
13. All liquids in reactors were drained by opening valves V5 and V6.
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_______________________________________ CONTINUOUS STIRRED TANK REACTOR in SERIES
RESULTS
Experiment 1: The effect of step change input.
FT: 139.8 ml / min TT1: 25.5 oC TT2: 25.4 oC TT3 25.3 oC
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GRAPH: EXPERIMENT 1
Graph 1
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GRAPH: EXPERIMENT 2
Graph 2
SAMPLE OF CALCULATION
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DISCUSSIONS
The Continuous Flow Stirred Tank Reactor (CSTR) is probably the easiest way to
transfer a batch process to a continuous one since all engineering and scale-up
data can be used from the batch process. The very broad residence time
distribution (RTD) profile however can pose some sever complications, therefore
the pitfalls are mentioned first
A minor problem is that the lower volumetric reaction rate results in a lower
productivity, this can easily be compensated by the reduction of waiting times
(filling, heating, cooling, emptying of the batch reactor) and a more constant
product quality. The effect on the selectivity of reactions can either be good or
bad. In the case of production of homogeneous copolymers for example, the
CSTR can be an ideal reactor since composition drift is absent during steady
state operation. The main reason that a series of CSTRs is not suited for the
entire emulsion polymerisation process is that the first stage of the process, the
particle nucleation, is very sensitive towards residence time distribution.
First of all, compared to the batch process, the steady state operation results in
more constant product properties, an improved energy consumption (the heat of
reaction can be used to heat feed streams) and a higher productivity through the
reduction of inactive periods (filling, heating, cooling, emptying). The control over
local mixing independently from net flow is one of the key advantages compared
to a traditional tubular reactor.
The ideal mixing in a single vessel can, besides all the negative effects
mentioned above, also have its positive effects. For the production of
homogeneous copolymers, the steady state concentrations in each CSTR make
it a lot easier to calculate and feed additional monomer streams to each CSTR
compared to the time-based addition profile for the semi-batch process. Because
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_______________________________________ CONTINUOUS STIRRED TANK REACTOR in SERIES
In the first experiment of the effect of step change, the values of the conductivity
for those three stirrers were recorded in each three minutes. From the graph we
can see that the concentration of the deionized water was increasing with time.
The concentration of the tank 1 is higher than the others. This is because; the
300 g of sodium chloride was dissolved firstly in tank 1. Then, the deionized
water that was dissolved to the sodium in tank 1 was pumped to other one by
one which was full with deionized water. Though the concentration is uniform in
each reactor, nevertheless there are changes in concentration as fluid moves on
from 1st reactor to others. After 93 minutes, the concentration in the 3 reactors
becomes stable which is equivalent for each reactor. The resulted was shown in
graph 1.
This situation above is one of the draw back of using cstr in series if compared to
single STR. Although the series STR requires a lower reactor volumes but it take
longer to reach the conversion and it also requires more stirrer than the single
STR.
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_______________________________________ CONTINUOUS STIRRED TANK REACTOR in SERIES
CONCLUSIONS
o Both first experiment and second experiment has the graph pattern as the
standard graph (figure 9 and 10).
o For the first experiment, it takes more time to achieving equilibrium in
concentration which rather it can be said that the concentration on the
reactor are directly proportional with time .
o Time measuring very important because it is can affect the conductivity.
RECOMMENDATIONS
During the experiment there are some problem occur, so these is the list of the
recommendation that can be considered if we want to produce better results;
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REFERENCES
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APPENDICES
CE 442
DESIGN EXAMPLE
A chemical manufacturing facility is planning on a product modification that will result in a change in wastewater character.
Of significance is the anticipated presence of phenol, an organic chemical that has not been treated by the company's
wastewater treatment facility. Consequently, the ability of the existing facility to treat phenol is in question. In order to
predict the existing reactor performance, kinetic and dispersion information is needed.
Reaction kinetic data have been collected for the chemical destruction of phenol through batch reactor tests (Table 1).
The phenol-bearing wastewater flow is projected to be 0.45 MGD with an anticipated phenol concentration of 95 mg/L.
The reactor ( a chemical oxidation process) has a total liquid volume of 25,000 gal. (L=35 ft., W=12 ft., H=8 ft.). A reactor
dispersion analysis has been performed by injecting an impulse of non-reactive material into the reactor feed stream. The
flow rate was monitored during the dispersion study and was determined to be 0.45 MGD. The reactor dye trace data are
presented in Table 2.
The phenol discharge permit limit has been set at 0.1 mg/L by the state regulatory board. Estimate the effluent
concentration of phenol based on the available information. Determine what might be done to meet the discharge limit. It
would be desirable to maintain the existing reactor due to obvious economic reasons. However, any reasonable design
option may be considered. Justify your final design recommendation. Show all calculations in a clear and concise
fashion. State all assumptions that you make in the design process. It should be assumed that the kinetic relationship
(Table 1) are fixed and cannot be altered. That is, the reaction kinetic data represents optimum conditions.
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46.92 0.36
48 0.82
48.5 1.24
49 2.15
49.33 2.61
50 2.98
50.75 2.93
51.67 2.98
52.75 2.89
54 2.84
56 2.89
58 2.84
60 2.52
62 2.52
64 1.92
66 1.79
68 1.6
70 1.33
75 1.28
79 1.14
83 1.1
98 0.41
113 0.39
128 0.27
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Solution
The solution approach is based on utilizing the kinetic information (Table 1) and dispersion information (Table 2) to
estimate existing reactor performance and to develop alternatives for upgrading the treatment process. The solution
approach is presented below.
3. determine the number (N) of CSTR's in series that simulates the calculated dispersion (
2 = 1/N),
3. estimate the existing reactor effluent concentration, and
4. develop alternative reactor design modifications.
Reaction rate constant and order. Reaction rate and order is determined using the data in Table 1 of the problem
statement. The general rate expression (equation 1) is applied in the analysis process.
dC
kC n (1)
dt
where
k = reaction rate constant
n = reaction order
After assuming a reaction order, equation 1 is integrated and algebraically manipulated such that a general straight line
relationship (equation 2) is developed.
y mx b (2)
For example, if we assume n=0, the following solution applies.
Ct kt C 0 (3)
dC
kC 0 k
dt
dC kdt
Ct t
dC k dt
C0 0
C t C 0 kt
Equation 3 is a straight line relationship and indicates that if the reaction data is truly zero order, a plot of C t vs. t would
result in a straight line. If, however, the data is not linear, another order must be assumed and the process repeated.
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dC
kC
dt
dC
kdt
C
Ct t
dC
C C k 0 dt
0
ln C t ln C 0 kt
LnC t kt ln C 0
The result of performing these operations on the kinetic data is presented in Figure 1.
Kinetic Data
120 6
5
100 y = -0.0819x + 4.7085
4
C
80 3
Ln(C)
C (mg/L)
2
Ln(C)
60
1
40 0
-1
20
-2
0 -3
0 20 40 60 80 100
Time (min)
Figure 1. C and ln(C) vs. time for the rate data from Table 1.
The data in Figure 1 indicate that a zero (n=0) order assumption does not result in a linear relationship (C vs. t data is
non-linear). ln(C) vs. t, however, does fall on a straight line. The reaction rate is therefore first order with the slope equal
to k = 0.08 min-1.
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