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No Title Page
1 Abstract………………………………. 2
2 Introduction………………………….. 3
3 Objectives…………………………….. 4
4 Theory………………………………... 5–6
5 Material And Apparatus……………… 7–9
6 Methodology…………………………. 10 – 11
7 Data and Results……………………… 12 – 14
8 Calculations…………………………... 15 – 19
9 Discussion……………………………. 20 – 25
10 Conclusion……………………………. 26
11 Recommendations……………………. 27
12 Reference……………………………... 28
13 Appendix……………………………... 29
The Continuous Flow Stirred-tank Reactor (CSTR) are also called vat- or backmix
reactor. It is a common ideal reactor type in chemical engineering. The calculation for ideal
CSTR are always be assume perfect mixing means no accumulation. This assumption is used to
simplify engineering calculations and can be used to describe the research factors.
Others assumption that usually been made when using the CSTR are, constant density,
isothermal condition, steady state, and first order reactor. The CSTR is equip with a stirring
blade or agitator, water jacket, heat exchanger and also the water inlet and outlet. The CSTR
usually used for a homogenous reaction in a industrial processing where constant mixing is
required.
aA + bB cC + dD
Residence time, is the average amount of time that a particle spends in a particular
system. The residence time, is a representation of how long it takes for the concentration to
significantly change in the sediment.
Where VCSTR is the reactor volume and v0 is the total feed flow rates. The reactor volume and the
total feed flow rates for each experiment remain unchanged.
Conversion is an improved way of quantifying exactly how far has the reaction moved, or
how many moles of products are formed for every mole of A has consumed. Conversion XA is
the number of moles of A that have reacted per mole of A fed to the system.
moles of A reacted
XA
moles of A fed
A reaction rate constant, k quantifies the rate of a chemical reaction. The reaction rate is
often found to have the form
rA kC A C B
Where C A and C B are the concentration of the species A and B respectively, each raised to the
powers and , while k is the reaction rate constant. The exponents and are the partial
reaction orders. In this experiment, we can calculate the reaction rate constant, k by the following
formula.
Where, k is the reaction rate constant, is the outlet concentration of reactant NaOH in the
reactor, is the inlet concentration of reactant NaOH in the reactor, and is the residence
time.
From the Arrhenius equation above, we can derive a new formula to find activation
energy, E.
( )
Where, E is the activation energy ,A is the Arrhenius constant, R is theUniversal Gas Constant
which is 8.314 J/mol.K , and T is the absolute temperature.
Activation energy, E is the minimum quantity of energy that the reacting species must
possess in order to undergo a specified reaction
5.2 APPARATUS
1) Reactor (R1)
i. 4-L vessel made of borosilicate glass
ii. Internal cooling coil
iii. Cartridge type heater (1.0 kW)
iv. Stainless steel impeller
v. Ports for:
vi. Stirrer (M1)
vii. Inlet for feed vessels (B1, B2)
viii. Condenser (W2)
ix. Sensors: Conductivity (QT201) and temperature (TT301)
x. Cartridge heater (W1)
xi. Cooling coil
xii. Gas sparger
2) Stirrer (M1)
i. Laboratory drive with LCD display
ii. Power: 230VAC / 50-60 Hz / 75 W
iii. Speed range: 50 – 2000 rpm, steplessly adjustable by hand
iv. Max torque: 30 Ncm
7) Instrumentation
i. Flow measurement (FT101, FT102, FT103)
ii. Temperature measurement (TT301)
iii. Conductivity measurement (QT201)
Valves List :-
10
Conductivity (mS)
0
0% 20% 40% 60% 80% 100% 120%
Conversion, X (%)
10
Conductivity(mS)
0
0 0.01 0.02 0.03 0.04 0.05 0.06
Concentration of NaOH (M)
250
Conversion (%)
200
150
100
50
0
0 50 100 150 200 250 300 350 400
Reaction Temperature ,T (K)
0
0 0.0005 0.001 0.0015 0.002 0.0025 0.003 0.0035
-2
ln k
-4
-6
-8
-10
1/T , (K-1)
No Calculations No Calculations
1 4
⁄ ⁄
2 5
⁄ ⁄
No Calculations No Calculations
1 4
% %
2 5
% %
No Calculations
1
Where,
k = Reaction rate constant
= Outlet concentration of reactant NaOH in the reactor (mol/L)
= Inlet concentration of reactant NaOH in the reactor (mol/L)
= Residence Time (min)
No Calculations No Calculations
1 4
2 5
ln k2 323
ln k3 333
ln k4 343
ln k5 353
( )
No Calculations
1
10
9.7
Conductivity (mS)
4
3.7
2
0
0% 20% 40% 60% 80% 100% 120%
Conversion, X (%)
The graph shows that the conductivity is inversely proportional with the conversion.
Conductivity decreases as the conversion increases. This graph shows the theotherical value and
relationship between conversion and conductivity. Based on the graph, we can relate
conductivity and conversion into linear equation where,
y = mx + c
7
6
5.8
5
4
3
2
1
0
0 10 20 30 40 50 5860 70
Conversion, X(%)
The graph shows the experimental value of data taken which the conductivity recorded is
inversely proportional with the conversion. However, when we compare the graph with the
theotherical graph, we can conclude that the experimental data deviated from the theotherical
data. Thus, the linear equation for the experimental value is a bit different from the theotherical
value, where
y = mx + c
250
200
Conversion (%)
150
100
50
0
0 50 100 150 200 250 300 350 400
Reaction Temperature ,T (K)
The graph shows that conversion is inversely proportional to the reaction temperature.
The conversion decreases as the reaction temperature increases. Theotherically, conversion
shoud have increase as the reaction temperature increases, however in the experiment, the data
obtained differ from the theory. From the graph , we can concluded that instead of being
consumed, the reactant actually being produced. This could happen due to reaction occurs in
backward direction. The relative corresponding equilibrium concentration have been achieved
before the data is taken. This could be the reason, why the result of the experiment differ from
the theory.
0
0 0.0005 0.001 0.0015 0.002 0.0025 0.003 0.0035
-2
ln k
-4
-6
-8
-10
1/T , (K-1)
The graph shows that ln k is directly proportional to 1/T . When ln k increases, 1/T will
increases. From the graph, we can obtained ln A which is the y-axis intercept. The linear
equation that relates ln k, 1/T and ln A is Arrhenius equation. Arrhenius equation show the
dependence of the rate constant , k of chemical reaction on the temperature, T and activation
energy, Ea.
( )
From the graph of ln k against 1/T , we can get the y-intercept of the graph which is ln A then
we can get the Arrhenius constant, A:-
The Continuous Flow Stirred-tank reactor (CSTR) or the backmix reactor, is a common
ideal reactor type in a chemical manufacturing. It is usually used to estimate the key unit
operation variables for continuous process to reach a specified output. In this reactor, he volume
input is equal to the volume of output. Thus we assume that the solution in the reactoe was well-
mixed.
In this experiment, we used the NaOH and Et(Ac) with a vary concentration by mixing
with a water. The reaction between the Sodium Hydroxide and Ethyl acetate are Saponification
process which produced Sodium Acetate and Ethyl Alcohol. This reaction are the main reaction
in the manufacturing of soap. The general equation of this reaction are
This reaction are known as the model reaction for second order reaction with the rate law
For this experiment, we used constant residence time for the solution which is 15
minutes. The residence time is calculated by dividing the reactor volume with the total flow rate.
As we used the same reactor and the same flow rate throughout our experiment, thus our
residence time is kept constant. Therefore, our solution of NaOH and Et(Ac) can be expect
resides in the reactor for 15 minutes.
Reaction Rate Constant (k) or the kinetic constant for this saponification process can be
calculated with the formula stated in the theory. The rate constant can be calculated by using the
inlet and outlet conductivity of the reactant, NaOH and the residence time that we already
calculated before this. The sample calculation for the rate constant, k can be refer in the
calculation section above. The rate constant thus can be tabulated in the table. The reaction rate
constant, k can be seen decreasing as the temperature increased. The unit for k is L/mol.min.
Our objective is to relate the rate law with the Arrhenius Equation, .
Based on the table that we tabulated, the graph of ln Reaction Rate Constant (ln k) against 1/T
were construct. The reason for this steps are to relate it to the equation of derived Arrhenius
equation which is ( ). In this new Arrhenius equation, we can relate in the
equation with the temperature, rate of reaction constant and the activation energy.
With the help of Arrhenius Equation above, and the graph of ln k against 1/T, we can get
the Arrhenius constant, ln A. The ln A is a slope or the gradient from the graph of ln k against
1/T. Thus the Arrhenius constant, A is defined with the value . As Arrhenius
equation relate the rate constant, k, Temperature, T, and the activation energy, Ea Then we can
calculate the activation energy for each equation. The Activation Energy, Ea is calculated by
using the formula for each of the repeated readings. The sample calculations for Activation
Energy can be refer in the sample calculation above. The activation energy for each reading for
this saponification reaction is between to . It is relatively
about constant with a different about 0.5 kJ / mol. As we finally get the activation energy for the
saponification of NaOH and Et(Ac), our objective was achieved.
Other than that, we were able to found out the reaction rate constant, k, thus we were able
to determine the value of the reaction’s activation energy. The value of the reaction rate constant
that we get was 12.6115 L/mol.min, 7.4995 L/mol.min, 5.4453 L/mol.min, 4.8247 L/mol.min,
and 4.0708 L/mol.min respectively while the value of the reaction’s activation energy that we get
was -29.6259 kJ/mol, -29.1766 kJ/mol, -29.1939 kJ/mol, -29.7253 kJ/mol and -30.0933 kJ/mol
respectively. The calculation for both reaction rate constant, k and the activation energy were
shown in the Sample Calculation section.
We can conclude that the experiment was successfully conducted since we were able to
fulfill the objective of this experiment.
First of all, it is important for students to fully understand the experiment that they need
to do. Thus, they need to read the lab manual and understand it before actually doing the
experiment. This can ensure that they follow the precautions and the guidelines of the
experiment which then enabling them to get the most accurate data for the experiment.
Besides, in order for the data and results of the experiment to be more accurate and
precise, the experiment should have been done at least three times per temperature and use the
average value obtained for the calculation. As for the calculation of the data, it is vital to take the
value approximately to at least 4 decimal places. This is to ensure that the data that being
calculated is more precise and accurate.
Other than that, students should be more focus and alert on the conductivity value which
will stabilize after some time. Errors might happen when students actually take the wrong value
on the conductivity measurement (QT201) as the conductivity values are not stabilize yet. This
then could lead to errors in conversion and oulet concentration that need to be calculated based
on the value of conductivity recorded.
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