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Lecture # 20 - Week # 12

This document provides information about the Chemical Reaction Engineering course offered at COMSATS University Islamabad, Lahore Campus. The course covers topics such as kinetics of homogeneous and heterogeneous reactions, analysis of batch reactor data using various methods, and design of different types of reactors. It lists recommended textbooks and outlines the course learning outcomes and their alignment with the program learning outcomes. Finally, it provides an example problem demonstrating the integral method for determining the reaction order and rate constant from experimental concentration-time data.

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Sufyan Khan
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© © All Rights Reserved
Available Formats
Download as PDF, TXT or read online on Scribd
0% found this document useful (0 votes)
12 views

Lecture # 20 - Week # 12

This document provides information about the Chemical Reaction Engineering course offered at COMSATS University Islamabad, Lahore Campus. The course covers topics such as kinetics of homogeneous and heterogeneous reactions, analysis of batch reactor data using various methods, and design of different types of reactors. It lists recommended textbooks and outlines the course learning outcomes and their alignment with the program learning outcomes. Finally, it provides an example problem demonstrating the integral method for determining the reaction order and rate constant from experimental concentration-time data.

Uploaded by

Sufyan Khan
Copyright
© © All Rights Reserved
Available Formats
Download as PDF, TXT or read online on Scribd
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Chemical Reaction Engineering

Course Code: CHE 331


Course Cr. Hrs.: 4(3,1)
Course Instructor:
Dr. Muhammad Haris Hamayun
Assistant Professor,
Department of Chemical Engineering,
COMSATS University Islamabad, Lahore Campus.
Contact Email: mhhamayun@cuilahore.edu.pk
1
Course Contents

Kinetics of homogeneous reactions: rate of reaction, variables affecting the rate of


reaction, order of reaction, rate constant; searching for a mechanism of reaction,
activation energy and temperature dependency. Interpretation of batch reactor data for
single and multiple reactions. Integral method and differential method of analysis for
constant volume and variable volume batch reactors, search for a rate equation. Design
of homogeneous reactors, Batch, Mixed flow, Plug flow reactors, Comparison of single
reactor, multiple reactor systems in parallel/series. Temperature and pressure effects.
Adiabatic and non-adiabatic operations. Surface phenomenon and catalysis,
Heterogeneous reaction systems, rate equations for heterogeneous reactions, fluid
particle reactions, determination of rate controlling steps. Catalysis desorption
isotherms, kinetics of solid catalyzed reactions. Catalyst deactivation and regeneration.
Design of fluid-solid catalytic reactors.

2
Recommended Books

1) H. Scott Fogler, Elements of Chemical Reaction Engineering, 5th edition, Prentice


Hall, 2016.

2) Octave Levenspiel, Chemical Reaction Engineering, 3rd edition, Wiley India Pvt.
Limited, 2006.

3) Elsie Perkins, Chemical Reaction Engineering, WILLFORD Press, 2022.

3
CLOs and Mapping with PLOs

Understand • Describe the fundamentals of chemical reaction


(C2, PLO1) engineering.

Apply • Apply the fundamentals of chemical reaction


(C3, PLO1) engineering.

Analysis • Analyze the kinetic data using different methods of


(C4, PLO2) data analysis.

Design • Design isothermal and nonisothermal reactors (e.g.,


(C6, PLO3) Batch, CSTR, PFR, PBR etc.)

4
OBE in a Nutshell

◼ What do you want the students to have or able


to do? ◼ Knowledge, Skill, Affective

◼ How can you best help students achieve it?


◼ Student Centred Delivery

◼ How will you know what they have achieved it?


◼ Assessment

◼ How do you close the loop


◼ Plan, Do, Check, Act (PDCA)
5
Lecture # 20 (CLO # 1, 2, and 3)

• Chapter # 7: Collection and Analysis of Rate Data

6
Enhancing Our Knowledge:
Reviewing What We've Learned!

7
Algorithm
for Data
Analysis

8
Algorithm
for Data
Analysis

9
Algorithm
for Data
Analysis

10
Method of Excess

• Batch reactors are used primarily to determine rate-law parameters for homogeneous
reactions.

• This determination is usually achieved by measuring concentration as a function of


time and then using either the integral, differential, or nonlinear regression method
of data analysis to determine the reaction order, α, and specific reaction-rate
constant, k.

• If some reaction parameter other than concentration is monitored, such as pressure,


the mole balance must be rewritten in terms of the measured variable (e.g., pressure)
11
Method of Excess

• For irreversible reaction: to determine the reaction order and the specific rate
constant by either nonlinear regression or by numerically differentiating
concentration versus time data.

• This latter method is most applicable when reaction conditions are such that the rate
is essentially a function of the concentration of only one reactant; for example, if, for
the decomposition reaction: A → Products

Differential method may


−rA = k A CAα
be used.

12
Method of Excess

13
Integral Method

• A quickest method used to determine the rate law if the order turns out to zero, first,
or second order.

• In the integral method, we guess the reaction order, α, in the combined batch reactor
mole balance and rate law equation:

dCA
= −kCAα
dt

• and integrate the differential equation to obtain the concentration as a function of


time.

14
Integral Method

• If the order we assume is correct, the appropriate plot (determined from this
integration) of the concentration–time data should be linear.

• The integral method is used most often when the reaction order is known, and it is
desired to evaluate the specific reaction rate constant at different temperatures to
determine the activation energy.

It is important to know how to generate linear plots of functions of versus t for


zero-, first-, and second-order reactions.
15
Integral Method
ln (CA0/CA) 1/CA
CA

t t t

Zeroth order First Order Second Order


dCA dCA dCA
= rA = −k = rA = −kCA = rA = −kCA2
dt dt dt

at t = 0, CA = CA 0 at t = 0, CA = CA 0 at t = 0, CA = CA 0
 CA 0  
  CA = CA 0 − kt  ln  = kt 
1

1
= kt
 CA  CA CA 0
  
16

Example # 7.1

17
Solution

18
Solution

19
Solution

20
Solution

21

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