Reactor Design for Complex Configurations

Slides:



Advertisements
Similar presentations
Reversible Reactions – Part II
Advertisements

Topic 7: Equilibrium SL Le Chatelier’s Principle
1 Ref: Seider et al, Product and process design principles, 3 rd ed., Wiley, 2010.
Chemical Equilibrium A Balancing Act.
ADVANCED PLACEMENT CHEMISTRY EQUILIBRIUM. Chemical equilibrium * state where concentrations of products and reactants remain constant *equilibrium is.
CHEMICAL AND PHASE EQUILIBRIUM (1)
Exercise 3. Solutions From Fujio Kida, JGC Co. All cases
Steady State Nonisothermal Reactor Design
Modelling & Simulation of Chemical Engineering Systems
First Law of Thermodynamics
Introduction to Chemical Equilibrium Chapter 15 CHEM 160.
Equilibrium DP Chemistry R. Slider.
ITK-233 Termodinamika Teknik Kimia I
Chemistry 1011 Slot 51 Chemistry 1011 TOPIC Gaseous Chemical Equilibrium TEXT REFERENCE Masterton and Hurley Chapter 12.
7. Equilibria Learning Outcomes Candidates should be able to:
S,S&L Chapter 7 Terry A. Ring ChE
P. 1 Wording Basic data Analysis Performance Flow pattern Concentration Temperature Pressure Practical reactor Diagram Actual process Ullmann 1 Ullmann.
EQUILIBRIUM TIER 5 & TIER 6 TIER 5:Apply the concepts of kinetics and equilibrium to industrial processes TIER 6: Make connections between equilibrium,
Simulating Ammonia Synthesis with COMSOL
Chapter 16 Chemical and Phase Equilibrium Study Guide in PowerPoint to accompany Thermodynamics: An Engineering Approach, 5th edition by Yunus.
Chapter 14: Chemical Equilibrium Renee Y. Becker Valencia Community College 1.
Chapter 16: Chemical Equilibrium- General Concepts WHAT IS EQUILIBRIUM?
Some reactions do not go to completion as we have assumed They may be reversible – a reaction in which the conversion of reactants to products and the.
Chapter 18: Chemical Equilibrium
SAMPLE EXERCISE 15.1 Writing Equilibrium-Constant Expressions
Chemical Reaction Engineering (CRE) is the field that studies the rates and mechanisms of chemical reactions and the design of the reactors in which they.
Lecture 19 Tuesday 3/18/08 Gas Phase Reactions Trends and Optimuns.
Tarek Moustafa1 Chemical Reaction Engineering An Introduction to Industrial Catalytic Reactors Tarek Moustafa, Ph.D. November 2011.
The Position of Equilibrium
1 Chemical Equilibrium You learned when we studied mechanisms that some rxns are reversible or equilibrium rxns The double arrow is used to show this.
Chemical Equilibrium Chapter 15.
Dr Saad Al-ShahraniChE 334: Separation Processes Absorption of Dilute Mixtures  Graphical Equilibrium Stage Method for Trayed Tower  Consider the countercurrent-flow,
Chemical Equilibrium.
Non Isothermal CSTR Chemical Reaction Engineering I Aug Dec 2011 Dept. Chem. Engg., IIT-Madras.
ITK-330 Chemical Reaction Engineering
© 2015 Carl Lund, all rights reserved A First Course on Kinetics and Reaction Engineering Class 34.
© 2014 Carl Lund, all rights reserved A First Course on Kinetics and Reaction Engineering Class 17.
© 2014 Carl Lund, all rights reserved A First Course on Kinetics and Reaction Engineering Class 29.
Chemical/Polymer Reactor Design
1 Ref: Seider et al, Product and process design principles, 2 nd ed., Chapter 4, Wiley, 2004.
© 2014 Carl Lund, all rights reserved A First Course on Kinetics and Reaction Engineering Class 25.
Energy Balance on Reactive Processes
Lecture 7 packed beds. Reactor Scale Considerations: Gas-Solid Systems Solid catalyzed gas reactions are mainly conducted in Adiabatic massive packed.
© 2015 Carl Lund, all rights reserved A First Course on Kinetics and Reaction Engineering Class 34.
Prentice Hall © 2003Chapter 15 Chapter 15 Chemical Equilibrium CHEMISTRY The Central Science 9th Edition David P. White.
Example of Process with Recycle: TOLUENE HYDRODEALKYLATION
© 2014 Carl Lund, all rights reserved A First Course on Kinetics and Reaction Engineering Class 17.
Kinetics and Reactor Design Kinetics and Reactor Design CHE-402 INSTRUCTOR: Dr. Nabeel Salim Abo-Ghander Chemical Reactions and Rate of Reactions Chapter.
© 2014 Carl Lund, all rights reserved A First Course on Kinetics and Reaction Engineering Class 25.
Chemical Reaction Engineering (CRE) is the field that studies the rates and mechanisms of chemical reactions and the design of the reactors in which they.
UNIT 10 COLLISION THEORY, RATE OF REACTION, LE CHATELIER PRINCIPLE.
SCHOOL OF CHEMICAL ENGINEERING, UNIVERSITI SAINS MALAYSIA EKC 334/3 ANALYSIS & OPERATION OF CATALYTIC REACTORS Experimental methods for finding rates 1)
Prentice Hall © 2003Chapter 15 Chapter 15 Chemical Equilibrium CHEMISTRY The Central Science 9th Edition David P. White.
CHAPTER 3 material balance part iI
Chemical Equilibrium. Unit Objectives  Define chemical equilibrium.  Explain the nature of the equilibrium constant.  Write chemical equilibrium expressions.
PRODUCTION OF SULFURIC ACID
Equilibrium.  In equilibrium, the concentrations of the chemical species are constant, not necessarily equal.  Equilibrium constants:  K = equilibrium.
Topic Extension Equilibrium Acid-Base Equilibrium Solubility Equilibrium Complex-Ions Equilibrium Qualitative Analysis.
Yousef Ghotok Joseph Havelin Wednesday, 23rd April 2008
Review: What size reactor(s) to use?
ChE 402: Chemical Reaction Engineering
Review: Equilibrium Conversion XAe
Steady-state Nonisothermal reactor Design Part I
P8-8 The elementary gas phase reaction A  B + C is carried out adiabatically in PFR packed with catalyst. Pure A enters the reactor at a volumetric flow.
Steady-state Nonisothermal reactor Design Part I
Reactor Design for Selective Product Distribution
Chapter 15 Chemical Equilibrium
Production of Sulfuric Acid
Steady-state Nonisothermal reactor Design Part I
Presentation transcript:

Reactor Design for Complex Configurations Ref: Seider et al, Product and process design principles, 3rd ed., Wiley, 2010.

Temperature Control Temperature control is an important consideration in reactor design. Adiabatic operation is always considered first because it provides the simplest and least-expensive reactor. However, when reactions are highly exothermic or endothermic, some methods must be used for controlling the temperature of reactor such as:

• Heat-exchanger reactor (a) • Use of diluent (b) • A series of beds with inter- heater or cooler (c) • Cold-shot cooling or hot-shot heating (d)

Industrial Examples A useful measure of the degree of exothermicity or endothermicity is the Adiabatic Temperature Rise (ATR) for complete reaction with reactants in the stoichiometric ratio. An industrial example of heat-exchanger reactor : Phthalic anhydide produced by the oxidation of ortho-xylene with air in the presence of vanadium pentoxide catalyst particles. The reaction, which is carried out at about 375 oC and 1.2 atm, is highly exothermic with an ATR of about 1170 oC, even with nitrogen in the air providing some dilution. Hundreds of long tubes of small diameter, inside the shell, are packed with catalyst particles and through which the reacting gas passes downward.

Industrial Examples A heat-transfer medium consisting of a sodium nitrite-potassi-um nitrate-fused salts circulates outside the tubes through the shell. The heat transfer rate distribution is not adequate to maintain isothermal condition, but its temperature changes is less than 40 oC. An industrial example of diluent usage : Styrene is produced by the catalytic dehydrogenation of ethylbenzene at 1.2 atm and 575 oC. The reaction is sufficiently endothermic, with an ATR of about -460 oC. To maintain a reasonable temperature, a large amount of steam (inert) that preheated to 625 oC, is added to the feed (molar ratio of steam to ethylbenzene is about 20:1).

Industrial Examples An industrial example of inter-cooler usage : Sulfur trioxide, which is used to make sulfuric acid, is produced by catalytic oxidation of sulfur dioxide in air with vanadium pentoxide catalyst particles at 1.2 atm and 450 oC. Adiabatic operation is not feasible because of an ATR of about 710 oC, even with nitrogen in the air providing some dilution. Hence, the reactor system consists of four adiabatic reactor beds, of the same diameter but different height, in series, with a heat exchanger between each pair of beds. When the ATR is higher, such as in the manufacture of ammonia from synthesis gas, the cold-shot design is recommended.

Desired Temperature Trajectory For 1-D fixed-bed catalytic reactors, it is desirable to reduce the vessel volume to a minimum. This objective can be achieved by matching the trajectory of the mass- and energy-balance equations along the length of reactor (X(z), T(z)), to the trajectory corresponding to the maximum reaction rate, (X*, T*), as closely as possible. Thus, tube-cooled (or heated) reactors, cold-shot (or hot-shot) converters, and multiple adiabatic beds with inter-coolers (or inter-heaters) need to be carefully designed in such a way that (X(z), T(z)) ≈ (X*, T*).

Desired Temperature Trajectory As an example , consider an exothermic reversible reaction in a PFR. For this case, the rate of the reverse reaction increases more rapidly with increasing temperature than the rate of forward reaction. Also, the reverse reaction is slow and the forward reaction is fast at low temperature. Thus, for a maximum rate of reaction, the temperature should be high at low conversions and low at high conversions.

Desired Temperature Trajectory The feed enters at point A (TA , X1). If the entering temperature cannot be increased, it is best to operate isoth-ermally at TA until the conversion at point C is reached, and than follow the optimal profile CB to the desired conversion (X4). Alternatively, a larger reactor volume will be needed, if isothermal operation is used (trajectory ACD). If instead of a PFR, a CSTR were used, the optimal operating temperature for achieving X4 would be TB, which corresponds to the maximum reaction rate for that conversion.

Multiple Steady States in an Auto-thermal Reactor The reactor feed temperature has an important effect on the stability of an auto-thermal reactor, that is, a reactor whose feed is preheated by its effluent. For a reversible exothermic reaction, as in ammonia synthesis, the heat generation rate varies nonlinearly with reaction temperature, with a maximum at some intermediate temperature. In contrast, the rate of heat removal is almost linear with the reaction temperature, with a slope dependent on the degree of heat exchange between the outlet and the inlet.

Multiple Steady States in an Auto-thermal Reactor The intersection of line (b) and curve (a) sometimes leads to three possible operating conditions: (O) the non-reacting state (stable), (I) the ignition point (unstable), and (S) the desired operating point (stable). The temperature difference between operating points I and S is called stability margin. Clearly, operation at S with larger stability margin would be more robust to disturbances. Thus a design with increased rate of heat transfer (line b’) and a design without considering the decreasing of catalyst activity (line a’), can lead to loss of stability.

Example 7.3: Optimal Bypass Distribution in a Three-Bed, Cold-Shot Ammonia Synthesis Converter A reactor for synthesis of ammonia consists of three cylindrical, 2-m-diameter adiabatic beds, packed with catalyst for bed lengths of 1.5 m, 2 m, and 2.5 m, respectively. The reactor feed is split into three branches, with the 1st branch becoming the main feed entering the 1st bed after being preheated by the hot reactor effluent from the 3rd bed. The 2nd and 3rd branches, with flow fractions of φ1 and φ2, provide cold-shot cooling at the 1st and 2nd bed effluents.

Example 7.3: Optimal Bypass Distribution in a Three-Bed, Cold-Shot Ammonia Synthesis Converter As summarized in the following Table, the reactor feed consists of two sources, the first of which is a make-up feed stream mainly hydrogen and nitrogen (synthesis gas) in stoichiometric molar ratio of 3:1. The second feed is a recycle stream consisting of unreacted synthesis gas, recovered after removing the ammonia product. It is desired to optimize the allocation of the bypass fractions to maximize the ammonia production.

Example 7.3: Solution Ammonia is synthesized by the following reversible reaction: After multiplying the rate equation by 2 and changing the unit of partial pressure to Pascal, we have:

Example 7.3: Solution At first, a value of 0.1 is assumed for each bypass fraction and the process was simulated in ASPEN PLUS (the PR EOS was used for property prediction). The simulated process was saved with filename: <example7_3_current.bkp>. For founding the optimum temperature trajectory based on the NH3 mole percent and the rate of reaction, the partial pressure of H2 and N2 must be expressed in terms of NH3 mole fraction. This can be done by component mass balance as follows: Where the F0 is the total molar flow rate of the combined feed and ξ is the molar extent of reaction.

Example 7.3: Solution Where xf,i is the feed mole fraction of species i. Consequently, the rate of reaction can be computed as a function of the temperature and mole percent of NH3, as shown in the following figure for operating pressure of 150 atm.

The above figure can be reproduced in MATLAB by running the m-file: <example7_3_current.m>. As can be seen from the results by using a value of 0.1 for each bypass fraction, the conc. of ammonia in the effluent stream is 12.9%.

Example 7.3: Solution To maximize the ammonia production in the reactor, the following optimization problem must be solved: The first constraint refers to the reactor model. The second and third constraints are selected for achieving a suitable stability margin. The last constraint is arbitrary.

Example 7.3: Solution The above optimization problem was solved by Successive Quadratic Programming (SQP) method in ASPEN PLUS (the filename is: <example7_3_optim.bkp>). The final ammonia composition in the reactor effluent is 16.1 mol%, obtained with optimal bypass fractions φ1=0.23 and φ2=0.24. The composition-temperature trajectories for the optimal bypass distribution, is shown in the following figure. This figure can be reproduced in MATLAB by running the m-file:<example7_3_optim.m>.

Example 7.3: Solution Investigate the performance of the optimized process, if the catalyst activity decreases by a factor of 0.2 (80% decrease in catalyst activity).