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<span class='text_page_counter'>(1)</span>Lecture 1 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 take place.. 1.
<span class='text_page_counter'>(2)</span> Lecture 1 Introduction Definitions General Mole Balance Equation . 2. Batch (BR) Continuously Stirred Tank Reactor (CSTR) Plug Flow Reactor (PFR) Packed Bed Reactor (PBR).
<span class='text_page_counter'>(3)</span> Chemical Reaction Engineering Chemical reaction engineering is at the heart of. virtually every chemical process. It separates the chemical engineer from other engineers. Industries that Draw Heavily on Chemical Reaction Engineering (CRE) are: CPI (Chemical Process Industries) Examples like Dow, Amoco, Chevron, BSR, SK Energy, etc.. 3.
<span class='text_page_counter'>(4)</span> 4.
<span class='text_page_counter'>(5)</span> Smog (Ch. 1) Wetlands (Ch. 7 DVD-ROM). Hippo Digestion (Ch. 2). Oil Recovery (Ch. 7). 5. Chemical Plant for Ethylene Glycol (Ch. 5). Lubricant Design (Ch. 9). Cobra Bites (Ch. 8 DVD-ROM). Plant Safety (Ch. 11,12,13).
<span class='text_page_counter'>(6)</span> Let’s Begin CRE 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 take place..
<span class='text_page_counter'>(7)</span> Chemical Identity • A chemical species is said to have reacted when it has lost its chemical identity..
<span class='text_page_counter'>(8)</span> Chemical Identity • A chemical species is said to have reacted when it has lost its chemical identity. • The identity of a chemical species is determined by the kind, number, and configuration of that species’ atoms..
<span class='text_page_counter'>(9)</span> Chemical Identity • A chemical species is said to have reacted when it has lost its chemical identity. 1. Decomposition.
<span class='text_page_counter'>(10)</span> Chemical Identity • A chemical species is said to have reacted when it has lost its chemical identity. 1. Decomposition. 2. Combination.
<span class='text_page_counter'>(11)</span> Chemical Identity • A chemical species is said to have reacted when it has lost its chemical identity. 1. Decomposition. 2. Combination. 3. Isomerization.
<span class='text_page_counter'>(12)</span> Chemical Identity A chemical species is said to have reacted when. it has lost its chemical identity. There are three ways for a species to loose its identity: 1. Decomposition CH3CH3 H2 + H2C=CH2 2. Combination N2 + O2 2 NO 3. Isomerization C2H5CH=CH2 CH2=C(CH3)2. 12.
<span class='text_page_counter'>(13)</span> Reaction Rate • The reaction rate is the rate at which a species looses its chemical identity per unit volume..
<span class='text_page_counter'>(14)</span> Reaction Rate • The reaction rate is the rate at which a species looses its chemical identity per unit volume. • The rate of a reaction (mol/dm3/s) can be expressed as either the rate of Disappearance: -rA or as the rate of Formation (Generation): rA.
<span class='text_page_counter'>(15)</span> Reaction Rate Consider the isomerization AB. rA = the rate of formation of species A per unit volume -rA = the rate of a disappearance of species A per unit volume rB = the rate of formation of species B per unit volume.
<span class='text_page_counter'>(16)</span> Reaction Rate • EXAMPLE: AB If Species B is being formed at a rate of 0.2 moles per decimeter cubed per second, ie, rB = 0.2 mole/dm3/s.
<span class='text_page_counter'>(17)</span> Reaction Rate • EXAMPLE: AB rB = 0.2 mole/dm3/s Then A is disappearing at the same rate: -rA= 0.2 mole/dm3/s.
<span class='text_page_counter'>(18)</span> Reaction Rate • EXAMPLE: AB rB = 0.2 mole/dm3/s Then A is disappearing at the same rate: -rA= 0.2 mole/dm3/s The rate of formation (generation of A) is rA= -0.2 mole/dm3/s.
<span class='text_page_counter'>(19)</span> Reaction Rate • For a catalytic reaction, we refer to -rA', which is the rate of disappearance of species A on a per mass of catalyst basis. (mol/gcat/s) NOTE: dCA/dt is not the rate of reaction.
<span class='text_page_counter'>(20)</span> Reaction Rate Consider species j: • rj is the rate of formation of species j per unit volume [e.g. mol/dm3/s].
<span class='text_page_counter'>(21)</span> Reaction Rate • rj is the rate of formation of species j per unit volume [e.g. mol/dm3*s] • rj is a function of concentration, temperature, pressure, and the type of catalyst (if any).
<span class='text_page_counter'>(22)</span> Reaction Rate • rj is the rate of formation of species j per unit volume [e.g. mol/dm3/s] • rj is a function of concentration, temperature, pressure, and the type of catalyst (if any) • rj is independent of the type of reaction system (batch reactor, plug flow reactor, etc.).
<span class='text_page_counter'>(23)</span> Reaction Rate • rj is the rate of formation of species j per unit volume [e.g. mol/dm3/s] • rj is a function of concentration, temperature, pressure, and the type of catalyst (if any) • rj is independent of the type of reaction system (batch, plug flow, etc.) • rj is an algebraic equation, not a differential equation.
<span class='text_page_counter'>(24)</span> Building Block 1:. General Mole Balances System Volume, V. Fj0. 24. Gj. Fj. Molar Flow Molar Flow Molar Rate Molar Rate Rateof − Rateof + Generation = Accumulation Species j in Species j out of Species j of Species j dN j Fj0 − Fj + Gj = dt mole mole mole mole − + = time time time time .
<span class='text_page_counter'>(25)</span> Building Block 1:. General Mole Balances If spatially uniform:. G j = r jV If NOT spatially uniform:. ∆V1 rj1 G j1 = rj1∆V1 25. ∆V2 rj 2 G j 2 = rj 2 ∆V2.
<span class='text_page_counter'>(26)</span> Building Block 1:. General Mole Balances n. G j = ∑ rji ∆Vi i =1. Take limit n. Gj = ∑. rji ∆Vi. i=1 lim ∆V → 0 n → ∞. 26. =. ∫ r dV j.
<span class='text_page_counter'>(27)</span> Building Block 1:. General Mole Balances System Volume, V. FA0. GA. FA. General Mole Balance on System Volume V. In − Out + Generation = Accumulation dN A FA 0 − FA + ∫ rA dV = dt 27.
<span class='text_page_counter'>(28)</span> Batch Reactor Mole Balance.
<span class='text_page_counter'>(29)</span> Batch Reactor - Mole Balances Batch. dN A FA0 − FA + ∫ rA dV = dt FA0 = FA = 0. Well-Mixed. 29 29. ∫r. A. dV = r A V. dN A = rAV dt.
<span class='text_page_counter'>(30)</span> Batch Reactor - Mole Balances Integrating. when. dN A dt = rAV. t = 0 N A = N A0 t = t NA = NA. t=. NA. ∫. N A0. dN A rAV. Time necessary to reduce the number of moles of A from NA0 to NA. 30.
<span class='text_page_counter'>(31)</span> Batch Reactor - Mole Balances NA. dN A t= ∫ rV N A0 A. NA. 31. t.
<span class='text_page_counter'>(32)</span> Continuously Stirred Tank Reactor Mole Balance.
<span class='text_page_counter'>(33)</span> CSTR (Cont.).
<span class='text_page_counter'>(34)</span> CSTR (Cont.).
<span class='text_page_counter'>(35)</span> CSTR (Cont.).
<span class='text_page_counter'>(36)</span> CSTR (Cont.).
<span class='text_page_counter'>(37)</span> CSTR (Cont.).
<span class='text_page_counter'>(38)</span> Plug Flow Reactor.
<span class='text_page_counter'>(39)</span> PFR Mole Balances PFR:.
<span class='text_page_counter'>(40)</span> PFR Mole Balances (Cont.).
<span class='text_page_counter'>(41)</span> PFR Mole Balances (Cont.).
<span class='text_page_counter'>(42)</span> PFR Mole Balances (Cont.).
<span class='text_page_counter'>(43)</span> PFR Mole Balances (Cont.).
<span class='text_page_counter'>(44)</span> PFR Mole Balances (Cont.).
<span class='text_page_counter'>(45)</span> Plug Flow Reactor - Mole Balances PFR. dN A FA0 − FA + ∫ rA dV = dt Steady State. dN A =0 dt. FA0 − FA + ∫ rA dV = 0 45.
<span class='text_page_counter'>(46)</span> Alternative Derivation. Plug Flow Reactor - Mole Balances Differientiate with respect to V. dFA = rA dV. dFA 0− = −rA dV. The integral form is:. V =. FA. ∫. FA 0. 46. dF A rA. This is the volume necessary to reduce the entering molar flow rate (mol/s) from FA0 to the exit molar flow rate of FA..
<span class='text_page_counter'>(47)</span> PFR Mole Balances (Cont.) PFR:. The integral form is:. dF A FA 0 r A. V=∫. FA. This is the volume necessary to reduce the entering molar flow rate (mol/s) from FA0 to the exit molar flow rate of FA..
<span class='text_page_counter'>(48)</span> Packed Bed Reactor Mole Balance PBR.
<span class='text_page_counter'>(49)</span> Packed Bed Reactor - Mole Balances ∆W. PBR FA. FA. W + ∆W. W. FA (W ) − FA (W + ∆W ) + rA′ ∆W =. Steady State. lim. 49. ∆W → 0. dN A =0 dt F A W + ∆W − F A. ∆W. W. dN A dt. = r A′.
<span class='text_page_counter'>(50)</span> Packed Bed Reactor - Mole Balances Rearrange:. dFA = rA′ dW. The integral form to find the catalyst weight is:. W=. FA. ∫. FA 0. dFA rA′. PBR catalyst weight necessary to reduce the entering molar flow rate FA0 to molar flow rate FA. 50.
<span class='text_page_counter'>(51)</span> Reactor Mole Balances Summary The GMBE applied to the four major reactor types (and the general reaction AB) Reactor. Differential. Algebraic. Integral NA. Batch. CSTR PFR. PBR 51. dN A t= ∫ rV N A0 A. dN A = rAV dt V=. dFA = rA dV dFA = rA′ dW. FA 0 − FA −rA. FA. dFA V= ∫ drA FA 0 W=. FA. ∫. FA 0. dFA rA′. NA t FA V FA W.
<span class='text_page_counter'>(52)</span> Homework 1: A 200-dm3 constant-volume batch reactor is pressurized to 20 atm with a mixture of 75% A and 25% inert. The gas-phase reaction is carried out isothermally at 227 C. V = 200-dm3 P = 20 atm T = 227 C a. Assuming that the ideal gas law is valid, how many moles of A are in the reactor initially? What is the initial concentration of A? b. If the reaction is first order: Calculate the time necessary to consume 99% of A. c. If the reaction is second order: Calculate the time to consume 80% of A. Also calculate the pressure in the reactor at this time if the temperature is 127 C..
<span class='text_page_counter'>(53)</span> Homework 2:.
<span class='text_page_counter'>(54)</span>