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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 AB. 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: AB 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: AB 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: AB 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 AB) 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>

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