Slides courtesy of Prof M L Kraft, Chemical & Biomolecular Engr Dept, University of Illinois at Urbana-Champaign. L21-1 Review: Heterogeneous Catalyst.

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Presentation transcript:

Slides courtesy of Prof M L Kraft, Chemical & Biomolecular Engr Dept, University of Illinois at Urbana-Champaign. L21-1 Review: Heterogeneous Catalyst We have looked at cases where 1)Adsorption, surface reaction, or desorption is rate limiting 2)External diffusion is rate limiting 3)Internal diffusion is rate limiting Next goal: Derive an overall rate law for heterogeneous catalyst where the rate limiting step as any of the 7 reaction steps. This new overall reaction rate would be inserted into the design equation to get W, X A, C A, etc

Slides courtesy of Prof M L Kraft, Chemical & Biomolecular Engr Dept, University of Illinois at Urbana-Champaign. L21-2 r R C As Review: Internal Diffusion Effects in Spherical Catalyst Particles Internal diffusion: diffusion of reactants or products from particle surface (pore mouth) to pellet interior Concentration at the pore mouth will be higher than that inside the pore Internal diffusion C Ab External diffusion Step 1) Mole balance over the shell thickness  r is: IN - OUT + GEN = ACCUM Volume of shell r’ A : rxn rate per mass of catalyst  c : catalyst density r m : mean radius between r and r -  r Divide by -  r & take limit as  r →0 Differential BMB in spherical catalyst particle

Slides courtesy of Prof M L Kraft, Chemical & Biomolecular Engr Dept, University of Illinois at Urbana-Champaign. L21-3 r R C As Review: Diffusion & Rxn in Spherical Catalyst r+  r System at steady state, so EMCD: W B = -W A (otherwise A or B would accumulate) Rate law: Insert diffusion eq & rate eq into BMB: Solve for C A (r) & get W Ar (r) from diffusion eq

Slides courtesy of Prof M L Kraft, Chemical & Biomolecular Engr Dept, University of Illinois at Urbana-Champaign. L21-4 Review:Dimensionless Variables Put into dimensionless form Boundary Conditions:  =1 at =1  =finite at =0 Thiele modulus for rxn of n th order ≡  n Subscript n = reaction order  n is small: surface reaction is rate limiting  n is large: internal diffusion is rate limiting The solution for a 1 st order rxn: R r=0 small  1 medium  1 large  1 small  1 : surface rxn control, significant amount of reactant diffuses into pellet interior w/out reacting large  1 : surface rxn is rapid, reactant is consumed very closed to the external surface of pellet (A waste of precious metal inside of pellet)

Slides courtesy of Prof M L Kraft, Chemical & Biomolecular Engr Dept, University of Illinois at Urbana-Champaign. L21-5 Review: Internal Effectiveness Factor,  eta 11  Internal diffusion limited Reaction limited Effectiveness factor vs  n As particle diameter ↓,  n ↓,  →1, rxn is surface rxn limited As particle diameter ↑,  n ↑,  →0, rxn is diffusion limited

Slides courtesy of Prof M L Kraft, Chemical & Biomolecular Engr Dept, University of Illinois at Urbana-Champaign. L21-6 surface-reaction-limited  1 is large, diffusion-limited reaction inside the pellet (external diffusion will have a negligible effect on the overall rxn rate because internal diffusion limits the rxn rate) Overall rate for 1st-order rxn When internal-diffusion-limited: To increase the overall rate of a rxn limited by internal diffusion (1) decrease the radius R(3) increase the concentration of A (2) increase the temperature(4) increase the internal surface area Review: Effectiveness Factor & Rxn Rate

Slides courtesy of Prof M L Kraft, Chemical & Biomolecular Engr Dept, University of Illinois at Urbana-Champaign. L21-7 L21: Simultaneous Internal Diffusion & External Diffusion C Ab C As C(r) At steady-state: transport of reactants from bulk fluid to external catalyst surface is equal to net rate of reactant consumption in/on the pellet Molar rate of mass transfer from bulk fluid to external surface: molar flux external surface area per unit reactor volume reactor volume This molar rate of mass transfer to surface is equal to net rxn rate on & in pellet! Goal: Derive a new rate eq that accounts for internal & external diffusion -r’ A is a function of reactant concentration Reactant conc is affected by internal & external diffusion Express reactant conc in terms of diffusion-related constants & variables →Use mole balance

Slides courtesy of Prof M L Kraft, Chemical & Biomolecular Engr Dept, University of Illinois at Urbana-Champaign. L21-8 Basic Molar Balance at Pellet Surface = Flux: bulk to external surface Actual rxn rate per unit total S.A. External S.A. x a c : external surface area per reactor volume (m 2 /m 3 )  V: reactor volume (m 3 ) -r’’ A : rate of reaction per unit surface area (mol/m 2 ·s) S a : surface area of catalyst per unit mass of catalyst (m 2 /g cat)  b : bulk density, catalyst mass/ reactor volume  b =  c (1-   : porosity of bed (void fraction)  c : catalyst density x external + internal S.A. Typically external surface area <<< internal surface area

Slides courtesy of Prof M L Kraft, Chemical & Biomolecular Engr Dept, University of Illinois at Urbana-Champaign. L21-9 Overall Molar Rate of Reaction Overall rxn rate = flux to surface = rxn rate on & in pellet For external mass transport: Since internal diffusion resistance is also significant, the reactant conc at the internal surface is lower that the reactant conc at the external surface: where the internal effectiveness factor: For a 1 st order rxn: -r’’ A =-  k 1 C As Plug flux & 1 st order rxn rate back into the mass balance: Solve mass balance for C As

Slides courtesy of Prof M L Kraft, Chemical & Biomolecular Engr Dept, University of Illinois at Urbana-Champaign. L21-10 Overall rxn rate with internal & external diffusion Overall Effectiveness Factors Finally insert C As into –r’’ A Is this the overall rxn rate that we ALWAYS use for a surface reaction that has internal & external? (a)Yes, we should always use this rate equation for a surface reaction (b)No, we should only use this rate eq for processes that use spherical catalyst pellets (c)No, we should only use this rate eq for processes that that involve catalyst particles that have a constant density & even catalyst loading on the surface (d) No, we should only use this rate eq for 1 st order irreversible reactions (e) b, c, & d

Slides courtesy of Prof M L Kraft, Chemical & Biomolecular Engr Dept, University of Illinois at Urbana-Champaign. L21-11 Overall rxn rate with internal & external diffusion Remember, the internal effectiveness factor (based on C As ) is: The overall effectiveness factor (based on C Ab ) is defined as: Overall Effectiveness Factors Finally insert C As into –r’’ A Put into design eq to account for internal & external diffusion Omega

Slides courtesy of Prof M L Kraft, Chemical & Biomolecular Engr Dept, University of Illinois at Urbana-Champaign. L21-12 Rxn Rate Variation vs Reactor Conditions Type of Limitation Variation of Reaction Rate with: Superficial velocityParticle sizeTemperature ExternalU 1/2 d p -3/2 Linear InternalIndependentd p -1 Exponential Surface reactionIndependent Exponential External diffusion Surface reaction -r’ A =kC A Internal diffusion

Slides courtesy of Prof M L Kraft, Chemical & Biomolecular Engr Dept, University of Illinois at Urbana-Champaign. L21-13 Consider an isothermal catalytic reaction in a PBR where there is no pressure drop and the catalyst pellets are uniformly packed & spherical. The kinetics are 1 st order, and k, all physical parameters, and the inlet conditions (pure A in feed, A→ products) are given. Derive an equation for X A, taking into account the diffusion to and within each catalyst particle, but ignore diffusion down the length of the reactor. PBR design eq: Rate must account for diffusion & be in terms of catalyst surface area 1. Put rate in terms of the unit surface area: 2. Account for diffusion limitations in rate eq: 3. Rate is 1 st order: 4. Put into design eq: 5. Put C ab in terms of X A : 6. Integrate:

Slides courtesy of Prof M L Kraft, Chemical & Biomolecular Engr Dept, University of Illinois at Urbana-Champaign. L21-14 Consider an isothermal catalytic reaction in a PBR where there is no pressure drop and the catalyst pellets are uniformly packed & spherical. The kinetics are 1 st order, and k, all physical parameters, and the inlet conditions (pure A in feed, A→ products) are given. Derive an equation for X A, taking into account the diffusion to and within each catalyst particle, but ignore diffusion down the length of the reactor. 6. Integrate: 7. Solve for X A :

Slides courtesy of Prof M L Kraft, Chemical & Biomolecular Engr Dept, University of Illinois at Urbana-Champaign. L21-15 For same conditions, eq derived in Fogler (12-71) for X A at end of reactor of length L is: X A for 1 st order rxn executed in an isothermal PBR packed with spherical catalyst particles with internal & external diffusion limitations Are these equations the same? They differ in the exponent: