Catalysis Introduction
Catalysis Introduction
CATALYSTS Used in Chemical and Allied Industries. Approximately 1/3 of Material GNP of U.S. involves a catalytic process somewhere between raw materials and finished products. TYPES OF CATALYTIC PROCESSES Homogeneous : Catalyst is in a solution with at least one of the reactants. Heterogeneous : Involves more than one phase where usually catalyst is in solid phase and reactants and products are gases or liquids.
LECTURE-1
Thermo. Fluid Flow Mathematics Design Economics
Chemical Kinetics
Chemical Reactor
Chemical Process
Product Marketing
Mass Transfer
Heat Transfer
Materials
Process Control
Pilot Plant
ChE311
LECTURE-1
ChE311
LECTURE-1 Typical Plant Capacity Price Tons/yr $/1b ___________________ _______ 6 8 Petroleum Refining 10 - 10 0.1 Commodity Chemicals 104 106 0.1-2 Fine Chemicals 102 104 2 10 Foods Materials 0- 3 Pharmaceuticals 10 - 10 Very different tasks in each category for a Ch.E. Important In petroleum + commodity Fine chemicals Foods & pharmaceuticals Low-cost Patent protection Patents, trademarks Marketing, advertising Category Waste Products lb/lb 0.1 1-3 2 10 1 50
ChE311
CHEMICAL ENGINEERING Chemical Diffusional Mechanical Process Analysis Reaction Engineering Economics
CATALYST RESEARCH Catalyst Prop. Catalytic Mech. Catalyst Rate Equation Support Reaction Steps Promoters Energetics Preparation Adsorption Pretreatment Mass & Heat Pellet Form Transfer
CATALYTIC CHEMISTRY Surface Chemistry and Physics Physical Chemistry Solid State Physics Patents Literature Experimental Programs
PATTERNS OF BEHAVIOR THEORIES OF CATALYSIS
CATALYST DESIGN
COMMERCIAL MANUFACTURE Scale-up of Procedures Plant Formulations Large Batches PILOT UNIT TESTING Real Feeds Process Conditions Process Variables Life-time Studies Scale-up Data PROCESS DESIGN Process and Economic Optimization Plant Design
REACTOR ENG. Unit Design and Operation Data Analysis Modeling CHEMICAL AND MECHANICAL ENG. Plant Design Materials Specifications
REACTION PATH CATALYST PROPERTIES CATALYTIC MATERIALS PROPOSED CATALYST Steps in catalyst design
TARGET REACTION CHEMISTRY DATA BASE THERMODYNAMIC DATA BASE REACTION DATA FILE
LIST STOICHIOMETRIC REACTIONS GENERATE THERMODYNAMIC PARAMETERS Operator Input Operator Input PROPOSE MOLECULAR MECHANISMS
Operator Input
Propylene Oxide Formation on Cu2O (001) Surface (by utilizing, DFT, VASP code)
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Relative Energy Profile of Propylene Oxide, Propionaldehyde and Allyl Radical Formation
1 0,5 TS (PO) 0 -0,5 -1 -1,5 -2 -2,5 -3 -3,5 -4 -4,5 C3H6 (ads)
Relative Energy (eV)
Allyl-radical(g)
PO (g)
PO(ads) Acetone (g) TS(Acetone) OMMP2(ads) TS(Acrolein) Acetone (ads) Allyl-radical (ads) Acrolein(ads) Acrolein (g)
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R1 A R2
B R3 C CH2
CH3CHO
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REACTION MECHANISM
SYNTHESIS OF CATALYSTS
SOLID STATE CHEMISTRY
CHARACTERIZATION OF CATALYSTS
STRUCTURE, TEXTURE, SPECTROSCOPY, AND DIFFRACTION
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HOMOGENEOUS CATALYSIS
Co
CH3 isobutylaldehyde
CH3-CH2-CH2-CHO n-butylaldehyde
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HETEROGENEOUS CATALYSIS
Solid Phase Catalyst Acid Catalyst
(Phosphoric Acid Type or ZSM-5 Type) C2H5 C2H5 Ethylbenzene
+ H2C=CH2
Benzene Ethylene
Dehydrogenation Catalyst
C2H5-CH=CH2
Styrene
Ethylbenzene
[Fe3O4-type]
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Coal or biomass
+Cellulose
Ru Alkanes, Fe, Alcohols, Co Alkenes (fuels, aviation or diesel), solvents, detergents CH2OH CH2OH And related glycols (antifreeze agents) CO+ H2
Ni/Al2O3
+ CO CH3OH
Acetic Acid
Cu/ZnO
Syn-gas
Methanol
CH3 Zeolite Ag Zeolite (CH2)n Petrol (fuel) Polymers (fabrics and building materials)
HCHO Formaldehyde
Toluene (solvent)
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Ehom Ehet
Potential Energy
Reactants
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Log10 (rate constant), arbitrary units
Ahom
Ahet
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Homogeneous Reaction
1 X 0 1 2 3 Y 4 5 6 7
103/T
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C2H6
Postulated Mechanisms:
For Homogeneous Reaction: G*
C2H4 + H2
C2H4 . H2
Activated Complex
C2H6
C2H4 + [S]1
G1 G2
H2 + C2H4[S]1 C2H4[S]1 H2
G3
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A difficult homogeneous reaction is replaced by a more easily executed heterogeneous surface reaction involving adsorbed C2H4 . (Eley-Rideal Mechanism)
These are simply phenomenological models, not mechanisms. The actual mechanism is quite complex.
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desorption C
adsorption
B Surface Reaction
Surface Migration
Two possible ways in which heterogeneous catalysis proceeds at a surface; the Langmuir-Hinshelwood Mechanism (left) and the Eley-Rideal Mechanism (right)
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H
Butane
C-C=C-C
C-C-C-C
Support Metal
A bifunctional catalyst such as platinum on Al2O3 facilitates the isomerization of methylcyclopropane to 2-butene as well as the hydrogenation of 2-butene to butane (after Boudart)
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Physical Adsorption
Weak Forces of Molecular Interaction (Van der Waals) Small Heats of Adsorption (10-40 kj/mol) Occurs only at ~Tb.p. Equilibrium rapidly attained, low E Highly reversible Multilayer coverage possible Nonspecific, almost indistinguishable from condensation In general, not responsible for catalysis; however may help to form chemisorption precursors Important for determination of total surface area and pore size of catalyst support
Chemisorption
Formation and Rupture of Chemical Bonds Large Heats of Adsorption (80-400 kj/mol) No such restriction at high T Nonactivated: Low E Activated: High Often Irreversible Less than a monolayer Highly specific (a function of a particular crystalline face) Necessary for catalysis Important for determination of activecenter surface area and elucidation of surface reaction kinetics
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DFT COMPUTATIONS
CO conversion energetics
COgp
0,0 1 20,0 40,0 3 5 7 9 11
RelativeEnergy(kcal/mol)
CO2des
60,0 80,0 100,0
O2gp
PdCeZrO2
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The Langmuir Treatment of Adsorption Ideal Surface Requirements 1. Energetically homogeneous or uniform surface; 2. Energy of interaction with the adsorbate is not affected by the presence or absence of adsorbate on adjoining sites; 3. Each site can accommodate only one adsorbate molecule or atom; 4. Adsorption would occur when an adsorbate molecule or atom with the required energy strikes an unoccupied site; 5. The energy contours would be unaffected by the extent of adsorption; 6. All adsorption has the same mechanism; each has the same structure; 7. The extent of adsorption is less than one complete monolayer
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If ra=Rate of adsorption, rs= No. of molecules striking the surf./ time-area (bare surf.) Then r a= s . rs ra=kaPA(1- ) where; ka=Ads. Rate Const. =Fraction occupied by already adsorbed molecules Also if rd= Rate of desorption rd=kd At Equilibrium: ra = r d
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and
Introduce
Where V=Vol. Adsorbed Vm= Vol. Adsorbed by all the active sites covered
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