Hydrocarbon activation propylene

The data of Table 5 show that propane activation with the formation of aromatic hydrocarbons and propylene is possible at appreciably lower temperatures. The possible mechanism of benzene dehydroalkylation by propane with the formation of IPB and propylene occurs with the carbenium ion formation by the scheme ... 

Many simple systems that could be expected to form ideal Hquid mixtures are reasonably predicted by extending pure-species adsorption equiUbrium data to a multicomponent equation. The potential theory has been extended to binary mixtures of several hydrocarbons on activated carbon by assuming an ideal mixture (99) and to hydrocarbons on activated carbon and carbon molecular sieves, and to O2 and N2 on 5A and lOX zeoHtes (100). Mixture isotherms predicted by lAST agree with experimental data for methane + ethane and for ethylene + CO2 on activated carbon, and for CO + O2 and for propane + propylene on siUca gel (36). A statistical thermodynamic model has been successfully appHed to equiUbrium isotherms of several nonpolar species on 5A zeoHte, to predict multicomponent sorption equiUbria from the Henry constants for the pure components (26). A set of equations that incorporate surface heterogeneity into the lAST model provides a means for predicting multicomponent equiUbria, but the agreement is only good up to 50% surface saturation (9). 

The partial oxidation of propylene occurs via a similar mechanism, although the surface structure of the bismuth-molybdenum oxide is much more complicated than in Fig. 9.17. As Fig. 9.18 shows, crystallographically different oxygen atoms play different roles. Bridging O atoms between Bi and Mo are believed to be responsible for C-H activation and H abstraction from the methyl group, after which the propylene adsorbs in the form of an allyl group (H2C=CH-CH2). This is most likely the rate-determining step of the mechanism. Terminal O atoms bound to Mo are considered to be those that insert in the hydrocarbon. Sites located on bismuth activate and dissociate the O2 which fills the vacancies left in the coordination of molybdenum after acrolein desorption. 

Light hydrocarbons consisting of oxygen or other heteroatoms are important intermediates in the chemical industry. Selective hydrocarbon oxidation of alkenes progressed dramatically with the discovery of bismuth molybdate mixed-metal-oxide catalysts because of their high selectivity and activity (>90%). These now form the basis of very important commercial multicomponent catalysts (which may contain mixed metal oxides) for the oxidation of propylene to acrolein and ammoxidation with ammonia to acrylonitrile and to propylene oxide. 

More recently phosphorus-containing zeolites developed by Union Carbide (alu-minophosphates, silicoaluminophosphates) were shown to be equally effective in methanol condensation.439-444 ZSM-5 was also shown to exhibit high activity and selectivity in the transformation of Fischer-Tropsch oxygenates to ethylene and propylene in high yields.445 Silicalite impregnated with transition-metal oxides, in turn, is selective in the production of C4 hydrocarbons (15-50% isobutane and 8-15% isobutylene).446... 

Minachev, Eidus et al. (25) found that Ca, Ni, Co, and NdY zeolites were active in the disproportionation of propylene to ethylene and butenes. The process was accompanied by hydrogen rearrangement to form saturated hydrocarbons and condensation products. The selectivity in this reaction depends on the composition of the catalysts, their pretreatment, and the experimental conditions (26). 

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