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Catalytic Conversion of Methane and Ethylene to Propylene

1998; American Chemical Society; Volume: 102; Issue: 1 Linguagem: Inglês

10.1021/jp9723628

1520-6106

Jack H. Lunsford, Ping Qiu, Michael P. Rosynek, Zhen‐Qiang Yu,

Catalytic Processes in Materials Science

Methane and ethylene react over several catalysts to form propylene as the principal product, with (LiCl + NaCl)/MgO being the most effective material. At 650 °C, it was possible to achieve 53% selectivity to C3H6 at a C2H4 conversion of 9.2%. Experiments utilizing 13CH4 demonstrated that one carbon atom in each C3H6 molecule was derived from methane. Methyl radicals, but not vinyl radicals, were detected over these catalysts using a matrix isolation electron spin resonance system. Moreover, it was found that C2H4 inhibited the formation of CH3• radicals. A model calculation, which included both heterogeneous and homogeneous reactions, indicated that most of the propylene was formed neither by the coupling of methyl and vinyl radicals nor via the addition of methyl radicals to ethylene in the gas phase. Rather, it appears that the primary pathway involves the reaction of methyl radicals with adsorbed ethylene to produce propyl radicals, which then lose a hydrogen atom to yield propylene. The instability of the vinyl radical limits the extent to which cross-coupling with methyl radicals can occur.