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Methane dehydroaromatization over Mo-modified H-MFI for gas to liquid catalysts 被引量:4
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作者 Hirofumi Aritani Hiromi Shibasaki +1 位作者 Hitoshi Orihara Atsushi Nakahira 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2009年第6期736-740,共5页
For direct gas to liquid(GTL),a novel process producing energy sources for methane dehydroaromatization is needed.Supporting MoO3 on H-MFI zeolite shows the high catalytic capacity and a selective activity for dehyd... For direct gas to liquid(GTL),a novel process producing energy sources for methane dehydroaromatization is needed.Supporting MoO3 on H-MFI zeolite shows the high catalytic capacity and a selective activity for dehydroaromatization of methane to benzene at 973 K in a fixed bed reactor.On the other hand,deactivation by coke on the active sites in all the catalysts is formed during the reaction.H2 co-feed suppressed the deactivation,which is probably due to the decrease in coking amount.Mo K-edge X-ray absorption fine structure(XAFS) results showed the formation of dispersed Mo2C species with low crystallinity after dehydroaromatization.Mo LIII-edge XANES(X-ray absorption near-edge structure) indicated the formation of active Mo species including Mo2C and Mo-oxycarbide(MoOxCy),where the redox state should be independent in the absence/presence of H2.It is concluded that Mo-oxycarbide species act as highly active species,and their stability affected the durable activity in the presence of H2. 展开更多
关键词 direct gas to liquid methane dehydroaromatization Mo/H-MFI L-XANES k-xafs
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