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Methanol to gasoline over zeolite H-ZSM-5

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Methanol to gasoline over zeolite H-ZSM-5 ( methanol-gasoline-over-zeolite-h-zsm-5 )

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50 M. Bjørgen et al. / Applied Catalysis A: General 345 (2008) 43–50 mechanism, whereas carbon atoms from methanol to a consider- able extent are incorporated and distributed among the C3+ alkenes in a series of alkene methylation and cracking steps [43,44]. Analysis of the product yields, rather than selectivities, indicates that the increase in propene/ethene ratio (Fig. 8c) is caused mainly by a decrease in the ethene yield, in particular for the 0.20M sample. This decrease in ethene yield is compensated by the increase in the yield of C5+. As stated above, ethene is formed from the aromatics, and a major difference between the untreated and the treated samples (0.20M in particular) is the speed with which the aromatics diffuse out of the catalyst and into the gas phase (Fig. 9). We hypothesize that as the diffusivity increases and the time each aromatics molecule resides in the micropores is shortened, the probability of undergoing the reaction steps required for ethene formation is diminished. Hence, the increase in propene/ethene ratio may be caused predominantly by a decline in the rate of ethene formation via the aromatics-based hydro- carbon pool mechanism, whereas the propene, which to a large extent is formed through alkene methylation and cracking steps, is less influenced by the reduction of the time the methylbenzenes spend within the catalyst. 4. Conclusions The catalytic performance of alkaline leached zeolite H-ZSM-5 in the conversion of methanol to gasoline has been studied both with respect to catalyst lifetime and product selectivities. After treatment with 0.20 M NaOH, the total conversion capacity, i.e. grams of methanol converted per gram catalyst until complete deactivation, increased by a factor of 3.3, and the selectivity towards the gasoline fraction increased by a factor of 1.7. Physical characterization indicated the presence of Lewis acidity, improved crystallinity and mesopore formation. Desilication of H-ZSM-5 with NaOH solution constitutes an effective and simple post- synthesis technique leading to substantial catalyst improvement. Work in progress indicates that similar improvements, in particular with respect to catalyst lifetime, is seen for samples that consist of smaller crystals and display less defects and therefore also a greater catalyst lifetime prior to the treatment with NaOH. References [1] G.A. Olah, A. Goeppert, G.K.S. Prakash, Beyond Oil and Gas: The Methanol Economy, Wiley VCH, Weinheim, Germany, 2006. [2] J. Cobb, in: G. 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