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Kinetics of the reactions of the light alkenes over SAPO-34

机译:SAPO-34上轻烯烃反应的动力学

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摘要

Many petrochemical processes produce light olefin byproducts that can be used to produce propene. This study reports the kinetics of the reactions of ethene, propene and n-butene isomers over a SAPO-34 catalyst at 450 °C and different space velocities and discusses suitable modes of reaction to maximize propene yield. The shape selectivity of SAPO-34 prevented the formation of i-butene and high alkenes. When a single alkene (ethene, propene, or n-butene) was used as the reactant, the other alkenes were rapidly produced by dimerization and cracking such that the final compositions of the light alkenes were close to the equilibrium composition, with propene as the main species. Hydrogen transfer reactions to form an alkane from an alkene were slower than alkene inter-conversion. A kinetic model for alkene inter-conversion was deduced. Experimental and simulation results indicated that a lower partial pressure of the reactant gave increased propene yield when ethene was the feed.
机译:许多石化工艺会产生可用于生产丙烯的轻质烯烃副产物。这项研究报告了SAPO-34催化剂在450°C和不同空速下乙烯,丙烯和正丁烯异构体反应的动力学,并讨论了使丙烯收率最大化的合适反应模式。 SAPO-34的形状选择性阻止了异丁烯和高烯烃的形成。当使用单一烯烃(乙烯,丙烯或正丁烯)作为反应物时,其他烯烃通过二聚和裂化快速生成,以使轻烯烃的最终组成接近于平衡组成,且丙烯为主要种类。由烯烃形成烷烃的氢转移反应比烯烃相互转化慢。推导了烯烃相互转化的动力学模型。实验和模拟结果表明,当以乙烯为原料时,较低的反应物分压可提高丙烯收率。

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