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A comparative study of PdZSM-5, Pd beta, and PdY in hybrid catalysts for syngas to hydrocarbon conversion

机译:合成酶与碳氢化合物转化的混合催化剂中PDZSM-5,PD Beta和PDY的比较研究

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摘要

The catalytic conversion of syngas into hydrocarbons over hybrid catalysts consisting of a methanol synthesis catalyst and Pd modified zeolites (PdZSM-5, Pd beta, and PdY) was investigated. The results indicate that the intermediate dehydration step of DME in the syngas to hydrocarbon process mainly occurs on the Bronsted acid sites of the Pd zeolite. The large pores and cavities of Pd beta and PdY promote the formation of C4+ hydrocarbons, which are mainly gasoline-type branched hydrocarbons. Moreover, the large pores and cavities provide enough space for the formation of higher aromatics which are the precursor of coke. The blockage of micropores of the Pd zeolites by hydrocarbon-type coke results in the deactivation of the hybrid catalysts.
机译:研究了由甲醇合成催化剂和PD修饰的沸石(PDZSM-5,PD Beta和PDY)组成的混合催化剂上的合核转化为烃的催化转化。 结果表明,在碳氢化合物过程中,同性体中DME的中间脱水步骤主要发生在PD沸石的Bronsted Acid位置。 PDβ和PDY的大孔和空腔促进了C4+烃的形成,C4+碳氢化合物主要是汽油型分支的烃。 此外,大毛孔和空腔为形成较高的芳香剂提供了足够的空间,这是可乐的前体。 碳氢化合物焦炭对PD沸石的微孔阻塞导致混合催化剂失活。

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