首页> 外文期刊>Journal of Catalysis >Insights into the promotional roles of palladium in structure and performance of cobalt-based zeolite capsule catalyst for direct synthesis of C-5-C-11 iso-paraffins from syngas
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Insights into the promotional roles of palladium in structure and performance of cobalt-based zeolite capsule catalyst for direct synthesis of C-5-C-11 iso-paraffins from syngas

机译:洞悉钯在钴基分子筛催化剂中的结构和性能中的促进作用,该催化剂可从合成气直接合成C-5-C-11异链烷烃

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Pd-promoted zeolite capsule catalyst (Co/Pd/SiO2-HZSM5) was developed by coating H-ZSM-5 zeolite shell over Pd-modified core catalyst (Co/Pd/SiO2), and employed for direct synthesis of C-5-C-11 iso-paraffins from syngas via Fischer-Tropsch synthesis (FTS). The roles of Pd promotion in structure and performance of the capsule catalyst for C-5-C-11 iso-paraffins synthesis were deeply studied. Structure characterizations (XRD, FTIR, TPR, and XPS) indicated that the main cobalt species in Pd-promoted capsule catalyst was cobalt silicate, while Co3O4 was the predominant cobalt species in un-promoted capsule catalyst (Co/SiO2-HZSM5). Evolution of cobalt species in the synthesis of Pd-promoted capsule catalyst revealed that Pd improved the formation of cobalt silicate in strong basic TPAOH solution during the hydrothermal synthesis of H-ZSM-5 zeolite shell. It was found that Pd not only promoted the reduction in cobalt oxides, but also improved the reduction in cobalt silicate, which could not be reduced under traditional reduction condition for cobalt-based FTS catalysts. Catalytic tests indicated that Pd-promoted capsule catalyst exhibited highly enhanced performance for C-5-C-11 iso-paraffins synthesis with molar ratio of iso-paraffins to n-paraffins up to 1.03. Long-chain hydrocarbons were completely eliminated in the capsule catalyst as a consequence of spatial confinement effect of the H-ZSM-5 zeolite shell. The hydrogenation of olefins to paraffins, which was enhanced by Pd promotion, together with the hydrocracking and isomerization of primary hydrocarbons, contributed to the high selectivity of C-5-C-11 iso-paraffins in Pd-promoted capsule catalyst. 2016 Elsevier Inc. All rights reserved.
机译:通过在Pd修饰的芯催化剂(Co / Pd / SiO2)上涂覆H-ZSM-5沸石壳,开发了Pd促进的沸石胶囊催化剂(Co / Pd / SiO2-HZSM5),并用于直接合成C-5-通过费-托合成(FTS)从合成气中提取C-11异链烷烃。深入研究了钯促进在C-5-C-11异链烷烃合成的胶囊催化剂结构和性能中的作用。结构表征(XRD,FTIR,TPR和XPS)表明,Pd促进的胶囊催化剂中主要的钴物种是硅酸钴,而Co3O4是未促进的胶囊催化剂(Co / SiO2-HZSM5)中的主要钴物种。在Pd促进的胶囊催化剂的合成中钴种类的演变表明,在H-ZSM-5沸石壳水热合成过程中,Pd改善了强碱性TPAOH溶液中硅酸钴的形成。发现Pd不仅促进了氧化钴的还原,而且还改善了硅酸钴的还原,这在钴基FTS催化剂的传统还原条件下是无法还原的。催化测试表明,Pd促进的胶囊催化剂对C-5-C-11异链烷烃的合成表现出高度增强的性能,异链烷烃与正链烷烃的摩尔比高达1.03。由于H-ZSM-5沸石壳的空间限制作用,胶囊催化剂中的长链碳氢化合物被完全消除。钯加氢促进了烯烃加氢成链烷烃的氢化,以及伯烃的加氢裂化和异构化,促进了钯促进胶囊催化剂中C-5-C-11异链烷烃的高选择性。 2016 Elsevier Inc.保留所有权利。

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