催化作用
沸石
双功能
化学
无机化学
甲醇
锆
金属
选择性
碳氢化合物
离子交换
协同催化
化学工程
有机化学
离子
工程类
作者
Yuhao Wang,Genyuan Wang,Lars I. van der Wal,Kang Cheng,Qinghong Zhang,Krijn P. de Jong,Ye Wang
标识
DOI:10.1002/ange.202107264
摘要
Abstract The catalytic performance of composite catalysts is not only affected by the physicochemical properties of each component, but also the proximity and interaction between them. Herein, we employ four representative oxides (In 2 O 3 , ZnO, Cr 2 O 3 , and ZrO 2 ) to combine with H‐ZSM‐5 for the hydrogenation of CO 2 to hydrocarbons directed by methanol intermediate and clarify the correlation between metal migration and the catalytic performance. The migration of metals to zeolite driven by the harsh reaction conditions can be visualized by electron microscopy, meanwhile, the change of zeolite acidity is also carefully characterized. The protonic sites of H‐ZSM‐5 are neutralized by mobile indium and zinc species via a solid ion‐exchange mechanism, resulting in a drastic decrease of C 2+ hydrocarbon products over In 2 O 3 /H‐ZSM‐5 and ZnO/H‐ZSM‐5. While, the thermomigration ability of chromium and zirconium species is not significant, endowing Cr 2 O 3 /H‐ZSM‐5 and ZrO 2 /H‐ZSM‐5 catalysts with high selectivity of C 2+ hydrocarbons.
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