选择性
纳米晶
双功能
催化作用
介孔材料
化学工程
材料科学
化学
二甲苯
组合化学
有机化学
纳米技术
甲苯
工程类
作者
Ting Wang,Chengguang Yang,Peng Gao,Shiju Zhou,Shenggang Li,Hui Wang,Yuhan Sun
标识
DOI:10.1016/j.apcatb.2021.119929
摘要
Direct CO2 hydrogenation to high-value chemicals and fuels have received considerable attention. Nevertheless, efficiently producing aromatics with controllable aromatics distribution remains a great challenge. Herein, we report a series of bifunctional catalysts composed of highly active ZnZrOx oxides and nanocrystal HZSM-5 zeolites with the b-axis length ranging from 0.06 to 1.41 μm, which enable direct CO2 hydrogenation into aromatics with high selectivity of 55∼75 %. The CO2 conversion is up to 17.5 % with CO selectivity as low as 23.8 % mainly due to the affluent Brønsted acid sites and a large number of mesopores in HZSM-5 nanocrystal clusters with chain-like morphology. We demonstrate that a proper extension of the b-axis length of HZSM-5 can increase the selectivity of para-xylene (PX) while shortening the length of b-axis favors the formation of tetramethylbenzene (TeMB). The maximum selectivities of PX and TeMB in aromatics can reach to 28.9 % and 74.1 %, respectively.
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