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在镍基ETS-10沸石催化剂上促进CO加氢制甲烷反应

Boosting CO hydrogenation to methane over Ni-based ETS-10 zeolite catalyst.

作者信息

Xiang Mei, Gao Zhangxi, Ji Xiaonan, Li Dantong, Deng Yaoyao, Ding Yalong, Yu Chi, Zhang Wei, Zhang Zhenwei, Wu Zeying, Zhou Jiancheng

机构信息

Research Center of Secondary Resources and Environment, School of Chemical Engineering and Materials, Changzhou Institute of Technology, Changzhou, China.

Department of Chemical Engineering, School of Chemistry and Chemical Engineering, Southeast University, Nanjing, China.

出版信息

Front Chem. 2022 Oct 11;10:1041843. doi: 10.3389/fchem.2022.1041843. eCollection 2022.

Abstract

The activation and conversion of the CO molecule have always been the most vexing challenge due to its chemical inertness. Developing highly active catalysts, which could overcome dynamic limitations, has emerged as a provable and effective method to promote CO activation-conversion. Herein, ETS-10 zeolite-based catalysts, with active nickel species introduced by doping and impregnation, have been employed for CO methanation. Conspicuous CO conversion (39.7%) and perfect CH selectivity (100%) were achieved over the Ni-doped ETS-10 zeolite catalyst at 280°C. Comprehensive analysis, which include X-ray diffraction, N adsorption-desorption, SEM, TEM, H chemisorption, CO temperature programmed desorption, and X-ray photoelectron spectroscopy, was performed. Also, the results indicated that the resultant hierarchical structure, high metal dispersion, and excellent CO adsorption-activation capacity of the Ni-doped ETS-10 zeolite catalyst played a dominant role in promoting CO conversion and product selectivity.

摘要

由于一氧化碳(CO)分子的化学惰性,其活化和转化一直是最棘手的挑战。开发能够克服动力学限制的高活性催化剂,已成为促进CO活化转化的一种可行且有效的方法。在此,通过掺杂和浸渍引入活性镍物种的ETS-10沸石基催化剂已被用于CO甲烷化反应。在280°C下,镍掺杂的ETS-10沸石催化剂实现了显著的CO转化率(39.7%)和完美的CH选择性(100%)。进行了包括X射线衍射、N吸附-脱附、扫描电子显微镜、透射电子显微镜、H化学吸附、CO程序升温脱附和X射线光电子能谱在内的综合分析。结果还表明,所得的分级结构、高金属分散性以及镍掺杂的ETS-10沸石催化剂优异的CO吸附活化能力在促进CO转化和产物选择性方面起主导作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbfa/9592893/eff638dbf241/fchem-10-1041843-g001.jpg

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