催化作用
二氧化碳重整
合成气
化学工程
材料科学
甲烷
氧气储存
X射线吸收精细结构
碳纤维
无机化学
化学
光谱学
复合数
工程类
复合材料
物理
有机化学
量子力学
生物化学
作者
Yadong Wang,Qing Hu,Ximing Wang,Yanpeng Huang,Yuanhao Wang,Fenghuan Wang
出处
期刊:Catalysts
[Multidisciplinary Digital Publishing Institute]
日期:2022-06-02
卷期号:12 (6): 606-606
被引量:2
标识
DOI:10.3390/catal12060606
摘要
Methane reforming with carbon dioxide (DRM) is one promising way to achieve carbon neutrality and convert methane to syngas for high-value chemical production. Catalyst development with better performance is the key to its potential large-scale industrial application due to its deactivation caused by carbon deposition and metal sintering. Hence, a Ni/CeO2 catalyst (Ni/CeO2-M) with higher CO2 conversion and better stability is prepared, supported on CeO2 precipitated via a novel microimpinging stream reactor. A series of ex-situ or in-situ characterizations, such as CO titration measurements, two-step transient surface reaction (two-step TSR), CO2 and CH4 temperature-programmed surface reaction (CO2-TPSR and CH4-TPSR), X-ray absorption fine structure (XAFS), and in-situ Raman spectroscopy study, were used to investigate its structure and mechanism. In contrast to Ni supported on commercial CeO2 (Ni/CeO2-C), the Ni/CeO2-M catalyst with stronger lattice oxygen mobility and higher oxygen storage capacity enhances its CO2 activation ability and carbon deposition. The Ni particle size of the Ni/CeO2-M catalyst decreased, and a higher oxidation state was obtained due to the strong metal–support interaction. Besides the reaction performance improvement of the Ni/CeO2-M catalyst, the novel microimpinging stream reactor could achieve catalyst continuous production with a high preparation efficiency. This work provides a novel method for the high-performance catalyst preparation for DRM reaction and its mechanism study gives a deep insight into high-performance catalyst development via bottom-up study.
科研通智能强力驱动
Strongly Powered by AbleSci AI