甲烷化
催化作用
非阻塞I/O
材料科学
化学工程
氧气
纳米颗粒
镍
金属
选择性
无机化学
纳米技术
化学
冶金
有机化学
工程类
作者
Yixiong Du,Chuan Qin,Yanfei Xu,Di Xu,Jingyang Bai,Guangyuan Ma,Mingyue Ding
标识
DOI:10.1016/j.cej.2021.129402
摘要
Developing efficient catalysts with superior low-temperature catalytic performance is highly promising yet challenging for CO2 methanation. Here we synthesized a nanoplate-shaped CeO2, which was rich in oxygen vacancies, as the carrier to disperse the nickel nanoparticles. The resultant catalyst (Ni/CeO2-P) showed remarkable low-temperature CO2 methanation performance with a CO2 conversion of high than 84% and 100% CH4 selectivity at a low temperature of 300 °C. A 100 h-on-stream test at 300 °C demonstrated the excellent stability of Ni/CeO2-P. Even when the WHSV rose as high as 30000 mL g−1 h−1, the Ni/CeO2-P catalyst still possessed a maximum CO2 conversion of approximately 79%. The surface characterization demonstrated that the abundant oxygen vacancies on the CeO2 nanoplates led to more amounts of NiO-CeO2 structures formed, which resulted in a stronger interaction between Ni metal and CeO2 support. This stronger NiO-CeO2 interaction was proved extraordinary in promoting the reaction performance as compared with metallic Ni. Also, by the in-situ DRIFTS technology, the reaction intermediates and possible reaction pathway were raised for CO2 methanation.
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