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Electronic structure modulating for supported Rh catalysts toward CO2 methanation
Catalysis Today ( IF 5.3 ) Pub Date : 2020-01-27 , DOI: 10.1016/j.cattod.2020.01.029
Yueyue Jiang , Junyu Lang , Xuechen Wu , Yun Hang Hu

Methanation of carbon dioxide is a promising approach to ameliorate greenhouse effect. Rhodium based catalysts have been intensively investigated due to its ability in cleavage of C-O bond, but the role of support in the catalysts was underestimated. In this regard, we explored the methanation of CO2 over Rh catalysts with three metal oxide supports (TiO2, Al2O3, and ZnO). It was found that Rh/TiO2 exhibited the highest catalytic activity with product yield of 455 mmol g-1 cat h-1 (CH4 and CO) at 370 °C and 2 MPa, which is 2 and 14 times higher than Rh/A12O3 and Rh/ZnO, respectively. Moreover, the CH4 selectivity over Rh/TiO2 was higher than 95%. The superior catalytic performance of Rh/TiO2 can be mainly attributed to its unique electronic structure associated with stronger Rh-TiO2 interaction and the existence of Ti3+ ions on TiO2.



中文翻译:

负载型Rh催化剂对CO 2甲烷化的电子结构调控。

二氧化碳的甲烷化是改善温室效应的一种有前途的方法。铑基催化剂因其裂解CO键的能力而被广泛研究,但低估了载体在催化剂中的作用。在这方面,我们探索了在具有三种金属氧化物载体(TiO 2,Al 2 O 3和ZnO)的Rh催化剂上CO 2的甲烷化反应。结果表明,在370℃和2 MPa条件下,Rh / TiO 2表现出最高的催化活性,产物收率为455 mmol g-1 cat h -1(CH 4和CO),分别是Rh / TiO 2和14倍。分别为Al 2 O 3和Rh / ZnO。而且,CH对于Rh / TiO 2的4选择性高于95%。的Rh / TiO 2的优良的催化性能2可主要归因于与更强的Rh-TIO关联其独特的电子结构2相互作用和Ti的存在3+离子在TiO 2

更新日期:2020-01-27
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