Enhanced low-temperature CO2 methanation over Ni/ZrO2-Al2O3 catalyst: Effect of Al addition on catalytic performance and reaction mechanism

被引:23
|
作者
Fu, Hao [1 ]
Sun, Shaohui [1 ]
Lian, Honglei [1 ,2 ]
机构
[1] Zhengzhou Univ, Engn Res Ctr Adv Funct Mat Mfg, Sch Chem Engn, Minist Educ, Zhengzhou 450001, Peoples R China
[2] Henan Prov Engn Lab Coal Based Ecol Fine Chem, Zhengzhou 450001, Peoples R China
关键词
Low -temperature CO 2 methanation; Reaction pathways; Operando DRIFTS; Composite support; CARBON-DIOXIDE; NI CATALYSTS; ALUMINA; NANOPARTICLES; HYDROGEN; NI/AL2O3; SURFACE; FTIR;
D O I
10.1016/j.jcou.2023.102415
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
It is desirable but challenging to obtain high CO2 conversion in low-temperature CO2 methanation and elucidate the reaction mechanism on nickel-based catalysts. In this work, we incorporated Al into Ni/ZrO2 to form nickel -based catalysts supported by ZrO2-Al2O3 composite support. The addition of the appropriate amount of Al increased the dispersion of metal Ni on the catalyst surface, promoted the activation and dissociation of H2, and thus significantly improved the activity of CO2 methanation at low-temperature (< 300 degrees C). The CO2 metha-nation on nickel-based catalysts supported on ZrO2-Al2O3 composite supports all follow the formate reaction pathway. Since adding Al removes the ability of ZrO2 to activate H2, the active sites of the catalyst change from the surrounding support to the support-Ni interface, which improves the efficiency of the hydrogenation reaction of the active intermediate.
引用
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页数:14
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