催化作用
甲醇
合成气
化学
无机化学
锰
动力学
核化学
有机化学
量子力学
物理
作者
Zhenzhou Zhang,Sifan Cheng,Wenqi Liu,Baojian Chen,Gao Xin-hua,Peng Wang,Jian Gao,Yisheng Tan,Shanshan Dang,Weifeng Tu
标识
DOI:10.1016/j.apcatb.2023.122985
摘要
This study unravels the regulation of Mn promoter in catalytic activity and surface identities of Cu/ZnO/Al2O3 catalysts by reaction kinetics, TPR/TPD, N2O titration experiments and in situ spectra techniques. The methanol formation EA of Cu/ZnO/Al2O3 catalyst almost remained unchanged with the addition of Mn, confirming the methanol synthesis pathways were not affected. With an increase in the content of Mn, the sizes of Cu and ZnO decreased whereas the reduction degree of ZnO to Zn0 on the catalyst surface increased, forming more Cu-ZnOx active sites in CAZ-2%Mn. TPSR confirmed that the amount of the surface CO and H species were highest in CAZ-2%Mn. Therefore, more Cu-ZnOx active site and surface species in CAZ-2%Mn accounts for the higher methanol formation activity. A detailed understanding of the regulation of Mn in the Cu-ZnOx sites formation is expected for the precise design of the CuZnAl catalysts for methanol synthesis.
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