Influence of valence state of cerium ion on dimethyl carbonate synthesis from methanol and carbon dioxide over CeO2

被引:4
|
作者
Zhang, Jingyang [1 ]
Zhao, Shuyang [1 ]
Zhao, Yujun [1 ]
Ma, Xinbin [1 ]
Wang, Shengping [1 ]
机构
[1] Tianjin Univ, Collaborat Innovat Ctr Chem Sci & Engn, Sch Chem Engn & Technol, Key Lab Green Chem Technol, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
CeO2; dimethyl carbonate; heterogeneous catalysis; in situ FTIR; valence state; OXIDATIVE CARBONYLATION; CATALYST; CO2; OXIDE; NANOPARTICLES;
D O I
10.1002/apj.2517
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The relationship between valence state of cerium ion and the catalytic activity for dimethyl carbonate (DMC) synthesis directly from carbon dioxide and methanol was investigated by using four CeO2 catalysts calcined at the different temperatures, which showed different concentrations of Ce4+ analyzed by XPS. In situ Fourier transform infrared spectroscopy (FTIR) was used to probe CO2 and methanol adsorption species on ceria surface. With the calcination temperature increasing from 323 to 973 K, the concentration of Ce4+ increased, leading to larger proportion of active methanol adsorptions (Types I and II methoxy) and CO2 adsorptions (bidentate carbonate). Meanwhile, high-calcination temperature also led to small surface area and more -OH group dehydration, which resulted in the less formation of active Types I and II methoxy and bidentate carbonate. As a result, the ceria calcined at 773 K showed the highest activity and the one calcined at 973 K performed the lowest.
引用
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页数:8
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