Effect of Ce additive on CO2 hydrogenation over Rh/SiO2 catalysts

被引:0
|
作者
Kusama, H [1 ]
Okabe, K [1 ]
Arakawa, H [1 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Tsukuba, Ibaraki 3058565, Japan
关键词
rhodium catalyst; cerium additive; carbon dioxide hydrogenation; in-situ FT-IR;
D O I
暂无
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
The effects. of Ce additive on CO2 hydrogenation over Rh/SiO2 catalysts were studied. Ce addition drastically increased CO2 conversion. The main product was CO over unpromoted Rh/SiO2 catalyst, but methane over Ce promoted Rh/SiO2 catalyst. Moreover, Ce additive promoted ethanol production. The mechanism of the promotion effect of Ce was investigated by XRD, TEM, EDX and FT-IR. The mean metal particle size of Rh-Ce/SiO2 estimated by XRD and TEM analysis was smaller than that for Rh/SiO2 and Ce/SiO2. In-situ FT-IR during reaction and CO2 adsorption on unpromoted catalyst showed CO2 molecules were adsorbed as CO species, as, found im CO adsorption. However, a new peak attributed to carboxylate species was observed at around 1570, cm(-1) by CO2 adsorption as well as during reaction over the Ce promoted Rh/SiO2 catalyst. This result indicates that the Ce additive enhanced CO2 adsorption on the catalyst, leading to increased activity. The new adsorption band at around 1700 cm(-1) may be attributed to a CO molecule bonded through both the carbon and oxygen atoms, due to higher metal dispersion. These findings suggest that the Ce additive enhanced CO dissociation and CO insertion over Rh/SiO2 catalysts, resulting in promotion of CH4 and ethanol formation.
引用
收藏
页码:384 / 391
页数:8
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