Highly stable Fe/CeO2 catalyst for the reverse water gas shift reaction in the presence of H2S

被引:3
|
作者
Watanabe, Ryo [1 ]
Karasawa, Fumiya [1 ]
Yokoyama, Chikamasa [1 ]
Oshima, Kazumasa [2 ]
Kishida, Masahiro [2 ]
Hori, Masahiro [3 ]
Ono, Yukinori [3 ]
Satokawa, Shigeo [4 ]
Verma, Priyanka [1 ]
Fukuhara, Choji [1 ]
机构
[1] Shizuoka Univ, Grad Sch Engn, Dept Appl Chem & Biochem Engn, 3-5-1 Johoku,Naka Ku, Hamamatsu, Shizuoka 4328561, Japan
[2] Kyushu Univ, Fac Engn, Dept Chem Engn, 744 Motooka,Nishi Ku, Fukuoka, Fukuoka 8190395, Japan
[3] Shizuoka Univ, Res Inst Elect, 3-5-1 Johoku,Naka Ku, Hamamatsu, Shizuoka 4328561, Japan
[4] Seikei Univ, Fac Sci & Technol, Dept Mat & Life Sci, 3-3-1 Kichijoji Kitamachi, Musashino, Tokyo 1808633, Japan
关键词
CO2; METHANATION; IONIC LIQUIDS; EFFICIENT; BIOGAS;
D O I
10.1039/d3ra01323e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This study focused on evaluating the catalytic properties for the reverse water gas shift reaction (RWGS: CO2 + H-2 -> CO + H2O Delta H-0 = 42.1 kJ mol(-1)) in the presence of hydrogen sulfide (H2S) over a Fe/CeO2 catalyst, commercial Cu-Zn catalyst for the WGS reaction (MDC-7), and Co-Mo catalyst for hydrocarbon desulfurization. The Fe/CeO2 catalyst exhibited a relatively high catalytic activity to RWGS, compared to the commercial MDC-7 and Co-Mo catalysts. In addition, the Fe/CeO2 catalyst showed stable performance in the RWGS environment that contained high concentrations of H2S. The role of cofeeding H2S was investigated over the Fe/CeO2 catalyst by the temperature programmed reaction (TPR) of CO2 and H-2 in the presence of H2S. The result of TPR indicated that the co-feeding H2S might enhance RWGS performance due to H2S acting as the hydrogen source to reduce CO2.
引用
收藏
页码:11525 / 11529
页数:5
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