Surface composition change of chlorine-doped catalyst Ni(Clx)/CeO2 in methanation reaction

被引:9
|
作者
Gao Zhiming [1 ]
Zhang Shan [1 ]
Ma Hongwei [2 ]
Li Zhanping [3 ]
机构
[1] Beijing Inst Technol, Sch Chem & Chem Engn, Beijing 102488, Peoples R China
[2] Beijing Inst Technol, Anal & Testing Ctr, Beijing 102488, Peoples R China
[3] Tsinghua Univ, Anal Ctr, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
hydrogen purification; selective methanation; compositional analysis; XPS; XRF; rare earths; SELECTIVE CO METHANATION; SUPPORTED NICKEL-CATALYSTS; PREFERENTIAL OXIDATION; RU-NI/TIO2; CATALYSTS; NI/CEO2; CARBON-MONOXIDE; PERFORMANCE; GAS; MECHANISM; NI/TIO2;
D O I
10.1016/S1002-0721(17)61002-0
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The oxide sample NiO/CeO2 with feed atomic ratio of Ni/Ce at 40%, prepared by co-precipitation method and calcination at 500 degrees C for 2 h, was impregnated by aqueous solution of NH4Cl to dope chlorine ions. After the impregnated samples were dried and calcined at 400 degrees C for 2 h, the calcined samples NiO(Cl-x)/CeO2 (x = 0.1-0.5) were characterized by means of X-ray diffraction (XRD) and temperature programmed reduction (TPR) techniques. It was comfirmed that the doped chlorine ions hindered reduction of Ni2+ ions in the calcined samples, and suppressed adsorption of CO2 and CO on the reduced sample Ni(Cl-0.3)/CeO2. The reduced samples Ni(Cl-x)/CeO2 (x = 0.0-0.5) were used as catalysts for selective methanation of CO in H-2-rich gas. When chlorine ions were doped at the feed atomic ratio of Cl/Ce(x) equal to 0.3-0.5, CO in the H-2-rich gas could be removed to below 10 ppm with a high selectivity more than 50% in a wide reaction temperature range of 220-280 degrees C. However, the selectivity of CO methanation decreased with reaction time in the durability tests over the catalyst Ni(Cl-0.3)/CeO2 at the reaction temperature of 260 degrees C and even at 220 degrees C. The lowering of the selectivity was found to be related with the surface composition change of the catalyst in the catalytic reaction.
引用
收藏
页码:977 / 983
页数:7
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