Molybdenum phosphide as a novel and stable catalyst for dry reforming of methane

被引:39
|
作者
Yao, Zhiwei [1 ]
Luan, Fubing [1 ]
Sun, Yue [1 ]
Jiang, Baojiang [2 ]
Song, Jia [3 ]
Wang, Haiyan [1 ]
机构
[1] Liaoning Shihua Univ, Coll Chem Chem Engn & Environm Engn, Fushun 113001, Peoples R China
[2] Heilongjiang Univ, Minist Educ Peoples Republ China, Key Lab Funct Inorgan Mat Chem, Harbin 150080, Peoples R China
[3] Liaoning Shihua Univ, Sch Foreign Languages, Fushun 113001, Peoples R China
基金
中国国家自然科学基金;
关键词
TRANSITION-METAL PHOSPHIDES; CARBIDE CATALYSTS; CARBON-DIOXIDE; TUNGSTEN CARBIDES; SYNGAS PRODUCTION; SYNTHESIS GAS; NI; STABILITY; BULK; HYDRODESULFURIZATION;
D O I
10.1039/c6cy00836d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this work, we proposed a novel catalyst, molybdenum phosphide (MoP), which exhibited high coking and oxidation resistance for dry reforming of CH4 with CO2 (DRM). The catalytic stability of MoP was found to be superior to that of Ni/Mo2C (recently known to be an efficient non-noble metal catalyst for DRM). At higher temperatures (>= 800 degrees C) and weight hourly space velocity (WHSV) values, the MoP catalyst would deactivate due to the oxidation of the catalyst to MoO2 with the loss of P, while operation at a lower temperature (750 degrees C) and WHSV resulted in stabilization of the MoP for the duration of the experiments (100 h). This might be due to a decrease in the oxidant-to-catalyst exposure. It was proposed that there were two possible DRM mechanisms (redox-type and noble metal-type) over the MoP catalyst, which were similar to those over the Ni/Mo2C catalyst. Nevertheless, the contribution of the noble metal-type mechanism to DRM activity on MoP was more than that on Ni/Mo2C, which accounted for the fact that the former showed better stability than the latter. It was suggested that the noble metal-type mechanism should be preferable for DRM over carbide and phosphide catalysts.
引用
收藏
页码:7996 / 8004
页数:9
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