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Application of Ni modified Mo2C/γ-Al2O3 catalyst in reverse water-gas shift reaction
被引:0
|作者:
Wu, Yong
[1
]
Ding, Wei
[1
]
Dai, Yongchuan
[1
]
Wang, Honghao
[1
]
Xu, Ming
[2
]
Song, Guanlong
[1
]
机构:
[1] College of Petrochemical Engineering, Liaoning Petrochemical University, Fushun,113001, China
[2] Bora Bioenergy Co., Ltd., Panjin,124119, China
来源:
关键词:
Alumina - Aluminum oxide - Carbonization - Catalyst activity - Catalyst selectivity - Chemical shift - Molecular sieves - Nickel - Temperature programmed desorption - Water gas shift;
D O I:
10.13550/j.jxhg.20211184
中图分类号:
学科分类号:
摘要:
Mo2C/γ-Al2O3 (MCAS) and Ni modified Ni-Mo2C/γ-Al2O3 (MNCAS) catalysts were prepared via co-impregnation and temperature-programmed carbonization using γ-Al2O3 doped Y molecular sieve as carrier, ammonium heptadolybdate (AMT) and hexamethylenetetramine (HMT) as raw materials, and NiCO3•2Ni(OH)2•4H2O as modifying agent. The synthesized catalysts were characterized by XRD, ICP, N2 adsorption-desorption, TEM and EDS, and their catalytic performances in reverse water-gas shift reaction were further investigated. The analyses revealed that MNCAS catalysts displayed the characteristic diffraction peaks of Ni3Mo3N with a good mesoporous structure, in which aggregation caused by Mo2C was effectively improved by the addition of Ni. Moreover, MCAS catalyst exhibited high catalytic activity for the reverse water-gas shift reaction at 300 ℃ with CO selectivity of 93.87%. Meanwhile, MNCAS-8 catalyst [n(AMT):n(HMT) = 1:8, the theoretical and actual loading amount of Mo were 30% and 28.52% respectively, and those of Ni were 5%, and 4.51%, respectively] showed a conversion tendency of CO2 into CH4, the CH4 selectivity reached up to 84.37% at low temperature range, which could be attributed to Ni3Mo3N generated after Ni addition. © 2022, Editorial Office of FINE CHEMICALS. All right reserved.
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页码:1190 / 1196
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