Hydrogen Production by Hydrogen Sulfide Decomposition Using Cobalt Catalysts Doped in SBA-15 Synthetized by EISA Method

被引:2
|
作者
Aguilar-Garcia, E. [1 ,2 ]
Perez-Cruz, M. A. [2 ]
Sanchez-Cruz, M. [2 ]
Yee-Madeira, H. [1 ]
Cruz-Leal, M. [3 ]
Rubio-Rosas, E. [4 ]
Ravelo-Acuna, D. [5 ]
Hernandez-Huesca, R. [2 ]
机构
[1] Inst Politecn Nacl, Escuela Super Fis & Matemat, Col San Pedro Zacatenco,Gustavo A, Mexico City 07738, Mexico
[2] Benemerita Univ Autonoma Puebla, Fac Ciencias Quim, Puebla 72570, PUE, Mexico
[3] Benemerita Univ Autonoma Puebla, Ctr Invest Fisicoquim Mat, Inst Ciencias, Eco Campus Valsequillo, San Pedro Zacachimalpa 72960, Puebla, Mexico
[4] Benemerita Univ Autonoma Puebla, Direcc Innovac & Transferencia Conocimiento, Puebla 72570, PUE, Mexico
[5] Inst Politecn Nacl, Unidad Profes Interdisciplinaria Energia & Movil, Col San Pedro Zacatenco,Gustavo A Madero, Mexico City 07738, Mexico
关键词
Hydrogen sulfide decomposition; Cobalt catalysts; EISA; SBA-15; MESOPOROUS MATERIALS; THERMAL-DECOMPOSITION; CO/SBA-15; CATALYSTS; H2S DECOMPOSITION; AL; CO; STABILITY;
D O I
10.1007/s10562-023-04515-8
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
Hydrogen production by H2S catalytic thermal decomposition was studied using Co mesostructured catalysts, directly synthesized by the Evaporation-Induced Self-Assembly method with molar ratios Co/Si of 0.01, 0.05, and 0.10. Cobalt was incorporated into the tetracoordinate silica structure, and lesser amounts of cobalt were left outside the structure in the spinel species of Co3O4. The H2S decomposition reaction was conducted at 400-800 degrees C under atmospheric pressure and continuous flow. The catalytic activity of catalysts was increased with the rising of temperature, reaching H2 maximum conversions at 800 degrees C; the conversion at this temperature for 0.01Co-SBA-15 was 28.4%, 0.05Co-SBA-15 was 29.5%, and 38.0% for 0.10Co-SBA-15. All catalysts showed high stability during the reaction without apparent deactivation, and the best activity was for 0.10Co-SBA-15, with a reaction rate of 0.63 mol h-1 g-1 and an energy activation of 51 kJ mol-1. During the reaction, cobalt oxidized phases were transformed into the sulphurated phase CoS by simultaneous reduction and sulphuration processes, which are due to the stream of H2S and the temperature. On the other hand, the sulfur formed was condensed as a yellow solid in the reactor outlet. The results showed that the experimental approach is an efficient alternative for synthesizing Co catalysts under soft conditions, with high activity and stability in H2 and sulfur production using a problematic gas.
引用
收藏
页码:3724 / 3737
页数:14
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