CO2 reforming of methane over the growth of hierarchical Ni nanosheets/Al2O3-MgO synthesized via the ammonia vapour diffusion impregnation

被引:5
|
作者
Dharmasaroja, Nichthima [1 ,2 ]
Ratana, Tanakorn [1 ,2 ]
Tungkamani, Sabaithip [1 ,2 ]
Sornchamni, Thana [3 ]
Simakov, David S. A. [4 ]
Phongaksorn, Monrudee [1 ,2 ]
机构
[1] King Mongkuts Univ Technol North Bangkok, Dept Ind Chem, Bangkok, Thailand
[2] King Mongkuts Univ Technol North Bangkok, Res & Dev Ctr Chem Engn, Unit Operat & Catalyst Design RCC, Bangkok, Thailand
[3] PTT Res & Technol Inst, Analyt & Petrochem Dept, Wangnoi, Thailand
[4] Univ Waterloo, Dept Chem Engn, Waterloo, ON, Canada
来源
关键词
coking resistance; hierarchical Ni nanosheets; impregnation; methane reforming; Ni/Al2O3-MgO catalyst; LAYERED DOUBLE HYDROXIDES; SYNTHESIS GAS-PRODUCTION; CARBON-DIOXIDE; SYNGAS PRODUCTION; LOW-TEMPERATURE; COMBINED STEAM; CATALYSTS; MG; CH4; CE;
D O I
10.1002/cjce.23992
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
A novel ammonia vapour diffusion-assisted impregnation technique was developed to synthesize the Al2O3-MgO-supported hierarchical Ni nanosheets. The resulting catalysts with different times for ammonia vapour treatments (at 12, 18, and 20 hours) were prepared to investigate the growth of Ni nanosheets on the catalyst surface. All catalysts were tested for CO2 reforming of methane and a comprehensive characterization study was conducted by XRD, N-2 adsorption-desorption, H-2-TPD, H-2-TPR, CO2-TPD, and TGA. The Ni nanosheets were obtained using the ammonia vapour treatment for 20 hours, improving the selectivity toward H-2 generation without a lower CH4 conversion. When compared to the reference catalyst prepared by a conventional impregnation method, the H-2/CO ratio for CO2 reforming of the methane process was enhanced by 0.35. Additionally, the carbon deposition was reduced by half using hierarchical Ni nanosheets for the CO2 reforming of methane at 620 degrees C for 20 hours. The mechanism of this improvement was achieved by the increase in medium basicity associated with a strong metal-support interaction that promotes the CO2 activation-dissociation pathways, preventing carbon formation and inhibiting the reverse water gas shift.
引用
收藏
页码:S585 / S595
页数:11
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