W-doped ordered mesoporous Ni–Al2O3 catalyst for methanation of carbon monoxide
Autor: | Qing Liu, Hongyuan Yang, Hongmei Ai |
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Rok vydání: | 2019 |
Předmět: |
Substitute natural gas
Materials science Renewable Energy Sustainability and the Environment Non-blocking I/O Energy Engineering and Power Technology Sintering 02 engineering and technology 010402 general chemistry 021001 nanoscience & nanotechnology Condensed Matter Physics 01 natural sciences 0104 chemical sciences Catalysis chemistry.chemical_compound Fuel Technology chemistry Chemical engineering Methanation 0210 nano-technology Mesoporous material Carbon monoxide Space velocity |
Zdroj: | International Journal of Hydrogen Energy. 44:23975-23982 |
ISSN: | 0360-3199 |
DOI: | 10.1016/j.ijhydene.2019.07.115 |
Popis: | In order to simultaneously inhibit the Ni sintering and coke formation as well as investigate the effects of WO3 promoter on catalytic performance, the ordered mesoporous Ni–WO3/Al2O3 catalysts were synthesized by a facile one-pot evaporation-induced self-assembly method for CO methanation reaction to produce synthetic natural gas. Addition of WO3 species could significantly promote the catalytic activity due to the enhancement of the Ni reducibility and the increase of active centers, and the optimal N10W5/OMA catalyst with NiO of 10 wt% and WO3 of 5 wt% achieved the maximum CH4 yield 80% at 425 °C, 0.1 MPa and a weight hourly space velocity of 60000 mL g−1 h−1. Besides, the reference catalyst N10W5/OMA-Im prepared by the conventional co-impregnation method was also evaluated. Compared with N10W5/OMA, N10W5/OMA-Im showed lower catalytic activity due to the partial block of channels by Ni and WO3 nanoparticles, which reduced active centers and restrict the mass transfer during the reaction. In addition, the N10W5/OMA catalyst showed superior anti-sintering and anti-coking properties in a 425oC-100 h-lifetime test, mainly because of confinement effect of ordered mesoporous structure to anchor the Ni particle in the alumina matrix. |
Databáze: | OpenAIRE |
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