4.8 Article

Ordered Mesoporous Metal Carbides with Enhanced Anisole Hydrodeoxygenation Selectivity

期刊

ACS CATALYSIS
卷 6, 期 6, 页码 3506-3514

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.6b00303

关键词

metal carbide; mesoporous; hydrodeoxygenation; biomass; vapor-phase reaction

资金

  1. University of Delaware Energy Institute Innovative Energy Research Grants Program (IERGP)
  2. Office of Basic Energy Sciences of the U.S. Department of Energy [DE-SC0008418]
  3. Directorate For Engineering
  4. Div Of Chem, Bioeng, Env, & Transp Sys [1350911] Funding Source: National Science Foundation
  5. U.S. Department of Energy (DOE) [DE-SC0008418] Funding Source: U.S. Department of Energy (DOE)

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Mesoporous metal carbides are of particular interest as catalysts for a variety of reactions because of their high surface areas, porous networks, nanosized walls, and unique electronic structures. Here, two ordered mesoporous metal carbides, Mo2C and W2C, were synthesized using a nanocasting approach coupled with a simultaneous decomposition/carburization process under a continuous methane flow. The as-synthesized mesoporous Mo2C and W2C have three dimensionally ordered porous structures, large surface areas (70-90 m(2) g(-1)), and crystalline walls. In vapor-phase anisole hydrodeoxygenation (HDO) reactions, they exhibited turnover frequencies of approximately 9 and 2 x 10(-4) mol molco(-1) s(-1), respectively, at relatively low reaction temperatures (423-443 K) and ambient hydrogen pressures. Notably, the ordered mesoporous W2C catalyst showed a greater than 96% benzene selectivity in anisole HDO, the highest benzene selectivity reported to date.

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