TiO2-supported molybdenum carbide: An active catalyst for the aqueous phase hydrogenation of succinic acid

被引:20
|
作者
Abou Hamdan, Marwa [1 ]
Loridant, Stephan [1 ]
Jahjah, Mohamad [2 ]
Pinel, Catherine [1 ]
Perret, Noemie [1 ]
机构
[1] Univ Claude Bernard Lyon 1, Univ Lyon, CNRS, IRCELYON,UMR5256, 2 Ave Albert Einstein, F-69626 Villeurbanne, France
[2] Univ Libanaise, Fac Sci 1, Lab Chim Coordinat Inorgan & Organometall, LCIO, Beirut, Lebanon
关键词
Succinic acid; Butyric acid; Hydrogenation; Aqueous phase; Mo carbide; TiO2 supported catalyst; TRANSITION-METAL CARBIDES; RAMAN-SPECTROSCOPY; GAMMA-BUTYROLACTONE; HYDRODEOXYGENATION; MO2C; CARBURIZATION; CARBON; RU; PD; 1,4-BUTANEDIOL;
D O I
10.1016/j.apcata.2018.11.009
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
Tio(2)-supported Mo carbides "MoC/TiO2" were prepared by impregnation of Mo salt followed by temperature programmed reduction-carburization using 20% v/v C2H6/H-2. Catalysts were characterized by XRD, XPS, TEM, STEM, 1CP, Raman, BET, and carbon elemental analysis. The catalytic activity was evaluated for aqueous phase hydrogenation of succinic acid at 160-240 degrees C, and 90-150 bar of H-2 in batch reactor. MoC/TiO2 is active for this reaction. The main products after 24 h are gamma-butyrolactone, and more remarkably butyric acid. These intermediates are then converted to tetrahydrofuran, butanol, 1,4-butanediol and butane. The reaction conditions (temperature, pressure) do not impact the products distribution. A larger amount of butyric acid is formed when catalysts were synthesized with a higher gas hourly space velocity. The deactivation observed while recycling the catalyst was mainly attributed to a decrease in the amounts of carbidic molybdenum and carbidic carbon, as demonstrated by XPS analysis.
引用
收藏
页码:71 / 81
页数:11
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