Hydroconversion of acetic acid over carbon aerogel supported molybdenum catalyst

被引:12
|
作者
Abraham, Daniel [1 ]
Nagy, Balazs [1 ]
Dobos, Gabor [2 ]
Madarasz, Janos [3 ]
Onyestyak, Gyoergy [4 ]
Trenikhin, Mikhail V. [5 ]
Laszlo, Krisztina [1 ]
机构
[1] Budapest Univ Technol & Econ, Dept Phys Chem & Mat Sci, H-1521 Budapest, Hungary
[2] Budapest Univ Technol & Econ, Dept Atom Phys, H-1521 Budapest, Hungary
[3] Budapest Univ Technol & Econ, Inst Gen & Analyt Chem, H-1521 Budapest, Hungary
[4] Hungarian Acad Sci, Inst Mat & Environm Chem, Res Ctr Nat Sci, Budapest, Hungary
[5] Russian Acad Sci, Siberian Branch, Omsk Sci Ctr, Inst Hydrocarbon Proc, Omsk 634055, Russia
关键词
Porous carbon support; Molybdenum; Biomass conversion; XPS; Catalysis; TRANSITION-METAL CARBIDES; SOL-GEL POLYCONDENSATION; THERMAL-DECOMPOSITION; ORGANIC AEROGELS; OXIDE CATALYSTS; PORE TEXTURE; RESORCINOL; TUNGSTEN; AROMATIZATION; ADSORPTION;
D O I
10.1016/j.micromeso.2014.01.021
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
High surface area carbon aerogels with increasing molybdenum content were obtained by carbonization of resorcinol-formaldehyde polymer aerogels after incipient wetness impregnation (IWI). The Mo(VI) form of the impregnant was converted into different molybdenum species during the heat treatment, resulting in samples with substantially different surface and bulk compositions. The samples were tested in the hydroconversion reaction of acetic acid, a model biomass. The reaction pathways and the product distribution were governed by the accessibility of the carbon surface as well as by the amount and form of Mo. The highest selectivity for ethanol was 16%, when 85% of the acetic acid was converted. Post-catalyst analysis of the aerogels revealed that their morphology and chemistry changed substantially during the redox processes. The products of each of the three potential pathways (hydrogenolysis, ketonization and consecutive reduction) oxidized the surface even in the reductive hydrogen flow. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:46 / 53
页数:8
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