Catalytic upgrading of biomass-derived vapors on carbon aerogel-supported Ni: Effect of temperature, metal cluster size and catalyst-to-biomass ratio

被引:21
作者
Arteaga-Perez, Luis E. [1 ,2 ]
Jimenez, Romel [3 ]
Grob, Nicolas [3 ]
Gomez, Oscar [3 ,4 ]
Romero, Romina [4 ]
Ronsse, Frederik [5 ]
机构
[1] Univ Bio Bio, Dept Wood Engn, Sch Chem Engn, Concepcion, Chile
[2] Univ Bio Bio, Dept Wood Engn, Nanomat & Catalysts Sustainable Proc NanoCatpSP, Concepcion, Chile
[3] Univ Concepcion, Dept Chem Engn, Concepcion, Chile
[4] Univ Concepcion, Technol Dev Unit, Coronel, Chile
[5] Univ Ghent, Dept Biosyst Engn, Coupure Links 653, B-9000 Ghent, Belgium
关键词
Carbon aerogel; Catalytic fast pyrolysis; Torrefaction; Reaction route; FAST PYROLYSIS; BIO-OIL; EUCALYPTUS-GLOBULUS; TORREFACTION; DEOXYGENATION; NANOCELLULOSE; HYDROCARBONS; QUALITY; CRUDE;
D O I
10.1016/j.fuproc.2018.05.036
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A comprehensive study of carbon aerogel-supported nickel (Ni/CAG) in the catalytic fast pyrolysis (CFP) of torrefied Eucalyptus globulus was performed in a micropyrolysis unit (Py-GCMS). Effects of pyrolysis temperatures (450-600 degrees C), catalyst-to-biomass ratio (1:1 < C-to-B < 10:1) and metal cluster sizes (9.6 < D-pi < 21) on upgrading reactions were analyzed. Catalysts were characterized by N-2 adsorption-desorption at 77 K, X-ray diffraction (XRD) and Transmission Electron Microscopy (TEM). Regardless the use of catalysts, the pyrolysis vapors produced from torrefied biomass were depleted in carboxylic acids (selectivity < 7%). Furthermore, the CFP decreased the selectivity to furans and ketones by almost 50%, while phenols increased in a similar proportion. Despite the similarities in the selectivity distribution of these functional groups in all the CFP experiments, their internal composition was rather different owing to the changes in temperature, C-to-B ratio and catalyst cluster sizes. Ni/CAG was active for hydrogenation under H-2-depleted atmosphere, presumably by a synergistic effect between water gas shift and reforming reactions with transalkylation and decarbonylation of phenolics and furanics. It was demonstrated that metal cluster sizes influenced the reaction routes by favoring hydrogenation on metal facets and deoxygenation on step/comers sites.
引用
收藏
页码:251 / 261
页数:11
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