期刊
BIOMASS & BIOENERGY
卷 124, 期 -, 页码 125-141出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.biombioe.2019.03.017
关键词
Catalytic pyrolysis; Biomass; Metal oxides; Bio-oil; Coke
资金
- Program of Taishan Scholars of Shandong Province Government
- Recruitment Program of Global Young Experts (Thousand Youth Talents Plan)
- Natural Science Fund of Shandong Province [ZR2017BB002]
- Strategic International Scientific and Technological Innovation Cooperation Special Funds of National Key R&D Program of China [2016YFE0204000]
Metal oxides are frequently used in the formulations of the catalysts for catalytic pyrolysis of biomass. This study aims to investigate the catalytic behaviors of the transition metal oxides (CoO, Cr2O3, CuO, Fe2O3, Mn2O3, NiO, TiO2 and V2O5) as well as CeO2 for the catalytic pyrolysis of poplar wood. The metal oxides, especially TiO2 and NiO could suppress further cracking of primary products, increasing the tar yield and simultaneously decreasing the gas yield. The V, Mn, Ti or Co-based catalyst promoted the formation of the heavy bio-oil, while the Ce, Cr, Cu or Fe-based catalysts were the opposite. The metal oxides (except Fe2O3) promoted the formation of alcohols, furan, ketones, acetic acid and phenolics in bio-oil. Fe2O3 catalysts suppressed formation of the derivatives from cellulose and hemicellulose except hydroxyl acetone. Hydroxyl acetone formation was promoted by almost all the oxide catalysts while hydroxyl aldehyde formation was the opposite. Remarkable coke formed over the V, Mn, Cu and Co-based catalysts. These oxides contain multiple valences and could be partially reduced to generate oxygen vacancies, which played important roles in the polymerisation reactions. In addition, the coke species formed on the oxide catalysts were mainly polymeric with low thermal stability.
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