Enhancement of Bio-based para-Xylene Selectivity in Catalytic Fast Pyrolysis of Cellulose Using a Surface-modified Mg/P/HZSM-5 Catalyst  被引量:4

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作  者:WANG Yulan FAN Minghui ZHU Lijuan WANG Shengfei HE Yuting LI Quanxin 

机构地区:[1]Department of Chemical Physics,CAS Key Laboratory of Urban Pollutant Conversion,Chinese Academy of Sciences,Anhui Key Laboratory of Biomass Clean Energy,University of Science & Technology of China,Hefei 230026,P.R.China

出  处:《Chemical Research in Chinese Universities》2019年第3期449-456,共8页高等学校化学研究(英文版)

摘  要:With the growing consumption of oil, the production of /?-xylene(PX) from renewable biomass has gained significant attention recently. This work demonstrated that cellulose, a main component in lignocellulosic biomass, was directly converted into PX over the Mg/P surface-modified zeolites. The catalysts modified by the incorporation of P2O5 and MgO into HZSM-5(HZ) promoted the isomerization of zw-/o-xylenes to p-xylene. The PX selectivity was greatly enhanced using the modified zeolites due to the deactivation of external surface and the adjustment of pore entrance. In addition, the addition of methanol to cellulose was beneficial to increase the selectivity of xylenes due to the alkylation reactions and the Diels-Alder reactions between cellulose-derived furans and methanol-derived olefins. The highest PX yield of 10.7%(molar fraction) with a high PX selectivity in xylenes(97.1%) was obtained over the 10%Mg/5%P/HZ catalyst. The reaction pathway for the formation ofp-xylene was addressed according to the study of the key reactions and the characterization of catalysts.

关 键 词:CELLULOSE P-XYLENE DIELS-ALDER reaction ISOMERIZATION ALKYLATION 

分 类 号:O6[理学—化学]

 

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