Hydrodeoxygenation of lignin model compounds to alkanes over Pd-Ni/HZSM-5 catalysts

被引:43
|
作者
Zhao, Yun-Peng [1 ,3 ]
Wu, Fa-Peng [1 ]
Song, Qing-Lu [1 ]
Fan, Xing [1 ]
Jin, Li-Jun [2 ]
Wang, Rui-Yu [3 ]
Cao, Jing-Pei [1 ]
Wei, Xian-Yong [1 ]
机构
[1] China Univ Min & Technol, Key Lab Coal Proc & Efficient Utilizat, Minist Educ, Xuzhou 221116, Jiangsu, Peoples R China
[2] Dalian Univ Technol, Sch Chem Engn, Inst Coal Chem Engn, State Key Lab Fine Chem, Dalian 116024, Peoples R China
[3] China Univ Min & Technol, Low Carbon Energy Inst, Xuzhou 221008, Jiangsu, Peoples R China
关键词
Hydrodeoxygenation; Lignin; Pd-Ni/HZSM-5; C-O bond; Alkanes; C-O BOND; BIMETALLIC CATALYSTS; PHENYL ETHER; IONIC LIQUID; NI; CLEAVAGE; HYDROGENOLYSIS; AROMATICS; NICKEL; HYDROGENATION;
D O I
10.1016/j.joei.2019.08.002
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
In this work, a bimetallic catalyst of Pd and Ni supported on HZSM-5 was designed and evaluated in the hydrodeoxygenation of model compounds representing various C-O bonds in lignin. The effects of temperature, holding time, and initial H-2 pressure on the catalytic performance of the Pd-Ni/HZSM-5 catalyst were investigated. The results indicated that the Pd-Ni/HZSM-5 catalyst exhibited superior catalytic activity towards the conversion of the model compounds to alkanes compared to its monometallic counterparts. Direct cleavage of the C-O bond in DPE was achieved under low H-2 pressure, mainly producing benzene and minor amounts of phenol and cyclohexane, while at high H-2 pressure, the reaction pathway was altered towards hydrogenation of the benzene ring, followed by then cleavage of the C-O bond to afford only cyclohexane. Moreover, the Pd-Ni/HZSM-5 catalyst showed high activities when applying other substrates including anisole, veratrole, guaiacol, benzyloxybenzene, phenethyl phenyl ether, and dibenzyl ether. (C) 2019 Energy Institute. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:899 / 910
页数:12
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