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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.
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页码:899 / 910
页数:12
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