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Efficient and Product-Controlled Depolymerization of Lignin Oriented by Raney Ni Cooperated with Cs x H3-x PW12O40
被引:18
|作者:
Shen, Xiao-Jun
[1
]
Wen, Jia-Long
[1
]
Huang, Pan-Li
[1
]
Zheng, Kai
[1
]
Wang, Shuang-Fei
[2
]
Liu, Qiu-Yun
[3
]
Charlton, Adam
[3
]
Sun, Run-Cang
[1
]
机构:
[1] Beijing Forestry Univ, Beijing Key Lab Lignocellulos Chem, Beijing 100083, Peoples R China
[2] Guangxi Univ, Light Ind & Food Engn Coll, Nanning 530004, Guangxi, Peoples R China
[3] Bangor Univ, BioComposites Ctr, Bangor LL57 2UW, Gwynedd, Wales
关键词:
Lignin isolation;
Depolymerization;
Raney Ni;
Cs-substituted tungstophosphate;
CHEMICALS;
HYDROGENOLYSIS;
CONVERSION;
CATALYSTS;
BIOMASS;
CESIUM;
NICKEL;
ACID;
D O I:
10.1007/s12155-017-9855-2
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:
A representative lignin was firstly prepared and characterized as well as an efficient lignin depolymerization process with highly controllable products was presented using Cs-substituted tungstophosphate (CsTP) cooperated with Raney Ni in the present study. The double enzymatic lignin (DEL) was depolymerized efficiently in the temperature range of 250-280 A degrees C. The synergistic effects of Raney Ni with CsTP and temperature on the degradation of lignin were investigated by FT-IR, NMR, GPC, and GC-MS techniques. Under the optimal condition with tandem catalyst at 270 A degrees C for 3 h, the yield of depolymerized DEL was over 70 wt% and phenolic monomers were over 20%. The weight average molecular weight of the lignin was reduced significantly from 15,770 to 1150 g/mol (for aqueous phase lignin) and about 420 g/mol (organic phase lignin). In addition, only a few syringols and cyclohexanols were obtained, indicating that this tandem catalyst facilitates the depolymerization and demethoxylation but prevents hydrogenation of benzene ring of lignin. More importantly, the formation of char was restrained effectively in this process.
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页码:1155 / 1162
页数:8
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