Oxovanadium complexes catalyzed oxidation of lignin and lignin dimers in acetonitrile/water under O2

被引:3
|
作者
Liu, Chao [1 ]
Lin, Fei [1 ]
Kong, Xiangchen [1 ]
Fan, Yuyang [1 ]
Xu, Weicong [1 ]
Xiao, Rui [1 ]
机构
[1] Southeast Univ, Sch Energy & Environm, Key Lab Energy Thermal Convers & Control, Minist Educ, Nanjing 210096, Peoples R China
基金
中国博士后科学基金; 国家重点研发计划;
关键词
Lignin; Oxidation; Oxovanadium complexes; Homogeneous catalysis; O BOND-CLEAVAGE; C-O; MODEL COMPOUNDS; STRUCTURAL-CHARACTERIZATION; CHEMICAL-STRUCTURE; AEROBIC OXIDATION; WOOD LIGNIN; VALORIZATION; CONVERSION; PYROLYSIS;
D O I
10.1007/s13399-021-02175-5
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
Selective oxidation of lignin is increasingly investigated due to its advantage of retaining the aromatic rings to produce value-added platform chemicals. In this paper, oxovanadium complexes catalyzed oxidation of lignin and lignin dimers in acetonitrile/water system under O-2 was reported. Under optimal conditions of VO(acac)(2) catalyzed oxidation, 95 mol% of lignin dimer 2-phenoxy acetophenone was converted, producing 43 mol% of phenol and 83 mol% of benzoic acid. The catalytic ability of V(acac) 3 was higher than that of VO(acac)(2), but it caused heavier repolymerization and lower product yields. VO(acac)(2) catalyzed oxidation system also cleaved various beta-O-4 lignin dimers, achieving > 95 mol% conversion. Whereas, yields of phenols from these dimers were lower than 5 mol%. These phenolics were shown to polymerize under reaction conditions. Furthermore, this oxidation system depolymerized poplar organosolv lignin. After oxidation, aromatic and C-O aliphatic functionalities in the heavy fractionation largely disappeared, and the weight-average molecular weight decreased from 5720 to 1140 Da.
引用
收藏
页码:607 / 619
页数:13
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