Catalytic hydrogenolysis of lignin in ethanol/isopropanol over an activated carbon supported nickel-copper catalyst

被引:59
|
作者
Cheng, Chongbo [1 ]
Li, Pengfei [1 ]
Yu, Wenbing [1 ]
Shen, Dekui [1 ]
Gu, Sai [2 ]
机构
[1] Southeast Univ, Sch Energy & Environm, Minist Educ, Key Lab Energy Thermal Convers & Control, Nanjing 210096, Peoples R China
[2] Univ Warwick, Gibbet Hill Rd, Coventry CV4 7AL, W Midlands, England
基金
中国国家自然科学基金;
关键词
Lignin; Hydrogenolysis; Catalysis; Mixed solvent; MALDI-TOF MS; IN-SITU HYDROGENOLYSIS; MASS-SPECTROMETRY; FAST PYROLYSIS; KRAFT LIGNIN; DEPOLYMERIZATION; BIOMASS; CONVERSION; CHEMICALS; VALORIZATION; STRATEGIES;
D O I
10.1016/j.biortech.2020.124238
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
Lignin is the renewable and abundant source of aromatics on earth, and the depolymerization of lignin provides significant potential for producing valuable monophenols. In this work, catalytic hydrogenolysis of organosolv poplar lignin (OPL) in ethanol/isopropanol solvent over monometallic and bimetallic nonprecious catalysts was investigated. Ni/C and a series of NiCu/C catalyst with different Cu loadings were prepared and applied for depolymerization of OPL. The highest yield of phenolic monomers was 63.4 wt% achieved over the Ni10Cu5/C catalyst at 270 degrees C without external H-2. The introduction of Cu in catalysts further promoted the hydrogen donor process of ethanol/isopropanol solvent and facilitated the cleavage of lignin linkages, resulting in the decreased molecular weight of bio-oil. The possible lignin dimer type structures, such as diphenylethane (beta-1) type, phenylcoumaran (beta-5) type, and pinoresinol (beta-beta) type structures, were proposed and identified by MALDI-TOF MS, giving a better understanding of the NiCu/C catalyzed lignin depolymerization.
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页数:8
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