Thio-assisted reductive electrolytic cleavage of lignin β-O-4 models and authentic lignin

被引:33
作者
Fang, Zhen [1 ,2 ]
Flynn, Michael G. [1 ]
Jackson, James E. [3 ]
Hegg, Eric L. [1 ,2 ]
机构
[1] Michigan State Univ, Dept Biochem & Mol Biol, 603 Wilson Rd, E Lansing, MI 48824 USA
[2] Michigan State Univ, Great Lakes Bioenergy Res Ctr, 1129 Farm Lane, E Lansing, MI 48824 USA
[3] Michigan State Univ, Dept Chem, 578 S Shaw Ln, E Lansing, MI 48824 USA
关键词
ELECTROCATALYTIC HYDROGENATION; FAST PYROLYSIS; RANEY-NICKEL; DEPOLYMERIZATION; OXIDATION; HYDROGENOLYSIS; CONVERSION; OIL; FRACTIONATION; CHEMICALS;
D O I
10.1039/d0gc03597a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Avoiding the use of expensive catalysts and harsh conditions such as elevated temperatures and high pressures is a critical goal in lignin depolymerization and valorization. In this study, we present a thio-assisted electrocatalytic reductive approach using inexpensive reticulated vitreous carbon (RVC) as the working cathode to cleave the beta-O-4-type linkages in keto aryl ethers. In the presence of a pre-electrolyzed disulfide (2,2 '-dithiodiethanol) and a radical inhibitor (BHT) at room temperature at a current density of 2.5 mA cm(-2), cathodic reduction of nonphenolic beta-O-4 dimers afforded over 90% of the corresponding monomeric C-O cleavage products in only 1.5 h. Extended to DDQ-oxidized poplar lignin, this combination of electric current and disulfide, applied over 6 h, released 36 wt% of ethyl acetate soluble fragments and 26 wt% of aqueous soluble fragments, leaving only 38 wt% of insoluble residue. These findings represent a significant improvement over the current alone values (24 wt% ethyl acetate soluble; 22 wt% aqueous soluble; 54 wt% insoluble residue) and represent an important next step in our efforts to develop a mild electrochemical method for reductive lignin deconstruction.
引用
收藏
页码:412 / 421
页数:10
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