催化作用
解聚
氢解
双金属片
木质素
煅烧
愈创木酚
化学
有机化学
材料科学
无机化学
作者
Zhu Jin,Fuqiang Chen,Zhiguo Zhang,Min Li,Qiwei Yang,Yiwen Yang,Zongbi Bao,Qilong Ren
出处
期刊:ACS Sustainable Chemistry & Engineering
[American Chemical Society]
日期:2019-07-01
卷期号:7 (15): 12955-12963
被引量:83
标识
DOI:10.1021/acssuschemeng.9b02005
摘要
Lignin is the only renewable source of aromatic compounds in nature, and high value-added monophenolic compounds can be obtained by depolymerizing lignin. This work reported a facile strategy for preparation of monometallic and bimetallic nonprecious catalysts for hydrogenolysis of lignin. Both Ni/C and bimetallic Ni–Co/C catalysts are synthesized starting from gallate-based MOFs, namely, M-gallate (M = Ni, Co), as a self-sacrificing precursor for calcination treatment. Gallic acid was used as the supporter of metal and a carbon source for carbothermal reduction of metal oxide to form well-dispersed metal nanoparticles during the calcination process. The prepared catalyst was characterized by PXRD, XPS, and STEM. The bimetallic catalyst NixCo1–x/C could form an alloy structure to produce a synergistic catalytic effect and greatly improve catalytic activity of lignin depolymerization. The highest yield of monophenols with Ni0.5Co0.5/C catalysts can reach 55.2%, and the guaiacol selectivity was as high as 70.3%. The depolymerization reaction of the lignin model compound guaiacylglycerol-β-guaiacyl ether (GG) revealed that the β-O-4 bond will be selectively broken, and the benzene ring will not overhydrogenated with Ni/C and the Ni0.5Co0.5/C catalyst.
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