4.6 Article

M-Gallate (M = Ni, Co) Metal-Organic Framework-Derived Ni/C and Bimetallic Ni-Co/C Catalysts for Lignin Conversion into Monophenols

期刊

ACS SUSTAINABLE CHEMISTRY & ENGINEERING
卷 7, 期 15, 页码 12955-12963

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.9b02005

关键词

Lignin; Hydrogenolysis; Bimetallic catalyst; Monophenols; Ni-Co/C

资金

  1. National Key R&D Program of China [2016YFB0301500]
  2. National Natural Science Foundation of China [21722609, 21436010]
  3. Zhejiang Provincial Natural Science Foundation of China [LR17B060001]
  4. Fundamental Research Funds for the Central Universities [2018XZZX002-14]

向作者/读者索取更多资源

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-beta-guaiacyl ether (GG) revealed that the beta-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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