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Catalytic hydrogenolysis of alkali lignin in supercritical ethanol over copper monometallic catalyst supported on a chromium-based metal–organic framework for the efficient production of aromatic monomers
  • Tran, My Ha ;
  • Phan, Dieu Phuong ;
  • Nguyen, Thuy Ha ;
  • Kim, Han Bom ;
  • Kim, Jinsoo ;
  • Park, Eun Duck ;
  • Lee, Eun Yeol
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Publication Year
2021-12-01
Publisher
Elsevier Ltd
Citation
Bioresource Technology, Vol.342
Keyword
Alkali ligninAromatic monomersCatalytic hydrogenolysisCopper catalystSupercritical ethanol
Mesh Keyword
Alkali ligninAromatic monomersCatalytic hydrogenolysisChromium-basedCopper catalystEffective approachesLignin depolymerizationMetalorganic frameworks (MOFs)Monometallic catalystsSupercritical ethanolAlkaliesCatalysisChromiumCopperEthanolLigninMetal-Organic Frameworks
All Science Classification Codes (ASJC)
BioengineeringEnvironmental EngineeringRenewable Energy, Sustainability and the EnvironmentWaste Management and Disposal
Abstract
The catalytic hydrogenolysis of lignin has been reported as an effective approach for lignin depolymerization owing to its high efficiency for aromatic monomer production. In this study, a series of copper monometallic catalysts over an MIL-101(Cr) support were synthesized and used for the catalytic hydrogenolysis of alkali lignin using supercritical ethanol. First, the optimal copper catalyst for lignin hydrogenolysis was selected. Subsequently, the reaction conditions for catalytic hydrogenolysis were systematically optimized to maximize the total monomer yield. The optimal conditions were determined to be 6 h of reaction time, 20 min of sonication pretreatment, 50% catalyst loading, and 5% lignin loading. Under these conditions, an aromatic monomer yield of 38.5% was obtained; this depolymerized lignin stream, which is mainly composed of G-type monomers, can serve as a promising aromatic feedstock and carbon source for further microbial upgrading and bioconversion to produce various value-added products.
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/32264
DOI
https://doi.org/10.1016/j.biortech.2021.125941
Fulltext

Type
Article
Funding
This research was supported by the C1 Gas Refinery Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science and ICT ( 2015M3D3A1A01064882 & 2015M3D3A1A01064899 ).
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PARK, EUN DUCK박은덕
Department of Chemical Engineering
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