期刊
ACS SUSTAINABLE CHEMISTRY & ENGINEERING
卷 9, 期 9, 页码 3379-3407出版社
AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.0c06715
关键词
Lignin; Biorefinery; Catalysis; Hydrogenolysis; Transfer hydrogenolysis
资金
- IIT Ropar [9-35/2009/IITRPR/3121]
- Australian Research Council [DP 200100204, DP200100313]
- SERB New Delhi [CRG/2020/00028]
- Australian Research Council [DP200100313] Funding Source: Australian Research Council
Global temperature rise has led to adverse climate impacts, mainly due to anthropogenic greenhouse gas emissions; Lignin, a renewable resource, can replace aromatic hydrocarbons from fossil sources; Hydrogenolysis reaction has gained significant attention as an effective way for cleavage of lignin-derived aromatic ethers.
Global temperature has risen >1 degrees C since the preindustrial era, resulting in well-documented adverse climate impacts including extreme weather (floods, droughts, storms, and heat waves), a rise in sea level accompanying melting polar and glacial ice, and disrupted crop growth. These changes are closely correlated with anthropogenic greenhouse gas emissions, predominantly arising from the combustion of nonrenewable fossil fuels. Lignin derived from lignocellulose is the second most abundant biopolymer on Earth, and a rich source of renewable aromatic hydrocarbons to replace those currently obtained from fossil resources. Lignin depolymerization by cleavage of C-O and C-C linkages in the biopolymer can be achieved by direct pyrolysis or catalytic transformations, involving oxidation, hydrolysis, or hydrogenolysis reactions. Hydrogenolysis, in which H-2 gas (or in-situ generated reactive H species) is supplied to lignin under relatively mild conditions, has attracted significant attention. This Perspective summarizes recent progress in the development of heterogeneous catalysts for the cleavage of C-O linkages in lignin-derived aromatic ethers by hydrogenolysis: it encompasses strategies using H-2, hydrogen transfer, and photocatalysis for aromatic monomers production, and the determination of structure-activity relationships and underlying reaction mechanisms.
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