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木质素的催化自转移氢解与内源氢:通向碳中和的未来之路。

Catalytic self-transfer hydrogenolysis of lignin with endogenous hydrogen: road to the carbon-neutral future.

机构信息

State Key Laboratory of Catalysis, Dalian National Laboratory for Clean Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.

Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Colloid and Interface and Thermodynamics, CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.

出版信息

Chem Soc Rev. 2022 Mar 7;51(5):1608-1628. doi: 10.1039/d1cs00908g.

Abstract

Due to the depletion of fossil sources, it is imperative to develop a sustainable and carbon-neutral biorefinery for supporting the fuel and chemical supply in modern society. Lignin, the only renewable aromatic source, is still an underutilized component in lignocellulose. Very recently, it has been found that hydrogenolysis is a promising technology for lignin valorization. However, high-pressure H is necessary during lignin hydrogenolysis, resulting in safety problems. Furthermore, H is mainly produced from steam reforming of fossil sources in industry, which makes the conversion of renewable lignin unsustainable and costly. Plentiful aliphatic hydroxyl and methoxy groups exist in native lignin and offer a renewable alternative to H, and can be hydrogen sources for the depolymerization and upgradation of lignin the intramolecular catalytic transfer hydrogenation. The hydrogen source generated from lignin is a type of green hydrogen, decreasing the carbon footprint. The purpose of this review is to provide a summary and perspective of lignin valorization self-transfer hydrogenolysis, mainly focusing on a comprehensive understanding of the mechanism of catalytic self-transfer hydrogenolysis at the molecular level and developing highly effective catalytic systems. Moreover, some opportunities and challenges within this attractive field are given to discuss future research directions.

摘要

由于化石资源的枯竭,开发一种可持续的、碳中和的生物炼制厂来支持现代社会的燃料和化学品供应势在必行。木质素是唯一可再生的芳香族资源,但它仍然是木质纤维素中未充分利用的成分。最近,人们发现氢解是一种很有前途的木质素增值技术。然而,木质素氢解需要高压 H,这会带来安全问题。此外,H 主要是在工业中通过化石资源的蒸汽重整来生产的,这使得可再生木质素的转化既不可持续又昂贵。天然木质素中存在丰富的脂肪族羟基和甲氧基,为 H 提供了一种可再生的替代品,也可以作为木质素解聚和升级的氢源,即分子内催化转移氢化。木质素产生的氢是一种绿色氢,减少了碳足迹。本文的目的是对木质素增值 自转移氢解进行综述和展望,主要侧重于在分子水平上全面理解催化自转移氢解的机制,并开发高效的催化体系。此外,还讨论了该有吸引力的领域内的一些机遇和挑战,以探讨未来的研究方向。

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