Sequential oxidation-depolymerization strategies for lignin conversion to low molecular weight aromatic chemicals

• Published in: Advances in inorganic chemistry Vol. 77
• Main Authors: Cui, Yanbin, Goes, Shannon L., Stahl, Shannon S.
• Format: Journal Article
• Language: English
• Published: United States Elsevier 01-01-2021
• Subjects: Aromatics; Depolymerization; Hydrolysis; INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; Lignin Valorization; Oxidation
• ISSN: 0898-8838; 1557-8917
• DOI: 10.1016/bs.adioch.2021.02.003

Lignin is the largest source of bio-derived aromatic chemicals, and oxidative conversion of this polymeric material can generate valuable oxygenated aromatic compounds. Oxidative depolymerization of lignosulfonate feedstocks under alkaline conditions is used commercially for vanillin production. Recent studies have led to other oxidation methods that access different aromatic products from lignin in good yields. A particularly effective strategy that accesses some of the highest yields of aromatic monomers to date features a two-step process in which the oxidation of specific alcohol groups in lignin is followed by an oxidative, reductive, or redoxneutral step that cleaves the polymer into aromatic monomers and oligomers. Studies of model compounds have provided crucial mechanistic insights and contributed to the development of effective lignin depolymerization methods. Furthermore, this review provides a general overview of lignin depolymerization methods, followed by a survey of oxidation-depolymerization methods that access oxygenated aromatic monomers in good yields.