Lignin is the largest source of renewable aromatic compounds, making the recovery of aromatic compounds from this material a significant scientific goal. Recently, many studies have reported on lignin depolymerization and upgrading strategies. Electrochemical approaches are considered to be low cost, reagent free, and environmentally friendly, and can be carried out under mild reaction conditions. In this Review, different electrochemical lignin conversion strategies, including electrooxidation, electroreduction, hybrid electro‐oxidation and reduction, and combinations of electrochemical and other processes (e. g., biological, solar) for lignin depolymerization and upgrading are discussed in detail. In addition to lignin conversion, electrochemical lignin fractionation from biomass and black liquor is also briefly discussed. Finally, the outlook and challenges for electrochemical lignin conversion are presented.

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It has been known that the yield of lignin monomers during lignin depolymerization is limited by the irreversible condensations of lignin in the fractionation and/or depolymerization process. In this study, we report a new oxidative catalytic fractionation (OCF) process with a simple and effective one-pot but two-step approach to depolymerize lignin to lignin-derived chemicals (LDCs) using polyoxometalate (POM) as the only catalyst. First, the POM effectively catalyzed the methoxylation of the active α-OH groups of lignin in a methanol and water mixture at low temperature (100 °C), and 96% of the stabilized lignin in the lignocellulose sawdust was extracted to the solution simultaneously. Then the lignin solution was heated to an elevated temperature (140 °C) in the same solvent. As a result, 74.0 wt % of the lignin (based on the weight of the Klason lignin in the wood) was converted to LDCs, including 45.9 wt % aromatic monomers.

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The composites made‐up from renewable fillers and polymer matrix have drawn great attention due to the renewable nature, improved thermal and mechanical properties, environmental issues and most importantly to reduce dependency on fossil fuel resources. In this work, kraft lignin in its modified form (butylated lignin) was used to make composites with polystyrene successfully through bulk polymerization and high internal phase emulsion (HIPE) polymerization. The kraft lignin was first modified to butyrated lignin by esterification using 1‐Methylimidazole as a catalyst in order to increase the compatibility as fillers with both monomer and polymer, which was further studied and verified through Hansen solubility parameter model. The thermal, mechanical, and structural properties of the lignin/polymer composites were systematically investigated. The incorporation of lignin in the composites could increase the modulus significantly and almost double (1,391 MPa) at 15 wt% of lignin loading as compared with bare composites. Excellent porous structure and mechanical properties are maintained with the lignin content as high as 10 wt% of the total foam mass. POLYM. ENG. SCI., 59:964–972, 2019. © 2018 Society of Plastics Engineers