“…Firstly, modification such as etherification of phenolic groups in lignin using epochlorihydrin 26 , alkyl oxide 27 , or organic carbonates [28][29][30][31][32] always is accompanied by side reactions, causing unknown structural changes and increased molar mass with a significant change in the molecular weight distribution; in some cases, the molar mass and polydispersity will rise to over 20-fold of its original value. 24,[26][27][28][29][33][34][35] Also, these derivatization processes, such as esterification, utilized toxic and water-reactive reagent (e.g., halogenated compounds) with the harmful catalysts (e.g., pyridine) and solvents (e.g., DMF, THF). [36][37][38] Beyond the "greenness" issues that cloud these chemicals, the multiple solvent mixtures lead to a more complex solvent parameter and additional difficulties to realize the separation of reagents mixture (solvents, reaction reagents, and catalysts) and the isolation of lignin from this mixture.…”