Related Experiment Video
Updated: Dec 13, 2025

Extraction of Lignin with High β-O-4 Content by Mild Ethanol Extraction and Its Effect on the Depolymerization Yield
Published on: January 7, 2019
Microwave-assisted selective acetylation of Kraft lignin: Acetic acid as a sustainable reactant for lignin
Davi Rabelo de Oliveira1, Francisco Avelino2, Selma Elaine Mazzetto1
1Department of Organic and Inorganic Chemistry, Federal University of Ceará, 60440-900 Fortaleza, CE, Brazil.
Abstract:
Lignin acetylation, one of the most widespread chemical modifications used for improve the solubility of this biopolymer in organic solvents and increase polymer-lignin compatibility, has been performed for decades using time-consuming methodologies and acetylating agents with serious drawbacks. Moreover, traditional acetylation reactions generally conduce to non-selective acetylation of both aliphatic and phenolic groups. In this work, we demonstrated that partial and selective acetylation of kraft lignin can be carried out through a greener, simple and fast microwave-assisted process using acetic acid as solvent and acetylating agent. Structural characterization via FTIR, 1H-13C HSQC and 31P NMR demonstrated that acetylation reaction occurs selectively only in aliphatic hydroxyls, preserving the phenolic hydroxyls. Optimal reaction conditions were obtained using 1% (v/v) of H2SO4 as catalyst and only 5 min as reaction time. The acetylated Kraft lignin (AKL) obtained, have enhanced solubility in organic solvents (ethyl acetate, chloroform and dichloromethane) compared to unmodified Kraft lignin (KL) and antioxidant capacity almost 8 times higher than a commercial antioxidant BHT. These characteristics make the partially and selectively acetylated Kraft lignin a potential green antioxidant additive to be used in polymers blends.
More Related Videos
Related Concept Videos
Alkylation of β-Ketoester Enolates: Acetoacetic Ester Synthesis
Reactions of Aldehydes and Ketones: Baeyer–Villiger Oxidation
The carbonyl center is activated by...
α-Hydroxy Ketones via Reductive Coupling of Esters: Acyloin Condensation Overview
Alkylation of β-Diester Enolates: Malonic Ester Synthesis

