1. Mild and efficient approach to aromatic backbone cleavage using copper-lignosulfonate/hydrogen peroxide system.
- Author
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Manassa A, Kim BS, Rachtanapun P, Chaiyaso T, Techapun C, and Seesuriyachan P
- Subjects
- Hydroxyl Radical chemistry, Catalysis, Copper chemistry, Hydrogen Peroxide chemistry, Lignin chemistry, Lignin analogs & derivatives, Oxidation-Reduction
- Abstract
This study investigates the dual role of copper ions in catalysis and complexation during the oxidation of lignosulfonates with hydrogen peroxide (H
2 O2 ) under alkaline conditions. The presence of copper ions reduces partial oxidation by 86 % compared to H2 O2 treatment alone, enhancing overall conversion efficiency to 63 % under increased oxidative conditions. Analyses reveal that copper-lignosulfonate complexes facilitate redox cycling and hydroxyl radical generation through interactions with H2 O2 , confirming copper's dual functions. This mechanism mitigates the hindrance of sulfonic groups on hydroperoxide anions, leading to lignosulfonate degradation into dicarboxylic acids. These findings provide novel insights into the copper-lignosulfonate/H2 O2 system, expanding the understanding of oxidative degradation mechanisms beyond traditional Fenton-like reactions. Furthermore, this system offers a simplified and efficient alternative for industrial applications, particularly in integration with the sulfite pretreatment process of woody biomass for producing valuable co-products., Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Phisit Seesuriyachan reports financial support was provided by the Thailand Science Research and Innovation, Thailand Research Fund (TRF), and National Research Council of Thailand. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)- Published
- 2025
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