Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/46284
Title: Identification and characterisation of the reaction path of β-O-4 dimerisation of monolignols by means of first-principles calculations
Authors: CASTENETTO, Pauline 
GUILLAUME, Emerick Y. 
BUI, Minh-Thu 
VANPOUCKE, Danny E.P. 
Issue Date: 2025
Source: Belgian Physical Society 2025, UC Louvain, Belgium, 2025, May 28
Abstract: Lignin is a naturally occurring substance found in plant cells, which confer their rigidity and therefore, their structural support. It is primarily composed of three monolignol units: p-coumaryl alcohol (H), coniferol alcohol (G) and sinapyl alcohol (S). In the paper industry, lignin is a by-product often regarded as low-value and incinerated for energy production. However, with increasing interest in sustainable materials, this by-product has emerged as a promising candidate for the development of bio-based plastics due to its potential to form durable and robust products [1]. Although early industrial processes have been established, the molecular details of lignin polymerisation remain unclear. This study uses first principles methods to investigate the dimerisation of monolignols. Focusing on the formation of the β-O-4 linkage, the most prevalent in native lignin, the energy profile of the reaction is investigated in detail to gain fundamental understanding of the physics behind the dimerformation. Contrary to earlier studies [2, 3, 4], we find that monolignol dimerization is not a straightforward process but possess a small barrier. Additionally, the role of solvents, both including and excluding van der Waals interactions, is examined. These results shed new light on the dimerisation of monolignols, thus unravelling part of the (de)polymerisation process of lignin.
Document URI: http://hdl.handle.net/1942/46284
Category: C2
Type: Conference Material
Appears in Collections:Research publications

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