TY - JOUR
T1 - Hydrothermal depolymerization of different lignins: Insights into structures and reactivities
AU - Lui, Yuen Wai
AU - Tao, Qingqing
AU - Akien, Geoffrey R.
AU - Yuen, Alexander K.L.
AU - Montoya, Alejandro
AU - Chan, Bun
AU - Lui, Matthew Y.
N1 - We gratefully acknowledge research funding from the General Research Fund (No. 12301421) provided by the Research Grants Council of Hong Kong (MYL), the Japan Society for the Promotion of Science (Project 22H02080), and the generous allocation of computer time by the RIKEN Information Systems Division (Project RB230026), Japan (BC). Additionally, funding from the Australian Research Council (Grant No. CE230100032) is also acknowledged (AKLY).
Publisher copyright:
© 2025 The Authors. Published by Elsevier B.V.
PY - 2025/6
Y1 - 2025/6
N2 - Hydrothermal depolymerization techniques such as hydrothermal liquefaction (HTL) are promising methods for converting biomass into fuel and valuable chemicals. While the HTL of lignin has been extensively studied, its fundamental chemistry remains underexplored, particularly regarding the reactivity differences among various major technical lignins under HTL conditions. A deeper understanding of these variations is essential for optimizing HTL processes. In this report, four major types of technical lignins—dioxane lignin, Kraft lignin, ethanosolv lignin, and soda lignin—derived from the same pine sawdust were thoroughly characterized and subjected to neutral or base-catalyzed HTL at 330 °C for 1 h. The bio-oils derived from these lignins were analyzed for their physical and chemical properties. The data indicate that, while the structural differences between the lignins influenced the HTL outcomes, their impact was significantly smaller compared to the effect of the presence of a catalyst. To better understand the relationship between lignin structure and the resulting monomeric products, model compounds representing key structural motifs in technical lignins (namely β-O-4, styryl ether, and phenyl glycerol) were synthesized and tested under HTL conditions to simulate the lignin depolymerization process. Additionally, computational methods were employed to elucidate its reaction pathways.
AB - Hydrothermal depolymerization techniques such as hydrothermal liquefaction (HTL) are promising methods for converting biomass into fuel and valuable chemicals. While the HTL of lignin has been extensively studied, its fundamental chemistry remains underexplored, particularly regarding the reactivity differences among various major technical lignins under HTL conditions. A deeper understanding of these variations is essential for optimizing HTL processes. In this report, four major types of technical lignins—dioxane lignin, Kraft lignin, ethanosolv lignin, and soda lignin—derived from the same pine sawdust were thoroughly characterized and subjected to neutral or base-catalyzed HTL at 330 °C for 1 h. The bio-oils derived from these lignins were analyzed for their physical and chemical properties. The data indicate that, while the structural differences between the lignins influenced the HTL outcomes, their impact was significantly smaller compared to the effect of the presence of a catalyst. To better understand the relationship between lignin structure and the resulting monomeric products, model compounds representing key structural motifs in technical lignins (namely β-O-4, styryl ether, and phenyl glycerol) were synthesized and tested under HTL conditions to simulate the lignin depolymerization process. Additionally, computational methods were employed to elucidate its reaction pathways.
KW - Depolymerization
KW - Hydrothermal liquefaction
KW - Lignin
UR - http://www.scopus.com/inward/record.url?scp=105005253476&partnerID=8YFLogxK
U2 - 10.1016/j.ijbiomac.2025.144293
DO - 10.1016/j.ijbiomac.2025.144293
M3 - Journal article
SN - 0141-8130
VL - 314
JO - International Journal of Biological Macromolecules
JF - International Journal of Biological Macromolecules
M1 - 144293
ER -