Efficient fractionation of woody biomass by cooking with active oxygen species and solid alkali

The fractionation of lignocellulosic biomass via pretreatment is a critical step for its valorization. However, the efficiency of pretreatment is often limited by the robust lignin-carbohydrate complex (LCC) structure. This study employed the cooking with activated oxygen and solid-alkali (CAOSA) pretreatment, using H 2 O 2 and O 2 as the dual oxidant sources, to pretreat various types of woody biomass. The CAOSA pretreatment with H 2 O 2 and O 2 achieved over 90% removal of hemicellulose and lignin, and over 90% retention of cellulose. In addition, the enzymatic hydrolysis efficiency of various cellulose pulps was obtained around 90% after the CAOSA pretreatment. Notably, the hemicellulose was degraded into organic acids like formic acid during the CAOSA pretreatment with H 2 O 2 and O 2 , which could be served as an in-situ hydrogen source for the hydrodeoxygenation reaction of the lignin dissolved in the cooking liquor, directly producing lignin monophenols with a yield close to the theoretical yield (based on β-O-4 linkage). Mechanism studies revealed that introducing H 2 O 2 as an oxidation additive to CAOSA pretreatment promoted the generation of reactive oxygen species (ROS), thereby enhancing the cleavage of glycosidic and C-C bonds in hemicellulose, resulting in more hemicellulose degradation into small-molecular-weight acids. It also promoted cleavage of β-O-4 and C-C bonds in lignin. In-situ generated small-molecular-weight acids from hemicellulose suppressed the cleavage of lignin aromatic structures, thereby improving lignin recovery with a high delignification rate. This study provides theoretical guidance and technical support for efficient alkali-oxygen pretreatment and comprehensive utilization of woody biomass. • The incorporation of H 2 O 2 led to an enhancement in the CAOSA pretreatment efficacy • H 2 O 2 promote cleaving of C-C bonds, thereby enhance formic acid formation • The Formic acid from hemicellulose acts as an in-situ H donor for the HDO of lignin • Mechanistic studies revealed H 2 O 2 promoted the ROS activated, enhancing cleavage of lignin linkage

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Journal
Industrial Crops and Products
Published
2026-04-17
DOI
https://doi.org/10.1016/j.indcrop.2026.123287
Primary Topic
Thermochemical Biomass Conversion Processes
Type
article
Field-Weighted Citation Impact
0.00

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article

Efficient fractionation of woody biomass by cooking with active oxygen species and solid alkali

Yintao Song, Xing Tang, Lihui Gan, Tong Sun et al.
Industrial Crops and Products
Thermochemical Biomass Conversion Processes
article

Efficient fractionation of woody biomass by cooking with active oxygen species and solid alkali

Yintao Song, Xing Tang, Lihui Gan, Tong Sun, Zhidong Yang, Mengyuan Huang, Yong Sun, Lu Lin, Zexing Zheng
article en

Abstract

The fractionation of lignocellulosic biomass via pretreatment is a critical step for its valorization. However, the efficiency of pretreatment is often limited by the robust lignin-carbohydrate complex (LCC) structure. This study employed the cooking with activated oxygen and solid-alkali (CAOSA) pretreatment, using H 2 O 2 and O 2 as the dual oxidant sources, to pretreat various types of woody biomass. The CAOSA pretreatment with H 2 O 2 and O 2 achieved over 90% removal of hemicellulose and lignin, and over 90% retention of cellulose. In addition, the enzymatic hydrolysis efficiency of various cellulose pulps was obtained around 90% after the CAOSA pretreatment. Notably, the hemicellulose was degraded into organic acids like formic acid during the CAOSA pretreatment with H 2 O 2 and O 2 , which could be served as an in-situ hydrogen source for the hydrodeoxygenation reaction of the lignin dissolved in the cooking liquor, directly producing lignin monophenols with a yield close to the theoretical yield (based on β-O-4 linkage). Mechanism studies revealed that introducing H 2 O 2 as an oxidation additive to CAOSA pretreatment promoted the generation of reactive oxygen species (ROS), thereby enhancing the cleavage of glycosidic and C-C bonds in hemicellulose, resulting in more hemicellulose degradation into small-molecular-weight acids. It also promoted cleavage of β-O-4 and C-C bonds in lignin. In-situ generated small-molecular-weight acids from hemicellulose suppressed the cleavage of lignin aromatic structures, thereby improving lignin recovery with a high delignification rate. This study provides theoretical guidance and technical support for efficient alkali-oxygen pretreatment and comprehensive utilization of woody biomass. • The incorporation of H 2 O 2 led to an enhancement in the CAOSA pretreatment efficacy • H 2 O 2 promote cleaving of C-C bonds, thereby enhance formic acid formation • The Formic acid from hemicellulose acts as an in-situ H donor for the HDO of lignin • Mechanistic studies revealed H 2 O 2 promoted the ROS activated, enhancing cleavage of lignin linkage

Industrial Crops and ProductsVol. 245
Xiamen University (CN), Putian University (CN)
National Natural Science Foundation of China
Zero hunger
Openalex Percentile: Top 16%
Thermochemical Biomass Conversion Processes
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