Lignin Valorization from Lignocellulosic Biomass: Extraction, Depolymerization, and Applications in the Circular Bioeconomy

Lignocellulosic biomass—the non-edible fraction of plants composed of cellulose, hemicellulose, and lignin—is the most abundant renewable carbon resource and a key lever for shifting from fossil to bio-based production. Agro-industrial residues (straws, cobs, shells, bagasse, brewery spent grains, etc.) offer low-cost, widely available feedstocks but are difficult to process because their polymers form a tightly integrated, three-dimensional matrix. Within this matrix, lignin provides rigidity, hydrophobicity, and defense, yet its heterogeneity and recalcitrance impede saccharification and upgrading. Today, most technical lignin from pulping and emerging biorefineries is burned for energy, despite growing opportunities to valorize it directly as a macromolecule (e.g., adhesives, foams, carbon precursors, UV/antioxidant additives) or via depolymerization to low-molecular-weight aromatics for fuels and chemicals. Extraction route and severity strongly condition lignin structure linkages (coumaryl-, coniferyl-, and sinapyl-alcohol ratios), determining reactivity, solubility, and product selectivity. Advances in selective fractionation, reductive/oxidative catalysis, and hybrid chemo-biological routes are improving yields while limiting condensation. Remaining barriers include feedstock variability, solvent and catalyst recovery, hydrogen and energy intensity, and market adoption (e.g., low-emission adhesives). Elevating lignin from fuel to product within integrated biorefineries can unlock significant environmental and economic benefits.

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Publication Details

Journal
Sustainability
Published
2025-11-06
DOI
https://doi.org/10.3390/su17219913
Citations
4
Primary Topic
Lignin and Wood Chemistry
Type
article
Field-Weighted Citation Impact
2.70
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article

Lignin Valorization from Lignocellulosic Biomass: Extraction, Depolymerization, and Applications in the Circular Bioeconomy

Tomas Makaveckas, Aušra Šimonėlienė, Vilma Šipailaitė-Ramoškienė
4 citations
Sustainability
Lignin and Wood Chemistry
2.70
article

Lignin Valorization from Lignocellulosic Biomass: Extraction, Depolymerization, and Applications in the Circular Bioeconomy

Tomas Makaveckas, Aušra Šimonėlienė, Vilma Šipailaitė-Ramoškienė
article en
4 citations

Abstract

Lignocellulosic biomass—the non-edible fraction of plants composed of cellulose, hemicellulose, and lignin—is the most abundant renewable carbon resource and a key lever for shifting from fossil to bio-based production. Agro-industrial residues (straws, cobs, shells, bagasse, brewery spent grains, etc.) offer low-cost, widely available feedstocks but are difficult to process because their polymers form a tightly integrated, three-dimensional matrix. Within this matrix, lignin provides rigidity, hydrophobicity, and defense, yet its heterogeneity and recalcitrance impede saccharification and upgrading. Today, most technical lignin from pulping and emerging biorefineries is burned for energy, despite growing opportunities to valorize it directly as a macromolecule (e.g., adhesives, foams, carbon precursors, UV/antioxidant additives) or via depolymerization to low-molecular-weight aromatics for fuels and chemicals. Extraction route and severity strongly condition lignin structure linkages (coumaryl-, coniferyl-, and sinapyl-alcohol ratios), determining reactivity, solubility, and product selectivity. Advances in selective fractionation, reductive/oxidative catalysis, and hybrid chemo-biological routes are improving yields while limiting condensation. Remaining barriers include feedstock variability, solvent and catalyst recovery, hydrogen and energy intensity, and market adoption (e.g., low-emission adhesives). Elevating lignin from fuel to product within integrated biorefineries can unlock significant environmental and economic benefits.

SustainabilityVol. 17(21)
Alytus College (LT), Kauno kolegija Higher Education Institution (LT)
Openalex Percentile: Top 9%
Lignin and Wood Chemistry
2.70
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