Lignin-reinforced phosphorus–boron synergy enabling adhesive-free bamboo biocomposites with coupled mechanical, flame-retardant, and UV-shielding performance

Abstract Replacing petroleum-derived feedstocks with renewable biomass is key to low-carbon material development, yet simultaneously achieving mechanical reinforcement, flame retardancy, water resistance, and ultraviolet (UV) shielding remains a central challenge for biocomposites. Here, formic-acid-pretreated Phyllostachys edulis (moso bamboo) powder served as the matrix, and adhesive-free multifunctional biocomposites were fabricated by co-impregnation with ammonium polyphosphate (APP) and boric acid, blending with lignin, and hot pressing (170 °C, 10–20 MPa, 60 min). Formic acid pretreatment (85 wt% formic acid, 100 °C, 120 min) afforded a 68.2% solid-phase yield, enriching cellulose from 50.72% to 68.85% while removing 61.9% of hemicellulose and 56.6% of lignin, thereby exposing reactive surface hydroxyls for hot-press self-bonding. Lignin (purity 96.43%, T g ≈ 157.4 °C) softened at the pressing temperature, infiltrated interparticle voids, and reinforced interfacial bonding. Structural analyses confirmed that hot pressing preserved the cellulose I framework, with XRD peaks at 2θ ≈ 15.9°, 22.2°, and 34.8°. Additional peaks at 16.6°, 23.7°, and 29.1° verified inorganic-phase incorporation. XPS detected B and P, while lignin reduced the O/C ratio to 0.671. FTIR further confirmed P–O, P–O–C, B–O, and lignin aromatic structures. At 6 wt% lignin and 20 MPa, the composite reached tensile and flexural strengths of 21.02 and 40.06 MPa, 2.6- and 4.3-fold higher than the lignin-free counterpart. Across the formulation series, the limiting oxygen index rose from 20.1% to 37.7%, the residual char at 800 °C reached 44.8%, and the material self-extinguished upon flame removal. The water contact angle exceeded 100°, and aromatic chromophores afforded broadband UV shielding across 200–400 nm, together with enhanced broadband absorption extending into the visible range (400–800 nm). The multifunctionality arises from a phosphorus–boron–lignin ternary synergy, offering a coupled processing–structure–property framework for valorizing formic-acid pretreatment products in construction and packaging.

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Publication Details

Journal
Advanced Composites and Hybrid Materials
Published
2026-08-03
DOI
https://doi.org/10.1007/s42114-026-02004-1
Primary Topic
Natural Fiber Reinforced Composites
Type
article
Field-Weighted Citation Impact
0.00

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article

Lignin-reinforced phosphorus–boron synergy enabling adhesive-free bamboo biocomposites with coupled mechanical, flame-retardant, and UV-shielding performance

Feng Peng, Yuan Liu, Mingfei Li, Cataldo De Blasio et al.
Advanced Composites and Hybrid Materials
Natural Fiber Reinforced Composites
article

Lignin-reinforced phosphorus–boron synergy enabling adhesive-free bamboo biocomposites with coupled mechanical, flame-retardant, and UV-shielding performance

Feng Peng, Yuan Liu, Mingfei Li, Cataldo De Blasio, Xin Jin, Jia-Xuan Long, Deng-Peng Song
article en

Abstract

Abstract Replacing petroleum-derived feedstocks with renewable biomass is key to low-carbon material development, yet simultaneously achieving mechanical reinforcement, flame retardancy, water resistance, and ultraviolet (UV) shielding remains a central challenge for biocomposites. Here, formic-acid-pretreated Phyllostachys edulis (moso bamboo) powder served as the matrix, and adhesive-free multifunctional biocomposites were fabricated by co-impregnation with ammonium polyphosphate (APP) and boric acid, blending with lignin, and hot pressing (170 °C, 10–20 MPa, 60 min). Formic acid pretreatment (85 wt% formic acid, 100 °C, 120 min) afforded a 68.2% solid-phase yield, enriching cellulose from 50.72% to 68.85% while removing 61.9% of hemicellulose and 56.6% of lignin, thereby exposing reactive surface hydroxyls for hot-press self-bonding. Lignin (purity 96.43%, T g ≈ 157.4 °C) softened at the pressing temperature, infiltrated interparticle voids, and reinforced interfacial bonding. Structural analyses confirmed that hot pressing preserved the cellulose I framework, with XRD peaks at 2θ ≈ 15.9°, 22.2°, and 34.8°. Additional peaks at 16.6°, 23.7°, and 29.1° verified inorganic-phase incorporation. XPS detected B and P, while lignin reduced the O/C ratio to 0.671. FTIR further confirmed P–O, P–O–C, B–O, and lignin aromatic structures. At 6 wt% lignin and 20 MPa, the composite reached tensile and flexural strengths of 21.02 and 40.06 MPa, 2.6- and 4.3-fold higher than the lignin-free counterpart. Across the formulation series, the limiting oxygen index rose from 20.1% to 37.7%, the residual char at 800 °C reached 44.8%, and the material self-extinguished upon flame removal. The water contact angle exceeded 100°, and aromatic chromophores afforded broadband UV shielding across 200–400 nm, together with enhanced broadband absorption extending into the visible range (400–800 nm). The multifunctionality arises from a phosphorus–boron–lignin ternary synergy, offering a coupled processing–structure–property framework for valorizing formic-acid pretreatment products in construction and packaging.

Advanced Composites and Hybrid Materials
Åbo Akademi University (FI), Beijing Forestry University (CN), Wuhan Textile University (CN)
Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 19%
Natural Fiber Reinforced Composites
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