An Efficient, Low-Cost Surface Activation toward Multifunctional Wood Manufacturing

With sustainable development, wood is functionalized for use in energy-efficient buildings, lightweight vehicles, and water treatment applications. However, complex chemical or physical treatments hinder its practical application. Here, we propose a simple and efficient surface activation that uses UV-assisted hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) treatment for photoassisted oxidation in multifunctional wood manufacturing. The oxidized wood cell walls increase the number of hydroxyl groups on lignin. Combined with the aligned cellulose nanofibers, this creates strong capillary forces that enable automatic impregnation of functional precursors for nanomodification. The ammonium polyphosphate-activated wood shows enhanced fire resistance and mold prevention, with a 39% lower average heat release rate, a 1.71-fold longer ignition time, and complete resistance against typical mold species. Techno-economic analysis reveals that the preparation of surface-activated functional wood reduces 92.5% in energy, 76.8% in reagent cost, and a 169.1% increase in the market profitability than traditional impregnation. Life cycle assessment indicates that the surface activation strategy has 43% lower carbon emissions than vacuum-pressure impregnation. The surface activation is adaptable for both fluorophore nanomodification and graphite impregnation, endowing fluorescence and photothermal conversion to wood. This low-cost, efficient, and customizable surface activation approach represents a significant advance in the low-carbon manufacturing of multifunctional wood materials.

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Publication Details

Journal
ACS Nano
Published
2025-12-18
DOI
https://doi.org/10.1021/acsnano.5c12508
Primary Topic
Advanced Cellulose Research Studies
Type
article
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article

An Efficient, Low-Cost Surface Activation toward Multifunctional Wood Manufacturing

Xiaofei Dong, Longxiang Sun, Wentao Gan, Xiaozhen Liu et al.
ACS Nano
Advanced Cellulose Research Studies
article

An Efficient, Low-Cost Surface Activation toward Multifunctional Wood Manufacturing

Xiaofei Dong, Longxiang Sun, Wentao Gan, Xiaozhen Liu, Jianfu Tang, Minghui Guo, Xueqi Li, Ran Yin, C. P. Sun, Xueqin Fan, Baoxing Liang, Yang Zhang, Kun Zhang
article en

Abstract

With sustainable development, wood is functionalized for use in energy-efficient buildings, lightweight vehicles, and water treatment applications. However, complex chemical or physical treatments hinder its practical application. Here, we propose a simple and efficient surface activation that uses UV-assisted hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) treatment for photoassisted oxidation in multifunctional wood manufacturing. The oxidized wood cell walls increase the number of hydroxyl groups on lignin. Combined with the aligned cellulose nanofibers, this creates strong capillary forces that enable automatic impregnation of functional precursors for nanomodification. The ammonium polyphosphate-activated wood shows enhanced fire resistance and mold prevention, with a 39% lower average heat release rate, a 1.71-fold longer ignition time, and complete resistance against typical mold species. Techno-economic analysis reveals that the preparation of surface-activated functional wood reduces 92.5% in energy, 76.8% in reagent cost, and a 169.1% increase in the market profitability than traditional impregnation. Life cycle assessment indicates that the surface activation strategy has 43% lower carbon emissions than vacuum-pressure impregnation. The surface activation is adaptable for both fluorophore nanomodification and graphite impregnation, endowing fluorescence and photothermal conversion to wood. This low-cost, efficient, and customizable surface activation approach represents a significant advance in the low-carbon manufacturing of multifunctional wood materials.

ACS NanoVol. 20(1)
ArtCenter College of Design (US), Zhejiang Hisun Pharmaceutical (China) (CN), Northeast Forestry University (CN)
Openalex Percentile: Top 72%
Advanced Cellulose Research Studies
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