A series of activated carbon hollow fibers doped with charcoal powder (WC-ACHFs) were prepared from wood waste with great potential for application in the gas adsorption of CO2 and H2. The hydrogen storage of WC-ACHF-1.0% increased approximately 10.5% more than that of activated carbon hollow fibers (ACHF), and the highest hydrogen uptake reached 4.51 wt% at 77 K and 100 bar. Regarding the CO2 adsorption, the highest adsorption amount reached 7.13 mmol g-1 and the mass content was 31.35 at 273 K, which was 49.8% higher than the sample without doping. In addition, the multiple heteroatoms (N, P) from wood waste liquefaction had a synergistic effect on the gas adsorption properties of WC-ACHFs. These results showed that a facile method was promising for the preparation of wood-derived activated carbon hollow fibers from forestry and agricultural residues in the application of gas adsorption.

This study examined the degradation of oil paint coatings on wood under UV light and heat, focusing on three drying oils: tung oil (TO), linseed oil (LO), and walnut oil (WO). Model coatings were prepared with malachite pigment on rubber wood, then exposed to 240 h of UV light at temperatures of 40 °C, 50 °C, and 60 °C. The results showed that tung oil (TO) was the most prone to degradation. After exposure to 60 °C, the lightness (L value) of TO decreased from 51.44 to 50.98, while LO and WO maintained higher lightness. The color differences (ΔE) for TO, LO, and WO were 3.08, 3.26, and 2.87, respectively. Gloss measurements revealed that TO had the lowest initial gloss (3.87 GU), while WO had the highest gloss value. After UV exposure, all three coatings showed a decrease in gloss to varying degrees. Fourier transform infrared spectroscopy (FTIR) analysis confirmed oxidative degradation in TO, characterized by increased hydroxyl and carbonyl bands, while LO and WO exhibited better chemical stability. Scanning electron microscopy (SEM) images revealed that the surface of TO was the roughest, while the WO surface was the smoothest. After UV exposure, the surface of TO became significantly rougher, while the WO coating showed almost no changes, maintaining better structural integrity. The results suggest that LO and WO are more resilient to UV light and thermal stress, making them more suitable for protecting wooden products.

Wooden magnetic activated carbon fibers (WMACFs) with hierarchical pore structures were obtained by adding magnetic iron oxide (Fe₃O₄) nanoparticles into the liquefied wood. The structures and properties of WMACFs were analyzed by scanning electronmicroscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), N₂ adsorption, and vibrating sample magnetometer (VSM). The results showed that WMACFs had high Brunauer-Emmett-Teller (BET) surface area (1578 m²/g) and total pore volume (0.929 cm³/g), of which 45% was the contribution of small mesopores of 2–3 nm. It is believed that Fe₃O₄ nanoparticles play an important role in the formation of hierarchical pores. With the Fe₃O₄ content increasing, the yield rate of WMACFs decreased, and the Fe₃O₄ crystal plane diffraction peaks and characteristic adsorption peaks were obviously observed. At the same time, it was also found that WMACFs had favorable magnetic properties when the Fe₃O₄ content was above 1.5%. As a result, WMACFs could be a promising candidate for high efficiency, low cost, and convenient separation for the magnetic field.

Teak (Tectona grandis) has been popularly known in the wood industry as a precious material due to its natural dimensional stability. To explore the main components affecting the dimensional stability of teak wood, the teak wood samples were extracted with different polar solvents, and the extractives were impregnated into rubberwood specimens to determine their effect on the dimensional stability of the modified rubberwood. The results showed that the methanol extractives of the teak wood exhibited the most significant effect on the dimensional stability of the rubberwood. The extractives were characterized by infrared (IR) and gas chromatograph/ mass spectrum (GC/MS). The GC/MS results showed that the methanol extractives primarily contained 9,10-anthracenedione, 1,1-dimethyl-3,4-bis(1-methylethenyl), and alcohol compounds. It was speculated that the alcohol compounds in the methanol extractives reacted with polar hydroxyl groups in the cell wall, which resulted in a decrease in the size of the site combined with bound water. Moreover, the hydrophobic hydrocarbon compound was impregnated into rubberwood to form a thin layer of protective film in the cells into which the water could not enter under 20 °C and 80% RH.

Lignocellulosic agro-forestry residues (LARs), such as rice straw, sugarcane bagasse, and wood wastes, are abundant and low-cost feedstocks for polyhydroxyalkanoate (PHA) bioplastics. However, their complex cellulose–hemicellulose–lignin matrix requires integrated valorization strategies. This review presents a dual-framework approach: “pretreatment–co-substrate compatibility” and “pretreatment–microbial platform matching”, to align advanced pretreatment methods (including deacetylation–microwave integration, deep eutectic solvents, and non-sterilized lignin recovery) with engineered or extremophilic microbial hosts. A “metabolic interaction” perspective on co-substrate fermentation, encompassing dynamic carbon flux allocation, synthetic consortia cooperation, and one-pot process coupling, is used to elevate PHA titers and tailor copolymer composition. In addition, we synthesize comprehensive kinetic analyses from the literature that elucidate microbial growth, substrate consumption, and dynamic carbon flux allocation under feast–famine conditions, thereby informing process optimization and scalability. Microbial platforms are reclassified as broad-substrate, process-compatible, or product-customized categories to emphasize adaptive evolution, CRISPR-guided precision design, and consortia engineering. Finally, next-generation techno-economic analyses, embracing multi-product integration, regional adaptation, and carbon-efficiency metrics, are surveyed to chart viable paths for scaling LAR-to-PHA into circular bioeconomy manufacturing.