In this study, the effects of tung oil heat treatment on the physico-mechanical properties of moso bamboo were investigated. Here, heat treatment in tung oil at 100–200 °C was used to modify natural bamboo materials. The changes in the nanostructures of cell walls in bamboo caused by oil heat treatment, like density, chemical compositions, and cellulose crystalline, were evaluated to study their correlation with mechanical properties. Results showed that the mechanical performance of bamboo, such as ultimate stress, modulus of elasticity (MOE), and modulus of rupture (MOR), didn’t reduce after heat treatment below 200 °C, compared with the untreated bamboo, which was mainly due to the tung oil uptake, stable cellulose content, and the increment of cellulose crystalline. No remarkable change in the ultimate strain occurred for bamboo materials thermally treated below 140 °C, but it decreased obviously at the heating temperature over 180 °C, mainly due to the degradation of hemicellulose resulting in a decrease in the viscoelasticity of cell wall.

The direct reductive amination of carbonyl compounds with NH3 and H2 is an alternative route to produce primary amines in practical production. The search for efficient and selective catalysts has attracted great interest. In the present work, the reductive amination of heptaldehyde with NH3 was investigated over a Ru-based catalyst. The product selectivities were found to be related with the supports of Ru. The alumina with spinel structure (γ-Al2O3, θ-Al2O3)-supported Ru catalysts exhibited selectivity favoring primary amines (94% yield) at 100% heptaldehyde conversion under optimal conditions. Purely basic (MgO, CaO) and relative acidic (Nb2O5, SnO2, MCM-41, HZSM-5) supports showed relatively poor selectivity towards primary amines (0%–53% yield). The reductive amination mechanism was also proposed. The Schiff base N-[heptylene]heptyl-1-amine was a key intermediate. Ru/γ-Al2O3 was shown to be an excellent hydrogenolysis catalyst to selectively produce primary amine by amination and hydrogenolysis of N-[heptylene]heptyl-1-amine.

Bamboo materials with improved antibacterial performance based on ZnO and graphene oxide (GO) were fabricated by vacuum impregnation and hydrothermal strategies. The Zn2+ ions and GO nanosheets were firstly infiltrated into the bamboo structure, followed by dehydration and crystallization upon hydrothermal treatment, leading to the formation of ZnO/GO nanocomposites anchored in the bulk bamboo. The bamboo composites were characterized by several techniques including scanning electron microscopy (SEM), Fourier transform infrared spectra (FTIR), and X-ray diffraction (XRD), which confirmed the existence of GO and ZnO in the composites. Antibacterial performances of bamboo samples were evaluated by the bacteriostatic circle method. The introduction of ZnO/GO nanocomposites into bamboo yielded ZnO/GO/bamboo materials which exhibited significant antibacterial activity against Escherichia coli (E. coli, Gram-negative) and Bacillus subtilis (B. subtilis, Gram-positive) bacteria and high thermal stability. The antimicrobial bamboo would be expected to be a promising material for the application in the furniture, decoration, and construction industry.

Hierarchical porous carbon materials made from cork were fabricated using a facile and green method combined with air activation, without any templates and chemical agents. The influence of air activation on the texture and other surface characteristics of the carbon materials were evaluated by various characterization techniques. Results indicate that air oxidation can effectively improve the surface area and the hierarchical porous structure of carbon materials, as well as increase the number of oxygen-containing functional groups on the carbon surface. The specific surface area and the pore volume of the carbon material activated by air at 450 °C (C800-M450) can reach 580 m²/g and 0.379 cm³/g, respectively. These values are considerably higher than those for the non-activated material (C800, 376 m²/g, 0.201 cm³/g). The contents of the functional groups (C–O, C=O and O–H) increased with rising activation temperature. After air activation, the adsorption capacity of the carbon materials for methylene blue (MB) and methyl orange (MO) was increased from 7.7 and 6.4 mg/g for C800 to 312.5 and 97.1 mg/g for C800-M450, respectively. The excellent dye removal of the materials suggests that the porous carbon obtained from biomass can be potentially used for wastewater treatment.

Chinese fir (Cunninghamia lanceolata (Lamb.) Hook.) has been an important afforestation species in northeast China. It has obvious defects of buckling and cracking easily, which are caused by its chemical components. Trametes versicolor (L.) Lloyd, a white-rot fungus, can decompose the cellulose, hemicellulose, and lignin in the wood. White-rot fungus was used to biologically degrade Chinese fir wood. The effects of different degradation time on the Chinese fir wood’s mechanical properties, micromorphology, chemical components, and crystallinity were studied. The results showed that the heartwood of Chinese fir was more durable than the sapwood and the durability class of Chinese fir was III. Trametes versicolor (L.) Lloyd had a greater influence on the mechanical properties (especially with respect to the modulus of elasticity (MOE)) for the sapwood. Trametes versicolor (L.) Lloyd degraded Chinese fir and colonized the lumen of various wood cell types in Chinese fir, penetrated cell walls via pits, caused erosion troughs and bore holes, and removed all cell layers. The ability of white-rot fungus to change the chemical composition mass fraction for Chinese fir was: hemicellulose > lignin > cellulose. The durability of the chemical compositions was: lignin > cellulose > hemicellulose. The crystallinity of the cellulose decreased and the mean size of the ordered (crystalline) domains increased after being treated by white-rot fungus.