Understanding the interfacial changes of wood during heat treatment can facilitate the improvement of the bonding and coating processes of heat-treated wood. Steam was used as the medium to modify Pinusmassoniana wood through heat treatment at 160, 180, 200, and 220 °C. Changes to the surface characteristics after heat treatment were characterized by Fourier transform-infrared spectroscopy (FT-IR), X-ray diffraction (XRD), scanning electron microscope (SEM) and contact angle measurement. The results showed that: (1) hemicelluloses were the first to experience degradation at 160 °C, and this degradation was the most intense at 200 °C. The cellulose started experiencing obvious degradation at 200 °C, while there was less degradation of lignin at this temperature. (2) Oxygen-containing groups like hydroxyl and carbonyl were gradually reduced as temperature increased with deepened color and passivated surface. (3) Cellulose crystallinity presented a variable trend of increasing–decreasing–increasing. (4) Surface porosity and roughness of Pinus massoniana wood both increased after heat treatment. (5) The Pinus massoniana wood interface turned from hydrophilic to hydrophobic, and 180 °C was a turning point for the wettability of the Pinus massoniana wood interface.

Bamboo fibers are considered as a more attractive option for the reinforcement of wood plastic composites as compared to wood fiber due to its fast growth rate and good toughness. Heat treatment is an environment-friendly method of improving the integrated performance of bamboo materials. This paper highlights the heat treatment of bamboo fiber for suitable properties as reinforcements in bamboo plastic composites. The effects of vacuum heat treatment on the surface characteristics of bamboo fibers and the properties of bamboo plastic composites were analyzed by studying the chemical composition, surface elements and polarity of bamboo fiber before and after treatment, and the physical and mechanical properties of bamboo plastic composite. The results showed that after vacuum heat treatment, the bamboo fibers became darker and experienced a transition from green to red. Moreover, FTIR, XPS and contact angle analysis indicated that the hemicellulose content, the oxygen/carbon ratio and the polar component of the bamboo fiber had a decreasing trend as the treatment temperature increased. In addition, the 24 h water absorption and the 24 h thickness expansion rate of the water absorption showed a trend of first decreasing and then increasing as the treatment temperature increased, while the bending performance of bamboo plastic composite showed a trend of increasing first and then decreasing as a result of increased treatment temperature. Therefore, a combined process of vacuum heat treatment and the addition of MAPE could improve the physical and mechanical properties of bamboo plastic composites to a certain extent.

Soybean protein hydrolysate, melamine, urea, and concentrated formaldehyde were used to synthesize an environmentally friendly soybean protein-melamine-urea-formaldehyde (SMUF) co-condensation resin. (NH₄)₂SO₄, (NH₄)₂HPO₄, (NH₄)₂HPO₄ + (NH₄)₂SO₄, (NH₄)₂HPO₄ + (NH₄)₂S₂O₈, and (NH₄)₂HPO₄ + (NH₄)₂SO₄ + (NH₄)₂S₂O₈ were employed as curing agents for SMUF resin. The curing and thermal behaviors of the SMUF resin were investigated using differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and scanning electron microscopy (SEM). The results revealed the following: (1) (NH₄)₂SO₄ alone could not cure the SMUF resin completely; thus, the final shear strength accomplished plywood with the resin was low, and its water resistance was poor, while the adhesive section was loose and porous/brittle after curing. (2) (NH4)2HPO4 could be hydrolyzed to generate H⁺ and promote SMUF curing, but it could also form polyphosphoric acids, resulting in crosslinking reactions with SMUF in parallel; thereby, the curing properties were improved. (3) When (NH₄)₂HPO₄ + (NH₄)₂SO₄ + (NH₄)₂S₂O₈ were engaged collectively as curing agent, the shear strength, water resistance, and heat resistance of SMUF attained were the best possible whereas the curing temperature was decreased and the heat released by curing was elevated substantially, which signifies maximized extent of crosslinking was achieved. Further, the adhesive section exhibited mostly a crosslinking intertexture as demonstrated by means of SEM. Accordingly, this study may serve as a guide for the curing of amino resins, with low-molar ratio of formaldehyde to amine in adhesives, which are applied to plywood production.

The wettability, bonding strength and flexibility of modified melamine–urea–formaldehyde resin adhesive with hydroxymethyl lignin (LMUF) were investigated. Moreover, the curing performance, thermal properties and chemical structure of LMUF were analyzed by differential scanning calorimetry (DSC), thermogravimetry (TG), scanning electronmicroscopy (SEM), X–ray diffraction (XRD), Fourier–transform infrared spectroscopy (FTIR) and ¹³C nuclear magnetic resonance (¹³C–NMR). The synthesis mechanism of LMUF was also discussed. The results demonstrated that: (1) LMUF resin is characterized by low free formaldehyde and a short pot life. (2) With the increase in hydroxymethyl lignin, the bonding strength and flexibility of the LMUF increased first and then decreased. They reached their maximum when the hydroxymethyl lignin content was 6%–8%, which represented increases of 36% and 102%, respectively. (3) The DSC and TG analyses showed that the LMUF resin had a high hot-pressing temperature, but its thermostability was increased. (4) The XRD and SEM analyses proved that the LMUF resin was characterized by flexibility failure, especially at 6% of hydroxymethyl lignin. (5) Hydroxymethyl lignin is a type of flexible long-chain molecule, which was introduced into spaces between the rigid triazine rings through adhesion and penetration, thus improving the regular single structural form of MUF resin and increasing the compactness of the system. As a result, the resin had stronger deformability and cohesion in the molecules. The bonding strength and flexibility were improved to different degrees.

Pinus massoniana wood was modified by steam heat-treatment at 160°C, 180°C, 200°C and 220°C respectively and effects of the changes of density, pH, surface wettability and apparent morphology of Pinus massoniana heat-treated wood on its bonding performance were studied in this paper. The results showed that Pinus massoniana wood underwent a series of physical and chemical changes during heat-treatment as the the following: (1) The degradation of hemicellulose and cellulose with low degree of polymerization, degradation and migration of the extract resulting in the decline of density and pH of heat-treated Pinus massoniana wood. (2) Brittle fracture occured on the cell wall surface, and the pit collapse, shrink and deformation, resulting in the formation of roughness and porosity on the wood surface. (3) The surface energy decreased with the improvement of temperature, the surface wettability of Pinus massoniana wood treated at 160°C–180°C was good, while that at 200°C–220°C showed hydrophobicity. (4) Changes of density, pH, surface roughness and porosity, and wettability resulted in a reduction in the bonding strength and reliability of heat-treated Pinus massoniana wood with MUF resin adhesive. (5) When the temperature was at 160°C–180°C, the better wettability of heat-treated Pinus massoniana wood could guarantee the better bonding performance.

(1) A compound protectant was prepared using manganese chloride, phosphoric acid, boric acid and ammonium chloride, and then a veneer was immersed in the prepared protectant to prepare plywood in this paper. Great attention was paid to discussing influences of such protectant on fire resistance, decay resistance, anti-mold property and bonding performance of plywood. Results demonstrated that after protectant treatment, the plywood showed not only good fire resistance and smoke inhibition, but also strong char-formation ability, slow flame spreading, long time to ignition, small fire risk and high safety level. (2) The mass loss rates of plywood with protectant treatment after infection and erosion in wood-destroying Coriolus versicolor and Gloeophyllum trabeum were 19.73% and 17.27%, reaching the II-level corrosion grade. (3) There is not a significant difference with Aspergillus niger V.; however, it was possible to observe a strong difference with Trichoderma viride Pers. ex Fr., indicating that the protectant acted as a good anti-mold product for plywood. (4) The protectant influenced the bonding interface of wood and bonding conditions of the adhesive. The bonding strength of plywood was weakened, but it still met the requirements on bonding strength of GB/T 9846-2015. (5) The protectant changed the thermal decomposition and thermal degradation of plywood, inhibiting the generation of inflammable goods, blocking transmission of heats and lowering the thermal decomposition temperature of plywood. These promoted dehydrations and charring of wood and the generated carbon had a high thermal stability. (6) Compared with untreated plywood, the prepared protectant treatment significantly enhanced the fire resistance of plywood, reduced its biodegradability by wood-decaying fungi and showed good mold resistance.