Fully bio-based adhesives are beneficial to reduce the dependence of the wood adhesive industry on synthetic resins based on petrochemical resources and enhance the market competitiveness of adhesives. A fully bio-based wood adhesive composed of tannin and sucrose was developed and successfully used in the preparation of plywood. Effects of the preparation technology on the bonding strength and water resistance of plywood were investigated, and the properties of the adhesive were analyzed by Fourier transform infrared spectroscopy (FT-IR), thermogravimetry (TG) and X-ray diffraction (XRD) in this study. The results showed that: (1) Compared with other biomass adhesives, tannin–sucrose adhesive had the characteristics of high-solid content and low viscosity, which had the potential to prepare particleboard and fiberboard. (2) A proper mass ratio of tannin to sucrose was key to obtaining a tannin–sucrose adhesive with better properties. (3) The optimum preparation process of tannin–sucrose adhesive for plywood was as follows: hot-pressing temperature of 210 °C, hot-pressing time of 1.2 min/mm, m(tannin):m(sucrose) of 60:40 and adhesive loading of 160 g/m². Under these conditions, the water-resistant bonding strength of the plywood was 0.89 MPa, which met the strength requirements of the Type II standard of plywood in GB/T 17657-2013. (4) The hot-pressing temperature played a decisive role in the tannin–sucrose adhesive, and the good performance of the plywood was maintained when the temperature was 210 °C or above. Thus, the prepared tannin–sucrose adhesive had high-bonding strength, good water resistance and thermal stability.

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.

Wood adhesive was prepared using Broussonetia papyrifera waste leaf protein as the raw material. The performance of the B. papyrifera leaf protein adhesive compared to soy protein was investigated using X-ray diffraction, Fourier transform infrared spectroscopy, and differential scanning calorimetry. The results indicated that both B. papyrifera leaf protein and soy protein were spherical proteins that could easily form three-dimensional crosslinked network structures and were of potential for protein adhesive preparation. The B. papyrifera leaf and soy protein-based adhesives had similar curing behaviors, but the crosslinking reaction of B. papyrifera leaf protein-based adhesive seems to be more complex than that of the soy protein-based adhesive. The B. papyrifera leaf protein-based adhesive had a lower increasing trend of particle size and crystallinity than the soy-based protein adhesive, and its water resistance and bonding strength were also weaker. The plywood with BP leaf protein adhesive had dry and wet shear strengths of 0.93 MPa and 0.59 MPa, respectively. These results are promising for future industrial production using Broussonetia papyrifera waste leaf protein as a new protein wood adhesive in the wood industry.

Alkali lignin was processed by plasma and then used in modification of phenol formaldehyde resin in this study. Chemical structural changes of lignin which was processed by plasma as well as bonding strength, tensile property, curing performance and thermal property of the prepared phenol formaldehyde resin which was modified by the plasma processed lignin were analyzed. Results demonstrated that: (1) Alkali lignin was degraded after the plasma processing. The original groups were destroyed, and the aromatic rings collected abundant free radicals and oxygen-containing functional groups like hydroxyls, carbonyls, carboxyls and acyls were introduced into increase the reaction activity of lignin significantly. (2) The introduction of alkali lignin decreased the free formaldehyde content and increased bonding strength and toughness of the prepared phenol formaldehyde resin, especially after the introduction of lignin treated with plasma. (3) The introduction of alkali lignin led to high curing temperature for the prepared phenol formaldehyde resin, but that was reduced by the plasma processed alkali lignin. (4) The introduction of alkali lignin could also increase thermal stability of phenol formaldehyde resin, but that was modified by plasma processed alkali lignin was better than the unprocessed lignin. Based on the results, the plasma processed lignin was used to modify phenol formaldehyde resin, which could increase the strength and toughness of phenol formaldehyde resin significantly.

The base-catalyzed melamine-formaldehyde (MF) reactions were studied in both diluted and concentrated solutions. The influences of F/M molar ratio and pH on the polymer structures were investigated based on the quantitative ¹³C-NMR analysis. The results show that both F/M molar ratio and pH influence the competitive formation of ether and methylene bridges. For the cases of F/M = 2.0, and 3.0, methylene bridge formation is minor in contrast to ether bridges either at pH = 9.3–9.8 or at 7.3–7.8. When the molar ratio was lowered to 1.0, methylene bridges became competitive with ether bridges at pH = 9.3–9.8, but the latter is still more favorable. When the lower molar ratio overlaps with the lower pH, significant changes were found. The content of methlylene bridges was over three times that of ether bridges with M/F = 1.0 and at pH = 7.3–7.8. The results in this study were compared with those previously obtained for base-catalyzed urea-formaldehyde reactions. It was found that molar ratio and pH influence the structures of the MF and UF polymers in similar ways. The different synthesis conditions of UF and MF resin were also addressed by comparing the structures of UF polymers with MF polymers.