The effects of soil burial on the biodegradation of biocomposite flower pots (BFP) made from straw fiber (SF) and hydrolyzed soy protein isolate/urea/formaldehyde (HSPI/U/F) copolymer resin were studied in detail. The microstructure, crystallinity, functional groups, mechanical, degradation and thermal property of the prepared SF with HSPI/U/F copolymer resin have been studied, and the degradation mechanism was also elucidated. XRD results showed that the bond breakage between SF and HSPI/U/F copolymer resin induced a decrease in relative degradation-resistant crystal structures. FTIR spectra showed that the methylolated HSPI units could form a cross-linking network with U/F and SF. The BFP degradation after soil burial was mainly attributed to the effects of microorganisms. The degradation products were environmentally friendly, because they were degradable and could fertilize the soil. In addition, the U/F adhesives were slightly degraded by the microorganisms due to the HSPI in the pots. The TG and DSC results showed that the molecular motion of the BFP matrix could be restricted by the degradation action and the content of HSPI, resulting in decreased crystallization enthalpy and showing good thermal property. The tensile strength of different reinforced samples was not significantly reduced in comparison to U/F resin, and still kept good mechanical performance. Thus, the prepared SF reinforced HSPI/U/F copolymer resins could have good potential for use in the field of biodegradable flower pots because of their good thermal property, mechanical property, biodegradability, and relatively low cost.

In this study, a phenol–formaldehyde resin–montmorillonite intercalation composite solution was used as a modifier to treat Chinese fir via impregnation and compression. The basic characteristics and wettability of the PF (phenol–formaldehyde)–montmorillonite impregnation solution were analyzed. The effects of the solid content of PF, the quantity of montmorillonite, and the impregnation time on the impregnation weight gain of Chinese fir were studied through orthogonal experiments. The results showed that when the amount of montmorillonite was 1%, the wettability of the PF–montmorillonite impregnation solution performed the best, the curing time was short, and the curing strength was high. The optimal impregnation process consists of a PF solid content of 25%, an impregnation time of 120 min, and a montmorillonite ratio of 1%. Under these conditions, the modified Chinese fir was prepared via hot pressing. The effects of the addition of montmorillonite and different levels of compressibility on the physical and mechanical properties of modified wood were studied. The physical and mechanical properties were found to be better when the compression ratio was 33%: the density increased from 0.33 g/cm³ to 0.58 g/cm³; the surface hardness increased from 33.6 HD to 70.9 HD; the static bending strength increased from 60.4 MPa to 98.7 MPa; and the elastic modulus increased from 6 390 MPa to 11 498 MPa. After 30 days of release, the compression rebound rate was 3.97%. Meanwhile, the micromorphology and heat resistance of the impregnated compressed Chinese fir showed that the PF–montmorillonite impregnation solution entered into the cell cavity and intercellular space of the Chinese fir and formed a good composite, thus improving the water resistance, heat resistance, and physical and mechanical properties.

Lignin is a renewable aromatic feedstock for wood adhesives, but its structural heterogeneity complicates control over curing and water resistance. This review examines how lignin structure and functionalization govern curing reactions, kinetics, and crosslinked network development in lignin-based wood adhesives, and how these processes relate to bondline formation and wet bonding performance. Across condensation, epoxy, and polyurethane-based systems, molecular weight, aromatic condensation, and reactive-site accessibility influence lignin incorporation into polymer networks. However, chemical conversion, gelation, and effective network formation do not necessarily proceed in parallel; adhesive flow, penetration, and wood moisture further affect bondline development. Although crosslinking can reduce swelling and improve wet strength, faster curing or higher reactivity does not invariably yield better water resistance. The wet performance of wood joints also depends on network chemical stability, residual hydrophilic groups, interfacial bonding, and moisture-induced deformation and damage. Comparisons among studies remain limited by differences in lignin feedstocks, processing conditions, and water-exposure protocols. Future research should link curing kinetics, network architecture, moisture response, and interfacial failure under controlled testing conditions to establish verifiable structure–property relationships and guide formulation and processing.