The possibility of using commercial bayberry tannin (BT) from a Chinese source as a cross-linker and functional additive to develop soybean protein isolate (SPI)-based films was explored in this study by using the solvent casting method. In particular, the impacts of BT loading on the tensile strength, microstructure, thermal stability, water resistance and antioxidant capacity were fully investigated. The results reveal that SPI incorporated with BT yielded a phenolic–protein hybrid whose relevant films exhibited an improvement in tensile strength of around two times greater compared with native SPI as a result of the formed interactions and covalent cross-links, which could be proven using FTIR spectroscopy. The introduction of BT also led to the compact microstructure of SPI–BT films and enhanced the thermal stability, while the water vapor permeability was reduced compared with the control SPI film, especially at high loading content of tannin. Additionally, the use of BT significantly promoted the antioxidant capacity of the SPI-based films according to DPPH radical scavenging assay results. On this basis, Chinese bayberry tannin is considered a promising natural cross-linker and multifunctional additive that can be dedicated to developing protein-derived films with antioxidant activity for food packaging applications.

Bamboo was carbonized and further modified via co-doping with graphene oxide (GO) and polyaniline (PANI) to prepare microwave absorption composites (GO/PANI/CB) by in situ polymerization of 1R-(-)-Camphorsulfonic acid (L-CSA). The conductivity of GO/PANI/CB reached 2.17 ± 0.05 S/cm under the optimized process conditions. The oxygen-containing group of GO reacts with PANI to form hydrogen bonds and thus polymerize. The GO and PANI particles covered the carbonized bamboo (CB) surface in a disordered aggregation form. Based on the measuring method of the vector network analyzer (VNA), the microwave-absorption performance of GO/PANI/CB was investigated. With 30% addition of GO/PANI/CB, the minimum reflection loss (RL_min) at 7.12 GHz with a thickness of 3.5 mm of samples reached −49.83 dB. The effective absorption bandwidth (<−10 dB) is as high as 4.72 GHz with a frequency range of 11.68–16.40 GHz and a thickness of 2 mm. Compared with many PANI based electromagnetic wave absorbing materials reported in recent years, GO/PANI/CB provides improved microwave-absorption performance while maintaining high absorption bandwidth. GO/PANI/CB exhibited the advantages of simple preparation, low cost, renewability, light texture, thinness, wide absorption bandwidth, and strong absorption ability, and can be used for new microwave absorption materials.

Cellulose-based aerogel has attracted considerable attention for its excellent adsorption capacity, biodegradability, and renewability. However, it is considered eco-unfriendly due to defibrillation of agriculture waste and requires harmful/expensive chemical agents. In this study, cornstalk rind-based aerogel was obtained via the following steps: green H₂O₂/HAc delignification of cornstalk rind to obtain cellulose fibers, binding with carboxymethyl cellulose (CMC)/polyvinyl alcohol (PVA) and freeze-drying treatment, and hydrophobic modification with stearic acid. The obtained aerogel showed high compressive strength (200 KPa), which is apparently higher (about 32 kPa) than NaClO-delignified cornstalk-based cellulose/PVA aerogel. Characterization of the obtained aerogel through SEM, water contact angle, etc., showed high porosity (95%), low density (0.0198 g/cm⁻³), and hydrophobicity (water contact angle, 159°), resulting in excellent n-hexane adsorption capacity (35 g/g), higher (about 29.5 g/g) than NaClO-delignified cornstalk-based cellulose/PVA aerogel. The adsorbed oil was recovered by the extrusion method, and the aerogel showed excellent recyclability in oil adsorption.

Wood possesses several advantageous qualities including innocuity, low cost, aesthetic appeal, and excellent biocompatibility, and its naturally abundant functional groups and diverse structural forms facilitate functionalization modification. As the most sustainable bio-based material, the combination of wood with triboelectric nanogenerators (TENGs) stands poised to significantly advance the cause of green sustainable production while mitigating the escalating challenges of energy consumption. However, the inherent weak polarizability of natural wood limits its development for TENGs. Herein, we present the pioneering development of a flexible transparent wood-based triboelectric nanogenerator (TW-TENG) combining excellent triboelectrical properties, optical properties, and wood aesthetics through sodium chlorite delignification and epoxy resin impregnation. Thanks to the strong electron-donating groups in the epoxy resin, the TW-TENG obtained an open-circuit voltage of up to ~127 V, marking a remarkable 530% enhancement compared to the original wood. Furthermore, durability and stability were substantiated through 10,000 working cycles. In addition, the introduction of epoxy resin and lignin removal endowed the TW-TENG with excellent optical characteristics, with optical transmittance of up to 88.8%, while preserving the unique texture and aesthetics of the wood completely. Finally, we show the application prospects of TW-TENGs in the fields of self-power supply, motion sensing, and smart home through the demonstration of a TW-TENG in the charging and discharging of capacitors and the output of electrical signals in different scenarios.

In order to improve the interface compatibility of HDPE/bamboo fiber composites, O₂ and N₂ plasma were used to treat the HDPE surface, the effects of plasma treatment power, time, and different flow rates on HDPE surface wettability were analyzed, the optimal process of plasma to improve HDPE surface wettability was determined, and a mathematical model between HDPE surface energy and the plasma treatment process was established. The effect of plasma treatment on the mechanical properties of HDPE/bamboo fiber composites was further studied, and the surface morphology and surface chemical structure of the materials before and after plasma treatment were analyzed. The results show that the surface wettability of HDPE can be significantly improved after O₂ and N₂ plasma treatment, which can further enhance the interface compatibility of HDPE/bamboo fiber composites and improve the impact and tensile strength of the composites (impact strength increased by 19.91% and 19.55% after O₂ and N₂ plasma treatment, respectively; tensile strength increased by 16.47% and 12.48%, respectively). The optimal process parameters for enhancing the interface compatibility of the two plasma composites are 1100 W, 13 s, and 1.75 L/min (O₂ plasma), and 1100 W, 13 s, 2.5 L/min (N₂ plasma); between the two, N₂ plasma has a better effect on the surface wettability of HDPE than O₂ plasma treatment.

Wood adhesives play a critical role in the wood processing industry; however, traditional formaldehyde-based adhesives pose health risks and are reliant on non-renewable resources. This study aims to develop a bio-based wood adhesive with excellent water resistance, focusing on environmentally friendly solutions. The synthesis of an oxidized starch-lignin (OSTL) composite adhesive was accomplished by modifying starch via oxidation and subsequent cross-linking with lignin. Ammonium persulfate (APS) was employed for oxidation of starch, introducing aldehyde groups that upgrade its reactivity with lignin. Subsequently, the oxidized starch (OST) was cross-linked with the phenolic rings of lignin, resulting in a strong network structure. The oxidation of starch and its cross-linking mechanism with lignin were investigated using the Fourier transform infrared (FT-IR), proton nuclear magnetic resonance (1H-NMR), and X-ray photoelectron spectroscopy (XPS) techniques, proving the formation of aldehyde and carboxyl groups with subsequent reaction possibilities. The effects of oxidant dosage, oxidation time, and the ratio of starch to lignin on the adhesive properties were systematically studied. The results demonstrated that the OSTL adhesive, prepared under optimized conditions, exhibited outstanding adhesion strength (1.23 MPa in dry state) and water resistance (0.94 MPa after 24 h cold water immersion, 1.04 MPa after 3 h in hot water, and 0.69 MPa after 3 h in boiling water), significantly outperforming conventional wood adhesives in terms of cold water, hot water, and boiling water resistance. In addition, the thermal behavior of the OSTL adhesive was further validated using differential scanning calorimetry (DSC) as well as thermogravimetric analysis (TGA). This study presents new insights and technical support for the development of green, environmentally friendly, and highly water-resistant lignin-based bio-adhesives.