The effects of heat treatment at various temperatures on mechanically separated bamboo fibers and parenchyma cells were examined in terms of color, microstructure, chemical composition, crystallinity, and thermal properties. The heat-treated parenchyma cells and fibers were characterized by scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR), chemical composition analysis, and thermogravimetric analysis (TGA). The results revealed that the colors of bamboo fibers and parenchyma cells were darkened as treatment temperature increased. The microstructure of the treated fibers and parenchyma cells slightly changed, yet the shape of starch granules in parenchyma cells markedly altered at a temperature of above 160 °C. The chemical compositions varied depending on the heat treatment temperature. When treated at 220 °C, the cellulose content was almost unchanged in fibers but increased by 15% in parenchyma cells; the hemicellulose content decreased and the lignin content increased regardless of fibers and parenchyma cells. The cellulose crystal structure was nearly unaffected by heat treatment, but the cellulose crystallinity of fibers changed more pronouncedly than that of parenchyma cells. The thermal stability of parenchyma cells after heat treatment was affected more substantially compared to fibers.

In order to study the performance of the bamboo fiber composites prepared by filament winding, composites reinforced with jute fiber and glass fiber were used as control samples. The structure and mechanical properties of the composites were investigated by scanning electric microscope (SEM), tensile testing, bending testing, and dynamic mechanical analysis. The results demonstrated that the bamboo fiber composites exhibited lower density (0.974 g/cm³) and mechanical properties in comparison of to fiber composite and glass fiber composite, because the inner tissue structure of bamboo fiber was preserved without resin adsorbed into the cell cavity of fibrous parenchyma. The bamboo fibers in composites were pulled out, while the fibers in the surface of composites were torn, resulting in the lowest mechanical performance of bamboo fiber composites. The glass transition temperature of twisting bamboo fiber Naval Ordnance Laboratory (TBF-NOL) composite (165.89 °C) was the highest in general, which indicated that the TBF circumferential composite had the best plasticizing properties and better elasticity, the reason being that the fiber-reinforced epoxy circumferential composite interface joint is a physical connection, which restricts the movement of the molecular chain of the epoxy matrix, making the composite have a higher storage modulus (6000 MPa). In addition, The TBF-NOL had the least frequency dependence, and the circumferential composite prepared by TBF had the least performance variability. Therefore, the surface and internal structures of the bamboo fiber should be further processed and improved by decreasing the twisting bamboo fiber (TBF) diameter and increasing the specific surface area of the TBF and joint surface between fibers and resin, to improve the comprehensive properties of bamboo fiber composites.

The focus of this report was to understand the tensile properties and dynamic mechanical properties of bamboo powder (BP) reinforced polylactic acid (PLA) composite filaments which were treated with nano calcium carbonate (CaCO₃), cellulose nanofibers (CNF), and micro-crystalline cellulose (MCC) using impregnation modification technology. The storage modulus (E’) of nano CaCO₃-BP/PLA, MCC-BP/PLA, and CNF-BP/PLA composite filaments increased compared with BP/PLA composite filaments before the glass transition temperature T_g. When the temperature was above T_g, the reinforcement effect of nano CaCO₃, MCC, and CNF gradually became less apparent. The loss modulus (E’’) and loss factor (tan δ_max) of the nano CaCO₃-BP/PLA, MCC-BP/PLA, and CNF-BP/PLA composite filaments was higher than that of BP/PLA composite filaments produced by the “one-step” method. The tensile strength (TS) results showed a similar trend. Compared with the control samples, the TS of nano CaCO₃-BP/PLA, MCC-BP/PLA, and CNF-BP/PLA composite filaments produced by the “one-step” method (and the “two-step” method) increased by 40.33% (and 10.10%), 32.35% (and −8.61%), and 12.32% (and −12.85%), respectively. The TS of nano CaCO₃-BP/PLA, MCC-BP/PLA, and CNF-BP/PLA composite filaments produced by the “one-step” method was slightly higher than those produced by the “two-step” method. The elongation at break (EAB) of BP/PLA composite filaments was higher than that of BP/PLA samples treated with nano CaCO₃, MCC, or CNF. The PLA and modified BP were readily accessible through a simple mixing process. The rheological investigation of such mixtures showed that nano CaCO₃, CNF, and MCC have different effects on the processability and rheological properties of composites.

In order to improve the flame-retardant properties of bamboo scrimber, chitosan (CS) and polyvinyl alcohol (PVA) were used as the film-forming substances, and hexagonal boron nitride (h-BN) was used as the flame-retardant substance to prepare h-BN flame-retardant coatings, which were coated on the surface of the bamboo scrimber. The effects of the h-BN flame-retardant coatings with different quality concentrations on the flame-retardant properties of the bamboo scrimber, as well as on the morphology of the residual carbon, were investigated using the analytical methods of FTIR, environmental scanning electron microscopy, thermogravimetric analysis, combustion test, and coating adhesion test. The results showed that the h-BN flame-retardant coating could improve the thermal stability of the bamboo scrimber and that the higher the mass concentration, the better the thermal stability of the h-BN. Compared to the control, the time to ignition (TTI) of the 5% h-BN flame-retardant-treated specimens increased by 56%; the peak heat release rate (Pk-HRR), total heat release (THR), and total smoke production (TSP) decreased by 9.92%, 7.54%, and 32.35%, respectively; however, due to the presence of PVA, the peak smoke production rate (Pk-SPR) increased by 17.78%. The 5% h-BN coating had very good adhesion, with an adhesion grade of zero. In conclusion, the h-BN coating could be well-adhered to the surface of the bamboo scrimber, and the 5% h-BN flame-retardant coating had a better flame retardancy compared to other treatments, meaning that it could provide a new strategy for improving the flame-retardant properties of bamboo scrimber for construction use.

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.