As a most attractive renewable resource, biomass has the advantages of low pollution, wide distribution and abundant resources, promoting its applications in lithium ion batteries (LIBs). Herein, cellulose-derived carbon nanospheres (CCS) were successfully synthesized by hydrothermal carbonization (HTC) from corn straw for use as an anode in LIBs. The uniform distribution and cross-linked structure of carbon nanospheres were obtained by carefully controlling reaction time, which could not only decrease the transport pathway of lithium ions, but also reduce the structural damage caused by the intercalation of lithium ions. Especially, obtained after hydrothermal carbonization for 36 h, those typical characteristics make it deliver excellent cycling stability as well as the notable specific capacity of 577 mA h g⁻¹ after 100 cycles at 0.2C. Hence, this efficient and environment-friendly method for the fabrication of CCS from corn straw could realize the secondary utilization of biomass waste, as well as serve as a new choice for LIBs anode materials.

In this study, cellulose acetate (CA)/polyvinylpyrrolidone (PVP) core–shell nanofibers were successfully fabricated by electrospinning their homogeneous blending solution. Uniform and cylindrical nanofibers were obtained when the PVP content increased from 0 to 2 wt %. Because of the concentration gradient associated with the solvent volatilization, the composite fibers flattened when the PVP increased to 5 wt %. Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) results confirmed the existence of a hydrogen bond between the CA and PVP molecules, which enhanced the thermodynamic properties of the CA/PVP nanofibers, as shown by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA) results. To analyze the interior structure of the CA/PVP fibers, the water-soluble PVP was selectively removed by immersing the fiber membranes in deionized water. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) indicated that the PVP component, which has a low surface tension, was driven to the exterior of the fiber to form a discontinuous phase, whereas the high-content CA component inclined to form the internal continuous phase, thereby generating a core–shell structure. After the water-treatment, the CA/PVP composite fibers provided more favorable conditions for mineral crystal deposition and growth. Energy-dispersive spectroscopy (EDS) and FTIR proved that the crystal was hydroxyapatite (HAP) and that the calcium to phosphorus ratio was 1.47, which was close to the theoretical value of 1.67 in HAP. Such nanofiber membranes could be potentially applicable in bone tissue engineering.

Improving the corrosion resistance of epoxy resin coatings has become the focus of current research. This study focuses on synthesizing a functionalized silane coupling agent (2-(3,4-epoxycyclohexyl)ethyl triethoxysilane) to modify the surface of graphene oxide to address nanomaterial agglomeration and enhance the coating resistance of the epoxy resin coating to corrosion by filling the coating with functionalized graphene oxide. Functionalized graphene oxide and coatings filled with functionalized graphene oxide were characterized by Fourier transform infrared spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, and transmission electron microscopy. The corrosion performance of each coating was studied by electrochemical impedance spectroscopy and a salt spray test. Results showed that the incorporation of functionalized graphene oxide enhances the corrosion protection performance of the epoxy composite coating, and the composite coating exhibited the best anticorrosion performance when the amount of functionalized graphene oxide was 0.7 wt %.

Epoxy resin composites with improved thermal resistance and flame retardancy were fabricated based on P(H) microcapsules.