H-Beta zeolite is a solid acid catalyst commonly utilized in the catalytic conversion of biomass resources. In this study, H-Beta zeolite was calcined at different temperatures (350, 550, 750, and 1000 °C) to explore the effects of high temperature-induced dealumination on its physicochemical properties and its catalytic ability to convert glucose into 5-hydroxymethylfurfural (HMF). It was shown that as the calcination temperature increased, the Si-O-Al bond of H-Beta zeolite was broken and its dealumination effect was enhanced. Dealumination led to the collapse of the framework of H-Beta zeolite and a reduction in the number of acid sites, which in turn reduced its catalytic performance and the efficiency of HMF formation from glucose. Furthermore, H-Beta zeolite exhibited an extraordinary catalytic ability for the production of HMF from carbohydrates. Using glucose and cellulose as substrates, superior HMF yields of 91% and 46%, respectively, were achieved under optimal reaction conditions. Further, calcination removes carbon deposits in the recovered H-Beta zeolite, but it affects the cycling stability of the catalyst. Meanwhile, the by-products formed during the synthesis of HMF from glucose catalyzed by H-Beta zeolite catalyst were also clearly detected.

Jute fibers are renewable, light, and strong, allowing them to be considered as attractive materials in composite manufacturing. In the present work, a simple and effective method for preparing continuous pre-preg tapes from short jute fiber bundles (without twist) is developed and its application in winding forming is evaluated. Linear low-density polyethylene film (LLDPE) with good flexibility and weather resistance was used as the thermoplastic matrix; jute fiber bundles were first spread parallel to each other on an LLDPE film and then rolled up to form a pre-roll. The pre-roll enclosing fiber bundles was hot-pressed in a designed mold to form a pre-preg tape, where the fiber bundles were more parallel to the tape than the fibers in twine. Although the untwisted structure exhibited a lower tensile strength for the fiber bundle, it could be processed into a continuous pre-preg with higher tensile strength than the jute twine-impregnated pre-preg. This is based on the good impregnation of the short fiber bundle and its unidirectional, uniform strengthening in the continuous pre-preg. The tensile strength and modulus of the fiber bundle-reinforced pre-preg increased by 16.70% and 257.14%, respectively, compared with jute twine-reinforced pre-preg (within the fiber proportion of 40.wt%). When applied to winding, the fiber bundle-reinforced pre-preg showed advantages of interlayer fusion, surface flatness, and ring stiffness. In contrast, the twisted continuous structure did not retain its advantage in pre-preg. The development of pre-preg tapes by discontinuous fibers might be a good way for utilizing natural fibers in the field of green engineering due to its diverse secondary processing.

Wood–plastic composites (WPCs) have received growing attention due to their good water resistance, environmental friendliness, and recyclability. For the application of WPCs in interior decoration and other high–value fields, it is necessary to preserve these characteristics whilst enhancing their mechanical properties and surface aesthetics. In this study, we used a sandwich structure and four interface modifiers to prepare wood veneer/wood flour–polyvinyl chloride composites (WWPVCs). The results revealed that the WWPVCs treated with a silane coupling agent exhibited superior interfacial bonding and mechanical properties compared to those obtained using other interface modifiers. The interfacial bonding strength of the treated sample reached 1.22 MPa, which was 122% higher than that of the untreated sample. In addition, the wood failure ratio of the optimal sample reached 80%. Furthermore, the dipping–peeling length was found to be shorter than those achieved using other interface modifiers after tests at 63 and 100 °C, indicating that the material treated using the silane coupling agent exhibits an excellent resistance to moisture and heat. Notably, silane coupling agents are easily prepared as solvent–based modifiers, and they do not release harmful gases (e.g., formaldehyde), thereby rendering them highly effective in the preparation of environmentally friendly WPC products.

Core–shell composites with strong weather resistance, mechanical strength and creep resistance can be prepared using co-extrusion technology. Considering the weak bonding strength between core–shell interfaces, this study started from the concept of a mortise and tenon combination; three types of conical, rectangular and trapezoidal mortise and tenon joints were prepared, and their bending properties, long-term creep properties, interfacial bonding properties, and dimensional stability properties were tested. Results showed that the mortise and tenon structure could form a mechanical interlock between the outer-shell-layer polyvinyl chloride (PVC) wood–plastic composite (WPVC) and the inner-core-layer laminated veneer lumber (LVL), which could effectively improve the interface bonding property between the two layers. Among them, the trapezoidal mortise and tenon structure had the largest interface bonding force compared with the tapered and rectangular mortise and tenon structure, where the interface bonding strength reached 1.01 MPa. Excellent interface bonding can effectively transfer and disperse stress, so the trapezoidal mortise and tenon structure had the best bending properties and creep resistance, with a bending strength of 59.54 MPa and a bending modulus of 5.56 GPa. In the long-term creep test, the deformation was also the smallest at about 0.2%, and its bending properties, creep resistance and interface bonding performance were also the best. The bending strength was 59.54 MPa and the bending modulus was 5.56 GPa; in the long-term creep test, the strain curve was the lowest, about 0.2%. In addition, the mortise and tenon structure could disperse the stress of the inner shell LVL after water absorption and expansion, thus significantly improving the dimensional stability of the co-extruded composite after water absorption.