ABSTRACT:The coupling efficiency of seven coupling agents in wood-polymer composites (WPC) was investigated in this study. The improvement on the interfacial bonding strength, flexural modulus, and other mechanical properties of the resultant wood fiber/high-density polyethylene (HDPE) composites was mainly related to the coupling agent type, function groups, molecular weight, concentration, and chain structure. As a coupling agent, maleated polyethylene (MAPE) had a better performance in WPC than oxidized polyethylene (OPE) and pure polyethylene (PPE) because of its stronger interfacial bonding. A combination of the acid number, molecular weight, and concentration of coupling agents had a significant effect on the interfacial bonding in WPC. The coupling agents with a high molecular weight, moderate acid number, and low concentration level were preferred to improve interfacial adhesion in WPC. The backbone structure of coupling agents also affected the interfacial bonding strength. Compared with the untreated composites, modified composites improved the interfacial bonding strength by 140% on maximum and the flexural storage modulus by 29%. According to the statistical analysis, 226D and 100D were the best of the seven coupling agents. The coupling agent performance was illustrated with the brush, switch, and amorphous structures.

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ABSTRACT:The compounding process directly influenced the compounding quality of wood-polymer blends and finally affected the interfacial bonding strength and flexural modulus of the resultant composites. With 50 wt % wood fiber, the optimum compounding parameters for the wood-fiber/high-density-polyethylene blends at 60 rpm were a temperature of 180°C and a mixing time of 10 min for the one-step process with a rotor mixer. The optimum compounding conditions at 90 rpm were a temperature of 165°C and a mixing time of 10 min. Therefore, a short compounding time, appropriate mixing temperatures, and a moderate rotation speed improved the compounding quality of the modified blends and the dynamic mechanical properties of the resultant composites. The melt torque and blend temperature followed a polynomial relationship with the loading ratio of the wood fiber. The highest melt torque and blend temperature were obtained with 50% wood fiber. The coupling treatment was effective for improving the compatibility and adhesion at the interface. The two-step process was better than the one-step process because the coupling agents were more evenly distributed at the interface with the two-step process.

The fiber characteristics (i.e., the fiber type, morphology, and dimension) and polymer melt flow index (MFI) significantly affected mechanical properties of sugarcane fiber/HDPE composites. The length and diameter of sugarcane fibers followed a lognormal distribution before and after compounding. The long fibers had a significant reduction in the dimension and aspect ratio during compounding. However, the short fibers had close values in these two properties before and after compounding. For the resultant sugarcane fiber/polymer composites, the HDPE resins with a low MFI value presented high tensile and impact strengths. Because of high sugar content, the pure rind fiber had a poor performance as filler in the HDPE resins with respect to the raw bagasse fiber and alkali-extracted bagasse fiber. On the other hand, the aspect ratio was proportional to the mechanical performance of the fibers in the HDPE resins. As a result, the fibers with a large aspect ratio and low sucrose content improved the strength properties of the resultant composites.

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