Crystallization behavior of organo-nanoclay treated and untreated kraft fiber–HDPE composites

Abstract

Both non-isothermal and isothermal crystallization behaviors of neat HDPE and organo-nanoclay treated and untreated kraft fiber–high density polyethylene (HDPE) or HDPE–maleic anhydride polyethylene (MAPE) composites were analyzed using differential scanning calorimetry (DSC). The isothermal crystallization process was studied by the Avrami model. The crystallization patterns and organo-nanoclay distribution was characterized by X-ray diffraction (XRD). It was found that both organo-nanoclay treated and untreated kraft fibers could act as nucleating agent for the HDPE polymer when the fiber length was comparatively small. All composites crystallized much faster than the neat HDPE, while their crystallinity levels were lower. The organo-nanoclay treatment of kraft fibers made the crystallinity level lower, but the nucleation rate increased in the composites compared to the untreated kraft fiber–HDPE composites. But both the crystallinity level and the nucleation rate of the composites were increased by adding MAPE compatibilizer to the composites. MAPE increased the d-spacing of the organo-nanoclay layers in the composites and resulted in exfoliated clay platelets when the fiber loading was as high as 40wt%.