Nanocellulose was prepared by acid hydrolysis of microcrystalline cellulose (MCC) at different hydrobromic acid (HBr) concentrations. Polyvinyl alcohol (PVA) composite films were prepared by the reinforcement of nanocellulose into a PVA matrix at different filler loading levels and subsequent film casting. Chemical characterization of nanocelluloses was performed for the analysis of crystallinity (X c ), degree of polymerization (DP), and molecular weight (M w ). The mechanical and thermal properties of the nanocellulose reinforced PVA films were also measured for tensile strength and thermogravimetric analysis (TGA). The acid hydrolysis decreased steadily the DP and M w of MCC. The crystallinity of MCC with 1.5 M and 2.5 M HBr showed a significant increase due to the degradation of amorphous domains in cellulose. Higher crystalline cellulose showed the higher thermal stability than MCC. From X-ray diffraction (XRD) analysis, nanocellulose samples showed the higher peak intensity than MCC cases. Reduction of MCC particle by acid hydrolysis was clearly observed from scanning electron microscope (SEM) images. The tensile and thermal properties of PVA composite films were significantly improved with the increase of the nanocellulose loading.
Abstract. Nanocomposites with polypropylene/clay/wood flour were prepared by melt compounding. Thermal, mechanical and morphological properties were characterized. The addition of clay, compatibilizer and wood flour considerably improved the thermal stability (i.e., decomposition and melting temperatures) of the hybrids. The tensile modulus and strength of most hybrids were highly increased with the increased loading of clay, MAPP and wood flour, compared to the hybrids without wood flour. The wide angle X-ray diffraction (WAXD) patterns showed the increased d-spacing of clay layers, indicating enhanced compatibility between PP and clay with the addition of maleated polypropylene (MAPP). The transmission electron microscopy (TEM) photomicrographs illustrated the intercalated and partially exfoliated structures of the hybrids with clay, MAPP and wood flour.
The effects of chemical modification (silane coupling) and filler loading on the fundamental properties of the bamboo fiber (BF) filled polypropylene (PP) bio-composites were investigated in this study. Mechanical properties of the PP/ BF composites, such as the tensile strength, flexural strength, and impact strength decreased as BF loading increased. However, the tensile modulus, flexural modulus, and water absorption were increased by the increase of the BF loading. The addition of aminopropyltrimethoxysilane (AS) and tetramethoxy orthosilicate (TMOS) after the alkali pretreatment for the BF increased all the tensile, flexural, impact strength, and water desorption of the resultant composites, resulting from the improved adhesion between the BF and PP matrix. This tendency was more obvious with the increase of the BF loading. The melting temperature, melting enthalpy, crystallization enthalpy, and crystallinity were decreased by the increase of BF loading and the AS and TMOS treatments. One the other hand, the crystalline temperature was increased by the addition of the BF, AS, and TMOS. Hence, AS and TMOS are considered as effectual coupling agents for the PP/BF composite systems.
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