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.

No abstract

We prepared poly(vinyl alcohol) (PVA)/SiO 2 and PVA/SiO 2 /glutaraldehyde (GA) nanocomposite membranes in a single step using the solution casting method. The structure, morphology, and properties of these nanocomposite membranes were characterized by Raman spectroscopy, atomic force microscopy, small-and wideangle X-ray scattering, thermogravimetric analysis, differential scanning calorimetry, and dynamic mechanical analysis (DMA). The influence of silica and GA loading on the meso-scale characteristics of the composite membranes was investigated. The results showed that silica deposited in the form of small nanoparticles (*1 nm) in the PVA/ SiO 2 membranes, while bigger submicron particles ([25 nm) were formed in the PVA/SiO 2 /GA membranes. The water uptake of the PVA/SiO 2 membranes increased with temperature, but the PVA/SiO 2 /GA membranes were completely dissolved above 50°C. We can therefore conclude that the addition of GA deteriorated the properties of PVA/SiO 2 membranes. The thermal stability of the PVA/ SiO 2 membranes increased with the increasing silica loading with a maximum char yield of 46 % for PVA/SiO 2 / 4T. Even DMA profiles indicated a promising increase in E R (rubbery modulus) from 6 MPa (PVA membrane) to 1015 MPa (PVA/SiO 2 /4T) at 250°C, showing high mechanical strength of these membranes.

No abstract

No abstract