The extraction of nanocrystalline cellulose from agro-residues is an interesting alternative to recover these materials. In the present study, nanocrystalline cellulose was extracted from pine wood and corncob. In addition, microcrystalline cellulose was used as a reference to compare results. Initially, the lignocellulosic residues were submitted to delignification pre-treatments. At the end of the process, the bleached fibre was submitted to acid hydrolysis. Additionally, microparticles were obtained from the spray-drying of the nanocrystalline cellulose suspensions. The nanocrystalline cellulose yield for the pine wood was 9.0-% of the value attained for the microcrystalline cellulose. For the corncob, the value was 23.5-%. Therefore, complementary studies are necessary to improve the yield. The spray-dried microparticles showed a crystallinity index of 67.8-% for the pine wood, 70.9-% for the corncob and 79.3-% for the microcrystalline cellulose. These microparticles have great potential for use in the production of polymer composites processed by extrusion.

SYNOPSISThe crystallization kinetics of a polyetheretherketone (PEEK)/liquid crystalline polymer (LCP) blend was studied by using differential scanning calorimetry. Nonisothermal runnings were performed on heating and on cooling at different rates. Isothermal crystallization experiments at 315, 312, 310, and 307"C, from the melt state (380°C) were performed in order to calculate the Avrami parameters n and k and the fold surface free energy, a , . Polarized light optical micrographs were also obtained to confirm the Avrami predictions. It was observed that the LCP retarded the PEEK crystallization process and that the PEEK melting temperature decreased with the amount of LCP, but the LCP melting temperature increased with the amount of PEEK. Probably the PEEK improves the perfection of the LCP crystalline domains. A spherulitic morphology in pure PEEK and its blends was predicted by the Avrami analysis; however this morphology was only observed for pure PEEK and for the 80/20 composition. The other compositions presented a droplet and fibrillar-like morphology. The overall crystallization rate was observed to decrease with the crystallization temperature for all compositions. Finally, u, was found to decrease with the increase of LCP in the blends, having unrealistic negative values. Thus, calculations were made assuming a, constant at all compositions. It was observed that u, the interfacial lateral free energy, decreased but still remained positive. It was concluded that in these blends neither a, nor u could be considered constant.

ABSTRACT:The quiescent isothermal crystallization kinetics of polypropylene was studied as a function of molecular weight (M w ), amount of ethene, and amount of maleic anhydride and acrylic acid grafting. Differential scanning calorimetry and polarized light optical microscopy were used to follow this kinetics. It was observed that the linear growth rate, G, decreased with the increase of M w , but increased with the amount of ethene. In the grafted polymers, as the amount of grafting increased, G decreased. The fold surface free energy, s e , was found to increase with the increase in M w . The heterophasic and grafted polymers had s e values higher than the homopolymers. All samples showed spherulitic morphology, except the acrylic acid-grafted polypropylene that showed axialitic morphology.

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Poly(vinylidene fluoride) (PVDF) nanocomposites have plenty of applications in the electronic realm. In this study, we produced nanocomposites based on PVDF and multiwalled carbon nanotubes (MWCNTs), with various MWCNT loadings, using three different processing routes: solution mixing, melt mixing, and electrospinning. The broadband electrical behavior of these nanocomposites was studied and compared via impedance spectroscopy. The morphologies of the nanocomposites were characterized by transmission electron microscopy and scanning electron microscopy. The results reveal that the electrical behaviors of the samples were completely different according to the processing route used. Solution mixing was the most suitable method for producing nanocomposites with the highest conductivities, at low MWCNT loadings, whereas electrospinning was the most suitable method for producing nanocomposites with the lowest dielectric permittivity. These differences were attributed to the different arrangements of the MWCNTs caused by the different processes. Although the solution‐mixed samples exhibited long and twisted MWCNTs, the melt‐mixed samples had shorter MWCNTs, and the electrospun samples had MWCNTs embedded and aligned inside the insulating polymer nanofibers. Thus, these results project a vast horizon for tailoring the structure and thereby the broadband electrical behavior of PVDF–MWCNT nanocomposites for different types of applications. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019, 136, 47409.