Structural characterization of a series of novel bio-polyamides based on renewable raw materials-PA 4.10, PA 6.10, PA 10.10, and PA 10.12-was performed by Fourier transform infrared spectroscopy (FTIR) and wideangle X-ray diffraction (WAXD). Infrared spectra and the WAXD patterns indicate the coexistence of different crystalline forms, a-and c-triclinic and b-pseudohexagonal. Thermal properties in the glass transition (T g ) and melting region were then investigated using temperaturemodulated DSC (TOPEM Ò DSC). The melting point (T m ) was found to increase with increasing amide/methylene ratio in the polymer backbone, which is consistent with the increase in linear density of hydrogen bonds. Studies on the molecular dynamics by dynamic mechanical analysis show three distinct regions associated with the c-and the b-relaxation and the dynamic glass transition. TOPEM Ò DSC data reveal that at low frequency/long timescales, the materials with significantly different amide/methylene ratios have similar segmental dynamics.

This article presents an overview of the preparation and characterization of poly(vinyl chloride)/montmorillonite (PVC/MMT) nanocomposites. Different methods of PVC/MMT nanocomposite preparation are discussed. The incorporation of MMT into the PVC matrix results in an increase of thermal stability and induces changes in the mechanical properties. However, the properties of PVC/MMT nanocomposites depend strongly on the MMT organic modification procedure that governs the extent of MMT penetration by PVC macrochains and plays an important role with regard to the morphology formation. Flammability as well as other properties—barrier, optical, etc.—of PVC/MMT nanomaterials are also described. Finally, a future outlook is given. J. VINYL ADDIT. TECHNOL., 2009. © 2009 Society of Plastics Engineers

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Polyhedral oligomeric silsesquioxane moieties with poly­(ethylene glycol) groups attached on the cage (PEG–POSS) were blended with an elastomeric polyurethane matrix, in contents up to 10 wt %. Several experimental techniques in agreement with each other show that the PEG–POSS moieties disperse well on the molecular level and act as diluents plasticizing the molecular dynamics. Although the degree of microphase separation is only weakly affected in all the compositions, changes in the macromorphology related to the POSS moieties have an impact on the matrix properties, decreasing the storage modulus. The PEG–POSS themselves display segmental dynamics, glass transition, and crystallinity; however, none of these properties are observed in the blends, providing additional support for excellent miscibility with the matrix. The results are compared to those of previous works where different synthesis approaches resulting in different POSS topologies were used.

In this work, isothermal crystallization kinetics of polyoxymethylene copolymer (POM) in POM/hydroxyapatite (HAp) nanocomposites has been investigated. Melting behavior and crystalline structure formation were studied using TOPEM DSC, positron lifetime spectroscopy (PALS), atomic force microscopy (AFM) and 13C and 31P solid‐state NMR. The highest degree of crystallinity was found for POM/0.5% HAp nanocomposite and the lowest for POM/2.5% HAp. Isothermal crystallization analysis showed that an introduction of HAp nanoparticles led to effective heterogeneous nucleation and formation of crystals with higher Avrami exponent. Besides, changes in overall crystallization rate were observed – the highest overall crystallization rate was found for POM/0.5% HAp sample, while the lowest for POM/2.5% HAp was observed. Generally, for POM in POM/HAp nanocomposites, a significant decrease in nucleation activation energy (Kg), and the fold surface free energy (σe) was found. For nanocomposite containing 2.5% HAp, heterogeneous nucleation takes place as well, but too high concentration of nanoparticles hinders POM crystallization and enhances formation of more defected crystals as confirmed by AFM data. The presence of HAp nanoparticles in the POM matrix was confirmed by 31P MAS‐NMR, but their influence on the crystallization process was not observed in the 13C CP‐MAS‐NMR spectra. Copyright © 2012 John Wiley & Sons, Ltd.

This work focuses on the influence of weathering factors—UV radiation, humidity, and temperature on the structure and morphology of poly(vinyl chloride)/montmorillonite (PVC/MMT) nanocomposites obtained by melt blending. It has been observed that organically modified MMT (OMMT) deteriorates the weathering resistance, the thermal behavior, as well as the long‐term stability of PVC. Decomposition of the organic modifier of MMT causes substantial color changes in the PVC nanocomposites as it facilitates the dehydrochlorination process of the polymer. However, the nonmodified MMT provides some stabilization during PVC weathering. The nanocomposites after annealing are characterized by higher glass transition temperature. The increase in heat capacity step (Δcp) during glass transition suggests that in the PVC composites with nonmodified MMT stronger molecular interactions between the polymer and clay platelets occur than in PVC/OMMT nanocomposites. The scanning electron microscopy images on the surface and the cross section show that thermal aging and weathering proceed by different mechanisms. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015, 132, 42090.

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