A X-ray study of β-phase and molecular orientation in nucleated and non-nucleated injection molded polypropylene resins

The development of α and β-phases and the molecular orientation of injection molded disks of two isotactic polypropylene (i-PP) resins were studied by wide angle X-ray diffraction (WAXD) and pole figures. A nucleated (NPP) and non-nucleated (HPP) polymers were analyzed. The main proposal of this article was the comprehensive study of the interrelations between the processing conditions, phase contents and PP α-phase molecular orientation of injection molded PP resins. In both resins, it was observed that the α-phase was present in all regions along the thickness while the β-phase was present mainly in the external layers, decreasing from the surface to the core; however this last phase was present in a very small amount in the NPP resin. For both polymers, the orientation of the macromolecules c-axis was higher along the flow direction (RD) than along the transverse direction (TD). The b-axis of the PP α-phase molecules was oriented to the thickness direction (ND). The orientation of the c-axis along RD and b-axis along ND of the NPP samples was considerably higher than of the HPP samples, due to the NPP faster crystallization kinetics. For both polymers, the most influential processing parameters on the molecular orientation were the mold temperature and flow rate. The results indicate that, as the mold temperature increased, the characteristic molecular orientation of PP α-phase, with c-axis along RD and b-axis along ND, decreased. With increase in the flow rate an increase of the c-axis molecular orientation of the samples along RD was observed

Interfacial tension of PBT/SAN blends by the drop retraction method

The aim of this work was to evaluate the interfacial tension from the poly(butylene terephtalate) and poly(styrene-co-acrylonitrile) (PBT/SAN) interface region using the drop retraction method. SAN filaments were sandwiched between two PBT films; the whole system was heated up to 240 °C, in a hot stage coupled to an optical microscope. The rheological parameters of the PBT/SAN system were obtained by parallel plates rheometry. An increase of the interfacial tension with the PBT molecular weight was observed with values between 0.57 and 1.06 mN/m, depending on the molecular weight. Theoretical values were calculated using the geometric-mean and harmonic-mean equations and were found to be similar to the experimental results. Viscosity measurements showed that the higher the SAN/PBT viscosity ratio, the lower the interfacial tension of these blends

Nanocomposites of polyamide 6/residual monomer with organic-modified montmorillonite and their nanofibers produced by electrospinning

Nanocomposites of an organic-modified montmorillonite (MMT) and polyamide 6 (PA6) with a residual monomer were produced by melt mixing in a torque rheometer. By wide angle X-rays diffraction (WAXD), intercalated/exfoliated structures were observed in the PA6/MMT nanocomposites with 3 and 5 wt. (%) of MMT; on the other hand, when 7 wt. (%) of MMT was added, a nanocomposite with exfoliated structures was obtained due to the predominant linking reactions between the residual monomer and the "nanoclays" organic surfactant. Solutions of these PA6/MMT nanocomposites at 15, 17 and 20 wt. (%) in formic acid were prepared. The 3 and 5 wt. (%) nanocomposites were successfully electrospun; however, electrospinning of the 7 wt. (%) nanocomposite was not possible. WAXD, scanning and transmission electron microscopy results showed that the 3 and 5 wt. (%) nanofibers with average diameter between 80-250 nm had exfoliated structures. These results indicate that the high elongational forces developed during the electrospinning process changed the initial intercalated/exfoliated structure of the nanocomposites to an exfoliated one

Electrospinning and characterization of polyamide 66 nanofibers with different molecular weights

Polyamide 66 (PA66) nanofibers of different molecular weights were obtained by electrospinning of formic acid solutions. An ionic salt, NaCl, was also added to the solutions to increase the conductivity. PA66 concentrations between 15-17 wt.(%)/v and electrical fields between 2.0 and 2.5 kV/cm were the best conditions to produce the smallest nanofibers; however, the addition of NaCl increased the fibers average diameters.The characterization of the fibers was done by scanning electron microscopy (SEM), differential scanning calorimetry (DSC), wide angle X rays diffraction (WAXD) and Fourier Transformed Infrared (FTIR). As the molecular weight decreased, the nanofibers average diameters also decreased; however, critical number average and weight average molecular weights were necessary for electrospinning. As the amounts of carboxyl terminal groups (CTG) increased, the nanofibers average diameters decreased; however, above CTG's critical values of 8.7 x 10-5 mol.g-1 no electrospinning was possible. The addition of ionic salt increased the electrical conductivity of the solutions and increased the nanofibers' average diameters. By DSC, residual solvent in all the electrospun mats was found; two melting endotherms, one between 248 and 258 °C and the other one between 258 and 267 °C, depending on the sample were also observed. These endotherms were attributed to the melting, re-crystallization and re-melting of the PA66 α-phase. The nanofibers had low % of crystallinity compared to a textile fiber. By WAXS and FTIR, confirmation of the presence of α-phase crystals, of small dimensions and highly imperfect and of a very small amount of β and γ-phases crystals in the nanofibers structure was obtained