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This work aims at identifying defects called deformation heterogeneities developing in polylactide (PLA)‐based materials upon drawing at room temperature. The influence of the initial crystallinity and of the plasticization methodology (physical blending vs. reactive blending) on the type of defect is also investigated. Defects are characterized in situ by (a) calculating the volume strain from digital image correlation (DIC), (b) measuring their surface density from optical microscopy, and (c) assessing their scattering invariant from small‐angle X‐ray scattering. Complementary structural analyses are done by microcomputed X‐ray tomography and atomic force microscopy. Drawing is accompanied by crazing in the case of low‐crystalline PLA, cracking in the case of annealed PLA, no defect in the case of plasticized PLA by physical blending, and shear bands and cracking in the case of plasticized PLA by reactive blending. These observations are discussed based on the initial structural features of the materials. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2018, 56, 1452–1468 Defects developing in PLA‐based materials upon drawing are studied by a multiscale and in situ approach. Low crystalline PLA exhibits crazing, while after annealing, tortuous defects are noted. These defects may be induced by the opening of crystallization‐induced cracks. Physical plasticization of PLA engenders no defect, while reactive plasticization of PLA induces shear bands and localized cracks. A multiscale correlation of defect characterization is performed in the case of crazing, showing the relevancy of this approach. [ABSTRACT FROM AUTHOR]

ABSTRACT PCL was blended with pristine multiwalled carbon nanotubes (MWCNT) and with a nanohybrid obtained from the same MWCNT but grafted with low molecular weight PCL, employing concentrations of 0.25 to 5 wt % of MWCNT and MWCNT- g-PCL. Excellent CNT dispersion was found in all samples leading to supernucleation of both nanofiller types. Nanohybrids with 1 wt % or less MWCNTs crystallize faster than nanocomposites (due to supernucleation), while the trend eventually reverses at higher nanotubes content (because of plasticization). Rheological results show that yield-like behavior develops in both nanocomposites, even for the minimum content of carbon nanotubes. In addition, the MWCNT- g-PCL family, when compared with the neat polymer, exhibits lower values of viscosity and modulus in oscillatory shear, and higher compliance in creep. These rheological differences are discussed in terms of the plasticization effect caused by the existence of low molecular weight free and grafted PCL chains in the nanohybrids. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2017, 55, 1310-1325 [ABSTRACT FROM AUTHOR]

ABSTRACT Poly(butylene succinate- ran-butylene azelate) random copolyesters were thermally fractionated by successive self-nucleation and annealing (SSA). The samples before and after SSA were analyzed by differential scanning calorimetry (DSC) and X-ray diffraction (WAXS and SAXS). WAXS results indicate that a small degree of comonomer inclusion is present in the crystalline phases that are formed in the copolymers depending on composition: a PBS-like unit cell or/and a PBAz-like unit cell, thus confirming the isodimorphic behavior of the samples. SSA on the other hand demonstrated that the degree of comonomer exclusion during crystallization is far larger than comonomer inclusion, as judged by the increase in fractionation degree with compositions leading to the pseudo-eutectic point. Furthermore, WAXS, SAXS, and SSA results show that the isodimorphic behavior is not highly dependent on kinetic factors, as the degree of comonomer inclusion or exclusion in the samples was not significantly altered by SSA thermal fractionation, a thermal treatment that promotes annealing and molecular segregation of defects to the amorphous regions of the material. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016, 54, 2346-2358 [ABSTRACT FROM AUTHOR]

ABSTRACT The effectiveness of hydrophobically modified nanosilica (NS) as interfacial modifying agent for immiscible polymer blends is evaluated. Blends of polypropylene (PP) with 20% of polyamide 6 (PA) and 5% hydrophobic NS were prepared by melt mixing. Compression molded sheets and extruded films were evaluated by scanning electron microscopy, transmission electron microscopy, tensile testing, and rheological measurements. Hydrophobic NS particles strongly reduce the polydispersity and droplet size of the dispersed phase, as a result of their preferential location at the interface. NS promotes outstanding stability of blend dispersion regardless of the processing or post-processing technique employed. The viscoelastic terminal zone shows a plateau for PP/PA/NS, which corresponds to a suspension-like behavior. Under large amplitude oscillatory shear, the increment in the non-linearity parameter Q evidences the interactions between NS and blend components. Therefore, NS is an excellent morphological stabilizer that prevents coalescence, but cannot promote interfacial adhesion between immiscible PP and PA phases. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2015, 53, 1567-1579 [ABSTRACT FROM AUTHOR]

The thermal properties, crystallization, and morphology of amphiphilic poly( D-lactide)- b-poly( N, N-dimethylamino-2-ethyl methacrylate) (PDLA- b-PDMAEMA) and poly ( L-lactide)- b-poly( N, N-dimethylamino-2-ethyl methacrylate) (PLLA- b-PDMAEMA) copolymers were studied and compared to those of the corresponding poly(lactide) homopolymers. Additionally, stereocomplexation of these copolymers was studied. The crystallization kinetics of the PLA blocks was retarded by the presence of the PDMAEMA block. The studied copolymers were found to be miscible in the melt and the glassy state. The Avrami theory was able to predict the entire crystallization range of the PLA isothermal overall crystallization. The melting points of PLDA/PLLA and PLA/PLA- b-PDMAEMA stereocomplexes were higher than those formed by copolymer mixtures. This indicates that the PDMAEMA block is influencing the stability of the stereocomplex structures. For the low molecular weight samples, the stereocomplexes particles exhibited a conventional disk-shape structure and, for high molecular weight samples, the particles displayed unusual star-like shape morphology. © 2011 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 49: 1397-1409, 2011 [ABSTRACT FROM AUTHOR]