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PLA/SiO2 composites: Influence of the filler modifications on the morphology,crystallization behavior,and mechanical properties
Authors:R. H. Hakim  J. Cailloux  O. O. Santana  J. Bou  M. Sánchez‐Soto  J. Odent  J. M. Raquez  P. Dubois  F. Carrasco  M. Ll. Maspoch
Affiliation:1. Centre Català del Plàstic (CCP), Universitat Politécnica de Catalunya Barcelona Tech (EEBE‐UPC), Terrassa, Spain;2. Department of Chemical Engineering, Universitat Politécnica de Catalunya Barcelona Tech (ETSEIB‐UPC), Pavellò G, planta 1, Barcelona, Spain;3. Laboratory of Polymeric and Composite Materials, Center of Innovation and Research in Materials & Polymers (CIRMAP), University of Mons UMONS, Mons, Belgium;4. Department of Chemical Engineering, Agriculture and Food Technology, Universitat de Girona (UdG), Girona, Spain
Abstract:Films of an architecturally modified poly(lactic acid) (PLAREx) with three different types of fumed silica nanofillers (SiO2) were processed through reactive extrusion‐calendering in a pilot plant. The effects of the SiO2 type on both the dispersion and the crystallization behavior under dynamic and isothermal conditions are investigated using transmission electron microscopy (TEM) and differential scanning calorimetry (DSC). The mechanical properties are assessed by tensile testing. TEM micrographs showed that the improved chemical affinity of both surface‐treated SiO2 toward PLAREx end groups did not improve particle dispersion. DSC results revealed that untreated SiO2 nucleated PLAREx more efficiently than both surface‐modified silicas. The activation energy for the isothermal crystallization process, as determined by an Arrhenius method, suggests that addition of untreated SiO2 enhances the crystallization rate of PLAREx. However, it seems that the tensile behavior remained unchanged whether silicas were added or not. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45367.
Keywords:biopolymers and renewable polymers  crystallization  extrusion  films  nanoparticles  nanowires and nanocrystals
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