1,720,997 research outputs found

    Thermal degradation of poly(lactic acid) (PLA) and poly(butylene adipate-co-terephtalate) (PBAT) as a consequence of melt processing: effects on pure materials and their blends

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    Poly(lactic acid) (PLA) and poly(butylene adipate-co-terephthalate) (PBAT) are biodegradable aliphatic polyesters, which being semicrystalline and thermoplastic can be processed by conventional methods. Their blends give interesting materials for industrial packaging applications, due to their increased ductility as PBAT content increases. However, like many aliphatic polyesters, the PLA matrix degrades upon melt processing thus affecting the thermo-mechanical features of the blended material. In this work, we studied the effect of processing at high temperature on the molecular weight distribution, morphology, and thermo-mechanical properties of both homopolymers, as well as the PLA/PBAT 75/25 blend. Notably, different processing conditions were adopted in terms of temperature (range 150–200 C) and other relevant processing parameters (moisture removal and nitrogen atmosphere). Analysis of PLA/ PBAT blends indicated that intermolecular chain reactions took place under strong degradative conditions of PLA, yielding PLA/PBAT mixed chains (copolymers). Increasing amounts of copolymers resulted in improved phase dispersion and increased ductility, as SEM and mechanical tests indicated. Conversely, reduced PLA degradation with less copolymer formation, afforded higher modulus materials, owing to poorer dispersion of the soft phase (PBAT) into the PLA matrix

    Amorphous/crystal and polymer/filler interphases in biocomposites from poly(butylene succinate)

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    Poly(butylene succinate)-hemp composites (PBS-hemp), with hemp content in the range 0-40 wt.\%, were prepared in the melt and characterized. This paper focuses on the detailed analysis of the thermal behaviour of the PBS-hemp composites, investigated by differential scanning calorimetry (DSC), to enlighten the polymer/fibre interphase features. The occurrence of specific intermolecular interactions between PBS and hemp was assessed from specific heat capacity data. Different degrees of mobility of the PBS amorphous segments were found at the amorphous/crystal interphases. A broadening of the bulk glass transition was observed, and attributed to the presence of polymer segments slightly constrained. Moreover, a rigid amorphous fraction that devitrifies at temperatures higher than the bulk glass transition, partly before the melting region and partly simultaneously with the fusion, was observed and quantified, and attributed to the presence of major constraints probably occurring in geometrically restricted areas. (C) 2012 Elsevier B.V. All rights reserved

    Radical functionalization of poly(butylene succinate-co-adipate): Effect of cinnamic co-agents on maleic anhydride grafting

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    Maleic anhydride (MAH), trans cinnamic acid (AcCin) and ethyl cinnamate (EtCin) were radically graft onto poly(butylene succinate-co-adipate) (PBSA). Samples were prepared in Brabender at 175 degrees C by addition of increasing amounts of MAH, AcCin, EtCin and their combinations, i.e. MAH/AcCin and MAH/EtCin, setting DCP content in the 0.2-0.6 wt\% range. Monomer grafting was quantitatively determined by FT-IR. MAH grafting degrees (FD(M)) resulted up to 1 molt Conversely, AcCin grafting degrees (FD(A)) were found almost negligible in all cases. EtCin was found grafted in the 0.3-1.0 mol\% range when the binary system MAH/EtCin was applied. Same MAH feeds returned almost doubled MAH grafting degrees (FD(M)) when AcCin was the stoichiometric co-agent, and even three times higher FD(M) when EtCin was the stoichiometric co-agent. On accounts of all the collected results, a kinetic model of the investigated systems is proposed. (C) 2011 Elsevier Ltd. All rights reserved

    Development of new PLA-based biodegradable compounds for micro-irrigation applications

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    New biodegradable compounds having high renewable resources starting materials content were developed and formulated at Lab, pilot and industrial level. Pipes were prepared using the here developed compounds, and perfectly mimic the mechanical behavior as well as the chemical resistance of the currently used polyethylene based materials. This work is currently developed within the EC founded HYDRUS project
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