| POLYMER | 卷:150 |
| Reduced physical aging rates of polylactide in polystyrene/polylactide multilayer films from fast scanning calorimetry | |
| Article | |
| Monnier, Xavier1,4,5  Nassar, Samira Fernandes2  Domenek, Sandra2  Guinault, Alain3  Sollogoub, Cyrille3  Dargent, Eric1  Delpouve, Nicolas1  | |
| [1] Normandie Univ, UNIROUEN Normandie, INSA Rouen, CNRS,Grp Phys Mat, F-76000 Rouen, France | |
| [2] Univ Paris Saclay, INRA, AgroParisTech, UMR Ingn Proc Aliments, 1 Ave Olympiades, F-91300 Massy, France | |
| [3] CNRS, CNAM, Arts & Metiers ParisTech, PIMM, 151 Bd Hop, F-75013 Paris, France | |
| [4] Univ Basque Country, CSIC, Ctr Fis Mat, Paseo Manuel de Lardizabal 4, San Sebastian 20018, Spain | |
| [5] DIPC, Paseo Manuel de Lardizabal 4, San Sebastian 20018, Spain | |
| 关键词: Confinement; Structural relaxation; Glass transition; | |
| DOI : 10.1016/j.polymer.2018.07.017 | |
| 来源: Elsevier | |
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【 摘 要 】
The physical aging behavior of amorphous polylactide constrained against polystyrene in layers of 300 nm, thanks to the layer-multiplying co-extrusion process, was investigated by fast-scanning calorimetry (FSC). By cooling down the sample from the liquid state to the glassy one at very fast scanning rates, it was possible to investigate the structural relaxation of the polymer glass at high temperatures for which the time needed to reach the equilibrium was shortened. Therefore it was possible to perform the study of physical aging in experimental conditions providing an expanded view of the structural relaxation for short aging times. Taking benefit of this property, it was highlighted that the aging kinetics of polylactide occurred significantly slower in the multilayer film, in comparison with a bulk amorphous film. The process of recovery in the multilayer system was found to occur at similar rates, or even slower, than in a three-layer film in which polylactide reached its maximum extent of crystallinity. This was attributed to mobility hindrance that might be inherent to the extrusion conditions or associated with the presence of capped interfaces with polystyrene. (C) 2018 Published by Elsevier Ltd.
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| 10_1016_j_polymer_2018_07_017.pdf | 3479KB |
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