2011
DOI: 10.1016/j.tca.2010.12.024
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Crystalline, mobile amorphous and rigid amorphous fractions in poly(L-lactic acid) by TMDSC

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Cited by 94 publications
(108 citation statements)
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“…This seems consistent with the results of Guinault et al [14] who described that important formation of RAF was linked to imperfect crystallization of PLA. It is assumed that at low crystallization temperature, typically 85 C, the lack of chain mobility hinders the reorganization of polymeric segments in crystals and induces many chain segments subjected to geometrical restrictions in the amorphous phase [47]. Most interestingly, we show here that this observation could be extended to imperfect conditions of crystallization in general, including the predominance of germination over growth that led to the formation of low-size spherulites.…”
supporting
confidence: 58%
“…This seems consistent with the results of Guinault et al [14] who described that important formation of RAF was linked to imperfect crystallization of PLA. It is assumed that at low crystallization temperature, typically 85 C, the lack of chain mobility hinders the reorganization of polymeric segments in crystals and induces many chain segments subjected to geometrical restrictions in the amorphous phase [47]. Most interestingly, we show here that this observation could be extended to imperfect conditions of crystallization in general, including the predominance of germination over growth that led to the formation of low-size spherulites.…”
supporting
confidence: 58%
“…However, as can be seen from Fig. 1a, b, they revealed a small endothermic peak due to cold crystallization of amorphous PLA chains (Fortunati et al 2012;Liao et al 2007;Mano et al 2004;Righetti and Tombari 2011;Salmerón Sánchez et al 2007;Wu et al 2007;Zhang et al 2004). Cold crystallization occurs due to rearrangement of the amorphous region of PLA into a crystalline phase during heating at low heating rates.…”
Section: Resultsmentioning
confidence: 89%
“…The drying process of the pellets at 80°C for 22 h results in a broadening of glass transition and a slight increase of the T g up to 64.0°C, without modifying the melting temperature and crystallinity degree (Figure 5a). According to Mago) et al [49] and Zuza et al [50], this increase in the T g value may be due to the confinement of the mobile amorphous phase fraction (MAF) [51,52]. Indeed, a three phases model (mobile amorphous, rigid amorphous and crystalline phases) can be used to explain the glass transition dynamics.…”
Section: Thermal Propertiesmentioning
confidence: 97%