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Polymer solidification under pressure and high cooling rates / Valerio Brucato in INTERNATIONAL POLYMER PROCESSING, Vol. XV, N° 1 (03/2000)
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Titre : Polymer solidification under pressure and high cooling rates Type de document : texte imprimé Auteurs : Valerio Brucato, Auteur ; Vincenzo La Carrubba, Auteur ; G. Titomanlio, Auteur ; S. Piccarolo, Auteur Année de publication : 2000 Article en page(s) : p. 103-110 Note générale : Bibliogr. Langues : Anglais (eng) Index. décimale : 668.9 Polymères Résumé : Polymer solidification under processing conditions is a complex phenomenon in which the kinetics of flow, high thermal gradients and high pressures determine the product morphology. The study of polymer structure formed under pressure has been mainly made using conventional techniques such as dilatometry and differential scanning calorimetry under isothermal conditions or non isothermal conditions but at cooling rates several orders of magnitude lower than those experienced in industrial processes. A new equipment has been recently developed and improved to study the crystallization of polypropylene when subjected to pressure and cooled rapidly. An experimental apparatus essentially constituted of a special injection mould has been employed. Polymer samples can be cooled at a known cooling rate and under a known pressure. Micro Hardness (MH), Wide angle x-ray diffraction (WAXD), Polarised Optical Microscopy (POM) and density measurements are then used to characterize the sample morphology. The results of rapid cooling experiments under pressure on an iPP sample display a lower density and a lower density dependence on cooling rate for increasing pressure. Micro hardness confirms the trend.
A deconvolution technique of WAXD patterns is used to evaluate the final phase content of samples and to assess a crystallization kinetics behaviour. Phase distribution results indicate that the decrease of alpha phase with pressure is balanced by an increase of the mesomorphic phase leaving unaffected the amorphous phase content. This peculiar behaviour can be easily related to a negative influence of pressure on the kinetics of the crystallization of alpha phase.Note de contenu : - EXPERIMENTAL : Apparatus development - Material employed - Sample preparation - Sample characterization - Heat-transfer modelling of cooling inside the polymer
- RESULTS AND DISCUSSION : Density and microhardness dependence on cooling rate and pressure - Properties-structure relationshipsDOI : 10.3139/217.1572 En ligne : https://drive.google.com/file/d/1ewmLxSkxdwt6FVg-Y8NCLwNzMQfwP6bT/view?usp=drive [...] Format de la ressource électronique : Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=16089
in INTERNATIONAL POLYMER PROCESSING > Vol. XV, N° 1 (03/2000) . - p. 103-110[article]Réservation
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Code-barres Cote Support Localisation Section Disponibilité 001011 - Périodique Bibliothèque principale Documentaires Disponible Solidification behaviour of PA6/iPP blends at high cooling rates / C. Colletti in INTERNATIONAL POLYMER PROCESSING, Vol. XV, N° 1 (03/2000)
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Titre : Solidification behaviour of PA6/iPP blends at high cooling rates Type de document : texte imprimé Auteurs : C. Colletti, Auteur ; S. Piccarolo, Auteur ; A. Valenza, Auteur Année de publication : 2000 Article en page(s) : p. 46-52 Note générale : Bibliogr. Langues : Anglais (eng) Index. décimale : 668.9 Polymères Résumé : The non isothermal crystallization behaviour of two model blends of immiscible polymers (an isotactic polypropylene and a polyamide-6) was examined by a quenching procedure within a range of cooling rates from 0.1 to above 1000°C/s in order to emulate the solidification conditions arising during polymer processing. The final structure of the blends was analyzed by density and WAXD and the transition from stable to metastable phases in the blends and the pure homopolymers was compared examining their dependence on cooling rate. This shows that crystallization in the blends is always faster since the transitions move to larger cooling rates. Observation of morphological details suggests that this can be due to enhanced nucleation at the interface. The density variation in the case of the polyamide-6 rich blend is larger than expected from an additive volume contribution which may be ascribed to development of microvoids at the interface. In the case of the isotactic polypropylene rich blend the additive volume contribution is consistent with experimental observations. DOI : 10.3139/217.1573 En ligne : https://drive.google.com/file/d/1pckF6tJ1S6jgy56fTmLPcvOsHVP6VOfl/view?usp=drive [...] Format de la ressource électronique : Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=16073
in INTERNATIONAL POLYMER PROCESSING > Vol. XV, N° 1 (03/2000) . - p. 46-52[article]Réservation
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Exemplaires (1)
Code-barres Cote Support Localisation Section Disponibilité 001011 - Périodique Bibliothèque principale Documentaires Disponible