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Advanced Modeling of Polymer Non-Linear Stress Relaxation – Poly(methylmethacrylate) and Polycarbonate

Bibliographic Details
Main Author: André, José Reinas
Publication Date: 2013
Other Authors: José, Cruz Pinto
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10314/3389
Summary: Sound models of temperature- and strain-dependent (non-linear) stress relaxation are still lacking. Recent work has shown that focusing on polymers’ local backbone strains and stresses provides an adequate basis for developing such models and accurately predicting experimental stress relaxation moduli (to within 1-2% relative errors), the values of meaningful physical parameters and long time behavior, from experiments spanning only a few hours. The modeling strategy is summarized and physically discussed, and applied to two amorphous polymers – PMMA and PC. The numerical values obtained for the model parameters are also physically discussed in detail, supporting a view of the stress relaxation process where a temperature-dependent, truncated log-normal, distribution of local cooperative (or clustering) transitions become involved, at and above a minimum (or primitive) relaxor size. Within this view, cooperativity (average and maximum cluster size) increases with decreasing temperatures. Beyond the reasonably accurate description of the experiments, the model succeeds in predicting (1) the effect of increases in the fully relaxed modulus, E∞, as in semi-crystalline or strongly cross-linked polymers, (2) the strict inapplicability of time-temperature and strain-time super-positions, (3) an extended, Kohlrausch-Williams-Watts, type of relaxation response spanning 12 or more time decades, and (4) specific, meaningful, physical parameters - a minimum activation energy (similar to those of corresponding β-type transitions), the (occupied + free) volume of the primitive relaxor, and the approximate crossover temperature, Tc, and frequency, νc, both of critical importance in condensed matter dynamics. The model also has the potential of incorporating the effect of changes in free volume.
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spelling Advanced Modeling of Polymer Non-Linear Stress Relaxation – Poly(methylmethacrylate) and PolycarbonatePoly(methylmethacrylate)PolycarbonateSound models of temperature- and strain-dependent (non-linear) stress relaxation are still lacking. Recent work has shown that focusing on polymers’ local backbone strains and stresses provides an adequate basis for developing such models and accurately predicting experimental stress relaxation moduli (to within 1-2% relative errors), the values of meaningful physical parameters and long time behavior, from experiments spanning only a few hours. The modeling strategy is summarized and physically discussed, and applied to two amorphous polymers – PMMA and PC. The numerical values obtained for the model parameters are also physically discussed in detail, supporting a view of the stress relaxation process where a temperature-dependent, truncated log-normal, distribution of local cooperative (or clustering) transitions become involved, at and above a minimum (or primitive) relaxor size. Within this view, cooperativity (average and maximum cluster size) increases with decreasing temperatures. Beyond the reasonably accurate description of the experiments, the model succeeds in predicting (1) the effect of increases in the fully relaxed modulus, E∞, as in semi-crystalline or strongly cross-linked polymers, (2) the strict inapplicability of time-temperature and strain-time super-positions, (3) an extended, Kohlrausch-Williams-Watts, type of relaxation response spanning 12 or more time decades, and (4) specific, meaningful, physical parameters - a minimum activation energy (similar to those of corresponding β-type transitions), the (occupied + free) volume of the primitive relaxor, and the approximate crossover temperature, Tc, and frequency, νc, both of critical importance in condensed matter dynamics. The model also has the potential of incorporating the effect of changes in free volume.Guarda Polytechnic Institute, Technology and Management School, UDI-Research Unit for Inland Development,American Institute of Physics2016-11-27T22:49:01Z2016-11-272013-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10314/3389http://hdl.handle.net/10314/3389engdoi:10.1063/1.4849227, 2013André, José ReinasJosé, Cruz Pintoinfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-01-05T02:59:04Zoai:bdigital.ipg.pt:10314/3389Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T19:24:16.081267Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Advanced Modeling of Polymer Non-Linear Stress Relaxation – Poly(methylmethacrylate) and Polycarbonate
title Advanced Modeling of Polymer Non-Linear Stress Relaxation – Poly(methylmethacrylate) and Polycarbonate
spellingShingle Advanced Modeling of Polymer Non-Linear Stress Relaxation – Poly(methylmethacrylate) and Polycarbonate
André, José Reinas
Poly(methylmethacrylate)
Polycarbonate
title_short Advanced Modeling of Polymer Non-Linear Stress Relaxation – Poly(methylmethacrylate) and Polycarbonate
title_full Advanced Modeling of Polymer Non-Linear Stress Relaxation – Poly(methylmethacrylate) and Polycarbonate
title_fullStr Advanced Modeling of Polymer Non-Linear Stress Relaxation – Poly(methylmethacrylate) and Polycarbonate
title_full_unstemmed Advanced Modeling of Polymer Non-Linear Stress Relaxation – Poly(methylmethacrylate) and Polycarbonate
title_sort Advanced Modeling of Polymer Non-Linear Stress Relaxation – Poly(methylmethacrylate) and Polycarbonate
author André, José Reinas
author_facet André, José Reinas
José, Cruz Pinto
author_role author
author2 José, Cruz Pinto
author2_role author
dc.contributor.author.fl_str_mv André, José Reinas
José, Cruz Pinto
dc.subject.por.fl_str_mv Poly(methylmethacrylate)
Polycarbonate
topic Poly(methylmethacrylate)
Polycarbonate
description Sound models of temperature- and strain-dependent (non-linear) stress relaxation are still lacking. Recent work has shown that focusing on polymers’ local backbone strains and stresses provides an adequate basis for developing such models and accurately predicting experimental stress relaxation moduli (to within 1-2% relative errors), the values of meaningful physical parameters and long time behavior, from experiments spanning only a few hours. The modeling strategy is summarized and physically discussed, and applied to two amorphous polymers – PMMA and PC. The numerical values obtained for the model parameters are also physically discussed in detail, supporting a view of the stress relaxation process where a temperature-dependent, truncated log-normal, distribution of local cooperative (or clustering) transitions become involved, at and above a minimum (or primitive) relaxor size. Within this view, cooperativity (average and maximum cluster size) increases with decreasing temperatures. Beyond the reasonably accurate description of the experiments, the model succeeds in predicting (1) the effect of increases in the fully relaxed modulus, E∞, as in semi-crystalline or strongly cross-linked polymers, (2) the strict inapplicability of time-temperature and strain-time super-positions, (3) an extended, Kohlrausch-Williams-Watts, type of relaxation response spanning 12 or more time decades, and (4) specific, meaningful, physical parameters - a minimum activation energy (similar to those of corresponding β-type transitions), the (occupied + free) volume of the primitive relaxor, and the approximate crossover temperature, Tc, and frequency, νc, both of critical importance in condensed matter dynamics. The model also has the potential of incorporating the effect of changes in free volume.
publishDate 2013
dc.date.none.fl_str_mv 2013-01-01T00:00:00Z
2016-11-27T22:49:01Z
2016-11-27
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10314/3389
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dc.relation.none.fl_str_mv doi:10.1063/1.4849227, 2013
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dc.publisher.none.fl_str_mv American Institute of Physics
publisher.none.fl_str_mv American Institute of Physics
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