Modeling nonlinear stress relaxation of polymers

Detalhes bibliográficos
Autor(a) principal: André, José Reinas
Data de Publicação: 2014
Outros Autores: José, Cruz Pinto
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10314/3388
Resumo: Non-linear stress relaxation is far more difficult to model than creep. The present work shows that, in the case of a polymer, focusing on the polymer chains’ non-affine local strains and stresses provides a sound basis for modeling stress relaxation in a physically realistic way. This new, though still simplified, model (1) describes a clearly non-linear (strain-dependent) behavior that only becomes linear at very low strains, (2) has the potential to predict faster stress relaxation than creep, (3) is the first to account for the effect of reduced differences between the initial and final plateau modulus in the case of semi-crystalline materials, which increase the longest relaxation times, (4) explicitly quantifies the effect of temperature, when one considers the whole distribution of relaxation times, (5) may be extended to also account for the effect of changes in free volume, and (6) ensure very fast computation of relevant physical parameters and extrapolated long time behavior from experiments spanning only a few hours. All predicted features generally agree with known experimental behavior, and initial comparisons with experimental stress relaxation modulus data for a poly(methylmethacrylate) validate the formulation to within relative errors of 1.34%. The model may nevertheless still be upgraded beyond the much simplified physical picture adopted here by relaxing most the present assumptions (e.g. by upgrading the two-level process description) and, eventually, by also taking into account the effect of the fast initial strain ramp up to its nominal value. The work also discusses in detail the values and physical meaning of the model parameters.
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spelling Modeling nonlinear stress relaxation of polymersStress relaxationpolymersNon-linear stress relaxation is far more difficult to model than creep. The present work shows that, in the case of a polymer, focusing on the polymer chains’ non-affine local strains and stresses provides a sound basis for modeling stress relaxation in a physically realistic way. This new, though still simplified, model (1) describes a clearly non-linear (strain-dependent) behavior that only becomes linear at very low strains, (2) has the potential to predict faster stress relaxation than creep, (3) is the first to account for the effect of reduced differences between the initial and final plateau modulus in the case of semi-crystalline materials, which increase the longest relaxation times, (4) explicitly quantifies the effect of temperature, when one considers the whole distribution of relaxation times, (5) may be extended to also account for the effect of changes in free volume, and (6) ensure very fast computation of relevant physical parameters and extrapolated long time behavior from experiments spanning only a few hours. All predicted features generally agree with known experimental behavior, and initial comparisons with experimental stress relaxation modulus data for a poly(methylmethacrylate) validate the formulation to within relative errors of 1.34%. The model may nevertheless still be upgraded beyond the much simplified physical picture adopted here by relaxing most the present assumptions (e.g. by upgrading the two-level process description) and, eventually, by also taking into account the effect of the fast initial strain ramp up to its nominal value. The work also discusses in detail the values and physical meaning of the model parameters.Unidade de Investigação para o Desenvolvimento do Interior (UDI)Wiley Online Library - Polymer Engineering & Science2016-11-27T22:39:33Z2016-11-272014-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10314/3388http://hdl.handle.net/10314/3388engdoi: 10.1002/pen.23581André, José ReinasJosé, Cruz Pintoinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-30T03:00:07ZPortal AgregadorONG
dc.title.none.fl_str_mv Modeling nonlinear stress relaxation of polymers
title Modeling nonlinear stress relaxation of polymers
spellingShingle Modeling nonlinear stress relaxation of polymers
André, José Reinas
Stress relaxation
polymers
title_short Modeling nonlinear stress relaxation of polymers
title_full Modeling nonlinear stress relaxation of polymers
title_fullStr Modeling nonlinear stress relaxation of polymers
title_full_unstemmed Modeling nonlinear stress relaxation of polymers
title_sort Modeling nonlinear stress relaxation of polymers
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 Stress relaxation
polymers
topic Stress relaxation
polymers
description Non-linear stress relaxation is far more difficult to model than creep. The present work shows that, in the case of a polymer, focusing on the polymer chains’ non-affine local strains and stresses provides a sound basis for modeling stress relaxation in a physically realistic way. This new, though still simplified, model (1) describes a clearly non-linear (strain-dependent) behavior that only becomes linear at very low strains, (2) has the potential to predict faster stress relaxation than creep, (3) is the first to account for the effect of reduced differences between the initial and final plateau modulus in the case of semi-crystalline materials, which increase the longest relaxation times, (4) explicitly quantifies the effect of temperature, when one considers the whole distribution of relaxation times, (5) may be extended to also account for the effect of changes in free volume, and (6) ensure very fast computation of relevant physical parameters and extrapolated long time behavior from experiments spanning only a few hours. All predicted features generally agree with known experimental behavior, and initial comparisons with experimental stress relaxation modulus data for a poly(methylmethacrylate) validate the formulation to within relative errors of 1.34%. The model may nevertheless still be upgraded beyond the much simplified physical picture adopted here by relaxing most the present assumptions (e.g. by upgrading the two-level process description) and, eventually, by also taking into account the effect of the fast initial strain ramp up to its nominal value. The work also discusses in detail the values and physical meaning of the model parameters.
publishDate 2014
dc.date.none.fl_str_mv 2014-01-01T00:00:00Z
2016-11-27T22:39:33Z
2016-11-27
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10314/3388
http://hdl.handle.net/10314/3388
url http://hdl.handle.net/10314/3388
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv doi: 10.1002/pen.23581
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.publisher.none.fl_str_mv Wiley Online Library - Polymer Engineering & Science
publisher.none.fl_str_mv Wiley Online Library - Polymer Engineering & Science
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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