Physical ageing and short-term creep in amorphous and semicrystalline polymers
Studies have been made of the effect of physical ageing at 23°C on the short-term creep of polycarbonate (PC), poly(butylene terephthalate) (PBT) and high density polyethylene (HDPE) at creep times between 10 −8 and 10 5 s. The age state of each polymer sample was specified by the elapsed time t e a...
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Veröffentlicht in: | Polymer 1990-07, Vol.31 (7), p.1204-1215 |
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creator | Read, B.E. tomlins, P.E. Dean, G.D. |
description | Studies have been made of the effect of physical ageing at 23°C on the short-term creep of polycarbonate (PC), poly(butylene terephthalate) (PBT) and high density polyethylene (HDPE) at creep times between 10
−8 and 10
5 s. The age state of each polymer sample was specified by the elapsed time
t
e at 23°C between quenching from a temperature at which the structure is close to equilibrium with respect to the α-retardation process and the start of a creep test. With increasing age, a small decrease was evident in the relaxed compliance
D
R
β
of the β-retardation process in each polymer and relationships between
D
R
β
and
t
e were derived from quantitative analyses of the data. For the amorphous PC and semicrystalline PBT, this decrease could reflect a slight reduction in the number of groups participating in the localized secondary process. It also appeared for PC and PBT that the average retardation time for the glass-rubber α-process increased with
t
e, with negligible change in the shape of the retardation time distribution or the magnitude of the α-retardation. For HDPE, the small decrease in
D
R
β
with increasing
t
e for the glass-rubber β-process is similar to that found for polypropylene and might involve conformational changes of amorphous tie-molecules. The results for HDPE deviate from the predictions of Struik's model of ageing in semicrystalline polymers and suggest that, for the crystal-related α-process, changes in retardation magnitude or shape of the retardation time distribution may occur with increasing age. |
doi_str_mv | 10.1016/0032-3861(90)90209-H |
format | Article |
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−8 and 10
5 s. The age state of each polymer sample was specified by the elapsed time
t
e at 23°C between quenching from a temperature at which the structure is close to equilibrium with respect to the α-retardation process and the start of a creep test. With increasing age, a small decrease was evident in the relaxed compliance
D
R
β
of the β-retardation process in each polymer and relationships between
D
R
β
and
t
e were derived from quantitative analyses of the data. For the amorphous PC and semicrystalline PBT, this decrease could reflect a slight reduction in the number of groups participating in the localized secondary process. It also appeared for PC and PBT that the average retardation time for the glass-rubber α-process increased with
t
e, with negligible change in the shape of the retardation time distribution or the magnitude of the α-retardation. For HDPE, the small decrease in
D
R
β
with increasing
t
e for the glass-rubber β-process is similar to that found for polypropylene and might involve conformational changes of amorphous tie-molecules. The results for HDPE deviate from the predictions of Struik's model of ageing in semicrystalline polymers and suggest that, for the crystal-related α-process, changes in retardation magnitude or shape of the retardation time distribution may occur with increasing age.</description><identifier>ISSN: 0032-3861</identifier><identifier>EISSN: 1873-2291</identifier><identifier>DOI: 10.1016/0032-3861(90)90209-H</identifier><identifier>CODEN: POLMAG</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>amorphous polymers ; Applied sciences ; creep ; Exact sciences and technology ; Organic polymers ; physical ageing ; Physicochemistry of polymers ; Properties and characterization ; Rheology and viscoelasticity ; semicrystalline polymers</subject><ispartof>Polymer, 1990-07, Vol.31 (7), p.1204-1215</ispartof><rights>1990</rights><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c426t-86868d8c99d39df58438973928335936fbdbfc05cb9f860d3ba0b4c56392927d3</citedby><cites>FETCH-LOGICAL-c426t-86868d8c99d39df58438973928335936fbdbfc05cb9f860d3ba0b4c56392927d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0032-3861(90)90209-H$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>313,314,780,784,792,3548,27921,27923,27924,45994</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5089725$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Read, B.E.</creatorcontrib><creatorcontrib>tomlins, P.E.</creatorcontrib><creatorcontrib>Dean, G.D.</creatorcontrib><title>Physical ageing and short-term creep in amorphous and semicrystalline polymers</title><title>Polymer</title><description>Studies have been made of the effect of physical ageing at 23°C on the short-term creep of polycarbonate (PC), poly(butylene terephthalate) (PBT) and high density polyethylene (HDPE) at creep times between 10
−8 and 10
5 s. The age state of each polymer sample was specified by the elapsed time
t
e at 23°C between quenching from a temperature at which the structure is close to equilibrium with respect to the α-retardation process and the start of a creep test. With increasing age, a small decrease was evident in the relaxed compliance
D
R
β
of the β-retardation process in each polymer and relationships between
D
R
β
and
t
e were derived from quantitative analyses of the data. For the amorphous PC and semicrystalline PBT, this decrease could reflect a slight reduction in the number of groups participating in the localized secondary process. It also appeared for PC and PBT that the average retardation time for the glass-rubber α-process increased with
t
e, with negligible change in the shape of the retardation time distribution or the magnitude of the α-retardation. For HDPE, the small decrease in
D
R
β
with increasing
t
e for the glass-rubber β-process is similar to that found for polypropylene and might involve conformational changes of amorphous tie-molecules. The results for HDPE deviate from the predictions of Struik's model of ageing in semicrystalline polymers and suggest that, for the crystal-related α-process, changes in retardation magnitude or shape of the retardation time distribution may occur with increasing age.</description><subject>amorphous polymers</subject><subject>Applied sciences</subject><subject>creep</subject><subject>Exact sciences and technology</subject><subject>Organic polymers</subject><subject>physical ageing</subject><subject>Physicochemistry of polymers</subject><subject>Properties and characterization</subject><subject>Rheology and viscoelasticity</subject><subject>semicrystalline polymers</subject><issn>0032-3861</issn><issn>1873-2291</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><recordid>eNqNkU1LAzEQhoMoWKv_wMMeRPSwOpvsR3IRpKgVinrQc8gms21kv0y2wv57U1t6FJnDXJ53ZniGkPMEbhJI8lsARmPG8-RKwLUACiKeH5BJwgsWUyqSQzLZI8fkxPtPAKAZTSfk5W01eqtVHakl2nYZqdZEftW5IR7QNZF2iH1k20g1netX3dpvCWysdqMfVF3bFqO-q8cGnT8lR5WqPZ7t-pR8PD68z-bx4vXpeXa_iHVK8yHmeSjDtRCGCVNlPGVcFExQzlgmWF6Vpqw0ZLoUFc_BsFJBmeosD4ighWFTcrmd27vua41-kI31GutatRhulDTjSQpp8S-QFYL9CwTO8wCmW1C7znuHleydbZQbZQJy8w65cS03rqUA-fsOOQ-xi9185YPuyqlWW7_PZhAE0Cxgd1sMg71vi056bbHVaKxDPUjT2b_3_ACgvJ2R</recordid><startdate>19900701</startdate><enddate>19900701</enddate><creator>Read, B.E.</creator><creator>tomlins, P.E.</creator><creator>Dean, G.D.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>7SR</scope><scope>JG9</scope><scope>7U5</scope><scope>L7M</scope></search><sort><creationdate>19900701</creationdate><title>Physical ageing and short-term creep in amorphous and semicrystalline polymers</title><author>Read, B.E. ; tomlins, P.E. ; Dean, G.D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c426t-86868d8c99d39df58438973928335936fbdbfc05cb9f860d3ba0b4c56392927d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>amorphous polymers</topic><topic>Applied sciences</topic><topic>creep</topic><topic>Exact sciences and technology</topic><topic>Organic polymers</topic><topic>physical ageing</topic><topic>Physicochemistry of polymers</topic><topic>Properties and characterization</topic><topic>Rheology and viscoelasticity</topic><topic>semicrystalline polymers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Read, B.E.</creatorcontrib><creatorcontrib>tomlins, P.E.</creatorcontrib><creatorcontrib>Dean, G.D.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Engineered Materials Abstracts</collection><collection>Materials Research Database</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Polymer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Read, B.E.</au><au>tomlins, P.E.</au><au>Dean, G.D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Physical ageing and short-term creep in amorphous and semicrystalline polymers</atitle><jtitle>Polymer</jtitle><date>1990-07-01</date><risdate>1990</risdate><volume>31</volume><issue>7</issue><spage>1204</spage><epage>1215</epage><pages>1204-1215</pages><issn>0032-3861</issn><eissn>1873-2291</eissn><coden>POLMAG</coden><abstract>Studies have been made of the effect of physical ageing at 23°C on the short-term creep of polycarbonate (PC), poly(butylene terephthalate) (PBT) and high density polyethylene (HDPE) at creep times between 10
−8 and 10
5 s. The age state of each polymer sample was specified by the elapsed time
t
e at 23°C between quenching from a temperature at which the structure is close to equilibrium with respect to the α-retardation process and the start of a creep test. With increasing age, a small decrease was evident in the relaxed compliance
D
R
β
of the β-retardation process in each polymer and relationships between
D
R
β
and
t
e were derived from quantitative analyses of the data. For the amorphous PC and semicrystalline PBT, this decrease could reflect a slight reduction in the number of groups participating in the localized secondary process. It also appeared for PC and PBT that the average retardation time for the glass-rubber α-process increased with
t
e, with negligible change in the shape of the retardation time distribution or the magnitude of the α-retardation. For HDPE, the small decrease in
D
R
β
with increasing
t
e for the glass-rubber β-process is similar to that found for polypropylene and might involve conformational changes of amorphous tie-molecules. The results for HDPE deviate from the predictions of Struik's model of ageing in semicrystalline polymers and suggest that, for the crystal-related α-process, changes in retardation magnitude or shape of the retardation time distribution may occur with increasing age.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/0032-3861(90)90209-H</doi><tpages>12</tpages></addata></record> |
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language | eng |
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source | ScienceDirect Journals (5 years ago - present) |
subjects | amorphous polymers Applied sciences creep Exact sciences and technology Organic polymers physical ageing Physicochemistry of polymers Properties and characterization Rheology and viscoelasticity semicrystalline polymers |
title | Physical ageing and short-term creep in amorphous and semicrystalline polymers |
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