Crystallization and thermoreversible gelation of poly(butylene terephthalate)-epoxy mixtures
The thermoreversible gelation of solutions of poly(butylene terephthalate) (PBT) and a liquid diglycidyl ether of bisphenol‐A epoxy has been investigated. The morphology of the gels and the conditions under which they form have been characterized by optical microscopy, thermal analysis, and x‐ray sc...
Gespeichert in:
Veröffentlicht in: | Journal of polymer science. Part B, Polymer physics Polymer physics, 1994-07, Vol.32 (9), p.1607-1616 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1616 |
---|---|
container_issue | 9 |
container_start_page | 1607 |
container_title | Journal of polymer science. Part B, Polymer physics |
container_volume | 32 |
creator | Nichols, Mark E. Robertson, Richard E. |
description | The thermoreversible gelation of solutions of poly(butylene terephthalate) (PBT) and a liquid diglycidyl ether of bisphenol‐A epoxy has been investigated. The morphology of the gels and the conditions under which they form have been characterized by optical microscopy, thermal analysis, and x‐ray scattering. Gels were found to form under two different conditions and with different morphologies. Gels formed after a considerable delay when homogenous PBT‐epoxy solutions were cooled to slightly below the dissolution temperature of crystalline PBT. These gels contained large, irregular PBT spherulites and smaller birefringent interspherulitic matter. The melting of these gels and the onset of macroscopic flow coincided with the melting of the interspherulitic matter, and occurred before the melting of the large spherulites. Thermoreversible gels formed very quickly when PBT‐epoxy solutions were self‐nucleated by heating a dispersion of crystalline PBT in epoxy slightly and briefly above the dissolution temperature and then cooling. These gels displayed only a weak background birefringence and were molten when the weak birefringence disappeared. In both cases, gelation occurred by the formation of a three‐dimensional PBT network in the epoxy liquid, and the nodes of the network were crystalline PBT particles. $ 1994 John Wiley & Sons, Inc. |
doi_str_mv | 10.1002/polb.1994.090320903 |
format | Article |
fullrecord | <record><control><sourceid>wiley_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_polb_1994_090320903</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>POLB090320903</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4353-b654cdf4daed2859ad6ad9768d23f396e0dda01d467473a45da7c842d149f3a43</originalsourceid><addsrcrecordid>eNqNkE9Lw0AQxRdRsFY_gZccPOghdZPdbLIXQYu2QrUi_ulBWLbZiY1uk7C71cZPb0JK8ehlhmHe-z14CB0HeBBgHJ5XpZ4PAs7pAHNMwnbsoF6AOfcxTZJd1MNJEvssZGwfHVj7gXHzi3gPvQ1NbZ3UOv-RLi8LTxbKcwswy9LAFxibzzV476C7b5l5TVZ9Ol-5WkMBngMD1cItZCOAMx-qcl17y3ztVgbsIdrLpLZwtNl99Hxz_TQc-5Pp6HZ4OfFTSiLiz1lEU5VRJUGFScSlYlLxmCUqJBnhDLBSEgeKspjGRNJIyThNaKgCyrPmJn1EOm5qSmsNZKIy-VKaWgRYtAWJtiDRFiS2BTWuk85VSZtKnRlZpLndWmmQbGQXnew711D_hyweppOrvzl-B8itg_UWIM2nYDGJI_F6PxLju8cZfhnNREh-ATxWi0k</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Crystallization and thermoreversible gelation of poly(butylene terephthalate)-epoxy mixtures</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Nichols, Mark E. ; Robertson, Richard E.</creator><creatorcontrib>Nichols, Mark E. ; Robertson, Richard E.</creatorcontrib><description>The thermoreversible gelation of solutions of poly(butylene terephthalate) (PBT) and a liquid diglycidyl ether of bisphenol‐A epoxy has been investigated. The morphology of the gels and the conditions under which they form have been characterized by optical microscopy, thermal analysis, and x‐ray scattering. Gels were found to form under two different conditions and with different morphologies. Gels formed after a considerable delay when homogenous PBT‐epoxy solutions were cooled to slightly below the dissolution temperature of crystalline PBT. These gels contained large, irregular PBT spherulites and smaller birefringent interspherulitic matter. The melting of these gels and the onset of macroscopic flow coincided with the melting of the interspherulitic matter, and occurred before the melting of the large spherulites. Thermoreversible gels formed very quickly when PBT‐epoxy solutions were self‐nucleated by heating a dispersion of crystalline PBT in epoxy slightly and briefly above the dissolution temperature and then cooling. These gels displayed only a weak background birefringence and were molten when the weak birefringence disappeared. In both cases, gelation occurred by the formation of a three‐dimensional PBT network in the epoxy liquid, and the nodes of the network were crystalline PBT particles. $ 1994 John Wiley & Sons, Inc.</description><identifier>ISSN: 0887-6266</identifier><identifier>EISSN: 1099-0488</identifier><identifier>DOI: 10.1002/polb.1994.090320903</identifier><identifier>CODEN: JPLPAY</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>Applied sciences ; Crystallization ; epoxy ; Exact sciences and technology ; nucleation ; Organic polymers ; Physicochemistry of polymers ; poly(butylene terephthalate) ; Properties and characterization ; spherulites ; thermoreversible gels</subject><ispartof>Journal of polymer science. Part B, Polymer physics, 1994-07, Vol.32 (9), p.1607-1616</ispartof><rights>Copyright © 1994 John Wiley & Sons, Inc.</rights><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4353-b654cdf4daed2859ad6ad9768d23f396e0dda01d467473a45da7c842d149f3a43</citedby><cites>FETCH-LOGICAL-c4353-b654cdf4daed2859ad6ad9768d23f396e0dda01d467473a45da7c842d149f3a43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fpolb.1994.090320903$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpolb.1994.090320903$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4180903$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Nichols, Mark E.</creatorcontrib><creatorcontrib>Robertson, Richard E.</creatorcontrib><title>Crystallization and thermoreversible gelation of poly(butylene terephthalate)-epoxy mixtures</title><title>Journal of polymer science. Part B, Polymer physics</title><addtitle>J. Polym. Sci. B Polym. Phys</addtitle><description>The thermoreversible gelation of solutions of poly(butylene terephthalate) (PBT) and a liquid diglycidyl ether of bisphenol‐A epoxy has been investigated. The morphology of the gels and the conditions under which they form have been characterized by optical microscopy, thermal analysis, and x‐ray scattering. Gels were found to form under two different conditions and with different morphologies. Gels formed after a considerable delay when homogenous PBT‐epoxy solutions were cooled to slightly below the dissolution temperature of crystalline PBT. These gels contained large, irregular PBT spherulites and smaller birefringent interspherulitic matter. The melting of these gels and the onset of macroscopic flow coincided with the melting of the interspherulitic matter, and occurred before the melting of the large spherulites. Thermoreversible gels formed very quickly when PBT‐epoxy solutions were self‐nucleated by heating a dispersion of crystalline PBT in epoxy slightly and briefly above the dissolution temperature and then cooling. These gels displayed only a weak background birefringence and were molten when the weak birefringence disappeared. In both cases, gelation occurred by the formation of a three‐dimensional PBT network in the epoxy liquid, and the nodes of the network were crystalline PBT particles. $ 1994 John Wiley & Sons, Inc.</description><subject>Applied sciences</subject><subject>Crystallization</subject><subject>epoxy</subject><subject>Exact sciences and technology</subject><subject>nucleation</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>poly(butylene terephthalate)</subject><subject>Properties and characterization</subject><subject>spherulites</subject><subject>thermoreversible gels</subject><issn>0887-6266</issn><issn>1099-0488</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><recordid>eNqNkE9Lw0AQxRdRsFY_gZccPOghdZPdbLIXQYu2QrUi_ulBWLbZiY1uk7C71cZPb0JK8ehlhmHe-z14CB0HeBBgHJ5XpZ4PAs7pAHNMwnbsoF6AOfcxTZJd1MNJEvssZGwfHVj7gXHzi3gPvQ1NbZ3UOv-RLi8LTxbKcwswy9LAFxibzzV476C7b5l5TVZ9Ol-5WkMBngMD1cItZCOAMx-qcl17y3ztVgbsIdrLpLZwtNl99Hxz_TQc-5Pp6HZ4OfFTSiLiz1lEU5VRJUGFScSlYlLxmCUqJBnhDLBSEgeKspjGRNJIyThNaKgCyrPmJn1EOm5qSmsNZKIy-VKaWgRYtAWJtiDRFiS2BTWuk85VSZtKnRlZpLndWmmQbGQXnew711D_hyweppOrvzl-B8itg_UWIM2nYDGJI_F6PxLju8cZfhnNREh-ATxWi0k</recordid><startdate>19940715</startdate><enddate>19940715</enddate><creator>Nichols, Mark E.</creator><creator>Robertson, Richard E.</creator><general>John Wiley & Sons, Inc</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19940715</creationdate><title>Crystallization and thermoreversible gelation of poly(butylene terephthalate)-epoxy mixtures</title><author>Nichols, Mark E. ; Robertson, Richard E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4353-b654cdf4daed2859ad6ad9768d23f396e0dda01d467473a45da7c842d149f3a43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Applied sciences</topic><topic>Crystallization</topic><topic>epoxy</topic><topic>Exact sciences and technology</topic><topic>nucleation</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>poly(butylene terephthalate)</topic><topic>Properties and characterization</topic><topic>spherulites</topic><topic>thermoreversible gels</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nichols, Mark E.</creatorcontrib><creatorcontrib>Robertson, Richard E.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Journal of polymer science. Part B, Polymer physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nichols, Mark E.</au><au>Robertson, Richard E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Crystallization and thermoreversible gelation of poly(butylene terephthalate)-epoxy mixtures</atitle><jtitle>Journal of polymer science. Part B, Polymer physics</jtitle><addtitle>J. Polym. Sci. B Polym. Phys</addtitle><date>1994-07-15</date><risdate>1994</risdate><volume>32</volume><issue>9</issue><spage>1607</spage><epage>1616</epage><pages>1607-1616</pages><issn>0887-6266</issn><eissn>1099-0488</eissn><coden>JPLPAY</coden><abstract>The thermoreversible gelation of solutions of poly(butylene terephthalate) (PBT) and a liquid diglycidyl ether of bisphenol‐A epoxy has been investigated. The morphology of the gels and the conditions under which they form have been characterized by optical microscopy, thermal analysis, and x‐ray scattering. Gels were found to form under two different conditions and with different morphologies. Gels formed after a considerable delay when homogenous PBT‐epoxy solutions were cooled to slightly below the dissolution temperature of crystalline PBT. These gels contained large, irregular PBT spherulites and smaller birefringent interspherulitic matter. The melting of these gels and the onset of macroscopic flow coincided with the melting of the interspherulitic matter, and occurred before the melting of the large spherulites. Thermoreversible gels formed very quickly when PBT‐epoxy solutions were self‐nucleated by heating a dispersion of crystalline PBT in epoxy slightly and briefly above the dissolution temperature and then cooling. These gels displayed only a weak background birefringence and were molten when the weak birefringence disappeared. In both cases, gelation occurred by the formation of a three‐dimensional PBT network in the epoxy liquid, and the nodes of the network were crystalline PBT particles. $ 1994 John Wiley & Sons, Inc.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><doi>10.1002/polb.1994.090320903</doi><tpages>10</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0887-6266 |
ispartof | Journal of polymer science. Part B, Polymer physics, 1994-07, Vol.32 (9), p.1607-1616 |
issn | 0887-6266 1099-0488 |
language | eng |
recordid | cdi_crossref_primary_10_1002_polb_1994_090320903 |
source | Wiley Online Library Journals Frontfile Complete |
subjects | Applied sciences Crystallization epoxy Exact sciences and technology nucleation Organic polymers Physicochemistry of polymers poly(butylene terephthalate) Properties and characterization spherulites thermoreversible gels |
title | Crystallization and thermoreversible gelation of poly(butylene terephthalate)-epoxy mixtures |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T20%3A20%3A23IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wiley_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Crystallization%20and%20thermoreversible%20gelation%20of%20poly(butylene%20terephthalate)-epoxy%20mixtures&rft.jtitle=Journal%20of%20polymer%20science.%20Part%20B,%20Polymer%20physics&rft.au=Nichols,%20Mark%20E.&rft.date=1994-07-15&rft.volume=32&rft.issue=9&rft.spage=1607&rft.epage=1616&rft.pages=1607-1616&rft.issn=0887-6266&rft.eissn=1099-0488&rft.coden=JPLPAY&rft_id=info:doi/10.1002/polb.1994.090320903&rft_dat=%3Cwiley_cross%3EPOLB090320903%3C/wiley_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |