Morphology and Molecular Motion of Poly(ethylene terephthalate) in Polymer/Oligomer Gel
The structural heterogeneity and molecular motion in a thermoreversible gel consisting of poly(ethylene terephthalate) (PET) and a liquid ethylene glycol oligomer (PEG) was investigated by solid-state NMR and FT−Raman spectroscopies. PET was dissolved in PEG at elevated temperatures to form a concen...
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Veröffentlicht in: | Macromolecules 1998-11, Vol.31 (22), p.7706-7711 |
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description | The structural heterogeneity and molecular motion in a thermoreversible gel consisting of poly(ethylene terephthalate) (PET) and a liquid ethylene glycol oligomer (PEG) was investigated by solid-state NMR and FT−Raman spectroscopies. PET was dissolved in PEG at elevated temperatures to form a concentrated solution (30 wt %), and the solution formed a gel rapidly on cooling. For the purpose of comparison, a PET/phenol binary system and PET crystallized by annealing methods were also investigated. The longest solid-state NMR relaxation times of 13C ( 13C T 1) in PET of PET/PEG gel among the samples indicated the slowest molecular motion and the highest rigidity PET chains. The structural heterogeneity of the PET/PEG gel investigated by H T 1 measurement and confirmed by FT−Raman spectroscopy indicated phase transition during gelation. The crystallinity of PET recovered from polymer/oligomer gels is near 70% as measured by wide-angle X-ray diffraction, which is about 20% higher than that for PET samples crystallized by solution crystallization and high-temperature annealing techniques. |
doi_str_mv | 10.1021/ma9802576 |
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PET was dissolved in PEG at elevated temperatures to form a concentrated solution (30 wt %), and the solution formed a gel rapidly on cooling. For the purpose of comparison, a PET/phenol binary system and PET crystallized by annealing methods were also investigated. The longest solid-state NMR relaxation times of 13C ( 13C T 1) in PET of PET/PEG gel among the samples indicated the slowest molecular motion and the highest rigidity PET chains. The structural heterogeneity of the PET/PEG gel investigated by H T 1 measurement and confirmed by FT−Raman spectroscopy indicated phase transition during gelation. The crystallinity of PET recovered from polymer/oligomer gels is near 70% as measured by wide-angle X-ray diffraction, which is about 20% higher than that for PET samples crystallized by solution crystallization and high-temperature annealing techniques.</description><identifier>ISSN: 0024-9297</identifier><identifier>EISSN: 1520-5835</identifier><identifier>DOI: 10.1021/ma9802576</identifier><identifier>CODEN: MAMOBX</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Applied sciences ; Exact sciences and technology ; Organic polymers ; Physicochemistry of polymers ; Properties and characterization ; Solution and gel properties</subject><ispartof>Macromolecules, 1998-11, Vol.31 (22), p.7706-7711</ispartof><rights>Copyright © 1998 American Chemical Society</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a324t-c820cb37e4fb519b03f105620189dfcb8f32843a5dfe87e071d843534b590f293</citedby><cites>FETCH-LOGICAL-a324t-c820cb37e4fb519b03f105620189dfcb8f32843a5dfe87e071d843534b590f293</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ma9802576$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ma9802576$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1587558$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Xue, Gi</creatorcontrib><creatorcontrib>Ji, Gending</creatorcontrib><creatorcontrib>Yan, Hong</creatorcontrib><creatorcontrib>Guo, Mingming</creatorcontrib><title>Morphology and Molecular Motion of Poly(ethylene terephthalate) in Polymer/Oligomer Gel</title><title>Macromolecules</title><addtitle>Macromolecules</addtitle><description>The structural heterogeneity and molecular motion in a thermoreversible gel consisting of poly(ethylene terephthalate) (PET) and a liquid ethylene glycol oligomer (PEG) was investigated by solid-state NMR and FT−Raman spectroscopies. PET was dissolved in PEG at elevated temperatures to form a concentrated solution (30 wt %), and the solution formed a gel rapidly on cooling. For the purpose of comparison, a PET/phenol binary system and PET crystallized by annealing methods were also investigated. The longest solid-state NMR relaxation times of 13C ( 13C T 1) in PET of PET/PEG gel among the samples indicated the slowest molecular motion and the highest rigidity PET chains. The structural heterogeneity of the PET/PEG gel investigated by H T 1 measurement and confirmed by FT−Raman spectroscopy indicated phase transition during gelation. The crystallinity of PET recovered from polymer/oligomer gels is near 70% as measured by wide-angle X-ray diffraction, which is about 20% higher than that for PET samples crystallized by solution crystallization and high-temperature annealing techniques.</description><subject>Applied sciences</subject><subject>Exact sciences and technology</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>Properties and characterization</subject><subject>Solution and gel properties</subject><issn>0024-9297</issn><issn>1520-5835</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNptkM1OwzAQhC0EEqVw4A1yAIkeQv0T184RVdAitaKIIrhZjmM3KW4c2alE3p5AULlw2lnNt7vaAeASwVsEMRrvZMohpmxyBAaIYhhTTugxGECIkzjFKTsFZyFsIUSIJmQA3pbO14WzbtNGssqjpbNa7a30nWpKV0XORCtn2xvdFK3VlY4a7XVdNIW0stGjqKx-_J324ydbblwnopm25-DESBv0xW8dgteH-_V0Hi-eZo_Tu0UsCU6aWHEMVUaYTkxGUZpBYhCkEwwRT3OjMm4I5gmRNDeaMw0ZyruWkiSjKTQ4JUMw6vcq70Lw2ojalzvpW4Gg-E5EHBLp2KuerWVQ0hovK1WGvwHKGe3iGoK4x8rQ6M-DLf2HmDDCqFivXgR9J3g1589i0fHXPS9VEFu391X38D_nvwA9MXqj</recordid><startdate>19981103</startdate><enddate>19981103</enddate><creator>Xue, Gi</creator><creator>Ji, Gending</creator><creator>Yan, Hong</creator><creator>Guo, Mingming</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19981103</creationdate><title>Morphology and Molecular Motion of Poly(ethylene terephthalate) in Polymer/Oligomer Gel</title><author>Xue, Gi ; Ji, Gending ; Yan, Hong ; Guo, Mingming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a324t-c820cb37e4fb519b03f105620189dfcb8f32843a5dfe87e071d843534b590f293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Applied sciences</topic><topic>Exact sciences and technology</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>Properties and characterization</topic><topic>Solution and gel properties</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xue, Gi</creatorcontrib><creatorcontrib>Ji, Gending</creatorcontrib><creatorcontrib>Yan, Hong</creatorcontrib><creatorcontrib>Guo, Mingming</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xue, Gi</au><au>Ji, Gending</au><au>Yan, Hong</au><au>Guo, Mingming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Morphology and Molecular Motion of Poly(ethylene terephthalate) in Polymer/Oligomer Gel</atitle><jtitle>Macromolecules</jtitle><addtitle>Macromolecules</addtitle><date>1998-11-03</date><risdate>1998</risdate><volume>31</volume><issue>22</issue><spage>7706</spage><epage>7711</epage><pages>7706-7711</pages><issn>0024-9297</issn><eissn>1520-5835</eissn><coden>MAMOBX</coden><abstract>The structural heterogeneity and molecular motion in a thermoreversible gel consisting of poly(ethylene terephthalate) (PET) and a liquid ethylene glycol oligomer (PEG) was investigated by solid-state NMR and FT−Raman spectroscopies. PET was dissolved in PEG at elevated temperatures to form a concentrated solution (30 wt %), and the solution formed a gel rapidly on cooling. For the purpose of comparison, a PET/phenol binary system and PET crystallized by annealing methods were also investigated. The longest solid-state NMR relaxation times of 13C ( 13C T 1) in PET of PET/PEG gel among the samples indicated the slowest molecular motion and the highest rigidity PET chains. The structural heterogeneity of the PET/PEG gel investigated by H T 1 measurement and confirmed by FT−Raman spectroscopy indicated phase transition during gelation. The crystallinity of PET recovered from polymer/oligomer gels is near 70% as measured by wide-angle X-ray diffraction, which is about 20% higher than that for PET samples crystallized by solution crystallization and high-temperature annealing techniques.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ma9802576</doi><tpages>6</tpages></addata></record> |
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subjects | Applied sciences Exact sciences and technology Organic polymers Physicochemistry of polymers Properties and characterization Solution and gel properties |
title | Morphology and Molecular Motion of Poly(ethylene terephthalate) in Polymer/Oligomer Gel |
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