Synthesis and thermal properties of poly(urethane-imide)

The synthesis and thermal properties of thermoplastic poly(urethane‐imide) (PUI) resins were studied. Model reaction studies on the reactions of 4,4′‐diphenylcarbamatodiphenylmethane and 4,4′‐diisocyanatodiphenylmethane with phthalic anhydride were performed. We found that the reaction of anhydrides...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of applied polymer science 2001-07, Vol.81 (3), p.773-781
Hauptverfasser: Jiang, Bibiao, Hao, Jianjun, Wang, Wenyun, Jiang, Luxia, Cai, Xinxian
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 781
container_issue 3
container_start_page 773
container_title Journal of applied polymer science
container_volume 81
creator Jiang, Bibiao
Hao, Jianjun
Wang, Wenyun
Jiang, Luxia
Cai, Xinxian
description The synthesis and thermal properties of thermoplastic poly(urethane‐imide) (PUI) resins were studied. Model reaction studies on the reactions of 4,4′‐diphenylcarbamatodiphenylmethane and 4,4′‐diisocyanatodiphenylmethane with phthalic anhydride were performed. We found that the reaction of anhydrides with urethane groups could take place under certain reaction conditions. According to the model reaction studies, N‐2‐methyl‐pyrrolidone was employed as a solvent, and no catalyst was used in the polymerization. To restrain the side reaction of anhydrides with urethane groups, we adopted a two‐step chain‐extending procedure in a chain‐extending reaction. The inherent viscosity of PUI was 0.83–0.99 dL/g. The prepared polymers not only exhibited improved solubility in organic solvents but also formed flexible films. Thermogravimetric analysis showed that PUI exhibited a two‐step thermal weight‐loss pattern. The first step of the thermal degradation of PUI was attributed to the thermooxidizing cleavage of weak and labile linkage, such as urethane groups, isopropylidene, and methylene, except for imide rings. The polymer inherent viscosity decreased sharply during the first step of thermal degradation. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 81: 773–781, 2001
doi_str_mv 10.1002/app.1494
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_26984631</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>26984631</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3604-eed8353e12862ab296e93e1cd62cd7dfb8c76ae04a50f2a2476ba8723278ad7c3</originalsourceid><addsrcrecordid>eNp1kF1LwzAUhoMoOKfgTygIohed-WiT9HIM3YQxJ35dhiw9ZdF2rUmH9t-bsbI7r845nIeHlxehS4JHBGN6p5tmRJIsOUIDgjMRJ5zKYzQILxLLLEtP0Zn3nxgTkmI-QPKl27Rr8NZHepNHYXWVLqPG1Q241oKP6iJq6rK72Tpo13oDsa1sDrfn6KTQpYeLfg7R28P962QWz5-mj5PxPDaM4yQGyCVLGRAqOdUrmnHIwmVyTk0u8mIljeAacKJTXFBNE8FXWgrKqJA6F4YN0fXeGyJ9b8G3qrLeQFmGKPXWK8ozmXBGAnizB42rvXdQqMbZSrtOEax21ahQjdpVE9Cr3qm90WXh9MZYf-CDkBEeqHhP_dgSun9tarxc9taet76F3wOv3ZfigolUfSym6p1MZpPseaYW7A_fiYA-</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>26984631</pqid></control><display><type>article</type><title>Synthesis and thermal properties of poly(urethane-imide)</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Jiang, Bibiao ; Hao, Jianjun ; Wang, Wenyun ; Jiang, Luxia ; Cai, Xinxian</creator><creatorcontrib>Jiang, Bibiao ; Hao, Jianjun ; Wang, Wenyun ; Jiang, Luxia ; Cai, Xinxian</creatorcontrib><description>The synthesis and thermal properties of thermoplastic poly(urethane‐imide) (PUI) resins were studied. Model reaction studies on the reactions of 4,4′‐diphenylcarbamatodiphenylmethane and 4,4′‐diisocyanatodiphenylmethane with phthalic anhydride were performed. We found that the reaction of anhydrides with urethane groups could take place under certain reaction conditions. According to the model reaction studies, N‐2‐methyl‐pyrrolidone was employed as a solvent, and no catalyst was used in the polymerization. To restrain the side reaction of anhydrides with urethane groups, we adopted a two‐step chain‐extending procedure in a chain‐extending reaction. The inherent viscosity of PUI was 0.83–0.99 dL/g. The prepared polymers not only exhibited improved solubility in organic solvents but also formed flexible films. Thermogravimetric analysis showed that PUI exhibited a two‐step thermal weight‐loss pattern. The first step of the thermal degradation of PUI was attributed to the thermooxidizing cleavage of weak and labile linkage, such as urethane groups, isopropylidene, and methylene, except for imide rings. The polymer inherent viscosity decreased sharply during the first step of thermal degradation. © 2001 John Wiley &amp; Sons, Inc. J Appl Polym Sci 81: 773–781, 2001</description><identifier>ISSN: 0021-8995</identifier><identifier>EISSN: 1097-4628</identifier><identifier>DOI: 10.1002/app.1494</identifier><identifier>CODEN: JAPNAB</identifier><language>eng</language><publisher>New York: John Wiley &amp; Sons, Inc</publisher><subject>Applied sciences ; Exact sciences and technology ; Organic polymers ; Physicochemistry of polymers ; poly(urethane-imide) ; Polycondensation ; polyimide ; polyurethane ; Preparation, kinetics, thermodynamics, mechanism and catalysts ; thermal properties ; thermogravimetric analysis</subject><ispartof>Journal of applied polymer science, 2001-07, Vol.81 (3), p.773-781</ispartof><rights>Copyright © 2001 John Wiley &amp; Sons, Inc.</rights><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3604-eed8353e12862ab296e93e1cd62cd7dfb8c76ae04a50f2a2476ba8723278ad7c3</citedby><cites>FETCH-LOGICAL-c3604-eed8353e12862ab296e93e1cd62cd7dfb8c76ae04a50f2a2476ba8723278ad7c3</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%2Fapp.1494$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fapp.1494$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=984316$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Jiang, Bibiao</creatorcontrib><creatorcontrib>Hao, Jianjun</creatorcontrib><creatorcontrib>Wang, Wenyun</creatorcontrib><creatorcontrib>Jiang, Luxia</creatorcontrib><creatorcontrib>Cai, Xinxian</creatorcontrib><title>Synthesis and thermal properties of poly(urethane-imide)</title><title>Journal of applied polymer science</title><addtitle>J. Appl. Polym. Sci</addtitle><description>The synthesis and thermal properties of thermoplastic poly(urethane‐imide) (PUI) resins were studied. Model reaction studies on the reactions of 4,4′‐diphenylcarbamatodiphenylmethane and 4,4′‐diisocyanatodiphenylmethane with phthalic anhydride were performed. We found that the reaction of anhydrides with urethane groups could take place under certain reaction conditions. According to the model reaction studies, N‐2‐methyl‐pyrrolidone was employed as a solvent, and no catalyst was used in the polymerization. To restrain the side reaction of anhydrides with urethane groups, we adopted a two‐step chain‐extending procedure in a chain‐extending reaction. The inherent viscosity of PUI was 0.83–0.99 dL/g. The prepared polymers not only exhibited improved solubility in organic solvents but also formed flexible films. Thermogravimetric analysis showed that PUI exhibited a two‐step thermal weight‐loss pattern. The first step of the thermal degradation of PUI was attributed to the thermooxidizing cleavage of weak and labile linkage, such as urethane groups, isopropylidene, and methylene, except for imide rings. The polymer inherent viscosity decreased sharply during the first step of thermal degradation. © 2001 John Wiley &amp; Sons, Inc. J Appl Polym Sci 81: 773–781, 2001</description><subject>Applied sciences</subject><subject>Exact sciences and technology</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>poly(urethane-imide)</subject><subject>Polycondensation</subject><subject>polyimide</subject><subject>polyurethane</subject><subject>Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><subject>thermal properties</subject><subject>thermogravimetric analysis</subject><issn>0021-8995</issn><issn>1097-4628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNp1kF1LwzAUhoMoOKfgTygIohed-WiT9HIM3YQxJ35dhiw9ZdF2rUmH9t-bsbI7r845nIeHlxehS4JHBGN6p5tmRJIsOUIDgjMRJ5zKYzQILxLLLEtP0Zn3nxgTkmI-QPKl27Rr8NZHepNHYXWVLqPG1Q241oKP6iJq6rK72Tpo13oDsa1sDrfn6KTQpYeLfg7R28P962QWz5-mj5PxPDaM4yQGyCVLGRAqOdUrmnHIwmVyTk0u8mIljeAacKJTXFBNE8FXWgrKqJA6F4YN0fXeGyJ9b8G3qrLeQFmGKPXWK8ozmXBGAnizB42rvXdQqMbZSrtOEax21ahQjdpVE9Cr3qm90WXh9MZYf-CDkBEeqHhP_dgSun9tarxc9taet76F3wOv3ZfigolUfSym6p1MZpPseaYW7A_fiYA-</recordid><startdate>20010718</startdate><enddate>20010718</enddate><creator>Jiang, Bibiao</creator><creator>Hao, Jianjun</creator><creator>Wang, Wenyun</creator><creator>Jiang, Luxia</creator><creator>Cai, Xinxian</creator><general>John Wiley &amp; Sons, Inc</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20010718</creationdate><title>Synthesis and thermal properties of poly(urethane-imide)</title><author>Jiang, Bibiao ; Hao, Jianjun ; Wang, Wenyun ; Jiang, Luxia ; Cai, Xinxian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3604-eed8353e12862ab296e93e1cd62cd7dfb8c76ae04a50f2a2476ba8723278ad7c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Applied sciences</topic><topic>Exact sciences and technology</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>poly(urethane-imide)</topic><topic>Polycondensation</topic><topic>polyimide</topic><topic>polyurethane</topic><topic>Preparation, kinetics, thermodynamics, mechanism and catalysts</topic><topic>thermal properties</topic><topic>thermogravimetric analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jiang, Bibiao</creatorcontrib><creatorcontrib>Hao, Jianjun</creatorcontrib><creatorcontrib>Wang, Wenyun</creatorcontrib><creatorcontrib>Jiang, Luxia</creatorcontrib><creatorcontrib>Cai, Xinxian</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Journal of applied polymer science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jiang, Bibiao</au><au>Hao, Jianjun</au><au>Wang, Wenyun</au><au>Jiang, Luxia</au><au>Cai, Xinxian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and thermal properties of poly(urethane-imide)</atitle><jtitle>Journal of applied polymer science</jtitle><addtitle>J. Appl. Polym. Sci</addtitle><date>2001-07-18</date><risdate>2001</risdate><volume>81</volume><issue>3</issue><spage>773</spage><epage>781</epage><pages>773-781</pages><issn>0021-8995</issn><eissn>1097-4628</eissn><coden>JAPNAB</coden><abstract>The synthesis and thermal properties of thermoplastic poly(urethane‐imide) (PUI) resins were studied. Model reaction studies on the reactions of 4,4′‐diphenylcarbamatodiphenylmethane and 4,4′‐diisocyanatodiphenylmethane with phthalic anhydride were performed. We found that the reaction of anhydrides with urethane groups could take place under certain reaction conditions. According to the model reaction studies, N‐2‐methyl‐pyrrolidone was employed as a solvent, and no catalyst was used in the polymerization. To restrain the side reaction of anhydrides with urethane groups, we adopted a two‐step chain‐extending procedure in a chain‐extending reaction. The inherent viscosity of PUI was 0.83–0.99 dL/g. The prepared polymers not only exhibited improved solubility in organic solvents but also formed flexible films. Thermogravimetric analysis showed that PUI exhibited a two‐step thermal weight‐loss pattern. The first step of the thermal degradation of PUI was attributed to the thermooxidizing cleavage of weak and labile linkage, such as urethane groups, isopropylidene, and methylene, except for imide rings. The polymer inherent viscosity decreased sharply during the first step of thermal degradation. © 2001 John Wiley &amp; Sons, Inc. J Appl Polym Sci 81: 773–781, 2001</abstract><cop>New York</cop><pub>John Wiley &amp; Sons, Inc</pub><doi>10.1002/app.1494</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0021-8995
ispartof Journal of applied polymer science, 2001-07, Vol.81 (3), p.773-781
issn 0021-8995
1097-4628
language eng
recordid cdi_proquest_miscellaneous_26984631
source Wiley Online Library Journals Frontfile Complete
subjects Applied sciences
Exact sciences and technology
Organic polymers
Physicochemistry of polymers
poly(urethane-imide)
Polycondensation
polyimide
polyurethane
Preparation, kinetics, thermodynamics, mechanism and catalysts
thermal properties
thermogravimetric analysis
title Synthesis and thermal properties of poly(urethane-imide)
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-13T05%3A02%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20and%20thermal%20properties%20of%20poly(urethane-imide)&rft.jtitle=Journal%20of%20applied%20polymer%20science&rft.au=Jiang,%20Bibiao&rft.date=2001-07-18&rft.volume=81&rft.issue=3&rft.spage=773&rft.epage=781&rft.pages=773-781&rft.issn=0021-8995&rft.eissn=1097-4628&rft.coden=JAPNAB&rft_id=info:doi/10.1002/app.1494&rft_dat=%3Cproquest_cross%3E26984631%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=26984631&rft_id=info:pmid/&rfr_iscdi=true