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...
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Veröffentlicht in: | Journal of applied polymer science 2001-07, Vol.81 (3), p.773-781 |
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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 |
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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</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 & 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 & 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&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 & 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 & 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 & Sons, Inc. J Appl Polym Sci 81: 773–781, 2001</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><doi>10.1002/app.1494</doi><tpages>9</tpages></addata></record> |
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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) |
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