Shape memory crosslinked polyurethanes containing thermoreversible Diels-Alder couplings
ABSTRACT Crosslinked polyurethanes (PUs) containing irreversible (allophanate) and reversible Diels‐Alder chemical bonds were synthesized using various diisocyanates (methylene diphenyl diisocyanate MDI, 1,6‐hexamethylenediisocyanate HDI) and poly(ɛ‐caprolactone) ((PCL) with different molecular weig...
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creator | Lakatos, Csilla Czifrák, Katalin Karger-Kocsis, József Daróczi, Lajos Zsuga, Miklós Kéki, Sándor |
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Crosslinked polyurethanes (PUs) containing irreversible (allophanate) and reversible Diels‐Alder chemical bonds were synthesized using various diisocyanates (methylene diphenyl diisocyanate MDI, 1,6‐hexamethylenediisocyanate HDI) and poly(ɛ‐caprolactone) ((PCL) with different molecular weights (Mn = 10 kg/mol, 25 kg/mol, 50 kg/mol) as diol component. The melting/crystallization of PCL and the reversible DA bonds acted as temperature‐activated switches for shape memory performances, while allophanate network provided the permanent crosslinks for these PUs. The reversible DA bonds were obtained by the reaction of diisocyanate‐ended prepolymers with furfurylamine (FA) followed by the addition of bismaleimide (BMI). The permanent crosslinks between the linear chains containing DA bonds were achieved using additional amounts of diisocyanates (MDI or HDI). The above reaction path was supported by infrared spectroscopic results and swelling experiments. Tensile mechanical and shape memory properties in tension of the PUs were determined and discussed as a function of composition and crosslink densities deduced from swelling and dynamic mechanical analysis. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016, 133, 44145. |
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Crosslinked polyurethanes (PUs) containing irreversible (allophanate) and reversible Diels‐Alder chemical bonds were synthesized using various diisocyanates (methylene diphenyl diisocyanate MDI, 1,6‐hexamethylenediisocyanate HDI) and poly(ɛ‐caprolactone) ((PCL) with different molecular weights (Mn = 10 kg/mol, 25 kg/mol, 50 kg/mol) as diol component. The melting/crystallization of PCL and the reversible DA bonds acted as temperature‐activated switches for shape memory performances, while allophanate network provided the permanent crosslinks for these PUs. The reversible DA bonds were obtained by the reaction of diisocyanate‐ended prepolymers with furfurylamine (FA) followed by the addition of bismaleimide (BMI). The permanent crosslinks between the linear chains containing DA bonds were achieved using additional amounts of diisocyanates (MDI or HDI). The above reaction path was supported by infrared spectroscopic results and swelling experiments. Tensile mechanical and shape memory properties in tension of the PUs were determined and discussed as a function of composition and crosslink densities deduced from swelling and dynamic mechanical analysis. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016, 133, 44145.</description><identifier>ISSN: 0021-8995</identifier><identifier>EISSN: 1097-4628</identifier><identifier>DOI: 10.1002/app.44145</identifier><identifier>CODEN: JAPNAB</identifier><language>eng</language><publisher>Hoboken: Blackwell Publishing Ltd</publisher><subject>Bismaleimides ; Chemical bonds ; Chemical synthesis ; copolymers ; Couplings ; Crosslinking ; Crystallization ; Diisocyanates ; Diphenyl methane diisocyanate ; Dynamic mechanical analysis ; Materials science ; MDI ; morphology ; Polymers ; Polyurethane resins ; polyurethanes ; Prepolymers ; Shape memory ; structure-property relations ; Swelling ; Switches</subject><ispartof>Journal of applied polymer science, 2016-11, Vol.133 (43), p.np-n/a</ispartof><rights>2016 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3965-c3928630e52d2135ae083f34df7c9412f7fe33fa3186480deb10c3e3263be76b3</citedby><cites>FETCH-LOGICAL-c3965-c3928630e52d2135ae083f34df7c9412f7fe33fa3186480deb10c3e3263be76b3</cites><orcidid>0000-0001-9699-7471</orcidid></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.44145$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fapp.44145$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids></links><search><creatorcontrib>Lakatos, Csilla</creatorcontrib><creatorcontrib>Czifrák, Katalin</creatorcontrib><creatorcontrib>Karger-Kocsis, József</creatorcontrib><creatorcontrib>Daróczi, Lajos</creatorcontrib><creatorcontrib>Zsuga, Miklós</creatorcontrib><creatorcontrib>Kéki, Sándor</creatorcontrib><title>Shape memory crosslinked polyurethanes containing thermoreversible Diels-Alder couplings</title><title>Journal of applied polymer science</title><addtitle>J. Appl. Polym. Sci</addtitle><description>ABSTRACT
Crosslinked polyurethanes (PUs) containing irreversible (allophanate) and reversible Diels‐Alder chemical bonds were synthesized using various diisocyanates (methylene diphenyl diisocyanate MDI, 1,6‐hexamethylenediisocyanate HDI) and poly(ɛ‐caprolactone) ((PCL) with different molecular weights (Mn = 10 kg/mol, 25 kg/mol, 50 kg/mol) as diol component. The melting/crystallization of PCL and the reversible DA bonds acted as temperature‐activated switches for shape memory performances, while allophanate network provided the permanent crosslinks for these PUs. The reversible DA bonds were obtained by the reaction of diisocyanate‐ended prepolymers with furfurylamine (FA) followed by the addition of bismaleimide (BMI). The permanent crosslinks between the linear chains containing DA bonds were achieved using additional amounts of diisocyanates (MDI or HDI). The above reaction path was supported by infrared spectroscopic results and swelling experiments. Tensile mechanical and shape memory properties in tension of the PUs were determined and discussed as a function of composition and crosslink densities deduced from swelling and dynamic mechanical analysis. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016, 133, 44145.</description><subject>Bismaleimides</subject><subject>Chemical bonds</subject><subject>Chemical synthesis</subject><subject>copolymers</subject><subject>Couplings</subject><subject>Crosslinking</subject><subject>Crystallization</subject><subject>Diisocyanates</subject><subject>Diphenyl methane diisocyanate</subject><subject>Dynamic mechanical analysis</subject><subject>Materials science</subject><subject>MDI</subject><subject>morphology</subject><subject>Polymers</subject><subject>Polyurethane resins</subject><subject>polyurethanes</subject><subject>Prepolymers</subject><subject>Shape memory</subject><subject>structure-property relations</subject><subject>Swelling</subject><subject>Switches</subject><issn>0021-8995</issn><issn>1097-4628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp90U1P3DAQBmCrKlK3wKH_IFIv9BDw-DM5rvgWCJAAFfVieZMJa_AmwU6A_fcYlvaARC_2wc87mvEQ8gPoNlDKdmzfbwsBQn4hE6ClzoVixVcySW-QF2Upv5HvMd5RCiCpmpCby7ntMVvgogvLrApdjN6191hnfeeXY8BhbluMWdW1g3Wta2-zYY4haXzEEN3MY7bn0Md86msMyY19KnAbN8haY33Ezfd7nVwf7F_tHuWn54fHu9PTvOKlkq8nKxSnKFnNgEuLtOANF3Wjq1IAa3SDnDeWQ6FEQWucAa04cqb4DLWa8XWytarbh-5hxDiYhYsVep_a7sZooOBS6jQ-S_TnB3rXjaFN3SVVSsqUBv1_BVSDFBKS-rVSb18WsDF9cAsblgaoed2ESZswb5tIdmdln5zH5efQTC8u_ibyVcLFAZ__JWy4N0pzLc3vs0MjSpA3Byd_TMFfAA3cmLI</recordid><startdate>20161115</startdate><enddate>20161115</enddate><creator>Lakatos, Csilla</creator><creator>Czifrák, Katalin</creator><creator>Karger-Kocsis, József</creator><creator>Daróczi, Lajos</creator><creator>Zsuga, Miklós</creator><creator>Kéki, Sándor</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope><orcidid>https://orcid.org/0000-0001-9699-7471</orcidid></search><sort><creationdate>20161115</creationdate><title>Shape memory crosslinked polyurethanes containing thermoreversible Diels-Alder couplings</title><author>Lakatos, Csilla ; Czifrák, Katalin ; Karger-Kocsis, József ; Daróczi, Lajos ; Zsuga, Miklós ; Kéki, Sándor</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3965-c3928630e52d2135ae083f34df7c9412f7fe33fa3186480deb10c3e3263be76b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Bismaleimides</topic><topic>Chemical bonds</topic><topic>Chemical synthesis</topic><topic>copolymers</topic><topic>Couplings</topic><topic>Crosslinking</topic><topic>Crystallization</topic><topic>Diisocyanates</topic><topic>Diphenyl methane diisocyanate</topic><topic>Dynamic mechanical analysis</topic><topic>Materials science</topic><topic>MDI</topic><topic>morphology</topic><topic>Polymers</topic><topic>Polyurethane resins</topic><topic>polyurethanes</topic><topic>Prepolymers</topic><topic>Shape memory</topic><topic>structure-property relations</topic><topic>Swelling</topic><topic>Switches</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lakatos, Csilla</creatorcontrib><creatorcontrib>Czifrák, Katalin</creatorcontrib><creatorcontrib>Karger-Kocsis, József</creatorcontrib><creatorcontrib>Daróczi, Lajos</creatorcontrib><creatorcontrib>Zsuga, Miklós</creatorcontrib><creatorcontrib>Kéki, Sándor</creatorcontrib><collection>Istex</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>Lakatos, Csilla</au><au>Czifrák, Katalin</au><au>Karger-Kocsis, József</au><au>Daróczi, Lajos</au><au>Zsuga, Miklós</au><au>Kéki, Sándor</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Shape memory crosslinked polyurethanes containing thermoreversible Diels-Alder couplings</atitle><jtitle>Journal of applied polymer science</jtitle><addtitle>J. Appl. Polym. Sci</addtitle><date>2016-11-15</date><risdate>2016</risdate><volume>133</volume><issue>43</issue><spage>np</spage><epage>n/a</epage><pages>np-n/a</pages><issn>0021-8995</issn><eissn>1097-4628</eissn><coden>JAPNAB</coden><abstract>ABSTRACT
Crosslinked polyurethanes (PUs) containing irreversible (allophanate) and reversible Diels‐Alder chemical bonds were synthesized using various diisocyanates (methylene diphenyl diisocyanate MDI, 1,6‐hexamethylenediisocyanate HDI) and poly(ɛ‐caprolactone) ((PCL) with different molecular weights (Mn = 10 kg/mol, 25 kg/mol, 50 kg/mol) as diol component. The melting/crystallization of PCL and the reversible DA bonds acted as temperature‐activated switches for shape memory performances, while allophanate network provided the permanent crosslinks for these PUs. The reversible DA bonds were obtained by the reaction of diisocyanate‐ended prepolymers with furfurylamine (FA) followed by the addition of bismaleimide (BMI). The permanent crosslinks between the linear chains containing DA bonds were achieved using additional amounts of diisocyanates (MDI or HDI). The above reaction path was supported by infrared spectroscopic results and swelling experiments. Tensile mechanical and shape memory properties in tension of the PUs were determined and discussed as a function of composition and crosslink densities deduced from swelling and dynamic mechanical analysis. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016, 133, 44145.</abstract><cop>Hoboken</cop><pub>Blackwell Publishing Ltd</pub><doi>10.1002/app.44145</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-9699-7471</orcidid></addata></record> |
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subjects | Bismaleimides Chemical bonds Chemical synthesis copolymers Couplings Crosslinking Crystallization Diisocyanates Diphenyl methane diisocyanate Dynamic mechanical analysis Materials science MDI morphology Polymers Polyurethane resins polyurethanes Prepolymers Shape memory structure-property relations Swelling Switches |
title | Shape memory crosslinked polyurethanes containing thermoreversible Diels-Alder couplings |
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