Production of “Green” Thermoplastic Polyurethanes from Decamethylene Sebacate‐co‐Isosorbide Copolymers
Long‐chain aliphatic copolyesters based on sebacic acid (SA) and isosorbide (IS), of renewable origin, are synthesized by a “green” and sustainable route, without the use of solvents, for the synthesis of polyurethanes (PUs). The polyesters are characterized by size exclusion chromatography (SEC), p...
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Veröffentlicht in: | Macromolecular symposia. 2022-12, Vol.406 (1), p.n/a |
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description | Long‐chain aliphatic copolyesters based on sebacic acid (SA) and isosorbide (IS), of renewable origin, are synthesized by a “green” and sustainable route, without the use of solvents, for the synthesis of polyurethanes (PUs). The polyesters are characterized by size exclusion chromatography (SEC), proton nuclear magnetic resonance (¹H NMR), Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), and thermogravimetry (TG). ¹H NMR and FTIR analyses confirm the production of copolyesters with the incorporation of IS, while SEC indicates that the addition of IS to copolyesters decreases the molecular weights. The results suggest the formation of random copolymers in the presence of IS, which makes the polymer chains more rigid. The formation of PUs by the reaction of copolyesters with 1,8‐diisocyanatooctane is confirmed by FTIR. Thermal behavior is compatible with thermoplastic processing and use in different biomedical applications. |
doi_str_mv | 10.1002/masy.202200051 |
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L. L. ; Pezzin, Sérgio H.</creator><creatorcontrib>Andrade, Ângela G. L. L. ; Pezzin, Sérgio H.</creatorcontrib><description>Long‐chain aliphatic copolyesters based on sebacic acid (SA) and isosorbide (IS), of renewable origin, are synthesized by a “green” and sustainable route, without the use of solvents, for the synthesis of polyurethanes (PUs). The polyesters are characterized by size exclusion chromatography (SEC), proton nuclear magnetic resonance (¹H NMR), Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), and thermogravimetry (TG). ¹H NMR and FTIR analyses confirm the production of copolyesters with the incorporation of IS, while SEC indicates that the addition of IS to copolyesters decreases the molecular weights. The results suggest the formation of random copolymers in the presence of IS, which makes the polymer chains more rigid. The formation of PUs by the reaction of copolyesters with 1,8‐diisocyanatooctane is confirmed by FTIR. Thermal behavior is compatible with thermoplastic processing and use in different biomedical applications.</description><identifier>ISSN: 1022-1360</identifier><identifier>EISSN: 1521-3900</identifier><identifier>DOI: 10.1002/masy.202200051</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>aliphatic polyesters ; Biomedical materials ; Copolymers ; Differential scanning calorimetry ; fatty acids ; Fourier transforms ; green chemistry ; Infrared spectroscopy ; isosorbide ; NMR ; Nuclear magnetic resonance ; Polyester resins ; Polyesters ; polyurethanes ; Sebacic acid ; Size exclusion chromatography ; Thermodynamic properties ; Thermogravimetry ; Urethane thermoplastic elastomers</subject><ispartof>Macromolecular symposia., 2022-12, Vol.406 (1), p.n/a</ispartof><rights>2022 Wiley‐VCH GmbH</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2021-142e00fff2a4f6368ac6e037c022799419abb567df5441214a535a80f04583a3</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%2Fmasy.202200051$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmasy.202200051$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids></links><search><creatorcontrib>Andrade, Ângela G. L. L.</creatorcontrib><creatorcontrib>Pezzin, Sérgio H.</creatorcontrib><title>Production of “Green” Thermoplastic Polyurethanes from Decamethylene Sebacate‐co‐Isosorbide Copolymers</title><title>Macromolecular symposia.</title><description>Long‐chain aliphatic copolyesters based on sebacic acid (SA) and isosorbide (IS), of renewable origin, are synthesized by a “green” and sustainable route, without the use of solvents, for the synthesis of polyurethanes (PUs). The polyesters are characterized by size exclusion chromatography (SEC), proton nuclear magnetic resonance (¹H NMR), Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), and thermogravimetry (TG). ¹H NMR and FTIR analyses confirm the production of copolyesters with the incorporation of IS, while SEC indicates that the addition of IS to copolyesters decreases the molecular weights. The results suggest the formation of random copolymers in the presence of IS, which makes the polymer chains more rigid. The formation of PUs by the reaction of copolyesters with 1,8‐diisocyanatooctane is confirmed by FTIR. Thermal behavior is compatible with thermoplastic processing and use in different biomedical applications.</description><subject>aliphatic polyesters</subject><subject>Biomedical materials</subject><subject>Copolymers</subject><subject>Differential scanning calorimetry</subject><subject>fatty acids</subject><subject>Fourier transforms</subject><subject>green chemistry</subject><subject>Infrared spectroscopy</subject><subject>isosorbide</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Polyester resins</subject><subject>Polyesters</subject><subject>polyurethanes</subject><subject>Sebacic acid</subject><subject>Size exclusion chromatography</subject><subject>Thermodynamic properties</subject><subject>Thermogravimetry</subject><subject>Urethane thermoplastic elastomers</subject><issn>1022-1360</issn><issn>1521-3900</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqFkM9Kw0AQxoMoqNWr54Dn1NnNbv4cS9VaqFhoL56WzXaWpiTZuJsiufURfAB9uT6JWyp69DIzfHy_GeYLghsCQwJA72rp-iEFSgGAk5PggnBKojgHOPWz1yMSJ3AeXDq38ZY8T8lF0MytWW1VV5omNDrc7z4nFrHZ777C5RptbdpKuq5U4dxU_dZit5YNulBbU4f3qGTtlb7CBsMFFlLJDve7D2V8mTrjjC3KFYZj03q6RuuugjMtK4fXP30QLB8fluOnaPYymY5Hs0j5B0hEGEUArTWVTCdxkkmVIMSp8l-kec5ILouCJ-lKc8YIJUzymMsMNDCexTIeBLfHta01b1t0ndiYrW38RUFTnrAs5pB41_DoUtY4Z1GL1pa1tL0gIA6RikOk4jdSD-RH4L2ssP_HLZ5Hi9c_9ht1en-Z</recordid><startdate>202212</startdate><enddate>202212</enddate><creator>Andrade, Ângela G. L. L.</creator><creator>Pezzin, Sérgio H.</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>202212</creationdate><title>Production of “Green” Thermoplastic Polyurethanes from Decamethylene Sebacate‐co‐Isosorbide Copolymers</title><author>Andrade, Ângela G. L. 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L. L.</creatorcontrib><creatorcontrib>Pezzin, Sérgio H.</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Macromolecular symposia.</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Andrade, Ângela G. L. L.</au><au>Pezzin, Sérgio H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Production of “Green” Thermoplastic Polyurethanes from Decamethylene Sebacate‐co‐Isosorbide Copolymers</atitle><jtitle>Macromolecular symposia.</jtitle><date>2022-12</date><risdate>2022</risdate><volume>406</volume><issue>1</issue><epage>n/a</epage><issn>1022-1360</issn><eissn>1521-3900</eissn><abstract>Long‐chain aliphatic copolyesters based on sebacic acid (SA) and isosorbide (IS), of renewable origin, are synthesized by a “green” and sustainable route, without the use of solvents, for the synthesis of polyurethanes (PUs). The polyesters are characterized by size exclusion chromatography (SEC), proton nuclear magnetic resonance (¹H NMR), Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), and thermogravimetry (TG). ¹H NMR and FTIR analyses confirm the production of copolyesters with the incorporation of IS, while SEC indicates that the addition of IS to copolyesters decreases the molecular weights. The results suggest the formation of random copolymers in the presence of IS, which makes the polymer chains more rigid. The formation of PUs by the reaction of copolyesters with 1,8‐diisocyanatooctane is confirmed by FTIR. Thermal behavior is compatible with thermoplastic processing and use in different biomedical applications.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/masy.202200051</doi><tpages>4</tpages></addata></record> |
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subjects | aliphatic polyesters Biomedical materials Copolymers Differential scanning calorimetry fatty acids Fourier transforms green chemistry Infrared spectroscopy isosorbide NMR Nuclear magnetic resonance Polyester resins Polyesters polyurethanes Sebacic acid Size exclusion chromatography Thermodynamic properties Thermogravimetry Urethane thermoplastic elastomers |
title | Production of “Green” Thermoplastic Polyurethanes from Decamethylene Sebacate‐co‐Isosorbide Copolymers |
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