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Aliphatic-aromatic copolyesters derived from 2,2,4,4-tetramethyl-1,3-cyclobutanediol
With the massive changes taking place in the world today, the development of new thermally and mechanically stable polymeric materials is of utmost importance. This article focuses on the synthesis and thermal characterization of a new series of copolyesters that incorporate both aromatic as well as...
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Published in: | Journal of polymer science. Part A, Polymer chemistry Polymer chemistry, 2004-07, Vol.42 (14), p.3473-3478 |
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description | With the massive changes taking place in the world today, the development of new thermally and mechanically stable polymeric materials is of utmost importance. This article focuses on the synthesis and thermal characterization of a new series of copolyesters that incorporate both aromatic as well as aliphatic diols. This is of interest because most polymer materials that exhibit high thermal and/or mechanical properties contain aromatic monomer units only. These aromatic units usually contribute to either the thermal or mechanical properties but typically not both. An example of this is bisphenol A polycarbonate, which has high mechanical properties but only moderate thermal properties when compared, for example, to polyimides. In recent years there has been an interest in copolyesters that contain 2,2,4,4‐tetramethyl‐1,3‐cyclobutanediol (CBDO). This aliphatic monomer imparts some very unique thermal as well as mechanical properties. This article will report the thermal properties of a new series of CBDO‐based copolyesters. These polymers include CBDO, a series of bisphenols, and terephthaloyl chloride. The series of bisphenols discussed here include bisphenol A, AF, F, and HPF. These polymers display glass transition temperatures near 200 °C and decomposition temperatures from 390–420 °C (Argon) and from 385–410 °C (Air). © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 3473–3478, 2004
2,2,4,4‐tetramethyl‐1,3‐cyclobutanediol (CBDO) is an aliphatic diol monomer that has been incorporated into both polycarbonates and polyesters. This article reports the thermal data obtained from a series of random poly(CBCO/Bisphenol)terephthalates. These polymers have Tg's around 200 °C and Td's near 400 °C. |
doi_str_mv | 10.1002/pola.20197 |
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2,2,4,4‐tetramethyl‐1,3‐cyclobutanediol (CBDO) is an aliphatic diol monomer that has been incorporated into both polycarbonates and polyesters. This article reports the thermal data obtained from a series of random poly(CBCO/Bisphenol)terephthalates. These polymers have Tg's around 200 °C and Td's near 400 °C.</description><identifier>ISSN: 0887-624X</identifier><identifier>EISSN: 1099-0518</identifier><identifier>DOI: 10.1002/pola.20197</identifier><identifier>CODEN: JPLCAT</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>2,2,4,4‐tetramethyl‐1,3‐cyclobutanediol (CBDO) ; 3-cyclobutanediol (CBDO) ; 4-tetramethyl-1 ; Applied sciences ; bisphenol ; copolyester ; Exact sciences and technology ; Organic polymers ; Physicochemistry of polymers ; Polycondensation ; Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><ispartof>Journal of polymer science. Part A, Polymer chemistry, 2004-07, Vol.42 (14), p.3473-3478</ispartof><rights>Copyright © 2004 Wiley Periodicals, Inc.</rights><rights>2004 INIST-CNRS</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3027-45e59b8411c5e28bb2d5af6ae87cfd80af918b59749d0d8d7a9ae36b99c8d0e83</citedby><cites>FETCH-LOGICAL-c3027-45e59b8411c5e28bb2d5af6ae87cfd80af918b59749d0d8d7a9ae36b99c8d0e83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15916794$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Hoppens, Nathan C.</creatorcontrib><creatorcontrib>Hudnall, Todd W.</creatorcontrib><creatorcontrib>Foster, Adam</creatorcontrib><creatorcontrib>Booth, Chad J.</creatorcontrib><title>Aliphatic-aromatic copolyesters derived from 2,2,4,4-tetramethyl-1,3-cyclobutanediol</title><title>Journal of polymer science. Part A, Polymer chemistry</title><addtitle>J. Polym. Sci. A Polym. Chem</addtitle><description>With the massive changes taking place in the world today, the development of new thermally and mechanically stable polymeric materials is of utmost importance. This article focuses on the synthesis and thermal characterization of a new series of copolyesters that incorporate both aromatic as well as aliphatic diols. This is of interest because most polymer materials that exhibit high thermal and/or mechanical properties contain aromatic monomer units only. These aromatic units usually contribute to either the thermal or mechanical properties but typically not both. An example of this is bisphenol A polycarbonate, which has high mechanical properties but only moderate thermal properties when compared, for example, to polyimides. In recent years there has been an interest in copolyesters that contain 2,2,4,4‐tetramethyl‐1,3‐cyclobutanediol (CBDO). This aliphatic monomer imparts some very unique thermal as well as mechanical properties. This article will report the thermal properties of a new series of CBDO‐based copolyesters. These polymers include CBDO, a series of bisphenols, and terephthaloyl chloride. The series of bisphenols discussed here include bisphenol A, AF, F, and HPF. These polymers display glass transition temperatures near 200 °C and decomposition temperatures from 390–420 °C (Argon) and from 385–410 °C (Air). © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 3473–3478, 2004
2,2,4,4‐tetramethyl‐1,3‐cyclobutanediol (CBDO) is an aliphatic diol monomer that has been incorporated into both polycarbonates and polyesters. This article reports the thermal data obtained from a series of random poly(CBCO/Bisphenol)terephthalates. These polymers have Tg's around 200 °C and Td's near 400 °C.</description><subject>2,2,4,4‐tetramethyl‐1,3‐cyclobutanediol (CBDO)</subject><subject>3-cyclobutanediol (CBDO)</subject><subject>4-tetramethyl-1</subject><subject>Applied sciences</subject><subject>bisphenol</subject><subject>copolyester</subject><subject>Exact sciences and technology</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>Polycondensation</subject><subject>Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><issn>0887-624X</issn><issn>1099-0518</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNp9kM1OAyEURonRxPqz8QlmowtTFJhhgGVjbDVprCY1uiMMMBGlToWpOm8vdaruXJBLcs93cvMBcITRGUaInC8br84IwoJtgQFGQkBEMd8GA8Q5gyUpHnfBXozPCKUd5QMwH3m3fFKt01CFZrH-ZLpJms7G1oaYGRvcuzVZnbYZGZJhMSxga9ugFrZ96jzEwxzqTvumWrXq1RrX-AOwUysf7eFm7oP78eX84gpOZ5Pri9EU6hwRBgtqqah4gbGmlvCqIoaqulSWM10bjlQtMK-oYIUwyHDDlFA2LyshNDfI8nwfnPTeZWjeVulguXBRW-_THc0qSsIJKjnOE3jagzo0MQZby2VwCxU6iZFcFyfXxcnv4hJ8vLGqqJWvg3rVLv4lqMAlE0XicM99OG-7f4zydjYd_bhhn3Gp3c_fjAovsmQ5o_LhZpLeHXoUnMlx_gW3PIzt</recordid><startdate>20040715</startdate><enddate>20040715</enddate><creator>Hoppens, Nathan C.</creator><creator>Hudnall, Todd W.</creator><creator>Foster, Adam</creator><creator>Booth, Chad J.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</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>20040715</creationdate><title>Aliphatic-aromatic copolyesters derived from 2,2,4,4-tetramethyl-1,3-cyclobutanediol</title><author>Hoppens, Nathan C. ; Hudnall, Todd W. ; Foster, Adam ; Booth, Chad J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3027-45e59b8411c5e28bb2d5af6ae87cfd80af918b59749d0d8d7a9ae36b99c8d0e83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>2,2,4,4‐tetramethyl‐1,3‐cyclobutanediol (CBDO)</topic><topic>3-cyclobutanediol (CBDO)</topic><topic>4-tetramethyl-1</topic><topic>Applied sciences</topic><topic>bisphenol</topic><topic>copolyester</topic><topic>Exact sciences and technology</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>Polycondensation</topic><topic>Preparation, kinetics, thermodynamics, mechanism and catalysts</topic><toplevel>online_resources</toplevel><creatorcontrib>Hoppens, Nathan C.</creatorcontrib><creatorcontrib>Hudnall, Todd W.</creatorcontrib><creatorcontrib>Foster, Adam</creatorcontrib><creatorcontrib>Booth, Chad J.</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 polymer science. Part A, Polymer chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hoppens, Nathan C.</au><au>Hudnall, Todd W.</au><au>Foster, Adam</au><au>Booth, Chad J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aliphatic-aromatic copolyesters derived from 2,2,4,4-tetramethyl-1,3-cyclobutanediol</atitle><jtitle>Journal of polymer science. Part A, Polymer chemistry</jtitle><addtitle>J. Polym. Sci. A Polym. Chem</addtitle><date>2004-07-15</date><risdate>2004</risdate><volume>42</volume><issue>14</issue><spage>3473</spage><epage>3478</epage><pages>3473-3478</pages><issn>0887-624X</issn><eissn>1099-0518</eissn><coden>JPLCAT</coden><abstract>With the massive changes taking place in the world today, the development of new thermally and mechanically stable polymeric materials is of utmost importance. This article focuses on the synthesis and thermal characterization of a new series of copolyesters that incorporate both aromatic as well as aliphatic diols. This is of interest because most polymer materials that exhibit high thermal and/or mechanical properties contain aromatic monomer units only. These aromatic units usually contribute to either the thermal or mechanical properties but typically not both. An example of this is bisphenol A polycarbonate, which has high mechanical properties but only moderate thermal properties when compared, for example, to polyimides. In recent years there has been an interest in copolyesters that contain 2,2,4,4‐tetramethyl‐1,3‐cyclobutanediol (CBDO). This aliphatic monomer imparts some very unique thermal as well as mechanical properties. This article will report the thermal properties of a new series of CBDO‐based copolyesters. These polymers include CBDO, a series of bisphenols, and terephthaloyl chloride. The series of bisphenols discussed here include bisphenol A, AF, F, and HPF. These polymers display glass transition temperatures near 200 °C and decomposition temperatures from 390–420 °C (Argon) and from 385–410 °C (Air). © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 3473–3478, 2004
2,2,4,4‐tetramethyl‐1,3‐cyclobutanediol (CBDO) is an aliphatic diol monomer that has been incorporated into both polycarbonates and polyesters. This article reports the thermal data obtained from a series of random poly(CBCO/Bisphenol)terephthalates. These polymers have Tg's around 200 °C and Td's near 400 °C.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><doi>10.1002/pola.20197</doi><tpages>6</tpages></addata></record> |
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subjects | 2,2,4,4‐tetramethyl‐1,3‐cyclobutanediol (CBDO) 3-cyclobutanediol (CBDO) 4-tetramethyl-1 Applied sciences bisphenol copolyester Exact sciences and technology Organic polymers Physicochemistry of polymers Polycondensation Preparation, kinetics, thermodynamics, mechanism and catalysts |
title | Aliphatic-aromatic copolyesters derived from 2,2,4,4-tetramethyl-1,3-cyclobutanediol |
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