Deconvolution of the excess heat capacity of the Brill transition in nylon 66
The Brill transition in nylon 66, crystallized from solution, is a small, diffuse endotherm extending between roughly 130-230 deg C. The excess heat capacity in this region has been deconvoluted using established methods of statistical mechanics. As have been found for the unfolding transitions in s...
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Veröffentlicht in: | Macromolecules 1989-04, Vol.22 (4), p.2000-2003 |
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description | The Brill transition in nylon 66, crystallized from solution, is a small, diffuse endotherm extending between roughly 130-230 deg C. The excess heat capacity in this region has been deconvoluted using established methods of statistical mechanics. As have been found for the unfolding transitions in several globular proteins, the data can be characterized by a model having two energy states within 5% of their fractions. The transition appears to involve a mass corresponding to approx 25 chemical repeat units or about five stems in a folded-chain crystal. This is much smaller than the size of the crystals calculated from small- and wide-angle X-ray data. Spectra, graphs. 9 ref.--AA |
doi_str_mv | 10.1021/ma00194a079 |
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The excess heat capacity in this region has been deconvoluted using established methods of statistical mechanics. As have been found for the unfolding transitions in several globular proteins, the data can be characterized by a model having two energy states within 5% of their fractions. The transition appears to involve a mass corresponding to approx 25 chemical repeat units or about five stems in a folded-chain crystal. This is much smaller than the size of the crystals calculated from small- and wide-angle X-ray data. Spectra, graphs. 9 ref.--AA</description><identifier>ISSN: 0024-9297</identifier><identifier>EISSN: 1520-5835</identifier><identifier>DOI: 10.1021/ma00194a079</identifier><identifier>CODEN: MAMOBX</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Applied sciences ; Exact sciences and technology ; Organic polymers ; Physicochemistry of polymers ; Properties and characterization ; Structure, morphology and analysis</subject><ispartof>Macromolecules, 1989-04, Vol.22 (4), p.2000-2003</ispartof><rights>1989 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a497t-cd3e04bec93a2c98b177f9fddf83ae55b585436d71c6add27702a339e29f511b3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ma00194a079$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ma00194a079$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7373048$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Starkweather, Howard W</creatorcontrib><title>Deconvolution of the excess heat capacity of the Brill transition in nylon 66</title><title>Macromolecules</title><addtitle>Macromolecules</addtitle><description>The Brill transition in nylon 66, crystallized from solution, is a small, diffuse endotherm extending between roughly 130-230 deg C. The excess heat capacity in this region has been deconvoluted using established methods of statistical mechanics. As have been found for the unfolding transitions in several globular proteins, the data can be characterized by a model having two energy states within 5% of their fractions. The transition appears to involve a mass corresponding to approx 25 chemical repeat units or about five stems in a folded-chain crystal. This is much smaller than the size of the crystals calculated from small- and wide-angle X-ray data. Spectra, graphs. 9 ref.--AA</description><subject>Applied sciences</subject><subject>Exact sciences and technology</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>Properties and characterization</subject><subject>Structure, morphology and analysis</subject><issn>0024-9297</issn><issn>1520-5835</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><recordid>eNptkEtPwzAQhC0EEqVw4g_kgOCAAn7EcX2EQgtSEY8WxM3aOo7qkibFTlD773FpqThw2pXm29HsIHRM8AXBlFzOAGMiE8BC7qAW4RTHvMP4LmphTJNYUin20YH304ARnrAWergxuiq_qqKpbVVGVR7VExOZhTbeRxMDdaRhDtrWy1_t2tmiiGoHpbc_N7aMymURljQ9RHs5FN4cbWYbvfZuR927ePDYv-9eDWJIpKhjnTGDk7HRkgHVsjMmQuQyz7K8w8BwPuadEC7NBNEpZBkVAlNgTBoqc07ImLXR6dp37qrPxvhazazXpiigNFXjFeWESxpeb6PzNahd5b0zuZo7OwO3VASrVWXqT2WBPtnYgtdQ5OFHbf32RDDBcLIyjdeY9bVZbGVwHyoNDFejp6F667-8D3v9RD0H_mzNg_ZqWjWuDN38G-AbsJiGqA</recordid><startdate>19890401</startdate><enddate>19890401</enddate><creator>Starkweather, Howard W</creator><general>American Chemical Society</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>19890401</creationdate><title>Deconvolution of the excess heat capacity of the Brill transition in nylon 66</title><author>Starkweather, Howard W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a497t-cd3e04bec93a2c98b177f9fddf83ae55b585436d71c6add27702a339e29f511b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Applied sciences</topic><topic>Exact sciences and technology</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>Properties and characterization</topic><topic>Structure, morphology and analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Starkweather, Howard W</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>Macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Starkweather, Howard W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Deconvolution of the excess heat capacity of the Brill transition in nylon 66</atitle><jtitle>Macromolecules</jtitle><addtitle>Macromolecules</addtitle><date>1989-04-01</date><risdate>1989</risdate><volume>22</volume><issue>4</issue><spage>2000</spage><epage>2003</epage><pages>2000-2003</pages><issn>0024-9297</issn><eissn>1520-5835</eissn><coden>MAMOBX</coden><abstract>The Brill transition in nylon 66, crystallized from solution, is a small, diffuse endotherm extending between roughly 130-230 deg C. The excess heat capacity in this region has been deconvoluted using established methods of statistical mechanics. As have been found for the unfolding transitions in several globular proteins, the data can be characterized by a model having two energy states within 5% of their fractions. The transition appears to involve a mass corresponding to approx 25 chemical repeat units or about five stems in a folded-chain crystal. This is much smaller than the size of the crystals calculated from small- and wide-angle X-ray data. Spectra, graphs. 9 ref.--AA</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ma00194a079</doi><tpages>4</tpages></addata></record> |
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subjects | Applied sciences Exact sciences and technology Organic polymers Physicochemistry of polymers Properties and characterization Structure, morphology and analysis |
title | Deconvolution of the excess heat capacity of the Brill transition in nylon 66 |
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