Crystallization and Stress Relaxation in Highly Stretched Samples of Natural Rubber and Its Synthetic Analogue
Vulcanizates of natural rubber (NR) and its synthetic analogue (IR) were quickly stretched to 6 times the original length. The post stretch relaxation of tensile stress and the development of strain-induced crystallization (SIC) were studied by simultaneous measurements of the stress and the diffrac...
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Veröffentlicht in: | Macromolecules 2006-07, Vol.39 (15), p.5100-5105 |
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creator | Tosaka, Masatoshi Kawakami, Daisuke Senoo, Kazunobu Kohjiya, Shinzo Ikeda, Yuko Toki, Shigeyuki Hsiao, Benjamin S |
description | Vulcanizates of natural rubber (NR) and its synthetic analogue (IR) were quickly stretched to 6 times the original length. The post stretch relaxation of tensile stress and the development of strain-induced crystallization (SIC) were studied by simultaneous measurements of the stress and the diffraction intensities using the synchrotron X-ray source. In the range of 8 s, NR crystallized much faster than IR. Accordingly, the origin of the superior toughness of NR was thought to come from the ability of rapid SIC. Time constants of the post-stretch crystallization were estimated from the X-ray study. Then the crystallization time constants were used to decompose the contribution of SIC from the total magnitude of the post-stretch relaxation. The contribution of SIC was dominant for the total magnitude of the post-stretch relaxation during several seconds. |
doi_str_mv | 10.1021/ma060407+ |
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The post stretch relaxation of tensile stress and the development of strain-induced crystallization (SIC) were studied by simultaneous measurements of the stress and the diffraction intensities using the synchrotron X-ray source. In the range of 8 s, NR crystallized much faster than IR. Accordingly, the origin of the superior toughness of NR was thought to come from the ability of rapid SIC. Time constants of the post-stretch crystallization were estimated from the X-ray study. Then the crystallization time constants were used to decompose the contribution of SIC from the total magnitude of the post-stretch relaxation. The contribution of SIC was dominant for the total magnitude of the post-stretch relaxation during several seconds.</description><identifier>ISSN: 0024-9297</identifier><identifier>EISSN: 1520-5835</identifier><identifier>DOI: 10.1021/ma060407+</identifier><identifier>CODEN: MAMOBX</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Applied sciences ; CRYSTALLIZATION ; DIFFRACTION ; Exact sciences and technology ; MATERIALS SCIENCE ; Mechanical properties ; national synchrotron light source ; Natural polymers ; NATURAL RUBBER ; Organic polymers ; ORIGIN ; PARTICLE ACCELERATORS ; Physicochemistry of polymers ; Properties and characterization ; RELAXATION ; STRESS RELAXATION ; SYNCHROTRONS ; SYNTHETIC MATERIALS ; X-RAY SOURCES</subject><ispartof>Macromolecules, 2006-07, Vol.39 (15), p.5100-5105</ispartof><rights>Copyright © 2006 American Chemical Society</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a356t-9152c9acfcf535a265d5c52f18cb17f6df152556d662dd03a49ece150a24ae1b3</citedby><cites>FETCH-LOGICAL-a356t-9152c9acfcf535a265d5c52f18cb17f6df152556d662dd03a49ece150a24ae1b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ma060407+$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ma060407+$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,885,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17971872$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/959893$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Tosaka, Masatoshi</creatorcontrib><creatorcontrib>Kawakami, Daisuke</creatorcontrib><creatorcontrib>Senoo, Kazunobu</creatorcontrib><creatorcontrib>Kohjiya, Shinzo</creatorcontrib><creatorcontrib>Ikeda, Yuko</creatorcontrib><creatorcontrib>Toki, Shigeyuki</creatorcontrib><creatorcontrib>Hsiao, Benjamin S</creatorcontrib><creatorcontrib>Brookhaven National Laboratory (BNL) National Synchrotron Light Source</creatorcontrib><title>Crystallization and Stress Relaxation in Highly Stretched Samples of Natural Rubber and Its Synthetic Analogue</title><title>Macromolecules</title><addtitle>Macromolecules</addtitle><description>Vulcanizates of natural rubber (NR) and its synthetic analogue (IR) were quickly stretched to 6 times the original length. The post stretch relaxation of tensile stress and the development of strain-induced crystallization (SIC) were studied by simultaneous measurements of the stress and the diffraction intensities using the synchrotron X-ray source. In the range of 8 s, NR crystallized much faster than IR. Accordingly, the origin of the superior toughness of NR was thought to come from the ability of rapid SIC. Time constants of the post-stretch crystallization were estimated from the X-ray study. Then the crystallization time constants were used to decompose the contribution of SIC from the total magnitude of the post-stretch relaxation. The contribution of SIC was dominant for the total magnitude of the post-stretch relaxation during several seconds.</description><subject>Applied sciences</subject><subject>CRYSTALLIZATION</subject><subject>DIFFRACTION</subject><subject>Exact sciences and technology</subject><subject>MATERIALS SCIENCE</subject><subject>Mechanical properties</subject><subject>national synchrotron light source</subject><subject>Natural polymers</subject><subject>NATURAL RUBBER</subject><subject>Organic polymers</subject><subject>ORIGIN</subject><subject>PARTICLE ACCELERATORS</subject><subject>Physicochemistry of polymers</subject><subject>Properties and characterization</subject><subject>RELAXATION</subject><subject>STRESS RELAXATION</subject><subject>SYNCHROTRONS</subject><subject>SYNTHETIC MATERIALS</subject><subject>X-RAY SOURCES</subject><issn>0024-9297</issn><issn>1520-5835</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNpl0FFLwzAQB_AgCs7pg98ggoIg1SRt2uVxDHWDobDpc7mmyZqRpSPJwPnpravig08Hdz_-3B1Cl5TcU8LowwZITjJS3B2hAeWMJHyU8mM0IIRliWCiOEVnIawJoZRn6QC5id-HCNaaT4imdRhcjZfRqxDwQln46LvG4alZNXZ_mEXZqE7BZmtVwK3GLxB3Hixe7KpK-UPGLAa83LvYqGgkHjuw7WqnztGJBhvUxU8dovenx7fJNJm_Ps8m43kCKc9jIrrVpQCppeYpB5bzmkvONB3JihY6r3UHOM_rPGd1TVLIhJKKcgIsA0WrdIiu-tw2RFMGaaKSjWydUzKWgouRSDtz2xvp2xC80uXWmw34fUlJ-f3M8veZHb3p6RaCBKs9OGnCny9EQUcF69x170CGct3ufHd2-B_3Bb2SgCA</recordid><startdate>20060725</startdate><enddate>20060725</enddate><creator>Tosaka, Masatoshi</creator><creator>Kawakami, Daisuke</creator><creator>Senoo, Kazunobu</creator><creator>Kohjiya, Shinzo</creator><creator>Ikeda, Yuko</creator><creator>Toki, Shigeyuki</creator><creator>Hsiao, Benjamin S</creator><general>American Chemical Society</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>OTOTI</scope></search><sort><creationdate>20060725</creationdate><title>Crystallization and Stress Relaxation in Highly Stretched Samples of Natural Rubber and Its Synthetic Analogue</title><author>Tosaka, Masatoshi ; Kawakami, Daisuke ; Senoo, Kazunobu ; Kohjiya, Shinzo ; Ikeda, Yuko ; Toki, Shigeyuki ; Hsiao, Benjamin S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a356t-9152c9acfcf535a265d5c52f18cb17f6df152556d662dd03a49ece150a24ae1b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Applied sciences</topic><topic>CRYSTALLIZATION</topic><topic>DIFFRACTION</topic><topic>Exact sciences and technology</topic><topic>MATERIALS SCIENCE</topic><topic>Mechanical properties</topic><topic>national synchrotron light source</topic><topic>Natural polymers</topic><topic>NATURAL RUBBER</topic><topic>Organic polymers</topic><topic>ORIGIN</topic><topic>PARTICLE ACCELERATORS</topic><topic>Physicochemistry of polymers</topic><topic>Properties and characterization</topic><topic>RELAXATION</topic><topic>STRESS RELAXATION</topic><topic>SYNCHROTRONS</topic><topic>SYNTHETIC MATERIALS</topic><topic>X-RAY SOURCES</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tosaka, Masatoshi</creatorcontrib><creatorcontrib>Kawakami, Daisuke</creatorcontrib><creatorcontrib>Senoo, Kazunobu</creatorcontrib><creatorcontrib>Kohjiya, Shinzo</creatorcontrib><creatorcontrib>Ikeda, Yuko</creatorcontrib><creatorcontrib>Toki, Shigeyuki</creatorcontrib><creatorcontrib>Hsiao, Benjamin S</creatorcontrib><creatorcontrib>Brookhaven National Laboratory (BNL) National Synchrotron Light Source</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>OSTI.GOV</collection><jtitle>Macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tosaka, Masatoshi</au><au>Kawakami, Daisuke</au><au>Senoo, Kazunobu</au><au>Kohjiya, Shinzo</au><au>Ikeda, Yuko</au><au>Toki, Shigeyuki</au><au>Hsiao, Benjamin S</au><aucorp>Brookhaven National Laboratory (BNL) National Synchrotron Light Source</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Crystallization and Stress Relaxation in Highly Stretched Samples of Natural Rubber and Its Synthetic Analogue</atitle><jtitle>Macromolecules</jtitle><addtitle>Macromolecules</addtitle><date>2006-07-25</date><risdate>2006</risdate><volume>39</volume><issue>15</issue><spage>5100</spage><epage>5105</epage><pages>5100-5105</pages><issn>0024-9297</issn><eissn>1520-5835</eissn><coden>MAMOBX</coden><abstract>Vulcanizates of natural rubber (NR) and its synthetic analogue (IR) were quickly stretched to 6 times the original length. The post stretch relaxation of tensile stress and the development of strain-induced crystallization (SIC) were studied by simultaneous measurements of the stress and the diffraction intensities using the synchrotron X-ray source. In the range of 8 s, NR crystallized much faster than IR. Accordingly, the origin of the superior toughness of NR was thought to come from the ability of rapid SIC. Time constants of the post-stretch crystallization were estimated from the X-ray study. Then the crystallization time constants were used to decompose the contribution of SIC from the total magnitude of the post-stretch relaxation. The contribution of SIC was dominant for the total magnitude of the post-stretch relaxation during several seconds.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ma060407+</doi><tpages>6</tpages></addata></record> |
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subjects | Applied sciences CRYSTALLIZATION DIFFRACTION Exact sciences and technology MATERIALS SCIENCE Mechanical properties national synchrotron light source Natural polymers NATURAL RUBBER Organic polymers ORIGIN PARTICLE ACCELERATORS Physicochemistry of polymers Properties and characterization RELAXATION STRESS RELAXATION SYNCHROTRONS SYNTHETIC MATERIALS X-RAY SOURCES |
title | Crystallization and Stress Relaxation in Highly Stretched Samples of Natural Rubber and Its Synthetic Analogue |
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