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Comparison of covalent and noncovalent interactions of carbon nanotubes on the crystallization behavior and thermal properties of poly(3-hydroxybutyrate-co-3-hydroxyvalerate)
ABSTRACT In this study, multiwalled carbon nanotubes (MWCNTs) were dispersed into a poly(3‐hydroxybutyrate‐co−3‐hydroxyvalerate) (PHBV) matrix, in which PHBV was either covalently attached to the nanotubes through an esterification reaction between the carboxylic groups of functionalized MWCNTs and...
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Published in: | Journal of applied polymer science 2013-12, Vol.130 (6), p.4299-4307 |
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creator | Yu, Hou-Yong Yao, Ju-Ming Qin, Zong-Yi Liu, Lin Yang, Xiao-Gang |
description | ABSTRACT
In this study, multiwalled carbon nanotubes (MWCNTs) were dispersed into a poly(3‐hydroxybutyrate‐co−3‐hydroxyvalerate) (PHBV) matrix, in which PHBV was either covalently attached to the nanotubes through an esterification reaction between the carboxylic groups of functionalized MWCNTs and the hydroxyl groups of PHBV with toluene diisocyanate as a coupling agent or physically mixed to result in only noncovalent interactions. The structure, crystallization behavior, and thermal properties of the resulting nanocomposites were studied. We found that the crystallization of PHBV grafted onto the MWCNTs (PHBV‐g‐MWCNTs) was markedly hindered and exhibited an exothermic peak caused by cold crystallization, whereas the nonisothermal crystallization of PHBV was enhanced because a heterogeneous nucleation effect appeared in the PHBV/MWCNTs. Moreover, the maximum decomposition temperature of the PHBV‐g‐MWCNTs was improved by about 14.4°C compared with that of the PHBV/MWCNTs and by about 23.7°C compared with that of the original PHBV. Furthermore, the PHBV‐g‐MWCNTs exhibited the wider melt‐processing window than the PHBV/MWCNTs and original PHBV. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 4299–4307, 2013 |
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In this study, multiwalled carbon nanotubes (MWCNTs) were dispersed into a poly(3‐hydroxybutyrate‐co−3‐hydroxyvalerate) (PHBV) matrix, in which PHBV was either covalently attached to the nanotubes through an esterification reaction between the carboxylic groups of functionalized MWCNTs and the hydroxyl groups of PHBV with toluene diisocyanate as a coupling agent or physically mixed to result in only noncovalent interactions. The structure, crystallization behavior, and thermal properties of the resulting nanocomposites were studied. We found that the crystallization of PHBV grafted onto the MWCNTs (PHBV‐g‐MWCNTs) was markedly hindered and exhibited an exothermic peak caused by cold crystallization, whereas the nonisothermal crystallization of PHBV was enhanced because a heterogeneous nucleation effect appeared in the PHBV/MWCNTs. Moreover, the maximum decomposition temperature of the PHBV‐g‐MWCNTs was improved by about 14.4°C compared with that of the PHBV/MWCNTs and by about 23.7°C compared with that of the original PHBV. Furthermore, the PHBV‐g‐MWCNTs exhibited the wider melt‐processing window than the PHBV/MWCNTs and original PHBV. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 4299–4307, 2013</description><identifier>ISSN: 0021-8995</identifier><identifier>EISSN: 1097-4628</identifier><identifier>DOI: 10.1002/app.39529</identifier><identifier>CODEN: JAPNAB</identifier><language>eng</language><publisher>Hoboken, NJ: Blackwell Publishing Ltd</publisher><subject>Applied sciences ; biopolymers and renewable polymers ; Composites ; Covalence ; Crystallization ; Exact sciences and technology ; Forms of application and semi-finished materials ; Grafting ; Graphene ; graphene and fullerenes ; Hydroxyl groups ; Materials science ; Nanotubes ; Polymer industry, paints, wood ; Polymers ; Reproduction ; Technology of polymers ; Thermal properties</subject><ispartof>Journal of applied polymer science, 2013-12, Vol.130 (6), p.4299-4307</ispartof><rights>Copyright © 2013 Wiley Periodicals, Inc.</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3139-e854486db4113d4c37958882b8f29f98c39515b35cc4eb5d7e2dae3b5b1e9b233</citedby><cites>FETCH-LOGICAL-c3139-e854486db4113d4c37958882b8f29f98c39515b35cc4eb5d7e2dae3b5b1e9b233</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27761880$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Yu, Hou-Yong</creatorcontrib><creatorcontrib>Yao, Ju-Ming</creatorcontrib><creatorcontrib>Qin, Zong-Yi</creatorcontrib><creatorcontrib>Liu, Lin</creatorcontrib><creatorcontrib>Yang, Xiao-Gang</creatorcontrib><title>Comparison of covalent and noncovalent interactions of carbon nanotubes on the crystallization behavior and thermal properties of poly(3-hydroxybutyrate-co-3-hydroxyvalerate)</title><title>Journal of applied polymer science</title><addtitle>J. Appl. Polym. Sci</addtitle><description>ABSTRACT
In this study, multiwalled carbon nanotubes (MWCNTs) were dispersed into a poly(3‐hydroxybutyrate‐co−3‐hydroxyvalerate) (PHBV) matrix, in which PHBV was either covalently attached to the nanotubes through an esterification reaction between the carboxylic groups of functionalized MWCNTs and the hydroxyl groups of PHBV with toluene diisocyanate as a coupling agent or physically mixed to result in only noncovalent interactions. The structure, crystallization behavior, and thermal properties of the resulting nanocomposites were studied. We found that the crystallization of PHBV grafted onto the MWCNTs (PHBV‐g‐MWCNTs) was markedly hindered and exhibited an exothermic peak caused by cold crystallization, whereas the nonisothermal crystallization of PHBV was enhanced because a heterogeneous nucleation effect appeared in the PHBV/MWCNTs. Moreover, the maximum decomposition temperature of the PHBV‐g‐MWCNTs was improved by about 14.4°C compared with that of the PHBV/MWCNTs and by about 23.7°C compared with that of the original PHBV. Furthermore, the PHBV‐g‐MWCNTs exhibited the wider melt‐processing window than the PHBV/MWCNTs and original PHBV. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 4299–4307, 2013</description><subject>Applied sciences</subject><subject>biopolymers and renewable polymers</subject><subject>Composites</subject><subject>Covalence</subject><subject>Crystallization</subject><subject>Exact sciences and technology</subject><subject>Forms of application and semi-finished materials</subject><subject>Grafting</subject><subject>Graphene</subject><subject>graphene and fullerenes</subject><subject>Hydroxyl groups</subject><subject>Materials science</subject><subject>Nanotubes</subject><subject>Polymer industry, paints, wood</subject><subject>Polymers</subject><subject>Reproduction</subject><subject>Technology of polymers</subject><subject>Thermal properties</subject><issn>0021-8995</issn><issn>1097-4628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNp1kdFqFDEUhgdRcK1e-AYDIrQX0yaTySS5rItthaIVKr0MJ5kMm5pNxiRbOz6Uz2h2t-6F4FXIyfd__ORU1VuMTjFC7RlM0ykRtBXPqgVGgjVd3_Ln1aK84YYLQV9Wr1K6RwhjivpF9XsZ1hNEm4Kvw1jr8ADO-FyDH2of_OFufTYRdLbBpx0IUZWIBx_yRpky83VemVrHOWVwzv6CLVsrs4IHG-JOWIC4BldPMUwmZmt2qim4-Zg0q3mI4XFWmzxHyKbRoTkMtyW2w5PX1YsRXDJvns6j6tvFx9vlVXP95fLT8vy60QQT0RhOu473g-owJkOnCROUc94qPrZiFFyXL8JUEap1ZxQdmGkHMERRhY1QLSFH1fHeW6r-2JiU5dombZwDb8ImSVz0rGM9aQv67h_0PmyiL-0KRRgWiFJWqJM9pWNIKZpRTtGuIc4SI7ndnCybk7vNFfb9kxGSBjdG8NqmQ6BlrMeco8Kd7bmf1pn5_0J5fnPz19zsEzZl83hIQPwue0YYlXefL2X79YpdfFjeyjvyBxTPut8</recordid><startdate>20131215</startdate><enddate>20131215</enddate><creator>Yu, Hou-Yong</creator><creator>Yao, Ju-Ming</creator><creator>Qin, Zong-Yi</creator><creator>Liu, Lin</creator><creator>Yang, Xiao-Gang</creator><general>Blackwell Publishing Ltd</general><general>Wiley</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope><scope>7U5</scope><scope>L7M</scope></search><sort><creationdate>20131215</creationdate><title>Comparison of covalent and noncovalent interactions of carbon nanotubes on the crystallization behavior and thermal properties of poly(3-hydroxybutyrate-co-3-hydroxyvalerate)</title><author>Yu, Hou-Yong ; Yao, Ju-Ming ; Qin, Zong-Yi ; Liu, Lin ; Yang, Xiao-Gang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3139-e854486db4113d4c37958882b8f29f98c39515b35cc4eb5d7e2dae3b5b1e9b233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Applied sciences</topic><topic>biopolymers and renewable polymers</topic><topic>Composites</topic><topic>Covalence</topic><topic>Crystallization</topic><topic>Exact sciences and technology</topic><topic>Forms of application and semi-finished materials</topic><topic>Grafting</topic><topic>Graphene</topic><topic>graphene and fullerenes</topic><topic>Hydroxyl groups</topic><topic>Materials science</topic><topic>Nanotubes</topic><topic>Polymer industry, paints, wood</topic><topic>Polymers</topic><topic>Reproduction</topic><topic>Technology of polymers</topic><topic>Thermal properties</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yu, Hou-Yong</creatorcontrib><creatorcontrib>Yao, Ju-Ming</creatorcontrib><creatorcontrib>Qin, Zong-Yi</creatorcontrib><creatorcontrib>Liu, Lin</creatorcontrib><creatorcontrib>Yang, Xiao-Gang</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><collection>Solid State and Superconductivity Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of applied polymer science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yu, Hou-Yong</au><au>Yao, Ju-Ming</au><au>Qin, Zong-Yi</au><au>Liu, Lin</au><au>Yang, Xiao-Gang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of covalent and noncovalent interactions of carbon nanotubes on the crystallization behavior and thermal properties of poly(3-hydroxybutyrate-co-3-hydroxyvalerate)</atitle><jtitle>Journal of applied polymer science</jtitle><addtitle>J. Appl. Polym. Sci</addtitle><date>2013-12-15</date><risdate>2013</risdate><volume>130</volume><issue>6</issue><spage>4299</spage><epage>4307</epage><pages>4299-4307</pages><issn>0021-8995</issn><eissn>1097-4628</eissn><coden>JAPNAB</coden><abstract>ABSTRACT
In this study, multiwalled carbon nanotubes (MWCNTs) were dispersed into a poly(3‐hydroxybutyrate‐co−3‐hydroxyvalerate) (PHBV) matrix, in which PHBV was either covalently attached to the nanotubes through an esterification reaction between the carboxylic groups of functionalized MWCNTs and the hydroxyl groups of PHBV with toluene diisocyanate as a coupling agent or physically mixed to result in only noncovalent interactions. The structure, crystallization behavior, and thermal properties of the resulting nanocomposites were studied. We found that the crystallization of PHBV grafted onto the MWCNTs (PHBV‐g‐MWCNTs) was markedly hindered and exhibited an exothermic peak caused by cold crystallization, whereas the nonisothermal crystallization of PHBV was enhanced because a heterogeneous nucleation effect appeared in the PHBV/MWCNTs. Moreover, the maximum decomposition temperature of the PHBV‐g‐MWCNTs was improved by about 14.4°C compared with that of the PHBV/MWCNTs and by about 23.7°C compared with that of the original PHBV. Furthermore, the PHBV‐g‐MWCNTs exhibited the wider melt‐processing window than the PHBV/MWCNTs and original PHBV. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 4299–4307, 2013</abstract><cop>Hoboken, NJ</cop><pub>Blackwell Publishing Ltd</pub><doi>10.1002/app.39529</doi><tpages>9</tpages></addata></record> |
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subjects | Applied sciences biopolymers and renewable polymers Composites Covalence Crystallization Exact sciences and technology Forms of application and semi-finished materials Grafting Graphene graphene and fullerenes Hydroxyl groups Materials science Nanotubes Polymer industry, paints, wood Polymers Reproduction Technology of polymers Thermal properties |
title | Comparison of covalent and noncovalent interactions of carbon nanotubes on the crystallization behavior and thermal properties of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) |
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