Comparing Crystallization Kinetics between Polyamide 6 and Polyketone via Chip‐Calorimeter Measurement
Polyamide 6 and aliphatic polyketone exhibit similar melting points and heats of fusion, which expose the kinetic effects of intermolecular interactions on their crystallization kinetics. The commercial chip‐calorimeter Flash DSC1 is employed to measure their crystallization rates in a broad tempera...
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Veröffentlicht in: | Macromolecular chemistry and physics 2018-02, Vol.219 (3), p.n/a |
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description | Polyamide 6 and aliphatic polyketone exhibit similar melting points and heats of fusion, which expose the kinetic effects of intermolecular interactions on their crystallization kinetics. The commercial chip‐calorimeter Flash DSC1 is employed to measure their crystallization rates in a broad temperature range. The results show that polyamide crystallizes faster than polyketone at high temperatures, but slower at low temperatures. The faster crystallization is attributed to a lower lateral‐surface free energy for crystal nucleation at high temperatures on account of the sheet‐like hydrogen bonding in polyamide crystals. The slower crystallization is attributed to the lower molecular mobility for crystal nucleation at low temperatures on account of the higher glass transition temperature of polyamide.
Polyamide 6 (PA) and polyketone (PK) share similar thermodynamic factors in crystallization kinetics, such as melting points and fusion heats; therefore, their different crystallization rates expose the kinetic factors: A higher molecular mobility for PK crystallizing faster at low temperatures, and a lower surface free energy of crystal nuclei for PA crystallizing faster at high temperatures. |
doi_str_mv | 10.1002/macp.201700385 |
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Polyamide 6 (PA) and polyketone (PK) share similar thermodynamic factors in crystallization kinetics, such as melting points and fusion heats; therefore, their different crystallization rates expose the kinetic factors: A higher molecular mobility for PK crystallizing faster at low temperatures, and a lower surface free energy of crystal nuclei for PA crystallizing faster at high temperatures.</description><identifier>ISSN: 1022-1352</identifier><identifier>EISSN: 1521-3935</identifier><identifier>DOI: 10.1002/macp.201700385</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>Aliphatic compounds ; Chemical bonds ; Crystallization ; Crystals ; DSC ; Free energy ; Glass transition temperature ; Hydrogen bonding ; Kinetics ; Melting points ; Nucleation ; polyamides ; polyketone</subject><ispartof>Macromolecular chemistry and physics, 2018-02, Vol.219 (3), p.n/a</ispartof><rights>2017 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3175-7fe5c4d9fe53ac46b4e56e38956da2283eff8f2497e321528a1482795701b89e3</citedby><cites>FETCH-LOGICAL-c3175-7fe5c4d9fe53ac46b4e56e38956da2283eff8f2497e321528a1482795701b89e3</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%2Fmacp.201700385$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmacp.201700385$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids></links><search><creatorcontrib>He, Yucheng</creatorcontrib><creatorcontrib>Luo, Ruiqi</creatorcontrib><creatorcontrib>Li, Zhaolei</creatorcontrib><creatorcontrib>Lv, Ruihua</creatorcontrib><creatorcontrib>Zhou, Dongshan</creatorcontrib><creatorcontrib>Lim, Soonho</creatorcontrib><creatorcontrib>Ren, Xiaoning</creatorcontrib><creatorcontrib>Gao, Hongxu</creatorcontrib><creatorcontrib>Hu, Wenbing</creatorcontrib><title>Comparing Crystallization Kinetics between Polyamide 6 and Polyketone via Chip‐Calorimeter Measurement</title><title>Macromolecular chemistry and physics</title><description>Polyamide 6 and aliphatic polyketone exhibit similar melting points and heats of fusion, which expose the kinetic effects of intermolecular interactions on their crystallization kinetics. The commercial chip‐calorimeter Flash DSC1 is employed to measure their crystallization rates in a broad temperature range. The results show that polyamide crystallizes faster than polyketone at high temperatures, but slower at low temperatures. The faster crystallization is attributed to a lower lateral‐surface free energy for crystal nucleation at high temperatures on account of the sheet‐like hydrogen bonding in polyamide crystals. The slower crystallization is attributed to the lower molecular mobility for crystal nucleation at low temperatures on account of the higher glass transition temperature of polyamide.
Polyamide 6 (PA) and polyketone (PK) share similar thermodynamic factors in crystallization kinetics, such as melting points and fusion heats; therefore, their different crystallization rates expose the kinetic factors: A higher molecular mobility for PK crystallizing faster at low temperatures, and a lower surface free energy of crystal nuclei for PA crystallizing faster at high temperatures.</description><subject>Aliphatic compounds</subject><subject>Chemical bonds</subject><subject>Crystallization</subject><subject>Crystals</subject><subject>DSC</subject><subject>Free energy</subject><subject>Glass transition temperature</subject><subject>Hydrogen bonding</subject><subject>Kinetics</subject><subject>Melting points</subject><subject>Nucleation</subject><subject>polyamides</subject><subject>polyketone</subject><issn>1022-1352</issn><issn>1521-3935</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqFkLtOwzAUhiMEEqWwMltiTvElTuyxiriJVjDAbLnJCXVJnGC7VGHiEXhGnoSUIhiZ_nOk_z-XL4pOCZ4QjOl5o4tuQjHJMGaC70UjwimJmWR8f6gxpTFhnB5GR96vMMYCy2wULfO26bQz9gnlrvdB17V508G0Ft0aC8EUHi0gbAAsum_rXjemBJQibcvv_hlCawG9Go3ypek-3z9yXbfONBDAoTlov3bQgA3H0UGlaw8nPzqOHi8vHvLreHZ3dZNPZ3HBSMbjrAJeJKUchOkiSRcJ8BSYkDwtNaWCQVWJiiYyA0aHB4UmiaCZ5BkmCyGBjaOz3dzOtS9r8EGt2rWzw0pFpEwGPEmaDq7JzlW41nsHleqGm7XrFcFqS1NtaapfmkNA7gIbU0P_j1vNp_n9X_YL9ex6zA</recordid><startdate>201802</startdate><enddate>201802</enddate><creator>He, Yucheng</creator><creator>Luo, Ruiqi</creator><creator>Li, Zhaolei</creator><creator>Lv, Ruihua</creator><creator>Zhou, Dongshan</creator><creator>Lim, Soonho</creator><creator>Ren, Xiaoning</creator><creator>Gao, Hongxu</creator><creator>Hu, Wenbing</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>201802</creationdate><title>Comparing Crystallization Kinetics between Polyamide 6 and Polyketone via Chip‐Calorimeter Measurement</title><author>He, Yucheng ; Luo, Ruiqi ; Li, Zhaolei ; Lv, Ruihua ; Zhou, Dongshan ; Lim, Soonho ; Ren, Xiaoning ; Gao, Hongxu ; Hu, Wenbing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3175-7fe5c4d9fe53ac46b4e56e38956da2283eff8f2497e321528a1482795701b89e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Aliphatic compounds</topic><topic>Chemical bonds</topic><topic>Crystallization</topic><topic>Crystals</topic><topic>DSC</topic><topic>Free energy</topic><topic>Glass transition temperature</topic><topic>Hydrogen bonding</topic><topic>Kinetics</topic><topic>Melting points</topic><topic>Nucleation</topic><topic>polyamides</topic><topic>polyketone</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>He, Yucheng</creatorcontrib><creatorcontrib>Luo, Ruiqi</creatorcontrib><creatorcontrib>Li, Zhaolei</creatorcontrib><creatorcontrib>Lv, Ruihua</creatorcontrib><creatorcontrib>Zhou, Dongshan</creatorcontrib><creatorcontrib>Lim, Soonho</creatorcontrib><creatorcontrib>Ren, Xiaoning</creatorcontrib><creatorcontrib>Gao, Hongxu</creatorcontrib><creatorcontrib>Hu, Wenbing</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Macromolecular chemistry and physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>He, Yucheng</au><au>Luo, Ruiqi</au><au>Li, Zhaolei</au><au>Lv, Ruihua</au><au>Zhou, Dongshan</au><au>Lim, Soonho</au><au>Ren, Xiaoning</au><au>Gao, Hongxu</au><au>Hu, Wenbing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparing Crystallization Kinetics between Polyamide 6 and Polyketone via Chip‐Calorimeter Measurement</atitle><jtitle>Macromolecular chemistry and physics</jtitle><date>2018-02</date><risdate>2018</risdate><volume>219</volume><issue>3</issue><epage>n/a</epage><issn>1022-1352</issn><eissn>1521-3935</eissn><abstract>Polyamide 6 and aliphatic polyketone exhibit similar melting points and heats of fusion, which expose the kinetic effects of intermolecular interactions on their crystallization kinetics. The commercial chip‐calorimeter Flash DSC1 is employed to measure their crystallization rates in a broad temperature range. The results show that polyamide crystallizes faster than polyketone at high temperatures, but slower at low temperatures. The faster crystallization is attributed to a lower lateral‐surface free energy for crystal nucleation at high temperatures on account of the sheet‐like hydrogen bonding in polyamide crystals. The slower crystallization is attributed to the lower molecular mobility for crystal nucleation at low temperatures on account of the higher glass transition temperature of polyamide.
Polyamide 6 (PA) and polyketone (PK) share similar thermodynamic factors in crystallization kinetics, such as melting points and fusion heats; therefore, their different crystallization rates expose the kinetic factors: A higher molecular mobility for PK crystallizing faster at low temperatures, and a lower surface free energy of crystal nuclei for PA crystallizing faster at high temperatures.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/macp.201700385</doi><tpages>6</tpages></addata></record> |
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subjects | Aliphatic compounds Chemical bonds Crystallization Crystals DSC Free energy Glass transition temperature Hydrogen bonding Kinetics Melting points Nucleation polyamides polyketone |
title | Comparing Crystallization Kinetics between Polyamide 6 and Polyketone via Chip‐Calorimeter Measurement |
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