Small-Angle Neutron Scattering Study on Defect-Controlled Polymer Networks
Tetra-PEG gels are classified to near-“ideal” networks with significantly low inhomogeneities, which were confirmed by small-angle neutron scattering (SANS). In this study, we systematically introduced two types of defects into Tetra-PEG gels and investigated effects of defects on structure. First,...
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Veröffentlicht in: | Macromolecules 2014-03, Vol.47 (5), p.1801-1809 |
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container_title | Macromolecules |
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creator | Nishi, Kengo Asai, Hanako Fujii, Kenta Han, Young-Soo Kim, Tae-Hwan Sakai, Takamasa Shibayama, Mitsuhiro |
description | Tetra-PEG gels are classified to near-“ideal” networks with significantly low inhomogeneities, which were confirmed by small-angle neutron scattering (SANS). In this study, we systematically introduced two types of defects into Tetra-PEG gels and investigated effects of defects on structure. First, we prepared defect-rich networks by simply reducing prepolymer concentration, and observed the evolution of network structure by time-resolved SANS during gelation process. In this case, both the scattering intensity and the correlation length increased with reaction time in the ϕ < ϕ* region, while they scarcely changed in the ϕ > ϕ* region. Here, ϕ and ϕ* are the polymer volume fractions at observation and that at chain-overlap concentration, respectively. Second, we prepared “p-tuned” Tetra-PEG gels by tuning the reaction probability, p, and soaked them in water to expose the inhomogeneities. It was revealed that SANS profiles of as-prepared gels did not change noticeably, while those of swollen gels systematically changed with decreasing p. On the basis of these results, we discuss the relationship between the defects of polymer network and inhomogeneities by using simple schematic pictures of polymer network. |
doi_str_mv | 10.1021/ma402590n |
format | Article |
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In this study, we systematically introduced two types of defects into Tetra-PEG gels and investigated effects of defects on structure. First, we prepared defect-rich networks by simply reducing prepolymer concentration, and observed the evolution of network structure by time-resolved SANS during gelation process. In this case, both the scattering intensity and the correlation length increased with reaction time in the ϕ < ϕ* region, while they scarcely changed in the ϕ > ϕ* region. Here, ϕ and ϕ* are the polymer volume fractions at observation and that at chain-overlap concentration, respectively. Second, we prepared “p-tuned” Tetra-PEG gels by tuning the reaction probability, p, and soaked them in water to expose the inhomogeneities. It was revealed that SANS profiles of as-prepared gels did not change noticeably, while those of swollen gels systematically changed with decreasing p. On the basis of these results, we discuss the relationship between the defects of polymer network and inhomogeneities by using simple schematic pictures of polymer network.</description><identifier>ISSN: 0024-9297</identifier><identifier>EISSN: 1520-5835</identifier><identifier>DOI: 10.1021/ma402590n</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 ; Solution and gel properties</subject><ispartof>Macromolecules, 2014-03, Vol.47 (5), p.1801-1809</ispartof><rights>Copyright © 2014 American Chemical Society</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a355t-4849f955bd19123f80972ddc01ff39447cdeb4c7036ceafa28b6b9ccb1b0d8f73</citedby><cites>FETCH-LOGICAL-a355t-4849f955bd19123f80972ddc01ff39447cdeb4c7036ceafa28b6b9ccb1b0d8f73</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/ma402590n$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ma402590n$$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=28451807$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Nishi, Kengo</creatorcontrib><creatorcontrib>Asai, Hanako</creatorcontrib><creatorcontrib>Fujii, Kenta</creatorcontrib><creatorcontrib>Han, Young-Soo</creatorcontrib><creatorcontrib>Kim, Tae-Hwan</creatorcontrib><creatorcontrib>Sakai, Takamasa</creatorcontrib><creatorcontrib>Shibayama, Mitsuhiro</creatorcontrib><title>Small-Angle Neutron Scattering Study on Defect-Controlled Polymer Networks</title><title>Macromolecules</title><addtitle>Macromolecules</addtitle><description>Tetra-PEG gels are classified to near-“ideal” networks with significantly low inhomogeneities, which were confirmed by small-angle neutron scattering (SANS). In this study, we systematically introduced two types of defects into Tetra-PEG gels and investigated effects of defects on structure. First, we prepared defect-rich networks by simply reducing prepolymer concentration, and observed the evolution of network structure by time-resolved SANS during gelation process. In this case, both the scattering intensity and the correlation length increased with reaction time in the ϕ < ϕ* region, while they scarcely changed in the ϕ > ϕ* region. Here, ϕ and ϕ* are the polymer volume fractions at observation and that at chain-overlap concentration, respectively. Second, we prepared “p-tuned” Tetra-PEG gels by tuning the reaction probability, p, and soaked them in water to expose the inhomogeneities. It was revealed that SANS profiles of as-prepared gels did not change noticeably, while those of swollen gels systematically changed with decreasing p. On the basis of these results, we discuss the relationship between the defects of polymer network and inhomogeneities by using simple schematic pictures of polymer network.</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>Solution and gel properties</subject><issn>0024-9297</issn><issn>1520-5835</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNptkEtLAzEcxIMoWB8Hv8FePHiI_vPqJsdS3xQVquclm0dpzWZLkiL99q5U6sXTwPCbgRmELghcE6DkptMcqFAQD9CICApYSCYO0QiAcqyoqo_RSc4rAEIEZyP0PO90CHgSF8FVL25TUh-rudGluLSMi2peNnZbDd6t884UPO3jgITgbPXWh23n0pAqX336zGfoyOuQ3fmvnqKP-7v36SOevT48TSczrJkQBXPJlVdCtJYoQpmXoGpqrQHiPVOc18a6lpsa2Ng47TWV7bhVxrSkBSt9zU7R1a7XpD7n5HyzTstOp21DoPk5odmfMLCXO3ats9HBJx3NMu8DVHJBJNR_nDa5WfWbFIcF__R9Az65aKo</recordid><startdate>20140311</startdate><enddate>20140311</enddate><creator>Nishi, Kengo</creator><creator>Asai, Hanako</creator><creator>Fujii, Kenta</creator><creator>Han, Young-Soo</creator><creator>Kim, Tae-Hwan</creator><creator>Sakai, Takamasa</creator><creator>Shibayama, Mitsuhiro</creator><general>American Chemical Society</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20140311</creationdate><title>Small-Angle Neutron Scattering Study on Defect-Controlled Polymer Networks</title><author>Nishi, Kengo ; Asai, Hanako ; Fujii, Kenta ; Han, Young-Soo ; Kim, Tae-Hwan ; Sakai, Takamasa ; Shibayama, Mitsuhiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a355t-4849f955bd19123f80972ddc01ff39447cdeb4c7036ceafa28b6b9ccb1b0d8f73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</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>Solution and gel properties</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nishi, Kengo</creatorcontrib><creatorcontrib>Asai, Hanako</creatorcontrib><creatorcontrib>Fujii, Kenta</creatorcontrib><creatorcontrib>Han, Young-Soo</creatorcontrib><creatorcontrib>Kim, Tae-Hwan</creatorcontrib><creatorcontrib>Sakai, Takamasa</creatorcontrib><creatorcontrib>Shibayama, Mitsuhiro</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nishi, Kengo</au><au>Asai, Hanako</au><au>Fujii, Kenta</au><au>Han, Young-Soo</au><au>Kim, Tae-Hwan</au><au>Sakai, Takamasa</au><au>Shibayama, Mitsuhiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Small-Angle Neutron Scattering Study on Defect-Controlled Polymer Networks</atitle><jtitle>Macromolecules</jtitle><addtitle>Macromolecules</addtitle><date>2014-03-11</date><risdate>2014</risdate><volume>47</volume><issue>5</issue><spage>1801</spage><epage>1809</epage><pages>1801-1809</pages><issn>0024-9297</issn><eissn>1520-5835</eissn><coden>MAMOBX</coden><abstract>Tetra-PEG gels are classified to near-“ideal” networks with significantly low inhomogeneities, which were confirmed by small-angle neutron scattering (SANS). In this study, we systematically introduced two types of defects into Tetra-PEG gels and investigated effects of defects on structure. First, we prepared defect-rich networks by simply reducing prepolymer concentration, and observed the evolution of network structure by time-resolved SANS during gelation process. In this case, both the scattering intensity and the correlation length increased with reaction time in the ϕ < ϕ* region, while they scarcely changed in the ϕ > ϕ* region. Here, ϕ and ϕ* are the polymer volume fractions at observation and that at chain-overlap concentration, respectively. Second, we prepared “p-tuned” Tetra-PEG gels by tuning the reaction probability, p, and soaked them in water to expose the inhomogeneities. It was revealed that SANS profiles of as-prepared gels did not change noticeably, while those of swollen gels systematically changed with decreasing p. On the basis of these results, we discuss the relationship between the defects of polymer network and inhomogeneities by using simple schematic pictures of polymer network.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ma402590n</doi><tpages>9</tpages></addata></record> |
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subjects | Applied sciences Exact sciences and technology Organic polymers Physicochemistry of polymers Properties and characterization Solution and gel properties |
title | Small-Angle Neutron Scattering Study on Defect-Controlled Polymer Networks |
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