Loading…
The Polyelectrolyte Complex/Coacervate Continuum
Stoichiometric polyelectrolyte complexes (PECs) of the strong polyelectrolytes poly(styrenesulfonate) (PSS) and poly(diallyldimethylammonium) (PDADMA) were dissociated and dissolved in aqueous KBr. Water was added to dilute the salt, allowing polyelectrolytes to reassociate. After appropriate equi...
Saved in:
Published in: | Macromolecules 2014-05, Vol.47 (9), p.3108-3116 |
---|---|
Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-a324t-9b4f9ce2ef449f08176e487d8e53a389aaa1eddf0c658dcb8d17d84db2b1b8cb3 |
---|---|
cites | cdi_FETCH-LOGICAL-a324t-9b4f9ce2ef449f08176e487d8e53a389aaa1eddf0c658dcb8d17d84db2b1b8cb3 |
container_end_page | 3116 |
container_issue | 9 |
container_start_page | 3108 |
container_title | Macromolecules |
container_volume | 47 |
creator | Wang, Qifeng Schlenoff, Joseph B |
description | Stoichiometric polyelectrolyte complexes (PECs) of the strong polyelectrolytes poly(styrenesulfonate) (PSS) and poly(diallyldimethylammonium) (PDADMA) were dissociated and dissolved in aqueous KBr. Water was added to dilute the salt, allowing polyelectrolytes to reassociate. After appropriate equilibration, these mixtures yielded compositions spanning complexes (solid) to coacervates (elastic liquid) to dissolved solutions with increasing [KBr]. These compositions were defined by a ternary polymer/water/salt phase diagram. For coacervates, transient microphase separation could be induced by a small departure from equilibration temperature. A boundary between complex and coacervate states was defined by the crossover point between loss and storage modulus. Salt ions within the complex/coacervate were identified as either ion paired with polyelectrolytes (“doping”) or unassociated. The fraction of ion pair cross-links between polyelectrolytes as a function of KBr concentration was used to account for viscosity using a model of “sticky” reptation. |
doi_str_mv | 10.1021/ma500500q |
format | article |
fullrecord | <record><control><sourceid>acs_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1021_ma500500q</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>c785257944</sourcerecordid><originalsourceid>FETCH-LOGICAL-a324t-9b4f9ce2ef449f08176e487d8e53a389aaa1eddf0c658dcb8d17d84db2b1b8cb3</originalsourceid><addsrcrecordid>eNptj01Lw0AQhhdRMFYP_oNePHiInf1qdo8S_IKCHuo5TDazmJIvd1Ox_95opV6EgRlmnnnhYeySww0HwRctaoCp3o9YwrWAVBupj1kCIFRqhc1O2VmMGwDOtZIJg_UbzV_6ZkcNuTFMw0jzvG-Hhj4XeY-Owgf-rLqx7rbb9pydeGwiXfz2GXu9v1vnj-nq-eEpv12lKIUaU1sqbx0J8kpZD4ZnS1ImqwxpidJYRORUVR7cUpvKlabi01FVpSh5aVwpZ-x6n-tCH2MgXwyhbjHsCg7Ft2pxUJ3Yqz07YHTY-ICdq-PhQRgN1hr-x6GLxabfhm4y-CfvCw36X_k</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>The Polyelectrolyte Complex/Coacervate Continuum</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)</source><creator>Wang, Qifeng ; Schlenoff, Joseph B</creator><creatorcontrib>Wang, Qifeng ; Schlenoff, Joseph B</creatorcontrib><description>Stoichiometric polyelectrolyte complexes (PECs) of the strong polyelectrolytes poly(styrenesulfonate) (PSS) and poly(diallyldimethylammonium) (PDADMA) were dissociated and dissolved in aqueous KBr. Water was added to dilute the salt, allowing polyelectrolytes to reassociate. After appropriate equilibration, these mixtures yielded compositions spanning complexes (solid) to coacervates (elastic liquid) to dissolved solutions with increasing [KBr]. These compositions were defined by a ternary polymer/water/salt phase diagram. For coacervates, transient microphase separation could be induced by a small departure from equilibration temperature. A boundary between complex and coacervate states was defined by the crossover point between loss and storage modulus. Salt ions within the complex/coacervate were identified as either ion paired with polyelectrolytes (“doping”) or unassociated. The fraction of ion pair cross-links between polyelectrolytes as a function of KBr concentration was used to account for viscosity using a model of “sticky” reptation.</description><identifier>ISSN: 0024-9297</identifier><identifier>EISSN: 1520-5835</identifier><identifier>DOI: 10.1021/ma500500q</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, 2014-05, Vol.47 (9), p.3108-3116</ispartof><rights>Copyright © 2014 American Chemical Society</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a324t-9b4f9ce2ef449f08176e487d8e53a389aaa1eddf0c658dcb8d17d84db2b1b8cb3</citedby><cites>FETCH-LOGICAL-a324t-9b4f9ce2ef449f08176e487d8e53a389aaa1eddf0c658dcb8d17d84db2b1b8cb3</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=28509981$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Qifeng</creatorcontrib><creatorcontrib>Schlenoff, Joseph B</creatorcontrib><title>The Polyelectrolyte Complex/Coacervate Continuum</title><title>Macromolecules</title><addtitle>Macromolecules</addtitle><description>Stoichiometric polyelectrolyte complexes (PECs) of the strong polyelectrolytes poly(styrenesulfonate) (PSS) and poly(diallyldimethylammonium) (PDADMA) were dissociated and dissolved in aqueous KBr. Water was added to dilute the salt, allowing polyelectrolytes to reassociate. After appropriate equilibration, these mixtures yielded compositions spanning complexes (solid) to coacervates (elastic liquid) to dissolved solutions with increasing [KBr]. These compositions were defined by a ternary polymer/water/salt phase diagram. For coacervates, transient microphase separation could be induced by a small departure from equilibration temperature. A boundary between complex and coacervate states was defined by the crossover point between loss and storage modulus. Salt ions within the complex/coacervate were identified as either ion paired with polyelectrolytes (“doping”) or unassociated. The fraction of ion pair cross-links between polyelectrolytes as a function of KBr concentration was used to account for viscosity using a model of “sticky” reptation.</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><sourceid>N~.</sourceid><recordid>eNptj01Lw0AQhhdRMFYP_oNePHiInf1qdo8S_IKCHuo5TDazmJIvd1Ox_95opV6EgRlmnnnhYeySww0HwRctaoCp3o9YwrWAVBupj1kCIFRqhc1O2VmMGwDOtZIJg_UbzV_6ZkcNuTFMw0jzvG-Hhj4XeY-Owgf-rLqx7rbb9pydeGwiXfz2GXu9v1vnj-nq-eEpv12lKIUaU1sqbx0J8kpZD4ZnS1ImqwxpidJYRORUVR7cUpvKlabi01FVpSh5aVwpZ-x6n-tCH2MgXwyhbjHsCg7Ft2pxUJ3Yqz07YHTY-ICdq-PhQRgN1hr-x6GLxabfhm4y-CfvCw36X_k</recordid><startdate>20140513</startdate><enddate>20140513</enddate><creator>Wang, Qifeng</creator><creator>Schlenoff, Joseph B</creator><general>American Chemical Society</general><scope>N~.</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20140513</creationdate><title>The Polyelectrolyte Complex/Coacervate Continuum</title><author>Wang, Qifeng ; Schlenoff, Joseph B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a324t-9b4f9ce2ef449f08176e487d8e53a389aaa1eddf0c658dcb8d17d84db2b1b8cb3</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>Wang, Qifeng</creatorcontrib><creatorcontrib>Schlenoff, Joseph B</creatorcontrib><collection>American Chemical Society (ACS) Open Access</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Qifeng</au><au>Schlenoff, Joseph B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Polyelectrolyte Complex/Coacervate Continuum</atitle><jtitle>Macromolecules</jtitle><addtitle>Macromolecules</addtitle><date>2014-05-13</date><risdate>2014</risdate><volume>47</volume><issue>9</issue><spage>3108</spage><epage>3116</epage><pages>3108-3116</pages><issn>0024-9297</issn><eissn>1520-5835</eissn><coden>MAMOBX</coden><abstract>Stoichiometric polyelectrolyte complexes (PECs) of the strong polyelectrolytes poly(styrenesulfonate) (PSS) and poly(diallyldimethylammonium) (PDADMA) were dissociated and dissolved in aqueous KBr. Water was added to dilute the salt, allowing polyelectrolytes to reassociate. After appropriate equilibration, these mixtures yielded compositions spanning complexes (solid) to coacervates (elastic liquid) to dissolved solutions with increasing [KBr]. These compositions were defined by a ternary polymer/water/salt phase diagram. For coacervates, transient microphase separation could be induced by a small departure from equilibration temperature. A boundary between complex and coacervate states was defined by the crossover point between loss and storage modulus. Salt ions within the complex/coacervate were identified as either ion paired with polyelectrolytes (“doping”) or unassociated. The fraction of ion pair cross-links between polyelectrolytes as a function of KBr concentration was used to account for viscosity using a model of “sticky” reptation.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ma500500q</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0024-9297 |
ispartof | Macromolecules, 2014-05, Vol.47 (9), p.3108-3116 |
issn | 0024-9297 1520-5835 |
language | eng |
recordid | cdi_crossref_primary_10_1021_ma500500q |
source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | Applied sciences Exact sciences and technology Organic polymers Physicochemistry of polymers Properties and characterization Solution and gel properties |
title | The Polyelectrolyte Complex/Coacervate Continuum |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T10%3A17%3A17IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-acs_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20Polyelectrolyte%20Complex/Coacervate%20Continuum&rft.jtitle=Macromolecules&rft.au=Wang,%20Qifeng&rft.date=2014-05-13&rft.volume=47&rft.issue=9&rft.spage=3108&rft.epage=3116&rft.pages=3108-3116&rft.issn=0024-9297&rft.eissn=1520-5835&rft.coden=MAMOBX&rft_id=info:doi/10.1021/ma500500q&rft_dat=%3Cacs_cross%3Ec785257944%3C/acs_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a324t-9b4f9ce2ef449f08176e487d8e53a389aaa1eddf0c658dcb8d17d84db2b1b8cb3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |