Loading…
Nonequilibrium polymer chains induced by conformational transitions in densely interfacial layers
Nonequilibrium poly(N-isopropylacrylamide) (PNIPAM) chains are generated by temperature-induced conformational transitions in the densely interfacial PNIPAM layer at high adsorbed amounts in aqueous solution. The interleaving chains relax in a spatially heterogeneous space of adsorbed layer which is...
Saved in:
Published in: | The Journal of chemical physics 2012-09, Vol.137 (10), p.104903-104903 |
---|---|
Main Author: | |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c278t-99566b8a8bf5978241baf8eaa18ea015e9cc93d765cedad3df839f97bcfd7b33 |
container_end_page | 104903 |
container_issue | 10 |
container_start_page | 104903 |
container_title | The Journal of chemical physics |
container_volume | 137 |
creator | Zhu, Peng-Wei |
description | Nonequilibrium poly(N-isopropylacrylamide) (PNIPAM) chains are generated by temperature-induced conformational transitions in the densely interfacial PNIPAM layer at high adsorbed amounts in aqueous solution. The interleaving chains relax in a spatially heterogeneous space of adsorbed layer which is filled with the domains via the hydrogen bonding and hydrophobic interactions. The relaxation dynamics of interleaving chains is changed from the weekly stretched exponential behaviour at the lower adsorbed amount to the strongly stretched exponential behaviour at the higher adsorbed amount. The kinetic constraints for the relaxation dynamics depend on the segment density of the adsorbed layer which is controlled by the temperature. The stretched exponential relaxation is related to an ensemble of relaxations confined in the domains with different physical origins for the heterogeneous dynamics. The range of energy barriers for the relaxation is estimated from the stretched exponent based on the random first order transition theory. |
doi_str_mv | 10.1063/1.4751479 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1671520592</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1671520592</sourcerecordid><originalsourceid>FETCH-LOGICAL-c278t-99566b8a8bf5978241baf8eaa18ea015e9cc93d765cedad3df839f97bcfd7b33</originalsourceid><addsrcrecordid>eNqF0LtOwzAUBmALgWgpDLwAyghDwJfE9hlRxU1CsHSPfBVGTtLayZC3J1ULK8u5SJ-Ojn6Ergm-J5izB3JfiZpUAk7QkmAJpeCAT9ESY0pK4Jgv0EXO3xhjImh1jhaUggAp-RKpj75zuzHEoFMY22Lbx6l1qTBfKnS5CJ0djbOFngrTd75PrRpC36lYDEl1OeyXvSqs67KL0zwOLnllwkyimlzKl-jMq5jd1bGv0Ob5abN-Ld8_X97Wj--loUIOJUDNuZZKal-DkLQiWnnplCJzwaR2YAwwK3g9_6Mss14y8CC08VZoxlbo9nB2m_rd6PLQtCEbF6PqXD_mhnBBaoproP9TXGEASRnM9O5ATepzTs432xRalaYZNfvsG9Ics5_tzfHsqFtn_-Rv2OwHaTKA0w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1040998239</pqid></control><display><type>article</type><title>Nonequilibrium polymer chains induced by conformational transitions in densely interfacial layers</title><source>American Institute of Physics:Jisc Collections:Transitional Journals Agreement 2021-23 (Reading list)</source><source>AIP_美国物理联合会现刊(与NSTL共建)</source><creator>Zhu, Peng-Wei</creator><creatorcontrib>Zhu, Peng-Wei</creatorcontrib><description>Nonequilibrium poly(N-isopropylacrylamide) (PNIPAM) chains are generated by temperature-induced conformational transitions in the densely interfacial PNIPAM layer at high adsorbed amounts in aqueous solution. The interleaving chains relax in a spatially heterogeneous space of adsorbed layer which is filled with the domains via the hydrogen bonding and hydrophobic interactions. The relaxation dynamics of interleaving chains is changed from the weekly stretched exponential behaviour at the lower adsorbed amount to the strongly stretched exponential behaviour at the higher adsorbed amount. The kinetic constraints for the relaxation dynamics depend on the segment density of the adsorbed layer which is controlled by the temperature. The stretched exponential relaxation is related to an ensemble of relaxations confined in the domains with different physical origins for the heterogeneous dynamics. The range of energy barriers for the relaxation is estimated from the stretched exponent based on the random first order transition theory.</description><identifier>ISSN: 0021-9606</identifier><identifier>EISSN: 1089-7690</identifier><identifier>DOI: 10.1063/1.4751479</identifier><identifier>PMID: 22979886</identifier><language>eng</language><publisher>United States</publisher><subject>Acrylamides - chemistry ; Acrylic Resins ; Adsorption ; Aqueous solutions ; Barriers ; Chains (polymeric) ; Density ; Dynamics ; Hydrodynamics ; Hydrogen bonding ; Kinetics ; Molecular Conformation ; Origins ; Polymers - chemistry ; Segments ; Solutions ; Temperature ; Water - chemistry</subject><ispartof>The Journal of chemical physics, 2012-09, Vol.137 (10), p.104903-104903</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c278t-99566b8a8bf5978241baf8eaa18ea015e9cc93d765cedad3df839f97bcfd7b33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,782,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22979886$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhu, Peng-Wei</creatorcontrib><title>Nonequilibrium polymer chains induced by conformational transitions in densely interfacial layers</title><title>The Journal of chemical physics</title><addtitle>J Chem Phys</addtitle><description>Nonequilibrium poly(N-isopropylacrylamide) (PNIPAM) chains are generated by temperature-induced conformational transitions in the densely interfacial PNIPAM layer at high adsorbed amounts in aqueous solution. The interleaving chains relax in a spatially heterogeneous space of adsorbed layer which is filled with the domains via the hydrogen bonding and hydrophobic interactions. The relaxation dynamics of interleaving chains is changed from the weekly stretched exponential behaviour at the lower adsorbed amount to the strongly stretched exponential behaviour at the higher adsorbed amount. The kinetic constraints for the relaxation dynamics depend on the segment density of the adsorbed layer which is controlled by the temperature. The stretched exponential relaxation is related to an ensemble of relaxations confined in the domains with different physical origins for the heterogeneous dynamics. The range of energy barriers for the relaxation is estimated from the stretched exponent based on the random first order transition theory.</description><subject>Acrylamides - chemistry</subject><subject>Acrylic Resins</subject><subject>Adsorption</subject><subject>Aqueous solutions</subject><subject>Barriers</subject><subject>Chains (polymeric)</subject><subject>Density</subject><subject>Dynamics</subject><subject>Hydrodynamics</subject><subject>Hydrogen bonding</subject><subject>Kinetics</subject><subject>Molecular Conformation</subject><subject>Origins</subject><subject>Polymers - chemistry</subject><subject>Segments</subject><subject>Solutions</subject><subject>Temperature</subject><subject>Water - chemistry</subject><issn>0021-9606</issn><issn>1089-7690</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqF0LtOwzAUBmALgWgpDLwAyghDwJfE9hlRxU1CsHSPfBVGTtLayZC3J1ULK8u5SJ-Ojn6Ergm-J5izB3JfiZpUAk7QkmAJpeCAT9ESY0pK4Jgv0EXO3xhjImh1jhaUggAp-RKpj75zuzHEoFMY22Lbx6l1qTBfKnS5CJ0djbOFngrTd75PrRpC36lYDEl1OeyXvSqs67KL0zwOLnllwkyimlzKl-jMq5jd1bGv0Ob5abN-Ld8_X97Wj--loUIOJUDNuZZKal-DkLQiWnnplCJzwaR2YAwwK3g9_6Mss14y8CC08VZoxlbo9nB2m_rd6PLQtCEbF6PqXD_mhnBBaoproP9TXGEASRnM9O5ATepzTs432xRalaYZNfvsG9Ics5_tzfHsqFtn_-Rv2OwHaTKA0w</recordid><startdate>20120914</startdate><enddate>20120914</enddate><creator>Zhu, Peng-Wei</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7U5</scope><scope>8FD</scope><scope>H8D</scope><scope>L7M</scope></search><sort><creationdate>20120914</creationdate><title>Nonequilibrium polymer chains induced by conformational transitions in densely interfacial layers</title><author>Zhu, Peng-Wei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c278t-99566b8a8bf5978241baf8eaa18ea015e9cc93d765cedad3df839f97bcfd7b33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Acrylamides - chemistry</topic><topic>Acrylic Resins</topic><topic>Adsorption</topic><topic>Aqueous solutions</topic><topic>Barriers</topic><topic>Chains (polymeric)</topic><topic>Density</topic><topic>Dynamics</topic><topic>Hydrodynamics</topic><topic>Hydrogen bonding</topic><topic>Kinetics</topic><topic>Molecular Conformation</topic><topic>Origins</topic><topic>Polymers - chemistry</topic><topic>Segments</topic><topic>Solutions</topic><topic>Temperature</topic><topic>Water - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhu, Peng-Wei</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Aerospace Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>The Journal of chemical physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhu, Peng-Wei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nonequilibrium polymer chains induced by conformational transitions in densely interfacial layers</atitle><jtitle>The Journal of chemical physics</jtitle><addtitle>J Chem Phys</addtitle><date>2012-09-14</date><risdate>2012</risdate><volume>137</volume><issue>10</issue><spage>104903</spage><epage>104903</epage><pages>104903-104903</pages><issn>0021-9606</issn><eissn>1089-7690</eissn><abstract>Nonequilibrium poly(N-isopropylacrylamide) (PNIPAM) chains are generated by temperature-induced conformational transitions in the densely interfacial PNIPAM layer at high adsorbed amounts in aqueous solution. The interleaving chains relax in a spatially heterogeneous space of adsorbed layer which is filled with the domains via the hydrogen bonding and hydrophobic interactions. The relaxation dynamics of interleaving chains is changed from the weekly stretched exponential behaviour at the lower adsorbed amount to the strongly stretched exponential behaviour at the higher adsorbed amount. The kinetic constraints for the relaxation dynamics depend on the segment density of the adsorbed layer which is controlled by the temperature. The stretched exponential relaxation is related to an ensemble of relaxations confined in the domains with different physical origins for the heterogeneous dynamics. The range of energy barriers for the relaxation is estimated from the stretched exponent based on the random first order transition theory.</abstract><cop>United States</cop><pmid>22979886</pmid><doi>10.1063/1.4751479</doi><tpages>1</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-9606 |
ispartof | The Journal of chemical physics, 2012-09, Vol.137 (10), p.104903-104903 |
issn | 0021-9606 1089-7690 |
language | eng |
recordid | cdi_proquest_miscellaneous_1671520592 |
source | American Institute of Physics:Jisc Collections:Transitional Journals Agreement 2021-23 (Reading list); AIP_美国物理联合会现刊(与NSTL共建) |
subjects | Acrylamides - chemistry Acrylic Resins Adsorption Aqueous solutions Barriers Chains (polymeric) Density Dynamics Hydrodynamics Hydrogen bonding Kinetics Molecular Conformation Origins Polymers - chemistry Segments Solutions Temperature Water - chemistry |
title | Nonequilibrium polymer chains induced by conformational transitions in densely interfacial layers |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T13%3A09%3A38IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Nonequilibrium%20polymer%20chains%20induced%20by%20conformational%20transitions%20in%20densely%20interfacial%20layers&rft.jtitle=The%20Journal%20of%20chemical%20physics&rft.au=Zhu,%20Peng-Wei&rft.date=2012-09-14&rft.volume=137&rft.issue=10&rft.spage=104903&rft.epage=104903&rft.pages=104903-104903&rft.issn=0021-9606&rft.eissn=1089-7690&rft_id=info:doi/10.1063/1.4751479&rft_dat=%3Cproquest_cross%3E1671520592%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c278t-99566b8a8bf5978241baf8eaa18ea015e9cc93d765cedad3df839f97bcfd7b33%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1040998239&rft_id=info:pmid/22979886&rfr_iscdi=true |