Amphiphilic derivatives of dextran: Adsorption at air/water and oil/water interfaces

Ionic amphiphilic dextran derivatives were synthesized by the attachment of sodium sulfopropyl and phenoxy groups on the native polysaccharide. A family of dextran derivatives was thus obtained with varying hydrophobic content and charge density in the polymer chains. The surface-active properties o...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of colloid and interface science 2004-11, Vol.279 (1), p.68-77
Hauptverfasser: Rotureau, E., Leonard, M., Dellacherie, E., Durand, A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 77
container_issue 1
container_start_page 68
container_title Journal of colloid and interface science
container_volume 279
creator Rotureau, E.
Leonard, M.
Dellacherie, E.
Durand, A.
description Ionic amphiphilic dextran derivatives were synthesized by the attachment of sodium sulfopropyl and phenoxy groups on the native polysaccharide. A family of dextran derivatives was thus obtained with varying hydrophobic content and charge density in the polymer chains. The surface-active properties of polymers were studied at the air–water and dodecane–water interfaces using dynamic surface/interfacial tension measurements. The adsorption was shown to begin in a diffusion-limited regime at low polymer concentrations, that is to say, with the diffusion of macromolecules in the bulk solution. In contrast, at long times the interfacial adsorption is limited by interfacial phenomena: adsorption kinetics or transfer into the adsorbed layer. A semiempirical equation developed by Filippov was shown to correctly fit the experimental curves over the whole time range. The presence of ionic groups in the chains strongly lowers the adsorption kinetics. This effect can be interpreted by electrostatic interactions between the free molecules and the already adsorbed ones. The adsorption kinetics at air–water and oil–water interfaces are compared.
doi_str_mv 10.1016/j.jcis.2004.06.040
format Article
fullrecord <record><control><sourceid>proquest_hal_p</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_00079357v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0021979704005594</els_id><sourcerecordid>66899433</sourcerecordid><originalsourceid>FETCH-LOGICAL-c453t-b122fed4a5a4054d396ded63c8472580ec9288ea710fef16d499a091f1398d393</originalsourceid><addsrcrecordid>eNp9kE1r3DAQhkVpaLZJ_0APxZcWcrAzsj5slVyW0DaFhVySs1CkEdHitbaSd9P--8qsSW8FMWKGZ16kh5CPFBoKVF5vm60NuWkBeAOyAQ5vyIqCEnVHgb0lK4CW1qpT3Tl5n_MWgFIh1DtyTgXrgVO2Ig_r3f45lDMEWzlM4WimcMRcRV_a31My49dq7XJM-ynEsTJTZUK6fjETpsqMrophWLowluqNxXxJzrwZMn5Y7gvy-P3bw-1dvbn_8fN2vaktF2yqn2jbenTcCMNBcMeUdOgksz3vWtEDWtX2PZryG4-eSseVMqCop0z1hWYX5OqU-2wGvU9hZ9IfHU3Qd-uNnmcA0CkmuiMt7JcTu0_x1wHzpHchWxwGM2I8ZC1lrxRnrIDtCbQp5pzQvyZT0LN3vdWzdz171yB18V6WPi3ph6cdun8ri-gCfF4Ak60ZfPE6Z7xysgUl-65wNycOi7djwKSzDThadCGhnbSL4X_v-Av2k5_t</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>66899433</pqid></control><display><type>article</type><title>Amphiphilic derivatives of dextran: Adsorption at air/water and oil/water interfaces</title><source>MEDLINE</source><source>ScienceDirect Journals (5 years ago - present)</source><creator>Rotureau, E. ; Leonard, M. ; Dellacherie, E. ; Durand, A.</creator><creatorcontrib>Rotureau, E. ; Leonard, M. ; Dellacherie, E. ; Durand, A.</creatorcontrib><description>Ionic amphiphilic dextran derivatives were synthesized by the attachment of sodium sulfopropyl and phenoxy groups on the native polysaccharide. A family of dextran derivatives was thus obtained with varying hydrophobic content and charge density in the polymer chains. The surface-active properties of polymers were studied at the air–water and dodecane–water interfaces using dynamic surface/interfacial tension measurements. The adsorption was shown to begin in a diffusion-limited regime at low polymer concentrations, that is to say, with the diffusion of macromolecules in the bulk solution. In contrast, at long times the interfacial adsorption is limited by interfacial phenomena: adsorption kinetics or transfer into the adsorbed layer. A semiempirical equation developed by Filippov was shown to correctly fit the experimental curves over the whole time range. The presence of ionic groups in the chains strongly lowers the adsorption kinetics. This effect can be interpreted by electrostatic interactions between the free molecules and the already adsorbed ones. The adsorption kinetics at air–water and oil–water interfaces are compared.</description><identifier>ISSN: 0021-9797</identifier><identifier>EISSN: 1095-7103</identifier><identifier>DOI: 10.1016/j.jcis.2004.06.040</identifier><identifier>PMID: 15380413</identifier><identifier>CODEN: JCISA5</identifier><language>eng</language><publisher>San Diego, CA: Elsevier Inc</publisher><subject>Adsorption ; Air ; Amphiphilic polymers ; Chemistry ; Dextran ; Dextrans - chemical synthesis ; Dextrans - chemistry ; Engineering Sciences ; Exact sciences and technology ; General and physical chemistry ; Interfacial tension ; Molecular Structure ; Oils - chemistry ; Other ; Polysaccharides - chemical synthesis ; Polysaccharides - chemistry ; Surface physical chemistry ; Surface Properties ; Surface-Active Agents - chemical synthesis ; Surface-Active Agents - chemistry ; Water - chemistry</subject><ispartof>Journal of colloid and interface science, 2004-11, Vol.279 (1), p.68-77</ispartof><rights>2004 Elsevier Inc.</rights><rights>2005 INIST-CNRS</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c453t-b122fed4a5a4054d396ded63c8472580ec9288ea710fef16d499a091f1398d393</citedby><cites>FETCH-LOGICAL-c453t-b122fed4a5a4054d396ded63c8472580ec9288ea710fef16d499a091f1398d393</cites><orcidid>0000-0003-1330-5631</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jcis.2004.06.040$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,777,781,882,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=16209687$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15380413$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00079357$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Rotureau, E.</creatorcontrib><creatorcontrib>Leonard, M.</creatorcontrib><creatorcontrib>Dellacherie, E.</creatorcontrib><creatorcontrib>Durand, A.</creatorcontrib><title>Amphiphilic derivatives of dextran: Adsorption at air/water and oil/water interfaces</title><title>Journal of colloid and interface science</title><addtitle>J Colloid Interface Sci</addtitle><description>Ionic amphiphilic dextran derivatives were synthesized by the attachment of sodium sulfopropyl and phenoxy groups on the native polysaccharide. A family of dextran derivatives was thus obtained with varying hydrophobic content and charge density in the polymer chains. The surface-active properties of polymers were studied at the air–water and dodecane–water interfaces using dynamic surface/interfacial tension measurements. The adsorption was shown to begin in a diffusion-limited regime at low polymer concentrations, that is to say, with the diffusion of macromolecules in the bulk solution. In contrast, at long times the interfacial adsorption is limited by interfacial phenomena: adsorption kinetics or transfer into the adsorbed layer. A semiempirical equation developed by Filippov was shown to correctly fit the experimental curves over the whole time range. The presence of ionic groups in the chains strongly lowers the adsorption kinetics. This effect can be interpreted by electrostatic interactions between the free molecules and the already adsorbed ones. The adsorption kinetics at air–water and oil–water interfaces are compared.</description><subject>Adsorption</subject><subject>Air</subject><subject>Amphiphilic polymers</subject><subject>Chemistry</subject><subject>Dextran</subject><subject>Dextrans - chemical synthesis</subject><subject>Dextrans - chemistry</subject><subject>Engineering Sciences</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Interfacial tension</subject><subject>Molecular Structure</subject><subject>Oils - chemistry</subject><subject>Other</subject><subject>Polysaccharides - chemical synthesis</subject><subject>Polysaccharides - chemistry</subject><subject>Surface physical chemistry</subject><subject>Surface Properties</subject><subject>Surface-Active Agents - chemical synthesis</subject><subject>Surface-Active Agents - chemistry</subject><subject>Water - chemistry</subject><issn>0021-9797</issn><issn>1095-7103</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1r3DAQhkVpaLZJ_0APxZcWcrAzsj5slVyW0DaFhVySs1CkEdHitbaSd9P--8qsSW8FMWKGZ16kh5CPFBoKVF5vm60NuWkBeAOyAQ5vyIqCEnVHgb0lK4CW1qpT3Tl5n_MWgFIh1DtyTgXrgVO2Ig_r3f45lDMEWzlM4WimcMRcRV_a31My49dq7XJM-ynEsTJTZUK6fjETpsqMrophWLowluqNxXxJzrwZMn5Y7gvy-P3bw-1dvbn_8fN2vaktF2yqn2jbenTcCMNBcMeUdOgksz3vWtEDWtX2PZryG4-eSseVMqCop0z1hWYX5OqU-2wGvU9hZ9IfHU3Qd-uNnmcA0CkmuiMt7JcTu0_x1wHzpHchWxwGM2I8ZC1lrxRnrIDtCbQp5pzQvyZT0LN3vdWzdz171yB18V6WPi3ph6cdun8ri-gCfF4Ak60ZfPE6Z7xysgUl-65wNycOi7djwKSzDThadCGhnbSL4X_v-Av2k5_t</recordid><startdate>20041101</startdate><enddate>20041101</enddate><creator>Rotureau, E.</creator><creator>Leonard, M.</creator><creator>Dellacherie, E.</creator><creator>Durand, A.</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><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>1XC</scope><orcidid>https://orcid.org/0000-0003-1330-5631</orcidid></search><sort><creationdate>20041101</creationdate><title>Amphiphilic derivatives of dextran: Adsorption at air/water and oil/water interfaces</title><author>Rotureau, E. ; Leonard, M. ; Dellacherie, E. ; Durand, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c453t-b122fed4a5a4054d396ded63c8472580ec9288ea710fef16d499a091f1398d393</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adsorption</topic><topic>Air</topic><topic>Amphiphilic polymers</topic><topic>Chemistry</topic><topic>Dextran</topic><topic>Dextrans - chemical synthesis</topic><topic>Dextrans - chemistry</topic><topic>Engineering Sciences</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Interfacial tension</topic><topic>Molecular Structure</topic><topic>Oils - chemistry</topic><topic>Other</topic><topic>Polysaccharides - chemical synthesis</topic><topic>Polysaccharides - chemistry</topic><topic>Surface physical chemistry</topic><topic>Surface Properties</topic><topic>Surface-Active Agents - chemical synthesis</topic><topic>Surface-Active Agents - chemistry</topic><topic>Water - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rotureau, E.</creatorcontrib><creatorcontrib>Leonard, M.</creatorcontrib><creatorcontrib>Dellacherie, E.</creatorcontrib><creatorcontrib>Durand, A.</creatorcontrib><collection>Pascal-Francis</collection><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>Hyper Article en Ligne (HAL)</collection><jtitle>Journal of colloid and interface science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rotureau, E.</au><au>Leonard, M.</au><au>Dellacherie, E.</au><au>Durand, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Amphiphilic derivatives of dextran: Adsorption at air/water and oil/water interfaces</atitle><jtitle>Journal of colloid and interface science</jtitle><addtitle>J Colloid Interface Sci</addtitle><date>2004-11-01</date><risdate>2004</risdate><volume>279</volume><issue>1</issue><spage>68</spage><epage>77</epage><pages>68-77</pages><issn>0021-9797</issn><eissn>1095-7103</eissn><coden>JCISA5</coden><abstract>Ionic amphiphilic dextran derivatives were synthesized by the attachment of sodium sulfopropyl and phenoxy groups on the native polysaccharide. A family of dextran derivatives was thus obtained with varying hydrophobic content and charge density in the polymer chains. The surface-active properties of polymers were studied at the air–water and dodecane–water interfaces using dynamic surface/interfacial tension measurements. The adsorption was shown to begin in a diffusion-limited regime at low polymer concentrations, that is to say, with the diffusion of macromolecules in the bulk solution. In contrast, at long times the interfacial adsorption is limited by interfacial phenomena: adsorption kinetics or transfer into the adsorbed layer. A semiempirical equation developed by Filippov was shown to correctly fit the experimental curves over the whole time range. The presence of ionic groups in the chains strongly lowers the adsorption kinetics. This effect can be interpreted by electrostatic interactions between the free molecules and the already adsorbed ones. The adsorption kinetics at air–water and oil–water interfaces are compared.</abstract><cop>San Diego, CA</cop><pub>Elsevier Inc</pub><pmid>15380413</pmid><doi>10.1016/j.jcis.2004.06.040</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-1330-5631</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0021-9797
ispartof Journal of colloid and interface science, 2004-11, Vol.279 (1), p.68-77
issn 0021-9797
1095-7103
language eng
recordid cdi_hal_primary_oai_HAL_hal_00079357v1
source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Adsorption
Air
Amphiphilic polymers
Chemistry
Dextran
Dextrans - chemical synthesis
Dextrans - chemistry
Engineering Sciences
Exact sciences and technology
General and physical chemistry
Interfacial tension
Molecular Structure
Oils - chemistry
Other
Polysaccharides - chemical synthesis
Polysaccharides - chemistry
Surface physical chemistry
Surface Properties
Surface-Active Agents - chemical synthesis
Surface-Active Agents - chemistry
Water - chemistry
title Amphiphilic derivatives of dextran: Adsorption at air/water and oil/water interfaces
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-18T02%3A41%3A50IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_hal_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Amphiphilic%20derivatives%20of%20dextran:%20Adsorption%20at%20air/water%20and%20oil/water%20interfaces&rft.jtitle=Journal%20of%20colloid%20and%20interface%20science&rft.au=Rotureau,%20E.&rft.date=2004-11-01&rft.volume=279&rft.issue=1&rft.spage=68&rft.epage=77&rft.pages=68-77&rft.issn=0021-9797&rft.eissn=1095-7103&rft.coden=JCISA5&rft_id=info:doi/10.1016/j.jcis.2004.06.040&rft_dat=%3Cproquest_hal_p%3E66899433%3C/proquest_hal_p%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=66899433&rft_id=info:pmid/15380413&rft_els_id=S0021979704005594&rfr_iscdi=true