Dilational viscoelasticity and relaxation properties of interfacial electrostatic complexes between oppositely charged hydrophobic and hydrophilic polyelectrolytes
Strongly adsorbing hydrophobic cationic polyelectrolyte, Eudragit RS, containing ∼2.5 mol% of pendent hydrophilic trimethylammonium (TMA) groups irreversibly adsorbs from its methylene chloride (MCl) solution at the MCl/water interface and forms solid-like adsorption layers (ALs). Submitted to perio...
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creator | Babak, Valery G. Baros, Francis Boury, Frank Desbrières, Jacques |
description | Strongly adsorbing hydrophobic cationic polyelectrolyte, Eudragit RS, containing ∼2.5
mol% of pendent hydrophilic trimethylammonium (TMA) groups irreversibly adsorbs from its methylene chloride (MCl) solution at the MCl/water interface and forms solid-like adsorption layers (ALs). Submitted to periodic dilational deformations with the standard radial frequency
ω
0
=
0.63
rad/s, these ALs exhibit relatively high dilational storage modulus
E′
∼
20
mN/m and practically zero loss modulus
E′′ at the bulk concentration
C
Eud
=
4
×
10
−3
g/L. The frequency scanning of these ALs in the diapason
ω
=
0.01–0.63
rad/s and the approximation of the experimental dependences
E′(
ω) and
E′′(
ω) by two relaxation times rheological model makes it possible to estimate the crossing frequency of these ALs determined from the condition
E′(
ω
c)
=
E′′(
ω
c) as
ω
c
∼
5
×
10
−4
rad/s. Upon dissolving the hydrophilic anionic polyelectrolyte, chitosan sulfate (ChS), in the water phase (
C
ChS
=
3
×
10
−2
g/L) the electrostatic interpolyelectrolyte complexes form at the MCl/water interface. The elasticity moduli
E′ and
E′′ of these mixed AL did not undergo remarkable variations, but the crossing frequency is sharply increased by ∼10 times becoming equal to
ω
c
≅
3
×
10
−3
rad/s. The increase of
ω
c certifies for the liquefaction of mixed Eudragit RS/ChS adsorption layers. A remarkable decrease of the storage modulus down to
E′
=
8
mN/m and simultaneous increase of the crossing frequency up to
ω
c
≅
10
−2
rad/s occurs upon increasing the concentrations of both components, Eudragit RS and ChS, up to 0.1
g/L. The liquefaction effect in the mixed ALs of oppositely charged polyelectrolytes was explained on the basis of the proposed relaxation mechanism. The effect of the liquefaction of adsorption layers of strongly adsorbing hydrophobic polyelectrolytes by formation of interpolyelectrolyte complexes with hydrophilic polyelectrolytes must be taken into account in the production of nano-capsules and nano-fibers. |
doi_str_mv | 10.1016/j.colsurfb.2008.02.019 |
format | Article |
fullrecord | <record><control><sourceid>proquest_hal_p</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_00320812v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S092777650800091X</els_id><sourcerecordid>20725084</sourcerecordid><originalsourceid>FETCH-LOGICAL-c431t-d95d3d1b6dd48437026d140d0e13fcb05df008f55a42c48ef010e9b58ae3c9d23</originalsourceid><addsrcrecordid>eNqFkUGP0zAQhS0EYkvhL6xyQuKQMHacOL2xWmAXqRIXOFuOPaGu3DjYbtn8Hv4o7jbAcU_Ws743M3qPkGsKFQXavt9X2rt4DENfMYCuAlYB3TwjK9qJuuR1K56TFWyYKIVomyvyKsY9ADBOxUtyRTsOwAVfkd8frVPJ-lG54mSj9uhUTFbbNBdqNEXI-uERKKbgJwzJYiz8UNgxYRiUttmIDnUKPqYM6kL7w-TwIWM9pl-IY-GnyUeb0M2F3qnwA02xm00et_N9Npz3LNq6rCfv5mWkmxPG1-TFoFzEN8u7Jt8_f_p2e19uv959ub3ZlprXNJVm05ja0L41hne8FsBaQzkYQFoPuofGDDmpoWkUZ5p3OAAF3PRNp7DWG8PqNXl3mbtTTk7BHlSYpVdW3t9s5fkPoGbQUXaimX17YXMqP48Ykzzk9NA5NaI_Rilo29ZcwJMgA8EayPeuSXsBdU4yBhz-nUBBnjuXe_m3c3nuXAKTufNsvF42HPsDmv-2peQMfLgAmMM7WQwyaoujRmNDTlkab5_a8Qc2xsa5</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>20725084</pqid></control><display><type>article</type><title>Dilational viscoelasticity and relaxation properties of interfacial electrostatic complexes between oppositely charged hydrophobic and hydrophilic polyelectrolytes</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Babak, Valery G. ; Baros, Francis ; Boury, Frank ; Desbrières, Jacques</creator><creatorcontrib>Babak, Valery G. ; Baros, Francis ; Boury, Frank ; Desbrières, Jacques</creatorcontrib><description>Strongly adsorbing hydrophobic cationic polyelectrolyte, Eudragit RS, containing ∼2.5
mol% of pendent hydrophilic trimethylammonium (TMA) groups irreversibly adsorbs from its methylene chloride (MCl) solution at the MCl/water interface and forms solid-like adsorption layers (ALs). Submitted to periodic dilational deformations with the standard radial frequency
ω
0
=
0.63
rad/s, these ALs exhibit relatively high dilational storage modulus
E′
∼
20
mN/m and practically zero loss modulus
E′′ at the bulk concentration
C
Eud
=
4
×
10
−3
g/L. The frequency scanning of these ALs in the diapason
ω
=
0.01–0.63
rad/s and the approximation of the experimental dependences
E′(
ω) and
E′′(
ω) by two relaxation times rheological model makes it possible to estimate the crossing frequency of these ALs determined from the condition
E′(
ω
c)
=
E′′(
ω
c) as
ω
c
∼
5
×
10
−4
rad/s. Upon dissolving the hydrophilic anionic polyelectrolyte, chitosan sulfate (ChS), in the water phase (
C
ChS
=
3
×
10
−2
g/L) the electrostatic interpolyelectrolyte complexes form at the MCl/water interface. The elasticity moduli
E′ and
E′′ of these mixed AL did not undergo remarkable variations, but the crossing frequency is sharply increased by ∼10 times becoming equal to
ω
c
≅
3
×
10
−3
rad/s. The increase of
ω
c certifies for the liquefaction of mixed Eudragit RS/ChS adsorption layers. A remarkable decrease of the storage modulus down to
E′
=
8
mN/m and simultaneous increase of the crossing frequency up to
ω
c
≅
10
−2
rad/s occurs upon increasing the concentrations of both components, Eudragit RS and ChS, up to 0.1
g/L. The liquefaction effect in the mixed ALs of oppositely charged polyelectrolytes was explained on the basis of the proposed relaxation mechanism. The effect of the liquefaction of adsorption layers of strongly adsorbing hydrophobic polyelectrolytes by formation of interpolyelectrolyte complexes with hydrophilic polyelectrolytes must be taken into account in the production of nano-capsules and nano-fibers.</description><identifier>ISSN: 0927-7765</identifier><identifier>EISSN: 1873-4367</identifier><identifier>DOI: 10.1016/j.colsurfb.2008.02.019</identifier><identifier>PMID: 18400474</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Acrylic Resins - chemistry ; Adsorption ; Biocompatible Materials - chemistry ; Chemical Physics ; Chitosan sulfate ; Crossing frequency ; Dilational storage and loss moduli ; Dilational viscoelasticity of adsorption layers ; Elasticity ; Electrolytes - chemistry ; Eudragit RS ; Hydrophobic and Hydrophilic Interactions ; Nano-fibers ; Nano-particles ; Physics ; Polymers - chemistry ; Static Electricity ; Surface Tension ; Trimethyl Ammonium Compounds - chemistry ; Viscosity</subject><ispartof>Colloids and surfaces, B, Biointerfaces, 2008-08, Vol.65 (1), p.43-49</ispartof><rights>2008 Elsevier B.V.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c431t-d95d3d1b6dd48437026d140d0e13fcb05df008f55a42c48ef010e9b58ae3c9d23</citedby><cites>FETCH-LOGICAL-c431t-d95d3d1b6dd48437026d140d0e13fcb05df008f55a42c48ef010e9b58ae3c9d23</cites><orcidid>0000-0002-3457-3988</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S092777650800091X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18400474$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00320812$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Babak, Valery G.</creatorcontrib><creatorcontrib>Baros, Francis</creatorcontrib><creatorcontrib>Boury, Frank</creatorcontrib><creatorcontrib>Desbrières, Jacques</creatorcontrib><title>Dilational viscoelasticity and relaxation properties of interfacial electrostatic complexes between oppositely charged hydrophobic and hydrophilic polyelectrolytes</title><title>Colloids and surfaces, B, Biointerfaces</title><addtitle>Colloids Surf B Biointerfaces</addtitle><description>Strongly adsorbing hydrophobic cationic polyelectrolyte, Eudragit RS, containing ∼2.5
mol% of pendent hydrophilic trimethylammonium (TMA) groups irreversibly adsorbs from its methylene chloride (MCl) solution at the MCl/water interface and forms solid-like adsorption layers (ALs). Submitted to periodic dilational deformations with the standard radial frequency
ω
0
=
0.63
rad/s, these ALs exhibit relatively high dilational storage modulus
E′
∼
20
mN/m and practically zero loss modulus
E′′ at the bulk concentration
C
Eud
=
4
×
10
−3
g/L. The frequency scanning of these ALs in the diapason
ω
=
0.01–0.63
rad/s and the approximation of the experimental dependences
E′(
ω) and
E′′(
ω) by two relaxation times rheological model makes it possible to estimate the crossing frequency of these ALs determined from the condition
E′(
ω
c)
=
E′′(
ω
c) as
ω
c
∼
5
×
10
−4
rad/s. Upon dissolving the hydrophilic anionic polyelectrolyte, chitosan sulfate (ChS), in the water phase (
C
ChS
=
3
×
10
−2
g/L) the electrostatic interpolyelectrolyte complexes form at the MCl/water interface. The elasticity moduli
E′ and
E′′ of these mixed AL did not undergo remarkable variations, but the crossing frequency is sharply increased by ∼10 times becoming equal to
ω
c
≅
3
×
10
−3
rad/s. The increase of
ω
c certifies for the liquefaction of mixed Eudragit RS/ChS adsorption layers. A remarkable decrease of the storage modulus down to
E′
=
8
mN/m and simultaneous increase of the crossing frequency up to
ω
c
≅
10
−2
rad/s occurs upon increasing the concentrations of both components, Eudragit RS and ChS, up to 0.1
g/L. The liquefaction effect in the mixed ALs of oppositely charged polyelectrolytes was explained on the basis of the proposed relaxation mechanism. The effect of the liquefaction of adsorption layers of strongly adsorbing hydrophobic polyelectrolytes by formation of interpolyelectrolyte complexes with hydrophilic polyelectrolytes must be taken into account in the production of nano-capsules and nano-fibers.</description><subject>Acrylic Resins - chemistry</subject><subject>Adsorption</subject><subject>Biocompatible Materials - chemistry</subject><subject>Chemical Physics</subject><subject>Chitosan sulfate</subject><subject>Crossing frequency</subject><subject>Dilational storage and loss moduli</subject><subject>Dilational viscoelasticity of adsorption layers</subject><subject>Elasticity</subject><subject>Electrolytes - chemistry</subject><subject>Eudragit RS</subject><subject>Hydrophobic and Hydrophilic Interactions</subject><subject>Nano-fibers</subject><subject>Nano-particles</subject><subject>Physics</subject><subject>Polymers - chemistry</subject><subject>Static Electricity</subject><subject>Surface Tension</subject><subject>Trimethyl Ammonium Compounds - chemistry</subject><subject>Viscosity</subject><issn>0927-7765</issn><issn>1873-4367</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUGP0zAQhS0EYkvhL6xyQuKQMHacOL2xWmAXqRIXOFuOPaGu3DjYbtn8Hv4o7jbAcU_Ws743M3qPkGsKFQXavt9X2rt4DENfMYCuAlYB3TwjK9qJuuR1K56TFWyYKIVomyvyKsY9ADBOxUtyRTsOwAVfkd8frVPJ-lG54mSj9uhUTFbbNBdqNEXI-uERKKbgJwzJYiz8UNgxYRiUttmIDnUKPqYM6kL7w-TwIWM9pl-IY-GnyUeb0M2F3qnwA02xm00et_N9Npz3LNq6rCfv5mWkmxPG1-TFoFzEN8u7Jt8_f_p2e19uv959ub3ZlprXNJVm05ja0L41hne8FsBaQzkYQFoPuofGDDmpoWkUZ5p3OAAF3PRNp7DWG8PqNXl3mbtTTk7BHlSYpVdW3t9s5fkPoGbQUXaimX17YXMqP48Ykzzk9NA5NaI_Rilo29ZcwJMgA8EayPeuSXsBdU4yBhz-nUBBnjuXe_m3c3nuXAKTufNsvF42HPsDmv-2peQMfLgAmMM7WQwyaoujRmNDTlkab5_a8Qc2xsa5</recordid><startdate>20080801</startdate><enddate>20080801</enddate><creator>Babak, Valery G.</creator><creator>Baros, Francis</creator><creator>Boury, Frank</creator><creator>Desbrières, Jacques</creator><general>Elsevier B.V</general><general>Elsevier</general><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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-3457-3988</orcidid></search><sort><creationdate>20080801</creationdate><title>Dilational viscoelasticity and relaxation properties of interfacial electrostatic complexes between oppositely charged hydrophobic and hydrophilic polyelectrolytes</title><author>Babak, Valery G. ; Baros, Francis ; Boury, Frank ; Desbrières, Jacques</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c431t-d95d3d1b6dd48437026d140d0e13fcb05df008f55a42c48ef010e9b58ae3c9d23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Acrylic Resins - chemistry</topic><topic>Adsorption</topic><topic>Biocompatible Materials - chemistry</topic><topic>Chemical Physics</topic><topic>Chitosan sulfate</topic><topic>Crossing frequency</topic><topic>Dilational storage and loss moduli</topic><topic>Dilational viscoelasticity of adsorption layers</topic><topic>Elasticity</topic><topic>Electrolytes - chemistry</topic><topic>Eudragit RS</topic><topic>Hydrophobic and Hydrophilic Interactions</topic><topic>Nano-fibers</topic><topic>Nano-particles</topic><topic>Physics</topic><topic>Polymers - chemistry</topic><topic>Static Electricity</topic><topic>Surface Tension</topic><topic>Trimethyl Ammonium Compounds - chemistry</topic><topic>Viscosity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Babak, Valery G.</creatorcontrib><creatorcontrib>Baros, Francis</creatorcontrib><creatorcontrib>Boury, Frank</creatorcontrib><creatorcontrib>Desbrières, Jacques</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Colloids and surfaces, B, Biointerfaces</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Babak, Valery G.</au><au>Baros, Francis</au><au>Boury, Frank</au><au>Desbrières, Jacques</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dilational viscoelasticity and relaxation properties of interfacial electrostatic complexes between oppositely charged hydrophobic and hydrophilic polyelectrolytes</atitle><jtitle>Colloids and surfaces, B, Biointerfaces</jtitle><addtitle>Colloids Surf B Biointerfaces</addtitle><date>2008-08-01</date><risdate>2008</risdate><volume>65</volume><issue>1</issue><spage>43</spage><epage>49</epage><pages>43-49</pages><issn>0927-7765</issn><eissn>1873-4367</eissn><abstract>Strongly adsorbing hydrophobic cationic polyelectrolyte, Eudragit RS, containing ∼2.5
mol% of pendent hydrophilic trimethylammonium (TMA) groups irreversibly adsorbs from its methylene chloride (MCl) solution at the MCl/water interface and forms solid-like adsorption layers (ALs). Submitted to periodic dilational deformations with the standard radial frequency
ω
0
=
0.63
rad/s, these ALs exhibit relatively high dilational storage modulus
E′
∼
20
mN/m and practically zero loss modulus
E′′ at the bulk concentration
C
Eud
=
4
×
10
−3
g/L. The frequency scanning of these ALs in the diapason
ω
=
0.01–0.63
rad/s and the approximation of the experimental dependences
E′(
ω) and
E′′(
ω) by two relaxation times rheological model makes it possible to estimate the crossing frequency of these ALs determined from the condition
E′(
ω
c)
=
E′′(
ω
c) as
ω
c
∼
5
×
10
−4
rad/s. Upon dissolving the hydrophilic anionic polyelectrolyte, chitosan sulfate (ChS), in the water phase (
C
ChS
=
3
×
10
−2
g/L) the electrostatic interpolyelectrolyte complexes form at the MCl/water interface. The elasticity moduli
E′ and
E′′ of these mixed AL did not undergo remarkable variations, but the crossing frequency is sharply increased by ∼10 times becoming equal to
ω
c
≅
3
×
10
−3
rad/s. The increase of
ω
c certifies for the liquefaction of mixed Eudragit RS/ChS adsorption layers. A remarkable decrease of the storage modulus down to
E′
=
8
mN/m and simultaneous increase of the crossing frequency up to
ω
c
≅
10
−2
rad/s occurs upon increasing the concentrations of both components, Eudragit RS and ChS, up to 0.1
g/L. The liquefaction effect in the mixed ALs of oppositely charged polyelectrolytes was explained on the basis of the proposed relaxation mechanism. The effect of the liquefaction of adsorption layers of strongly adsorbing hydrophobic polyelectrolytes by formation of interpolyelectrolyte complexes with hydrophilic polyelectrolytes must be taken into account in the production of nano-capsules and nano-fibers.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>18400474</pmid><doi>10.1016/j.colsurfb.2008.02.019</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-3457-3988</orcidid></addata></record> |
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language | eng |
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source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Acrylic Resins - chemistry Adsorption Biocompatible Materials - chemistry Chemical Physics Chitosan sulfate Crossing frequency Dilational storage and loss moduli Dilational viscoelasticity of adsorption layers Elasticity Electrolytes - chemistry Eudragit RS Hydrophobic and Hydrophilic Interactions Nano-fibers Nano-particles Physics Polymers - chemistry Static Electricity Surface Tension Trimethyl Ammonium Compounds - chemistry Viscosity |
title | Dilational viscoelasticity and relaxation properties of interfacial electrostatic complexes between oppositely charged hydrophobic and hydrophilic polyelectrolytes |
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