Interactions of a hydrophobically modified polymer with oppositely charged surfactants

The interaction of a hydrophobically modified anionic polymer (PMAOVE) with a cationic surfactant (DTAB) was studied using a multi-technique approach: turbidity, surface tension, and viscosity measurements, as well as EPR (5-doxyl stearic acid) and fluorescence (pyrene) probe techniques were used. I...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 23(2007), 11 vom: 22. Mai, Seite 5906-13
1. Verfasser: Deo, Puspendu (VerfasserIn)
Weitere Verfasser: Deo, Namita, Somasundaran, P, Moscatelli, Alberto, Jockusch, Steffen, Turro, Nicholas J, Ananthapadmanabhan, K P, Ottaviani, M Francesca
Format: Aufsatz
Sprache:English
Veröffentlicht: 2007
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article
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520 |a The interaction of a hydrophobically modified anionic polymer (PMAOVE) with a cationic surfactant (DTAB) was studied using a multi-technique approach: turbidity, surface tension, and viscosity measurements, as well as EPR (5-doxyl stearic acid) and fluorescence (pyrene) probe techniques were used. In the investigated pH range (4-10), the cationic surfactant headgroups interact with the anionic carboxylic groups of the polymer backbone. In addition, nonpolar interactions of the surfactant chains with the n-octyl chains of PMAOVE stabilize the PMAOVE-DTAB complexes. Charge neutralization of the anionic polymer by the cationic surfactant leads to precipitation of the PMAOVE-DTAB complex at a certain DTAB concentration range. Further addition of DTAB causes a charge reversal of the complex and, subsequently, resolubilization of the precipitate. At an acidic pH (pH = 4), a second precipitation was observed, which is probably caused by conformational changes in the PMAOVE-DTAB complex. This second precipitate can be resolubilized by further addition of surfactant. At a neutral and basic pH, this second precipitation is absent. EPR analysis indicates that the surfactants form an ordered structure at the extended polymer chain at a neutral and basic pH, whereas at an acidic pH, a less ordered surfactant layer is formed on the coiled polymer with more hydrophobic microdomains 
650 4 |a Journal Article 
700 1 |a Deo, Namita  |e verfasserin  |4 aut 
700 1 |a Somasundaran, P  |e verfasserin  |4 aut 
700 1 |a Moscatelli, Alberto  |e verfasserin  |4 aut 
700 1 |a Jockusch, Steffen  |e verfasserin  |4 aut 
700 1 |a Turro, Nicholas J  |e verfasserin  |4 aut 
700 1 |a Ananthapadmanabhan, K P  |e verfasserin  |4 aut 
700 1 |a Ottaviani, M Francesca  |e verfasserin  |4 aut 
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