Mixtures of hydrogenated and fluorinated lactobionamide surfactants with cationic surfactants: Study of hydrogenated and fluorinated chains miscibility through potentiometric techniques

被引:18
作者
Peyre, Veronique [1 ]
Patil, Sandeep
Durand, Gregory
Pucci, Bernard
机构
[1] Univ Paris 06, LECA, UMR7575, F-75005 Paris, France
[2] ENSCP, UMR7575, F-75005 Paris, France
[3] CNRS, UMR7575, F-75005 Paris, France
[4] Univ Avignon & Pays Vaucluse, Fac Sci, Lab Chim Bioorgan & Syst Mol Vectoriels, F-84000 Avignon, France
关键词
D O I
10.1021/la701579e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The work reported herein deals with the aqueous behavior of hydrocarbon and/or fluorocarbon ionic and nonionic surfactants mixtures. These mixtures were studied using potentiometric techniques in NaBr (0.1 mol L-1) aqueous solution as well as in pure water. Mixed micelles were formed from a cationic surfactant (dodecyl or tetradecyltrimethylammonium bromide respectively called DTABr or TTABr) and neutral lactobionamide surfactants bearing a hydrogenated dodecyl chain (H(12)Lac) or a fluorinated chain (CF3-(CF2)(5)-(CH2)(2)- or CF3-(CF2)(7)(CH2)(2)-)- We showed that concentrations of ionic and nonionic surfactants in the monomeric form as well as the composition of the mixed micelles can be specified thanks to a potentiometric technique. The complete characterization does not request any model of micellization a priori. The activities of the micellar phase constituents, as well as the free enthalpies of mixing, were calculated. The subsequent interpretation only relies on the experimental characterization. Comparison of the behaviors of the various systems with a model derived from the regular solution theory reveals the predominant part of electrostatic interactions in the micellization phenomenon. It also appears that the energy of interaction between hydrogenated and fluorinated chains is unfavorable to mixing and is of much lower magnitude than the electric charges interactions.
引用
收藏
页码:11465 / 11474
页数:10
相关论文
共 38 条
[1]   Small angle neutron scattering study of demixing in micellar solutions containing CTAC and a partially fluorinated cationic surfactant [J].
Almgren, M ;
Garamus, VM .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (22) :11348-11353
[2]   Micellar properties of nonionic saccharide surfactants with amide linkage in aqueous solution [J].
Arai, T ;
Takasugi, K ;
Esumi, K .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 1996, 119 (01) :81-85
[3]   Thermodynamic consideration of mixtures of surfactants in adsorbed films and micelles [J].
Aratono, M ;
Villeneuve, M ;
Takiue, T ;
Ikeda, N ;
Iyota, H .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1998, 200 (01) :161-171
[4]   A theoretical analysis of synergistic effects in mixed surfactant systems [J].
Bergström, M ;
Eriksson, JC .
LANGMUIR, 2000, 16 (18) :7173-7181
[5]   Regarding the effect that different hydrocarbon/fluorocarbon surfactant mixtures have on their complexation with HSA [J].
Blanco, Elena ;
Messina, Paula ;
Ruso, Juan M. ;
Prieto, Gerardo ;
Sarmiento, Felix .
JOURNAL OF PHYSICAL CHEMISTRY B, 2006, 110 (23) :11369-11376
[6]   Mixed fluorinated-hydrogenated surfactant-based system:: Preparation of ordered mesoporous materials [J].
Blin, J. L. ;
Henzel, N. ;
Stebe, M. J. .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2006, 302 (02) :643-650
[7]   Demixing of mixed micelles. Thermodynamics of sodium perfluorooctanoate sodium dodecanoate mixtures in water [J].
DeLisi, R ;
Inglese, A ;
Milioto, S ;
Pellerito, A .
LANGMUIR, 1997, 13 (02) :192-202
[8]   NMR studies of binary surfactant mixture thermodynamics: Molecular size model for asymmetric activity coefficients [J].
Eads, CD ;
Robosky, LC .
LANGMUIR, 1999, 15 (08) :2661-2668
[9]  
Fletcher P.D.I., 1997, SPECIALIST SURFACTAN
[10]  
FUNASAKI N, 1993, MIXED SURFACTANTS SY, pCH5