Role of the surfactant headgroup on the counterion specificity in the micelle-to-vesicle transition through salt addition

被引:125
|
作者
Vlachy, Nina [1 ]
Drechsler, Markus [2 ]
Verbavatz, Jean-Marc [3 ]
Touraud, Didier [1 ]
Kunz, Werner [1 ]
机构
[1] Univ Regensburg, Inst Phys & Theoret Chem, D-93040 Regensburg, Germany
[2] Univ Bayreuth, Inst Macromol Chem, D-95440 Bayreuth, Germany
[3] CE Saclay, DBCM SBCe, F-91191 Gif Sur Yvette, France
关键词
specific-ion effects; micelle-to-vesicle transition; catanionic surfactant mixtures;
D O I
10.1016/j.jcis.2007.11.048
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A transition from micelles to vesicles is reported when salts are added to a catanionic micellar solution composed of sodium dodecylcarboxylate (SL) and dodecyltrimethylammonium bromide (DTAB), with an excess of SL. The counterion binding and increase in aggregate size was monitored by mass spectrometry, rheology and dynamic light scattering measurements, whereas the vesicles were characterized by freeze-fracture and cryo-transmission microscopy experiments. The effect of counterions on the formation of vesicles was studied and compared to a previously studied catanionic system with a sulfate head group, SDS/DTAB. As in the latter case, no anion specificity was found, while large differences in the hydrodynamic radii of the formed objects were observed, when the cation of the added salt was varied. A classification of the cations could be made according to their ability to increase the measured hydrodynamic radii. It is observed that, if the sulfate headgroup of the anionic surfactant is replaced by a carboxylic group, the order of the ions is reversed, i.e. it follows the reversed Hofmeister series. Different morphologies are observed as the ionic strength of the system is increased. The aggregates are analogous to those found in the SDS/DTAB system. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:542 / 548
页数:7
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