Zou Aihua, Hoffmann Heinz, Freiberger Norbert, Glatter Otto
Bayreuth Center for Colloid and Interface, University Bayreuth, 95448 Bayreuth, Germany.
Langmuir. 2007 Mar 13;23(6):2977-84. doi: 10.1021/la063148q. Epub 2007 Feb 10.
The influence of ionic charges on the mesophases in the ternary system of C(12-16)E(6) (LA 070), ethylhexylglycerid (EHG), and water was studied. The charge was introduced by adding the ionic surfactant SDS (sodium dodecyl sulfate). The single lamellar phase (5 wt % LA 070 and 240 mM EHG in water) yields a bluish homogeneous solution. With the addition of SDS, the samples become more and more clear. Rheology measurements indicate that increased charge density increases the storage modulus G', and the lamellar phases show typical behavior of a viscoelastic fluid with a yield stress at higher SDS concentration. SAXS measurements show that the interlamellar distance D decreases with SDS concentration. The addition of ionic surfactants suppresses the Helfrich undulations, flattens the bilayers, and decreases interbilayer spacing due to electrostatic repulsions of the ionic surfactant head groups. Furthermore, the L(alpha) phase transforms into vesicle phases as the SDS concentration is increased. Second, it is shown that with added NaCl electrolyte the phase with charged surfactant behaves again in the same way as the initial uncharged system. The addition of salt screens the electrostatic interaction, which leads to a higher flexibility of the bilayers and a decrease of the storage modulus G'. Theoretical calculations show that the shear moduli of the L(alpha) phases are much smaller than the osmotic pressure of the systems. Several models are proposed for the explanation of the shear moduli. The model due to Lekkerkerker for the electric contribution of the bending constant of the bilayer seems to yield good results for the transition to vesicles.
研究了离子电荷对C(12 - 16)E(6)(LA 070)、乙基己基甘油(EHG)和水的三元体系中间相的影响。通过添加离子表面活性剂十二烷基硫酸钠(SDS)引入电荷。单片层相(水中5 wt% LA 070和240 mM EHG)产生蓝色均匀溶液。随着SDS的添加,样品变得越来越澄清。流变学测量表明,电荷密度增加会提高储能模量G',并且在较高SDS浓度下,片层相表现出具有屈服应力的粘弹性流体的典型行为。小角X射线散射(SAXS)测量表明,层间距离D随SDS浓度降低。离子表面活性剂的添加抑制了赫尔弗里希波动,使双层变平,并由于离子表面活性剂头部基团的静电排斥而减小了双层间距。此外,随着SDS浓度增加,L(α)相转变为囊泡相。其次,结果表明,添加NaCl电解质后,含有带电表面活性剂的相的行为再次与初始不带电体系相同。盐的添加屏蔽了静电相互作用,这导致双层具有更高的柔韧性并降低了储能模量G'。理论计算表明,L(α)相的剪切模量远小于体系的渗透压。提出了几种模型来解释剪切模量。Lekkerkerker提出的关于双层弯曲常数电贡献的模型似乎对向囊泡的转变给出了很好的结果。