Ziserman Lior, Abezgauz Ludmila, Ramon Ory, Raghavan Srinivasa R, Danino Dganit
Department of Biotechnology and Food Engineering, Technion-Istrael Institute of Technology, Haifa, Israel.
Langmuir. 2009 Sep 15;25(18):10483-9. doi: 10.1021/la901189k.
The rheology of wormlike micelles ("worms") formed by surfactants in water often follows nonmonotonic trends as functions of composition. For example, a study by Raghavan et al. (Langmuir 2002, 18, 3797) on mixtures of the anionic surfactant sodium oleate (NaOA) and the cationic surfactant octyl trimethylammonium bromide (OTAB) reported a pronounced peak in the zero-shear viscosity eta0 as a function of NaOA/OTAB ratio at a constant surfactant concentration (3 wt %). In this work, we study the origins of rheological changes in the NaOA/OTAB system and the relations between the composition and structural characteristics using cryo-transmission electron microscopy (cryo-TEM). When either surfactant is in large excess, the dominating morphology is that of spherical micelles. As oppositely charged surfactant is added to the mixture, the spheres grow into linear worms and these continue to elongate as the viscosity peak (which occurs at a 70/30 NaOA/OTAB ratio) is approached from either end. At the viscosity peak, the sample shows numerous long worms as well as a small number of branched worms. Taken together, NaOA/OTAB rheology can be primarily understood on the basis of micellar growth, which is explained primarily by packing arguments. While the size of the hydrophobic micellar core continuously decreases as the short amphiphile OTAB is added at the expense of NaOA, screening of charges goes through a maximum, which contributes to the asymmetry of the viscosity curve. With regard to micellar branching, there is no significant difference in the density of branched worms on either side of the viscosity peak. Therefore, it appears that in contrast to the behavior of some surfactant/salt systems, branching does not have a significant influence on the rheology of this mixed catanionic surfactant system. Instead, our data clearly indicate that the origin of the viscosity peak is linked with micellar growth and micellar shortening.
表面活性剂在水中形成的蠕虫状胶束(“蠕虫”)的流变学通常随组成呈现非单调趋势。例如,Raghavan等人(《朗缪尔》2002年,第18卷,第3797页)对阴离子表面活性剂油酸钠(NaOA)和阳离子表面活性剂溴化辛基三甲基铵(OTAB)混合物的研究报告称,在恒定表面活性剂浓度(3 wt%)下,零剪切粘度η0随NaOA/OTAB比例呈现明显峰值。在这项工作中,我们使用冷冻透射电子显微镜(cryo-TEM)研究了NaOA/OTAB体系中流变学变化的起源以及组成与结构特征之间的关系。当任何一种表面活性剂大量过量时,主要形态是球形胶束。随着带相反电荷的表面活性剂添加到混合物中,球体生长成线性蠕虫,并且当从两端接近粘度峰值(出现在70/30的NaOA/OTAB比例时)时,这些蠕虫会继续伸长。在粘度峰值处,样品显示出许多长蠕虫以及少量分支蠕虫。综合来看,NaOA/OTAB的流变学主要可以基于胶束生长来理解,这主要通过堆积理论来解释。虽然随着短两亲物OTAB的添加,以NaOA为代价,疏水性胶束核心的尺寸不断减小,但电荷屏蔽会经历一个最大值,这导致了粘度曲线的不对称性。关于胶束分支,在粘度峰值两侧分支蠕虫的密度没有显著差异。因此,与一些表面活性剂/盐体系的行为相反,分支似乎对这种混合阳离子 - 阴离子表面活性剂体系的流变学没有显著影响。相反,我们的数据清楚地表明,粘度峰值的起源与胶束生长和胶束缩短有关。