Aramaki Kenji, Iemoto Suzuka, Ikeda Naoaki, Saito Keitaro
Graduate School of Environment and Information Sciences, Yokohama National University, Yokohama, Japan.
J Oleo Sci. 2010;59(4):203-12. doi: 10.5650/jos.59.203.
We investigated phase behavior and rheological properties of aqueous micellar phase formed in water/cocoyl glutamate neutralized with triethanol amine (CGT-n)/hexadecyl trimethylammonium salt (CTAB or CTAC) systems, where n is a degree of neutralization. Micellar phase appears in wide composition range with respect to the surfactant mixing fraction in ternary phase diagrams at 25 degrees C. At high mixing fraction of cationic surfactant in the water/CGT-n/CTAB systems, one can observe a highly viscous micellar phase in which worm-like micelles are expected to form. Contrary to conventional systems in which worm-like micelles are formed, the zero-shear viscosity of the micellar solution in the water/CGT-n/CTAB system with n=1.2 increases with the addition of cationic cosurfactant and once decreases after a maximum, then increases again and decreases after the second maximum. At n=1.5 and 2, highly viscous solution is observed in the relatively wide range of surfactant mixing fraction instead of two maxima of the viscosity curve observed at n=1.2. In the case of CTAC instead of CTAB we can observe narrow composition range for the maximum viscosity. Frequency sweep measurements were performed on the highly viscous samples in the water/CGT-1.5/CTAB system. Typical viscoelastic behavior of worm-like micellar solutions is observed; i.e. the curves of storage (G') and loss (G") moduli make a crossover and the data points of G' and G" can be fitted to the Maxwell model. Relaxation time against the mixing fraction of two surfactants behaves similarly to the zero-shear viscosity change, whereas the plateau modulus continuously increases in the plateau region for the zero-shear viscosity curve.
我们研究了在水/用三乙醇胺中和的椰油酰谷氨酸(CGT-n)/十六烷基三甲基铵盐(CTAB或CTAC)体系中形成的水相胶束相的相行为和流变性质,其中n为中和度。在25℃下的三元相图中,相对于表面活性剂混合分数,胶束相出现在很宽的组成范围内。在水/CGT-n/CTAB体系中阳离子表面活性剂的混合分数较高时,可以观察到一种高粘性的胶束相,预计其中会形成蠕虫状胶束。与形成蠕虫状胶束的传统体系相反,n = 1.2的水/CGT-n/CTAB体系中胶束溶液的零剪切粘度随着阳离子共表面活性剂的加入而增加,在达到最大值后一度下降,然后再次上升,在第二个最大值后又下降。在n = 1和2时,在相对较宽的表面活性剂混合分数范围内观察到高粘性溶液,而不是在n = 1.2时观察到的粘度曲线的两个最大值。在用CTAC代替CTAB的情况下,我们可以观察到最大粘度的组成范围较窄。对水/CGT-1.5/CTAB体系中的高粘性样品进行了频率扫描测量。观察到了蠕虫状胶束溶液典型的粘弹性行为;即储能模量(G')和损耗模量(G'')的曲线出现交叉,并且G'和G''的数据点可以拟合到麦克斯韦模型。弛豫时间相对于两种表面活性剂的混合分数的变化与零剪切粘度的变化类似,而在零剪切粘度曲线的平台区域,平台模量持续增加。