Yamashita Yuji, Kunieda Hironobu, Oshimura Eiko, Sakamoto Kazutami
Graduate School of Environment and Information Sciences, Yokohama National University, Tokiwadai 79-7, Hodogaya-ku, Yokohama 240-8501, Japan.
J Colloid Interface Sci. 2007 Aug 1;312(1):172-8. doi: 10.1016/j.jcis.2006.10.045. Epub 2006 Oct 26.
The phase behavior in the brine/sodium N-dodecanoyl sarcosinate (Sar)/isopropyl N-dodecanoyl sarcosinate (SLIP) system has been investigated by means of phase study, static light scattering, and small-angle X-ray scattering. The liquid crystal phases, hexagonal (H(1)) and discontinuous cubic (I(1)), melt upon the addition of NaCl, which shows the similar effect to the increasing of temperature. The addition of SLIP to the brine/Sar solution at high Sar concentration induces the phase transition from H(1) to I(1) via the isotropic micellar solution (W(m2)). The micellar structure in the W(m2) phase also changes from the wormlike to the globular micelle with SLIP concentration. Adding NaCl reduces the repulsive force between the Sar head groups and simultaneously the space of the solubilized SLIP in the palisade layer, leading SLIP to shift their location further into the micelle core. As a consequence, the hexagonal symmetry breaks into the micelle solution and the liquid crystal order is destabilized entropically.
通过相研究、静态光散射和小角X射线散射等手段,对盐水/ N-十二烷酰肌氨酸钠(Sar)/ N-十二烷酰肌氨酸异丙酯(SLIP)体系的相行为进行了研究。液晶相,即六方相(H(1))和不连续立方相(I(1)),在加入NaCl后会熔化,这与温度升高显示出相似的效果。在高Sar浓度下,向盐水/Sar溶液中添加SLIP会诱导相从H(1)通过各向同性胶束溶液(W(m2))转变为I(1)。W(m2)相中的胶束结构也会随着SLIP浓度的变化从蠕虫状胶束转变为球状胶束。添加NaCl会降低Sar头基之间的排斥力,同时降低SLIP在栅栏层中增溶空间,导致SLIP进一步向胶束核心移动。结果,六方对称性破坏形成胶束溶液,液晶有序性因熵而变得不稳定。