Donina Liva, Porcar Lionel, Cabral João T
Department of Chemical Engineering, Imperial College London, UK.
Institut Laue-Langevin, 71 Avenue des Martyrs, B.P. 156, F-38042 Grenoble CEDEX, France.
Soft Matter. 2023 Nov 15;19(44):8542-8551. doi: 10.1039/d3sm01098h.
We investigate the solution structures of model sodium dodecyl sulfate/octanol/brine ternary mixtures across the lamellar (L), vesicle (L) and micellar (L) phases employing small angle neutron scattering (SANS), optical microscopy and nuclear magnetic resonance (NMR). Specifically, we examine the effect of co-surfactant octanol (0.2-9.48 w/v%) and temperature (25-65 °C) along dilution lines at fixed octanol : SDS ratios (0.08-1.21). A transition from L to sponge phase (L) above 35 °C is found along the octanol : SDS = 1.21 isopleth, with phase coexistence above ≈ 0.14 weight fraction of surfactant and co-surfactant. The lamellar bilayers swell upon dilution, with an approximately linear increase of -spacing, accompanied by a decrease of the Caillé parameter, indicative of greater membrane rigidity. At a lower octanol : SDS ratio of 0.62, coexistence of oblate micelles and vesicles is observed with preferential formation of vesicles at low concentrations. Dilution of the L phase, along octanol : SDS = 0.08, results in elongated micelles, as the NaCl : SDS ratio increases, while higher temperatures favour the formation of less elongated micelles. Our results provide a detailed map of the equilibrium structures found in the L vicinity of this extensively investigated flow-responsive surfactant system.
我们采用小角中子散射(SANS)、光学显微镜和核磁共振(NMR)研究了十二烷基硫酸钠/辛醇/盐水模型三元混合物在层状(L)、囊泡(L)和胶束(L)相中的溶液结构。具体而言,我们研究了共表面活性剂辛醇(0.2 - 9.48 w/v%)和温度(25 - 65 °C)沿稀释线在固定辛醇∶SDS比例(0.08 - 1.21)下的影响。发现在辛醇∶SDS = 1.21等压线上,温度高于35 °C时会从L相转变为海绵相(L),在表面活性剂和共表面活性剂的重量分数约高于0.14时会出现相共存。层状双层在稀释时会膨胀,-间距近似线性增加,同时凯莱参数减小,这表明膜刚性增强。在较低的辛醇∶SDS比例0.62时,观察到扁长胶束和囊泡共存,且在低浓度时优先形成囊泡。沿辛醇∶SDS = 0.08稀释L相时,随着NaCl∶SDS比例增加会形成拉长的胶束,而较高温度有利于形成拉长程度较小的胶束。我们的结果提供了在这个经过广泛研究的流动响应表面活性剂体系的L附近发现的平衡结构的详细图谱。