Agrawal Niti R, Yue Xiu, Feng Yujun, Raghavan Srinivasa R
Department of Chemical & Biomolecular Engineering , University of Maryland , College Park , Maryland 20742 , United States.
Xinjiang Technical Institute of Physics & Chemistry , Chinese Academy of Sciences , Urumqi 830011 , China.
Langmuir. 2019 Oct 1;35(39):12782-12791. doi: 10.1021/acs.langmuir.9b02125. Epub 2019 Sep 17.
Wormlike micelles (WLMs) are long, flexible cylindrical chains formed by the self-assembly of surfactants in semidilute solutions. Scientists have been fascinated by WLMs because of their similarities to polymers, while at the same time, the viscoelastic properties of WLM solutions have made them useful in a variety of industrial applications. To date, most studies on WLMs have been performed in water (i.e., a highly polar liquid), while there are a few examples of "reverse" WLMs in oils (i.e., highly nonpolar liquids). However, in organic solvents with lower polarity than water such as glycerol, formamide, and ethylene glycol, there have been no reports of WLMs thus far. Here, we show that it is indeed possible to induce a long-tailed cationic surfactant to assemble into WLMs in several of these solvents. To form WLMs, the surfactant is combined with a "binding" salt, i.e., one with a large organic counterion that is capable of binding to the micelles. Examples of such salts include sodium salicylate and sodium tosylate, and we find self-assembly to be maximized when the surfactant and salt concentrations are near-equimolar. Interestingly, the addition of a simple, inorganic salt such as sodium chloride (NaCl) to the same surfactant does not induce WLMs in polar solvents (although it does so in water). Thus, the design rules for WLM formation in polar solvents are distinct from those in water. Aqueous WLMs have been characterized at temperatures from 25 °C and above, but few studies have examined WLMs at much lower (e.g., subzero) temperatures. Here, we have selected a surfactant with a very low Krafft point (i.e., the surfactant does not crystallize out of solution upon cooling due to a cis-unsaturation in its tail) and a low-freezing solvent, viz. a 90/10 mixture of glycerol and ethylene glycol. In these mixtures, we find evidence for WLMs that persist down to temperatures as low as -20 °C. Rheological techniques as well as small-angle neutron scattering (SANS) have been used to characterize the WLMs under these conditions. Much like their aqueous counterparts, WLMs in polar solvents show viscoelastic properties, and accordingly, these fluids could find applications as synthetic lubricants or as improved antifreezing fluids.
蠕虫状胶束(WLMs)是表面活性剂在半稀释溶液中自组装形成的长而灵活的圆柱形链。科学家们对蠕虫状胶束很感兴趣,因为它们与聚合物有相似之处,同时,蠕虫状胶束溶液的粘弹性使其在各种工业应用中很有用。迄今为止,大多数关于蠕虫状胶束的研究都是在水中(即高极性液体)进行的,而在油中(即高非极性液体)有一些“反相”蠕虫状胶束的例子。然而,在极性低于水的有机溶剂中,如甘油、甲酰胺和乙二醇,到目前为止还没有关于蠕虫状胶束的报道。在这里,我们表明在其中几种溶剂中确实有可能诱导一种长尾阳离子表面活性剂组装成蠕虫状胶束。为了形成蠕虫状胶束,表面活性剂与一种“结合”盐混合,即一种带有能够与胶束结合的大有机抗衡离子的盐。这种盐的例子包括水杨酸钠和对甲苯磺酸钠,我们发现当表面活性剂和盐的浓度接近等摩尔时,自组装达到最大化。有趣的是,向相同的表面活性剂中添加一种简单的无机盐,如氯化钠(NaCl),在极性溶剂中不会诱导形成蠕虫状胶束(尽管在水中会)。因此,在极性溶剂中形成蠕虫状胶束的设计规则与在水中不同。水相蠕虫状胶束已在25℃及以上的温度下进行了表征,但很少有研究在低得多(例如零下)的温度下研究蠕虫状胶束。在这里,我们选择了一种具有非常低的克拉夫特点(即由于其尾部的顺式不饱和键,表面活性剂在冷却时不会从溶液中结晶出来)的表面活性剂和一种低凝固点溶剂,即甘油和乙二醇的90/10混合物。在这些混合物中,我们发现了蠕虫状胶束在低至零下二十摄氏度的温度下仍然存在的证据。在这些条件下,流变技术以及小角中子散射(SANS)已被用于表征蠕虫状胶束。与它们的水相类似物非常相似,极性溶剂中的蠕虫状胶束表现出粘弹性,因此,这些流体可以用作合成润滑剂或改进的抗冻液。