首页> 外文期刊>Canadian Journal of Chemistry >Thermodynamics of micellization and solubilisation in systems of water sodium n-alkylcarboxylates alkoxyethanols at 25 degrees C
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Thermodynamics of micellization and solubilisation in systems of water sodium n-alkylcarboxylates alkoxyethanols at 25 degrees C

机译:正烷基羧酸钠在25°C的水中的胶束化和溶解的热力学

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摘要

The apparent molar volumes and adiabatic compressibilities, Y-phi,Y-S, of carboxylate surfactants, CnNa (n = 8, 10, 12), in aqueous solutions in the absence and presence of medium-chain-length alkoxyethanols, C4EOX (EO = ethylene oxide group, X = 0-4), and of alkoxyethanols, Y-phi,Y-A, in aqueous solutions in the absence and presence of surfactant, were determined at 25 degrees C from density and sound velocity measurements as a function of both the surfactant and alcohol concentrations. The partial molar volumetric properties of CnNa and the transfer functions of C4EOX from water to aqueous surfactant solutions were calculated from the apparent molar properties. Values of the thermodynamic parameters of micellization for CnNa, i.e., the critical micelle concentration, the partial molar property of the monomer at infinite dilution, Y-S(0), and in the micellar state, Y-S(M), were obtained from simulations of the experimental data, Y-phi,Y-S, using a mass-action model. As expected, these properties are strongly dependent on the surfactant chain length. The distribution coefficient of C4EOX between the micelle and aqueous phases, K-D, and the change in the molar property of alcohols due to micellization, Y-A(M), extracted from fitting the transfer function data of C4EOX using a chemical equilibrium model, show that the solubilization of alkoxyethanols in carboxylate micelles is enhanced by increasing the surfactant chain length and the number of EO groups in the alcohol. The deeper penetration of C4EOX into the micelles of longer chain surfactants is associated with increasingly stronger interactions between surfactant head groups and EO segments of the alcohol on (or near) the micelle surface. Aggregation numbers of CnNa-C4EOX mixed micelles show that addition of a small amount of C4EOX has little effect on the structure of the micelles formed from C8Na and C10Na, but leads to significant change in C12Na micelles.
机译:在不存在和存在中链长度的烷氧基乙醇C4EOX(EO =乙烯)的情况下,水溶液中羧酸盐表面活性剂CnNa(n = 8,10,12)的表观摩尔体积和绝热压缩率Y-phi,YS在25°C下根据密度和声速测量值测定表面活性剂的存在和不存在时在水溶液中不存在和存在表面活性剂的情况下的氧化基团(X = 0-4)和烷氧基乙醇的Y-phi,YA的含量和酒精浓度。由表观摩尔特性计算出CnNa的部分摩尔体积特性和C4EOX从水到表面活性剂水溶液的传递函数。 CnNa的胶束化热力学参数值,即临界胶束浓度,无限稀释下单体的部分摩尔特性YS(0)和胶束态下的YS(M),是通过模拟CnNa获得的。使用质量作用模型的实验数据Y-phi,YS。如预期的那样,这些性质在很大程度上取决于表面活性剂链的长度。 C4EOX在胶束和水相之间的分布系数KD以及由于胶束化引起的醇的摩尔特性变化YA(M)是通过使用化学平衡模型拟合C4EOX的传递函数数据而提取的,表明通过增加表面活性剂链的长度和醇中EO基团的数量,可以增强烷氧基乙醇在羧酸盐胶束中的增溶作用。 C4EOX更深入地渗透到较长链表面活性剂的胶束中,这与表面活性剂头部基团与胶束表面(或附近)上的醇的EO链段之间的相互作用越来越强相关。 CnNa-C4EOX混合胶束的聚集数表明,添加少量C4EOX对由C8Na和C10Na形成的胶束的结构影响很小,但会导致C12Na胶束的显着变化。

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