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非离子/离子混合表面活性剂体系中的胶束相互作用。

Micellar Interactions in Nonionic/Ionic Mixed Surfactant Systems.

作者信息

Goloub TP, Pugh RJ, Zhmud BV

机构信息

Institute for Surface Chemistry, Stockholm, SE-114 86, Sweden

出版信息

J Colloid Interface Sci. 2000 Sep 1;229(1):72-81. doi: 10.1006/jcis.2000.6954.

Abstract

To study the influence of the chemical nature of headgroups and the type of counterion on the process of micellization in mixed surfactant systems, the cmc's of several binary mixtures of surfactants with the same length of hydrocarbon tail but with different headgroups have been determined as a function of the monomer composition using surface tension measurements. Based on these results, the interaction parameter between the surfactant species in mixed micelles has been determined using the pseudophase separation model. Experiments were carried out with (a) the nonionic/anionic C(12)E(6)/SDS ((hexa(ethyleneglycol) mono-n-dodecyl ether)/(sodium dodecyl sulfate)), (b) amphoteric/anionic DDAO/SDS ((dodecyldimethylamine oxide)/(sodium dodecyl sulfate)), and (c) amphoteric/nonionic C(12)E(6)/DDAO mixed surfactant systems. In the case of the mixed surfactant systems containing DDAO, experiments were carried out at pH 2 and pH 8 where the surfactant was in the cationic and nonionic form, respectively. It was shown that the mixtures of the nonionic surfactants with different kinds of headgroups exhibit almost ideal behavior, whereas for the nonionic/ionic surfactant mixtures, significant deviations from ideal behavior (attractive interactions) have been found, suggesting binding between the head groups. Molecular orbital calculations confirmed the existence of the strong specific interaction between (1) SDS and nonionic and cationic forms of DDAO and between (2) C(12)E(6) and the cationic form of DDAO. In the case for the C(12)E(6)/SDS system, an alternative mechanism for the stabilization of mixed micelles was suggested, which involved the lowering in the free energy of the hydration layer. Copyright 2000 Academic Press.

摘要

为了研究混合表面活性剂体系中头基化学性质和抗衡离子类型对胶束化过程的影响,通过表面张力测量,测定了几种具有相同碳氢链长度但头基不同的表面活性剂二元混合物的临界胶束浓度(cmc)随单体组成的变化关系。基于这些结果,使用假相分离模型确定了混合胶束中表面活性剂物种之间的相互作用参数。实验分别在以下混合表面活性剂体系中进行:(a)非离子/阴离子型的C(12)E(6)/SDS((六(乙二醇)单正十二烷基醚)/(十二烷基硫酸钠));(b)两性离子/阴离子型的DDAO/SDS((十二烷基二甲基氧化胺)/(十二烷基硫酸钠));(c)两性离子/非离子型的C(12)E(6)/DDAO。对于含有DDAO的混合表面活性剂体系,实验分别在pH 2和pH 8条件下进行,此时表面活性剂分别处于阳离子和非离子形式。结果表明,具有不同头基的非离子表面活性剂混合物表现出几乎理想的行为,而对于非离子/离子表面活性剂混合物,则发现明显偏离理想行为(存在吸引相互作用),这表明头基之间存在结合。分子轨道计算证实了(1)SDS与DDAO的非离子和阳离子形式之间以及(2)C(12)E(6)与DDAO的阳离子形式之间存在强烈的特异性相互作用。对于C(12)E(6)/SDS体系,提出了一种混合胶束稳定化的替代机制,该机制涉及水化层自由能的降低。版权所有2000年,学术出版社。

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