Binary Mixed Systems of Anionic/Nonionic Surfactants

T. Okano, Y. Abe, Daisuke Hotta, T. Nakano, G. Sugihara, Seong-Geun Oh
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引用次数: 11

Abstract

Micelle formation in water and adsorbed film formation at air/water interface were studied by surface tension measurement for two mixed surfactant systems : combinations of sodium salts of α-sulfonatomyristic acid methyl ester (α-SMy·Me) and the propyl ester (α-SMy·Pr) with n-decanoyl-N-methyl glucamide (MEGA-10). The α-SMy·Pr/MEGA-10 and the α-SMy·Me/MEGA-10 mixed systems were found to synergistically enhance surface activity and form well-mixed micelles with the aid of strong interaction between head groups. Critical micellization concentration (CMC) as a function of mole fraction of MEGA-10 in the surfactant mixture (XMEGA-10) for both mixed systems was noted to deviate negatively from ideal mixing. Micellar phase (CMC vs YMEGA-10 relation) curves were simulated through use of the interaction parameter, ωR=-2.1 for α-SMy·Me/MEGA-10 and ωR=-2.0 for α-SMy·Pr/MEGA-10 and indicated the presence of azeotropes. Based on equations for estimating composition (Zi) and the interaction parameter (ωA) in adsorbed film equilibrated with monomers in bulk solution, phase diagrams were constructed that included the two relations of CMC vs XMEGA-10 and CMC vs ZMEGA-10. Adsorbed film of the respective mixed systems was formed through stronger interactions between anionic and nonionic surfactants compared to those of mixed micelles (-ωA>-ωR). The diagrams demonstrated that composition in micelles (Yi) differs from that in the adsorbed film (Zi). From the slope of surface tension (γ) vs logarithmic molality (ln mt) curve, just below CMC, surface excess (Γ) was determined and mean molecular area (Am) was computed as a function of XMEGA-10 or ZMEGA-10. From Am data, partial molecular area (PMA) of each component was determined as a function of ZMEGA-10; a large deviation from ideal mixing (the additivity rule) was observed for the respective mixed systems. Effects of differences in head group moiety, i.e., either methyl or propyl, were clearly evident with respect to hydrophobicity difference, but physicochemical behavior appeared essentially the same.
阴离子/非离子表面活性剂二元混合体系
通过表面张力测量,研究了α-磺酰基酸甲酯钠盐(α-SMy·Me)和丙基酯(α-SMy·Pr)与正癸烷酰- n-甲基葡萄糖酰胺(meg10)的混合表面活性剂体系在水中的胶束形成和空气/水界面的吸附膜形成。α-SMy·Pr/MEGA-10和α-SMy·Me/MEGA-10混合体系通过头基之间的强相互作用增强了表面活性,形成了混合良好的胶束。两种混合体系的临界胶束浓度(CMC)作为表面活性剂混合物(XMEGA-10)中MEGA-10摩尔分数的函数与理想混合情况呈负向偏离。采用α-SMy·Me/MEGA-10的相互作用参数ωR=-2.1和α-SMy·Pr/MEGA-10的ωR=-2.0模拟胶束相(CMC与YMEGA-10的关系)曲线,表明共共物的存在。基于估算吸附膜中单体平衡的组分(Zi)和相互作用参数(ωA)的方程,构建了CMC与XMEGA-10和CMC与ZMEGA-10的相图。与混合胶束相比(-ωA>-ωR),阴离子表面活性剂和非离子表面活性剂通过更强的相互作用形成了各自的混合体系的吸附膜。图显示胶束(Yi)的组成与吸附膜(Zi)的组成不同。从表面张力(γ)对对数质量摩尔浓度(ln mt)曲线的斜率,在CMC下方,确定了表面过剩(Γ),并计算了平均分子面积(Am)作为XMEGA-10或ZMEGA-10的函数。根据Am数据,确定了各组分的部分分子面积(PMA)与ZMEGA-10的函数关系;对于各自的混合系统,观察到与理想混合(可加性规则)的较大偏差。无论是甲基还是丙基,不同的头基部分对疏水性的影响是明显的,但物理化学行为基本相同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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