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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Micellization and adsorbed film formation of a binary mixed system of anioniconionic surfactants
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Micellization and adsorbed film formation of a binary mixed system of anioniconionic surfactants

机译:阴离子/非离子表面活性剂二元混合体系的胶束化和吸附膜形成

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Micelle formation in water and adsorbed film formation at the air/water interface were investigated by surface tension measurement of a mixed surfactant system: the combination of sodium salt of alpha-sulfonatomyristic acid methyl ester (alpha-SMy.Me) with decanoyl-N-methylglucamide (MEGA-10). alpha-SMy.Me and MEGA-10 can form well-mixed micelles with the aid of a strong interaction between headgroups, and accordingly the critical micelle concentration (cmc) as a function of mole fraction of MEGA-10 in the surfactant mixture (X-MEGA10) deviates negatively from ideal mixing. The micellar phase curve (cmc-Y-MEGA10 relation) was simulated by using the interaction parameter omega(R) = -2.1; the curve indicated the existence of an azeotrope formed by a 3:2 mixture (at X-MEGA10 = Y-MEGA10 = 0.4) Further, we derived equations related to the composition in the adsorbed film (Z(i)) equilibrated with monomers in bulk solution and to the interaction parameter (W-A), and then constructed a phase diagram including two relations of cmc vs X-MEGA10 and cme vs Z(MEGA10). From the diagram an azeotrope was found to be formed by the 1:1 mixture (at X-MEGA10 = Z(MEGA10) = 0.5), suggesting that the composition in micelles (Y-i) differs from that in the adsorbed film (Z(i)). The surface tension (gamma) vs logarithmic molality (ln m) curve at every 0.1 increment in X-MEGA10 showed synergistically enhanced surface activity. From the slope of the gamma vs ln m curve just below cmc, the surface excess (Gamma) was determined and then the mean molecular area (A(m)) was calculated as a function of X-MEGA10 BY analysis of A(m) data, the partial molecular area (PMA) of each component was determined as a function of X-MEGA10; this also showed a large deviation from ideal mixing (the additivity rule). [References: 41]
机译:通过混合表面活性剂系统的表面张力测量研究了水中的胶束形成和在空气/水界面处的吸附膜形成:α-磺基原子苯乙烯酸甲酯的钠盐(alpha-SMy.Me)与癸酰基-N-的组合甲基葡糖酰胺(MEGA-10)。 alpha-SMy.Me和MEGA-10可以通过头基团之间的强相互作用而形成充分混合的胶束,因此临界胶束浓度(cmc)是表面活性剂混合物中MEGA-10摩尔分数的函数(X -MEGA10)偏离理想混合。通过使用相互作用参数ω= -2.1模拟胶束相曲线(cmc-Y-MEGA10关系)。曲线表明存在由3:2混合物形成的共沸物(在X-MEGA10 = Y-MEGA10 = 0.4时)。此外,我们推导了与单体中平衡的吸附膜(Z(i))中的组成有关的方程。体积解和相互作用参数(WA),然后构造了一个相图,包括cmc与X-MEGA10和cme与Z(MEGA10)的两个关系。从该图发现,由1:1混合物形成共沸物(在X-MEGA10 = Z(MEGA10)= 0.5时),表明胶束(Yi)中的组成与吸附膜中的组成不同(Z(i ))。 X-MEGA10中每增加0.1,表面张力(γ)对数摩尔浓度(ln m)曲线显示出协同增强的表面活性。从恰好低于cmc的gamma与ln m曲线的斜率确定表面过量(Gamma),然后通过分析A(m)计算平均分子面积(A(m))作为X-MEGA10的函数数据确定每个组分的部分分子面积(PMA)作为X-MEGA10的函数。这也表明与理想混合(相加规则)存在较大偏差。 [参考:41]

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