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首页> 外文期刊>Colloids and Surfaces, A. Physicochemical and Engineering Aspects >1-butanol and 3,3-dimethyl-1-butanol as cosurfactants of the laurylsulfobetaine/water system
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1-butanol and 3,3-dimethyl-1-butanol as cosurfactants of the laurylsulfobetaine/water system

机译:1-丁醇和3,3-二甲基-1-丁醇作为月桂基磺基甜菜碱/水体系的助表面活性剂

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摘要

Phase and theological behaviors for laurylsulfobetaine with 1-butanol and with 3,3-dimethyl-1-butanol at 30.0 +/- 0.1 degreesC are presented. Both systems show three liquid crystal phases: lamellar, hexagonal and cubic. Only one micellar phase appears with l-butanol while two different micellar phases (L-1 and L-2) appear with the branched alcohol. For the system with 1-butanol, the transition from normal to reverse micelles goes through bicontinuous structures without phase separation. The shape of the mixed laurylsulfobetaine/1-butanol micelles in water change from spherical to large cylindrical micelles with the surfactant content. For the system with 3,3-dimethyl-1-butanol, the normal micelles in water solution are small and spherical and they exist in a narrow range of alcohol content. The reverse micelles in l-butanol are larger than in 3,3-dimethyl-1-butanol. The extension of the cubic phase is the same for both systems. This phase is the most viscous phase with elastic properties which fits to the Maxwell model at low frequencies. On the contrary, the extension of lamellar and hexagonal phases is different depending of the alcohol structure. The formation of lamellar phase is favoring for the branched alcohol while the hexagonal region is larger for the system with the linear alcohol. Both phases show also viscoelastic properties but they do no fit to Maxwell model. (C) 2001 Elsevier Science B.V. All rights reserved. [References: 30]
机译:提出了月桂基磺基甜菜碱与1-丁醇和3,3-二甲基-1-丁醇在30.0 +/- 0.1摄氏度下的相和神学行为。这两个系统都显示三个液晶相:层状,六方和立方。异丁醇只出现一个胶束相,而支链醇出现两个不同的胶束相(L-1和L-2)。对于具有1-丁醇的系统,从正向胶束的转变通过双连续结构进行而没有相分离。具有表面活性剂含量的水中混合的月桂基磺基甜菜碱/ 1-丁醇胶束的形状从球形变成大的圆柱形胶束。对于含3,3-二甲基-1-丁醇的体系,水溶液中的正常胶束很小且呈球形,并且它们的醇含量范围很窄。 1-丁醇中的反胶束大于3,3-二甲基-1-丁醇中的胶束。两种系统的立方相扩展相同。该相是最粘的相,具有弹性,适合低频下的麦克斯韦模型。相反,层状相和六角相的延伸取决于醇的结构而不同。层状相的形成对于支链醇是有利的,而对于线性醇的体系,六角形区域更大。这两个阶段都显示出粘弹性,但它们不适合麦克斯韦模型。 (C)2001 Elsevier Science B.V.保留所有权利。 [参考:30]

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