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在阳离子双子表面活性剂和阴离子 SDS 的混合物中形成单分散带电囊泡。

Formation of monodisperse charged vesicles in mixtures of cationic gemini surfactants and anionic SDS.

机构信息

Stranski-Laboratorium für Physikalische und Theoretische Chemie, Institut für Chemie, Technische Universität Berlin, Strasse des 17. Juni 124, Sekr. TC7, D-10623 Berlin, Germany.

出版信息

Langmuir. 2011 Jan 18;27(2):582-91. doi: 10.1021/la103976p. Epub 2010 Dec 10.

Abstract

The aggregation behavior of catanionics formed by the mixture of cationic geminis derived from dodecyltrimethylammonium chloride (DTAC) and anionic sodium dodecylsulfate (SDS) was studied by means of phase studies and comprehensive small-angle neutron scattering (SANS) experiments at 25 °C and 50 mM overall concentration. The results are compared to those for the previously studied SDS + DTAC system. Various gemini spacers of different natures and geometries were used, but all of them had similar lengths: an ethoxy bridge, a double bond, and an aromatic ring binding the two DTACs in three different substitutions (ortho, meta, and para). SANS and SAXS data analysis indicates that the spacer has no large effect on the spheroidal micelles of pure surfactants formed at low concentration in water; however, specific effects appear with the addition of electrolytes. Microstructures formed in the catanionic mixtures are rather strongly dependent on the nature of the spacer. The most important finding is that for the hydrophilic, flexible ethoxy bridge, monodisperse vesicles with a fixed anionic/cationic charge ratio (depending only on the surfactant in excess) are formed. Furthermore, the composition of these vesicles shows that strongly charged aggregates are formed. This study therefore provides new opportunities for developing tailor-made gemini surfactants that allow for the fine tuning of catanionic structures.

摘要

通过相态研究和综合小角中子散射(SANS)实验,在 25°C 和 50mM 总浓度下,研究了由十二烷基三甲基氯化铵(DTAC)衍生的阳离子双子体与阴离子十二烷基硫酸钠(SDS)混合物形成的反离子的聚集行为。将结果与之前研究过的 SDS+DTAC 体系进行了比较。使用了各种不同性质和几何形状的双子体间隔基,但它们的长度都相似:一个乙氧基桥、一个双键和一个芳环,将两个 DTAC 以三种不同的取代方式(邻位、间位和对位)结合在一起。SANS 和 SAXS 数据分析表明,间隔基对低浓度水中形成的纯表面活性剂的球形胶束没有大的影响;然而,随着电解质的加入,会出现特定的影响。在反离子混合物中形成的微结构强烈依赖于间隔基的性质。最重要的发现是,对于亲水、柔性的乙氧基桥,形成了具有固定阴离子/阳离子电荷比的单分散囊泡(仅取决于过量的表面活性剂)。此外,这些囊泡的组成表明形成了带强电荷的聚集体。因此,这项研究为开发定制的双子表面活性剂提供了新的机会,可以精细调整反离子结构。

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