离子型表面活性剂的第一种聚集状态由球形胶束组成,这并不是一种规则。以十四烷基三甲基水杨酸铵为例

IF 4.7 3区 材料科学 Q2 CHEMISTRY, PHYSICAL
Álvaro Javier Patiño-Agudelo, Suelen Gauna Trindade, Larissa de Almeida Ueti, Edvaldo Sabadini
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引用次数: 0

摘要

离子表面活性剂可在高浓度下聚集成蠕虫状胶束(WLM),形成与聚合物溶液相似的超分子结构。虽然人们对这些超分子聚集体的流变学有了很好的了解,但低浓度下的实验热力学研究仍处于早期阶段。在本研究中,我们首次采用了十四烷基三甲基水杨酸铵(TTASal),利用等温滴定量热法、电导率测量法和低温透射电子显微镜研究了 WLM 形成背后的驱动力。我们的研究结果表明,TTASal 最初聚集成的是 WLM 而不是球形胶束,这表明 WLM 的形成受到表面活性剂离子-计数器相互作用的影响,而不仅仅是浓度的影响。值得注意的是,与聚集过程相关的焓变是决定游离单体聚集成球形或 WLM 的关键因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

It is not a rule that the first aggregation state of an ionic surfactant consists of spherical micelles. The case of tetradecyltrimethylammonium salicylate

It is not a rule that the first aggregation state of an ionic surfactant consists of spherical micelles. The case of tetradecyltrimethylammonium salicylate

Ionic surfactants can assemble into wormlike micelles (WLM) at high concentrations, forming supramolecular structures that exhibit similarities to polymeric solutions. Although the rheology of these supramolecular aggregates is well understood, experimental thermodynamic studies at low concentrations are still in their early stages. In this study, we employed tetradecyltrimethylammonium salicylate (TTASal) to investigate the driving forces behind WLM formation for the first time, using isothermal titration calorimetry, electrical conductivity measurements, and cryogenic transmission electron microscopy. Our findings indicate that TTASal initially aggregates into WLM rather than spherical micelles, demonstrating that WLM formation is influenced by surfactant ion-counterion interactions rather than concentration alone. Notably, the enthalpy change associated with the aggregation process emerges as a key determinant in dictating the aggregation of free monomers into spherical or WLM.

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来源期刊
Colloid and Interface Science Communications
Colloid and Interface Science Communications Materials Science-Materials Chemistry
CiteScore
9.40
自引率
6.70%
发文量
125
审稿时长
43 days
期刊介绍: Colloid and Interface Science Communications provides a forum for the highest visibility and rapid publication of short initial reports on new fundamental concepts, research findings, and topical applications at the forefront of the increasingly interdisciplinary area of colloid and interface science.
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