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长链正烷醇的添加对阳离子表面活性剂/阴离子聚离子复合物盐和水体系相行为的控制。

Phase Behavior Controlled by the Addition of Long-Chain n-Alcohols in Systems of Cationic Surfactant/Anionic Polyion Complex Salts and Water.

机构信息

Institute of Chemistry , University of Campinas (UNICAMP) , PO Box 6154, 13084-970 Campinas , São Paulo , Brazil.

Department of Chemistry , Pontifical Catholic University of Rio de Janeiro , 22451-900 Rio de Janeiro , Rio de Janeiro , Brazil.

出版信息

J Phys Chem B. 2018 May 10;122(18):4861-4869. doi: 10.1021/acs.jpcb.8b01788. Epub 2018 May 1.

Abstract

Phase behavior of surfactants in water may be affected by the addition of a third component, and the present study discusses how long-chain n-alcohols affect phase transitions of systems formed by the surfactant hexadecyltrimethylammonium bromide, CTAB, or its complex salts formed with polyacrylate, CTAPA, as well as other previously reported complex salts/water/alcohol systems. Structural characterization by X-ray diffraction patterns at small and wide angles and different temperatures was performed for samples containing n-decanol, n-dodecanol, or n-tetradecanol. Differential scanning calorimetry (DSC) was also used to study the phase transition. The results allowed us to observe and understand the coexistence of lamellar gel (L) and lamellar liquid-crystal (L) phases, elucidating the structure of a previously reported mesophase, proposing an alternative assignment. Whereas the chain-melting transition is well-known to be sharp for lipids, we have found that it is broader for CTAB and CTAPA in the presence of these n-alcohols. We have investigated the effects of their composition and chain length on the temperature and enthalpy of transition. This elucidates why the addition of n-alcohols with chains slightly shorter than that of the surfactants leads to the formation of an ordered gel-like lamellar phase (L). n-Alcohols act as neutral cosurfactants, leading to more packing, and all of the factors converge to a limit situation, associated with a common critical area occupied by each alkyl chain. We compared our results with other mesophase systems from the literature, demonstrating that the same trends of phase behavior occur for complex salts of other polyelectrolytes with alkyltrimethylammonium surfactants.

摘要

表面活性剂在水中的相行为可能会受到第三种成分的影响,本研究讨论了长链醇如何影响由表面活性剂十六烷基三甲基溴化铵(CTAB)或其与聚丙烯酸形成的复合盐(CTAPA)以及其他先前报道的复合盐/水/醇系统形成的体系的相变。通过小角和广角 X 射线衍射图案以及不同温度下的结构表征,对含有正癸醇、正十二醇或正十四醇的样品进行了研究。差示扫描量热法(DSC)也用于研究相变。结果使我们能够观察和理解层状凝胶(L)和层状液晶(L)相的共存,阐明了先前报道的介相的结构,提出了替代的分配。虽然众所周知脂质的链熔化转变是急剧的,但我们发现,在这些 n-醇存在下,CTAB 和 CTAPA 的转变更为广泛。我们研究了它们的组成和链长对转变温度和焓的影响。这阐明了为什么添加比表面活性剂链稍短的 n-醇会导致有序凝胶状层状相(L)的形成。n-醇作为中性助表面活性剂,导致更紧密的堆积,所有因素都汇聚到一个极限情况,与每个烷基链占据的共同临界面积相关。我们将我们的结果与文献中的其他介相系统进行了比较,证明了具有烷基三甲基铵表面活性剂的其他聚电解质的复合盐的相行为也呈现出相同的趋势。

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