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核心冷冻时胶束中增溶物的释放。

Release of Solubilizate from Micelle upon Core Freezing.

作者信息

Dai Jing, Alaei Zahra, Plazzotta Beatrice, Pedersen Jan Skov, Furó István

机构信息

Division of Applied Physical Chemistry, Department of Chemistry, KTH Royal Institute of Technology , SE-10044 Stockholm, Sweden.

Interdisciplinary Nanoscience Center (iNANO) and Department of Chemistry, Aarhus University , Gustav Wieds Vej 14, 8000 Aarhus C, Denmark.

出版信息

J Phys Chem B. 2017 Nov 16;121(45):10353-10363. doi: 10.1021/acs.jpcb.7b08912. Epub 2017 Nov 1.

Abstract

By combining NMR (yielding H chemical shift, spin relaxation, and self-diffusion data) and small-angle X-ray scattering experiments, we investigate the complex temperature dependence of the molecular and aggregate states in aqueous solutions of the surfactant [CH(CH)(OCHCH)OH], abbreviated as C18E20, and hexamethyldisiloxane, HMDSO. The latter molecule serves as a model for hydrophobic solubilizates. Previously, the pure micellar solution was demonstrated to exhibit core freezing at approximately 7-8 °C. At room temperature, we find that HMDSO solubilizes at a volume fraction of approximately 10% in the core of the C18E20 micelles, which consists of molten and thereby highly mobile alkyl chains. Upon lowering the temperature, core freezing is found, just like in pure micelles, but at a temperature shifted significantly to 3 °C. The frozen cores contain immobile alkyl chains and exhibit a higher density but are essentially devoid (volume fraction below 1%) of the solubilizate. The latter molecules are released, first gradually and then rather steeply, from the core in the temperature range that is roughly delimited by the two core freezing temperatures, one for pure micelles and one for micelles with solubilizates. The release behavior of systems with different initial HMDSO loading follows the same master curve. This feature is rationalized in terms of loading capacity being strongly temperature dependent: upon lowering the temperature, release commences once the loading capacity descends below the actual solubilizate content. The sharp release curves and the actual release mechanism with its molecular features shown in rich detail have some bearing on a diverse class of possible applications.

摘要

通过结合核磁共振(可得出氢化学位移、自旋弛豫和自扩散数据)和小角X射线散射实验,我们研究了表面活性剂[CH(CH)(OCHCH)OH](简称为C18E20)与六甲基二硅氧烷(HMDSO)的水溶液中分子和聚集体状态复杂的温度依赖性。后一种分子用作疏水增溶物的模型。此前已证明,纯胶束溶液在约7 - 8°C时会出现核心冻结现象。在室温下,我们发现HMDSO在C18E20胶束核心中的增溶体积分数约为10%,该胶束核心由熔融且因此高度可移动的烷基链组成。随着温度降低,与纯胶束一样,会出现核心冻结现象,但温度明显偏移至3°C。冻结的核心包含不可移动的烷基链,密度更高,但基本上不含(体积分数低于1%)增溶物。后一种分子在大致由两个核心冻结温度界定的温度范围内,首先逐渐然后相当急剧地从核心中释放出来,一个核心冻结温度对应纯胶束,另一个对应含有增溶物的胶束。不同初始HMDSO负载量的体系的释放行为遵循相同的主曲线。这一特征可以从负载能力强烈依赖温度的角度来解释:随着温度降低,一旦负载能力降至实际增溶物含量以下,释放就会开始。详细展示的尖锐释放曲线及其具有分子特征的实际释放机制与多种可能的应用有关。

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