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溶致液晶体系中受限扩散的核磁共振研究。

NMR studies of restricted diffusion in lyotropic systems.

作者信息

Szutkowski Kosma, Klinowski Jacek, Jurga Stefan

机构信息

Department of Macromolecular Physics, Adam Mickiewicz University, Umultowska 85, 61-614 Poznan, Poland.

出版信息

Solid State Nucl Magn Reson. 2002 Sep-Nov;22(2-3):394-408. doi: 10.1006/snmr.2002.0087.

DOI:10.1006/snmr.2002.0087
PMID:12469822
Abstract

Tortuosity, 1/alpha, and surface-to-volume ratio, S/V, were determined in aqueous solutions of decylammonium, dodecylammonium and tetradecylammonium chlorides of various concentrations by measuring the apparent diffusion coefficient of water, D(app)(delta). This was found to be much smaller than in the bulk state. Such restricted diffusion is interpreted in terms of the Mitra model, where D(delta) depends on diffusion time and is controlled primarily by S/V. The samples exhibit lamellar (L), hexagonal (H) and isotropic (I) liquid crystalline phases. We observed changes in S/V upon phase transition. In the lamellar and hexagonal phases, the system is ordered, resulting in relatively small S/V ratios, compared to the micellar-isotropic phase. We did not observe a dependence on the diffusion time, delta, in the isotropic phase, because the duration of the experiment was not sufficiently short to observe the change from D(app)(delta) to D(eff). We observed the effective diffusion coefficient of water, which directly probes the tortuosity of the system. The S/V ratios were obtained by fitting the Mitra model, using known values of the bulk water diffusion coefficients, and the assumption that D(app) --> D0 for delta --> 0. S/V is correlated with the type of structure, increasing on transition to the isotropic phase and decreasing on transition to other phases. The change in tortuosity is small, but slightly larger for the isotropic phase.

摘要

通过测量水的表观扩散系数D(app)(δ),确定了不同浓度的癸基氯化铵、十二烷基氯化铵和十四烷基氯化铵水溶液中的曲折度、1/α以及表面积与体积比S/V。结果发现,该表观扩散系数比在本体状态下小得多。这种受限扩散根据米特拉模型进行解释,其中D(δ)取决于扩散时间,并且主要由S/V控制。样品呈现层状(L)、六方(H)和各向同性(I)液晶相。我们观察到相变时S/V的变化。在层状和六方相中,体系是有序的,与胶束-各向同性相相比,导致S/V比值相对较小。在各向同性相中,我们没有观察到对扩散时间δ的依赖性,因为实验持续时间不够短,无法观察到从D(app)(δ)到D(eff)的变化。我们观察到了水的有效扩散系数,它直接探测了体系的曲折度。通过拟合米特拉模型,利用本体水扩散系数的已知值以及δ→0时D(app)→D0的假设,获得了S/V比值。S/V与结构类型相关,在转变为各向同性相时增加,在转变为其他相时减小。曲折度的变化很小,但在各向同性相中略大一些。

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