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木糖醇-水混合物中的长程扩散。

Long-range diffusion in xylitol-water mixtures.

机构信息

Department of Applied Physics, Chalmers University of Technology, SE-412 96 Göteborg, Sweden.

出版信息

J Phys Chem B. 2013 Jun 20;117(24):7363-9. doi: 10.1021/jp401633g. Epub 2013 Jun 10.

Abstract

Dynamic light scattering (DLS) and small-angle neutron scattering (SANS) were employed to study mixtures of xylitol and water. The results were also related to a previous dielectric relaxation study on the same system. In the temperature range of the DLS measurements the viscosity related structural (α) relaxation is too fast to be observed on the experimental time scale, but a considerably slower exponential and hydrodynamic relaxation process is clearly observable in the polarized light scattering data. A similar ultraslow process has been observed in many other types of binary liquids and commonly assigned to long-range concentration or density fluctuations. In some studies this interpretation has been supported by observations of substantial structural inhomogeneities in static light scattering or SANS experiments. However, in this study we observe such an ultraslow process without any indication of structural inhomogeneities on length-scales above 2 nm. Hence, we suggest that our observed ultraslow process is due to long-range diffusion of single xylitol molecules or small clusters of a few xylitol molecules (and perhaps some associated water molecules) which are randomly dispersed and sufficiently small to not be structurally detected in our SANS study. In the q-range of the DLS measurements this ultraslow relaxation process is around room temperature several orders of magnitude slower than the structural α-relaxation. However, if its 1/q(2)-dependent relaxation time is extrapolated to q-values where relaxation times from dielectric spectroscopy and quasielastic neutron scattering are compatible (about 10 nm(-1)), a relaxation time similar to that of the dielectric α-relaxation is obtained. Thus, the large difference in time scale between the two relaxation processes in the q-range of a DLS study is due to the fact that the α-relaxation is cooperative in nature, rather than caused by long-range single particle diffusion, and thus q-independent at low q-values.

摘要

动态光散射(DLS)和小角中子散射(SANS)被用来研究木糖醇和水的混合物。研究结果还与之前对同一体系的介电弛豫研究有关。在 DLS 测量的温度范围内,与粘度有关的结构(α)弛豫太快,无法在实验时间尺度上观察到,但在偏振光散射数据中可以清楚地观察到一个相当慢的指数和流体力学弛豫过程。在许多其他类型的二元液体中都观察到了类似的超慢过程,通常归因于长程浓度或密度波动。在一些研究中,这种解释得到了静态光散射或 SANS 实验中观察到的大量结构不均匀性的支持。然而,在这项研究中,我们观察到了这样一个超慢过程,而在 2nm 以上的长度尺度上没有任何结构不均匀性的迹象。因此,我们认为我们观察到的超慢过程是由于单个木糖醇分子或几个木糖醇分子(可能还有一些相关的水分子)的长程扩散造成的,这些分子随机分散,并且足够小,在我们的 SANS 研究中无法在结构上检测到。在 DLS 测量的 q 范围内,这个超慢弛豫过程在室温下比结构α弛豫慢几个数量级。然而,如果将其 1/q(2)依赖性弛豫时间外推到介电光谱和准弹性中子散射相容的 q 值(约 10nm(-1)),则得到与介电α弛豫相似的弛豫时间。因此,在 DLS 研究的 q 范围内,两个弛豫过程之间的时间尺度差异很大,是因为α弛豫本质上是协同的,而不是由长程单个粒子扩散引起的,因此在低 q 值时与 q 无关。

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