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The anomalous behavior of the density of water in the range 30 K < T < 373 K

机译:30 K <T <373 K范围内水密度的异常行为

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The temperature dependence of the density of water, ρ(T). is obtained by means of optical scattering data, Raman and Fourier transform infrared, in a very wide temperature range, 30 < T < 373 K. This interval covers three regions: the thermodynamically stable liquid phase, the metastable supercooled phase, and the low-density amorphous solid phase, at very low T. From analyses of the profile of the OH stretching spectra, we determine the fractional weight of the two main spectral components characterized by two different local hydrogen bond structures. They are, as predicted by the liquid-liquid phase transition hypothesis of liquid water, the low- and the high-density liquid phases. We evaluate contributions to the density of these two phases and thus are able to calculate the absolute density of water as a function of T. We observe in ρ(T) a complex thermal behavior characterized not only by the well known maximum in the stable liquid phase at T = 277 K, but also by a well defined minimum in the deeply supercooled region at 203 ± 5 K, in agreement with suggestions from molecular dynamics simulations.
机译:水密度ρ(T)与温度的关系。是通过在30 <T <373 K的非常宽的温度范围内通过拉曼光谱和傅立叶变换红外光谱获得的光学散射数据而获得的。此间隔涵盖了三个区域:热力学稳定的液相,亚稳态的过冷相和低热稳定性。密度非常高的非晶态固相,在非常低的T下。通过分析OH拉伸光谱的分布图,我们确定了以两个不同的局部氢键结构为特征的两个主要光谱成分的分数重量。正如液态水的液相-液相转变假说所预测的那样,它们是低密度和高密度液相。我们评估了这两个相的密度的贡献,因此能够计算出水的绝对密度作为T的函数。我们在ρ(T)中观察到复杂的热行为,其特征不仅在于稳定液体中的已知最大值。 T = 277 K时的相变,但在203±5 K处的深过冷区域也有明确定义的最小值,这与分子动力学模拟的建议一致。

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