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254至298K以及高达100MPa条件下冷态和过冷重水的相对密度和等压膨胀系数

Relative density and isobaric expansivity of cold and supercooled heavy water from 254 to 298 K and up to 100 MPa.

作者信息

Blahut A, Hykl J, Peukert P, Vinš V, Hrubý J

机构信息

Institute of Thermomechanics of the Czech Academy of Sciences, Dolejškova 5, CZ-18200 Praha 8, Czech Republic.

出版信息

J Chem Phys. 2019 Jul 21;151(3):034505. doi: 10.1063/1.5100604.

Abstract

A dual-capillary apparatus was developed for highly accurate measurements of density of liquids, including the supercooled liquid region. The device was used to determine the density of supercooled heavy water in the temperature range from 254 K to 298 K at pressures ranging from atmospheric to 100 MPa, relative to density at reference isotherm 298.15 K. The measurements of relative density were reproducible within 10 ppm, and their expanded (k = 2) uncertainty was within 50 ppm. To obtain absolute values of density, thermodynamic integration was performed using recent accurate speed of sound measurements in the stable liquid region. An empirical equation of state (EoS) was developed, giving specific volume as a rational function of pressure and temperature. The new experimental data are represented by EoS within their experimental uncertainty. Gibbs energy was obtained by EoS integration allowing computation of all thermodynamic properties of heavy water using Gibbs energy derivatives. Although based on data in relatively narrow temperature and pressure ranges, the developed EoS shows an excellent agreement with literature data for densities, isothermal compressibilities, and isobaric expansivities of deeply supercooled heavy water. The curvature of the thermodynamic surface steeply increases toward low temperatures and low pressures, thus supporting the existence of the hypothesized liquid-liquid coexistence boundary in a close vicinity of existing experimental data.

摘要

开发了一种双毛细管装置,用于高精度测量液体密度,包括过冷液体区域。该装置用于在254 K至298 K的温度范围内,在大气压力至100 MPa的压力下,相对于参考等温线298.15 K处的密度,测定过冷重水的密度。相对密度的测量重复性在10 ppm以内,其扩展(k = 2)不确定度在50 ppm以内。为了获得密度的绝对值,利用最近在稳定液体区域进行的精确声速测量进行了热力学积分。建立了一个经验状态方程(EoS),将比容表示为压力和温度的有理函数。新的实验数据在其实验不确定度范围内由EoS表示。通过EoS积分获得吉布斯自由能,从而利用吉布斯自由能导数计算重水的所有热力学性质。尽管基于相对较窄的温度和压力范围内的数据,但所开发的EoS与文献中关于深度过冷重水的密度、等温压缩率和等压膨胀率的数据显示出极好的一致性。热力学表面的曲率朝着低温和低压急剧增加,从而支持了在现有实验数据附近存在假设的液 - 液共存边界。

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