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

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388998%3A_____%2F19%3A00509586" target="_blank" >RIV/61388998:_____/19:00509586 - isvavai.cz</a>

Výsledek na webu

<a href="https://aip.scitation.org/doi/10.1063/1.5100604" target="_blank" >https://aip.scitation.org/doi/10.1063/1.5100604</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1063/1.5100604" target="_blank" >10.1063/1.5100604</a>

Jazyk výsledku

angličtina

Název v původním jazyce

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

Popis výsledku v původním jazyce

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 heavynwater 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.

Název v anglickém jazyce

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

Popis výsledku anglicky

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 heavynwater 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.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

20303 - Thermodynamics

Projekt

Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.

Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2019

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Journal of Chemical Physics

ISSN

0021-9606

e-ISSN

—

Svazek periodika

151

Číslo periodika v rámci svazku

3

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

18

Strana od-do

034505

Kód UT WoS článku

000476588700016

EID výsledku v databázi Scopus

2-s2.0-85069463336