The (p,ρ,T,x) properties for {xNH3+(1−x)H2O} at T=(450 and 500)K over the pressure range from (10 to 200)MPa
Clicks: 247
ID: 272381
2008
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This
article has not been analysed, so there is no overall score —
reader engagement is measured and shown alongside.
Reader Engagement
Steady Performance
30.0
/100
247 views
35 readers
AI Quality Assessment
Not analyzed
Readership in this journal
SteadyRanked #6 of 8 articles by views in The Journal of Chemical Thermodynamics
Most read
Least read
Bar heights use a square-root scale.
Mint this article as an NFT
Not yet mintedCreate a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.
5
SUSD
one-off · no wallet required
Abstract
The (p , ρ , T , x ) properties for {x NH3 + (1 − x )H2O} with x = (0.1048, 0.2046, 0.3807, 0.5565, 0.7008, 0.8010, 0.9102, and 1.0000) in the compressed liquid phase were measured by means of a metal-bellows variable volumometer at temperatures of (450 and 500) K and pressures from (10 to 200) MPa. The volume fraction purities of the ammonia used in the measurements were 0.99999. The water employed was deionised, distilled, and degassed to 3.0 ≅ 10−4 Pa by freeze–thaw cycling with liquid nitrogen before use. In order to carry out these measurements at higher ranges of temperature (above T = 450 K) and pressure (up to p = 200 MPa), we have implemented several reconstructions to the apparatus, including the replacement of the sample cell containing the metal-bellows, and the development of a thermostatted air bath, in which the temperature of the air and sample cell can be raised up to 600 K. The expanded uncertainties (k = 2) in temperature, pressure, density, and composition measurements have been estimated to be less than 5 mK; 1.3 × 10−2%; 0.48%; and 8.2 × 10−4, respectively. Comparisons of the available equations of state (EoS) with the present measurements are reported. On the basis of the present results, moreover, the excess molar volume vmE of the mixtures was calculated and illustrated as a function of temperature and pressure.
| Reference Key |
uematsu2008thethe
Use this key to autocite in the manuscript while using
SciMatic Manuscript Manager or Thesis Manager
|
|---|---|
| Authors | S. Muromachi,H. Miyamoto,M. Uematsu;S. Muromachi;H. Miyamoto;M. Uematsu; |
| Journal | The Journal of Chemical Thermodynamics |
| Year | 2008 |
| DOI |
10.1016/j.jct.2008.06.009
|
| URL | |
| Keywords |
Citations
No citations found. To add a citation, contact the admin at info@scimatic.org
Comments
No comments yet. Be the first to comment on this article.