openHSU logo
  • English
  • Deutsch
  • Log In
  • Communities & Collections
  1. Home
  2. Helmut-Schmidt-University / University of the Federal Armed Forces Hamburg
  3. Publications
  4. 3 - Publication references (without full text)
  5. Ab initio virial equation of state for argon using a new nonadditive three-body potential
 
Options
Show all metadata fields

Ab initio virial equation of state for argon using a new nonadditive three-body potential

Publication date
2011-08-28
Document type
Research article
Author
Jäger, Benjamin
Hellmann, Robert 
Bich, Eckard
Vogel, Eckhard
Organisational unit
Universität Rostock
DOI
10.1063/1.3627151
URI
https://openhsu.ub.hsu-hh.de/handle/10.24405/14500
Scopus ID
2-s2.0-80052408612
Pubmed ID
21895186
ISSN
0021-9606
1089-7690
Series or journal
The journal of chemical physics : JCP
Periodical volume
135
Periodical issue
8
Peer-reviewed
✅
Part of the university bibliography
Nein
  • Additional Information
Abstract
An ab initio nonadditive three-body potential for argon has been developed using quantum-chemical calculations at the CCSD(T) and CCSDT levels of theory. Applying this potential together with a recent ab initio pair potential from the literature, the third and fourth to seventh pressure virial coefficients of argon were computed by standard numerical integration and the Mayer-sampling Monte Carlo method, respectively, for a wide temperature range. All calculated virial coefficients were fitted separately as polynomials in temperature. The results for the third virial coefficient agree with values evaluated directly from experimental data and with those computed for other nonadditive three-body potentials. We also redetermined the second and third virial coefficients from the best experimental pρT data utilizing the computed higher virial coefficients as constraints. Thus, a significantly closer agreement of the calculated third virial coefficients with the experimental data was achieved. For different orders of the virial expansion, pρT data have been calculated and compared with results from high quality measurements in the gaseous and supercritical region. The theoretically predicted pressures are within the very small experimental errors of ±0.02% for p ≤ 12 MPa in the supercritical region near room temperature, whereas for subcritical temperatures the deviations increase up to +0.3%. The computed pressure at the critical density and temperature is about 1.3% below the experimental value. At pressures between 200 MPa and 1000 MPa and at 373 K, the calculated values deviate by 1% to 9% from the experimental results.
Version
Not applicable (or unknown)
Access right on openHSU
Metadata only access

  • Cookie settings
  • Privacy policy
  • Send Feedback
  • Imprint