Volume 595, November 2016
|Number of page(s)||23|
|Section||Atomic, molecular, and nuclear data|
|Published online||16 November 2016|
I. Improved partition functions and thermodynamic quantities for normal, equilibrium, and ortho and para molecular hydrogen⋆
Niels Bohr Institute & Centre for Star and Planet Formation, University of Copenhagen, Øster Voldgade 5–7, 1350 Copenhagen K, Denmark
Received: 19 August 2015
Accepted: 25 June 2016
Context. Hydrogen is the most abundant molecule in the Universe. Its thermodynamic quantities dominate the physical conditions in molecular clouds, protoplanetary disks, etc. It is also of high interest in plasma physics. Therefore thermodynamic data for molecular hydrogen have to be as accurate as possible in a wide temperature range.
Aims. We here rigorously show the shortcomings of various simplifications that are used to calculate the total internal partition function. These shortcomings can lead to errors of up to 40 percent or more in the estimated partition function. These errors carry on to calculations of thermodynamic quantities. Therefore a more complicated approach has to be taken.
Methods. Seven possible simplifications of various complexity are described, together with advantages and disadvantages of direct summation of experimental values. These were compared to what we consider the most accurate and most complete treatment (case 8). Dunham coefficients were determined from experimental and theoretical energy levels of a number of electronically excited states of H2. Both equilibrium and normal hydrogen was taken into consideration.
Results. Various shortcomings in existing calculations are demonstrated, and the reasons for them are explained. New partition functions for equilibrium, normal, and ortho and para hydrogen are calculated and thermodynamic quantities are reported for the temperature range 1–20 000 K. Our results are compared to previous estimates in the literature. The calculations are not limited to the ground electronic state, but include all bound and quasi-bound levels of excited electronic states. Dunham coefficients of these states of H2 are also reported.
Conclusions. For most of the relevant astrophysical cases it is strongly advised to avoid using simplifications, such as a harmonic oscillator and rigid rotor or ad hoc summation limits of the eigenstates to estimate accurate partition functions and to be particularly careful when using polynomial fits to the computed values. Reported internal partition functions and thermodynamic quantities in the present work are shown to be more accurate than previously available data.
Key words: miscellaneous / molecular data / astrochemistry / equation of state
The full datasets in 1 K temperature steps are only available at the CDS via anonymous ftp to cdsarc.u-strasbg.fr (188.8.131.52) or via http://cdsarc.u-strasbg.fr/viz-bin/qcat?J/A+A/595/A130
© ESO, 2016
Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.
Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.
Initial download of the metrics may take a while.