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Henry's Law Constants

www.henrys-law.org

Rolf Sander

Atmospheric Chemistry Division

Max-Planck Institute for Chemistry
Mainz, Germany

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Henry's Law Constants

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When referring to the compilation of Henry's Law Constants, please cite this publication:

R. Sander: Compilation of Henry's law constants (version 5.0.0) for water as solvent, Atmos. Chem. Phys., 23, 10901-12440 (2023), doi:10.5194/acp-23-10901-2023

The publication from 2023 replaces that from 2015, which is now obsolete. Please do not cite the old paper anymore.

Henry's Law Constants → Inorganic species → Hydrogen (H) → hydroperoxy radical

FORMULA:HO2
CAS RN:3170-83-0
STRUCTURE
(FROM NIST):
InChIKey:MHAJPDPJQMAIIY-UHFFFAOYSA-M

Hscp d ln Hs cp / d (1/T) References Type Notes
[mol/(m3Pa)] [K]
5.7×101 Régimbal and Mozurkewich (1997) R
6.8 Burkholder et al. (2019) T 47)
6.8 Burkholder et al. (2015) T 47)
6.8 Sander et al. (2011) T 47)
6.8 Sander et al. (2006) T 47)
3.8×101 5900 Hanson et al. (1992) T
8.9×101 Weinstein-Lloyd and Schwartz (1991) T
8.9×101 Chameides (1984) T
1.2×101 Schwartz (1984) T 50)
4.6×101 4800 Berdnikov and Bazhin (1970) T 48)
6600 Jacob (1986) E 51)

Data

The first column contains Henry's law solubility constant Hscp at the reference temperature of 298.15 K.
The second column contains the temperature dependence d ln Hs cp / d (1/T), also at the reference temperature.

References

  • Berdnikov, V. M. & Bazhin, N. M.: Oxidation-reduction potentials of certain inorganic radicals in aqueous solutions, Russ. J. Phys. Chem., 44, 395–398 (1970).
  • Burkholder, J. B., Sander, S. P., Abbatt, J., Barker, J. R., Huie, R. E., Kolb, C. E., Kurylo, M. J., Orkin, V. L., Wilmouth, D. M., & Wine, P. H.: Chemical Kinetics and Photochemical Data for Use in Atmospheric Studies, Evaluation No. 18, JPL Publication 15-10, Jet Propulsion Laboratory, Pasadena, URL https://jpldataeval.jpl.nasa.gov (2015).
  • Burkholder, J. B., Sander, S. P., Abbatt, J., Barker, J. R., Cappa, C., Crounse, J. D., Dibble, T. S., Huie, R. E., Kolb, C. E., Kurylo, M. J., Orkin, V. L., Percival, C. J., Wilmouth, D. M., & Wine, P. H.: Chemical Kinetics and Photochemical Data for Use in Atmospheric Studies, Evaluation No. 19, JPL Publication 19-5, Jet Propulsion Laboratory, Pasadena, URL https://jpldataeval.jpl.nasa.gov (2019).
  • Chameides, W. L.: The photochemistry of a remote marine stratiform cloud, J. Geophys. Res., 89, 4739–4755, doi:10.1029/JD089ID03P04739 (1984).
  • Hanson, D. R., Burkholder, J. B., Howard, C. J., & Ravishankara, A. R.: Measurement of OH and HO2 radical uptake coefficients on water and sulfuric acid surfaces, J. Phys. Chem., 96, 4979–4985, doi:10.1021/J100191A046 (1992).
  • Jacob, D. J.: Chemistry of OH in remote clouds and its role in the production of formic acid and peroxymonosulfate, J. Geophys. Res., 91, 9807–9826, doi:10.1029/JD091ID09P09807 (1986).
  • Régimbal, J.-M. & Mozurkewich, M.: Peroxynitric acid decay mechanisms and kinetics at low pH, J. Phys. Chem. A, 101, 8822–8829, doi:10.1021/JP971908N (1997).
  • Sander, S. P., Friedl, R. R., Golden, D. M., Kurylo, M. J., Moortgat, G. K., Keller-Rudek, H., Wine, P. H., Ravishankara, A. R., Kolb, C. E., Molina, M. J., Finlayson-Pitts, B. J., Huie, R. E., & Orkin, V. L.: Chemical Kinetics and Photochemical Data for Use in Atmospheric Studies, Evaluation Number 15, JPL Publication 06-2, Jet Propulsion Laboratory, Pasadena, CA, URL https://jpldataeval.jpl.nasa.gov (2006).
  • Sander, S. P., Abbatt, J., Barker, J. R., Burkholder, J. B., Friedl, R. R., Golden, D. M., Huie, R. E., Kolb, C. E., Kurylo, M. J., Moortgat, G. K., Orkin, V. L., & Wine, P. H.: Chemical Kinetics and Photochemical Data for Use in Atmospheric Studies, Evaluation No. 17, JPL Publication 10-6, Jet Propulsion Laboratory, Pasadena, URL https://jpldataeval.jpl.nasa.gov (2011).
  • Schwartz, S. E.: Gas- and aqueous-phase chemistry of HO2 in liquid water clouds, J. Geophys. Res., 89, 11 589–11 598, doi:10.1029/JD089ID07P11589 (1984).
  • Weinstein-Lloyd, J. & Schwartz, S. E.: Low-intensity radiolysis study of free-radical reactions in cloudwater: H2O2 production and destruction, Environ. Sci. Technol., 25, 791–800, doi:10.1021/ES00016A027 (1991).

Type

Table entries are sorted according to reliability of the data, listing the most reliable type first: L) literature review, M) measured, V) VP/AS = vapor pressure/aqueous solubility, R) recalculation, T) thermodynamical calculation, X) original paper not available, C) citation, Q) QSPR, E) estimate, ?) unknown, W) wrong. See Section 3.1 of Sander (2023) for further details.

Notes

47) The free energy of solution was calculated based on electrochemical reduction potentials and related free energies.
48) Calculated from correlation between the polarizabilities and solubilities of stable gases. The temperature dependence is an estimate of the upper limit.
50) In the abstract, Schwartz (1984) gives a range of 9.9 mol m−3 Pa−1 < Hscp < 3.0×101 mol m−3 Pa−1. The mean value of this range (2.0×101 mol m−3 Pa−1) has been used by Lelieveld and Crutzen (1991), Pandis and Seinfeld (1989), and Jacob (1986).
51) The value of Hs⊖ was taken from Schwartz (1984).

The numbers of the notes are the same as in Sander (2023). References cited in the notes can be found here.

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