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Henry's Law Constants

www.henrys-law.org

Rolf Sander

NEW: Version 5.0.0 has been published in October 2023

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 Please do not cite the old paper anymore.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 ConstantsOrganic species with chlorine (Cl)Polychlorinated biphenyls (PCBs) → 2,2'-dichlorobiphenyl

FORMULA:C12H8Cl2
TRIVIAL NAME: PCB-4
CAS RN:13029-08-8
STRUCTURE
(FROM NIST):
InChIKey:JAYCNKDKIKZTAF-UHFFFAOYSA-N

Hscp d ln Hs cp / d (1/T) References Type Notes
[mol/(m3Pa)] [K]
4.6×10−2 6000 Bamford et al. (2002) M
4.0×10−2 Fendinger and Glotfelty (1990) M
2.9×10−2 Dunnivant et al. (1988) M
2.9×10−2 Dunnivant and Elzerman (1988) M 725)
3.3×10−2 Murphy et al. (1987) M 12)
4.5×10−2 Murphy et al. (1983a) M 24)
7.1×10−3 5500 Paasivirta and Sinkkonen (2009) V
1.7×10−2 Mackay et al. (2006b) V
1.7×10−2 Mackay et al. (1992a) V
1.7×10−2 Shiu and Mackay (1986) V
1.8×10−2 Burkhard et al. (1985) V
2.6×10−2 Chiou et al. (1980) V
4.5×10−2 Murphy et al. (1983b) X 24) 726)
4.5×10−2 Keshavarz et al. (2022) Q
5.5×10−2 Duchowicz et al. (2020) Q 300)
2.5×10−2 Hilal et al. (2008) Q
6.9×10−2 Modarresi et al. (2007) Q 68)
2.7×10−2 Lee (2007) Q 723)
2.1×10−2 Lee (2007) Q 724)
4.8×10−2 English and Carroll (2001) Q 231) 232)
3.0×10−2 Dunnivant et al. (1992) Q
4.3×10−2 Duchowicz et al. (2020) ? 21) 186)

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

  • Bamford, H. A., Poster, D. L., Huie, R. E., & Baker, J. E.: Using extrathermodynamic relationships to model the temperature dependence of Henry’s law constants of 209 PCB congeners, Environ. Sci. Technol., 36, 4395–4402, doi:10.1021/ES020599Y (2002).
  • Burkhard, L. P., Armstrong, D. E., & Andren, A. W.: Henry’s law constants for the polychlorinated biphenyls, Environ. Sci. Technol., 19, 590–596, doi:10.1021/ES00137A002 (1985).
  • Chiou, C. T., Freed, V. H., Peters, L. J., & Kohnert, R. L.: Evaporation of solutes from water, Environ. Int., 3, 231–236, doi:10.1016/0160-4120(80)90123-3 (1980).
  • Duchowicz, P. R., Aranda, J. F., Bacelo, D. E., & Fioressi, S. E.: QSPR study of the Henry’s law constant for heterogeneous compounds, Chem. Eng. Res. Des., 154, 115–121, doi:10.1016/J.CHERD.2019.12.009 (2020).
  • Dunnivant, F. M. & Elzerman, A. W.: Aqueous solubility and Henry’s law constant data for PCB congeners for evaluation of quantitative structure-property relationships (QSPRs), Chemosphere, 17, 525–541, doi:10.1016/0045-6535(88)90028-8 (1988).
  • Dunnivant, F. M., Coates, J. T., & Elzerman, A. W.: Experimentally determined Henry’s law constants for 17 polychlorobiphenyl congeners, Environ. Sci. Technol., 22, 448–453, doi:10.1021/ES00169A013 (1988).
  • Dunnivant, F. M., Elzerman, A. W., Jurs, P. C., & Hasan, M. N.: Quantitative structure-property relationships for aqueous solubilities and Henry’s law constants of polychlorinated biphenyls, Environ. Sci. Technol., 26, 1567–1573, doi:10.1021/ES00032A012 (1992).
  • English, N. J. & Carroll, D. G.: Prediction of Henry’s law constants by a quantitative structure property relationship and neural networks, J. Chem. Inf. Comput. Sci., 41, 1150–1161, doi:10.1021/CI010361D (2001).
  • Fendinger, N. J. & Glotfelty, D. E.: Henry’s law constants for selected pesticides, PAHs and PCBs, Environ. Toxicol. Chem., 9, 731–735, doi:10.1002/ETC.5620090606 (1990).
  • Hilal, S. H., Ayyampalayam, S. N., & Carreira, L. A.: Air-liquid partition coefficient for a diverse set of organic compounds: Henry’s law constant in water and hexadecane, Environ. Sci. Technol., 42, 9231–9236, doi:10.1021/ES8005783 (2008).
  • Keshavarz, M. H., Rezaei, M., & Hosseini, S. H.: A simple approach for prediction of Henry’s law constant of pesticides, solvents, aromatic hydrocarbons, and persistent pollutants without using complex computer codes and descriptors, Process Saf. Environ. Prot., 162, 867–877, doi:10.1016/J.PSEP.2022.04.045 (2022).
  • Lee, F. F.: Comprehensive analysis, Henry’s law constant determination, and photocatalytic degradation of polychlorinated biphenyls (PCBs) and/or other persistent organic pollutants (POPs), Ph.D. thesis, University at Albany, State University of New York, USA, ISBN 978-0-549-42141-2 (2007).
  • Mackay, D., Shiu, W. Y., & Ma, K. C.: Illustrated Handbook of Physical-Chemical Properties and Environmental Fate for Organic Chemicals, vol. I of Monoaromatic Hydrocarbons, Chlorobenzenes, and PCBs, Lewis Publishers, Boca Raton, ISBN 0873715136 (1992a).
  • Mackay, D., Shiu, W. Y., Ma, K. C., & Lee, S. C.: Handbook of Physical-Chemical Properties and Environmental Fate for Organic Chemicals, vol. II of Halogenated Hydrocarbons, CRC/Taylor & Francis Group, doi:10.1201/9781420044393 (2006b).
  • Modarresi, H., Modarress, H., & Dearden, J. C.: QSPR model of Henry’s law constant for a diverse set of organic chemicals based on genetic algorithm-radial basis function network approach, Chemosphere, 66, 2067–2076, doi:10.1016/J.CHEMOSPHERE.2006.09.049 (2007).
  • Murphy, T. J., Pokojowczyk, J. C., & Mullin, M. D.: Vapor exchange of PCBs with Lake Michigan: The atmosphere as a sink for PCBs, Tech. Rep. EPA/600/D-83/097 (NTIS PB83250316), United States Environmental Protection Agency, URL https://ntrl.ntis.gov/NTRL/dashboard/searchResults.xhtml?searchQuery=PB83250316 (1983a).
  • Murphy, T. J., Pokojowczyk, J. C., & Mullin, M. D.: Vapor exchange of PCBs with Lake Michigan: The atmosphere as a sink for PCBs, in: Physical Behavior of PCBs in the Great Lakes, edited by Mackay, D., Patterson, S., Eisenreich, S. J., & Simmons, M. S., pp. 49–58, Ann Arbor Science, Ann Arbor, Mich. (1983b).
  • Murphy, T. J., Mullin, M. D., & Meyer, J. A.: Equilibration of polychlorinated biphenyls and toxaphene with air and water, Environ. Sci. Technol., 21, 155–162, doi:10.1021/ES00156A005 (1987).
  • Paasivirta, J. & Sinkkonen, S. I.: Environmentally relevant properties of all 209 polychlorinated biphenyl congeners for modeling their fate in different natural and climatic conditions, J. Chem. Eng. Data, 54, 1189–1213, doi:10.1021/JE800501H (2009).
  • Shiu, W. Y. & Mackay, D.: A critical review of aqueous solubilities, vapor pressures, Henry’s law constants, and octanol-water partition coefficients of the polychlorinated biphenyls, J. Phys. Chem. Ref. Data, 15, 911–929, doi:10.1063/1.555755 (1986).

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

12) Value at T = 293 K.
21) Several references are given in the list of Henry's law constants but not assigned to specific species.
24) Value at "room temperature".
68) Modarresi et al. (2007) use different descriptors for their calculations. They conclude that a genetic algorithm/radial basis function network (GA/RBFN) is the best QSPR model. Only these results are shown here.
186) Experimental value, extracted from HENRYWIN.
231) English and Carroll (2001) provide several calculations. Here, the preferred value with explicit inclusion of hydrogen bonding parameters from a neural network is shown.
232) Value from the training dataset.
300) Value from the test set for true external validation.
723) Calculated with the principal component regression (PCR) method; see Lee (2007) for details.
724) Calculated with the partial least-square regression (PLSR) method; see Lee (2007) for details.
725) The same data were also published in Dunnivant et al. (1988).
726) Value given here as quoted by Dunnivant et al. (1988).

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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