Thermochemical Evaluation of Hydroxyl and Peroxyl Radical Precursors in the Formation of Tropospheric Ozone Reactions

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The thermochemical properties of varieties of species needed to assess the most prominent pathways of tropospheric ozone transformation have been established. In the troposphere, ozone which is a secondary pollution produced by photochemical induced transformation, acts as an oxidizing agent to numerous atmospheric reactions leading to the formation of particulate matter. Based on the climate related problems resulting from the precursor of particulate matter, it is adequate to establish the feasible routes of ozone formation. In this study, the electronic structure methods which approximate the Schrödinger equation to compute Gibbs free energies and enthalpies of formation of the various chemical species participating in the reactions were used. These thermodynamic properties were determined using four computational model chemistry methods integrated in the Gaussian 03 (G03) chemistry package. Five known reaction pathways for the formation of NO2 (the O3 precursor specie), as well as the dominant ozone formation route from NO2 were examined and their energies determined. Of all the computational methods, the complete basis set (CBS-4M) method produced energies for all species of the five reaction routes. Out of the five routes, only the reactions involving radical species were favoured to completion over a temperature range of -100 and +100oC. The most relevant reaction route for the formation of NO2 and subsequently O3 is that involving the peroxyl acetyl nitrate (PAN) and hydroxyl radicals. Chemical equilibrium analyses of the reaction routes also indicated that reduction in temperature encourages NO2 formation while increase in temperature favours O3 production.

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74-83

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November 2010

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© 2010 Trans Tech Publications Ltd. All Rights Reserved

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[1] C. D Ahrens, Meteorology Today: An Introductory to Weather, Climate and the Environment, Sixth Edition, Modesto Junior College Pub., USA, (2000).

Google Scholar

[2] J. H. Seinfeld and S. N. Pandis, Atmospheric Chemistry and Physics: From Air Pollution to Climate Change, Wiley Interscience, New York, (1998).

Google Scholar

[3] P. Warneck, Chemistry of the Natural Atmosphere, Int. Geophysics Series, 41, Academic Press, New York, (1988).

Google Scholar

[4] P. Warneck, The relative importance of various pathways for the oxidation of sulphur dioxide and nitrogen dioxide in sunlit continental fair weather clouds, Physical Chemistry Chemical Physics 1 (1999), 5471 – 5483.

DOI: 10.1039/a906558j

Google Scholar

[5] J. J. Pienaar and G. Helas, The kinetics of chemical process affecting acidity in the atmosphere, South African Journal of Science 92 (1996) 128 – 132.

Google Scholar

[6] R. P. Wayne, Chemistry of Atmospheres, Third Edition, Oxford University Press, New York, (2000).

Google Scholar

[7] A. I. Igbafe and S. A. Omhenke: Evaluation of thermochemical properties of tropospheric ozone reactions, International Journal of Engineering Research in Africa 1 (2010) 39 – 45.

DOI: 10.4028/www.scientific.net/jera.1.39

Google Scholar

[8] M. L. Bell, A. McDermott, S. L. Zeger, J. M. Samet and F. Dominici, Ozone and short- term mortality in 95 US urban communities, 1987-2000 Journal American Medical Association, 292 (2004) 2372 – 2378.

DOI: 10.1001/jama.292.19.2372

Google Scholar

[9] http: /en. wikipedia. org/wiki/Tropospheric_ozone, Source Date: 30th April (2010).

Google Scholar

[10] J. M. Smith, H. C. Van Ness and M. M. Abbort, Introduction to Chemical Engineering Thermodynamics, Seventh Edition, McGraw Hill Co. Inc., New York, (2004).

Google Scholar

[11] A. I. Igbafe, L. L. Jewell and S. J. Piketh, Thermochemical analyses of sulphur compounds: Implications for atmospheric sulphur oxidation, Research Journal of Applied Science 3 (2008) 393 – 406.

Google Scholar

[12] C. Cramer, Essentials of Computational Chemistry, John Wiley and Sons, Chichester, (2002).

Google Scholar

[13] J. B. Foresman and Æ. Frisch, Exploring Chemistry with Electronic Structure Methods, Second Edition, Gaussian, Inc., Carnergie, Pittsburgh, USA, (1996).

Google Scholar

[14] G. H. Grant and W. G. Richards, Computational Chemistry, Oxford University Press, New York, (1995).

Google Scholar

[15] D. M. Hirst, A Computational Approach to Chemistry, Blackwell Scientific, London, (1990).

Google Scholar

[16] F. Jensen: Introduction to Computational Chemistry, John Wiley and Sons Ltd., Chichester, (1999).

Google Scholar

[17] M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria, M. A. Robb, Gaussian 03, Revision C. 02, Gaussian, Inc., Wallingford CT, (2004).

Google Scholar