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Solubility of HOBr in Acidic Solution and Implications for Liberation of Halogens Via Aerosol ProcessingHalogen species are known to catalytically destroy ozone in several regions of the atmosphere. In addition to direct catalytic losses, bromine compounds can indirectly enhance ozone loss through coupling to other radical families. Hypobromous acid (HOBr) is a key species in the linkage of BrOx to ClOx and HOx. The aqueous- phase coupling reaction HOBr + HCI (right arrow) BrCl + H2O may provide a pathway for chlorine activation on sulfate aerosols at temperatures warmer than those required for polar stratospheric cloud formation. We have measured t h e solubility of HOBr in 45 - 70 wt% sulfuric acid solutions. Over the temperature range 201 - 252 K, HOBr is quite soluble in sulfuric acid, H* = 10(exp 4) - 10(exp 7) mol dm(exp -3) atm(exp -1). The expected inverse dependence of H* on temperature was observed, but only a weak dependence on acidity was found. The solubility of HOBr is comparable to that of HBr, indicating that equilibrium concentrations of HOBr could equal or exceed those of HBr in upper tropospheric and lower stratospheric aerosols. Despite the high solubility of HOBr, aerosol volumes are not large enough to sequester a significant fraction of inorganic bromine from the gas phase. Our measurements of HOBr uptake in aqueous sulfuric acid in the presence of other brominated gases show the evolution of gaseous products including Br2O and Br2.
Document ID
20040087038
Acquisition Source
Ames Research Center
Document Type
Conference Paper
Authors
Iraci, Laura T.
(NASA Ames Research Center Moffett Field, CA, United States)
Michelsen, R. R.
(NASA Ames Research Center Moffett Field, CA, United States)
Rammer, T. A.
(NASA Ames Research Center Moffett Field, CA, United States)
Ashbourn, S. F. M.
(NASA Ames Research Center Moffett Field, CA, United States)
Date Acquired
August 21, 2013
Publication Date
January 1, 2004
Subject Category
Inorganic, Organic And Physical Chemistry
Meeting Information
Meeting: 8th International Global Atmospheric Chemistry Conference
Country: Unknown
Start Date: September 4, 2004
End Date: September 9, 2004
Distribution Limits
Public
Copyright
Work of the US Gov. Public Use Permitted.

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