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Heterogeneous processes: Laboratory, field, and modeling studiesThe efficiencies of chemical families such as ClO(x) and NO(x) for altering the total abundance and distribution of stratospheric ozone are controlled by a partitioning between reactive (active) and nonreactive (reservoir) compounds within each family. Gas phase thermodynamics, photochemistry, and kinetics would dictate, for example, that only about 1 percent of the chlorine resident in the lower stratosphere would be in the form of active Cl or ClO, the remainder existing in the reservoir compounds HCl and ClONO2. The consistency of this picture was recently challenged by the recognition that important chemical transformations take place on polar regions: the Airborne Antarctic Ozone Experiment (AAOE) and the Airborne Arctic Stratospheric Expedition (AASA). Following the discovery of the Antarctic ozone hole, Solomon et al. suggested that the heterogeneous chemical reaction: ClONO2(g)+HCl(s) yields Cl2(g)+HNO3(s) could play a key role in converting chlorine from inactive forms into a species (Cl2) that would rapidly dissociate in sunlight to liberate atomic chlorine and initiate ozone depletion. The symbols (s) and (g) denote solid phase, or adsorbed onto a solid surface, and gas phase, respectively, and represent the approach by which such a reaction is modeled rather than the microscopic details of the reaction. The reaction was expected to be most important at altitudes where PSC's were most prevalent (10 to 25 km), thereby extending the altitude range over which chlorine compounds can efficiently destroy ozone from the 35 to 45 km region (where concentrations of active chlorine are usually highest) to lower altitudes where the ozone concentration is at its peak. This chapter will briefly review the current state of knowledge of heterogeneous processes in the stratosphere, emphasizing those results obtained since the World Meteorological Organization (WMO) conference. Sections are included on laboratory investigations of heterogeneous reactions, the characteristics and climatology of PSC's, stratospheric sulfate aerosols, and evidence of heterogeneous chemical processing.
Document ID
19930001902
Acquisition Source
Legacy CDMS
Document Type
Other
Authors
Poole, Lamont R.
(NASA Langley Research Center Hampton, VA, United States)
Kurylo, Michael J.
(NASA Headquarters Washington, DC United States)
Jones, Rod L.
(Cambridge Univ. United Kingdom)
Wahner, Andreas
(Kernforschungsanlage Juelich, Germany)
Calvert, Jack G.
(National Center for Atmospheric Research Boulder, CO., United States)
Leu, M.-T.
(Jet Propulsion Lab. California Inst. of Tech., Pasadena., United States)
Fried, A.
(National Center for Atmospheric Research Boulder, CO., United States)
Molina, Mario J.
(Massachusetts Inst. of Tech. Cambridge., United States)
Hampson, Robert F.
(National Inst. of Standards and Technology Gaithersburg, MD., United States)
Pitts, M. C.
(Hughes STX, Inc. Greenbelt, MD., United States)
Date Acquired
September 6, 2013
Publication Date
January 1, 1991
Publication Information
Publication: NASA, Washington, Scientific Assessment of Ozone Depletion: 1991
Subject Category
Environment Pollution
Accession Number
93N11090
Distribution Limits
Public
Copyright
Work of the US Gov. Public Use Permitted.
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