Abstract

Overwhelming evidence now exists that perchlorate is produced through natural processes and can be ubiquitously found at environmentally relevant concentrations in arid and semi-arid locations. A number of potential production mechanisms have been hypothesized and ClO 4 − production by ozone oxidation of surface bound Cl − was demonstrated. However, no information concerning the impact of concentration, final reaction products distribution, impact of reaction phase, or oxidation of important oxychlorine intermediates has been reported. Using IC-MS–MS analysis and replicate oxidation experiments, we show that exposing aqueous solutions or Cl − coated sand or glass surfaces to O 3 (0.96%) generated ClO 4 − with molar yields of 0.007 and 0.01% for aqueous Cl − solutions and 0.025 and 0.42% for Cl − coated sand and glass, respectively. Aqueous solutions of Cl − produced less ClO 4 − than Cl − coated sand or glass as well as a higher ratio of ClO 3 − to ClO 4 −. Reduction of the initial Cl − mass resulted in substantially higher molar yields of ClO 4 − and ClO 3 −. In addition, alkaline absorbers that captured gaseous products contained substantial quantities of Cl −, ClO 3 −, and ClO 4 −. Solutions of possible oxychlorine intermediates (OCl − and ClO 3 −) exposed to O 3 produced only scant amounts of ClO 4 − while a ClO 2 − solution exposed to O 3 produced substantial molar yields of ClO 4 − (4% molar yield). Scanning electron microscopy coupled with energy energy-dispersive X-ray analysis demonstrated a significant loss of Cl − and an increase in oxygen on the Cl − coated silica sand exposed to O 3. While the experimental conditions are not reflective of natural conditions this work clearly demonstrates the relative potential of Cl − precursors in perchlorate production and the likely importance of dry aerosol oxidation over solution phase reactions. It also suggests that ClO 2 − may be a key intermediate while ClO 3 − and OCl − are unlikely to play a significant role.

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