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Heterogeneous interactions of BrO and ClO: Evidence for BrO surface recombination and reaction with HSO 3 − /SO 3 2−
Author(s) -
Abbatt Jonathan P. D.
Publication year - 1996
Publication title -
geophysical research letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.007
H-Index - 273
eISSN - 1944-8007
pISSN - 0094-8276
DOI - 10.1029/96gl01430
Subject(s) - radical , chemistry , sulfuric acid , atmosphere (unit) , analytical chemistry (journal) , phase (matter) , aqueous solution , inorganic chemistry , thermodynamics , organic chemistry , physics
The uptake coefficients (γ) for loss of BrO and ClO radicals on surfaces characteristic of participate material in the atmosphere have been measured using a coated‐wall flow tube coupled to a resonance fluorescence detector. Neither radical is lost efficiently at 213 K on sulfuric acid (60 to 70 wt%), pyrex or ice surfaces, with BrO uptake coefficients ranging from 5 × 10 −4 to 1 × 10 −3 on these surfaces and with ClO uptake coefficients smaller than 1×10 −4 . Based on the observation by mass spectrometry of Br 2 formation coincident with BrO loss on ice surfaces, it is believed that radical self‐reaction is occurring on the surface. Finally, for BrO it was observed that the uptake coefficient on 23 wt% aqueous solutions of NaCl at 253 K was small (< 3 × 10 −3 ) but that it could be significantly enhanced when sulfur(IV) species were added to the solution, either by exposure to gas phase SO 2 or by the addition of Na 2 SO 3 . Aside from the BrO/S(IV) reactions which may promote condensed‐phase free‐radical chemistry, these findings imply that heterogeneous interactions of BrO and ClO in the atmosphere will be insignificant with respect to gas‐phase processes.

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