Wc. Keene et al., MEASUREMENT TECHNIQUE FOR INORGANIC CHLORINE GASES IN THE MARINE BOUNDARY-LAYER, Environmental science & technology, 27(5), 1993, pp. 866-874
A technique was developed to measure inorganic Cl gases in the marine
boundary layer. The inlet inertially removed coarse aerosol (>1-mum di
ameter), and an in-line filter removed fine aerosol. A trace gas conce
ntrator positioned downstream incorporated an acidic mist chamber whic
h sampled HCI (including HCl, NOCl, ClNO2, and ClNO3), followed by an
alkaline mist chamber which sampled Cl2 (including Cl2 and a portion
of HOCl). Mist solutions were analyzed by ion chromatography. Estimat
ed detection limits for HCl and Cl2* were 39 and 13 pptv, respectivel
y. Standard additions of calibration gases from permeation sources to
ambient air were recovered quantitatively within source uncertainties.
The sampler appears to discriminate against organic Cl gases. HCl in
coastal air near Miami varied from <39 to 268 pptv with lower mixing
ratios at night. Ambient Cl2 Varied from <13 to 127 pptv with highest
mixing ratios before dawn.