Abstract

The chemical species and source of gaseous chlorine in the marine atmosphere have been the subject of controversy for many years. Cauer [1951] suggested that the gaseous chlorine is Cl2 released from sea-salt particles in the atmosphere by the reaction of chloride ion with ozone. Eriksson [1960] pointed out that the rate of this reaction was too slow to account for the observed amounts of gaseous chlorine in the atmosphere. Robbins et al. [1959] suggested that atmospheric NO2 may be hydrolyzed in the vapor phase to form HNO3, the latter subsequently dissolving in the sea-salt particles, which are liquid droplets at relative humidities above 70%.

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