Abstract

Measurements of gaseous hydrogen peroxide (H 2O 2) and organoperoxides (ROOH) in clear air and cloudy air were made from a Twin Otter aircraft over central Ontario, Canada, during March and April of 1990 as part of the Eulerian Model Evaluation Field Study (EMEFS). In clear boundary layer air (altitude 500 m to 1750 m), unperturbed by the presence of cloud, the ratio [H 2O 2]/[ROOH] depends on NO 2 mixing ratios, while in the presence of cloud perturbing H 2O 2, the ratio [H 2O 2]/[ROOH] was significantly decreased compared with those in clear air mainly due to the high solubility of H 2O 2. In order to examine the effects of cloud processing on air that was detrained from cloud, we selected measurements made in cloud-free air located between two passes made in air with high liquid water content. Gaseous H 2O 2 concentrations in these detrained air masses were often higher than those in the cloudy air, and sometimes higher than those in the clear air for high NO 2 conditions (> 500 ppt) but lower than clear-sky levels for low NO 2 (< 500 ppt) conditions. This result is in general agreement with that from photochemical modeling, namely, for chemical regimes typical of high-NO 2 (more polluted) conditions, where aqueous-phase reactions of dissolved HO 2 lead to net production of H 2O 2(aq) that can subsequently be detrained from the cloud.

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