Abstract

The absorption of UV, visible and near IR radiation by O3 produces transient, electronically excited O3. The absorption of thermal IR radiation ( = 9.065, 9.596 and 14.267 µm) produces vibrationally excited O3 molecules. Thermal absorption is likely the main factor in the self-decay of O3. Photoexcitation of ground state by IR and red light radiation produces singlet oxygens and . Chemical reactions in the stratosphere produce them as well. When reacting with ozone, singlet oxygen produces O (3P) and . By doing so, they tend to maintain the prevailing ozone concentration and are thereby important for the stability of the ozone layer. During the daytime, O(1D), and reach their maximum concentrations at altitudes of 45 to 48 km. This manifests fast ozone turnover which generates the maximum stratospheric temperature at those particular altitudes. During the night-time, the self-decay of ozone and absorption of light from the nightglows, moon and stars by O3 and O2 generates so much heat that the stratospheric temperature decreases by only a couple of degrees. Being a heavier gas than O2 and N2, ozone lacks buoyancy in the atmosphere, and it starts to descend immediately when formed. Chapman calculated that ozone in the stratosphere would descend 20 m per day. At the North and South Poles, during the four to six months of darkness in the winter, ozone descends by 2.4 to 3.6 km. This descent is likely the main reason for the stratospheric ozone depletion above the poles during winter.

Highlights

  • At the beginning of the 20th century, it was found that the emissions of stars contribute to only a part of the total night-sky emission intensity in the visible range [1]

  • Ultraviolet radiation (UV) nightglow was explained to be due to the relaxation of even more highly excited oxygen molecules [4]

  • The aim of this meta-study is to provide a basic understanding of the dynamics related to the formation of the stratospheric ozone layer

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Summary

Introduction

At the beginning of the 20th century, it was found that the emissions of stars contribute to only a part of the total night-sky emission intensity in the visible range [1]. By the late 1920s, it became obvious that Earth’s atmosphere exists at high altitudes as well, and important chemical processes occur there, such as the green line nightglow of oxygen atoms (OI 5577Å) [2]. It became evident that excited O and O2 are present in the atmosphere, because features of the day and night airglows derive optical transitions from these species. 1O2 (present notation O2 (a1∆g)), was first observed in 1924 [3] and it was defined as a more reactive form of oxygen molecule. UV nightglow was explained to be due to the relaxation of even more highly excited oxygen molecules [4]. The study of excited oxygen molecules has since become an important goal in physical chemistry [6, 7]

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