{"title":"Effect of Particles of the Junge Layer on the Length of Ozone Depletion Chains in the Atmosphere","authors":"I. K. Larin, G. B. Pronchev, A. N. Yermakov","doi":"10.1134/S1990793124700258","DOIUrl":null,"url":null,"abstract":"<p>This paper presents the results of calculations of the length of ozone destruction chains in the lower stratosphere in HO<sub><i>x</i></sub>-, NO<sub><i>x</i></sub>-, and ClO<sub><i>x</i></sub>-catalytic cycles, taking into account heterogeneous chemical reactions (HCRs) involving particles of the Junge layer. Taking into account these reactions leads to a change in the type of high-altitude profiles of the length of the chains in these cycles, calculated in the approximation of the absence of HCRs. At the lower boundary of the Junge layer, a degeneration of the chain destruction of ozone in the NO<sub><i>x</i></sub> cycle is observed, caused by a sharp decline in the concentrations of components of this family due to the capture of N<sub>2</sub>O<sub>5</sub> gas molecules. At the same time, there is an increase in the chain length in the HO<sub><i>x</i></sub> cycle by more than an order of magnitude due to the decrease in the concentrations of OH and HO<sub>2</sub> radicals and, as a result, a decrease in the rate of chain breakage with their participation. At high altitudes, the length of the ozone destruction chains, taking into account HCRs, on the contrary, are higher; this is due to the acceleration of the destruction of O<sub>3</sub> by chain carriers in HO<sub><i>x</i></sub>- and ClO<sub><i>x</i></sub>-cycles. The increase in their concentrations is due to the reduced content of NO and NO<sub>2</sub> in the air. The considered effect of HCR practically disappears at the upper boundary of the Young layer due to the evaporation of particles.</p>","PeriodicalId":768,"journal":{"name":"Russian Journal of Physical Chemistry B","volume":"18 3","pages":"675 - 681"},"PeriodicalIF":1.4000,"publicationDate":"2024-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Russian Journal of Physical Chemistry B","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1134/S1990793124700258","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PHYSICS, ATOMIC, MOLECULAR & CHEMICAL","Score":null,"Total":0}
引用次数: 0
Abstract
This paper presents the results of calculations of the length of ozone destruction chains in the lower stratosphere in HOx-, NOx-, and ClOx-catalytic cycles, taking into account heterogeneous chemical reactions (HCRs) involving particles of the Junge layer. Taking into account these reactions leads to a change in the type of high-altitude profiles of the length of the chains in these cycles, calculated in the approximation of the absence of HCRs. At the lower boundary of the Junge layer, a degeneration of the chain destruction of ozone in the NOx cycle is observed, caused by a sharp decline in the concentrations of components of this family due to the capture of N2O5 gas molecules. At the same time, there is an increase in the chain length in the HOx cycle by more than an order of magnitude due to the decrease in the concentrations of OH and HO2 radicals and, as a result, a decrease in the rate of chain breakage with their participation. At high altitudes, the length of the ozone destruction chains, taking into account HCRs, on the contrary, are higher; this is due to the acceleration of the destruction of O3 by chain carriers in HOx- and ClOx-cycles. The increase in their concentrations is due to the reduced content of NO and NO2 in the air. The considered effect of HCR practically disappears at the upper boundary of the Young layer due to the evaporation of particles.
期刊介绍:
Russian Journal of Physical Chemistry B: Focus on Physics is a journal that publishes studies in the following areas: elementary physical and chemical processes; structure of chemical compounds, reactivity, effect of external field and environment on chemical transformations; molecular dynamics and molecular organization; dynamics and kinetics of photoand radiation-induced processes; mechanism of chemical reactions in gas and condensed phases and at interfaces; chain and thermal processes of ignition, combustion and detonation in gases, two-phase and condensed systems; shock waves; new physical methods of examining chemical reactions; and biological processes in chemical physics.