Vibrationally Excited Ozone Relaxation by CO


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Abstract

Time profiles of ozone concentration after pulsed UV laser photolysis in the O2- O3-Ar-CO mixture, measured using time-resolved absorption spectroscopy, are presented. The experimental results show the dominance of the stabilization channel over the reactive one for the interaction between the vibrationally excited ozone molecule O3(υ) and carbon monoxide CO. The rate constant of the process O3(υ)+CO→O3 + CO, obtained by processing experimental data by the kinetic modeling method is (1.5 ± 0.2) · 10−13 cm3/s.

About the authors

A. P. Torbin

Samara Branch of the Lebedev Physical Institute; Samara National Research University

Author for correspondence.
Email: torbinalex@gmail.com
Russian Federation, ul. Novo-Sadovaya 221, Samara, 443011; Moskovskoye shosse 34, Samara, 443086

A. A. Pershin

Samara Branch of the Lebedev Physical Institute; Samara National Research University

Email: torbinalex@gmail.com
Russian Federation, ul. Novo-Sadovaya 221, Samara, 443011; Moskovskoye shosse 34, Samara, 443086

A. M. Mebel

Samara National Research University; Florida International University.

Email: torbinalex@gmail.com
Russian Federation, Moskovskoye shosse 34, Samara, 443086; 11200 SW 8th St, Miami, FL, 33199

V. N. Azyazov

Samara Branch of the Lebedev Physical Institute; Samara National Research University

Email: torbinalex@gmail.com
Russian Federation, ul. Novo-Sadovaya 221, Samara, 443011; Moskovskoye shosse 34, Samara, 443086

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