Rate constants for the reactions of O+ with N2 and O2 as a function of temperature (300–1800 K)
Author(s) -
Peter M. Hierl,
I. Dotan,
John V. Seeley,
Jane M. Van Doren,
Robert A. Morris,
Albert A. Viggiano
Publication year - 1997
Publication title -
the journal of chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.071
H-Index - 357
eISSN - 1089-7690
pISSN - 0021-9606
DOI - 10.1063/1.473450
Subject(s) - reaction rate constant , atmospheric temperature range , constant (computer programming) , chemistry , range (aeronautics) , thermodynamics , analytical chemistry (journal) , materials science , physics , kinetics , organic chemistry , quantum mechanics , computer science , composite material , programming language
We have measured the rate constants for the reactions of Ar+ with CO2 and SO2 from 300 to 1500 K in a high temperature flowing afterglow. For the reaction with CO2, we have found that all modes of energy, i.e., translation, rotation, and vibration, affect the rate constant to the same degree up to a total energy of 0.4 eV. Above 0.4 eV total energy, internal energy decreases the rate constants more effectively than does translational energy. For the reaction of Ar+ with SO2, the rate constants go through a minimum at about 900 K. By comparing our results to drift tube data, we derive rate constants for reaction from the υ=0 and υ>0 vibrational levels. At low energy, the vibrationally excited SO2 molecules react with Ar+ approximately twice as fast as the ground state molecules. Both vibrational modes have similar temperature dependences.
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