Temperature, Kinetic Energy, and Internal Energy Dependences of the Rate Constant and Branching Fraction for the Reaction of O(+) (4S) with CO2

Abstract

Rate constants and branching fractions were measured for the reaction of O (+) (4S) with CO sub 2 as a function of average ion-neutral center-of-mass kinetic energy (<KE(+) cm>) at several temperatures. The reaction produces both O sub 2 and CO(+) sub 2 as product ions. The total rate constants were found to be nearly collisional at low <KE sub cm> and to decrease slightly at higher <KE sub cm>. No temperature dependence of the rate constants was found at any given <KE sub cm>, indicating that neither CO sub 2 rotational excitation nor CO sub 2 bending mode excitation has much effect on the overall reactivity. In contrast, the branching fraction for the endothermic charge transfer channel leading to CO(+) sub 2 was found to increase with increasing <KE sub cm> and also to increase with temperature at fixed <KE sub cm>. Analysis of the data indicates that the branching fraction depends on the total energy in the system (electronic, kinetic, rotational, and vibrational).

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Document Details

Document Type
Technical Report
Publication Date
Jan 01, 1992
Accession Number
ADA248041

Entities

People

  • Albert A Viggiano
  • Jane M. Van Doren
  • John F. Paulson
  • Robert A. Morris

Organizations

  • Phillips Laboratory

Tags

Communities of Interest

  • Energy and Power Technologies

DTIC Thesaurus Topics

  • Air Force
  • Charge Transfer
  • Collisions
  • Efficiency
  • Endothermic Reactions
  • Energy
  • Energy Levels
  • Errors
  • Excitation
  • Ground State
  • Ions
  • Kinetic Energy
  • Measurement
  • Metastable State
  • Molecules
  • United States
  • United States Government

Fields of Study

  • Physics

Readers

  • Mathematics or Statistics
  • Plasma Physics / Magnetohydrodynamics
  • Solar Physics

Technology Areas

  • Microelectronics