COMPUTED ACTIVATION ENERGIES FOR REACTIONS OF O2, N2, NO, N2O, NO2, CO, AND CO2

Abstract

A method is described for calculating the activation energies of bimolecular reactions of such multivalent gaseous compounds as O2, N2, NO, N2O, NO2, CO, and CO2. It is also applicable to the monatomic reactants O, N, and H and to the OH radical. The method uses relationships between dissociation energy, bond length, vibrational wavenumber, and bond order. It avoids the use of adjustable parameters. The agreement between calculated and experimental activation energies is very good when spin conservation in the transition state is considered in the computation procedure. A convenient rule has also been formulated that predicts the activation energy will be negligible in bimolecular reactions between radicals when the transition-state formula corresponds to that of a compound having stable bonds. No exceptions to this rule have been found. The method is applicable to computing rates needed for nonequilibrium calculations of propellant performance and of reentry behavior.

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Document Details

Document Type
Technical Report
Publication Date
Dec 01, 1967
Accession Number
AD0665473

Entities

People

  • Stanley W. Mayer

Organizations

  • The Aerospace Corporation

Tags

Communities of Interest

  • Energy and Power Technologies

DTIC Thesaurus Topics

  • Abstracts
  • Agreements
  • Air Force
  • Chemical Reaction Properties
  • Chemical Reactions
  • Combustion
  • Computational Science
  • Computations
  • Dissociation
  • Energy
  • Exothermic Reactions
  • Explosive Testing
  • Ground State
  • Heat Of Activation
  • Potential Energy
  • Propellants
  • Transitions

Readers

  • Combustion science or combustion engineering.
  • Electromagnetic Wave Scattering and Antenna Radiation Engineering
  • Quantum Chemistry