NON-EQUILIBRIUM EFFECTS IN THE KINETICS OF GAS PHASE REACTIONS.

Abstract

A theoretical rate equation derived for exchange reactions in the gas phase from an assumed Boltzmann equation yields statistical rate expressions for theoretical rate coefficients which in general are functions of concentration with a ratio not equal to the equilibrium constant, K. However, the theoretical rate equation may be rearranged to yield rate coefficients defined to obey the relation K sub F.C/K sub R.C. = K. The rate coefficients K sub F.C. and K sub R.C. are also functions of concentration except in three linear cases: (1) a reaction with one of the components present in large excess; (2) a chemical reaction proceeding unaffected by inelastic processes; (3) an isomerization reaction proceeding in a large excess of inert gas. Thus for these three cases the usual phenomenological rate equation applies. In cases 1 and 3 the rate constants are determined not by chemical reaction cross sections but also by inelastic cross sections for at least some and possibly all reactants and products. (Author)

Document Details

Document Type
Technical Report
Publication Date
Jul 01, 1965
Accession Number
AD0468565

Entities

People

  • John Ross
  • Neil S. Snider

Organizations

  • University of Virginia

Tags

DTIC Thesaurus Topics

  • Arrhenius Equation
  • Boltzmann Equation
  • Chemical Reaction Properties
  • Chemical Reactions
  • Coefficients
  • Cooperation
  • Equations
  • Exchange Reactions
  • Isomerization
  • Kinetics
  • Mathematics

Readers

  • Calculus or Mathematical Analysis
  • Materials Science and Engineering.
  • Quantum Chemistry