Vib-Rotational Energy Transfer and Relaxation Patterns in Non-Equilibrium Chemical Systems.

Abstract

The characteristics of vibrational relaxation of diatomic molecules are analyzed using a combined kinetic-thermodynamic approach based on the master equation formalism on the one hand and the maximal entropy procedure on the other. The complex and detailed solutions for the vibrational relaxation of diatomic molecules (HF as a specific system) can be greatly compacted and systemized. The physical-mathematical significance of detailed balancing and quasi-equilibrium distributions in non-isothermal systems are discussed. It is shown that the increased efficiency of rotationally relaxed chemical lasers is due to the removal of thermodynamic constraints from the molecular distribution function. The different roles of reagent internal excitation on the rates of endoergic reactions at a given temperature and a given total energy are discussed and demonstrated. (Author)

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Document Details

Document Type
Technical Report
Publication Date
Mar 01, 1980
Accession Number
ADA084132

Entities

People

  • A. Ben-shaul

Organizations

  • Hebrew University of Jerusalem

Tags

Communities of Interest

  • Energy and Power Technologies

DTIC Thesaurus Topics

  • Air Force
  • Chemical Lasers
  • Chemical Reactions
  • Chemistry
  • Demography
  • Diatomic Molecules
  • Energy Levels
  • Energy Transfer
  • Molecular Dynamics
  • Molecular Physics
  • Molecules
  • New York
  • Physical Chemistry
  • Polyatomic Molecules
  • Spectra
  • Spectroscopy
  • Vibrational Relaxation

Readers

  • Molecular Photonics/Laser Physics
  • Theoretical Analysis.

Technology Areas

  • Directed Energy
  • Directed Energy - Lasers