Electronically Excited Oxygen

Abstract

The specific aim of this research project was to explore the role of electronically excited oxygen in a variety of processes: combustion, spontaneous ignition, cool flames, and unusual structural forms of oxygen. The results show that electronically excited oxygen participates in cool flame combustion through a chain mechanism involving a manifold of electronically excited molecular species. At elevated temperatures of 600 K that are much lower than normal combustion temperatures, electronically excited oxygen reacts with hydrocarbons (for instance, through ene-reactions) at rates that are 10-20 times faster than quenching of the excited state. The significance of this result is that the oxygen excitation process can be exploited to enhance the fuel burning properties of internal combustion engines and that the spontaneous oxidation (combustion) of liquid fuels can be explained. A further result is that a valence bond analysis of assemblies of oxygen molecules provides insight into their electronic structure. The significance of this result is in explaining the nature of bonding between oxygen atoms in an extended molecular system.

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Document Details

Document Type
Technical Report
Publication Date
Mar 01, 2002
Accession Number
ADA414664

Entities

People

  • David M. Silver

Organizations

  • Johns Hopkins University

Tags

Communities of Interest

  • Human Systems

DTIC Thesaurus Topics

  • Abstracts
  • Chemical Reactions
  • Combustion
  • Cool Flames
  • Energy Transfer
  • Engines
  • Excitation
  • Flames
  • Hydrocarbons
  • Ignition
  • Ignition Lag
  • Internal Combustion Engines
  • Molecules
  • Oxidation
  • Oxygen
  • Physics Laboratories
  • Quenching

Fields of Study

  • Chemistry
  • Physics

Readers

  • Combustion science or combustion engineering.
  • Molecular Photonics/Laser Physics

Technology Areas

  • Microelectronics