Measurements and kinetic modeling of O2 vibrational kinetics in O2–Ar mixtures partially dissociated by a Ns pulse discharge
Journal Article
·
· Plasma Sources Science and Technology
- Ohio State University, Columbus, OH (United States); THE OHIO STATE UNIVERSITY
- CNR ISTP (Consiglio Nazionale delle Ricerche Istituto per la Scienza e Tecnologia dei Plasmi), Bari (Italy)
- Netherlands Organization for Applied Scientific Research (TNO), RD Geleen (The Netherlands)
- Ohio State University, Columbus, OH (United States)
Vibrational kinetics of O2 is studied during the O atom recombination in an O2–Ar mixture, partially dissociated by a burst of ns discharge pulses in a heated plasma flow reactor. The time-resolved temperature in the discharge afterglow is determined by Rayleigh scattering. Time-resolved O atom number density is measured by ps Two-Photon absorption Laser Induced Fluorescence, calibrated in xenon. Time-resolved vibrational level populations of molecular oxygen, O2(v= 8–20), are measured by ps Laser Induced Fluorescence (LIF), with the absolute calibration by NO LIF. Time-resolved ozone number density is monitored by broadband UV absorption. The results are compared with the predictions of a state-specific kinetic model. The experimental data indicate a rapid initial decay of O2(v) populations generated by electron impact in the discharge, due to the vibration-translation (V–T) relaxation by O atoms. This is followed by a slower population reduction, on the time scale much longer compared to that for V–T relaxation or vibration-vibration (V–V) exchange. Both O atoms and the O2(v) populations decay on the same time scale, indicating that chemical reactions initiated by the O atom recombination result in the generation of vibrationally excited O2 molecules. These trends are reproduced by the kinetic model, which shows that the reaction of O atoms with ozone is the dominant pathway of O2(v) generation at the present conditions. The predicted relative O2(v) populations are close to the experimental results, but absolute number densities differ from the experimental data. This is likely due to uncertainties in the absolute calibration of LIF measurements and in the spectroscopic model used in the data reduction. The present work demonstrates the capability for the absolute, time-resolved measurements of vibrationally excited O2 in recombining gas flows, to quantify the energy partition in the recombination reactions.
- Research Organization:
- The Ohio State University, Columbus, OH (United States)
- Sponsoring Organization:
- USDOE
- Grant/Contract Number:
- SC0020232
- OSTI ID:
- 2566731
- Journal Information:
- Plasma Sources Science and Technology, Journal Name: Plasma Sources Science and Technology Journal Issue: 1 Vol. 34; ISSN 0963-0252
- Publisher:
- IOP PublishingCopyright Statement
- Country of Publication:
- United States
- Language:
- English
Similar Records
O{sub 3} photolysis and reactions of O{sub 2}(b{sup 1}S{sub g}{sup +}) with O{sub 3}
Time-resolved CO 2 , CO, and N 2 vibrational population measurements in Ns pulse discharge plasmas
Photochemical kinetics of excited states of O sub 3 and O sub 2 : Laboratory studies and atmospheric implications
Conference
·
Sat Dec 30 23:00:00 EST 1995
·
OSTI ID:215134
Time-resolved CO 2 , CO, and N 2 vibrational population measurements in Ns pulse discharge plasmas
Journal Article
·
Thu Sep 01 00:00:00 EDT 2022
· Plasma Sources Science and Technology
·
OSTI ID:1982448
Photochemical kinetics of excited states of O sub 3 and O sub 2 : Laboratory studies and atmospheric implications
Thesis/Dissertation
·
Mon Dec 31 23:00:00 EST 1990
·
OSTI ID:5019675