H2F2 chain reaction rate investigation

Experimental performance of chemical lasers pumped by the H2 + F2 chain reaction has consistently fallen below expectations, although the 'hot' H + F2 yields HF(v) + F pumping reaction produces greater vibrational excitation than the 'cold' F + H2 yields HF(v) + H reaction used i...

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Veröffentlicht in:Journal of quantitative spectroscopy & radiative transfer 1977-02, Vol.17 (2), p.97-116
Hauptverfasser: Cummings, John C., Broadwell, J.Eugene, Shackleford, William L., Witte, Arvel B., Trost, Jack E., Emanuel, George
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container_end_page 116
container_issue 2
container_start_page 97
container_title Journal of quantitative spectroscopy & radiative transfer
container_volume 17
creator Cummings, John C.
Broadwell, J.Eugene
Shackleford, William L.
Witte, Arvel B.
Trost, Jack E.
Emanuel, George
description Experimental performance of chemical lasers pumped by the H2 + F2 chain reaction has consistently fallen below expectations, although the 'hot' H + F2 yields HF(v) + F pumping reaction produces greater vibrational excitation than the 'cold' F + H2 yields HF(v) + H reaction used in most HF CW chemical lasers. The reasons for this discrepancy are examined by measuring spatially-resolved HF(v) number density and the temperature profiles in a laminar parallel-flow hydrogen-fluorine mixing layer and comparing the results with theoretical computations. By dissociating either the hydrogen or fluorine molecules with arc heaters, kinetics of the hot and cold reaction systems are separately investigated. From a comparison of the experimental vibrational populations and the theoretical predictions, it is concluded that: (1) previously-used pumping and deactivation rates associated with the cold reaction are approximately correct; (2) the deactivation of high vibrational levels populated by the hot reaction is much faster than previously stated; and (3) the inclusion of multiquantum HF(v) V-T (or V-R) deactivation reactions, which sharply decreases the number density of the upper vibrational levels, greatly improves the agreement between theory and experiment.
doi_str_mv 10.1016/0022-4073(77)90145-5
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title H2F2 chain reaction rate investigation
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