1981
DOI: 10.1016/0009-2614(81)85111-1
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Spectroscopy and reaction kinetics of HS radicals

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Cited by 46 publications
(16 citation statements)
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“…An even higher upper limit by Black [148], based on the lack of SH decay, may have been complicated by SH regeneration. Much less sensitive upper limits have been calculated by Tiee et al [1308], Nielsen [974], and Cupitt and Glass [336]. Stachnik and Molina [1229] also report a somewhat higher upper limit (< 1.0 × 10 -18 ) for the rate constant for the sum of the two SH + O 2 reaction channels (producing OH + SO and H + SO 2 ).…”
Section: -104mentioning
confidence: 89%
“…An even higher upper limit by Black [148], based on the lack of SH decay, may have been complicated by SH regeneration. Much less sensitive upper limits have been calculated by Tiee et al [1308], Nielsen [974], and Cupitt and Glass [336]. Stachnik and Molina [1229] also report a somewhat higher upper limit (< 1.0 × 10 -18 ) for the rate constant for the sum of the two SH + O 2 reaction channels (producing OH + SO and H + SO 2 ).…”
Section: -104mentioning
confidence: 89%
“…For high temperature all curves approach each other with a tendency to a plateau. Figure 3 also displays the experimental rate constant values reported in literature for title reaction [30][31][32][33][34]. For completeness we report vibrationally averaged reactive thermal rate coefficients, obtained as:…”
Section: Reactive Thermal Rate Coefficientsmentioning
confidence: 99%
“…On the other hand, under typical experimental conditions [30][31][32][33][34], the use of O 2 as vibrational quencher of excited HS radical introduces vibrational-vibrational energy transferences between both molecules producing vibrational excited oxygen and hence the possibility of allowing reaction (1) to occur. This argument also supports the concordance of our calculations with experimental results.…”
Section: Comparison Between Hs Excited and O 2 Excited Casesmentioning
confidence: 99%
“…Thus the fluorescence quantum yield of this state is not only small, but internal quantum state dependent. Consequently, there have been relatively few quantitative measurements of SH(X) or SD(X) radical concentrations using LIF on the A-X transition as the radical probe [5][6][7][8], and even fewer attempts at determining internal quantum state population distributions for these species [9].…”
Section: Introductionmentioning
confidence: 99%