Rate constants have ba:en determined for the reaction OH + NO\* (+ N2) + HNOz (+ N2), using time-resolved resonance absorption to follow the removal of OH radicals produced by flash photolysis of HN03. 'Ike measurements cover the ranges: 220 C T 4 3.58 K and 3.2 X IO" 4 [Nz] G 4.0 X IO" molecule cme
Absolute Rate constants for O + No + N2 → NO2 + N2 from 217–500 K
✍ Scribed by D.A. Whytock; J.V. Michael; W.A. Payne
- Publisher
- Elsevier Science
- Year
- 1976
- Tongue
- English
- Weight
- 468 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0009-2614
No coin nor oath required. For personal study only.
✦ Synopsis
Flash photolysis of NO coupled with time resolved detection of 0 via resonance fluorescence has been used to obtain rate constants for the reaction 0 + NO f N2 --, NO2 + Na ar temperatures from 217 to 500 K. The measured rate constxrts obey the Arrhenius equation k = (is.5 + 2.0) X 1O-33 -2 exp[(ll60 i 70)/l-987 T] cm6 molecule s-' _ An equally accept-abIe equatron describing the temperature dependence of k is k = 3.80 X 10-27/T1-81-cm6 molecule-2 s-r . These results are discussed and compared with previous work. I. htroduction * We calculate, from the intercepts of fig. 1 in ref. [ 191 and the pressures listed, that k(296 K) = 5.60 X 10m3* cm6 moIecuId2 s-' and k(241 K) = 9.96 cm6 molecule-2s-x, which yields E = 1.48 kcal mole-' . Volume 42, number 3 CHEMICAL PHYSICS LETTERS 1.
📜 SIMILAR VOLUMES
## Abstract The reaction NO + O~3~ → NO~2~ + O~2~ has been studied in a 220‐m^3^ spherical stainless steel reactor under stopped‐flow conditions below 0.1 mtorr total pressure. Under the conditions used, the mixing time of the reactants was negligible compared with the chemical reaction time. The p
Using a pulse radiolysis UV absorption technique and subsequent simulations of experimental NO1 and FNO absorption transients, rate constants for reaction between CF90 and CFsO2 radicals with NO were determined, CFp02+NO+CF,O+N02 (3 ), CF,OtNO~CF,OtFNO(5).k~wasderivedtobe(1.68~0.26)X10~~'cm3molecuIe
The hinetics of the reactions of the (CI13)2K rrtduxl wthX0.N02,and O2 rrere studied usins FTIR spectroscopy. The tutwe of the products and the ratio ofr.~tc constants for these reactions acre dctermmed\_ The results were used to evalu.rte the potenti.n for nitros.unine .md nitramine formation in X0