c-111 UK-.\L l'li\ SKS I I ITI KS I5 Octobtr 1979 Recently, Hack et al\_ [9] confirmed that reaction (I) is f&st and therefore, reaction (Ie), which is cndothermic, can be negIected at room temperature.
Kinetics of reactions of NH with NO and NO2
โ Scribed by J.A. Harrison; A.R. Whyte; L.F. Phillips
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- English
- Weight
- 501 KB
- Volume
- 129
- Category
- Article
- ISSN
- 0009-2614
No coin nor oath required. For personal study only.
โฆ Synopsis
Ground-state NH radicals were generated by 248 mn KrF laser photolysis of NsH4 and their concentration monitored by laser-induced fluorescence at 336 mn, at total pressures near 1 Torr and temperatures between 269 and 377 K. He, Ar, Ns and NsO were used as carrier gases. Rate constants obtained at 300 K are (1.61 f 0.14) X lo-** for NH + NO2 and (5.78 * 0.64) X lo-"
for NH + NO (units cm3 molecule-1 s-l). For NH + NO the rate constant is independent of temperature over the range studied; for NH + NO2 there is a smalI negative temperature dependence. Within experimental error, results at 300 K are independent of the choice of carrier gas. The results are discussed in terms of a mechanism involving an intermediate MN0 or HNNO2 complex.
๐ SIMILAR VOLUMES
The rate coefficients of the reactions of NCO radicals with NO and NOz: (1) NCO + NOproducts (293-836 K) and : (2) NCO + NO2products (294-774 K) were measured by means of laser photolysis and laser induced fluorescence technique in the indicated temperature ranges. NCO radicals were produced from th
The reactions of GeH 3 with 02, NO, and NO 2 were studied via time-resolved infrared diode laser absorption spectroscopy over the temperature range 232-468 K for 02 and NO, and 252-407 for NO 2. The measured rate constants (in cm 3 molecule -1 s -1) were kGert3+o2 = (10 -13"18+ยฐ"18) exp[(874 + 146)/
The products of reaction cf NO Gth breakdown products of NH3 in nn H2/N2/02 flame at 1500 K were investigated by mass spectromctric analysis of the hot gases. It is concluded that the nxjor process invobing NO 2nd NH is NO + NH -N2 + 0 + H and thnt not more than 10% of reactive collisions Ixtwcen th
The reactions Br + NO2 + M -+ BrNOZ + M (1) and I + NOz have been studied at low pressure (0.6-2.2 torr) at room temperature and with helium as the third body by the discharge-flow technique with EPR and mass spectrometric analysis of t h e species. The following third order rate constants were fou