## Abstract The full vibrational Hamiltonian for the inversion of NH~3~ and H~2~NO has been diagonalized in a basis set that is the direct product of functions of the inversion coordinate and of harmonic vibrational functions independent of this inversion coordinate. The kinetic part of the Hamilto
Vibrational dependence of the NH3+ (v2)+NO and NO+(v)+NH3 charge transfer cross sections
โ Scribed by Takayuki Ebata; Richard N. Zare
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- English
- Weight
- 546 KB
- Volume
- 130
- Category
- Article
- ISSN
- 0009-2614
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โฆ Synopsis
A tandem quadrupole mass spectrometer is used to study the charge transfer reactions NH: + NO and NO+ + NH, over a collision energy range 1.5-l 3 eV. The vibrational state of the reagent ions is selected by resonance-enhanced multiphoton ionization. For the 0.9 eV exothermic process NHf +NO+NH,+NO+ excitation of the u2 umbrella bending mode ( vz=O-12) causes no marked change in the charge transfer cross section, while in the reverse process NO+ +NH,+NO+NH: excitation of the NO+ vibration (v= O-6) strongly enhanced the charge transfer cross section.
๐ SIMILAR VOLUMES
The rate constants for the reactions OH(X 'II, kl k2 u=O) + NH3 --t HzO+ NH? and OII(X '11, u=O) + O3 -HO, + O2 were measured at 296K by the flash photolysis resonance fluorescence technique. The values of the rate constants thus obtained are kl = (4.1 +-0.6) X lo-l4 nndkz = (6.5 t 1.0) X lo-l4 in u
The rate constant for the NH 3 ฯฉ NO 2 L NH 2 ฯฉ HONO reaction (1) has been kinetically modeled by using the photometrically measured NO 2 decay rates available in the literature. The rates of NO 2 decay were found to be strongly dependent on reaction (1) and, to a significant extent, on the secondary
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