The results of an experimental investigation designed to determine t-he vibrational energy content in the praducts of the reaction OH + CO + CO\* + H are presented. No 1R emission wm observed in any of the fundamental or strong combination bands of C02, 3nd thus OUT results are expressed as bounds o
Reaction dynamics, OH energy partitioning, and OH product angular momentum alignment studies: H+H2O→OH+H2 versus H+CO2→OH+CO
✍ Scribed by A. Jacobs; H.-R. Volpp; J. Wolfrum
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 813 KB
- Volume
- 218
- Category
- Article
- ISSN
- 0009-2614
No coin nor oath required. For personal study only.
✦ Synopsis
Using translationally
excited H atoms generated by laser photolysis of H2S at 193 nm, the reaction dynamics of H + H,O+OH + H2 and H + COIdOH + CO was investigated at collision energies of 2.2 and 2.3 eV, respectively. Nascent OH rotational and vibrational quantum-state distributions and OH product translational energies were measured by means of the laser photolysis/laser-induced fluorescence pump-probe technique. A markedly non-statistical distribution of the available energy was found: H+H1O+OH+H1: f,,=O.O4+0.01,
10m3, f-,=0.65+0.26; H+CO,+OH+CO: f,,= 0.14 f 0.02, ftib = 0.11 f 0.04, l;_S= 0.59 k 0.16. In addition, velocity-aligned H atoms generated via polarized HZ!3 photodissociation were used to investigate vector correlations for both reactions.
📜 SIMILAR VOLUMES
We have studied the O ϩ OH 4 O 2 ϩ H reaction on Varandas's DMBE IV potential using a variety of statistical methods, all involving the RRKM assumption for the HO complex. \* 2 Comparing our results using microcanonical variational transition-state theory (VT) with those using microcanonical/fixed-
The rate coefficients for the reactions were determined using mixtures of HN03/CO/Ar and HN03/HNCO/Ar in incident shock wave experiments Simultaneous OH and COz absorption time-histories were obtained via cw uv narrow-linewidth absorption at 32606 56 cm-' ( A = 306 687 nm) and cw infrared narrowlin
Photolysis of HCI with an ArF excimer laser at 193 nm yields H atoms with well-defined high translational energy ( I .86 eV) which react with CO2 to form OH and CO. The product OH radicals are detected by laser-induced fluorescence (LIF). From LIF spectra the nascent OH vibrational, rotational and t
The title reaction was studied under single-collision conditions using 227-285 nm HI photolysis. A large decrease in the OH yield was obsenred as the photolysis wavelength was increased. Rotational distributions were obtained at 227,239,251,263 and 280 MI. Similar yield versus wavelength data were o