DYNAMICS OF OH AND OD RADICAL REACTIONS WITH HI AND GEH4 AS STUDIED BY INFRARED CHEMILUMINESCENCE OF THE H2O AND HDO PRODUCTS

Citation
Ni. Butkovskaya et Dw. Setser, DYNAMICS OF OH AND OD RADICAL REACTIONS WITH HI AND GEH4 AS STUDIED BY INFRARED CHEMILUMINESCENCE OF THE H2O AND HDO PRODUCTS, The Journal of chemical physics, 106(12), 1997, pp. 5028-5042
Citations number
75
Categorie Soggetti
Physics, Atomic, Molecular & Chemical
ISSN journal
00219606
Volume
106
Issue
12
Year of publication
1997
Pages
5028 - 5042
Database
ISI
SICI code
0021-9606(1997)106:12<5028:DOOAOR>2.0.ZU;2-D
Abstract
The infrared chemiluminescence of vibrationally excited H2O and HDO fr om the highly exothermic reactions of OH and OD radicals with HI and G eH4 was observed in the 2200-5500 cm(-1) range. The experiments utiliz ed a fast-flow reactor with 0.3-1 Torr of Ar carrier gas at 300 K; the OH(OD) radicals were produced via the H(D) + NO2 reaction and the H o r D atoms were generated by a discharge in a H-2(D-2)/Ar mixture. The H2O and HOD vibrational distributions were determined by computer simu lation of the emission spectra in the 2200-3900 cm(-1) range. The tota l vibrational energy released to H2O and HOD molecules is, respectivel y, [f(upsilon)] = 0.36 and 0.41 from HI and [f(upsilon)] = 0.46 and 0. 51 from GeH4. These values are significantly smaller than for the reac tions of OH and OD with HBr, [f(upsilon)] = 0.61 and 0.65. The populat ions of the O-H stretching vibration of HOD and the collisionally coup led nu(1) and nu(3) stretching modes of H2O decrease with increasing v ibrational energy. In contrast, the vibrational distribution from the HBr reaction is inverted. The bending mode distributions in all stretc hing states of H2O and HOD extend to the thermodynamic limit of each r eaction. A surprisal analysis was made for H2O(HOD) distributions from the title reactions and compared with that for OH(OD) + HBr. The surp risal analysis tends to confirm that the dynamics for the HI and GeH4 reactions differ from the HBr reaction. The HI reaction may proceed ma inly via addition-migration, while the GeH4 reaction may involve both direct abstraction and addition-migration, A rate constant for the OHGeH4-->H2O+GeH3 reaction was evaluated by comparing the H2O emission i ntensities with that of the OH+HBr-->H2O+Br reaction, k(GeH4)/k(HBr) = 6.5 +/- 0.9. Secondary kinetic-isotope effects, k(OH)/k(OD) = 1.4 +/- 0.1, 1.0 +/- 0.2, and 1.3 +/- 0.2, were determined for reactions of O H and OD with GeH4, HI, and HBr, respectively, by comparing the relati ve H2O and HOD emission intensities. (C) 1997 American Institute of Ph ysics.