TY - JOUR
T1 - Kinetic energy dependence of the branching ratios of the reaction of N + ions with O2
AU - Howorka, F.
AU - Dotan, I.
AU - Fehsenfeld, F. C.
AU - Albritton, D. L.
PY - 1980
Y1 - 1980
N2 - The kinetic energy dependence of the branching ratios of the reaction of N+ with O2 has been determined in the collision energy range from 0.06 to 1.8 eV using a selected-ion flow-drift tube. At energies near thermal, the branching ratios were found to be the following percentages: O2+ 51±4, NO+ 43±4, and O + 6±4, in good agreement with the results of some of the earlier thermal-energy studies. At relative kinetic energies above about 0.1 eV, the O2+ channel increases and eventually becomes dominant, at the expense of the NO+ channel. At the highest energy investigated in the present study, the branching ratios obtained are 79%, 19%, and 2%, respectively, and join rather smoothly with crossed-beam data extending to higher energies. The O+ channel remains a minor channel over the energy range studied here. These energy-dependent branching ratios are in striking contrast to the total rate constant for this reaction, which is virtually energy-independent for energies below 1 eV.
AB - The kinetic energy dependence of the branching ratios of the reaction of N+ with O2 has been determined in the collision energy range from 0.06 to 1.8 eV using a selected-ion flow-drift tube. At energies near thermal, the branching ratios were found to be the following percentages: O2+ 51±4, NO+ 43±4, and O + 6±4, in good agreement with the results of some of the earlier thermal-energy studies. At relative kinetic energies above about 0.1 eV, the O2+ channel increases and eventually becomes dominant, at the expense of the NO+ channel. At the highest energy investigated in the present study, the branching ratios obtained are 79%, 19%, and 2%, respectively, and join rather smoothly with crossed-beam data extending to higher energies. The O+ channel remains a minor channel over the energy range studied here. These energy-dependent branching ratios are in striking contrast to the total rate constant for this reaction, which is virtually energy-independent for energies below 1 eV.
UR - http://www.scopus.com/inward/record.url?scp=0001418257&partnerID=8YFLogxK
U2 - 10.1063/1.440181
DO - 10.1063/1.440181
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AN - SCOPUS:0001418257
SN - 0021-9606
VL - 73
SP - 758
EP - 764
JO - Journal of Chemical Physics
JF - Journal of Chemical Physics
IS - 2
ER -