Nitric oxide chemiexcitation occurring in the reaction between metastable nitrogen atoms and oxygen molecules

The infrared emission spectrum of the NO Δv=1 bands, chemiexcited in the reaction between metastable atomic nitrogen and molecular oxygen, has been studied at temperatures of 90–180 K and pressures near 5×10−6 atm. It is concluded that the observed radiation corresponds to an NO vibrational distribution created solely by the chemical reaction, unaffected by any relaxation process(es). Relative rate constants for production of NO into individual vibrational levels are found to be very nearly constant for levels v=1–7 and decrease monotonically for levels v=8–12. The average degree of excitation is about 4.5 vibrational quanta per NO molecule, and, assuming that N(2P) atoms play a negligible role, it is determined that 27% of the N(2D)+O2 exothermicity is converted to vibrational excitation of the nitric oxide product. Both the nature of the distribution and the results of a surprisal analysis suggest that those reactions which produce NO in levels higher than v=7 may also be producing O(1D).

[1]  D. Kley,et al.  The yield of N/2D/ atoms in the dissociative recombination of NO/+/ , 1977 .

[2]  T. Slanger,et al.  Quenching of N(2D) by N2 and H2O , 1976 .

[3]  M. E. Whitson,et al.  Vibrational energy distribution in the NO produced by the reaction of N(4S) with O2 , 1976 .

[4]  F. Billingsley Calculated vibration-rotation intensities for NO(X2Π) , 1976 .

[5]  R. Levine,et al.  Vibrational energy transfer in molecular collisions: An information theoretic analysis and synthesis , 1975 .

[6]  R. E. Murphy,et al.  Quenching of vibrationally excited nitric oxide by molecular oxygen and nitrogen , 1975 .

[7]  T. Shimazaki,et al.  Diurnal variations of odd nitrogen and ionic densities in the mesosphere and lower thermosphere: Simultaneous solution of photochemical‐diffusive equations , 1975 .

[8]  D. Perner,et al.  Rate constants for the quenching of N2(A 3Σ+u; vA=1–6,8) by rare gases , 1975 .

[9]  E. Oran,et al.  The aeronomy of odd nitrogen in the thermosphere , 1975 .

[10]  R. Levine,et al.  Analysis of electronically nonadiabatic chemical reactions: An information theoretic approach , 1975 .

[11]  D. Perner,et al.  Rate constants for the quenching of N2 (A 3Σu+, vA = 0 – 8) by CO, CO2, NH3, NO, and O2 , 1974 .

[12]  J. D. Mcdonald,et al.  Infrared chemiluminescence studies of the reaction of fluorine atoms with monosubstituted ethylene compounds , 1974 .

[13]  R. L. Taylor Energy Transfer Processes in the Stratosphere , 1974 .

[14]  L. G. Piper,et al.  Quenching cross sections for electronic energy transfer reactions between metastable argon atoms and noble gases and small molecules , 1973 .

[15]  M. Bourène,et al.  Pulse radiolysis study of argon‐nitrogen mixtures. Measurement of the rate constant of metastable argon de‐excitation by nitrogen , 1973 .

[16]  D. Perner,et al.  Deactivation of N2 (A3Σu+, v=0–7) by ground state nitrogen, ethane, and ethylene measured by kinetic absorption spectroscopy , 1973 .

[17]  R. Levine,et al.  Entropy and Chemical Change. II. Analysis of Product Energy Distributions: Temperature and Entropy Deficiency , 1972 .

[18]  A. T. Stair,et al.  Further Comments on the Chemiluminescent Reaction N + O(2) ? NO + O and Its Overtone Photon Efficiency. , 1972, Applied optics.

[19]  B. Wood,et al.  Temperature coefficients for N(2 D) quenching by O2 and N2O , 1971 .

[20]  F. Kaufman,et al.  Reactions of Metastable Nitrogen Atoms , 1971 .

[21]  J. Polanyi,et al.  Formation of Vibrationally Excited OH by the Reaction H + O(3). , 1971, Applied optics.

[22]  A. T. Stair,et al.  Infrared Chemiluminescence of the Reaction N + O(2) ? NO + O. , 1971, Applied optics.

[23]  D. Stedman,et al.  Chemical Applications of Metastable Argon Atoms. IV. Excitation and Relaxation of Triplet States of N2 , 1970 .

[24]  D. Husain,et al.  Recent advances in the chemistry of electronically excited atoms , 1970 .

[25]  D. Stedman,et al.  Energy transfer reactions of N2(A3.SIGMA.u+). II. Quenching and emission by oxygen and nitrogen atoms , 1970 .

[26]  B. McCarroll An improved microwave discharge cavity for 2450 MHz (Notes) , 1970 .

[27]  R. Young,et al.  Vacuum‐Ultraviolet Photolysis of N2O. IV. Deactivation of N(2D) , 1969 .

[28]  A. Dalgarno A discussion on infared astronomy - Infrared day and night airglow of Earth's upper atmosphere , 1969, Philosophical Transactions of the Royal Society of London. Series A, Mathematical and Physical Sciences.

[29]  Roger C. Millikan,et al.  Systematics of Vibrational Relaxation , 1963 .

[30]  Walter J. Murphy,et al.  ADVANCES IN CHEMISTRY SERIES: Numbers 15 and 17 Demonstrate Rapidly Crowing Interest in Documentation; International Conference To Be Held in 1958 , 1956 .

[31]  R. Wayne,et al.  Collisional quenching of N2(A3∑+u; v= 0, 1) by N atoms, ground state N2 and a pyrex surface , 1976 .

[32]  D. Husain,et al.  Kinetic study of electronically excited nitrogen atoms, N(22DJ, 22PJ), by attenuation of atomic resonance radiation in the vacuum ultra-violet , 1974 .

[33]  F. Kaufman The production of atoms and simple radicals in glow discharges , 1967 .

[34]  Benjamin Bederson,et al.  Advances in atomic and molecular physics , 1965 .

[35]  H. P. Broida,et al.  Microwave Discharge Cavities Operating at 2450 MHz , 1964 .