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74 G a s , C h e m i c a l , a n d F r e e - E l e c t r o n L a s e r s Chemical Lasers 75
3.5.2 Carbon Monoxide Lasers
Chemically driven carbon monoxide devices have also been dem-
onstrated. They typically rely on the highly exothermal pumping
reaction:
CS + O → CO* + S, ∆Q = 334 kJ (3.34)
where the CS radical is often produced by the reaction
CS + O → CS + SO (3.35)
2
The pumping reaction produces highly vibrationally excited CO that
is redistributed by V-V transfer processes. Furthermore, the VT deac-
tivation rates for CO* are much more favorable than are those for HF.
Unfortunately, due to the high O bond energy, oxygen atoms are
2
almost as difficult to produce as hydrogen atoms. Because the oxygen
atoms are typically produced electrically, there is no real advantage to
using an all–electrically driven CO laser. Furthermore, interest is lim-
ited by the relatively poor propagation characteristics of CO in the
atmosphere.
References
1. Polanyi, J. C., “On iraser detectors for radiation emitted from diatomic
gases and coherent infrared sources,” J. Chem. Phys., 34: 347, 1961; Penner,
S. S., “Proposal for an infrared maser dependent on vibrational excitation,”
J. Quant. Spectrosc. Radiative Transfer, 1: 163, 1961.
2. Kasper, J. V. V., and Pimentel, G. C., “HCl Chemical Laser,” Phys. Rev. Lett., 14:
352, 1965.
3. Pimentel, G. C., “The significance of chemical lasers in chemistry,” IEE J.
Quantum Electron, 6: 174, 1970.
4. Gross, R. W. F., and Bott, J. F., Handbook of Chemical Lasers, John Wiley & Sons,
New York, 1976.
5. Stitch, M. L., Laser Handbook, Volume 3, North-Holland Publishing Company,
Amsterdam, 1979.
6. Cheo, P., Handbook of Molecular Lasers, Dekker, New York, 1987.
7. Endo, M., and Walter, R., Gas Lasers, CRC Press, New York, 2007.
8. Hertzberg, G., Spectra of Diatomic Molecules, Van Nostrand Reinhold Company,
New York, 1950.
9. Zissis, G. J., and Wolf, W. L., The Infrared Handbook, Environmental Research
Institute of Michigan, Ann Arbor, 1985.
10. Polanyi, J. C., and Woodall, K. B., “Energy distribution among reaction prod-
ucts VI F + H ,D ,” J. Chem. Phys., 57: 1574, 1972; Polanyi, J.C., and Sloan, J .J.,
2
2
“Energy distribution amoung reaction products VII H + F ,” J. Chem. Phys., 57:
2
4988, 1972.
11. Cohen, N., and Bott, J. F., “Review of Rate Data for Reactions of Interest in
HF and DF Lasers,” Aerospace Corporation TR SD-TR-82-86, Segundo, CA,
1982.
12. Derwent, R.G., and Thrush, B.A., “The radiative lifetime of the metastable
iodine atom I(5 P 1/2 ),” Chem. Phys. Lett., 9: 591, 1971.
2
13. McDermott, W., Pchelkin, W. E., Bernard, D. J., and Bousek, R. R., “An electronic
transition chemical laser,” Appl. Phys. Lett., 32: 469, 1970.