Reaction of CH radical with O2 by time-resolved FTIR spectroscopy

Chinese Science Bulletin

Volumn 48, Issue 12, 2003, Pages 1225-1229

  Ren, Li ^a,b   Kong, Fanao ^a  

^a INSTITUTE OF CHEMISTRY   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

Author keywords

CH radical; CO; CO2; IR emission; Time resolved Fourier transform

Indexed keywords

EID: 4043141517     PISSN: 10016538     EISSN: 18619541     Source Type: Journal    
DOI: 10.1360/02wb0219     Document Type: Article

References (24)

1. Sanders, W. A., Lin, M. C., In Chemical Kinetics of Small Organic Radicals (Alfassi, Z. B.), CRC: Boca Raton, FL, 1986, Vol. III, 103.
2. Miller, J. A., Bowman, C. T., Mechanism and modeling of nitrogen chemistry in combustion. Prog. Energy Combustion Sci., 1989, 15: 287-338.
3. Lichtin, D. A., Berman, M. R., Lin, M. C., NH (A3Π→X3Τ-) chemiluminescence from the CH+ NO reaction, Chem. Phys. Lett., 1984, 108: 18-24.
4. Dean, A. J., Hanson, R. K., Bowman, C. T., A shock tube study of reactions of C atom and CH with NO including product channel measurements, J. Phys. Chem., 1991, 95: 3180-3189.
5. Vinckier, C., Determination of the rate constant of the reaction CH + O→CHO++e, J. Phys. Chem., 1979, 83: 1234-1235.
6. Fenimore, C. P., Formation of nitric oxide in premixed hydrocarbon flames. Thirteenth Symposium (International) on Combustion, The Combustion Institute: Pittsburgh, PA, 1971, 373-379.
7. Barin, I., Thermochemical Data of Pure Substances, Weinheim:, VCH Publishers, 1989.
8. 2 lasers produced from the CH + O2 reaction, J. Chem. Phys., 1974, 61: 1835-1843.
9. 2, 19th Symposium (International) on Combustion/The Combustion Institute, 1982, 73-79.
10. Anderson, S. M., Freedman, A., Kolb, C. E., Fast-flow studies of CH radical kinetics at 290 K, J. Phys. Chem., 1987, 91: 6272-6277.
11. 2 and NO (T=13-708 K) and with NH3 (T=23-295 K), J. Phys. Chem., 1996, 100: 3036-3069.
12. 2 reaction, J. Phys. Chem., 1996, 100: 17840-17845.
13. Becker, K. H., Engelhardt, B., Wiesen, P. et al., Rate constants for CH reaction at low total pressures, Chem. Phys. Lett., 1989, 154: 342-348.
14. 2, Chem. Phys. Lett., 1979, 66: 95-99.
15. 2 at 296≤T/K≤873, J. Chem. Soc. Faraday Trans., 1996, 92: 2335-2341.
16. 2, J. Phys. Chem. A, 1999, 103: 7395-7400.
17. Kulda, K., Schatz, G. C., Wagner, A. F., A quasiclassical trajectory study of the OH + CO reaction, J. Chem. Phys., 1991, 95: 1635-1647.
18. 2 reactions, J. Phys. Chem., 2002, 106: 5490-5497.
19. Zhu, Q. H., Huang, S. L., Wang, X. B. et al., The time-resolved FTIR emission spectroscopy initiated by laser photolysin, Chin. J. Chem. Phys., 1993, 6: 87-93.
20. 3 at 248 and 193 nm: observation of the electronically electronically excited CH(A2A) product, Chem. Phys., 1998, 238: 329-341.
21. 2 studied by TR-FTIR emission spectroscopy, Chem. Phys. Lett., 2000, 326: 73-79.
22. 2 studied by time-resolved FTIR spectroscopy, Chem. Phys. Lett., 2000, 322: 21-26.
23. Wang, H., Wang, B. S., He, Y. et al., The gaseous reaction of vinyl radical with oxygen, J. Chem. Phys., 2001, 115: 1742-1746.
24. Su, H. M., He, Y., Kong, F. A., Photodissociation of formic acid, J. Chem. Phys., 2000, 113: 1891-1897.