Kinetics of the reaction between oxygen atoms and carbon disulfide

1974 ◽  
Vol 61 (2) ◽  
pp. 704-709 ◽  
Author(s):  
Irene R. Slagle ◽  
James R. Gilbert ◽  
David Gutman
Keyword(s):  
Carbon Disulfide ◽  
Kinetics Of ◽  
Oxygen Atoms

Correlation between the dynamics of oxygen atoms and oxidation kinetics of solid solutions based on Bi2Sr2CaCu2O8

2004 ◽  
Vol 46 (3) ◽  
pp. 424-429
Author(s):  
A. V. Knotko ◽  
A. V. Garshev ◽  
M. N. Pulkin ◽  
V. I. Putlyaev ◽  
S. I. Morozov
Keyword(s):  
Solid Solutions ◽  
Oxidation Kinetics ◽  
Kinetics Of ◽  
Oxygen Atoms

ChemInform Abstract: Kinetics of the Reaction Between Oxygen Atoms and Allyl Radicals.

ChemInform ◽  
1990 ◽  
Vol 21 (33) ◽  
Author(s):  
I. R. SLAGLE ◽  
J. R. BERNHARDT ◽  
D. GUTMAN ◽  
M. A. HANNING-LEE ◽  
M. J. PILLING
Keyword(s):  
Kinetics Of ◽  
Oxygen Atoms

Kinetics of the process of eliminating carbon disulfide from high-modulus viscose rayon tow

1976 ◽  
Vol 8 (4) ◽  
pp. 408-409 ◽  
Author(s):  
S. V. Belokonev ◽  
G. T. Glichev ◽  
A. T. Serkov
Keyword(s):  
Carbon Disulfide ◽  
Viscose Rayon ◽  
High Modulus ◽  
Kinetics Of

Effect of oxygen atoms on the vibrational kinetics of CO2 and CO revealed by the use of a large surface area material

2020 ◽  
Vol 54 (9) ◽  
pp. 095208 ◽  
Author(s):  
A S Morillo-Candas ◽  
B L M Klarenaar ◽  
C Amoedo ◽  
V Guerra ◽  
O Guaitella
Keyword(s):  
Surface Area ◽  
Large Surface Area ◽  
Vibrational Kinetics ◽  
Effect Of Oxygen ◽  
Kinetics Of ◽  
Oxygen Atoms

Kinetics of reactions involving CN emission IV. Study of the reactions of CN by electronic absorption spectroscopy

1968 ◽  
Vol 305 (1480) ◽  
pp. 107-123 ◽  
Keyword(s):  
Absorption Spectroscopy ◽  
Rate Constant ◽  
Electronic Absorption ◽  
Flow Reactor ◽  
Initial Step ◽  
Electronic Absorption Spectroscopy ◽  
Kinetics Of ◽  
Cn Radicals ◽  
Limiting Values ◽  
Oxygen Atoms

The kinetics of the reaction between oxygen atoms and cyanogen have been studied in a capacity flow reactor at temperatures between 570 and 687 °K. The concentration of CN radicals was measured by electronic absorption spectroscopy. This work confirms the previously proposed mechanism (part II). The initial step has a rate constant of k 1 = 2∙5 (± 0∙3) x 10 13 exp ( – 11000±2000/ RT ) cm 3 mole –1 s –1 . CN radicals are removed mainly by reactions (4) and (2) for which k 4 = 6∙3 (±3∙5) x 10 13 exp (–2400±700/ RT ) cm 3 mole –1 s –1 and k 2 = 4∙4 (±2∙0) x 10 12 cm 3 mole –1 s –1 . CN+O = CO+N, (4) CN+O 2 = NCO+O. (2) The rates of reaction of CN with NO and NH 3 were also measured; for CH 4 and H 2 limiting values were obtained.

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