CATALYZED RECOMBINATION OF NITROGEN ATOMS, AND THE POSSIBLE PRESENCE OF A SECOND ACTIVE SPECIESIN ACTIVE NITROGEN

1960 ◽  
Vol 38 (12) ◽  
pp. 2514-2522 ◽  
Author(s):  
Roger Kelly ◽  
C. A. Winkler

The reactions of ethylene, ethane, and ammonia with active nitrogen have been studied over the pressure range 0.3 to 4 mm usinganunheatedreaction vessel. The object was to determine why each reactant shows, as is well-known, a smaller extent of reaction at lower temperatures than would be predicted from the atom concentration. It was concluded that ethylene probably brought about homogeneouscatalyzedrecombination, i.e. the process [Formula: see text] followed by N + N•C2H4 → N2 + C2H4. The over-all third-order rate constant appeared to be very large, about 1.8 × 10−28 cc2 molecule−2 sec−1. The behavior of ammonia was quite different from that of ethylene and it was, in fact, possible to show that the extent of reaction was not governed by the instantaneous atom concentration at all. The results can be explained qualitatively, however, if it is assumed that excited molecules formed in the course of homogeneous atom decay constitute a second active species in active nitrogen. This view serves also to explain the failure in such work as that of Kistiakowsky etal. to observe ammonia destruction or excited molecules when especially low atom concentrations are used. The few experiments involving ethane were sufficient to show that the reactivity was low for a different reason than with ethylene.

1980 ◽  
Vol 33 (7) ◽  
pp. 1425 ◽  
Author(s):  
GK Farquharson ◽  
RH Smith

The rate of disappearance of hydroxyl radicals (generated by H+NO2 → OH+NO) along a discharge flow tube both with and without ethene present was measured by resonance fluorescence. Stoichiometry was simultaneously measured with a mass spectrometer, the leak into which was located downstream of the resonance fluorescence cell. After allowing for loss of hydroxyl by known homogeneous reactions and for wall loss (when applicable) it was found that for OH+C2H4 the low pressure limiting third-order rate constant kter was (3.1 � 0.5)x 10-29 cm6 s-1 at approximately 298 K. In addition an estimate for the second- order rate constant for OH+OH was obtained, namely (1.7 � 0.2) × 10-12 cm3 s-1. These results are discussed in relation to previous measurements.


Sign in / Sign up

Export Citation Format

Share Document