Pressure broadening of water and carbon monoxide transitions by molecular hydrogen at high temperatures

Author(s):  
A. Faure ◽  
L. Wiesenfeld ◽  
B.J. Drouin ◽  
J. Tennyson
1973 ◽  
Vol 95 (4) ◽  
pp. 535-538 ◽  
Author(s):  
J. C. Lin ◽  
R. Greif

The absorption of a vibrational-rotational band has been studied and the contribution from the first hot band has been included. A specific application has been made to carbon monoxide and good agreement with experimental results has been obtained.


Methods for determining the true widths of lines in simple vibration-rotation bands have been considered, and a procedure has been devised for studying the effect of added gases upon the line widths in the fundamental vibration bands of deuterium chloride and carbon monoxide


1972 ◽  
Vol 27 (1) ◽  
pp. 41-46 ◽  
Author(s):  
C. v. Sonntag

In the 185 nm photolysis of liquid O2-free isopropanol the following products (quantum yields) are formed: hydrogen (0.75), acetone (0.72), pinacol (0.036), methane (0.046), acetaldehyde (0.04), propane (0.02β), ane (0.0023) and carbon monoxide (0.0015). A detailed reaction scheme is proposed. The major primary processes are the formation of H-atoms by homolytic scission of the O —H-bond (61 — 69%), elimination of molecular hydrogen (21%) and molecular methane (5%). Φ(Η2) is strongly decreased by adding water which does not absorb an appreciable portion of the 185 nm light in the mixtures down to 1 mole/l isopropanol (Φ(Η2) =0.21). In contrast to the strong effect of water there is no effect on Φ(Η2) by diluting isopropanol with n-hexane. From experiments with isopropanol-OD and 2-deutero-isopropanol it is tentatively concluded that H-atoms stemming from the O—H-group of the alcohol are to about 65% the precursors of the hydrogen in these mixtures.


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