MilliganD. E. and JacoxM. E., in Molecular Spectroscopy, Modern Research, ed. by RaoK. N. and MatthewsC. W. (Academic Press, New York, 1972), pp. 259–286.
2.
MilliganD. E. and JacoxM. E., Adv. High Temp. Chem.4, 1 (1971).
3.
GordonR.RebbertR. E., and AusloosP., Rare Gas Resonance Lamps, NBS Technical Note 496, (National Bureau of Standards, Washington, D.C., 1969).
4.
DavisD. and BraunW., Appl. Opt.7, 2071 (1968).
5.
LauferA. H. and McNesbyJ. R., J. Chem. Phys.42, 3329 (1965).
6.
McNesbyJ. R.BraunW., and BallJ., in Creation and Detection of the Excited State, ed. by LamolaA. A. (Dekker, New York, 1971), pp. 548–551.
7.
At pressures of a few Torr or less, the principal atomic emission lines of argon are the 106.67 and 104.82 nm lines with the lower wavelength line being approximately twice as intense as the 106.67 nm emission; DieblerV. H. and ReeseR. M., J. Res. Natl. Bur. Stand.68A, 409 (1964).
8.
SmardzewskiR. R. and FoxW. B., J. Fluorine Chem.7, 353 (1976).
9.
SmardzewskiR. R. and FoxW. B., J. Fluroine Chem.7, 453 (1976).
10.
SmardzewskiR. R. and FoxW. B., J. Fluorine Chem.7, 456 (1976).
11.
FehsenfeldF. C.EvensonK. M., and BroidaH. P., Rev. Sci. Instrum.36, 294 (1965).
12.
The most probable metastable species having sufficient energies to dissociate SF6 are the 3P2 (11.54 eV) and 3P0 (11.72 eV) states of argon.
13.
SetserD. W.StedmanD. H., and CoxonJ. A., J. Chem. Phys.53, 1004 (1970).
14.
Experimentally, the probability of quenching of Ar(3P0,2) metastables by a glass surface was found to be 0.97; AllisonW.DunningF. B., and SmithA. C. H., J. Phys.B5, 1175 (1972).
15.
After emerging from the discharge, the argon is subsequently deactivated to its ground state and condensed onto the 8°K window and must therefore be taken into account in the calculation of the final M/R (M = moles matrix, R = moles solute) ratios. An additional advantage realized when argon is used both as an excitation source and a matrix is that any mixed-matrix effects are avoided.
16.
ComptonR. N.NelsonD. R., and ReinhardtP. W., Int. J. Mass Spectrom. Ion Phys.6, 117 (1971).
17.
WightC. A.AultB. S., and AndrewsL., J. Chem. Phys.65, 1244 (1976).