Engineering topics
Publications and source records attributed to Slanger, T. G..
Measurements of the photodissociation quantum yields of CO2 have been carried out using various atomic line sources between 1200 and 1500 A. The production of CO was monitored by resonance fluorescence, and the results indicate that where the CO2 absorption spectrum is continuous, the CO quantum yield is high, but where there is structure, the yield is low.
The principal subjects of investigation were the determination of the CO2 photodissociation quantum yields at the wavelengths from 1200 A to 1500 A, and the efficiency of electronic-to-vibrational energy transfer in the systems 0(1D) + CO, N2, CO2 yields 0(3P) + CO N2, CO2 vibrational energies. Measurements on the photodissociation quantum yield of CO2 in the 1200-1500 A region show that it is wavelength dependent, and for the six atomic line sources used, the quantum yield varied from 0.2 to 0.8. The data appear to fit the interpretation of stable CO2 bound states mixed with repulsive or predissociating states, since the low quantum yields coincide with the maximum structure in the CO2 absorption spectrum. The first reliable measurements were made on the efficiency of electronic-to-vibrational energy transfer in the systems 0(1D)-CO and 0(1D)-N2, using a uv resonance fluorescence technique. The 0(1D)-CO2 interaction was investigated by infrared techniques.
With the aid of a molecular resonance fluorescence technique, which utilizes optical pumping from the v = 1 level of the ground state of CO by A 1 Pi-X 1 Sigma radiation, a study is made of the efficiency of E-V transfer from O(1 D) to CO. O(1 D) is generated at a known rate by O2 photodissociation at 1470 A in an intermittent mode, and the small modulation of the fluorescent signal associated with CO (v = 1) above the normal thermal background is interpreted in terms of E-V transfer efficiency. The CO (v = 1) lifetime in this system is determined mainly by resonance trapping of the IR fundamental band, and is found to be up to ten times longer than the natural radiative lifetime. For CO, (40 plus or minus 8)% of the O(1 D) energy is converted into vibrational energy. By observing the effect of N2 on the CO (v = 1) fluorescent intensity and lifetime, it is possible to obtain the E-V transfer efficiency for the system O(1 D)-N2 relative to that for O(1 D)-CO. The results indicate that the efficiency for N2 is (83 plus or minus 10)% of that for CO.
Measurement of rate coefficients over the temperature range from 250 to 370 K for the three-body recombination of O(super 3P) with CO. Earlier results at 300 K have been re-evaluated and were found to have been influenced by unknown impurities in the CO, which have now been removed by more elaborate purification methods. For CO as the third body, the rate constant is given by K = 6.5 x 10 to the minus 33rd exp (-4340 plus or minus 550/RT) cm to the 6th power per sq molecule per sec. For N2 and CO2, the 296 K rate constants are 2.3 and 6.2 x 10 to the minus 36th cm to the 6th power per sq molecule per sec, respectively.
The CO(a 3II) state, the upper state of the Cameron bands, was characterized with respect to its average radiative lifetime and its quenching coefficients for a series of simple molecules. The CO2 recombination reaction (O(3P) + CO + M yields CO2 + M) was studied as a function of temperature. For M = CO, the rate constant can be expressed as k = 6.5 x 10/33 exp(-4340 plus or minus 550/RT) cm to the 6th power molec/2 sec/1, whereas the rate for M = CO2, the pertinent species in the planetary atmospheres, is 1.6 times greater. The quantum yield for CO2 photodissociation was measured in the 1200-1500 A region, using atomic line sources. The yield throughout this spectral region was much lower than that measured at 1470 A, the lowest value obtained being 8% at 1304 A.
Deactivation and radiative lifetime of CO Cameron forbidden transition spectral bands produced by photon absorption
Quantum yield of carbon dioxide photolysis at 1470 A concerning Mars and Venus atmospheres
Photodissociation produced O/P3/ atoms detection and reaction rate measurements by resonance fluorescence scattering
Photolysis of CO-2 in UV spectral region applied to models of Martian and Venusian atmospheres
Oxygen and carbon dioxide UV photolysis studied with resonance fluorescence to analyze planetary atmospheric processes
Perturbation rotational levels in triplet states of CO emission spectra attributed to resonance fluorescence process involving optically forbidden transitions