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Davis, D. D.

Publications and source records attributed to Davis, D. D..

47 records · Page 3
All sourcesNASA NTRSDOE OSTI
NASA NTRS1977

High resolution absorption cross sections for the A2Pi-X2Pi system of ClO

High-resolution ultraviolet absorption cross-sections for the ClO molecule are obtained, with the aim of facilitating studies of ozone depletion resulting from the injection of chlorofluorocarbons into the atmosphere. The spectroscopic analysis, which involves a frequency-doubled tunable dye laser with a bandwidth of 0.015 A, is described. Studies of the rotational lines of the ClO A 2Pi 3/2-X2Pi 3/2 9-10 band were conducted. Peak cross-sections for the P and R lines of the 9-0 band are found to be 10.0, 9.6, 8.6, 10.6, 10.3, and 9.2 times ten to the negative seventeenth power cm squared, with estimated accuracy of plus or minus 25%. Problems in distinguishing between Cl-35 and Cl-37 absorption are also considered.

Wine, P. H.↗
NASA NTRS1977

A study of the chemical degradation of ClONO2 in the stratosphere

The flash photolysis-resonance fluorescence system described by Davis et al. (1974) is used to measure the rate constants for the reactions of chlorine nitrate (ClONO2) with stratospheric O(3-P) and OH. Both reactions are examined in a pyrex cell with an internal volume of about 150 cu cm, where the reaction mixture was maintained at 245 K by circulating methanol from a thermostated circulation bath through the outer jacket of the reaction cell. The relative chemical degradation rates as a function of altitude for both reactions are tabulated, which shows that the chemical degradation pathways contribute less than 10% to the total rate of ClONO2 destruction at altitudes less than 30 km. Since the concentration of ClONO2 is calculated to be near its maximum around 25 km and drops off very significantly at higher altitudes, it is concluded that the photochemical decomposition of ClONO2 in the stratosphere is by far the most important degradation path for this molecule.

Ravishankara, A. R.↗
NASA NTRS1976

A temperature dependence kinetics study of the reactions of Cl/2-P-3/2/ with O3, CH4, and H2O2

The temperature dependence of two chlorine atom reactions of considerable fundamental importance to stratospheric chemistry was studied using the technique of flash photolysis-resonance fluorescence. The reactions of interest were: (1) Cl + O3 yields ClO + O2 studied at 220-350 K, and (2) Cl + CH4 yields CH3 + HCl studied at 218-401 K. In addition, the reaction Cl + H2O2 yields HCl + HO2 was studied at 300 K. The corresponding rate constants are provided for the three reactions. The new rate data implies the need to revise downward by a factor of 2.4-3 the magnitude of the ozone perturbation due to the presence of ClO/x/ species in the stratosphere, predicted by earlier model calculations.

Watson, R.↗
NASA NTRS1976

A frequency doubled pressure-tunable oscillator-amplifier dye laser system

A tunable high-repetition-rate oscillator-amplifier dye-laser system is reported. The dye laser described was longitudinally pumped with the second harmonic of a Nd-YAG laser operating at 10 Hz. Using three Faraday-Perot etalons and pressure tuning, a maximum fundamental output power of the order of 6 MW with a corresponding spectral width of less than 0.003 nm at 564 nm was obtained. The fundamental at 564 nm was frequency doubled to give a maximum power level of 0.6 MW of second-harmonic output power with a spectral width less than 0.0015 nm at 282 nm. Frequency stability could be maintained to within approximately 15% of the line-width.

Moriarty, A.↗
NASA NTRS1974

A flash photolysis-resonance fluorescence kinetics study of the reaction S/3P/ + OCS

Using the technique of flash photolysis-resonance fluorescence, the reaction of ground-state atomic sulfur with carbonyl sulfide has been investigated over the temperature range from 233 to 445 K. Over this temperature range, the experimental data were fitted to an Arrhenius equation of the form k sub 1 = (1.52 plus or minus 0.20) x 10 to the minus 12th power exp(-3.63 plus or minus 0.12 kcal/mol/RT) cu cm/molecule/sec. A comparison of these results with previous investigations on this reaction system is presented.

Klemm, R. B.↗
NASA NTRS1973

The hydroperoxyl radical in atmospheric chemical dynamics - Reaction with carbon monoxide.

Discussion of laboratory measurements which indicate that the reaction of the thermalized HO(2) radical with CO is exceedingly slow and that this reaction should not, therefore, be of any significance in atmospheric chemistry. The large discrepancy between the new results and data obtained earlier by Westenberg and de Haas (1972) is explained in terms of the reacting hydroperoxyl radical being in a non-Boltzmann distribution in the former study. It appears that the most important reactions of thermalized HO(2) in the atmosphere are those involving the trace gases of NO and sulfur dioxide.

Davis, D. D.↗
NASA NTRS1973

The color bar phase meter: A simple and economical method for calibrating crystal oscillators

Comparison of crystal oscillators to the rubidium stabilized color burst is made easy and inexpensive by use of the color bar phase meter. Required equipment consists of an unmodified color TV receiver, a color bar synthesizer and a stop watch (a wrist watch or clock with sweep second hand may be used with reduced precision). Measurement precision of 1 x 10 to the minus 10th power can be realized in measurement times of less than two minutes. If the color bar synthesizer were commercially available, user cost should be less than $200.00, exclusive of the TV receiver. Parts cost for the color bar synthesizer which translates the crystal oscillator frequency to 3.579MHz and modulates the received RF signal before it is fed to the receiver antenna terminals is about $25.00. A more sophisticated automated version, with precision of 1 x 10 to the minus 11th power would cost about twice as much.

Davis, D. D.↗