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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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At least 379 records · Page 21

Neutral cometary atmospheres. II - The production of CN in comets

Brightness profiles of the CN (0-0) band at 3883 A have been constructed from spectrograms of comets Bennett (1979 II) and West (1976 VI). The subsequent analysis of these profiles shows that the parent molecule of CN had a radial scale length of (2.19 plus or minus 0.07) x 10 to the 4th r (H-squared), in kilometers. This, combined with current theories as well as photochemistry, is consistent with production by simple photodissociation of HCN. The rather random variation of the radial scale length for the apparent decay of CN is indicative not of a true decay scale length, but of the fact that no steady state in the CN parent production rate is achieved for the time scale necessary to build up the observed profile. A revision of the average CN production law with heliocentric distance from published photometry indicates an r(H to the -2nd) law for comet West out to at least 2.555 AU. This implies that the vaporization of this comet was controlled by some species more volatile than water. Based on this and other evidence, CO2 is suggested, but even more volatile molecules like CO cannot be ruled out.

Combi, M. R.↗

F region airglow - Are ground-based observations consistent with recent satellite results

The Atmosphere Explorer photochemistry is used to interpret simultaneous observations made at the Arecibo Observatory of the OI (6300 A) and NI (5200 A) airglow surface brightness and electron density and temperature profiles measured by incoherent scatter radar. It was found that the theory and the experiment agree for the 5200-A emission; however, it was not possible to obtain to a complete agreement for the 6300-A nightglow. It is suggested that the source of the discrepancy results from one of the parameters used to calculate the production rate of O(lD); the data show evidence of an asymmetrical behavior of the ionosphere between times when the F layer is descending and when it is ascending, with asymmetry probably reflecting the effects of transport on molecular ion densities in the bottom side of the F region.

Cogger, L. L.↗

A model of comet comae. II - Effects of solar photodissociative ionization

Improvements to a computer model of coma photochemistry are described. These include an expansion of the chemical reactions network and new rate constants that have been measured only recently. Photolytic reactions of additional molecules are incorporated, and photolytic branching ratios are treated in far greater detail than previously. A total of 25 photodissociative ionization (PDI) reactions are now considered (as compared to only 3 PDI reactions previously). Solar PDI of the mother molecule CO2 is shown to compete effectively with photoionization of CO in the production of observed CO(+). The CO(+) density peak predicted by the improved model, for CO2 or CO mother molecules, is deep in the inner coma, in better agreement with observation than the old CO2 model. However, neither CO2 nor CO mother molecule calculations reproduce the CO(+)/H2O(+) ratio observed in comet Kohoutek. PDI products of CO2, CO, CH4, and NH3 mother molecules fuel a complex chemistry scheme, producing inner coma abundances of CN, C2, and C3 much greater than previously calculated.

Huebner, W. F.↗

A two-dimensional model of odd nitrogen in the thermosphere and mesosphere

Satellite measurements of the global nitric oxide distribution demonstrating the need for a two dimensional model of odd nitrogen photochemistry and transport in the thermosphere and mesosphere are reviewed. The main characteristics of a new code solving the transport equation for N(4S), N(2D), and N0 are given. This model extends from pole to pole between 75 and 275 km and reacts to the magnetic activity, the ultraviolet solar flux, and the neutral wind field. The effects of ionization and subsequent odd nitrogen production by high latitude particle precipitation are also included. Preliminary results are illustrated for a magnetically quiet solar minimum period with no neutral wind.

Gerard, J. C.↗

The 1980 summer research fellowship program

The problem of incorporating visual input into robot systems is described. The photochemistry of the stratosphere, particularly possible permutations of the ozone layer, is discussed. Photoelectrochemical properties of metal thio-hypodiphosphates are investigated. Extreme eigenvalues are computed by the Lancqos approach. The rotational Raman spectra of the molecular atmosphere is studied. A computer operated mathematical symbolic manipulation system is described. Preparation of polycrystalline semiconductor electrodes of tungsten and molybdenum dichalcogenides is received.

Darden, G. C.↗

Two-dimensional zonal mean flow model

The interactions of dynamics, photochemistry and radiation in the stratosphere can be described by the continuity, momentum, and energy equations. A more comprehensive model for stratospheric transport theory was developed for the purpose of aiding predictions of changes in the stratospheric ozone content as a consequence of natural and anthropogenic processes. This model is time dependent and the dependent variables are zonal means of the relevant meteorological quantities which are functions of latitude and height. The detailed formulation of a numerical model both in physics and mathematics is given. A set of fundamental dynamical equations, and the numerical method used in the integration are described.

Chen, H. C.↗

Evolution of the atmosphere of Venus

The photochemistry of the stratosphere of Venus was modeled using an updated and expanded chemical scheme, and the results of recent laboratory studies. The model satisfactorily accounts for the observations of CO, O2, (1) and SO2 in the stratosphere. Oxygen, derived from CO2 photolysis, is primarily consumed by CO2 recombination and oxidation of SO2 to H2SO4. Photolysis of HCl in the upper stratosphere provides a major source of odd hydrogen radicals essential for the catalytic oxidation of CO. Oxidation of SO2 by O occurs in the lower stratosphere, with the O-O bond broken by S + O2 and SO + HO2. The sensitivity of stratospheric chemistry to ambient H2 abundance was studied and the model prefers the high value (1 10 ppm) recently inferred from the Pioneer Venus ionospheric measurements. The importance of the photochemical production of S2O, (SO)2, S2, H2S2O2 and H2S2O3 is speculated. A number of previously unsuspected similarities between the chemistry of the stratospheres of Venus and the Earth, presented and discussed.

Yung, Y. L.↗

Oceanic Lidar

Instrument concepts which measure ocean temperature, chlorophyll, sediment and Gelbstoffe concentrations in three dimensions on a quantitative, quasi-synoptic basis were considered. Coastal zone color scanner chlorophyll imagery, laser stimulated Raman temperaure and fluorescence spectroscopy, existing airborne Lidar and laser fluorosensing instruments, and their accuracies in quantifying concentrations of chlorophyll, suspended sediments and Gelbstoffe are presented. Lidar applications to phytoplankton dynamics and photochemistry, Lidar radiative transfer and signal interpretation, and Lidar technology are discussed.

Carder, K. L.↗

Stratospheric constituent measurements using UV solar occultation technique

The photochemistry of the stratospheric ozone layer was studied as the result of predictions that trace amounts of pollutants can significantly affect the layer. One of the key species in the determination of the effects of these pollutants is the OH radical. A balloon flight was made to determine whether data on atmospheric OH could be obtained from lower resolution solar spectra obtained from high altitude during sunset.

Murcray, D. G.↗

Evaluated kinetic and photochemical data for atmospheric chemistry

This paper contains a critical evaluation of the kinetics and photochemistry of gas phase chemical reactions of neutral species involved in middle atmosphere chemistry (10-55 km altitude). Data sheets have been prepared for 148 thermal and photochemical reactions, containing summaries of the available experimental data with notes giving details of the experimental procedures. For each reaction a preferred value of the rate coefficient at 298 K is given together with a temperature dependency where possible. The selection of the preferred value is discussed, and estimates of the accuracies of the rate coefficients and temperature coefficients have been made for each reaction. The data sheets are intended to provide the basic physical chemical data needed as input for calculations which model atmospheric chemistry. A table summarizing the preferred rate data is provided, together with an appendix listing the available data on enthalpies of formation of the reactant and product species.

Baulch, D. L.↗

Ionospheres of the terrestrial planets

The theory and observations relating to the ionospheres of the terrestrial planets Venus, the earth, and Mars are reviewed. Emphasis is placed on comparing the basic differences and similarities between the planetary ionospheres. The review covers the plasma and electric-magnetic field environments that surround the planets, the theory leading to the creation and transport of ionization in the ionospheres, the relevant observations, and the most recent model calculations. The theory section includes a discussion of ambipolar diffusion in a partially ionized plasma, diffusion in a fully ionized plasma, supersonic plasma flow, photochemistry, and heating and cooling processes. The sections on observations and model calculations cover the neutral atmosphere composition, the ion composition, the electron density, and the electron, ion, and neutral temperatures.

Schunk, R. W.↗

The two-dimensional diagnostic model for tropospheric OH - An uncertainty analysis

Tropospheric OH is believed to play a major role in atmospheric photochemistry, and, via its chemical interactions OH ultimately may affect the climate, stratospheric ozone levels, and the pH of rain. A valuable tool for predicting the global OH abundance as a function of latitude and altitude is the two-dimensional diagnostic model for tropospheric OH. This model can also be applied to budget studies of species which interact with OH, such as CH4, CO, and O3. In addition to laboratory-obtained kinetic data, important variables include the rate constants for several reactions, the rate of heterogeneous removal of soluble species, and the global abundance and spatial variability in H2O, O3, CO, and NOx. The uncertainties in these parameters imply over a factor of 3 variability in the calculated global OH concentration as well as significant uncertainties in the latitudinal and vertical OH distribution.

Chameides, W. L.↗

The Stratosphere 1981: Theory and measurements

Measurements of trace species are compared with theoretical estimates and the similarities and the differences between the two sets of data are discussed. The theoretical predictions are compared with long term trends in both column content and altitude profile of ozone as observed from ground-based and satellite instruments. The chemical kinetics and photochemistry of the stratosphere were reviewed.

Source record↗

Spectroscopic measurements of Mars and Venus with heterodyne techniques

Measurements were made of the exact shape of CO2 absorption lines in Mars and Venus to determine the vertical pressure temperature structure using high resolution heterodyne spectroscopy. Accurate measurements of absolute wind velocities in both the mesosphere and stratosphere of Venus were made from Doppler shifts of narrow CO2 lines, and searches were made for minor molecular species of interest in modeling the stratospheric photochemistry for Mars and Venus.

Betz, A.↗

A review of acetylene, ethylene and ethane molecular spectroscopy for planetary applications

Spectroscopic work in acetylene, ethylene and ethane, are of particular interest since the Voyager IRIS observations of Jupiter. Acetylene and ethane but not ethylene were observed in the Jovian spectrum. Two fundamental bands of the observed gases are used to determine the spatial distribution of these hydrocarbons on Jupiter and to illuminate the photochemistry of these species. The 100 to 1000 cm region is discussed and selected examples of current laboratory work are given.

Maguire, W. C.↗

Organic chemistry in Titan's atmosphere

Laboratory photochemical simulations and other types of chemical simulations are discussed. The chemistry of methane, which is the major known constituent of Titan's atmosphere was examined with stress on what can be learned from photochemistry and particle irradiation. The composition of dust that comprises the haze layer was determined. Isotope fractionation in planetary atmospheres is also discussed.

Scattergood, T.↗

Ozone Uncertainties Study Algorithm (OUSA)

An algorithm to carry out sensitivities, uncertainties and overall imprecision studies to a set of input parameters for a one dimensional steady ozone photochemistry model is described. This algorithm can be used to evaluate steady state perturbations due to point source or distributed ejection of H2O, CLX, and NOx, besides, varying the incident solar flux. This algorithm is operational on IBM OS/360-91 computer at NASA/Goddard Space Flight Center's Science and Applications Computer Center (SACC).

Bahethi, O. P.↗

A photochemical study of the kinetics of the reactions of NH2 with phosphine, ethylene, and acetylene using flash photolysis-laser induced fluorescence

The photochemistry of the reactions of NH2 was investigated in an attempt to explain the existence of an abundance of ammonia in the Jovian atmosphere. The production of ammonia reservoirs from the coupling of ammonia with other atmospheric constituents was considered. The rate constants for the reactions of NH2 radicals with phosphine, acetylene, and ethylene were measured. Flash photolysis was used for the production of NH2 radicals and laser induced fluorescence was employed for radical detection. It was determined that the rates of the reactions were too slow to be significant as a source of ammonia reservoirs in the Jovian atmosphere.

Bosco, S. R.↗