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At least 109 records · Page 6

Photodissociation regions. I - Basic model. II - A model for the Orion photodissociation region

A theoretical parameter study of the temperature and chemical structure of dense photodissociation regions and their resultant spectrum is presented. Models are discussed which are relevant not only to the dust and gas between molecular clouds and H II regions, but also apply to any neutral cloud illuminated by intense FUV fluxes. The models relate observed line and continuum emission from these regions to physical parameters such as the gas density and temperature, the elemental and chemical abundances, the local radiation field, and the grain properties. The results are applied to observational data from the OMC-1 region. The model shows that the observed high brightness temperature of the C I 609 microns line can be explained by emission from the C(+)/C/CO transition region. This difference with previous chemical models is due to a higher gas phase elemental abundance of carbon, to the charge exchange reactions of C(+) with S and SiO, and to carbon self-shielding.

Tielens, A. G. G. M.↗

Planetary fast neutral emission and effects on solar wind - A cometary exosphere analog

Ion-neutral charge exchange reactions occurring in planetary magnetospheres produce a copious supply of fast neutrals in the form of high-speed magnetospheric neutral winds. Theoretical models of such processes and their subsequent effects on the solar wind are investigated. Source strengths for emission from earth's ring current (10 to the 25th - 10 to the 26th/s), Jupiter's Io plasma torus (1-2 x 10 to the 28th/s), and both the Dione-Tethys torus and the Titan hydrogen torus (10 to the 26th - 10 to the 27th/s) of Saturn are evaluated. The effects of an extensive atomic nitrogen cloud surrounding the orbit of Titan are also considered in connection with the Saturnian aurora. Reionization and pickup of sulfur atoms in the circumplanetary region of Jupiter lead to a small mass-loading effect on the solar wind velocity (less than 10 percent); however, the heat input is substantial, resulting in a large increase in the effective ion temperature (not less than 100 percent). The pickup ion model is also applied tot the generation of electromagnetic ion cyclotron waves in the local neighborhood of the central body. The model suggests the preferential excitation of left-hand-polarized waves in regions where the solar wind-magnetic field angle is large (outer sheath) and right-hand waves in regions where the angle is small (near-tail).

Barbosa, D. D.↗

Mesospheric ionization and O2 1Delta(g) depletion

Observations of O2 1Delta(g) emission during solar proton events reveal large depletions below 80 and near 90 km. The lower-altitude depletions are believed to be due to odd hydrogen production and associated depletion of ozone, but the mechanism producing the depletion near 90 km has not yet been established. In this paper, it is proposed that an exothermic charge exchange reaction between O2(+) and O2 1Delta(g) is likely to be responsible for these high-altitude depletions. In particular, it is shown that the vertical structure of the observed change in airglow emission is consistent with this mechanism.

Spear, K. A.↗

Current review of the Jupiter, Saturn, and Uranus ionospheres

The ionospheres of the major planets Jupiter, Saturn, and Uranus are reviewed in light of Pioneer and Voyager observations. Some refinements to pre-Voyager theoretical models are required to explain the results, most notably the addition of significant particle ionization from 'electroglow' and auroral processes and the need for additional chemical loss of protons via charge exchange reactions with water. Water from the Saturn rings has been identified as a major modifier of the Saturn ionosphere and water influx from satellites and/or meteorites may also be important at Jupiter and Uranus as well, as evidenced by the observed ionospheric structure and the identification of cold stratospheric carbon monoxide at Jupiter.

Waite, J. H., Jr.↗

Energetic Neutral Atom Precipitation (ENAP)

The Energetic Neutral Atom Precipitation experiment is scheduled to be flown on the Atmospheric Laboratory for Applications and Science (ATLAS 1) NASA mission. The objective of this experiment is to measure very faint emissions at nighttime arising from fluxes of energetic neutral atoms in the thermosphere. These energetic atoms have energies ranging up to about 50 keV, and arise from ions of hydrogen, helium, and oxygen trapped in the inner magnetosphere. Some of these ions become neutralized in charge exchange reactions with neutral hydrogen in the hydrogen geocorona that extends through the region. The ions are trapped on magnetic field lines which cross the equatorial plane at 2 to 6 earth radii distance, and they mirror at a range of heights on these field lines, extending down to the thermosphere at 500 km altitude. The ATLAS 1 measurements will not be of the neutral atoms themselves but of the optical emission produced by those on trajectories that intersect the thermosphere. The ENAP measurements are to be made using the Imaging Spectrometric Observatory (ISO) which is being flown on the ATLAS mission primarily for daytime spectral observations, and the ENAP measurements will all be nighttime measurements because of the faintness of the emissions and the relatively low level of magnetic activity expected.

Tinsley, B. A.↗

A time-dependent wave packet approach to atom-diatom reactive collision probabilities - Theory and application to the H + H2(J = 0) system

This paper describes a new approach to the study of atom-diatom reactive collisions in three dimensions employing wave packets and the time-dependent Schroedinger equation. The method uses a projection operator approach to couple the inelastic and reactive portions of the total wave function and optical potentials to circumvent the necessity of using product arrangement coordinates. Reactive transition probabilities are calculated from the state resolved flux of the wave packet as it leaves the interaction region in the direction of the reactive arrangement channel. The present approach is used to obtain such vibrationally resolved probabilities for the three-dimensional H + H2 (J = 0) hydrogen exchange reaction, using a body-fixed system of coordinates.

Neuhauser, Daniel↗

Comment on 'A non-mass-dependent isotopic fractionation effect' by F. Robert, J. Halbout and J. Baudon

The fractionation model of Robert et al. (1988) treats the gas-phase isotopic exchange reaction between kinetically excited atoms aX and diatomic MbX yielding bX and MaX and finds an abundance-dependent fractionation superimposed on the usual mass dependent fractionation. This paper shows that the treatment of Robert et al. is in error and presents a more straightforward treatment of the same system. This model shows only mass-dependent fractionation.

Sund, Mark T.↗

Validation of chemistry models employed in a particle simulation method

The chemistry models employed in a statistical particle simulation method, as implemented in the Intel iPSC/860 multiprocessor computer, are validated and applied. Chemical relaxation of five-species air in these reservoirs involves 34 simultaneous dissociation, recombination, and atomic-exchange reactions. The reaction rates employed in the analytic solutions are obtained from Arrhenius experimental correlations as functions of temperature for adiabatic gas reservoirs in thermal equilibrium. Favorable agreement with the analytic solutions validates the simulation when applied to relaxation of O2 toward equilibrium in reservoirs dominated by dissociation and recombination, respectively, and when applied to relaxation of air in the temperature range 5000 to 30,000 K. A flow of O2 over a circular cylinder at high Mach number is simulated to demonstrate application of the method to multidimensional reactive flows.

Haas, Brian L.↗

The Carlisle Lakes-type chondrites - A new grouplet with high Delta(17)O and evidence for nebular oxidation

The petrogenesis of the Carlisle Lakes-type chondrites and their relationship to other chondrites are studied using new petrologic data, especially on mineralogical zoning patterns, and oxygen isotopic analyses of the whole chondrites and some of chondrules. Detailed zoning profiles of mafic silicates are measured in order to determine the environment(s) in which their oxidation states are established. It is concluded that the zoning did not form during crystallization from a melt droplet chondrule but post-dated chondrule formation. Parent-body thermal metamorphism and nebular gas-solid exchange reactions accompanied by condensation of new FeO-rich olivine, utilizing existing olivine surfaces as nucleation sites are considered as hypotheses explaining the zoning. The occurrence of zoned grains in a host that is mainly equilibrated suggests that the equilibration of the Carlisle Lakes-type chondrites occurred prior to final lithification.

Weisberg, Michael K.↗

Processible Polyazomethines

Processibility enhanced by incorporating trifluoromethylbenzene units into molecules. Results of two unexpected properties: high solubility in common organic solvents and lack of crystallinity. Properties coupled with ability of this class of polymers to undergo exchange reactions at elevated temperatures allow these materials to moderate their molecular weights during processing, which affects resulting mechanical properties after processing. Fluorinated polyazomethines form amorphous films that have excellent mechanical properties. Used in moisture-free environments as electronic semiconducting films and adhesives, and as matrix resins for advanced structural composites.

Bryant, Robert G.↗

Mechanistic investigations of shuttle glow

A series of laboratory measurements have been performed in order to provide a mechanistic interpretation for the visible shuttle glow. These studies involved interactions of an 8 km/s oxygen atom beam with both contaminant dosed surfaces and gaseous targets. We conclude that visible shuttle glow arises from surface mediated O + NO recombination via a Langmuir-Hinshelwood mechanism and that the gas-phase exchange reaction O + N2 - NO + N provides a viable source of precursor NO above surfaces oriented in the ram direction.

Caledonia, G. E.↗

High temperature conductivity of potassium-beta(double prime)-alumina

Potassium beta(double prime)-alumina (BDPA) single crystals have been reported by several groups to leave higher ionic conductivity than sodium BDPA crystals at room temperature, and similar conductivities are obtained at temperatures up to 600-700 K. Potassium BDPA ceramics have been reported to have significantly poorer conductivities than those of sodium BDPA ceramics, but conductivity measurements at temperatures above 625 K have not been reported. In this study, K(+)-BDPA ceramics were prepared from Na(+)-BDPA ceramic using a modified version of the exchange reaction with KCl vapor reported by Crosbie and Tennenhouse (1982), and the conductivity has been measured in K vapor at temperatures up to 1223 K, using the method of Cole et al. (1979). The results indicate reasonable agreement with earlier data on K(+)-BDPA ceramic measured in a liquid K cell, but show that the K(+)-BDPA ceramic's conductivity approaches that of Na(+)-BDPA ceramic at higher temperatures, being within a factor of four at 700 K and 60 percent of the conductivity of Na(+)-BDPA at T over 1000 K. Both four-probe dc conductivity and four probe ac impedance measurements were used to characterize the conductivity. A rather abrupt change in the grain boundary resistance suggesting a possible phase change in the intergranular material, potassium aluminate, is seen in the ac impedance behavior.

Williams, R. M.↗

Characterization of in-flight performance of ion propulsion systems

In-flight measurements of ion propulsion performance, ground test calibrations, and diagnostic performance measurements were reviewed. It was found that accelerometers provided the most accurate in-flight thrust measurements compared with four other methods that were surveyed. An experiment has also demonstrated that pre-flight alignment of the thrust vector was sufficiently accurate so that gimbal adjustments and use of attitude control thrusters were not required to counter disturbance torques caused by thrust vector misalignment. The effects of facility background pressure, facility enhanced charge-exchange reactions, and contamination on ground-based performance measurements are also discussed. Vacuum facility pressures for inert-gas ion thruster life tests and flight qualification tests will have to be less than 2 mPa to ensure accurate performance measurements.

Sovey, James S.↗

Characterization of in-flight performance of ion propulsion systems

In-flight measurements of ion propulsion performance, ground test calibrations, and diagnostic performance measurements were reviewed. It was found that accelerometers provided the most accurate in-flight thrust measurements compared with four other methods that were surveyed. An experiment has also demonstrated that pre-flight alignment of the thrust vector was sufficiently accurate so that gimbal adjustments and use of attitude control thrusters were not required to counter disturbance torques caused by thrust vector misalignment. The effects of facility background pressure, facility enhanced charge-exchange reactions, and contamination on ground-based performance measurements are also discussed. Vacuum facility pressures for inert-gas ion thruster life tests and flight qualification tests will have to be less than 2 mPa to ensure accurate performance measurements.

Sovey, James S.↗

Carbonates and sulfates in the Chassigny meteorite: Further evidence for aqueous chemistry on the SNC parent planet

Scanning electron microscopy and energy-dispersive X-ray spectrometry of untreated interior chips from three different specimens of the Chassigny meteorite confirm the presence of discrete grains of Ca-carbonate, Mg-carbonate, and Ca-sulfate. Morphologies of these salt grains suggest that the Ca-carbonate is calcite (CaCO3) and that the Ca-sulfate is gypsum (CaSO4-2H2O) or bassanite (CaSO4-1/2H2O). The morphologic identification of the Mg-carbonate is equivocal, but rhombohedral and acicular crystal habits suggest magnesite and hydromagnesite, respectively. The salts in Chassigny occur as discontinuous veins in primary igneous minerals and are similar to those previously documented in the nakhlites, Nakhla and Lafayette, and in shergottite EETA79001. Unlike those in nakhlites, however, the Chassigny salts occur alone, without associated ferric oxides or aluminosilicates clays. Traces of Cl and P in Chassigny salts are consistent with precipitation of the salts from short-lived, saline, aqueous solutions that postdated igneous crystallization. In contrast with the clear case for nakhlites, stratigraphic evidence for a preterrestrial origin of the salts in Chassigny is ambiguous; however, a preterrestrial origin of the Chassigny salts best explains all available evidence. The water-precipitated salts provide clear physical evidence for the hypothesis, proposed by other workers, that the igneous amphiboles in Chassigny might have experienced isotope-exchange reactions with near-surface water, thereby compromising the original stable-isotope signature of any magmatic water in melt inclusions.

Wentworth, Susan J.↗

Interstellar carbon monoxide toward zeta Ophiuchi

Interstellar CO A-X bands in the spectrum of zeta Oph were recorded at high Sound-to-Noise (S/N) with grating G160M of the Goddard High Resolution Spectrograph on the Hubble Space Telescope. Isotopic fractionation of CO is severe: CO-12/CO-13 = 167, C(16)O/C(18)O approximately equal to 1550 and C(16)O/C(17)O is greater than 5900 are found where C-12/C-13 = 70, O-16/O-18 = 500, and O-16.O-17 = 2600 are observed or expected. Standard models of the zeta Oph cloud predict CO-12/CO-13 is less than or approximately 70. The higher observed ratio suggests that photodissociation of CO, not the isotopic charge exchange reaction ((13)C(+) + CO reversible reaction (12)C(+) + (13)(CO), is the dominant influence on the CO-12/CO-13 ratio.

Lambert, David L.↗

Application of Chlorine-Assisted Chemical Vapor Deposition of Diamond at Low Temperatures

Low temperature deposition of diamond has been achieved by a chlorine-assisted diamond chemical vapor deposition (CA-CVD) process. This method begins with the thermal dissociation of molecular chlorine into atomic chlorine in a resistively heated graphite furnace at temperatures between 1300 and 1500 deg. C. The atomic chlorine, upon mixing, subsequently reacts with molecular hydrogen and hydrocarbons. The rapid exchange reactions between the atomic chlorine, molecular hydrogen, and hydrocarbons give rise to the atomic hydrogen and carbon precursors required for diamond deposition. Homoepitaxial diamond growth on diamond substrates has been studied over the substrate temperature range of 100-950 C. It was found that the diamond growth rates are approximately 0.2 microns/hr in the temperature range between 102 and 300 C and that the growth rates do not decrease significantly with a decrease in substrate temperature. This is unique because the traditional diamond deposition using H2/CH4 systems usually disappears at substrate temperatures below approx. 500 deg. C. This opens up a possible route to the deposition of diamond on low-melting point materials such as aluminum and its alloys.

Pan, Chenyu↗