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At least 847 records · Page 47
All sourcesNASA NTRSDOE OSTI
NASA NTRS1985

Clathrate hydrates in the solar system

Clathrate hydrates are crystalline compounds in which an expanded ice lattice forms cages that contain gas molecules. There are two principal hydrate structures. Structure I, with a 12 A cubic unit cell, contains 46 water molecules and 8 cages of two types, giving an ideal formula (for CH4) of CH4.5.75H2O. The actual formula contains somewhat more water as the cages are not completely filled. Other examples that form Structure I hydrates are C2H6, C2H4, C2H2, CO2, SO2, OCS, Xe, H2S. Structure II, with a 17 A cubic unit cell, contains 136 water molecules, and 8 large and 16 small cages. The ideal formula for CHCl3 is CHCL3.17H2O. Other examples of Structure II hydrates include C3H8, C2H5Cl, acetone, and tetrahydrofuran. Small molecules such as Ar, Kr and probably N2 and O2 also form a Structure II hydrate. The small molecules occupy both the large and small cages, giving an ideal formula of Ar.5.67H2O. The conditions of pressure and temperature for hydrate formation are discussed.

Miller, S. L.↗
NASA NTRS1986

On the colors of Jupiter's satellite Io - Irradiation of solid sulfur at 77 K

The colors of seven sulfur allotropes at 77 K have been investigated both before and after irradiation by a high-pressure mercury lamp. S8 is white at 77 K but turns intense yellow within a few minutes on irradiation through quartz or DURAN. On warming, the yellow species (presumably chain-like sulfur diradicals characterized by an absorption at 430 nm) decomposes near 260 K and polymeric sulfur (S-infinity) is formed; the sample color changes gradually to the very similar color of an S8-S-infinity mixture, resulting in no visually detectable color change with temperatures from 77 K to 260 K. This is consistent with the lack of posteclipse brightening on Io. Other sulfur forms also turn intense yellow (S7, S10), grayish yellow (S12, S20, S-infinity), or brownish yellow (S6) on irradiation at 77 K, and these colors also change to the normal colors of the starting materials on warming to 298 K. It is suggested that the yellowish features on Io are caused by the effect of solar radiation on elemental sulfur. The yellow color thus produced may subsequently be modified by deposits of SO2 frosts and volcanic ash.

Steudel, R.↗
NASA NTRS1986

Vertical distribution of dimethylsulphide in the marine atmosphere

The first data on the vertical distribution of dimethylsulfide (DMS) in the marine troposphere are presented. The observations agree well with the distributions predicted by a two dimensional model calculation which includes convective transport and chemical processes. This agreement supports the validity of a previous estimate of about 40 Tg-S/yr for the input of DMS from the oceans to the atmosphere, and suggests that the oxidation of DMS can contribute significantly to the SO2 levels observed in the free troposphere.

Ferek, R. J.↗
NASA NTRS1986

Possible role of NO3 in the nighttime chemistry of a cloud

The NO3 radical in the aqueous phase is a strong oxidizing agent which reacts rapidly with a wide variety of inorganic and organic species. Within nighttime clouds the production of gaseous NO3 from the reaction of NO2 with O3 followed by heterogeneous scavenging of NO3 by cloud droplets can represent a significant source of these reactive radicals to cloud water. Model calculations indicate that in addition to leading to the production of NO3(-) in cloud water, this aqueous-phase source of NO3 can, under the appropriate conditions and depending upon the values for a number of uncertain rate constants, have a significant impact upon the rate of conversion of SO2 to H2SO4.

Chameides, W. L.↗
NASA NTRS1986

Vacuum ultraviolet photoabsorption study of SO

The photoabsorption of SO was investigated by producing the radicals from a pulsed discharge of a trace of SO2 in Ar. The photoabsorption cross section of SO in the 115-135 nm region was measured. A repulsive potential curve is constructed from the observed photoabsorption spectrum.

Nee, J. B.↗
NASA NTRS1986

Laser heterodyne system for obtaining height profiles of minor species in the atmosphere

An infrared laser heterodyne system for obtaining height profiles of minor constituents of the atmosphere was developed and erected. A brief discription of the system is given. The system consists of a tunable CO2 waveguide laser in the 9 to 11 micrometer band, that is used as a local oscillator and a heliostat that follows the sun and brings in solar radiation, that is mixed with the laser beam in a high speed liquid nitrogen cooled mercury cadmium telluride detector. The detected signal is analysed in a RF spectrum analyser that allows tracing absorption line profiles. Absorption lines of a number of minor constituents in the troposphere and stratosphere, such as O3, NH3, H2O, SO2, ClO, N2O, are in the 9 to 11 micrometer band and overlap with that of CO2 laser range. The experimental system has been made operational and trial observations taken. Current measurements are limited to ozone height profiles. Results are presented.

Jain, S. L.↗
NASA NTRS1986

OH measurement by laser light absorption

Since the first attempt to measure atmospheric hydroxyl radicals by optical absorption in 1975 (Perner et al., 1976) this method has been continuously developed further and its major obstacles and limitations are known today. The laser beam needs to be expanded in order to reduce the beam divergence. At the same time the energy density of the laser beam which produces OH via ozone photolysis is reduced to such an extent that the self-produced OH concentration ranges well below the atmospheric value. Atmospheric absorptions should be observed over a wide spectral range so that not only the OH radicals are properly identified by several rotational lines but their absorption can be corrected for interfering absorptions from other air constituents as SO2, CH2O, CS2, etc., which can be identified in a wide spectral range with more confidence. Air turbulence demands fast spectral scanning or probing on and off the absorption line. Energy requirements should be kept small in field operations. In the experiment frequency doubled dye laser pulses at 308 nm are produced. The picosecond light pulses are expected to show a smooth profile (light intensity against wavelength) which will be broadened to the required spectral width according to the uncertainty principle. The pump laser will be an optoacoustically modulated Nd:YAG laser.

Perner, D.↗
NASA NTRS1986

Tunable-diode laser absorption spectrometry

Tunable-diode laser absorption spectrometry (TDLAS) affords a number of advantages for atmospheric measurements. It is a universal method, applicable, in principle, to all gases of atmospheric interest. Because of its extremely high spectral resolution it provides unequivocal identification of the target species, with no interferences from other gases. It provides real-time, in situ measurements with time resolutions better than 1 minute. The sensitivity of the current TDLAS system is marginally capable of measuring HO2. This species exists in the troposphere at concentrations which are up to 2 orders of magnitude higher than those of HO and, in addition, is much less susceptible to removal by the surfaces of the instrument and its sampling system. HO2 is an important HO sub x species in its own right but can also give direct information on the HO concentration by virtue of the rapid partitioning between these two species. The addition of the high-frequency modulation technique to the TDLAS system would ensure its ability to measure HO2 under most atmospheric conditions. The ability of the TDLAS to measure hydrogen peroxide (H2O2) in the ambient atmosphere was also demonstrated. H2O2 measurements give a clear indication of HO sub x mixing ratios and are also important as a photolytic source of HO and as an important oxidant for other atmospheric consitituents such as SO2.

Schiff, H. I.↗
NASA NTRS1986

Photochemical production of H2SO4 aerosols on Venus

The quantum yields for producing O2(a (1 delta g)) and O2(b(1 sigma g +)) for the reaction, O + ClO yields Cl + O2, are summarized. Also included are results for other simple reactions capable of producing the singlet oxygen states. An episodic injection of SO2 into the upper atmosphere of Venus is considered as a possible explanation for the airglow values.

Yuk, L. Yung↗
NASA NTRS1987

Atlas of Absorption Lines from 0 to 17900 Cm (sup)-1

Plots of logarithm (base 10) of absorption line strength versus wavenumber from 0 to 17900/cm(sup)-1 are shown for the 28 atmospheric gases (H2O, CO2, O3, N2O, CO, CH4, O2, NO, SO2, NO2, NH3, HNO3, OH, HF, HCl, HBr, HI, ClO, OCS, H2CO, HOCl, N2, HCN, CH3Cl, H2O2, C2H2, C2H6, PH3), which appear in the 1986 Air Force Geophysics Laboratory high-resolution transmission molecular absorption data base (HITRAN) compilation, and for O(P-3), O-18 isotopic ozone, and HO2 from the 1984 JPL compilation in the 0- to 200/cm(sup)-1 region, and infrared solar CO lines at 4500 K. Also shown are plots of logarithm (base 10) of approximate infrared absorption cross sections of 11 heavy molecules versus wavenumber. The cross-section data cover 700 to 1800/cm(sup)-1 and are included as a separate data file in the 1986 HITRAN database.

Park, J. H.↗
NASA NTRS1986

Mass and energy balance of the cold Io torus

A new model of the cold Io torus is described. Ions and energy are injected into the system by independent processes so that the mass balance is isolated from the energy balance. The primary source of energy is local ionization and acceleration of hot pickup ions resulting from charge exchange between thermal ions and an extended cloud of Iogenic sulfur and oxygen atoms. The primary energy loss mechanism of the plasma is collisionally excited line emission at optical wavelengths. The primary ion source is radial diffusion inward from the hot torus on a time scale of 140-710 days. The primary ion loss mechanism is a novel two-step enhanced recombination mechanism involving charge exchange between thermal ions and an extended cloud of neutral SO2 molecules, followed by rapid dissociative recombination of the resultant molecular ion. The model provides a self-consistent solution which reconciles a number of diverse observations with known physical processes.

Moreno, M. A.↗
NASA NTRS1986

Galileo probe battery systems design

NASA's Galileo mission to Jupiter will consist of a Jovian orbiter and an atmospheric entry probe. The power for the probe will be derived from two primary power sources. The main source is composed of three Li-SO2 battery modules containing 13 D-size cell strings per module. These are required to retain capacity for 7.5 years, support a 150 day clock, and a 7 hour mission sequence of increasing loads from 0.15 to 9.5 amperes for the last 30 minutes. This main power source is supplemented by two thermal batteries (CaCrO4-Ca) for use in firing the pyrotechnic initiators during the atmospheric staging events. This paper describes design development and testing of these batteries at the system level.

Dagarin, B. P.↗
NASA NTRS1986

Radiative forcing of the Venus mesosphere. I - Solar fluxes and heating rates

A radiative-transfer model has been used to derive the structure and amplitude of the solar fluxes and heating rates in the Venus mesosphere, accounting for absorption and scattering extinction sources that encompass CO2, H2O, SO2, and H2SO4 aerosols as well as an unidentified UV absorber. The unknown substance that causes the observed cloud-top UV contrasts is responsible for most of the absorption of sunlight within the upper cloud deck; this contributes to solar heating rates of the order of 6 K/day at levels near 65 km. These results are judged sufficiently reliable for use in numerical dynamical models of the Venus atmosphere.

Crisp, D.↗
NASA NTRS1986

Reactions occurring during the sulfation of sodium chloride deposited on alumina substrates

The reaction between solid NaCl and air containing 1 pct SO2 has been studied between 500 and 700 C. The reaction product, Na2SO4, forms not only on the surface of the NaCl but also on surrounding areas of the substrate due to the volatility of the NaCl at these temperatures. At the higher temperatures, the vapor pressure of NaCl is so high that the majority of the reaction product is distributed on the substrate. Above 625 C, the reaction product is a liquid solution of NaCl and Na2SO4 that exists only so long as NaCl is supplied from the original crystal source. Eventually, the liquid solidifies by constitutional solidification as the NaCl is converted to Na2SO4. While it exists, the liquid NaCl-Na2SO4 solution is shown to be highly corrosive to Al2O3 and, on a scale of Al2O3 growing on alloy HOS 875, particularly attacks the grain boundaries of the scale at preferred sites where chromium and iron oxides and sulfides rapidly develop. This is proposed as one mechanism by which NaCl deposition contributes to the initiation of low temperature hot corrosion.

Wu, C. S.↗
NASA NTRS1986

Evaluation of the microwave spectrum of Venus in the 1.2-22 centimeter wavelength range based on laboratory measurements of constituent gas opacities

Laboratory measurements of the microwave (1.2-22.3 cm) spectrum properties of Venus' gaseous atmospheric constituents were performed using an apparatus for simulating conditions of the middle atmosphere of Venus (gaseous H2SO4 + CO2 at 1 to 6 atm). The results have shown that at wavelengths longer than 1.8 cm, gaseous H2SO4 and CO2 are the predominant microwave absorbers, while at wavelengths from 1.2 to 1.8 cm, SO2 and CO2 are the predominant absorbers. These results were used to develop a model for the microwave emission spectrum of Venus, which correlated well with microwave observations of this planet.

Steffes, Paul G.↗
NASA NTRS1986

Space opportunities for tropospheric chemistry research

The use of the Space Shuttle to measure tropospheric trace species is examined. Factors which affect the measurement of tropospheric trace species are discussed. The Academy of Sciences 1985 report categorized the trace species into levels: first-level gases include water vapor, O3, CO, and CH4, and the second-level gases are N2O, NO2, NH3, SO2, chlorofluoromethanes, and HCl. The effects of first-level gases on the earth's climate, the photochemistry/chemistry of the troposphere, and the photochemical/chemical production and destruction of the hydroxyl radical are studied; the distribution and magnitude of the hydroxyl radical in the troposphere are analyzed in terms of water vapor, O3, CO, and CH4.

Levine, Joel S.↗
NASA NTRS1986

Phase curves of materials on Io - Interpretation in terms of Hapke's function

Disk-resolved near-opposition phase curves, derived for regions on Io suggest differences in surface texture among materials of different color on the satellite. This suggestion is tested quantitatively, using a photometric function having physically meaningful parameters. Derived values of the Hapke compaction parameter suggest that (1) a large percentage of the material on Io's surface has a porosity significantly greater than 60 percent and (2) average and polar materials are significantly more porous than Bright material, a contrast consistent with the Matson and Nash (1983) SO2 cold trap model. For the color classes, and for Io as a whole, the degree of backscattering tends to increase toward longer wavelengths. The average macroscopic roughness of the Ionian surface, characterized by a mean slope angle of about 25 degrees, is similar to that of other solid surfaces in the solar system.

Simonelli, Damon P.↗
NASA NTRS1987

Atlas of reflectance spectra of terrestrial, lunar, and meteoritic powders and frosts from 92 to 1800 nm

The spectra of samples of several powder and frost materials are presented to serve in a reference database for future far-UV scans of solar system bodies. The spectra cover in the 92-1800 nm wavelengths, i.e., wavenumbers 110,000-5600/cm and photon energies from 13.5-1.5 eV. Preparation procedures for the particulates are delineated. The survey includes feldspars, orthopyroxenes, clinopyroxenes, olivines, assorted minerals, achondrites, carbonaceous chondrites and ordinary chondrites, lunar soils and rocks. Frosts of H2O, CO2, NH3 and SO2 gases were also examined. The data are expected to aid in obtaining spectral matches for asteroids and meteoroids when far-UV telescopy of solar system bodies is performed.

Wagner, Jeffrey K.↗