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At least 127 records · Page 7
All sourcesNASA NTRSDOE OSTI
NASA NTRS1980

An upper limit to the global SO2 abundance on Io

An upper limit to the global abundance of SO2 gas in the atmosphere of Io has been derived from observations of near-UV reflectivity made from earth orbit. Spectra in the range 2900-3100 A were obtained by the long-wavelength spectrograph of the IUE, and compared with the convolved solar spectrum of Broadfoot (1972). From the apparent solar origin of all the spectral features, an upper limit of 0.008 cm atm was calculated for the abundance of SO2, which was confirmed by ratio spectra of Vesta. Discrepancies between the upper limit obtained and the detection of a column abundance of 0.2 cm atm by the Voyager 1 IRIS experiment have a number of possible explanations, the most likely of which is that the SO2 atmosphere in Io is patchy, being confined to regions over solid deposits and volcanic vents.

Butterworth, P. S.↗
NASA NTRS1981

Study of sulfur-containing molecules in the EUV region. I - Photoabsorption cross section of SO2

Using synchrotron radiation as a continuum background, the absorption cross sections of SO2 have been measured using a double ionization chamber. The cross sections range from 10 to a maximum value of 56 Mb in the 175-760 A region. A possible window resonance series was observed and tentatively assigned to a Ryberg series converging to the (6a sub 1) to the -1st ion state. From the fluorescence excitation function the vibrational progressions of the SO2(+) ion states have been measured and found in good agreement with those observed from photoelectron spectroscopy. The same correspondence between peaks in the fragment fluorescence excitation function and the photoelectron spectrum suggests that these ion states of SO2 are dissociative in nature.

Wu, C. Y. R.↗
NASA NTRS1981

SO2 and CS2 cross section data in the ultraviolet region

Using synchrotron radiation as a continuum background, the cross sections of SO2 in the 208-228 and 299-340 nm region and of CS2 in the 318-350 nm region have been measured with a bandwidth of 0.06 nm. It has been confirmed that the reported band positions of SO2 in the 170-315 nm region by Warneck et al. (1964) should all be shifted by about 0.3 nm toward shorter wavelengths. An important application of the present results is found in the SO2 and CS2 mixing ratio calculations for Venus and Io.

Wu, C. Y. R.↗
NASA NTRS1982

Carbon-catalyzed oxidation of SO2 by NO2 and air

A series of experiments was performed using carbon particles (commercial furnace black) as a surrogate for soot particles. Carbon particles were suspended in water, and gas mixtures were bubbled into the suspensions to observe the effect of carbon particles on the oxidation of SO2 by air and NO2. Identical gas mixtures were bubbled into a blank containing only pure water. After exposure each solution was analyzed for pH and sulfate. It was found that NO2 greatly enhances the oxidation of SO2 to sulfate in the presence of carbon particles. The amount of sulfate found in the blanks was significantly less. Under the conditions of these experiments no saturation of the reaction was observed and SO2 was converted to sulfate even in a highly acid medium (pH or = 1.5).

Rogowski, R. S.↗
NASA NTRS1982

Fluorescence yields from photodissociation of SO2 at 1060-1330 A

The absorption and fluorescence cross sections of SO2 were measured in the 1060-1330 A region using synchrotron radiation as the light source. Several absorption bands were observed and assigned tentatively to the Rydberg states converging to the SO2(+) states. It is shown that the apparent quantum yields for excitation wavelengths longer than 1200 A are small, and are presumably emitted from the O(1S) and S(1S) metastable species. At shorter excitation wavelengths, the fluorescence cross sections increase at the threshold wavelengths of possible SO2 dissociation processes.

Suto, M.↗
NASA NTRS1982

Oxidation of SO2 by NO2 and air in an aqueous suspension of carbon

A series of experiments has been performed using carbon black as a surrogate for soot particles. Carbon black was suspended in water and gas mixtures were bubbled into the suspensions to observe the effect of carbon particles on the oxidation of SO2 by air and NO2. Identical gas mixtures were bubbled into a black containing only pure water. After exposure each solution was analyzed for pH and sulfate. It was found that NO2 greatly enhances the oxidation of SO2 to sulfate in the presence of carbon black. The amount of sulfate in the blanks was significantly less. Under the conditions of the experiments no saturation of the reaction was observed and SO2 was converted to sulfate even in a highly acid medium (pH not less than 1.5).

Rogowski, R. S.↗
NASA NTRS1983

Limits on Venus' SO2 abundance profile from interferometric observations at 3.4 mm wavelength

The role of SO2 in the chemistry of the clouds of Venus has been investigated by deducing its mixing ratio profile in the atmosphere through millimeter wavelength interferometric measurements of the planet's limb darkening. The first zero crossing of the Venus visibility function was measured to be 0.6221 + or - 0.0007 at a wavelength of 3.4 mm, using a reference radius for Venus of 6100 km. This measurement constrains the amount of limb darkening and shows that the high concentrations of SO2 found in the lower atmosphere do not persist above an altitude of 42 km. Thus, a sink for SO2 exists below the level of the lowest cloud deck.

Good, J. C.↗
NASA NTRS1983

Sputtering of SO2 by high energy ions

Sputtering yields of solid SO2 by high energy ions were measured in order to study the mechanism for sputtering dielectrics with ions in the electronic stopping power region. The incident ions were helium and fluorine with energies ranging from 1.5 MeV to 25 MeV. Yields as high as 7000 SO2 molecules/incident F ion were measured; the 1.5 MeV He-4 beam had a sputtering yield of 50. The data are compared to yield measurements made on UF4 and H2O targets. There is a striking similarity in the yield as a function of the incident F energy for all three targets. The data compare favorably with theoretical yield curves based on a new model for the sputtering which considers the electronic excitations induced in the target by the incident beam. Measurements and calculations of this sort are also useful in understanding processes which occur on the surface of Jupiter's satellite Io, which is covered with SO2 frost and bombarded by energetic ions trapped in the Jovian magnetosphere.

Lepoire, D. J.↗
NASA NTRS1983

Observations of SO2 and HCS(+) in cold molecular clouds

The first instance of SO2 emission from a dark dust cloud (L183), and the first astronomical detections of the J = 1-0 rotational transition of the HCS(+) ion and the J = 16-15 transition of HC5N, both towards the cold cloud TMC-1, are reported. The HCS(+)/CS abundance ratio in TMC-1 is greater than about 0.1. Unlike HCS(+) and the cyanopolyynes, SO2 appears to be more abundant in L183 than in TMC-1. SO2 was also detected in the Orion ambient molecular cloud and in the Rho Oph cloud.

Irvine, W. M.↗
NASA NTRS1983

Measurements of stratospheric SO2 after the EL Chichon eruptions

Samples of stratospheric trace gases were obtained on eight flights of NASA high-altitude aircraft from April 16 through December 13, 1982. The sampling occurred at altitudes from 15 to 22 km, latitudes from 23 to 52 deg N, and longitudes from 108 to 130 deg W. The cryogenically concentrated samples were analyzed by gas chromatography for SO2, a primary precursor of the gas-to-particle conversion process. The measured mixing ratio of SO2 varied between 8 and 132 pptv. Evidence from aerosol measurements indicates that a few of our early samples may have been collected in the fringes of the volcanic cloud from El Chichon. Samples obtained on some later flights may have been from the eruption cloud but were taken at times when most of the volcanically injected SO2 should have been converted to H2SO4.

Vedder, J. F.↗
NASA NTRS1984

An Eulerian transport/transformation/removal model for SO2 and sulfate. I - Model development. II - Model calculation of SO(x) transport in the eastern United States

A three-dimensional, time dependent Eulerian atmospheric SO2 and sulfate transport/transformation/removal model is described and applied to the eastern U.S. The model was developed in anticipation of increased input to the atmospheric sulfur content by coal-burning power plants in the near future and is intended as an aid in identifying sources of SO2. The Eulerian transport model incorporates functions for chemical transformations, dry deposition, spatial topographical variations, spatial and temporal variations of mixing layer heights, the wind field, eddy diffusivities, deposition velocities, and temperature and water concentration profiles. Attention is also given to the SO2 photochemical oxidation mechanism and rates. Results from a 72-hr simulation of SO(x) transport over the eastern U.S., using actual 1974 meteorological data, illustrate the model's capability to depict interactions between emissions, transport, chemistry and removal. Concentration distributions are demonstrated to have significant spatial and temporal variations.

Carmichael, G. R.↗
NASA NTRS1984

Sulfur and oxygen escape from Io and a lower limit to atmospheric SO2 at Voyager 1 encounter

Estimates of the abundance of sulfur, sodium and oxygen ions and neutrals observed by Voyager 1 in the plasma torus and neutral cloud associated with the Jovian satellite Io are used to investigate the physical characteristics of the Io atmosphere. Specific attention is given to two questions about the Io atmosphere: the necessity of an atmosphere to account for the supply of sulfur and oxygen observed in the plasma torus, and, if an atmosphere is necessary, the lower limit to such atmosphere. It is found that an SO2 atmosphere is most likely needed on Io as an intermediate buffer so that the sulfur and oxygen can be transported to the plasma torus. The minimum atmosphere needed for this process is calculated to be 1.4 x 10 to the -10th bar with an SO2 column density of about 10 to the 16th per sq cm and an SO2 surface density of about 1.2 x 10 to the 10th per cu cm. A complete list of all the atmospheric escape fluxes for Io is provided.

Kumar, S.↗
NASA NTRS1986

Rate constant for the reaction SO + BrO yields SO2 + Br

The rate of the radical-radical reaction SO + BrO yields SO2 + Br has been determined at 298 K in a discharge flow system near 1 torr pressure with detection of SO and BrO via collision-free sampling mass spectrometry. The rate constant was determined using two different methods: measuring the decay of SO radicals in the presence of an excess of BrO and measuring the decay of BrO radicals in excess SO. The results from the two methods are in reasonable agreement and the simple mean of the two values gives the recommended rate constant at 298 K, k = (5.7 + or - 2.0) x 10 to the -11th cu cm/s. This represents the first determination of this rate constant and it is consistent with a previously derived lower limit based on SO2 formation. Comparison is made with other radical-radical reactions involving SO or BrO. The reaction SO + BrO yields SO2 + Br is of interest for models of the upper atmosphere of the earth and provides a potential coupling between atmospheric sulfur and bromine chemistry.

Brunning, J.↗
NASA NTRS1987

Episodic vs. epochal release of SO2 on Mars

Erosion of the Martian surface by the flow of liquid water has apparently taken place at different times and locations on the planet. Many attempts were made to explain the valley networks by invoking a strong atmospheric CO2/H2O greenhouse early in the history of the planet. It was assumed that the large amounts of CO2 necessary to cause the greenhouse would have disappeared due to carbonate formation. Carbonates have yet to be positively identified. Volcanism has occurred throughout much of the history of Mars. Presumably gases such as SO2 were released along with CO2 and H2O. Estimates of amounts and rates with which SO2 were released into the Martian atmosphere, and how this would effect the global climate were made. Studies are continuing on the effects of SO2 and other volcanic gases on Martian climatic history.

Postawko, S. E.↗
NASA NTRS1992

SO and SO2 in mass-loss envelopes of red giants - Probes of nonequilibrium circumstellar chemistry and mass-loss rates

SO emission was searched for in one or more of four transitions toward 23 oxygen-rich red giant or supergiant stars and one S star, selected primarily on the basis of their nonmaser SiO emission. SO was detected in a total of 14 circumstellar envelopes, 13 of which are new detections. The circumstellar abundance of SO (and SO2) is significantly enhanced over the equilibrium value achieved in the photospheres of these stars. In general, the SO abundances are significantly larger than predicted by nonequilibrium circumstellar chemistry models. Sulfur cannot be significantly depleted onto circumstellar grains, and probably exists as H2S (and/or SH) in the inner regions of the envelopes. The SO rotational-level population in most circumstellar envelopes observed is characterized by excitation temperatures less than or approximately equal to 50 K. The circumstellar abundance of SO2 is comparable to, or larger than, that of SO, ruling out the 'large' value adopted for the unshielded photodissociation rate for SO2 in recent models.

Sahai, Raghvendra↗
NASA NTRS1992

SO2 on Venus: A final cross-calibration with Pioneer Venus

In our previous report, we noted that we had successfully completed all of the IUE observations which were proposed. A total of 7 Venus spectra were obtained. In the present reporting period, essentially all of the associated data reduction and analysis activities were completed, and Drs. Stern, Barker, and Na met to collaborate on data interpretation. The model atmosphere used in this analysis is similar to the one used in the analysis of the Pioneer Venus observations (Esposito, et al. 1979, 1988) and the previous IUE observations (Na, et al. 1990). In this model, sulfuric acid aerosols with a radius of about 1 micron are mixed uniformly with Rayleigh scattering gases throughout the cloud layer. There are two wavelength-independent absorbers. First, the aerosols are assumed to have a single scattering albedo of 0.98, and second a pure absorbing layer with an optical depth of 0.2 is added at an altitude of 75 mbar. The variable parameters in this model are the mixing ratios of SO2 at the cloud top (40 mbar level), and the scale height of SO2 at the same altitude. Model spectra were calculated using a radiative transfer code utilizing a Markov Chain method. Each model calculation takes into account the multiple scattering and the vertical inhomogeneity of the atmosphere. We reported those initial results at the 1992 meeting of the AAS Division of Planetary Sciences (Barker, Stern, and Na 1992) The important finding we have reached is that the 1991 IUE observations indicate that the long-term decline in Venus SO2 abundance has either halted or reversed. Our simultaneous groundbased measurements made on the McDonald Observatory 2.7 m corroborate this result. We are now preparing a paper describing these IUE results for publication in Icarus. With the IUE results reduced, we are also beginning a project to compare the 1991 IUE results to Pioneer Venus UV spectra made on the same dates.

Stern, S. Alan↗
NASA NTRS1993

Microwave Limb Sounder measurement of stratospheric SO2 from the Mt. Pinatubo volcano

The Microwave Limb Sounder (MLS) experiment on the Upper Atmosphere Research Satellite (UARS) began atmospheric measurements on September 19, 1991. Residual SO2 from the Pinatubo eruption was detected immediately after instrument activation. The SO2 was 1ocated in a tropical band with peak mixing ratios of about 15 ppbv near 26 km altitude. The observed decay of SO2 has provided an estimate of the OH concentration in the plume.

Read, W. G.↗
NASA NTRS1992

The use of TIMS data to estimate the SO2 concentrations of volcanic plumes: A case study at Mount Etna, Sicily

Thermal Infrared Multispectral Scanner (TIMS) data were acquired over Mount Etna, Sicily, on 29 July 1986. The volcanic activity at that time was characterized by the steady effusion of gas from the Bocca Nuova (BN), Chasm, and Southeast craters. The Northeast crater, quiet at the time of the TIMS overflight, was the site of Strombolian eruptive activity between 31 July and 24 Sep. 1986. In aerial photographs of the Etna summit region acquired during the TIMS overflight, the SO2-rich plume is visible due to the scattering of sunlight by the entrained aerosols. In the TIMS imagery, the plume is revealed by the strong absorption of SO2 between 8 and 9 microns. This absorption feature falls within the first three channels of TIMS, with the strongest absorption falling within Channel 2. Following decorrelation processing, the plume is visible in color-composites of TIMS channels 2, 3, and 5. To estimate the concentration of SO2 within the plume, the LOWTRAN 7 radiative transfer code was used to model the radiance spectra measured by TIMS.

Realmuto, Vincent J.↗