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At least 1,135 records · Page 63

Oxidation of CS2 and COS - sources for atmospheric SO2

The oxidation of COS and CS2 by reaction with hydroxyl radicals is investigated as a possible source of atmospheric SO2 in remote marine regions. Calculations of the vertical profiles of SO2 were performed based on a one-dimensional photochemical model of the formation and destruction of SO2 by various processes for observed O3, CO, CH4 and H2O profiles at 15 deg S. Variations in the rate of SO2 destruction, the chosen deposition velocity and the loss due to aerosols are shown to lead to similar SO2 profiles, which indicate higher mixing ratios at high altitude, while the oxidation of dimethyl sulfide or hydrogen sulfide can not account for the profiles observed. Possible diffuse sources of CS2 and COS are indicated, and it is concluded that the oxidation of COS and possibly CS2 may provide an explanation for the existence of a uniform background level of SO2.

Logan, J. A.↗

Fast-response atmospheric-pollutant monitor

Fast infrared spectrometer measures atmospheric C0, CH4, and HC1 over range of 1 to 12 ppm. With modifications it could measure other pollutants and use natural light as source. Cell filled with sample to be measured filters out spectral lines of interest. Infrared beam passes through rotating cell holder that produces chopped signals at two frequencies. Difference in signal amplitudes depends on amount of test gas in sample. Signal processing circuitry amplifies and separates test-gas and reference signals.

Sebacher, D. I.↗

Large area silicon sheet by EFG

Recent advances toward silicon growth stations and improved electronic quality of multiplesilicon are discussed. These advances were made in large measure by studies in which the composition of the gas environment around the meniscus area was varied. By introducing gases such as CO2, CO, and CH4 into this region, reproducible increases in diffusion length and cell performance were realized, with the best large area (5 cm x 10 cm) cells exceeding 11% efficiency.

Source record↗

Jupiter and Saturn - Near-infrared spectral albedos

The near-infrared (0.65-2.5 micron) spectral albedo of Jupiter and Saturn with 1.5% spectral resolution is presented for the center of disk and for the limb. There is a distinct difference in the continuum slope between Jupiter and Saturn which may be attributed to a difference in the dust content or composition of the two atmospheres. There is an indication of limb brightening in the deepest CH4 bands on Saturn. No limb brightening is found for Jupiter.

Clark, R. N.↗

Phosphine absorption in the 5-micron window of Jupiter

Since the original suggestion by Gillett et al. (1969) it has generally been assumed that the region of partial transparency near 5 micron in Jupiter's atmosphere (the 5-micron window) is bounded by the nu sub 4 NH3 at 6.1 micron and the nu sub 3 CH4 band at 3.3 micron. New measurements of Jupiter and of laboratory phosphine (PH3) samples show that PH3 is a significant contributor to the continuum opacity in the window and in fact defines its short-wavelength limit. This has important implications for the use of 5-micron observations as a means to probe the deep atmospheric structure of Jupiter. The abundance of PH3 which results from a comparison of Jovian and laboratory spectra is about 3 to 5 cm-am. This is five to eight times less than that found by Larson et al. (1977) in the same spectral region, but is in good agreement with the result of Tokunaga et al. (1979) from 10-micron observations.

Beer, R.↗

On the clouds of Uranus

Several models for the atmosphere of Uranus are considered. If the H2 abundance is less than 250 km-am and the internal heat source is only a few percent of the total emitted energy then the cloud at the base of the atmosphere may be composed of solid CH4 particles, while if the H2 abundance is greater than 250 km-am or if the internal heat source is near the current upper limit of 35% of the total emitted energy the cloud at the base of the atmosphere may be composed of either solid NH3 or H2S particles.

Macy, W., Jr.↗

The infrared spectra of Uranus, Neptune, and Titan from 0.8 to 2.5 microns

The paper combines the results of two projects that significantly augment previous studies: exploratory IR spectroscopic observations of Uranus, Neptune, and Titan using a 4-m telescope; and new long-path laboratory comparison spectra of methane at abundances appropriate for these planetary spectra. The observations of these previously unexplored spectral regimes provide new insights into the composition and structures of these atmospheres. The spectra of Uranus, Neptune, and Titan are discussed and analyzed from several complementary points of view. A number of specific topics are discussed in detail: methane abundance determinations, limitations in using the 3nu3 CH4 band at high abundances, upper limits to a number of molecules, implications from the pressure-induced spectrum of H2, and consequences of Rayleigh scattering in Uranus's upper atmosphere.

Fink, U.↗

Trace gas concentrations, intertropical convergence, atmospheric fronts, and ocean currents in the tropical Pacific

Descriptions of the intertropical convergence zones (ITCZ) in the tropical Pacific have been obtained from shipboard measurements of Rn-222, CO, and CH4 in combination with conventional meteorological data and satellite images. The intertropical convergence zone is marked by light shifting waves near an area of heavy cloud cover and precipitation, and appears to be located north and south of the south equatorial current. A 'second' ITCZ with the same atmospheric features was encountered just north of the south equatorial current in the Southern Hemisphere. Atmospheric Rn-222 increases north of the ITCZ and serves as a sensitive indicator for this atmospheric boundary.

Wilkniss, P. E.↗

Variability of Lyman-alpha emission from Jupiter

The Jovian Lyman-alpha emission line was reobserved in 1978 March using the high-resolution spectrometer of the Copernicus satellite. An intensity of 8.3 plus or minus 2.9 kilorayleighs was measured. This value represents a significant increase in intensity over previous (1976) Copernicus observations, but is lower than the recent (1979) values obtained by Voyager 1 and IUE. The increase in intensity has been accompanied by a significant increase in line width giving strong support to the theory that the emission results from resonant scattering of the solar Lyman-alpha line by H atoms in the upper Jovian atmossphere. The strength of Jovian Lyman-alpha emission correlates well with the level of solar activity. The solar extreme ultraviolet radiation varies with the solar cycle. This radiation causes the dissociation of H2 and CH4 into H atoms in the Jovian atmosphere. Therefore, in times of high solar activity, the H column density will increase, causing the observed strong Jovian Lyman-alpha emission.

Cochran, W. D.↗

Climatic effects due to halogenated compounds in the earth's atmosphere

Using a one-dimensional radiative-convective model, a sensitivity study is performed of the effect of ozone depletion in the stratosphere on the surface temperature. There could be a cooling of the surface temperature by approximately 0.2 K due to chlorofluoromethane-induced ozone depletion at steady state (assuming 1973 release rates). This cooling reduces significantly the greenhouse effect due to the presence of chlorofluoromethanes. Carbon tetrafluoride has a strong nu sub 3 band at 7.8 microns, and the atmospheric greenhouse effect is shown to be 0.07 and 0.12 K/ppbv with and without taking into account overlap with CH4 and N2O bands. At concentrations higher than 1 ppbv, absorption by the nu sub 3 band starts to saturate and the greenhouse effect becomes less efficient.

Wang, W.-C.↗

Product distribution for the reaction of HO2 with ClO

The paper reports the direct measurement of the reaction product HOCl from the reaction of H2O with ClO, and sets an upper limit for the possible product O3, using a discharge flow/mass spectrometry/resonance fluorescence apparatus. The upper limits of the reaction channel producing HCl + O3 are 1.5% at 298 K and 3.0% at 248 K. It is seen that the HCl production rate from the HO2 + ClO reaction could be as large as that from the Cl + CH4 reaction in the lower and middle stratosphere. Thus, this reaction may possibly increase the HCl production rate appreciably and thereby reduce the calculated O3 destruction by chlorofluoromethanes.

Leu, M.-T.↗

The fate of the hydroxyl radical in the earth's primitive atmosphere and implications for the production of molecular oxygen

Behavior of the hydroxyl radical produced by the photolysis of water vapor in the earth's early atmosphere is examined. Because of the substantial OH radical reactivity with trace species (CO, HCl, SO2, H2S, NH3, and CH4) the formation of molecular oxygen may be prevented, even at a trace species mixing ratio. The photolysis rate of H2O, with corrections for hydrogen exospheric escape, is capable of describing the oxidation of the atmosphere and crust but may not be used to determine the rate of molecular oxygen generation without consideration of the various OH-trace species reactions.

Vander Wood, T. B.↗

Longitudinal variability of methane and ammonia bands on Jupiter

Results of a quantitative study of the longitudinal variations of methane and ammonia absorption on Jupiter are presented. A total of 78 high signal-to-noise ratio photoelectric spectra in the range 6000 to 6600 A were obtained on two consecutive nights, with complete longitudinal equatorial coverage each night through 9-min exposures covering a total of over 9 h. Analysis of the equivalent widths of the CH4 6190 A and NH3 6450 A absorption bands by means of a blind, automated, self-consistent method of continuum determination reveals large equivalent widths in both bands near longitudes of 35 and 340 deg and small equivalent widths near 150 deg, with a high degree of correlation between the equivalent widths of the bands. Continuum molecular absorption is found to be slightly negatively correlated with band equivalent widths. Radiative transfer calculations based on the model of Sato and Hansen (1979) using a doubling and adding technique indicate that the observed longitudinal variables of equivalent widths and continuum reflectivity are the results of longitudinal variations in ammonia cloud altitude.

Cochran, W. D.↗

Kinetic inhibition of CO and N2 reduction in the solar nebula

It is shown that the conversion of CO to methane and of N2 to ammonia in the primitive solar nebula was probably so slow relative to radial mixing rates or nebula evolutionary rates that only small amounts of NH3 and CH4 could have been present. Thus most of the nitrogen was present as N2 and most of the carbon as CO and CO2 throughout the nebula. The consequences of this kinetic effect upon the composition of cometary ices and of the Jovian planets, the melting and outgassing behavior of ice rich planetary satellites, and the abundance of carbon in the terrestrial planets are briefly discussed.

Lewis, J. S.↗

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.↗

An experiment concept to measure stratospheric trace constituents by Laser Heterodyne Spectroscopy

The concept and techniques of a Laser Heterodyne Spectrometer experiment for measuring the vertical profiles of several stratospheric trace gases are discussed. The goal of the experiment is to develop a laser heterodyne receiver capable of measuring 2-4 gases simultaneously from Spacelab and, ultimately, from free-flying platforms. Sensitivity analyses are currently being performed for tenuous molecules such as ClO, ClONO2, NOCl, HO2, H2O2, and N2O5, although the capability exists for measuring more abundant gases, such as O3, HNO3, N2O, NO2, and CH4. Results indicate that O3 and ClO vertical profiles can be measured with an accuracy equal to or better than 95% and 80%, respectively, over the total profile. Laboratory measurements of the performance characteristics of the local oscillator and heterodyne detector are discussed with reference to 'excess-noise' and Doppler-shift effects.

Allario, F.↗

Stratospheric H2O

The present state of our knowledge and understanding of H2O in the stratosphere is reviewed. This reveals continuing discrepancies between observations and expectations following from the Brewer-Dobson hypothesis of stratospheric circulation. In particular, available observations indicate unexplained upward and poleward directed H2O gradients immediately downstream from the tropical tropopause and variable vertical gradients above 20 km which generally disagree with those expected from oxidation of CH4.

Ellsaesser, H. W.↗

A model for gas phase chemistry in interstellar clouds. II - Nonequilibrium effects and effects of temperature and activation energies

The chemical evolution of diffuse and dense interstellar clouds is examined via the time-dependent model outlined by Prasad and Huntress (1980). This paper presents specific results for CH, CO, CH4, O2, CH2O, CN, C2, C2H, HC3N, and NH3. Comparison with observations and predictions of other contemporary models show that cloud temperature plays a very important role through the inverse temperature dependence of radiative association reactions and through activation energies in neutral reactions and selected ion-molecule reactions. The observed fractional abundance of CN with respect to H2 and more accurate recent laboratory data on CN + O and CN + O2 reactions suggest that there is an unidentified, yet efficient, mechanism for conversion of O and O2 into polyatomic species. C2H and HC3N are synthesized early in the history of dense clouds. The value of the fractional abundance of C2H remains high, because as the cloud cools down the activation energy in the C2H + O reaction closes down this most important loss channel. A rapidly decreasing fractional abundance of O with time can also accomplish the same result. The value of the fractional abundance of HC3N remains high because it is an unreactive molecule and probably does not condense readily onto grains.

Prasad, S. S.↗