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At least 469 records · Page 26
All sourcesNASA NTRSDOE OSTI
NASA NTRS1992

Volatiles in interplanetary dust particles - A review

The paper presents a review of the volatiles found within interplanetary dust particles. These particles have been shown to represent primitive material from early in the solar system's formation and also may contain records of stellar processes. The organogenic elements (i.e., H, C, N, O, and S) are among the most abundant elements in our solar system, and their abundances, distributions, and isotopic compositions in early solar system materials permit workers to better understand the processes operating early in the evolutionary history of solar system materials. Interplanetary dust particles have a range of elemental compositions, but generally they have been shown to be similar to carbonaceous chondrites, the solar photosphere, Comet Halley's chondritic cores, and matrix materials of chondritic chondrites. Recovery and analysis of interplanetary dust particles have opened new opportunities for analysis of primitive materials, although interplanetary dust particles represent major challenges to the analyst because of their small size.

Gibson, Everett K., Jr.↗
NASA NTRS1992

Volatile processes in Triton's atmosphere and surface

A basic model for latitudinal transport of nitrogen is reviewed focusing on its limitations and some complications associated with surface and atmospheric physics. Data obtained by 1989 Voyager encounter with the Neptune system revealed the complexity in the pure nitrogen transport which is caused by the nonuniform albedo of the frosts. It is concluded that Triton is similar to Mars in terms of the complexity of volatile transport and to understand Triton's surface-atmosphere system, Mars may be a very good analog.

Lunine, J. I.↗
NASA NTRS1992

The effect of a non-volatile dust mantle on the energy balance of cometary surface layers

It is likely that large parts of a cometary surface layer consist of porous ices, which are covered by a thin layer of non-volatile debris, whose structure is also fluffy and porous. In this paper the results of model calculations are presented. The calculations show the effect of ice and dust pore sizes and of the dust mantle thickness upon the thermal behavior of such a dust-ice system, when it is irradiated by the sun. In particular, it is found that the average pore size of the ice and the dust material has a large influence both on the dust surface temperature and on the temperature at the dust-ice interface.

Koemle, Norbert I.↗
NASA NTRS1993

Thermal Analyzer for Planetary Soil (TAPS): an in Situ Instrument for Mineral and Volatile-element Measurements

Thermal Analyzer for Planetary Soil (TAPS) offers a specific implementation for the generic thermal analyzer/evolved-gas analyzer (TA/EGA) function included in the Mars Environmental Survey (MESUR) strawman payload; applications to asteroids and comets are also possible. The baseline TAPS is a single-sample differential scanning calorimeter (DSC), backed by a capacitive-polymer humidity sensor, with an integrated sampling mechanism. After placement on a planetary surface, TAPS acquires 10-50 mg of soil or sediment and heats the sample from ambient temperature to 1000-1300 K. During heating, DSC data are taken for the solid and evolved gases are swept past the water sensor. Through ground based data analysis, multicomponent DSC data are deconvolved and correlated with the water release profile to quantitatively determine the types and relative proportions of volatile-bearing minerals such as clays and other hydrates, carbonates, and nitrates. The rapid-response humidity sensors also achieve quantitative analysis of total water. After conclusion of soil-analysis operations, the humidity sensors become available for meteorology. The baseline design fits within a circular-cylindrical volume less than 1000 cm(sup 3), occupies 1.2 kg mass, and consumes about 2 Whr of power per analysis. Enhanced designs would acquire and analyze multiple samples and employ additional microchemical sensors for analysis of CO2, SO2, NO(x), and other gaseous species. Atmospheric pumps are also being considered as alternatives to pressurized purge gas.

Gooding, J. L.↗
NASA NTRS1992

Implications for volcanogenic volatile release on the weathering of Mars

Volcanism on Mars has been widespread in both space and time. Notwithstanding important specific differences between the mantles of Earth and Mars, the similarities are such that the suite of gases emitted from martian volcanic activity surely includes gases such as H2O, CO2, S-containing gases (H2S, SO3, or SO2), and Cl-containing gases (e.g. Cl or HCl). Both H2O and CO2 are present in the atmosphere of Mars; both are also present as surface condensates. Spectroscopic observations of the martian atmosphere clearly show that the S- and Cl-containing gases are severely depleted. Likewise, there is no evidence of surface condensates of compounds of these elements. Within the soil, there is direct evidence of incorporation of H2O and some compounds of sulfur and chlorine. None of the resultant weathering products have been directly identified, but both clays and salts have been indirectly implicated. Other aspects of the implications for volcanogenic volatile release on the weathering of Mars are discussed.

Clark, Benton C.↗
NASA NTRS1992

Volatile history of Mangala Valles, Mars

The Mangala Valles channel system differs from other Mars outflow channels as they emanate from a point source determined by the local interplay of tectonism, volcanism, and volatiles that led directly to the release of groundwater. Water discharge rates through the southern reaches of Mangala Valles may have been substantially lower than estimates determined fron the canyon system as a whole, suggesting that the accumulation and release of water may have lasted longer than previously envisioned. The sequence of events determined from mapping of units along the southern reaches of Mangala Valles is closely related to the area structures.

Zimbelman, James R.↗
NASA NTRS1992

Mars - Epochal climate change and volatile history

The epochal climate change and volatile history of Mars are examined, with special attention given to evidence for and mechanisms of long-term climate change. Long-term climate change on Mars is indicated most directly by the presence, age, and distribution of the valley networks. They were almost certainly formed by running water, but it seems more likely that they were formed by groundwater sapping than by rainfall. It is argued to be physically plausible that a higher early intensity of surface insolation caused by a CO2 greenhouse effect could have overcompensated for an early weak sun and raised temperatures to the freezing point near the equator under favorable conditions of obliquity and eccentricity. This could account for the morphological changes.

Fanale, Fraser P.↗
NASA NTRS1992

Measurement of volatile organic chemicals at selected sites in California

Urban air concentrations of 24 selected volatile organic chemicals that may be potentially hazardous to human health and environment were measured during field experiments conducted at two California locations, at Houston, and at Denver. Chemicals measured included chlorofluorocarbons, halomethanes, haloethanes, halopropanes, chloroethylenes, and aromatic hydrocarbons. With emphasis on California sites, data from these studies are analyzed and interpreted with respect to variabilities in ambient air concentrations, diurnal changes, relation to prevailing meteorology, sources and trends. Except in a few instances, mean concentrations are typically between 0 and 5 ppb. Significant variabilities in atmospheric concentrations associated with intense sources and adverse meteorological conditions are shown to exist. In addition to short-term variability, there is evidence of systematic diurnal and seasonal trends. In some instances it is possible to detect declining trends resulting from the effectiveness of control strategies.

Singh, Hanwant B.↗
NASA NTRS1951

Effect of fuel volatility on performance of tail-pipe burner

Fuels having Reid vapor pressures of 6.3 and 1.0 pounds per square inch were investigated in a tail-pipe burner on an axial-flow-type turbojet engine at a simulated flight Mach number of 0.6 and altitudes from 20,000 to 45,000 feet. With the burner configuration used in this investigation, having a mixing length of only 8 inches between the fuel manifold and the flame holder, the low-vapor-pressure fuel gave lower combustion efficiency at a given tail-pipe fuel-air ratio. Because the exhaust-nozzle area was fixed, the lower efficiency resulted in lower thrust and higher specific fuel consumption. The maximum altitude at which the burner would operate was practically unaffected by the change in fuel volatility.

FUELS - TURBINE ENGINES, RAM JETS, AND PULSE JETS↗
NASA NTRS1993

The correlation of alkalis and aluminum during high-temperature volatilization of albite and nepheline

Our previous study of high-temperature evaporation of mafic targets has shown a systematic enrichment of newly-formed condensates in silicon and alkalis and depletion in refractory elements (Al, Ca, Ti). This effect, which is consistent with the volatility of the elements, was also tested for several experiments with acidic targets. In one case it was the impact evaporation of granite targets using a light-gas gun facility. Analyses of the condensate which was collected during the impact show that it was enriched in Al and Na so that the composition of the condensate became close to nepheline. In the work of Nagahara, an incongruent evaporation of alkali feldspars under stationary conditions has been also proposed. These discoveries required a more detailed study of high-temperaure evaporation of monomineralic Al-silicate targets. In these experiments, we have used samples of oligoclase and of nepheline. Vaporization of samples was performed in a hermetic cell filled with helium at normal temperature and pressure using a powerful Nd-laser focused on the sample. Laser pulses had the following parameters: luminous energy approximately 600 J, duration approximately 10(exp -3) s, density of luminosity was approximately 5 x 10(exp 6) W/sq cm, the temperature of vaporization is about 3000-4000 K. About 4 cm from the sample, a nickel foil was placed on which the condensate was collected. Films of condensate were analyzed using X-Ray Photo-Electron spectrometer ES-2401. The measurement of internal chemical composition and of the charging state of elements through the whole depth of the condensed films was made layer by layer with argon-ion etching of 200 A of the film per step. Results of this study are given. The bottom layers of condensed film correspond to the front parts of the evaporated cloud or to condensation at the beginning of the evaporative process and surface layers to condensation at the end of the process.

Dikov, Yu. P.↗
NASA NTRS1993

Trace element content of chondritic cosmic dust: Volatile enrichments, thermal alterations, and the possibility of contamination

Trace element abundances in 51 chondritic Interplanetary Dust Particles (IDP's) were measured by Synchrotron X-Ray Fluorescence (SXRF). The data allow us to determine an average composition of chondritic IDP's and to examine the questions of volatile loss during the heating pulse experienced on atmospheric entry and possible element addition due to contamination during atmospheric entry, stratospheric residence, and curation.

Flynn, G. J.↗
NASA NTRS1992

Factors controlling fluxes of volatile sulfur compounds in Sphagnum peatlands

Exchange of DMS and OCS between the surface of Sphagnum peatlands and the atmosphere were measured with dynamic (S-free sweep air) and static enclosures. DMS emission rates determined by both methods were comparable. The dynamic method provided positive OCS flux rates (emission) for measurements performed at sites containing Sphagnum. Conversely, data from the static method indicated that OCS was consumed from the atmosphere. Short and long-term impacts of increased S deposition on fluxes of volatile S compounds (VSC's) from Sphagnum peatlands were investigated in a poor fen (Mire 239) at the Experimental Lakes Area, Ontario, Canada. Additional experiments were conducted in a poor fen (Sallie's Fen in Barrington, NH, USA). At Mire 239, emissions of VSC's were monitored, before and after acidification, at control and experimental sections within two major physiographic areas of the mire (oligotrophic and minerotrophic). DMS was the predominant VSC released from Mire 239 and varied largely with time and space. Sulfur addition did not affect DMS emissions in a period of hours to a few days. DMS emissions in the experimental oligotrophic area of the mire was approximately 3-fold greater than in the control oligotrophic area, and approximately 10-fold greater than in the minerotrophic zones. These differences could be due to a combination of differences in types of vegetation, nutritional status, and S input. At Sallie's Fen, DMS fluxes were not significantly affected by sulfate amendments, while DMS and MSH concentrations increased greatly with time in the top 10 cm of the peat column. The major environmental factors controlling fluxes of DMS in a Sphagnum-dominated peatland were investigated in Sallie's Fen, NH. DMS emissions from the surface of the peatland varied greatly over 24 hours and seasonally. Temperature seemed to be the major environmental factor controlling these variabilities. Concentrations of dissolved VSC's varied with time and space throughout the fen. Dissolved DMS, MSH, and OCS in the surface of the water table were supersaturated with respect to their concentrations in the atmosphere. Sphagnum mosses did not appear to be a direct source of VSC's, however they increase transport of DMS from the peat surface to the atmosphere.

Demello, William Zamboni↗
NASA NTRS1992

Effects of inorganic sulfur addition on fluxes of volatile sulfur compounds in Sphagnum peatlands

Short and long-term impacts of increased S deposition on fluxes of volatile S compounds (VSC's) from Sphagnum peatlands were investigated in an artificially acidified (sulfuric and nitric acids) poor fen (Mire 239) at the Experimental Lakes Area (ELA), Ontario, Canada. Additional experiments were conducted in a poor fen (Sallie's Fen) in Barrington, NH, USA. At Mire 239, emissions of VSC's were monitored, before and after acidification, at control (unacidified) and experimental sections within two major physiographic zones of the mire (oligotrophic and minerotrophic). The experimental segments of the mire received S amendments since 1983, in amounts equivalent to the annual S deposition in the highest polluted areas of Canada and U.S. Dimethyl sulfide (DMS) was the predominant VSC released from the mire and varied largely with time and space (i.e., from 2.5 to 127 nmol/m(sup -2)h(sup -1)). Sulfur addition did not affect DMS emissions in a period of hours to a few days, although it stimulated production of DMS and MSH in the anoxic surficial regions of the peat. DMS emissions in the experimental oligotrophic segment of the mire was approximately 3-fold greater than in the control oligotrophic segment, and approximately 10-fold greater than in the minerotrophic zones. These differences could be due to a combination of differences in types of vegetation, nutritional status, and S input. At Sallie's Fen, DMS fluxes were approximately 8 times higher from a Sphagnum site than from a bare peat site. Fluxes of VSC's were not significantly affected by sulfate amendments at both sites, while DMS and MSH concentrations increases greatly with time in the top 10 cm of the peat column. Our data indicated that although Sphagnum is not the direct source of DMS released from Sphagnum peatlands, it might play a role in regulating DMS emissions to the atmosphere.

Demello, William Zamboni↗
NASA NTRS1993

Volatility in the lunar crust: Trace element analyses of lunar minerals by PIXE proton microprobe

In situ determination of mineral compositions using microbeam techniques can characterize magma compositions through mineral-melt partitioning, and be used to investigate fine-grained or rare phases which cannot be extracted for analysis. Abundances of Fe, Mn, Sr, Ga, Zr, Y, Nb, Zn, Cu, Ni, Se, and Sb were determined for various mineral phases in a small number of lunar highlands rocks using the PIXE proton microprobe. Sr/Ga ratios of plagioclase and Mn/Zn ratios of mafic silicates show that the ferroan anorthosites and Mg-suite cumulates are depleted in volatile lithophile elements to about the same degree compared with chondrites and the Earth. This links the entire lunar crust to common processes or source compositions. In contrast, secondary sulfides in Descartes breccia clasts are enriched in chalcophile elements such as Cu, Zn, Ni, Se, and Sb, and represent a potential resource in the lunar highlands.

Norman, M. D.↗
NASA NTRS1993

Elevation and igneous crater modification on Venus: Implications for magmatic volatile content

Although most impact craters on Venus preserve nearly pristine crater rim and ejecta features, a small number of craters have been identified showing clear evidence of either igneous intrusion emplacement (floor-fracturing) beneath the crater floor or of volcanically embayed exterior ejecta deposits. Since the volcanically embayed craters consistently occur at higher elevations than the identified floor-fractured craters, this report proposes that igneous crater modification on Venus is elevation dependent. This report describes how regional variations in magmatic neutral buoyancy could produce such elevation dependent crater modification and considers the implications for typical magmatic volatile contents on Venus.

Wichman, R. W.↗
NASA NTRS1994

Non-volatile, solid state bistable electrical switch

A bistable switching element is made of a material whose electrical resistance reversibly decreases in response to intercalation by positive ions. Flow of positive ions between the bistable switching element and a positive ion source is controlled by means of an electrical potential applied across a thermal switching element. The material of the thermal switching element generates heat in response to electrical current flow therethrough, which in turn causes the material to undergo a thermal phase transition from a high electrical resistance state to a low electrical resistance state as the temperature increases above a predetermined value. Application of the electrical potential in one direction renders the thermal switching element conductive to pass electron current out of the ion source. This causes positive ions to flow from the source into the bistable switching element and intercalate the same to produce a non-volatile, low resistance logic state. Application of the electrical potential in the opposite direction causes reverse current flow which de-intercalates the bistable logic switching element and produces a high resistance logic state.

Williams, Roger M.↗
NASA NTRS1994

Volatiles in the Earth: All shallow and all recycled

A case can be made that accretion of the Earth was a high-temperature process and that the primordial Earth was dry. A radial zone-refining process during accretion may have excluded low-melting point and volatile material, including large-ion lithophile elements toward the surface, leaving a refractory and zoned interior. Water, sediments and altered hydrous oceanic crust are introduced back into the interior by subduction, a process that may be more efficient today than in the past. Seismic tomography strongly suggests that a large part of the uppermantle is above the solidus, and this implies wet melting. The mantle beneath Archean cratons has very fast seismic velocities and appears to be strong to 150 km or greater. This is consistent with very dry mantle. It is argued that recycling of substantial quantities of water occurs in the shallow mantle but only minor amounts recycle to depths greater than 200 km. Recycling also oxidizes that mantle; ocean island ('hotspot') basalts are intermediate in oxidation state to island-arc and midocean ridge basalts (MORB). This suggests a deep uncontaminated reservoir for MORB. Plate tectonics on a dry Earth is discussed in order to focus attention on inconsistencies in current geochemical models of terrestrial evolution and recycling.

Anderson, Don L.↗
NASA NTRS1994

Dynamics of volatile delivery from outer to inner solar system

Owen et al. propose that the Ar excess of Venus compared to Earth was caused by impact of a large icy planetesimal from the outer solar system, where temperatures were low enough for Ar to adhere to ice, about 30 K. A body of solar Ar/Si and C/H similar to Pluto and Triton less than 100 km diameter would suffice. However, direct delivery from the Uranus-Neptune zone to Venus would result in a very high approach velocity, causing erosion rather than accretion of volatiles. It would also be an extremely improbable event. Virtually all icy bodies scattered from the Uranus-Neptune zone to the terrestrial zone were strongly perturbed by Jupiter, but even then arrived at Venus (or Earth) at too-high velocities. What is needed is a 'deboost' of bodies scattered inward from Jupiter by Earth and Venus perturbations, prior to impact into Venus. This has low probability, since the influence radii of Venus and Earth for the high velocities are small compared to that of Jupiter for the lower velocities further out. It is desirable that this problem be examined by an integerator that allows for close approaches, such as developed by Levison and Duncan. However, it would be a long and expensive computation compared to explaining short-period comets to accomplish the third 'deboost' phase. But since close encounters dominate in such distant scattering, an Opik algorithm seems the appropriate reconnaissance tool.

Kaula, W. M.↗