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At least 253 records · Page 14

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NASA NTRS1980

A meteoritic component rich in volatile elements - Its characterization and implications

An analysis of a study of minerals unique to enstatite chondrites, an unusual group of meteorites characterized by highly reduced mineral assemblages, is presented. Various samples of crushed fragments of the Abee meteorite were studied and the normal procedures for identifying the minerals in sections and then extracting them were reversed. An unusual carbon-rich material was found that is highly enriched in volatile elements by factors of 10000 relative to the case for nonvolatile elements. It is believed that this volatile-rich material forms in the solar nebula toward the end of accretion, when small amounts of residual dust acquire all the uncondensed volatile elements.

Ganapathy, R.↗

NASA NTRS1980

Moon and earth - Compositional differences inferred from siderophiles, volatiles, and alkalis in basalts

A comparison of RNAA analyses of 18 trace elements in 25 low-Ti lunar and 10 terrestrial oceanic basalts indicated that the volatiles such as Ag, Bi, and Br are depleted in lunar basalts by nearly constant factors of 0.026 relative to terrestrial basalts. This constancy is not consistent with models that derive the moon's volatiles from partial recondensation of the earth's mantle or from partial degassing of a captured body; it is consistent with models which derive planetary volatiles from a thin veneer of C-chondrite material. Chalcogens (Se and Te) have almost constant and identical abundances in lunar and terrestrial basalts; siderophiles show abundant Ni in lunar basalts, while Ir, Re, Ge, and Au are depleted.

Wolf, R.↗

NASA NTRS1980

Redistribution of volatiles during lunar metamorphism

Thermal release profiles of Pb, Zn, and Cd in sample 66095 (highly shocked breccia with melt rock matrix) showed that these volatiles were mostly present on the surface of the grains. Zn in rusty grains from 66095 was also mostly surface Zn, probably from sphalerite in grain boundaries and cracks. Simulation experiments of volatile transfer showed that Fe, FeCl2, iron phosphide, and troilite (FeS) can be produced and transported during subsolidus reactions. These results suggest that volatiles, rust, schreibersite, and possible siderophiles which are observed in lunar highland samples might have been redistributed during disequilibrium thermal metamorphism in hot ejecta blankets, and were not necessarily introduced by volcanic activity or meteoritic addition.

Cirlin, E. H.↗

NASA NTRS1982

Conference on Planetary Volatiles

Initial and present volatile inventories and distributions in the Earth, other planets, meteorites, and comets; observational evidence on the time history of volatile transfer among reservoirs; and volatiles in planetary bodies, their mechanisms of transport, and their relation to thermal, chemical, geological and biological evolution were addressed.

Hrametz, K.↗

NASA NTRS1982

Conference on Planetary Volatiles

Pepin, R. O.↗

NASA NTRS1982

The infrared spectral properties of frozen volatiles

Since Whipple's dirty snowball model of comet nuclei, it has been generally accepted that volatile ices help to explain cometary phenomena. The infrared spectral properties of many substances that are potential candidates for frozen volatiles in the solar system are being pursued; indeed some of these frozen materials have been found in the solar system: H2O, CO2, and SO2. A review of laboratory spectra in the range 1 to 20 microns of H2O, CO2, SO2, CH4, NH3, H2S, CO, NH4HS and NH3.H2O is presented. Both reflection spectra of thick frosts and transmission spectra of thin films are shown, and their main characteristics are described. Hydrates, clathrates, and composite spectra are discussed. When it is possible to observe the nuclei of comets at close range, it may be possible to identify frozen volatiles by their infrared spectra.

Fink, U.↗

NASA NTRS1982

Absence of silicic volcanism on Mars - Implications for crustal composition and volatile abundance

It is believed that explosive basic to ultrabasic eruptions may be responsible for small cinder conelike features on Mars and perhaps for the ancient flank-scoured paterae. Eruptions of this type may have been driven by near-surface water/ice-magma interactions or volatile rich magmas. Noting that the paterae represent a unique style of volcanism that stopped approximately 2 b.y. ago, it is suggested that the volatiles associated with these features were derived from mantle sources and that the cessation of patera formation may coincide with the termination of the period of maximum planetary degassing. Since approximately 2 b.y. ago volcanism has been dominantly effusive, except for such minor explosive ash events as those that blanketed part of the summit of Hecates Tholus. It is proposed that such eruptions were driven by volatiles generated by differentiation of a magma chamber, similar to Icelandic explosive eruptions.

Francis, P. W.↗

NASA NTRS1986

Volatile components and continental material of planets

It is shown that the continental material of the terrestrial planets varies in composition from planet to planet according to the abundances and composition of true volatiles (H20, CO2, etc.) in the outer shells of the planets. The formation of these shells occurs very early in a planet's evolution when the role of endogenous processes is indistinct and continental materials are subject to melting and vaporizing in the absence of an atmosphere. As a result, the chemical properties of continental materials are related not only to fractionation processes but also to meltability and volatility. For planets retaining a certain quantity of true volatile components, the chemical transformation of continental material is characterized by a close interaction between impact melting vaporization and endogeneous geological processes.

Florenskiy, K. P.↗

NASA NTRS1986

The effect of oxygen pressure on volatility and morphology of LaB6 single crystal cathodes

The effect of oxygen pressure on the volatility and morphology of single crystal LaB6 cathodes, heated to different temperatures, was investigated. At a temperature of 1600 K, an increase of oxygen pressure from 1 x 10 to the -8th torr to 1 x 10 to the -6th torr has led to a 100-fold enhancement in cathode volatility. The enhancement effect of oxygen pressure diminished with increasing temperature: at a cathode operating temperature of 1900 K, the volatility enhancement due to the same oxygen pressure was negligible. It was shown that the faceting frequently observed during evaporation of conically shaped emitters is due to a crystallograpic anisotropy of the oxidation rate of LaB6. No facet formation occurs during evaporation at oxygen pressures below -110 to the -8th torr.

Davis, P. R.↗

NASA NTRS1986

Origin of the earth's moon - Constraints from alkali volatile trace elements

Although the moon is depleted in volatile elements compared to the earth, these depletions are not in accord with simple volatility. For example, the Cs/Rb ratios of the earth and moon inferred from basalt are approximately one seventh and one half of the CI ratio, respectively. Volatility considerations alone predict that the lunar Cs/Rb ratio should be equal to or lower than the terrestrial ratio if the moon was derived entirely from earth mantle material. Thus hypotheses such as rotational fission which invoke derivation of lunar material entirely from the earth's mantle may be excluded. The collisional ejection hypothesis of lunar origin requires at least 18 percent of lunar material to be derived from a projectile with dehydrated CI composition to match the lunar Cs/Rb ratio, and 25-50 percent to match both the lunar Cs/Rb ratio and absolute concentrations of Cs and Rb. It remains to be demonstrated that this relatively large contribution of projectile material is consistent with other elemental abundances and element ratios in the moon.

Kreutzberger, M. E.↗

NASA NTRS1986

The formation of volatile corrosion products during the mixed oxidation-chlorination of cobalt at 650 C

The reaction of cobalt with 1 pct Cl2 in 1, 10, and 50 pct O2/Ar atmospheres has been studied at 650 C with thermogravimetry and mass spectrometry. The principal vapor species appear to be CoCl2 and CoCl3. In all cases, CoCl2(s) forms at the oxide/metal interface and equilibration of the volatile chlorides with Co3O4 does not occur in the early stages of the reaction. In the 1 pct Cl2 1 pct O2-Ar case, continuous volatilization occurs. In the 1 pct Cl2-10 pct O2-Ar and 1 pct CL2-50 pct O2-Ar cases, volatilization occurs only in the first few minutes of reaction. Afterwards, the reaction is predominantly oxidation.

Jacobson, N. S.↗

NASA NTRS1988

Cosmochemical trends of volatile elements in the solar system

Chemical interactions between gases and grains in the solar nebula played a central role in establishing the presently observed volatile element inventories of the planets, their satellites, and the other bodies in the solar system. Kinetic constraints relevant to gas-grain chemical interactions in the solar nebula are reviewed. The abundant, chemically active volatiles H, O, C, N, and S are emphasized; however, less abundant volatiles such as P, Cl, and F are discussed where appropriate.

Fegley, Bruce, Jr.↗

NASA NTRS1987

Comets, volcanism, the salt rich regolith and cycling of volatiles on Mars

The composition of the Martian surface and its evolution are examined, reviewing the results of recent theoretical models and composition estimates based on Viking lander analyses. The data are compiled in tables and characterized in detail, and a high degree of variation among the predictions is noted. The discussion centers on the possible roles of comets (as sources of volatiles), the salt rich regolith (as an important water sink), and volcanic activity (interfering with volatile-recycling processes and eventually producing a volatile depleted surface layer).

Clark, Benton C.↗

NASA NTRS1988

Moderately volatile elements

That the fractionation of moderately volatile and highly volatile elements was a major process in the early solar system is reflected in the variable concentrations of Rb and associated variations in initial Sr-isotopic ratios in chondritic meteorites. Greater knowledge of processes leading to volatile depletion would place stronger constraints on the formation conditions of solid material in the solar system. It will especially become possible to ascertain whether evaporation or incomplete condensation was the major process in establishing the elemental abundance patterns observed in primitive meteorites and planets.

Palme, H.↗

NASA NTRS1989

Asteroid volatiles inventory

Asteroids appear in light of telescopic and meteority studies to be the most accessible repositories of early solar system history available. In the cooler regions of the outer asteroid belt, apparently unaffected by severe heating, the C, P, and D populations appear to harbor significant inventories of volatiles; the larger primordial belt population may have had an even greater percentage of volatile-rich, low-albedo asteroids, constituting a potent asteroid for veneering early terrestrial planet atmospheres. The volatile-rich asteroids contain carbon, structurally bound and adsorbed water, as well as remnants of interstellar material predating the solar system.

Lebofsky, L. A.↗

NASA NTRS1989

Volatile fractionation and tektite source material

The arguments used by Love and Woronow (1988) to assess the role played in the origin of bediasites by extensive volatile fractionation are critically examined. Using the ratios of 'refractory' oxides, CaO, Al2O3, and MgO, to the 'volatile' oxides, Na2O and K2O, these authors concluded that vapor fractionation did not play a significant role. In this paper, experimental evidence is presented that shows that the assumption of volatility for the alkali elements (as least with respect to silica) to be not valid under the conditions under which tektites formed. It is shown that the results of vapor fractionation in experiments on glasses of tektite composition are approximately parallel the trends seen in bediasite analysis.

Walter, Louis S.↗

NASA NTRS1990

In situ extraction and analysis of volatiles and simple molecules in interplanetary dust particles, contaminants, and silica aerogel

Results are presented for the analyses of eight interplanetary dust particles (IDPs) for the volatile elements H, C, N, O, and S and their molecular species, as well as of the volatiles associated with contaminants (i.e., the compounds used during the collection and curation of IDPs), which were carried out using a laser microprobe interfaced with a quadrupole mass spectrometer. It was found that the volatile species from contaminants were always present in the spectra of IDPs. Despite the contamination problems, several indigenous molecular species could be identified, including OH, CO2 or C2H4, C and CS2, CO2 along with CO (possibly indicating the presence of carbonate), H2S, SO, COS, SO2, and CS2. In some cases, the sulfur components can be attributed to aerosols; however, in one of the IDPs, the presence of H2S, SO, COS, and SO2 indicates the possible presence of elemental sulfur.

Hartmetz, C. P.↗

NASA NTRS1989

Thermal evolution of the earth - Effects of volatile exchange between atmosphere and interior

The thermal history of the earth is investigated using a parameterized model of mantle convection, that includes the effects of volatile exchange between the mantle and the surface reservoir and the softening of the mantle by the dissolved volatiles. The mantle degassing rate is taken to be directly proportional to the rate of seafloor spreading which depends on the mantle heat flow. It is shown that the dependence of the mantle viscosity on the volatile content has important effects on the thermal evolution of planetary interiors and the evolution of planetary atmospheres. Degassing is compensated by an increase in temperature, while regassing is compensated by a decrease in temperature. Reasonable degassing scenarios can account for an early rapid formation of the earth's atmosphere inferred from noble gas abundances.

Mcgovern, Patrick J.↗