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NASA NTRS1973

Volatile elements in Apollo 16 samples - Possible evidence for outgassing of the moon.

Several Apollo 16 breccias, including one containing goethite, are strikingly enriched in volatile elements such as bromine, cadmium, germanium, antimony, thallium, and zinc. Similar but smaller enrichments are found in all highland soils. It appears that volcanic processes took place in the lunar highlands, involving the release of volatiles including water. The lunar thallium/uranium ratio is .0002 of the cosmic ratio, which suggests that the moon's original water content could not have exceeded the equivalent of a layer 22 meters deep. The cataclastic anorthosites at the Apollo 16 site may represent deep ejecta from the Nectaris basin.

Krahenbuhl, U.↗
NASA NTRS1973

Volatile element chemistry of selected lunar, meteoritic, and terrestrial samples

Using vacuum pyrolysis and high resolution mass spectrometry, a study is made of the gas release patterns of representative lunar samples, meteorites, terrestrial samples, and synthetic samples doped with various sources of carbon and nitrogen. The pyrolytic gas evolution patterns were intercorrelated, allowing an assessment of the possible sources of the volatilizable material in the lunar samples to be made. Lightly surface adsorbed species and more strongly chemisorbed species are released from ambient to 300 C and from 300 to 500 C, respectively. The low-temperature volatiles (less than 500 C) derived from various chondrites correlate well with the gas evolution patterns of volatile-rich samples, as for example 74220 and 61221. Solar wind entrapped species and molecules derived from reactions probably in the grain surfaces are evolved from about 500 to 700 C, respectively. Solar wind implanted C, N, and S species are generated from 750 to 1150 C, probably by reaction with the mineral matrix during the annealing process. Possible indigenous and/or refractory carbide, nitride, and sulfide C, N, and S are released in the region from 1200 C to fusion.

Simoneit, B. R.↗
NASA NTRS1975

Distribution, movement, and evolution of the volatile elements in the lunar regolith

The abundances and distributions of carbon, nitrogen, and sulfur in lunar soils are reviewed. Carbon and nitrogen have a predominantly extra-lunar origin in lunar soils and breccias, while sulfur is mostly indigeneous to the moon. The lunar processes which effect the movement, distribution, and evolution of carbon, nitrogen, and sulfur, along with the volatile alkali elements sodium, potassium, and rubidium during regolith processes are discussed. Possible mechanisms which may result in the addition to or loss from the moon of these volatile elements are considered.

Gibson, E. K., Jr.↗
NASA NTRS1975

On the depletion of moderately volatile elements in ordinary chondrites

Within the accuracy of present data, elements of intermediate volatility (condensation temperatures between about 1100 and 600 K) do not show a correlation of abundance with volatility in equilibrated ordinary chondrites. There is no need to postulate continuous loss of gas during condensation.

Anders, E.↗
NASA NTRS1975

Siderophiles and volatiles in Apollo-16 rocks and soils

The duplicate and mean concentrations of eight trace elements (Ni, Zn, Ga, Ge, Cd, In, Ir, Au) in eight Apollo-16 soils, five rocks, and a metallic spherule were determined by radiochemical neutron-activation analysis (RNAA) following radiochemical separation. Data are presented and compared with analyses of Apollo-14 samples. The concentration of extralunar components in mature Apollo-16 soils is about 3.8%, and the samples contain a large amount of pre-Imbrium regolith. Volatiles, siderophiles, and cosmogenic isotopes are intercorrelated, largely as a result of mixing of North Ray crater ejecta having low concentrations with mature soils containing high concentrations. Light soils have higher concentrations of Zn, Ga, and Cd than dark mature and submature soils, which contain comparatively higher concentration of Sc and Fe. Volatility largely controls the distributions of Zn, Cd, and In in soils and soil breccias and probably affects the Ga distribution.

Wasson, J. T.↗
NASA NTRS1976

Volatile inventories on Mars

Predictions for the total inventory of outgassed volatiles on Mars can be developed by studying volatiles in meteorites, terrestrial rocks, and the atmospheres of Venus, the moon, and the earth. Two models are presented, following the basic assumption that the devolatilization of Mars has been analogous to that of the earth. The recent discovery of a high abundance of argon in the Martian atmosphere appears to indicate that Mars has outgassed as completely as the earth, but present uncertainties and lacunae in the essential data set permit several other interpretations.

Owen, T.↗
NASA NTRS1977

Volatilization of oxides during oxidation of some superalloys at 1200 C

Volatilization of oxides during cyclic oxidation of commercial Nichrome, Inconel 750, Rene 41, Stellite 6B, and GE-1541 was studied at 1200 C in static air. Quantitative analysis of oxide vapor deposits revealed that oxides of tungsten, molybdenum, niobium, manganese, and chromium volatilized preferentially from the oxide scales. Aluminum and silicon were not detected in vapor deposits. For all the alloys except GE-1541, chromium was found to be the main metallic element in the oxide scales.

Zaplatynsky, I.↗
NASA NTRS1977

Volatilization of oxides during oxidation of some superalloys at 1200 C

Volatilization of oxides during cyclic oxidation of commercial Nichrome, Inconel 750, Rene 41, Stellite 6B, and GE-1541 was studied at 1200 C in static air. Quantitative analysis of oxide vapor deposits revealed that oxides of tungsten, molybdenum, niobium, manganese, and chromium volatilized preferentially from the oxide scales. Aluminum and silicon were not detected in vapor deposits. For all the alloys except GE-1541 chromium was found to be the main metallic element in the oxide scales.

Zaplatynsky, I.↗
NASA NTRS1979

On volatile element trends in gas-rich meteorites

Ten volatile elements (and non-volatile Co) in co-existing light and dark portions of 5 gas-rich chondrites were studied. Patterns of distinct but non-uniform enrichment by dark admixing material are revealed. The dark admixing material is enriched in Cs; Bi and Tl covary in it. It is compositionally unique from known types of primitive materials and is apparently not derived by secondary processes from such materials.

Bart, G.↗
NASA NTRS1978

Lonar crater glasses and high-magnesium australites - Trace element volatilization and meteoritic contamination

Radiochemical neutron activation analysis was used to detect six siderophile elements (Ni, Re, Os, Pd, Ir and Au) and three volatile elements (Zn, Se and Cd) in two basalts, a pumice and three impact glasses from Lonar crater, India, and in six high-magnesium australites. Significant depletions in Re and Se with respect to the parent basalts were found in the Lonar glasses. These depletions, apparently correlated with the degree of shock, are probably due to volatilization under the oxidizing conditions characteristic of earth. One of the australites is substantially enriched in siderophiles relative to the level of these elements in the other five tektites. The element patterns in the australites resemble those of the carbonaceous or cometary component of an Apollo 16 soil.

Morgan, J. W.↗
NASA NTRS1979

Scanning Auger Microprobe and atomic absorption studies of lunar volcanic volatiles

Results on lunar volatile transport processes have been obtained by studying green and brown glass droplets, orange and black core tube samples and the surface sample 74241 with the Scanning Auger Microprobe (SAM) and by Flameless Atomic Absorption Analysis (FLAA). SAM analyses show that the most dominant volatiles in the top few atomic layers of droplets are Zn and S, confirming that the surface Zn and S are good indicators of pyroclastic origin, and they are not entirely present as ZnS. In addition, FLAA thermal release profiles show that almost all the Zn and Cd are on grain surfaces, indicating that Zn and Cd were completely outgassed from lava fountain products during the volcanic eruption, were recondensed during or after the eruptions, and are thus present as surface coating.

Cirlin, E. H.↗
NASA NTRS1980

Spatial distribution of volatile compounds in graphite composites

The distribution of water and other volatile compounds such as acetone and phenol was measured as a function of depth in four graphite resin matrix composites. Precision abrasion mass spectrometry was used to qualitatively and quantitatively characterize the indigenous volatile compounds in the as received condition and after drying in an environmentally controlled oven. The total amount of water in the composites varied from 0.12 wt% to 1.1 wt% and the times required to dry the samples ranged from less than 96 h to much greater than 555 h.

Grayson, M. A.↗
NASA NTRS1980

Evolution of Io's volatile inventory

Voyager data are used to make crude estimates of the rate at which Io loses volatiles, by a variety of processes, to the surrounding magnetosphere, for the case of both the current, SO2-dominated atmosphere and hypothetical paleoatmospheres in which such other gases as N2 may have been the dominant constituent. Among the mechanisms making significant contributions to the prodigious rate at which Io is losing volatiles are: the interaction of the magnetospheric plasma with volcanic plume particles and the background atmosphere; the sputtering of ices on the surface, if the nightside atmospheric pressure is low enough; and Jeans' escape of O as a dissociation product of SO2 gas. It is also argued that in the case of paleoatmospheres only the first two alternatives would have been possible and, nevertheless, insufficient to account for N2 loss over the life of the satellite.

Pollack, J. B.↗
NASA NTRS1982

Venus: Halide cloud condensation and volatile element inventories

Several Venus cloud condensates, including A12C16 as well as halides, oxides and sulfides of arsenic and antimony, are assessed for their thermodynamic and geochemical plausibility. Aluminum chloride can confidently be ruled out, and condensation of arsenic sulfides on the surface will cause arsenic compounds to be too rare to produce the observed clouds. Antimony may conceivably be sufficiently volatile, but the expected molecular form is gaseous SbS, not the chloride. Arsenic and antimony compounds in the atmosphere will be regulated at very low levels by sulfide precipitation, irrespective of the planetary inventory of As and Sb. Thus the arguments for a volatile-deficient origin for Venus based on the depletion of water and mercury (relative to Earth) cannot be tested by a search for atmospheric arsenic or antimony.

Lewis, J. S.↗
NASA NTRS1984

Identification of a volatile phytotoxin from algae

The objectives were to develop a trap system for isolating fractions of volatile algal phytotoxin and to characterize the major components of the isolated phytotoxin fractions. A bioassay using Phaseolus vulgaris seedlings was developed to aid in investigating the properties of the phytotoxin produced by cultures of Euglena gracilis var. bacillaris and Chlorella vulgaris. Two traps were found, 1.0 M hydrochloric acid and 0 C, which removed the phytotoxin from the algal effluent and which could be treated to release that phytotoxin as judged with the bioassay procedure. It was also determined that pretraps of 1.0 M sodium hydroxide and 1.0 M potassium biocarbonate could be used without lowering the phytotoxin effect. Ammonia was identified in trap solutions by ninhydrin reaction, indophenol reaction and derivatization with dansyl chloride and phenylisothiocyanate. Ammonia at the gaseous concentrations detected was found to have the same effects in the bioassay system as the volatile phytotoxin. It is possible that other basic, nitrogen containing compounds which augment the effects of ammonia were present at lower concentrations in the algal effluent.

Garavelli, J. S.↗
NASA NTRS1984

Origin of the Moon: Constraints from volatile elements

Supporting arguments for the lunar fusion hypothesis include the low density of the Moon corresponding to the density of the Earth's mantle and the low volatile content of the lunar rocks vs. those of terrestrial origin. Vapor pressures of the alkali elements and their oxides increase in the following order: Na, K, Rb and Cs. The Moon should, therefore, be more depleted in Cs relative to Rb, Rb relative to K, and K relative to Na than the Earth if the fission model is correct. Analyses of lunar mare basalts and terrestrial mid-ocean ridge and other young basalts indicate that this behavior is not observed. It is possible that monovalent alkali elements might be lost from silicate materials in a different order than that inferred from elemental and oxide vapor pressures, as a result of differences in the way they are bound in silicate materials. To test this hypothesis a series of experiments was conducted to investigate alkali loss at high temperatures. Analyses indicate that the behavior of volatiles dissolved in a silicate melt is similar to that inferred from elemental and oxide vapor pressures. It is concluded that alkali element ratios in the Earth and Moon are not readily interpreted in terms of the fission hypothesis.

Kreutzberger, M. E.↗
NASA NTRS1985

Nebular volatile fractionations associated with chondrule formation

Chondrules are ubiquitous constituents of primitive solar system matter, indicating that chondrule formation was an important and widespread process in the early history of the solar system. If chondrules formed from fine grained CI like precursors, some volatile fractionation must have accompanied chondrule formation. This is not likely related to a separation of chondrules from gas (and dust, fine enough to be coupled to gas) shortly after formation, a process required by most models of chondrule formation. If chondrules are continuously formed in and removed from a region of the solar nebula, the chemical environment in this region will change. Vaporization of solid increases both oxygen and sulfur in the gas relative to H. Depending on the oxygen/sulfur ratio, which may vary widely as a function of precursor composition and temperature, two cases can be distinguished: (1) sulfur requires reaction with solid to condense, and thus may become much more enriched than 0; (2) if a significant amount of silicate is vaporized together with sulfides and does not recondense, changes in H/O outweigh S enrichment. In combination, these two effects may be able to account for much of the chemical variation among various types of chondrites. Opaque, fine grained matrix in unequilibrated chondrites, which is thought to derive from dust, has indeed been found to have a volatile element abundance complementary to chondrules.

Kracher, A.↗
NASA NTRS1985

Unequilibrated ordinary chondrites - A tentative subclassification based on volatile-element content

In view of the lack of correlation sometimes encountered between the volatile content and metamorphism measures of primitiveness for unequilibrated ordinary chondrites (UOCs), a tentative classification scheme is developed which is based on volatile content and complements the Sears et al. (1980) scheme based on metamorphism. The classification is based primarily on C and Xe, which are not significantly affected by shock-induced reheating. It is noted that novel clues to the formation of chondrites may be derivable from Xe and C; their concentrations in UOCs vary by a factor greater than 5, yet the Xe/C ratio remains nearly constant at 0.0034 of the solar system ratio.

Anders, E.↗