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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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At least 325 records · Page 18
All sourcesNASA NTRSDOE OSTI
NASA NTRS1994

The stability of hibonite, melilite and other aluminous phases in silicate melts: Implications for the origin of hibonite-bearing inclusions from carbonaceous chondrites

Phase fields in which hibonite and silicate melt coexist with spinel CaAl4O7, gehlenitic melilite, anorthite or corundum at 1 bar in the system CaO-MgO-Al2O3-SiO2-TiO2 were determined. The hibonites contain up to 1.7 wt% SiO2. For TiO2, the experimentally determined partition coefficients between hibonite and coexisting melt D(sub i)(sup Hib/L), vary from 0.8 to 2.1 and generally decrease with increasing TiO2 in the liquid. Based on Ti partitioning between hibonite and melt, bulk inclusion compositions and hibonite-saturated liquidus phase diagrams, the hibonite in hibonite-poor fluffy Type A inclusions from Allende and at least some hibonite from hibonite-rich inclusions is relict, although much of the hibonite from hibonite-glass spherules probably crystallized metasably from a melt. Bulk compositions for all of these CAIs are consistent with an origin as melite + hibonite + spinel + perovskite phase assembalges that were partially altered and in some cases partially or completely melted. The duration of the melting event was sufficient to remove any Na introduced by the alteration process but frequently insufficient to dissolve all of the original hibonite. Simple thermochemical models developed for meteoritic melilite and hibonite solid solutions were used to obtain equilibration temperatures of hibonite-bearing phase assemblages with vapor. Referenced to 10(exp -3) atm, hibonite + corundum + vapor equilibrated at approximately 1260 C and hibonite + spinel +/- melilite + vapor at 1215 +/- 10 C. If these temperatures reflect condensation in a cooling gas of solar composition, then hibonite +/- corundum condensed first, followed by spinel and then melilite. The position of perovskite within this sequence is uncertain, but it probably began to condense before spinel. This sequence of phase appearances and relative temperatures is generally consistent with observed textures but differs from expectations based on classical condensation calculations in that equilibration temperatures are generally lower than predicted and melilite initially condenses with or even after spinel. Simple thermochemical modes for the substitution of trace elements into the Ca site of meteoritic hibonites suggest that virtually all Eu is divalent in early condensate hibonites but that Eu(2+)/Eu(#+) decreases by a factor of 20 or more during the course of condensation primarily because the ratio is proportional to the partial pressure of Al, which decreases dramatically as aluminous phase condense. The relative sizes of Eu and Yb anomalies in meteoritic hibonites and inclusions may be partly due to this effect.

Beckett, J. R.↗
NASA NTRS1994

Origin of the O(+) pick-up ions in the hehiosphere

The main sources for the ions in the interplanetary medium are the solar wind and the interstellar gas intruding into the heliosphere. Other sources, i.e. comets and planets can, however, contribute significantly locally. We present approximate expressions for deriving fluxes of pick-up ions originating from local neutral gas sources. Since the Io-torus is thought to be a relatively strong emitter of fast atoms, particular O and S, we used the O(+) data obtained by SWICS-Ulysses as a function of distance from Jupiter, both in and out-off the ecliptic plane in order to recognize a possible contribution of the Ionian source to the measured O(+). We find that - except for a very limited zone near the Jovian magnetosphere - the contribution of the Io-torus to the O(+) fluxes is minor, thus confirming our previous results on the pick-up H(+), He(+), N(+), O(+), and Ne(+) fluxes of interstellar origin.

Geiss, J.↗
NASA NTRS1994

Discovery of intense gamma-ray flashes of atmospheric origin

Observations have been made of a new terrestrial phenomenon: brief (approx. millisecond), intense flashes of gamma rays, observed with space-borne detectors. These flashes must originate at altitudes in the atmosphere above at least 30 km in order to be observable by orbiting detectors aboard the Compton Gamma-Ray Observatory (CGRO). At least a dozen events have been detected over the past 2 years. The photon spectra from the events are very hard and are consistent with bremsstrahlung emission from energetic (MeV) electrons. The most likely origin of these high energy electrons, while speculative at this time, is a rare type of high altitude electrical discharge above thunderstorm regions.

Fishman, G. J.↗
NASA NTRS1994

Discovery of Intense Gamma-Ray Flashes of Atmospheric Origin

Detectors aboard the Compton Gamma Ray Observatory have observed an unexplained terrestrial phenomenon: brief, intense flashes of gamma rays. These flashes must originate in the atmosphere at altitudes above at least 30 kilometers in order to escape atmospheric absorption and reach the orbiting detectors. At least a dozen such events have been detected over the past 2 years. The photon spectra from the events are very hard (peaking in the high-energy portion of the spectrum) and are consistent with bremsstrahlung emission from energetic (million-electron volt) electrons. The most likely origin of these high- energy electrons, although speculative at this time, is a rare type of high-altitude electrical discharge above thunderstorm regions.

Fishman, G. J.↗
NASA NTRS1996

A Glass Spherule of Questionable Impact Origin from the Apollo 15 Landing Site: Unique Target Mare Basalt

A 6 mm-diameter dark spherule, 15434,28, from the regolith on the Apennine Front at the Apollo 15 landing site has a homogeneous glass interior with a 200 microns-thick rind of devitrified or crystallized melt. The rind contains abundant small fragments of Apollo 15 olivine-normative mare basalt and rare volcanic Apollo 15 green glass. The glass interior of the spherule has the chemical composition, including a high FeO content and high CaO/Al2O3, of a mare basalt. Whereas the major element and Sc, Ni, and Co abundances are similar to those of low-Ti mare basalts, the incompatible elements and Sr abundances are similar to those of high-Ti mare basaits. The relative abundance patterns of the incompatible trace elements are distinct from any other lunar mare basalts or KREEP; among these distinctions are a much steeper slope of the heavy rare earth elements. The 15434,28 glass has abundances of the volatile element Zn consistent with both impact glasses and crystalline mare basalts, but much lower than in glasses of mare volcanic origin. The glass contains siderophile elements such as Ir in abundances only slightly higher than accepted lunar indigenous levels, and some, such as Au, are just below such upper limits. The age of the glass, determined by the Ar-40/Ar-39 laser incremental heating technique, is 1647 +/- 11 Ma (2 sigma); it is expressed as an age spectrum of seventeen steps over 96% of the Ar-38 released, unusual for an impact glass. Trapped argon is negligible. The undamaged nature of the sphere demonstrates that it must have spent most of its life buried in regolith; Ar-38 cosmic ray exposure data suggest that it was buried at less than 2m but more than a few centimeters if a single depth is appropriate. That the spherule solidified to a glass is surprising; for such a mare composition, cooling at about 50 C/s is required to avoid crystallization, and barely attainable in such a large spherule. The low volatile abundances, slightly high siderophile abundances, and the young age are perhaps all most consistent with an impact origin, but nonetheless not absolutely definitive.

Ryder, Graham↗
NASA NTRS1996

The Origin of Eucrites: An Experimental Perspective

The origin of eucrites has been the subject of debate. At issue is whether high-Mg# eucrites such as Sioux County are primitive or evolved liquids. We believe that the problem of the origin of eucrites is essentially solved. Problems associated with the petrogenesis of other achondrite groups remain, but the eucrites, taken as a whole, seem to present a clear and understandable story that we will present using experiments, analyses, and calculations. The two traditional eucrite groupings, the partial melting trend a.k.a. Stannem trend) and the fractional crystallization trend (a.k.a. Nuevo Laredo trend) have both been reproduced experimentally. The partial melting trend culminates in Sioux County. Sioux County is also an acceptable starting point for the fractional crystallization trend. The implication of these experimental results is that it is extremely difficult to relate the eucrites to diogenites, a group of pyroxene cumulates that conceivably could have crystallized from eucrite parent magmas.

Jones, J. H.↗
NASA NTRS1998

Chasma Australe Mars: Structural Framework for a Catastrophic Outflow Origin

Chasma Australe is the most remarkable of the martian south pole erosional reentrants carved in the polar layered deposits. Ms chasma originates near the south pole and runs across the polar troughs over a distance of about 500 km. Its width varies between 20 and 80 km and, with a depth up to 1000 m, it reaches the bedrock. Following an idea put forward originally for Chasma Boreale, we propose for the genesis of Chasma Australe a mechanism of catastrophic outflow preceded by a tectonically induced powerful sapping process. A detailed geomorphological analysis of Chasma Australe shows erosional and depositional features that can be interpreted as produced by the motion of a fluid. Like other polar reentrants, Chasma Australe is clearly assymetric, with a steep eastern margin where basal and lateral erosion prevailed, and a gentler western side, where the stepped topography and bedrock spurs favored deposition.

Anguita, F.↗
NASA NTRS1998

Prebiotic Polymer Synthesis and the Origin of Glycolytic Metabolism

Our research resulted in several discoveries which contributed to understanding the origin and operation of life. (1) Most importantly, we discovered a new pathway of prebiotic amino acid synthesis in which formaldehyde and glycolaldehyde (formose reaction substrates) react with ammonia to give alanine and homoserine in the presence of thiol catalysts. The thiol-dependent synthesis of amino acids undoubtedly occurs via amino acid thioester intermediates capable of forming peptides. This 'one-pot' reaction system operates under mild aqueous conditions, and like modern amino acid biosynthesis, uses sugar intermediates which are converted to amino acids by energy-yielding redox disproportionation. Preliminary evidence suggests that this type of process can be "evolved" by a serial transfer methods that lead to enrichment of autocatalytic molecules. (2) We established that prebiotic peptide polymers can be made by condensation of amino acid thioesters (homocysteine thiolactone and S-(N-beta-orotidyl- diaminopropionic acid) ethanethiol), and that prebiotic polydisulfide polymers can be generated by oxidation of dithiols with iron(III) in minerals. (3) In our analysis of metabolism we discovered the primary energy source of biosynthesis -- chemical energy made available by the redox disproportionation of substrate carbon groups. We concluded that the energy and reactivity of sugars make them the optimal substrate for the origin and operation of terrestrial (or extraterrestrial) life. (4) Since it is likely that the use of optimal sugar substrates in biosynthesis sets the average oxidation number of functional biocarbon throughout the Universe near 0.0 (the reduction level of formaldehyde), we proposed that a line(s) in the microwave spectrum of formaldehyde could be rationally selected as a frequency for interstellar communication that symbolizes life. (5) Finally, in preparation for the analysis of Martian meteorite samples, we upgraded our HPLC system to one femtomole sensitivity, and developed a new electrophoretic method of sample preparation for HPLC analysis of the meteoritic amino acids. In a sample of the KT boundary layer from Sussex Wyoming, we found about 300 picomoles per gram of meteoritic alpha-aminoisobutyric acid per gram of KT layer.

Weber, Arthur L.↗
NASA NTRS1999

Original Size of the Sudbury Structure: Evidence from Field Investigations and Imaging Radar

This paper summarizes results of continuing studies of the original size of the Sudbury impact structure, including imaging radar and field investigations of supposed "Sudbury breccia" north of the Sudbury Igneous Comples (SIC). Imaging radar acquired from Canada Centre for Remote Sensing (CCRS) aircraft, European Space Agency Remote Sensing Satellite (ERS-1), and RADARSAT shows no evidence of outer rings concentric with the North Range. Illumination directions are such that these rings, presumably extension fractures, would be conspicuous by look azimuth highlighting if they existed. Field mapping supports this interpretation, showing that supposed ring fractures occupied by Huronian sediments are essentially synclines older than the 1850 Ma impact and are not related to the impact. Field investigations of "Sudbury breccia" north of the SIC shows that most if not all of it is inside or along contacts with diabase dykes of the Sudbury Swarm (ca. 1238 Ma), and hence is far too young to be related to the impact. A recently-discovered occurrence of "Sudbury breccia" south of the SIC, near Creighton, is similarly associated with a NW-trending diabase dyke cutting the SIC, supporting the post-impact age of the breccia. It is concluded that the original north rim of the Sudbury crater was not more than 5 to 10 km north of the present North Range SIC contact, and that published estimates of the crater size (ca 200 km diameter) are incorrect.

Lowmman, Paul D., Jr.↗
NASA NTRS1998

The Origin and Time Dependence of the Amount and Composition of Non-Constituent Gases Present in Crystal Growth Systems

Presence of different, non-constituent gases may be a critical factor in crystal growth systems. In Physical Vapor Transport processes the cras(es) can be used intentionally (to prevent excessively high, unstable growth conditions), or can evolve unintentionally during the course of the process (which may lead to undesired reduction in the -rowth rate). In melt growth, particularly under low gravity conditions (reduced hydrostatic pressure) the gas present in the system may contribute to formation of voids in the growing crystals and even to a separation of the crystal and the liquid phase [1]. On the other hand, some amount of gas may facilitate 'contactless' crystal growth particularly under reduced gravity conditions [2 - 6]. Different non-constituent gases may be present in growth ampoules, and their amount and composition may change during the crystallization process. Some gases can appear even in empty ampoules sealed originally under high vacuum: they may diffuse in from the outside, and/or desorb from the ampoule walls. Residual gases can also be generated by the source materials: even very high purity commercial elements and compounds may contain trace amounts of impurities, particularly oxides. The oxides may have low volatilities themselves but their reaction with other species, particularly carbon and hydrogen, may produce volatile compounds like water or carbon oxides. The non-constituent gases, either added initially to the system or evolved during the material processing, may diffuse out of the ampoule during the course of the experiment. Gases present outside (e.g. as a protective atmosphere or thermal conductor) may diffuse into the ampoule. In either case the growth conditions and the quality of the crystals may be affected. The problem is of a particular importance in sealed systems where the amount of the gases cannot be directly controlled. Therefore a reasonable knowledge and understanding of the origin, composition, magnitude, and change with time of gases present in sealed ampoules may be important for a meaningful control and interpretation of crystal growth processes. This problem is of a particular importance for processing of electronic materials in space because (i) safety considerations require using sealed systems only, and (ii) high cost of crystal growth experiments in microgravity calls for a throughout, accurate description of the processing conditions necessary for a meaningful, efficient, and conclusive interpretation of the space results. In this paper we present the results of our extensive studies on gases in closed crystal growth systems which include: (a) Degassing properties of fused silica; (b) Generation of inert gases by source materials (CdTe, ZnTe, CdZnTe, ZnSe, PbTe, PbSe, PbSeTe); (c) Diffusive cas losses from silica glass ampoules.

Palosz, Witold↗
NASA NTRS1999

Enstatite Meteorites and the Original Heterogeneity of Mn-53 Distribution in the Solar Nebula

We have shown earlier that the relative abundance of radiogenic Cr-53 in bulk ordinary chondrites (approximately 0.48 epsilon) is clearly different from that in the earth-moon system (0 epsilon). The SNC parent body (Mars) is characterized by an intermediate Cr-53 excess (approximately 0.23 epsilon). We have also shown that the Mn-Cr systematics of the howardite-eucrite-diogenite parent body (HED PB, the asteroid Vesta) is consistent with the chondritic Mn/Cr ratio in the bulk HED PB and that it has a Cr-53 excess of approximately 0.5 epsilon units which is within error the same as that of chondrites. It appears that the excesses of Cr-53 in these planets are a function of their present heliocentric distance. The study of some other meteorite classes (angrites, pallasites, primitive achondrites) has shown that their Mn-CR systematics is consistent with that of the ordinary chondrites. The observed gradient in the radiogenic Cr-53 abundances can be explained by a). an early volatility controlled radial Mn/Cr fractionation in the nebula or b). an original heterogeneity of Mn-53. The first assumption, however, requires the Mn/Cr ratios of the bulk Earth and Mars to be considerably lower than the inferred model Mn/Cr ratios for these two planets. For this reason, we suggested that the observed gradient is due to an original radial Mn-53 heterogeneity in the late nebula.

Lugmair, Guenter W.↗
NASA NTRS1999

Origin and Reactivity of the Martian Soil: A 2003 Micromission

The role of water in the development of the martian surface remains a fundamental scientific question. Did Mars have one or more "warm and wet" climatic episodes where liquid water was stable at the surface? If so, the mineral phases present in the soils should be consistent with a history of aqueous weathering. More generally, the formation of hydrated mineral phases on Mars is a strong indicator of past habitable surface environments. The primary purpose of this investigation is to help resolve the question of whether such aqueous indicators are present on Mars by probing the upper meter for diagnostic mineral species. According to Burns [1993], the formation of the ferric oxides responsible for the visible color of Mars are the result of dissolution of Fe (+2) phases from basalts followed by aqueous oxidation and precipitation of Fe" mineral assemblages. These precipitates likely included iron oxyhydroxides such as goethite (a-FeOOH) and lepidocrocite (g-FeOOH), but convincing evidence for these phases at the surface is still absent. The stability of these minerals is enhanced beneath the surface, and thus we propose a subsurface search for hydroxylated iron species as a test for a large-scale chemical weathering process based on interactions with liquid water. It is also possible that the ferric minerals on Mars are not aqueous alteration products of the rocks. A chemical study of the Pathfinder landing site concluded that the soils are not directly derived from the surrounding rocks and are enhanced in Mg and Fe. The additional source of these elements might be from other regions of Mars and transported by winds, or alternatively, from exogenic sources. Gibson [1970] proposed that the spectral reflectivity of Mars is consistent with oxidized meteoritic material. Yen and Murray [1998] further extend Gibson's idea and show, in the laboratory, that metallic iron can be readily oxidized to maghemite and hematite under present-day martian surface conditions (in the absence of liquid water). A test for a meteoritic component of the soil can be conducted, as described below, by searching for the presence of Ni at the martian surface. The average abundance of nickel in an Fe-Ni meteorite is about 7% and, if present at measurable levels in the soil, would be indicative of an exogenic contribution. In addition, it may be possible to directly search for mineral phases common in meteorites. An understanding of the formation and evolution of the martian soil would not be complete without addressing the unusual reactivity discovered by the Viking Landers The presence of an inorganic oxidant, possibly one produced as a results of photochemical processes, is the most widely accepted explanation of the Viking results. Are these chemical species simply adsorbed on soil grains, or have they reacted with the metal oxide substrates and altered the mineral structures? Could a completely different (non-photochemical) process be responsible for the soil reactivity? The various ideas for the nature of this putative oxidant could be constrained by a measurement of the change in reactivity with depth. Different compositions will have different lifetimes and mobilities and thus will have different vertical profiles. Because the oxidizing compounds are believed to actively destroy organic molecules, determination of the reactivity gradient also has significant implications for the search for life on Mars. A DS2-based microprobe system can be instrumented for a 2003 micromission to investigate the origin and reactivity of the martian soil. These measurements would provide invaluable information regarding the climate history and exobiological potential of the planet. The NMR, X ray and chemiresistor measurement approach described embodies a highly synergistic and general set of soil interrogation methods for elements, compounds, and crystal structures and can also be applied to other geologic questions of interest. For example, if the capability for precise targeting of the probes is available, then in-situ investigations of suspected evaporite and hydrothermal deposits would be possible with the same set of instruments. Additional information is contained in the original.

Yen, Albert S.↗
NASA NTRS1999

Physical and Chemical Study of Minerals and Rocks Containing Low-Z Compounds of Interest to Astrobiology and Origin of Life

Understanding the origins of Life requires a good understanding of the physics and chemistry of biogenic low-z elements H, C, N, O, P, S in terrestrial environments, on Mars, on extraterrestrial bodies such as meteorite parent bodies and comets, and in interstellar space. In this Proposal five Tasks form a coherent program aimed at elucidating various aspects of low-z element geo- and cosmochemistry with special reference to the origin of Life on Earth and to the search for life on Mars, extant or extinct. (i) Formation of organic molecules, in particular oxygenated H-C-0 molecules or precursors thereof of the composition H(x)C(y)O(z)(n-), inside the hard matrix of structurally dense magmatic minerals; (ii) Formation of organic molecules inside the soft matrix of amorphous and crystalline water ice; (iii) Preservation of organic molecules in cherts and other siliceous rocks formed in hot spring or submarine hydrothermal vent environments; (iv) The nature of the elusive Martian soil oxidant; and (v) Prototype development of an XRD instrument, using a new patented XRD camera concept that utilizes a Charge Coupled Device (CCD) as a camera and as a energy-dispersive analyzer.

Source record↗
NASA NTRS2000

Spallogenic Light Elements and Cosmic Ray Origin

Most of the Galactic Li-6, all of the Be and the bulk of the B are cosmic ray produced. I will discuss the production mechanisms and detail a recently developed evolutionary code for Fe,O and these light elements. I will review the leading models for Li, Be and B origin and discuss their implications on cosmic ray origin. I will also show evidence for extragalactic production of Li-6.

Ramaty, Reuven↗
NASA NTRS2000

Origin of the Valley Networks On Mars: A Hydrological Perspective

The geomorphology of the Martian valley networks is examined from a hydrological perspective for their compatibility with an origin by rainfall, globally higher heat flow, and localized hydrothermal systems. Comparison of morphology and spatial distribution of valleys on geologic surfaces with terrestrial fluvial valleys suggests that most Martian valleys are probably not indicative of a rainfall origin, nor are they indicative of formation by an early global uniformly higher heat flow. In general, valleys are not uniformly distributed within geologic surface units as are terrestrial fluvial valleys. Valleys tend to form either as isolated systems or in clusters on a geologic surface unit leaving large expanses of the unit virtually untouched by erosion. With the exception of fluvial valleys on some volcanoes, most Martian valleys exhibit a sapping morphology and do not appear to have formed along with those that exhibit a runoff morphology. In contrast, terrestrial sapping valleys form from and along with runoff valleys. The isolated or clustered distribution of valleys suggests localized water sources were important in drainage development. Persistent ground-water outflow driven by localized, but vigorous hydrothermal circulation associated with magmatism, volcanism, impacts, or tectonism is, however, consistent with valley morphology and distribution. Snowfall from sublimating ice-covered lakes or seas may have provided an atmospheric water source for the formation of some valleys in regions where the surface is easily eroded and where localized geothermal/hydrothermal activity is sufficient to melt accumulated snowpacks.

Gulick, Virginia C.↗