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At least 91 records · Page 5
All sourcesNASA NTRSDOE OSTI
NASA NTRS2020

Aqueous Alteration in the Kuiper Belt: Evidence from Hydrated Interplanetary Dust Particles

Edgeworth-Kuiper belt objects (EKBOs) formed in the outer reaches of the protoplanetary disk and thus avoided much of the high tempera-ture processing experienced by bodies in the inner solar system. For this reason, they contain a wealth of information on the nature of nebular solids and the chemical conditions in the earliest solar system. Astronomical observations of EKBOs have been limited largely to the surface chemistry of the ices covering these small and difficult to observe bodies. The mineralogy of EKBO objects are poorly known, but clues regarding their mineralogical makeup come from studies of samples from short period comets (e.g. Wild2), and interplanetary dust particles (IDPs) produced by collisions in the Kuiper belt. Interplanetary dust particles from objects in the solar system (mainly comets and asteroids) spiral in to-wards the Sun under the influence of Poynting-Robertson (PR) drag forces and accumulate solar flare energetic particle tracks. Recent work has shown that the observed solar flare track densities (~1010-1011/sq.cm) in these IDPs are ~two orders of magnitude higher than expected if they were derived from main belt asteroids or Jupiter family comets and thus require an origin from outer solar system source bodies such as EKBOs. The track-rich IDPs include representatives from the two major groups of IDPs: the chondritic-porous, anhydrous IDPs and the chondritic-smooth, hydrated IDPs, although rare IDPs with mineralogies intermediate between these two groups are known. Here, we report on the mineralogy, composition, organic matter content, and isotopic characteristics of track-rich hydrated IDPs, and implications for aqueous alteration in outer solar system bodies.

Keller, L. P.↗
NASA NTRS2020

Telescopic Observations of Lunar Hydration: Variations and Abundance

Prior to 2009, the Moon was believed to be anhydrous. However, observations by three spacecraft revealed a hydrated surface by reporting a 3 μm absorption band attributed to hydroxyl and possibly molecular water. The Moon Mineralogy Mapper (M3) spectrometer, onboard the Chandrayaan-1 spacecraft is mainly used to study the lunar 3 μm band but its spectral range ends at 3 μm. The limited wavelength range of M3 has allowed observed variations in the 3 μm band to be called into question due to uncertainties in thermal corrections. To investigate the validity of variations in the lunar 3 μm band, we used the SpeX infrared spectrograph at the NASA InfraRed Telescope Facility at Maunakea Observatory in Hawaiʻi. With SpeX, we are able to obtain lunar data over a wavelength range of 1.67 to 4.2 μm at 1 – 2 km spatial resolution. The long wavelengths provide strong constraints on thermal emission corrections. We confirm that the 3 μm band varies with lunar time of day as well as with latitude and composition. Each observation reveals strong variations in abundances of hydroxyl and possibly molecular water. The data reveal a decrease in abundance with increasing lunar local time, an asymmetric trend about the equator that favors the southern latitudes, and higher concentrations in highland regions. The longer wavelengths provided by SpeX have allowed us to examine variations in the 3 μm band and provide definitive evidence that the variations are due to changes in hydration.

C. I. Honniball↗
NASA NTRSDate not supplied

The Carbonate Mineralogy of Hydrated Interplanetary Dust Particles

Hydrated interplanetary dust particles (IDPs) are a major component of the stratospheric dust population and are widely believed to be derived from asteroidal parent bodies. Recent work has shown that many, if not most, hydrated IDPs represent samples of outer solar system parent bodies, namely Kuiper Belt objects (KBOs) [1]. Coordinated analyses of these IDPs provide important constraints on the nature and extent of water:rock interactions in these outer solar system parent bodies.

Lindsay P. Keller↗
NASA NTRS2000

On the possibilty of clathrate hydrates on the Moon

One of the most important inferences of the Lunar Prospector mission data was the existence of subsurface water ice in the permanently shadowed craters near both lunar poles [Feldman et al., 1998]. We propose and substantiate an alternative explanation that hydrogen can exist in the shallow lunar subsurface in the form of clathrate hydrates: CH4 . 6H(2)o and/or CO2 . 6H(2)o.

Lunar subsurface calthrate hydrates↗
NASA NTRS1974

Evidence about hydrate and solid water in the Martian surface from the 1969 Mariner infrared spectrometer

Results of laboratory simulation studies and comparative computer analyses of infrared spectral data regarding the presence, distribution, and form of condensed-phase water in the Martian surface. The data were obtained with the aid of the Mariner 6 and 7 spacecraft which were equipped with infrared spectrometers recording the infrared spectrum from 1.9 to 14.4 microns. From the analysis of these data evidence is obtained which signifies some sort of compositional and/or particle size variability of the extent and nature of hydration. Changes are noted which could be due to ice thinly covering a small fraction of the planetary surface in particularly cold spots, possibly on partially shaded slopes. At southerly latitudes, the fraction so covered seems to increase as the polar cap edge is approached. It is therefore concluded that there is strong evidence of ice formation on the planetary surface at the edge of the polar cap.

Pimentel, G. C.↗
NASA NTRS1974

The formation of goethite and hydrated clay minerals on Mars

Laboratory studies reported by Huguenin (1973) on the kinetics and mechanism of the photostimulated oxidation of magnetic and preliminary laboratory data on the weathering of silicates, reported herein, are applied to Mars. Basalts in the Martian dark areas are predicted to alter to hydrated Fe(2 plus or minus) depleted clay minerals, minor goethite, and minor to trace amounts of transition metal oxides such as TiO2, MnO2, and Cr2O3 at a rate of 10 to the minus 1.5 plus or minus 1.5 micron/yr. Some Ca-Mg carbonates are also expected to be formed. The clay minerals are predicted to be more silica-rich than the silicate source material, SiO2 contents of 60% or higher being expected, and strongly depleted in Fe(2+). The oxygen, OH, and H2O contents of the bulk weathering product are predicted to be significantly greater than those of the dark-area source materials, whereas the relative bulk metal abundances should be the same.

Huguenin, R. L.↗
NASA NTRS1978

Asteroid 1 Ceres - Evidence for water of hydration

An absorption feature centred near 3.0 microns has been discovered in the infrared spectrum of asteroid 1 Ceres. This spectrum has been compared with laboratory spectra of meteorites and shows great similarity to the spectra of type II carbonaceous chondrites. By analogy this suggests the presence of about 10-15 per cent water in the form of water of hydration on the surface of Ceres. This is the first evidence of water in the surface material of an asteroid.

Lebofsky, L. A.↗
NASA NTRS1980

Thermal reaction of ethynylphthalimides and hydration of N-/4-ethynylphenyl/phthalimide

Three ethynyl substituted phenylphthalimides were prepared and characterized by high pressure liquid chromatography, differential scanning calorimetry, and mass spectroscopy. When the preparation of N-(4-ethynylphenyl)phthalimide was attempted by the thermal cyclodehydration of N-(4-ethynylphenyl)-2-carboxybenzamide, N-(4-acetylphenyl)phthalimide was obtained as the major component. This unusual hydration of an ethynyl group was investigated and a mechanism was proposed to explain it.

Hergenrother, P. M.↗
NASA NTRS1981

The infrared spectrum of ammonia hydrate - Explanation for a reported ammonia phase

A number of anomalous spectra of solid NH3 deposited from the vapor phase have appeared in the literature. These spectra have been ascribed to a new phase of NH3. In the experiment reported here these anomalous spectra were reproduced by depositing a thin film from a mixture of gaseous NH3 and H2O and annealing this film at a temperature of 162 K. The thin film spectra showed excellent agreement with recent data on NH3.H2O. The anomalous 'NH3' spectra are, therefore, seen to be caused by H2O contamination of solid NH3 with formation of NH3 hydrate.

Still, G.↗