Na22, Al26, Th and U in Apollo 11 lunar samples
Apollo 11 lunar samples composition for Na 22, Al 26, Th and U, investigating positron activities
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Apollo 11 lunar samples composition for Na 22, Al 26, Th and U, investigating positron activities
Mossbauer effect spectrometry application to Apollo 11 lunar rocks composition, using nuclear gamma resonance measurements for nuclide Fe 57
Apollo 12 specimens elemental abundance from neutron activation analysis, discussing fractional crystallization, partial melting, rare earth abundances and soil mixing model
Microprobe measurements of rare gas composition for lunar rock 12013,10,31 mineral separates, noting cosmic ray bombardment role in K and Ar production
Spectrometer measures chemical composition of lunar rocks by remote sensing from orbit and senses lunar X-rays produced by interaction of solar X-rays and elements on the lunar surface. Instrument features high sensitivity, data handling system that accumulates and prepares data for telemetry, and automatic calibration.
Analyses of rare earth elements in various lunar samples are shown. The elements are listed in order of increasing atomic number, and the abundances are relative to primordial abundances as determined from stony meteorites. Analyses of soils from Apollo 11, 12, and 14 and Luna 16 missions are also shown. These elements show small regular differences in chemical and physical properties with atomic number.
The petrology of Luna 20 lithic fragments is described and compared to that of other highland sites. An identification of the major types of rocks that compose the lunar terrae is attempted, and their probable petrogenesis is discussed.
The existence in the lunar atmosphere of helium, neon, argon, and possibly molecular hydrogen has been confirmed by the Apollo 17 mass spectrometer. The observed helium concentrations and distribution agree closely with model predictions for a non-condensable gas based on a solar wind source, thermal escape and a Monte Carlo random walk calculated longitudinal distribution. Heavier gases are lost by photoionization and subsequent sweeping away by the solar wind electric field. The observed nighttime neon concentration of 80,000 molecules per cu cm is consistent with expected amounts. Argon, however, is adsorbed on the lunar surface late at night when the surface temperature is lowest. It shows the expected predawn enhancement exhibited by condensable gases released into the atmosphere at the sunrise terminator. Hydrogen appears to exist in the molecular rather than atomic state. Its observed concentration is less than a factor of 3 higher than that predicted by a model similar to that used for helium.
The accomplishments of the Apollo 17 flight are summarized. The basic objective of the mission was to sample basin-rim highland material and adjacent mare material and to investigate the geological evolutionary relationship between these two major units. The lunar experiments which were conducted include: (1) lunar field geology, (2) surface electrical experiments, (3) lunar traverse gravimeter experiments, (4) lunar seismic profiling experiment, (5) lunar ejecta and meteorites experiment, (6) analysis of lunar atmosphere composition, and (7) heat flow experiments.
Forty-nine sub-samples of the polymict breccia 14321,184 have been excavated from the rock and analyzed by instrumental activation analysis techniques, specially modified to allow examination of small samples. Two distinct types of microbreccia clasts were analysed. A mare-type basalt of unusual composition is present as several discrete clasts. Mixing models for the clastic components of the breccia illustrate that at least three stages of assembly may be distinguished on compositional grounds. The first was at a site such that KREEP-rich materials dominated the clastic rocks formed, although a variety of lithic fragments were apparently present. The second assembly stage may have been primarily that of comminution and mixing of the more primitive materials, with addition of mare-type basalt clasts. The third stage saw addition of clasts of 14321-type basalt. In the final assembly stage, the light matrix was apparently formed entirely by mutual abrasion of the pre-existing clasts, resulting in little or no change in bulk composition.
Melting experiments in vacuum at Fe-saturation for high-Ti lunar basalt compositions 70215 and 15318 Red Glass, and low-Ti basalt composition 15555-15016, have defined equilibrium crystallization sequences and the liquid lines of descent, and show that much of the chemical variety in the samples is due to near-surface fractionation processes. The various groups within the high-Ti suite, however, cannot be interrelated by such processes, nor can the high-Ti suite be a near-surface derivative of a low-Ti parent magma.
The concentrations of aluminum, manganese, sodium, chromium, iron, cobalt, and 12 rare earth elements were determined by neutron activation analysis using slow neutrons. Oxygen and silicon were determined using a fast neutron generator. Mossbauer spectroscopy was used to investigate iron compounds in Luna 16 regolith samples from the upper part of the core.
In most lunar terrae samples a trend of decreasing Ab-content of plagioclase with increasing Fa-content of olivine is observed. This covariance of composition is the opposite of the trend observed in terrestrial layered intrusions, and contradicts Bowen's reaction series. The 'anomalous' trend is considered in terms of olivine-melt and plagioclase-melt equilibria. The composition of plagioclase crystallizing from a melt depends directly upon the activity of silica in the melt, while the composition of olivine does not. It is proposed that the inverse correlation of plagioclase and olivine compositions in most lunar terrae rocks is a predictable consequence of crystallization from a lunar bulk composition which is poorer in silica than the bulk compositions of terrestrial layered intrusions. The data of Roedder and Weiblen (1974) lend support to this hypothesis.
The overall objectives of this research were to evaluate the role of C-O-S-Cl degassing processes in explaining vesiculation, oxidation state and fire-fountaining of lunar magmas by analysis of individual lunar glass spherules, and by experimental determination of equilibrium abundances and diffusion rates of C, S and Cl melt species in lunar glass compositions; and to determine possible primitive SNC magma compositions and the mineralogy of the mantle from which they were derived, and to evaluate P, T, XH2O etc. conditions at which they crystallize to form the SNC meteorites. After funding for one year, a project on the A15 volcanic green glass has been completed to the point of writing a first manuscript. Carbon-oxygen species C-O and CO2 are below detection limits (20 ppm) in these glasses, but there is up to 500 ppm S with concentrations both increasing and decreasing toward the spherule margins. Calculations and modeling indicate that C species could have been present in the volcanic gases, however. In a second project, experiments with low PH2O have resulted in refined estimates of the early intercumulus melt composition in the Chassigny meteorite which is generally accepted as a sample from Mars.
Some considerations are discussed on how information on site geology can be obtained from the distribution of data points on 2-element plots of composition of lunar regolith samples collected along a traverse.
Clementine spectral reflectance and compositional data, Lunar Prospector gamma ray and neutron spectrometer data, and sample analysis of lunar soils are used to examine the origin of high-Th in Eratosthenian basalts of the Procellarum KREEP. Additional information is contained in the original extended abstract.
NASA's long-term vision for space exploration includes developing human habitats and conducting scientific investigations on planetary bodies, especially on Moon and Mars. Processing and utilization of planetary in-situ resources is recognized as an important element of this vision since it can minimize the level of up-mass that will have to be transported from earth to the planetary bodies. Within this scope and context, we have undertaken a general effort aimed primarily at extracting and refining metals, developing glass, glass-ceramic, or traditional ceramic type materials using lunar soil simulants. In this paper we will present preliminary results on our effort on simultaneous carbothermal reduction of oxides for elemental extraction and zone refining for obtaining high purity metals. In additions we will demonstrate the possibility of developing glass fibers as reinforcement agents for planetary habitat construction, glasses for fixing nuclear waste from potential nuclear power generators, and glasses for magnetic applications. The paper will also include initial thermal characterization of the glasses produced from lunar simulant. Compositional analysis of processed samples will be presented.
It has generally been accepted that the Moon is depleted in volatile elements. However, the recent discovery of measurable water in lunar glasses and apatites suggests that volatiles are not as depleted as was once thought. And, in fact, some authors have claimed that water contents of the lunar and terrestrial mantles are similar. Moderately volatile alkali elements may have a bearing on this issue. In general, bulk Moon alkalis are depleted relative to the bulk silicate Earth. Although the bulk lunar chemical composition is difficult to reconstruct, good correlations of alkali elements with refractory lithophile incompatible trace elements make this conclusion robust. These observations have been taken to mean that the Moon overall is depleted in volatiles relative to the Earth. Since water is more volatile than any of the alkali elements, presumably this conclusion is true for water, or even more so.