Chemical composition of the lunar surface in Mare Tranquillitatis.
Mare Tranquillitatis surface chemical composition data from Surveyor 5, comparing element abundances with meteorites and terrestrial rocks
Franzgrote, E. J.↗
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X-ray spectral microanalysis of composition of individual lunar regolith particles
Determinations were made of the chemical compositions of selected olivine crystals, spherical particles ranging in size from 170 to 350 micrometer, spinels, and magnetic particles. The olivines contain 30 to 50 mole percent fayalite. The spherical particles of various colors are aluminosilicate glasses, significantly enriched in CaO compared with the mean composition of the regolith. The degree of coloration depends on the FeO content and also the admixtures TiO2, MnO, and Cr2O3. Compositionally, the spinel was interpreted to be chromopicotites. Magnetic particles were shown to be complex intergrowths of nickelous iron and aluminosilicates. The composition of the metallic phase of one particle (in percent) was: Fe - 86, Ni - 13.6, and Co - 0.16 in combination with plagioclase and microinclusions of ilmenite in silicate. Kamacite was determined in another intergrowth of Fe, Ni, and Co.
Ilin, N. P.↗
Investigation of glass particles recovered from Apollo 11 and 12 fines: Implications concerning the composition of the lunar surface
Investigation of glass particles recovered from Apollo 11 and Apollo 12 fines, and composition and heteorogeneity of lunar surface
Glass, B. P.↗
The average chemical composition of the lunar surface
The available analytical data from twelve locations on the moon are used to estimate the average amounts of the principal chemical elements (O, Na, Mg, Al, Si, Ca, Ti, and Fe) in the mare, the terra, and the average lunar surface regolith. These chemical elements comprise about 99% of the atoms on the lunar surface. The relatively small variability in the amounts of these elements at different mare (or terra) sites, and the evidence from the orbital measurements of Apollo 15 and 16, suggest that the lunar surface is much more homogeneous than the surface of the earth. The average chemical composition of the lunar surface may now be known as well as, if not better than, that of the solid part of the earth's surface.
Turkevich, A. L.↗
Mineralogy and composition of Apollo 11 lunar samples
Apollo 11 lunar samples mineralogical and compositional studies concerning lunar origin hypothesis
Bunch, T. E.↗
Compositions of Three Lunar Meteorites: Meteorite Hills 01210, Northeast Africa 001, and Northwest Africa 3136
We report on compositions obtained by instrumental neutron activation analysis on three new lunar meteorites, MET 01210 (Meteorite Hills, Antarctica; 23 g), NEA 001 (Northeast Africa, Sudan; 262 g), and NWA 3136 (Northwest Africa, Algeria or Morocco; 95 g). As in previous similar studies, we divided our samples into many (8-9) small (approximately 30 mg) subsamples prior to analysis.
Korotev, R. L.↗
In-situ Lunar Launch and Landing Pad Construction with Regolith-Thermoset Polymer Composite Materials
Lunar launch and landing pads are necessary to mitigate risks to lander/ascent vehicles and surrounding surface assets from rocket plume ejected regolith. The current state of the art of landing and launching from the lunar surface is to land/launch on unprepared regolith surfaces. Significant risks exist for the larger landers proposed for the Artemis Program due to higher thrust levels leading to increased ejecta and cratering, presence of co-located assets in the ejecta path, and potential strict surface levelness requirements for tall vehicles.
Launch Pad↗
Phase Equilibria of a S- and C-Poor Lunar Core
The composition of the lunar core can have a large impact on its thermal evolution, possible early dynamo creation, and physical state. Geochemical measurements have placed better constraints on the S and C content of the lunar mantle. In this study we have carried out phase equilibrium studies of geochemically plausible S- and C-poor lunar core compositions in the Fe-Ni-S-C system, and apply them to the early history of the Moon. We chose two bulk core compositions, with differing S and C content based on geochemical analyses of S and C trapped melts in Apollo samples, and on the partitioning of S and C between metal and silicate. This approach allowed calculation of core S and C contents - 90% Fe, 9% Ni, 0.5% C, and 0.375% S by weight; a second composition contained 1% each of S and C. Experiments were carried out from 1473K to 1973K and 1 GPa to 5 GPa, in piston cylinder and multi- anvil apparatuses. Combination of the thermal model of with our results, shows that a solid inner core (and therefore initiation of a dynamo) may have been possible in the earliest history of the Moon (approximately 4.2 Ga ago), in agreement with. Thus a volatile poor lunar core may explain the thermal and magnetic history of the Moon.
Righter, K.↗
On compositional modeling of lunar highlands soils, including application to the orbiting gamma-ray experimental data
The compositions of remotely sensed highlands soils are compared with those of acquired highlands soils through the use of a compositional model. This model previously demonstrated its ability to describe compositions of acquired highlands soils with an accuracy approximating the present knowledge of the compositions. The principal question addressed here is whether the compositional end-members used to describe the acquired highlands soils are adequate to describe the remotely sensed ones or whether in some remotely sensed regions volumetrically significant components of different composition are required. Owing to the large analytical uncertainties in the gamma-ray data, only the presence of substantial proportions of significantly different components would be detectable by this (or any other) analysis of those data.
Haskin, L. A.↗
Lunar and Asteroid Composition Using a Remote Secondary Ion Mass Spectrometer
Laboratory experiments simulating solar wind sputtering of lunar surface materials have shown that solar wind protons sputter secondary ions in sufficient numbers to be measured from low-altitude lunar orbit. Secondary ions of Na, Mg, Al, Si, K, Ca, Mn, Ti, and Fe have been observed sputtered from sample simulants of mare and highland soils. While solar wind ions are hundreds of times less efficient than those used in standard secondary ion mass spectrometry, secondary ion fluxes expected at the Moon under normal solar wind conditions range from approximately 10 to greater than 10(exp 4) ions cm(sup -2)s(sup -1), depending on species. These secondary ion fluxes depend both on concentration in the soil and on probability of ionization; yields of easily ionized elements such as K and Na are relatively much greater than those for the more electronegative elements and compounds. Once these ions leave the surface, they are subject to acceleration by local electric and magnetic fields. For typical solar wind conditions, secondary ions can be accelerated to an orbital observing location. The same is true for atmospheric atoms and molecules that are photoionized by solar EUV. The instrument to detect, identify, and map secondary ions sputtered from the lunar surface and photoions arising from the tenuous atmosphere is discussed.
Elphic, R. C.↗
Compositional analysis of lunar and planetary surfaces using neutron capture gamma rays Quarterly report, 1 Jul. - 30 Sep. 1968
Compositional analysis of basalt using neutron capture gamma rays
Mandler, J. W.↗
Feasibility of remote compositional mapping of the lunar surface - effects of surface roughness.
Remote compositional mapping of lunar surface, using surface roughness effects on infrared spectral emission
INFRARED SPECTRUM↗
Nanoscale Compositional Relations in Lunar Rock Patina: Deciphering Sources for Patina Components on an Apollo 17 Station 6 Boulder
Space weathering on the Moon and other airless bodies modifies the surfaces of regolith grains as well as the space-exposed surfaces of larger rocks and boulders. As space weathering witness plates, rocks and boulders are distinguished from regolith grains based on their ability to persist as physically intact substrates over longer time scales before being disaggregated by impact processes. Because lunar surfaces, including exposed rocks, quickly develop an optically thick layer of patina, it is important to understand the compositional relationship between patinas and their underlying rock substrates, particularly to support remote-sensing of rocky lunar terrains. Based on analytical TEM techniques, supported by focused ion beam (FIB) cross-sectioning, we have begun to systematize the multi-layer microstructural complexity of patinas on rock samples with a range of space exposure histories. Our on-going work has particularly focused on lunar rock 76015, both because it has a long (approx. 22 my) exposure history, and because its surface was exposed to patina development approximately 1 m off the regolith surface on a boulder in the Apollo 17 Station 6 boulder field. Potential sources for the 76015 patina therefore include impact-melted and vaporized material derived from the local rock substrate, as well as from the mix of large boulders and regolith in the Station 6 area. While similar, there are differences in the mineralogy and chemistry of the rocks and regolith at Station 6. We were interested to see if these, or other sources, could be distinguished in the average composition, as well as the compositional nanostratigraphy of the 76015 patina. To date we have acquired a total of 9 TEM FIB cross-sections from the 76015 patina, giving us reasonable confidence of being able to arrive at an integrated average for the patina major element composition based on analytical TEM methods.
Christoffersen, R.↗
Chemical composition of Luna 16 lunar regolith
Data on the chemical composition of regolith returned by the Luna 16 automatic station and two fragments of basalts from the lower layer of the core are presented. Spark mass spectrometric, primary X-ray spectral, emission spectral, and atomic absorption methods were used in the analysis. The regolith of mare provinces were shown to be a mixture of material of various origins. The source of the material of the mare regolith was principally basalts of the corresponding lunar lava maria. The regolith is genetically related to it. This follows from a comparison of the chemical composition, mineralogical, and petrochemical features of the basesalts and the regolith from the Sea of Fertility, Sea of Tranquillity, and Ocean of Storms, respectively.
Vinogradov, A. P.↗
On compositional variations among lunar anorthosites
Ferroan anorthosite (FAN) is the most abundant 'pristine' highlands igneous rock in the Apollo sample collection. The presence of substantial FAN in the lunar crust is one argument used in favor of a global magma ocean on which crystallizing plagioclase could float. Information about the composition of the proposed magma ocean or whatever liquids might have been parental to FAN is sparse. As a first step toward learning about the nature of the FAN parent and the processes by which FAN attained its compositional characteristics, attention is given to the concentrations for a number of major and trace elements whose behavior during magmatic processes is somewhat understood. Serious difficulties are found with both FAN and the Marcy anorthosite in interpreting incompatible trace element concentrations in the plagioclases or the whole rocks in terms of residues from parent liquids. A description is presented of the nature of these difficulties.
Haskin, L. A.↗
Mineral compositions in pristine lunar highland rocks and the diversity of highland magmatism
High precision electron microprobe analyses of olivine and pyroxene in pristine lunar highland rocks confirm the dichotomy between ferroan anorthosites and the Mg-suite. Ferroan-anorthosites plot as coherent trends, consistent with formation in a complex global magma system. Lack of coherent compositional trends in the Mg-suite rocks indicates derivation from numerous magmas.
Bersch, Michael G.↗
Pickup Ion Mass Spectrometry for Surface Bounded Exospheres and Composition Mapping of Lunar and Planetary Surfaces
Many of the small to medium sized objects in the solar system can be characterized as having surface bounded exospheres, or atmospheres so tenuous that scale lengths for inter-particle collisions are much larger than the dimensions of the objects. The atmospheres of these objects are the product of their surfaces, both the surface composition and the interactions that occur on them and also their interiors when gases escape from there. Thus by studying surface bounded exospheres it is possible to develop insight into the composition and processes that are taking place on the surface and interiors of these objects. The Moon and Mercury are two examples of planetary bodies with surface bounded exospheres that have been studied through spectroscopic observations of sodium, potassium, and, on the moon, mass spectrometric measurements of lunar gases such as argon and helium.
Keller, J. W.↗
Remote compositional mapping of lunar titanium and surface maturity
Lunar ilmenite (FeTiO3) is a potential resource capable of providing oxygen for life support and spacecraft propellant for future lunar bases. Estimates of TiO2 content in mature mare soils can be made using an empirical relation between the 400/500 nm reflectance ratio and TiO2 wt percent. A TiO2 abundance map was constructed for the entire near-side lunar maria accurate to + or - 2 wt percent TiO2 using CCD images obtained at the Tumamoc Hill 0.5 m telescope in Tucson, employing bandpass filters centered at 400 and 560 nm. Highest TiO2 regions in the maria are located in western Mare Tranquillitatis. Greater contrast differences between regions on the lunar surface can be obtained using 400/730 nm ratio images. The relation might well be refined to accommodate this possibly more sensitive indicator of TiO2 content. Another potential lunar resource is solar wind-implanted He-3 which may be used as a fuel for fusion reactors. Relative soil maturity, as determined by agglutinate content, can be estimated from 950/560 nm ration images. Immature soils appear darker in this ratio since such soils contain abundant pyroxene grains which cause strong absorption centered near 950 nm due Fe(2+) crystal field transitions. A positive correlation exists between the amount of He-3 and TiO2 content in lunar soils, suggesting that regions high in TiO2 should also be high in He-3. Reflectance spectrophotometry in the region 320 to 870 nm was also obtained for several regions. Below about 340 nm, these spectra show variations in relative reflectance that are caused by as yet unassigned near-UV absorptions due to compositional differences.
Johnson, J. R.↗