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At least 37 records · Page 2
All sourcesNASA NTRSDOE OSTI
NASA NTRS1972

The Oro Grande, New Mexico, chondrite and its lithic inclusion.

The Oro Grande, New Mexico, U.S.A., chondrite was found in 1971. Electron microprobe analyses and microscopic examination show the following mineralogy: olivine (Fa 19.3 mole %), orthopyroxene (Fs 16.2 mole %), diopside, feldspar (An 13.6 mole %), chlorapatite, whitlockite, kamacite, taenite, troilite, chromite, and an iron-bearing terrestrial weathering product. A bulk chemical analysis of the meteorite shows the following results (weight %): Fe 0.84, Ni 1.46, Co 0.07, FeS 3.62, SiO2 34.18, TiO2 0.14, Al2O3 1.83, Cr2O3 0.55, Fe2O3 21.25, FeO 9.13, MnO 0.31, MgO 21.52, CaO 1.72, Na2O 0.70, K2O 0.08, P2O5 0.25, H2O(+) 2.14, H2O(-) 0.40, C 0.22, sum 100.41. On the basis of composition and texture the Oro Grande meteorite is classified as an H5 chondrite.

Fodor, R. V.↗
NASA NTRS1973

Volatile trace elements and the characterization of the Cayley Formation and the primitive lunar crust

Two types of highland terrain appear to be present at the Apollo 16 landing site. The Plains Formation called Cayley is ubiquitous and blankets even those regions that were presumably a part of the mountainous Descartes Formation. The second type of terrain is that associated with the ejectae from North and South Ray craters. The stratigraphy sampled by the ejectae underlays the Cayley layer as characterized above and may permit a redefinition of Descartes Formation as that which underlays the smooth Plains deposits. These conclusions are based on the concentrations and chemical coherence between elements such as Cl-F-P2O5 and Ru-Os. The primitive lunar crust may be characterized by the type of feldspathic rocks which are enriched in trace elements, such as Cl, Br, U, Te, Ru, and Os, as found in 'rusty' rock 66095 and in 61016; other feldspathic rocks are depleted and may be of secondary origin.

Jovanovic, S.↗
NASA NTRS1974

Regolith compositions from the Apollo 17 mission

An investigation of the chemical, mineralogical, and petrographic data from six Apollo 17 regolith samples is summarized. The samples from the center of the Taurus-Littrow valley are very similar in composition and consist of mare basalt and a minor admixture (about 25%) of plagioclase-rich material. The material from Station 9 (Van Serg Crater) contains much less basalt and more breccia and are higher in Al2O3 and lower in TiO2 and FeO than the other mare sites. The chemical compositions of the samples from the North Massif, the South Massif, and the light mantle believed to be of landslide origin, are very similar and correspond to an olivine norite; the relatively high K2O and P2O5 content indicate the presence of a KREEP component. Additional results are described in detail.

Mason, B.↗
NASA NTRS1974

Labile and nonlabile element relationships among Apollo 17 samples

Volatile and nonvolatile trace element contents in a suite of Apollo 17 soils and rocks are studied. It is found that the halogens exhibit a remarkable degree of coherence because of their apparent diverse geochemistry, that the F-Cl-P2O5 coherence previously noted persists among Apollo 17 samples, that both U and Ru-Os support lateral mixing of regolith on a local scale, and that the meteoritic Ru/Os ratios found in a few samples are attributed to primitive lunar material that has not been extensively recycled.

Jovanovic, S.↗
NASA NTRS1975

History of Boulder 1 at Station 2, Apollo 17 based on trace element interrelationships

Correlations among the trace and minor element pairs Cl and Br, Cl and P2O5, and Ru and Os, present in parent igneous rocks, generally survived the processes of boulder breccia formation. Fractions of Cl, Br, and Hg that are mobilized by water leaching or volatilization at moderate temperatures place constraints on the thermal history of Boulder 1 and its component breccias. Since, and possibly during, consolidation, the boulder has probably not been subjected to temperatures in excess of 450 C. The parent rocks of the Apollo 17 boulder and breccia samples studied could have been derived from two initial magmas. Vapor clouds from apparently external sources permeated the source regions of the boulders.

Jovanovic, S.↗
NASA NTRS1978

Reactions of yttria-stabilized zirconia with oxides and sulfates of various elements

The reactions between partially stabilized zirconia, containing 8 weight-percent yttria, and oxides and sulfates of various elements were studied at 1200, 1300, and 1400 C for times to 800, 400, and 200 hours, respectively. These oxides and sulfates represent impurities and additives potentially present in gas turbine fuels or impurities in the turbine combustion air as well as the elements of the substrate alloys in contact with zirconia. Based on the results, these compounds can be classified in four groups: (1) compounds which did not react with zirconia (Na2SO4, K2SO4, Cr2O3, Al2O3 and NiO); (2) compounds that reached completely with both zirconia phases (CaO, BaO, and BaSO4); (3) compounds that reacted preferentially with monoclinic zirconia (Na2O, K2O, CoO, Fe2O3, MgO, SiO2, and ZnO); and (4) compounds that reacted preferentially with cubic zirconia (V2O5, P2O5).

Zaplatynsky, I.↗
NASA NTRS1977

Mineralogy, petrology and chemistry of ANT-suite rocks from the lunar highlands

Anorthositic-noritic-troctolitic (ANT) rocks are the oldest and most abundant rocks of the lunar surface, and comprise about 90% of the suite of the lunar highlands. Consideration is given to the mineralogy, petrology, bulk chemistry, and origin of ANT-suite rocks. Problems associated in classifying and labeling lunar highland rocks because of textural complexities occurring from impact modifications are discussed. The mineralogy of ANT-suite rocks, dominated by plagioclase, olivine and pyrozene, and containing various minor minerals, is outlined. The petrology of ANT-suite rocks is reviewed along with the major element bulk composition of these rocks, noting that they are extremely depleted in K2O and P2O5. Various models describing the origin of ANT-suite rocks are summarized, and it is suggested that this origin involves a parental liquid of high-alumina basalt with low Fe/Fe+Mg.

Prinz, M.↗
NASA NTRS1977

Trace element geochemistry and the early lunar differentiation

The results are considered of experiments in which thermal neutron activation analysis was used to measure the halogens, U, Te, Ru, Os, and Hg in lunar samples. A calorimetric method was used for P2O5. Three Apollo 17 basalts, one Apollo 11 basalt, and one Apollo 15 basalt were used for the Ru-Os study. Os and Ru were measured in seven samples of breccia 14305 in a series of experiments to check an apparent anomaly in the isotopic composition of the Hg which it contains. A lunar model for Ru-Os partition is discussed. It is suggested that Ru and Os were partitioned and fractionated in the original differentiation of the lunar surface ocean. Fractionation among near-surface materials was less than a factor of 2 according to the lithic breccia data. Fractionations among basaltic sources were very large, exceeding 100, and primarily due to Ru. A clue to Ru and Os distributions at the depths from which mare basalts were derived may be provided by the relative ages of the basalts. These are interpreted as being related to partial melting in response to temperature increases at depth with time.

Jovanovic, S.↗
NASA NTRS1979

Reactions of calcium orthosilicate and barium zirconate with oxides and sulfates of various elements

Calcium orthosilicate and barium zirconate were evaluated as the insulation layer of thermal barrier coatings for air cooled gas turbine components. Their reactions with various oxides and sulfates were studied at 1100 C and 1300 C for times ranging up to 400 and 200 hours, respectively. These oxides and sulfates represent potential impurities or additives in gas turbine fuels and in turbine combustion air, as well as elements of potential bond coat alloys. The phase compositions of the reaction products were determined by X-ray diffraction analysis. BaZrO3 and 2CaO-SiO2 both reacted with P2O5, V2O5, Cr2O3, Al2O3, and SiO2. In addition, 2CaO-SiO2 reacted with Na2O, BaO, MgO, and CoO and BaZrO3 reacted with Fe2O3.

Zaplatynsky, I.↗
NASA NTRS1981

Derivation of a heterogeneous lithic fragment in the Bovedy L-group chondrite from impact-melted porphyritic chondrules

Results are presented of petrographic, compositional and dating analyses of a light-colored lithic fragment in the L-group Bovedy meteorite that has a composition different from that of the host chondrite. Polished thin sections of the lithic fragment, host, and the fragment-host boundary were examined microscopically and analyzed by electron microprobe, metallic Ni-Fe, and instrumental neutron activation techniques; chips of the fragment were also used for Ar-39/Ar-40 dating and oxygen isotope analyses. The poikilitic textures, olivine, low-Ca pyroxene and kamacite composition and low Na2O, K2O and P2O5 contents of the fragment indicate that it represents a solidified, slightly fractionated impact melt formed from a source rich in porphyritic chondrules. A progressive increase on MgO content across the fragment is accounted for by the heterogeneous nucleation of MgO-rich phases. The Ar data indicate that the Bovedy lithic fragment and its host were partly degassed of radiogenic Ar less than 0.94 billion years ago, probably due to shock. The data are consistent with a cooling rate of about 5 C/million years through 500 C, which must have resulted from the burial of the assemblage beneath insulating material on the parent body at depths of at least several km.

Rubin, A. E.↗
NASA NTRS1987

Experimental geochemistry of Pu and Sm and the thermodynamics of trace element partitioning

An experimental study of the partitioning of Pu and Sm between diopside/liquid and whitlockite/liquid supports the hypothesis that Pu behaves as a light rare earth element during igneous processes in reducing environments. D-Pu/D-Sm is found to be about 2 for both diopsidic pyroxene and whitlockite, and the amount of fractionation would be decreased further if Pu were compared to Ce or Nd. Data indicate that temperature, rather than melt composition, is the most important control on elemental partitioning, and that P2O5 in aluminosilicate melts serves as a complexing agent for the actinides and lanthanides.

Jones, John H.↗
NASA NTRS1989

Gas atomization of cobalt ferrite-phosphate melts

XRD, Moessbauer spectroscopy, and EDXS have been used to characterize a rapidly-solidified (Co,Fe)3O4 spinel generated in a cobalt-iron-phosphate glass matrix by gas atomization of melts. Of the two compositions tested, that containing 20 mol pct P2O5 exhibited randomly-oriented ferrite crystallization whose growth appears to have been diffusion-controlled. Unlike the ferrite, in which the iron has both tetrahedral and octahedral coordination, the iron in the glassy matrix was primarily of distorted-octahedral coordination. Calculations indicate that the cooling rates obtained with oxide melts vary strongly with droplet size, but less strongly with melt temperature.

De Guire, Mark R.↗
NASA NTRS1989

Metasomatic products of the lunar magma ocean - The role of KREEP dissemination

The 'urKREEP' hypothesis of Warren and Wasson (1979) is extended by defining KREEP in terms of specific (i.e., constrained) lunar components. It is shown that, the presilicate liquid immiscibility (pre-SLI) composition can be obtained by recombining experimental data on KREEP basalt components, or by calculating from liquid-liquid Kd's. Both calculated urKREEP compositions were lower in MgO and Al2O3 and higher in FeO and P2O5 than reported low- and high-K KREEP compositions. The calculated REE abundances were higher and the REE profiles were slightly more LREE-enriched than the previously reported KREEP compositions.

Neal, Clive R.↗
NASA NTRS1989

'Nose method' of calculating critical cooling rates for glass formation

The use of the so-called 'nose method' for computing critical cooling rates for glass formation is examined and compared with other methods, presenting data for the glass-forming systems SiO2, GeO2, and P2O5. It is shown that, for homogeneous crystallization, the nose-method will give an overestimate of Rc, a conclusion which was drawn after assessing the enfluence of a range of values for the parameters which control crystal growth and nucleation. The paper also proposes an alternative simple procedure (termed the 'cutoff method') for computing critical cooling rates from T-T-T diagrams, which was shown in the SiO2 and GeO2 systems to be superior to the nose method.

Weinberg, Michael C.↗
NASA NTRS1991

Investigation of anodic and chemical oxides grown on p-type InP with applications to surface passivation for n(+)-p solar cell fabrication

Most of the previously reported InP anodic oxides were grown on a n-type InP with applications to fabrication of MISFET structures and were described as a mixture of In2O3 and P2O5 stoichiometric compounds or nonstoichiometric phases which have properties similar to crystalline compounds In(OH)3, InPO4, and In(PO3)3. Details of the compositional change of the anodic oxides grown under different anodization conditions were previously reported. The use of P-rich oxides grown either by anodic or chemical oxidation are investigated for surface passivation of p-type InP and as a protective cap during junction formation by closed-ampoule sulfur diffusion. The investigation is based on but not limited to correlations between PL intensity and X-ray photoelectron spectroscopy (XPS) chemical composition data.

Faur, Maria↗
NASA NTRS1990

Cation distributions on rapidly solidified cobalt ferrite

The cation distributions in two rapidly solidified cobalt ferrites have been determined using Moessbauer spectroscopy at 4.2 K in an 8-T magnetic field. The samples were obtained by gas atomization of a Co0-Fe2O3-P2O5 melt. The degree of cation disorder in both cases was greater than is obtainable by cooling unmelted cobalt ferrite. The more rapidly cooled sample exhibited a smaller departure from the equilibrium cation distribution than did the more slowly cooled sample. This result is explained on the basis of two competing effects of rapid solidification: high cooling rate of the solid, and large undercooling.

De Guire, Mark R.↗
NASA NTRS1991

Impact melts in the MAC88105 lunar meteorite - Inferences for the lunar magma ocean hypothesis and the diversity of basaltic impact melts

The MAC88105 lunar meteorite, as represented by thin section 78, contains three major types of impact melt breccias. The most abundant type is clast-laden, fine-grained, and rich in Al2O3 (28 wt pct); these clasts constitute most of the meteorite. Their abundance and aluminous nature indicate that the MAC88105 source area was very aluminous. This is consistent with formation of the primordial lunar crust from a global magma ocean. The second type of impact melt is represented by only one clast in 78. It has a basaltic bulk composition similar to many other lunar impact melts, but is significantly richer in P2O5 than most and has a much lower MgO/(MgO + FeO). The third impact-melt type resembles a prominent melt group at Apollo 16, but has lower MgO/(MgO + FeO). These data show that basaltic impact melts are compositionally diverse. Dating samples of the Al-rich impact melts and the new types of basaltic impact melts from this meteorite can test the idea that the Moon suffered a terminal cataclysm 3.9 Ga ago.

Taylor, G. J.↗
NASA NTRS1991

Geochemistry and petrogenesis of proterozoic mafic dykes in north Kerala, southwestern Indian Shield - Preliminary results

Mafic dyke intrusions occur in three distinct orientations ( NNW-SSE and NW-SE and NE-SW) in north Kerala regions, the southwestern part of the Indian Shield. Dating of two NNW-SSE trending dykes by K-Ar method has yielded Middle Proterozoic ages (ca. 1660 Ma and ca. 1420 Ma respectively). Our initial geochemical results on these dyke rocks (0.65-0.15 wt pct K2O, 0.37-0.38 wt pct P2O5, 3.30-1.00 wt pct TiO2, 11-1 p.p.m. Rb, 250-90 p.p.m. Sr, 230-40 p.p.m. Ba, 160-40 p.p.m. Zr, and 30-10 x chondrite rare earth elemental abundances) indicate a transitional character between abyssal and plateau tholeiites. Petrogenetic modelling suggests that the dyke compositions have been derived by different degrees of partial melting of a heterogenous source mantle. The mantle sources with accessory amphibole and/or garnet, variably enriched in LREE and LIL elements, are compatible with the observed geochemical data.

Radhakrishna, T.↗