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Rare earth alloys spin disorder resistivity in crystalline electric field absence and presence
Apollo 12 lunar soils, rocks and core samples, determining rare earth, alkali and alkaline earth elements concentrations
Apollo 12 lunar rock rare earth element abundances, comparing to Icelandic basalt flow
Rare earth elements and trace elements abundance in Apollo 12 igneous rocks, breccia and lunar soil
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Measurements were made of the magnetic entropy and magnetization of powered samples of the compounds Dy2Ti2O7 and Gd3Al5O12. The magnetization was measured for temperatures at and below 4.2 K, in applied fields ranging to 7.0 tesla. Isothermal changes in magnetic entropy were measured for temperatures from 1.2 to 20 K, in applied fields up to 10 tesla. The results of the measurements are consistent with a doublet ground state for Dy2Ti2O7, and an eight-fold degenerate ground state for Gd3Al5O12. Absolute values of magnetic entropy have been obtained at the lower temperatures, permitting the isotherms to be properly located in the S-H plane with the use of adiabatic magnetization data. The iso-field lines in the S-T plane were determined. The results indicate that Dy2Ti2O7 can absorb a maximum of 71 + or - 4 joules/kg of heat at 4.2 K, while Gd3Al5O12 can absorb 233 + or - joules/kg at the same temperature. The large difference between the two is most likely a result of crystal field interactions in the dysoprosium compound. Both materials can be cycled adiabatically between 4.2 and 20 K.
An analysis was made of regolith from layer A of the Luna 16 sample for rare earth elements, by a chemical spectral method. Chemical and ion exchange concentrations were used to determine the content of 12 elements and Y at the level 0.001 to 0.0001 percent with 10 to 15 percent reproducibility of the emission determination. Results within the limits of reproducibility agree with data obtained by mass spectra, activation, and X-ray fluorescent methods.
The search for a new high-modulus, high-temperature glass fiber involved the preparation of 500 glass compositions lying in 12 glass fields. These systems consisted primarily of low atomic number oxides and rare-earth oxides. Direct optical measurements of the kinetics of crystallization of the cordierite-rare earth system, for example, showed that the addition of rare-earth oxides decreased the rate of formation of cordierite crystals. Glass samples prepared from these systems proved that the rare-earth oxides made large specific contributions to the Young's modulus of the glasses. The best glasses have moduli greater than 21 million psi, the best glass fibers have moduli greater than 18 million psi, and the best glass fiber-epoxy resin composites have tensile strengths of 298,000 psi, compressive strengths of at least 220,000 psi, flexural strengths of 290,000 psi, and short-beam shear strengths of almost 17,000 psi.
Ultraviolet photometry by OAO-2 was made of alpha 2 CVn covering the entire 5.5d period of this magnetic Ap variable. The light curves ranging from 1330 A to 3320 A indicate the dominant role of rare-earth line-blanketing in redistributing flux. In a broad depression of the continuum covering 2300-2600 A, scanner observations possibly identify strong lines of Eu III as major contributors to this feature. At maximum intensity of the rare-earth lines, the ultraviolet continuum shortward of 2900 A is greatly diminished while the longer wavelength regions into the visual become brighter. In addition, there is evidence that the hydrogen line opacity is variable and the photoionization edge of Si I at 1680 A is identified.
K, Rb, Sr, Ba and rare-earth concentrations in some Japanese lavas have been determined by mass-spectrometric stable-isotope dilution. The samples fall into three rare-earth groups corresponding to tholeiitic, high alumina and alkali basalts. Japanese tholeiites have trace element characteristics similar to those of oceanic ridge tholeiites except for distinctly higher relative concentrations of Ba. Japanese lavas may result from various degrees of partial fusion of amphibole eclogite.
Determination of rare-earth elemental abundances in meteorites
Rare-earth element abundance patterns in Hawaiian basalts determined by neutron activation analysis
Data are presented on major and trace element concentrations determined by atomic absorption spectrophotometry, colorimetry, and isotope dilution in Apollo 15 mare basalt 15555 from the Hadley Rille area, as well as on trace element concentrations determined in plagioclase and pyroxene separates from basalt 15555 and in soil 15531 from the same area. Most of the chemical differences between basalt 15555 and soil 15531 could be accounted for if the soil were a mixture of 88% basalt, 6% KREEP (a component, identified in other Apollo soils, rich in potassium, rare-earth elements, and phosphorus), and 6% plagioclase.
Far-ultraviolet photometry by OAO-2 is presented for alpha squared CVn covering the entire 5.47-day period of this magnetic Ap variable. The light curves ranging from 1330 to 3320 A indicate that there are two important sources of back warming from far-ultraviolet absorption. Strong line blanketing by the rare earths redistributes flux longward of the Balmer discontinuity, causing the major observed photometric variations. In addition, a second source, which may be due to a combination of continuous opacities and line blanketing from the iron-peak and rare-earth groups below 1600 A, apparently redistributes flux into the region of the Balmer discontinuity. It is also found that ground-based determinations of the effective temperature are overestimated due to the flux redistribution from far-ultraviolet absorption. The effective temperature of alpha squared CVn derived from OAO and ground-based absolute fluxes is found to be 11,200 K, which remains constant over the cycle.
Niobian rutile was found in a KREEP lithic fragment of basaltic texture. The niobian rutile contains 85.3% TiO2, 7.1% Nb2O5, 2.65% Cr2O3, 0.70% ZrO2, 0.61% SiO2, 0.82% Al2O3 0.61% FeO, 0.52% CaO, 0.22% V2O3 in addition to minor amounts of MnO, MgO, and CeO2. Rare-earth elements were not detected, in contrast with lunar niobian rutile of Marvin (1971). Coexisting minerals in the KREEP fragment are major amounts of plagioclase and orthopyroxene, and minor amounts of olivine, ilmenite, augite, barian K-feldspar, whitlockite, troilite, Ni-Fe, zirkelite, and chromite.
The results of the analysis by neutron activation of six samples from the Luna 20 mission and one sample of less than 1 mm fines from Apollo 16 are reported. The concentrations of the rare-earth elements (REE) in the samples of fines from Luna 20 and Apollo 16 are less than those found for corresponding materials from the mare areas but a negative Eu anomaly is still present. The concentrations of the REE in fines from Luna 20 are only about two-thirds as great as in the sample of Apollo 16 fines, but the concentration of Co, Sc and Cr are greater by factors ranging from 1.5 to 2.3.
The concentrations of major and trace elements have been determined in igneous rocks from Apollo 15. All materials analyzed have typical depletions of Eu except for minerals separated from sample 15085. Four samples have concentrations of trace elements that are similar to those of KREEP. The samples of mare basalt from Apollo 15 have higher concentrations of FeO, MgO, Mn, and Cr and lower concentrations of CaO, Na2O, K2O, and rare-earth elements (REE) as compared to the samples of mare basalt from Apollos 11, 12, and 14. The samples can be divided into two groups on the basis of their normative compositions. One group is quartz normative and has low concentrations of FeO while the other is olivine normative and has high concentrations of FeO. The trace element data indicate that the samples of olivine normative basalt could be from different portions of a single lava flow.
The compressional velocities are estimated for materials thought to be important in the lunar interior and compared with lunar seismic results. The lower lunar crust has velocities appropriate for basalts or anorthosites. Anorthosite is preferred if lunar basalts result from a small degree of partial melting. The high velocities associated with the uppermost mantle imply high densities and a change to a lighter assemblage at depths of the order of 120 km. Ca- and Al-rich minerals are important components of both the lower crust and the upper mantle. Most of the moon may have accreted from refractory material rich in Ca, Al, U, and the rare-earth elements. The important mineral of the upper mantle is garnet; possible accessory minerals are kyanite, spinel and rutile. If the seismic results stand up, the high-velocity layer in the moon is more likely to be a high-pressure form of anorthosite than eclogite, pyroxenite, or dunite.