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At least 55 records · Page 3

Os, Sr, Nd, and Pb isotope systematics of southern African peridotite xenoliths - Implications for the chemical evolution of subcontinental mantle

Isotope analyses of Os, Sr, Nd, and Pb elements were caried out on twelve peridotite xenoliths from the Jagersfontein, Letseng-la-terae, Thaba Patsoa, Mothae, and Premier kimberlites of southern Africa, to investigate the timing and the nature of melt extraction from the continental lithosphere and its relation to the continent formation and stabilization. The distinct Os and Pb isotopic characteristics found in these samples suggested that both the low- and the high-temperature peridotites reside in an ancient stable lithospheric 'keel' to the craton that has been isolated from chemical exchange with the sublithospheric mantle for time periods in excess of 2 Ga.

Walker, R. J.↗

Comparison of Os and Cr Isotopic Methods for the Detection of Meteoritic Components in Impact Melt Rocks from the Morokweng and Vredefort Impact Structures, South Africa

The verification of an extraterrestrial component in impact-derived melt rocks or breccias can be of diagnostic value to provide confirming evidence for an impact origin of a geological structure. Geochemical methods are used to determine the presence of the traces of such a component. In the absence of actual meteorite fragments, it is necessary to search for traces of meteoritic material that is mixed in with the target rocks in breccias and melt rocks. Meteoritic components have been identified for just over 40 impact structures (out of more than 160 known on Earth), which reflects also the detail in which these structures were studied. The identification of a meteoritic component can be achieved by determining the concentrations and interelement ratios of siderophile elements, especially the platinum group elements (PGE), which are several orders of magnitude more abundant in meteorites than in terrestrial upper crustal rocks. The usage of platinum group element abundances and ratios avoids some of the ambiguities that may result if only common siderophile elements (e.g., Cr, Co, Ni) are considered. However, problems may arise if the target rocks have high abundances of siderophile elements, or if the siderophile element concentrations in the impactites are very low. In such cases, the Os and Cr isotopic systems have recently been used for establishing the presence of a meteoritic component in a number of impact melt rocks and breccias. In the past it was attempted to use PGE data to determine the type or class of meteorite for the impactor, but these attempts were not always successful. It is difficult to decide between chondrite types based on PGE abundances, which has led to conflicting identifications for a number of impact structures. Clearly, the identification of a meteoritic component in impactites is not a trivial problem. In this study, we are using a combination of trace element (PGE) analyses and the results from both, Os and Cr isotopic studies, to illustrate the pros and cons of each method on two case studies, namely the Vredefort and Morokweng impact structures. Additional information is contained in the original extended abstract.

Koeberl, Christian↗

Os-187/Os-188 and Highly Siderophile Element Systematics of Apollo 17 Aphanitic Melt Rocks

Introduction: Generally chondritic relative abundances and high absolute abundances of the highly siderophile elements (HSE: Ru, Rh, Pd, Re, Os, Ir, Pt, Au) in Earth s upper mantle provide strong evidence that these elements were added to the Earth following the last major interaction between its metallic core and silicate fraction. So called "late accretion" may have added materials comprising as much as 0.8% of the total mass of the Earth and possibly a similar proportion of mass to the Moon. We have begun to study the chemical nature of late accreted materials to the Earth - Moon system by examining the HSE contained in lunar impact-melt rocks. The HSE contained in melt rocks were largely added to the Moon during the period of time from the origin of the lunar highlands crust (4.4- 4.5 Ga) to the end of the late bombardment period (ca. 3.9 Ga). These materials provide the only direct chemical link to the late accretionary period. The chemical fingerprints of the HSE in late accreted materials may enable us to ascertain under what conditions and where in the solar system the late accreted materials formed. The Os-187/Os-188 ratios (reflecting long-term Re/Os), coupled with ratios of other HSE, can be diagnostic for identifying the nature of the impactor. A critical issue, however, will be deconvolving the exogenous from indigenous components.

Puchtel, I. S.↗

Effect of Silicon on the Activity Coefficient of Rhenium in Fe-Si Liquids: Implications for HSE and Os Isotopes in Planetary Mantles

Metallic cores contain light alloying elements that can be a combination of S, C, Si, and O, all of which have important chemical and physical influences. For Earth, Si may be the most abundant light element in the core. Si dissolved into Fe liquids can have a large effect on the magnitude of the activity coefficient of siderophile elements (SE), and thus the partitioning behavior of those elements between core and mantle. The effect of Si on the highly siderophile elements is only beginning to be studied and the effects on Au, Pd and Pt are significant. Here we report new experiments designed to quantify the effect of Si on the partitioning of Re between metal and silicate melt. A solid understanding of Re partitioning is required for a complete understanding of the Re-Os isotopic systems. The results will be applied to understanding the HSEs and Os isotopic data for planetary mantles, and especially Earth.

Righter, K.↗

Materials Data on Os(SeBr6)2 by Materials Project

OsSe2Br12 crystallizes in the monoclinic C2/m space group. The structure is zero-dimensional and consists of two OsSe2Br12 clusters. Os8+ is bonded to six Br1- atoms to form OsBr6 octahedra that share faces with two equivalent SeBr6 octahedra. All Os–Br bond lengths are 2.50 Å. Se2+ is bonded to six Br1- atoms to form distorted SeBr6 octahedra that share a faceface with one OsBr6 octahedra. There are a spread of Se–Br bond distances ranging from 2.41–2.98 Å. There are four inequivalent Br1- sites. In the first Br1- site, Br1- is bonded in a distorted L-shaped geometry to one Os8+ and one Se2+ atom. In the second Br1- site, Br1- is bonded in a single-bond geometry to one Se2+ atom. In the third Br1- site, Br1- is bonded in a distorted L-shaped geometry to one Os8+ and one Se2+ atom. In the fourth Br1- site, Br1- is bonded in a single-bond geometry to one Se2+ atom.

36 MATERIALS SCIENCE↗

First-principles studies of the unconventional spin-phonon coupling mediated by spin-orbit coupling in pyrochlore Cd 2 Os 2 O 7

Here, we perform systematic first-principles calculations to investigate the spin-phonon coupling (SPC) mediated by spin-orbit coupling in pyrochlore Cd 2 Os 2 O 7 which has the peculiar all-in-all-out noncollinear magnetic ground state. A large SPC coefficient up to 34 cm –1 is found, showing the potential of using this material in thermal spin devices.We further split the SPC coefficients to contributions from symmetric exchange interaction, Dzyaloshinskii-Moriya interaction (DMI), and the single ion anisotropy. Unlike what was assumed in previous studies, the DMI contributions are rather important for most modes. These results provide insights for the understanding of the SPC in 5d transition metal oxides and useful guidance for the search of excellent spin caloritronic materials.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Heat capacity of URu 2 - x Os x Si 2 at low temperatures

Here we perform measurements of the heat capacity as a function of temperature on URu 2-x Os x Si 2 alloys. Our experimental results show that the critical temperature of the second-order phase transition increases while the value of the Sommerfeld coefficient in the ordered state decreases with an increase in osmium concentration. We also observe an increase in the values of the heat capacity at the critical temperature as well as a broadening of the critical fluctuation region with an increase in x. We analyze the experimental data using the Haule-Kotliar model which, in particular, identifies the “hidden order” transition in the parent material UR u2 Si 2 as a transition to a state with a nonzero hexadecapole moment. We demonstrate that our experimental results are consistent with the predictions of that model.

36 MATERIALS SCIENCE↗

Muon spin rotation and relaxation in Pr 1 - x Nd x Os 4 Sb 12 : Superconductivity and magnetism in Pr-rich alloys

The Pr-rich end 0 ≤ x ≤ 0.25 of the alloy series Pr 1-x Nd x ⁢Os 4 ⁢Sb 12 has been studied using muon spin rotation and relaxation. The end compound PrOs 4 ⁢Sb 12 is an unconventional heavy-fermion superconductor, which exhibits a spontaneous magnetic field associated with broken time-reversal symmetry (TRS) in the superconducting phase. Further, no such field is observed in the Nd-doped alloys for x ≥ 0.05, indicating that TRS has been restored. The superfluid density from the vortex-lattice field distribution is insensitive to Nd concentration for x ≲ 0.2, indicating that TRS restoration does not have a strong effect on the superconducting state. No Nd 3+ static magnetism, ordered or disordered, is found down to the lowest temperatures of measurement.

72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS↗

Optimization techniques for FORTRAN 4 (G and H) programs written for the IBM 360 under OS

A fairly complete list is reported of programming techniques which are available to the programmer for optimizing the execution time of production programs written in FORTRAN IV (G and H) for the IBM 360 under OS. After the program has been complied under FORTRAN H, OPT=2, then the process of actually changing code begins. The bulk of execution time of FORTRAN programs can almost always be attributed to a few loops, and primary consideration is given to these.

Dean, J. L.↗

Modification of os calcis bone mineral profiles during bedrest

The mineral content of the left central os calcis was determined using the photon absorptiometric technique modified for the space missions to permit area scanning, and was compared with total body calcium balance changes. The instrument consists of a rectilinear scanner that is programmed by a specially designed control module to move a low energy X-ray emitting radionuclide placed in opposition to a detector to scan the foot which is places between them. The foot is placed in a plexiglas box filled with water to provide tissue equivalence and to compensate for irregularities in thickness of tissue cover that surrounds the bone. The mineral content is obtained from basic attenuation equation.

Vogel, J. M.↗

Determination of CA-41, I-129 and OS-187 in the Rochester tandem accelerator and some applications of these isotopes

The measurement of Ca-41 and I-129 utilizing the Rochester Tanden Accelerator Mass Spectrometer (TAMS) is discussed. Ca-41, having a half-life of 100,000 yrs., is of potential use for the dating of ground water as well as of bones in the age range between 50,000 and 1 million yrs. A major problem for the measurement of Ca-41 with TAMS is the fact that calcium does not readily form negative atomic ions. It does, however, form negative molecular ions. The production of CaO ions from compounds such as CaO and CaCO3 and from free Ca molecules sprayed with oxygen gas was studied. A project to utilize I-129 as a tracer for hydrothermal convection in sediment-covered oceanic crust is also briefly described. Finally, plans to use the Os-187/Os-186 ratio for the determination of extraterrestrial material in the Ries crater in Germany are summarized.

Fehn, U.↗

Ultraviolet light curves of galactic and extra-galactic classical CNO novae: PW Vul, OS, and LMC 1988 no. 1 and no. 2

In order to determine the comparative energy budgets of novae in outburst, the ultraviolet light curves for a number of novae are determined. The low dispersion IUE (International Ultraviolet Explorer) spectra of PW Vul 1984, OS And 1986, LMC 1988 number 1 and number 2 and obtained values for the integrated energy emitted in the wavelength interval from 1200 to 3400 A, not including the geocoronal Lyman-alpha emission line are re-examined. The light curves show that the brightness of the nova declines much more slowly in the ultraviolet than the optical, that the maximum brightness of the nova occurs much later in the ultraviolet than in the optical, and the peak luminosity is super Eddington for LMC 1988 number 2.

Austin, S.↗

Re-Os Isotope Systematics in Lunar Soils and Breccias

Lunar soil and breccia samples show a narrow range in 187Os/188Os, in the range for H-chondrites and unfractionated irons. All samples show enrichments in 187Re/188Os, possibly reflecting loss of Os, associated with the terminal lunar cataclysm. Additional information is contained in the original extended abstract.

Chen, J. H.↗

Re-187 Os-187 Isotopic and Highly Siderophile Element Systematics of Group IVB Irons

Study of the magmatic iron meteorite groups permits constraints to be placed on the chemical and isotopic composition of parent bodies, and the timing of, and crystal-liquid fractionation processes involved in the crystallization of asteroidal cores. Here we examine Re-Os isotopic and trace elemental systematics of group IVB irons. Compared to most irons, the irons comprising this group are enriched in some of the most refractory siderophile elements, yet highly-depleted in most volatile siderophile elements. These characteristics have been attributed to processes such as high temperature condensation of precursor materials and oxidation in the parent body. Most recently it has been suggested that both processes may be involved in the chemical complexity of the group. Here, high precision isotopic and highly siderophile element (HSE) concentrations are used to further examine these possible origins, and the crystallization history of the group. In addition, we have begun to assess the possibility of relating certain ungrouped irons with major groups via multi-element, trace element modeling. In a companion abstract, the isotopic and trace element systematics of the ungrouped iron Tishomingo are compared with the IVB irons.

Honesto, J.↗

Materials Data on Os(NCl3)2 by Materials Project

OsCl6N2 is Fluorite structured and crystallizes in the cubic Fm-3m space group. The structure is zero-dimensional and consists of eight ammonia molecules and four hexachloroosmium molecules.

36 MATERIALS SCIENCE↗