Search NASA⌕ Search

SEARCH · Search NASA

Results for “trace elements”

Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 955 records · Page 53

Utilization of nuclear methods for materials analysis and the determination of concentration gradients

The various types of nuclear chemical analysis methods are discussed. The possibilities of analysis through activation and direct observation of nuclear reactions are described. Such methods make it possible to analyze trace elements and impurities with selectivity, accuracy, and a high degree of sensitivity. Such methods are used in measuring major elements present in materials which are available for analysis only in small quantities. These methods are well suited to superficial analyses and to determination of concentration gradients; provided the nature and energy of the incident particles are chosen judiciously. Typical examples of steels, pure iron and refractory metals are illustrated.

Darras, R.↗

Viscosity and thermal conductivity of model Jupiter atmospheres

The viscosity and thermal conductivity coefficient are estimated for three models of the atmosphere of Jupiter: a heavy model consisting of 22% helium and 78% hydrogen, a nominal model consisting of 11% helium and 89% hydrogen, and a light model consisting of pure hydrogen. The effect of trace elements is neglected. Linearized approximations are used for the transport coefficients of the mixtures; these are found to be in almost constant ratio to the values for pure hydrogen, independent of temperature. Short Basic language programs for computing the coefficients are listed.

Hansen, C. F.↗

Diffusion and phase change characterization by mass spectrometry

The high temperature diffusion of trace elements in metals and alloys was investigated. Measurements were made by high sensitivity mass spectrometry in which individual atoms were detected, and quantitative data was obtained for zircaloy-2, 304 stainless steel, and tantalum. Additionally, a mass spectrometer was also an analytical tool for determining an allotropic phase change for stainless steel at 955 C, and a phase transition region between 772 C and 1072 C existing for zircaloy-2. Diffusion rates were measured in thin (0.001" (0.0025 cm) and 0.0005" (0.0013 cm)) ribbons which were designed as high temperature thermal ion sources, with the alkali metals as naturally occurring impurities. In the temperature and pressure regime where diffusion measurements were made, the solute atoms evaporated from the ribbon filaments when the impurities diffused to the surface, with a fraction of these impurity atoms ionized according to the Langmuir-Saha relation. The techniques developed can be applied to many other alloys important to space vehicles and supersonic transports; and, with appropriate modifications, to the diffusion of impurities in composites.

Koslin, M. E.↗

Comparison of the properties of some synthetic crudes with petroleum crudes

Physical properties and chemical compositions of six synthetic crudes were determined. The results were compared to those of typical petroleum crudes, with the interest being the feasibility of making jet fuels from oil shale and coal syncrudes. The specific gravity, viscosity, and pour point were measured, showing that these crudes would be described as heavier rather than lighter crudes. The boiling range distribution of the crudes was determined by distillation and by gas chromatography. In addition, gel permeation chromatograms were obtained, giving a unique molecular weight distribution profile for each crude. Analyses for carbon, hydrogen, nitrogen and sulfur concentrations were performed, as well as for hydrocarbon group type and trace element concentrations. It was found that the range in concentration of vanadium, an element whose presence in turbine fuels is of major concern, was lower than that of petroleum crudes. Sodium and potassium, other elements of concern, were present in comparatively high concentrations.

Antoine, A. C.↗

Measurement techniques for trace metals in coal-plant effluents: A brief review

The strong features and limitations of techniques for determining trace elements in aerosols emitted from coal plants are discussed. Techniques reviewed include atomic absorption spectroscopy, charged particle scattering and activation, instrumental neutron activation analysis, gas/liquid chromatography, gas chromatographic/mass spectrometric methods, X-ray fluorescence, and charged-particle-induced X-ray emission. The latter two methods are emphasized. They provide simultaneous, sensitive multielement analyses and lend themselves readily to depth profiling. It is recommended that whenever feasible, two or more complementary techniques should be used for analyzing environmental samples.

Singh, J. J.↗

Luna 24 - Lateral heterogeneity in the lunar crust

Results of petrological investigations of Luna 24 soil samples are compared with data from Apollo and other Luna missions in order to determine the large scale composition of the lunar surface and crust. Modal analysis of the 90 to 150 micron soil fraction and electron microprobe analysis of glass spheres and fragments of the Luna 24 core sample are presented. High and low MgO mare basalt compositional clusters are found, suggesting the derivation of southern Mare Crisium basalts from two magmas. A model of Luna 24 soils as being composed of a mixture of glass-poor mare material and glass-rich highland material is found to be consistent with glass and agglutinate modal abundances. Comparisons show that potassium, and by inference all lithophile trace elements, are depleted on the eastern limb of the moon relative to the central nearside. The observed depletion is interpreted to be characteristic of the underlying crust and mantle as well as the surface.

Warner, J. L.↗

Chemistry, mineralogy and petrology of seven greater than 1 mm fragments from Mare Crisium

Results are summarized for a consortium study of the chemistry, mineralogy, and petrology of seven Luna 24 fragments greater than 1 mm in size and having a mass of about 2 mg each. The fragments include four samples of mare ferrobasalt composition, one vitrophyre with the composition of a Mg-rich VLT mare basalt, one agglutinate, and one plagioclase fragment. It is found that: (1) the ferrobasalt is a highly fractionated mare rock very low in alkalis and TiO2, is similar to the less fractionate Apollo 17 VLT basalts, and is quite low in large-ion lithophile trace-element content; (2) the rare-earth-element patterns of the ferrobasalts are typical of VLT basalt, but some ophitic basalts have positive Eu anomalies, while others have negative Eu anomalies typical of mare basalts; and (3) the agglutinate is feldspathic and similar in composition to soil fines in Fe, Cr, Ca, and Al.

Laul, J. C.↗

Chemical and Sr-isotopic characteristics of the Luna 24 samples

The chemical and Sr isotopic characteristics of Luna 24 bulk soil samples are determined and interpreted within the framework of lunar mare basalt evolution. Major and trace element compositions lead to the suggestion of candidate rock types consisting of a basalt/gabbro with very low TiO2 and MgO content (52%), a very low TiO2 basalt with 10% MgO (23%), olivine vitrophyre (20%), low K Fra Mauro basalt (4%) and anorthositic gabbro (1%). The proposed compositions are supported by the agreement of mixing models based on the proposed compositions with observed soil compositions. Sr ratios for plagioclase samples imply a lower Sr-87/Sr-86 value for low Mg soils than for other mare basalts and higher Rb/Sr and a more evolved Sr ratio in high Mg basalts. Rb, Sr and rare earth element compositions for low Mg basalts fit a model of partial remelting of cumulates containing small amounts of plagioclase.

Nyquist, L. E.↗

Petrology, chemistry, age and irradiation history of Luna 24 samples

The results of petrological, chemical, isotopic age determination and irradiation studies of sample 24170 from the 170 cm depth of the regolith core returned from Mare Crisium by Luna 24 are presented. The sample is found to be comprised of fragments from a single igneous rock, with mineralogical evidence indicating it to be a mare basalt. The crystallization age is determined by Sm-Nd and Ar(40)-Ar(39) ages to be 3.30 AE, establishing the presence of relatively young flows. All soil samples show low trace element compositions with minimum contamination by KREEPUTh-rich materials. Rb-Sr and Sm-Nd relations reflect the absence of significant fractionation at ages younger than 4.5 AE. One soil sample shows extremely large neutron capture effects, imposing a new lower limit to the neutron production rate in the regolith and requiring the addition of irradiated materials from depth.

Wasserburg, G. J.↗

Mesosiderites and howardites - Igneous formation and possible genetic relationships

Neutron activation data are presented for major, minor, and trace elements in whole rock howardites and silicates from mesosiderites. Compositions of howardites and mesosiderites are similar and intermediate between those of eucrites and diogenites. It is indicated that mesosiderites have a higher normative silica component than howardites. It appears that this results partly from a higher content of a highly evolved igneous component and partly from in situ reduction of FeO to Fe followed by magnetic separation of metal prior to analysis. It is shown that light rare earth elements are enriched in some mesosiderites.

Mittlefehldt, D. W.↗

The origin of metal clasts in the Bencubbin meteoritic breccia

The Bencubbin meteorite is a shock-welded breccia consisting of a diverse collection of metal and silicate clasts. Several types of evidence suggest that the metal clasts in Bencubbin retain chemical abundances that were established during condensation. The Cr, Ni, P and trace element abundances are consistent with condensation calculations and are much closer to the predicted compositions of metal condensates than the CM metal particles. In addition, petrographic and chemical evidence strongly suggest that the breccia components were incorporated as solid clasts within the breccia prior to a shock heating event of very short duration, which did not produce significant metamorphic effects.

Newsom, H. E.↗

Compositional-petrographic investigation of pristine nonmare rocks

Twenty-six highlands rocks and clasts are characterized petrographically and by determinations of major and trace elements, including key incompatibles and siderophiles. Most samples were selected in the hope that they would prove to be pristine, i.e., unremelted, monomict products of endogenous lunar magmatism. About 3/5 are almost certainly pristine, while about 1/4 are definitely non-pristine, and the remainder await further study before pristinity may be either proven or disproven. All of the major conclusions of Warren and Wasson (1977) about the significance of pristine nonmare rocks and the nature of the lunar crust still appear correct. Probably none, or virtually none, of the samples possessing the attributes by which 'pristinity' is judged formed as 'secondary differentiates' in giant impact melt pools, as Delano and Ringwood (1978) propose. Those which possess markedly plutonic textures (e.g., 62236) almost certainly did not.

Warren, P. H.↗

Pyroxene stability and the composition of the lunar magma ocean

Data on the liquidus stability fields of pyroxene phases in lunar-like systems are used to predict the crystallization sequence and residual liquid composition of lunar magma oceans. Fractional and equilibrium crystallization of major and trace elements are modeled quantitatively through use of analytical expressions for liquidus phase boundaries. According to the model, a magma ocean that differentiated chiefly at low pressure and contained 6-8 wt% A1203 and a subchondritic Ca/Al ratio probably formed the lunar crust. The chondrite-normalized pattern of heavy REE depletion in the magma ocean could have developed by self-contamination of extensively fractionated liquids, or could have been imparted during accretion.

Longhi, J.↗

Chemistry of orange/black soils from core 74001/2

Double core 74001/2 soils were studied. Bulk soils and the 90-150 micrometer and less than 20 micrometer size fractions of 13 soils from the core for both major and trace elements by instrumental neutron activation analysis were analyzed. The orange and black glassy soils in the core 74001/2 are homogeneous in composition and due to their unusual compositional characteristics probably have derived from a single source with the same composition. The top of the core has been reworked to a depth of about 5 cm. The reworked layer is marked by compositional differences in the first 3 cm which reflect the addition (at least 10%) of materials including mare basalt and a CaO-rich component. The maturity profile (I sub s/FeO) clearly indicates reworking depth of about 5 cm. It is likely that at least some of the ferro-magnetically active component (including agglutinitic glass) has been 'inherited' with the added material.

Blanchard, D. P.↗

Chemistry and petrology of size fractions of Apollo 17 deep drill core 70009-70006

Instrumental neutron activation analysis was used to examine 34 major, minor and trace elements in 48 bulk soils and size fractions (90-1000 microns, 20-90 microns and less than 20 microns) of the Apollo 17 deep drill core sections 70009-70006 (upper 130 cm). Modal data were also obtained for the less than 20 micron size fraction. Preliminary results indicate that (1) the chemistry of the greater than 90 micron and 20-90 micron coarse fractions is identical but quite different from the less than 20 micron fine fraction; (2) the upper 50 cm of the drill core is highly enriched in mare material; (3) the dominant source of highland material is KREEPy instead of anorthositic; and (4) indigenous volatiles such as Zn are quite high in all size fractions.

Laul, J. C.↗

The petrogenesis of L-6 chondrites - Insights from the chemistry of minerals

Measurements of the major, minor and trace element abundances of the major minerals of the L-6 chondrites Alfianello, Colby (WI) and Leedey are used to investigate the formation mechanisms of L-6 chondrites. Electron microprobe analysis was performed on individual grains of each mineral, and separated minerals were analyzed by instrumental and radiochemical neutron activation analysis. The compositions of the three meteorites are observed to be generally uniform, however different abundances and distributions of rare earth elements and Co and Ni indicate that the meteorites have different petrogenetic histories. Alkali element distributions are found to be incompatible with internal equilibration of a closed system.

Curtis, D. B.↗

The upper mantle transition region - Eclogite

The upper mantle transition region is usually considered to be peridotite which undergoes a series of phase changes involving spinel and post-spinel assemblages. There are difficulties associated with attempts to explain the 220, 400 and 670 km discontinuities in terms of phase changes in a peridotitic mantle. Moreover, in a differentiated earth there should be large quantities of eclogite in the upper mantle. Eclogite is denser than Al2O3-poor mantle to depths of 670 km, but it stays in the garnet stability field to pressures in excess of those required to transform depleted mantle to denser phases such as ilmenite and perovskite. Eclogite, therefore, remains above 670 km. The seismic properties of the transition region are more consistent with eclogite than peridotite. Most of the mantle's inventory of incompatible trace elements may be in this layer, which is a potential source region for some basalt magmas. The radioactivity in this layer is the main source of mantle heat flow, 0.7 microcalorie/sq cm-sec, and drives upper mantle convection.

Anderson, D. L.↗

Hotspots and the evolution of the mantle

Trace element patterns show that continental and ocean island basalts are complementary to mid-ocean ridge basalts (MORB). The relative sizes of the two source regions can be estimated from enrichment/depletion patterns. Their combined volume, computed from estimates of whole mantle abundances, occupies the entire upper mantle. The source regions appear to be the result of an early differentiation of the mantle. The MORB source evolved from the melt fraction which lost its late stage enriched fluids to the overlying plume source. The MORB source is primarily garnet and clinopyroxene, consistent with it being an eclogite cumulate.

Anderson, D. L.↗