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At least 37 records · Page 2

Chemical abundances in Hg-Mn stars

An abundance analysis has been conducted of 21 elements in 21 Hg-Mn, two Si-Cr, and six normal stars using model atmospheres and high-dispersion spectroscopy in the visible and UV. Manganese line strengths imply abundances that correlate well with stellar effective temperature. Within the studied sample of Hg-Mn stars there appears to be no correlation of abundances of any element with projected rotational velocity. Abundances in several Hg-Mn stars show patterns that are probably consistent with diffusion but difficult to reconcile with equilibrium nucleosynthesis. In general, no combination of gross stellar physical parameters is sufficient to characterize the patterns of line strengths observed in Hg-Mb Hg-Mn stars.

Heacox, W. D.↗

Eutectic equilibria in the quaternary system Fe-Cr-Mn-C

The constitution of the quaternary system, Fe-Cr-Mn-C and to a lesser extent of the quinary system, Fe-Cr-Mn-Al-C were examined for in situ composite alloy candidates. Multivariant eutectic compositions were determined from phase equilibria studies wherein M7C3 carbides (approximately 30% by volume) formed from the melt within gamma iron. An extended field of the hexagonal carbide, (Cr, Fe, Mn)7 C3, was found without undergoing transformation to the orthorhombic structure. Increasing stability for this carbide was found for higher ratios of Cr/Fe(+) Cr + Mn. Aluminum additions promoted a ferritic matrix while manganese favored the desired gamma austenitic matrix. In coexistence with the matrix phase, chromium enters preferentially the carbide phase while manganese distributes equally between the gamma matrix and the M7C3 carbide. The composition and lattice parameters of the carbide and matrix phases were determined to establish their respective stabilities.

Nowotny, H.↗

Cosmogenic Mn-53 in meteorites

The distributions of the Mn-53 contents in 106 nonantarctic and 112 antarctic chondrites were analyzed. A correlation analysis of these distributions showed that the correlation coefficient is a maximum r sub max = 0.75 plus or minus 0.03) when the histogram for antarctic chondrites is displaced by 40 plus or minus 8 dpm kg-1Fe towards lower Mn-53 contents. The distribution of Mn-53 saturated contents in nonantarctic ordinary chondrites was investigated as a function of their radiation age (T). It is found that the Mn-53 average content is higher by (21 plus or minus 9)% in H-chondrites with radiation age T approximately 12 Myr than in thse with T 12 Myr. This effect can be attributed to the fact that a considerable proportion of H-chondrites with T 12 Myr originates from a comet or from the objects of Chiron like, with the orbits more inclined to the ecliptic plane and/or more extended, which caused their irradiation by cosmic rays of higher intensity.

Alexeev, V. A.↗

Directional solidification of Bi-Mn alloys using an applied magnetic field

Off-eutectic compositions of Bi-Mn were directionally solidified in applied transverse magnetic fields up to 3 kG, to determine the effects on thermal and solutal convection. Plane front directional solidification of eutectic and near-eutectic Bi-Mn results in a two-phase rodlike morphology consisting of ferromagnetic MnBi rods in a Bi solid solution matrix. Compositions of either side of the eutectic were studied in growth orientations vertically up and down. Temperature gradient was monitored during growth by means of an in-situ thermocouple. For Bi-rich compositions, the magnetic field appeared to increase mixing as determined from thermal, morphological, chemical, and magnetic analyses. For Mn-rich compositions, morphological and chemical analyses suggest some reduction in mixing due to application of the magnetic force. The capability for carrying out directional solidification of Bi-Mn in high longitudinal magnetic fields was established.

Decarlo, J. L.↗

Iron-base superalloys - A phase analysis of the multicomponent system (Fe-Mn-Cr-Mo-Nb-Al-Si-C)

In the course of studies on the iron-rich multicomponent system Fe-Mn-Cr-Mo-Nb-Al-Si-C, work was concentrated on pertinent quinary and six-component combinations namely Fe-Mn-Al-Si-C, Fe-Cr-Al-Si-C and Fe-Mn-Cr-Al-Si-C which had been elaborated at 65, 72, and 80 wt pct Fe. Manganese acts as a strong stabilizer for the cementite carbide. Chromium seems to stabilize the iron aluminide Fe2Al5 which forms in a considerable amount within an alloy of nominal composition Fe(65)Mn(15)Cr(12)Al(5)Si(2)C(1) (percent by weight). Although the Mn3AlC carbide is, like Fe3AlC, a perovskite carbide, manganese does not appear to favor the formation of the perovskite carbide. Because of the relatively low sintering temperature (700 C), for al large portion of the samples equilibria conditions are not always reached.

Gupta, H.↗

V, Cr, and Mn in the earth, moon, EPB, and SPB and the origin of the moon - Experimental studies

The abundances of V, Cr, and Mn inferred for the mantles of the earth and moon decrease in that order and are similar in both mantles (but distinct from those in the mantles of the Eucrite Parent Body and Shergottite Parent Body), suggesting a common origin for the mantles of the earth and the moon. This hypothesis was investigated on the basis of a comparison between the depletions of V, Cr, and Mn in the mantles of the earth and the moon, and the metal/silicate partition coefficients of these elements at 1260 C and 1 bar pressure among a S-bearing metallic liquid, a silicate melt, and a FeNi alloy. It was found that the earth and the moon depletions of V, Cr, and Mn are not correlated with metal/silicate partition coefficients; the V and Cr partitioned into S-rich metallic liquids under reducing conditions more strongly than Mn, consistent with the relative volatilities of these elements. This indicates that the depletion patterns of these elements in the mantles of the earth and moon cannot be attributed primarily to terrestrial core formation.

Drake, Michael J.↗

Near Infrared Luminescence Properties of Mn(5+): Ca5(PO4)3F

We report a spectroscopic investigation of Mn(5+) doped Ca5(PO4)(sub 3)F or FAP. Mn(5+) doped crystals have recently attracted world wide attention for potential solid-state laser applications. Following optical excitation of Mn: FAP with the 600 nm output of a Nd: YAG OPO laser system, we observed a strong near infrared luminescence centered at around 1150 nm. The room temperature luminescence decay time was measured to be approximately 635 microseconds. We attribute the infrared luminescence to the(1)E yields (3)A2 transition of tetrahedrally coordinated Mn5+ ions located in a strong crystal field environment. Absorption, luminescence and lifetime data of Mn: FAP will be presented and discussed.

Davis, Valetta R.↗

Enstatite Meteorites and the Original Heterogeneity of Mn-53 Distribution in the Solar Nebula

We have shown earlier that the relative abundance of radiogenic Cr-53 in bulk ordinary chondrites (approximately 0.48 epsilon) is clearly different from that in the earth-moon system (0 epsilon). The SNC parent body (Mars) is characterized by an intermediate Cr-53 excess (approximately 0.23 epsilon). We have also shown that the Mn-Cr systematics of the howardite-eucrite-diogenite parent body (HED PB, the asteroid Vesta) is consistent with the chondritic Mn/Cr ratio in the bulk HED PB and that it has a Cr-53 excess of approximately 0.5 epsilon units which is within error the same as that of chondrites. It appears that the excesses of Cr-53 in these planets are a function of their present heliocentric distance. The study of some other meteorite classes (angrites, pallasites, primitive achondrites) has shown that their Mn-CR systematics is consistent with that of the ordinary chondrites. The observed gradient in the radiogenic Cr-53 abundances can be explained by a). an early volatility controlled radial Mn/Cr fractionation in the nebula or b). an original heterogeneity of Mn-53. The first assumption, however, requires the Mn/Cr ratios of the bulk Earth and Mars to be considerably lower than the inferred model Mn/Cr ratios for these two planets. For this reason, we suggested that the observed gradient is due to an original radial Mn-53 heterogeneity in the late nebula.

Lugmair, Guenter W.↗

Measurement of cosmic ray produced Mn-53 in deep sea metallic spherules

Cosmic ray originated Mn-53 nuclides were measured in deep sea metallic spherules by neutron activation analysis. The spherules may be fused micrometeoroids or ablation droplets from larger objects; the low activities of Mn-53 may indicate its evaporation loss resulting from the heating in the earth's atmosphere or short exposure age. The Mn-53 nuclide is now being measured in chondritic spherules, and Be-10 and Cl-36 concentrations are determined in individual spherules using ion counting methods.

Nishiizumi, K.↗

Optical conductivity of alpha-Mn

The optical constants were measured at room temperature in the photon-energy range 0.6 to 6.5 eV on evaporated thin films. Evaporation conditions were chosen that gave the alpha-Mn crystal structure with reasonably large grains. The optical conductivity was separated into intraband and interband contributions by fitting to the Drude formula at low energies. The results are anomalous in comparison to other 3d transition metals. The free-electron lifetime is exceptionally sort (in agreement with the large dc resistivity of Mn), and the interband transitions seem unusually weak at the lower energies. Possible explanations related to the complicated crystal structure of alpha-Mn are discussed.

Scoles, K. J.↗

Surface chemistry, friction and wear of Ni-Zn and Mn-Zn ferrites in contact with metals

X-ray photoelectron and Auger electron spectroscopy analysis were used in sliding friction experiments. These experiments were conducted with hot-pressed polycrystalline Ni-Zn and Mn-Zn ferrites, and single-crystal Mn-Zn ferrite in contact with various transition metals at room temperature in both vacuum and argon. The results indicate that Ni2O3 and Fe3O4 were present on the Ni-Zn ferrite surface in addition to the nominal bulk constituents, while MnO2 and Fe3O4 were present on the Mn-Zn ferrite surface in addition to the nominal bulk constituents. The coefficients of friction for the ferrites in contact with metals were related to the relative chemical activity of these metals. The more active the metal, the higher is the coefficient of friction. The coefficients of friction for the ferrites were correlated with the free energy of formation of the lowest metal oxide. The interfacial bond can be regarded as a chemical bond between the metal atoms and the oxygen anions in the ferrite surfaces. The adsorption of oxygen on clean metal and ferrite does strengthen the metal-ferrite contact and increase the friction. The ferrites exhibit local cracking and fracture with sliding under adhesive conditions. All the metals transferred to he surfaces of the ferrites in sliding.

Miyoshi, K.↗

Optical conductivity of alpha-Mn

The optical constants were measured at room temperature in the photon-energy range 0.6-6.5 eV on evaporated thin films. Evaporation conditions were chosen that gave the alpha-Mn crystal structure with relatively large grains. The optical conductivity was separated into intraband and interband contributions by fitting to the Drude formula at low energies. The results are anomalous in comparison to other 3d transition metals: the free-electron lifetime is exceptionally short (in agreement with the large dc resistivity of Mn), and the interband transitions seem unusually weak at the lower energies. Possible explanations related to the complicated crystal structure of alpha-Mn with its loss of point symmetry at the atom sites are discussed.

Scoles, K. J.↗

Surface chemistry, friction, and wear of Ni-Zn and Mn-Zn ferrites in contact with metals

X-ray photoelectron and Auger electron spectroscopy analysis were used in sliding friction experiments. These experiments were conducted with hot-pressed polycrystalline Ni-Zn and Mn-Zn ferrites, and single-crystal Mn-Zn ferrite in contact with various transition metals at room temperature in both vacuum and argon. The results indicate that Ni2O3 and Fe3O4 were present on the Ni-Zn ferrite surface in addition to the nominal bulk constituents, while MnO2 and Fe3O4 were present on the Mn-Zn ferrite surface in addition to the nominal bulk constituents. The coefficients of friction for the ferrites in contact with metals were related to the relative chemical activity of these metals. The more active the metal, the higher is the coefficient of friction. The coefficients of friction for the ferrites were correlated with the free energy of formation of the lowest metal oxide. The interfacial bond can be regarded as a chemical bond between the metal atoms and the oxygen anions in the ferrite surfaces. The adsorption of oxygen on clean metal and ferrite does strengthen the metal-ferrite contact and increase the friction. The ferrites exhibit local cracking and fracture with sliding under adhesive conditions. All the metals transferred to the surfaces of the ferrites in sliding. Previously announced in STAR as N83-19901

Miyoshi, K.↗

Sputtering and native oxide formation on (110) surfaces of Cd(1-x)Mn(x)Te

Native oxides on the surface of Cd(1-x)Mn(x)Te (X between 0 and 0.7) have been analyzed on the basis of X-ray photoemission spectroscopy measurements. Depth profile analysis revealed a significant increase in the thickness at higher Mn concentrations and a strong Mn segregation to the surface, respectively. Sputter-induced damage on cleaved (110)-oriented surfaces was analyzed by photoreflectance and photoluminescence measurements. The damage was found to be larger on CdTe than on the alloy. Thermal annealing showed nearly complete restoration for the surface of the alloy, while CdTe revealed irreversible modifications in the near-surface regime upon sputtering and post annealing.

Neff, H.↗

Characterization of Mn-doped In(1-x)Ga(x)As(y)P(1-y) grown by LPEE

Mn-doped In(1-x)Ga(x)As(y)P(1-y) epilayers lattice matched to InP substrate have been grown by the liquid phase electroepitaxial (LPEE) technique. The variation of growth velocity of the epilayers with current density and the doping characteristics of Mn in the epilayer has been studied. The temperature dependence of the hole concentration and the mobility has been analyzed to determine the donor and acceptor densities, thermal activation energy of the level associated with Mn and the dominant scattering mechanisms that limit the hole mobility. The photoluminescence spectra of the doped epilayers are examined at 10 K as a function of the excitation level.

Iyer, Shanthi N.↗

The roles of Zr and Mn in processing and superplasticity of Al-Mg alloys

Processing studies have been conducted on two alloys, of nominal compositions Al-10Mg-0.1Zr or Al-10Mg-0.5Mn, in order to clarify the role of the dispersoid forming Zr or Mn additions. Mechanical property data reveal that the Mn-containing alloy has a lower maximum elongation but exhibits superplastic response over a broader range of temperature. Microstructural investigations and texture analyses were utilized to assess the effect of the presence of Al8Mg5 precipitates in combination with either Al3Zr or Al6Mn dispersoid particles during isothermal rolling at 300 C and subsequent tensile deformation at temperatures from 200-425 C.

Mcnelley, Terry R.↗

Mn-Cr isotopic systematics of Chainpur chondrules and bulk ordinary chondrites

We report on ongoing study of the Mn-Cr systematics of individual Chainpur (LL3.4) chondrules and compare the results to those for bulk ordinary chondrites. Twenty-eight chondrules were surveyed for abundances of Mn, Cr, Na, Fe, Sc, Hf, Ir, and Zn by INAA. Twelve were chosen for SEM/EDX and high-precision Cr-isotopic studies on the basis of LL-chondrite-normalized Mn(LL), Sc(LL), (Mn/Fe)(LL), and (Sc/Fe)(LL) as well as their Mn/Cr ratios. Classification into textural types follows from SEM/EDX examination of interior surfaces.

Nyquist, L.↗

Mn-Cr isotopic systematics of individual Chainpur chondrules

Twenty-eight chondrules separated from Chainpur (LL3.4) were surveyed for abundances of Mn, Cr, Na, Fe, Sc, Hf, Ir, and Zn by Instrumental Neutron Activation Analysis (INAA). Six, weighting 0.6-1.5 mg each, were chosen for Scanning Electron Microscopy (SEM)/Energy Dispersive X-ray (EDX) and high-precision Ce-isotopic studies. LL-chondrite-normalized (Mn/Fe)(sub LL) and (Sc/Fe)(sub LL) were found to be useful in categorizing them. Five chondrules (CH-16, -17, -18, -23, and -28) were in the range 0.5 less than (Mn/Fe)(sub LL) less than 1. 4 and 0.5 less than (Sc/Fe)(sub LL) less than 1.4. The sixth (CH-25) had (Mn/Fe)(sub LL) and (Sc/Fe)(sub LL) ratios of 0.40 and 8.1, respectively, and was enriched in the refractory lithophile elements Sc and Hf and the refractory siderophile element Ir by 2.7 and 4.4x LL abundances respectively. SEM/EDX of exterior surfaces of the chondrules showed they consisted of varying proportions of low- and high-Ca pyroxenes, olivine, glass, kamacite/taenite, and Fe-sulfides. Chromium-53/chromium-52 for the six chondrules and bulk Chainpur (WR) are presented. Chromium-54/chromium-52 is close to terrestrial and does not correlate with Mn/Cr. We provisionally ignore the possibility of initial Cr isotopic heterogeneities among the chondrules. Omitting both the CH-25 and WR data, a linear regression gives initial (Mn-53/Mn-55)(sub I) = 8 +/- 4 x 10(exp -6), corresponding to chondrule formation at Delta(t)(sub LEW) = -9 +/- 4 Ma prior to igneous crystallization of the LEW 86010 angrite. If initial (Mn-53/Mn-55)(sub 0) in the solar system were as high as approximately 4.4 x 10(exp -5) when Allende CAI formed, our data suggest Chainpur chondrules formed approximately 9 Ma later, in qualitative agreement with 'late' I-Xe formation ages for most Chainpur chondrules.

Nyquist, L.↗