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Sample records for al iron fe

  1. Peculiarities of the iron reduction mechanism in Fe-Al-K system

    NASA Astrophysics Data System (ADS)

    Krylova, A. Yu.; Chernavskii, P. A.; Lyadov, A. S.; Sagitov, S. A.; Krylova, M. V.; Khadzhiev, S. N.

    2011-01-01

    Temperature-programmed reduction was used in combination with measurements of magnetization to determine the peculiarities of iron reduction in the Fe-K-Al system. It was found that reduction by hydrogen proceeds with the formation of metallic iron through the stage of magnetite formation (Fe3O4); the effective activation energies are 63 and 39 kJ/mol for the I and II stages, respectively. It was shown that substituting carbon oxide for hydrogen leads to iron reduction proceeding only to the stage of magnetite formation ( E Fe 3O4 = 94 kJ/mol). The magnetite interacts with CO to produce carbide (presumably Hegge carbide Fe2C). Iron reduction in the synthesis gas occurs with the preferential participation of hydrogen or carbon dioxide, depending on the rate of temperature rise.

  2. Iron spin state and site distribution in FeAlO3-bearing bridgmanite

    NASA Astrophysics Data System (ADS)

    Mohn, Chris E.; Trønnes, Reidar G.

    2016-04-01

    DFT at the GGA, GGA + U and hybrid functional levels were used to investigate thousands of different Al and Fe3+ configurations of MgSiO3-FeAlO3 (MS-FA) and MgSiO3-FeAlO3-Al2O3 bridgmanite at deep mantle conditions. Comparison of the different functionals and atomic charge analysis suggests that GGA, frequently used to explain high to low spin transitions observed in several Mössbauer and X-ray emission spectroscopy experiments, is hampered by spurious self-interaction errors in the exchange-correlation energy. Configurational Boltzmann averaging shows that the B site is thermally inaccessible to Fe3+ at the GGA + U and hybrid levels, and we find no evidence for a spin-pairing transition in fully (thermodynamically) equilibrated samples of bridgmanite, even at the lowermost mantle conditions. The comparison of the cation radii of Fe3+ and Mg supports a spin transition accompanied by a site exchange, but the flexibility of Fesbnd O bonds to locally adapt promotes the incorporation of iron in the irregularly coordinated A-site. The concept of ionic radii is therefore unsuitable for analysis of spin state and site exchange in bridgmanite at these conditions. Consistent with previous computational work and experimental studies with glass and gel as starting material, we find that ferric iron kinetically trapped at the B site undergoes a spin transition under lowermost mantle conditions. In bridgmanite with mole fraction of Fe3+ >Al a charge-balancing amount of low spin Fe3+ will be thermodynamically stable at the B site, but because bridgmanite in peridotitic and basaltic lithologies mostly has Al/Fetotal above unity, FA with high spin Fe3+ in the A-site will be the dominant iron component. The lack of a Fe3+ spin transition in the FA-component has important implications for bridgmanite-ferropericlase partitioning of iron and magnesium and the mineral physics of the lowermost mantle.

  3. Preparation of iron aluminate (FeAl2O4) nanoparticles from FeAl2O4 hollow particles fabricated by using a spray pyrolysis process

    NASA Astrophysics Data System (ADS)

    Yun, Jaecheol; Kim, Yangdo; Park, Dahee; Yun, Jung-Yeul

    2015-05-01

    Iron aluminate (FeAl2O4) hollow particles with a spinel structure were synthesized by using a spray pyrolysis process. FeAl2O4 hollow particles were formed at a reaction temperature of 900 °C at a flow rate of 40 L/min as a result of the rapid solvent evaporation and decomposition gases from the droplets in the spray solution prepared from metal salts and organic reagents. FeAl2O4 hollow particles were fabricated at a reaction temperature of 900 °C with a flow rate of 40 L/min. The FeAl2O4 hollow particles were heat treated for 3 hours at 600 °C in a 5% H2/Ar atmosphere to form the crystal particles. Subsequently, FeAl2O4 nanoparticles were fabricated from the FeAl2O4 hollow particles by using the wet milling process. After milling for 60 minutes, transmission electron microscopy revealed the FeAl2O4 particles to have a mean size of approximately 50 nm. The FeAl2O4 nanoparticles were fabricated successfully by using a two-step process, spray pyrolysis and wet milling.

  4. Hot Tear Susceptibility of Al-Mg-Si-Fe Alloys with Varying Iron Contents

    NASA Astrophysics Data System (ADS)

    Sweet, Lisa; Easton, Mark A.; Taylor, John A.; Grandfield, John F.; Davidson, Cameron J.; Lu, Liming; Couper, Malcolm J.; StJohn, David H.

    2013-12-01

    Hot tear susceptibility in cast Al-0.52Si-0.34Mg- xFe 6060 aluminum alloys was investigated using a hot tearing test apparatus to simulate hot tearing in DC casting. The test apparatus has two cast bars, one that is used to measure the load response and one which is fixed at both ends to restrain thermal contraction so that hot tearing can be observed and rated where it occurred. The iron (Fe) content, ranging from 0.02 to 0.5 wt pct, was seen to have a major influence on the load response during solidification and the tear rating of these alloys. The findings are discussed in terms of Rappaz-Drezet-Gremaud (RDG) model sensitivity analysis and related to the effect of Fe content on the morphology and prevalence of the β-Al5FeSi and α-AlFeSi intermetallic phases and their influence on the coherency and coalescence of the microstructure.

  5. Development of weldable, corrosion-resistant iron-aluminide (FeAl) alloys

    SciTech Connect

    Maziasz, P.J.; Goodwin, G.M.; Wang, X.L.; Alexander, D.J.

    1997-04-01

    A boron-microalloyed FeAl alloy (Fe-36Al-0.2Mo-0.05Zr-0.13C, at.%, with 100-400 appm B) with improved weldability and mechanical properties was developed in FY 1994. A new scale-up and industry technology development phase for this work began in FY 1995, pursuing two parallel paths. One path was developing monolithic FeAl component and application technology, and the other was developing coating/cladding technology for alloy steels, stainless steels and other Fe-Cr-Ni alloys. In FY 1995, it was found that cast FeAl alloys had good strength at 700-750{degrees}C, and some (2.5%) ductility in air at room-temperature. Hot-extruded FeAl with refined grain size was found to have ductility and to also have good impact-toughness at room-temperature. Further, it was discovered that powder-metallurgy (P/M) FeAl, consolidated by direct hot-extrusion at 950-1000{degrees}C to have an ultra fine-grained microstructure, had the highest ductility, strength and impact-toughness ever seen in such intermetallic alloys.

  6. Two-stage spin transition of iron in FeAl-bearing phase D at lower mantle

    NASA Astrophysics Data System (ADS)

    Wu, Xiang; Wu, Ye; Lin, Jung-Fu; Liu, Jin; Mao, Zhu; Guo, Xinzhuan; Yoshino, Takashi; McCammon, Catherine; Prakapenka, Vitali B.; Xiao, Yuming

    2016-09-01

    Hydrous magnesium silicate phase D plays a key role in the transport of water from the upper to the lower mantle via subducted slabs. Here we report pressure dependence hyperfine and lattice parameters of FeAl-bearing phase D up to megabar pressures using synchrotron nuclear forward scattering and X-ray diffraction in a diamond anvil cell at room temperature. FeAl-bearing phase D undergoes a two-stage high-spin to low-spin transition of iron for Fe2+ at 37-41 GPa and for Fe3+ at 64-68 GPa. These transitions are accompanied by an increase in density and a significant softening in the bulk modulus and bulk velocity at their respective pressure range. The occurrence of the dense low-spin FeAl-bearing phase D with relatively high velocity anisotropies in deep-subducted slabs can potentially contribute to small-scale seismic heterogeneities in the middle-lower mantle beneath the circum-Pacific area.

  7. Carbides in iron-rich Fe-Mn-Cr-Mo-Al-Si-C systems

    NASA Technical Reports Server (NTRS)

    Lemkey, F. D.; Gupta, H.; Nowotny, H.; Wayne, S. F.

    1984-01-01

    The optimization of high carbon iron-base superalloy properties with duplex microstructure gamma + M7C3 carbide requires analysis in the context of a seven-component system. Data are first provided here for the Fe-Mn-Cr-Mo-C quinary system, at 30 at. pct carbon. A characterization of competing carbides, according to a pseudoternary phase diagram at 35 wt pct iron, is made from isothermal sections. It is noted that while M7C3 and M3C carbides' occurrences are respectively favored at the Cr and Mn corners, the M2C carbide and molybdenum cementite are predominant with increasing amounts of Mo. Lattice parameters are reported for the various carbides.

  8. The ductile-brittle size transition of iron aluminide ligaments in an FeAl/TiC composite

    SciTech Connect

    Subramanian, R.; Schneibel, J.H.

    1998-08-10

    The fracture surfaces of FeAl/TiC composites containing 70 vol% TiC were investigated. Since thin iron aluminide ligaments in the composites fractured in a ductile manner, whereas thicker ones fractured by cleavage, a systematic correlation of the fracture mode to the ligament thickness was performed. The results clearly show that FeAl ligaments thicker than about 1--2 {micro}m fracture by cleavage and those smaller in size fracture predominantly in a ductile manner. The ductile failure mode is attributed to the limited dislocation pile-up distance available for very thin ligaments, which prevents high stresses from building up and eliminates cleavage fracture. It is also shown that the ductile-brittle transition size is controlled by alloying and/or heat treatment. No significant dependence of the fracture toughness on the fracture mode would be found.

  9. Microstructural and magnetic characterization of iron precipitation in Ni-Fe-Al alloys

    SciTech Connect

    Duman, Nagehan; Mekhrabov, Amdulla O.; Akdeniz, M. Vedat

    2011-06-15

    The influence of annealing on the microstructural evolution and magnetic properties of Ni{sub 50}Fe{sub x}Al{sub 50-x} alloys for x = 20, 25, and 30 has been investigated. Solidification microstructures of as-cast alloys reveal coarse grains of a single B2 type {beta}-phase and typical off eutectic microstructure consisting of proeutectic B2 type {beta} dendrites and interdendritic eutectic for x = 20 and x > 20 at.% Fe respectively. However, annealing at 1073 K results in the formation of FCC {gamma}-phase particles along the grain boundaries as well as grain interior in x = 20 at.% Fe alloy. The volume fraction of interdentritic eutectic regions tend to decrease and their morphologies start to degenerate by forming FCC {gamma}-phase for x > 20 at.% Fe alloys with increasing annealing temperatures. Increasing Fe content of alloys induce an enhancement in magnetization and a rise in the Curie transition temperature (T{sub C}). Temperature scan magnetic measurements and transmission electron microscopy reveal that a transient rise in the magnetization at temperatures well above the T{sub C} of the alloys would be attributed to the precipitation of a nano-scale ferromagnetic BCC {alpha}-Fe phase. Retained magnetization above the Curie transition temperature of alloy matrix, together with enhanced room temperature saturation magnetization of alloys annealed at favorable temperatures support the presence of ferromagnetic precipitates. These nano-scale precipitates are shown to induce significant precipitation hardening of the {beta}-phase in conjunction with enhanced room temperature saturation magnetization in particular when an annealing temperature of 673 K is used. - Research Highlights: {yields} Evolution of microstructure and magnetic properties with varying Fe content. {yields} Transient rise in magnetization via the formation of ferromagnetic phase. {yields} Enhancements in saturation magnetization owing to precipitated ferromagnetic phase. {yields} Nanoscale

  10. Aluminum Deoxidation Equilibria in Liquid Iron: Part III—Experiments and Thermodynamic Modeling of the Fe-Mn-Al-O System

    NASA Astrophysics Data System (ADS)

    Paek, Min-Kyu; Do, Kyung-Hyo; Kang, Youn-Bae; Jung, In-Ho; Pak, Jong-Jin

    2016-10-01

    Deoxidation equilibria in high-Mn- and high-Al-alloyed liquid steels were studied over the entire Fe-Mn-Al composition range by both experiments and thermodynamic modeling. Effect of Mn on the Al deoxidation equilibria in liquid iron was measured by the different experimental techniques depending on the Al content. In order to confirm the reproducibility of the experimental results, the deoxidation experiments were carried out reversibly from high oxygen state by addition of Al as a deoxidizer, and from low oxygen state by addition of Fe2O3 or MnO as an oxygen source. For the Al-rich side, CaO flux was added on top of liquid iron in order to remove suspended Al2O3 inclusions in the melt. Based on the present experimental result and available critically evaluated literature data, the Al deoxidation equilibria in Fe-Mn-Al-O liquid alloy were thermodynamically modeled. The Modified Quasichemical Model was used in order to take into account a strong short-range ordering of atoms in molten state. Deoxidation equilibria and inclusion stability diagram for entire Fe-Mn-Al melt were successfully reproduced by the present model.

  11. High-temperature corrosion-resistant iron-aluminide (FeAl) alloys exhibiting improved weldability

    DOEpatents

    Maziasz, Philip J.; Goodwin, Gene M.; Liu, Chain T.

    1996-01-01

    This invention relates to improved corrosion-resistant iron-aluminide intermetallic alloys. The alloys of this invention comprise, in atomic percent, from about 30% to about 40% aluminum alloyed with from about 0.1% to about 0.5% carbon, no more than about 0.04% boron such that the atomic weight ratio of boron to carbon in the alloy is in the range of from about 0.01:1 to about 0.08:1, from about 0.01 to about 3.5% of one or more transition metals selected from Group IVB, VB, and VIB elements and the balance iron wherein the alloy exhibits improved resistance to hot cracking during welding.

  12. High-temperature corrosion-resistant iron-aluminide (FeAl) alloys exhibiting improved weldability

    DOEpatents

    Maziasz, P.J.; Goodwin, G.M.; Liu, C.T.

    1996-08-13

    This invention relates to improved corrosion-resistant iron-aluminide intermetallic alloys. The alloys of this invention comprise, in atomic percent, from about 30% to about 40% aluminum alloyed with from about 0.1% to about 0.5% carbon, no more than about 0.04% boron such that the atomic weight ratio of boron to carbon in the alloy is in the range of from about 0.01:1 to about 0.08:1, from about 0.01 to about 3.5% of one or more transition metals selected from Group IVB, VB, and VIB elements and the balance iron wherein the alloy exhibits improved resistance to hot cracking during welding. 13 figs.

  13. Orientation relationship between α-Fe precipitate and α-Al2O3 matrix in iron-implanted sapphire.

    PubMed

    Wang, Y; Liu, X P; Qin, G W

    2014-07-01

    Fe ions were implanted into α-Al2O3 single crystals (sapphire) at room temperature and annealed in a reducing atmosphere. The orientation relationships (ORs) between α-Fe particles and sapphire matrix were investigated using transmission electron microscopy (TEM). All the α-Fe particles have the orientation relationship (OR) of (111)α-Fe||(0001)sapphire and [11¯0]α-Fe||[112¯0]sapphire with sapphire. This OR is predicted precisely by the coincidence of reciprocal lattice points (CRLP) method. The other OR of (110)α-Fe||(0001)sapphire and [111]α-Fe||[51¯4¯0]sapphire reported before is confirmed by the same method to be one of the secondary preferred orientation relationships in the α-Fe/sapphire system.

  14. Experimental determination of coexisting iron titanium oxides in the systems FeTiAlO, FeTiAlMgO, FeTiAlMnO, and FeTiAlMgMnO at 800 and 900°C, 1 4 kbar, and relatively high oxygen fugacity

    NASA Astrophysics Data System (ADS)

    Evans, Bernard W.; Scaillet, Bruno; Kuehner, Scott M.

    2006-08-01

    A synthetic, low-melting rhyolite composition containing TiO2 and iron oxide, with further separate additions of MgO, MnO, and MgO + MnO, was used in hydrothermal experiments to crystallize Ilm-Hem and Usp-Mt solid solutions at 800 and 900°C under redox conditions slightly below nickel nickel oxide (NNO) to ≈ 3 log_{10} f_{{{text{O}}2}} units above the NNO oxygen buffer. These experiments provide calibration of the FeTi-oxide thermometer + oxygen barometer at conditions of temperature and oxygen fugacity poorly covered by previous equilibrium experiments. Isotherms for our data in Roozeboom diagrams of projected %usp vs. %ilm show a change in slope at ≈ 60% ilm, consistent with the second-order transition from FeTi-ordered Ilm to FeTi-disordered Ilm-Hem. This feature of the system accounts for some, but not all, of the differences from earlier thermodynamic calibrations of the thermobarometer. In rhyolite containing 1.0 wt.% MgO, 0.8 wt.% MnO, or MgO + MnO, Usp-Mt crystallized with up to 14% of aluminate components, and Ilm-Hem crystallized with up to 13% geikielite component and 17% pyrophanite component. Relative to the FeTiAlO system, these components displace the ferrite components in Usp-Mt, and the hematite component in Ilm-Hem. As a result, projected contents of ulvöspinel and ilmenite are increased. These changes are attributed to increased non-ideality along joins from end-member hematite and magnetite to their respective Mg- and Mn-bearing titanate and aluminate end-members. The compositional shifts are most pronounced in Ilm-Hem in the range Ilm50 80, a solvus region where the chemical potentials of the hematite and ilmenite components are nearly independent of composition. The solvus gap widens with addition of Mg and even further with Mn. The Bacon Hirschmann correlation of Mg/Mn in Usp-Mt and coexisting Ilm-Hem is displaced toward increasing Mg/Mn in ilmenite with passage from ordered ilmenite to disordered hematite. Orthopyroxene and biotite

  15. Missing Fe: hydrogenated iron nanoparticles

    NASA Astrophysics Data System (ADS)

    Bilalbegović, G.; Maksimović, A.; Mohaček-Grošev, V.

    2017-03-01

    Although it was found that the FeH lines exist in the spectra of some stars, none of the spectral features in the interstellar medium (ISM) have been assigned to this molecule. We suggest that iron atoms interact with hydrogen and produce Fe-H nanoparticles which sometimes contain many H atoms. We calculate infrared spectra of hydrogenated iron nanoparticles using density functional theory methods and find broad, overlapping bands. Desorption of H2 could induce spinning of these small Fe-H dust grains. Some of hydrogenated iron nanoparticles possess magnetic and electric moments and should interact with electromagnetic fields in the ISM. FenHm nanoparticles could contribute to the polarization of the ISM and the anomalous microwave emission. We discuss the conditions required to form FeH and FenHm in the ISM.

  16. Liquid-solid equilibria involving spinel, ilmenite, and ferropseudobrookite in the system 'FeO'-Al2O3-TiO2 in contact with metallic iron

    NASA Technical Reports Server (NTRS)

    Schreifels, W. A.; Muan, A.

    1975-01-01

    Phase relations in the liquidus temperature region of the system 'FeO'-Al2O3-TiO2 in contact with metallic iron, at a total pressure below 1 atm, have been determined by the quenching technique. Four invariant points have been located, with phase assemblages and temperatures as follows; wuestite, ulvoespinel, nercynite and liquid, 1306 C; ulvoespinel, ilmenite, ferropseudobrookite and liquid, 1340 C; ulvoespinel, hercynite, ferropseudobrookite and liquid, 1367 C; hercynite, ferropseudobrookite, corundum and liquid, 1465 C. The data obtained confirm the presence of a miscibility gap between titanate and aluminate spinels, and provide quantitative data for the effect of Al2O3 on mutual stability relations among spinel, ilmenite, and ferropseudobrookite phases in the presence of liquid at high temperatures and strongly reducing conditions. It is shown that Al2O3 has a strong stabilizing effect on the phase assemblage ferropseudobrookite and spinel relative to ilmenite.

  17. Comparison of Fe-AlPILC and Fe-ZSM-5 catalysts used for degradation of methomyl

    NASA Astrophysics Data System (ADS)

    Lázár, Károly; Tomašević, Andjelka; Bošković, Goran; Kiss, Ernő

    2009-07-01

    Catalytic performances of Fe-AlPILC (14 wt.% Fe) and Fe-ZSM-5 (5 wt.% Fe) catalysts are compared in the wet oxidative degradation of methomyl. Fe-ZSM-5 exhibits outstanding whereas Fe-AlPILC shows only mediocre activity. Positions of iron are analysed in the two catalysts by Mössbauer spectroscopy. Iron is in highly dispersed state in Fe-AlPILC whereas in the other case a hematite/ZSM-5 composite is formed. The catalytic activity is attributed to iron located and stabilized in ionic dispersion.

  18. Fabrication of Fe-Al nanoparticles by selective oxidation of Fe-Al thin films

    NASA Astrophysics Data System (ADS)

    Jang, Pyungwoo; Shin, Seungchan; Jung, Chip-Sup; Kim, Kwang-Ho; Seomoon, Kyu

    2013-04-01

    The possibility of a new technique for fabricating nanoparticles from thin films using selective oxidation in an atmosphere mixture of water vapor and hydrogen was investigated. Fe-5wt.%Al films were RF-sputtered and annealed in the atmosphere mixture at 900°C for up to 200 min, in order to oxidize aluminum selectively. Thermodynamics simulation showed that temperatures exceeding 800°C are necessary to prevent iron from being oxidized, as confirmed by the depth profile of XPS. As the annealing time increased, the morphology of the 200-nm Fe-Al films changed from the continuous to the discontinuous type; thus, particulate Fe-Al films formed after 100 min. The particulate 10- to 100-nm Fe-Al films showed super-paramagnetic behavior after the oxidation. Thus, a new technique for fabricating nanoparticles was successfully introduced using selective oxidation.

  19. Understanding the reentrant superconducting phase diagram of the iron pnictide Ca4Al2O6Fe2(As1-xPx)2: First-principles calculations

    NASA Astrophysics Data System (ADS)

    Usui, Hidetomo; Suzuki, Katsuhiro; Kuroki, Kazuhiko; Takeshita, Nao; Shirage, Parasharam Maruti; Eisaki, Hiroshi; Iyo, Akira

    2013-05-01

    Recently, a very rich phase diagram has been obtained for an iron-based superconductor Ca4Al2O6Fe2(As1-xPx)2. It has been revealed that nodeless (x˜0) and nodal (x=1) superconductivity are separated by an antiferromagnetic phase. Here we study the origin of this peculiar phase diagram using a five orbital model constructed from first-principles band calculation, and applying the fluctuation exchange approximation assuming spin-fluctuation-mediated pairing. At x=1, there are three hole Fermi surfaces, but the most inner one around the wave vector (0,0) has strong dX2-Y2 orbital character, unlike in LaFeAsO, where the most inner Fermi surface has dXZ/YZ character. Since the Fermi surfaces around (0,0), (π,0), and (π,π) all have dX2-Y2 orbital character, the repulsive pairing interaction mediated by the spin fluctuations gives rise to a frustration in momentum space, thereby degrading superconductivity despite the bond angle being close to the regular tetrahedron angle. As x decreases and the bond angle is reduced, the inner hole Fermi surface disappears, but the frustration effect still remains because the top of the band with dX2-Y2 character lies close to the Fermi level. On the other hand, the loss of the Fermi surface itself gives rise to a very good nesting of the Fermi surface because the number of electron and hole Fermi surfaces are now the same. The pairing interaction frustration and the good nesting combined favors antiferromagnetism over superconductivity. Finally for x close to 0, the band sinks far below the Fermi level, reducing the frustration effect, so that superconductivity is enhanced. There, the Fermi surface nesting is also lost to some extent, once again favoring superconductivity over antiferromagnetism. To see whether the present theoretical scenario is consistent with the actual nature of the competition between superconductivity and antiferromagnetism, we also perform hydrostatic pressure experiment for Ca4Al2O6Fe2(As1-xPx)2. In the

  20. Al-Co-Fe (030)

    NASA Astrophysics Data System (ADS)

    Carow-Watamura, U.; Louzguine, D. V.; Takeuchi, A.

    This document is part of Part 1 http://dx.doi.org/10.1007/9getType="URL"/> 'Systems from Ag-Al-Ca to Au-Pd-Si' of Subvolume B 'Physical Properties of Ternary Amorphous Alloys' of Volume 37 'Phase Diagrams and Physical Properties of Nonequilibrium Alloys' of Landolt-Börnstein - Group III 'Condensed Matter'. It contains the Chapter 'Al-Co-Fe (030)' with the content:

  1. Phase equilibria in the system K2O-FeO-MgO-Al2O3-SiO2-H2O-CO2 and the stability limit of stilpnomelane in metamorphosed Precambrian iron-formations

    NASA Astrophysics Data System (ADS)

    Miyano, Takashi; Klein, Cornelis

    1989-08-01

    The phase relations of Al- and Fe-bearing silicates in the system K2O-FeO-MgO-Al2O3-SiO2-H2O-CO2, in the presence of quartz and magnetite, are discussed on the basis of mineralogic and petrologic data from Precambrian iron-formations and blueschist facies meta-ironstone from the Franciscan Formation, California. These relations allow an estimation of the physiochemical conditions during low-grade metamorphism of iron-formations. Petrologic data together with available experimental and predicted thermodynamic data on the associated minerals place the upper stability limit of stilpnomelane in iron-formations at about 430 470° C and 5 6 kilobars. Fe-end member stilpnomelane can persist to a maximum temperature of 500° C and pressures up to 6 7 kilobars, although it is unlikely to occur in metamorphosed iron-formations. In iron-formation occurrences the stilpnomelane stability field is bordered by four equilibrium reactions with the assemblages stilpnomelane-zussmanite-chlorite-minnesotaite, stilpnomelane-zussmanite-chlorite-grunerite, stilpnomelane-biotite-chlorite-grunerite, and stilpnomelane-biotite-almandine-grunerite. The stability field is reduced by increasing X(CO2) and X {Mg/Stil}, and is also a function of a( K +)/ a( H +) in the metamorphic fluid. If the value of a( K +)/ a( H +) is smaller than that defined by the above assemblages, stilpnomelane decomposes to chlorite, but if larger, it is replaced by biotite. At pressures less than 4 kilobars, the zussmanite field is restricted to a very high value of a( K +)/a( H +) (> 5.0 in log units at 1.0 kilobar) where iron-formation assemblages are not stable.

  2. Rapidly solidified NiAl and FeAl

    NASA Technical Reports Server (NTRS)

    Gaydosh, D. J.; Crimp, M. A.

    1984-01-01

    Melt spinning was used to produce rapidly solidified ribbons of the B2 intermetallics NiAl and FeAl. Both Fe-40Al and Fe-45Al possessed some bend ductility in the as spun condition. The bend ductility of Fe-40Al, Fe-45Al, and equiatomic NiAl increased with subsequent heat treatment. Heat treatment at approximately 0.85 T (sub m) resulted in significant grain growth in equiatomic FeAl and in all the NiAl compositions. Low bend ductility in both FeAl and NiAl generally coincided with intergranular failure, while increased bend ductility was characterized by increasing amounts of transgranular cleavage fracture.

  3. Oxidation Resistant Ti-Al-Fe Diffusion Barrier for FeCrAlY Coatings on Titanium Aluminides

    NASA Technical Reports Server (NTRS)

    Brady, Michael P. (Inventor); Smialke, James L. (Inventor); Brindley, William J. (Inventor)

    1996-01-01

    A diffusion barrier to help protect titanium aluminide alloys, including the coated alloys of the TiAl gamma + Ti3Al (alpha2) class, from oxidative attack and interstitial embrittlement at temperatures up to at least 1000 C is disclosed. The coating may comprise FeCrAlX alloys. The diffusion barrier comprises titanium, aluminum, and iron in the following approximate atomic percent: Ti-(50-55)Al-(9-20)Fe. This alloy is also suitable as an oxidative or structural coating for such substrates.

  4. Structural evolution in mechanically alloyed Al-Fe powders

    SciTech Connect

    Mukhopadhyay, D.K.; Suryanarayana, C.; Froes, F.H.

    1995-08-01

    The structural evolution in mechanically alloyed binary aluminum-iron powder mixtures containing 1, 4, 7.3, 10.7, and 25 at pct Fe was investigated using X-ray diffraction (XRD) and electron microscopic techniques. The constitution (number and identity of phases present), microstructure (crystal size, particle size), and transformation behavior of the powders on annealing were studied. The solid solubility of Fe in Al has been extended up to at least 4.5 at. pct, which is close to that observed using rapid solidification (RS) (4.4 at. pct), compared with the equilibrium value of 0.025 at. pct Fe at room temperature. Nanometer-sized grains were observed in as-milled crystalline powders in all compositions. Increasing the ball-to-powder weight ratio (BPR) resulted in a faster rate of decrease of crystal size. A fully amorphous phase was obtained in the Al-25 at. pct Fe composition, and a mixed amorphous phase plus solid solution of Fe in Al was developed in the Al-10.7 at. pct Fe alloy, agreeing well with the predictions made using the semiempirical Miedema model. Heat treatment of the mechanically alloyed powders containing the supersaturated solid solution or the amorphous phase resulted in the formation of the Al{sub 3}Fe intermetallic in all but the Al-25 at. pct Fe powders. In the Al-25 at. pct Fe powder, formation of nanocrystalline Al{sub 5}Fe{sub 2} was observed directly by milling. Electron microscope studies of the shock-consolidated mechanically alloyed Al-10.7 and 25 at. pct Fe powders indicated that nanometer-sized grains were retained after compaction.

  5. FeAl-TiC and FeAl-WC composites - melt infiltration processing, microstructure and mechanical properties

    SciTech Connect

    Subramanian, R.; Schneibel, J.H.

    1997-04-01

    TiC-based and WC-based cermets were processed with iron aluminide, an intermetallic, as a binder by pressureless melt infiltration to near full density (> 97 % theoretical density). Phase equilibria calculations in the quaternary Fe-Al-Ti-C and Fe-Al-W-C systems at 145{degrees}C were performed to determine the solubility of the carbide phases in liquid iron aluminide. This was done by using Thermocalc{trademark} and the results show that molten Fe-40 at.% Al in equilibrium with Ti{sub 0.512}C{sub 0.488} and graphite, dissolves 4.9 at% carbon and 64 atomic ppm titanium. In the Fe-Al-W-C system, liquid Fe-40 at.% Al in equilibrium with graphite dissolves about 5 at.% carbon and 1 at.% tungsten. Due to the low values for the solubility of the carbide phases in liquid iron aluminide, liquid phase sintering of mixed powders does not yield a dense, homogeneous microstructure for carbide volume fractions greater than 0.70. Melt infiltration of molten FeAl into TiC and WC preforms serves as a successful approach to process cermets with carbide contents ranging from 70 to 90 vol. %, to greater than 97% of theoretical density. Also, the microstructures of cermets prepared by melt infiltration were very homogeneous. Typical properties such as hardness, bend strength and fracture toughness are reported. SEM observations of fracture surfaces suggest the improved fracture toughness to result from the ductility of the intermetallic phase. Preliminary experiments for the evaluation of the oxidation resistance of iron aluminide bonded cermets indicate that they are more resistant than WC-Co cermets.

  6. Processing and properties of FeAl-bonded composites

    SciTech Connect

    Schneibel, J.H.; Subramanian, R.; Alexander, K.B.; Becher, P.F.

    1996-12-31

    Iron aluminides are thermodynamically compatible with a wide range of ceramics such as carbides, borides, oxides, and nitrides, which makes them suitable as the matrix in composites or cermets containing fine ceramic particulates. For ceramic contents varying from 30 to 60 vol.%, composites of Fe-40 at. % Al with WC, TiC, TiB{sub 2}, and ZrB{sub 2} were fabricated by conventional liquid phase sintering of powder mixtures. For ceramic contents from 70 to 85 vol.%, pressureless melt infiltration was found to be a more suitable processing technique. In FeAl-60 vol.% WC, flexure strengths of up to 1.8 GPa were obtained, even though processing defects consisting of small oxide clusters were present. Room temperature fracture toughnesses were determined by flexure testing of chevron-notched specimens. FeAl/WC and FeAl/TiC composites containing 60 vol.% carbide particles exhibited K{sub Q} values around 20 MPa m{sup 1/2}. Slow crack growth measurements carried out in water and in dry oxygen suggest a relatively small influence of water-vapor embrittlement. It appears therefore that the mechanical properties of iron aluminides in the form of fine ligaments are quite different from their bulk properties. Measurements of the oxidation resistance, dry wear resistance, and thermal expansion of iron aluminide composites suggest many potential applications for these new materials.

  7. Orientation relationship of eutectoid FeAl and FeAl2

    PubMed Central

    Scherf, A.; Kauffmann, A.; Kauffmann-Weiss, S.; Scherer, T.; Li, X.; Stein, F.; Heilmaier, M.

    2016-01-01

    Fe–Al alloys in the aluminium range of 55–65 at.% exhibit a lamellar microstructure of B2-ordered FeAl and triclinic FeAl2, which is caused by a eutectoid decomposition of the high-temperature Fe5Al8 phase, the so-called ∊ phase. The orientation relationship of FeAl and FeAl2 has previously been studied by Bastin et al. [J. Cryst. Growth (1978 ▸), 43, 745] and Hirata et al. [Philos. Mag. Lett. (2008 ▸), 88, 491]. Since both results are based on different crystallographic data regarding FeAl2, the data are re-evaluated with respect to a recent re-determination of the FeAl2 phase provided by Chumak et al. [Acta Cryst. (2010 ▸), C66, i87]. It is found that both orientation relationships match subsequent to a rotation operation of 180° about a 〈112〉 crystallographic axis of FeAl or by applying the inversion symmetry of the FeAl2 crystal structure as suggested by the Chumak data set. Experimental evidence for the validity of the previously determined orientation relationships was found in as-cast fully lamellar material (random texture) as well as directionally solidified material (∼〈110〉FeAl || solidification direction) by means of orientation imaging microscopy and global texture measurements. In addition, a preferential interface between FeAl and FeAl2 was identified by means of trace analyses using cross sectioning with a focused ion beam. On the basis of these habit planes the orientation relationship between the two phases can be described by (01)FeAl || (114) and [111]FeAl || [10]. There is no evidence for twinning within FeAl lamellae or alternating orientations of FeAl lamellae. Based on the determined orientation and interface data, an atomistic model of the structure relationship of Fe5Al8, FeAl and FeAl2 in the vicinity of the eutectoid decomposition is derived. This model is analysed with respect to the strain which has to be accommodated at the interface of FeAl and FeAl2. PMID:27047304

  8. Iron acquisition from Fe-pyoverdine by Arabidopsis thaliana.

    PubMed

    Vansuyt, Gérard; Robin, Agnès; Briat, Jean-François; Curie, Catherine; Lemanceau, Philippe

    2007-04-01

    Taking into account the strong iron competition in the rhizosphere and the high affinity of pyoverdines for Fe(III), these molecules are expected to interfere with the iron nutrition of plants, as they do with rhizospheric microbes. The impact of Fe-pyoverdine on iron content of Arabidopsis thaliana was compared with that of Fe-EDTA. Iron chelated to pyoverdine was incorporated in a more efficient way than when chelated to EDTA, leading to increased plant growth of the wild type. A transgenic line of A. thaliana overexpressing ferritin showed a higher iron content than the wild type when supplemented with Fe-EDTA but a lower iron content when supplemented with Fe-pyoverdine despite its increased reductase activity, suggesting that this activity was not involved in the iron uptake from pyoverdine. A mutant knock-out iron transporter IRT1 showed lower iron and chlorophyll contents when supplemented with Fe-EDTA than the wild type but not when supplemented with Fe-pyoverdine, indicating that, in contrast to iron from EDTA, iron from pyoverdine was not incorporated through the IRT1 transporter. Altogether these data suggest that iron from Fe-pyoverdine was not incorporated in planta through the strategy I, which is based on reductase activity and IRT1 transporter. This is supported by the presence of pyoverdine in planta as shown by enzyme-linked immunosorbent assay and by tracing 15N of 15N-pyoverdine.

  9. Composition and solidification microstructure selection in the interdendritic matrix between primary Al{sub 3}Fe dendrites in hypereutectic Al-Fe alloys

    SciTech Connect

    Liang, D.; Korgul, P.; Jones, H.

    1996-07-01

    The composition and constitution of matrix microstructure between plate-like Al{sub 3}Fe dendrites in Bridgman-grown hypereutectic Al-Fe alloys has been determined as a function of alloy concentration C{sub 0} and growth velocity V in the ranges 2.5 < C{sub 0} < 28.1 wt%Fe and 0.01 < V < 5.0 mm/s. The transition at V = 0.1 mm/s from a fully eutectic matrix at C{sub 0} = 3.5 wt%Fe to one containing {alpha}Al dendrites at C{sub 0} {ge} 4.7 wt%Fe is attributed to growth temperatures of {alpha}Al dendrites that are higher than those of eutectic in a matrix of lower iron-content, which results from these conditions. The matrix eutectic changes from irregular {alpha}-Al-Al{sub 3}Fe to regular {alpha}Al-Al{sub x}Fe with increasing V, the transition velocity increasing from 0.1 to 0.2 mm/s for C{sub 0} values of 9.5 and 14 wt%Fe up to 0.35--1.0 mm/s for C{sub 0} values of 18.7--28.1 wt%Fe. This increased transition velocity, compared with that for {alpha}-Al-Al{sub 3}Fe to {alpha}Al-Al{sub 6}Fe at lower concentration, is indicative of a lower formation temperature for the {alpha}Al-Al{sub x}Fe than the {alpha}Al-Al{sub 6}Fe eutectic.

  10. Electron Microprobe Analysis of Fe2+/Fe3+ in Minerals With low Total Iron Concentrations

    NASA Astrophysics Data System (ADS)

    Creighton, S. D.; Matveev, S.; Stachel, T.; Luth, R. W.

    2004-12-01

    The development of the `flank method' by Höfer et al. (1994) has made it possible to quantify ferrous and ferric iron concentrations in minerals using the electron microprobe. The flank method makes use of the changes in both the wavelength and intensity of soft Fe Lα and Fe Lβ X-ray emission lines of minerals containing Fe3+ and Fe2+.By measuring at energies off the peak maxima (on the peaksAƒAøAøâ_sA¬Aøâ_zAø flanks) the differences due to variable ferric iron ratios are maximized, thus making the flank method much more sensitive than methods relying on either peak shifts or peak area ratios. Using a correction for self-absorption, the Fe3+/Fe2+ ratio of minerals may be accurately and precisely determined. The original flank method was developed for minerals with high total iron concentration e.g. Fe-rich garnet end-members (almandine, andradite, and skiagite), and Fe-oxides (wüstite). To make it applicable to minerals with total iron concentrations of less than 10 wt.% as is common in mantle-derived minerals, we have modified, in three ways, the flank method to significantly improve the precision. Firstly, we have increased the number of analyses per mineral grain to 400 thereby providing a far more representative mean. Secondly, because it is necessary to accurately reproduce the exact position of the spectrometer crystal for each flank measurement, we have eliminated the need to reposition the spectrometer by serially measuring each flank position. Thirdly, we compensate for instrumental drift by measuring two 10 μ m by 10 μ m grids (1 μ m spot size and spacing) for both flank positions. Each mineral grain is measured sequentially, collecting 200 analyses on the first flank position. The procedure is identically repeated for measurements on the second flank position. The elapsed time between each grid measurement is the same for all samples and drift for either flank position is eliminated by averaging. Using these modifications to the flank

  11. Creep-rupture behavior of a developmental cast-iron-base alloy for use up to 800/sup 0/C. [NASAUT 4G-Al: Fe-15Mn-15Cr-2Mo-1. 5C-1Nb-1Si

    SciTech Connect

    Titran, R.H.; Scheuermann, C.M.

    1987-08-01

    As part of the DOE/NASA Stirling Engine Systems Project, an iron-base cast alloy was developed, designated NASAUT 4G-Al. Its nominal composition, in percent by weight, is Fe-15Mn-15Cr-2Mo-1.5C-1Nb-1Si. This report presents the results of a study of this alloy, 4G-Al, performed to determine its creep-rupture properties. The alloy was studied in the directionally solidified (DS) form with a 650/sup 0/C/100 h anneal recommended by UTRC to optimize properties and in the investment-cast (IC) form with either a 760/sup 0/C/20 h anneal recommended by UTRC to optimize properties, or a solution anneal of 790/sup 0/C/20 h followed by a simulated brazing cycle of 1065/sup 0/C/15 min + a heat treatment of 760/sup 0/C/16 h + 650/sup 0/C/16 h. Alloy 4G-Al exhibited typical 3-stage creep response under all conditions tested. The most creep resistant condition was the DS material. This condition compares very favorably to the prototype (HS-31) and prime candidate (XF-818) alloys for the automotive Stirling engine cylinder/regenerator housing. 14 refs., 7 figs., 6 tabs.

  12. Tetragonal magnetostriction and magnetoelastic coupling in Fe-Al, Fe-Ga, Fe-Ge, Fe-Si, Fe-Ga-Al, and Fe-Ga-Ge alloys

    NASA Astrophysics Data System (ADS)

    Restorff, J. B.; Wun-Fogle, M.; Hathaway, K. B.; Clark, A. E.; Lograsso, T. A.; Petculescu, G.

    2012-01-01

    This paper presents a comparative study on the tetragonal magnetostriction constant, λγ,2, [ = (3/2)λ100] and magnetoelastic coupling, b1, of binary Fe100-xZx (0 < x < 35, Z = Al, Ga, Ge, and Si) and ternary Fe-Ga-Al and Fe-Ga-Ge alloys. The quantities are corrected for magnetostrains due to sample geometry (the magnetostrictive form effect). Recently published elastic constant data along with magnetization measurements at both room temperature and 77 K make these corrections possible. The form effect correction lowers the magnetostriction by ˜10 ppm for high-modulus alloys and by as much as 30 ppm for low-modulus alloys. The elastic constants are also used to determine the values of the magnetoelastic coupling constant, b1. With the new magnetostriction data on the Fe-Al-Ga alloy, it is possible to show how the double peak magnetostriction feature of the binary Fe-Ga alloy flows into the single peak binary Fe-Al alloy. The corrected magnetostriction and magnetoelastic coupling data for the various alloys are also compared using the electron-per-atom ratio, e/a, as the common variable. The Hume-Rothery rules link the e/a ratio to the regions of phase stability, which appear to be intimately related to the magnetostriction versus the solute concentration curve in these alloys. Using e/a as the abscissa tends to align the peaks in the magnetostriction and magnetoelastic coupling for the Fe-Ga, Fe-Ge, Fe-Al, Fe-Ga-Al, and Fe-Ga-Ge alloys, but not for the Fe-Si alloys for which the larger atomic size difference may play a greater role in phase stabilization. Corrections for the form effect are also presented for the rhombohedral magnetostriction, λɛ,2, and the magnetoelastic coupling, b2, of Fe100-xGax (0 < x < 35) alloys.

  13. Iron [Fe(0)]-rich substrate based on iron-carbon micro-electrolysis for phosphorus adsorption in aqueous solutions.

    PubMed

    Deng, Shihai; Li, Desheng; Yang, Xue; Xing, Wei; Li, Jinlong; Zhang, Qi

    2017-02-01

    The phosphorus (P) adsorption properties of an iron [Fe(0)]-rich substrate (IRS) composed of iron scraps and activated carbon were investigated based on iron-carbon micro-electrolysis (IC-ME) and compared to the substrates commonly used in constructed wetlands (CWs) to provide an initial characterization of the [Fe(0)]-rich substrate. The results showed that P was precipitated by Fe(III) dissolved from the galvanic cell reactions in the IRS and the reaction was suppressed by the pH and stopped when the pH exceeded 8.90 ± 0.09. The adsorption capacity of the IRS decreased by only 4.6% in the second round of adsorption due to Fe(0) consumption in the first round. Substrates with high Ca- and Mg-oxide contents and high Fe- and Al-oxide contents had higher P adsorption capacities at high and low pH values, respectively. Substrates containing high Fe and Al concentrations and low Ca concentrations were more resistant to decreases in the P adsorption capacity resulting from organic matter (OM) accumulation. The IRS with an iron scrap to activated carbon volume ratio of 3:2 resulted in the highest P adsorption capacity (9.34 ± 0.14 g P kg(-1)), with minimal pH change and strong adaptability to OM accumulation. The Fe(0)-rich substrate has the considerable potential for being used as a CW substrate.

  14. FeCycle: Attempting an iron biogeochemical budget from a mesoscale SF6 tracer experiment in unperturbed low iron waters

    NASA Astrophysics Data System (ADS)

    Boyd, P. W.; Law, C. S.; Hutchins, D. A.; Abraham, E. R.; Croot, P. L.; Ellwood, M.; Frew, R. D.; Hadfield, M.; Hall, J.; Handy, S.; Hare, C.; Higgins, J.; Hill, P.; Hunter, K. A.; Leblanc, K.; Maldonado, M. T.; McKay, R. M.; Mioni, C.; Oliver, M.; Pickmere, S.; Pinkerton, M.; Safi, K.; Sander, S.; Sanudo-Wilhelmy, S. A.; Smith, M.; Strzepek, R.; Tovar-Sanchez, A.; Wilhelm, S. W.

    2005-12-01

    An improved knowledge of iron biogeochemistry is needed to better understand key controls on the functioning of high-nitrate low-chlorophyll (HNLC) oceanic regions. Iron budgets for HNLC waters have been constructed using data from disparate sources ranging from laboratory algal cultures to ocean physics. In summer 2003 we conducted FeCycle, a 10-day mesoscale tracer release in HNLC waters SE of New Zealand, and measured concurrently all sources (with the exception of aerosol deposition) to, sinks of iron from, and rates of iron recycling within, the surface mixed layer. A pelagic iron budget (timescale of days) indicated that oceanic supply terms (lateral advection and vertical diffusion) were relatively small compared to the main sink (downward particulate export). Remote sensing and terrestrial monitoring reveal 13 dust or wildfire events in Australia, prior to and during FeCycle, one of which may have deposited iron at the study location. However, iron deposition rates cannot be derived from such observations, illustrating the difficulties in closing iron budgets without quantification of episodic atmospheric supply. Despite the threefold uncertainties reported for rates of aerosol deposition (Duce et al., 1991), published atmospheric iron supply for the New Zealand region is ˜50-fold (i.e., 7- to 150-fold) greater than the oceanic iron supply measured in our budget, and thus was comparable (i.e., a third to threefold) to our estimates of downward export of particulate iron. During FeCycle, the fluxes due to short term (hours) biological iron uptake and regeneration were indicative of rapid recycling and were tenfold greater than for new iron (i.e. estimated atmospheric and measured oceanic supply), giving an "fe" ratio (uptake of new iron/uptake of new + regenerated iron) of 0.17 (i.e., a range of 0.06 to 0.51 due to uncertainties on aerosol iron supply), and an "Fe" ratio (biogenic Fe export/uptake of new + regenerated iron) of 0.09 (i.e., 0.03 to 0.24).

  15. Evolution of Fe Bearing Intermetallics During DC Casting and Homogenization of an Al-Mg-Si Al Alloy

    NASA Astrophysics Data System (ADS)

    Kumar, S.; Grant, P. S.; O'Reilly, K. A. Q.

    2016-06-01

    The evolution of iron (Fe) bearing intermetallics (Fe-IMCs) during direct chill casting and homogenization of a grain-refined 6063 aluminum-magnesium-silicon (Al-Mg-Si) alloy has been studied. The as-cast and homogenized microstructure contained Fe-IMCs at the grain boundaries and within Al grains. The primary α-Al grain size, α-Al dendritic arm spacing, IMC particle size, and IMC three-dimensional (3D) inter-connectivity increased from the edge to the center of the as-cast billet; both α c-AlFeSi and β-AlFeSi Fe-IMCs were identified, and overall α c-AlFeSi was predominant. For the first time in industrial billets, the different Fe-rich IMCs have been characterized into types based on their 3D chemistry and morphology. Additionally, the role of β-AlFeSi in nucleating Mg2Si particles has been identified. After homogenization, α c-AlFeSi predominated across the entire billet cross section, with marked changes in the 3D morphology and strong reductions in inter-connectivity, both supporting a recovery in alloy ductility.

  16. Iron Atom Exchange between Hematite and Aqueous Fe(II).

    PubMed

    Frierdich, Andrew J; Helgeson, Maria; Liu, Chengshuai; Wang, Chongmin; Rosso, Kevin M; Scherer, Michelle M

    2015-07-21

    Aqueous Fe(II) has been shown to exchange with structural Fe(III) in goethite without any significant phase transformation. It remains unclear, however, whether aqueous Fe(II) undergoes similar exchange reactions with structural Fe(III) in hematite, a ubiquitous iron oxide mineral. Here, we use an enriched (57)Fe tracer to show that aqueous Fe(II) exchanges with structural Fe(III) in hematite at room temperature, and that the amount of exchange is influenced by particle size, pH, and Fe(II) concentration. Reaction of 80 nm-hematite (27 m(2) g(-1)) with aqueous Fe(II) at pH 7.0 for 30 days results in ∼5% of its structural Fe(III) atoms exchanging with Fe(II) in solution, which equates to about one surface iron layer. Smaller, 50 nm-hematite particles (54 m(2) g(-1)) undergo about 25% exchange (∼3× surface iron) with aqueous Fe(II), demonstrating that structural Fe(III) in hematite is accessible to the fluid in the presence of Fe(II). The extent of exchange in hematite increases with pH up to 7.5 and then begins to decrease as the pH progresses to 8.0, likely due to surface site saturation by sorbed Fe(II). Similarly, when we vary the initial amount of added Fe(II), we observe decreasing amounts of exchange when aqueous Fe(II) is increased beyond surface saturation. This work shows that Fe(II) can catalyze iron atom exchange between bulk hematite and aqueous Fe(II), despite hematite being the most thermodynamically stable iron oxide.

  17. Mechanical properties and electronic structures of Fe-Al intermetallic

    NASA Astrophysics Data System (ADS)

    Liu, YaHui; Chong, XiaoYu; Jiang, YeHua; Zhou, Rong; Feng, Jing

    2017-02-01

    Using the first-principles calculations, the elastic properties, anisotropy properties, electronic structures, Debye temperature and stability of Fe-Al (Fe3Al, FeAl, FeAl2, Fe2Al5 and FeAl3) binary compounds were calculated. The formation enthalpy and cohesive energy of these Fe-Al compounds are negative, and show they are thermodynamically stable structures. Fe2Al5 has the lowest formation enthalpy, which shows the Fe2Al5 is the most stable of Fe-Al binary compounds. These Fe-Al compounds display disparate anisotropy due to the calculated different shape of the 3D curved surface of the Young's modulus and anisotropic index. Fe3Al has the biggest bulk modulus with the value 233.2 GPa. FeAl has the biggest Yong's modulus and shear modulus with the value 296.2 GPa and 119.8 GPa, respectively. The partial density of states, total density of states and electron density distribution maps of the binary Fe-Al binary compounds are analyzed. The bonding characteristics of these Fe-Al binary compounds are mainly combination by covalent bond and metallic bonds. Meanwhile, also exist anti-bond effect. Moreover, the Debye temperatures and sound velocity of these Fe-Al compounds are explored.

  18. Iron Corrosion Observations: Pu(VI)-Fe Reduction Studies

    SciTech Connect

    Reed, Donald T.; Swanson, Juliet S.; Richmann, Michael K.; Lucchini, Jean-Francois; Borkowski, Marian

    2012-09-11

    Iron and Pu Reduction: (1) Very different appearances in iron reaction products were noted depending on pH, brine and initial iron phase; (2) Plutonium was associated with the Fe phases; (3) Green rust was often noted at the higher pH; (4) XANES established the green rust to be an Fe2/3 phase with a bromide center; and (5) This green rust phase was linked to Pu as Pu(IV).

  19. Elevated Temperature Deformation of Fe-39.8Al and Fe-15.6Mn-39.4Al

    NASA Technical Reports Server (NTRS)

    Whittenberger, J. Daniel

    2004-01-01

    The elevated temperature compressive properties of binary Fe-39.8 at % Al and Fe-15.6Mn-39.4Al have been measured between 1000 and 1300 K at strain rates between 10(exp 7) and 10(exp 3)/ s. Although the Mn addition to iron aluminide did not change the basic deformation characteristics, the Mn-modified alloy was slightly weaker. In the regime where deformation of FeAl occurs by a high stress exponent mechanism (n = 6), strength increases as the grain size decreases at least for diameters between approx. 200 and approx. 10 microns. Due to the limitation in the grain size-flow stress-temperature-strain rate database, the influence of further reductions of the grain size on strength is uncertain. Based on the appearance of subgrains in deformed iron aluminide, the comparison of grain diameters to expected subgrain sizes, and the grain size exponent and stress exponent calculated from deformation experiments, it is believed that grain size strengthening is the result of an artificial limitation on subgrain size as proposed by Sherby, Klundt and Miller.

  20. Development of Fe-Mn-Al-X-C alloys

    NASA Technical Reports Server (NTRS)

    Schuon, S. R.

    1982-01-01

    Development of a low cost Cr-free, iron-base alloy for aerospace applications involves both element substitution and enhancement of microstructural strengthening. When Mn is substituted for Ni and Al or Si is substituted for Cr, large changes occur in the mechanical and thermal stability of austenite in FeMnAlC alloys. The in situ strength of MC or M2C (M = Ti, V, Hf, Ta, or Mo) in FeMnAlC alloys was determined. The high temperature tensile strength depends more on the distribution of carbides than the carbide composition. Precipitation of a high volume percent-ordered phase was achieved in Fe2OMnlONi6Al6Ti (lC) alloys. As case, these alloys have a homogeneous austenitic structure. After solutioning at 1100 C for 5 hr followed by aging at 600 C for 16 hr, gamma prime or a perovskite carbide is precipitated. Overaging occurs at 900 C where eta is precipitated.

  1. Higher Fe{sup 2+}/total Fe ratio in iron doped phosphate glass melted by microwave heating

    SciTech Connect

    Mandal, Ashis K.; Sinha, Prasanta K.; Das, Dipankar; Guha, Chandan; Sen, Ranjan

    2015-03-15

    Highlights: • Iron doped phosphate glasses prepared using microwave heating and conventional heating under air and reducing atmosphere. • Presence of iron predominantly in the ferrous oxidation state in all the glasses. • Significant concentrations of iron in the ferrous oxidation state on both octahedral and tetrahedral sites in all the glasses. • Ratio of Fe{sup 2+} with total iron is found higher in microwave prepared glasses in comparison to conventional prepared glasses. - Abstract: Iron doped phosphate glasses containing P{sub 2}O{sub 5}–MgO–ZnO–B{sub 2}O{sub 3}–Al{sub 2}O{sub 3} were melted using conventional resistance heating and microwave heating in air and under reducing atmosphere. All the glasses were characterised by UV–Vis–NIR spectroscopy, Mössbauer spectroscopy, thermogravimetric analysis and wet colorimetry analysis. Mössbauer spectroscopy revealed presence of iron predominantly in the ferrous oxidation state on two different sites in all the glasses. The intensity of the ferrous absorption peaks in UV–Vis–NIR spectrum was found to be more in glasses prepared using microwave radiation compared to the glasses prepared in a resistance heating furnace. Thermogravimetric analysis showed increasing weight gain on heating under oxygen atmosphere for glass corroborating higher ratio of FeO/(FeO + Fe{sub 2}O{sub 3}) in glass melted by direct microwave heating. Wet chemical analysis also substantiated the finding of higher ratio Fe{sup +2}/ΣFe in microwave melted glasses. It was found that iron redox ratio was highest in the glasses prepared in a microwave furnace under reducing atmosphere.

  2. Magnetic properties of Al/57Fe/Cr multilayers

    NASA Astrophysics Data System (ADS)

    Jani, Snehal; Lakshmi, N.; Jain, Vishal; Reddy, V. R.; Gupta, Ajay; Venugopalan, K.

    2013-06-01

    Conversion Electron Mössbauer Spectroscopy (CEMS) and DC magnetization are used to compare magnetic properties of as-deposited multilayer (MLS) and Fe2CrAl thin film made from Al/57Fe/Cr MLS deposited by ion beam sputtering and then annealed in UHV. Interdiffusion of elements on annealing sample-1 at 500°C leads to formation of a single, disordered film of Fe2CrAl as evidenced by hyperfine field values obtained by CEMS in the film which compares well with that in bulk Fe2CrAl. CEMS also shows contributions from Fe, Fe/Cr and Fe/Al interfaces in the MLS. Saturation magnetization of as-deposited sample-1 is much less than pure Fe due to reduced Fe thickness because of interface formation and also reduction in Fe-Fe interaction due to intervening Al and Cr layers.

  3. Al2O3 Scale Development on Iron Aluminides

    SciTech Connect

    Zhang, Xiao-Feng; Thaidigsmann, Katja; Ager, Joel; Hou, Peggy Y.

    2005-11-10

    The structure and phase of the Al{sub 2}O{sub 3} scale that forms on an Fe{sub 3}Al-based alloy (Fe-28Al-5Cr) (at %) was investigated by transmission electron microscopy (TEM) and photoluminescence spectroscopy (PL). Oxidation was performed at 900 C and 1000 C for up to 190 min. TEM revealed that single-layer scales were formed after short oxidation times. Electron diffraction was used to show that the scales are composed of nanoscale crystallites of the {theta}, {gamma}, and {alpha} phases of alumina. Band-like structure was observed extending along three 120{sup o}-separated directions within the surface plane. Textured {theta} and {gamma} grains were the main components of the bands, while mixed {alpha} and transient phases were found between the bands. Extended oxidation produced a double-layered scale structure, with a continuous {alpha} layer at the scale/alloy interface, and a {gamma}/{theta} layer at the gas surface. The mechanism for the formation of Al{sub 2}O{sub 3} scales on iron aluminide alloys is discussed and compared to that for nickel aluminide alloys.

  4. Stability of Fe,Al-bearing bridgmanite in the lower mantle and synthesis of pure Fe-bridgmanite

    PubMed Central

    Ismailova, Leyla; Bykova, Elena; Bykov, Maxim; Cerantola, Valerio; McCammon, Catherine; Boffa Ballaran, Tiziana; Bobrov, Andrei; Sinmyo, Ryosuke; Dubrovinskaia, Natalia; Glazyrin, Konstantin; Liermann, Hanns-Peter; Kupenko, Ilya; Hanfland, Michael; Prescher, Clemens; Prakapenka, Vitali; Svitlyk, Volodymyr; Dubrovinsky, Leonid

    2016-01-01

    The physical and chemical properties of Earth’s mantle, as well as its dynamics and evolution, heavily depend on the phase composition of the region. On the basis of experiments in laser-heated diamond anvil cells, we demonstrate that Fe,Al-bearing bridgmanite (magnesium silicate perovskite) is stable to pressures over 120 GPa and temperatures above 3000 K. Ferric iron stabilizes Fe-rich bridgmanite such that we were able to synthesize pure iron bridgmanite at pressures between ~45 and 110 GPa. The compressibility of ferric iron–bearing bridgmanite is significantly different from any known bridgmanite, which has direct implications for the interpretation of seismic tomography data. PMID:27453945

  5. Forging of FeAl intermetallic compounds

    SciTech Connect

    Flores, O.; Juarez, J.; Campillo, B.; Martinez, L.; Schneibel, J.H.

    1994-09-01

    Much activity has been concentrated on the development of intermetallic compounds with the aim of improving tensile ductility, fracture toughness and high notch sensitivity in order to develop an attractive combination of properties for high and low temperature applications. This paper reports experience in processing and forging of FeAl intermetallic of B2 type. During the experiments two different temperatures were employed, and the specimens were forged after annealing in air, 10{sup {minus}2} torr vacuum and argon. From the results it was learned that annealing FeAl in argon atmosphere prior to forging resulted in better deformation behavior than for the other two environments. For the higher forging temperature used in the experiments (700C), the as-cast microstructure becomes partially recrystallized.

  6. Iron isotope fractionation during microbially stimulated Fe(II) oxidation and Fe(III) precipitation

    USGS Publications Warehouse

    Balci, N.; Bullen, T.D.; Witte-Lien, K.; Shanks, Wayne C.; Motelica, M.; Mandernack, K.W.

    2006-01-01

    Interpretation of the origins of iron-bearing minerals preserved in modern and ancient rocks based on measured iron isotope ratios depends on our ability to distinguish between biological and non-biological iron isotope fractionation processes. In this study, we compared 56Fe/54Fe ratios of coexisting aqueous iron (Fe(II)aq, Fe(III)aq) and iron oxyhydroxide precipitates (Fe(III)ppt) resulting from the oxidation of ferrous iron under experimental conditions at low pH (<3). Experiments were carried out using both pure cultures of Acidothiobacillus ferrooxidans and sterile controls to assess possible biological overprinting of non-biological fractionation, and both SO42- and Cl- salts as Fe(II) sources to determine possible ionic/speciation effects that may be associated with oxidation/precipitation reactions. In addition, a series of ferric iron precipitation experiments were performed at pH ranging from 1.9 to 3.5 to determine if different precipitation rates cause differences in the isotopic composition of the iron oxyhydroxides. During microbially stimulated Fe(II) oxidation in both the sulfate and chloride systems, 56Fe/54Fe ratios of residual Fe(II)aq sampled in a time series evolved along an apparent Rayleigh trend characterized by a fractionation factor ??Fe(III)aq-Fe(II)aq???1.0022. This fractionation factor was significantly less than that measured in our sterile control experiments (???1.0034) and that predicted for isotopic equilibrium between Fe(II)aq and Fe(III)aq (???1.0029), and thus might be interpreted to reflect a biological isotope effect. However, in our biological experiments the measured difference in 56Fe/54Fe ratios between Fe(III)aq, isolated as a solid by the addition of NaOH to the final solution at each time point under N2-atmosphere, and Fe(II)aq was in most cases and on average close to 2.9??? (??Fe(III)aq-Fe(II)aq ???1.0029), consistent with isotopic equilibrium between Fe(II)aq and Fe(III)aq. The ferric iron precipitation experiments

  7. Evidence for a Fe3+-rich pyrolitic lower mantle from (Al,Fe)-bearing bridgmanite elasticity data

    NASA Astrophysics Data System (ADS)

    Kurnosov, A.; Marquardt, H.; Frost, D. J.; Ballaran, T. Boffa; Ziberna, L.

    2017-03-01

    The chemical composition of Earth’s lower mantle can be constrained by combining seismological observations with mineral physics elasticity measurements. However, the lack of laboratory data for Earth’s most abundant mineral, (Mg,Fe,Al)(Al,Fe,Si)O3 bridgmanite (also known as silicate perovskite), has hampered any conclusive result. Here we report single-crystal elasticity data on (Al,Fe)-bearing bridgmanite (Mg0.9Fe0.1Si0.9Al0.1)O3 measured using high-pressure Brillouin spectroscopy and X-ray diffraction. Our measurements show that the elastic behaviour of (Al,Fe)-bearing bridgmanite is markedly different from the behaviour of the MgSiO3 endmember. We use our data to model seismic wave velocities in the top portion of the lower mantle, assuming a pyrolitic mantle composition and accounting for depth-dependent changes in iron partitioning between bridgmanite and ferropericlase. We find excellent agreement between our mineral physics predictions and the seismic Preliminary Reference Earth Model down to at least 1,200 kilometres depth, indicating chemical homogeneity of the upper and shallow lower mantle. A high Fe3+/Fe2+ ratio of about two in shallow-lower-mantle bridgmanite is required to match seismic data, implying the presence of metallic iron in an isochemical mantle. Our calculated velocities are in increasingly poor agreement with those of the lower mantle at depths greater than 1,200 kilometres, indicating either a change in bridgmanite cation ordering or a decrease in the ferric iron content of the lower mantle.

  8. Synthesis of iron aluminide-Al{sub 2}O{sub 3} composites by in-situ displacement reactions

    SciTech Connect

    Subramanian, R.; McKamey, C.G.; Buck, L.R.; Schneibel, J.H.

    1997-09-01

    Composites consisting of an iron aluminide matrix with ceramic particle reinforcements, such as alumina, could improve the high temperature strength without compromising the oxidation resistance. In this paper, the feasibility of processing Fe-Al alloy/Al{sub 2}O{sub 3} composites by an in-situ displacement reaction between Fe-40 at.% Al and iron oxide, Fe{sub 2}O{sub 3}, is investigated. Simple powder metallurgical processing was performed without resorting to an externally applied pressures or deformations during the high temperature processing step. The microstructural features of the composites are rationalized based on results from diffusion couples. Preliminary mechanical properties such as fracture toughness, yield strength and hardness are determined and compared with the values obtained for monolithic iron aluminide - Fe-28 at.% Al. Results suggest that a significant improvement in the properties is needed and further avenues for modifications, such as changes in the interface strength and externally applied forces during processing, are suggested.

  9. A systematic ALCHEMI study of Fe-doped NiAl alloys

    SciTech Connect

    Anderson, I.M.; Bentley, J.; Duncan, A.J.

    1995-06-01

    ALCHEMI site-occupation studies of alloying additions to ordered aluminide intermetallic alloys have been performed with varying degrees of success, depending on the ionization delocalization correction. This study examines the variation in the site-occupancy of Fe in B2-ordered NiAl vs solute concentration and alloy stoichiometry. The fraction of Fe on the `Ni` site is plotted vs Fe concentration. The good separation among the data from alloys of the three stoichiometries shows that the site occupancy of iron depends on the relative concentrations of the Ni and Al host elements; however a preference for the `Ni` site is clearly indicated.

  10. On isoelectronic fluorides [H 3tren]ṡ(AlF 6)ṡH 2O, [H 3tren]ṡ(AlF 6)ṡHF, [H 4tren]ṡ(AlF 6)ṡ(F) and the iron analogue [H 4tren]ṡ(FeF 6)ṡ(F)

    NASA Astrophysics Data System (ADS)

    Adil, K.; Ben Ali, A.; Leblanc, M.; Maisonneuve, V.

    2006-06-01

    [H 3tren]ṡ(AlF 6)ṡH 2O, [H 3tren]ṡ(AlF 6)ṡHF and [H 4tren]ṡ( MF 6)ṡ(F) ( M=Al, Fe), are obtained by hydrothermal technique and microwave heating in the (Al(OH) 3,FeF 3)- tren-(HF/H 2O)-ethanol system. Structure determinations are performed from single crystal X-ray diffraction data. All phases are built up from ( MF 6) 3- anions linked by hydrogen bonds to [H 3tren] 3+ or [H 4tren] 4+ cations and to water or HF molecules or "isolated" fluoride anions. [H 3tren] 3+ and [H 4tren] 4+ cations adopt a "spider" shape configuration. Surprisingly, the HF molecule is strongly hydrogen bonded with one fluoride ion of the AlF 6 octahedron (d=2.38 Å) in [H 3tren]ṡ(AlF 6)ṡHF while "isolated" fluoride ion is weakly coordinated by three hydrogen atoms in [H 4tren]ṡ( MF 6)ṡ(F). The evolution of the formulations, from [H 3tren]ṡ(AlF 6)ṡH 2O to [H 3tren]ṡ(AlF 6)ṡHF and to [H 4tren]ṡ( MF 6)ṡ(F) ( M=Al, Fe), is linked with the increase of the HF content of the starting solution. The volumes per formula unit decrease from 321.3(1) Å 3 and 320.6(1) Å 3 in [H 3tren]ṡ(AlF 6)ṡH 2O and [H 3tren]ṡ(AlF 6)ṡHF, respectively, to 298.5(4) Å 3 in [H 4tren]ṡ(AlF 6)ṡ(F).

  11. [Reduction of chromium (VI) by nanoscale zero-valent iron supported on Al-pillared bentonite].

    PubMed

    Yin, Li-Jing; Li, Yi-Min; Zhang, Lu-Ji; Peng, Yuan-Fei; Ying, Zhe-Lan

    2009-04-15

    In the presence of Al-pillared bentonite with good sorption capacity, nanoscale zero-valent iron supported on Al-pillared bentonite (NZVI/Al-PILC) was prepared with NaBH4 and FeSO4 aqueous solution. The structure of NZVI/Al-PILC was characterized by X-ray diffraction (XRD) and Brunauer-Emmett-Teller (BET). The effects of pH values and initial chromium (VI) concentrations on its removal rate by NZVI/Al-PILC were investigated, and were compared with those of unsupported nanoscale zero-valent iron (NZVI) containing the same iron mount of NZVI/Al-PILC. The results indicate that in the same experimental condition, the chromium (VI) removal by NZVI/Al-PILC reached 100% after 120 min. The removal is not only much higher than that (63.0%) of the NZVI containing same iron mount, but also superior to the sum of removal (75.4%) by NZVI containing the same iron amount and the Al-pillared bentonite containing the same clay amount with NZVI/Al-PILC.

  12. The influence of the iron content on the reductive decomposition of A{sub 3−x}Fe{sub x}Al{sub 2}Si{sub 3}O{sub 12} garnets (A = Mg, Mn; 0.47 ≤ x ≤ 2.85)

    SciTech Connect

    Aparicio, Claudia Filip, Jan Mashlan, Miroslav Zboril, Radek

    2014-10-27

    Thermally-induced reductive decomposition of natural iron-bearing garnets of the almandine-pyrope and almandine-spessartine series were studied at temperatures up to 1200 °C (heating rate of 10 °C/min) under atmosphere of forming gas (10% of H{sub 2} in N{sub 2}). Crystallochemical formula of the studied garnet was calculated as {sup VIII}(A{sub 3−x}Fe{sub x}{sup 2+}){sup VI}(Al,Fe{sup 3+}){sub 2}Si{sub 3}O{sub 12}, where the amount of Fe{sup 3+} in the octahedral sites is negligible with the exception of pyrope, A = Mg, Mn, and 0.47 ≤ x ≤ 2.85. The observed decomposition temperature, determined from differential scanning calorimetry and thermogravimetry, is greater than 1000 °C in all cases and showed almost linear dependence on the iron content in the dodecahedral sites of the studied garnets, with the exception of garnet with a near-pyrope composition (Prp{sub 80}Alm{sub 20}). The initial garnet samples and decomposition products were characterized in details by means of X-ray powder diffraction and {sup 57}Fe Mössbauer spectroscopy. We found that all studied garnets have common decomposition products such as metallic iron (in general, rounded particles below 4 μm) and Fe-spinel; the other identified decomposition products depend on starting chemical composition of the garnet: Fe-cordierite, olivine (fayalite or tephroite), cristobalite, pyroxene (enstatite or pigeonite), and anorthite. Anorthite and pigeonite were only present in garnets with Ca in the dodecahedral site. All the identified phases were usually well crystallized.

  13. Tensile Properties of Al-Cu 206 Cast Alloys with Various Iron Contents

    NASA Astrophysics Data System (ADS)

    Liu, K.; Cao, X.; Chen, X.-G.

    2014-05-01

    The Al-Cu 206 cast alloys with varying alloy compositions ( i.e., different levels of Fe, Mn, and Si) were investigated to evaluate the effect of the iron-rich intermetallics on the tensile properties. It is found that the tensile strength decreases with increasing iron content, but its overall loss is less than 10 pct over the range of 0.15 to 0.5 pct Fe at 0.3 pct Mn and 0.3 pct Si. At similar iron contents, the tensile properties of the alloys with dominant Chinese script iron-rich intermetallics are generally higher than those with the dominant platelet phase. In the solution and artificial overaging condition (T7), the tensile strength of the 206 cast alloys with more than 0.15 pct Fe is satisfactory, but the elongation does not sufficiently meet the minimum requirement of ductility (>7 pct) for critical automotive applications. However, it was found that both the required ductility and tensile strength can be reached at high Fe levels of 0.3 to 0.5 pct for the alloys with well-controlled alloy chemistry and microstructure in the solution and natural aging condition (T4), reinforcing the motivation for developing recyclable high-iron Al-Cu 206 cast alloys.

  14. Iron Cycling in Marine Sediments - New Insights from Isotope Analysis on Sequentially Extracted Fe Fractions

    NASA Astrophysics Data System (ADS)

    Henkel, S.; Kasten, S.; Poulton, S.; Hartmann, J.; Staubwasser, M.

    2014-12-01

    Reactive Fe (oxyhydr)oxides preferentially undergo early diagenetic cycling and may cause a diffusive flux of dissolved Fe2+ from sediments towards the sediment-water interface. The partitioning of Fe in sediments has traditionally been studied by applying sequential extractions based on reductive dissolution of Fe minerals. We complemented the sequential leaching method by Poulton and Canfield [1] in order to be able to gain δ56Fe data for specific Fe fractions, as such data are potentially useful to study Fe cycling in marine environments. The specific mineral fractions are Fe-carbonates, ferrihydrite + lepidocrocite, goethite + hematite, and magnetite. Leaching was performed with acetic acid, hydroxylamine-HCl, Na-dithionite and oxalic acid. The processing of leachates for δ56Fe analysis involved boiling the samples in HCl/HNO3/H2O2, Fe precipitation and anion exchange column chromatography. The new method was applied to short sediment cores from the North Sea and a bay of King George Island (South Shetland Islands, Antarctica). Downcore mineral-specific variations in δ56Fe revealed differing contributions of Fe (oxyhydr)oxides to redox cycling. A slight decrease in easily reducible Fe oxides correlating with a slight increase in δ56Fe for this fraction with depth, which is in line with progessive dissimilatory iron reduction [2,3], is visible in the top 10 cm of the North Sea core, but not in the antarctic sediments. Less reactive (dithionite and oxalate leachable) fractions did not reveal isotopic trends. The acetic acid-soluble fraction displayed pronounced δ56Fe trends at both sites that cannot be explained by acid volatile sulfides that are also extracted by acetic acid [1]. We suggest that low δ56Fe values in this fraction relative to the pool of easily reducible Fe oxides result from adsorbed Fe(II) that was open to isotopic exchange with oxide surfaces, affirming the experimental results of Crosby el al. [2]. Hence, δ56Fe analyses on marine

  15. Evolutionary analysis of iron (Fe) acquisition system in Marchantia polymorpha.

    PubMed

    Lo, Jing-Chi; Tsednee, Munkhtsetseg; Lo, Ying-Chu; Yang, Shun-Chung; Hu, Jer-Ming; Ishizaki, Kimitsune; Kohchi, Takayuki; Lee, Der-Chuen; Yeh, Kuo-Chen

    2016-07-01

    To acquire appropriate iron (Fe), vascular plants have developed two unique strategies, the reduction-based strategy I of nongraminaceous plants for Fe(2+) and the chelation-based strategy II of graminaceous plants for Fe(3+) . However, the mechanism of Fe uptake in bryophytes, the earliest diverging branch of land plants and dominant in gametophyte generation is less clear. Fe isotope fractionation analysis demonstrated that the liverwort Marchantia polymorpha uses reduction-based Fe acquisition. Enhanced activities of ferric chelate reductase and proton ATPase were detected under Fe-deficient conditions. However, M. polymorpha did not show mugineic acid family phytosiderophores, the key components of strategy II, or the precursor nicotianamine. Five ZIP (ZRT/IRT-like protein) homologs were identified and speculated to be involved in Fe uptake in M. polymorpha. MpZIP3 knockdown conferred reduced growth under Fe-deficient conditions, and MpZIP3 overexpression increased Fe content under excess Fe. Thus, a nonvascular liverwort, M. polymorpha, uses strategy I for Fe acquisition. This system may have been acquired in the common ancestor of land plants and coopted from the gametophyte to sporophyte generation in the evolution of land plants.

  16. Soluble ferrous iron (Fe (II)) enrichment in airborne dust

    NASA Astrophysics Data System (ADS)

    Bhattachan, Abinash; Reche, Isabel; D'Odorico, Paolo

    2016-09-01

    The input of soluble iron in dust delivered to the ocean and lakes is critical to their biogeochemistry and phytoplankton productivity. Most iron in soils and sediment deposits is insoluble, while only a tiny fraction is soluble and therefore suitable to meet the phytoplankton's requirements for photosynthesis and nitrogen assimilation. Aerosol deposition constitutes a major source of soluble iron to oceans and lakes, and in some regions the low phytoplankton productivity has been related to limitations in the supply of soluble iron from terrestrial sources. It is suggested that during atmospheric transport part of the insoluble iron is converted into soluble form. While the understanding of increased bioavailability of iron during atmospheric transport is improving, there are only a limited number of studies that actually quantify the increase in iron bioavailability in dust. In this study we compare the soluble ferrous iron, Fe (II) content in dust collected at deposition sites in the high-altitude mountains of the Sierra Nevada, Spain, to the source of dust in North Africa. We found that the dust is greatly enriched (on average 15 times) in Fe (II) relative to the fine fraction (<45 µm) of the parent soil collected from North African dust sources.

  17. THE IRON PROJECT AND THE RMAX PROJECT: Radiative and CollisionalProcesses of Iron Ions - Fe I, Fe II, Fe XVI, Fe XVII

    NASA Astrophysics Data System (ADS)

    Montenegro, Maximiliano; Nahar, Sultana; Pradhan, Anil; Sur, Chiranjib

    2008-05-01

    Results from work in progress under the Iron Project and Rmax Project on electron impact excitation and radiative processes of photo-excitations, photoionization and electron-ion recombination will be reported. Whereas the Iron Project is involved in scattering and radiative atomic processes of iron and iron-peak elements, and the Rmax Project aims particularly at the X-ray spectroscopy of astrophysical objects. We will present (i) collision strengths of Fe II at low energies using an accurate wavefunction needed for spectral analysis of infrared region, (ii) oscillator strengths and radiative decay rates for allowed and forbidden transitions in Fe I and Fe II, (iii) photoionization and electron-ion recombination of ground state of Fe XVI for over a large energy/temperature range up to and including K-shell ionization and core excitations as observed in X-ray spectra, and (iv) photoionization cross sections of large number fine structure levels (n<=10 and 0 <= 10) needed for astrophysical and modeling work. Relativistic approach in the Breit-Pauli approximation is being employed to study these atomic processes.

  18. Overview of the development of FeAl intermetallic alloys

    SciTech Connect

    Maziasz, P.J.; Liu, C.T.; Goodwin, G.M.

    1995-09-01

    B2-phase FeAl ordered intermetallic alloys based on an Fe-36 at.% Al composition are being developed to optimize a combination of properties that includes high-temperature strength, room-temperature ductility, and weldability. Microalloying with boron and proper processing are very important for FeAl properties optimization. These alloys also have the good to outstanding resistance to oxidation, sulfidation, and corrosion in molten salts or chlorides at elevated temperatures, characteristic of FeAl with 30--40 at.% Al. Ingot- and powder-metallurgy (IM and PM, respectively) processing both produce good properties, including strength above 400 MPa up to about 750 C. Technology development to produce FeAl components for industry testing is in progress. In parallel, weld-overlay cladding and powder coating technologies are also being developed to take immediate advantage of the high-temperature corrosion/oxidation and erosion/wear resistance of FeAl.

  19. Iron allocation in leaves of Fe-deficient cucumber plants fed with natural Fe complexes.

    PubMed

    Zanin, Laura; Tomasi, Nicola; Rizzardo, Cecilia; Gottardi, Stefano; Terzano, Roberto; Alfeld, Matthias; Janssens, Koen; De Nobili, Maria; Mimmo, Tanja; Cesco, Stefano

    2015-05-01

    Iron (Fe) sources available for plants in the rhizospheric solution are mainly a mixture of complexes between Fe and organic ligands, including phytosiderophores (PS) and water-extractable humic substances (WEHS). In comparison with the other Fe sources, Fe-WEHS are more efficiently used by plants, and experimental evidences show that Fe translocation contributes to this better response. On the other hand, very little is known on the mechanisms involved in Fe allocation in leaves. In this work, physiological and molecular processes involved in Fe distribution in leaves of Fe-deficient Cucumis sativus supplied with Fe-PS or Fe-WEHS up to 5 days were studied combining different techniques, such as radiochemical experiments, synchrotron micro X-ray fluorescence, real-time reverse transcription polymerase chain reaction and in situ hybridization. In Fe-WEHS-fed plants, Fe was rapidly (1 day) allocated into the leaf veins, and after 5 days, Fe was completely transferred into interveinal cells; moreover, the amount of accumulated Fe was much higher than with Fe-PS. This redistribution in Fe-WEHS plants was associated with an upregulation of genes encoding a ferric(III) -chelate reductase (FRO), a Fe(2+) transporter (IRT1) and a natural resistance-associated macrophage protein (NRAMP). The localization of FRO and IRT1 transcripts next to the midveins, beside that of NRAMP in the interveinal area, may suggest a rapid and efficient response induced by the presence of Fe-WEHS in the extra-radical solution for the allocation in leaves of high amounts of Fe. In conclusion, Fe is more efficiently used when chelated to WEHS than PS and seems to involve Fe distribution and gene regulation of Fe acquisition mechanisms operating in leaves.

  20. Weldability of Fe[sub 3]Al-type Aluminide

    SciTech Connect

    David, S.A.; Zacharia, T. )

    1993-05-01

    An investigation was carried out to determine the weldability of a series of Fe[sub 3]Al-type alloys. Autogenous welds were made on thin sheets of iron aluminide alloys using gas tungsten arc (GTA) and electron beam (EB) welding processes at different travel speeds and power levels. The results indicate that although these alloys can be successfully welded using the EB welding process, some compositions may hot crack during GTA welding. Boron and zirconium additions have been found to promote hot cracking in these alloys. Among the alloys investigated, Fe[sub 3]Al modified with chromium, niobium and carbon (FA-129) showed the most promise for good weldability. Hot-cracking severity of this alloy was further investigated using the Sigmajig test. The minimum threshold stress of 25 ksi measured is within the material range of other aluminides and some commercial stainless steels. Also, some of these alloys exhibited a tendency for cold cracking. This is related to severe hydrogen embrittlement associated with this class of alloys.

  1. The Pressure-Volume-Temperature Equation of State of Iron-Rich (Mg,Fe)O

    NASA Astrophysics Data System (ADS)

    Wicks, J. K.; Jackson, J. M.; Zhuravlev, K. K.; Prakapenka, V.

    2012-12-01

    Seismic observations near the base of the core-mantle boundary (CMB) have detected 5-20 km thick patches in which the seismic wave velocities are reduced by up to 30%. These ultra-low velocity zones (ULVZs) have been interpreted as aggregates of partially molten material (e.g. Williams and Garnero 1996, Hernlund and Jellinek, 2010) or as solid, iron-enriched residues (e.g. Knittle and Jeanloz, 1991; Mao et al., 2006; Wicks et al., 2010), typically based on proposed sources of velocity reduction. The stabilities of these structure types have been explored through dynamic models that have assembled a relationship between ULVZ stability and density (Hernlund and Tackley, 2007; Bower et al., 2010). Now, to constrain the chemistry of ULVZs, more information is needed on the relationship between density and sound velocity of candidate phases. Recently, we have shown that the characteristically low sound speeds of ULVZs can be produced by small amounts of iron-rich (Mg,Fe)O, which is likely to be found in iron-rich assemblages based on current partitioning studies (eg. Sakai et al., 2010; Tange et al., 2009). We determined the Debye velocity (VD) of (Mg.1657Fe.84)O using nuclear resonant inelastic x-ray scattering (NRIXS), and calculated the seismically relevant compressional (VP) and shear (VS) wave velocities up to 120 GPa using an equation of state of a similar composition (Wicks et al., 2010). These densities and sound velocities, in turn, are consistent with reasonable morphologies of modeled solid ULVZs (Bower et al., 2011). To increase the accuracy of density and sound velocity predictions, measurements must be made at elevated temperatures to correctly predict the properties of iron-rich (Mg,Fe)O at mantle conditions. In this study, we present the pressure-volume-temperature equation of state of (Mg.0657Fe.94)O measured up to pressures of 120 GPa and temperatures of 2000 K. Volume was measured with x-ray diffraction at beamline 13-ID-D of the Advanced Photon

  2. Synthesis of Fe-MCM-41 Using Iron Ore Tailings as the Silicon and Iron Source.

    PubMed

    Li, Xin; Yu, Honghao; He, Yan; Xue, Xiangxin

    2012-01-01

    Highly ordered Fe-MCM-41 molecular sieve was successfully synthesized by using n-hexadecyl-trimethyl ammonium bromide (CTAB) as the template and the iron ore tailings (IOTs) as the silicon and iron source. X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), diffuse reflectance UV-visible spectroscopy, (29)Si magic-angle spinning (MAS) nuclear magnetic resonance (NMR), and nitrogen adsorption/desorption were used to characterize the samples. The results showed that the mesoporous materials had highly ordered 2-dimensional hexagonal structure. The synthesized sample had high surface area, and part of iron atoms is retained in the framework with formation of tetrahedron after removal of the template by calcinations. The results obtained in the present work demonstrate the feasibility of employing iron ore tailings as a potential source of silicon and iron to produce Fe-MCM-41 mesoporous materials.

  3. Synthesis of Fe-MCM-41 Using Iron Ore Tailings as the Silicon and Iron Source

    PubMed Central

    Li, Xin; Yu, Honghao; He, Yan; Xue, Xiangxin

    2012-01-01

    Highly ordered Fe-MCM-41 molecular sieve was successfully synthesized by using n-hexadecyl-trimethyl ammonium bromide (CTAB) as the template and the iron ore tailings (IOTs) as the silicon and iron source. X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), diffuse reflectance UV-visible spectroscopy, 29Si magic-angle spinning (MAS) nuclear magnetic resonance (NMR), and nitrogen adsorption/desorption were used to characterize the samples. The results showed that the mesoporous materials had highly ordered 2-dimensional hexagonal structure. The synthesized sample had high surface area, and part of iron atoms is retained in the framework with formation of tetrahedron after removal of the template by calcinations. The results obtained in the present work demonstrate the feasibility of employing iron ore tailings as a potential source of silicon and iron to produce Fe-MCM-41 mesoporous materials. PMID:22567574

  4. Iron Partitioning in the Lower Mantle: New Experimental Data from Al-Enriched Olivine

    NASA Astrophysics Data System (ADS)

    Piet, H.; Nabiei, F.; Gillet, P.; Badro, J.

    2014-12-01

    The partitioning of iron between the major phases of the lower mantle has an important impact on their physical and chemical properties. A series of experimental studies of Fe-Mg exchange between bridgemanite (magnesium silicate perovskite) and ferropericlase have shown that stark differences in partitioning are observed if olivine [1, 2] or a pyrolitic [3, 4] starting composition are used. The discrepancy has been attributed to the presence of alumina, to that of ferric iron, to multiphase equilibria and even to the activity of FeO in the system. In order to mitigate the discrepancy, we synthesized a sample with San Carlos olivine composition that was doped in alumina. We then used this as starting material for experiments in the laser-heated diamond anvil cell at lower mantle (P,T) conditions along the geotherm. Samples were pressurized, heated, transformed to bridgemanite and ferropericlase, equilibrated, quenched, and decompressed. Thin sections were recovered from the hotspot using a focused ion beam microscope and the composition of the two phases was analyzed using analytical transmission electron microscopy. Iron partitioning in Al-rich olivine will be discussed through a detailed comparison with the Al-rich pyrolitic trend and the Al-free olivine trend. References [1] A-L. Auzende et al., Earth Planet. Sci. Lett., 2008. [2] R. Sinmyo et al., J. Geophys. Res., 2008.[3] R. Irifune et al., Science, 2010. [4] R. Sinmyo et al., Phys. Chem. Minerals, 2013.

  5. Experimental Spinel Standards for Ferric Iron (Fe3+) Determination During Peridotite Partial Melting

    NASA Astrophysics Data System (ADS)

    Wenz, M. D.; Sorbadere, F.; Rosenthal, A.; Frost, D. J.; McCammon, C. A.

    2014-12-01

    The presence of ferric iron (Fe3+) in the mantle plays a significant role in the oxygen fugacity (fO2) of the Earth's interior. This has a wide range of implications for Earth related processes ranging from the composition of the atmosphere to magmatic phase relations during melting and crystallization processes [1]. A major source of Earth's mantle magmas is spinel peridotite. Despite its low abundance, spinel (Fe3+/ƩFe = 15-34%, [2]) is the main contributor of Fe3+to the melt upon partial melting. Analyses of Fe3+ on small areas of spinel and melt are required to study the Fe3+ behavior during partial melting of spinel peridotite. Fe K-edge X-ray Absorption Near Edge Structure (XANES) combines both high precision and small beam size, but requires standards with a wide range of Fe3+ content to obtain good calibration. Glasses with varying Fe3+ content are easily synthesized [3, 4]. Spinel, however, presents a challenge for experimental standards due to the low diffusion of Cr and Al preventing compositional homogeneity. Natural spinel standards are often used, but only cover a narrow Fe3+ range. Thus, there is a need for better experimental spinel standards over a wider range of fO2. Our study involves making experimental mantle spinels with variable Fe3+ content. We used a sol-gel auto-combustion method to synthesize our starting material [5]. FMQ-2, FMQ+0, and air fO2 conditions were established using a gas mixing furnace. Piston cylinder experiments were performed at 1.5GPa, and 1310 -1370°C to obtain solid material for XANES. To maintain distinct oxidizing conditions, three capsules were used: graphite for reduced, Re for intermediate and AuPd for oxidized conditions. The spinels were analyzed by Mössbauer spectroscopy. Fe3+/ƩFe ranged from 0.3 to 0.6. These values are consistent with the Fe edge position obtained using XANES analyses, between 7130 and 7132 eV, respectively. Our spinels are thus suitable standards for Fe3+ measurements in peridotite

  6. Ductility and fracture in B2 FeAl alloys. Ph.D. Thesis Final Report

    NASA Technical Reports Server (NTRS)

    Crimp, Martin A.

    1987-01-01

    The mechanical behavior of B2FeAl alloys was studied. Stoichiometric Fe-50Al exhibits totally brittle behavior while iron-rich Fe-40Al yields and displays about 3% total strain. This change in behavior results from large decreases in the yield strength with iron-rich deviations from stoichiometry while the fracture stress remains essentially constant. Single crystal studies show that these yield strength decreases are directly related to decreases in the critical resolved shear stress for a group of zone axes /111/ set of (110) planes slip. This behavior is rationalized in terms of the decrease in antiphase boundary energy with decreasing aluminum content. The addition of boron results in improvements in the mechanical behavior of alloys on the iron-rich side of stoichiometry. These improvements are increased brittle fracture stresses of near-stoichiometric alloys, and enhanced ductility of up to 6% in Fe-40Al. These effects were attributed to increased grain boundary adhesion as reflected by changes in fracture mode from intergranular to transgranular failure. The increases in yield strength, which are observed in both polycrystals and single crystals, result from the quenching in of large numbers of thermal vacancies. Hall-Petch plots show that the cooling rate effects are a direct result of changes in the Hall-Petch intercept/lattice resistance flow.

  7. Stabilization of itinerant (band) magnetism in FeAl by Ga substitution for Al

    NASA Astrophysics Data System (ADS)

    Papaconstantopoulos, D. A.; Mazin, I. I.; Hathaway, K. B.

    2001-06-01

    Band structure calculations of FeGa1-xAlx have been performed, to further investigate the stability of ferromagnetism in FeAl. The Stoner parameter increases by about 20% at the FeGa end. This is also confirmed by our spin-polarized calculations. We conclude that Ga substitution for Al is likely to stabilize the elusive (or illusive) ferromagnetic state in FeAl.

  8. Antiferromagnetic spin fluctuations and unconventional nodeless superconductivity in an iron-based new superconductor (Ca4Al2O(6-y))(Fe2As2): 75As nuclear quadrupole resonance study.

    PubMed

    Kinouchi, H; Mukuda, H; Yashima, M; Kitaoka, Y; Shirage, P M; Eisaki, H; Iyo, A

    2011-07-22

    We report 75As nuclear quadrupole resonance studies on (Ca4Al2O(6-y))(Fe2As2) with T(c) = 27  K. Measurement of nuclear-spin-relaxation rate 1/T1 has revealed a significant development of two-dimensional antiferromagnetic spin fluctuations down to T(c) in association with the smallest As-Fe-As bond angle. Below T(c), the temperature dependence of 1/T1 without any trace of the coherence peak is well accounted for by a nodeless s(±)-wave multiple-gaps model. From the fact that its T(c) is comparable to T(c) = 28  K in the optimally doped LaFeAsO(1-y) in which antiferromagnetic spin fluctuations are not dominant, we remark that antiferromagnetic spin fluctuations are not a unique factor for enhancing T(c) among Fe-based superconductors, but a condition for optimizing superconductivity should be addressed from the lattice structure point of view.

  9. Hydrogen permeation in FeCrAl alloys for LWR cladding application

    DOE PAGES

    Hu, Xunxiang; Terrani, Kurt A.; Wirth, Brian D.; ...

    2015-03-19

    FeCrAl is an advanced oxidation-resistant iron-based alloy class, is a highly prevalent candidate as an accident-tolerant fuel cladding material. Compared with traditional zirconium alloy fuel cladding, increased tritium permeation through FeCrAl fuel cladding to the primary coolant is expected, raising potential safety concerns. In our study, the hydrogen permeability of several FeCrAl alloys was obtained using a static permeation test station, which was calibrated and validated using 304 stainless steel. The high hydrogen permeability of FeCrAl alloys leads to concerns with respect to potentially significant tritium release when used for fuel cladding in LWRs. Also, the total tritium inventory insidemore » the primary coolant of a light water reactor was quantified by applying a 1-dimensional steady state tritium diffusion model to demonstrate the dependence of tritium inventory on fuel cladding type. Furthermore, potential mitigation strategies for tritium release from FeCrAl fuel cladding were discussed and indicate the potential for application of an alumina layer on the inner clad surface to serve as a tritium barrier. More effort is required to develop a robust, economical mitigation strategy for tritium permeation in reactors using FeCrAl clad fuel assemblies.« less

  10. Hydrogen permeation in FeCrAl alloys for LWR cladding application

    SciTech Connect

    Hu, Xunxiang; Terrani, Kurt A.; Wirth, Brian D.; Snead, Lance L.

    2015-03-19

    FeCrAl is an advanced oxidation-resistant iron-based alloy class, is a highly prevalent candidate as an accident-tolerant fuel cladding material. Compared with traditional zirconium alloy fuel cladding, increased tritium permeation through FeCrAl fuel cladding to the primary coolant is expected, raising potential safety concerns. In our study, the hydrogen permeability of several FeCrAl alloys was obtained using a static permeation test station, which was calibrated and validated using 304 stainless steel. The high hydrogen permeability of FeCrAl alloys leads to concerns with respect to potentially significant tritium release when used for fuel cladding in LWRs. Also, the total tritium inventory inside the primary coolant of a light water reactor was quantified by applying a 1-dimensional steady state tritium diffusion model to demonstrate the dependence of tritium inventory on fuel cladding type. Furthermore, potential mitigation strategies for tritium release from FeCrAl fuel cladding were discussed and indicate the potential for application of an alumina layer on the inner clad surface to serve as a tritium barrier. More effort is required to develop a robust, economical mitigation strategy for tritium permeation in reactors using FeCrAl clad fuel assemblies.

  11. Unusual Solidification Behavior of the Suction-Cast Cu-Zr-Al-Y Alloy Doped with Fe

    NASA Astrophysics Data System (ADS)

    Kozieł, Tomasz; Cios, Grzegorz; Latuch, Jerzy; Pajor, Krzysztof; Bała, Piotr

    2017-04-01

    The effect of iron addition on the microstructure of the Cu-Zr-Al-Y glass-forming alloy was studied. Despite a high superficial cooling rate, small Fe additions (1.5 and 3 pct) induced formation of crystalline CuZr and AlCu2Zr phases on the outer layers of suction-cast rods. As the melt composition near the solid/liquid interface was depleted in Fe, the remaining melt vitrified at a relatively low cooling rate.

  12. Molecular Structures of Al/Si and Fe/Si Coprecipitates and the Implication for Selenite Removal

    PubMed Central

    Chan, Ya-Ting; Kuan, Wen-Hui; Tzou, Yu-Min; Chen, Tsan-Yao; Liu, Yu-Ting; Wang, Ming-Kuang; Teah, Heng-Yi

    2016-01-01

    Aluminum and iron oxides have been often used in the coagulation processes during water purification due to their unique surface properties toward anions. In the presence of silica, the coprecipitation of Al/Si or Fe/Si might decrease the efficiency of wastewater purification and reuse. In this study, surface properties and molecular structures of Al/Si and Fe/Si coprecipitates were characterized using spectroscopic techniques. Also, the selenite removal efficiency of Al/Si and Fe/Si coprecipitates in relation to their surface and structural properties was investigated. While dissolved silicate increased with increasing pH from Fe/Si coprecipitates, less than 7% of silicate was discernible from Al/Si samples over the range from acidic to alkaline conditions. Our spectroscopic results showed that the associations between Al and Si were relatively stronger than that between Fe and Si in coprecipitates. In Al/Si coprecipitates, core-shell structures were developed with AlO6/AlO4 domains as the shells and Si frameworks polymerized from the SiO2 as the cores. However, Si framework remained relatively unchanged upon coprecipitation with Fe hydroxides in Fe/Si samples. The Si core with Al shell structure of Al/Si coprecipitates shielded the negative charges from SiO2 and thereby resulted in a higher adsorption capacity of selenite than Fe/Si coprecipitates. PMID:27095071

  13. Synthesis of Cd/(Al+Fe) layered double hydroxides and characterization of the calcination products

    SciTech Connect

    Perez, M.R.; Barriga, C.; Fernandez, J.M.; Rives, V.; Ulibarri, M.A.

    2007-12-15

    Layered double hydroxides (LDHs) containing Cd(II), Al(III), and Fe(III) in the brucite-like layers with different starting Fe/Al atomic ratios and with nitrate as counteranion have been prepared following the coprecipitation method at a constant pH value of 8. An additional Cd(II),Al(III)-LDH sample interlayered with hexacyanoferrate(III) ions has been prepared by ionic exchange at pH 9. The samples have been characterized by elemental chemical analysis, powder X-ray diffraction (PXRD), and FT-IR spectroscopy. Their thermal stability has been assessed by thermogravimetric and differential thermal analyses (TG-DTA) and mass spectrometric analysis of the evolved gases. The PXRD patterns of the solids calcined at 800 deg. C show diffraction lines corresponding to Cd(Al)O and spinel-type materials, which precise nature (CdAl{sub 2}O{sub 4}, Cd{sub 1-x}Fe{sub 2+x}O{sub 4}, or Cd{sub x}Fe{sub 2.66}O{sub 4}) depends on location and concentration of iron in the parent material or precursor. - Graphical abstract: Layered double hydroxides (LDHs) containing Cd(II), Al(III), and Fe(III) in the brucite-like layers with different starting Fe/Al atomic ratios and with nitrate as counteranion have been prepared following the coprecipitation method. An additional Cd(II),Al(III)-LDH sample interlayered with hexacyanoferrate(III) ions has been prepared by ionic exchange. Calcination at 800 deg. C shows diffraction lines corresponding to CdO and to spinel-type materials. SEM micrograph of sample CdAlFe-N-0.

  14. The blue of iron in mineral pigments: a Fe K-edge XANES study of vivianite

    NASA Astrophysics Data System (ADS)

    Figueiredo, M. O.; Silva, T. P.; Veiga, J. P.

    2010-05-01

    Iron is a powerful chromophore element whose pigmenting properties were the first to be recognized among transition metals. The interest in blue iron minerals as pigments for painting was enhanced with the use of vivianite—a natural hydrated ferrous phosphate, Fe3(PO4)2ṡ8H2O—which in medieval Europe became an alternative to the expensive lapis lazuli, (Na, Ca)4(AlSiO4)3(SO4, Cl, S), a member of the ultramarines whose appreciated blue tone is due to the presence of sulfur polyanions. Conversely, vivianite coloring is attributed to the intervalence charge transfer (IVCT) Fe2+-Fe3+ that in later decades was studied by optical techniques and Mössbauer spectroscopy. However, the aging of blue vivianite pigments in old paintings has become a serious concern for conservators, but the aging process still awaits a satisfactory explanation. As an input to this problem, an X-ray absorption near-edge structure (XANES) study at the Fe K-edge of vivianite with different colors and origins was undertaken at the European Synchrotron Radiation Facility using the instrumental facilities of beamline ID-21. The analysis of pre-edge features corroborates previous data on the origin of vivianite color and emphasizes the need for a precautious assessment of iron speciation on the exclusive basis of XANES data. Actual results are discussed and further work is outlined.

  15. Electrochemical corrosion behavior and elasticity properties of Ti-6Al-xFe alloys for biomedical applications.

    PubMed

    Lu, Jinwen; Zhao, Yongqing; Niu, Hongzhi; Zhang, Yusheng; Du, Yuzhou; Zhang, Wei; Huo, Wangtu

    2016-05-01

    The present study is to investigate the microstructural characteristics, electrochemical corrosion behavior and elasticity properties of Ti-6Al-xFe alloys with Fe addition for biomedical application, and Ti-6Al-4V alloy with two-phase (α+β) microstructure is also studied as a comparison. Microstructural characterization reveals that the phase and crystal structure are sensitive to the Fe content. Ti-6Al alloy displays feather-like hexagonal α phase, and Ti-6Al-1Fe exhibits coarse lath structure of hexagonal α phase and a small amount of β phase. Ti-6Al-2Fe and Ti-6Al-4Fe alloys are dominated by elongated, equiaxed α phase and retained β phase, but the size of α phase particle in Ti-6Al-4Fe alloy is much smaller than that in Ti-6Al-2Fe alloy. The corrosion resistance of these alloys is determined in SBF solution at 37 °C. It is found that the alloys spontaneously form a passive oxide film on their surface after immersion for 500 s, and then they are stable for polarizations up to 0 VSCE. In comparison with Ti-6Al and Ti-6Al-4V alloys, Ti-6Al-xFe alloys exhibit better corrosion resistance with lower anodic current densities, larger polarization resistances and higher open-circuit potentials. The passive layers show stable characteristics, and the wide frequency ranges displaying capacitive characteristics occur for high iron contents. Elasticity experiments are performed to evaluate the elasticity property at room temperature. Ti-6Al-4Fe alloy has the lowest Young's modulus (112 GPa) and exhibits the highest strength/modulus ratios as large as 8.6, which is similar to that of c.p. Ti (8.5). These characteristics of Ti-6Al-xFe alloys form the basis of a great potential to be used as biomedical implantation materials.

  16. Thermoelectric properties of Fe and Al co-added Ge

    NASA Astrophysics Data System (ADS)

    Sasaki, Takayuki; Kurosaki, Ken; Yusufu, Aikebaier; Ohishi, Yuji; Muta, Hiroaki; Yamanaka, Shinsuke

    2017-04-01

    The polycrystalline bulk samples of Fe and Al co-added Ge were synthesized by melt-spinning followed by spark plasma sintering and the thermoelectric properties were examined. Here, Al acts as a p-type dopant, while Fe is expected to form FeGe2 as precipitates. Since the lattice mismatch between Ge and FeGe2 is small (<4%), they would coherently connect with each other, reducing the thermal conductivity without affecting the electrical transport. In this study, a reduction in thermal conductivity was achieved by dispersing the FeGe2 precipitates in the Al-doped Ge matrix, while they had little influences on both the carrier mobility and the Seebeck coefficient. As the results, the maximum ZT value of 0.13 was obtained at 773 K, which is three times higher than that of single-crystal Ge reported by the authors’ group [Y. Ohishi et al., Jpn. J. Appl. Phys. 55, 051301 (2016)].

  17. Strength anomaly in B2 FeAl single crystals

    SciTech Connect

    Yoshimi, K.; Hanada, S.; Yoo, M.H.; Matsumoto, N.

    1994-12-31

    Strength and deformation microstructure of B2 Fe-39 and 48%Al single crystals (composition given in atomic percent), which were fully annealed to remove frozen-in vacancies, have been investigated at temperatures between room temperature and 1073K. The hardness of as-homogenized Fe-48Al is higher than that of as-homogenized Fe-39Al while after additional annealing at 698K the hardness of Fe-48Al becomes lower than that of Fe-39Al. Fe-39Al single crystals slowly cooled after homogenizing at a high temperature were deformed in compression as a function of temperature and crystal orientation. A peak of yield strength appears around 0.5T{sub m} (T{sub m} = melting temperature). The orientation dependence of the critical resolved shear stress does not obey Schmid`s law even at room temperature and is quite different from that of b.c.c. metals and B2 intermetallics at low temperatures. At the peak temperature slip transition from <111>-type to <001>-type is found to occur macroscopically and microscopically, while it is observed in TEM that some of the [111] dislocations decompose into [101] and [010] on the (1096I) plane below the peak temperature. The physical sources for the positive temperature dependence of yield stress of B2 FeAl are discussed based on the obtained results.

  18. 57Fe Mössbauer study of Lu2Fe3Si5 iron silicide superconductor

    DOE PAGES

    Ma, Xiaoming; Ran, Sheng; Pang, Hua; ...

    2015-03-28

    With the advent of Fe–As based superconductivity it has become important to study how superconductivity manifests itself in details of 57Fe Mössbauer spectroscopy of conventional, Fe-bearing superconductors. The iron-based superconductor Lu2Fe3Si5 has been studied by 57Fe Mössbauer spectroscopy over the temperature range from 4.4 K to room temperature with particular attention to the region close to the superconducting transition temperature (Tc=6.1 K). Consistent with the two crystallographic sites for Fe in this structure, the observed spectra appear to have a pattern consisting of two doublets over the whole temperature range. Furthermore, the value of Debye temperature was estimated from temperaturemore » dependence of the isomer shift and the total spectral area and compared with the specific heat capacity data. Neither abnormal behavior of the hyperfine parameters at or near Tc, nor phonon softening were observed.« less

  19. Fabric cutting application of FeAl-based alloys

    SciTech Connect

    Sikka, V.K.; Blue, C.A.; Sklad, S.P.; Deevi, S.C.; Shih, H.R.

    1998-11-01

    Four intermetallic-based alloys were evaluated for cutting blade applications. These alloys included Fe{sub 3}Al-based (FAS-II and FA-129), FeAl-based (PM-60), and Ni{sub 3}Al-based (IC-50). These alloys were of interest because of their much higher work-hardening rates than the conventionally used carbon and stainless steels. The FeAl-based PM-60 alloy was of further interest because of its hardening possibility through retention of vacancies. The vacancy retention treatment is much simpler than the heat treatments used for hardening of steel blades. Blades of four intermetallic alloys and commercially used M2 tool steel blades were evaluated under identical conditions to cut two-ply heavy paper. Comparative results under identical conditions revealed that the FeAl-based alloy PM-60 outperformed the other intermetallic alloys and was equal to or somewhat better than the commercially used M2 tool steel.

  20. Oxidation behavior of FeAl+Hf,Zr,B

    NASA Technical Reports Server (NTRS)

    Smialek, James L.; Doychak, Joseph

    1988-01-01

    The oxidation behavior of Fe-40Al-1Hf, Fe-40Al-1Hf-0.4B, and Fe-40Al-0.1Zr-0.4B (at. percent) alloys was characterized after 900, 1000, and 100 C exposures. Isothermal tests revealed parabolic kinetics after a period of transitional theta-alumina scale growth. The parabolic growth rates for the subsequent alpha-alumina scales were about five times higher than those for NiAl+0.1Zr alloys. The isothermally grown scales showed a propensity toward massive scale spallation due to both extensive rumpling from growth stresses and to an inner layer of HfO2. Cyclic oxidation for 200 1-hr cycles produced little degradation at 900 or 1000 C, but caused significant spallation at 1100 C in the form of small segments of the outer scale. The major difference in the cyclic oxidation of the three FeAl alloys was increased initial spallation for FeAl+Zr,B. Although these FeAl alloys showed many similarities to NiAl alloys, they were generally less oxidation resistant. It is believed that this resulted from nonoptimal levels of dopants and larger thermal expansion mismatch stresses.

  1. Electronic structure and properties of magnetic defects in Co(1+x)Al(1-x) and Fe(1+x)Al(1-x) alloys. Ph.D. Thesis - Paris Univ.

    NASA Technical Reports Server (NTRS)

    Abbe, D.

    1984-01-01

    CoAl and FeAl compounds are developed along two directions. Magnetic susceptibility and specific heat at low temperature on (NiCo)Al and (CoFe)Al ternary alloys are in good agreement with band calculations. Results on magnetization and specific heat under field at low temperature on nonstoichiometric compounds show clearly the importance of the nearest neighbor effects. In the case of CoAl, the isolated cobalt atoms substituting aluminum are characterized by a Kondo behavior, and, for FeAl, the isolated extra iron atoms are magnetic and polarize the matrix. Moreover, for the two compounds, clusters of higher order play a considerable part in the magnetic properties for CoAl, these clusters also seem to be characterized by a Kondo behavior, for FeAl, these clusters whose moment is higher than in the case of isolated atoms, could be constituted of excess parts of iron atoms.

  2. Structure and properties of iron oxide clusters: From Fe6 to Fe6 O20 and from Fe7 to Fe7 O24.

    PubMed

    Gutsev, Gennady L; Belay, Kalayu G; Gutsev, Lavrenty G; Ramachandran, Bala R

    2016-10-30

    Geometrical and electronic structures of the neutral and singly negatively charged Fe6 On and Fe7 Om clusters in the range of 1 ≤ n ≤ 20 and 1 ≤ m ≤ 24, respectively, are computed using density functional theory with the generalized gradient approximation. The largest clusters in the two series, Fe6 O20 and Fe7 O24 , can be described as Fe(FeO4 )5 and Fe(FeO4 )6 or alternatively as [FeO5 ](FeO3 )5 and [FeO6 ](FeO3 )6 , respectively. The Fe6 O20 and Fe7 O24 clusters possess adiabatic electron affinities (EAad ) of 5.64 eV and 5.80 eV and can be attributed to the class of hyperhalogens since FeO4 is an unique closed-shell superhalogen with the EAad of 3.9 eV. The spin character of the lowest total energy states in both series changes from ferromagnetic to ferrimagnetic or antiferromagnetic when the first FeOFe bridge is formed. Oxidation decreases substantially the polarizability per atom of the initial bare clusters; namely, from 5.98 Å(3) of Fe6 to 2.47 Å(3) of Fe6 O20 and from 5.67 Å(3) of Fe7 to 2.38 Å(3) of Fe7 O24 . The results of our computations pertaining to the binding energies of O, Fe, O2 , and FeO in the Fe7 Om series provide an explanation for the experimentally observed abundance of the iron oxide nanoparticles with stoichiometric compositions. © 2016 Wiley Periodicals, Inc.

  3. Mechanical Properties of In-Situ FeAl-TiB2 Intermetallic Matrix Composites

    NASA Astrophysics Data System (ADS)

    Kim, Jonghoon; Park, Bonggyu; Park, Yongho; Park, Ikmin; Lee, Heesoo

    Intermetallic matrix composites reinforced with ceramic particles have received a great deal of attention. Iron aluminide is known to be a good material for the matrix in such composites. Two processes were used to fabricate FeAl-TiB2 intermetallic matrix composites. One was liquid melt in-situ mixing, and the other was arc melting and suction casting processes. FeAl-TiB2 IMCs obtained by two different methods were investigated to elucidate the influence of TiB2 content. In both methods, the grain size in the FeAl alloy decreased with the presence of titanium diboride. The grain size of in-situ FeAl-TiB2 IMCs became smaller than that of arc FeAl-TiB2 IMCs. Significant increase in fracture stress and hardness was achieved in the composites. The in-situ process gives clean, contamination-free matrix/reinforcement interface which maintained good bonding causing high load bearing capability. This contributed to the increase in the mechanical properties of composites.

  4. A Description of an Acidophilic, Iron Reducer, Geobacter sp. FeAm09 Isolated from Tropical Soils

    NASA Astrophysics Data System (ADS)

    Healy, O.; Souchek, J.; Heithoff, A.; LaMere, B.; Pan, D.; Hollis, G.; Yang, W. H.; Silver, W. L.; Weber, K. A.

    2014-12-01

    Iron (Fe) is the fourth most abundant element in the Earth's crust and plays a significant role controlling the geochemistry in soils, sediments, and aquatic systems. As part of a study to understand microbially-catalysed iron biogeochemical cycling in tropical soils, an iron reducing isolate, strain FeAm09, was obtained. Strain FeAm09 was isolated from acidic, Fe-rich soils collected from a tropical forest (Luquillo Experimental Forest, Puerto Rico). Strain FeAm09 is a rod-shaped, motile, Gram-negative bacterium. Taxonomic analysis of the near complete 16S rRNA gene sequence revealed that strain FeAm09 is 94.7% similar to Geobacter lovleyi, placing it in the genus Geobacter within the Family Geobacteraceae in the Deltaproteobacteria. Characterization of the optimal growth conditions revealed that strain FeAm09 is a moderate acidophile with an optimal growth pH of 5.0. The optimal growth temperature was 37°C. Growth of FeAm09 was coupled to the reduction of soluble Fe(III), Fe(III)-NTA, with H2, fumarate, ethanol, and various organic acids and sugars serving as the electron donor. Insoluble Fe(III), in the form of synthetic ferrihydrite, was reduced by strain FeAm09 using acetate or H2 as the electron donor. The use of H2 as an electron donor in the presence of CO2 and absence of organic carbon and assimilation of 14C-labelled CO2 into biomass indicate that strain FeAm09 is an autotrophic Fe(III)-reducing bacterium. Together, these data describe the first acidophilic, autotrophic Geobacter species. Iron reducing bacteria were previously shown to be as abundant in tropical soils as in saturated sediments (lake-bottoms) and saturated soils (wetlands) where Fe(III) reduction is more commonly recognized as a dominant mode of microbial respiration. Furthermore, Fe(III) reduction was identified as a primary driver of carbon mineralization in these tropical soils (Dubinsky et al. 2010). In addition to mineralizing organic carbon, Geobacter sp. FeAm09 is likely to also

  5. High-temperature corrosion behavior of coatings and ODS alloys based on Fe{sub 3}Al

    SciTech Connect

    Tortorelli, P.F.; Pint, B.A.; Wright, I.G.

    1996-06-01

    Iron aluminides containing greater than about 20-25 @ % Al have oxidation/sulfidation resistance at temperatures well above those at which these alloys have adequate mechanical strength. In addition to alloying modifications for improved creep resistance of wrought material, this strength limitation is being addressed by development of oxide-dispersion- strengthened (ODS) iron aluminides and by evaluation of Fe{sub 3}Al alloy compositions as coatings or claddings on higher-strength, less corrosion-resistant materials. As part of these efforts, the high-temperature corrosion behavior of iron-aluminide weld overlays and ODS alloys is being characterized and compared to previous results for ingot-processed material.

  6. Towards advanced structural analysis of iron oxide clusters on the surface of γ-Al2O3 using EXAFS

    NASA Astrophysics Data System (ADS)

    Boubnov, Alexey; Roppertz, Andreas; Kundrat, Matthew D.; Mangold, Stefan; Reznik, Boris; Jacob, Christoph R.; Kureti, Sven; Grunwaldt, Jan-Dierk

    2016-11-01

    Iron oxide centres are structurally investigated in 0.1% Fe/γ-Al2O3, which is known as highly active catalyst, for instance in the oxidation of CO. The sample was characterised by using X-ray absorption spectroscopy (XAS) in terms of X-ray absorption near-edge structure (XANES) and extended X-ray absorption fine structure (EXAFS), Mössbauer spectroscopy, X-ray diffraction (XRD) and transmission electron microscopy (TEM). These analyses evidenced high dispersion of the iron oxide entities without significant presence of bulk-like aggregates associated with the low Fe content of the catalyst. A library of structural models of Al2O3-supported surface Fe was created as input for EXAFS fitting. Additionally, several model structures of Fe substituting Al ions in bulk γ-Al2O3 were created with optimised geometry based on density-functional theory (DFT) calculations. From EXAFS refinement of the best 8 out of 24 models, it was found that the trivalent Fe ions are coordinated by 4-5 oxygen atoms and are located on octahedral lattice sites of the exposed surfaces of γ-Al2O3. These iron oxide species exist mainly as a mixture of monomeric and binuclear species and due to the low concentration represent suitable model systems as alternative to single crystal systems for structure-function relationships.

  7. The Morphology and Chemistry Evolution of Inclusions in Fe-Si-Al-O Melts

    NASA Astrophysics Data System (ADS)

    Kwon, Youjong; Choi, Juhan; Sridhar, Seetharaman

    2011-08-01

    This study aims to elucidate the process of inclusion precipitation in Fe-Si and Fe-Si-Al melts. Deoxidation experiments were carried out in a vacuum induction furnace (VIF) at 1873 K (1600 °C). In the Si-deoxidation experiments, spherical SiO2 of 1~2 μm diameter was dominant. When 3 wt pct Si and 300 ppm Al were added, such that Al2O3 and mullite were thermodynamically stable, the resulting inclusions depended on the addition sequence. When aluminum was added before silicon, spherical aluminum oxides were dominant after the Al addition, but after the Si addition, the number and size of alumina decreased and Al-Si oxides and mullite appeared with increasing time. When silicon was added before aluminum, spherical SiO2 was dominant after the Si addition, but after the Al addition, spherical and polygonal alumina inclusions were dominant. When Al/Si was added simultaneously, polygonal alumina inclusions were dominant initially, but with time, Al-Si oxide and mullite inclusions increased in numbers. If the Al amount in the Al/Si addition was increased to 600 ppm, only alumina was found. This study shows how, under similar thermodynamic conditions, the transient evolution of inclusions in iron melts in the Si-Al-O system differ depending on the alloy addition sequence.

  8. Local structure study of Fe dopants in Ni-deficit Ni3Al alloys

    DOE PAGES

    V. N. Ivanovski; Umicevic, A.; Belosevic-Cavor, J.; ...

    2015-08-24

    We found that the local electronic and magnetic structure, hyperfine interactions, and phase composition of polycrystalline Ni–deficient Ni 3-x FexAl (x = 0.18 and 0.36) were investigated by means of 57 Fe Mössbauer spectroscopy. The samples were characterized by X–ray diffraction and magnetization measurements. The ab initio calculations performed with the projector augmented wave method and the calculations of the energies of iron point defects were done to elucidate the electronic structure and site preference of Fe doped Ni 3 Al. Moreover, the value of calculated electric field gradient tensor Vzz=1.6 1021Vm-2 matches well with the results of Mössbauer spectroscopymore » and indicates that the Fe atoms occupy Ni sites.« less

  9. Observations of Al, Fe and Ca(+) in Mercury's Exosphere

    NASA Technical Reports Server (NTRS)

    Bida, Thomas A.; Killen, Rosemary M.

    2011-01-01

    We report 5-(sigma) tangent column detections of Al and Fe, and strict 3-(sigma) tangent column upper limits for Ca(+) in Mercury's exosphere obtained using the HIRES spectrometer on the Keck I telescope. These are the first direct detections of Al and Fe in Mercury's exosphere. Our Ca(-) observation is consistent with that reported by The Mercury Atmospheric and Surface Composition Spectrometer (MASCS) on the MErcury Surface, Space ENvironment, GEochemistry, and Ranging (MESSENGER) spacecraft.

  10. Metastable Phases of Rapidly Solidified Al-Rich Al-Fe Alloys

    DTIC Science & Technology

    1984-01-01

    same contrast. 20 FIGURE 9. Convergent beam diffraction pattern taken from a single crystal globular "S" phase. 21 FIGURE 10. The flower -like phase. 21...FIGURE 11. Convergent beam diffraction pattern obtained from the flower -like phase. 21 iii "- "’., % i ’ % " PAGE FIGURE 12. At-i wt.% Fe. Cellular...any of the previously reported aluminum-rich phases (Al3Fe, AlxFe, AI6Fe, A19Fe2, or AlmFe) [2,3]. An additional flower - shaped phase was detected in

  11. Alloy development and processing of FeAl: An overview

    SciTech Connect

    Maziasz, P.J.; Goodwin, G.M.; Alexander, D.J.; Viswanathan, S.

    1997-03-01

    In the last few years, considerable progress has been made in developing B2-phase FeAl alloys with improved weldability, room-temperature ductility, and high-temperature strength. Controlling the processing-induced microstructure is also important, particularly for minimizing trade-offs in various properties. FeAl alloys have outstanding resistance to high-temperature oxidation, sulfidation, and corrosion in various kinds of molten salts due to formation of protective Al{sub 2}O{sub 3} scales. Recent work shows that FeAl alloys are carburization-resistant as well. Alloys with 36 to 40 at. % Al have the best combination of corrosion resistance and mechanical properties. Minor alloying additions of Mo, Zr, and C, together with microalloying additions of B, produce the best combination of weldability and mechanical behavior. Cast FeAl alloys, with 200 to 400 {mu}m grain size and finely dispersed ZrC, have 2 to 5% tensile ductility in air at room-temperature, and a yield strength > 400 MPa up to about 700 to 750{degrees}C. Extruded ingot metallurgy (I/M) and powder metallurgy (P/M) materials with refined grain sizes ranging from 2 to 50 {mu}m, can have 10 to 15% ductility in air and be much stronger, and can even be quite tough, with Charpy impact energies ranging from 25 to 105 J at room-temperature. This paper highlights progress made in refining the alloy composition and exploring processing effects on FeAl for monolithic applications. It also includes recent progress on developing FeAl weld-overlay technology, and new results on welding of FeAl alloys. It summarizes some of the current industrial testing and interest for applications.

  12. Evaluation of Magnetostrictive Shunt Damper Performance Using Iron (Fe)-Gallium (Ga) Alloy

    DTIC Science & Technology

    2013-09-01

    Evaluation of Magnetostrictive Shunt Damper Performance Using Iron (Fe)-Gallium (Ga) Alloy by Andrew James Murray and Dr. JinHyeong Yoo...Aberdeen Proving Ground, MD 21005 ARL-TN-0566 September 2013 Evaluation of Magnetostrictive Shunt Damper Performance Using Iron (Fe... Magnetostrictive Shunt Damper Performance Using Iron (Fe)- Gallium (Ga) Alloy 5a. CONTRACT NUMBER 5b. GRANT NUMBER 5c. PROGRAM ELEMENT NUMBER 6

  13. Formation of Al2O3/FeAl coatings on a 9Cr-1Mo steel, and corrosion evaluation in flowing Pb-17Li loop

    NASA Astrophysics Data System (ADS)

    Majumdar, Sanjib; Paul, Bhaskar; Chakraborty, Poulami; Kishor, Jugal; Kain, Vivekanand; Dey, Gautam Kumar

    2017-04-01

    Iron aluminide coating layers were formed on a ferritic martensitic grade 9Cr-1Mo (P 91) steel using pack aluminizing process. The formation of different aluminide compositions such as orthorhombic-Fe2Al5, B2-FeAl and A2-Fe(Al) on the pack chemistry and heat treatment conditions have been established. About 4-6 μm thick Al2O3 scale was formed on the FeAl phase by controlled heat treatment. The corrosion tests were conducted using both the FeAl and Al2O3/FeAl coated specimens in an electro-magnetic pump driven Pb-17Li Loop at 500 °C for 5000 h maintaining a flow velocity of 1.5 m/s. The detailed characterization studies using scanning electron microscopy, back-scattered electron imaging and energy dispersive spectrometry revealed no deterioration of the coating layers after the corrosion tests. Self-healing oxides were formed at the cracks generated in the aluminide layers during thermal cycling and protected the base alloy (steel) from any kind of elemental dissolution or microstructural degradation.

  14. Fe Segregation Effects on Grain Boundary Migration in Al

    NASA Astrophysics Data System (ADS)

    Mendelev, Mikhail; Srolovitz, David; Ackland, Graeme; Han, Seungwu

    2004-03-01

    We investigate the effect of Fe impurities on grain boundary migration in Al. We fit a new interatomic potential to experimental data and our first principles results. This potential is validated by comparing simulated and experimental liquid Al-Fe alloy structure factors. This potential was used to simulate boundary migration in pure Al. The boundary velocity vs. driving force data at several temperatures were used to extract the boundary mobility and the activation energy for boundary migration. The activation energy was found to be at least an order of magnitude smaller than that obtained from experiment. This discrepancy is presumably associated with impurities in the Al samples. Therefore, we examined the effect of Fe on boundary migration in Al by determining the heat of segregation and the Fe diffusivity in Al as input to the Cahn-Lücke-Stüwe analytical impurity drag model. This analysis showed that even extremely small quantities of Fe (less than 1 ppm) in Al can reduce the grain boundary mobility by two orders of magnitude at T=723 K and even more at lower T, consistent with the extant experimental data.

  15. The Parent Li(OH)FeSe Phase of Lithium Iron Hydroxide Selenide Superconductors.

    PubMed

    Woodruff, Daniel N; Schild, Francesca; Topping, Craig V; Cassidy, Simon J; Blandy, Jack N; Blundell, Stephen J; Thompson, Amber L; Clarke, Simon J

    2016-10-03

    Lithiation of hydrothermally synthesized Li1-xFex(OH)Fe1-ySe turns on high-temperature superconductivity when iron ions are displaced from the hydroxide layers by reductive lithiation to fill the vacancies in the iron selenide layers. Further lithiation results in reductive iron extrusion from the hydroxide layers, which turns off superconductivity again as the stoichiometric composition Li(OH)FeSe is approached. The results demonstrate the twin requirements of stoichiometric FeSe layers and reduction of Fe below the +2 oxidation state as found in several iron selenide superconductors.

  16. An Assessment of the Al- Fe- N System

    NASA Astrophysics Data System (ADS)

    Hillert, Mats; Jonsson, Stefan

    1992-11-01

    The thermodynamic properties of the Al-Fe-N system are assessed, taking various types of information into account. For solid AIN, a description very similar to that given by JANAF is found to yield reasonable predictions for the solubility of A1N in face-centered cubic (fcc) Fe and in liquid Fe. An ionic two-sublattice model is applied to the liquid phase, containing two N species, N-3 and N0 The melting point of A1N is taken as 3068 K, and a required gas pressure of 9.75 bar is predicted. A sublimation point of 2690 K at 1 bar is also predicted. A plot of the liquidus surfaces in the Fe-rich end of the Al-Fe-N system is presented.

  17. The role of FeS(aq) molecular clusters in microbial redox cycling and iron mineralization.

    NASA Astrophysics Data System (ADS)

    Druschel, G.; Oduro, H.; Sperling, J.; Johnson, C.

    2008-12-01

    Iron sulfide molecular clusters, FeS(aq), are a group of polynuclear Fe-S complexes varying in size between a few and a few hundred molecules that occur in many environments and are critical parts of cycling between soluble iron and iron sulfide minerals. These clusters react uniquely with voltammetric Au-amalgam electrodes, and the signal for these molecules has now been observed in many terrestrial and marine aquatic settings. FeS(aq) clusters form when aqueous sulfide and iron(II) interact, but the source of those ions can come from abiotic or microbial sulfate and iron reduction or from the abiotic non-oxidative dissolution of iron sulfide minerals. Formation of iron sulfide minerals, principally mackinawite as the first solid nanocrystalline phase in many settings, is necessarily preceeded by formation and evolution of these molecular clusters as mineralization proceeds, and the clusters have been suggested to additionally be part of the pyritization process (Rickard and Luther, 1997; Luther and Rickard, 2005). In several systems, we have also observed FeS(aq) clusters to be the link between Fe-S mineral dissolution and oxidation of iron and sulfide, with important implications for changes to the overall oxidation pathway. Microorganisms can clearly be involved in the formation of FeS(aq) through iron and sulfate reduction, but it is not clear to date if organisms can utilize these clusters either as metabolic components or as anabolic 'building blocks' for enzyme production. Cycling of iron in the Fe-S system linked to FeS(aq) would clearly be a critical part of understanding iron isotope dynamics preserved in iron sulfide minerals. We will review ongoing work towards understanding the role of FeS(aq) in iron cycling and isotope fractionation as well as the measurement and characterization of this key class of iron complexes using environmental voltammetry.

  18. Effect of thermomechanical processing on mechanical properties of Fe-16 at. % Al alloy

    SciTech Connect

    Sikka, V.K.

    1994-12-31

    An iron-aluminum alloy containing 16 at. % Al, which is essentially free from environmental effect on its ductility, has been developed. This alloy has over 20% elongation at room temperature. This paper presents in detail the effect of vacuum versus air melting on the properties of Fe-16 at. % Al alloy. The comparative results have shown air-induction melting to produce lower room-temperature ductility for the identical processing steps. Additional processing steps required to improve the ductility of air-melted material are also identified.

  19. Electron microscopy of iron chalcogenide FeTe(Se) films

    NASA Astrophysics Data System (ADS)

    Shchichko, I. O.; Presnyakov, M. Yu.; Stepantsov, E. A.; Kazakov, S. M.; Antipov, E. V.; Makarova, I. P.; Vasil'ev, A. L.

    2015-05-01

    The structure of Fe1 + δTe1 - x Se x films ( x = 0; 0.05) grown on single-crystal MgO and LaAlO3 substrates has been investigated by transmission and scanning transmission electron microscopy. The study of Fe1.11Te/MgO structures has revealed two crystallographic orientation relationships between the film and substrate. It is shown that the lattice mismatch between the film and substrate is compensated for by the formation of misfit dislocations. The Burgers vector projection is determined. The stresses in the film can partially be compensated for due to the formation of an intermediate disordered layer. It is shown that a FeTe0.5Se0.5 film grown on a LaAlO3 substrate is single-crystal and that the FeTe0.5Se0.5/LaAlO3 interface in a selected region is coherent. The orientation relationships between the film and substrate are also determined for this case.

  20. Electron microscopy of iron chalcogenide FeTe(Se) films

    SciTech Connect

    Shchichko, I. O.; Presnyakov, M. Yu.; Stepantsov, E. A.; Kazakov, S. M.; Antipov, E. V.; Makarova, I. P.; Vasil’ev, A. L.

    2015-05-15

    The structure of Fe{sub 1+δ}Te{sub 1−x}Se{sub x} films (x = 0; 0.05) grown on single-crystal MgO and LaAlO{sub 3} substrates has been investigated by transmission and scanning transmission electron microscopy. The study of Fe{sub 1.11}Te/MgO structures has revealed two crystallographic orientation relationships between the film and substrate. It is shown that the lattice mismatch between the film and substrate is compensated for by the formation of misfit dislocations. The Burgers vector projection is determined. The stresses in the film can partially be compensated for due to the formation of an intermediate disordered layer. It is shown that a FeTe{sub 0.5}Se{sub 0.5} film grown on a LaAlO{sub 3} substrate is single-crystal and that the FeTe{sub 0.5}Se{sub 0.5}/LaAlO{sub 3} interface in a selected region is coherent. The orientation relationships between the film and substrate are also determined for this case.

  1. Large magnetostriction in directionally solidified FeGa and FeGaAl alloys

    NASA Astrophysics Data System (ADS)

    Srisukhumbowornchai, N.; Guruswamy, S.

    2001-12-01

    The magnetostriction of Fe-x at. % Ga (x=15, 20, and 27.5) was measured, for alloys processed under different directional solidification conditions, and the effect of partial substitution of Ga with Al on the magnetostriction of the alloys was examined. Magnetostriction measurements were carried out at different prestress levels varying from 0 to 55 MPa. Ga additions in the range of 15-27.5 at. % Ga in Fe were found to improve the magnetostriction of the disordered bcc phase of Fe by as much as 1 order of magnitude. The applied fields for saturation magnetostriction and the hysteresis observed were small. Magnetostriction values as high as 271×10-6 were obtained in polycrystalline Fe-27.5 at. % Ga rods prepared using a directional growth (DG) process at a growth rate of 22.5 mm/h. This process, which is essentially a seedless vertical Bridgman technique, resulted in near [001] textured polycrystalline Fe-Ga alloys. The preferred [001] crystallographic orientation of the DG alloys was approximately 14° away from the rod direction. For Ga contents between 15 and 27.5 at. % in Fe, the Ga atoms increase the Fe-Fe spacing in the disordered bcc (A2) phase and reduce the magnetic moment of Fe. Substitution of Ga with Al has a significant effect on the magnetostriction of the Fe-Ga alloys. Small substitution of 5 at. % Al for Ga in the Fe-20 at. % Ga alloy increases the magnetostriction in Fe, and the value is slightly larger than that of the Fe-20 at. % Ga alloy. A higher substitution amount of Al tends to decrease the magnetostriction.

  2. Segregation-Induced Subsurface Restructuring of FeAl(100)

    NASA Astrophysics Data System (ADS)

    Kottche, M.; Graupner, H.; Hammer, L.; Heinz, K.; Zehner, D. M.

    1996-03-01

    For FeAl, the stacking sequence in the [100] direction of the bulk crystal (CsCl structure) consists of alternating, single element planes. After sputtering, the selvedge region is depleted in Al. Following annealing to 350 ^circC, Al segregates to the surface region and a c(2 x 2) structure develops.(H. Graupner, L. Hammer, K. Müller, and D. M. Zehner, Surf. Sci. 322 (1995) 103. Research is sponsored by the *University of Erlangen-Nürnberg, Germany and DAAD, and the **Division of Materials Sciences, U.S. Department of Energy, under contract DE-AC05-84OR21400 with Lockheed Martin Energy Systems, Inc.) We have used low-energy electron diffraction (LEED) and Auger electron spectroscopy to investigate the structure and composition of this surface. From a detailed LEED I-V analysis, it has been determined that the subsurface region of the (100) surface orders with annealing, to form a stable Fe_3Al slab which is capped by an Al top layer and acts as an interface to the bulk FeAl. Within the limits of error, the interfacial Fe_3Al is similar to the bulk phase with some slight geometric rippling of the layers containing both elements. Annealing to higher temperatures leads to additional Al diffusion and eliminates the restructuring, resulting in a (1 x 1) phase.

  3. Analysis of the FeCrAl Accident Tolerant Fuel Concept Benefits during BWR Station Blackout Accidents

    SciTech Connect

    Robb, Kevin R

    2015-01-01

    Iron-chromium-aluminum (FeCrAl) alloys are being considered for fuel concepts with enhanced accident tolerance. FeCrAl alloys have very slow oxidation kinetics and good strength at high temperatures. FeCrAl could be used for fuel cladding in light water reactors and/or as channel box material in boiling water reactors (BWRs). To estimate the potential safety gains afforded by the FeCrAl concept, the MELCOR code was used to analyze a range of postulated station blackout severe accident scenarios in a BWR/4 reactor employing FeCrAl. The simulations utilize the most recently known thermophysical properties and oxidation kinetics for FeCrAl. Overall, when compared to the traditional Zircaloy-based cladding and channel box, the FeCrAl concept provides a few extra hours of time for operators to take mitigating actions and/or for evacuations to take place. A coolable core geometry is retained longer, enhancing the ability to stabilize an accident. Finally, due to the slower oxidation kinetics, substantially less hydrogen is generated, and the generation is delayed in time. This decreases the amount of non-condensable gases in containment and the potential for deflagrations to inhibit the accident response.

  4. The structure-property relationships of powder processed Fe-Al-Si alloys

    SciTech Connect

    Prichard, Paul D.

    1998-02-23

    Iron-aluminum alloys have been extensively evaluated as semi-continuous product such as sheet and bar, but have not been evaluated by net shape P/M processing techniques such as metal injection molding. The alloy compositions of iron-aluminum alloys have been optimized for room temperature ductility, but have limited high temperature strength. Hot extruded powder alloys in the Fe-Al-Si system have developed impressive mechanical properties, but the effects of sintering on mechanical properties have not been explored. This investigation evaluated three powder processed Fe-Al-Si alloys: Fe-15Al, Fe-15Al-2.8Si, Fe-15Al-5Si (atomic %). The powder alloys were produced with a high pressure gas atomization (HPGA) process to obtain a high fraction of metal injection molding (MIM) quality powder (D84 < 32 μm). The powders were consolidated either by P/M hot extrusion or by vacuum sintering. The extruded materials were near full density with grain sizes ranging from 30 to 50 μm. The vacuum sintering conditions produced samples with density ranging from 87% to 99% of theoretical density, with an average grain size ranging from 26 μm to 104 μm. Mechanical property testing was conducted on both extruded and sintered material using a small punch test. Tensile tests were conducted on extruded bar for comparison with the punch test data. Punch tests were conducted from 25 to 550 C to determine the yield strength, and fracture energy for each alloy as a function of processing condition. The ductile to brittle transition temperature (DBTT) was observed to increase with an increasing silicon content. The Fe-15Al-2.8Si alloy was selected for more extensive testing due to the combination of high temperature strength and low temperature toughness due to the two phase α + DO3 structure. This investigation provided a framework for understanding the effects of silicon in powder processing and mechanical property behavior of Fe-Al-Si alloys.

  5. Fe behavior in iron-bearing phonolitic and pantelleritic melts and its significance for magma dynamics in the volcanic conduits

    NASA Astrophysics Data System (ADS)

    Borovkov, Nikita; Hess, Kai-Uwe; Fehr, Karl-Thomas; Cimarelli, Corrado; Dingwell, Donald Bruce

    2014-05-01

    . From functional analysis of Mössbauer spectra this increasing is due to transformation of iron coordination: Fe2+ [5]-Fe2+ [4] and Fe3+ [5]-Fe3+ [4], depending on Redox conditions. XANES data helps us to prove coordination transformation of Fe clearly. This methods (Giuli et al., 2011) reveal that Fe3+ is always in tetrahedral coordination and Fe2+ is in the form of both [4] and [5] species. The presence of minor [5] or even [6] cannot be excluded. Combining Mössbauer and XANES methods, we can suggest that more reduced samples include more high coordinated Fe species. Under oxidized conditions Fe3+ tends to be [4] - coordinated completely and amount of Fe2+ [5] decreases. Viscosity for phonolitic and pantelleritic melts increases as well with more oxidized conditions, suggesting more polymerized structure. Under reduced conditions, low viscosity means that some higher coordinated Fe2+ and Fe3+ sites occur in structure and function as a depolymerizing factor. Therefore, in the presence of iron-bearing peralkaline melts, the prediction of an eruptive style requires knowledge of the dependence of viscosity on thermodynamic parameters as well as dependence on RedOx conditions, which are responsible for ferric and ferrous iron structural transformations.

  6. Superconductivity in new iron pnictide oxide Fe2As2Sr4(Mg,Ti)2O6

    NASA Astrophysics Data System (ADS)

    Sato, Shinya; Ogino, Hiraku; Kishio, Kohji; Shimoyama, Jun-Ichi

    2010-03-01

    A new iron arsenide oxide Fe2As2Sr4MgTiO6, which is isostructural with the iron-based superconductor Fe2Pn2Sr4M2O6^[1,2], has been successfully synthesized by the solid-state reaction in quartz ampoules. Fe2As2Sr4MgTiO6 has antifluorite-type iron arsenide layer and K2NiF4-type oxide layer, while the M-site is composed of a combination of divalent (Mg^2+) and tetravalent (Ti^4+) cations as in the case of a double perovskite La(Mg,Ti)O3. This fact indicates chemical flexibility of the perovskite-related layer in this system. This compound showed bulk superconductivity with Tc of ˜20 K by partial substitution of Co for Fe. Moreover, high Tc above 35 K was recorded by samples starting from Co-free and Ti-rich compositions, Fe2As2Sr4(Mg1-xTix)2O6 (x =0.7˜0.8). [1] H. Ogino et al., Supercond. Sci. Technol. 22 (2009) 075008. [2] X. Zhu et al., Phys. Rev. B 79 (2009) 220512(R).

  7. Particulate iron dynamics during FeCycle in subantarctic waters southeast of New Zealand

    NASA Astrophysics Data System (ADS)

    Frew, R. D.; Hutchins, D. A.; Nodder, S.; Sanudo-Wilhelmy, S.; Tovar-Sanchez, A.; Leblanc, K.; Hare, C. E.; Boyd, P. W.

    2006-03-01

    The FeCycle experiment provided an SF6 labeled mesoscale patch of high-nitrate low-chlorophyll (HNLC) water in austral summer 2003. These labeled waters enabled a comparison of the inventory of particulate iron (PFe) in the 45-m-deep surface mixed layer with the concurrent downward export flux of PFe at depths of 80 and 120 m. The partitioning of PFe between four size fractions (0.2-2, 2-5, 5-20, and >20 μm) was assessed, and PFe was mainly found in the >20-μm size fraction throughout FeCycle. Estimates of the relative contribution of the biogenic and lithogenic components to PFe were based on an Al:Fe molar ratio (0.18) derived following analysis of dust/soil from the nearest source of aerosol Fe: the semi-arid regions of Australia. The lithogenic component dominated each of the four PFe size fractions, with medians ranging from 68 to 97% of PFe during the 10-day experiment. The Fe:C ratios for mixed-layer particles were ˜40 μmol/mol. PFe export was ˜300 nmol m-2 d-1 at 80 m depth representing a daily loss of ˜1% from the mixed-layer PFe inventory. There were pronounced increases in the Fe:C particulate ratios with depth, with a five-fold increase from the surface mixed layer to 80 m depth, consistent with scavenging of the remineralized Fe by sinking particles and concurrent solubilization and loss of particulate organic carbon. Significantly, the lithogenic fraction of the sinking PFe intercepted at both 80 m and 120 m was >40% that is, there was an approximately twofold decrease in the proportion of lithogenic iron exported relative to that in the mixed-layer lithogenic iron inventory. This indicates that the transformation of lithogenic to biogenic PFe takes place in the mixed layer, prior to particles settling to depth. Moreover, the magnitude of lithogenic Fe supply from dust deposition into the waters southeast of New Zealand is comparable to that of the export of PFe from the mixed layer, suggesting that a large proportion of the deposited dust

  8. Coherent cluster atomic ordering in the Fe-27Al intermetallic compound

    NASA Astrophysics Data System (ADS)

    Balagurov, A. M.; Bobrikov, I. A.; Mukhametuly, B.; Sumnikov, S. V.; Golovin, I. S.

    2016-10-01

    Neutron diffraction studies of the Fe0.735Al0.265 compound are performed in a wide temperature range (20-900°C) in order to determine its structural states and the mechanism of ordering of atoms. The combination of high-resolution diffraction and the real-time detection of diffraction spectra makes it possible to establish that, in contrast to traditional notions, the structure of this compound at room temperature is a phase with only a partially ordered arrangement of Fe and Al in a unit cell. A completely ordered phase (such as Fe3Al) is present in the form of mesoscopic ( 200Å) clusters coherently incorporated into the disordered matrix of the main phase. After the transition of the sample to a disordered state ( T> 740°C) and slow cooling to room temperature, the size of structurally ordered clusters increases to 900 Å. A high contrast in the coherent neutron scattering lengths of iron and gallium nuclei allows the accurate determination of the temperature dependence of the occupancy factors of sites by Fe and Al atoms up to a phase transition to the disordered state.

  9. Atomic data from the iron project. 3: Rate coefficients for electron impact excitation of boron-like ions: Ne VI, Mg VIII, Al IX, Si X, S XII, Ar XIV, Ca XVI and Fe XXII

    NASA Technical Reports Server (NTRS)

    Zhang, Hong Lin; Graziani, Mark; Pradhan, Anil K.

    1994-01-01

    Collison strengths and maxwellian averaged rate coefficients have been calculated for the 105 transitions among all 15 fine structure levels of the 8 LS terms 2s(sup 2) 2 P(P-2(sup 0 sub 1/, 3/2)), 2s2p(sup 2)(P-4(sub 1/2,3/2,5/2), D-2(sub 3/2, 5/2), S-2(sub 1/2), P-2(sub 1/2, 3/2)), 2p(sup 3)(S-4(sup 0)(sub 3/2), D-2(sup 0 sub 3/2, 5/2), P-2(sup 0 sub 1/2, 3/2)) in highly- charged B-like Ne, Mg, Al, Si, S, Ar, Ca and Fe. Rate coefficients have been tabulated at a wide range of temperatures, depending on the ion charge and abundance in plasma sources. Earlier work for O IV has also been extended to include the high temperature range. A brief discussion of the calculations, sample results, and comparison with earlier works is also given. While much of the new data should be applicable to UV spectral diagnostics, the new rates for the important ground state fine structure transition P-2(sup 0 sub 1/2)-P-2(sup 0 sub 3/2) should result in significant revision of the IR cooling rates in plasmas where B-like ions are prominent constituents, since the new rate coefficients are generally higher by several factors compared with the older data.

  10. Synthesis of granular Fe sbnd Al 2O 3 by the sol-gel method

    NASA Astrophysics Data System (ADS)

    Santos, A.; Ardisson, J. D.; Tambourgi, E. B.; Macedo, W. A. A.

    1998-01-01

    We have investigated the structural and magnetic properties of a granular composite of iron particles dispersed in alumina matrix, obtained starting from an aqueous solution containing Al(NO 3) 3 · 9H 2O and FeSO 4 · 7H 2O. The samples were characterized by X-ray diffraction and fluorescence, Mössbauer spectroscopy (MS) and vibrating sample magnetometry (VSM). Samples with 7.8 wt% Fe were submitted to two different heat treatments with the aim of reducing the iron oxides into metallic iron. Series A was submitted to calcination between 100°C and 1200°C, followed by reduction in ultra pure H 2 at 600°C during 2 h; Series B was submitted to reduction at 600°C or at 1000°C directly after drying at 80°C. As determined by MS, we have obtained a maximum of 24% metallic Fe in series A and of 74% α-Fe in series B, after reduction at 1000°C. By VSM, at 300 K, the maximum coercivity of 819 Oe was obtained for the samples calcinated at 800°C before reduction and an almost constant saturation magnetization of 2 emu/g. In series B, samples with 74% α-Fe presented a coercivity of 370 Oe and a saturation magnetization of 9.0 emu/g. The applied synthesis method seems to be an interesting alternative way to obtain magnetic Fe nanoparticles in a non-magnetic alumina matrix.

  11. Extreme Ultraviolet Emission Lines of Iron Fe XI-XIII

    NASA Astrophysics Data System (ADS)

    Lepson, Jaan; Beiersdorfer, P.; Brown, G. V.; Liedahl, D. A.; Brickhouse, N. S.; Dupree, A. K.

    2013-04-01

    The extreme ultraviolet (EUV) spectral region (ca. 20--300 Å) is rich in emission lines from low- to mid-Z ions, particularly from the middle charge states of iron. Many of these emission lines are important diagnostics for astrophysical plasmas, providing information on properties such as elemental abundance, temperature, density, and even magnetic field strength. In recent years, strides have been made to understand the complexity of the atomic levels of the ions that emit the lines that contribute to the richness of the EUV region. Laboratory measurements have been made to verify and benchmark the lines. Here, we present laboratory measurements of Fe XI, Fe XII, and Fe XIII between 40-140 Å. The measurements were made at the Lawrence Livermore electron beam ion trap (EBIT) facility, which has been optimized for laboratory astrophysics, and which allows us to select specific charge states of iron to help line identification. We also present new calculations by the Hebrew University - Lawrence Livermore Atomic Code (HULLAC), which we also utilized for line identification. We found that HULLAC does a creditable job of reproducing the forest of lines we observed in the EBIT spectra, although line positions are in need of adjustment, and line intensities often differed from those observed. We identify or confirm a number of new lines for these charge states. This work was supported by the NASA Solar and Heliospheric Program under Contract NNH10AN31I and the DOE General Plasma Science program. Work was performed in part under the auspices of the Department of Energy by Lawrence Livermore National Laboratory under Contract DEAC52-07NA27344.

  12. Preliminary study of heavy metal pollution from Fe-Al oxides in Peihuang Creek, North Taiwan

    NASA Astrophysics Data System (ADS)

    Lai, B.

    2012-12-01

    Tatun Volcano Group (TVG) is not active since late Pleistocene but the post-volcanic activities, such as hot spring and sulfur gas, still widespread around the volcano province. Peihuang Creek is the main watershed system in TVG. The creek water is characterized by higher temperature, low pH values (3.0-4.5) and high SO4 content (60-400 ppm) due to the mixing of hotspring. This would promote the geochemical interaction between water and andesitic rocks and results in waters with highly enriched iron, aluminum and silica. These elements prefer to form suspended colloidal particles in water and adsorb heavy metals. Once the pH of water increases under oxidation condition, the colloid would precipitate in the form of ochre colored powder on the riverbed. The previous study reports that the arsenic content can reach as high as hundreds ppm. It is very important to evaluate the desorption behavior of heavy metals, especially for the study area with highly developed agriculture. For the preliminary analysis, five samples of ochre colored powder were sampled along the creek. The results of XRF demonstrate that the powder is mainly composed of iron, aluminum and silica, which is Fe-Al hydroxide. The iron content of Fe-Al hydroxide decreases from 63% to 25% while the aluminum and silica contents gradually increase from 5% to 20% and from 9% to 30%, respectively. To evaluate the desorption of heavy metals, the sequential extraction procedure was conducted. In the first step for determining leachable metals, the Fe-Al oxides were extracted with deionized water in the room temperature for one week. All of the metals are in ppb level except copper. For determining reducible phase, Step 2 used reagent solution of 0.5 mol/L hydroxylamine hydrochloride, which was adjusted to pH=2 with ultrapure nitric acid, for one week. The extracted chromium, arsenic, lead and copper are in the dangerous level of tens to hundreds ppm. It is believed that only very small amounts of heavy metals

  13. FORMATION MECHANISM FOR THE NANOSCALE AMORPHOUS INTERFACE IN PULSE-WELDED AL/FE BIMETALLIC SYSTEM

    SciTech Connect

    Li, Jingjing; Yu, Qian; Zhang, Zijiao; Xu, Wei; Sun, Xin

    2016-05-20

    Pulse or impact welding traditionally has been referred to as “solid-state” welding. By integrating advanced interface characterizations and diffusion calculations, we report that the nanoscale amorphous interface in the pulse-welded Al/Fe bimetallic system is formed by rapid heating and melting of a thin Al layer at the interface, diffusion of iron atoms in the liquid aluminum, and subsequent rapid quenching with diffused iron atoms in solution. This finding challenges the commonly held belief regarding the solid-state nature of the impact-based welding process for dissimilar metals. Elongated ultra-fine grains with high dislocation density and ultra-fine equiaxed grains also are observed in the weld interface vicinity on the steel and aluminum sides, respectively, which further confirms that melting and the resulted recrystallization occurred on the aluminum side of the interface.

  14. Formation mechanism for the nanoscale amorphous interface in pulse-welded Al/Fe bimetallic systems

    NASA Astrophysics Data System (ADS)

    Li, Jingjing; Yu, Qian; Zhang, Zijiao; Xu, Wei; Sun, Xin

    2016-05-01

    Pulse or impact welding traditionally has been referred to as "solid-state" welding. By integrating advanced interface characterizations and diffusion calculations, we report that the nanoscale amorphous interface in the pulse-welded Al/Fe bimetallic system is formed by rapid heating and melting of a thin Al layer at the interface, diffusion of iron atoms in the liquid aluminum, and subsequent rapid quenching with diffused iron atoms in solution. This finding challenges the commonly held belief regarding the solid-state nature of the impact-based welding process for dissimilar metals. Elongated ultra-fine grains with high dislocation density and ultra-fine equiaxed grains also are observed in the weld interface vicinity on the steel and aluminum sides, respectively, which further confirms that melting and the subsequent recrystallization occurred on the aluminum side of the interface.

  15. Magnetic and structural properties of Fe87Pt13-Al2O3 composite thin films synthesized by solid-state reactions

    NASA Astrophysics Data System (ADS)

    Zhigalov, V. S.; Myagkov, V. G.; Bykova, L. E.; Bondarenko, G. N.; Matsynin, A. A.; Volochaev, M. N.

    2017-02-01

    The structural and magnetic properties of Fe87Pt13 films synthesized by solid-state reactions and Fe87Pt13-Al2O3 composite films fabricated by aluminothermy are investigated. It is shown that the synthesized samples of both types are characterized by the rotational magnetic anisotropy, when the easy magnetization axis in the film plane can be set by a magnetic field. It is established that the value of rotational magnetic anisotropy in the Fe87Pt13-Al2O3 composite films is higher than in the Fe87Pt13 samples by an order of magnitude. The rotational magnetic anisotropy is assumed to be caused by the exchange coupling of the L10-FePt phase with the L12-Fe3Pt phase in the Fe87Pt13 films and magnetic iron oxides in the Fe87Pt13-Al2O3 samples.

  16. Iron and phosphorus speciation in Fe-conditioned membrane bioreactor activated sludge.

    PubMed

    Wu, Hao; Ikeda-Ohno, Atsushi; Wang, Yuan; Waite, T David

    2015-06-01

    Iron dosing of membrane bioreactors (MBRs) is widely used as a means of meeting effluent phosphorus targets but there is limited understanding of the nature of iron and phosphorus-containing solids that are formed within the bioreactor (an important issue in view of the increasing interest in recovering phosphorus from wastewaters). Of particular challenge is the complexity of the MBR system and the variety of reactions that can occur on addition of iron salts to a membrane bioreactor. In this study, the performances of bench scale MBRs with dosing of either ferrous or ferric salts were monitored for a period of four months. The distributions of Fe and P-species in the Fe-conditioned sludges were determined using X-ray absorption spectroscopy (XAS) at the Fe K-edge and the P K-edge. Regardless of whether iron was dosed to the anoxic or aerobic chambers and regardless of whether ferrous (Fe(II)) or ferric (Fe(III)) iron was dosed, iron present in the minerals in the conditioned sludges was consistently in the +III oxidation state. Fitting of the Fe K-edge EXAFS spectra revealed that an Fe(III)-phosphate species was the main Fe species present in all cases with the remaining fraction dominated by lepidocrocite (γ-FeOOH) in the Fe(II)-dosed case and ferrihydrite (am-FeOOH) in the Fe(III)-dosed case. Approximately half the phosphorus in the activated sludge samples was present as a distinct Fe-PO4 mineral (such as strengite or an amorphous ferric hydroxyl phosphate analogue of strengite) and half as phosphorus adsorbed to an iron oxyhydroxide mineral phase indicating that both co-precipitation and adsorption of phosphorus by iron contribute to removal of phosphorus from the MBR supernatant.

  17. An experimental approach for synthesis of Fe-Al-O multiferroic fibrous material

    NASA Astrophysics Data System (ADS)

    Starbov, N.; Starbova, K.; Vanderbemden, Ph; Simeonova, P.; Lovchinov, V.

    2012-12-01

    Basic principles of the electro-hydrodynamics are applied for synthesis of solid state Fe-Al-O multi-ferroic fibrous material. For that purpose stable blend spinning solutions comprised of a high molecular assisting organic polymer and salts of iron and aluminum are developed. These solutions are tested under electrospinning conditions and synthesis of homogeneous as spun non-woven mats characterized by fibre mean diameters in the micro-and nano-size range is successfully demonstrated. Multi-step thermal procedure is applied for the consecutive solvent evaporation, polymer pyrolisis and final fibre calcination. Electron-optical imaging technique and XRD are applied for revealing the sample morphology and the phase composition correspondingly. The results obtained outline the wide possibilities for fabrication of multi-ferroics fibrous nano-materials on the basis of Fe-Al-O.

  18. Critical Assessment and Thermodynamic Modeling of the Al-Fe-O System

    NASA Astrophysics Data System (ADS)

    Shishin, Denis; Prostakova, Viktoria; Jak, Evgueni; Decterov, Sergei A.

    2016-02-01

    A complete literature review, critical evaluation, and thermodynamic modeling of the phase diagrams and thermodynamic properties of phases in the Al-Fe-O system at 1 atm total pressure are presented. Optimized model equations for the thermodynamic properties of all phases are obtained, which reproduce all available thermodynamic and phase-equilibrium data within experimental error limits from 298.15 K (25 °C) to above the liquidus temperatures at all compositions and oxygen partial pressures from metal saturation to 1 atm. The complex phase relationships in the system have been elucidated, and discrepancies among the data have been resolved. The database of the model parameters can be used along with software for Gibbs-energy minimization in order to calculate all thermodynamic properties and any type of phase diagram section. The modified quasichemical model was used for the liquid oxide phase. A sublattice model, based upon the Compound Energy Formalism, was developed for spinel, which expands from magnetite, Fe3O4, to hercynite, FeAl2O4. The distribution of cations between octahedral and tetrahedral sites and oxygen nonstoichiometry in spinel are taken into account. The model for metallic liquid assumes random mixing of associates: Fe, Al, O, AlO, and Al2O. It describes well the minimum that is observed on the solubility of oxygen in liquid iron as a function of the Al content. The solid solution between hematite and corundum exhibiting a miscibility gap, as well as a small solubility of Al2O3 in wüstite are quantitatively described by a simple Bragg-Williams model.

  19. The fate of iron nanoparticles in environmental waters treated with nanoscale zero-valent iron, FeONPs and Fe3O4NPs.

    PubMed

    Peeters, Kelly; Lespes, Gaëtane; Zuliani, Tea; Ščančar, Janez; Milačič, Radmila

    2016-05-01

    Among the different nanoparticles (NPs) that are used in the remediation of contaminated environmental waters, iron nanoparticles (FeNPs) are the most frequently applied. However, if these FeNPs remain in the waters after the treatment, they can cause a hazard to the environment. In this work the time dependent size distribution of iron particles was investigated in Milli-Q water, forest spring water and landfill leachate after a variety of FeNP treatments. The efficiency of the metal removal by the FeNPs was also examined. The concentrations of the metals in the aqueous samples were determined before and after the nano-remediation by inductively coupled plasma mass spectrometry (ICP-MS). The data revealed that the settling and removal of the FeNPs after the treatment of the waters was related to the sample characteristics and the ways of dispersing the NPs. When mixing was used for the dispersion, the nano zero-valent iron (nZVI), FeONPs and Fe3O4NPs settled quickly in the Milli-Q water, the forest spring water and the landfill leachate. Dispersion with tertramethylammonium hydroxide (TMAH) resulted in a slower settling of the iron aggregates. In the Milli-Q and forest spring waters treated with FeONPs and dispersed by TMAH, the nanosized iron remained in solution as long as 24 h after the treatment and could represent a potential threat in environmental waters with a low ionic strength. The removal of the metals strongly depended on the type of FeNPs, the chemical speciation of the elements and the sample matrix. If the FeNPs are contaminated by a particular metal, this contaminant could be, during the NPs treatment, released into the water that is being remediated.

  20. Search for pressure-induced superconductivity in CeFeAsO and CeFePO iron pnictides

    SciTech Connect

    Zocco, D. A.; Baumbach, R. E.; Hamlin, J. J.; Janoschek, M.; Lum, I. K.; McGuire, Michael A; Safa-Sefat, Athena; Sales, Brian C; Jin, Rongying; Mandrus, David; Jeffries, J. R.; Weir, S. T.; Vohra, Y. K.; Maple, M. B.

    2011-01-01

    The CeFeAsO and CeFePO iron pnictide compounds were studied via electrical transport measurements under high pressure. In CeFeAsO polycrystals, the magnetic phases involving the Fe and Ce ions coexist for hydrostatically applied pressures up to 15 GPa, and with no signs of pressure-induced superconductivity up to 50 GPa for the less hydrostatic pressure techniques. For the CeFePO single crystals, pressure further stabilizes the Kondo screening of the Ce 4f-electron magnetic moments.

  1. Spin Transition of Iron and Crystal Structure in FeO from X-ray Emission Spectroscopy and Diffraction Measurements

    NASA Astrophysics Data System (ADS)

    Ozawa, H.; Hirose, K.; Ishii, H.; Hiraoka, N.; Ohishi, Y.

    2010-12-01

    FeO is definitely an important component in the Earth’s core because of high oxygen solubility into liquid iron at high pressure. High-pressure behavior of FeO is, therefore, of our great interest to geophysics. However, phase relationships in FeO at high pressure and high temperature still remain controversial, which is mainly due to lack of information on magnetic state of iron. The spin state of iron in FeO has been experimentally investigated by Mössbauer spectroscopy and X-ray emission spectroscopy (XES) to Mbar pressures [Pasternak et al., 1997 PRL; Badro et al., 1999 PRL]. However, there is a discrepancy between these studies probably because of sluggish structural transition at room temperature from rhombohedral to NiAs-type (B8) in FeO. Here we examined the spin state of iron and the crystal structure in FeO with combination of XES and X-ray diffraction (XRD) measurements at SPring-8. Starting material was commercially available Fe0.95O powder. The high-pressure phases of FeO were synthesized at high pressure and high temperature using a laser-heated diamond-anvil cell and examined by in-situ XRD measurements. XES spectra of the Fe Kβ fluorescence lines were collected up to 146 GPa. At 36 GPa, FeO with rhombohedral structure shows high-spin state, which is consistent with the previous studies. The satellite peak Kβ’ of iron in B8 phase completely disappeared at 146 GPa, indicating the loss of the 3d magnetic moment. We further collected XES spectra at 119 and 103 GPa with decreasing pressure. The presence of the Kβ’ peak of iron in B8 phase was clearly observed at 103 GPa whereas it was absent at 119 GPa, which suggests that the spin collapse occurred between these pressures. Furthermore, the volume measurements of B8 phase were conducted at P=77-132 GPa and 88-139 GPa at T=300 K and 1500-1700 K, respectively, using in-situ XRD. Sharp density discontinuity was observed at around 120 GPa at both 300 K and 1500-1700 K, which is most likely

  2. Development of ODS-Fe{sub 3}Al alloys

    SciTech Connect

    Wright, I.G.; Pint, B.A.; Tortorelli, P.F.; McKamey, C.G.

    1997-12-01

    The overall goal of this program is to develop an oxide dispersion-strengthened (ODS) version of Fe{sub 3}Al that has sufficient creep strength and resistance to oxidation at temperatures in the range 1000 to 1200 C to be suitable for application as heat exchanger tubing in advanced power generation cycles. The main areas being addressed are: (a) alloy processing to achieve the desired alloy grain size and shape, and (b) optimization of the oxidation behavior to provide increased service life compared to semi-commercial ODS-FeCrAl alloys intended for the same applications. The recent studies have focused on mechanically-alloyed powder from a commercial alloy vendor. These starting alloy powders were very clean in terms of oxygen content compared to ORNL-produced powders, but contained similar levels of carbon picked up during the milling process. The specific environment used in milling the powder appears to exert a considerable influence on the post-consolidation recrystallization behavior of the alloy. A milling environment which produced powder particles having a high surface carbon content resulted in a consolidated alloy which readily recrystallized, whereas powder with a low surface carbon level after milling resulted in no recrystallization even at 1380 C. A feature of these alloys was the appearance of voids or porosity after the recrystallization anneal, as had been found with ORNL-produced alloys. Adjustment of the recrystallization parameters did not reveal any range of conditions where recrystallization could be accomplished without the formation of voids. Initial creep tests of specimens of the recrystallized alloys indicated a significant increase in creep strength compared to cast or wrought Fe{sub 3}Al, but the specimens failed prematurely by a mechanism that involved brittle fracture of one of the two grains in the test cross section, followed by ductile fracture of the remaining grain. The reasons for this behavior are not yet understood. The

  3. Biostimulation of Iron Reduction and Subsequent Oxidation of Sediment Containing Fe-silicates and Fe-oxides: Effect of Redox Cycling on Fe(III) Bioreduction

    SciTech Connect

    Komlos, John; Kukkadapu, Ravi K.; Zachara, John M.; Jaffe, Peter R.

    2007-07-01

    Microbial reduction of iron has been shown to be important in the transformation and remediation of contaminated sediments. Re-oxidation of microbially reduced iron may occur in sediments that experience oxidation-reduction cycling and can thus impact the extent of contaminant remediation. The purpose of this research was to quantify iron oxidation in a flow-through column filled with biologically-reduced sediment and to compare the iron phases in the re-oxidized sediment to both the pristine and biologically-reduced sediment. The sediment contained both Fe(III)-oxides (primarily goethite) and silicate Fe (illite/vermiculite) and was biologically reduced in phosphate buffered (PB) medium during a 497 day column experiment with acetate supplied as the electron donor. Long-term iron reduction resulted in partial reduction of silicate Fe(III) without any goethite reduction, based on Mössbauer spectroscopy measurements. This reduced sediment was treated with an oxygenated PB solution in a flow-through column resulting in the oxidation of 38% of the biogenic Fe(II). Additional batch experiments showed that the Fe(III) in the oxidized sediment was more quickly reduced compared to the pristine sediment, indicating that oxidation of the sediment not only regenerated Fe(III) but also enhanced iron reduction compared to the pristine sediment. Oxidation-reduction cycling may be a viable method to extend iron-reducing conditions during in-situ bioremediation.

  4. A flow-through fluorescent sensor to determine Fe(III) and total inorganic iron.

    PubMed

    Pulido-Tofiño, P; Moreno, J M; Pérez-Conde, M C

    2000-03-06

    A flow-through fluorescent sensor for the consecutive determination of Fe(III) and total iron is described. The reactive phase of the proposed sensor, which has a high affinity for complexed Fe(III), consists of pyoverdin immobilized on controlled pore glass (CPG) by covalent bonding. This pigment selectively reacts with Fe(III) decreasing its fluorescence emission. Total inorganic iron is determined as Fe(III) after on-line oxidation in a mini-column containing persulphate immobilized on an ion exchange resin. The developed method allows the determination of Fe(III) in the 3-200 (g l(-1) range. The relative standard deviations of 10 determinations of 60 (g l(-1) of Fe(III) and 20 (g l(-1) of Fe(III)+Fe(II) are 3 and 5%, respectively. The sensor has been satisfactorily applied to speciate iron in synthetic, tap and well waters and wines. There were no significant differences for total inorganic iron determination between this new method and the atomic absorption spectroscopy reference method at the 95% confidence level. The sensor allows the concentration of Fe(II) to be calculated as the difference between total inorganic iron and Fe(III). The lifetime of the sensor is at least 3 months in continuous use or the equivalent of 1000 determinations.

  5. The effects of composition on the environmental embrittlement of Fe{sub 3}Al alloys

    SciTech Connect

    Alven, D.A.; Stoloff, N.S.

    1997-12-01

    This paper reviews recent research on embrittlement of iron aluminides at room temperature brought about by exposure to moisture or hydrogen. The tensile and fatigue crack growth behavior of several Fe-28Al-5Cr alloys with small additions of Zr and C are described. It will be shown that fatigue crack growth behavior is dependent on composition, environment, humidity level, and frequency. Environments studied include vacuum, oxygen, hydrogen gas, and moist air. All cases of embrittlement are ultimately traceable to the interaction of hydrogen with the crack tip.

  6. Morphological evolution and strengthening behavior of α-Al(Fe,Mn)Si in Al-6Si-2Fe-xMn alloys

    NASA Astrophysics Data System (ADS)

    Gao, Tong; Hu, Kaiqi; Wang, Longshuai; Zhang, Bangran; Liu, Xiangfa

    β-Al5FeSi is preferred to form in Al-Si-Fe alloys, normally exhibiting needlelike, which is harmful for the mechanical properties. In this paper, with the addition of 1%, 1.5% and 3% Mn into an Al-6Si-2Fe alloy, β-Al5FeSi phase was found to transform to skeleton, flower-like and coarse dendritic α-Al(Fe,Mn)Si, respectively. The novel flower-like α-Al(Fe,Mn)Si crystals contain developed branches with the average diameter of ∼200 nm, performing strengthening effect on the tensile property. Detailed morphologies of α-Al(Fe,Mn)Si phase and the formation mechanism were discussed.

  7. BISON Fuel Performance Analysis of FeCrAl cladding with updated properties

    SciTech Connect

    Sweet, Ryan; George, Nathan M.; Terrani, Kurt A.; Wirth, Brian

    2016-08-30

    In order to improve the accident tolerance of light water reactor (LWR) fuel, alternative cladding materials have been proposed to replace zirconium (Zr)-based alloys. Of these materials, there is a particular focus on iron-chromium-aluminum (FeCrAl) alloys due to much slower oxidation kinetics in high-temperature steam than Zr-alloys. This should decrease the energy release due to oxidation and allow the cladding to remain integral longer in the presence of high temperature steam, making accident mitigation more likely. As a continuation of the development for these alloys, suitability for normal operation must also be demonstrated. This research is focused on modeling the integral thermo-mechanical performance of FeCrAl-cladded fuel during normal reactor operation. Preliminary analysis has been performed to assess FeCrAl alloys (namely Alkrothal 720 and APMT) as a suitable fuel cladding replacement for Zr-alloys, using the MOOSE-based, finite-element fuel performance code BISON and the best available thermal-mechanical and irradiation-induced constitutive properties. These simulations identify the effects of the mechanical-stress and irradiation response of FeCrAl, and provide a comparison with Zr-alloys. In comparing these clad materials, fuel rods have been simulated for normal reactor operation and simple steady-state operation. Normal reactor operating conditions target the cladding performance over the rod lifetime (~4 cycles) for the highest-power rod in the highest-power fuel assembly under reactor power maneuvering. The power histories and axial temperature profiles input into BISON were generated from a neutronics study on full-core reactivity equivalence for FeCrAl using the 3D full core simulator NESTLE. Evolution of the FeCrAl cladding behavior over time is evaluated by using steady-state operating conditions such as a simple axial power profile, a constant cladding surface temperature, and a constant fuel power history. The fuel rod designs and

  8. Iron oxidation in Mops buffer. Effect of EDTA, hydrogen peroxide and FeCl3.

    PubMed

    Tadolini, B

    1987-01-01

    The effect of EDTA and H2O2 on iron autoxidation in Mops buffer depends on the pH of the solution. At acidic pH, EDTA caused the oxidation of a stoichiometric amount of iron. At neutral and alkaline pH, EDTA and H2O2 not only oxidizes a stoichiometric amount of iron but also causes the oxidation of the Fe2+ exceeding the concentration of these compounds. In the presence of EDTA, oxidation of Fe2+ in exceeding the concentration of these compounds has a shorter lag phase and an increased rate compared with that in the absence. The solution develops a yellow colour whose intensity is proportional to the amount of Fe2+ exceeding the concentration of these compounds in solution. When the reaction is conducted in the presence of NBT, formazan formation is greatly reduced compared to the control without EDTA and H2O2. The Fe3+-EDTA complex and Fe3+ affected iron oxidation, development of the yellow colour and NBT reduction in a similar fashion. In all these experimental conditions, iron oxidation is greatly reduced in the presence of mannitol, sorbitol and catalase. In phosphate buffer, EDTA oxidized a stoichiometric amount of iron without affecting free Fe2+ oxidation. Fe3+ has no effect on iron oxidation in this buffer.

  9. Ferromagnetism in CuFeSb: Evidence of competing magnetic interactions in iron-based superconductors

    NASA Astrophysics Data System (ADS)

    Qian, B.; Lee, J.; Hu, J.; Wang, G. C.; Kumar, P.; Fang, M. H.; Liu, T. J.; Fobes, D.; Pham, H.; Spinu, L.; Wu, X. S.; Green, M.; Lee, S. H.; Mao, Z. Q.

    2012-04-01

    We have synthesized a new layered iron-pnictide CuFeSb. This material shares a similar layered tetragonal structure with iron-based superconductors, with Fe square planar sheets forming from the edge-sharing iron antimony tetrahedral network. CuFeSb differs remarkably from Fe-based superconductors in the height of anion Zanion from the Fe plane; ZSb for CuFeSb is ˜1.84 Å, much larger than ZAs (1.31-1.51 Å) in FeAs compounds and ZTe (˜1.77 Å) in Fe1+yTe. In contrast with the metallic antiferromagnetic (AFM) or superconducting state of iron pnictides and chalcogenides under current studies, CuFeSb exhibits a metallic, ferromagnetic (FM) state with Tc=375 K. This finding suggests that the competition between AFM and FM coupling may exist in Fe-based superconductors and that the nature of magnetic coupling within the Fe plane is indeed dependent on the height of anion as predicted in theories.

  10. Gamma-resonance study of nanopowders with different dispersion and quasicrystalline phases in the Al-Cu-Fe system

    SciTech Connect

    Frolov, K. V. Mikheeva, M. N.; Lyubutin, I. S.; Nikonov, A. A.; Teplov, A. A.; Shaitura, D. S.; Abuzin, Yu. A.

    2007-11-15

    {sup 57}Fe Moessbauer spectroscopy has been used to monitor synthesis of quasicrystals in the Al-Cu-Fe system and study the influence of the size of quasicrystalline particles in powder samples of the Al{sub 63.1}Cu{sub 25.6}Fe{sub 11.3} alloy on the properties of synthesized materials. Quasicrystalline samples of different dispersion with particle sizes from 0.3 to 15 {mu}m have been studied in the temperature range 80-295 K. It is established that iron atoms in an Al{sub 63.1}Cu{sub 25.6}Fe{sub 11.3} quasicrystals occupy four types of structural positions, which differ in the atomic composition of the nearest environment. The results of the analysis suggest the dependence of the hyperfine-interaction parameters on the degree of sample dispersion. The components corresponding to iron atoms in both the surface layer and bulk of microparticles are isolated in the Moessbauer spectra. No magnetic hyperfine splitting has been found in the Moessbauer spectra in the entire temperature range. This fact suggests that a localized magnetic moment is absent in iron atoms.

  11. Corrosion performance of Fe-Cr-Al and Fe aluminide alloys in complex gas environments

    SciTech Connect

    Natesan, K.; Johnson, R.N.

    1995-05-01

    Alumina-forming structural alloys can offer superior resistance to corrosion in the presence of sulfur-containing environments, which are prevalent in coal-fired fossil energy systems. Further, Fe aluminides are being developed for use as structural materials and/or cladding alloys in these systems. Extensive development has been in progress on Fe{sub 3}Al-based alloys to improve their engineering ductility. In addition, surface coatings of Fe aluminide are being developed to impart corrosion resistance to structural alloys. This paper describes results from an ongoing program that is evaluating the corrosion performance of alumina-forming structural alloys, Fe-Al and Fe aluminide bulk alloys, and Fe aluminide coatings in environments typical of coal-gasification and combustion atmospheres. Experiments were conducted at 650-1000{degrees}C in simulated oxygen/sulfur gas mixtures. Other aspects of the program are corrosion evaluation of the aluminides in the presence of HCl-containing gases. Results are used to establish threshold Al levels in the alloys for development of protective alumina scales and to determine the modes of corrosion degradation that occur in the materials when they are exposed to S/Cl-containing gaseous environments.

  12. First-principles study of the effect of iron on the crystal structure, stability and chemical bonding in the β-based AlCu ordered η2-phase and the pretransition state of a solid solution

    NASA Astrophysics Data System (ADS)

    Shalaeva, E. V.; Medvedeva, N. I.

    2012-05-01

    First-principles calculations showed that the thermodynamic stability of β-based ordered η2-AlCu phase doped with Fe is due to iron substitution in the copper sublattice (FeCu), which corresponds to the maximum number of Fe-Al bonds in the first cubic coordination polyhedron. This iron localisation leads to stable ω-like atomic displacements and pentagonal Al-nets in the (010) plane of η2-AlCu(Fe). This phase with iron substituting copper (e/a = 1.925) is an energetically preferred η-based non-canonical approximant of the icosahedral phase (e/a = 1.86). The energy gain for the FeCu position is determined by strong covalent Fe3d-Al3p bonding, while there is a weak Fe3d-Cu4s3d hybridisation for the FeAl substitution. Using a composite cluster model, we demonstrate that short-range order in the pretransition state of the β-Al-Cu-Fe solid solution observed prior to the precipitation of η-phase is stabilised due to formation of Fe-Al bonds in the first cubic coordination polyhedron of the composite cluster.

  13. Regulation of high affinity iron uptake in the yeast Saccharomyces cerevisiae. Role of dioxygen and Fe.

    PubMed

    Hassett, R F; Romeo, A M; Kosman, D J

    1998-03-27

    High affinity iron uptake in Saccharomyces cerevisiae requires a metal reductase, a multicopper ferroxidase, and an iron permease. Fet3, the apparent ferroxidase, is proposed to facilitate iron uptake by catalyzing the oxidation of reductase-generated Fe(II) to Fe(III) by O2; in this model, Fe(III) is the substrate for the iron permease, encoded by FTR1 (Kaplan, J., and O'Halloran, T. V. (1996) Science 271, 1510-1512). We show here that dioxygen also plays an essential role in the expression of these iron uptake activities. Cells grown anaerobically exhibited no Fe(III) reductase or high affinity iron uptake activity, even if assayed for these activities under air. Northern blot analysis showed that the amount of those mRNAs encoding proteins associated with this uptake was repressed in anaerobic cultures but was rapidly induced by exposure of the culture to dioxygen. The anaerobic repression was reduced in cells expressing an iron-independent form of the trans-activator, Aft1, a protein that regulates the expression of these proteins. Thus, the effect of oxygenation on this expression appeared due at least in part to the state or distribution of iron in the cells. In support of this hypothesis, the membrane-permeant Fe(II) chelator, 2, 2'-bipyridyl, in contrast to the impermeant chelator bathophenanthroline disulfonate, caused a strong and rapid induction of these transcripts under anaerobic conditions. An increase in the steady-state levels of iron-regulated transcripts upon oxygenation or 2,2'-bipyridyl addition occurred within 5 min, indicating that a relatively small, labile intracellular pool of Fe(II) regulates the expression of these activities. The strength of the anaerobic repression was dependent on the low affinity, Fe(II)-specific iron transporter, encoded by FET4, suggesting that this Fe(II) pool was linked in part to iron brought into the cell via Fet4 protein. The data suggest a model in which dioxygen directly or indirectly modulates the Fe(III)/Fe

  14. Investigation of Phase Equilibria and Some Properties of Alloys of Ti-Al-Fe and Ti-Al-V Systems,

    DTIC Science & Technology

    Some data on the structure and properties of Ti-Al-Fe alloys are presented. The phase equilibria in alloys in the system Ti-Al-V were studies...However, the data available in the literature on phase equilibria in the systems Ti-Al-Fe and Ti-Al-V require refinement, as they are insufficiently

  15. Disappearance of superconductivity in the solid solution between (Ca4Al2O6)(Fe2As2) and (Ca4Al2O6)(Fe2P2) superconductors.

    PubMed

    Shirage, Parasharam M; Kihou, Kunihiro; Lee, Chul-Ho; Takeshita, Nao; Eisaki, Hiroshi; Iyo, Akira

    2012-09-19

    The effect of alloying the two perovskite-type iron-based superconductors (Ca(4)Al(2)O(6))(Fe(2)As(2)) and (Ca(4)Al(2)O(6))(Fe(2)P(2)) was examined. While the two stoichiometric compounds possess relatively high T(c)'s of 28 and 17 K, respectively, their solid solutions of the form (Ca(4)Al(2)O(6))(Fe(2)(As(1-x)P(x))(2)) do not show superconductivity over a wide range from x = 0.50 to 0.95. The resultant phase diagram is thus completely different from those of other typical iron-based superconductors such as BaFe(2)(As,P)(2) and LaFe(As,P)O, in which superconductivity shows up when P is substituted for As in the non-superconducting "parent" compounds. Notably, the solid solutions in the non-superconducting range exhibit resistivity anomalies at temperatures of 50-100 K. The behavior is reminiscent of the resistivity kink commonly observed in various non-superconducting parent compounds that signals the onset of antiferromagnetic/orthorhombic long-range order. The similarity suggests that the suppression of the superconductivity in the present case also has a magnetic and/or structural origin.

  16. Effects of iron status on transpulmonary transport and tissue distribution of Mn and Fe.

    PubMed

    Brain, Joseph D; Heilig, Elizabeth; Donaghey, Thomas C; Knutson, Mitchell D; Wessling-Resnick, Marianne; Molina, Ramon M

    2006-03-01

    Manganese transport into the blood can result from inhaling metal-containing particles. Intestinal manganese and iron absorption is mediated by divalent metal transporter 1 (DMT1) and is upregulated in iron deficiency. Since iron status alters absorption of Fe and Mn in the gut, we tested the hypothesis that iron status may alter pulmonary transport of these metals. DMT1 expression in the lungs was evaluated to explore its role in metal transport. The pharmacokinetics of intratracheally instilled 54Mn or 59Fe in repeatedly bled or iron oxide-exposed rats were compared with controls. Iron oxide exposure caused a reduction in pulmonary transport of 54Mn and 59Fe, and decreased uptake in other major organs. Low iron status from repeated bleeding also reduced pulmonary transport of iron but not of manganese. However, uptake of manganese in the brain and of iron in the spleen increased in bled rats. DMT1 transcripts were detected in airway epithelium, alveolar macrophages, and bronchial-associated lymphoid tissue in all rats. Focal increases were seen in particle-containing macrophages and adjacent epithelial cells, but no change was observed in bled rats. Although lung DMT1 expression did not correlate with iron status, differences in pharmacokinetics of instilled metals suggest that their potential toxicity can be modified by iron status.

  17. Effect of Heat Treatment on Morphology of Fe-Rich Intermetallics in Hypereutectic Al-Si-Cu-Ni Alloy with 1.26 pct Fe

    NASA Astrophysics Data System (ADS)

    Sha, Meng; Wu, Shusen; Wan, Li; Lü, Shulin

    2013-12-01

    Cobalt is generally considered as the element that can neutralize the negative effects of iron in Al alloys, such as inducing fracture and failure for stress concentration. Nevertheless, Fe-rich intermetallics would be inclined to form coarse plate-like δ-Al4(Fe, Co, Ni)Si2 particles when the content of Fe was high, which could also cause inferior mechanical properties. The dissolution and transformation of δ-Al4(Fe, Co, Ni)Si2 phase in solution heat-treated samples of Al-20Si-1.85Cu-1.05Ni-1.26Fe-1.35Co alloy were studied using optical microscopy, image analysis, and scanning electron microscopy. The effects of solution heat treatment time ranging from 0 to 9 hours at 783.15 K (510 °C) on mechanical properties were also investigated. The coarse plate-like δ-Al4(Fe, Co, Ni)Si2 particles varied slowly through concurrent dissolution along widths and at the plate tips as solution treatment time increased, which could be explained from diffusion-induced grain boundary migration. Solution heat treatment also has an important influence on mechanical properties. The maximum ultimate tensile strength and yield strength after T6 treatment were 258 and 132 MPa, respectively, while the maximum hardness was 131 HB. Compared with those of the samples in the as-cast state, they increased by 53, 42, and 28 pct, respectively. Moreover, δ-Al4(Fe, Co, Ni)Si2 phase, which appears as a coarse plate-like particle in two dimensions, is actually a cuboid in three dimensions. The length of this cuboid is close to the width, while the height is much smaller.

  18. Effect of iron ions (Fe(2+), Fe(3+)) on the formation and structure of aerobic granular sludge.

    PubMed

    Yilmaz, Gulsum; Bozkurt, Umit; Magden, Karin Aleksanyan

    2017-02-01

    Aerobic granulation is a promising technology for wastewater treatment, but problems regarding its formation and stability need to be solved. Divalent metal ions, especially Ca(2+), Mg(2+) and Mn(2+), have been demonstrated to play an important role in the process of aerobic granulation. Here, we studied whether iron ions can affect aerobic granulation. Granular sludge formed without iron ion addition (<0.02 mg Fe(2+) L(-1)) was fluffy and had a finger-type structure and filamentous out-growth. The addition of iron ions to concentrations of 1 and 10 mg Fe(2+) L(-1) repressed the finger-type structure and filamentous out-growth. The results show that chemical precipitation in the granules with iron ion addition was higher than that in the granules without ferrous addition. The amount of precipitates was higher inside the granules than outside. This study demonstrates that iron ions (Fe(2+)/Fe(3+)) increase the size and stability of aerobic granular sludge but do not affect the granulation time, which is the time that the first granular sludge is observed. The study shows that aerobic granular sludge technology can be confidently applied to actual wastewater containing a high concentration of iron compounds.

  19. Development of ductile Fe{sub 3}Al-based aluminides

    SciTech Connect

    McKamey, C.G.; Sikka, V.K.; Goodwin, G.M.

    1993-07-01

    Iron aluminides based on Fe{sub 3}Al are of interest because of their excellent oxidation and corrosion resistance, especially in sulfur-bearing atmospheres. Work at ORNL has centered on developing Fe{sub 3}Al-based alloys with improved ambient temperature ductilities and increased strengths at temperatures of 600--700C. Ambient temperature brittleness in this system is not ``inherent,`` but is caused by atomic hydrogen which is produced by an environmental reaction between aluminum in the alloy and water vapor in the atmosphere. Great strides have been made in understanding this embrittlement Phenomenon, and the production of alloys with room temperature ductilities of over 10% and tensile yield strengths at 600C of as high as 500 MPa is now possible through modifications in alloy composition and control of thermomechanical processing techniques. Creep rupture lifes of over 200 h at 593C (1100{degrees}F) and 207 MPa (30 ksi) can also be produced through control of alloy composition and microstructure. This paper summarizes our present efforts to improve the tensile and creep rupture properties and gives the status of efforts to commercialize Fe{sub 3}Al-based alloy compositions.

  20. Evaluation of nickel for positive electrode components in Li-Al/FeS cells

    NASA Astrophysics Data System (ADS)

    Smaga, J. A.; Battles, J. E.

    1982-03-01

    A series of tests were performed to examine the suitability of pure Ni positive electrodes, which have an oxidation potential of 2.2 V, in Li-Al/FeS batteries. A prismatic bicell was employed for the trials with the positive current collector sandwiched between the positive electrode halves, which were covered with Ni screens. The battery was run at 450 C for 31-153 days using different cells. Electrodes were then sectioned, cleaned, measured for thickness, evaluated for reactions, and examined microscopically and metallographically. Largest utilization gains were observed with a LiCl-rich electrolyte. Iron layers, with a thickness up to 6 microns, were found on the Ni components, but were considered too small to display significant life-shortening effects. Cells assembled in less than fully charged conditions showed noticeable intergranular corrosion, a process which was eliminated by using finer Fe particles in the positive electrode mix.

  1. Determination of the ferric iron (Fe3+) behaviour during MORB petrogenesis

    NASA Astrophysics Data System (ADS)

    Sorbadere, F.; Frost, D. J.; McCammon, C. A.

    2013-12-01

    The oxidation state of iron in MORB glasses is proposed to be directly related to the oxygen fugacity of the upper mantle from which it derives [e.g., 1]. Fe3+/ΣFe ratios of MORB recently measured by Cottrell and Kelley [2, 3], show a very narrow range, from 0.15 to 0.18, with a global average of 0.16×0.01, which corresponds to a fO2 very close to the Fayalite-Magnetite-Quartz (FMQ) buffer. For comparison, oceanic island basalts which derive from lower degrees of melting than MORB display higher Fe3+/ΣFe ratio, i.e., about 0.29 [4]. This is consistent with the Fe3+ behaving incompatibly during partial melting (i.e., from 0.1; [5] to 0.2; [6]). Hence, MORB Fe3+/ΣFe ratios are expected to be essentially controlled by magmatic processes of partial melting and fractional crystallisation, similar to other incompatible elements. Correlations between Fe3+/ΣFe ratios and indices of low pressure fractional crystallization have been recognized in global MORB [2], but are not systematic [7]. However, Fe3+/ΣFe ratios do not vary with melt-fraction related parameters, such as the Na2O(8) [7, 2], reflecting a relatively constant oxygen fugacity (fO2). Studies of other redox sensitive elements such as V and Cr, which have variable valence states and partition coefficients as a function of fO2 [e.g., 6, 8] also seem to imply that mantle melting occurs over a relatively small range of fO2. The absence of a correlation between magmatic processes and the Fe3+/ΣFe ratio of MORB implies that this ratio is controlled or even buffered by some processes. One possibility to account for this Fe3+/ΣFe paradox might be a change in the Fe3+ partition coefficient as a function of the degree of peridotite melting [2]. The decrease in the Fe3+ content of the melt expected for increasing melt extraction would have to be off-set by a process that would make Fe3+ more incompatible at higher degrees of melting [2]. To determine the effect of P, T and fO2 on the Fe3+ partition coefficient

  2. Distribution of Al{sub 12}Fe{sub 3}Si and (FeAl{sub 6})Si in a HIPed Al-10.71 wt. % Si casting

    SciTech Connect

    Chama, C.C.

    1996-10-01

    An investigation on microstructural development in a hot isostatically pressed (HIPed) Al-10.71 wt. % Si casting is described. The as-cast material contained 0.006 total volume fraction of Al{sub 12}Fe{sub 3}Si and (FeAl{sub 6})Si particles but HIPing at 550 C and 68.95 MPa produced a moderate increase in this fraction, to a maximum value of 0.061 when HIPed for 120 min. Dislocations appeared to be the dominant nucleation sites for the particles in both the as-cast and the HIPed materials.

  3. Al-26-Mg-26 ages of iron meteorites

    NASA Technical Reports Server (NTRS)

    Herzog, G. F.; Souzis, A. E.; Xue, S.; Klein, J.; Juenemann, D.; Middleton, R.

    1993-01-01

    An exposure age for an iron meteorite can be calculated from measurements of a radioactive nuclide and a stable nuclide that are produced by similar sets of nuclear reactions, provided that the stable nuclide is present with low initial abundance. The standard methods rely on either K-40 (t(sub 1/2) = 1.26 Gy), K-39, and K-41 or on a shorter-lived radionuclide and a stable, noble gas isotope. Widely used pairs of this type include Cl-36/Ar-36 and Al-26/Ne-21. Other pairs that may serve the purpose for iron meteorites contain many stable isotopes besides those of K and the noble gases that are produced partly by cosmic rays. We consider here the calculation of exposure ages, t(sub 26), from measurements of Al-26 (t(sub 1/2) = 0.7 My) and (stable) Mg-26. Ages based on Al-26/Mg-26 ratios, like those based on Cl-36/Ar-36 ratios, are 'buffered' against changes in relative production rates due to shielding because decay of the radioactive nuclide accounts for a good part of the inventory of the stable nuclide.

  4. High-valent iron (Fe(VI), Fe(V), and Fe(IV)) species in water: characterization and oxidative transformation of estrogenic hormones.

    PubMed

    MachalováŠišková, Karolína; Jančula, Daniel; Drahoš, Bohuslav; Machala, Libor; Babica, Pavel; Alonso, Paula Godoy; Trávníček, Zdeněk; Tuček, Jiří; Maršálek, Blahoslav; Sharma, Virender K; Zbořil, Radek

    2016-07-28

    This paper presents solid state synthesis and characterization of tetra-oxy iron(iv) and iron(v) species in their salt forms (Na4FeO4-Fe(IV) and K3FeO4-Fe(V)). Stability of the synthesized salts, commonly called ferrates, in water was determined by applying the (57)Fe Mössbauer spectroscopy technique. Within 2 s in water, Fe(IV) converted into Fe(III) while Fe(V) transformed into Fe(VI) and Fe(III) at pH = 8.2. Comparatively, Fe(VI) (bought as K2FeO4) remained stable in aqueous solution during the short time period. The oxidative removal efficiency of the high-valent iron species was then tested against five environmentally important estrogenic hormones (estron (E1), 17-β-estradiol (E2), estriol (E3), 17-α-ethinylestradiol (EE2), and diethylstibestrol (DES)) in effluent water of a wastewater treatment plant. Three dosages of iron species (1, 10, and 100 mg L(-1)) were applied to the effluent water. An increase in the concentration of dosages enhanced the removal of estrogens. Both Fe(V) and Fe(VI) were effective in degrading estrogens, but Fe(IV) showed limited oxidation capacity to transform estrogens. The oxidized products of the estrogens were analyzed using Raman spectroscopy and high-performance liquid chromatography-mass spectrometry (HPLC-MS) techniques. Results demonstrated the transformation of estrogens into low molecular weight oxygenated compounds such as quinone-like and opened-aromatic ring species. A detailed study on E1 by using excess Fe(VI) showed the mineralization of the parent compound. The results demonstrate great potential of high-valent iron species in the degradation of endocrine disruptor chemicals like estrogens with several superior aspects including fast reactions, complete degradation and/or formation of benign organic species, and environmentally-acceptable iron oxide by-products.

  5. Welding and mechanical properties of cast FAPY (Fe-16 at. % Al-based) alloy slabs

    SciTech Connect

    Sikka, V.K.; Goodwin, G.M.; Alexander, D.J.; Howell, C.R.

    1995-08-01

    The low-aluminum-content iron-aluminum program deals with the development of a Fe-Al alloy with aluminum content such as a produce the minimum environmental effect at room temperature. The FAPY is an Fe-16 at. % Al-based alloy developed at the Oak Ridge National Laboratory as the highest aluminum-containing alloy with essentially no environmental effect. The chemical composition for FAPY in weight percent is: aluminum = 8.46, chromium = 5.50, zirconium = 0.20, carbon = 0.03, molybdenum = 2.00, yttrium = 0.10, and iron = 83.71. The cast ingots of the alloy can be hot worked by extrusion, forging, and rolling processes. The hot- worked cast structure can be cold worked with intermediate anneals at 800{degrees}C. Typical room-temperature ductility of the fine-grained wrought structure is 20 to 25% for this alloy. In contrast to the wrought structure, the cast ductility at room temperature is approximately 1% with a transition temperature of approximately 100 to 150{degrees}C, above which ductility values exceed 20%. The alloy has been melted and processed into bar, sheet, and foil. The alloy has also been cast into slabs, step-blocks of varying thicknesses, and shapes. The purpose of this section is to describe the welding response of cast slabs of three different thicknesses of FAPY alloy. Tensile, creep, and Charpy-impact data of the welded plates are also presented.

  6. Influence of Fe(2+)-catalysed iron oxide recrystallization on metal cycling.

    PubMed

    Latta, Drew E; Gorski, Christopher A; Scherer, Michelle M

    2012-12-01

    Recent work has indicated that iron (oxyhydr-)oxides are capable of structurally incorporating and releasing metals and nutrients as a result of Fe2+-induced iron oxide recrystallization. In the present paper, we briefly review the current literature examining the mechanisms by which iron oxides recrystallize and summarize how recrystallization affects metal incorporation and release. We also provide new experimental evidence for the Fe2+-induced release of structural manganese from manganese-doped goethite. Currently, the exact mechanism(s) for Fe2+-induced recrystallization remain elusive, although they are likely to be both oxide-and metal-dependent. We conclude by discussing some future research directions for Fe2+-catalysed iron oxide recrystallization.

  7. Concentration dependent structural parameters of liquid Al-Fe alloys

    NASA Astrophysics Data System (ADS)

    Lalnuntluanga, C.; Mishra, Raj Kumar

    2016-10-01

    Square well potential is perturbed over Lebowtiz solution of hard sphere mixtures to determine direct correlation function,C(0) ij(r) in repulsive and attractive regions under Mean Spherical Model Approximation [1]. Obtained direct correlation functions were employed to derive partial structure factors and then total structure factor, S(k) in liquid Al-Fe alloy at different atomic percent of Al. Fourier transform of partial and total structure factors gives partial and total radial distribution functions, g(r) from which partial and total coordination numbers and the partial nearest-neighbor distances were computed.

  8. Role of Fe and sign reversal of the Hall coefficient in quasicrystalline Al-Cu-Fe

    NASA Astrophysics Data System (ADS)

    Lindqvist, P.; Berger, C.; Klein, T.; Lanco, P.; Cyrot-Lackmann, F.; Calvayrac, Y.

    1993-07-01

    Electronic transport properties were measured for the stable icosahedral phase of Al-Cu-Fe for a large number of high-structural-quality samples of different compositions. At low temperature, the Hall coefficient RH and the conductivity σ are found to best correlate with the Fe content rather than with the electron per atom parameter which is usually used; RH changes sign at a concentration of 12.5 at. % Fe, where σ is at minimum. RH has a strong temperature dependence and can change sign with temperature. These features put the focus on the Fe d states and can be interpreted by a Hume-Rothery type of behavior including the sp-d hybridization effects.

  9. Iron bioavailability of common beans (Phaseolus vulgaris L.) intrinsically labeled with (59)Fe.

    PubMed

    Brigide, Priscila; Ataide, Terezinha da R; Canniatti-Brazaca, Solange G; Baptista, Antônio S; Abdalla, Adibe L; Filho, Virgílio F Nascimento; Piedade, Sônia M S; Bueno, Nassib B; Sant'Ana, Antônio E G

    2014-07-01

    A radiobioassay was performed in rats with or without iron depletion to evaluate the iron bioavailability of diets enriched with common beans and with "multimixture", a nutritional supplement based on parts of foods that are not usually eaten. The full-body (59)Fe level was determined after 5h, the absorbed (59)Fe level was determined after 48 h, and the amount of (59)Fe retained was determined after 7 days. Iron bioavailability was assessed by the full-body radioactivity of the animals, determined using a solid scintillation detector. The iron bioavailability of common beans was higher in the iron-depleted animals (55.7%) than in the non-depleted animals (25.12%) because of the higher absorption rate in the iron-depleted animals. The multimixture did not influence dietary iron bioavailability. In addition, the iron bioavailability of common beans was similar to that observed in the standard source of iron for Wistar rats. Hence, common beans may be considered an adequate dietary iron source because of its high bioavailability.

  10. Comment on “Isotopic fractionation between Fe(III) and Fe(II) in aqueous solutions” by Clark Johnson et al., [Earth Planet. Sci. Lett. 195 (2002) 141–153

    USGS Publications Warehouse

    Bullen, Thomas D.; White, Arthur F.; Childs, Cyril W.

    2003-01-01

    In a recent contribution [1], Johnson et al. reported the equilibrium isotope fractionation factor between dissolved Fe(II) and Fe(III) in aqueous solutions at pH=2.5 and 5.5. They suggest that because the iron isotope fractionation observed in their experiments spans virtually the entire range observed in sedimentary rocks, Fe(II)–Fe(III) aqueous speciation may play a major role in determining iron isotope variations in nature where Fe(II) and Fe(III) can become physically separated. They discounted earlier conclusions by us and others [2] ;  [3] that significant equilibrium fractionation between specific coexisting Fe(II)- or Fe(III)-aqueous complexes (e.g., between aqueous Fe(II)(OH)x(aq)and Fe(II)(aq) ion) is capable of producing iron isotope contrasts that can be preserved in nature. This is an important contribution not only because the authors recognize the importance of abiotic equilibrium iron isotope fractionation in nature in contrast to previous assertions [4], but also because it will help to focus discussion on the development and evaluation of experimental approaches that can reveal abiotic fractionation mechanisms. However, in this Comment we propose that the experiments presented in this paper cannot be interpreted as straightforwardly as Johnson et al. contend. In particular, we show that in one of their critical experiments attainment of either isotope mass balance or equilibrium was not demonstrated, and thus the results of that experiment cannot be used to calculate an Fe(II)–Fe(III) equilibrium fractionation factor.

  11. Towards a Superplastic Forming of Fe-Mn-Al Alloys

    SciTech Connect

    Guanabara, Paulo Jr.; Bueno, Levi de O.; Ferreira Batalha, Gilmar

    2011-01-17

    The aim is to study the characteristics of superplasticity, mostly on non qualified materials, such as austenitic steel of the Fe-Mn-Al alloy, which has some of the specific material parameters closely related to microstructural mechanisms. These parameters are used as indicators of material superplastic potentiality. The material was submitted to hot tensile testing, within a temperature range from 600 deg. C to 1000 deg. C and strain-rates varying from 10{sup -6} to 1 s{sup -1}. The strain rate sensitivity parameter (m) and observed maximum elongation until rupture ({epsilon}{sub r}) could be determined and also obtained from the hot tensile test. The experiments stated a possibility of superplastic behaviour in a Fe-Mn-Al alloy within a temperature range from 700 deg. C to 900 deg. C with grain size around 3 {mu}m (ASTM grain size 12) and average strain rate sensitivity of m {approx} 0.54, as well as a maximum elongation at rupture around 600%. The results are based on a more enhanced research from the authors; however, this paper has focused just on the hot tensile test, as further creep tests results are not available herein. There are rare examples of superplasticity study of an austenitic steel Fe-Mn-Al alloy, thus this work showed some possibility of exploring the potential use of such materials in this regime at temperatures {>=}700 deg. C.

  12. Yield stress anomaly in B2 FeAl

    SciTech Connect

    Yoshimi, K.; Hanada, S.; Yoo, M.H.

    1996-12-31

    The studies on yield stress anomaly of B2 FeAl single crystals are reviewed in this paper. A positive temperature dependence of yield stress, so-called yield stress anomaly, is observed in B2 FeAl in which excess vacancies are fully annealed out. Associated with the anomaly, characteristic asymmetry is found between tension and compression. While the strain-rate sensitivity is almost zero in the temperature range of the yield stress anomaly, the stress relaxation becomes significant with increasing temperature, indicating that a recovery process is thermally activated. It is ascertained by the two-surface trace analysis that slip transition from <111> direction at intermediate temperature to <100> at high temperature occurs around the peak temperature. Even at the peak temperature, in addition, operative slip vector for yielding is confirmed to be predominantly <111> by TEM. Also, it is observed that <111>-type superdislocations are frequently climb-dissociated in the temperature range of the anomaly. APB formation on {l_brace}111{r_brace} plane is energetically favorable, which is in agreement with the Flinn`s calculation for the B2 superlattice that APB energy on {l_brace}111{r_brace} plane is lower than that on {l_brace}110{r_brace} plane. Such an anisotropy of APB energy would offer specific driving force for the climb dissociation on <111> superdislocations. On the basis of the observed results, the anomalous strengthening behavior of B2 FeAl single crystals is discussed.

  13. Melting and casting of FeAl-based cast alloy

    SciTech Connect

    Sikka, V.K.; Wilkening, D.; Liebetrau, J.; Mackey, B.

    1998-11-01

    The FeAl-based intermetallic alloys are of great interest because of their low density, low raw material cost, and excellent resistance to high-temperature oxidation, sulfidation, carburization, and molten salts. The applications based on these unique properties of FeAl require methods to melt and cast these alloys into complex-shaped castings and centrifugal cast tubes. This paper addresses the melting-related issues and the effect of chemistry on the microstructure and hardness of castings. It is concluded that the use of the Exo-Melt{trademark} process for melting and the proper selection of the aluminum melt stock can result in porosity-free castings. The FeAl alloys can be melted and cast from the virgin and revert stock. A large variation in carbon content of the alloys is possible before the precipitation of graphite flakes occurs. Titanium is a very potent addition to refine the grain size of castings. A range of complex sand castings and two different sizes of centrifugal cast tubes of the alloy have already been cast.

  14. Zeta-Fe2O3 - A new stable polymorph in iron(III) oxide family

    NASA Astrophysics Data System (ADS)

    Tuček, Jiří; Machala, Libor; Ono, Shigeaki; Namai, Asuka; Yoshikiyo, Marie; Imoto, Kenta; Tokoro, Hiroko; Ohkoshi, Shin-Ichi; Zbořil, Radek

    2015-10-01

    Iron(III) oxide shows a polymorphism, characteristic of existence of phases with the same chemical composition but distinct crystal structures and, hence, physical properties. Four crystalline phases of iron(III) oxide have previously been identified: α-Fe2O3 (hematite), β-Fe2O3, γ-Fe2O3 (maghemite), and ɛ-Fe2O3. All four iron(III) oxide phases easily undergo various phase transformations in response to heating or pressure treatment, usually forming hexagonal α-Fe2O3, which is the most thermodynamically stable Fe2O3 polymorph under ambient conditions. Here, from synchrotron X-ray diffraction experiments, we report the formation of a new iron(III) oxide polymorph that we have termed ζ-Fe2O3 and which evolved during pressure treatment of cubic β-Fe2O3 ( space group) at pressures above 30 GPa. Importantly, ζ-Fe2O3 is maintained after pressure release and represents the first monoclinic Fe2O3 polymorph (I2/a space group) that is stable at atmospheric pressure and room temperature. ζ-Fe2O3 behaves as an antiferromagnet with a Néel transition temperature of ~69 K. The complex mechanism of pressure-induced transformation of β-Fe2O3, involving also the formation of Rh2O3-II-type Fe2O3 and post-perovskite-Fe2O3 structure, is suggested and discussed with respect to a bimodal size distribution of precursor nanoparticles.

  15. Preparation and Pore Structure Stability at High Temperature of Porous Fe-Al Intermetallics

    NASA Astrophysics Data System (ADS)

    Shen, P. Z.; Gao, H. Y.; Song, M.; He, Y. H.

    2013-12-01

    Porous Fe-Al intermetallics with different nominal compositions (from Fe-8 wt.% Al to Fe-50 wt.% Al) were fabricated by Fe and Al elemental powders through reaction synthesis. The effects of the Al content on the pore structure properties, and the comparison of pore structure stabilities at high-temperatures among the porous Fe-Al intermetallics and porous Ti, Ni, 316L stainless steel samples, were systematically studied. Results showed that the open porosity, maximum pore size, and permeability vary with the Al content. Porous Fe-(25-30 wt.%) Al intermetallics show good shape controllability and excellent pore structure stability at 1073 K in air, which suggests that these porous Fe-Al intermetallics could be used for filtration at high temperatures.

  16. Al-26 and Be-10 production in iron meteorites

    NASA Technical Reports Server (NTRS)

    Aylmer, D.; Bonanno, V.; Herzog, G. F.; Weber, H.; Klein, J.

    1988-01-01

    To compare the Al-26/Ne-21 ages with K-40/K-41 ages, the contents of Al-26 were determined in seven iron meteorites using accelerator mass spectrometry and the light noble gas contents were determined using conventional mass spectrometry, for samples for which these values were not available. In addition, contents of Be-10 were measured. Due to the presence of boron in the samples, the values of Al-26 were found to be at least 30 percent lower than the literature values obtained by low-level counting techniques, while the Be-10 values were 10-15 percent lower. The production rates of these nuclides at different He-4/Ne-21 ratios were estimated, showing that the increase in He-4/Ne-21 ratios corresponded with decreases in Al-26 and Be-10. It was shown that the exposure ages calculated from the Ne-21/Al-26 ratio cannot be calibrated so as to agree with both the K-40/K-41 ages and ages based on the shorter-lived nuclides Ar-39 and Cl-36.

  17. The 57Fe hyperfine interactions in human liver ferritin and its iron-polymaltose analogues: the heterogeneous iron core model

    NASA Astrophysics Data System (ADS)

    Oshtrakh, M. I.; Alenkina, I. V.; Semionkin, V. A.

    2016-12-01

    Human liver ferritin and its iron-polymaltose pharmaceutical analogues Ferrum Lek, Maltofer® and Ferrifol® were studied using Mössbauer spectroscopy at 295 and 90 K. The Mössbauer spectra were fitted on the basis of a new model of heterogeneous iron core structure using five quadrupole doublets. These components were related to the corresponding more or less close-packed iron core layers/regions demonstrating some variations in the 57Fe hyperfine parameters for the studied samples.

  18. Reduction Kinetics of Electric Arc Furnace Oxidizing Slag by Al-Fe Alloy

    NASA Astrophysics Data System (ADS)

    Lee, Jaehong; Oh, Joon Seok; Lee, Joonho

    2016-09-01

    Effects of temperature and slag basicity on the reduction rate of iron oxide in molten synthetic electric arc furnace oxidizing slag by Al-40 wt.%Fe alloy was investigated. An alloy sample was dropped into molten slag in an MgO crucible. When the initial slag temperature was 1723 K, there was no reduction. However, when the initial slag temperature was 1773 K and the slag basicity was 1.1, the reduction was initiated and the temperature of the slag rapidly increased. When the slag basicity was 1.1, increasing the initial slag temperature from 1773 K to 1823 K increases the reaction rate. As the slag basicity increased from 1.1 to 1.4 at 1773 K, the reaction rate increased. From SEM analysis, it was found that an Al2O3 or a spinel phase at the slag-metal interface inhibited the reaction at a lower temperature and a lower slag basicity.

  19. First principles investigation of Fe and Al bearing phase H

    NASA Astrophysics Data System (ADS)

    Tsuchiya, J.; Tsuchiya, T.

    2015-12-01

    The global circulation of water in the earth is important to investigate the evolution history and dynamics of the earth, since the physical properties (e.g. atomic diffusivity, melting temperature, electrical conductivity and seismic velocities) of the constituent minerals are considerably changed by the presence of water. It has been believed that water is carried into the deep Earth's interior by hydrous minerals such as the dense hydrous magnesium silicates (DHMSs) which are also known as alphabet phases (phase A, superhydrous phase B, and phase D etc.) in the descending cold plate. It has been thought that the relay of these hydrous phases was terminated at ~1200 km depth by the dehydration of phase D which was the highest pressure phase of DHMSs. Recently, we have theoretically predicted the high pressure phase of phase D and experimentally confirmed the existence of this new DHMS in lower mantle pressure conditions above ~45 GPa. This phase has MgSiO4H2chemical composition and named as phase H. At the lower mantle pressure conditions, Al and H-bearing SiO2, δ-AlOOH, ɛ-FeOOH and phase H may be the relevant hydrous phases in the subducting slabs. Interestingly, the crystal structure of these hydrous phases are almost same and have CaCl2type structure. This suggests that these hydrous phases may potentially be able to make the wide range of solid solution. Some experimental studies already reported that Al preferentially partitioned into phase H and the stability of phase H drastically increased by incorporation of Al (Nishi et al. 2014, Ohira et al. 2014). The density of subducted MORB is reported to be denser than that of pyrolite in the lower mantle (e.g. Kawai et al. 2009). Therefore, there is a possibility that phase H containing Al and Fe in subducted MORB survive down to the bottom of lower mantle and the melting of phase H at the core mantle boundary may contribute to the cause of ultra-low velocity zones. In this study, we further extends our

  20. Al-Ca and Al-Fe metal-metal composite strength, conductivity, and microstructure relationships

    SciTech Connect

    Kim, Hyong June

    2011-01-01

    Deformation processed metal-metal composites (DMMC’s) are composites formed by mechanical working (i.e., rolling, swaging, or wire drawing) of two-phase, ductile metal mixtures. Since both the matrix and reinforcing phase are ductile metals, the composites can be heavily deformed to reduce the thickness and spacing of the two phases. Recent studies have shown that heavily drawn DMMCs can achieve anomalously high strength and outstanding combinations of strength and conductivity. In this study, Al-Fe wire composite with 0.07, 0.1, and 0.2 volume fractions of Fe filaments and Al-Ca wire composite with 0.03, 0.06, and 0.09 volume fractions of Ca filaments were produced in situ, and their mechanical properties were measured as a function of deformation true strain. The Al-Fe composites displayed limited deformation of the Fe phase even at high true strains, resulting in little strengthening effect in those composites. Al-9vol%Ca wire was deformed to a deformation true strain of 13.76. The resulting Ca second-phase filaments were deformed to thicknesses on the order of one micrometer. The ultimate tensile strength increased exponentially with increasing deformation true strain, reaching a value of 197 MPa at a true strain of 13.76. This value is 2.5 times higher than the value predicted by the rule of mixtures. A quantitative relationship between UTS and deformation true strain was determined. X-ray diffraction data on transformation of Al + Ca microstructures to Al + various Al-Ca intermetallic compounds were obtained at the Advanced Photon Source at Argonne National Laboratory. Electrical conductivity was measured over a range of true strains and post-deformation heat treatment schedules.

  1. Toxicity of chelated iron (Fe-DTPA) in American cranberry

    Technology Transfer Automated Retrieval System (TEKTRAN)

    American cranberry (Vaccinium macrocarpon) is naturally adapted to environments with high concentrations of soluble iron. Yet, there is a need to further explore iron nutrition in cranberry given concerns of toxicity problems from irrigation with iron-rich water. This study investigated the threat o...

  2. Metal transports and enrichments in iron depositions hosted in basaltic rocks. II: Metal rich fluids and Fe origin

    NASA Astrophysics Data System (ADS)

    Zhang, Ronghua; Zhang, Xuetong; Hu, Shumin

    2015-12-01

    This study focuses on revealing the mechanism of metal transport, enrichment and Fe origin of iron deposition during water basalt interactions occurred in basaltic rocks. Observations of the iron deposits (anhydrite-magnetite-pyroxene type deposits) hosted in K-rich basaltic rocks in the Mesozoic volcanic area of the Middle-Lower Yangtze River valley, China, indicate that the mechanism of metal transport and enrichment for those deposits are significant objective to scientists, and the Fe origin problem is not well resolved. Here the metal transport, enrichment and iron origin have been investigated in high temperature experiments of water basaltic interactions. These deposits were accompanying a wide zone with metal alteration. The effects of hydrothermal alteration on major rock-forming element concentrations in basaltic rock were investigated by systematically comparing the chemical compositions of altered rocks with those of fresh rocks. In the deposits, these metals are distributed throughout altered rocks that exhibit vertical zoning from the deeper to the shallow. Then, combined with the investigations of the metal-alterations, we performed kinetic experiments of water-basaltic rock interactions using flow-through reactors in open systems at temperatures from 20 °C to 550 °C, 23-34 MPa. Release rates for the rock-forming elements from the rocks have been measured. Experiments provide the release rates for various elements at a large temperature range, and indicate that the dissolution rates (release rates) for various elements vary with temperature. Si, Al, and K have high release rates at temperatures from 300 °C to 500 °C; the maximum release rates (RMX) for Si are reached at temperatures from 300 °C to 400 °C. The RMXs for Ca, Mg, and Fe are at low temperatures from 20 °C to 300 °C. Results demonstrate that Fe is not released from 400 °C to 550 °C, and indicate that when deep circling fluids passed through basaltic rocks, Fe was not mobile, and

  3. Inhibition of trace element release during Fe(II)-activated recrystallization of Al-, Cr-, and Sn-substituted goethite and hematite.

    PubMed

    Frierdich, Andrew J; Scherer, Michelle M; Bachman, Jonathan E; Engelhard, Mark H; Rapponotti, Brett W; Catalano, Jeffrey G

    2012-09-18

    Aqueous Fe(II) reacts with Fe(III) oxides by coupled electron transfer and atom exchange (ETAE) resulting in mineral recrystallization, contaminant reduction, and trace element cycling. Previous studies of Fe(II)-Fe(III) ETAE have explored the reactivity of either pure iron oxide phases or those containing small quantities of soluble trace elements. Naturally occurring iron oxides, however, contain substantial quantities of insoluble impurities (e.g., Al) which are known to affect the chemical properties of such minerals. Here we explore the effect of Al(III), Cr(III), and Sn(IV) substitution (1-8 mol %) on trace element release from Ni(II)-substituted goethite and Zn(II)-substituted hematite during reaction with aqueous Fe(II). Fe(II)-activated trace element release is substantially inhibited from both minerals when an insoluble element is cosubstituted into the structure, and the total amount of release decreases exponentially with increasing cosubstituent. The limited changes in surface composition that occur following reaction with Fe(II) indicate that Al, Cr, and Sn do not exsolve from the structure and that Ni and Zn released to solution originate primarily from the bulk rather than the particle exterior (upper ~3 nm). Incorporation of Al into goethite substantially decreases the amount of iron atom exchange with aqueous Fe(II) and, consequently, the amount of Ni release from the structure. This implies that trace element release inhibition caused by substituting insoluble elements results from a decrease in the amount of mineral recrystallization. These results suggest that naturally occurring iron oxides containing insoluble elements are less susceptible to Fe(II)-activated recrystallization and exhibit a greater retention of trace elements and contaminants than pure mineral phases.

  4. Inhibition of trace element release during Fe(II)-activated recrystallization of Al-, Cr-, and Sn-substituted goethite and hematite

    SciTech Connect

    Frierdich, Andrew J.; Scherer, M.; Bachman, Jonathan E.; Engelhard, Mark H.; Rapponotti, Brett W.; Catalano, Jeffrey G.

    2012-09-18

    Aqueous Fe(II) reacts with Fe(III) oxides by coupled electron transfer and atom exchange (ETAE) resulting in mineral recrystallization, contaminant reduction, and trace element cycling. Previous studies of Fe(II)-Fe(III) ETAE have explored the reactivity of either pure iron oxide phases or those containing small quantities of soluble trace elements. Naturally occurring iron oxides, however, contain substantial quantities of insoluble impurities (e.g., Al) which are known to affect the chemical properties of such minerals. Here we explore the effect of Al(III), Cr(III), and Sn(IV) substitution on trace element release from Ni(II)-substituted goethite and Zn(II)-substituted hematite during reaction with aqueous Fe(II). Fe(II)-activated trace element release is substantially inhibited from both minerals when an insoluble element is co-substituted into the structure, and the total amount of release decreases exponentially with increasing co substituent. The limited changes in surface composition that occur following reaction with Fe(II) indicate that Al, Cr, and Sn do not exsolve from the structure and that Ni and Zn released to solution originate primarily from the bulk rather than the particle exterior (upper ~3 nm). Incorporation of Al into goethite substantially decreases the amount of iron atom exchange with aqueous Fe(II) and, consequently, the amount of Ni release from the structure. This implies that trace element release inhibition caused by substituting insoluble elements results from a decrease in the amount of mineral recrystallization. These results suggest that naturally occurring iron oxides containing insoluble elements are less susceptible to Fe(II)-activated recrystallization and exhibit a greater retention of trace elements and contaminants than pure mineral phases.

  5. Identification of an incommensurate FeAl{sub 2} overlayer on FeAl(110) using x-ray diffraction and reflectivity

    SciTech Connect

    Baddorf, A.P.; Chandavarkar, S.S.

    1995-06-30

    FeAl, like NiAl, crystallizes in the CsCl structure. Consequently the (110) planes contain equal amounts of Fe and Al distributed as interlocking rectangles. Unlike the NiAI(110) surface, which retains the (1{times}l) in-plane symmetry of the bulk, FeAl(l10) reconstructs to form an ordered, incommensurate overlayer. The reconstructed layer introduces x-ray diffraction rods at half-order positions along the [1{bar 1}0] direction, and displaced {plus_minus}0.2905 from integer positions along the [001] direction. Peak widths reveal excellent long range order. Specular reflectivity measurements above and below the Fe K{alpha} edge can be reproduced using a model containing a single reconstructed overlayer with an Fe:Al ratio of 1:2, consistent with FeA{sub I}2.

  6. Local structure study of Fe dopants in Ni-deficit Ni3Al alloys

    SciTech Connect

    V. N. Ivanovski; Umicevic, A.; Belosevic-Cavor, J.; Lei, Hechang; Li, Lijun; Cekic, B.; Koteski, V.; Petrovic, C.

    2015-08-24

    We found that the local electronic and magnetic structure, hyperfine interactions, and phase composition of polycrystalline Ni–deficient Ni 3-x FexAl (x = 0.18 and 0.36) were investigated by means of 57 Fe Mössbauer spectroscopy. The samples were characterized by X–ray diffraction and magnetization measurements. The ab initio calculations performed with the projector augmented wave method and the calculations of the energies of iron point defects were done to elucidate the electronic structure and site preference of Fe doped Ni 3 Al. Moreover, the value of calculated electric field gradient tensor Vzz=1.6 1021Vm-2 matches well with the results of Mössbauer spectroscopy and indicates that the Fe atoms occupy Ni sites.

  7. Response of pore water Al, Fe and S concentrations to waterlogging in a boreal acid sulphate soil.

    PubMed

    Virtanen, Seija; Simojoki, Asko; Hartikainen, Helinä; Yli-Halla, Markku

    2014-07-01

    Environmental hazards caused by acid sulphate (AS) soils are of worldwide concern. Among various mitigation measures, waterlogging has mainly been studied in subtropical and tropical conditions. To assess the environmental relevance of waterlogging as a mitigation option in boreal AS soils, we arranged a 2.5-year experiment with monolithic lysimeters to monitor changes in the soil redox potential, pH and the concentrations of aluminium (Al), iron (Fe) and sulphur (S) in pore water in response to low and high groundwater levels in four AS soil horizons. The monoliths consisted of acidic oxidized B horizons and a reduced C horizon containing sulphidic material. Eight lysimeters were cropped (reed canary grass, Phalaris arundinacea) and two were bare without a crop. Waterlogging was conducive to reduction reactions causing a slight rise in pH, a substantial increase in Fe (Fepw) and a decrease in Al (Alpw) in the pore water. The increase in Fepw was decisively higher in the cropped waterlogged lysimeters than in the bare ones, which was attributable to the microbiologically catalysed reductive dissolution of poorly ordered iron oxides and secondary minerals. In contrast to warmer climates, Fepw concentrations remained high throughout the experiment, indicating that the reduction was poised in the iron range, while sulphate was not reduced to sulphide. Therefore, the precipitation of iron sulphide was negligible in the environment with a low pH and abundant with poorly ordered Fe oxides. Increased Fe in pore water counteracts the positive effects of waterlogging, when water is flushed from fields to watercourses, where re-oxidation of Fe causes acidity and oxygen depletion. However, waterlogging prevented further oxidation of sulphidic materials and decreased Alpw to one-tenth of the initial concentrations, and even to one-hundredth of the levels in the low water table lysimeters.

  8. The Property of Phonon Gap in Iron-Based Superconductors FeSe, LiFeAs and SrFeAsF

    NASA Astrophysics Data System (ADS)

    Wang, Wei; Li, Bin; He, Junqi; Sun, Jiafa

    2017-03-01

    First-principles calculations are performed for iron-based superconductors FeSe, LiFeAs and SrFeAsF, and the reasons of generation and loss of the phonon gaps in them are analyzed by analogy with electronic energy band theory. In iron-based superconductors FeSe and LiFeAs, lattice vibrations are affected by so strong changes in the periodic potential that the phonon spectra open a full gap. After considering electron-spin interactions, the enhancement of the periodic potential results in a broadening of the gap. From binary FeSe to ternary LiFeAs to quaternary SrFeAsF, the full phonon gap undergoes the process from decrease to disappearance, which is closely related to the frequencies overlapping of different atoms by vibrations. The fewer the material components and the larger the atomic number ratio, the more possible the production of the full phonon gap or the appearance of wider gap. In addition, the phonon gaps of FeSe and LiFeAs locate around the frequency of 10^{12} Hz, whose filtering properties for elastic waves are hopefully to be applied in quantum acoustics.

  9. Decomposition of Al2.7Fe0.3Ti in heated Al-Al2.7Fe0.3Ti refiner fabricated by spark plasma sintering and its refining performance

    NASA Astrophysics Data System (ADS)

    Watanabe, Yoshimi; Hamada, Takayuki; Sato, Hisashi

    2017-01-01

    In our previous study, a novel Al-L12-type Al2.7Fe0.3Ti refiner was fabricated by spark plasma sintering (SPS) and its refining performance was studied. It was found that L12-type Al2.7Fe0.3Ti particles can be favorable heterogeneous nucleation sites for Al casts, since the lattice matching between Al2.7Fe0.3Ti and Al is good. It was also found that the thermal stability of heterogeneous nucleation sites affects the grain-refining performance. In this study, the decomposition phenomena of the Al2.7Fe0.3Ti phase in a refiner are studied by heating an Al-Al2.7Fe0.3Ti refiner fabricated by SPS. In addition, the refining performance of a heated Al-Al2.7Fe0.3Ti refiner is investigated.

  10. Enhanced Cr(VI) removal from groundwater by Fe(0)-H2O system with bio-amended iron corrosion.

    PubMed

    Yin, Weizhao; Li, Yongtao; Wu, Jinhua; Chen, Guocai; Jiang, Gangbiao; Li, Ping; Gu, Jingjing; Liang, Hao; Liu, Chuansheng

    2017-02-27

    A one-pot bio-iron system was established to investigate synergetic abiotic and biotic effects between iron and microorganisms on Cr(VI) removal. More diverse iron corrosion and reactive solids, such as green rusts, lepidocrocite and magnetite were found in the bio-iron system than in the Fe(0)-H2O system, leading to 4.3 times higher Cr(VI) removal efficiency in the bio-iron system than in the Fe(0)-H2O system. The cycling experiment also showed that the Cr(VI) removal capacity of Fe(0) in the bio-iron system was 12.4 times higher than that in the Fe(0)-H2O system. A 62days of life-span could be achieved in the bio-iron system, while the Fe(0)-H2O system lost its efficacy after 30days. Enhanced effects of extra Fe(2+) on Cr(VI) removal was observed, largely contributed to the adsorbed Fe(2+) on iron surface, which could function as an extra reductant for Cr(VI) and promote the electron transfer on the solid phase. The results also showed that the reduction of Cr(VI) by microorganisms was insignificant, indicating the adsorption/co-precipitation of Cr by iron oxides on iron surface was responsible for the overall Cr(VI) removal. Our study demonstrated that the bio-amended iron corrosion could improve the performance of Fe(0) for Cr(VI) removal from groundwater.

  11. Crystallographic and magnetic properties of the hyperthermia material CoFe2O4@AlFe2O4

    NASA Astrophysics Data System (ADS)

    Choi, Hyunkyung; An, Mijeong; Eom, Wonyoung; Lim, Sae Wool; Shim, In-Bo; Kim, Chul Sung; Kim, Sam Jin

    2017-01-01

    Hard/soft CoFe2O4@AlFe2O4 core/shell nanoparticles were prepared by using a high temperature thermal decomposition method with seed-mediated growth. The structural, magnetic and thermal properties of the nanoparticles were investigated by using X-ray diffraction, vibrating sample magnetometer, MagneTherm, and Mössbauer spectroscopy. The crystal structure of nanoparticles was determined to be cubic spinel ferrite with space group Fd-3m. The CoFe2O4 nanoparticles were found to show high magnetization and coercivity while AlFe2O4 nanoparticles were found to show low magnetization and coercivity. The CoFe2O4@AlFe2O4 core/shell nanoparticles showed intermediate values of magnetization and the coercivity between those of CoFe2O4 and AlFe2O4. Also, the blocking temperature ( T B ) of the nanoparticles (NPs) was observed to be 280, 50, and 225 K for CoFe2O4, AlFe2O4 and CoFe2O4@AlFe2O4, respectively. The core/shell ferrite shows a T B near 225 K, associated with the harder CoFe2O4 NPs. Temperatures below 225 K, the zero-field-cooled curves show changes in their slopes at a temperature near 50 K, corresponding to the second blocking temperature associated with the softer AlFe2O4 NPs.

  12. Discovery of the recoverable high-pressure iron oxide Fe4O5.

    PubMed

    Lavina, Barbara; Dera, Przemyslaw; Kim, Eunja; Meng, Yue; Downs, Robert T; Weck, Philippe F; Sutton, Stephen R; Zhao, Yusheng

    2011-10-18

    Phases of the iron-oxygen binary system are significant to most scientific disciplines, directly affecting planetary evolution, life, and technology. Iron oxides have unique electronic properties and strongly interact with the environment, particularly through redox reactions. The iron-oxygen phase diagram therefore has been among the most thoroughly investigated, yet it still holds striking findings. Here, we report the discovery of an iron oxide with formula Fe(4)O(5), synthesized at high pressure and temperature. The previously undescribed phase, stable from 5 to at least 30 GPa, is recoverable to ambient conditions. First-principles calculations confirm that the iron oxide here described is energetically more stable than FeO + Fe(3)O(4) at pressure greater than 10 GPa. The calculated lattice constants, equation of states, and atomic coordinates are in excellent agreement with experimental data, confirming the synthesis of Fe(4)O(5). Given the conditions of stability and its composition, Fe(4)O(5) is a plausible accessory mineral of the Earth's upper mantle. The phase has strong ferrimagnetic character comparable to magnetite. The ability to synthesize the material at accessible conditions and recover it at ambient conditions, along with its physical properties, suggests a potential interest in Fe(4)O(5) for technological applications.

  13. In situ measurement of ferric iron in lunar glass beads using Fe-XAS

    NASA Astrophysics Data System (ADS)

    McCanta, Molly C.; Dyar, M. Darby; Rutherford, Malcolm J.; Lanzirotti, Antonio; Sutton, Stephen R.; Thomson, Bradley J.

    2017-03-01

    Through use of a new X-ray Absorption Spectroscopy (XAS) calibration for Fe3+ analysis in silicate glasses, the first direct measurements of ferric iron in natural lunar picritic glasses are presented. Lunar glass beads from the Apollo sample collection contain up to 60.0% Fe3+. No correlation with melt chemical properties, such as Mg# or weight % TiO2, or physical properties, such as bead diameter, was observed. Fe3+/ΣFe is negatively correlated with NBO/T. These elevated Fe3+/ΣFe values reflect eruption and post-eruption oxidation due to magmatic degassing of H or OH. Glass beads observed to be zoned to lower Fe3+/ΣFe rims may represent a subsequent reduction in the lunar vacuum prior to cooling through the glass transition temperature.

  14. Chemical mixing at “Al on Fe” and “Fe on Al” interfaces

    SciTech Connect

    Süle, P.; Horváth, Z. E.; Kaptás, D.; Bujdosó, L.; Balogh, J.; Nakanishi, A.

    2015-10-07

    The chemical mixing at the “Al on Fe” and “Fe on Al” interfaces was studied by molecular dynamics simulations of the layer growth and by {sup 57}Fe Mössbauer spectroscopy. The concentration distribution along the layer growth direction was calculated for different crystallographic orientations, and atomically sharp “Al on Fe” interfaces were found when Al grows over (001) and (110) oriented Fe layers. The Al/Fe(111) interface is also narrow as compared to the intermixing found at the “Fe on Al” interfaces for any orientation. Conversion electron Mössbauer measurements of trilayers—Al/{sup 57}Fe/Al and Al/{sup 57}Fe/Ag grown simultaneously over Si(111) substrate by vacuum evaporation—support the results of the molecular dynamics calculations.

  15. Direct Observation of an Iron-Bound Terminal Hydride in [FeFe]-Hydrogenase by Nuclear Resonance Vibrational Spectroscopy.

    PubMed

    Reijerse, Edward J; Pham, Cindy C; Pelmenschikov, Vladimir; Gilbert-Wilson, Ryan; Adamska-Venkatesh, Agnieszka; Siebel, Judith F; Gee, Leland B; Yoda, Yoshitaka; Tamasaku, Kenji; Lubitz, Wolfgang; Rauchfuss, Thomas B; Cramer, Stephen P

    2017-03-29

    [FeFe]-hydrogenases catalyze the reversible reduction of protons to molecular hydrogen with extremely high efficiency. The active site ("H-cluster") consists of a [4Fe-4S]H cluster linked through a bridging cysteine to a [2Fe]H subsite coordinated by CN(-) and CO ligands featuring a dithiol-amine moiety that serves as proton shuttle between the protein proton channel and the catalytic distal iron site (Fed). Although there is broad consensus that an iron-bound terminal hydride species must occur in the catalytic mechanism, such a species has never been directly observed experimentally. Here, we present FTIR and nuclear resonance vibrational spectroscopy (NRVS) experiments in conjunction with density functional theory (DFT) calculations on an [FeFe]-hydrogenase variant lacking the amine proton shuttle which is stabilizing a putative hydride state. The NRVS spectra unequivocally show the bending modes of the terminal Fe-H species fully consistent with widely accepted models of the catalytic cycle.

  16. Competing redox reactions in Fe-containing AlO(OH) and Al2O3 matrices: A combined investigation by Mössbauer, ESR spectroscopy and thermal analysis

    NASA Astrophysics Data System (ADS)

    Stößer, R.; Menzel, M.; Feist, M.; Nofz, M.; Renz, F.

    2010-03-01

    The investigation of iron-doped AlO(OH)/Al2O3 systems revealed that the combined employment of Mössbauer and ESR spectroscopies together with thermal analysis yields meaningful data with complementary information. This mutual complementarity is based on the coexistence of Fe point defects with the corresponding aggregated FeOx species which has been observed even for very low Fe concentrations. Competing redox processes between the dopant, the AlOx matrix, and the gas atmosphere during the thermal treatment enable the generation of solid phases exhibiting specific chemical properties. The entire reaction process is influenced by a specific mechanical and thermal pre-treatment that affects predominantly oxydative processes in the matrix. A protecting influence of the matrix preventing further reductive attack of the Fe3+ Fe2+ ions by hydrogen has been established.

  17. Magnetic properties of ball milled Fe-40Al at.% alloys

    SciTech Connect

    Amils, X.; Nogues, J.; Surinach, S.; Baro, M.D.; Munoz, J.S.

    1998-07-01

    A direct correlation between the lattice parameter and the saturation magnetization, during the disordering (ball milling) and posterior reordering (annealing) processes, has been found in Fe-40Al At.% compounds. These results indicate that the paramagnetic-ferromagnetic-paramagnetic transitions induced by ball milling and subsequent annealing could be related to the changes in volume, and not only to nearest neighbors effects as is commonly assumed. Moreover, these alloys have been found to become spin glass at low temperatures, independently of their structural state (ordered or disordered).

  18. MOKE Study of Fe/Co/Al Multilayers

    SciTech Connect

    Jani, Snehal; Lakshmi, N.; Venugopalan, K.; Rajput, Parasmani; Zajaoc, M.; Rueffer, R.; Reddy, V. R.; Gupta, Ajay

    2011-07-15

    The multilayer system (MLS)-[{sup 57}Fe{sub 25}A/Co{sub 11}A/Al{sub 17}A]x20 has been deposited by Ion beam sputtering (IBS) technique. The MLS has been annealed at 700 deg. C for 1 h. Overall composition of as deposited and annealed MLS have been characterized by EDX and magnetic properties have been studied through angular dependent magneto optic Kerr effect (MOKE) hysteresis curves. The study shows that the as-deposited MLS has excellent soft magnetic properties coupled with perpendicular magnetic isotropy which is destroyed on annealing.

  19. Electronic structure in a one-Fe Brillouin zone of the iron pnictide superconductors CsFe2As2 and RbFe2As2

    NASA Astrophysics Data System (ADS)

    Kong, S.; Liu, D. Y.; Cui, S. T.; Ju, S. L.; Wang, A. F.; Luo, X. G.; Zou, L. J.; Chen, X. H.; Zhang, G. B.; Sun, Z.

    2015-11-01

    Using angle-resolved photoemission spectroscopy, we studied the electronic structures of CsFe2As2 and RbFe2As2 . Contrary to other iron-based superconductors where the band structures are usually depicted in the two-Fe Brillouin zone (BZ), we found that the distribution of electronic spectral weight in CsFe2As2 and RbFe2As2 follows the one-Fe BZ, and that the emerging band structure is qualitatively consistent with theoretical band calculations of the one-Fe BZ except for some shadow band effect. Our data suggest that the interlayer separation is an important tuning factor for the physics of FeAs layers, the increase of which can reduce the coupling between Fe and As and lead to the emergence of the electronic structure in accord with the one-Fe symmetry of the Fe square lattice. Our finding puts strong constraints on the theoretical models constructed on the basis of the one-Fe BZ.

  20. Cyclic Oxidation of FeCrAlY/Al2O3 Composites

    NASA Technical Reports Server (NTRS)

    Nesbitt, James A.; Draper, Susan L.; Barrett, Charles A.

    1999-01-01

    Three-ply FeCrAlY/Al2O3 composites and FeCrAlY matrix-only samples were cyclically oxidized at 1000 C and 1100 C for up to 1000 1-hr cycles. Fiber ends were exposed at the ends of the composite samples. Following cyclic oxidation, cracks running parallel to and perpendicular to the fibers were observed on the large surface of the composite. In addition, there was evidence of increased scale damage and spallation around the exposed fiber ends, particularly around the middle ply fibers. This damage was more pronounced at the higher temperature. The exposed fiber ends showed cracking between fibers in the outer plies, occasionally with Fe and Cr-rich oxides growing out of the cracks. Large gaps developed at the fiber/matrix interface around many of the fibers, especially those in the outer plies. Oxygen penetrated many of these gaps resulting in significant oxide formation at the fiber/matrix interface far within the composite sample. Around several fibers, the matrix was also internally oxidized showing Al2O3 precipitates in a radial band around the fibers. The results show that these composites have poor cyclic oxidation resistance due to the CTE mismatch and inadequate fiber/matrix bond strength at temperatures of 1000 C and above.

  1. Development and property evaluation of nuclear grade wrought FeCrAl fuel cladding for light water reactors

    NASA Astrophysics Data System (ADS)

    Yamamoto, Y.; Pint, B. A.; Terrani, K. A.; Field, K. G.; Yang, Y.; Snead, L. L.

    2015-12-01

    Development of nuclear grade, iron-based wrought FeCrAl alloys has been initiated for light water reactor (LWR) fuel cladding to serve as a substitute for zirconium-based alloys with enhanced accident tolerance. Ferritic alloys with sufficient chromium and aluminum additions can exhibit significantly improved oxidation kinetics in high-temperature steam environments when compared to zirconium-based alloys. In the first phase, a set of model FeCrAl alloys containing 10-20Cr, 3-5Al, and 0-0.12Y in weight percent, were prepared by conventional arc-melting and hot-working processes to explore the effect of composition on the properties of FeCrAlY alloys. It was found that the tensile properties were insensitive to the alloy compositions studied; however, the steam oxidation resistance strongly depended on both the chromium and the aluminum contents. The second phase development focused on strengthening Fe-13Cr-5Al with minor alloying additions of molybdenum, niobium, and silicon. Combined with an optimized thermo-mechanical treatment, a thermally stable microstructure was produced with improved tensile properties at temperatures up to 741 °C.

  2. Development and property evaluation of nuclear grade wrought FeCrAl fuel cladding for light water reactors

    DOE PAGES

    Yamamoto, Yukinori; Pint, Bruce A.; Terrani, Kurt A.; ...

    2015-10-19

    Development of nuclear grade, iron-based wrought FeCrAl alloys has been initiated for light water reactor (LWR) fuel cladding to serve as a substitute for zirconium-based alloys with enhanced accident tolerance. Ferritic alloys with sufficient chromium and aluminum additions can exhibit significantly improved oxidation kinetics in high-temperature steam environments when compared to zirconium-based alloys. In the first phase, a set of model FeCrAl alloys containing 10–20Cr, 3–5Al, and 0–0.12Y in weight percent, were prepared by conventional arc-melting and hot-working processes to explore the effect of composition on the properties of FeCrAlY alloys. It was found that the tensile properties were insensitivemore » to the alloy compositions studied; however, the steam oxidation resistance strongly depended on both the chromium and the aluminum contents. The second phase development focused on strengthening Fe-13Cr-5Al with minor alloying additions of molybdenum, niobium, and silicon. Combined with an optimized thermo-mechanical treatment, a thermally stable microstructure was produced with improved tensile properties at temperatures up to 741°C.« less

  3. Development and property evaluation of nuclear grade wrought FeCrAl fuel cladding for light water reactors

    SciTech Connect

    Yamamoto, Yukinori; Pint, Bruce A.; Terrani, Kurt A.; Field, Kevin G.; Yang, Ying; Snead, Lance Lewis

    2015-10-19

    Development of nuclear grade, iron-based wrought FeCrAl alloys has been initiated for light water reactor (LWR) fuel cladding to serve as a substitute for zirconium-based alloys with enhanced accident tolerance. Ferritic alloys with sufficient chromium and aluminum additions can exhibit significantly improved oxidation kinetics in high-temperature steam environments when compared to zirconium-based alloys. In the first phase, a set of model FeCrAl alloys containing 10–20Cr, 3–5Al, and 0–0.12Y in weight percent, were prepared by conventional arc-melting and hot-working processes to explore the effect of composition on the properties of FeCrAlY alloys. It was found that the tensile properties were insensitive to the alloy compositions studied; however, the steam oxidation resistance strongly depended on both the chromium and the aluminum contents. The second phase development focused on strengthening Fe-13Cr-5Al with minor alloying additions of molybdenum, niobium, and silicon. Combined with an optimized thermo-mechanical treatment, a thermally stable microstructure was produced with improved tensile properties at temperatures up to 741°C.

  4. Phase Separation kinetics in an Fe-Cr-Al alloy

    SciTech Connect

    Capdevila, C.; Miller, Michael K; Chao, J.

    2012-01-01

    The {alpha}-{alpha}{prime} phase separation kinetics in a commercial Fe-20 wt.% Cr-6 wt.% Al oxide dispersion-strengthened PM 2000{trademark} steel have been characterized with the complementary techniques atom probe tomography and thermoelectric power measurements during isothermal aging at 673, 708, and 748 K for times up to 3600 h. A progressive decrease in the Al content of the Cr-rich {alpha}{prime} phase was observed at 708 and 748 K with increasing time, but no partitioning was observed at 673 K. The variation in the volume fraction of the {alpha}{prime} phase well inside the coarsening regime, along with the Avrami exponent 1.2 and activation energy 264 kJ mol{sup -1}, obtained after fitting the experimental results to an Austin-Rickett type equation, indicates that phase separation in PM 2000{trademark} is a transient coarsening process with overlapping nucleation, growth, and coarsening stages.

  5. Phase relations of Fe3C and Fe7C3 up to 185 GPa and 5200 K: Implication for the stability of iron carbide in the Earth's core

    NASA Astrophysics Data System (ADS)

    Liu, Jin; Lin, Jung-Fu; Prakapenka, Vitali B.; Prescher, Clemens; Yoshino, Takashi

    2016-12-01

    We have investigated phase relations and melting behavior of Fe3C and Fe7C3 using X-ray diffraction in a laser-heated diamond cell up to 185 GPa and 5200 K. Our results show that the starting Fe3C sample decomposes into a mixture of solid orthorhombic Fe7C3 and hcp-Fe at above 145 GPa upon laser heating and then transforms into Fe-C liquid and solid Fe7C3 at temperatures above 3400 K. Using the intensity of the diffuse scattering as a primary criteria for detecting melting, the experimentally derived liquidus for a bulk composition of Fe3C fitted with the Simon-Glatzel equation is Tm(K) = 1800 × [1 + (Pm - 5.7)/15.10 ± 2.55]1/2.41 ± 0.17 at 24-185 GPa, which is 500 K higher than the melting curve of iron reported by Anzellini et al. (2013) at Earth's core pressures. The higher melting point and relative stability of Fe7C3 in Fe-rich Fe-C system at Earth's core conditions indicate that Fe7C3 could solidify out of the early Earth's molten core to become a constituent of the innermost inner core.

  6. [Determination of Total Iron and Fe2+ in Basalt].

    PubMed

    Liu, Jian-xun; Chen, Mei-rong; Jian, Zheng-guo; Wu, Gang; Wu, Zhi-shen

    2015-08-01

    Basalt is the raw material of basalt fiber. The content of FeO and Fe2O3 has a great impact on the properties of basalt fibers. ICP-OES and dichromate method were used to test total Fe and Fe(2+) in basalt. Suitable instrument parameters and analysis lines of Fe were chosen for ICP-OES. The relative standard deviation (RSD) of ICP-OES is 2.2%, and the recovery is in the range of 98%~101%. The method shows simple, rapid and highly accurate for determination of total Fe and Fe(2+) in basalt. The RSD of ICP-OES and dichromate method is 0.42% and 1.4%, respectively.

  7. Formation of layered Fe(II)-Al(III)-hydroxides during reaction of Fe(II) with aluminum oxide.

    PubMed

    Elzinga, Evert J

    2012-05-01

    The reactivity of aqueous Fe(II) with aluminum oxide in anoxic solutions was investigated with batch kinetic experiments combined with Fe K edge X-ray absorption spectroscopy measurements to characterize Fe(II) sorption products. Formation of Fe(II)-Al(III)-layered double hydroxides with an octahedral sheet structure similar to nikischerite (NaFe(II)(6) Al(3)(SO(4))(2)(OH)(18) (H(2)O)(12)) was observed within a few hours during sorption at pH 7.5 and aqueous Fe(II) concentrations of 1-3 mM. These Fe(II) phases are composed of brucite-like Fe(II)(OH)(2) sheets with partial substitution of Al(III) for Fe(II), charge balanced by anions coordinated along the basal planes. Their fast rate of formation suggests that these previously unrecognized Fe(II) phases, which are structurally and compositionally similar to green rust, may be an important sink of Fe(II) in suboxic and anoxic geochemical environments, and impact the fate of structurally compatible trace metals, such as Co(II), Ni(II), and Zn(II), as well as redox-reactive species including Cr(VI) and U(VI). Further studies are required to assess the thermodynamics, formation kinetics, and stability of these Fe(II) minerals under field conditions.

  8. Importance of doping and frustration in itinerant Fe-doped Cr2Al

    DOE PAGES

    Susner, M. A.; Parker, D. S.; Sefat, A. S.

    2015-05-12

    We performed an experimental and theoretical study comparing the effects of Fe-doping of Cr2Al, an antiferromagnet with a N el temperature of 670 K, with known results on Fe-doping of antiferromagnetic bcc Cr. (Cr1-xFex)2Al materials are found to exhibit a rapid suppression of antiferromagnetic order with the presence of Fe, decreasing TN to 170 K for x=0.10. Antiferromagnetic behavior disappears entirely at x≈0.125 after which point increasing paramagnetic behavior is exhibited. Moreover, this is unlike the effects of Fe doping of bcc antiferromagnetic Cr, in which TN gradually decreases followed by the appearance of a ferromagnetic state. Theoretical calculations explainmore » that the Cr2Al-Fe suppression of magnetic order originates from two effects: the first is band narrowing caused by doping of additional electrons from Fe substitution that weakens itinerant magnetism; the second is magnetic frustration of the Cr itinerant moments in Fe-substituted Cr2Al. In pure-phase Cr2Al, the Cr moments have an antiparallel alignment; however, these are destroyed through Fe substitution and the preference of Fe for parallel alignment with Cr. This is unlike bulk Fe-doped Cr alloys in which the Fe anti-aligns with the Cr atoms, and speaks to the importance of the Al atoms in the magnetic structure of Cr2Al and Fe-doped Cr2Al.« less

  9. Precursors to [FeFe]-Hydrogenase Models: Syntheses of Fe2(SR)2(CO)6 from CO-Free Iron Sources

    PubMed Central

    Chen, Jinzhu; Boyke, Christine; Rauchfuss, Thomas B.; Volkers, Phillip I.; Whaley, C. Matthew; Wilson, Scott R.; Yao, Haijun

    2008-01-01

    This report describes routes to iron dithiolato carbonyls that do not require preformed iron carbonyls. The reaction of FeCl2, Zn, and Q2S2CnH2n (Q+ = Na+, Et3NH+) under an atmosphere of CO affords Fe2(S2CnH2n)(CO)6 (n = 2, 3) in yields >70%. The method was employed to prepare Fe2(S2C2H4)(13CO)6. Treatment of these carbonylated mixtures with tertiary phosphines gave the ferrous species Fe3(S2C3H6)3(CO)4(PR3)2, for R = Et, Bu, and Ph. Like the related complex Fe3(SPh)6(CO)6, these compounds consist of a linear arrangement of three conjoined face-shared octahedral centers. Omitting the phosphine but with an excess of dithiolate, we obtained the related mixed-valence triiron species [Fe3(S2CnH2n)4(CO)4]−. The highly reducing all-ferrous species [Fe3(S2CnH2n)4(CO)4]2− is implicated as an intermediate in this transformation. Reactive forms of iron, prepared by the method of Rieke, also combined with dithiols under a CO atmosphere to give Fe2(S2CnH2n)(CO)6 in modest yields under mild conditions. Studies on the order of addition indicate that ferrous thiolates are formed prior to the onset of carbonylation. Crystallographic characterization demonstrated that the complexes Fe3(S2C3H6)3(CO)4(PEt3)2 and PBnPh3[Fe3(S2C3H6)4(CO)4] feature high spin ferrous and low spin ferric as the central metal, respectively. PMID:18610969

  10. Oxidized and Reduced [2Fe-2S] Clusters from an Iron(I) Synthon

    PubMed Central

    Reesbeck, Megan E.; Rodriguez, Meghan M.; Brennessel, William W.; Mercado, Brandon Q.; Vinyard, David; Holland, Patrick L.

    2016-01-01

    Synthetic [2Fe-2S] clusters are often used to elucidate ligand effects on the reduction potentials and spectroscopy of natural electron transfer sites, which can have anionic Cys ligands or neutral His ligands. Current synthetic routes to [2Fe-2S] clusters are limited in their feasibility with a range of supporting ligands. Here we report a new synthetic route to synthetic [2Fe-2S] clusters, through oxidation of an iron(I) source with elemental sulfur. This method yields a neutral diketiminate-supported [2Fe-2S] cluster in the diiron(III) oxidized form. The oxidized [2Fe-2S] cluster can be reduced to a mixed valent iron(II)-iron(III) compound. Both the diferric and reduced mixed valent clusters are characterized using X-ray crystallography, Mössbauer spectroscopy, EPR spectroscopy and cyclic voltammetry. The reduced compound is particularly interesting because its X-ray crystal structure shows a difference in Fe-S bond lengths to one of the iron atoms, consistent with valence localization. The valence localization is also evident from Mössbauer spectroscopy. PMID:26044124

  11. Mg, Al, Si, Ca, Ti, Fe, and Ni abundance for a sample of solar analogues

    NASA Astrophysics Data System (ADS)

    López-Valdivia, Ricardo; Bertone, Emanuele; Chávez, Miguel

    2017-01-01

    We report on the determination of chemical abundances of 38 solar analogues, including 11 objects previously identified as super metal-rich stars. We have measured the equivalent widths for 34 lines of 7 different chemical elements (Mg, Al, Si, Ca, Ti, Fe, and Ni) in high-resolution (R ˜ 80 000) spectroscopic images, obtained at the Observatorio Astrofísico Guillermo Haro (Sonora, Mexico), with the Cananea High-resolution Spectrograph. We derived chemical abundances using ATLAS12 model atmospheres and the Fortran code MOOG. We confirmed the super metallicity status of 6 solar analogues. Within our sample, BD+60 600 is the most metal-rich star ([Fe/H]=+0.35 dex), while for HD 166991 we obtained the lowest iron abundance ([Fe/H]=-0.53 dex). We also computed the so-called [Ref] index for 25 of our solar analogues, and we found, that BD+60 600 ([Ref]=+0.42) and BD+28 3198 ([Ref]=+0.34) are good targets for exoplanet search.

  12. Unraveling the complexity of iron oxides at high pressure and temperature: Synthesis of Fe5O6

    DOE PAGES

    Lavina, Barbara; Meng, Yue

    2015-06-26

    The iron-oxygen system is the most important reference of rocks’ redox state. Even as minor components, iron oxides can play a critical role in redox equilibria, which affect the speciation of the fluid phases chemical differentiation, melting, and physical properties. Until our recent finding of Fe4O5, iron oxides were assumed to comprise only the polymorphs of FeO, Fe3O4, and Fe2O3. Combining synthesis at high pressure and temperature with micro- diffraction mapping, we have identified yet another distinct iron oxide, Fe5O6. The new compound, which has an orthorhombic structure, was obtained in the pressure range from 10 to 20 GPa uponmore » laser heating mixtures of iron and hematite at ~2000 K, and is recoverable to ambient conditions. The high-pressure orthorhombic iron oxides Fe5O6, Fe4O5, and h-Fe3O4 display similar iron coordination geometries and structural arrangements, and indeed exhibit coherent systematic behavior of crystallographic parameters and compressibility. Fe5O6, along with FeO and Fe4O5, is a candidate key minor phase of planetary interiors; as such, it is of major petrological and geo- chemical importance. Here, we are revealing an unforeseen complexity in the Fe-O system with four different compounds—FeO, Fe5O6, Fe4O5, and h-Fe3O4—in a narrow compositional range (0.75 < Fe/O < 1.0). New, finely spaced oxygen buffers at conditions of the Earth’s mantle can be defined.« less

  13. Unraveling the complexity of iron oxides at high pressure and temperature: Synthesis of Fe5O6

    PubMed Central

    Lavina, Barbara; Meng, Yue

    2015-01-01

    The iron-oxygen system is the most important reference of rocks’ redox state. Even as minor components, iron oxides can play a critical role in redox equilibria, which affect the speciation of the fluid phases chemical differentiation, melting, and physical properties. Until our recent finding of Fe4O5, iron oxides were assumed to comprise only the polymorphs of FeO, Fe3O4, and Fe2O3. Combining synthesis at high pressure and temperature with microdiffraction mapping, we have identified yet another distinct iron oxide, Fe5O6. The new compound, which has an orthorhombic structure, was obtained in the pressure range from 10 to 20 GPa upon laser heating mixtures of iron and hematite at ~2000 K, and is recoverable to ambient conditions. The high-pressure orthorhombic iron oxides Fe5O6, Fe4O5, and h-Fe3O4 display similar iron coordination geometries and structural arrangements, and indeed exhibit coherent systematic behavior of crystallographic parameters and compressibility. Fe5O6, along with FeO and Fe4O5, is a candidate key minor phase of planetary interiors; as such, it is of major petrological and geochemical importance. We are revealing an unforeseen complexity in the Fe-O system with four different compounds—FeO, Fe5O6, Fe4O5, and h-Fe3O4—in a narrow compositional range (0.75 < Fe/O < 1.0). New, finely spaced oxygen buffers at conditions of the Earth’s mantle can be defined. PMID:26601196

  14. The life cycle of iron Fe(III) oxide: impact of fungi and bacteria

    NASA Astrophysics Data System (ADS)

    Bonneville, Steeve

    2014-05-01

    Iron oxides are ubiquitous reactive constituents of soils, sediments and aquifers. They exhibit vast surface areas which bind a large array of trace metals, nutrients and organic molecules hence controlling their mobility/reactivity in the subsurface. In this context, understanding the "life cycle" of iron oxide in soils is paramount to many biogeochemical processes. Soils environments are notorious for their extreme heterogeneity and variability of chemical, physical conditions and biological agents at play. Here, we present studies investigating the role of two biological agents driving iron oxide dynamics in soils, root-associated fungi (mycorrhiza) and bacteria. Mycorrhiza filaments (hypha) grow preferentially around, and on the surface of nutrient-rich minerals, making mineral-fungi contact zones, hot-spots of chemical alteration in soils. However, because of the microscopic nature of hyphae (only ~ 5 µm wide for up to 1 mm long) and their tendency to strongly adhere to mineral surface, in situ observations of this interfacial micro-environment are scarce. In a microcosm, ectomycorrhiza (Paxillus involutus) was grown symbiotically with a pine tree (Pinus sylvestris) in the presence of freshly-cleaved biotite under humid, yet undersaturated, conditions typical of soils. Using spatially-resolved ion milling technique (FIB), transmission electron microscopy and spectroscopy (TEM/STEM-EDS), synchrotron based X-ray microscopy (STXM), we were able to quantify the speciation of Fe at the biotite-hypha interface. The results shows that substantial oxidation of biotite structural-Fe(II) into Fe(III) subdomains occurs at the contact zone between mycorrhiza and biotite. Once formed, iron(III) oxides can reductively dissolve under suboxic conditions via several abiotic and microbial pathways. In particular, they serve as terminal electron acceptors for the oxidation of organic matter by iron reducing bacteria. We aimed here to understand the role of Fe(III) mineral

  15. Development and commercialization status of Fe{sub 3}Al-based intermetallic alloys

    SciTech Connect

    Sikka, V.K.; Viswanathan, S.; McKamey, C.G.

    1993-06-01

    The Fe{sub 3}Al-based intermetallic alloys offer unique benefits of excellent oxidation and sulfidation resistance, limited by poor room-temperature (RT) ductility and low high-temperature strength. Recent understanding of environmental effects on RT ductility of these alloys has led to progress toward taking commercial advantage of Fe{sub 3}Al-based materials. Cause of low ductility appears to be related to hydrogen formed from reaction with moisture. The environmental effect has been reduced in these intermetallic alloys by two methods. The first deals with producing a more hydrogen-resistant microstructure through thermomechanical processing, and the second dealed with compositional modification. The alloys showing reduced environmental effect have been melted and processed by many different methods. Laboratory and commercial heats have been characterized. Tests have been conducted in both air and controlled environments to quantify environmental effects on these properties. These materials were also tested for aqueous corrosion and resistance to stress corrosion cracking. Oxidation and sulfidation data were generated and effects of minor alloying elements on were also investigated. Several applications have been identified for the newly developed iron aluminides. Commercialization status of these alloys is described.

  16. Zinc and iron metabolism in Euglena gracilis: metal redistribution during Zn and Fe deficiency

    SciTech Connect

    Taylor, P.; Gingrich, D.; Antholine, W.E.; Petering, D.H.

    1986-05-01

    The normal cytosolic distribution of Zn and Fe in Euglena gracilis and their changes during Zn and Fe deficiency and repletion in relationship to cell proliferation were examined. Using Sephadex G-75 chromatography, two metal pools were found-Zn and Fe bound to high molecular weight (HMW) proteins and a pool of low molecular weight (LMW) Zn and Fe of less than 2000 daltons (ZnL, FeL), containing 80-90% of the cytosolic Zn and Fe. ZnL and FeL can be separated on Sephadex G-15 and by HPLC techniques. According to ESR analysis both HMW and LMW iron is high spin Fe(III). Under conditions of Zn deficiency, cell proliferation is halted after 48 hrs. in concert with the depletion of the ZnL. Within error, HMW protein bound Zn is unaffected. ZnL appears to be a labile store of Zn to supply the cell with this essential metal. In contrast, during Fe deficiency cell proliferation is unaffected. Yet both HMW and LMW pools are depleted within 48 hrs. Both bands of Fe appear to be storage forms of the metal. Proliferative capacity of the alga is evidently more sensitive to Zn deficiency than to Fe depletion, possibly because Euglena can scavenge adventitious Fe from the medium by a siderophore-mediated mechanism.

  17. Comparison of iron isotope variations in modern and Ordovician siliceous Fe oxyhydroxide deposits

    NASA Astrophysics Data System (ADS)

    Moeller, Kirsten; Schoenberg, Ronny; Grenne, Tor; Thorseth, Ingunn H.; Drost, Kerstin; Pedersen, Rolf B.

    2014-02-01

    Formation pathways of ancient siliceous iron formations and related Fe isotopic fractionation are still not completely understood. Investigating these processes, however, is difficult as good modern analogues to ancient iron formations are scarce. Modern siliceous Fe oxyhydroxide deposits are found at marine hydrothermal vent sites, where they precipitate from diffuse, low temperature fluids along faults and fissures on the seafloor. These deposits exhibit textural and chemical features that are similar to some Phanerozoic iron formations, raising the question as to whether the latter could have precipitated from diffuse hydrothermal fluids rather than from hydrothermal plumes. In this study, we present the first data on modern Fe oxyhydroxide deposits from the Jan Mayen hydrothermal vent fields, Norwegian-Greenland Sea. The samples we investigated exhibited very low δ56Fe values between -2.09‰ and -0.66‰. Due to various degrees of partial oxidation, the Fe oxyhydroxides are with one exception either indistinguishable from low-temperature hydrothermal fluids from which they precipitated (-1.84‰ and -1.53‰ in δ56Fe) or are enriched in the heavy Fe isotopes. In addition, we investigated Fe isotope variations in Ordovician jasper beds from the Løkken ophiolite complex, Norway, which have been interpreted to represent diagenetic products of siliceous ferrihydrite precursors that precipitated in a hydrothermal plume, in order to compare different formation pathways of Fe oxyhydroxide deposits. Iron isotopes in the jasper samples have higher δ56Fe values (-0.38‰ to +0.89‰) relative to modern, high-temperature hydrothermal vent fluids (ca. -0.40‰ on average), supporting the fallout model. However, formation of the Ordovician jaspers by diffuse venting cannot be excluded, due to lithological differences of the subsurface of the two investigated vent systems. Our study shows that reliable interpretation of Fe isotope variations in modern and ancient marine

  18. Magnetic characterization of iron oxides formed after thermal treatment of nontronite and the formation of three polymorphs of Fe2O3: α-Fe2O3, γ-Fe2O3, ɛ-Fe2O3

    NASA Astrophysics Data System (ADS)

    Berquo, T. S.; Moskowitz, B. M.

    2011-12-01

    Nontronite is an Fe-rich smectite clay that occurs widely in terrestrial soils, sediments and weathering formations and may also be present in the Martian regolith. The thermal decomposition of nontronite is known to form various magnetic iron oxides but their compositions, magnetic properties, and formation pathways remain poorly understood. The magnetic alteration products of nontronite have been proposed as a source for the magnetic phases in the surface layers and dust on Mars as well as in some archeological fired-bricks and ceramic pottery. One alteration product of nontronite is ɛ-Fe2O3 which is ferrimagnetic with a Curie temperature of ~ 500 K and extremely large coercivity (HC ~ 1-2 T) at 300 K. In this work nontronite samples from eight source localities were heated to 1000°C in air for one hour. The magnetic properties of the alteration products were investigated with low-temperature (LT) magnetization and AC susceptibility curves, hysteresis loops, Mossbauer spectroscopy, and X-ray diffraction. The thermal treatment was effective in converting the nontronite to a combination of different polymorphs of ferric oxide depending on source locality and included: hematite (α-Fe2O3), ɛ-Fe2O3, and a cubic spinel phase that suggest the presence of maghemite (γ-Fe2O3). Mossbauer spectra at 300 K identified hematite and ɛ-Fe2O3 as the main phases in 7 samples with amounts ranging from 26-100% for hematite 0-69% for ɛ-Fe2O3. One sample showed a paramagnetic Fe3+ doublet and a broad sextet characteristic of magnetic relaxation effects. Upon cooling to 4.2 K, the Mossbauer spectrum was consistent with maghemite. In all samples except one, the magnetic hyperfine fields for the hematite phase are slightly reduced as compared with its stoichiometric form indicating some iron substitution with ions such as Al. This is consistent with the observation that all but one sample lacked the characteristic Morin transition for pure hematite on LT-remanence warming curves

  19. Microstructural characterization of the dispersed phases in Al-Ce-Fe system

    NASA Astrophysics Data System (ADS)

    Ayer, Raghavan; Angers, L. M.; Mueller, R. R.; Scanlon, J. C.; Klein, C. F.

    1988-07-01

    Analytical electron microscopy studies were conducted on a rapidly solidified Al-8.8Fe-3.7Ce alloy and arc melted buttons of aluminum rich Al-Fe-Ce alloys to determine the characteristics of the metastable and equilibrium phases. The rapidly solidified alloy consisted of binary and ternary metastable phases in the as-extruded condition. The binary metastable phase was identified to be Al6Fe, while the ternary metastable phases were identified to be Al10Fe2Ce and Al20Fe5Ce. The Al20Fe5Ce was a decagonal quasicrystal while the Al10Fe2Ce phase was determined to have an orthorhombic crystal structure belonging to space group Cmmm, Cmm2, or C222. Microscopy studies of RS alloy and cast buttons annealed at 700 K established the equilibrium phases to be Al13Fe4, Al4Ce, and an Al13Fe3Ce ternary phase which was first identified in the present study. The crystal structure of the equilibrium ternary phase was determined to be orthorhombic with a Cmcm or Cmc2 space group. The details of X-ray microanalysis and convergent beam electron diffraction analysis are described.

  20. Structural investigation of the (010) surface of the Al13 Fe4 catalyst.

    PubMed

    Ledieu, J; Gaudry, É; Loli, L N Serkovic; Villaseca, S Alarcón; de Weerd, M-C; Hahne, M; Gille, P; Grin, Y; Dubois, J-M; Fournée, V

    2013-02-15

    We have investigated the structure of the Al(13)Fe(4)(010) surface using both experimental and ab initio computational methods. The results indicate that the topmost surface layers correspond to incomplete puckered (P) planes present in the bulk crystal structure. The main building block of the corrugated termination consists of two adjacent pentagons of Al atoms, each centered by a protruding Fe atom. These motifs are interconnected via additional Al atoms referred to as "glue" atoms which partially desorb above 873 K. The surface structure of lower atomic density compared to the bulk P plane is explained by a strong Fe-Al-Fe covalent polar interaction that preserves intact clusters at the surface. The proposed surface model with identified Fe-containing atomic ensembles could explain the Al(13)Fe(4) catalytic properties recently reported in line with the site-isolation concept [M. Armbrüster et al., Nat. Mater. 11, 690 (2012)].

  1. Discovery of Fe7O9: a new iron oxide with a complex monoclinic structure

    NASA Astrophysics Data System (ADS)

    Sinmyo, Ryosuke; Bykova, Elena; Ovsyannikov, Sergey V.; McCammon, Catherine; Kupenko, Ilya; Ismailova, Leyla; Dubrovinsky, Leonid

    2016-09-01

    Iron oxides are fundamentally important compounds for basic and applied sciences as well as in numerous industrial applications. In this work we report the synthesis and investigation of a new binary iron oxide with the hitherto unknown stoichiometry of Fe7O9. This new oxide was synthesized at high-pressure high-temperature (HP-HT) conditions, and its black single crystals were successfully recovered at ambient conditions. By means of single crystal X-ray diffraction we determined that Fe7O9 adopts a monoclinic C2/m lattice with the most distorted crystal structure among the binary iron oxides known to date. The synthesis of Fe7O9 opens a new portal to exotic iron-rich (M,Fe)7O9 oxides with unusual stoichiometry and distorted crystal structures. Moreover, the crystal structure and phase relations of such new iron oxide groups may provide new insight into the cycling of volatiles in the Earth’s interior.

  2. Discovery of Fe7O9: a new iron oxide with a complex monoclinic structure

    PubMed Central

    Sinmyo, Ryosuke; Bykova, Elena; Ovsyannikov, Sergey V.; McCammon, Catherine; Kupenko, Ilya; Ismailova, Leyla; Dubrovinsky, Leonid

    2016-01-01

    Iron oxides are fundamentally important compounds for basic and applied sciences as well as in numerous industrial applications. In this work we report the synthesis and investigation of a new binary iron oxide with the hitherto unknown stoichiometry of Fe7O9. This new oxide was synthesized at high-pressure high-temperature (HP-HT) conditions, and its black single crystals were successfully recovered at ambient conditions. By means of single crystal X-ray diffraction we determined that Fe7O9 adopts a monoclinic C2/m lattice with the most distorted crystal structure among the binary iron oxides known to date. The synthesis of Fe7O9 opens a new portal to exotic iron-rich (M,Fe)7O9 oxides with unusual stoichiometry and distorted crystal structures. Moreover, the crystal structure and phase relations of such new iron oxide groups may provide new insight into the cycling of volatiles in the Earth’s interior. PMID:27605075

  3. Effect of nitrogen upon structural and magnetic properties of FePt in FePt/AlN multilayer structures

    SciTech Connect

    Gao, Tenghua Zhang, Cong; Sannomiya, Takumi; Muraishi, Shinji; Nakamura, Yoshio; Shi, Ji

    2014-09-01

    This paper investigates the effect of the addition of nitrogen in FePt layers for ultrathin FePt/AlN multilayer structures. X-ray diffraction results reveal that a compressive stress relaxation occurs after annealing owing to the release of interstitial nitrogen atoms in the FePt layers. The introduction of nitrogen also induces a large in-plane compressive strain during grain growth not seen in FePt deposited without nitrogen. This strain is considered to decrease the driving force for (111) grain growth and FePt ordering.

  4. Inhibition of Fe(2+)- and Fe(3+)- induced hydroxyl radical production by the iron-chelating drug deferiprone.

    PubMed

    Timoshnikov, V A; Kobzeva, T V; Polyakov, N E; Kontoghiorghes, G J

    2015-01-01

    Deferiprone (L1) is an effective iron-chelating drug that is widely used for the treatment of iron-overload diseases. It is known that in aqueous solutions Fe(2+) and Fe(3+) ions can produce hydroxyl radicals via Fenton and photo-Fenton reactions. Although previous studies with Fe(2+) have reported ferroxidase activity by L1 followed by the formation of Fe(3+) chelate complexes and potential inhibition of Fenton reaction, no detailed data are available on the molecular antioxidant mechanisms involved. Similarly, in vitro studies have also shown that L1-Fe(3+) complexes exhibit intense absorption bands up to 800nm and might be potential sources of phototoxicity. In this study we have applied an EPR spin trapping technique to answer two questions: (1) does L1 inhibit the Fenton reaction catalyzed by Fe(2+) and Fe(3+) ions and (2) does UV-Vis irradiation of the L1-Fe(3+) complex result in the formation of reactive oxygen species. PBN and TMIO spin traps were used for detection of oxygen free radicals, and TEMP was used to trap singlet oxygen if it was formed via energy transfer from L1 in the triplet excited state. It was demonstrated that irradiation of Fe(3+) aqua complexes by UV and visible light in the presence of spin traps results in the appearance of an EPR signal of the OH spin adduct (TMIO-OH, a(N)=14.15G, a(H)=16.25G; PBN-OH, a(N)=16.0G, a(H)=2.7G). The presence of L1 completely inhibited the OH radical production. The mechanism of OH spin adduct formation was confirmed by the detection of methyl radicals in the presence of dimethyl sulfoxide. No formation of singlet oxygen was detected under irradiation of L1 or its iron complexes. Furthermore, the interaction of L1 with Fe(2+) ions completely inhibited hydroxyl radical production in the presence of hydrogen peroxide. These findings confirm an antioxidant targeting potential of L1 in diseases related to oxidative damage.

  5. Solubility and release of fenbufen intercalated in Mg, Al and Mg, Al, Fe layered double hydroxides (LDH): The effect of Eudragit S 100 covering

    SciTech Connect

    Arco, M. del; Fernandez, A.; Martin, C.; Rives, V.

    2010-12-15

    Following different preparation routes, fenbufen has been intercalated in the interlayer space of layered double hydroxides with Mg{sup 2+} and Al{sup 3+} or Mg{sup 2+}, Al{sup 3+} and Fe{sup 3+} in the layers. Well crystallized samples were obtained in most of the cases (intercalation was not observed by reconstruction of the MgAlFe matrix), with layer heights ranging between 16.1 and 18.8 A. The presence of the LDH increases the solubility of fenbufen, especially when used as a matrix. The dissolution rate of the drug decreases when the drug is intercalated, and is even lower in those systems containing iron; release takes place through ionic exchange with phosphate anions from the solution. Preparation of microspheres with Eudragit S 100 leads to solids with an homogeneous, smooth surface with efficient covering of the LDH surface, as drug release was not observed at pH lower than 7. - Graphical abstract: LDHs containing Mg, Al, Fe increase fenbufen solubility, release takes place through ionic exchange with phosphate anions from the medium. Spherical solids with homogeneous, smooth surface are formed when using Eudragit S 100, efficiently covering the LDH surface. Display Omitted

  6. High-pressure high-temperature behavior of iron silicide (Fe5Si3) to 58 GPa and 2400K

    NASA Astrophysics Data System (ADS)

    McGuire, C. P.; Kavner, A.; Santamaria, D.

    2015-12-01

    Silicon is an important candidate for the light element in the outer core. Here we present new measurements of the equation-of-state, thermal expansion, melting temperature, and thermal conductivity of iron silicide (Fe5Si3) at high pressures and temperatures. We performed a series of X-ray diffraction experiments in the laser-heated diamond anvil cell on Fe5Si3 at ALS beamline 12.2.2. Diffraction patterns and temperature-versus-laser power curves were measured in situ at pressures up to 58 GPa and temperatures up to 2300 K. In one set of experiments both NaCl and Ne were used as the pressure transmitting, thermal insulator and pressure calibrant. In a second set of experiments, only NaCl was present and served those three purposes. The measurements yield a new thermoelastic equation of state for Fe5Si3, including bulk modulus, high-pressure thermal expansion, and the Grüneisen parameter. In addition, we have determined a lower bound on the melting behavior up to 58 GPa. This information helps constrain compositionally-sensitive models describing the density, compressibility, and dynamics of Earth's core. The temperature-versus-laser power measurements provide information about the heat flow environment in the diamond anvil cell. A comparison of the temperature-versus-laser power measurements for pure iron and Fe5Si3 yields a measure of how the presence of Si influences the thermal conductivity of iron at high pressures and temperatures. Our measurements also show a jump in thermal conductivity of NaCl across the B1- B2 phase transition. This information is important for interpreting thermal conductivity values in the present work and also has broader implications for experimental design and data interpretation in laser-heated diamond anvil cell experiments.

  7. Drosophila Frataxin: an Iron Chaperone During Cellular [2Fe-2S] Cluster Bioassembly

    SciTech Connect

    Kondapalli,K.; Kok, N.; Dancis, A.; Stemmler, T.

    2008-01-01

    Frataxin, a mitochondrial protein that is directly involved in regulating cellular iron homeostasis, has been suggested to serve as an iron chaperone during cellular Fe-S cluster biosynthesis. In humans, decreased amounts or impaired function of frataxin causes the autosomal recessive neurodegenerative disorder Friedreich's ataxia. Cellular production of Fe-S clusters is accomplished by the Fe cofactor assembly platform enzymes Isu (eukaryotes) and IscU (prokaryotes). In this report, we have characterized the overall stability and iron binding properties of the Drosophila frataxin homologue (Dfh). Dfh is highly folded with secondary structural elements consistent with the structurally characterized frataxin orthologs. While the melting temperature (TM {approx} 59 C) and chemical stability ([urea]50% {approx} 2.4 M) of Drosophila frataxin, measured using circular dichroism (CD) and fluorescence spectroscopy, closely match values determined for the human ortholog, pure Dfh is more stable against autodegradation than both the human and yeast proteins. The ferrous iron binding affinity (Kd {approx} 6.0 {mu}M) and optimal metal to protein stoichiometry (1:1) for Dfh have been measured using isothermal titration calorimetry (ITC). Under anaerobic conditions with salt present, holo-Dfh is a stable iron-loaded protein monomer. Frataxin prevents reactive oxygen species-induced oxidative damage to DNA when presented with both Fe(II) and H2O2. Ferrous iron bound to Dfh is high-spin and held in a partially symmetric Fe-(O/N)6 coordination environment, as determined by X-ray absorption spectroscopy (XAS). Extended X-ray absorption fine structure (EXAFS) simulations indicate the average Fe-O/N bond length in Dfh is 2.13 Angstroms, consistent with a ligand geometry constructed by water and carboxylate oxygens most likely supplied in part by surface-exposed conserved acidic residues located on helix 1 and strand 1 in the structurally characterized frataxin orthologs. The iron

  8. Drosophila Frataxin: An Iron Chaperone During Cellular Fe-S Cluster Bioassembly

    SciTech Connect

    Kondapalli, K.C.; Kok, N.M.; Dancis, A.; Stemmler, T.L.

    2009-05-20

    Frataxin, a mitochondrial protein that is directly involved in regulating cellular iron homeostasis, has been suggested to serve as an iron chaperone during cellular Fe-S cluster biosynthesis. In humans, decreased amounts or impaired function of frataxin causes the autosomal recessive neurodegenerative disorder Friedreich's ataxia. Cellular production of Fe-S clusters is accomplished by the Fe cofactor assembly platform enzymes Isu (eukaryotes) and IscU (prokaryotes). In this report, we have characterized the overall stability and iron binding properties of the Drosophila frataxin homologue (Dfh). Dfh is highly folded with secondary structural elements consistent with the structurally characterized frataxin orthologs. While the melting temperature (T{sub M} {approx} 59 C) and chemical stability ([urea]{sub 50} {approx} 2.4 M) of Drosophila frataxin, measured using circular dichroism (CD) and fluorescence spectroscopy, closely match values determined for the human ortholog, pure Dfh is more stable against autodegradation than both the human and yeast proteins. The ferrous iron binding affinity (K{sub d} {approx} 6.0 {micro}M) and optimal metal to protein stoichiometry (1:1) for Dfh have been measured using isothermal titration calorimetry (ITC). Under anaerobic conditions with salt present, holo-Dfh is a stable iron-loaded protein monomer. Frataxin prevents reactive oxygen species-induced oxidative damage to DNA when presented with both Fe(II) and H{sub 2}O{sub 2}. Ferrous iron bound to Dfh is high-spin and held in a partially symmetric Fe-(O/N){sub 6} coordination environment, as determined by X-ray absorption spectroscopy (XAS). Extended X-ray absorption fine structure (EXAFS) simulations indicate the average Fe-O/N bond length in Dfh is 2.13 {angstrom}, consistent with a ligand geometry constructed by water and carboxylate oxygens most likely supplied in part by surface-exposed conserved acidic residues located on helix 1 and strand 1 in the structurally

  9. Preparation and biodistribution of 59Fe-radiolabelled iron oxide nanoparticles

    NASA Astrophysics Data System (ADS)

    Pospisilova, Martina; Zapotocky, Vojtech; Nesporova, Kristina; Laznicek, Milan; Laznickova, Alice; Zidek, Ondrej; Cepa, Martin; Vagnerova, Hana; Velebny, Vladimir

    2017-02-01

    We report on the 59Fe radiolabelling of iron oxide nanoparticle cores through post-synthetic isotope exchange (59Fe-IONPex) and precursor labelling (59Fe-IONPpre). Scanning electron microscopy and dynamic light scattering measurements showed no impact of radiolabelling on nanoparticle size or morphology. While incorporation efficiencies of these methods are comparable—83 and 90% for precursor labelling and post-synthetic isotope exchange, respectively—59Fe-IONPpre exhibited much higher radiochemical stability in citrated human plasma. Quantitative ex vivo biodistribution study of 59Fe-IONPpre coated with triethylene glycol was performed in Wistar rats. Following the intravenous administration, high 59Fe concentration was observed in the lung and the organs of the reticuloendothelial system such as the liver, the spleen and the femur.

  10. Anomalous Dilatometric Response in Fe-Mn-Al-Si Steel

    NASA Astrophysics Data System (ADS)

    Ghosh, S. K.

    2012-04-01

    The present study deals with the transformation of an aggregate consisting of ferrite and pearlite into austenite in a Fe-0.36C-1.98Mn-1.97Al-0.30Si (wt%) steel. The transformation phenomenon has been studied using dilatometry which confirms that austenite starts to nucleate due to dissolution of ferrite and pearlite and subsequently it commences to grow when the appropriate elevated temperature is reached. The austenite formation has been accompanied with the formation of a hump in the dilatation curve which is different with respect to the results reported earlier. The non-conventional behaviour associated with the austenite formation has been explained using the X-ray diffraction data, microstructural investigation and also with MT-DATA theoretical calculations.

  11. Fe-doped ZnO nanoparticles: the oxidation number and local charge on iron, studied by 57Fe Mößbauer spectroscopy and DFT calculations.

    PubMed

    Xiao, Jianping; Kuc, Agnieszka; Pokhrel, Suman; Mädler, Lutz; Pöttgen, Rainer; Winter, Florian; Frauenheim, Thomas; Heine, Thomas

    2013-03-04

    Iron bru: Fe-doped ZnO may contain Fe(2+) and Fe(3+) species. Whilst Mößbauer spectroscopy can distinguish these sites in pure oxides FeO and Fe(2)O(3), it gives very similar shifts for Fe-doped phases. This result is rationalized by electron redistribution from the dopant site to the crystal matrix. Mößbauer shifts correlate with the local charge on the Fe sites and different dopant sites can be identified by the Mößbauer quadrupole splitting (see figure).

  12. Replacing electrolytic iron in a fortification-mix with NaFeEDTA increases both iron and zinc availabilities in traditional African maize porridges.

    PubMed

    Kruger, Johanita

    2016-08-15

    While replacing electrolytic iron with NaFeEDTA in multi-micronutrient fortification-mixes is a popular option, there is no information about the effect on the iron and zinc availabilities in African staple foods. This study evaluated the effects of adding a multi-micronutrient fortification-mix, with no iron, electrolytic iron or NaFeEDTA on the availabilities of iron and zinc from thick and fermented special-grade maize porridges using a Caco-2 cell model. Replacing electrolytic iron with NaFeEDTA significantly (p ⩽ 0.05) increased iron and, importantly zinc, availabilities in both the thick (2.16% vs. 1.45% and 2.51% vs. 2.29%, respectively) and fermented (3.35% vs. 2.66% and 3.04% vs. 2.61%, respectively) porridges. Some of the NaFeEDTA complexes perhaps partially dissociated because of pH changes during simulated digestion, binding with zinc and increasing its availability. NaFeEDTA in a multi-micronutrient fortification-mix, added to less refined, high phytate maize meal, would be more effective than electrolytic iron in addressing both iron and zinc deficiencies in low socio-economic populations of sub-Saharan Africa.

  13. Coexistence of localized and itinerant magnetism in intercalated iron-selenide (Li,Fe)OHFeSe

    NASA Astrophysics Data System (ADS)

    Liu, Da-Yong; Sun, Zhe; Zou, Liang-Jian

    2017-02-01

    The electronic structure and magnetism of a new magnetic intercalation compound (Li0.8Fe0.2)OHFeSe are investigated theoretically. The electronic structure calculations predict that the Fe in the (Li,Fe)OH intercalated layer is in a +2 valence state, i.e. there is electron doping to the FeSe layer, resulting in the shrinking of the Fermi surface (FS) pocket around Γ and a strong suppression of dynamical spin susceptibility at M in comparison with the bulk FeSe compound. The ground state of the FeSe layer is a striped antiferromagnetic (SAFM) metal, while the (Li,Fe)OH layer displays a very weak localized magnetism, with an interlayer ferromagnetic (FM) coupling between the FeSe and intercalated (Li,Fe)OH layers. Moreover, the (Li,Fe)OH is more than a block layer; it is responsible for enhancing the antiferromagnetic (AFM) correlation in the FeSe layer through interlayer magnetic coupling. We propose that the magnetic spacer layer introduces a tuning mechanism for spin fluctuations associated with superconductivity in iron-based superconductors.

  14. Wet hydrogen peroxide catalytic oxidation of phenol with FeAC (iron-embedded activated carbon) catalysts.

    PubMed

    Liou, Rey-May; Chen, Shih-Hsiung; Huang, Cheng-Hsien; Hung, Mu-Ya; Chang, Jing-Song; Lai, Cheng-Lee

    2010-01-01

    This investigation aims at exploring the catalytic oxidation activity of iron-embedded activated carbon (FeAC) and the application for the degradation of phenol in the wet hydrogen peroxide catalytic oxidation (WHPCO). FeAC catalysts were prepared by pre-impregnating iron in coconut shell with various iron loadings in the range of 27.5 to 46.5% before they were activated. The FeAC catalysts were characterised by measuring their surface area, pore distribution, functional groups on the surface, and X-ray diffraction patterns. The effects of iron loading strongly inhibited the pore development of the catalyst but benefited the oxidation activity in WHPCO. It was found that the complete conversion of phenol was observed with all FeAC catalysts in oxidation. High level of chemical oxygen demand (COD) abatement can be achieved within the first 30 minutes of oxidation. The iron embedded in the activated carbon showed good performance in the degradation and mineralisation of phenol during the oxidation due to the active sites as iron oxides formed on the surface of the activated carbon. It was found that the embedding irons were presented in gamma-Fe(2)O(3), alpha-Fe(2)O(3), and alpha-FeCOOH forms on the activated carbon. The aging tests on FeAC catalysts showed less activity loss, and less iron leaching was found after four oxidation runs.

  15. Selective oxidation catalysts obtained by immobilization of iron(III) porphyrins on thiosalicylic acid-modified Mg-Al layered double hydroxides.

    PubMed

    de Freitas Castro, Kelly Aparecida Dias; Wypych, Fernando; Antonangelo, Ariana; Mantovani, Karen Mary; Bail, Alesandro; Ucoski, Geani Maria; Ciuffi, Kátia Jorge; Cintra, Thais Elita; Nakagaki, Shirley

    2016-09-15

    Nitrate-intercalated Mg-Al layered double hydroxides (LDHs) were synthesized and exfoliated in formamide. Reaction of the single layer suspension with thiosalicylic acid under different conditions afforded two types of solids: LDHA1, in which the outer surface was modified with the anion thiosalicylate, and LDHA2, which contained the anion thiosalicylate intercalated between the LDH layers. LDHA1 and LDHA2 were used as supports to immobilize neutral (FeP1 and FeP2) and anionic (FeP3) iron(III) porphyrins. For comparison purposes, the iron(III) porphyrins (FePs) were also immobilized on LDH intercalated with nitrate anions obtained by the co-precipitation method. Chemical modification of LDH facilitated immobilization of the FePs through interaction of the functionalizing groups in LDH with the peripheral substituents on the porphyrin ring. The resulting FePx-LDHAy solids were characterized by X-ray diffraction (powder) and UV-Vis and EPR spectroscopies and were investigated as catalysts in the oxidation of cyclooctene and cyclohexane. The immobilized neutral FePs and their homogeneous counterparts gave similar product yields in the oxidation of cyclooctene, suggesting that immobilization of the FePs on the thiosalicylate-modified LDHs only supported the catalyst species without interfering in the catalytic outcome. On the other hand, in the oxidation of cyclohexane, the thiosalicylate anions on the outer surface of LDHA1 or intercalated between the LDHA2 layers influenced the catalytic activity of FePx-LDHAy, leading to different efficiency and selectivity results. FeP1-LDHA2 performed the best (29.6% alcohol yield) due to changes in the polarity of the surface of the support and the presence of FeP1. Interestingly, FeP1 also performed better in solution as compared to the other FePs. Finally, it was possible to recycle FeP1-LDHA2 at least three times.

  16. Iron uptake by Caco-2 cells from NaFeEDTA and FeSO4: Effects of ascorbic acid, pH, and a Fe(II) chelating agent.

    PubMed

    Zhu, Le; Glahn, Raymond P; Yeung, Chi Kong; Miller, Dennis D

    2006-10-04

    Sodium iron(III) ethylenediaminetetraacetate (NaFeEDTA) has considerable promise as an iron fortificant because of its high bioavailability in foods containing iron absorption inhibitors. In this study, uptakes of iron from NaFeEDTA, FeSO4, and FeCl3 by Caco-2 cells were compared in the absence or presence of ascorbic acid (AA), an iron absorption enhancer; at selected pH levels; and in the absence or presence of an iron absorption inhibitor, bathophenanthroline disulfonic acid (BPDS). Ferritin formation in the cells was used as the indicator of iron uptake. Uptake from all three Fe sources was similar in the absence of AA. Adding AA at a 5:1 molar excess as compared to Fe increased uptake by 5.4-, 5.1-, and 2.8-fold for FeSO4, FeCl3, and NaFeEDTA, respectively. The smaller effect of AA on uptake from NaFeEDTA may be related to the higher solubility of NaFeEDTA and/or the strong binding affinity of EDTA for Fe3+, which may prevent AA and duodenal cytochrome b from effectively reducing EDTA-bound Fe. Uptake was inversely related to the pH of the media over a range of 5.8-7.2. Because uptake by DMT-1 is proton-coupled, the inverse relationship between pH and Fe uptake in all three iron sources suggests that they all follow the DMT-1 pathway into the cell. Adding BPDS to the media inhibited uptake from all three iron compounds equally. Because BPDS binds Fe2+ but not Fe3+ and because only Fe2+ is transported by DMT-1, the finding that BPDS inhibited uptake from NaFeEDTA suggests that at least some iron dissociates from EDTA and is reduced just as simple inorganic iron at the brush border membrane of the enterocyte. Taken together, these results suggest that uptake of iron from NaFeEDTA by intestinal enterocytes is regulated similarly to uptake from iron salts.

  17. His86 from the N-terminus of frataxin coordinates iron and is required for Fe-S cluster synthesis

    PubMed Central

    Gentry, Leslie E.; Thacker, Matthew A.; Doughty, Reece; Timkovich, Russell; Busenlehner, Laura S.

    2013-01-01

    Human frataxin has a vital role in the biosynthesis of iron–sulfur (Fe-S) clusters in mitochondria and its deficiency causes the neurodegenerative disease Friedreich’s ataxia. Proposed functions for frataxin in the Fe-S pathway include iron donation to the Fe-S cluster machinery and regulation of cysteine desulfurase activity to control the rate of Fe-S production, although further molecular detail is required to distinguish these two possibilities. It is well established that frataxin can coordinate iron using glutamate and aspartate side chains on the protein surface; however, in this work we identify a new iron coordinating residue in the Nterminus of human frataxin using complementary spectroscopic and structural approaches. Further, we demonstrate that His86 in this N-terminal region is required for high affinity iron coordination and iron assembly of Fe-S clusters by ISCU as part of the Fe-S cluster biosynthetic complex. If a binding site that includes His86 is important for Fe-S cluster synthesis as part of its chaperone function, this raises the possibility that either iron binding at the acidic surface of frataxin may be spurious or that it is required for protein–protein interactions with the Fe-S biosynthetic quaternary complex. Our data suggest that iron coordination to frataxin may be significant to the Fe-S cluster biosynthesis pathway in mitochondria. PMID:23909240

  18. Nanostructure evolution in joining of Al and Fe nanoparticles with femtosecond laser irradiation

    SciTech Connect

    Jiao, Z.; Huang, H.; Zhou, Y. E-mail: nzhou@uwaterloo.ca; Liu, L.; Hu, A.; Duley, W.; He, P. E-mail: nzhou@uwaterloo.ca

    2014-04-07

    The joining of Al-Fe nanoparticles (NPs) by femtosecond (fs) laser irradiation is reported in this paper. Fe and Al NPs were deposited on a carbon film in vacuum via fs laser ablation. Particles were then exposed to multiple fs laser pulses at fluences between 0.5 and 1.3 mJ/cm{sup 2}. Transmission Electron Microscopy (TEM) and Electron Diffraction X-ray observations indicate that Al and Fe NPs bond to each other under these conditions. For comparison, bonding of Al to Al and Fe to Fe NPs was also investigated. The nanostructure, as observed using TEM, showed that individual Al NPs were monocrystalline while individual Fe NPs were polycrystalline prior to joining and that these structures are retained after the formation of Al-Al and Fe-Fe NPs. Al-Fe NPs produced by fs laser joining exhibited a mixed amorphous and crystalline phase at the interface. Bonding is suggested to originate from intermixing within a region of high field intensity between particles.

  19. Ba2F2Fe(1.5)Se3: An Intergrowth Compound Containing Iron Selenide Layers.

    PubMed

    Driss, Dalel; Janod, Etienne; Corraze, Benoit; Guillot-Deudon, Catherine; Cario, Laurent

    2016-03-21

    The iron selenide compound Ba2F2Fe(1.5)Se3 was synthesized by a high-temperature ceramic method. The single-crystal X-ray structure determination revealed a layered-like structure built on [Ba2F2](2+) layers of the fluorite type and iron selenide layers [Fe(1.5)Se3](2-). These [Fe1.5Se3](2-) layers contain iron in two valence states, namely, Fe(II+) and Fe(III+) located in octahedral and tetrahedral sites, respectively. Magnetic measurements are consistent with a high-spin state for Fe(II+) and an intermediate-spin state for Fe(III+). Moreover, susceptibility and resistivity measurements demonstrate that Ba2F2Fe(1.5)Se3 is an antiferromagnetic insulator.

  20. Formation of a paramagnetic Al complex and extrusion of Fe during the reaction of (diiminepyridine)Fe with AlR3 (R = Me, Et).

    PubMed

    Scott, Jennifer; Gambarotta, Sandro; Korobkov, Ilia; Knijnenburg, Quinten; de Bruin, Bas; Budzelaar, Peter H M

    2005-12-14

    The reaction of the {2,6-[2,6-(iPr)2PhN=C(CH3)]2(C5H3N)}FeCl2 catalyst precursor with R3Al [R = Me, Et] afforded {2,6-[2,6-(iPr)2PhN=C(CH3)]2(C5H3N)}AlMe2 (1) and [eta4-LAl2Et3(mu-Cl)]Fe-(eta6-C7H8) (2), respectively. These paramagnetic species arises from both transmetalation, during which the strong terdentate ligand loses the Fe center, and reduction. The extent of reduction depends on the nature of the Al alkylating agent. The electrons necessary for the reduction are likely to be provided by cleavage of Fe-C bond of transient low-valent organo-Fe species.

  1. Uranium(VI) reduction by nanoscale zero-valent iron in anoxic batch systems: The role of Fe(II) and Fe(III)

    SciTech Connect

    Yan, Sen; Chen, Yongheng; Xiang, Wu; Bao, Zhengyu; Liu, Chongxuan; Deng, Baolin

    2014-12-01

    The role of Fe(II) and Fe(III) on U(VI) reduction by nanoscale zerovalent iron (nanoFe0) was investigated using two iron chelators 1,10-phenanthroline and triethanolamine (TEA) under a CO2-free anoxic condition. The results showed U(VI) reduction was strongly inhibited by 1,10-phenanthroline and TEA in a pH range from 6.92 to 9.03. For instance, at pH 6.92 the observed U(VI) reduction rates decreased by 80.7% and 82.3% in the presence of 1,10-phenanthroline and TEA, respectively. The inhibition was attributed to the formation of stable complexes between 1,10-phenanthroline and Fe(II) or TEA and Fe(III). In the absence of iron chelators, U(VI) reduction can be enhanced by surface-bound Fe(II) on nanoFe0. Our results suggested that Fe(III) and Fe(II) probably acted as an electron shuttle to mediate the transfer of electrons from nanoFe0 to U(VI), therefore a combined system with Fe(II), Fe(III) and nanoFe0 can facilitate the U(VI) reductive immobilization in the contaminated groundwater.

  2. High stability of magnetic parameters in Fe-Al nanocomposite powders

    NASA Astrophysics Data System (ADS)

    Jani, S.; Sebastian, V.; Sudheesh, V.; Nehra, J.; Lakshmi, N.; Venugopalan, K.

    2016-09-01

    The structural and magnetic properties of Fe75Al25 nanosystem prepared by high energy ball milling for 15 h milling time have been studied. Structural analysis shows the formation of distinct Fe-Al portions with Al at grain boundaries, indicating that Fe-Al nanocomposite formation is favored over alloying due to the formation of diffusion hindering Fe-Al phase at grain boundaries. The saturation magnetization (Ms) of the nanocomposite at 8 nm grain size is 117 emu/g (i.e. 55 % that of pure Fe). The Curie temperature (TC) 1053 K matches the value of pure bcc α-Fe. M-H curves recorded after M-T studies are the same as before indicating the extreme stability of this system against high temperatures. Low temperature M-T measurements and room temperature remanence measurements show that interparticle interactions are demagnetizing kind and dipolar in nature.

  3. Correlation Of 2-Chlorobiphenyl Dechlorination By Fe/Pd With Iron Corrosion At Different pH

    EPA Science Inventory

    The rate of 2-chlorobiphenyl dechlorination by palladized iron (Fe/Pd) decreased with increasing pH until pH > 12.5. Iron corrosion potential (Ec) and current (jc), obtained from polarization curves of a rotating disk electrode of iron, followed the Tafel e...

  4. Microbial Fe(III) oxide reduction and Fe cycling in iron-rich freshwater wetland sediments

    SciTech Connect

    Roden, E.E.

    1995-12-31

    The dynamics of Fe cycling and the interaction between microbial Fe(III) oxide reduction and other anaerobic microbial respiratory processes were examined in Fe-rich, sulfate-poor freshwater wetland sediments. Sediment incubation experiments demonstrated that reduction of Fe(III) oxides (amorphous, soluble in dilute HCl) dominated anaerobic carbon mineralization at Fe(III) concentrations in excess of 10 mmol per liter wet sediment. The kinetics of Fe(III) reduction were found to be first-order with respect to the concentration of Fe(III) oxide, although estimated first-order rate constants varied in relation to the absolute rates of Fe(III) reduction, suggesting a co-dependency on the concentration of easily degradable organic carbon. High concentrations of amorphous Fe(III) oxides (10-100 mmol L wet sed {sup -1}) were found in surface sediments (0-3 cm) of unvegetated zones of the wetland and in the rhizosphere (0-10 cm) of emergent aquatic plants, sufficient (based on sediment incubation experiments) to allow Fe(III)-reducing bacteria (FeRB) to dominate anaerobic carbon mineralization. A rapid redox cycling of Fe is apparent in these localized zones based on observed rates of Fe(III) reduction and the abundance/depth distribution of Fe(Ill) oxides. Preliminary culture enrichment studies indicate that FeRB present in these sediments are capable of metabolizing a range of both natural and contaminant aromatic hydrocarbons, which suggests a potential for utilization of natural and/or artificial Fe-rich wetland systems for organic contaminant bioremediation.

  5. Enhanced Homogenization of Vanadium in Spark Plasma Sintering of Ti-10V-2Fe-3Al Alloy from Titanium and V-Fe-Al Master Alloy Powder Blends

    NASA Astrophysics Data System (ADS)

    Yang, Y. F.; Imai, H.; Kondoh, K.; Qian, M.

    2017-02-01

    Strong and ductile powder metallurgy (PM) Ti-10V-2Fe-3Al alloy has been fabricated by spark plasma sintering (SPS) of titanium and V-Fe-Al master alloy powder blends at 1100°C for 30 min under 30 MPa. The homogenization of vanadium, which dictates the realization of a uniform microstructure of the Ti-10V-2Fe-3Al alloy, was markedly accelerated by SPS. The mechanism is attributed to the intensive Joule heating effect produced by the direct current passing through the electric conducting powder blends, rather than through spark plasma discharge, because homogenization occurred mainly after near full identification had been achieved. The chemical and microstructural homogeneity ensured the achievement of excellent tensile properties of PM Ti-10V-2Fe-3Al in the as-sintered state, with tensile strength >1250 MPa and elongation >10%.

  6. Brillouin light scattering study of Co2Cr0.6Fe0.4Al and Co2FeAl Heusler compounds

    NASA Astrophysics Data System (ADS)

    Gaier, O.; Hamrle, J.; Trudel, S.; Conca Parra, A.; Hillebrands, B.; Arbelo, E.; Herbort, C.; Jourdan, M.

    2009-04-01

    The thermal magnonic spectra of Co2Cr0.6Fe0.4Al (CCFA) and Co2FeAl were investigated using Brillouin light scattering (BLS) spectroscopy. For CCFA, the exchange constant A (exchange stiffness D) is found to be 0.48 ± 0.04 µerg cm-1 (203 ± 16 meV Å2), while for Co2FeAl the corresponding values of 1.55 ± 0.05 µerg cm-1 (370 ± 10 meV Å2) were found. The observed asymmetry in the BLS spectra between the Stokes and anti-Stokes frequencies was assigned to an interplay between the asymmetrical profiles of hybridized Damon-Esbach and perpendicular standing spin-wave modes, combined with the optical sensitivity of the BLS signal to the upper side of the CCFA or Co2FeAl film.

  7. Al13Fe4 as a low-cost alternative for palladium in heterogeneous hydrogenation

    NASA Astrophysics Data System (ADS)

    Armbrüster, M.; Kovnir, K.; Friedrich, M.; Teschner, D.; Wowsnick, G.; Hahne, M.; Gille, P.; Szentmiklósi, L.; Feuerbacher, M.; Heggen, M.; Girgsdies, F.; Rosenthal, D.; Schlögl, R.; Grin, Yu.

    2012-08-01

    Replacing noble metals in heterogeneous catalysts by low-cost substitutes has driven scientific and industrial research for more than 100 years. Cheap and ubiquitous iron is especially desirable, because it does not bear potential health risks like, for example, nickel. To purify the ethylene feed for the production of polyethylene, the semi-hydrogenation of acetylene is applied (80 × 106 tons per annum refs , , ). The presence of small and separated transition-metal atom ensembles (so-called site-isolation), and the suppression of hydride formation are beneficial for the catalytic performance. Iron catalysts necessitate at least 50 bar and 100 °C for the hydrogenation of unsaturated C-C bonds, showing only limited selectivity towards semi-hydrogenation. Recent innovation in catalytic semi-hydrogenation is based on computational screening of substitutional alloys to identify promising metal combinations using scaling functions and the experimental realization of the site-isolation concept employing structurally well-ordered and in situ stable intermetallic compounds of Ga with Pd (refs , , , , ). The stability enables a knowledge-based development by assigning the observed catalytic properties to the crystal and electronic structures of the intermetallic compounds. Following this approach, we identified the low-cost and environmentally benign intermetallic compound Al13Fe4 as an active and selective semi-hydrogenation catalyst. This knowledge-based development might prove applicable to a wide range of heterogeneously catalysed reactions.

  8. Oxygenic photosynthesis as a protection mechanism for cyanobacteria against iron-encrustation in environments with high Fe2+ concentrations

    PubMed Central

    Ionescu, Danny; Buchmann, Bettina; Heim, Christine; Häusler, Stefan; de Beer, Dirk; Polerecky, Lubos

    2014-01-01

    If O2 is available at circumneutral pH, Fe2+ is rapidly oxidized to Fe3+, which precipitates as FeO(OH). Neutrophilic iron oxidizing bacteria have evolved mechanisms to prevent self-encrustation in iron. Hitherto, no mechanism has been proposed for cyanobacteria from Fe2+-rich environments; these produce O2 but are seldom found encrusted in iron. We used two sets of illuminated reactors connected to two groundwater aquifers with different Fe2+ concentrations (0.9 μM vs. 26 μM) in the Äspö Hard Rock Laboratory (HRL), Sweden. Cyanobacterial biofilms developed in all reactors and were phylogenetically different between the reactors. Unexpectedly, cyanobacteria growing in the Fe2+-poor reactors were encrusted in iron, whereas those in the Fe2+-rich reactors were not. In-situ microsensor measurements showed that O2 concentrations and pH near the surface of the cyanobacterial biofilms from the Fe2+-rich reactors were much higher than in the overlying water. This was not the case for the biofilms growing at low Fe2+ concentrations. Measurements with enrichment cultures showed that cyanobacteria from the Fe2+-rich environment increased their photosynthesis with increasing Fe2+ concentrations, whereas those from the low Fe2+ environment were inhibited at Fe2+ > 5 μM. Modeling based on in-situ O2 and pH profiles showed that cyanobacteria from the Fe2+-rich reactor were not exposed to significant Fe2+ concentrations. We propose that, due to limited mass transfer, high photosynthetic activity in Fe2+-rich environments forms a protective zone where Fe2+ precipitates abiotically at a non-lethal distance from the cyanobacteria. This mechanism sheds new light on the possible role of cyanobacteria in precipitation of banded iron formations. PMID:25228899

  9. Infrared Brazing Fe3Al Using Ag-Based Filler Metals

    NASA Astrophysics Data System (ADS)

    Shiue, Ren-Kae; Li, Yao; Wu, Shyi-Kaan; Wu, Ling-Mei

    2010-11-01

    The microstructural evolution and bonding shear strength of infrared brazed Fe3Al using Ag and BAg-8 (72Ag-28Cu in wt pct) braze alloys have been studied. The Ag-rich phase alloyed with Al dominates the entire Ag brazed joints, and the shear strength is independent of the brazing time. The BAg-8 brazed joint contains Ag-Cu eutectic for all brazing conditions, and its shear strength increases slightly with increasing brazing time. The highest shear strength of 181 MPa is acquired from the joint infrared brazed at 1073 K (800 °C) for 600 seconds. A thin layer of Fe3Al is identified at the interface between the brazed zone and the substrate for both braze alloys. An Al depletion zone in the Fe3Al substrate next to the interfacial Fe3Al is identified as the α-Fe phase. The dissolution of Al from the Fe3Al substrate into the molten braze causes the formation of α-Fe in the Fe3Al substrate.

  10. THE IRON PROJECT AND THE RMAX PROJECT: Photoionization, Electron-IonRecombination and Oscillator Strengths of Fe Ions, Fe XVII and Fe XIX

    NASA Astrophysics Data System (ADS)

    Eissner, Werner; Nahar, Sultana; Pradhan, Anil

    2010-03-01

    The aims of the Iron Project and the Rmax Project are detailed study of radiative and collisional processes of astrophysically abundant atoms and ions, mainly iron and iron-peak elements, over a wide energy range, from infra-red to X-rays. We will present the complete results on photoionization, partial and total, of fine structure levels with n <= 10 of Fe XVII. They correspond to a large-scale computation using a wave function expansion containing 60 levels of the core. Preliminary results on total recombination rate coefficients ranging over low to very high temperatures, especially where the ion is abundant in astrophysical plasmas, will be presented. We will also report the latest results on oscillator strengths for photo-excitations in Fe XIX. This highly charged nitrogen-like iron ion has over thousands of bound fine structure levels. The calculations have been carried out in relativistic Breit-Pauli R-matrix (BPRM) method. The forbidden electric quadrupole, electric octupole, magnetic dipole and magnetic quadrupole transitions for Fe XIX correspond to fine structure levels upto 4p obtained from atomic structure calculations in Breit-Pauli approximation.

  11. High-temperature corrosion behavior of coatings and ODS alloys based on Fe{sub 3}Al

    SciTech Connect

    Tortorelli, P.F.; Pint, B.A.; Wright, I.G.

    1996-08-01

    Iron-aluminide coatings were prepared by gas tungsten arc and gas metal arc weld-overlay techniques. All the weld overlays showed good oxidation/sulfidation behavior under isothermal conditions, including a gas metal arc deposit with only 21 at.% Al. A rapid degradation in corrosion resistance was observed under thermal cycling conditions when the initially grown scales spalled and the subsequent rate of reaction was not controlled by the formation of slowly growing aluminum oxides. Higher starting aluminum concentrations (>{approximately}25 at.%) are needed to assure adequate oxidation/sulfidation lifetimes of the weld overlays. A variety of stable oxides was added to a base Fe-28 at.% Al-2 % Cr alloy to assess the effect of these dopants on the oxidation behavior at 1200{degrees}C. A Y{sub 2}O{sub 3} dispersion improved the scale adhesion relative to a Zr alloy addition, but wasn`t as effective as it is in other alumina-forming alloys. Preliminary data for powder-processed Fe-28 at.% Al-2% Cr exposed to the H{sub 2}S-H{sub 2}-H{sub 2}O-Ar gas at 800{degrees}C showed that the oxidation/sulfidation rate was similar to that of many Fe{sub 3}Al alloys produced by ingot metallurgy routes.

  12. Temperature control of the growth of iron oxide nanoislands on Fe(001)

    NASA Astrophysics Data System (ADS)

    Kazu Yamada, Toyo; Sakaguchi, Yuki; Gerhard, Lukas; Wulfhekel, Wulf

    2016-08-01

    The control of atomically flat interfaces between iron (Fe) and insulating oxide films, such as the Fe/MgO(001) interface, is crucial for tunnel-magnetoresistance (TMR) devices. However, the realization of an ideal atomically flat and clean interface is rather difficult since iron easily binds to impurities such as oxygen. Atomic step defects and iron oxide at the interface could reduce TMR. In this study, the oxidization of an atomically flat and clean Fe(001)-whisker single crystal at different substrate and annealing temperatures was investigated with an ultrahigh-vacuum scanning tunneling microscope (STM). Annealing up to a temperature of 850 K was required to obtain ordered and atomically flat Fe(001)-p(1×1)O terraces after the oxidization with the coexistence of Fe-O nanoislands (˜1 nm in height, ˜50 nm in size). We found that the growth of such nanoislands, which enhances interface roughness, strongly depends on the substrate temperature (T S) during the oxidization. A T S lower than 300 K reduces the coverage by the nanoislands to less than 10%.

  13. The Effect of Iron Fortification on Iron (Fe) Status and Inflammation: A Randomized Controlled Trial

    PubMed Central

    Ma, Jingqiu; Sun, Qianqian; Liu, Jinrong; Hu, Yanqi; Liu, Shanshan; Zhang, Jie; Sheng, Xiaoyang; Hambidge, K. Michael

    2016-01-01

    Background Iron deficiency (ID) is common in toddlers in developing countries. Iron fortified or meat-based complementary foods may be effective to prevent ID. Objective Our objective was to compare iron status at 18 months and growth from 6 to 18 months in rural poor toddlers fed 3 different complementary foods. Methods The study was nested within a larger trial in which 6-month-old infants were randomized to receive 50g/d meat (MG), an equi-caloric fortified cereal supplement (FG) or local cereal supplement (LG) for 1 year. Hb, sTfR, HsCRP, ferritin and AGP were measured in 410 blood samples collected by a random sampling (MG, 137; FG, 140; LG, 133); calprotectin was measured in feces. Body iron = -[log (sTfR ×1000/ferritin)-2.8229] /0.1207. ID = ferritin<12ug/L. Results The toddlers in FG had the significantly highest levels in serum ferritin and body iron (P = 0.043, 0.004), and the rates of both ID and iron deficiency anemia (IDA) were the lowest in FG (P = 0.010, 0.021). The rate of systemic inflammation in FG was 30.71%, which was the highest among three groups (P = 0.042). No intervention effects on either the rates of ID and IDA or iron stores (serum ferritin and body iron) were shown in MG. The change in length-for-age z scores (LAZ) from 6 to 18 months among three groups was significantly different (P = 0.021) and a smaller decrease of LAZ in MG and a larger decrease of LAZ in FG were observed. Conclusion Iron fortified cereal improved iron status of poor rural toddlers but was also associated with systemic inflammation which was likely to impair their growth. PMID:27923057

  14. Binding of ligands containing carbonyl and phenol groups to iron(iii): new Fe6, Fe10 and Fe12 coordination clusters.

    PubMed

    Kitos, Alexandros A; Papatriantafyllopoulou, Constantina; Tasiopoulos, Anastasios J; Perlepes, Spyros P; Escuer, Albert; Nastopoulos, Vassilios

    2017-03-07

    The initial use of ligands 2'-hydroxyacetophenone (HL(1)), 2-hydroxybenzophenone (HL(2)) and 2,2'-dihydroxybenzophenone (H2L(3)) in iron(iii) chemistry is described. The syntheses and crystal structures are reported for five iron(iii) clusters: [Fe10O4(OMe)14(L(1))6(MeOH)2](NO3)2·3MeOH (1·3MeOH), [Fe12O4(OH)(OMe)17(L(1))8](ClO4)2·2H2O (2·2H2O), [Fe10O4(OMe)14Cl4(L(2))4(MeOH)2] (3), [Fe10O4(OMe)14(L(2))6(py)2](ClO4)2·MeOH (4·MeOH), where py = pyridine, and [Fe6O2(OEt)6(O2CMe)2(L(3))2(HL(3))2] (5). The molecular structures of the decanuclear clusters 1, 3 and 4 are organized around a {Fe10(μ4-O)4(μ3-OMe)2(μ-OMe)12}(8+) core consisting of ten {Fe3O4} face-sharing defective cubane units. The core of 2 consists of a {Fe12(μ4-O)4(μ3-OMe)4(μ-OH)(μ-OMe)13}(10+) unit composed of twelve {Fe3O4} face-sharing defective cubanes. The ligands (L(1))(-) and (L(2))(-) in 1-4 adopt the O,O'-bidentate chelating coordination mode and their roles are to terminate the further aggregation of the Fe(III)/O(2-)/RO(-) cores. Complex 5 contains the {Fe6(μ4-O)2(μ-OEt)6(μ-Ocarbonyl)2}(4+) core, where the μ-Ocarbonyl atoms are the bridging carbonyl oxygens of the two η(1):η(2):η(1):μ (L(3))(2-) ligands; the (HL(3))(-) groups behave as Ophenolate, Ocarbonyl-bidentate chelating ligands with the neutral hydroxyl group being unbound to the Fe(III) atoms. The core is composed of four {Fe3O4} face-sharing defective cubanes. The Fe(III) atoms in 1-5 are all six-coordinate with distorted octahedral geometries. The IR spectra of the complexes are discussed in terms of the known coordination modes of the ligands and the ionic character of nitrates and perchlorates. Variable-temperature magnetic susceptibility and variable-field magnetization measurements establish that 2, 3 and 5 have S = 3, 0 and 5 ground states, respectively. The susceptibility data for 5 were fitted using a 3-J model indicating the simultaneous presence of both antiferromagnetic and ferromagnetic Fe(III)Fe

  15. Effect of rapid solidification on the microstructure and mechanical properties of hot-pressed Al-20Si-5Fe alloys

    SciTech Connect

    Rajabi, M.; Vahidi, M.; Simchi, A.; Davami, P.

    2009-11-15

    The aim of this work is to study the effect of cooling rate and subsequent hot consolidation on the microstructural features and mechanical strength of Al-20Si-5Fe-2X (X = Cu, Ni and Cr) alloys. Powder and ribbons were produced by gas atomization and melt spinning processes at two different cooling rates of 1 x 10{sup 5} K/s and 5 x 10{sup 7} K/s. The microstructure of the products was examined using optical microscopy, scanning electron microscopy, transmission electron microscopy, and X-ray diffraction. The particles were consolidated by hot pressing at 400 deg. C/250 MPa/1 h under a high purity argon atmosphere and the microstructure, hardness and compressive strength of the compacts were evaluated. Results showed a profound effect of the cooling rate, consolidation stage, and transition metals on the microstructure and mechanical strength of Al-20Si-5Fe alloys. While microstructural refining was obtained at both cooling rates, the microstructure of the atomized powder exhibited the formation of fine primary silicon ({approx} 1 {mu}m), eutectic Al-Si phase with eutectic spacing of {approx} 300 nm, and {delta}-iron intermetallic. Supersaturated Al matrix containing 5-7 at.% silicon and nanometric Si precipitates (20-40 nm) were determined in the microstructure of the melt-spun ribbons. The hot consolidation resulted in coarsening of Si particles in the atomized particles, and precipitation of Si and Fe-containing intermetallics from the supersaturated Al matrix in the ribbons. The consolidated ribbons exhibited higher mechanical strength compared to the atomized powders, particularly at elevated temperatures. The positive influence of the transition metals on the thermal stability of the Al-20Si-5Fe alloy was noticed, particularly in the Ni-containing alloy.

  16. Studies on water transport through the sweet cherry fruit surface. 7. Fe3+ and Al3+ reduce conductance for water uptake.

    PubMed

    Beyer, Marco; Peschel, Stefanie; Weichert, Holger; Knoche, Moritz

    2002-12-18

    The effects of the chloride salts LiCl, CaCl(2), MgCl(2), AlCl(3), EuCl(3), and FeCl(3) and the iron salts FeCl(2), FeCl(3), Fe(NO(3))(3), FeSO(4), and Fe(2)(SO(4))(3) on water conductance of exocarp segments (ES) and rates of water uptake into detached sweet cherry fruit (Prunus avium L. cv. Adriana, Early Rivers, Namare, Namosa, and Sam) were studied. ES were excised from the cheek of mature fruit and mounted in stainless steel diffusion cell; water penetration was monitored gravimetrically from donor solutions containing the above mineral salts into a PEG 6000 (osmolality = 1.14 osM, pH 4.8, 25 degrees C) receiver solution. Conductance of ES was calculated from the amount of water taken up per unit of surface area and time by dividing by the gradient in water activity across ES. LiCl, CaCl(2), MgCl(2), FeCl(2), and FeSO(4) had no significant effect on conductance, but AlCl(3), FeCl(3), Fe(NO(3))(3), and Fe(2)(SO(4))(3) significantly reduced conductance compared to water only as a donor. Also, EuCl(3) lowered conductance; however, this effect was not always significant. Effects of salts on water conductance of ES and rates of water uptake into detached fruit were closely related (R 2 = 0.97***). Upon application of an FeCl(3)-containing donor conductance decreased instantaneously. FeCl(3) concentrations of <6.6 x 10(-)(4) M had no effect on conductance, but concentrations at or above this threshold decreased conductance. FeCl(3) lowered water conductance at a receiver pH of 4.8, but not at pH < or =2.6. The effect of FeCl(3) on conductance was largest in cv. Namare and smallest in cv. Adriana. There was no significant effect of FeCl(3) on conductance for transpiration. Formation of aluminum and iron oxides and hydroxides in the exocarp as a result of a pH gradient between donor and receiver solution is discussed as the potential mechanism for Fe(3+) and Al(3+) reducing conductance for water uptake.

  17. The role of microaerophilic Fe-oxidizing micro-organisms in producing banded iron formations.

    PubMed

    Chan, C S; Emerson, D; Luther, G W

    2016-09-01

    Despite the historical and economic significance of banded iron formations (BIFs), we have yet to resolve the formation mechanisms. On modern Earth, neutrophilic microaerophilic Fe-oxidizing micro-organisms (FeOM) produce copious amounts of Fe oxyhydroxides, leading us to wonder whether similar organisms played a role in producing BIFs. To evaluate this, we review the current knowledge of modern microaerophilic FeOM in the context of BIF paleoenvironmental studies. In modern environments wherever Fe(II) and O2 co-exist, microaerophilic FeOM proliferate. These organisms grow in a variety of environments, including the marine water column redoxcline, which is where BIF precursor minerals likely formed. FeOM can grow across a range of O2 concentrations, measured as low as 2 μm to date, although lower concentrations have not been tested. While some extant FeOM can tolerate high O2 concentrations, many FeOM appear to prefer and thrive at low O2 concentrations (~3-25 μm). These are similar to the estimated dissolved O2 concentrations in the few hundred million years prior to the 'Great Oxidation Event' (GOE). We compare biotic and abiotic Fe oxidation kinetics in the presence of varying levels of O2 and show that microaerophilic FeOM contribute substantially to Fe oxidation, at rates fast enough to account for BIF deposition. Based on this synthesis, we propose that microaerophilic FeOM were capable of playing a significant role in depositing the largest, most well-known BIFs associated with the GOE, as well as afterward when global O2 levels increased.

  18. CEMS study of defect annealing in Fe implanted AlN

    NASA Astrophysics Data System (ADS)

    Bharuth-Ram, K.; Geburt, S.; Ronning, C.; Masenda, H.; Naidoo, D.

    2016-12-01

    An AlN thin film grown on sapphire substrate was implanted with 45 keV 57Fe and 56Fe ions at several energies to achieve a homogeneous concentration profile of approximately 2.6 at.%. in the AlN film. Conversion electron Mössbauer Spectroscopy data were collected after annealing the sample up to 900 °C. The spectra were fitted with three components, a single line attributed to small Fe clusters, and two quadrupole split doublets attributed to Fe substituting Al in the wurtzite AlN lattice and to Fe located in implantation induced lattice damage. The damage component shows significant decrease on annealing up to 900 °C, accompanied by corresponding increases in the singlet component and the substitutional Fe.

  19. Formation of pyrite (FeS{sub 2}) thin films by thermal sulfurization of dc magnetron sputtered iron

    SciTech Connect

    Soukup, R. J.; Prabukanthan, P.; Ianno, N. J.; Sarkar, A.; Kamler, C. A.; Sekora, D. G.

    2011-01-15

    Iron films deposited by direct current magnetron sputtering onto glass substrates were converted into FeS{sub 2} films by thermal sulfurization. Experiments were carried out to optimize the sulfurization process, and the formation of FeS{sub 2} thin films was investigated under different annealing temperatures and times. High quality FeS{sub 2} films were fabricated using this process, and single phase pyrite films were obtained after sulfurization in a sulfur and nitrogen atmosphere at 450 deg. C for 1 h. Film crystallinity and phase identification were determined by using x-ray diffraction. The cubic phase pyrite films prepared were p-type, and scanning electron microscopy studies exhibited a homogeneous surface of pyrite. The authors have found that the best Ohmic contact for their pyrite thin films, using inexpensive metals, was Ni. The following were chosen for the study: Al, Mo, Fe, and Ni, and the one that led to the lowest resistance, 333 {Omega}, was Ni.

  20. Effect of Composite Fabrication on the Strength of Single Crystal Al2O3 Fibers in Two Fe-Base Alloy Composites

    NASA Technical Reports Server (NTRS)

    Draper, Susan L.; Aiken, Beverly J. M.

    1998-01-01

    Continuous single-crystal Al2O3 fibers have been incorporated into a variety of metal and intermetallic matrices and the results have consistently indicated that the fiber strength had been reduced by 32 to 50% during processing. Two iron-based alloys, FeNiCoCrAl and FeAlVCMn, were chosen as matrices for Al2O3 fiber reinforced metal matrix composites (MMC) with the goal of maintaining Al2O3 fiber strength after composite processing. The feasibility of Al2O3/FeNiCoCrAl and Al2O3/FeAlVCMn composite systems for high temperature applications were assessed in terms of fiber-matrix chemical compatibility, interfacial bond strength, and composite tensile properties. The strength of etched-out fibers was significantly improved by choosing matrices containing less reactive elements. The ultimate tensile strength (UTS) values of the composites could generally be predicted with existing models using the strength of etched-out fibers. However, the UTS of the composites were less than desired due to a low fiber Weibull modulus. Acoustic emission analysis during tensile testing was a useful tool for determining the efficiency of the fibers in the composite and for determining the failure mechanism of the composites.

  1. Iron nanoparticle growth induced by Kr-F excimer laser photolysis of Fe(CO)5

    NASA Astrophysics Data System (ADS)

    Eremin, A. V.; Gurentsov, E. V.; Priemchenko, K. Yu

    2013-06-01

    In this article the process of nanoparticle formation under the condensation of highly supersaturated atomic vapor produced by the photodissociation of metal-bearing compounds was investigated. The iron nanoparticles were synthesized by Kr-F laser pulse photolysis of Fe(CO)5. The measurements of an optical density of condensed phase were performed using a laser light extinction at a wavelength 633 nm. The particle size during their formation process was measured by a two-color time-resolved laser-induced incandescence. The final iron particle sizes and their structure were analyzed by a transmission electron microscopy. It has been shown that the process of iron particle formation in the investigated conditions could be divided onto three stages: the fast nucleation of iron atoms during 1-2 μs, the surface growth of particles up to the sizes of 1-6 nm with increasing volume fraction of condensed phase during 100-250 μs, and the relatively slow particle coagulation up to the final sizes of 5-9 nm. The effective rate constants of iron clusters and particle growth were extracted using laser light extinction measurements. The essential role of the reactions of iron clusters and particles with the parental Fe(CO)5 molecules was established. The kinetic mechanism of iron nanoparticle growth induced by photo-dissociation of Fe(CO)5 at room temperature based on obtained experimental results and known literature data has been suggested. The results obtained could be used for the developments of methods of synthesis of catalysts, magnetic nanopowders, and others nanomaterials at room temperature. Besides that, the presented experimental data could be useful for the validation of kinetic models of gas-phase condensation of supersaturated vapor of solids.

  2. Fe electron transfer and atom exchange in goethite: influence of Al-substitution and anion sorption.

    PubMed

    Latta, Drew E; Bachman, Jonathan E; Scherer, Michelle M

    2012-10-02

    The reaction of Fe(II) with Fe(III) oxides and hydroxides is complex and includes sorption of Fe(II) to the oxide, electron transfer between sorbed Fe(II) and structural Fe(III), reductive dissolution coupled to Fe atom exchange, and, in some cases mineral phase transformation. Much of the work investigating electron transfer and atom exchange between aqueous Fe(II) and Fe(III) oxides has been done under relatively simple aqueous conditions in organic buffers to control pH and background electrolytes to control ionic strength. Here, we investigate whether electron transfer is influenced by cation substitution of Al(III) in goethite and the presence of anions such as phosphate, carbonate, silicate, and natural organic matter. Results from (57)Fe Mössbauer spectroscopy indicate that both Al-substitution (up to 9%) and the presence of common anions (PO(4)(3-), CO(3)(2-), SiO(4)(4-), and humic acid) does not inhibit electron transfer between aqueous Fe(II) and Fe(III) in goethite under the conditions we studied. In contrast, sorption of a long-chain phospholipid completely shuts down electron transfer. Using an enriched isotope tracer method, we found that Al-substitution in goethite (10%), does, however, significantly decrease the extent of atom exchange between Fe(II) and goethite (from 43 to 12%) over a month's time. Phosphate, somewhat surprisingly, appears to have little effect on the rate and extent of atom exchange between aqueous Fe(II) and goethite. Our results show that electron transfer between aqueous Fe(II) and solid Fe(III) in goethite can occur under wide range of geochemical conditions, but that the extent of redox-driven Fe atom exchange may be dependent on the presence of substituting cations such as Al.

  3. Soft chemical control of superconductivity in lithium iron selenide hydroxides Li(1-x)Fe(x)(OH)Fe(1-y)Se.

    PubMed

    Sun, Hualei; Woodruff, Daniel N; Cassidy, Simon J; Allcroft, Genevieve M; Sedlmaier, Stefan J; Thompson, Amber L; Bingham, Paul A; Forder, Susan D; Cartenet, Simon; Mary, Nicolas; Ramos, Silvia; Foronda, Francesca R; Williams, Benjamin H; Li, Xiaodong; Blundell, Stephen J; Clarke, Simon J

    2015-02-16

    Hydrothermal synthesis is described of layered lithium iron selenide hydroxides Li(1-x)Fe(x)(OH)Fe(1-y)Se (x ∼ 0.2; 0.02 < y < 0.15) with a wide range of iron site vacancy concentrations in the iron selenide layers. This iron vacancy concentration is revealed as the only significant compositional variable and as the key parameter controlling the crystal structure and the electronic properties. Single crystal X-ray diffraction, neutron powder diffraction, and X-ray absorption spectroscopy measurements are used to demonstrate that superconductivity at temperatures as high as 40 K is observed in the hydrothermally synthesized samples when the iron vacancy concentration is low (y < 0.05) and when the iron oxidation state is reduced slightly below +2, while samples with a higher vacancy concentration and a correspondingly higher iron oxidation state are not superconducting. The importance of combining a low iron oxidation state with a low vacancy concentration in the iron selenide layers is emphasized by the demonstration that reductive postsynthetic lithiation of the samples turns on superconductivity with critical temperatures exceeding 40 K by displacing iron atoms from the Li(1-x)Fe(x)(OH) reservoir layer to fill vacancies in the selenide layer.

  4. Dietary iron depletion at weaning imprints low microbiome diversity and this is not recovered with oral Nano Fe(III).

    PubMed

    Pereira, Dora I A; Aslam, Mohamad F; Frazer, David M; Schmidt, Annemarie; Walton, Gemma E; McCartney, Anne L; Gibson, Glenn R; Anderson, Greg J; Powell, Jonathan J

    2015-02-01

    Alterations in the gut microbiota have been recently linked to oral iron. We conducted two feeding studies including an initial diet-induced iron-depletion period followed by supplementation with nanoparticulate tartrate-modified ferrihydrite (Nano Fe(III): considered bioavailable to host but not bacteria) or soluble ferrous sulfate (FeSO4: considered bioavailable to both host and bacteria). We applied denaturing gradient gel electrophoresis and fluorescence in situ hybridization for study-1 and 454-pyrosequencing of fecal 16S rRNA in study-2. In study-1, the within-community microbial diversity increased with FeSO4 (P = 0.0009) but not with Nano Fe(III) supplementation. This was confirmed in study-2, where we also showed that iron depletion at weaning imprinted significantly lower within- and between-community microbial diversity compared to mice weaned onto the iron-sufficient reference diet (P < 0.0001). Subsequent supplementation with FeSO4 partially restored the within-community diversity (P = 0.006 in relation to the continuously iron-depleted group) but not the between-community diversity, whereas Nano Fe(III) had no effect. We conclude that (1) dietary iron depletion at weaning imprints low diversity in the microbiota that is not, subsequently, easily recovered; (2) in the absence of gastrointestinal disease iron supplementation does not negatively impact the microbiota; and (3) Nano Fe(III) is less available to the gut microbiota.

  5. Multiple diffraction in an icosahedral Al-Cu-Fe quasicrystal

    NASA Astrophysics Data System (ADS)

    Fan, C. Z.; Weber, Th.; Deloudi, S.; Steurer, W.

    2011-07-01

    In order to reveal its influence on quasicrystal structure analysis, multiple diffraction (MD) effects in an icosahedral Al-Cu-Fe quasicrystal have been investigated in-house on an Oxford Diffraction four-circle diffractometer equipped with an Onyx™ CCD area detector and MoKα radiation. For that purpose, an automated approach for Renninger scans (ψ-scans) has been developed. Two weak reflections were chosen as the main reflections (called P) in the present measurements. As is well known for periodic crystals, it is also observed for this quasicrystal that the intensity of the main reflection may significantly increase if the simultaneous (H) and the coupling (P-H) reflections are both strong, while there is no obvious MD effect if one of them is weak. The occurrence of MD events during ψ-scans has been studied based on an ideal structure model and the kinematical MD theory. The reliability of the approach is revealed by the good agreement between simulation and experiment. It shows that the multiple diffraction effect is quite significant.

  6. Single-Crystal 57Fe Q-Band ENDOR Study of the 4 Iron-4 Sulfur Cluster in its Reduced [4Fe-4S] 1+ State

    NASA Astrophysics Data System (ADS)

    Moriaud, Fabrice; Gambarelli, Serge; Lamotte, Bernard; Mouesca, Jean-Marie

    2001-12-01

    57Fe Q-band ENDOR has been used to study the [4Fe-4S]1+ state created by γ irradiation of single crystals of the synthetic model compound [N(C2H5)4]2[Fe4S4(SCH2C6H5)4] enriched in 57Fe. This compound is an excellent biomimetic model of the active sites of many 4 iron-4 sulfur proteins, enabling detailed and systematic studies of its oxidized [4Fe-4S]3+ and reduced [4Fe-4S]1+ paramagnetic states. Taking advantage of the fact that Q-band ENDOR, in contrast with X-Band ENDOR, allows for a very good separation of the 57Fe transitions from those of the protons, the complete hyperfine tensors of the four iron atoms for the [4Fe-4S]1+ species has been measured with precision. For each iron atom, the electron orbital and electron spin isotropic contributions have been determined separately. Moreover, it is remarkable that two 57Fe hyperfine tensors attributed to the ferrous pair of iron atoms are very different. In effect, one tensor presents a much larger anisotropic part and a much smaller isotropic part than those of the other. This difference has been interpreted in terms of a differential electron orbital hyperfine interaction among the two ferrous ions.

  7. Observational Evidence of Iron Hydride in the ISM - Search for FeH in the Supernova Remnant IC 443

    NASA Astrophysics Data System (ADS)

    Remijan, Anthony

    2013-10-01

    The most abundant molecular species in astronomical environments are light hydrides - of course with the bulk of the abundance in H2. The presence of these species are enigmatic - the formation route to many light hydrides are highly endothermic and many of these species are not thermodynamically stable with respect to collisions with common ISM species or strong UV radiation. Yet, numerous hydrides have been detected in the ISM (CH,OH,NH,FH,SH,ClH,SiH).The detection of all of these species implies significantly energetic conditions/processing in interstellar environments. This is particularly true of SiH and SH, the two least energetically favorable hydrides detected. SOFIA provides the unique observing platform to continue the search for metal hydrides in astronomical environments. With a cosmic abudance comparable to sulfur, iron is one of the highest mass atomic species that could react with hydrogen to form iron hydride (FeH). The FeH radical has been the focus of many spectroscopic studies due to the complexity of its electronic, vibrational and rotational structure. It is also an important species for astronomical searches in determining the formation properties of metal hydrides in astronomical environment. For example, it is present in the atmosphere of the sun and has been detected in M-dwarf stars (Wende et al 2010). This proposal will search for the cosmic origins of FeH by targeting an extremently energetic Fe rich environment interacting with ambient molecular H gas - the Supernova Remnant IC 443. Given the high sensitivity and frequency range available to the GREAT instrument, SOFIA is the only astronomical facility in the world that can conduct this experiment.

  8. Itenerant spin glass states and asperomagnetism of amorphous Fe and iron-rich Fe/Zr alloys

    NASA Astrophysics Data System (ADS)

    Krey, U.; Krauss, U.; Krompiewski, S.

    1992-01-01

    A realistic tight-binding approach for the self-consistent calculation of the itinerant spin configurations of disordered metallic systems has been developed and is used to study numerically the problem of the magnetic states at T = 0 K of iron-rich amorphous alloys of the type Fe 1- xZr xH y, and of fictitious amorphous Fe of different densities. In our approach, the local spin polarization is not restricted to the z-direction, i.e. the polarization magnitude as well as its direction can vary from site to site. The calculations show that the spin configurations depend strongly on the preparation, and that changes of the relative spin orientations can lead to drastic changes of the itinerant atomic moments. Metastable spin configurations with essentially isotropic distribution can be prepared by relaxing the system in gradually vanishing external fields with isotropically distributed randomness and zero spatial average, whereas with a non-vanishing average the so-called asperomagnetic configurations are obtained, i.e. ferromagnetic states with randomly frozen transverse components. For iron-rich Fe 1- xZr x alloys with x = 0.07, according to our calculation, the isotropic spin glass configuration would have slightly lower energy than the asperomagnetic state, by amounts corresponding to ≈ 0.003 eV per electron, while for the hydrogenated system Fe 1- xZr xH y with y ≈ 2 x, the asperomagnetic state would be favoured by ≈ 0.004 eV. For two computer models of (fictitious) amorphous Fe with densities of 7.39 and 9.19 g cm -3, the spin-glass and the asperomagnetic states have roughly the same energy, although for the low-density sample the magnitudes of the moments are quite different in both states.

  9. Thermodynamic analysis of compatibility of several reinforcement materials with FeAl alloys

    NASA Technical Reports Server (NTRS)

    Misra, Ajay K.

    1988-01-01

    Chemical compatibility of several reinforcement materials with FeAl alloys within the concentration range 40 to 50 at pct Al have been analyzed from thermodynamic considerations at 1173 and 1273 K. The reinforcement materials considered in this study include carbides, borides, oxides, nitrides, and silicides. Although several chemically compatible reinforcement materials are identified, the coefficients of thermal expansion for none of these materials match closely with that of FeAl alloys and this might pose serious problems in the design of composite systems based on FeAl alloys.

  10. Iron redox reactions in the tourmaline structure: High-temperature treatment of Fe3+-rich schorl

    NASA Astrophysics Data System (ADS)

    Filip, Jan; Bosi, Ferdinando; Novák, Milan; Skogby, Henrik; Tuček, Jiří; Čuda, Jan; Wildner, Manfred

    2012-06-01

    We present a detailed study of thermally-driven oxidation and reduction of Fe in the structure of schorl (as the most widespread tourmaline), Fe2+-bearing olenite and fluor-schorl. The principal Fe3+-rich tourmaline investigated in this study is a natural schorl sample from a unique occurrence in peralkaline rocks near Cancrinite Hill, east of Bancroft, southern Ontario. Tourmaline samples were thermally-treated in air and hydrogen at temperatures of 700, 800 and 900 °C to oxidize or reduce the structural Fe. High-temperature changes were continuously monitored using 57Fe Mössbauer and infrared spectroscopy. Proportions of Fe2+ and Fe3+ vary as a function of the heat treatment. An increase in Fe3+ up to 100% after heating in air at 700 °C was observed, whereas only small changes in the Fe/Fetot ratio after heating under hydrogen at 700 °C was revealed. Partial deprotonation/protonation represents charge compensation for the oxidation/reduction of Fe at the Y and Z sites. Critical samples of Cancrinite Hill tourmaline were investigated in detail by means of 57Fe Mössbauer and infrared spectroscopy, single-crystal X-ray diffraction, electron microprobe and magnetometry. The optimized structural formulae are: X(Na0.93K0.02□0.05)Y(Ti0.13Al0.20Fe1.263+Fe1.102+Mn0.022+□0.30)Z(Al5.16Fe0.532+Mg0.31)BB3T(Si5.88Al0.12)O27V(OH)3W(O0.12OH0.88) - untreated tourmaline (schorl); X(Na0.93K0.02□0.05)Y(Ti0.13Al0.52Fe1.143+Fe0.842+Mg0.05Mn0.022+□0.30)Z(Al4.85Fe0.902+Mg0.25)BB3T(Si5.88Al0.12)O27V(OH)3W(OH) - tourmaline reduced in hydrogen (schorl); X(Na0.93K0.02□0.05)Y(Ti0.13Al0.40Fe2.003+Mg0.15Mn0.022+□0.30)Z(Al4.99Fe0.873+Mg0.14)BB3T(Si5.90Al0.10)O27V(O1.05OH1.95)W(O0.70OH0.30) - tourmaline oxidized in air (H+-rich “buergerite”). There is evident disorder of Al over the Y, Z and T sites as well as disorder of Fe2+ over the Y and Z sites, and ordering of Fe3+ at the Y site and Mg at the Z site. The fully oxidized tourmaline shows disorder of Fe3+ and Mg over the

  11. Carbo-Iron - An Fe/AC composite - As alternative to nano-iron for groundwater treatment.

    PubMed

    Mackenzie, Katrin; Bleyl, Steffen; Georgi, Anett; Kopinke, Frank-Dieter

    2012-08-01

    Carbo-Iron(®)(1) is a novel colloidal composite consisting of activated carbon colloids (ACC) with a d(50) particle size of 0.8 μm and anchored deposits of zero-valent iron clusters. This study discusses the principal material properties of Carbo-Iron colloids (CIC) relevant for groundwater treatment in comparison to commercially available nano-sized zero-valent iron (nZVI). CIC with 10-25 wt% Fe(0) have been developed and tested in laboratory studies for their suitability as dehalogenation reagent and are especially designed to overcome some limitations known from the utilization of nZVI: CIC combine the sorption properties of ACC and the chemical reactivity of nZVI. In column tests, flushed-in CIC showed an enhanced mobility in sediment material compared to nZVI, without the need for colloid stabilizers. However, adding 1-3 wt-% of carboxymethyl cellulose (CMC) related to CIC as colloid stabilizer was found to assure long-lived stable suspensions under laboratory conditions which may additionally support the already improved mobility of the CIC and the homogeneity of particle deposition on the sediment matrix. The hydrophobic character of the ACC carrier provides a high affinity of CIC to non-aqueous phase liquids (NAPL). In undisturbed flow, the reactive particles are collected at the water-NAPL interface. The reagent accumulation at the organic phase is necessary for a successful source attack.

  12. Effects of Composition and Iron Spin State on the Structural Transition of (Mg,Fe)CO3 in the Earth's Lower Mantle

    NASA Astrophysics Data System (ADS)

    Hsu, H.; Huang, S. C.; Wei, C. M.; Hsing, C. R.

    2015-12-01

    Iron-bearing magnesium carbonates (Mg,Fe)CO3 are believed the major carbon carriers in the Earth's deep lower mantle; they may play a crucial role in the Earth's deep carbon cycle. Knowledge of the physical and chemical properties of these carbonates is thus essential for our understanding of the mantle's role in global carbon cycle. Experiments have shown that (Mg,Fe)CO3 ferromagnesite (calcite structure) can be stable up to 80-100 GPa. At 45-50 GPa, ferromangsite undergoes a high-spin to low-spin transition, accompanied by a volume reduction and elastic anomalies. Starting ~100 GPa, ferromagnesite goes through a complicated structural transition. The detail of this transition and the atomic structures of high-pressure (Mg,Fe)CO3 phases are still highly debated. Experimental observations and theoretical results are inconsistent so far. In experiments, several distinct high-pressure (Mg,Fe)CO3 structures have been reported, including a P21/c phase [1] and a Pmm2 phase [2]. In theory, a C2/m phase [3] and a P-1 phase [4] have been suggested, while the Pmm2 phase is not found. One possible reason for such a discrepancy is that all available theoretical calculations so far are based on pure MgCO3, while experimental works are performed using (Mg,Fe)CO3 with high iron concentration ( > 50%). Clearly, the concentration of iron and the possible iron spin crossover can significantly affect the stability of these high-pressure (Mg,Fe)CO3 phases. Here, we use density functional theory + self-consistent Hubbard U (DFT+Usc) calculations to study this structural transition. The effects of composition and iron spin state on these (Mg,Fe)CO3 phases are also discussed. Our results can be expected to provide insightful information for better understanding the Earth's deep carbon cycle.[1] E. Boulard et al., Proc. Natl. Acad. Sci. USA 108, 5184 (2011).[2] J. Liu et al., Sci. Rep. 5, 7640 (2015). [3] A. R. Oganov et al., Earth Planet. Sci. Lett. 273, 38 (2008). [4] C. J. Pickard and

  13. Iron absorption differs in piglets fed extrinsically and intrinsically 59Fe-labeled sow's milk.

    PubMed

    Gislason, J; Jones, B; Lönnerdal, B; Hambraeus, L

    1992-06-01

    Iron bioavailability from species-specific milk is assumed to be high for the offspring, possibly due to species-specific iron-binding proteins in the milk. To assess this bioavailability using radioisotopes, the validity of extrinsic labeling technique needs to be proven. Using the suckling piglet as an animal model, we have compared iron bioavailability from sow's milk labeled extrinsically and intrinsically. During intrinsic labeling transfer into milk of 59Fe given intramuscularly was slow and was found to be at maximum 14 h post-injection. Recovery of isotope in the milk was only 0.00014%. Extrinsic and intrinsic labels were distributed differently among milk fractions; intrinsic iron bound primarily to the fat fraction but the extrinsic iron bound primarily to the casein fraction. Iron retention from intrinsically labeled milk was considerably higher than from extrinsically labeled milk. These results show that the extrinsic tag method is not valid for studies on iron absorption from sow's milk and suggest that the situation may be the same for human milk.

  14. Resilient carbon encapsulation of iron pyrite (FeS2) cathodes in lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Yoder, Tara S.; Tussing, Matthew; Cloud, Jacqueline E.; Yang, Yongan

    2015-01-01

    Converting iron pyrite (FeS2) from a non-cyclable to a cyclable cathode material for lithium ion batteries has been an ongoing challenge in recent years. Herein we report a promising mitigation strategy: wet-chemistry based conformal encapsulation of synthetic FeS2 nanocrystals in a resilient carbon (RC) matrix (FeS2@RC). The FeS2@RC composite was fabricated by dispersing autoclave-synthesized FeS2 nanocrystals in an aqueous glucose solution, polymerizing the glucose in a hydrothermal reactor, and finally heating the polymer/FeS2 composite in a tube furnace to partially carbonize the polymer. The FeS2@RC electrodes showed superior cyclability compared with the FeS2 electrodes, that is, 25% versus 1% of retention at the 20th cycle. Based on electrochemical analysis, XRD study, and SEM characterization, the performance enhancement was attributed to RC's ability to accommodate volume fluctuation, enhance charge transfer, alleviate detrimental side reactions, and suppress loss of the active material. Furthermore, the remaining issues associated with the current system were identified and future research directions were proposed.

  15. Abiotic transformation of high explosives by freshly precipitated iron minerals in aqueous Fe¹¹ solutions

    SciTech Connect

    Boparai, Hardiljeet K.; Comfort, Steve; Satapanajaru, Tunlawit; Szecsody, James E.; Grossl, Paul; Shea, Patrick

    2010-05-11

    Zerovalent iron barriers have become a viable treatment for field-scale cleanup of various ground water contaminants. While contact with the iron surface is important for contaminant destruction, the interstitial pore water within and near the iron barrier will be laden with aqueous, adsorbed and precipitated FeII phases. These freshly precipitated iron minerals could play an important role in transforming high explosives (HE). Our objective was to determine the transformation of RDX (hexahydro-1,3,5-trinitro-1,3,5-triazine), HMX (octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine), and TNT (2,4,6-trinitrotoluene) by freshly precipitated iron FeII/FeIII minerals. This was accomplished by quantifying the effects of initial FeII concentration, pH, and the presence of aquifer solids (FeIII phases) on HE transformation rates. Results showed that at pH 8.2, freshly precipitated iron minerals transformed RDX, HMX, and TNT with reaction rates increasing with increasing FeII concentrations. RDX and HMX transformations in these solutions also increased with increasing pH (5.8-8.55). By contrast, TNT transformation was not influenced by pH (6.85-8.55) except at pH values <6.35. Transformations observed via LC/MS included a variety of nitroso products (RDX, HMX) and amino degradation products (TNT). XRD analysis identified green rust and magnetite as the dominant iron solid phases that precipitated from the aqueous FeII during HE treatment under anaerobic conditions. Geochemical modeling also predicted FeII activity would likely be controlled by green rust and magnetite. These results illustrate the important role freshly precipitated FeII/FeIII minerals in aqueous FeII solutions play in the transformation of high explosives.

  16. Preparation of Al-Cu-Fe-(Sn,Si) quasicrystalline bulks by laser multilayer cladding

    NASA Astrophysics Data System (ADS)

    Feng, Li-ping; Fleury, Eric; Zhang, Guo-sheng

    2012-05-01

    (Al65Cu20Fe15)100- x Sn x ( x=0, 12, 20, 30) and Al57Si10Cu18Fe15 powders were cladded on a medium carbon steel (45# steel) substrate by laser multilayer cladding, respectively. The phases and properties of the produced quasicrystalline bulks were investigated. It was found that the main phases in the Al65Cu20Fe15 sample were crystalline λ-Al13Fe4 and icosahedral quasicrystal together with a small volume fraction of θ-Al2Cu phase. The volume fraction of icosahedral phase decreased as the Sn content in the (Al65Cu20Fe15)100- x Sn x samples increased owing to the formation of β-CuSn phase. The increase of Sn content improved the brittleness of the quasicrystal samples. The morphology of the solidification microstructure in the Al57Si10Cu18Fe15 sample changed from elongated shape to spherical shape due to the addition of Si. The nanohardness of the laser multilayer cladded quasicrystal samples was equal to that of the as-cast sample prepared by vacuum quenching. In terms of hardness, the laser cladded Al57Si10Cu18Fe15 quasicrystalline alloy has the highest value among all the investigated samples.

  17. Addition of Al and Fe salts during treatment of paper mill effluents to improve activated sludge settlement characteristics.

    PubMed

    Agridiotis, V; Forster, C F; Carliell-Marquet, C

    2007-11-01

    Metal salts, ferrous sulphate and aluminium chloride, were added to laboratory-scale activated sludge plant treating paper mill effluents to investigate the effect on settlement characteristics. Before treatment the sludge was filamentous, had stirred sludge volume index (SSVI) values in excess of 300 and was moderately hydrophobic. The use of FeSO4.7H2O took three weeks to reduce the SSVI to 90. Microscopic examination showed that Fe had converted the filamentous flocs into a compact structure. When the iron dosing was stopped, the sludge returned to its bulking state within four weeks. In a subsequent trial, the addition of AlCl3 initially resulted in an improvement of the settlement index but then caused deterioration of the sludge properties. It is possible that aluminium was overdosed and caused charge reversal, increasing the SSVI.

  18. Activities of the components in a spinel solid solution of the Fe-Al-O system

    NASA Astrophysics Data System (ADS)

    Lykasov, A. A.; Kimyashev, A. A.

    2011-09-01

    The conditions of the equilibrium between the Fe3O4-FeAl2O4 solution and wustite are determined by measuring the EMF of galvanic cells containing a solid electrolyte, and the activities of the components in the Fe3O4-FeAl2O4 solution are calculated by treating the results of the experiment on the equilibrium between the spinel solution and wustite. Their properties are found to be different from those of ideal solutions at temperatures of 1000-1300 K. A significant positive deviation from the Raoult's law is believed to indicate the tendency of the solution to decompose. The experimental data are treated in terms of the theory of regular solutions, assuming the energy of mixing to be a function of temperature only. The critical temperature of decomposition for the Fe3O4-FeAl2O4 solution is found to be 1084 K.

  19. Experiments of eliminating the destructive effects of excessive Fe inclusions for Al secondary products

    NASA Astrophysics Data System (ADS)

    Sun, D. Q.; Dai, G. H.; Geng, F.; Yang, K.

    2017-02-01

    Excessive Fe content in Al alloys caused the serious decline of mechanical properties, such as the ductility and impact toughness. Carried out the experiments of eliminating the destructive effects of excessive Fe content by flux-adding technology, which including removing a part of Fe content from Al scrap melt and modifying the morphology of Fe rich precipitates. The experimental results showed that, the ratio of removing Fe element was above 20%, and the morphology of Fe rich precipitates changed from Lamellar to bulk or lath precipitations under the process parameters: the fluxing-agents composed of borax, and MnCl2 (mixed by mass ratio of 1:1), and the adding amount of fluxing-agents was about 1.5%; thrown the fluxing-agents into the Al scrap melt by powder injection process and kept for 30 min.

  20. Influence of Be and Al on the magnetostrictive behavior of FeGa alloys

    SciTech Connect

    Mungsantisuk, Pinai; Corson, Robert P.; Guruswamy, Sivaraman

    2005-12-15

    The rare-earth-free body-centered-cubic FeGa-based alloys have an attractive combination of large low-field magnetostriction at room temperature, good mechanical properties, low hysteresis, and relatively low cost for use in sensor and actuator devices. This paper examines the influence of partially substituting Ga in FeGa alloys with Be and Al on their magnetostrictive behavior. Magnetic and magnetostrictive properties of the various ternary FeGaAl and FeGaBe alloys prepared by directional growth process are presented. It is shown that substitution of Ga with Al and Be can be made in FeGa alloys in certain composition ranges without a significant reduction in magnetostriction. Minimal reductions in magnetostriction when Ga is partially substituted by smaller Be or larger Al atoms in certain composition ranges indicate that local electronic environments are more important and that the effects of Ga and Be are additive.

  1. Point defect concentrations and solid solution hardening in NiAl with Fe additions

    SciTech Connect

    Pike, L.M.; Chang, Y.A.; Liu, C.T.

    1997-08-01

    The solid solution hardening behavior exhibited when Fe is added to NiAl is investigated. This is an interesting problem to consider since the ternary Fe additions may choose to occupy either the Ni or the Al sublattice, affecting the hardness at differing rates. Moreover, the addition of Fe may affect the concentrations of other point defects such as vacancies and Ni anti-sites. As a result, unusual effects ranging from rapid hardening to solid solution softening are observed. Alloys with varying amounts of Fe were prepared in Ni-rich (40 at. % Al) and stoichiometric (50 at. % Al) compositions. Vacancy concentrations were measured using lattice parameter and density measurements. The site occupancy of Fe was determined using ALCHEMI. Using these two techniques the site occupancies of all species could be uniquely determined. Significant differences in the defect concentrations as well as the hardening behavior were encountered between the Ni-rich and stoichiometric regimes.

  2. Influence of Be and Al on the magnetostrictive behavior of FeGa alloys

    NASA Astrophysics Data System (ADS)

    Mungsantisuk, Pinai; Corson, Robert P.; Guruswamy, Sivaraman

    2005-12-01

    The rare-earth-free body-centered-cubic FeGa-based alloys have an attractive combination of large low-field magnetostriction at room temperature, good mechanical properties, low hysteresis, and relatively low cost for use in sensor and actuator devices. This paper examines the influence of partially substituting Ga in FeGa alloys with Be and Al on their magnetostrictive behavior. Magnetic and magnetostrictive properties of the various ternary FeGaAl and FeGaBe alloys prepared by directional growth process are presented. It is shown that substitution of Ga with Al and Be can be made in FeGa alloys in certain composition ranges without a significant reduction in magnetostriction. Minimal reductions in magnetostriction when Ga is partially substituted by smaller Be or larger Al atoms in certain composition ranges indicate that local electronic environments are more important and that the effects of Ga and Be are additive.

  3. Slow-release formulations of the herbicide picloram by using Fe-Al pillared montmorillonite.

    PubMed

    Marco-Brown, Jose L; Undabeytia, Tomás; Torres Sánchez, Rosa M; Dos Santos Afonso, María

    2017-04-01

    Slow-release formulations of the herbicide picloram (PCM, 4-amino-3,5,6-trichloropyridine-2-carboxylic acid) were designed based on its adsorption on pillared clays (pillared clays (PILCs)) for reducing the water-polluting risk derived from its use in conventional formulations. Fe-Al PILCs were synthesized by the reaction of Na(+)-montmorillonite (SWy-2) with base-hydrolyzed solutions of Fe and Al. The Fe/(Fe + Al) ratios used were 0.15 and 0.50. The PCM adsorption isotherms on Fe-Al PILCs were well fitted to Langmuir and Freundlich models. The PCM adsorption capacity depended on the Fe content in the PILCs. Slow-release formulations were prepared by enhanced adsorption of the herbicide from PCM-cyclodextrin (CD) complexes in solution. CDs were able to enhance up to 2.5-fold the solubility of PCM by the formation of inclusion complexes where the ring moiety of the herbicide was partially trapped within the CD cavity. Competitive adsorption of anions such as sulfate, phosphate, and chloride as well as the FTIR analysis of PCM-PILC complexes provided evidence of formation of inner sphere complexes of PCM-CD on Fe-Al PILCs. Release of the herbicide in a sandy soil was lower from Fe-Al PILC formulations relative to a PCM commercial formulation.

  4. A Pyrolitic Lower Mantle with (Mg,Fe3+)(Si,Al3+)O3 Bridgmanite

    NASA Astrophysics Data System (ADS)

    Wang, X.; Tsuchiya, T.

    2014-12-01

    To better understand the Earth's lower mantle (LM), thermodynamic properties (TDPs) of LM minerals should be illustrated clearly. We have so far reported the TDPs of Fe (and Al)-bearing MgO, MgSiO3 bridgmanite (Br) and post bridgmanite [1-5] by using the internally consistent LSDA+U method and the lattice dynamics method. In this work, two spin states, the high (HS) and low spin (LS) state, and several possible distribution configurations are considered in the LM pressure range. For Fe incorporated in Br, only Fe3+ at the Si site undergoes a HS to LS transition. However, this is suppressed by Al incorporation, because Al3+ prefers the Si site and attracts HS Fe3+ at the adjacent Mg site forming Fe3+-Al3+ pair. Br with geophysically relevant 6.25 mol% Fe2+ or Fe3+-Al3+ pair is found vibrationally stable. Incorporation of these elements increases the Br volume a little but gives marginal effects on the TDPs. Simulated densities, adiabatic bulk moduli, and bulk sound velocities of possible LM mineral aggregations show that a composition close to pyrolite with (Mg,Fe3+)(Si,Al3+)O3 Br is accountable for the reference Earth model, while Fe2+-bearing Br instead gives unignorable disagreements in deeper part. Neither Si-richer nor Si-poorer composition improves the disagreements. This indicates that Fe in LM bridgmanite should predominantly be ferric acquiring the HS state, and pyrolitic composition with (Mg,Fe3+)(Si,Al3+)O3 Br is a reasonable LM model. References:[1] A. Metsue, and T. Tsuchiya, J. Geophys. Res. 116, B08207 (2011). [2] A. Metsue, and T. Tsuchiya, Geophys. J. Int. 190, 310 (2012). [3] H. Fukui, T. Tsuchiya, and A. Q. R. Baron, J. Geophys. Res. 117, B12202 (2012). [4] T. Tsuchiya, and X. Wang, J. Geophys. 118, 83 (2013). [5] X. Wang, and T. Tsuchiya, under reviewing.

  5. Development of ODS FeCrAl alloys for accident-tolerant fuel cladding

    SciTech Connect

    Dryepondt, Sebastien N.; Hoelzer, David T.; Pint, Bruce A.; Unocic, Kinga A.

    2015-09-18

    FeCrAl alloys are prime candidates for accident-tolerant fuel cladding due to their excellent oxidation resistance up to 1400 C and good mechanical properties at intermediate temperature. Former commercial oxide dispersion strengthened (ODS) FeCrAl alloys such as PM2000 exhibit significantly better tensile strength than wrought FeCrAl alloys, which would alloy for the fabrication of a very thin (~250 m) ODS FeCrAl cladding and limit the neutronic penalty from the replacement of Zr-based alloys by Fe-based alloys. Several Fe-12-Cr-5Al ODS alloys where therefore fabricated by ball milling FeCrAl powders with Y2O3 and additional oxides such as TiO2 or ZrO2. The new Fe-12Cr-5Al ODS alloys showed excellent tensile strength up to 800 C but limited ductility. Good oxidation resistance in steam at 1200 and 1400 C was observed except for one ODS FeCrAl alloy containing Ti. Rolling trials were conducted at 300, 600 C and 800 C to simulate the fabrication of thin tube cladding and a plate thickness of ~0.6mm was reached before the formation of multiple edge cracks. Hardness measurements at different stages of the rolling process, before and after annealing for 1h at 1000 C, showed that a thinner plate thickness could likely be achieved by using a multi-step approach combining warm rolling and high temperature annealing. Finally, new Fe-10-12Cr-5.5-6Al-Z gas atomized powders have been purchased to fabricate the second generation of low-Cr ODS FeCrAl alloys. The main goals are to assess the effect of O, C, N and Zr contents on the ODS FeCrAl microstructure and mechanical properties, and to optimize the fabrication process to improve the ductility of the 2nd gen ODS FeCrAl while maintaining good mechanical strength and oxidation resistance.

  6. Electronic structure and soft magnetic properties of Se/FeSiAl (110) films

    NASA Astrophysics Data System (ADS)

    Schwindt, V. Cardoso; Ardenghi, J. S.; Bechthold, P.; Juan, A.; Batic, B. Setina; Jenko, M.; González, E. A.; Jasen, P. V.

    2015-11-01

    The Se adsorption at different coverages on DO3 FeSiAl(110) surface is studied using density functional theory (DFT). Se adsorption is favorable in almost all surface high-symmetry sites, except for the bridge site formed by Fe-Si atoms. The most stable is a hollow site formed by four Fe atoms with adsorption energy of -5.30 eV. When the coverages increase, the energies decrease in the case of hollow sites. The surface present a reconstruction after Se adsorption, being the most important at 1/2 ML. The local magnetic moment for Fe atoms increase for the type A (all nearst neighbours (nn) are Fe atoms) and decrease for the type B (nn are Fe, Si and Al atoms). The most affected metal orbitals are Fe 4s and 4p. In the case of the hollow site the surface Fe-Fe bond is weakened after Se adsorption. A Fe-Se bond is developed at all coverages in both sites being the most important on top (dFe-Se = 2.23 Å, OP: 0.774 at 1/4 ML). The first and second layer Fe-Fe bond increase at 1/4 ML and decrease at 1/2 and 1 ML. Small Se-Se bonding interaction appear at 1/2 ML and increase noticeable for 1 ML. For the top site, the Se-Se bond appears at all coverage. The Fe-Fe surface bonds also decrease its strength with respect to the clean surface at all coverage. The first and second layer Fe-Fe bond increase at all coverage.

  7. Composition dependence of the electronic properties of Al-Cu-Fe and Al-Cu-Ru-Si semimetallic quasicrystals

    NASA Astrophysics Data System (ADS)

    Pierce, F. S.; Bancel, P. A.; Biggs, B. D.; Guo, Q.; Poon, S. J.

    1993-03-01

    Electronic transport properties and specific heats of ordered icosahedral phase alloys in the Al-Cu-Ru-Si and Al-Cu-Fe systems are examined, and comparison with high-quality rhombohedral (3/2) approximant phase samples of Al-Cu-Fe is made. Strong temperature dependence and sensitivity to composition changes of these properties are observed. The similarity of transport properties between the icosahedral (i) and rhombohedral (r) phases of Al62.5Cu26.5Fe11 is noted. The results can be qualitatively interpreted in terms of band structure. There appears to be sufficient evidence for a rapidly varying conductivity spectrum σ(E) in the ordered i phases. However, important questions concerning the physics of these semimetallic quasicrystals remain to be answered.

  8. Quantum many-body intermetallics: Phase stability of Fe3Al and small-gap formation in Fe2VAl

    NASA Astrophysics Data System (ADS)

    Kristanovski, Oleg; Richter, Raphael; Krivenko, Igor; Lichtenstein, Alexander I.; Lechermann, Frank

    2017-01-01

    Various intermetallic compounds harbor subtle electronic correlation effects. To elucidate this fact for the Fe-Al system, we perform a realistic many-body investigation based on a combination of density functional theory with dynamical mean-field theory in a charge self-consistent manner. A better characterization and understanding of the phase stability of bcc-based D 03-Fe3Al through an improved description of the correlated charge density and the magnetic energy is achieved. Upon replacement of one Fe sublattice with V, the Heusler compound Fe2VAl is realized, known to display bad-metal behavior and increased specific heat. Here we document a charge-gap opening at low temperatures in line with previous experimental work. The gap structure does not match conventional band theory and is reminiscent of (pseudo)gap characteristics in correlated oxides.

  9. Phase equilibria and structural investigations in the system Al-Fe-Si.

    PubMed

    Marker, Martin C J; Skolyszewska-Kühberger, Barbara; Effenberger, Herta S; Schmetterer, Clemens; Richter, Klaus W

    2011-12-01

    The Al-Fe-Si system was studied for an isothermal section at 800 °C in the Al-rich part and at 900 °C in the Fe-rich part, and for half a dozen vertical sections at 27, 35, 40, 50 and 60 at.% Fe and 5 at.% Al. Optical microscopy and powder X-ray diffraction (XRD) was used for initial sample characterization, and Electron Probe Microanalysis (EPMA) and Scanning Electron Microscopy (SEM) of the annealed samples was used to determine the exact phase compositions. Thermal reactions were studied by Differential Thermal Analysis (DTA). Our experimental results are generally in good agreement with the most recent phase diagram versions of the system Al-Fe-Si. A new ternary high-temperature phase τ12 (cF96, NiTi2-type) with the composition Al48Fe36Si16 was discovered and was structurally characterized by means of single-crystal and powder XRD. The variation of the lattice parameters of the triclinic phase τ1 with the composition Al2+x Fe3Si3-x (-0.3 < x < 1.3) was studied in detail. For the binary phase FeSi2 only small solubility of Al was found in the low-temperature modification LT-FeSi2 (ζβ ) but significant solubility in the high-temperature modification HT-FeSi2 (ζα ) (8.5 at.% Al). It was found that the high-temperature modification of FeSi2 is stabilized down to much lower temperature in the ternary, confirming earlier literature suggestions on this issue. DTA results in four selected vertical sections were compared with calculated sections based on a recent CALPHAD assessment. The deviations of liquidus values are significant suggesting the need for improvement of the thermodynamic models.

  10. Phase separation in equiatomic AlCoCrFeNi high-entropy alloy.

    PubMed

    Manzoni, A; Daoud, H; Völkl, R; Glatzel, U; Wanderka, N

    2013-09-01

    The microstructure of the as-cast AlCoCrFeNi high entropy alloy has been investigated by transmission electron microscopy and atom probe tomography. The alloy shows a very pronounced microstructure with clearly distinguishable dendrites and interdendrites. In both regions a separation into an Al-Ni rich matrix and Cr-Fe-rich precipitates can be observed. Moreover, fluctuations of single elements within the Cr-Fe rich phase have been singled out by three dimensional atom probe measurements. The results of investigations are discussed in terms of spinodal decomposition of the alloying elements inside the Cr-Fe-rich precipitates.

  11. Magneto-optical imaging of iron-oxypnictide superconductor LaFeAs(O,F)

    NASA Astrophysics Data System (ADS)

    Nakajima, Yasuyuki; Maruoka, Toshihide; Tamegai, Tsuyoshi; Kamihara, Yoichi; Hirano, Masahiro; Hosono, Hideo

    2010-12-01

    We report the magneto-optical imaging for polycrystalline LaFeAsO0.95F0.05 and LaFeAsO0.892F0.108. We find a significant magneto-optical contrast with marked inhomogeneities and with a typical superconducting grain size ˜20-40 μm. Although intergrain critical current density is negligibly small, intragrain critical current density obtained from magneto-optical image is about 1 × 105 A/cm2 at 5 K, which is smaller than other rare-earth-based iron-oxypnictide superconductors but is potentially attractive for technological applications.

  12. Elucidation of the Fe(III) Gallate Structure in Historical Iron Gall Ink.

    PubMed

    Ponce, Aldo; Brostoff, Lynn B; Gibbons, Sarah K; Zavalij, Peter; Viragh, Carol; Hooper, Joseph; Alnemrat, Sufian; Gaskell, Karen J; Eichhorn, Bryan

    2016-05-17

    Synthetic, structural, spectroscopic and aging studies conclusively show that the main colorant of historical iron gall ink (IGI) is an amorphous form of Fe(III) gallate·xH2O (x = ∼1.5-3.2). Comparisons between experimental samples and historical documents, including an 18th century hand-written manuscript by George Washington, by IR and Raman spectroscopy, XRD, X-ray photoelectron spectroscopy, and Mössbauer spectroscopy confirm the relationship between the model and authentic samples. These studies settle controversy in the cultural heritage field, where an alternative structure for Fe(III) gallate has been commonly cited.

  13. Potentiometric and electrokinetic signatures of iron(II) interactions with (a,y)-Fe2O3

    SciTech Connect

    Toczydlowska, Diana; Kedra-Krolik, Karolina; Nejbert, Krzysztof; Preocanin, Tajana; Rosso, Kevin M.; Zarzycki, Piotr P.

    2015-05-29

    The role of surface electrostatics on the reductive dissolution of iron (III) oxides is poorly understood, despite its importance in controlling the amount of mobilized iron. We report the potentiometric titration of the a; y -Fe2O3 oxides exposed to reductants and complexing ligands (Fe(II), ascorbate, oxalate, malonate). We monitored in situ surface and potentials, the ratio of mobilized ferric to ferrous ions, and periodically analyzed nanoparticle crystal structure using X-ray diffraction. We found that addition of Fe2+ ions produces a response consistent with the iron solubilityactivity curve, whereas the presence of ascorbate significantly decreases the amount of mobilized Fe(III) due to reduction to Fe(II). In addition, XRD analysis proved that y-Fe2O3 particles remain structurally unchanged along the titration pathway despite iron cycling between aqueous and solid reservoirs. Our studies, suggest that the surface redoxactivity of iron oxides is primarily governed by the balance between Fe(III) and Fe(II) ions in aqueous phase, which may be easily altered by complexing and reducing agents.

  14. Synthesis and properties of new multinary silicides R5Mg5Fe4Al(x)Si(18-x) (R = Gd, Dy, Y, x ≈ 12) grown in Mg/Al flux.

    PubMed

    Ma, Xiaowei; Chen, Banghao; Latturner, Susan E

    2012-06-04

    Reactions of iron, silicon, and R = Gd, Dy, or Y in 1:1 Mg/Al mixed flux produce well-formed crystals of R(5)Mg(5)Fe(4)Al(x)Si(18-x) (x ≈ 12). These phases have a new structure type in tetragonal space group P4/mmm (a = 11.655(2) Å, c = 4.0668(8) Å, Z = 1 and R(1) = 0.0155 for the Dy analogue). The structure features two rare earth sites and one iron site; the latter is in monocapped trigonal prismatic coordination surrounded by silicon and aluminum atoms. Siting of Al and Si was investigated using bond length analysis and (27)Al and (29)Si MAS NMR studies. The magnetic properties are determined by the R elements, with the Gd and Dy analogues exhibiting antiferromagnetic ordering at T(N) = 11.9 and 6.9 K respectively; both phases exhibit complex metamagnetic behavior with varying field.

  15. Structure and physical properties of the layered iron oxychalcogenide BaFe2Se2O

    NASA Astrophysics Data System (ADS)

    Lei, Hechang; Ryu, Hyejin; Ivanovski, V.; Warren, J. B.; Frenkel, A. I.; Cekic, B.; Yin, Wei-Guo; Petrovic, C.

    2012-11-01

    We have successfully synthesized a layered iron oxychalcogenide BaFe2Se2O single crystal. This compound is built up of Ba and Fe-Se(O) layers alternatively stacked along the c axis. The Fe-Se(O) layers contain double chains of edge-shared Fe-Se(O) tetrahedra that propagate along the b axis and are bridged by oxygen along the a axis. Physical property measurements indicate that BaFe2Se2O is a semiconductor without the Curie-Weiss behavior up to 350 K. There is a possible long-range antiferromagnetic transition at 240 K, corresponding to the peak in specific-heat measurement, and two transitions at 115 K and 43 K where magnetic susceptibility drops abruptly. The magnetic entropy up to 300 K is much smaller than the expected value for Fe2+ in tetrahedral crystal fields and the Mössbauer spectrum indicates that long-range magnetic order is unlikely at 294 K. Our results suggest that BaFe2Se2O is a magnetic insulator at the borderline between a long-range antiferromagnetic spin ordering and possible spin dimerization.

  16. Impact of a long term fire retardant (Fire Trol 931) on the leaching of Na, Al, Fe, Mn, Cu and Si from a Mediterranean forest soil: a short-term, lab-scale study.

    PubMed

    Koufopoulou, Sofia; Michalopoulos, Charalampos; Tzamtzis, Nikolaos; Pappa, Athina

    2014-06-01

    Long term fire retardant (LTR) application for forest fire prevention purposes as well as wildland fires can result in chemical leaching from forest soils. Large quantities of sodium (Na), aluminium (Al), iron (Fe), manganese (Mn), copper (Cu) and silicon (Si) in leachates, mainly due to ammonium (one of the major LTR components) soil deposition, could affect the groundwater quality. The leaching of Na, Al, Fe, Mn, Cu and Si due to nitrogen based LTR application (Fire Trol 931) was studied at laboratory scale. The concentrations of Na(+), Al(3+), Fe(3+)/Fe(2+), Mn(2+), Cu(2+) and Si(4+) were measured in the resulting leachates from pots with forest soil and pine trees alone and in combination with fire. The leaching of Na, Fe and Si from treated pots was significantly greater than that from control pots. The leaching of Al, Mn and Cu was extremely low.

  17. Thermodynamic analysis of chemical compatibility of several compounds with Fe-Cr-Al alloys

    NASA Technical Reports Server (NTRS)

    Misra, Ajay K.

    1993-01-01

    Chemical compatibility between Fe-19.8Cr-4.8Al (weight percent), which is the base composition for the commercial superalloy MA956, and several carbides, borides, nitrides, oxides, and silicides was analyzed from thermodynamic considerations. The effect of addition of minor alloying elements, such as Ti, Y, and Y2O3, to the Fe-Cr-Al alloy on chemical compatibility between the alloy and various compounds was also analyzed. Several chemically compatible compounds that can be potential reinforcement materials and/or interface coating materials for Fe-Cr-Al based composites were identified.

  18. Structural Disorder and Magnetism in the Spin-Gapless Semiconductor CoFeCrAl

    DTIC Science & Technology

    2016-08-24

    semiconductor CoFeCrAl into a half- metallic ferrimagnet and increases the half- metallic band gap by 0.12 eV. Compared CoFeCrAl, the moment of...magnets. However, Si addition improves the degree of Heusler ordering and changes the electronic structure from a SGS to a half- metal with increased...total moment per relaxed unit cell are 1.71 µB (I), –0.60 µB (II), and 1.05 µB (III). None of the disordered CoFeCrAl structures is energetically

  19. X-ray powder diffraction and 57Fe Mössbauer spectroscopy of synthetic trioctahedral micas {K}[Me3]Fe2+; T = Al3+, Fe3+

    NASA Astrophysics Data System (ADS)

    Redhammer, G. J.; Amthauer, G.; Lottermoser, W.; Bernroider, M.; Tippelt, G.; Roth, G.

    2005-11-01

    Trioctahedral 1 M micas have been synthesized along (pseudo)binary joins using hydrothermal techniques and controlled oxygen fugacities. Octahedrally coordinated iron in annite {K}[Fe3]<AlSi3rangleO10(OH)2 was successively replaced by Co2+, Mg2+ and Ni2+ and tetrahedrally coordinated aluminum by Fe3+. Unit cell parameters decrease almost linearly with decreasing average radius of the octahedral cation/average M O bond length within the octahedral sheet. With increasing substitution of Fe2+ the octahedral sheet becomes more flattened, the ditrigonal distortion of the tetrahedral sheet increases up to a maximum value of ≈10° for micas with tetrahedral sheet compositions close to <AlSi3rangle and up to ≈14° for those containing a <FeSi3rangle tetrahedral sheet. All iron-bearing samples were studied by 57Fe Mössbauer spectroscopy. With increasing substitution of iron by smaller divalent cations the quadrupole splitting distribution (QSD) evolves from a broad bimodal distribution in annite to a smaller unimodal distribution in Mg2+ and Ni2+-rich samples so that for high substitution rates more regular local environments are dominating. These results, however, can not be interpreted in terms of an octahedral cation ordering scheme. For none of the micas investigated reliable Fe2+ M2/M1 area ratios can be extracted. fMoreover, the complete QSD is shifted towards higher quadrupole splitting values. Similar observations were obtained for substituting Fe2+ by Mg2+ and Ni2+ in tetra-ferri-annite free of octahedral coordinated trivalent cations. Unlike in the Al3+ bearing micas a third QSD component is missing which supports the claim that the appearance of this third QSD component is closely related to the presence of trivalent cations (Al3+, Fe3+) in octahedra coordination.

  20. What makes the nematic phase of FeSe different than other iron-based superconductors?

    NASA Astrophysics Data System (ADS)

    Fernandes, Rafael

    Most iron-based superconductors display, in their normal state, a transition to a magnetic stripe state that is either accompanied or preceded by a tetragonal-to-orthorhombic transition. The proximity between these two transitions has led to the proposal that they correspond to a two-stage melting of the magnetic stripe state, resulting in a vestigial orthorhombic-paramagnetic nematic phase. Despite the success of this scenario to describe many iron-based materials, the simplest of them, FeSe, displays a high-temperature nematic transition but no long-range magnetic order. Interestingly, in its monolayer form, FeSe displays the highest Tc of all iron-based materials, raising the question of whether the nematic state of its bulk form could be related to the superconducting state of its monolayer form. In this talk, we investigate theoretically the microscopic origin of the nematic phase of FeSe. By extending the standard RPA formalism, we compare the orbital-order susceptibility and the spin-driven nematic susceptibility of a generic multi-orbital Hubbard model. We find that the former cannot in general drive the nematic transition, and that high-energy magnetic fluctuations play a fundamental role in stabilizing the nematic state in the absence of long-range magnetic order. Focusing on FeSe, we identify two features that distinguish it from all other iron-based materials: a very small Fermi energy and a large degeneracy of the magnetic ground state. We show that both effects enhance the nematic transition temperature at the same time as they suppress the magnetic transition. These results may explain why, in FeSe, the onset of nematic order does not require strong magnetic fluctuations, in contrast to other iron-based materials. Finally, we discuss how the interplay between magnetic fluctuations and small Fermi energy in FeSe can lead to the emergence of different types of Pomeranchuk instabilities, and discuss their experimental manifestations. This work was

  1. Electrochemical capacitance of iron oxide nanotube (Fe-NT): effect of annealing atmospheres.

    PubMed

    Sarma, Biplab; Jurovitzki, Abraham L; Ray, Rupashree S; Smith, York R; Mohanty, Swomitra K; Misra, Mano

    2015-07-03

    The effect of annealing atmosphere on the supercapacitance behavior of iron oxide nanotube (Fe-NT) electrodes has been explored and reported here. Iron oxide nanotubes were synthesized on a pure iron substrate through an electrochemical anodization process in an ethylene glycol solution containing 3% H2O and 0.5 wt.% NH4F. Subsequently, the annealing of the nanotubes was carried out at 500 °C for 2 h in various gas atmospheres such as air, oxygen (O2), nitrogen (N2), and argon (Ar). The morphology and crystal phases evolved after the annealing processes were examined via field emission scanning electron microscopy, x-ray diffraction, Raman spectroscopy, and x-ray photoelectron spectroscopy. The electrochemical capacitance properties of the annealed Fe-NT electrodes were evaluated by conducting cyclic voltammetry (CV), galvanostatic charge-discharge, and electrochemical impedance spectroscopy tests in the Li2SO4 electrolyte. Based on these experiments, it was found that the capacitance of the Fe-NT electrodes annealed in air and O2 atmospheres shows mixed behavior comprising both the electric double layer and pseudocapacitance. However, annealing in N2 and Ar environments resulted in well-defined redox peaks in the CV profiles of the Fe-NT electrodes, which are therefore attributed to the relatively higher pseudonature of the capacitance in these electrodes. Based on the galvanostatic charge-discharge studies, the specific capacitance achieved in the Fe-NT electrode after annealing in Ar was about 300 mF cm(-2), which was about twice the value obtained for N2-annealed Fe-NTs and three times higher than those annealed in air and O2. The experiments also demonstrated excellent cycle stability for the Fe-NT electrodes with 83%-85% capacitance retention, even after many charge-discharge cycles, irrespective of the gas atmospheres used during annealing. The increase in the specific capacitance was discussed in terms of increased oxygen vacancies as a result of the

  2. The effects of Ni, Mo, Ti and Si on the mechanical properties of Cr free Mn steel (Fe-25Mn-5Al-2C)

    NASA Technical Reports Server (NTRS)

    Schuon, S. R.

    1982-01-01

    The FeMnAlC alloys may hold potential as Cr-free replacements for high strategic material iron base superalloys, but little is known about their intermediate temperature (650 C to 870 C) mechanical properties. The effects of alloying elements on the mechanical properties of model FeMnAlC alloys were studied. Results showed that modified FeMnAlC alloys had promising short term, intermediate temperature properties but had relatively poor stress rupture lives at 172 MPa and 788 C. Room temperature and 788 C tensile strength of FeMnAlC alloys were better than common cast stainless steels. Changes in room temperature tensile and 788 C tensile strength and ductility, and 788 C stress rupture life were correlated with changes in Ni, Mo, Ti, and Si levels due to alloying effects on interstitial carbon levels and carbide morphology. Fe-25Mn-5Al-2C had a very poor stress rupture life at 172 MPa and 788 C. Addition of carbide-forming elements improved the stress rupture life.

  3. Effect of CeO{sub 2} addition on the properties of FeAl based alloy produced by mechanical alloying technique

    SciTech Connect

    Khaerudini, Deni S.; Muljadi,; Sardjono, P.; Tetuko, Anggito P.; Sebayang, P.; Ginting, M.

    2013-09-03

    Iron aluminides based on FeAl is notable for their low materials cost, ease of fabrication and good corrosion, suffixation and oxidation resistance. However, the application based on these unique properties still require the development of Fe-Al based alloy since it shows some drawbacks such as a lack of high temperature strength and low ductility. To improve the mechanical properties of FeAl based alloy, ceria (CeO{sub 2}) will be added to this compound. FeAl based alloy produced by the mechanical alloying (MA) technique. The developed specimens then assessed with respect to oxidation behaviour in high temperature, scale microstructure and hardness. The surface morphologies of the alloy evaluated and observed using scanning electron microscopy (SEM) with an energy dispersive X-ray spectroscopy (EDX). The phase structures of oxide scale formed on them were identified by X-ray diffraction (XRD). The results found that the FeAl intermetallic compound containing CeO{sub 2} 0.5 wt.% is less pores and CeO{sub 2} 1.0 wt.% is more homogen in powder and solid form, higher hardness and increase in their resistance to oxidation behaviour in high temperature compared with another percentage of CeO{sub 2}.

  4. Genetic and biochemical effects induced by iron ore, Fe and Mn exposure in tadpoles of the bullfrog Lithobates catesbeianus.

    PubMed

    Veronez, Alexandra Caroline da Silva; Salla, Rômulo Victor; Baroni, Vinícius Dadalto; Barcarolli, Indianara Fernanda; Bianchini, Adalto; Dos Reis Martinez, Claudia Bueno; Chippari-Gomes, Adriana Regina

    2016-05-01

    For decades, the extraction of minerals has intensified in order to meet the demand of industry. Iron ore deposits are important sources of metals, such as iron (Fe) and manganese (Mn). The particulate ores can be dispersed during extraction, transport and storage, with potential to induce biological impacts. Amphibians are very sensitive to environmental stressors. Therefore, the present study aimed to assess the effects of iron ore, Fe and Mn exposure during the metamorphosis of Lithobates catesbeianus. Endpoints analyzed included morphological (biometrical and developmental analyses), whole body Fe and Mn concentration in, plasma ferritin concentration, erythrocyte DNA damage (measured through comet assay and micronucleus test) and liver activity of enzymes involved in oxidative status [glutathione S-transferase (GST) and catalase (CAT)]. Tadpoles were kept under control condition (no contaminant addition) or exposed to iron ore (3.79mg/L as fine particulate matter); Fe (nominal concentration: 0.51mg/L Fe as C10H12FeN2NaO8; Fe-EDTA); and Mn (nominal concentration: 5.23mg/L Mn as 4H2O.MnCl2) for 30 days. Virtually, no mortality was observed, except for one tadpole found dead in the iron ore treatment. However, tadpoles exposed to iron ore had longer tail than those kept under control conditions while tadpoles exposed to manganese chloride showed higher body length than control ones. Exposure to Fe and Mn induced a delay in tadpole metamorphosis, especially when these metals are presented not as a mixture (iron ore). Tadpoles exposed to iron ore had increased whole body Fe and Mn while those exposed to Fe and Mn accumulated each metal individually. Tadpoles exposed to any of the contaminants tested showed a significant increase in erythrocyte DNA damage and frequency of micronuclei. In addition, they showed higher liver GST activity respect with those kept under control conditions. Plasma ferritin concentration and liver CAT activity were higher only in tadpoles

  5. Heterogeneous oxidation of Fe(II) on iron oxides in aqueous systems: Identification and controls of Fe(III) product formation

    NASA Astrophysics Data System (ADS)

    Larese-Casanova, Philip; Kappler, Andreas; Haderlein, Stefan B.

    2012-08-01

    The aqueous Fe(II)-oxide Fe(III) system is a reactant for many classes of redox sensitive compounds via an interfacial Fe(II) sorption and electron transfer process. The poorly soluble Fe(III) products formed as a result of contaminant reduction and Fe(II) oxidation on iron oxides may be capable of modifying iron oxide surfaces and affecting subsequent reduction rates of contaminants such as halogenated ethenes or nitroaromatic compounds. The scope of this study was to identify the secondary Fe(III) mineral phases formed after Fe(II) oxidation on common iron oxides during heterogeneous contaminant reduction by directly targeting the secondary minerals using Mössbauer-active isotopes. Fe(III) mineral characterization was performed using 57Fe-Mössbauer spectroscopy, μ-X-ray diffraction, and electron microscopy after oxidation of dissolved 57Fe(II) using nitrobenzenes as a model oxidant in pH-buffered suspensions of 56hematite, 56goethite, 56magnetite, and 56maghemite. Mössbauer spectra confirmed sorbed 57Fe(II) becomes oxidized by the parent 56Fe(III)-oxide sorbent and assimilated as the sorbent oxide prior to any nitrobenzene reduction, consistent with several reports in the literature. In addition to oxide sorbent growth, Fe(II) sorption and oxidation by nitrobenzene result also in the formation of secondary Fe(III) minerals. Goethite formed on three hematite morphologies (rhombohedra, needles, and hexagonal platelets), and acicular needle shapes typical of goethite appeared on the micron-sized hexagonal platelets, at times aligned in 60° orientations on (0 0 1) faces. The proportion of goethite formation on the three hematites was linked to number of surface sites. Only goethite was observed to form on a goethite sorbent. In contrast, lepidocrocite was observed to form on magnetite and maghemite sorbents (consistent with homogeneous Fe(II) oxidation by O2) and assumed spherulite morphologies. All secondary Fe(III) phases were confirmed within

  6. Directional solidification of Al-8 wt. %Fe alloy under high magnetic field gradient

    NASA Astrophysics Data System (ADS)

    Wu, Mingxu; Liu, Tie; Dong, Meng; Sun, Jinmei; Dong, Shulin; Wang, Qiang

    2017-02-01

    We investigated applying a magnetic field (up to 6 T) during directional solidification of a hypereutectic Al-8 wt. %Fe alloy, finding that it dramatically affected the final microstructure. A eutectic area appeared at the top of the samples, and as the magnetic flux density increased, the eutectic area clearly enlarged. In addition, the Al3Fe phase was twisted and fractured, and some phases aggregated and distributed randomly in the samples. We also investigated the volume fraction distribution of the Al3Fe phase, revealing that applying the magnetic field during solidification caused dramatic disorder in the solute and phase distributions. The magnetic force induced by the interaction between the magnetic field gradient and the magnetic materials appeared to be the main reason not only for the occurrence and enlargement of the eutectic area but also for the movement of Fe-enriched zones during directional solidification. Otherwise, the deformation and fracture of the Al3Fe phase, the morphological instability in the interface between the eutectic area and the Al3Fe phase, and the random distribution of the aggregated Al3Fe phase appeared to come from the thermoelectric magnetic force/thermoelectric magnetic convection under the magnetic field.

  7. Tribological Properties of the Fe-Al-Cr Alloyed Layer by Double Glow Plasma Surface Metallurgy

    NASA Astrophysics Data System (ADS)

    Luo, Xixi; Yao, Zhengjun; Zhang, Pingze; Zhou, Keyin; Wang, Zhangzhong

    2016-09-01

    A Fe-Al-Cr alloyed layer was deposited onto the surface of Q235 low-carbon steel via double glow plasma surface metallurgy (DGPSM) to improve the steel's wear resistance. After the DGPSM treatment, the Fe-Al-Cr alloyed layer grown on the Q235 low-carbon steel was homogeneous and compact and had a thickness of 25 µm. The layer was found to be metallurgically adhered to the substrate. The frictional coefficient and specific wear rate of the sample with a Fe-Al-Cr alloyed layer (treated sample) were both lower than those of the bare substrate (untreated sample) at the measured temperatures (25, 250 and 450 °C). The results indicated that the substrate and the alloyed layer suffered oxidative wear and abrasive wear, respectively, and that the treated samples exhibited much better tribological properties than did the substrate. The formation of Fe2AlCr, Fe3Al(Cr), FeAl(Cr), Fe(Cr) sosoloid and Cr23C6 phases in the alloyed layer dramatically enhanced the wear resistance of the treated sample. In addition, the alloyed layer's oxidation film exhibited a self-healing capacity with lubrication action that also contributed to the improvement of the wear resistance at high temperature. In particular, at 450 °C, the specific wear rate of treated sample was 2.524 × 10-4 mm3/N m, which was only 45.2% of the untreated sample.

  8. Intramolecular iron-mediated C-H bond heterolysis with an assist of pendant base in a [FeFe]-hydrogenase model.

    PubMed

    Zheng, Dehua; Wang, Ning; Wang, Mei; Ding, Shengda; Ma, Chengbing; Darensbourg, Marcetta Y; Hall, Michael B; Sun, Licheng

    2014-12-03

    Although many metalloenzymes containing iron play a prominent role in biological C-H activation processes, to date iron-mediated C(sp(3))-H heterolysis has not been reported for synthetic models of Fe/S-metalloenzymes. In contrast, ample precedent has established that nature's design for reversible hydrogen activation by the diiron hydrogenase ([FeFe]-H2ase) active site involves multiple irons, sulfur bridges, a redox switch, and a pendant amine base, in an intricate arrangement to perform H-H heterolytic cleavage. In response to whether this strategy might be extended to C-H activation, we report that a [FeFe]-H2ase model demonstrates iron-mediated intramolecular C-H heterolytic cleavage via an agostic C-H interaction, with proton removal by a nearby pendant amine, affording Fe(II)-[Fe'(II)-CH-S] three-membered-ring products, which can be reduced back to 1 by Cp2Co in the presence of HBF4. The function of the pendant base as a proton shuttle was confirmed by the crystal structures of the N-protonated intermediate and the final deprotonated product in comparison with that of a similar but pendant-amine-free complex that does not show evidence of C-H activation. The mechanism of the process was backed up by DFT calculations.

  9. Preparation of iron oxide nanoparticles from FeCl3 solid powder using microemulsions

    NASA Astrophysics Data System (ADS)

    Nassar, Nashaat; Husein, Maen

    2006-05-01

    Nanoparticles of iron oxide were prepared by subjecting iron chloride powder to (w/o) microemulsions consisting of sodium bis(2-ethylhexyl) sulfosuccinate (AOT), isooctane and water. FeCl3 was first dissolved in the water pools of the microemulsion, and then reacted with NaOH added as an aqueous solution to form iron oxide. The amount of NaOH solution was limited so that single microemulsion phase is obtained. This technique serves as an in-situ nanoparticle preparation technique aimed at minimizing particle aggregation associated with particle transportation to required sites. In this study, the effects of AOT concentration and water to AOT mole ratio on the nanoparticle size were investigated. UV/Vis spectrophotometry and transmission electron microscopy (TEM) were used to measure the particle size distribution.

  10. Phenol Nitration Induced by an {Fe(NO)2}10 Dinitrosyl Iron Complex

    SciTech Connect

    N Tran; H Kalyvas; K Skodje; T Hayashi; P Moenne-Loccoz; P Callan; J Shearer; L Kirschenbaum; E Kim

    2011-12-31

    Cellular dinitrosyl iron complexes (DNICs) have long been considered NO carriers. Although other physiological roles of DNICs have been postulated, their chemical functionality outside of NO transfer has not been demonstrated thus far. Here we report the unprecedented dioxygen reactivity of a N-bound {l_brace}Fe(NO){sub 2}{r_brace}{sup 10} DNIC, [Fe(TMEDA)(NO){sub 2}] (1). In the presence of O{sub 2}, 1 becomes a nitrating agent that converts 2,4,-di-tert-butylphenol to 2,4-di-tert-butyl-6-nitrophenol via formation of a putative iron-peroxynitrite [Fe(TMEDA)(NO)(ONOO)] (2) that is stable below -80 C. Iron K-edge X-ray absorption spectroscopy on 2 supports a five-coordinated metal center with a bound peroxynitrite in a cyclic bidentate fashion. The peroxynitrite ligand of 2 readily decays at increased temperature or under illumination. These results suggest that DNICs could have multiple physiological or deleterious roles, including that of cellular nitrating agents.

  11. VizieR Online Data Catalog: Iron Project. XLIV. Fe VI. (Chen+, 2000)

    NASA Astrophysics Data System (ADS)

    Chen, G.-X.; Pradhan, A. K.

    2000-10-01

    Relativistic atomic structure calculations for electric dipole (E1), electric quadrupole (E2) and magnetic dipole (M1) transition probabilities among the first 80 fine-structure levels of Fe VI, dominated by configurations 3d3, 3d24s, and 3d24p, are carried out using the Breit-Pauli version of the code SUPERSTRUCTURE. Experimental energies are used to improve the accuracy of these transition probabilities. Employing the 80-level collision-radiative (CR) model with these dipole and forbidden transition probabilities, and Iron Project R-matrix collisional data, we present a number of [Fe VI] line ratios applicable to spectral diagnostics of photoionized H II regions. It is shown that continuum fluorescent excitation needs to be considered in CR models in order to interpret the observed line ratios of optical [Fe VI] lines in planetary nebulae NGC 6741, IC 351, and NGC 7662. The analysis leads to parametrization of line ratios as function of, and as constraints on, the electron density and temperature, as well as the effective radiation temperature of the central source and a geometrical dilution factor. The spectral diagnostics may also help ascertain observational uncertainties. The method may be generally applicable to other objects with intensive background radiation fields, such as novae and active galactic nuclei. The extensive new Iron Project radiative and collisional calculations enable a consistent analysis of many line ratios for the complex iron ions. (5 data files).

  12. Microbial mediated iron redox cycling in Fe (hydr)oxides for nitrite removal.

    PubMed

    Lu, Yongsheng; Xu, Lu; Shu, Weikang; Zhou, Jizhi; Chen, Xueping; Xu, Yunfeng; Qian, Guangren

    2017-01-01

    Nitrite, at an environmentally relevant concentration, was significantly reduced with iron (hydr)oxides mediated by Shewanella oneidensis MR-1. The average nitrite removal rates of 1.28±0.08 and 0.65±0.02(mgL(-1))h(-1) were achieved with ferrihydrite and magnetite, respectively. The results showed that nitrite removal was able to undergo multiple redox cycles with iron (hydr)oxides mediated by Shewanella oneidensis MR-1. During the bioreduction of the following cycles, biogenic Fe(II) was subsequently chemically oxidized to Fe(III), which is associated with nitrite reduction. There was 11.18±1.26mgL(-1) of NH4(+)-N generated in the process of redox cycling of ferrihydrite. Additionally, results obtained by using X-ray diffraction showed that ferrihydrite and magnetite remained mainly stable in the system. This study indicated that redox cycling of Fe in iron (hydr)oxides was a potential process associated with NO2(-)-N removal from solution, and reduced most nitrite abiotically to gaseous nitrogen species.

  13. Evidence of Multi-step Nucleation Leading to Various Crystallization Pathways from an Fe-O-Al Melt

    PubMed Central

    Wang, G. C.; Wang, Q.; Li, S. L.; Ai, X. G.; Fan, C. G.

    2014-01-01

    The crystallization process from a solution begins with nucleation, which determines the structure and size of the resulting crystals. Further understanding of multi-pathway crystallizations from solution through two-step nucleation mechanisms is needed. This study uses density functional theory to probe the thermodynamic properties of alumina clusters at high temperature and reveals the thermodynamic relationship between these clusters and the saturation levels of dissolved oxygen and aluminum in an Fe–O–Al melt. Based on the thermodynamics of cluster formation and the experimental evidence for both excess oxygen in the Fe-O-Al melt and for alumina with a polycrystalline structure in solidified iron, we demonstrate that the appearance of various types of clusters that depends on the saturation ratio determines the nucleation steps that lead to the various crystallization pathways. Such mechanisms may also be important in nucleation and crystallization from solution. PMID:24866413

  14. Durability of PEM fuel cell cathode in the presence of Fe 3+ and Al 3+

    NASA Astrophysics Data System (ADS)

    Li, Hui; Tsay, Ken; Wang, Haijiang; Shen, Jun; Wu, Shaohong; Zhang, Jiujun; Jia, Nengyou; Wessel, Silvia; Abouatallah, Rami; Joos, Nathan; Schrooten, Jeremy

    The contamination effects of Fe 3+ and Al 3+ on the performance of polymer electrolyte membrane fuel cells were investigated by continuously injecting Fe 3+ or Al 3+ salt solution into the air stream of an operating fuel cell. Both metal ions individually caused significant cell performance degradation at a level of only 5 ppm mol in air. In addition, elevated temperature accelerated fuel cell performance degradation in the presence of Fe 3+. Moreover, the presence of Fe 3+ in an operating fuel cell resulted in the cell's sudden death, due to the formation of membrane pinholes that may have been promoted by the enhanced production of peroxy radicals catalyzed by Fe species. Half-cell tests in liquid electrolyte revealed that the presence of Al 3+ in the electrolyte changed the kinetics and mechanisms of the oxygen reduction reaction by reducing the kinetic current densities and the electron transfer number.

  15. Iron deficiency chlorosis in plants as related to Fe sources in soil

    NASA Astrophysics Data System (ADS)

    Díaz, I.; Delgado, A.; de Santiago, A.; del Campillo, M. C.; Torrent, J.

    2012-04-01

    Iron deficiency chlorosis (IDC) is a relevant agricultural problem in many areas of the World where calcareous soils are dominant. Although this problem has been traditionally ascribed to the pH-buffering effect of soil carbonates, the content and type of Fe oxides in soil contribute to explain Fe uptake by plants and the incidence of this problem. During the last two decades, it has been demonstrated Fe extraction with oxalate, related to the content of poorly crystalline Fe oxides, was well-correlated with the chlorophyll content of plants and thus with the incidence of IDC. This reveals the contribution of poorly crystalline Fe oxides in soil to Fe availability to plants in calcareous soils, previously shown in microcosm experiments using ferrihydrite as Fe source in the growing media. In order to supply additional information about the contribution of Fe sources in soil to explain the incidence of IDC and to perform accurate methods to predict it, a set of experiments involving different methods to extract soil Fe and plant cultivation in pots to correlate amounts of extracted Fe with the chlorophyll content of plants (measured using the SPAD chlorophyll meter) were performed. The first experiment involved 21 soils and white lupin cultivation, sequential Fe extraction in soil to study Fe forms, and single extractions (DTPA, rapid oxalate and non-buffered hydroxylamine). After that, a set of experiments in pot involving growing of grapevine rootstocks, chickpea, and sunflower were performed, although in this case only single extractions in soil were done. The Fe fraction more closely related to chlorophyll content in plants (r = 0.5, p < 0.05) was the citrate + ascorbate (CA) extraction, which was the fraction that releases most of the Fe related to poorly crystalline Fe oxides, thus revealing the key role of these compounds in Fe supply to plants. Fe extracted with CA was more correlated with chlorophyll content in plants that oxalate extractable Fe, probably

  16. Iron isotope fractionation between pyrite (FeS 2), hematite (Fe 2O 3) and siderite (FeCO 3): A first-principles density functional theory study

    NASA Astrophysics Data System (ADS)

    Blanchard, Marc; Poitrasson, Franck; Méheut, Merlin; Lazzeri, Michele; Mauri, Francesco; Balan, Etienne

    2009-11-01

    In addition to equilibrium isotopic fractionation factors experimentally derived, theoretical predictions are needed for interpreting isotopic compositions measured on natural samples because they allow exploring more easily a broader range of temperature and composition. For iron isotopes, only aqueous species were studied by first-principles methods and the combination of these data with those obtained by different methods for minerals leads to discrepancies between theoretical and experimental isotopic fractionation factors. In this paper, equilibrium iron isotope fractionation factors for the common minerals pyrite, hematite, and siderite were determined as a function of temperature, using first-principles methods based on the density functional theory (DFT). In these minerals belonging to the sulfide, oxide and carbonate class, iron is present under two different oxidation states and is involved in contrasted types of interatomic bonds. Equilibrium fractionation factors calculated between hematite and siderite compare well with the one estimated from experimental data (ln α57Fe/ 54Fe = 4.59 ± 0.30‰ and 5.46 ± 0.63‰ at 20 °C for theoretical and experimental data, respectively) while those for Fe(III) aq-hematite and Fe(II) aq-siderite are significantly higher that experimental values. This suggests that the absolute values of the reduced partition functions ( β-factors) of aqueous species are not accurate enough to be combined with those calculated for minerals. When compared to previous predictions derived from Mössbauer or INRXS data [Polyakov V. B., Clayton R. N., Horita J. and Mineev S. D. (2007) Equilibrium iron isotope fractionation factors of minerals: reevaluation from the data of nuclear inelastic resonant X-ray scattering and Mössbauer spectroscopy. Geochim. Cosmochim. Acta71, 3833-3846], our iron β-factors are in good agreement for siderite and hematite while a discrepancy is observed for pyrite. However, the detailed investigation of the

  17. Constraints on silicates formation in the Si-Al-Fe system: Application to hard deposits in steam generators of PWR nuclear reactors

    NASA Astrophysics Data System (ADS)

    Berger, Gilles; Million-Picallion, Lisa; Lefevre, Grégory; Delaunay, Sophie

    2015-04-01

    Introduction: The hydrothermal crystallization of silicates phases in the Si-Al-Fe system may lead to industrial constraints that can be encountered in the nuclear industry in at least two contexts: the geological repository for nuclear wastes and the formation of hard sludges in the steam generator of the PWR nuclear plants. In the first situation, the chemical reactions between the Fe-canister and the surrounding clays have been extensively studied in laboratory [1-7] and pilot experiments [8]. These studies demonstrated that the high reactivity of metallic iron leads to the formation of Fe-silicates, berthierine like, in a wide range of temperature. By contrast, the formation of deposits in the steam generators of PWR plants, called hard sludges, is a newer and less studied issue which can affect the reactor performance. Experiments: We present here a preliminary set of experiments reproducing the formation of hard sludges under conditions representative of the steam generator of PWR power plant: 275°C, diluted solutions maintained at low potential by hydrazine addition and at alkaline pH by low concentrations of amines and ammoniac. Magnetite, a corrosion by-product of the secondary circuit, is the source of iron while aqueous Si and Al, the major impurities in this system, are supplied either as trace elements in the circulating solution or by addition of amorphous silica and alumina when considering confined zones. The fluid chemistry is monitored by sampling aliquots of the solution. Eh and pH are continuously measured by hydrothermal Cormet© electrodes implanted in a titanium hydrothermal reactor. The transformation, or not, of the solid fraction was examined post-mortem. These experiments evidenced the role of Al colloids as precursor of cements composed of kaolinite and boehmite, and the passivation of amorphous silica (becoming unreactive) likely by sorption of aqueous iron. But no Fe-bearing was formed by contrast to many published studies on the Fe

  18. Synthesis and Characterization of In Situ Dendritic/Particulate α-Al(Fe,TM)Si Phase Reinforced Al Matrix Composites

    NASA Astrophysics Data System (ADS)

    Hou, L. G.; Wang, Shuai; He, Z. B.; Zhang, D.; Wang, X. D.; Zhuang, L. Z.; Zhang, J. S.

    2016-12-01

    The strength and ductility of transition metallic element alloyed Al alloys could be inevitably and severely weakened if these elements appeared as coarse intermetallics. Present studies aimed to optimize the morphologies and sizes of these intermetallics via composition design and process selection so as to decrease their detrimental effects to the properties. It is shown that the dendritic α-Al(Fe,TM)Si phase solidified as primary phase can be refined into small dendrites or micro- and submicro-sized particles via controlling the cooling rate and alloy composition, and this phase exhibits better heat resistance. After spark plasma sintering (SPS) the atomized alloy powders, the bulk aluminum matrix composites (AMCs) were successfully prepared and well strengthened by the uniformly distributed particulate α-Al(Fe,TM)Si phase. These sintered bulk composites also possess good heat resistance that might facilitate their application for some heat-resistant parts. The transmission electron microscope (TEM) and high-resolution TEM (HRTEM) results indicate these α-Al(Fe,TM)Si phases possesses body-centered-cubic structure with a lattice constant of 1.25 to 1.27 nm. The solidification or phase formation of these alloys is discussed as well as the densification process for the SPS of powders. The present studies indicate a possibility to prepare in situ small dendritic/particulate α-Al(Fe,TM)Si phase reinforced AMCs by using the casting process and controlling the normal impurity elements in Al alloys.

  19. Theoretical analysis of compatibility of several reinforcement materials with NiAl and FeAl matrices

    NASA Technical Reports Server (NTRS)

    Misra, Ajay K.

    1989-01-01

    Several potential reinforcement materials were assessed for their chemical, coefficient of thermal expansion (CTE), and mechanical compatibility with the intermetallic matrices based on NiAl and FeAl. Among the ceramic reinforcement materials, Al2O3, TiC, and TiB2, appear to be the optimum choices for NiAl and FeAl matrices. However, the problem of CTE mismatch with the matrix needs to be solved for these three reinforcement materials. Beryllium-rich intermetallic compounds can be considered as potential reinforcement materials provided suitable reaction barrier coatings can be developed for these. Based on preliminary thermodynamic calculations, Sc2O3 and TiC appear to be suitable as reaction barrier coatings for the beryllides. Several reaction barrier coatings are also suggested for the currently available SiC fibers.

  20. Characterization of novel microstructures in Al-Fe-V-Si and Al-Fe-V-Si-Y alloys processed at intermediate cooling rates

    NASA Astrophysics Data System (ADS)

    Marshall, Ryan

    Samples of an Al-Fe-V-Si alloy with and without small Y additions were prepared by copper wedge-mold casting. Analysis of the microstructures developed at intermediate cooling rates revealed the formation of an atypical morphology of the cubic alpha-Al12(Fe/V)3Si phase (Im 3 space group with a = 1.26 nm) in the form of a microeutectic with alpha-Al that forms in relatively thick sections. This structure was determined to exhibit promising hardness and thermal stability when compared to the commercial rapidly solidified and processed Al-Fe-V-Si (RS8009) alloy. In addition, convergent beam electron diffraction (CBED) and selected area electron diffraction (SAD) were used to characterize a competing intermetallic phase, namely, a hexagonal phase identified as h-AlFeSi (P6/mmm space group with a = 2.45 nm c = 1.25 nm) with evidence of a structural relationship to the icosahedral quasicrystalline (QC) phase (it is a QC approximant) and a further relationship to the more desirable alpha-Al12(Fe/V) 3Si phase, which is also a QC approximant. The analysis confirmed the findings of earlier studies in this system, which suggested the same structural relationships using different methods. As will be shown, both phases form across a range of cooling rates and appear to have good thermal stabilities. Additions of Y to the alloy were also studied and found to cause the formation of primary YV2Al20 particles on the order of 1 microm in diameter distributed throughout the microstructure, which otherwise appeared essentially identical to that of the Y-free 8009 alloy. The implications of these results on the possible development of these structures will be discussed in some detail.

  1. The distribution alloying elements in alnico 8 and 9 magnets: Site preference of ternary Ti, Fe, Co, and Ni additions in DO3 Fe3Al, Co3Al, and Ni3Al based intermetallic phases

    NASA Astrophysics Data System (ADS)

    Samolyuk, G. D.; Újfalussy, B.; Stocks, G. M.

    2014-11-01

    Recently, interest in alnico magnetic alloys has been rekindled due to their potential to substitute for rare-earth based permanent magnets provided modest improvements in their coercivity can be achieved without loss of saturation magnetization. Recent experimental studies have indicated that atomic and magnetic structure of the two phases (one AlNi-based, the other FeCo-based) that comprise these spinodally decomposed alloy is not as simple as previously thought. A key issue that arises is the distribution of Fe, Co, and Ti within the AlNi-based matrix phase. In this paper, we report the results of first-principles calculations of the site preference of ternary alloying additions in DO3 Fe3Al, Co3Al, and Ni3Al alloys, as models for the aluminide phase. For compound compositions that are Al rich, which correspond to experimental situation, Ti and Fe are found to occupy the α sites, while Co and Ni prefer the γ sites of the DO3 lattice. An important finding is that the magnetic moments of transition metals in Fe3Al and Co3Al are ordered ferromagnetically, whereas the Ni3Al were found to be nonmagnetic unless the Fe or Co is added as a ternary element.

  2. The distribution alloying elements in alnico 8 and 9 magnets: Site preference of ternary Ti, Fe, Co, and Ni additions in DO3 Fe3Al, Co3Al, and Ni3Al based intermetallic phases

    DOE PAGES

    Samolyuk, G. D.; Újfalussy, B.; Stocks, G. M.

    2014-11-07

    Recently, interest in alnico magnetic alloys has been rekindled due to their potential to substitute for rare-earth based permanent magnets provided modest improvements in their coercivity can be achieved without loss of saturation magnetization. Recent experimental studies have indicated that atomic and magnetic structure of the two phases (one AlNi-based, the other FeCo-based) that comprise these spinodally decomposed alloy is not as simple as previously thought. A key issue that arises is the distribution of Fe, Co and Ti within the AlNi-based matrix phase. In our paper we report the results of first-principles calculations of the site preference of ternarymore » alloying additions in DO3 Fe3Al, Co3Al and Ni3Al alloys, as models for the aluminide phase. For compound compositions that are Al rich, which corresponds to experimental situation, Ti and Fe are found to occupy the sites, while Co and Ni prefer the sites of the DO3 lattice. Finally, an important finding is that the magnetic moments of transition metals in Fe3Al and Co3Al are ordered ferromagnetically, whereas the Ni3Al were found to be nonmagnetic unless the Fe or Co are added as a ternary element.« less

  3. Effect of interfacial iron oxidation on the exchange bias in CoO/Fe bilayers

    NASA Astrophysics Data System (ADS)

    Młyńczak, E.; Gurgul, J.; Przewoźnik, J.; Wilgocka-Ślęzak, D.; Freindl, K.; Spiridis, N.; Korecki, J.

    2014-06-01

    The relation between the interface structure and the exchange bias was studied in the epitaxial CoO/Fe(0 0 1) bilayers that were grown on MgO(0 0 1) using molecular beam epitaxy. Three samples with different interface structures were prepared. The CoO/Fe bilayer, which was prepared using the reactive evaporation of CoO, served as the reference sample. In the other two samples, the CoO/Fe interfaces were modified prior to the CoO growth using either (i) the deposition of a 2 Å thick Co layer or (ii) an exposure to molecular oxygen, which resulted in under- and over-oxidized CoO/Fe interfaces, respectively. The actual structures of the resulting interfaces were revealed using conversion electron Mössbauer spectroscopy. For each sample, an iron oxide was found at the interface, and its amount depended on the sample preparation recipe. The exchange bias effect (EB), as a function of the temperature, was experimentally studied in detail using VSM magnetometry. The coercivity showed a distinct peak near the blocking temperature for all samples; however, the peak's location and its width were diverse. The obtained EB values depended on the interface structure. The largest hysteresis loop shift (HEB = 180 Oe at 4 K) was obtained for the sample with the thickest interfacial iron oxide layer.

  4. Salivary Iron (Fe) Ion Levels, Serum Markers of Anemia and Caries Activity in Pregnant Women.

    PubMed

    Costa, Elisa Miranda; Azevedo, Juliana Aires Paiva de; Martins, Rafiza Félix Marão; Rodrigues, Vandilson Pereira; Alves, Cláudia Maria Coêlho; Ribeiro, Cecília Cláudia Costa; Thomaz, Erika Bárbara Abreu Fonseca

    2017-03-01

    Introduction Anemia is a very frequent event among pregnant women. There are evidences of differences in the incidence of dental caries between pregnant and non-pregnant women, but the relationship between salivary iron (Fe) and serum markers of anemia and caries development has not been investigated. Objective To evaluate the correlation between salivary (Fe) and serum iron (Fe, ferritin and hemoglobin) parameters in pregnant women with the development of dental caries. Methods A prospective cohort was conducted with 59 women. The outcome of interest was represented by new dental caries lesions during pregnancy, using the Nyvad criteria. Pregnant women were evaluated at three clinical times: up to the 16th week of gestational age (GA) (T1), in the last trimester of pregnancy (T2), and postpartum (T3), at the Mother and Child Unit of University Hospital of the Universidade Federal do Maranhão. A stimulated saliva sample was collected for biochemical analysis of salivary Fe, and a blood sample was collected early in the morning. The correlation between salivary and serum Fe was evaluated through the Pearson correlation test. Analysis of variance (ANOVA) and Kruskal-Wallis were used to compare the means of anemia parameters at different times. The Student's t and Mann-Whitney tests were used to compare the anemia parameters between the groups of pregnant women (with and without new caries lesions). Results Serum Fe concentrations were higher in the first trimester of pregnancy and lower after delivery (p = 0.036). It was also observed that the ferritin concentrations were higher in the first trimester and lower at the end of gestation (p = 0.011). There was no association between the expositions of salivary iron and anemia, and the development of dental caries. There was a positive correlation between serum Fe in T1 and salivary Fe in T2 (p < 0.05). Conclusion The serum markers of anemia were more prevalent in the last trimester of pregnancy.

  5. Mössbauer study of the effect of pH on Fe valence in iron-polygalacturonate as a medicine for human anaemia

    NASA Astrophysics Data System (ADS)

    Kuzmann, E.; Garg, V. K.; de Oliveira, A. C.; Klencsár, Z.; Szentmihályi, K.; Fodor, J.; May, Z.; Homonnay, Z.

    2015-02-01

    Iron-polygalacturonate complexes have been synthesized from polygalacturonic acid by applying a novel preparation method in order to develop medicine suitable for the effective iron supplementation of the human body in the case of anemia. Since the iron uptake depends on the oxidation state of iron, 57Fe Mössbauer spectroscopy was used to study the occurrence of different valence states in the iron-polygalacturonate complexes prepared under different circumstances. The Mössbauer-spectra indicated the presence of iron both in FeII and FeIII states in the investigated iron-polygalacturonate compounds, the occurrence of which varied with the preparation parameters. A correlation of the relative occurrence of iron valence states with the pH has been found. The relative occurrence of FeIII was found to increase with increasing pH. The knowledge of this correlation can help find optimum preparation conditions of iron-polygalacturonates to cure human anemia.

  6. Structure and electromagnetic properties of FeSiAl particles coated by MgO

    NASA Astrophysics Data System (ADS)

    Zhang, Yu; Zhou, Ting-dong

    2017-03-01

    FeSiAl particles with a layer of MgO surface coating have excellent soft magnetic and electromagnetic properties. In order to obtain the FeSiAl/MgO composites, Mg(OH)2 sol prepared by sol-gel process was well-mixed with FeSiAl flake particles, and then treated by calcination at 823 K in vacuum. The microstructural, morphological and electromagnetic parameters of FeSiAl/MgO particles were tested. Accordingly, the electromagnetic wave reflection loss in the frequency range of 0.5-18 GHz was calculated. The results show that the surface coating increases coercivity Hc and decreases complex permittivity, leading to a good impedance matching. When the coating amount was 7.5%, reflection loss of the composite particles can reach to -33 dB.

  7. Understanding phase stability of Al-Co-Cr-Fe-Ni high entropy alloys

    SciTech Connect

    Zhang, Chuan; Zhang, Fan; Diao, Haoyan; Gao, Michael C.; Tang, Zhi; Poplawsky, Jonathan D.; Liaw, Peter K.

    2016-07-19

    The concept of high entropy alloy (HEA) opens a vast unexplored composition range for alloy design. As a well-studied system, Al-Co-Cr-Fe-Ni has attracted tremendous amount of attention to develop new-generation low-density structural materials for automobile and aerospace applications. In spite of intensive investigations in the past few years, the phase stability within this HEA system is still poorly understood and needs to be clarified, which poses obstacles to the discovery of promising Al-Co-Cr-Fe-Ni HEAs. In the present work, the CALPHAD approach is employed to understand the phase stability and explore the phase transformation within the Al-Co-Cr-Fe-Ni system. As a result, the phase-stability mapping coupled with density contours is then constructed within the composition - temperature space, which provides useful guidelines for the design of low-density Al-Co-Cr-Fe-Ni HEAs with desirable properties.

  8. Magnetic states of multilayer Fe /Cr structures with ultrathin iron layers

    NASA Astrophysics Data System (ADS)

    Drovosekov, A. B.; Kreines, N. M.; Kholin, D. I.

    2010-08-01

    The evolution of the magnetic properties of Fe /Cr superlattices is studied as the nominal thickness of the iron layers is reduced to atomic values, when these layers are no longer continuous. The studies were done on multilayer samples with Fe thicknesses of 2-6Å and chromium spacer thicknesses of 10 and 20Å. The samples were prepared by molecular beam epitaxy. The static magnetization and complex magnetic susceptibility were measured and FMR spectra taken. It was found that, depending on the thickness of the Fe layers and temperature, different magnetic phases are realized in the system: supermagnetism, magnetic ordering, and a nonergodic state characterized by a dependence of the magnetization of a sample on its magnetic prehistory. The observed nonergodic phase is found to exhibit spin glass properties. A qualitative phase diagram of the magnetic states of this system is constructed.

  9. Vibrational spectroscopic characterization of the phosphate mineral kulanite Ba(Fe2+,Mn2+,Mg)2(Al,Fe3+)2(PO4)3(OH)3

    NASA Astrophysics Data System (ADS)

    Frost, Ray L.; López, Andrés; Xi, Yunfei; Granja, Amanda; Scholz, Ricardo

    2013-11-01

    The mineral kulanite BaFe2Al2(PO4)3(OH)3, a barium iron aluminum phosphate, has been studied by using a combination of electron microscopy and vibrational spectroscopy. Scanning electron microscopy with EDX shows the mineral is homogenous with no other phases present. The Raman spectrum is dominated by an intense band at 1022 cm-1 assigned to the PO43- ν1 symmetric stretching mode. Low intensity Raman bands at 1076, 1110, 1146, 1182 cm-1 are attributed to the PO43 - ν3 antisymmetric stretching vibrations. The infrared spectrum shows a complex spectral profile with overlapping bands. Multiple phosphate bending vibrations supports the concept of a reduction in symmetry of the phosphate anion. Raman spectrum at 3211, 3513 and 3533 cm-1 are assigned to the stretching vibrations of the OH units. Vibrational spectroscopy enables aspects on the molecular structure of kulanite to be assessed.

  10. Effect of solution chemistry on arsenic sorption by Fe- and Al-based drinking-water treatment residuals.

    PubMed

    Nagar, Rachana; Sarkar, Dibyendu; Makris, Konstantinos C; Datta, Rupali

    2010-02-01

    Drinking-water treatment residual (WTR) have been proposed as a low-cost alternative sorbent for arsenic (As) - contaminated aquatic and soil systems. However, limited information exists regarding the effect of solution chemistry on As sorption by WTR. A batch incubation study was carried out to investigate the effect of solution pH (3-9) on As(V) sorption by Al- and Fe-based WTR as a function of solid: solution ratio (SSR) and initial As concentration. The effect of competing ligands (phosphate-P(V) and sulfate), and complexing metal (calcium) on As(V) sorption envelopes at the optimum SSR (200gL(-1)) was also evaluated. At 200gL(-1) SSR, maximum As(V) sorption ( approximately 100%) exhibited by the Fe-WTR was limited at the pH range of 3-7, whereas, the Al-WTR demonstrated approximately 100% As(V) sorption in the entire pH range. The negative pH effect on As(V) sorption became more pronounced with increasing initial As concentrations and decreasing SSR. Sorption of As(V) by surfaces of both WTR decreased in the presence of P(V), exhibiting strong pH dependence. Only for the Fe-WTR, increased dissolved iron concentrations at pH>7 supported a Fe-hydroxide reductive dissolution mechanism to account for the enhanced As sorption at alkaline pH. Addition of sulfate did not influence As(V) sorption by both WTR. A cooperative effect of calcium on As(V) sorption was observed at alkaline pH due to the formation of a calcium-arsenate phase. The constant capacitance model provided reasonable fits to the sorption envelope data for both single ion and binary ion (As and P) systems, but it was unable to explain the enhanced As sorption by the Fe-WTR at pH>7.

  11. Role of Nitrosomonas europaea NitABC iron transporter in the uptake of Fe3+-siderophore complexes.

    PubMed

    Vajrala, Neeraja; Sayavedra-Soto, Luis A; Bottomley, Peter J; Arp, Daniel J

    2010-11-01

    Nitrosomonas europaea has a single three-gene operon (nitABC) encoding an iron ABC transporter system (NitABC). Phylogenetic analysis clustered the subunit NitB with Fe(3+)-ABC transporter permease components from other organisms. The N. europaea strain deficient in nitB (nitB::kan) grew well in either Fe-replete or Fe-limited media and in Fe-limited medium containing the catecholate-type siderophore, enterobactin or the citrate-based dihydroxamate-type siderophore, aerobactin. However, the nitB::kan mutant strain was unable to grow in Fe-limited media containing either the hydroxamate-type siderophores, ferrioxamine and ferrichrome or the mixed-chelating type siderophore, pyoverdine. Exposure of N. europaea cells to a ferrichrome analog coupled to the fluorescent moiety naphthalic diimide (Fhu-NI) led to increase in fluorescence in the wild type but not in nitB::kan mutant cells. Spheroplasts prepared from N. europaea wild type exposed to Fhu-NI analog retained the fluorescence, while spheroplasts of the nitB::kan mutant were not fluorescent. NitABC transports intact Fe(3+)-ferrichrome complex into the cytoplasm and is an atypical ABC type iron transporter for Fe(3+) bound to ferrioxamine, ferrichrome or pyoverdine siderophores into the cytoplasm. The mechanisms to transport iron in either the Fe(3+) or Fe(2+) forms or Fe(3+) associated with enterobactin or aerobactin siderophores into the cell across the cytoplasmic membrane are as yet undetermined.

  12. From Tetrahedral to Octahedral Iron Coordination: Layer Compression in Topochemically Prepared FeLa2Ti3O10.

    PubMed

    Gustin, Léa; Hosaka, Yoshiteru; Tassel, Cédric; Aharen, Tomoko; Shimakawa, Yuichi; Kageyama, Hiroshi; Wiley, John B

    2016-11-07

    Synthesis, characterization, and thermal modification of the new layered perovskite FeLa2Ti3O10 have been studied. FeLa2Ti3O10 was prepared by ion exchange of the triple-layered Ruddlesden-Popper phase Li2La2Ti3O10 with FeCl2 at 350 °C under static vacuum. Rietveld refinement on synchrotron X-ray diffraction data indicates that the new phase is isostructural with CoLa2Ti3O10, where Fe(II) cations occupy slightly compressed/flattened interlayer tetrahedral sites. Magnetic measurements on FeLa2Ti3O10 display Curie-Weiss behavior at high temperatures and a spin-glass transition at lower temperatures (<30 K). Thermal treatment in oxygen shows that FeLa2Ti3O10 undergoes a significant cell contraction (Δc ≈ -2.7 Å) with a change in the oxidation state of iron (Fe(2+) to Fe(3+)); structural analysis and Mössbauer studies indicate that upon oxidation the local iron environment goes from tetrahedral to octahedral coordination with some deintercalation of iron as Fe2O3 to produce Fe0.67La2Ti3O10.

  13. HIGH TEMPERATURE BRAZING ALLOY FOR JOINT Fe-Cr-Al MATERIALS AND AUSTENITIC AND FERRITIC STAINLESS STEELS

    DOEpatents

    Cost, R.C.

    1958-07-15

    A new high temperature brazing alloy is described that is particularly suitable for brazing iron-chromiumaluminum alloys. It consists of approximately 20% Cr, 6% Al, 10% Si, and from 1.5 to 5% phosphorus, the balance being iron.

  14. Plasma Nitriding Behavior of Fe-C-M (M = Al, Cr, Mn, Si) Ternary Martensitic Steels

    NASA Astrophysics Data System (ADS)

    Tomio, Yusaku; Kitsuya, Shigeki; Oh-ishi, Keilchiro; Hono, Kazuhiro; Miyamoto, Goro; Furuhara, Tadashi

    2014-01-01

    Change in surface hardness and nitrides precipitated in Fe-0.6C binary and Fe-0.6 mass pct C-1 mass pct M (M = Al, Cr, Mn, Si) ternary martensitic alloys during plasma nitriding were investigated. Surface hardness was hardly increased in the Fe-0.6C binary alloy and slightly increased in Fe-0.6C-1Mn and Fe-0.6C-1Si alloys. On the other hand, it was largely increased in Fe-0.6C-1Al and Fe-0.6C-1Cr alloys. In all the Fe-0.6C-1M alloys except for the Si-added alloy, fine platelet alloy nitrides precipitated inside martensite laths. In the Fe-0.6C-1Si alloy, Si-enriched film was observed mainly at a grain boundary and an interface between cementite and matrix. Crystal structure of nitrides observed in the martensitic alloys was similar to those in Fe-M binary ferritic alloys reported previously. However, there was a difference in hardening behavior between ferrite and martensite due to a high density of dislocations acting as a nucleation site of the nitrides and partitioning of an alloying element between martensite and cementite changing the driving force of precipitation of the nitrides.

  15. Structure and magnetism of granular Fe-Al 2O 3

    NASA Astrophysics Data System (ADS)

    Santos, A.; Ardisson, J. D.; Viegas, A. D. C.; Schmidt, J. E.; Persiano, A. I. C.; Macedo, W. A. A.

    2001-05-01

    The structural and magnetic properties of granular Fe-Al 2O 3 nanocomposite obtained starting from sol-gel processing are presented. Samples with nominal Fe content ranging from 20% to 62% in volume were prepared. The conversion of Fe oxides into metallic Fe was obtained by calcination at 800°C followed by reduction at 600°C for 2 h in H 2 atmosphere. After reduction, our results indicated up to 78% α-Fe, preserving the mean diameter of the metallic nanoparticles between 50 and 80 nm, ˜16% Fe oxides and ˜7% interstitial Fe 2+ and substitutional Fe 3+ cations in the Al 2O 3 lattice. Vibrating sample magnetometry at 300 K resulted in coercivity between 400 and 630 Oe and saturation magnetization between 40 and 134 emu/g. From transport measurements, the highest magnetoresistance, close to 2% at room temperature, was observed for samples with 25% α-Fe and 51 vol% total Fe.

  16. Mixed-valence iron minerals on Venus: Fe(2+)-Fe(3+) oxides and oxy-silicates formed by surface-atmosphere interactions

    NASA Technical Reports Server (NTRS)

    Burns, Roger G.; Straub, Darcy W.

    1992-01-01

    Inferences from these investigations are that Fe(3+)-bearing minerals such as hematite magnesioferrite, acmite, and epidote are thermodynamically unstable, and that magnetite is the predominant mixed-valence iron oxide mineral on venus. Recently, the Fe(2+)-Fe(3+) silicate mineral laihunite was proposed to be a reaction product of olivine with the venusian atmosphere. This possibility is discussed further here. We suggest that other mixed-valence Fe(2+)-Fe(3+)-Oz-OH(-) silicates could also result from surface-atmosphere interactions on Venus. Topics discussed include the following: (1) conversion of hematite to magnetite; (2) stability of laihunite; (3) the possible existence of oxy-amphiboles and oxy-micas on Venus; and (4) other mixed-valence Fe(2+)-Fe(3+) silicates likely to exist on Venus.

  17. Growth and characterization of insulating ferromagnetic semiconductor (Al,Fe)Sb

    SciTech Connect

    Anh, Le Duc Kaneko, Daiki; Tanaka, Masaaki; Hai, Pham Nam

    2015-12-07

    We investigate the crystal structure, transport, and magnetic properties of Fe-doped ferromagnetic semiconductor (Al{sub 1−x},Fe{sub x})Sb thin films up to x = 14% grown by molecular beam epitaxy. All the samples show p-type conduction at room temperature and insulating behavior at low temperature. The (Al{sub 1−x},Fe{sub x})Sb thin films with x ≤ 10% maintain the zinc blende crystal structure of the host material AlSb. The (Al{sub 1−x},Fe{sub x})Sb thin film with x = 10% shows intrinsic ferromagnetism with a Curie temperature (T{sub C}) of 40 K. In the (Al{sub 1−x},Fe{sub x})Sb thin film with x = 14%, a sudden drop of the hole mobility and T{sub C} was observed, which may be due to the microscopic phase separation. The observation of ferromagnetism in (Al,Fe)Sb paves the way to realize a spin-filtering tunnel barrier that is compatible with well-established III-V semiconductor devices.

  18. Viability of thin wall tube forming of ATF FeCrAl

    SciTech Connect

    Maloy, Stuart Andrew; Aydogan, Eda; Anderoglu, Osman; Lavender, Curt; Yamamoto, Yukinori

    2016-09-16

    Fabrication of thin walled tubing of FeCrAl alloys is critical to its success as a candidate enhanced accident-tolerant fuel cladding material. Alloys that are being investigated are Generation I and Generation II FeCrAl alloys produced at ORNL and an ODS FeCrAl alloy, MA-956 produced by Special Metals. Gen I and Gen II FeCrAl alloys were provided by ORNL and MA-956 was provided by LANL (initially produced by Special Metals). Three tube development efforts were undertaken. ORNL led the FeCrAl Gen I and Gen II alloy development and tube processing studies through drawing tubes at Rhenium Corporation. LANL received alloys from ORNL and led tube processing studies through drawing tubes at Century Tubing. PNNL led the development of tube processing studies on MA-956 through pilger processing working with Sandvik Corporation. A summary of the recent progress on tube development is provided in the following report and a separate ORNL report: ORNL/TM-2015/478, “Development and Quality Assessments of Commercial Heat Production of ATF FeCrAl Tubes”.

  19. Effect of parent body evolution on equilibrium and kinetic isotope fractionation: a combined Ni and Fe isotope study of iron and stony-iron meteorites

    NASA Astrophysics Data System (ADS)

    Chernonozhkin, Stepan M.; Goderis, Steven; Costas-Rodríguez, Marta; Claeys, Philippe; Vanhaecke, Frank

    2016-08-01

    Various iron and stony-iron meteorites have been characterized for their Ni and Fe isotopic compositions using multi-collector inductively coupled plasma-mass spectrometry (MC-ICP-MS) after sample digestion and chromatographic separation of the target elements in an attempt to further constrain the planetary differentiation processes that shifted these isotope ratios and to shed light on the formational history and evolution of selected achondrite parent body asteroids. Emphasis was placed on spatially resolved isotopic analysis of iron meteorites, known to be inhomogeneous at the μm to mm scale, and on the isotopic characterization of adjacent metal and silicate phases in main group pallasites (PMG), mesosiderites, and the IIE and IAB complex silicate-bearing iron meteorites. In a 3-isotope plot of 60/58Ni versus62/58Ni, the slope of the best-fitting straight line through the laterally resolved Ni isotope ratio data for iron meteorites reveals kinetically controlled isotope fractionation (βexper = 1.981 ± 0.039, 1 SD), predominantly resulting from sub-solidus diffusion (with the fractionation exponent β connecting the isotope fractionation factors, as α62/58 =α60/58β). The observed relation between δ56/54Fe and Ir concentration in the metal fractions of PMGs and in IIIAB iron meteorites indicates a dependence of the bulk Fe isotopic composition on the fractional crystallization of an asteroidal metal core. No such fractional crystallization trends were found for the corresponding Ni isotope ratios or for other iron meteorite groups, such as the IIABs. In the case of the IIE and IAB silicate-bearing iron meteorites, the Fe and Ni isotopic signatures potentially reflect the influence of impact processes, as the degree of diffusion-controlled Ni isotope fractionation is closer to that of Fe compared to what is observed for magmatic iron meteorite types. Between the metal and olivine counterparts of pallasites, the Fe and Ni isotopic compositions show clearly

  20. Spin crossover in (Mg,Fe3+)(Si,Fe3+)O3 bridgmanite: Effects of disorder, iron concentration, and temperature

    NASA Astrophysics Data System (ADS)

    Shukla, Gaurav; Wentzcovitch, Renata M.

    2016-11-01

    The spin crossover of iron in Fe3+ -bearing bridgmanite, the most abundant mineral of the Earth's lower mantle, is by now a well-established phenomenon, though several aspects of this crossover remain unclear. Here we investigate effects of disorder, iron concentration, and temperature on this crossover using ab initio LDA + Usc calculations. The effect of concentration and disorder are addressed using complete statistical samplings of coupled substituted configurations in super-cells containing up to 80 atoms. Vibrational/thermal effects on the crossover are addressed within the quasiharmonic approximation. The effect of disorder seems quite small, while increasing iron concentration results in considerable increase in the crossover pressure. Our calculated compression curves for iron-free, Fe2+ -, and Fe3+ -bearing bridgmanite compare well with the latest experimental measurements. The comparison also suggests that in a closed system, Fe2+ present in the sample may transform into Fe3+ by introduction of Mg and O vacancies with increasing pressure. As in the spin crossover in ferropericlase, this crossover in bridgmanite is accompanied by a clear volume reduction and an anomalous softening of the bulk modulus throughout the crossover pressure range. These effects reduce significantly with increasing temperature. Though the concentration of [Fe3+]Si in bridgmanite may be small, related elastic anomalies may impact the interpretation of radial and lateral velocity structures of the Earth's lower mantle.

  1. Coordinated induction of Nrf2 target genes protects against iron nitrilotriacetate (FeNTA)-induced nephrotoxicity

    SciTech Connect

    Tanaka, Yuji; Aleksunes, Lauren M. |; Goedken, Michael J.; Chen, Chuan; Reisman, Scott A.; Manautou, Jose E.; Klaassen, Curtis D.

    2008-09-15

    The iron chelate, ferric nitrilotriacetate (FeNTA), induces acute proximal tubular necrosis as a consequence of lipid peroxidation and oxidative tissue damage. Chronic exposure of FeNTA leads to a high incidence of renal adenocarcinomas in rodents. NF-E2-related factor 2 (Nrf2) is a transcription factor that is activated by oxidative stress and electrophiles, and regulates the basal and inducible expression of numerous detoxifying and antioxidant genes. To determine the roles of Nrf2 in regulating renal gene expression and protecting against oxidative stress-induced kidney damage, wild-type and Nrf2-null mice were administered FeNTA. Renal Nrf2 protein translocated to the nucleus at 6h after FeNTA treatment. FeNTA increased mRNA levels of Nrf2 target genes, including NQO1, GCLC, GSTpi1/2, Mrp1, 2, and 4 in kidneys from wild-type mice, but not Nrf2-null mice. Protein expression of NQO1, a prototypical Nrf2 target gene, was increased in wild-type mice, with no change in Nrf2-null mice. FeNTA produced more nephrotoxicity in Nrf2-null mice than wild-type mice as indicated by higher serum urea nitrogen and creatinine levels, as more urinary NAG, stronger 4-hydroxynonenal protein adduct staining, and more extensive proximal tubule damage. Furthermore, pretreatment with CDDO-Im, a potent small molecule Nrf2 activator, protected mice against FeNTA-induced renal toxicity. Collectively, these results suggest that activation of Nrf2 protects mouse kidneys from FeNTA-induced oxidative stress damage by coordinately up-regulating the expression of cytoprotective genes.

  2. Magnetic and microstructural properties of nanocrystalline Fe-25 at% Al and Fe-25 at% Al +0.2 at%B alloys prepared by mechanical alloying process

    NASA Astrophysics Data System (ADS)

    Ibn Gharsallah, H.; Makhlouf, T.; Escoda, L.; Suñol, J. J.; Khitouni, M.

    2016-04-01

    In the present work, structural and magnetic properties of nanocrystalline Fe-25at%Al and Fe-25at%Al+0.02at%B alloys produced by mechanical alloying were studied. Their microstructural properties were investigated by X-ray diffraction, scanning electron microscopy and vibrating sample magnetometer. A BCC-nanostructured Fe(Al,B) solid solution with an average crystallite size of about 18nm has been produced by milling for 4h. Whereas in Fe-25at%Al the alloying process has been accomplished after 16h of milling. It is found that B speeds up the formation of a bcc phase with finer microstructure (around 5nm) after 40h of milling. When increasing the milling time, the crystallite size decreases for all powders. An increase in microstrain was observed with increasing the milling time and also with addition of boron. Coercivity and the saturation magnetization of alloyed powders were measured at room temperature by a vibration sample magnetization. The magnetic measurements show a contrasting saturation magnetization and coercivity ( Hc) in both alloys. These variations are explained by crystallite size and strain variations in the samples during milling.

  3. Improvement of the Eakins and Brown method for measuring 59Fe and 55Fe in blood and other iron-containing materials by liquid scintillation counting and sample preparation using microwave digestion and ion-exchange column purification of iron.

    PubMed

    Viteri, F E; Kohaut, B A

    1997-01-01

    The simultaneous measurement of 59Fe and 55Fe in whole blood by liquid scintillation counting by the Eakins and Brown (EB) method is extensively used in iron absorption studies. The EB method requires many steps which increase the chances of error and decrease its sensitivity. We describe two modifications to the above method consisting of microwave digestion and column purification of iron. This "New Method" (NM) is simpler and more precise, and sensitive than the EB method. Counting efficiencies with the NM are similar for 59Fe (75%) as with the EB method but are better for 55Fe (29% for NM vs 22%), and cross counting from 59Fe into the 55Fe window is lower with the NM (3.7-4.5%) than with the EB method (10-12%). For the NM, recoveries of radioactive blood samples, in relation to processed standards ranged from 100 to 103% for 59Fe and 101 to 113% for 55Fe. For the EB method, recoveries ranged from 94 to 99% for 59Fe and from 88 to 93% for 55Fe. Even with very low counts, average intrarun CV with the NM was lower than 5.4% for either isotope, while it was as high as 10.0% for 55Fe with the EB method.

  4. Modeling of Iron K Lines: Radiative and Auger Decay Data for Fe II-Fe IX

    NASA Technical Reports Server (NTRS)

    Palmeri, P.; Mendoza, C.; Kallman, T. R.; Bautista, M. A.; Melendez, M.

    2003-01-01

    A detailed analysis of the radiative and Auger de-excitation channels of K-shell vacancy states in Fe II-Fe IX has been carried out. Level energies, wavelengths, A-values, Auger rates and fluorescence yields have been calculated for the lowest fine-structure levels populated by photoionization of the ground state of the parent ion. Different branching ratios, namely K alpha 2/K alpha 1, K beta/K alpha, KLM/KLL, KMM/KLL, and the total K-shell fluorescence yields, omega(sub k), obtained in the present work have been compared with other theoretical data and solid-state measurements, finding good general agreement with the latter. The Kalpha 2/K alpha l ratio is found to be sensitive to the excitation mechanism. From these comparisons it has been possible to estimate an accuracy of approx.10% for the present transition probabilities.

  5. Microstructured Al/Fe2O3/Nitrocellulose Energetic Fibers Realized by Electrospinning

    NASA Astrophysics Data System (ADS)

    Li, Rui; Xu, Hongmei; Hu, Hailong; Yang, Guangcheng; Wang, Jun; Shen, Jinpeng

    2014-01-01

    At present, metastable intermolecular composites (MICs) have been widely studied for their potential in high-density energetic materials and nanotechnology, but the relatively low-pressure discharge in a short period of time and the oxidation of Al powders have seriously impeded their applications in rocket solid fuels and explosives. In this work, the authors successfully fabricated microstructured Al/Fe2O3/nitrocellulose (Al/Fe2O3/NC) fibers via simple electrospinning, introducing nitrocellulose (NC), a gas generator to MICs. In view of previous reports, wrapping nAl in NC fibers might reduce their further oxidation during storage. In addition, the thermal properties and elastic modulus of NC fibers were measured before and after adding Al/Fe2O3.

  6. Microstructure properties and microhardness of rapidly solidified Al64Cu20Fe12Si4 quasicrystal alloy

    NASA Astrophysics Data System (ADS)

    Karaköse, Ercan; Keskin, Mustafa

    2012-04-01

    This paper presents differences in the microstructure and microhardness properties of conventional casting (ingot) and rapidly solidified Al64Cu20Fe12Si4 quasicrystal (QC) alloys. The phases present in the Al64Cu20Fe12Si4 ingot alloy were determined to be icosahedral quasicrystalline (IQC) Ψ-Al65Cu20Fe15, cubic β-AlFe, tetragonal θ-Al2Cu, and monoclinic λ-A13Fe4 phases, whereas only IQC Ψ-Al65Cu20Fe15 and cubic β-AlFe phases were identified in the rapidly solidified alloy. The microhardness value of the melt spun alloy was measured to be approximately 790 kg/mm2. Microhardness increases with increasing solidification rates.

  7. Comparative study using MS and XRD of Fe80Al20 alloy produced by mechanical alloying

    NASA Astrophysics Data System (ADS)

    Hadef, F.; Otmani, A.; Grenèche, J. M.

    2013-08-01

    An X-ray diffraction and 57Fe Mössbauer effect study of mechanically alloyed Fe80Al20 is presented. X-ray measurements indicate that the disordered bcc α-Fe(Al) solid solution was formed after 2 h of milling, while the analysis of Mössbauer spectra suggested that total dissolution of aluminium is achieved after 10 h of milling. These differences can be attributed to: (i) rapid nanocrystallization of aluminium and/or (ii) small particles with small amounts of aluminium cannot be detected by the X-ray diffraction technique.

  8. Perpendicular magnetic anisotropy in Ta|Co40Fe40B20|MgAl2O4 structures and perpendicular CoFeB|MgAl2O4|CoFeB magnetic tunnel junction

    NASA Astrophysics Data System (ADS)

    Tao, B. S.; Li, D. L.; Yuan, Z. H.; Liu, H. F.; Ali, S. S.; Feng, J. F.; Wei, H. X.; Han, X. F.; Liu, Y.; Zhao, Y. G.; Zhang, Q.; Guo, Z. B.; Zhang, X. X.

    2014-09-01

    Magnetic properties of Co40Fe40B20 (CoFeB) thin films sandwiched between Ta and MgAl2O4 layers have been systematically studied. For as-grown state, Ta/CoFeB/MgAl2O4 structures exhibit good perpendicular magnetic anisotropy (PMA) with interface anisotropy Ki = 1.22 erg/cm2, which further increases to 1.30 erg/cm2 after annealing, while MgAl2O4/CoFeB/Ta multilayer shows in-plane magnetic anisotropy and must be annealed in order to achieve PMA. For bottom CoFeB layer, the thickness window for PMA is from 0.6 to 1.0 nm, while that for top CoFeB layer is between 0.8 and 1.4 nm. Perpendicular magnetic tunnel junctions (p-MTJs) with a core structure of CoFeB/MgAl2O4/CoFeB have also been fabricated and tunneling magnetoresistance ratio of about 36% at room temperature and 63% at low temperature have been obtained. The intrinsic excitations in the p-MTJs have been identified by inelastic electron-tunneling spectroscopy.

  9. Environmental application of millimeter-scale sponge iron (s-Fe(0)) particles (II): the effect of surface copper.

    PubMed

    Ju, Yongming; Liu, Xiaowen; Liu, Runlong; Li, Guohua; Wang, Xiaoyan; Yang, Yanyan; Wei, Dongyang; Fang, Jiande; Dionysiou, Dionysios D

    2015-04-28

    To enhance the catalytic reactivity of millimeter-scale particles of sponge iron (s-Fe(0)), Cu(2+) ions were deposited on the surface of s-Fe(0) using a simple direct reduction reaction, and the catalytic properties of the bimetallic system was tested for removal of rhodamine B (RhB) from an aqueous solution. The influence of Cu(0) loading, catalyst dosage, particle size, initial RhB concentration, and initial pH were investigated, and the recyclability of the catalyst was also assessed. The results demonstrate that the 3∼5 millimeter s-Fe(0) particles (s-Fe(0)(3∼5mm)) with 5wt% Cu loading gave the best results. The removal of RhB followed two-step, pseudo-first-order reaction kinetics. Cu(0)-s-Fe(0) showed excellent stability after five reuse cycles. Cu(0)-s-Fe(0) possesses great advantages compared to nanoscale zero-valent iron, iron power, and iron flakes as well as its bimetals. The surface Cu(0) apparently catalyzes the production of reactive hydrogen atoms for indirect reaction and generates Fe-Cu galvanic cells that enhance electron transfer for direct reaction. This bimetallic catalyst shows great potential for the pre-treatment of recalcitrant wastewaters. Additionally, some oxides containing iron element are selected to simulate the adsorption process. The results prove that the adsorption process of FeOOH, Fe2O3 and Fe3O4 played minor role for the removal of RhB.

  10. Thermal Stability of the Dynamic Magnetic Properties of FeSiAl-Al2O3 and FeSiAl-SiO2 Films Grown by Gradient-Composition Sputtering Technique

    NASA Astrophysics Data System (ADS)

    Zhong, Xiaoxi; Phuoc, Nguyen N.; Soh, Wee Tee; Ong, C. K.; Peng, Long; Li, Lezhong

    2017-01-01

    We carry out a systematic investigation of the dynamic magnetic properties of FeSiAl-Al2O3 and FeSiAl-SiO2 thin films prepared by gradient-composition deposition technique with respect to temperature in the range of 300 K to 420 K. It was found that the magnetic anisotropy field ( H K) and ferromagnetic resonance frequency ( f FMR) are increased with increasing deposition angle ( β) due to the enhancement of stress ( σ) when concentrations of Al and O or Si and O are increased. The thermal stability of FeSiAl-Al2O3 films show a very interesting behavior with the magnetic anisotropy increasing with temperature when the deposition angle is increased. In contrast, when the deposition angle is lower, the usual trend of decreasing magnetic anisotropy with increasing temperature is observed. Moreover, the temperature-dependent behaviors of the dynamic permeability and effective Gilbert damping coefficient ( α eff) for FeSiAl-Al2O3 and FeSiAl-SiO2 films at different deposition angles are discussed in detail.

  11. Discovery of the recoverable high-pressure iron oxide Fe[subscript 4]O[subscript 5

    SciTech Connect

    Lavina, Barbara; Dera, Przemyslaw; Kim, Eunja; Meng, Yue; Downs, Robert T.; Weck, Philippe F.; Sutton, Stephen R.; Zhao, Yusheng

    2016-08-15

    Phases of the iron-oxygen binary system are significant to most scientific disciplines, directly affecting planetary evolution, life, and technology. Iron oxides have unique electronic properties and strongly interact with the environment, particularly through redox reactions. The iron-oxygen phase diagram therefore has been among the most thoroughly investigated, yet it still holds striking findings. Here, we report the discovery of an iron oxide with formula Fe{sub 4}O{sub 5}, synthesized at high pressure and temperature. The previously undescribed phase, stable from 5 to at least 30 GPa, is recoverable to ambient conditions. First-principles calculations confirm that the iron oxide here described is energetically more stable than FeO + Fe{sub 3}O{sub 4} at pressure greater than 10 GPa. The calculated lattice constants, equation of states, and atomic coordinates are in excellent agreement with experimental data, confirming the synthesis of Fe{sub 4}O{sub 5}. Given the conditions of stability and its composition, Fe{sub 4}O{sub 5} is a plausible accessory mineral of the Earth's upper mantle. The phase has strong ferrimagnetic character comparable to magnetite. The ability to synthesize the material at accessible conditions and recover it at ambient conditions, along with its physical properties, suggests a potential interest in Fe{sub 4}O{sub 5} for technological applications.

  12. Influence of addition of Si in FeAl alloys: Theory

    NASA Astrophysics Data System (ADS)

    Apiñaniz, E.; Legarra, E.; Plazaola, F.; Garitaonandia, J. S.

    The magnetic behaviour of Fe-based magnetic systems has been studied theoretically and experimentally for many years [E.P. Wohlfath, K.H.J. Buschow, Handbook of Ferromagnetic Materials, vol. 4, North-Holland Elsevier Science Publishers, Amsterdam, New York, Oxford, Tokyo, 1988 (Chapter 1)]. Starting with Al dissolved in Fe, the first stable structure is the D03 cubic structure and it exists over the range 23-37 at% Al. In this range these alloys present interesting magnetic properties. The other stable compound existing over a wide range of composition is FeAl which is also cubic, with the B2 structure (CsCl), and it exists over the range 37-50 at% Al. On the other hand, the FeAlSi alloys show the D03 structure, but do not show the B2 structure. The effect of Si in these alloys is double; on the one hand, it contributes to the decrease of the lattice parameter which, as reported by Nogues et al. [Phys. Rev. B 74 (2006) 024407], has a major influence on the magnetism and, on the other hand, having one more p electron than the Al atom, it promotes the charge transfer from Si to Fe atoms, as reported by Legarra et al. [Hyperfine Interact. 169 (2006) 1217-1222]. In this work, we perform ab-initio electronic calculations by means of tight binding linear muffin-tin orbital (TBLMTO) and Vienna Ab-initio Simulation Package (VASP) in order to study the magnetic contribution of Si/Al substitution in the FeAl alloys.

  13. An overview of the welding of Ni{sub 3}Al and Fe{sub 3}Al alloys

    SciTech Connect

    Santella, M.L.

    1996-12-31

    Weldability (degree to which defect formation is resisted when an alloy is welded) is an issue in fabrication of Ni{sub 3}Al and Fe{sub 3}Al. Work to define and improve welding of Ni{sub 3}Al and Fe{sub 3}Al alloys is reviewed and progress illustrated by examples of current activities. The cast Ni{sub 3}Al alloys currently under development, IC221M and IC396M, have low resistance to solidification cracking and hence difficult to weld. Modifications to the composition of both base alloys and weld deposits,however, increase their resistance to cracking. Crack-free, full-penetration welds were made in centrifugally cast tubes of IC221M. Tensile and stress- rupture properties of the weldments compare favorably with base metal properties. Weldability issues have limited the use of Fe{sub 3}Al alloys to weld overlay applications. Filler metal compositions suitable for weld overlay cladding were developed, and the preheat and postweld heat treatment needed to avoid cracking, were determined experimentally.

  14. Interfacial perpendicular magnetic anisotropy and damping parameter in ultra thin Co2FeAl films

    NASA Astrophysics Data System (ADS)

    Cui, Yishen; Khodadadi, Behrouz; Schäfer, Sebastian; Mewes, Tim; Lu, Jiwei; Wolf, Stuart A.

    2013-04-01

    B2-ordered Co2FeAl films were synthesized using an ion beam deposition tool. A high degree of chemical ordering ˜81.2% with a low damping parameter (α) less than 0.004 was obtained in a 50 nm thick film via rapid thermal annealing at 600 °C. The perpendicular magnetic anisotropy (PMA) was optimized in ultra thin Co2FeAl films annealed at 350 °C without an external magnetic field. The reduced thickness and annealing temperature to achieve PMA introduced extrinsic factors thus increasing α significantly. However, the observed damping of Co2FeAl films was still lower than that of Co60Fe20B20 films prepared at the same thickness and annealing temperature.

  15. Magnetic properties and microstructure of L10-FePt/AlN perpendicular nanocomposite films

    NASA Astrophysics Data System (ADS)

    Feng, C.; Zhang, E.; Xu, C. C.; Li, N.; Jiang, Y.; Yu, G. H.; Li, B. H.

    2011-09-01

    Based on interfacial manipulation of a MgO (100) substrate and non-magnetic AlN compound, L10-FePt/AlN perpendicular nanocomposite films were designed and prepared. Systematic studies on magnetic properties and microstructure of the films show that the MgO substrate controls crystal orientation of the FePt lattice and induces perpendicular magnetic anisotropy (PMA). The AlN compound helps to control the island growth mode and acts as isolators of FePt islands to pin the sites of FePt domains, resulting in manipulation of coercivity and magnetic exchange interaction of the films. Moreover, PMA of the film was optimized by appropriately decreasing film thickness or increasing substrate temperature.

  16. Status of FeCrAl ODS Irradiations in the High Flux Isotope Reactor

    SciTech Connect

    Field, Kevin G.; Howard, Richard H.

    2016-08-19

    FeCrAl oxide-dispersion strengthened (ODS) alloys are an attractive sub-set alloy class of the more global FeCrAl material class for nuclear applications due to their high-temperature steam oxidation resistance and hypothesized enhanced radiation tolerance. A need currently exists to determine the radiation tolerance of these newly developed alloys. To address this need, a preliminary study was conducted using the High Flux Isotope Reactor (HFIR) to irradiate an early generation FeCrAl ODS alloy, 125YF. Preliminary post-irradiation examination (PIE) on these irradiated specimens have shown good radiation tolerance at elevated temperatures (≥330°C) but possible radiation-induced hardening and embrittlement at irradiations of 200°C to a damage level of 1.9 displacement per atom (dpa). Building on this experience, a new series of irradiations are currently being conceptualized. This irradiation series called the FCAD irradiation program will irradiate the latest generation FeCrAl ODS and FeCr ODS alloys to significantly higher doses. These experiments will provide the necessary information to determine the mechanical performance of irradiated FeCrAl ODS alloys at light water reactor and fast reactor conditions.

  17. Observations of the Minor Species Al, Fe and Ca(+) in Mercury's Exosphere

    NASA Technical Reports Server (NTRS)

    Bida, Thomas A.; Killen, Rosemary M.

    2011-01-01

    We report the first detections of Al and Fe, and strict upper limits for Ca(+) in the exosphere of Mercury, using the HIRES spectrometer at the Keck I telescope. We report observed 4-sigma tangent columns of 1.5x10(exp 7) Al atoms per square centimeter at an altitude of 1220 km (1.5 Mercury radii (R(sub M)) from planet center), and that for Fe of 1.6 x 10 per square centimeter at an altitude of 950 km (1.4 R(sub M)). The observed 3-sigma Ca(+) column was 3.9x10(exp 6) ions per square centimeter at an altitude of 1630 km (1.67 R(sub M). A simple model for zenith column abundances of the neutral species were 9.5 x 10(exp 7) Al per square centimeter, and 3.0 x 10(exp 8) Fe per square centimeter. The observations appear to be consistent with production of these species by impact vaporization with a large fraction of the ejecta in molecular form. The scale height of the Al gas is consistent with a kinetic temperature of 3000 - 9000 K while that of Fe is 10500 K. The apparent high temperature of the Fe gas would suggest that it may be produced by dissociation of molecules. A large traction of both Al and Fe appear to condense in a vapor cloud at low altitudes.

  18. Large magnetization and high Curie temperature in highly disordered nanoscale Fe2CrAl thin films

    NASA Astrophysics Data System (ADS)

    Dulal, Rajendra P.; Dahal, Bishnu R.; Forbes, Andrew; Pegg, Ian L.; Philip, John

    2017-02-01

    We have successfully grown nanoscale Fe2CrAl thin films on polished Si/SiO2 substrates using an ultra-high vacuum deposition with a base pressure of 9×10-10 Torr. The thickness of thin films ranges from 30 to 100 nm. These films exhibit cubic crystal structure with lattice disorder and display ferromagnetic behavior. The Curie temperature is greater than 400 K, which is much higher than that reported for bulk Fe2CrAl. The magnetic moments of the films varies from 2.5 to 2.8 μB per formula unit, which is larger than the reported bulk values. Thus, the disordered nanoscale Fe2CrAl films exhibit strong Fe-Fe exchange interactions through Fe-Cr-Fe and Fe-Al-Fe layers, resulting in both a large magnetization and a high Curie temperature.

  19. Atomic origin of the spin-polarization of the Co2FeAl Heusler compound

    NASA Astrophysics Data System (ADS)

    Liang, Jaw-Yeu; Lam, Tu-Ngoc; Lin, Yan-Cheng; Chang, Shu-Jui; Lin, Hong-Ji; Tseng, Yuan-Chieh

    2016-02-01

    Using synchrotron x-ray techniques, we studied the Co2FeAl spin-polarization state that generates the half-metallicity of the compound during an A2 (low-spin)  →  B2 (high-spin) phase transition. Given the advantage of element specificity of x-ray techniques, we could fingerprint the structural and magnetic cross-reactions between Co and Fe within a complex Co2FeAl structure deposited on a MgO (0 0 1) substrate. X-ray diffraction and extended x-ray absorption fine structure investigations determined that the Co atoms preferably populate the (1/4,1/4,1/4) and (3/4,3/4,3/4) sites during the development of the B2 phase. X-ray magnetic spectroscopy showed that although the two magnetic elements were ferromagnetically coupled, they interacted in a competing manner via a charge-transfer effect, which enhanced Co spin polarization at the expense of Fe spin polarization during the phase transition. This means that the spin-polarization of Co2FeAl was electronically dominated by Fe in A2 whereas the charge transfer turned the dominance to Co upon B2 formation. Helicity-dependent x-ray absorption spectra also revealed that only the minority state of Co/Fe was involved in the charge-transfer effect whereas the majority state was independent of it. Despite an overall increase of Co2FeAl magnetization, the charge-transfer effect created an undesired trade-off during the Co-Fe exchange interactions, because of the presence of twice as many X sites (Co) as Y sites (Fe) in the Heusler X 2 YZ formula. This suggests that the spin-polarization of Co2FeAl is unfortunately regulated by compromising the enhanced X (Co) sites and the suppressed Y (Fe) sites, irrespective of the development of the previously known high-spin-polarization phase of B2. This finding provides a possible cause for the limited half-metallicity of Co2FeAl discovered recently. Electronic tuning between the X and Y sites is necessary to further increase the spin-polarization, and likely the half

  20. Understanding the role of iron in the magnetism of Fe doped ZnO nanoparticles.

    PubMed

    Beltrán, J J; Barrero, C A; Punnoose, A

    2015-06-21

    The actual role of transition metals like iron in the room temperature ferromagnetism (RTFM) of Fe doped ZnO nanoparticles is still an unsolved problem. While some studies concluded that the Fe ions participate in the magnetic interaction, others in contrast do not believe Fe to play a direct role in the magnetic exchange interaction. To contribute to the understanding of this issue, we have carefully investigated the structural, optical, vibrational and magnetic properties of sol-gel synthesized Zn1-xFexO (0 < x < 0.10) nanoparticles. No Fe(2+) was detected in any sample. We found that high spin Fe(3+) ions are substitutionally incorporated at the Zn(2+) in the tetrahedral-core sites and in pseudo-octahedral surface sites in ZnO. Superficial OH(-) was observed in all samples. For x ≤ 0.03, an increment in Fe doping concentration decreased a and c lattice parameters, average Zn-O bond length, average crystallite size and band gap; while it increased the degree of distortion and quadrupole splitting. Undoped ZnO nanoparticles exhibited very weak RTFM with a saturation magnetization (Ms) of ∼0.47 memu g(-1) and this value increased to ∼2.1 memu g(-1) for Zn0.99Fe0.01O. Very interestingly, the Ms for Zn0.99Fe0.01O and Zn0.97Fe0.03O increased by a factor of about ∼2.3 by increasing annealing for 1 h to 3 h. For x ≥ 0.05, ferrimagnetic disordered spinel ZnFe2O4 was formed and this phase was found to become more ordered with increasing annealing time. Fe does not contribute directly to the RTFM, but its presence promoted the formation of additional single charged oxygen vacancies, zinc vacancies, and more oxygen-ended polar terminations at the nanoparticle surface. These defects, which are mainly superficial, altered the electronic structure and are considered as the main sources of the observed ferromagnetism.

  1. Phase relationships in the iron-rich Fe-Cr-Ni-C system at solidification temperatures

    NASA Astrophysics Data System (ADS)

    Kundrat, D. M.; Elliott, J. F.

    1986-08-01

    The phase relationships between the liquid phase and the primary solid phases were investigated in the iron-rich comer of the Fe-Cr-Ni-C system as part of a larger study of the Fe-Cr-Mn-Ni-C system. The investigation consisted of measurements of tie-lines for the liquid-delta (bcc) and the liquid-gamma (fcc) equilibria in the iron-rich corner of the Gibbs tetrahedron bounded by 0 to 25 wt Pct Cr, 0 to 25 wt Pct Ni, and 1.2 wt Pct C (bal. Fe). The temperature ranged from 1811 to 1750 K. Compositions for the tie-lines were obtained from liquid-solid equilibrium couples and the temperatures of the equilibrium, by differential thermal analysis (DTA). A mathematical procedure was employed on the experimental data to obtain parameters for a thermodynamic model of the alloy system. This involved minimization of an error function. The details of this analysis are discussed fully in this paper. Calculations by the model employing the “best-set” parameters are in good agreement with the experimental results. The usefulness of the model is demonstrated by calculation of the three-phase equilibrium in the quaternary system as a function of temperature.

  2. The influence of cooling rate and Fe/Cr content on the evolution of Fe-rich compounds in a secondary Al-Si-Cu diecasting alloy

    NASA Astrophysics Data System (ADS)

    Fabrizi, A.; Timelli, G.

    2016-03-01

    This study investigates the morphological evolution of primary α-Al(Fe,Mn,Cr)Si phase in a secondary Al-Si-Cu alloy with respect to the initial Fe and Cr contents as well as to the cooling rate. The solidification experiments have been designed in order to cover a wide range of cooling rates, and the Fe and Cr contents have been varied over two levels. Metallographic and image analysis techniques have been used to quantitatively examine the microstructural changes occurring at different experimental conditions. The morphological evolution of the α-Fe phase has been also analysed by observing deep etched samples. By changing the cooling rate, α-Al15(Fe,Mn,Cr)3Si2 dodecahedron crystals, as well as Chinese- script, branched structures and dendrites form, while primary coarse β-Al5(Fe,Mn)Si needles appear in the alloy with the highest Fe content at low cooling rates.

  3. Transformation of α-Al(Fe,Mn)Si in Al-7Si-0.4Mg cast alloys after solution heat treatment

    NASA Astrophysics Data System (ADS)

    Han, Sang Won

    2013-01-01

    The α-Al(Fe,Mn)Si compound in an Al-7Si-0.35Mg-0.2Fe-xMn cast alloy has two shapes, a needle-like shape and a Chinese script shape. These two kinds of compounds are tinged with either white or gray tones irrespective of their shape. Unlike compounds with a white tone, during solution heat treatment, all α-Al (Fe,Mn)Si compounds with a gray tone experience severe dissolution. Concerning white-tinged α-Al (Fe,Mn)Si compounds, unlike the needle-like α-Al(Fe,Mn)Si, α-Al(Fe,Mn)Si that resembles Chinese script is rarely transformed.

  4. Magnetic properties of Nd-Fe-Co(Cu)-Al-B amorphous alloys prepared by nonequilibrium techniques

    NASA Astrophysics Data System (ADS)

    Kumar, G.; Eckert, J.; Roth, S.; Löser, W.; Ram, S.; Schultz, L.

    2002-03-01

    The amorphous alloys Nd40Fe40Co5Al8B7, Nd57Fe20Co5Al10B8, and Nd57Fe20Cu5Al10B8 were prepared by copper mold casting, melt spinning, and mechanical alloying. Despite their similar x-ray diffraction patterns, samples display different magnetic and thermal behavior correlated with the method of preparation. The fully amorphous melt-spun ribbons exhibit relatively soft magnetic properties with coercivities ≈40 kA/m at room temperature and a Curie temperature (TC)≈474 K. Apparently only the mold-cast cylinders of 3 mm diameter show hard magnetic behavior with a coercivity in the range of 258-270 kA/m (depending on composition) and have approximately the same TC as that of the melt-spun ribbons. An additional magnetic transition at 585 K due to the presence of Nd2Fe14B phase in the case of Nd40Fe40Co5Al8B7 cast rod has been observed. Heat treatment above crystallization temperature in as-cast Nd57Fe20Co5Al10B8 and Nd57Fe20Cu5Al10B8 samples destroys the hard magnetic properties. In contrast, mechanically alloyed amorphous samples are soft magnetic with maximum coercivity up to 11 kA/m but show an entirely different TC≈680-740 K, which is rather characteristic of an Fe solid solution. The magnetic properties are discussed in terms of different local atomic environment and cluster sizes in amorphous samples prepared by different methods.

  5. Phase Structure and High-Temperature Mechanical Properties of Two-Phase Fe-25Al- xZr Alloys Compared to Three-Phase Fe-30Al- xZr Alloys

    NASA Astrophysics Data System (ADS)

    Kejzlar, Pavel; Kratochvíl, Petr; Král, Robert; Vodičková, Věra

    2014-01-01

    The structure and high-temperature mechanical properties of Fe-30 at. pct Al and Fe-25 at. pct Al alloys with various Zr contents are compared. The scanning electron microscope images in chemical contrast mode (R-BSE) as well as EDS, EBSD, and X-ray diffraction were used to determine the structure and phase composition. The as-cast alloys (both Fe-30Al and Fe-25Al) were observed to be two-phase DO3/B2 + Laves phase λ 1 (Fe,Al)2Zr alloys with typical fine lamellar eutectic areas. During the heat treatment of the Fe-25Al alloys, their structure transformed from a DO3/B2 matrix with fine lamellar eutectic into λ 1 globular particles situated in a DO3/B2 matrix. The same structure of Fe-30Al alloys decomposed into three phases: λ 1 and τ 1 Zr(Fe,Al)12 particles in a DO3/B2 matrix. The hardening in both groups of alloys (Fe-25Al and Fe-30Al) due to the presence of Zr-containing λ 1 and τ 1 phases is compared.

  6. Optimized Gen-II FeCrAl cladding production in large quantity for campaign testing

    SciTech Connect

    Yamamoto, Yukinori; Sun, Zhiqian; Pint, Bruce A.; Terrani, Kurt A.

    2016-06-03

    There are two major objectives in this report; (1) to optimize microstructure control of ATF FeCrAl alloys during tube drawing processes, and (2) to provide an update on the progress of ATF FeCrAl tube production via commercial manufacturers. Experimental efforts have been made to optimize the process parameters balancing the tube fabricability, especially for tube drawing processes, and microstructure control of the final tube products. Lab-scale sheet materials of Gen II FeCrAl alloys (Mo-containing and Nb-containing FeCrAl alloys) were used in the study, combined with a stepwise warm-rolling process and intermediate annealing, aiming to simulate the tube drawing process in a commercial tube manufacturer. The intermediate annealing at 650ºC for 1h was suggested for the tube-drawing process of Mo-containing FeCrAl alloys because it successfully softened the material by recovering the work hardening introduced through the rolling step, without inducing grain coarsening due to recrystallization. The final tube product is expected to have stabilized deformed microstructure providing the improved tensile properties with sufficient ductility. Optimization efforts on Nb-containing FeCrAl alloys focused on the effect of alloying additions and annealing conditions on the stability of deformed microstructure. Relationships between the second-phase precipitates (Fe2Nb-Laves phase) and microstructure stability are discussed. FeCrAl tube production through commercial tube manufacturers is currently in progress. Three different manufacturers, Century Tubes, Inc. (CTI), Rhenium Alloys, Inc. (RAI), and Superior Tube Company, Inc. (STC), are providing capabilities for cold-drawing, warm-drawing, and HPTR cold-pilgering, respectively. The first two companies are currently working on large quantity tube production (expected 250 ft length) of Gen I model FeCrAl alloy (B136Y3, at CTI) and Gen II (C35M4, at RAI), with the process parameters obtained from the experimental

  7. Magnetic properties of the ternary aluminide TbFe2Al10

    NASA Astrophysics Data System (ADS)

    Khandelwal, Ashish; Sharma, V. K.; Sharath Chandra, L. S.; Singh, M. N.; Sinha, A. K.; Chattopadhyay, M. K.

    2013-09-01

    The magnetic properties of the ternary aluminide TbFe2Al10 have been studied with the help of magnetization measurements. From the temperature and field dependence of magnetization, a detailed magnetic phase diagram of TbFe2Al10 has been constructed. While the high- and low-temperature phases (in low fields) of TbFe2Al10 are paramagnetic and antiferromagnetic respectively, the signature of a field-induced ferromagnetic phase is obtained in the magnetization results in the intermediate temperature regime. While it was already known that TbFe2Al10 has a ferrimagnetic phase in between the low-field antiferromagnetic and the high-field ferromagnetic phases, the present results indicate the presence of a second intermediate-field-induced ferrimagnetic phase in the compound, in between the first ferrimagnetic and the high-field ferromagnetic phases. The possible magnetic structure for this second ferrimagnetic phase is proposed on the basis of existing neutron diffraction results. The successive field-induced or metamagnetic transitions in TbFe2Al10 are found to be induced by temperature as well, when the applied magnetic field is appropriate. The present magnetization results also indicate the presence of short-range magnetic correlations in TbFe2Al10 well inside the paramagnetic regime. Owing to the presence of successive temperature and field-induced magnetic phase transitions, TbFe2Al10 is found to exhibit a moderate magneto-caloric effect with a maximum of 7.86 J kg-1K-1 at 18.5 K. The magneto-caloric effect is found to persist well inside the paramagnetic regime because of the presence of short-range magnetic correlations at these temperatures. This leads to a substantial refrigerant capacity in the material, which could be useful information for future technology.

  8. Simultaneous spectrophotometric determination of Fe(III) and Al(III) using orthogonal signal correction-partial least squares calibration method after solidified floating organic drop microextraction

    NASA Astrophysics Data System (ADS)

    Rohani Moghadam, Masoud; Haji Shabani, Ali Mohammad; Dadfarnia, Shayessteh

    2015-01-01

    A solidified floating organic drop microextraction (SFODME) procedure was developed for the simultaneous extraction and preconcentration of Fe(III) and Al(III) from water samples. The method was based on the formation of cationic complexes between Fe(III) and Al(III) and 3,5,7,2‧,4‧-pentahydroxyflavone (morin) which were extracted into 1-undecanol as ion pairs with perchlorate ions. The absorbance of the extracted complexes was then measured in the wavelength range of 300-450 nm. Finally, the concentration of each metal ion was determined by the use of the orthogonal signal correction-partial least squares (OSC-PLS) calibration method. Several experimental parameters that may be affected on the extraction process such as the type and volume of extraction solvent, pH of the aqueous solution, morin and perchlorate concentration and extraction time were optimized. Under the optimum conditions, Fe(III) and Al(III) were determined in the ranges of 0.83-27.00 μg L-1 (R2 = 0.9985) and 1.00-32.00 μg L-1 (R2 = 0.9979) of Fe(III) and Al(III), respectively. The relative standard deviations (n = 6) at 12.80 μg L-1 of Fe(III) and 17.00 μg L-1 of Al(III) were 3.2% and 3.5%, respectively. An enhancement factors of 102 and 96 were obtained for Fe(III) and Al(III) ions, respectively. The procedure was successfully applied to determination of iron and aluminum in steam and water samples of thermal power plant; and the accuracy was assessed through the recovery experiments and independent analysis by electrothermal atomic absorption spectroscopy (ETAAS).

  9. Simultaneous spectrophotometric determination of Fe(III) and Al(III) using orthogonal signal correction-partial least squares calibration method after solidified floating organic drop microextraction.

    PubMed

    Rohani Moghadam, Masoud; Haji Shabani, Ali Mohammad; Dadfarnia, Shayessteh

    2015-01-25

    A solidified floating organic drop microextraction (SFODME) procedure was developed for the simultaneous extraction and preconcentration of Fe(III) and Al(III) from water samples. The method was based on the formation of cationic complexes between Fe(III) and Al(III) and 3,5,7,2',4'-pentahydroxyflavone (morin) which were extracted into 1-undecanol as ion pairs with perchlorate ions. The absorbance of the extracted complexes was then measured in the wavelength range of 300-450 nm. Finally, the concentration of each metal ion was determined by the use of the orthogonal signal correction-partial least squares (OSC-PLS) calibration method. Several experimental parameters that may be affected on the extraction process such as the type and volume of extraction solvent, pH of the aqueous solution, morin and perchlorate concentration and extraction time were optimized. Under the optimum conditions, Fe(III) and Al(III) were determined in the ranges of 0.83-27.00 μg L(-1) (R(2)=0.9985) and 1.00-32.00 μg L(-1) (R(2)=0.9979) of Fe(III) and Al(III), respectively. The relative standard deviations (n=6) at 12.80 μg L(-1) of Fe(III) and 17.00 μg L(-)(1) of Al(III) were 3.2% and 3.5%, respectively. An enhancement factors of 102 and 96 were obtained for Fe(III) and Al(III) ions, respectively. The procedure was successfully applied to determination of iron and aluminum in steam and water samples of thermal power plant; and the accuracy was assessed through the recovery experiments and independent analysis by electrothermal atomic absorption spectroscopy (ETAAS).

  10. Modeling of iron K lines: Radiative and Auger decay data for Fe II-Fe IX

    NASA Astrophysics Data System (ADS)

    Palmeri, P.; Mendoza, C.; Kallman, T. R.; Bautista, M. A.; Meléndez, M.

    2003-10-01

    A detailed analysis of the radiative and Auger de-excitation channels of K-shell vacancy states in Fe II-Fe IX has been carried out. Level energies, wavelengths, A-values, Auger rates and fluorescence yields have been calculated for the lowest fine-structure levels populated by photoionization of the ground state of the parent ion. Different branching ratios, namely Kalpha2 /Kalpha1, Kbeta/Kalpha, KLM/KLL, KMM/KLL, and the total K-shell fluorescence yields, omegaK, obtained in the present work have been compared with other theoretical data and solid-state measurements, finding good general agreement with the latter. The Kalpha2/Kalpha1 ratio is found to be sensitive to the excitation mechanism. From these comparisons it has been possible to estimate an accuracy of ~ 10% for the present transition probabilities. Tables 3 and 4 are only available in electronic form at the CDS via anonymous ftp to cdsarc.u-strasbg.fr (130.79.128.5) or via http://cdsweb.u-strasbg.fr/cgi-bin/qcat?J/A+A/410/359

  11. CaFeAl mixed oxide derived heterogeneous catalysts for transesterification of soybean oil to biodiesel.

    PubMed

    Lu, Yongsheng; Zhang, Zaiwu; Xu, Yunfeng; Liu, Qiang; Qian, Guangren

    2015-08-01

    CaAl layered double oxides (LDO) were prepared by co-precipitation and calcined at 750°C, and then applied to biodiesel production by transesterification reaction between methanol and soybean oil. Compared with characteristics of CaFe/LDO and CaAl/LDO, CaFeAl/LDO had the best performance based on prominent catalytic activity and stability, and achieved over 90% biodiesel yield, which stayed stable (over 85%) even after 8 cycles of reaction. The optimal catalytic reaction condition was 12:1M-ratio of methanol/oil, reaction temperatures of 60°C, 270rpm stirring rate, 60min reaction time, and 6% weight-ratio of catalyst/oil. In addition, the CaFeAl/LDO catalyst is insoluble in both methanol and methyl esters and can be easily separated for further reaction, turning it into an excellent alternative for biodiesel synthesis.

  12. Effects of Iron-Rich Intermetallics and Grain Structure on Semisolid Tensile Properties of Al-Cu 206 Cast Alloys near Solidus Temperature

    NASA Astrophysics Data System (ADS)

    Bolouri, Amir; Liu, Kun; Chen, X.-Grant

    2016-12-01

    The effects of iron-rich intermetallics and grain size on the semisolid tensile properties of Al-Cu 206 cast alloys near the solidus were evaluated in relation to the mush microstructure. Analyses of the stress-displacement curves showed that the damage expanded faster in the mush structure dominated by plate-like β-Fe compared to the mush structure dominated by Chinese script-like α-Fe. While there was no evidence of void formation on the β-Fe intermetallics, they blocked the interdendritic liquid channels and thus hindered liquid flow and feeding during semisolid deformation. In contrast, the interdendritic liquid flows more freely within the mush structure containing α-Fe. The tensile properties of the alloy containing α-Fe are generally higher than those containing β-Fe over the crucial liquid fraction range of 0.6 to 2.8 pct, indicating that the latter alloy may be more susceptible to stress-related casting defects such as hot tearing. A comparison of the semisolid tensile properties of the alloy containing α-Fe with different grain sizes showed that the maximum stress and elongation of the alloy with finer grains were moderately higher for the liquid fractions of 2.2 to 3.6 pct. The application of semisolid tensile properties for the evaluation of the hot tearing susceptibility of experimental alloys is discussed.

  13. Mössbauer characterisation of Fe-polygalacturonate as a medicine for human anaemia: the effect of iron concentration

    NASA Astrophysics Data System (ADS)

    Fodor, Judit; Kuzmann, Ernő; Vértes, Attila; Homonnay, Zoltán; Klencsár, Zoltán; May, Zoltán; Szentmihályi, Klára

    2009-04-01

    57Fe Mössbauer spectroscopy was used to study the effect of iron concentration on the oxidation state and microenvironments of iron in Fe-polygalacturonate compounds prepared by a novel method from pectin. The iron concentration of the coordination compounds was determined by inductively coupled plasma optical emission spectrometry analysis. The Mössbauer spectra of the studied compounds could be decomposed into three markedly different quadrupole doublets referring to three microenvironments. Two of these have ferrous and one has ferric oxidation state. In the applied concentration range the relative occurrence of the ferric component was found to increase considerably with iron concentration. At the same time, with increasing iron concentration the relative occurrence characteristic of the three components showed saturation behaviour up to the iron concentration at which for each pair of galacturonic acid units there is on average one iron atom in the system, which iron concentration value is interpreted as to be related to the complete fill up of certain iron complexation sites of the polygalacturonate chains.

  14. Chemical evaluation of HBED/Fe(3+) and the novel HJB/Fe(3+) chelates as fertilizers to alleviate iron chlorosis.

    PubMed

    López-Rayo, Sandra; Hernández, Diana; Lucena, Juan J

    2009-09-23

    Iron chelates such as ethylenediamine-N,N'-bis(2-hydroxyphenylacetic) acid (o,o-EDDHA) and their analogues are the most efficient soil fertilizers to treat iron chlorosis in plants growing in calcareous soil. A new chelating agent, HJB (N,N'-bis(2-hydroxy-5-methylphenyl)ethylendiamine-N,N'-diacetic acid) may be an alternative to o,o-EDDHA since its synthesis yields a purer product, but its chemical behavior and efficiency as chlorosis corrector should be evaluated. In this research, a known analogous HBED (N,N'-bis(2-hydroxyphenyl)ethylendiamine-N,N'-diacetic acid) has also been considered. First, an ion-pair high performance liquid chromatography (HPLC) method has been tested for the HJB/Fe(3+) and HBED/Fe(3+) determination. The ability of HJB and HBED to maintain Fe in solution has been compared with respect to o,o-EDDHA. Theoretical modelization for HBED and HJB in agronomic conditions has been done after the determination of the protonation and Ca(II), Mg(II), Fe(III), and Cu(II) stability constants for HJB. Also, batch interaction experiments with soils and soil materials have been conducted. According to our results, HJB/Fe(3+) and HBED/Fe(3+) present high stability, even when competing cations (Cu(2+), Ca(2+)) are present, and have low reactivity with soils and soil components. The chelating agent HJB dissolves a higher amount of Fe than o,o-EDDHA, and it seems as effective as o,o-EDDHA in keeping Fe in solution. These results indicate that these chelates may be very efficient products to correct Fe chlorosis, and additional plant experiments should demonstrate plants' ability to assimilate Fe from HJB/Fe(3+) and HBED/Fe(3+).

  15. Effect of CeO2 doping on catalytic activity of Fe2O3/gamma-Al2O(3) catalyst for catalytic wet peroxide oxidation of azo dyes.

    PubMed

    Liu, Yan; Sun, Dezhi

    2007-05-08

    In order to find a catalyst with high activity and stability for catalytic wet peroxide oxidation (CWPO) process under normal condition, with Fe(2)O(3)/gamma-Al(2)O(3) and Fe(2)O(3)-CeO(2)/gamma-Al(2)O(3) catalysts prepared by impregnation method, the effect of CeO(2) doping on the structure and catalytic activity of Fe(2)O(3)/gamma-Al(2)O(3) for catalytic wet peroxide oxidation of azo dyes at 25 degrees C and atmospheric pressure is evaluated using BET, SEM, XRF, XRD, XPS and chemical analysis techniques, and test results show that, better dispersion and smaller size of Fe(2)O(3) crystal can be achieved by adding CeO(2), and the content of chemisorbed oxygen can also be increased on the surface of catalyst. CWPO experimental results indicate that azo dyes in simulated wastewater can be efficiently mineralized and the catalytic activity of Fe(2)O(3)-CeO(2)/gamma-Al(2)O(3) can be increased by about 10% compared with that of Fe(2)O(3)/gamma-Al(2)O(3) because of the promotion of the structural and redox properties of the ferric oxide by ceria doped. Leaching tests indicate that Fe(2)O(3)/gamma-Al(2)O(3) and Fe(2)O(3)-CeO(2)/gamma-Al(2)O(3) are stable with a negligible amount of irons found in the aqueous solution after reaction for 2h. It can therefore be concluded from results and discussion that in comparison with Fe(2)O(3)/gamma-Al(2)O(3), Fe(2)O(3)-CeO(2)/gamma-Al(2)O(3) is a suitable catalyst, which can effectively degrade contaminants at normal temperature and atmospheric pressure.

  16. Predictions of the Hunt-Lu array model compared with measurements for the growth undercooling of Al{sub 3}Fe dendrites in Al-Fe alloys

    SciTech Connect

    Liang, D.; Jones, H.

    1997-10-01

    Earlier contributions by the authors reported the first measurements of growth temperature as a function of growth velocity V and alloy concentration C{sub 0} for a dendritic intermetallic phase (Al{sub 3}Fe, in Al-rich Al-Fe alloys). Comparison with predictions of the model of Kurz, Giovanola and Trivedi (KGT model) of dendrite growth of a needle gave predicted {Delta}T a factor between 1.1 and 2.5 above the measured values. A subsequent paper presented evidence that the Al{sub 3}Fe dendrite tips were indeed needle-like under the conditions studied, as distinct from the plate-like morphology that develops behind the dendrite tips. The KGT model predicts T{sub G} and {Delta}T on the basis that marginal stability determines the operating condition at the dendrite tip. The present purpose is to compare the measurements with predictions of the more recently developed array model of Hunt and Lu.

  17. A Microstructural and Kinetic Investigation of the KCl-Induced Corrosion of an FeCrAl Alloy at 600 °C

    DOE PAGES

    Israelsson, Niklas; Unocic, Kinga A.; Hellström, K.; ...

    2015-03-18

    In this paper, the corrosion behaviour of a FeCrAl alloy was investigated at 600 °C in O2 + H2O with solid KCl applied. A kinetics and microstructural investigation showed that KCl accelerates corrosion and that potassium chromate formation depletes the protective scale in Cr, thus triggering the formation of a fast-growing iron-rich scale. Iron oxide was found to grow both inward and outward, on either side of the initial oxide. A chromia layer is formed with time underneath the iron oxide. Finally, it was found that although the alloy does not form a continuous pure alumina scale at the investigatedmore » temperature, aluminium is, however, always enriched at the oxide/alloy interface.« less

  18. A Microstructural and Kinetic Investigation of the KCl-Induced Corrosion of an FeCrAl Alloy at 600 °C

    SciTech Connect

    Israelsson, Niklas; Unocic, Kinga A.; Hellström, K.; Jonsson, T.; Norell, M.; Svensson, J. -E.; Johansson, L. -G.

    2015-03-18

    In this paper, the corrosion behaviour of a FeCrAl alloy was investigated at 600 °C in O2 + H2O with solid KCl applied. A kinetics and microstructural investigation showed that KCl accelerates corrosion and that potassium chromate formation depletes the protective scale in Cr, thus triggering the formation of a fast-growing iron-rich scale. Iron oxide was found to grow both inward and outward, on either side of the initial oxide. A chromia layer is formed with time underneath the iron oxide. Finally, it was found that although the alloy does not form a continuous pure alumina scale at the investigated temperature, aluminium is, however, always enriched at the oxide/alloy interface.

  19. Kinetics and mechanism of the oxidation process of two-component Fe-Al alloys

    NASA Technical Reports Server (NTRS)

    Przewlocka, H.; Siedlecka, J.

    1982-01-01

    The oxidation process of two-component Fe-Al alloys containing up to 7.2% Al and from 18 to 30% Al was studied. Kinetic measurements were conducted using the isothermal gravimetric method in the range of 1073-1223 K and 1073-1373 K for 50 hours. The methods used in studies of the mechanism of oxidation included: X-ray microanalysis, X-ray structural analysis, metallographic analysis and marker tests.

  20. Autoionization resonances in the photoabsorption spectra of Fe n+ iron ions

    NASA Astrophysics Data System (ADS)

    Konovalov, A. V.; Ipatov, A. N.

    2016-11-01

    The photoabsorption cross sections of a neutral iron atom, as well as positive Fe+ and Fe2+ ions, are calculated in the relativistic random-phase approximation with exchange in the energy range 20-160 eV. The wavefunctions of the ground and excited states are calculated in the single-configuration Hartree-Fock-Dirac approximation. The resultant photoabsorption spectra are compared with experimental data and with the results of calculations based on the nonrelativistic spin-polarized version of the random-phase approximation with exchange. Series of autoionization resonance peaks, as well as giant autoionization resonance lines corresponding to discrete transitions 3 p → 3 d, are clearly observed in the photoabsorption cross sections. The conformity of the positions of calculated peaks of giant autoionization resonances with experimental data is substantially improved by taking into account additionally the correlation electron-electron interaction based on the model of the dynamic polarization potential.

  1. Iron and zinc concentrations and /sup 59/Fe retention in developing fetuses of zinc-deficient rats

    SciTech Connect

    Rogers, J.M.; Loennerdal, B.H.; Hurley, L.S.; Keen, C.L.

    1987-11-01

    Because disturbances in iron metabolism might contribute to the teratogenicity of zinc deficiency, we examined the effect of zinc deficiency on fetal iron accumulation and maternal and fetal retention of /sup 59/Fe. Pregnant rats were fed from mating a purified diet containing 0.5, 4.5 or 100 micrograms Zn/g. Laparotomies were performed on d 12, 16, 19 and 21 of gestation. Maternal blood and concepti were analyzed for zinc and iron. Additional groups of dams fed 0.5 or 100 micrograms Zn/g diet were gavaged on d 19 with a diet containing /sup 59/Fe. Six hours later maternal blood and tissues, fetuses and placentas were counted for /sup 59/Fe. Maternal plasma zinc, but not iron, concentration was affected by zinc deficiency on d 12. Embryo zinc concentration on d 12 increased with increasing maternal dietary zinc, whereas iron concentration was not different among groups. On d 16-21 plasma iron was higher in dams fed 0.5 micrograms Zn/g diet than in those fed 4.5 or 100 micrograms/g, whereas plasma zinc was lower in dams fed 0.5 or 4.5 micrograms Zn/g than in those fed 100 micrograms Zn/g diet. On d 19 zinc concentration in fetuses from dams fed 0.5 micrograms/g zinc was not different from that of those fed 4.5 micrograms/g zinc, and iron concentration was higher in the 0.5 microgram Zn/g diet group. The increase in iron concentration in zinc-deficient fetuses thus occurs too late to be involved in major structural teratogenesis. Although whole blood concentration of /sup 59/Fe was not different in zinc-deficient and control dams, zinc-deficient dams had more /sup 59/Fe in the plasma fraction.

  2. Report on fundamental modeling of irradiation-induced swelling and creep in FeCrAl alloys

    SciTech Connect

    Kohnert, Aaron A.; Dasgupta, Dwaipayan; Wirth, Brian; Linton, Kory D.

    2016-09-23

    In order to improve the accident tolerance of light water reactor (LWR) fuel, alternative cladding materials have been proposed to replace zirconium (Zr)-based alloys. Of these materials, there is a particular focus on iron-chromium-aluminum (FeCrAl) alloys due to much slower oxidation kinetics in high-temperature steam than Zr-alloys. This should decrease the energy release due to oxidation and allow the cladding to remain integral longer in the presence of high temperature steam, making accident mitigation more likely. As a continuation of the development for these alloys, the material response must be demonstrated to provide suitable radiation stability, in order to ensure that there will not be significant dimensional changes (e.g., swelling), as well as quantifying the radiation hardening and radiation creep behavior. In this report, we describe the use of cluster dynamics modeling to evaluate the defect physics and damage accumulation behavior of FeCrAl alloys subjected to neutron irradiation, with a particular focus on irradiation-induced swelling and defect fluxes to dislocations that are required to model irradiation creep behavior.

  3. Structural, electron transportation and magnetic behavior transition of metastable FeAlO granular films

    PubMed Central

    Bai, Guohua; Wu, Chen; Jin, Jiaying; Yan, Mi

    2016-01-01

    Metal-insulator granular film is technologically important for microwave applications. It has been challenging to obtain simultaneous high electrical resistivity and large saturation magnetization due to the balance of insulating non-magnetic and metallic magnetic components. FeAlO granular films satisfying both requirements have been prepared by pulsed laser deposition. The as-deposited film exhibits a high resistivity of 3700 μΩ∙cm with a negative temperature coefficient despite that Fe content (0.77) exceeds the percolation threshold. This originates from its unique microstructure containing amorphous Fe nanoparticles embedded in Al2O3 network. By optimizing the annealing conditions, superior electromagnetic properties with enhanced saturation magnetization (>1.05 T), high resistivity (>1200 μΩ∙cm) and broadened Δf (>3.0 GHz) are obtained. Phase separation with Al2O3 aggregating as inclusions in crystallized Fe(Al) matrix is observed after annealing at 673 K, resulting in a metallic-like resistivity. We provide a feasible way to achieve both high resistivity and large saturation magnetization for the FeAlO films with dominating metallic component and show that the microstructure can be tuned for desirable performance. PMID:27075955

  4. Machinability of Intermetallic Compound Fe3Al from the Viewpoint of Tool Wear

    NASA Astrophysics Data System (ADS)

    Sasaki, Tomohiro; Yakou, Takao

    The intermetallic compound Fe3Al was processed by a reactive sintering process, and its machinability from the viewpoint of tool wear was investigated using dry turning. In cutting Fe3Al with a cemented carbide tool, the tool life was approximately one tenth that of cutting carbon tool steel SK3 because of intense flank wear. The tool life for cutting Fe3Al using the cemented carbide P20(WC-TiC-TaC-Co) tool was longer than for cemented carbide K10(WC-Co). In addition, a cermet tool reached its tool life limit by chipping for the whole cutting speed range measured. The roughness of the machined surface of Fe3Al cut using a cemented carbide tool was much smaller than for SK3. However, for cutting using the cermet tool, the roughness showed a sharp rise due to chipping. It was found that the wear rate of the WC particles in the tool material is larger than TiC particles. The results of the study suggest that the cemented carbide P20 is suitable for cutting Fe3Al.

  5. Microstructural Investigation and Phase Relationships of Fe-Al-Hf Alloys

    NASA Astrophysics Data System (ADS)

    Yildirim, Mehmet; Akdeniz, M. Vedat; Mekhrabov, Amdulla O.

    2014-07-01

    The effect of Hf addition on microstructures, phase relationships, microhardness, and magnetic properties of Fe50Al50- n Hf n alloys for n = 1, 3, 5, 7, and 9 at. pct has been investigated. At all investigated compositions, the ternary intermetallic HfFe6Al6 τ 1 phase forms due to the limited solid solubility of Hf in FeAl phase and tends to develop a eutectic phase mixture with the Fe-Al-based phase. The Hf concentration of the eutectic composition is found to be 7 at. pct from the microstructural examinations and the eutectic phase transition temperature is determined as 1521 K (1248 °C) independent of Hf amount by differential scanning calorimetry measurements. Furthermore, the enthalpies and activation energies (based on Kissinger and Ozawa methods) of eutectic phase transitions are reported. The minimum activation energy is calculated for the fully eutectic composition. Moreover, variation of the microhardness of Fe-Al-based alloys as a function of the Hf content is investigated, and its dependence on the thermal history of the alloys is explained.

  6. Structure evolution of Fe-50%Al coating prepared by mechanical alloying

    NASA Astrophysics Data System (ADS)

    Aryanto, D.; Wismogroho, A. S.; Sudiro, T.

    2016-08-01

    The deposition of Fe-50%Al coating (in at%) on low carbon steel was successfully prepared by using mechanical alloying (MA). The coating process was performed in a shaker mill with variation of milling times from 30 minute to 180 minutes. The deposited coating was then heat treated at 600°C for 2 hour in a vacuum furnace of 5.6 Pa. The structure evolution of mechanical alloyed samples before and after heat treatment was investigated by scanning electron microscopy (SEM) equipped with energy dispersive X-ray spectrometer (EDX) and X-ray diffractometer (XRD). The results revealed that before heat treatment, the deposited coating on low carbon steel is composed of Fe and Al. The Fe(Al) solid solution was mostly formed after 180 minutes of milling time. Metallographic observation indicated that the surface of Fe-Al coating was rough and the coating thickness was increased with increasing milling time. Meanwhile, the heat treatment process led to structural evolution by forming FeAl intermetallic phase on the surface of low carbon steel.

  7. Development of a new graded-porosity FeAl alloy by elemental reactive synthesis

    SciTech Connect

    Shen, P Z; He, Y H; Gao, H Y; Zou, J; Xu, N P; Jiang, Y; Huang, B; Lui, C T

    2009-01-01

    A new graded-porosity FeAl alloy can be fabricated through Fe and Al elemental reactive synthesis. FeAl alloy with large connecting open pores and permeability were used as porous supports. The coating was obtained by spraying slurries consisting of mixtures of Fe powder and Al powder with 3 5 m diameter onto porous FeAl support and then sintered at 1100 C. The performances of the coating were compared in terms of thickness, pore diameter and permeability. With an increase in the coating thickness up to 200 m, the changes of maximum pore size decreased from 23.6 m to 5.9 m and the permeability decreased from 184.2 m3m 2kPa 1h 1 to 76.2 m3m 2kPa 1h 1, respectively, for a sintering temperature equal to 1100 C. The composite membranes have potential application for excellent filters in severe environments.

  8. [Release of Si, Al and Fe in red soil under simulated acid rain].

    PubMed

    Liu, Li; Song, Cun-yi; Li, Fa-sheng

    2007-10-01

    bstract:A laboratory leaching experiment on simulated acid rain was carried out using soil columns. The release of Si, Al and Fe from soils and pH values of eluates were investigated. The results showed that under the given leaching volume, the release amounts of cations were influenced by the pH value of simulated acid rain, while their response to acid rain was different. Acid rain led to Si release, nearly none of Fe. Within the range from pH 3.0 to 5.6, a little Al release but mass Al only release at the pH below 3.0, both Si and Al had a declining release ability with the undergoing eluviation. At pH 2.5, the release amounts of Si and Al, especially Al, increased significantly with the strengthened weathering process of soil mineral. With an increase of the leaching amount of acid rain, the release of Si and Al increased, but acceleration of Si was slower than Al which was slower and slower. When the soil pH falling down to a certain grade, there are negative correlation between pH and both Al and DOC concentration of eluate. released, but most of Al derived from the aluminosilicates dissolved. Acid deposition can result in solid-phase alumino-organics broken and Al released, but most of Al derived from the aluminosilicates dissolved.

  9. Fermi surface deformation in a simple iron-based superconductor, FeSe

    NASA Astrophysics Data System (ADS)

    Coldea, Amalia; Watson, Matthew; Kim, Timur; Haghighirad, Amir; McCollam, Alix; Hoesch, Moritz; Schofield, Andrew

    2015-03-01

    One of the outstanding problems in the field superconductivity is the identification of the normal state out of which superconductivity emerges. FeSe is one of the simplest and most intriguing iron-based superconductors, since in its bulk form it undergoes a structural transition before it becomes superconducting, whereas its single-layer form is believed to be a high-temperature superconductor. The nature of the structural transition, occurring in the absence of static magnetism, is rather unusual and how the electronic structure is stabilized by breaking of the rotational symmetry is the key to understand the superconductivity in bulk FeSe. Here we report angle-resolved photoemission spectroscopy measurements on FeSe that gives direct access to the band structure and orbital-dependent effects. We complement our studies on bulk FeSe with low-temperature angular-dependent quantum oscillation measurements using applied magnetic fields that are sufficiently strong to suppress superconductivity and reach the normal state. These studies reveal a strong deformation of Fermi surface through the structural transition driven by electronic correlations and orbital-dependent effects. . This work was supported by EPSRC, UK (EP/I004475/1), Diamond Light Source, UK and HFML, Nijmegen.

  10. Symmetry-Defying Iron Pyrite (FeS2) Nanocrystals through Oriented Attachment

    PubMed Central

    Gong, Maogang; Kirkeminde, Alec; Ren, Shenqiang

    2013-01-01

    Iron pyrite (fool's gold, FeS2) is a promising earth abundant and environmentally benign semiconductor material that shows promise as a strong and broad absorber for photovoltaics and high energy density cathode material for batteries. However, controlling FeS2 nanocrystal formation (composition, size, shape, stoichiometry, etc.) and defect mitigation still remains a challenge. These problems represent significant limitations in the ability to control electrical, optical and electrochemical properties to exploit pyrite's full potential for sustainable energy applications. Here, we report a symmetry-defying oriented attachment FeS2 nanocrystal growth by examining the nanostructure evolution and recrystallization to uncover how the shape, size and defects of FeS2 nanocrystals changes during growth. It is demonstrated that a well-controlled reaction temperature and annealing time results in polycrystal-to-monocrystal formation and defect annihilation, which correlates with the performance of photoresponse devices. This knowledge opens up a new tactic to address pyrite's known defect problems. PMID:23807691

  11. Rusty Old Stars: A Source of the Missing Interstellar Iron

    DTIC Science & Technology

    2010-06-18

    et al. 2008). Iron is also de- pleted by >90% in the gas phase of planetary nebulae (Delgado Inglada et al. 2009). Direct evidence for iron...planetary nebulae ; as well as isotopic ratios in FeO grains in meteorites. While iron increases opacity in oxygen-rich winds, it remains unclear

  12. FeS/S/FeS(2) redox system and its oxidoreductase-like chemistry in the iron-sulfur world.

    PubMed

    Wang, Wei; Yang, Bin; Qu, Youpeng; Liu, Xiaoyang; Su, Wenhui

    2011-06-01

    The iron-sulfur world (ISW) theory is an intriguing prediction regarding the origin of life on early Earth. It hypothesizes that life arose as a geochemical process from inorganic starting materials on the surface of sulfide minerals in the vicinity of deep-sea hot springs. During the last two decades, many experimental studies have been carried out on this topic, and some interesting results have been achieved. Among them, however, the processes of carbon/nitrogen fixation and biomolecular assembly on the mineral surface have received an inordinate amount of attention. To the present, an abiotic model for the oxidation-reduction of intermediates participating in metabolic pathways has been ignored. We examined the oxidation-reduction effect of a prebiotic FeS/S/FeS(2) redox system on the interconversion between several pairs of α-hydroxy acids and α-keto acids (i.e., lactate/pyruvate, malate/oxaloacetate, and glycolate/glyoxylate). We found that, in the absence of FeS, elemental sulfur (S) oxidized α-hydroxy acids to form corresponding keto acids only at a temperature higher than its melting point (113°C); in the presence of FeS, such reactions occurred more efficiently through a coupled reaction mechanism, even at a temperature below the phase transition point of S. On the other hand, FeS was shown to have the capacity to reversibly reduce the keto acids. Such an oxidoreductase-like chemistry of the FeS/S/FeS(2) redox system suggests that it can determine the redox homeostasis of metabolic intermediates in the early evolutionary phase of life. The results provide a possible pathway for the development of primordial redox biochemistry in the iron-sulfur world. Key Words: Iron-sulfur world-FeS/S/FeS(2) redox system-Oxidoreductase-like chemistry. Astrobiology 11, 471-476.

  13. On-line solid-phase extraction and multisyringe flow injection analysis of Al(III) and Fe(III) in drinking water.

    PubMed

    Vanloot, Pierre; Branger, Catherine; Margaillan, André; Brach-Papa, Christophe; Boudenne, Jean-Luc; Coulomb, Bruno

    2007-11-01

    A new analytical method was developed for on-line monitoring of residual coagulants (aluminium and iron salts) in potable water. The determination was based on a sequential procedure coupling an extraction/enrichment step of the analytes onto a modified resin and a spectrophotometric measurement of a surfactant-sensitized binary complex formed between eluted analytes and Chrome Azurol S. The optimization of the solid phase extraction was performed using factorial design and a Doehlert matrix considering six variables: sample percolation rate, sample metal concentration, flow-through sample volume (all three directly linked to the extraction step), elution flow rate, concentration and volume of eluent (all three directly linked to the elution step). A specific reagent was elaborated for sensitive and specific spectrophotometric determination of Al(III) and Fe(III), by optimizing surfactant and ligand concentrations and buffer composition. The whole procedure was automated by a multisyringe flow injection analysis (MSFIA) system. Detection limits of 4.9 and 5.6 microg L(-1) were obtained for Al(III) and Fe(III) determination , respectively, and the linear calibration graph up to 300 microg L(-1) (both for Al(III) and Fe(III)) was well adapted to the monitoring of drinking water quality. The system was successfully applied to the on-site determination of Al(III) and Fe(III) at the outlet of two water treatment units during two periods of the year (winter and summer conditions).

  14. Photoassisted Fenton degradation of phthalocyanine dyes from wastewater of printing industry using Fe(II)/γ-Al2O3 catalyst in up-flow fluidized-bed.

    PubMed

    Cheng, Hsuhui; Chou, Shihjie; Chen, Shiaoshing; Yu, Chiajen

    2014-06-01

    Fe(II)/γ-Al2O3 powders synthesized using the dipping method were produced from a mixed aqueous solution containing aluminium oxide (γ-Al2O3) and iron(II)-precursor (FeSO4), and used for photo-Fenton degradation of phthalocyanine dyes (PCS) under ultraviolet (UV) irradiation in an up-flow fluidized bed. The catalysts were characterized by XRD, ESCA, BET, EDS and SEM. The results showed that Fe(2+) ion was compounded on the γ-Al2O3 carrier. The effects of different reaction parameters such as catalyst activity, dosage and solution pH on the decolorization of PCS were assessed. Results indicated that maximum decolorization (more than 95%) of PCS occurred with 20 wt% Fe(II)/γ-Al2O3 catalyst (dosage of 60 g/L) using a combination of UV irradiation and heterogeneous Fenton system. The degradation efficiency of PCS increases as pH decreases, exhibiting a maximum efficiency at pH 3.5. The recycled catalyst was capable of repeating three runs without a significant decrease in treatment efficiency, and this demonstrated the stability and reusability of catalyst.

  15. Processing and Properties of Mechanical Alloyed Al93Fe3Cr2Ti2 Alloys

    DTIC Science & Technology

    2004-10-01

    Nanomaterials, Aluminum Alloys ABSTRACT Nanostructured A193Fe3Ti2Cr2 alloys were prepared via mechanical alloying (MA) starting from elemental powders...2Cr2 . The aluminum powder had a purity of 99.5 wt% with a mean particle size of 70 ^rn, while the corresponding values for iron, chromium and...increases. 2) All aluminum reflections exhibit broadening even after only 2-hours of milling, indicating the grain size reduction and possibly the

  16. Large anisotropic Fe orbital moments in perpendicularly magnetized Co2FeAl Heusler alloy thin films revealed by angular-dependent x-ray magnetic circular dichroism

    NASA Astrophysics Data System (ADS)

    Okabayashi, Jun; Sukegawa, Hiroaki; Wen, Zhenchao; Inomata, Koichiro; Mitani, Seiji

    2013-09-01

    Perpendicular magnetic anisotropy (PMA) in Heusler alloy Co2FeAl thin films sharing an interface with a MgO layer is investigated by angular-dependent x-ray magnetic circular dichroism. Orbital and spin magnetic moments are deduced separately for Fe and Co 3d electrons. In addition, the PMA energies are estimated using the orbital magnetic moments parallel and perpendicular to the film surfaces. We found that PMA in Co2FeAl is determined mainly by the contribution of Fe atoms with large orbital magnetic moments, which are enhanced at the interface between Co2FeAl and MgO. Furthermore, element specific magnetization curves of Fe and Co are found to be similar, suggesting the existence of ferromagnetic coupling between Fe and Co PMA directions.

  17. Control of spin current by a magnetic YIG substrate in NiFe/Al nonlocal spin valves

    NASA Astrophysics Data System (ADS)

    Dejene, F. K.; Vlietstra, N.; Luc, D.; Waintal, X.; Ben Youssef, J.; van Wees, B. J.

    2015-03-01

    We study the effect of a magnetic insulator [yttrium iron garnet (YIG)] substrate on the spin-transport properties of Ni80Fe20/Al nonlocal spin valve (NLSV) devices. The NLSV signal on the YIG substrate is about two to three times lower than that on a nonmagnetic SiO2 substrate, indicating that a significant fraction of the spin current is absorbed at the Al/YIG interface. By measuring the NLSV signal for varying injector-to-detector distances and using a three-dimensional spin-transport model that takes spin-current absorption at the Al/YIG interface into account, we obtain an effective spin-mixing conductance G↑↓≃5 -8 ×1013Ω-1m-2 . We also observe a small, but clear, modulation of the NLSV signal when rotating the YIG magnetization direction with respect to the fixed spin polarization of the spin accumulation in the Al. Spin relaxation due to thermal magnons or roughness of the YIG surface may be responsible for the observed small modulation of the NLSV signal.

  18. Iron-[S,S']-EDDS (FeEDDS) Chelate as an Iron Source for Horticultural Crop Production: Marigold Growth and Nutrition, Spectral Properties, and Photodegradation

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Aminopolycarboxylic acid (APCA) complexones, commonly referred to as ligands or chelating agents, like ethylenediaminetetraacetic acid (EDTA) and diethylenetriaminepentaacetic acid (DTPA) are commonly used in soluble fertilizers to supply copper (Cu), iron (Fe), manganese (Mn), and/or zinc (Zn) to p...

  19. Effect of Al substitution for Ga on the mechanical properties of directional solidified Fe-Ga alloys

    NASA Astrophysics Data System (ADS)

    Liu, Yangyang; Li, Jiheng; Gao, Xuexu

    2017-02-01

    Alloys of Fe82Ga18-xAlx (x=0, 4.5, 6, 9, 12, 13.5) were prepared by directional solidification technique and exhibited a <001> preferred orientation along the axis of alloy rods. The saturation magnetostriction value of the Fe82Ga13.5Al4.5 alloy was 247 ppm under no pre-stress. The tensile properties of alloys of Fe82Ga18-xAlx at room temperature were investigated. The results showed that tensile ductility of binary Fe-Ga alloy was significantly improved with Al addition. The fracture elongation of the Fe82Ga18 alloy was only 1.3%, while that of the Fe82Ga9Al9 alloy increased up to 16.5%. Addition of Al increased the strength of grain boundary and cleavage, resulting in the enhancement of tensile ductility of the Fe-Ga-Al alloys. Analysis of deformation microstructure showed that a great number of deformation twins formed in the Fe-Ga-Al alloys, which were thought to be the source of serrated yielding in the stress-strain curves. The effect of Al content in the Fe-Ga-Al alloys on tensile ductility was also studied by the analysis of deformation twins. It indicated that the joint effect of slip and twinning was beneficial to obtain the best ductility in the Fe82Ga9Al9 alloy.

  20. Hydrogenic Lamb shift in iron Fe{sup 25+} and fine-structure Lamb shift

    SciTech Connect

    Chantler, C. T.; Laming, J. M.; Dietrich, D. D.; Hallett, W. A.; McDonald, R.; Silver, J. D.

    2007-10-15

    1s-2p Lyman {alpha} transitions in hydrogenic iron Fe{sup 25+} have been observed from a beam-foil source in fourth-order diffraction off ADP 101 and PET 002 crystals, simultaneously with the n=2 to n=4 Balmer {beta} transitions diffracted in first order. Calibration of the local dispersion relation of the spectrometer using Balmer {beta} lines provides measurements of Lyman {alpha} wavelengths. The approach of fitting the full two-dimensional dispersion relation, including other members of Balmer and Lyman series, limits random and systematic correlation of parameters, and reveals a major systematic due to dynamical diffraction depth penetration into a curved crystal. The development of a theory of x-ray diffraction from mosaic crystals was necessary for the accurate interpretation of the experimental data. Photographic theory was also developed in the process of this research. Several systematics are discussed and quantified for the first time for these medium-Z QED comparisons. 2s-1s and 4f-2p satellites are explicitly investigated, and a dominant systematic is uncovered, which is due to the variable location of spectral emission downstream of the beam-foil target. 1s-2p{sub 3/2}, 1s-2p{sub 1/2} iron Lamb shifts are measured to be 35 376{+-}1900 cm{sup -1} and 35 953{+-}1800 cm{sup -1}. These agree with but lie higher than theory. This represents a 5.7% measurement of the hydrogenic 1s-2p{sub 1/2} Lamb shift in iron. The technique also reports the iron 2p{sub 3/2}-2p{sub 1/2} fine structure as 171 108 cm{sup -1}{+-}180 cm{sup -1}, which represents a 51% measurement of the hydrogenic iron fine-structure Lamb shift, and reports measurements of secondary lines.

  1. High spatial resolution PEELS characterization of FeAl nanograins prepared by mechanical alloying

    SciTech Connect

    Valdre, G. |; Botton, G.A.; Brown, L.M.

    1999-05-28

    The authors investigate the nanograin ``chemical`` structure in a nanostructured material of possible industrial application (Fe-Al system) prepared by conventional mechanical alloying via ball milling in argon atmosphere. They restrict themselves to the structural and nanochemical behavior of ball-milled nanocrystalline Fe-Al powders with atomic composition Fe{sub 3}Al, corresponding to a well-known intermetallic compound of the Fe-Al system. Scanning transmission electron microscopy (STEM) equipped with a parallel detection electron energy loss spectrometer (PEELS) has provided an insight on the ``chemical`` structure of both nanograins and their surface at a spatial resolution of better than 1 nm. The energy loss near edge structure of the Al L loss reveals that the Al coordination is similar to a B2 compound and the oxidation of the powder during processing may play a significant role in the stabilization of the intermetallic phases. Conventional transmission electron microscopy (TEM) was used for the structural characterization of the material after the ball milling; powder X-ray diffraction (XRD) aided the investigation.

  2. Synthesis of Imine-Naphthol Tripodal Ligand and Study of Its Coordination Behaviour towards Fe(III), Al(III), and Cr(III) Metal Ions

    PubMed Central

    Kaur, Kirandeep

    2014-01-01

    A hexadentate Schiff base tripodal ligand is synthesized by the condensation of tris (2-aminoethyl) amine with 2-hydroxy-1-naphthaldehyde and characterized by various spectroscopic techniques like UV-VIS, IR, NMR, MASS, and elemental analysis. The solution studies by potentiometric and spectrophotometric methods are done at 25 ± 1°C, µ = 0.1 M KCl, to calculate the protonation constants of the ligand and formation constants of metal complexes formed by the ligand with Fe(III), Al(III), and Cr(III) metal ions. The affinity of the ligand towards Fe(III) is compared with deferiprone (a drug applied for iron intoxication) and transferrin (the main Fe(III) binding protein in plasma). Structural analysis of the ligand and the metal complexes was done using semiempirical PM6 method. Electronic and IR spectra are calculated by semiempirical methods and compared with experimental one. PMID:25294978

  3. Effect of the Chalcogenide Element Doping on the Electronic Properties of Co2FeAl Heusler Alloys

    NASA Astrophysics Data System (ADS)

    Huang, Ting; Cheng, Xiao-min; Guan, Xia-wei; Miao, Xiang-shui

    2016-02-01

    The electronic properties of the typical Heusler compound Co2FeAl with chalcogenide element doping were investigated by means of first principles calculations within the local spin-density approximation (LSDA) + Hubbard U parameter (U). The calculations indicate that, only when 25% of the number of Al atoms is substituted by the chalcogenide element, the chalcogenide element-doped Co2FeAl shows the half metallic properties. The Fermi energy ( E F) of the 25% chalcogenide element-doped Co2FeAl is located in the middle of the gap of the minority states instead of around the top of the valence band as in Co2FeAl. Moreover, the band gap of 25% Te-doped Co2FeAl (0.80 eV) is wider than that of Co2FeAl (0.74 eV). These improved electronic structures will make 25% chalcogenide element-doped Co2FeAl more stable against temperature variation. Therefore, the expected excellent stability of the 25% chalcogenide element-doped Co2FeAl make it more suitable for spintronic applications than Co2FeAl.

  4. Flaky FeSiAl alloy-carbon nanotube composite with tunable electromagnetic properties for microwave absorption

    PubMed Central

    Huang, Lina; Liu, Xiaofang; Chuai, Dan; Chen, Yaxin; Yu, Ronghai

    2016-01-01

    Flaky FeSiAl alloy/multi-wall carbon nanotube (FeSiAl/MWCNT) composite was fabricated by facile and scalable ball milling method. The morphology and electromagnetic properties of the FeSiAl alloy can be well tuned by controlling the milling time. It is found that the magnetic loss of the FeSiAl alloy is improved by optimizing the milling time due to the increased anisotropy field. Meanwhile the addition of MWCNTs enhances the dielectric loss of the composite by increasing the interfacial polarizations, dipolar polarizations and conductive paths. Relative to conventional FeSiAl absorbers, the FeSiAl/MWCNT composite exhibits greatly improved microwave absorption performance with advantages of strong absorption and small thickness. The minimum reflection loss of the composite reaches −42.8 dB at 12.3 GHz at a very thin thickness of 1.9 mm. PMID:27762327

  5. Flaky FeSiAl alloy-carbon nanotube composite with tunable electromagnetic properties for microwave absorption.

    PubMed

    Huang, Lina; Liu, Xiaofang; Chuai, Dan; Chen, Yaxin; Yu, Ronghai

    2016-10-20

    Flaky FeSiAl alloy/multi-wall carbon nanotube (FeSiAl/MWCNT) composite was fabricated by facile and scalable ball milling method. The morphology and electromagnetic properties of the FeSiAl alloy can be well tuned by controlling the milling time. It is found that the magnetic loss of the FeSiAl alloy is improved by optimizing the milling time due to the increased anisotropy field. Meanwhile the addition of MWCNTs enhances the dielectric loss of the composite by increasing the interfacial polarizations, dipolar polarizations and conductive paths. Relative to conventional FeSiAl absorbers, the FeSiAl/MWCNT composite exhibits greatly improved microwave absorption performance with advantages of strong absorption and small thickness. The minimum reflection loss of the composite reaches -42.8 dB at 12.3 GHz at a very thin thickness of 1.9 mm.

  6. Flaky FeSiAl alloy-carbon nanotube composite with tunable electromagnetic properties for microwave absorption

    NASA Astrophysics Data System (ADS)

    Huang, Lina; Liu, Xiaofang; Chuai, Dan; Chen, Yaxin; Yu, Ronghai

    2016-10-01

    Flaky FeSiAl alloy/multi-wall carbon nanotube (FeSiAl/MWCNT) composite was fabricated by facile and scalable ball milling method. The morphology and electromagnetic properties of the FeSiAl alloy can be well tuned by controlling the milling time. It is found that the magnetic loss of the FeSiAl alloy is improved by optimizing the milling time due to the increased anisotropy field. Meanwhile the addition of MWCNTs enhances the dielectric loss of the composite by increasing the interfacial polarizations, dipolar polarizations and conductive paths. Relative to conventional FeSiAl absorbers, the FeSiAl/MWCNT composite exhibits greatly improved microwave absorption performance with advantages of strong absorption and small thickness. The minimum reflection loss of the composite reaches ‑42.8 dB at 12.3 GHz at a very thin thickness of 1.9 mm.

  7. Magnetic properties of fibrous Fe-Al-O prepared by electrospinning

    NASA Astrophysics Data System (ADS)

    Lovchinov, V.; Simeonova, P.; Vanderbemden, Ph; Krezhov, K.

    2014-12-01

    Recently, we obtained a new Fe-Al-O fibrous material by applying the novel route of electrospinning. Here we report on the properties of the as prepared material established by PPMS magnetometry and X-ray diffraction. X-ray diffractograms revealed the coexistence of the orthorhombic multiferroic phase FeAlO3 along with traces of unreacted impurities. The structure of the FeAlO3 phase is described in the orthorhombic Pna21 space group and is of great current interest since the compound features piezoelectricity, ferrimagnetism and magnetoelectric effects at low temperatures. In contrast to known bulk material obtained by classical routes the new fibrous material shows a lower value of saturation magnetization and the magnetic transition occurs at a much lower temperature. In the discussion an attempt is made to disclose the reasons for the observed differences.

  8. Surface magneto-optical and Mössbauer observations of Fe-Al

    NASA Astrophysics Data System (ADS)

    Jirásková, Y.; Hendrych, A.; Životský, O.; Buršík, J.; Žák, T.; Procházka, I.; Janičkovič, D.

    2013-07-01

    The paper is devoted to detailed surface studies of the Fe82Al18 alloy prepared from high purity Fe and Al by arc melting. The results summarize observations of the surface sensitive methods - high resolution scanning electron microscopy (HRSEM), slow energy electron microscopy (SLEEM), magneto-optical Kerr effect (MOKE), and conversion electron Mössbauer spectrometry (CEMS). Morphology of grains and grain boundaries obtained by HRSEM is observed in more detail by SLEEM. The CEMS results analyzed using free components with characteristic hyperfine parameters and by theoretical model, give evidence for A2 order of the as-prepared and as-quenched Fe82Al18 sample surfaces. A small contribution of the oxide layer influences the shape of hysteresis loops and domain structure of the sample surface above all in the as-quenched state.

  9. Microstructural characterization of Ni-22Fe-22Cr-6Al metallic foam by transmission electron microscopy.

    PubMed

    Kim, Hyung Giun; Lee, Taeg Woo; Lee, Jae Young; Lee, Eui Sung; Oh, Kwon Oh; Lee, Chang Woo; Lim, Sung Hwan

    2012-01-01

    Ni-22Fe-22Cr-6Al metallic foam, prepared using a thermomechanical treatment and alloying elements, was studied via transmission electron microscopy (TEM) in order to clarify the relationship between the mechanical properties and the nanoscale microstructural characteristics. Due to the unique porous structure of the metallic foam, TEM specimens were prepared using an embedding-process-assisted-ion-milling technique and a focused-ion-beam method. The Cr-, Fe- and Al-clustered regions around the surface of the metallic foam were investigated using elemental maps. The Ni(3)Al (γ') precipitates, which can affect the mechanical properties of the Ni-Fe-Cr (γ) matrix, were characterized in the metallic foam.

  10. Irradiation-enhanced α' precipitation in model FeCrAl alloys

    SciTech Connect

    Edmondson, Philip D.; Briggs, Samuel A.; Yamamoto, Yukinori; Howard, Richard H.; Sridharan, Kumar; Terrani, Kurt A.; Field, Kevin G.

    2016-02-17

    We have irradiated the model FeCrAl alloys with varying compositions (Fe(10–18)Cr(10–6)Al at.%) with a neutron at ~ 320 to damage levels of ~ 7 displacements per atom (dpa) to investigate the compositional influence on the formation of irradiation-induced Cr-rich α' precipitates using atom probe tomography. In all alloys, significant number densities of these precipitates were observed. Cluster compositions were investigated and it was found that the average cluster Cr content ranged between 51.1 and 62.5 at.% dependent on initial compositions. Furthermore, this is significantly lower than the Cr-content of α' in binary FeCr alloys. As a result, significant partitioning of the Al from the α' precipitates was also observed.

  11. Irradiation-enhanced α' precipitation in model FeCrAl alloys

    DOE PAGES

    Edmondson, Philip D.; Briggs, Samuel A.; Yamamoto, Yukinori; ...

    2016-02-17

    We have irradiated the model FeCrAl alloys with varying compositions (Fe(10–18)Cr(10–6)Al at.%) with a neutron at ~ 320 to damage levels of ~ 7 displacements per atom (dpa) to investigate the compositional influence on the formation of irradiation-induced Cr-rich α' precipitates using atom probe tomography. In all alloys, significant number densities of these precipitates were observed. Cluster compositions were investigated and it was found that the average cluster Cr content ranged between 51.1 and 62.5 at.% dependent on initial compositions. Furthermore, this is significantly lower than the Cr-content of α' in binary FeCr alloys. As a result, significant partitioning ofmore » the Al from the α' precipitates was also observed.« less

  12. Electrochemical deposition and microstructural characterization of AlCrFeMnNi and AlCrCuFeMnNi high entropy alloy thin films

    NASA Astrophysics Data System (ADS)

    Soare, V.; Burada, M.; Constantin, I.; Mitrică, D.; Bădiliţă, V.; Caragea, A.; Târcolea, M.

    2015-12-01

    Al-Cr-Fe-Mn-Ni and Al-Cr-Cu-Fe-Mn-Ni high entropy alloy thin films were prepared by potentiostatic electrodeposition and the microstructure of the deposits was investigated. The thin films were co-deposited in an electrolyte based on a DMF (N,N-dimethylformamide)-CH3CN (acetonitrile) organic compound. The energy dispersive spectrometry investigation (EDS) indicated that all the five respectively six elements were successfully co-deposited. The scanning electron microscopy (SEM) analysis revealed that the film consists of compact and uniform particles with particle sizes of 500 nm to 4 μm. The X-ray diffractometry (XRD) patterns indicated that the as-deposited thin films were amorphous. Body-centered-cubic (BCC) structures were identified by XRD after the films were annealed at various temperatures under inert Ar atmosphere. The alloys adhesion on the substrate was determined by the scratch-testing method, with higher values obtained for the Al-Cr-Cu-Fe-Mn-Ni alloy.

  13. Influence of recrystallization on phase separation kinetics of oxide dispersion strengthened Fe Cr Al alloy

    SciTech Connect

    Capdevila, C.; Miller, Michael K; Pimentel, G.; Chao, J.

    2012-01-01

    The effect of different starting microstructures on the kinetics of Fe-rich ({alpha}) and Cr-rich ({alpha}') phase separation during aging of Fe-Cr-Al oxide dispersion strengthened (ODS) alloys has been analyzed with a combination of atom probe tomography and thermoelectric power measurements. The results revealed that the high recrystallization temperature necessary to produce a coarse grained microstructure in Fe-base ODS alloys affects the randomness of Cr-atom distributions and defect density, which consequently affect the phase separation kinetics at low annealing temperatures.

  14. Heat capacity and phase equilibria of almandine, Fe3Al2Si3O12

    USGS Publications Warehouse

    Anovitz, Lawrence M.; Essene, E.J.; Metz, G.W.; Bohlen, S.R.; Westrum, E.F.; Hemingway, B.S.

    1993-01-01

    The heat capacity of a synthetic almandine, Fe3Al2Si3O12, was measured from 6 to 350 K using equilibrium, intermittent-heating quasi-adiabatic calorimetry and from 420 to 1000 K using differential scanning calorimetry. These measurements yield Cp298 = 342.80 ?? 1.4 J/mol ?? K and S298o = 342.60 J/mol ?? K. Mo??ssbauer characterizations show the almandine to contain less than 2 ?? 1% of the total iron as Fe3+. X-ray diffraction studies of this synthetic almandine yield a = 11.521 ?? 0.001 A?? and V298o = 115.11 +- 0.01 cm3/mol, somewhat smaller than previously reported. The low-temperature Cp data indicate a lambda transition at 8.7 K related to an antiferromagnetic-paramagnetic transition with TN = 7.5 K. Modeling of the lattice contribution to the total entropy suggests the presence of entropy in excess of that attributable to the effects of lattice vibrations and the magnetic transition. This probably arises from a low-temperature electronic transition (Schottky contribution). Combination of the Cp data with existing thermodynamic and phase equilibrium data on almandine yields ??Gf,298o = -4938.3 kJ/mol and ??Hf,298o= -5261.3 kJ/mol for almandine when calculated from the elements. The equilibrium almandine = hercynite + fayalite + quartz limits the upper T P for almandine and is metastably located at ca. 570??C at P = 1 bar, with a dP dT of +17 bars/??C. This agrees well with reversed experiments on almandine stability when they are corrected for magnetite and hercynite solid-solutions. In {norm of matrix}O2-T space, almandine oxidizes near QFM by the reactions almandine + O2 = magnetite + sillimanite + quartz and almandine + 02 = hercynite + magnetite + quartz. With suitable correction for reduced activities of solid phases, these equilibria provide useful oxygen barometers for medium- to high-grade metamorphic rocks. ?? 1993.

  15. A Fe3O4/FeAl2O4 composite coating via plasma electrolytic oxidation on Q235 carbon steel for Fenton-like degradation of phenol.

    PubMed

    Wang, Jiankang; Yao, Zhongping; Yang, Min; Wang, Yajing; Xia, Qixing; Jiang, Zhaohua

    2016-08-01

    The Fe3O4/FeAl2O4 composite coatings were successfully fabricated on Q235 carbon steel by plasma electrolytic oxidation technique and used to degrade phenol by Fenton-like system. XRD, SEM, and XPS indicated that Fe3O4 and FeAl2O4 composite coating had a hierarchical porous structure. The effects of various parameters such as pH, phenol concentration, and H2O2 dosage on catalytic activity were investigated. The results indicated that with increasing of pH and phenol content, the phenol degradation efficiency was reduced significantly. However, the degradation rate was improved with the addition of H2O2, but dropped with further increasing of H2O2. Moreover, 100 % removal efficiency with 35 mg/L phenol was obtained within 60 min at 303 K and pH 4.0 with 6.0 mmol/L H2O2 on 6-cm(2) iron oxide coating. The degradation process consisted of induction period and rapid degradation period; both of them followed pseudo-first-order reaction. Hydroxyl radicals were the mainly oxidizing species during phenol degradation by using n-butanol as hydroxyl radical scavenger. Based on Fe leaching and the reaction kinetics, a possible phenol degradation mechanism was proposed. The catalyst exhibited excellent stability.

  16. Growth of Zinc Phosphide (Zn3P2) and Iron Disulfide (FeS2) using pulsed laser deposition

    NASA Astrophysics Data System (ADS)

    Vaddi, Rajesh

    The growing energy needs of society have triggered tremendous interest in the development of photovoltaics formed from earth abundant materials. Zinc Phosphide (Zn3P2) and Iron Pyrite (FeS2) are two materials formed from elements with large Earth crustal abundances that have nearly ideal band gap energies (1.5eV and 0.96 eV, respectively) and optical absorption coefficients (~104 /cm) for use as absorber layers in solar cells. In this work, the structural, optical, and electronic properties of these materials produced in thin film form using pulsed laser deposition have been explored. Stoichiometric Zn3P2 thin films were obtained at a laser energy density of 3 J/cm2. However, these films were found to be amorphous. Crystallization of these highly resistive amorphous thin films was possible after rapid thermal annealing (RTA). A near optimal band gap of 1.6 eV and a high absorption coefficient of >104/cm were observed for samples annealed at 500 C for 60 seconds when high ramp rates of 150 °C/sec were used for annealing. XPS studies showed the presence of a trace amount of oxygen in the samples upon depth profiling. Schottky barrier heights were extracted for samples annealed at 350 °C and 500 °C with different metals. Al and Mg showed higher barrier heights with good diode rectification behavior. Fermi level pinning was shown to be a significant concern in both cases due to the large values of interface states observed (> 1013/cm2-eV). A Schottky barrier solar cell was fabricated using these films and showed low efficiency with a low Voc of 410 mV that was impacted by Fermi level pinning. Growth of Iron pyrite thin films from an FeS target was demonstrated for the first time using pulsed laser deposition. For the different laser energy densities and substrate temperatures explored, amorphous FeS (Pyrrhotite) was mainly produced. Conversion of FeS to FeS2 was obtained by sulfurization of thin films at 350 °C for times of 30 minutes at a N2 flow rates of 200

  17. Magnetotransport and magnetothermal properties of the ternary intermetallic compound TbFe2Al10

    NASA Astrophysics Data System (ADS)

    Khandelwal, Ashish; Chattopadhyay, M. K.; Roy, S. B.

    2016-09-01

    We have studied the temperature and field dependences of electrical resistivity and heat capacity of TbFe2Al10, and have also complimented the above studies with low field magnetization measurements. In zero magnetic field, TbFe2Al10 exhibits paramagnetic (PM) to ferrimagnetic (Ferri-I) and Ferri-I to antiferromagnetic (AFM) phase transitions below 17.6 and 10 K respectively. We have found that the electrical resistivity of TbFe2Al10 exhibits a sharp rise across the PM to Ferri-I phase transition in this compound. Our analysis indicates that this sharp rise of electrical resistivity is related to the formation of new zone boundaries (across the PM to Ferri-I phase transition) that reduce the area of the Fermi surface. We have found that TbFe2Al10 exhibits large magnetoresistance (MR) below 100 K. Overall, the MR behaviour of TbFe2Al10 below 17.6 K in different magnetic fields reveals strong competition between AFM and ferromagnetic (FM) correlations, which seems to be quite intrinsic to the magnetic structure of the compound. Our analysis indicates that the large MR and magnetocaloric effect persisting deep inside the PM regime of TbFe2Al10 is mainly related to the presence of FM spin fluctuations and the formation of a Griffiths like (GL) phase consisting of FM clusters within the PM regime. The formation of the GL phase may be mediated by the static crystal defects in the midst of the competing inter and intra layer magnetic interactions.

  18. Degradation of Aluminide Coatings in Fe-Al-Cr Alloy on the Isothermal Oxidation

    NASA Astrophysics Data System (ADS)

    Juwita, L.; Prajitno, D. H.; Soedarsono, J. W.; Manaf, A.

    2008-03-01

    Fe base superalloy has a good mechanical strength to be used as component operating at high temperature with oxidative environment. Although, the oxidation rate can not be tolerated as it will be oxidized and form oxide scale of un-protective FeO. Coating is a proper solution that this alloy can be used at high temperature. In this research, pack aluminizing on sample was conducted with temperatures of 900 °C, 1000 °C and 1100 °C for 10 hours in inert (argon) environment and then an oxidation test was carried out at temperature of 650 °C by an isothermal method for 10 hours in air environment. It was carried out an analysis for characteristics of coating and oxide scale formed in Fe-Al-Cr super alloy resulted from pack aluminizing. From this experiment, it was indicated by XRD analysis that the coating formed on substrate was a layer of FeAl2 compound, other than coating it was found a diffused zone, where in this area it occurred movement of Fe and Cr atoms from substrate toward coating, while Al atoms moved from coating to substrate. The increase of temperature of pack aluminizing process will affect settling rate of Al and coating growth.

  19. Synthesis of novel magnetic iron metal-silica (Fe-SBA-15) and magnetite-silica (Fe(3)O(4)-SBA-15) nanocomposites with a high iron content using temperature-programed reduction.

    PubMed

    Yiu, H H P; Keane, M A; Lethbridge, Z A D; Lees, M R; El Haj, A J; Dobson, J

    2008-06-25

    Magnetic iron metal-silica and magnetite-silica nanocomposites have been prepared via temperature-programed reduction (TPR) of an iron oxide-SBA-15 (SBA: Santa Barbara Amorphous) composite. TPR of the starting SBA-15 supported Fe(2)O(3) generated Fe(3)O(4) and FeO as stepwise intermediates in the ultimate formation of Fe-SBA-15. The composite materials have been characterized by means of x-ray diffraction, high resolution transmission electron microscopy and SQUID (superconducting quantum interference device) magnetometry. The Fe oxide and metal components form a core, as nanoscale particles, that is entrapped in the SBA-15 pore network. Fe(3)O(4)-SBA-15 and Fe-SBA-15 exhibited superparamagnetic properties with a total magnetization value of 17 emu g(-1). The magnetite-silica composite (at an Fe(3)O(4) loading of 30% w/w) delivered a magnetization that exceeded values reported in the literature or obtained with commercial samples. Due to the high pore volume of the mesoporous template, the magnetite content can be increased to 83% w/w with a further enhancement of magnetization.

  20. (4Fe-4S)-cluster-depleted Azotobacter vinelandii ferredoxin I: a new 3Fe iron-sulfur protein

    SciTech Connect

    Stephens, P.J.; Morgan, T.V.; Devlin, F.; Penner-Hahn, J.E.; Hodgson, K.O.; Scott, R.A.; Stout, C.D.; Burgess, B.K.

    1985-09-01

    Fe(CN)6T oxidation of the aerobically isolated 7Fe Azotobacter vinelandii ferredoxin I, (7Fe)FdI, is a degradative reaction. Destruction of the (4Fe-4S) cluster occurs first, followed by destruction of the (3Fe-3S) cluster. At a Fe(CN)6T /(7Fe)FdI concentration ratio of 20, the product is a mixture of apoprotein and protein containing only a (3Fe-3S) cluster, (3Fe)FdI. This protein mixture, after partial purification, has been characterized by absorption, CD, magnetic CD, and EPR and Fe x-ray absorption spectroscopies. EPR and magnetic CD spectra provide strong evidence that the (3Fe-3S) cluster in (3Fe)FdI is essentially identical in structure to that in (7Fe)FdI. Analysis of the extended x-ray absorption fine structure (EXAFS) of (3Fe)FdI finds Fe scattering at an average Fe...Fe distance of approx. =2.7 A. The structure of the oxidized (3Fe-3S) cluster in solutions of oxidized (3Fe)FdI, and, by extension, of oxidized (7Fe)FdI, is thus different from that obtained by x-ray crystallography on oxidized (7Fe)FdI. Possible interpretations of this result are discussed.

  1. Pharmacokinetics and red cell utilization of 52Fe/59Fe-labelled iron polymaltose in anaemic patients using positron emission tomography.

    PubMed

    Beshara, Soheir; Sörensen, Jens; Lubberink, Mark; Tolmachev, Vladimir; Långström, Bengt; Antoni, Gunnar; Danielson, Bo G; Lundqvist, Hans

    2003-03-01

    Parenteral iron-polysaccharide complexes are increasingly applied. The pharmacokinetics of iron sucrose have been assessed by our group using positron emission tomography (PET). A single intravenous injection of 100 mg iron as iron (III) hydroxide-polymaltose complex, labelled with a tracer in the form of 52Fe/59Fe, was similarly assessed in six patients using PET for about 8 h. Red cell utilization was followed for 4 weeks. Iron polymaltose was similarly distributed to the liver, spleen and bone marrow. However, a larger proportion of this complex was rapidly distributed to the bone marrow. The shorter equilibration phase for the liver, about 25 min, indicates the minimal role of the liver for direct distribution. Splenic uptake also reflected the reticuloendothelial handling of this complex. Red cell utilization ranged from 61% to 99%. Despite the relatively higher uptake by the bone marrow, there was no saturation of marrow transport systems at this dose level. In conclusion, high red cell utilization of iron polymaltose occurred in anaemic patients. The major portion of the injected dose was rapidly distributed to the bone marrow. In addition, the reticuloendothelial uptake of this complex may reflect the safety of polysaccharide complexes. Non-saturation of transport systems to the bone marrow indicated the presence of a large interstitial transport pool, which might possibly be transferrin.

  2. Geochemistry of dissolved aluminum at low pH: Extent and significance of Al-Fe(III) coprecipitation below pH 4.0

    NASA Astrophysics Data System (ADS)

    Sánchez-España, Javier; Yusta, Iñaki; Gray, Jennifer; Burgos, William D.

    2016-02-01

    This work examines the geochemical behavior of dissolved aluminum in sulfate-rich acidic waters. Our observations were obtained during several years of geochemical and mineralogical research in the San Telmo acidic pit lake and other pit lakes of SW Spain. The work includes scanning and transmission electron microscopy (SEM, TEM) of suspended mineral colloids found in deep lake waters. Energy dispersive spectroscopy (EDS) coupled to scanning and high resolution transmission electron microscopy (STEM, HRTEM) revealed not only the presence and formation of discrete, sub-micron Al solids like alunite, but also the abundance and distribution of Al into Fe(III) phases typical of acid mine drainage, such as schwertmannite and jarosite, at a nanometric resolution. The main conclusion emerging from our work is that the fate and transport of Al at low pH (<4.0) can be largely influenced by adsorption on and/or coprecipitation with both schwertmannite and jarosite. Under the geochemical conditions studied (SO42- = 10-2 M, Fe(III) ∼ Al = 10-3 M), alunite formation may occur at pH > 3.3, as suggested by mineralogical observations and geochemical modelling. Below this pH, and contrary to the extended assumption, Al is not truly conservative, and in the presence of ferric iron, both metals may co-precipitate at a substantial extent to form either particles of Al-rich schwertmannite (containing up to ca. 8 at.% Al with [Fe/(Fe + Al)] = 0.77) and/or crystals of H3O+- to K+-jarosite (containing up to ca. 10 at.% Al with [Fe/(Fe + Al)] = 0.54). This Al incorporation seems to take place by adsorption on particle surfaces in schwertmannite and by atomic substitution for Fe3+ in jarosite. Alunite is also unstable at this low pH range with respect to jarosite, which may lead either to isomorphic transformation and/or to chemically zoned crystals with jarositic rims around previously formed alunite cores. As a whole, the compositional spectrum of the analyzed jarosites and alunites

  3. Influence of Ti and V substitution for Al on the properties of Nd 60Fe 30Al 10 alloys

    NASA Astrophysics Data System (ADS)

    Chau, N.; Luong, N. H.; Huu, C. X.; Thep, N. T.; Anh, H. D.

    2003-06-01

    Systems with compositions Nd 60Fe 30Al 10- xTi x and Nd 60Fe 30Al 10- xV x ( x=2, 4, 6, 8, and 10) have been prepared by arc melting and copper mold suction-casting. The cast surface of the samples is partially crystalline. At increasing the Ti or V content, the crystalline fraction in the samples increases and for x=10, the alloys are fully crystalline. Melting temperatures also increase with increasing Ti or V content in the samples. All samples, some of them in a partly crystalline state, exhibit good hard magnetic properties at room temperature. With increasing Ti or V content, the magnetization continuously decreases, whereas both the coercivity and the Curie temperature increase. Thermomagnetic curves measured for all samples at low field exhibit an interesting shape. The temperature dependence of the coercivity of the samples has been determined.

  4. Solid state amorphization in the Al-Fe binary system during high energy milling

    SciTech Connect

    Urban, P. Montes, J. M.; Cintas, J.

    2013-12-16

    In the present study, mechanical alloying (MA) of Al75Fe25 elemental powders mixture was carried out in argon atmosphere, using a high energy attritor ball mill. The microstructure of the milled products at different stages of milling was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and differential scanning calorimetry (DSC). The results showed that the amorphous phase content increased by increasing the milling time, and after 50 hours the amorphization process became complete. Heating the samples resulted in the crystallization of the synthesized amorphous alloys and the appearance of the equilibrium intermetallic compounds Al{sub 5}Fe{sub 2}.

  5. Microstructural Influence on Dynamic Properties of Age Hardenable FeMnAl Alloys

    DTIC Science & Technology

    2011-04-01

    dependent on the separation distance between the two crystal slabs and modeled using the universal binding energy relation ( UBER ) 28, 29: GC (x... UBER fit results for pure Fe3AlC gave a cleavage energy of GC=5.04 J/m2 and an ideal stress ζ max=40 GPa with the maximum stress and separation...distance λ at 163 0.46 Å, which corresponds to an ideal strain of 12.3%. The UBER fit results for a phosphorus doped Fe3AlC supercell showed that the

  6. Equation of State of an AlCoCrCuFeNi High-Entropy Alloy

    NASA Astrophysics Data System (ADS)

    Li, Gong; Xiao, Daihong; Yu, Pengfei; Zhang, Lijun; Liaw, Peter K.; Li, Yanchun; Liu, Riping

    2015-08-01

    The pressure-volume (P-V) relationship of the AlCoCrCuFeNi high-entropy alloy (HEA) at room temperature has been studied using in situ high-pressure energy-dispersive x-ray diffraction with synchrotron radiation at high pressures. The equation of state of the AlCoCrCuFeNi HEA is determined by the calculation of the radial distribution function. The experimental results indicate that the HEA keeps a stable face-centered-cubic + body-centered-cubic structure in the experimental pressure range from 0 GPa to 24 GPa.

  7. ALCHEMI of Fe-doped B2-ordered NiAl alloys with different doping levels

    SciTech Connect

    Anderson, I.M.; Bentley, J.; Duncan, A.J.

    1994-09-01

    The ALCHEMI technique yields exact expressions for best-fit parameters in terms of ionization localization constants and site distributions of 3 elements distributed over two sublattices. In this paper, a graphical plotting technique is applied to Fe-doped NiAl B2-ordered alloys Ni{sub 0.5-x}Fe{sub x}Al{sub 0.5}, with x=0.02 or 0.10. The thin foil samples were examined in an electron microscope with an x-ray spectrometer.

  8. Elastic Modulus Measurement of ORNL ATF FeCrAl Alloys

    SciTech Connect

    Thompson, Zachary T.; Terrani, Kurt A.; Yamamoto, Yukinori

    2015-10-01

    Elastic modulus and Poisson’s ratio for a number of wrought FeCrAl alloys, intended for accident tolerant fuel cladding application, are determined via resonant ultrasonic spectroscopy. The results are reported as a function of temperature from room temperature to 850°C. The wrought alloys were in the fully annealed and unirradiated state. The elastic modulus for the wrought FeCrAl alloys is at least twice that of Zr-based alloys over the temperature range of this study. The Poisson’s ratio of the alloys was 0.28 on average and increased very slightly with increasing temperature.

  9. Development and quality assessments of commercial heat production of ATF FeCrAl tubes

    SciTech Connect

    Yamamoto, Yukinori

    2015-09-01

    Development and quality assessment of the 2nd generation ATF FeCrAl tube production with commercial manufacturers were conducted. The manufacturing partners include Sophisticated Alloys, Inc. (SAI), Butler, PA for FeCrAl alloy casting via vacuum induction melting, Oak Ridge National Laboratory (ORNL) for extrusion process to prepare the master bars/tubes to be tube-drawn, and Rhenium Alloys, Inc. (RAI), North Ridgeville, OH, for tube-drawing process. The masters bars have also been provided to Los Alamos National Laboratory (LANL) who works with Century Tubes, Inc., (CTI), San Diego, CA, as parallel tube production effort under the current program.

  10. Interdiffusion in epitaxial ultrathin Co2FeAl/MgO heterostructures with interface-induced perpendicular magnetic anisotropy

    NASA Astrophysics Data System (ADS)

    Wen, Zhenchao; Hadorn, Jason Paul; Okabayashi, Jun; Sukegawa, Hiroaki; Ohkubo, Tadakatsu; Inomata, Koichiro; Mitani, Seiji; Hono, Kazuhiro

    2017-01-01

    The interfacial atomic structure of epitaxial ultrathin Co2FeAl/MgO(001) heterostructures, which is related to the interface-induced perpendicular magnetic anisotropy (PMA), was investigated using scanning transmission electron microscopy, energy dispersive X-ray spectroscopy, and X-ray magnetic circular dichroism. Al atoms from the Co2FeAl layer significantly interdiffused into MgO, forming an Al-deficient Co-Fe-Al/Mg-Al-O structure near the Co2FeAl/MgO interface. This atomic replacement may have enhanced the PMA, which is consistent with the observed large perpendicular orbital magnetic moments of Fe atoms at the interface. This work suggests that control of interdiffusion at ferromagnet/barrier interfaces is critical for designing an interface-induced PMA system.

  11. Phase diagram of (Li(1-x)Fe(x))OHFeSe: a bridge between iron selenide and arsenide superconductors.

    PubMed

    Dong, Xiaoli; Zhou, Huaxue; Yang, Huaixin; Yuan, Jie; Jin, Kui; Zhou, Fang; Yuan, Dongna; Wei, Linlin; Li, Jianqi; Wang, Xinqiang; Zhang, Guangming; Zhao, Zhongxian

    2015-01-14

    Previous experimental results have shown important differences between iron selenide and arsenide superconductors which seem to suggest that the high-temperature superconductivity in these two subgroups of iron-based families may arise from different electronic ground states. Here we report the complete phase diagram of a newly synthesized superconducting (SC) system, (Li1-xFex)OHFeSe, with a structure similar to that of FeAs-based superconductors. In the non-SC samples, an antiferromagnetic (AFM) spin-density-wave (SDW) transition occurs at ∼127 K. This is the first example to demonstrate such an SDW phase in an FeSe-based superconductor system. Transmission electron microscopy shows that a well-known √5×√5 iron vacancy ordered state, resulting in an AFM order at ∼500 K in AyFe2-xSe2 (A = metal ions) superconductor systems, is absent in both non-SC and SC samples, but a unique superstructure with a modulation wave vector q = (1)/2(1,1,0), identical to that seen in the SC phase of KyFe2-xSe2, is dominant in the optimal SC sample (with an SC transition temperature Tc = 40 K). Hence, we conclude that the high-Tc superconductivity in (Li1-xFex)OHFeSe stems from the similarly weak AFM fluctuations as FeAs-based superconductors, suggesting a universal physical picture for both iron selenide and arsenide superconductors.

  12. Very low sound velocities in iron-rich (Mg,Fe)O : Implications for the core-mantle boundary region.

    SciTech Connect

    Wicks, J. K.; Jackson, J. M.; Sturhahn, W.; X-Ray Science Division; California Inst. of Tech.; Jet Propulsion Lab.

    2010-08-10

    The sound velocities of (Mg{sub .16}Fe{sub .84})O have been measured to 121 GPa at ambient temperature using nuclear resonant inelastic x-ray scattering. The effect of electronic environment of the iron sites on the sound velocities were tracked in situ using synchrotron Moessbauer spectroscopy. We found the sound velocities of (Mg{sub .16}Fe{sub .84})O to be much lower than those in other presumed mantle phases at similar conditions, most notably at very high pressures. Conservative estimates of the effect of temperature and dilution on aggregate sound velocities show that only a small amount of iron-rich (Mg,Fe)O can greatly reduce the average sound velocity of an assemblage. We propose that iron-rich (Mg,Fe)O be a source of ultra-low velocity zones. Other properties of this phase, such as enhanced density and dynamic stability, strongly support the presence of iron-rich (Mg,Fe)O in localized patches above the core-mantle boundary.

  13. Strong electronic correlations in iron pnictides: Comparison of the optical spectra for BaFe2As2-related compounds

    NASA Astrophysics Data System (ADS)

    Nakajima, Masamichi

    2014-03-01

    The role of electronic correlations in iron pnictides is one of the hottest issues in research of iron-based superconductors. Utilizing optical spectroscopy, we quantified the strength of electronic correlations in BaFe2As2-related compounds. For the parent compound BaFe2As2, the fraction of the coherent spectral weight in the low-energy optical conductivity spectrum is distinctly small. Such a spectral feature is also observed in KFe2As2, indicating that the charge dynamics is highly incoherent in iron arsenides. It is found that the strength of electronic correlations significantly changes by chemical substitution, either through changing the electron filling and/or the As-Fe-As bond angle. The present result indicates that superconductivity of the iron pnictides emerges when the materials possess adequate amount of electronic correlations, and that either too weak or too strong correlations are not favorable for high-Tc superconductivity. The degree of electronic correlations in iron arsenides turns out to be comparable to that in the hole-underdoped cuprate superconductors. In this sense, the iron arsenides are classified into strongly correlated systems, probably arising from the Hund's rule coupling. This work was done in collaboration with S. Ishida, K. Kihou, Y. Tomioka, C. H. Lee, A. Iyo, T. Ito, H. Eisaki (AIST), T. Tanaka, T. Kakeshita, S. Uchida (University of Tokyo), T. Saito, H. Fukazawa, and Y. Kohori (Chiba University).

  14. Cobalt and iron segregation and nitride formation from nitrogen plasma treatment of CoFeB surfaces

    NASA Astrophysics Data System (ADS)

    Mattson, E. C.; Michalak, D. J.; Veyan, J. F.; Chabal, Y. J.

    2017-02-01

    Cobalt-iron-boron (CoFeB) thin films are the industry standard for ferromagnetic layers in magnetic tunnel junction devices and are closely related to the relevant surfaces of CoFe-based catalysts. Identifying and understanding the composition of their surfaces under relevant processing conditions is therefore critical. Here we report fundamental studies on the interaction of nitrogen plasma with CoFeB surfaces using infrared spectroscopy, x-ray photoemission spectroscopy, and low energy ion scattering. We find that, upon exposure to nitrogen plasma, clean CoFeB surfaces spontaneously reorganize to form an overlayer comprised of Fe2N3 and BN, with the Co atoms moved well below the surface through a chemically driven process. Subsequent annealing to 400 °C removes nitrogen, resulting in a Fe-rich termination of the surface region.

  15. Acetones Removal with Fe Doped Titanium Nano Tube Catalysts Prepared from Slag Iron in Steel Plant.

    PubMed

    Lin, Yu-Jung; Wen-ZhiCao; Chang, Chang-Tang

    2016-01-01

    TiO₂ has been studied most commonly because it has high stability, non-toxicity, high catalytic activity, and highly conductivity. Many studies have shown that TiO₂ would generate electron-hole pairs illuminated with UV and surround more energy than that before being illuminated. However, the surface area of TiO₂ is not large enough and the adsorption capacity is small. In this study, the titanium nano tube (TNT) catalysts were prepared to increase the surface area and adsorption capacity. The Fe-TNT was also prepared from slag iron since many slag iron cause waste treatment problems. In this study, the effect of Fe loading, including 0.77%, 1.13%, 2.24% and 4.50%, on acetone removal was also assessed since TNT doped with transitional or precious metals can be used to improve catalytic reaction efficiency. Furthermore, four kinds of VOCs concentration, including 250, 500, 1000 and 1500 ppm were tested. Four kinds of retention time, including 0.4, 0.8, 4.0 and 6.0 sec, and four kinds of dosage, including 0.15, 0.25, 0.30 and 0.45 g cm⁻³, were also assessed. In this study, the adsorption capacity of Fe-TNT was 18.8, 23.3, 28.9 and 32.6 mg g⁻¹ for acetone of 250, 500, 1000 and 1500 ppm, respectively. Four kinds of temperature, including 150, 200, 250 and 300 °C were tested in catalytic reaction system. The results showed removal efficiency increased with increasing temperature. The efficiency can be reached 95% under the conditions with the dosage higher than 0.3 g cm⁻³, temperature higher than 270 °C and retention time higher than 270 °C. Reaction efficiency was 20, 31, 41 and 96% at the temperature of 150, 200, 250 and 300 °C, respectively.

  16. Relative coronal abundances derived from X-ray observations 3: The effect of cascades on the relative intensity of Fe (XVII) line fluxes, and a revised iron abundance

    NASA Technical Reports Server (NTRS)

    Walker, A. B. C., Jr.; Rugge, H. R.; Weiss, K.

    1974-01-01

    Permitted lines in the optically thin coronal X-ray spectrum were analyzed to find the distribution of coronal material, as a function of temperature, without special assumptions concerning coronal conditions. The resonance lines of N, O, Ne, Na, Mg, Al, Si, S, and Ar which dominate the quiet coronal spectrum below 25A were observed. Coronal models were constructed and the relative abundances of these elements were determined. The intensity in the lines of the 2p-3d transitions near 15A was used in conjunction with these coronal models, with the assumption of coronal excitation, to determine the Fe XVII abundance. The relative intensities of the 2p-3d Fe XVII lines observed in the corona agreed with theoretical prediction. Using a more complete theoretical model, and higher resolution observations, a revised calculation of iron abundance relative to hydrogen of 0.000026 was made.

  17. Arsenic localization, speciation, and co-occurrence with iron on rice (Oryza sativa L.) roots having variable Fe coatings.

    PubMed

    Seyfferth, Angelia L; Webb, Samuel M; Andrews, Joy C; Fendorf, Scott

    2010-11-01

    Arsenic contamination of rice is widespread, but the rhizosphere processes influencing arsenic attenuation remain unresolved. In particular, the formation of Fe plaque around rice roots is thought to be an important barrier to As uptake, but the relative importance of this mechanism is not well characterized. Here we elucidate the colocalization of As species and Fe on rice roots with variable Fe coatings; we used a combination of techniques--X-ray fluorescence imaging, μXANES, transmission X-ray microscopy, and tomography--for this purpose. Two dominant As species were observed in fine roots-inorganic As(V) and As(III) -with minor amounts of dimethylarsinic acid (DMA) and arsenic trisglutathione (AsGlu(3)). Our investigation shows that variable Fe plaque formation affects As entry into rice roots. In roots with Fe plaque, As and Fe were strongly colocated around the root; however, maximal As and Fe were dissociated and did not encapsulate roots that had minimal Fe plaque. Moreover, As was not exclusively associated with Fe plaque in the rice root system; Fe plaque does not coat many of the young roots or the younger portion of mature roots. Young, fine roots, important for solute uptake, have little to no iron plaque. Thus, Fe plaque does not directly intercept (and hence restrict) As supply to and uptake by rice roots but rather serves as a bulk scavenger of As predominantly near the root base.

  18. Disorder-Sensitive Superconductivity and Bonding Network in the Iron-Silicide Superconductor Lu2Fe3Si5

    NASA Astrophysics Data System (ADS)

    Watanabe, Tadataka; Okuyama, Hiroaki; Takase, Kouichi; Takano, Yoshiki; Yoshida, Fumiko; Moriyoshi, Chikako; Kuroiwa, Yoshihiro

    2010-03-01

    Iron silicide superconductor Lu2Fe3Si5 exhibits relatively high Tc = 6.0 K among Fe-based substances. Recent specific heat, penetration depth, and thermal conductivity measurements have provided evidences for the multigap superconductivity. We have studied non-magnetic and magnetic impurity effects on superconductivity in Lu2Fe3Si5 by investigating Tc variations in non-magnetic (Lu1-xScx)2Fe3Si5, (Lu1-xYx)2Fe3Si5 and magnetic (Lu1-xDyx)2Fe3Si5. Small amount of non-magnetic impurities (Sc and Y) on the Lu-site rapidly depresses Tc in accordance with the increase in the residual resistivity. Such a disorder-sensitive superconductivity strongly suggests the sign reversal of the superconducting order parameter. Lu2Fe3Si5 has a complicated crystal structure compared to other multigap superconductors such as MgB2 and iron pnictides. Thus it is important to map out the accurate bonding network in the crystal structure for the better understanding of the electronic structure. We have observed the charge density distribution of Lu2Fe3Si5 by analyzing the synchrotron radiation powder diffraction data using the maximum entropy method/Rietveld method.

  19. Formation Mechanisms of Alloying Element Nitrides in Recrystallized and Deformed Ferritic Fe-Cr-Al Alloy

    NASA Astrophysics Data System (ADS)

    Akhlaghi, Maryam; Meka, Sai Ramudu; Jägle, Eric A.; Kurz, Silke J. B.; Bischoff, Ewald; Mittemeijer, Eric J.

    2016-09-01

    The effect of the initial microstructure (recrystallized or cold-rolled) on the nitride precipitation process upon gaseous nitriding of ternary Fe-4.3 at. pct Cr-8.1 at. pct Al alloy was investigated at 723 K (450 °C) employing X-ray diffraction (XRD) analyses, transmission electron microscopy (TEM), atom probe tomography (APT), and electron probe microanalysis (EPMA). In recrystallized Fe-Cr-Al specimens, one type of nitride develops: ternary, cubic, NaCl-type mixed Cr1- x Al x N. In cold-rolled Fe-Cr-Al specimens, precipitation of two types of nitrides occurs: ternary, cubic, NaCl-type mixed Cr1- x Al x N and binary, cubic, NaCl-type AlN. By theoretical analysis, it was shown that for the recrystallized specimens an energy barrier for the nucleation of mixed Cr1- x Al x N exists, whereas in the cold-rolled specimens no such energy barriers for the development of mixed Cr1- x Al x N and of binary, cubic AlN occur. The additional development of the cubic AlN in the cold-rolled microstructure could be ascribed to the preferred heterogeneous nucleation of cubic AlN on dislocations. The nitrogen concentration-depth profile of the cold-rolled specimen shows a stepped nature upon prolonged nitriding as a consequence of instantaneous nucleation of nitride upon arrival of nitrogen and nitride growth rate-limited by nitrogen transport through the thickening nitrided zone.

  20. Observation of Precipitation Evolution in Fe-Ni-Mn-Ti-Al Maraging Steel by Atom Probe Tomography

    NASA Astrophysics Data System (ADS)

    Pereloma, E. V.; Stohr, R. A.; Miller, M. K.; Ringer, S. P.

    2009-12-01

    We describe the full decomposition sequence in an Fe-Ni-Mn-Ti-Al maraging steel during isothermal annealing at 550 °C. Following significant pre-precipitation clustering reactions within the supersaturated martensitic solid solution, (Ni,Fe)3Ti and (Ni,Fe)3(Al,Mn) precipitates eventually form after isothermal aging for ~60 seconds. The morphology of the (Ni,Fe)3Ti particles changes gradually during aging from predominantly plate-like to rod-like, and, importantly, Mn and Al were observed to segregate to these precipitate/matrix interfaces. The (Ni,Fe)3(Al,Mn) precipitates occurred at two main locations: uniformly within the matrix and at the periphery of the (Ni,Fe)3Ti particles. We relate this latter mode of precipitation to the Mn-Al segregation.

  1. Observation of Precipitation Evolution in Fe-Ni-Mn-Ti-Al Maraging Steel using Atom Probe Tomography

    SciTech Connect

    Pereloma, E. V.; Stohr, R A; Miller, Michael K; Ringer, S. P.

    2009-01-01

    We describe the full decomposition sequence in an Fe-Ni-Mn-Ti-Al maraging steel during isothermal annealing at 550 C. Following significant pre-precipitation clustering reactions within the supersaturated martensitic solid solution, (Ni,Fe){sub 3}Ti and (Ni,Fe){sub 3}(Al,Mn) precipitates eventually form after isothermal aging for {approx}60 seconds. The morphology of the (Ni,Fe){sub 3}Ti particles changes gradually during aging from predominantly plate-like to rod-like, and, importantly, Mn and Al were observed to segregate to these precipitate/matrix interfaces. The (Ni,Fe){sub 3}(Al,Mn) precipitates occurred at two main locations: uniformly within the matrix and at the periphery of the (Ni,Fe){sub 3}Ti particles. We relate this latter mode of precipitation to the Mn-Al segregation.

  2. Stability of arsenate-bearing Fe(III)/Al(III) co-precipitates in the presence of sulfide as reducing agent under anoxic conditions.

    PubMed

    Doerfelt, Christoph; Feldmann, Thomas; Roy, Ranjan; Demopoulos, George P

    2016-05-01

    Currently, the co-precipitation of arsenate with ferric iron at molar ratios Fe(III)/As(V) ≥ 3 by lime neutralization produces tailings solids that are stable under oxic conditions. However not much is known about the stability of these hazardous co-precipitates under anoxic conditions. These can develop in tailings storage sites by the action of co-discharged reactive sulfides, organic reagent residuals or bacterial activity. The ferric matrix can then undergo reductive dissolution reactions, which could release arsenic into the pore water. Co-ions like aluminum could provide a redox-immune sink to scavenge any mobilized arsenic as a result of reduction of ferric. As such, in this work Fe(III)/As(V) = 4 and aluminum substituted Fe(III)/Al(III)/As(V) = 2/2/1 co-precipitates were produced in a mini continuous co-precipitation process circuit and subjected to excess sulfide addition under inert gas to evaluate their stability. It was found that the ferric-arsenate co-precipitate could retain up to 99% (30 mg/L in solution) of its arsenic content despite the high pH (10.5) and extremely reducing (Eh < -200 mV) environment. There was no significant reduction of arsenate and only 45% of ferric iron was reduced. Partial aluminum substitution was found to cut the amount of mobilized arsenic by 50% (down to 15 mg/L) hence mixed Fe(III)/Al(III)-arsenate co-precipitates may offer better resistance to reductive destabilization over the long term than all iron co-precipitates.

  3. The cyclic oxidation resistance at 1200 C of beta-NiAl, FeAl, and CoAl alloys with selected third element additions

    NASA Technical Reports Server (NTRS)

    Barrett, C. A.; Titran, R. H.

    1992-01-01

    The intermetallic compounds Beta-NiAl, FeAl, and CoAl were tested in cyclic oxidation with selected third element alloy additions. Tests in static air for 200 1-hr cycles at 1200 C indicated by specific weight change/time data and x-ray diffraction analysis that the 5 at percent alloy additions did not significantly improve the oxidation resistance over the alumina forming baseline alloys without the additions. Many of the alloy additions were actually deleterious. Ta and Nb were the only alloy additions that actually altered the nature of the oxide(s) formed and still maintained the oxidation resistance of the protective alumina scale.

  4. Al-Fe interactions and growth enhancement in Melastoma malabathricum and Miscanthus sinensis dominating acid sulphate soils.

    PubMed

    Watanabe, Toshihiro; Jansen, Steven; Osaki, Mitsuru

    2006-12-01

    Plants growing in acid sulphate soils are subject to high levels of Al availability, which may have effects on the growth and distribution of these species. Although Fe availability is also high in acid sulphate soils, little is known about the effect of Fe on the growth of native plants in these soils. Two species dominating this soil type in Asia, viz. Melastoma malabathricum and Miscanthus sinensis were grown hydroponically in a nutrient solution with different concentrations of Al and Fe. Melastoma malabathricum is found to be sensitive to Fe (40 and 100 microm). Application of 500 microm Al, however, completely ameliorates Fe toxicity and is associated with a decrease of Fe concentration in shoots and roots. The primary reason for the Al-induced growth enhancement of M. malabathricum is considered to be the Al-induced reduction of toxic Fe accumulation in roots and shoots. Therefore, Al is nearly essential for M. malabathricum when growing in acid sulphate soils. In contrast, application of both Fe and Al does not reduce the growth of M. sinensis, and Al application does not result in lower shoot concentrations of Fe, suggesting that this grass species has developed different mechanisms for adaptation to acid sulphate soils.

  5. Structural and Magnetic Properties of Fe and Au Ion-Implanted Al2O3 Single Crystals

    NASA Astrophysics Data System (ADS)

    Kinoshita, Ryosuke; Sakamoto, Isao; Hayashi, Nobuyuki; Nomura, Kiyoshi; Honda, Shigeo; Ishida, Tomoya; Iio, Satoshi; Tashiro, Hiroyuki; Toriyama, Tamotsu

    2011-01-01

    Au ion implantation in Fe ion-implanted Al2O3 (Fe/Al2O3) has been performed in order to tailor the structural, magnetic and optical properties of Fe granules in Al2O3 matrix. After Au ion implantation, Rutherford backscattering (RBS) measurements indicate the decrease and the redistribution of retained Fe atoms with the inclusion of Au atoms, and the patterns of X-ray diffraction (XRD) show the formation of Au granules in the Fe/Al2O3. Besides, the magnetization curves of the Fe/Al2O3 after Au ion implantation show still the superparamagnetic characteristics and the decrease of saturation magnetization, and the optical absorption measurements indicate the formation of Au granules in the Fe/Al2O3 in accordance with the XRD result. In addition, we investigated a behavior of Fe granules in Al2O3 matrix by conversion electron Mössbauer spectroscopy (CEMS), which indicates the decrease of superparamagnetic state as a function of Au ion dose. As a result, it is suggested that Au ion implantation has potentialities to tailor the physical properties of Fe granules in Al2O3 matrix.

  6. Long-term high-velocity oxidation and hot corrosion testing of several NiCrAl and FeCrAl base oxide dispersion strengthened alloys

    NASA Technical Reports Server (NTRS)

    Lowell, C. E.; Deadmore, D. L.; Whittenberger, J. D.

    1982-01-01

    Several oxide dispersion strengthened (ODS) alloys have been tested for cyclic, long-term, high gas-velocity resistance to oxidation at 1100 C and hot corrosion at 900 C. Both nominally Ni-16Cr-4Al and Fe-20Cr-4.5Al ODS alloys were subjected up to about 2500 cycles, where each cycle consisted of 1 hr in a hot, Mach 0.3 combusted gas stream followed by a 3-min quench in an ambient temperature, Mach 0.3 air blast. For comparison to existing technology, a coated superalloy was simultaneously tested. The ODS iron alloy exhibited clearly superior behavior, surviving 3800 oxidation and 2300 hot corrosion cycles essentially unscathed. While the ODS nickel alloys exhibited adequate oxidation resistance, the long-term hot corrosion resistance could be marginal, since the best life for such alloys under these conditions was only about 1100 cycles. However, the hot corrosion resistance of the ODS Ni-base alloys is excellent in comparison to that of traditional superalloys.

  7. Microstructures and superplastic behavior of eutectic Fe-C and Ni-Cr white cast irons produced by rapid solidification

    NASA Astrophysics Data System (ADS)

    Kum, D. W.; Frommeyer, G.; Grant, N. J.; Sherby, O. D.

    1987-10-01

    Superplastic behavior of two commercial grade white cast irons, eutectic Fe-C and Ni-Cr white cast irons, was investigated at intermediate temperatures (650 to 750 °C). For this purpose, rapidly solidified powders of the cast irons were fully consolidated by compaction and rolling at about 650 °C. The volume fractions of cementite in the eutectic cast iron and in the Ni-Cr cast iron were 64 pct and 51 pct, respectively, and both cast irons consisted of fine equiaxed grains of cementite (1 to 2 μm) and ferrite (0.5 to 2 μm). The cast iron compacts exhibited high strain-rate sensitivity (strain-rate-sensitivity exponent of 0.35 to 0.46) and high tensile ductility (total elongation of 150 pct to 210 pct) at strain rates of 10-4 to 10-3 s-1 and at 650 °C to 750 °C. Microstructure evaluations were made by TEM, SEM, and optical microscopy methods. The equiaxed grains in the as-compacted samples remained unchanged even after large tensile deformation. It is concluded that grain boundary sliding ( e.g., along cementite grain boundaries in the case of the eutectic cast iron) is the principal mode of plastic deformation in both cast irons during superplastic testing conditions.

  8. Formation and Yield of Multi-Walled Carbon Nanotubes Synthesized via Chemical Vapour Deposition Routes Using Different Metal-Based Catalysts of FeCoNiAl, CoNiAl and FeNiAl-LDH

    PubMed Central

    Hussein, Mohd Zobir; Mohamad Jaafar, Adila; Hj. Yahaya, Asmah; Masarudin, Mas Jaffri; Zainal, Zulkarnain

    2014-01-01

    Multi-walled carbon nanotubes (MWCNTs) were prepared via chemical vapor deposition (CVD) using a series of different catalysts, derived from FeCoNiAl, CoNiAl and FeNiAl layered double hydroxides (LDHs). Catalyst-active particles were obtained by calcination of LDHs at 800 °C for 5 h. Nitrogen and hexane were used as the carrier gas and carbon source respectively, for preparation of MWCNTs using CVD methods at 800 °C. MWCNTs were allowed to grow for 30 min on the catalyst spread on an alumina boat in a quartz tube. The materials were subsequently characterized through X-ray diffraction, Fourier transform infrared spectroscopy, surface area analysis, field emission scanning electron microscopy and transmission electron microscopy. It was determined that size and yield of MWCNTs varied depending on the type of LDH catalyst precursor that is used during synthesis. MWCNTs obtained using CoNiAl-LDH as the catalyst precursor showed smaller diameter and higher yield compared to FeCoNiAl and FeNiAl LDHs. PMID:25380526

  9. A Versatile Iron-Tannin-Framework Ink Coating Strategy to Fabricate Biomass-Derived Iron Carbide/Fe-N-Carbon Catalysts for Efficient Oxygen Reduction.

    PubMed

    Wei, Jing; Liang, Yan; Hu, Yaoxin; Kong, Biao; Simon, George P; Zhang, Jin; Jiang, San Ping; Wang, Huanting

    2016-01-22

    The conversion of biomass into valuable carbon composites as efficient non-precious metal oxygen-reduction electrocatalysts is attractive for the development of commercially viable polymer electrolyte membrane fuel-cell technology. Herein, a versatile iron-tannin-framework ink coating strategy is developed to fabricate cellulose-derived Fe3 C/Fe-N-C catalysts using commercial filter paper, tissue, or cotton as a carbon source, an iron-tannin framework as an iron source, and dicyandiamide as a nitrogen source. The oxygen reduction performance of the resultant Fe3C/Fe-N-C catalysts shows a high onset potential (i.e. 0.98 V vs the reversible hydrogen electrode (RHE)), and large kinetic current density normalized to both geometric electrode area and mass of catalysts (6.4 mA cm(-2) and 32 mA mg(-1) at 0.80 V vs RHE) in alkaline condition. This method can even be used to prepare efficient catalysts using waste carbon sources, such as used polyurethane foam.

  10. Hafnium influence on the microstructure of FeCrAl alloys

    NASA Astrophysics Data System (ADS)

    Geanta, V.; Voiculescu, I.; Stanciu, E.-M.

    2016-06-01

    Due to their special properties at high temperatures, FeCrAl alloys micro-alloyed with Zr can be regarded as potential materials for use at nuclear power plants, generation 4R. These materials are resistant to oxidation at high temperatures, to corrosion, erosion and to the penetrating radiations in liquid metal environments. Also, these are able to form continuously, by the self-generation process of an oxide coating with high adhesive strength. The protective oxide layers must be textured and regenerable, with a good mechanical strength, so that crack and peeling can not appear. To improve the mechanical and chemical characteristics of the oxide layer, we introduced limited quantities of Zr, Ti, Y, Hf, Ce in the range of 1-3%wt in the FeCrAl alloy. These elements, with very high affinity to the oxygen, are capable to stabilize the alumina structure and to improve the oxide adherence to the metallic substrate. FeCrAl alloys microalloyed with Hf were prepared using VAR (Vacuum Arc Remelting) unit, under high argon purity atmosphere. Three different experimental alloys have been prepared using the same metallic matrix of Fe-14Cr-5Al, by adding of 0.5%wt Hf, 1.0%wt Hf and respectively 1.5%wt Hf. The microhardness values for the experimental alloys have been in the range 154 ... 157 HV0.2. EDAX analyses have been performed to determine chemical composition on the oxide layer and in the bulk of sample and SEM analyze has been done to determine the microstructural features. The results have shown the capacity of FeCrAl alloy to form oxide layers, with different texture and rich in elements such as Al and Hf.

  11. Di/mono-nuclear iron(I)/(II) complexes as functional models for the 2Fe2S subunit and distal Fe moiety of the active site of [FeFe] hydrogenases: protonations, molecular structures and electrochemical properties.

    PubMed

    Gao, Shang; Fan, Jiangli; Sun, Shiguo; Song, Fengling; Peng, Xiaojun; Duan, Qian; Jiang, Dayong; Liang, Qingcheng

    2012-10-21

    Di/mono-nuclear iron(I)/(II) complexes containing conjugated and electron-withdrawing S-to-S linkers, [{(μ-S)(2)(C(4)N(2)H(2))}Fe(2)(CO)(6)] (1), [{(μ-S)(2)(C(4)N(2)H(2))}Fe(2)(CO)(5)(PMe(3))] (1P), and [{(μ-S)(2)(C(4)N(2)H(2))}Fe(CO)(2)(PMe(3))(2)] (2) were prepared as biomimetic models for the 2Fe2S subunit and distal Fe moiety of the active site of [FeFe] hydrogenases. The N atoms in the heterocyclic pyrazines of 1 and 2 were protonated in the presence of proton acid to generate one and two hydrides, [1(NH)](+) CF(3)SO(3)(-), [2(NH)](+) CF(3)SO(3)(-), and [2(NH)(2)](2+) (CF(3)SO(3)(-))(2), respectively. The protonation processes were evidenced by in situ IR and NMR spectroscopy. The molecular structures of the protonated species [1(NH)](+) CF(3)SO(3)(-) and [2(NH)(2)](2+) (CF(3)SO(3)(-))(2) together with their originating complexes and , and the mono-PMe(3) substituted diiron complex were identified by X-ray crystallography. The IR and single-crystal analysis data all suggested that the electron-withdrawing bridge, pyrazine, led to decreased electron density at the Fe centers of the model complexes, which was consistent with the electrochemical studies. The cyclic voltammograms indicated that complex exhibited a low primary reduction potential at -1.17 V vs. Fc-Fc(+) with a 270 mV positive shift compared with that of the benzene-1,2-dithiolate (bdt) bridged analogue [(μ-bdt)Fe(2)(CO)(6)]. Under the weak acid conditions, complexes 1 and 2 could electrochemically catalyze the proton reduction. More interestingly, the mononuclear ferrous complex 2 showed two catalytic peaks during the formation of hydrogen, confirming its potential as a catalyst for hydrogen production.

  12. Iron porphyrinate Fe(TPPS) reduces brain cell damage in rats intrastriatally lesioned by quinolinate.

    PubMed

    González-Cortés, Carolina; Salinas-Lara, Citlaltepetl; Gómez-López, Marcos Artemio; Tena-Suck, Martha Lilia; Pérez-De La Cruz, Verónica; Rembao-Bojórquez, Daniel; Pedraza-Chaverrí, José; Gómez-Ruiz, Celedonio; Galván-Arzate, Sonia; Ali, Syed F; Santamaría, Abel

    2008-01-01

    It has been recently demonstrated that the reactive nitrogen species (RNS) peroxynitrite (ONOO(-)) is involved in the neurotoxic pattern produced by quinolinic acid in the rat brain [V. Pérez-De La Cruz, C. González-Cortés, S. Galván-Arzate, O.N. Medina-Campos, F. Pérez-Severiano, S.F. Ali, J. Pedraza-Chaverrí, A. Santamaría, Excitotoxic brain damage involves early peroxynitrite formation in a model of Huntington's disease in rats: protective role of iron porphyrinate 5,10,15,20-tetrakis (4-sulfonatophenyl)porphyrinate iron (III), Neuroscience 135 (2005) 463-474.]. The aim of this work was to investigate whether ONOO(-) can also be responsible for morphological alterations and inflammatory events in the same paradigm. For this purpose, we evaluated the effect of a pre-treatment with the iron porphyrinate Fe(TPPS), a well-known ONOO(-) decomposition catalyst (10 mg/kg, i.p., 120 min before lesion), on the quinolinate-induced striatal cell damage and immunoreactivities to glial-fibrilar acidic protein (GFAP), interleukin 6 (IL-6) and inducible nitric oxide synthase (iNOS), one and seven days after the intrastriatal infusion of quinolinate (240 nmol/microl) to rats. The striatal tissue from animals lesioned by quinolinate showed a significant degree of damage and enhanced immunoreactivities to GFAP, IL-6 and iNOS, both at 1 and 7 days post-lesion. Pre-treatment of rats with Fe(TPPS) significantly attenuated or prevented all these markers at both post-lesion times tested, except for GFAP immunoreactivity at 7 days post-lesion and iNOS immunoreactivity at 1 day post-lesion. Altogether, our results suggest that ONOO(-) is actively participating in triggering inflammatory events and morphological alterations in the toxic model produced by quinolinate, since the use of agents affecting its formation, such as Fe(TPPS), are effective experimental tools to reduce the brain lesions associated to excitotoxic and oxidative damage.

  13. Assessment of Post-eutectic Reactions in Multicomponent Al-Si Foundry Alloys Containing Cu, Mg, and Fe

    NASA Astrophysics Data System (ADS)

    Javidani, Mousa; Larouche, Daniel; Grant Chen, X.

    2015-07-01

    Post-eutectic reactions occurring in Al-Si hypoeutectic alloys containing different proportions of Cu, Mg, and Fe were thoroughly investigated in the current study. As-cast microstructures were initially studied by optical and electron microscopy to investigate the microconstituents of each alloy. Differential scanning calorimetry (DSC) was then used to examine the phase transformations occurring during the heating and cooling processes. Thermodynamic calculations were carried out to assess the phase formation under equilibrium and in nonequilibrium conditions. The Q-Al5Cu2Mg8Si6 phase was predicted to precipitate from the liquid phase, either at the same temperature or earlier than the θ-Al2Cu phase depending on the Cu content of the alloy. The AlCuFe-intermetallic, which was hardly observed in the as-cast microstructure, significantly increased after the solution heat treatment in the alloys containing high Cu and Fe contents following a solid-state transformation of the β-Al5FeSi phase. After the solution heat treatment, the AlCuFe-intermetallics were mostly identified with the stoichiometry of the Al7Cu2Fe phase. Thermodynamic calculations and microstructure analysis helped in determining the DSC peak corresponding to the melting temperature of the N-Al7Cu2Fe phase. The effect of Cu content on the formation temperature of π-Al8Mg3FeSi6 is also discussed.

  14. Observation of clusters in Re60Fe30Al10 alloys and the associated magnetic properties

    NASA Astrophysics Data System (ADS)

    Z, Kong H.; J, Ding; L, Dong Z.; L, Wang; T, White; Y, Li

    2002-03-01

    Magnetic properties and microstructure of melt-spun ribbons of RE60Fe30Al10 alloys with RE{} = {}Nd, Sm, Dy, Gd and Y were studied in detail. High coercivity values in the range of MA m-1 were observed at low temperatures for amorphous ribbons. Presence of Fe-rich clusters and nanoscale rare-earth crystallites in the amorphous matrix in the ribbons were revealed by high-resolution transmission electron microscopy studies. The magnetic transition temperatures were estimated experimentally and compared with fitting results based on the cluster ferromagnetism model (Wang L et al 2001 Phys. Rev. B 64 214410). Possible mechanisms for the magnetic behaviour observed due to the presence of Fe-rich magnetic clusters are discussed.

  15. Synthesis of Waste Form in the Gd-Fe-Al-Ni-Mn-Cr-O System

    SciTech Connect

    Chae, S.C.; Jang, Y.N.; Bae, I.K.; Ryu, K.W.

    2006-07-01

    Poly-phase waste form which was the mixture of Gd{sub 3}Fe{sub 2}Al{sub 3}O{sub 12} and (Ni{sub x}Mn{sub 1-x})(Fe{sub y}Cr{sub 1-y}){sub 2}O{sub 4} was synthesized. Also, we are intended to examine phase relation and physicochemical properties of coexisted phases in the compositions and to confirm accommodation relation of elements and phases. Two types of phase series were observed: Garnet-perovskite-spinel and Garnet-spinel. The compositions of garnets and spinels were nonstoichiometric, and especially, this poly-phase ceramics may be in a good waste form. The excessive Gd in garnets indicated the immobilization of higher content of actinides. The nonstoichiometric compositions of garnet and spinel were attributed to the formation of perovskite in that perovskite contained Gd, Fe and Al from garnet and Cr from spinel. (authors)

  16. Weldability of high toughness Fe-12% Ni alloys containing Ti, Al or Nb

    NASA Technical Reports Server (NTRS)

    Devletian, J. H.; Stephens, J. R.; Witzke, W. R.

    1977-01-01

    Three exceptionally high-toughness Fe-12%Ni alloys designed for cryogenic service were welded using the GTA welding process. Evaluation of weldability included equivalent energy (KIed) fracture toughness tests, transverse-weld tensile tests at -196 and 25 C and weld crack sensitivity tests. The Fe-12%Ni-0.25%Ti alloy proved extremely weldable for cryogenic applications, having weld and HAZ properties comparable with those of the wrought base alloy. The Fe-12%Ni-0.5%Al had good weld properties only after the weld joint was heat treated. The Fe-12%Ni-0.25%Nb alloy was not considered weldable for cryogenic use because of its poor weld joint properties at -196 C and its susceptibility to hot cracking.

  17. Elevated Temperature Properties of a Dispersion Strengthened Al(Fe, V, Si) Alloy

    DTIC Science & Technology

    1991-12-01

    ASTM STP 890, M. E. Fine and E. A. Starke, Jr., Eds., American Society for Testing and Materials, pp. 211-236, 1986. 3. Raybould , D., "Forming of...and Materials Society, pp 181-197, 1988. 6. Skinner, D. J., Rye, D., Raybould , D., and Brown, A. M., "Dispersion Strengthened Al-Fe-V-Si Alloys

  18. A Study of Phase Composition and Structure of Alloys of the Al - Mg - Si - Fe System

    NASA Astrophysics Data System (ADS)

    Mailybaeva, A. D.; Zolotorevskii, V. S.; Smagulov, D. U.; Islamkulov, K. M.

    2017-03-01

    The Thermo-Calc software is used to compute the phase transformations occurring during cooling of alloys. Polythermal and isothermal sections of the phase diagram of the Al - Mg - Si - Fe system are plotted. The phase composition and the structure of aluminum alloys in cast condition and after a heat treatment are studied experimentally.

  19. Dislocations in nanostructured two-phase Fe30Ni20Mn20Al30.

    PubMed

    Wu, X; Baker, I

    2013-03-01

    In a previous study, the dislocations in Fe(30)Ni(20)Mn(25)Al(25) (at. %), which consist of 50 nm wide alternating b.c.c. and B2 phases, were shown to have a/2<111> Burgers vectors after room temperature deformation. The dislocations were found to glide in pairs on both {110} and {112} slip planes and were relatively widely separated in the b.c.c. phase, where the dislocations were uncoupled, and closely spaced in the B2 phase, where the dislocations were connected by an anti-phase boundary. In this article, we analyze the dislocations in the two ~5 nm-wide B2 phases in a related two-phase alloy Fe(30)Ni(20)Mn(20)Al(30), with compositions Fe-23Ni-21Mn-24Al and Fe-39Ni-12Mn-34Al, compressed to ~3% strain at a strain rate 5 × 10(-4) s(-1) at 873 K (the lowest temperature at which substantial plastic flow was observed). It is shown that slip occursby the glide of a<100> dislocations. A review of the literature suggests that the differences in the observed slip vector between these B2 phases could be due to the differences in composition, differences in deformation temperature, or possibly both.

  20. Database on Performance of Neutron Irradiated FeCrAl Alloys

    SciTech Connect

    Field, Kevin G.; Briggs, Samuel A.; Littrell, Ken; Parish, Chad M.; Yamamoto, Yukinori

    2016-08-01

    The present report summarizes and discusses the database on radiation tolerance for Generation I, Generation II, and commercial FeCrAl alloys. This database has been built upon mechanical testing and microstructural characterization on selected alloys irradiated within the High Flux Isotope Reactor (HFIR) at Oak Ridge National Laboratory (ORNL) up to doses of 13.8 dpa at temperatures ranging from 200°C to 550°C. The structure and performance of these irradiated alloys were characterized using advanced microstructural characterization techniques and mechanical testing. The primary objective of developing this database is to enhance the rapid development of a mechanistic understanding on the radiation tolerance of FeCrAl alloys, thereby enabling informed decisions on the optimization of composition and microstructure of FeCrAl alloys for application as an accident tolerant fuel (ATF) cladding. This report is structured to provide a brief summary of critical results related to the database on radiation tolerance of FeCrAl alloys.

  1. Understanding phase stability of Al-Co-Cr-Fe-Ni high entropy alloys

    DOE PAGES

    Zhang, Chuan; Zhang, Fan; Diao, Haoyan; ...

    2016-07-19

    The concept of high entropy alloy (HEA) opens a vast unexplored composition range for alloy design. As a well-studied system, Al-Co-Cr-Fe-Ni has attracted tremendous amount of attention to develop new-generation low-density structural materials for automobile and aerospace applications. In spite of intensive investigations in the past few years, the phase stability within this HEA system is still poorly understood and needs to be clarified, which poses obstacles to the discovery of promising Al-Co-Cr-Fe-Ni HEAs. In the present work, the CALPHAD approach is employed to understand the phase stability and explore the phase transformation within the Al-Co-Cr-Fe-Ni system. As a result,more » the phase-stability mapping coupled with density contours is then constructed within the composition - temperature space, which provides useful guidelines for the design of low-density Al-Co-Cr-Fe-Ni HEAs with desirable properties.« less

  2. Detection of Fe[superscript 3+] and Al[superscript 3+] by Test Paper

    ERIC Educational Resources Information Center

    Li, Lili; Xiang, Haifeng; Zhou, Xiangge; Li, Menglong; Wu, Di

    2012-01-01

    A porphyrin-based test paper has been designed and prepared. It can be used to analyze for Al[superscript 3+] and Fe[superscript 3+] in aqueous solution. An experiment employing the test paper can help students understand basic principles of spectrophotometry and how spectrophotometry is used in analyzing for metal ions. (Contains 1 scheme and 1…

  3. Ion irradiation testing and characterization of FeCrAl candidate alloys

    SciTech Connect

    Anderoglu, Osman; Aydogan, Eda; Maloy, Stuart Andrew; Wang, Yongqiang

    2014-10-29

    The Fuel Cycle Research and Development program’s Advanced Fuels Campaign has initiated a multifold effort aimed at facilitating development of accident tolerant fuels. This effort involves development of fuel cladding materials that will be resistant to oxidizing environments for extended period of time such as loss of coolant accident. Ferritic FeCrAl alloys are among the promising candidates due to formation of a stable Al₂O₃ oxide scale. In addition to being oxidation resistant, these promising alloys need to be radiation tolerant under LWR conditions (maximum dose of 10-15 dpa at 250 – 350°C). Thus, in addition to a number of commercially available alloys, nuclear grade FeCrAl alloys developed at ORNL were tested using high energy proton irradiations and subsequent characterization of irradiation hardening and damage microstructure. This report summarizes ion irradiation testing and characterization of three nuclear grade FeCrAl cladding materials developed at ORNL and four commercially available Kanthal series FeCrAl alloys in FY14 toward satisfying FCRD campaign goals.

  4. Experimentally observed iron redox kinetics in silicic liquids: Implications for Fe/sup 3 +//Fe/sup 2 +/ variations in rhyolite lava

    SciTech Connect

    Naney, M.T.; Swanson, S.E.

    1989-01-01

    Iron redox kinetics in silicate liquids were investigated by melting 100 mg pellets of compacted rhyolite, pantellerite, pantelleritic trachyte, and andesite rock powders at 1243 and 1343/degree/C in a moderately reducing furnace atmosphere (log fO/sub 2/ = /minus/7.83) for periods of 1 to 4320 minutes. The redox state of glasses produced by quenching these liquids was determined by colorimetric analysis of the ferrous iron and total iron content. Redox equilibrium, indicated by the attainment of a constant FeO/FeO/sub tot/ ratio, was observed for all temperature-composition conditions studied, except for 1243/degree/C experiments with USGS rhyolite standard RGM-1. This is consistent with the low diffusivity of reacting components in high viscosity rhyolite liquids. In the 1243/degree/C experiments with RGM-1, no change in the FeO/FeO/sub tot/ ratio was observed after 4320 minutes. This implies that redox equilibrium is not maintained in natural rhyolite lavas which erupt as significantly lower temperatures (720--850/degree/C). We conclude that sluggish redox kinetics precludes major changes in the oxidation state of a rhyolite magma during the eruption process. If this is true, then the quenched magma, represented by glassy rhyolites, preserves the pre-eruption redox signature of the magma. 2 refs.

  5. Importance of doping and frustration in itinerant Fe-doped Cr2Al

    SciTech Connect

    Susner, M. A.; Parker, D. S.; Sefat, A. S.

    2015-05-12

    We performed an experimental and theoretical study comparing the effects of Fe-doping of Cr2Al, an antiferromagnet with a N el temperature of 670 K, with known results on Fe-doping of antiferromagnetic bcc Cr. (Cr1-xFex)2Al materials are found to exhibit a rapid suppression of antiferromagnetic order with the presence of Fe, decreasing TN to 170 K for x=0.10. Antiferromagnetic behavior disappears entirely at x≈0.125 after which point increasing paramagnetic behavior is exhibited. Moreover, this is unlike the effects of Fe doping of bcc antiferromagnetic Cr, in which TN gradually decreases followed by the appearance of a ferromagnetic state. Theoretical calculations explain that the Cr2Al-Fe suppression of magnetic order originates from two effects: the first is band narrowing caused by doping of additional electrons from Fe substitution that weakens itinerant magnetism; the second is magnetic frustration of the Cr itinerant moments in Fe-substituted Cr2Al. In pure-phase Cr2Al, the Cr moments have an antiparallel alignment; however, these are destroyed through Fe substitution and the preference of Fe for parallel alignment with Cr. This is unlike bulk Fe-doped Cr alloys in which the Fe anti-aligns with the Cr atoms, and speaks to the importance of the Al atoms in the magnetic structure of Cr2Al and Fe-doped Cr2Al.

  6. Solid / Liquid Partitioning of Iron in (Mg0.9Fe0.1)2SiO4 Bulk Composition under Lower Mantle Conditions

    NASA Astrophysics Data System (ADS)

    Nomura, R.; Hirose, K.; Tateno, S.

    2009-12-01

    Melting causes strong chemical differentiation in the Earth’s interior. It is generally believed that ultra-low velocity zone (ULVZ) observed in the lowermost mantle represents the partially molten zone, but the nature of partial melting is not known yet. Is the partial melt enriched in iron? Is it denser than coexisting solid? Here we investigate the partitioning of iron between partial melt and solid residue in (Mg0.9Fe0.1)2SiO4 bulk composition up to 61 GPa using laser-heated diamond-anvil cell (LHDAC). We used the olivine from KLB-1 peridotite as starting material and loaded its powder between the argon pressure medium. The sample was heated from double side using the Nd:YLF laser. Melting was confirmed by a sudden increase in the absorption of the laser light by the sample. A recovered sample was processed to a thin film by Ar ion using the Ion Slicer, and subsequently examined under field emission-type microprobe (FE-EPMA). The X-ray mapping of the sample showed the extensive segregation of each phase under the temperature gradient. The center of the laser-heated hot spot had non-stoichiometric composition, indicating a quenched liquid. Liquidus phase was found to be ferropericlase (Fp) up to ~26 GPa and changed into Mg-silicate perovskite (MgPv) at about 31GPa, consistent with the results obtained by previous melting experiments in multi-anvil apparatus (Ohtani et al., 1998 PEPI; Ito et al., 2004 PEPI). MgPv remains the liquidus phase up to 61 GPa, the highest pressure condition examined so far in this study. We determined the iron partitioning between MgPv and melt (D= FeO (in crystal, wt.%) / FeO (in liquid, wt.%)) from the results of chemical analyses. The partition coefficient D increased weakly with increasing pressure from 31 to 61 GPa, though partial melt remains more iron-rich than perovskite up to 61GPa. The results up to the lowermost mantle condition will be discussed in the presentation.

  7. Elevated Fe(II) and dissolved Fe in hypoxic shelf waters off Oregon and Washington: an enhanced source of iron to coastal upwelling regimes.

    PubMed

    Lohan, Maeve C; Bruland, Kenneth W

    2008-09-01

    There has been a growing interest in the cause and impact of hypoxic regions known as "dead zones" that have increasingly appeared along the west coast of the United States and have caused widespread destruction to the crab and fishing industry in this upwelling region. Here, we present results that demonstrate that the hypoxic conditions in the water column over the continental shelf result in a marked increase in iron(II) concentrations, which contribute to elevated dissolved and labile particulate iron concentrations. These elevated dissolved iron(II) concentrations result from two factors: (1) the hypoxic water column allows extremely elevated iron(II) concentrations in reducing porewaters to exist close to the sediment water interface, leading to an increased flux of iron(II) from the sediments; (2) the low oxygen, low pH, and low temperatures within the bottom boundary layer act in concert to markedly slow down the oxidation rate of Fe(ll). During upwelling conditions, this process can result in a greatly enhanced source of Fe available to upwell to surface waters, potentially increasing phytoplankton productivity, which can, in turn, lead to enhanced export flux, driving the system further into hypoxic or suboxic conditions.

  8. Transformation of the pesticide 1,2-dibromo-3-chloropropane (DBCP) and nitrate by iron powder and by H{sub 2}/Pd/Al{sub 2}O{sub 3}

    SciTech Connect

    Siantar, D.P.; Schreier, C.G.; Reinhard, M.

    1995-12-01

    In this study, zero-valent iron powder (Fe{sup o}) was shown to reductively dehalogenate DBCP completely under sterile (abiotic) buffered and unbuffered conditions. DBCP transformation was evidenced by the appearance of bromide and chloride ions. The effect of pH, mass transport, iron content and of dissolved oxygen (O{sub 2}), sulfate (SO{sub 4}{sup 2-}), nitrate (NO{sub 3}{sup -}), and nitrite (NO{sub 2}{sup -}) on DBCP transformation was investigated. There was little effect on DBCP transformation rate between pH {approx}6 and 8. Mass transport was not limiting if the iron slurries in the batch system were shaken at >340 rpm. The rate of DBCP transformation was proportional to the amount of iron. The DBCP transformation rate decreased linearly with increasing oxygen content. Sulfate did not significantly affect the rate of DBCP transformation. The presence of nitrate appeared to temporarily inhibit DBCP transformation until the NO{sub 3} was removed. Nitrate was reduced by iron to nitrite. Nitrite was also removed by iron. This system appears to be able to effectively treat DBCP nitrate and/or nitrite containing water. Comparison of DBCP transformation in groundwater using the Fe{sup o} and H{sub 2}/Pd/Al{sub 2}O{sub 3} systems shows that the H{sub 2}/Pd/Al{sub 2}O{sub 3} system performs better in actual environmental conditions.

  9. Performance of Al-rich Oxidation Resistant Coatings for Fe-Base Alloys

    SciTech Connect

    Pint, Bruce A; Zhang, Ying

    2011-01-01

    Aluminum-rich coatings made by chemical vapor deposition and pack cementation on ferritic (e.g. Fe-9Cr-1Mo) and austenitic (Type 304L) substrates are being evaluated at 650-800 C. For oxidation testing, a humid air environment was used to quantify coating performance, as uncoated substrates experience rapid oxidation at these temperatures. A main goal of this work is to demonstrate the potential benefits and problems with alumina-forming coatings. The higher exposure temperatures were selected to accelerate the degradation of the coating by interdiffusion with the substrate. A general conclusion of this testing was that coatings with less Al and a ferritic Fe(Al) structure could be more durable than higher Al content aluminide coatings which have a large thermal expansion mismatch with these substrates. A lifetime model has been developed using diffusion and oxidation observations to predict coating performance as a function of temperature and initial coating composition. To test and improve the model, additional experiments are now being conducted to determine the effect of substrate composition (e.g. Cr content using Fe-12Cr and Fe-9Cr-2W substrates) and exposure temperature on the critical Al content for coating failure. Because of the unexpectedly low level of Al measured at coating failure ({approx}3.5 at.% at 700 C), exposures of specimens with thick ({approx}200 {micro}m) high Al content coatings were stopped after 10kh at 800 C and 20kh at 700 C because extremely long times to failure were predicted. Post-exposure Al concentration profiles for these specimens were measured using electron microprobe.

  10. {sup 60}Fe AND {sup 26}Al IN CHONDRULES FROM UNEQUILIBRATED CHONDRITES: IMPLICATIONS FOR EARLY SOLAR SYSTEM PROCESSES

    SciTech Connect

    Mishra, R. K.; Goswami, J. N.; Rudraswami, N. G.; Tachibana, S.; Huss, G. R.

    2010-05-10

    The presence of about a dozen short-lived nuclides in the early solar system, including {sup 60}Fe and {sup 26}Al, has been established from isotopic studies of meteorite samples. An accurate estimation of solar system initial abundance of {sup 60}Fe, a distinct product of stellar nucleosynthesis, is important to infer the stellar source of this nuclide. Previous studies in this regard suffered from the lack of exact knowledge of the time of formation of the analyzed meteorite samples. We present here results obtained from the first combined study of {sup 60}Fe and {sup 26}Al records in early solar system objects to remove this ambiguity. Chondrules from unequilibrated ordinary chondrites belonging to low petrologic grades were analyzed for their Fe-Ni and Al-Mg isotope systematics. The Al-Mg isotope data provide the time of formation of the analyzed chondrules relative to the first solar system solids, the Ca-Al-rich inclusions. The inferred initial {sup 60}Fe/{sup 56}Fe values of four chondrules, combined with their time of formation based on Al-Mg isotope data, yielded a weighted mean value of (6.3 {+-} 2) x 10{sup -7} for solar system initial {sup 60}Fe/{sup 56}Fe. This argues for a high-mass supernova as the source of {sup 60}Fe along with {sup 26}Al and several other short-lived nuclides present in the early solar system.

  11. Electric double-layer transistor using layered iron selenide Mott insulator TlFe1.6Se2

    PubMed Central

    Katase, Takayoshi; Hiramatsu, Hidenori; Kamiya, Toshio; Hosono, Hideo

    2014-01-01

    A1–xFe2–ySe2 (A = K, Cs, Rb, Tl) are recently discovered iron-based superconductors with critical temperatures (Tc) ranging up to 32 K. Their parent phases have unique properties compared with other iron-based superconductors; e.g., their crystal structures include ordered Fe vacancies, their normal states are antiferromagnetic (AFM) insulating phases, and they have extremely high Néel transition temperatures. However, control of carrier doping into the parent AFM insulators has been difficult due to their intrinsic phase separation. Here, we fabricated an Fe-vacancy-ordered TlFe1.6Se2 insulating epitaxial film with an atomically flat surface and examined its electrostatic carrier doping using an electric double-layer transistor (EDLT) structure with an ionic liquid gate. The positive gate voltage gave a conductance modulation of three orders of magnitude at 25 K, and further induced and manipulated a phase transition; i.e., delocalized carrier generation by electrostatic doping is the origin of the phase transition. This is the first demonstration, to the authors' knowledge, of an EDLT using a Mott insulator iron selenide channel and opens a way to explore high Tc superconductivity in iron-based layered materials, where carrier doping by conventional chemical means is difficult. PMID:24591598

  12. Elastic moduli of nanocrystalline binary Al alloys with Fe, Co, Ti, Mg and Pb alloying elements

    NASA Astrophysics Data System (ADS)

    Babicheva, Rita I.; Bachurin, Dmitry V.; Dmitriev, Sergey V.; Zhang, Ying; Kok, Shaw Wei; Bai, Lichun; Zhou, Kun

    2016-05-01

    The paper studies the elastic moduli of nanocrystalline (NC) Al and NC binary Al-X alloys (X is Fe, Co, Ti, Mg or Pb) by using molecular dynamics simulations. X atoms in the alloys are either segregated to grain boundaries (GBs) or distributed randomly as in disordered solid solution. At 0 K, the rigidity of the alloys increases with decrease in atomic radii of the alloying elements. An addition of Fe, Co or Ti to the NC Al leads to increase in the Young's E and shear μ moduli, while an alloying with Pb decreases them. The elastic moduli of the alloys depend on a distribution of the alloying elements. The alloys with the random distribution of Fe or Ti demonstrate larger E and μ than those for the corresponding alloys with GB segregations, while the rigidity of the Al-Co alloy is higher for the case of the GB segregations. The moduli E and μ for polycrystalline aggregates of Al and Al-X alloys with randomly distributed X atoms are estimated based on the elastic constants of corresponding single-crystals according to the Voigt-Reuss-Hill approximation, which neglects the contribution of GBs to the rigidity. The results show that GBs in NC materials noticeably reduce their rigidity. Furthermore, the temperature dependence of μ for the NC Al-X alloys is analyzed. Only the Al-Co alloy with GB segregations shows the decrease in μ to the lowest extent in the temperature range of 0-600 K in comparison with the NC pure Al.

  13. Optimization of High Temperature Hoop Creep Response in ODS-Fe3Al Tubes

    SciTech Connect

    Kad, B.K.; Heatherington, J.H.; McKamey, C.; Wright, I.; Sikka, V.; Judkins, R.

    2003-04-22

    Oxide dispersion strengthened (ODS) Fe3Al alloys are currently being developed for heat-exchanger tubes for eventual use at operating temperatures of up to 1100 C in the power generation industry. The development challenges include (a) efforts to produce thin walled ODS-Fe3Al tubes, employing powder extrusion methodologies, with (b) adequate increased strength for service at operating temperatures to (c) mitigate creep failures by enhancing the as-processed grain size. A detailed and comprehensive research and development methodology is prescribed to produce ODS-Fe3Al thin walled tubes. Current single step extrusion consolidation methodologies typically yield 8ft. lengths of 1-3/8 inch diameter, 1/8 inch wall thickness ODS-Fe3Al tubes. The process parameters for such consolidation methodologies have been prescribed and evaluated as being routinely reproducible. Recrystallization treatments at 1200 C produce elongated grains (with their long axis parallel to the extrusion axis), typically 200-2000 {micro}m in diameter, and several millimeters long. The dispersion distribution is unaltered on a micro scale by recrystallization, but the high aspect ratio grain shape typically obtained limits grain spacing and consequently the hoop creep response. Improving hoop creep in ODS-alloys requires an understanding and manipulating the factors that control grain alignment and recrystallization behavior. Current efforts are focused on examining the processing dependent longitudinal vs. transverse creep anisotropy, and exploring post-extrusion methods to improve hoop creep response in ODS-Fe3Al alloy tubes. In this report we examine the mechanisms of hoop creep failure and describe our efforts to improve creep performance via variations in thermal-mechanical treatments.

  14. Electronic Structure and Chemistry of Iron-Based Metal Oxide Nanostructured Materials: A NEXAFS Investigation of BiFeO3, Bi2Fe4O9, α-Fe2O3, γ-Fe2O3, and Fe/Fe3O4

    SciTech Connect

    Park,T.; Sambasivan, S.; Fischer, D.; Yoon, W.; Misewich, J.; Wong, S.

    2008-01-01

    We present a systematic and detailed near edge X-ray absorption fine structure (NEXAFS) experimental investigation of the electronic structure and chemistry of iron-based metal oxide nanostructured (FeMONS) materials including BiFeO3, Bi2Fe4O9, a-Fe2O3, ?-Fe2O3, and Fe/Fe3O4. Correlations of the electronic structure and structural chemistry of these intriguing nanomaterials are presented, ranging from the nano to the bulk scale. In this work, variations in the shape, position, and intensity of the O K-edge and Fe L-edge NEXAFS spectra have been analyzed in terms of electronic structure and surface chemistry of the FeMONS materials as compared with that of the bulk. We hypothesize that surface imperfection and surface strain anisotropies in nanoparticles induce distortion and site inequivalency of the oxygen Oh sites around the Fe ion located close to the surface, resulting in an increase in the degree of multiplicity as well as in nonstoichiometric effects in FeMONS materials.

  15. Impact of iron-site defects on superconductivity in LiFeAs

    NASA Astrophysics Data System (ADS)

    Chi, Shun; Aluru, Ramakrishna; Singh, Udai Raj; Liang, Ruixing; Hardy, Walter N.; Bonn, D. A.; Kreisel, A.; Andersen, Brian M.; Nelson, R.; Berlijn, T.; Ku, W.; Hirschfeld, P. J.; Wahl, Peter

    2016-10-01

    In conventional s -wave superconductors, only magnetic impurities exhibit impurity bound states, whereas for an s± order parameter they can occur for both magnetic and nonmagnetic impurities. Impurity bound states in superconductors can thus provide important insight into the order parameter. Here, we present a combined experimental and theoretical study of native and engineered iron-site defects in LiFeAs. A detailed comparison of tunneling spectra measured on impurities with spin-fluctuation theory reveals a continuous evolution from negligible impurity-bound-state features for weaker scattering potential to clearly detectable states for somewhat stronger scattering potentials. All bound states for these intermediate strength potentials are pinned at or close to the gap edge of the smaller gap, a phenomenon that we explain and ascribe to multiorbital physics.

  16. Location and oxidation state of iron in Fe-substituted CuInS{sub 2} chalcopyrites

    SciTech Connect

    Burnett, Johanna D.; Xu Tianhong; Sorescu, Monica; Strohmeier, Brian R.; Sturgeon, Jacqueline; Gourdon, Olivier; Baroudi, Kristen; Yao Jinlei; Aitken, Jennifer A.

    2013-01-15

    CuIn{sub 1-x}Fe{sub x}S{sub 2}(x=0-0.30) was synthesized via high-temperature, solid-state synthesis. Phase-pure materials were found in samples where x=0-0.15, after which a secondary phase became apparent. The materials were characterized with the use of X-ray powder diffraction (XRPD), and Reitveld refinement revealed a linear decrease in unit cell volume as the amount of iron substitution increases in accordance with Vegard's Law. Inductively coupled plasma (ICP) confirms that the actual stoichiometry is close to the nominal composition of the materials. The temperature for both the chalcopyrite-to-sphalerite and the sphalerite-to-wurtzite phase transitions decreases with increasing iron substitution for indium. These findings suggest that the Fe is being randomly incorporated into the crystal structure of the CuInS{sub 2}. X-ray photoelectron spectroscopy (XPS) measurements were used to determine the oxidation state of the ions (Cu{sup 1+}, In{sup 3+,} and S{sup 2-}), and Fe{sup 57} Moessbauer spectroscopy verified that the iron is in the 3{sup +} oxidation state. Band gaps of the solid solution were estimated to be in the range of 0.70-0.85 eV. Rietveld refinement of neutron diffraction data indicates that the iron is occupying the In site within the chalcopyrite structure. - Graphical abstract: CuIn{sub 1-x}Fe{sub x}S{sub 2} samples were prepared by solid-state synthesis. X-ray photoelectron spectroscopy and Moessbauer spectroscopy indicate Cu{sup +}, In{sup 3+}, Fe{sup 3+} and S{sup 2-} in the samples. Rietveld refinement of neutron powder diffraction data shows Fe{sup 3+} residing on the indium site. The band gaps of the iron-containing samples decrease to {approx}0.7 eV. Highlights: Black-Right-Pointing-Pointer X-ray photoelectron spectroscopy confirms the presence of Cu{sup +}, In{sup 3+} and S{sup 2-}. Black-Right-Pointing-Pointer Moessbauer spectroscopy indicates the presence of Fe{sup 3+}. Black-Right-Pointing-Pointer Rietveld refinement of neutron

  17. Electron spin-lattice relaxation of the (4Fe-4S) ferredoxin from B. stearothermophilus. Comparison with other iron proteins

    NASA Astrophysics Data System (ADS)

    Bertrand, Patrick; Gayda, Jean-Pierre; Rao, K. Krishna

    1982-05-01

    The temperature dependence of the electron spin-lattice relaxation time T1 of the (4Fe-4S) ferredoxin from Bacillus stearothermophilus is studied in the range 1.2 to 40 K. This dependence is similar to that observed for the (2Fe-2S) ferredoxin from Spirulina maxima and can be interpreted with the same relaxation processes [J.P. Gayda, P. Bertrand, A. Deville, C. More, G. Roger, J.F. Gibson, and R. Cammack, Biochim. Biophys. Acta 581, 15 (1979)]. In particular, between 4 and 15 K, the data are well fitted by a second-order Raman process involving three-dimensional phonons, with a Debye temperature of about 60 K (45 cm-1). This would give an estimation of the highest frequency of the vibrations which can propagate through the three-dimensional proteinic medium. In the highest temperature range (T≳30 K) the results are interpreted with an Orbach process involving an excited level of energy 120 cm-1. This process could be induced by the localized vibrations of the active site. Finally, these results are compared to those recently reported for some hemoproteins [H.J. Stapleton, J.P. Allen, C.P. Flynn, D.G. Stinson, and S.R. Kurtz, Phys. Rev. Lett. 45, 1456 (1980)]. Below 15 K, the temperature dependence of T1 for these samples is similar to that observed for the iron-sulfur proteins and may be interpreted in the same way. Our interpretation is compared to the fractal model proposed by Stapleton et al.

  18. Estimation of fracture parameters for Al-SiC and Al-Fe2O3 metal matrix composites

    NASA Astrophysics Data System (ADS)

    Jacob, S.; Sridhar, R.; Irudaya Raja, S. Joseph

    2017-03-01

    In this paper silicon carbide and iron oxide is reinforced with aluminum matrix. The prepared composite provide high strength than the commercial composite. It provides high elastic properties and high service temperature. Since this material have great scope in space application it has been chosen for estimation of fracture toughness. Hence grain size of the samples increased this is due to the effect of reinforcement bonding with aluminum matrix. The CMOD test has been carried out for this Purpose. Microscopic examination has shown that with increase in of reinforcement test confirmed that with increase in reinforcement ratio the fracture toughness also increased. In this work specimens have been preferred with and without addition of SiC and Fe2O3 to compare the influence. The results are compared and it has been studied that Fracture Toughness increased significantly by addition of inclusions.

  19. The conserved protein Dre2 uses essential [2Fe-2S] and [4Fe-4S] clusters for its function in cytosolic iron-sulfur protein assembly.

    PubMed

    Netz, Daili J A; Genau, Heide M; Weiler, Benjamin D; Bill, Eckhard; Pierik, Antonio J; Lill, Roland

    2016-07-15

    The cytosolic iron-sulfur (Fe-S) protein assembly (CIA) machinery comprises 11 essential components and matures Fe-S proteins involved in translation and genome maintenance. Maturation is initiated by the electron transfer chain NADPH-diflavin reductase Tah18-Fe-S protein Dre2 that facilitates the de novo assembly of a [4Fe-4S] cluster on the scaffold complex Cfd1-Nbp35. Tah18-Dre2 also play a critical role in the assembly of the diferric tyrosyl radical cofactor of ribonucleotide reductase. Dre2 contains eight conserved cysteine residues as potential co-ordinating ligands for Fe-S clusters but their functional importance and the type of bound clusters is unclear. In the present study, we use a combination of mutagenesis, cell biological and biochemical as well as UV-visible, EPR and Mössbauer spectroscopic approaches to show that the yeast Dre2 cysteine residues Cys(252), Cys(263), Cys(266) and Cys(268) (motif I) bind a [2Fe-2S] cluster, whereas cysteine residues Cys(311), Cys(314), Cys(322) and Cys(325) (motif II) co-ordinate a [4Fe-4S] cluster. All of these residues with the exception of Cys(252) are essential for cell viability, cytosolic Fe-S protein activity and in vivo (55)Fe-S cluster incorporation. The N-terminal methyltransferase-like domain of Dre2 is important for proper Fe-S cluster assembly at motifs I and II, which occurs in an interdependent fashion. Our findings further resolve why recombinant Dre2 from Arabidopsis, Trypanosoma or humans has previously been isolated with a single [2Fe-2S] instead of native [2Fe-2S] plus [4Fe-4S] clusters. In the presence of oxygen, the motif I-bound [2Fe-2S] cluster is labile and the motif II-bound [4Fe-4S] cluster is readily converted into a [2Fe-2S] cluster.

  20. X-ray absorption spectroscopic studies of iron framework-substituted and exchanged zeolites: Characterization and quantification of incorporated iron species

    NASA Astrophysics Data System (ADS)

    Stanfel, Christine Marie

    X-ray absorption spectroscopic (XAS) analysis methods were derived which allowed iron species within iron substituted and exchanged zeolites to be characterized, and the fractional contribution of each species to the zeolite iron population to be quantified. Framework (T-site occupant) and non-framework iron species simultaneously present within zeolites were differentiated. Non-framework iron was segregated further into phases respectively exhibiting and lacking long range order. The former was described as precipitate iron. Zeolitic precipitate iron was found to occur either as an ordered Goethite-type phase, or a disordered aggregate. Iron species lacking long range order were found to be approximated by hydrated ferric ions (Fe(Hsb2O)sb6sp{3+}). XAS methods allowed determination of the fractional contribution of each iron phase; framework, precipitate, and low long range order, to the zeolite. XAS analysis methods were applied to an iron framework-substituted LTL zeolite (Fe LTL2) and two ferric exchanged analogs of Fe LTL2 (Fesp{3+} exchanged Fe LTL2). Fesp{3+} exchanged Fe LTL2 zeolites differed according to ferric salt and acid exposure length. Fe LTL2 was found to contain 20% disordered aggregate precipitate iron, and 80% framework iron. Fesp{3+} exchanged Fe LTL2 zeolites contained three iron species; framework, precipitate, and low long range order. Exchange left Fe LTL2 precipitate type and quantity unchanged, while framework iron decreased. Elemental analysis indicated composition changes arose from framework iron removal by acid exposure. Iron lacking long range order served a charge-balancing function as increased levels correlated with decreased Ksp+/(Al + Fesbframework) ratios. XAS methods were additionally applied to six iron framework-substituted faujasites (Fe FAU) with Si/Al ratios consistent with zeolites X, Y, and ECR-32. Two iron substitution levels, low and high, were synthesized for each isotype. Iron within each faujasite partitioned into

  1. Hexaferrites and phase relations in the iron-rich part of the system Sr-La-Co-Fe-O

    SciTech Connect

    Langhof, N.; Goebbels, M.

    2009-10-15

    The iron rich part of the system was examined in the temperature range of 1200-1380 deg. C in air, with focus on the solid solutions of M-type hexaferrites. Samples of suitable compositions were studied by electronprobe microanalysis (EPMA). Substituted Sr-hexaferrites in the system Sr-La-Co-Fe-O do not follow the 1:1 substitution mechanism of La/Co in M-type ferrites. Due to the presence and limited Co{sup 2+}-incorporation Fe{sup 3+}-ions are reduced to Fe{sup 2+} within the crystal lattice to obtain charge balance. In all examined M-type ferrites divalent iron is formed, even at 1200 deg. C. The substitution principle Sr{sup 2+}+Fe{sup 3+}reversibleLa{sup 3+}+(Fe{sup 2+}, Co{sup 2+}) yields to the general substitution formula for the M-type hexaferrite Sr{sup 2+}{sub 1-x}La{sup 3+}{sub x}Fe{sup 2+}{sub x-y}Co{sup 2+}{sub y}Fe{sup 3+}{sub 12-x}O{sup 19} (0<=x<=1 and 0<=y<=x). In addition Sr/La-perovskite{sub SS} ({sub SS}=solid solution), Co/Fe-spinel{sub SS}, hematite and magnetite are formed. Sr-hexaferrite exhibits at 1200 deg. C a limited solid solution with small amounts of Fe{sup 2+} (SrFe{sub 12}O{sub 19}reversibleSr{sub 0.3}La{sub 0.7}Co{sub 0.5}Fe{sup 2+}{sub 0.2}Fe{sub 11.3}O{sub 19}). At 1300 and 1380 deg. C a continuous solid solution series of the M-type hexaferrite is stable. SrFe{sub 12}O{sub 19} and LaCo{sub 0.4}Fe{sup 2+}{sub 0.6}Fe{sub 11}O{sub 19} are the end members at 1300 deg. C. The maximum Fe{sup 2+}O content is about 13 mol% in the M-type ferrite at 1380 deg. C (LaCo{sub 0.1}Fe{sup 2+}{sub 0.9}Fe{sub 11}O{sub 19}). - Graphical abstract: M-type hexaferrite solid solution series Sr{sub 1-x}La{sub x}Fe{sup 2+}{sub x-y}Co{sup 2+}{sub y}Fe{sup 3+}{sub 12-x}O{sup 19} (0<=x<=1 and 0<=y<=0.40) at 1300 deg. C; M-type contains significant amounts of FeO even at 1200 deg. C; blue=data from electronprobe microanalyses; SF{sub 6}=SrFe{sup 3+}{sub 12}O{sub 19}; LCoFf{sub 6}=LaCo{sub 0.4}Fe{sup 2+}{sub 0.6}Fe{sup 3+}{sub 11}O{sub 19}; S=SrO; L=La{sub 2

  2. Sol-gel based optical sensor for determination of Fe (II): a novel probe for iron speciation.

    PubMed

    Samadi-Maybodi, Abdolraouf; Rezaei, Vida; Rastegarzadeh, Saadat

    2015-02-05

    A highly selective optical sensor for Fe (II) ions was developed based on entrapment of a sensitive reagent, 2,4,6-tri(2-pyridyl)-s-triazine (TPTZ), in a silica sol-gel thin film coated on a glass substrate. The thin films fabricated based on tetraethoxysilane (TEOS) as precursor, sol-gel pH∼3, water:alkoxyde ratio of 4:1 and TPTZ concentration of 0.112 mol L(-1). The influence of sol-gel parameters on sensing behavior of the fabricated sensor was also investigated. The fabricated sensor can be used for determination of Fe (II) ion with an outstanding high selectivity over a dynamic range of 5-115 ng mL(-1) and a detection limit of 1.68 ng mL(-1). It also showed reproducible results with relative standard deviation of 3.5% and 1.27% for 10 and 90 ng mL(-1) of Fe (II), respectively, along with a fast response time of ∼120 s. Total iron also was determined after reduction of Fe (III) to Fe (II) using ascorbic acid as reducing agent. Then, the concentration of Fe (III) was calculated by subtracting the concentration of Fe (II) from the total iron concentration. Interference studies showed a good selectivity for Fe (II) with trapping TPTZ into sol-gel matrix and appropriately adjusting the structure of doped sol-gel. The sensor was compared with other sensors and was applied to determine iron in different water samples with good results.

  3. Sol-gel based optical sensor for determination of Fe (II): A novel probe for iron speciation

    NASA Astrophysics Data System (ADS)

    Samadi-Maybodi, Abdolraouf; Rezaei, Vida; Rastegarzadeh, Saadat

    2015-02-01

    A highly selective optical sensor for Fe (II) ions was developed based on entrapment of a sensitive reagent, 2,4,6-tri(2-pyridyl)-s-triazine (TPTZ), in a silica sol-gel thin film coated on a glass substrate. The thin films fabricated based on tetraethoxysilane (TEOS) as precursor, sol-gel pH ∼ 3, water:alkoxyde ratio of 4:1 and TPTZ concentration of 0.112 mol L-1. The influence of sol-gel parameters on sensing behavior of the fabricated sensor was also investigated. The fabricated sensor can be used for determination of Fe (II) ion with an outstanding high selectivity over a dynamic range of 5-115 ng mL-1 and a detection limit of 1.68 ng mL-1. It also showed reproducible results with relative standard deviation of 3.5% and 1.27% for 10 and 90 ng mL-1 of Fe (II), respectively, along with a fast response time of ∼120 s. Total iron also was determined after reduction of Fe (III) to Fe (II) using ascorbic acid as reducing agent. Then, the concentration of Fe (III) was calculated by subtracting the concentration of Fe (II) from the total iron concentration. Interference studies showed a good selectivity for Fe (II) with trapping TPTZ into sol-gel matrix and appropriately adjusting the structure of doped sol-gel. The sensor was compared with other sensors and was applied to determine iron in different water samples with good results.

  4. Glycerol Steam Reforming Over Ni-Fe-Ce/Al2O3 Catalyst: Effect of Cerium.

    PubMed

    Go, Gwang-Sub; Go, Yoo-Jin; Lee, Hong-Joo; Moon, Dong-Ju; Park, Nam-Cook; Kim, Young-Chul

    2016-02-01

    In this work, hydrogen production from glycerol by steam reforming was studied using Ni-metal oxide catalysts. Ni-based catalyst becomes deactivated during steam reforming reactions because of coke deposits and sintering. Therefore, the aim of this study was to reduce carbon deposits and sintering on the catalyst surface by adding a promoter. Ni-metal oxide catalysts supported on Al2O3 were prepared via impregnation method, and the calcined catalyst was reduced under H2 flow for 2 h prior to the reaction. The characteristics of the catalysts were examined by XRD, TPR, TGA, and SEM. The Ni-Fe-Ce/Al2O3 catalyst, which contained less than 2 wt% Ce, showed the highest hydrogen selectivity and glycerol conversion. Further analysis of the catalysts revealed that the Ni-Fe-Ce/Al2O3 catalyst required a lower reduction temperature and produced minimum carbon deposit.

  5. Scanning Tunneling Microscopy Studies of Surface Structures of Icosahedral Al-Cu-Fe Quasicrystals

    SciTech Connect

    Cai, Tanhong

    2001-01-01

    Three papers are included in this dissertation. The first paper: ''Structural aspects of the fivefold quasicrystalline Al-Cu-Fe surface from STM and dynamical LEED studies'', is in press with ''Surface Science''. The second paper: ''An STM study of the atomic structure of the icosahedral Al-Cu-Fe fivefold surface'' is submitted to ''Physical Review B, Rapid Communication''. The third paper: ''Pseudomorphic starfish: arrangement of extrinsic metal atoms on a quasicrystalline substrate'' is submitted to ''Nature''. Following the third paper are general conclusions and appendices that document the published paper ''Structural aspects of the three-fold surface of icosahedral Al-Pd-Mn'' (appearing in volume 461, issue 1-3 of ''Surface Science'' on page L521-L527, 2000), the design as well as the specifications of the aluminum evaporator used in the aluminum deposition study in this dissertation, an extended discussion of the aluminum deposition on the quasicrystalline surface, and the STM database.

  6. Magnetic properties on the surface of FeAl stripes induced by nanosecond pulsed laser irradiation

    NASA Astrophysics Data System (ADS)

    Kaiju, H.; Yoshida, Y.; Watanabe, S.; Kondo, K.; Ishibashi, A.; Yoshimi, K.

    2014-05-01

    We demonstrate the formation of magnetic nanostripes on the surface of Fe52Al48 induced by nanosecond pulsed laser irradiation and investigate their magnetic properties. The magnetic stripe consists of a disordered A2 phase of Fe-Al alloys with Al-oxide along the [110] direction on the (111)-oriented plane. According to the focused magneto-optical Kerr effect measurement, the coercive force of the magnetic stripe obeys the 1/cos θ law, where θ is the field rotation angle estimated from the stripe direction. Also, the jump field can be observed in the magnetic hysteresis loop. These results indicate that the magnetization reversal in the magnetic stripe originates from the domain pinning, showing that the magnetization rotates incoherently.

  7. On pseudoelasticity in single crystals of the intermetallic compound Fe{sub 3}Al

    SciTech Connect

    Brinck, A.; Engelke, C.; Neuhaeuser, H.

    1997-09-01

    Only few notes can be found in literature which report on pseudoelastic effects in Fe{sub 3}Al intermetallic compounds. Reversible deformation on {l_brace}110{r_brace} and {l_brace}112{r_brace} planes was observed in shear and compression experiments by Guedou and Rieu and explained by microtwinning, while Kubin et al. showed by in-situ TEM observations that the motion of the front partial of a superdislocation appeared to cause the slip reversal on {l_brace}110{r_brace} planes. The authors have recently observed such a similar effect during in-situ slip line formation studies of Fe{sub 3}Al crystals with a special crystal orientation deformed in compression at and above room temperature. In the following these observations are described and the possible reasons are discussed in connection with the data from literature.

  8. The effect of various oxide dispersions on the oxidation resistance of Fe{sub 3}Al

    SciTech Connect

    Pint, B.A.; Alexander, K.B.; Tortorelli, P.F.

    1996-10-01

    Oxide-dispersed Fe-28at.%Al-2%Cr alloys were produced by a powder metallurgy technique followed by hot extrusion. Yttria and ceria were added to the base alloy to assess the effect of these dopants on the oxidation behavior. The amount of dopant was varied from 0.05-0.5 at.% Y in a series of Y{sub 2}O{sub 3}-dispersed alloys. isothermal and cyclic oxidation testing was conducted at temperatures from 800{degrees} to 1300{degrees}C. A CeO{sub 2} addition was detrimental to the oxidation behavior. The Y{sub 2}O{sub 3} improved the {alpha}-Al{sub 2}O{sub 3} scale adhesion relative to an undoped alloy, but was not as effective as similar additions to an oxide-dispersed FeCrAl alloy.

  9. The influence of engineered Fe(2)O(3) nanoparticles and soluble (FeCl(3)) iron on the developmental toxicity caused by CO(2)-induced seawater acidification.

    PubMed

    Kadar, E; Simmance, F; Martin, O; Voulvoulis, N; Widdicombe, S; Mitov, S; Lead, J R; Readman, J W

    2010-12-01

    An embryo development assay using a common test organism, the edible mussel (Mytilus galloprovincialis), exposed to both Fe(2)O(3) nanoparticles and soluble FeCl(3) at 3 acidic pHs, has provided evidence for the following: (1) CO(2) enriched seawater adjusted to pH projections for carbon capture leakage scenarios (CCS) significantly impaired embryo development; (2) under natural pH conditions, no significant effect was detected following exposure of embryos to Fe, no matter if in nano- or soluble form; (3) at pH of natural seawater nano-Fe particles aggregate into large, polydisperse and porous particles, with no biological impact detected; (4) at pH 6 and 7, such aggregates may moderate the damage associated with CO(2) enrichment as indicated by an increased prevalence of normal D-shell larvae when nano-Fe was present in the seawater at pH 7, while soluble iron benefited embryo development at pH 6, and (5) the observed effects of iron on pH-induced development toxicity were concentration dependent.

  10. Identification of a catalytic iron-hydride at the H-cluster of [FeFe]-hydrogenase

    SciTech Connect

    Mulder, David W.; Guo, Yisong; Ratzloff, Michael W.; King, Paul W.

    2016-12-14

    Hydrogenases couple electrochemical potential to the reversible chemical transformation of H2 and protons, yet the reaction mechanism and composition of intermediates are not fully understood. In this Communication we describe the biophysical properties of a hydride-bound state (Hhyd) of the [FeFe]-hydrogenase from Chlamydomonas reinhardtii. The catalytic H-cluster of [FeFe]-hydrogenase consists of a [4Fe-4S] subcluster ([4Fe-4S]H) linked by a cysteine thiol to an azadithiolate-bridged 2Fe subcluster ([2Fe]H) with CO and CN- ligands. Mossbauer analysis and density functional theory (DFT) calculations show that Hhyd consists of a reduced [4Fe-4S]H+ coupled to a diferrous [2Fe]H with a terminally bound Fe-hydride. The existence of the Fe-hydride in Hhyd was demonstrated by an unusually low Mossbauer isomer shift of the distal Fe of the [2Fe]H subcluster. As a result, a DFT model of Hhyd shows that the Fe-hydride is part of a H-bonding network with the nearby bridging azadithiolate to facilitate fast proton exchange and catalytic turnover.

  11. Identification of a catalytic iron-hydride at the H-cluster of [FeFe]-hydrogenase

    DOE PAGES

    Mulder, David W.; Guo, Yisong; Ratzloff, Michael W.; ...

    2016-12-14

    Hydrogenases couple electrochemical potential to the reversible chemical transformation of H2 and protons, yet the reaction mechanism and composition of intermediates are not fully understood. In this Communication we describe the biophysical properties of a hydride-bound state (Hhyd) of the [FeFe]-hydrogenase from Chlamydomonas reinhardtii. The catalytic H-cluster of [FeFe]-hydrogenase consists of a [4Fe-4S] subcluster ([4Fe-4S]H) linked by a cysteine thiol to an azadithiolate-bridged 2Fe subcluster ([2Fe]H) with CO and CN- ligands. Mossbauer analysis and density functional theory (DFT) calculations show that Hhyd consists of a reduced [4Fe-4S]H+ coupled to a diferrous [2Fe]H with a terminally bound Fe-hydride. The existence ofmore » the Fe-hydride in Hhyd was demonstrated by an unusually low Mossbauer isomer shift of the distal Fe of the [2Fe]H subcluster. As a result, a DFT model of Hhyd shows that the Fe-hydride is part of a H-bonding network with the nearby bridging azadithiolate to facilitate fast proton exchange and catalytic turnover.« less

  12. Structure and nuclearity of active sites in Fe-zeolites: comparison with iron sites in enzymes and homogeneous catalysts.

    PubMed

    Zecchina, Adriano; Rivallan, Mickaël; Berlier, Gloria; Lamberti, Carlo; Ricchiardi, Gabriele

    2007-07-21

    Fe-ZSM-5 and Fe-silicalite zeolites efficiently catalyse several oxidation reactions which find close analogues in the oxidation reactions catalyzed by homogeneous and enzymatic compounds. The iron centres are highly dispersed in the crystalline matrix and on highly diluted samples, mononuclear and dinuclear structures are expected to become predominant. The crystalline and robust character of the MFI framework has allowed to hypothe