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

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At least 55 records · Page 3
All sourcesNASA NTRSDOE OSTI
NASA NTRS1975

Morphology and composition of chalcopyrite, chromite, Cu, Ni-Fe, pentlandite, and troilite in vugs of 76015 and 76215

Vugs from 76015 and 76215 are lined with euhedral crystals of plagioclase, pyroxene, ilmenite, Ni-Fe, and troilite. Smaller crystals of chromite, pentlandite, and chalcopyrite occur on the surface of the troilite in 76015. Wire Cu and dendritic-metallic Cu occurs with metallic Ni-Fe and troilite in some vugs of 76215. Troilite in both samples may have crystallized from an immiscible sulfide liquid. With falling temperature, chalcopyrite, and pentlandite may have exsolved from the troilite in 76015. By contrast, metallic Cu may have formed in 76215 by thermal breakdown of a bornite, troilite, and Ni-Fe assemblage which originally crystallized from a low-Ni immiscible sulfide liquid.

Carter, J. L.↗
NASA NTRS1982

SEM, optical, and Moessbauer studies of submicrometer chromite in Allende

New scanning electron and optical microscope results are presented showing that sub-micrometer chromite is abundant along healed cracks and grain boundaries in Allende chondrule olivine. Some wider healed cracks also contain pentlandite and euhedral Ni3Fe grains. Also reported are Moessbauer measurements on Allende HF-HCl residues confirming a high Fe(+++)/Fe(++) ratio.

Housley, R. M.↗
DOE OSTI2016

Radio frequency abnormal dielectric response of manganese chromite (MnCr{sub 2}O{sub 4}) nanoparticles synthesized by coprecipitation method

Highlights: • Uniform MnCr{sub 2}O{sub 4} nanoparticles synthesized by surfactant-free coprecipitation route. • XRD analysis confirmed the single spinel phase formation in the material. • Dielectric loss was found abnormal over certain lower frequencies. • AC conductivity proved the involvement of small polarons in conduction process. - Abstract: Radio frequency dielectric behavior of nanocrystalline MnCr{sub 2}O{sub 4} synthesized via surfactant-free controlled coprecipitation route has been studied. Keeping in view the necessity of particle size uniformity and phase purity for genuine performance, experimental conditions were optimized accordingly. The scanning electron micrographs of the synthesized product revealed the formation of monodispersed particle system. X-ray diffraction analysis confirmed monophasic spinel structure formation with 65 nm crystallite size. Two characteristic peaks observed between 700 cm{sup −1} and 400 cm{sup −1} in the FTIR spectrum also supported the spinel phase purity of compound. The dielectric constant was found normal, but loss tangent of the sample showed abnormal behavior with frequency. The observed dielectric behavior of the synthesized product has been explained on the basis of space-charge polarization according to Maxwell–Wagner’s model and mutual contribution of n-type &p-type charge carriers (Rezlescu model). The ac conductivity linearly increased with frequency highlighting the existence of polaron hopping.

36 MATERIALS SCIENCE↗
DOE OSTI2016

Enhancement in magnetocaloric properties of holmium chromite by gadolinium substitution

HoCrO{sub 3}, Ho{sub 0.67}Gd{sub 0.33}CrO{sub 3}, and GdCrO{sub 3} bulk powder samples were prepared by citrate route. The phase purity and the structural properties of the samples were examined by x-ray diffraction and Raman spectroscopic measurements. The dc magnetization data revealed that the Cr{sup 3+} ordering temperatures (Néel temperature) for the HoCrO{sub 3}, Ho{sub 0.67}Gd{sub 0.33}CrO{sub 3}, and GdCrO{sub 3} samples are 140 K, 148 K, and 167 K, respectively, while the ac magnetization data revealed that the rare-earth (Ho) ordering occurs at ∼8 K for HoCrO{sub 3} and Ho{sub 0.67}Gd{sub 0.33}CrO{sub 3} samples. Temperature-induced magnetization reversal and spin reorientation were observed in GdCrO{sub 3} bulk sample, which depends on applied magnetic field and disappears at ∼1500 Oe and 500 Oe, respectively. By fitting the dc magnetic data with Curie-Weiss law, the effective magnetic moments were calculated to be 11.66 μ{sub B}, 10.23 μ{sub B}, and 9.90 μ{sub B} for the HoCrO{sub 3}, Ho{sub 0.67}Gd{sub 0.33}CrO{sub 3}, and GdCrO{sub 3} samples, respectively. The isothermal magnetization data showed that the magnetic behavior changed from canted antiferromagnetic in low temperature region (below Néel temperature) to paramagnetic at high temperature. It was found that Gd substitution considerably improves the magnetocaloric effect of HoCrO{sub 3}. Pure GdCrO{sub 3} bulk sample showed giant magnetocaloric entropy change (31.6 J/kg K at temperature ∼5 K and at ∼70 kOe), which is higher than that for polycrystalline RMnO{sub 3}, RCrO{sub 3}, and RFeO{sub 3} bulk powder samples. This renders GdCrO{sub 3} useful for potential applications in low-temperature magnetic refrigeration.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗
DOE OSTI2014

Disorder-induced Room Temperature Ferromagnetism in Glassy Chromites

We report an unusual robust ferromagnetic order above room temperature upon amorphization of perovskite [YCrO3] in pulsed laser deposited thin films. This is contrary to the usual expected formation of a spin glass magnetic state in the resulting disordered structure. To understand the underlying physics of this phenomenon, we combine advanced spectroscopic techniques and first-principles calculations. We find that the observed order-disorder transformation is accompanied by an insulator-metal transition arising from a wide distribution of Cr-O-Cr bond angles and the consequent metallization through free carriers. Similar results also found in YbCrO3-films suggest that the observed phenomenon is more general and should, in principle, apply to a wider range of oxide systems. The ability to tailor ferromagnetic order above room temperature in oxide materials opens up many possibilities for novel technological applications of this counter intuitive effect.

36 MATERIALS SCIENCE↗