Neutron powder diffraction analysis of (Tm{sub 0.50}Ca{sub 0.50})MnO{sub 3} and (Lu{sub 0.50}Ca{sub 0.50})MnO{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Martinelli, A., E-mail: alberto.martinelli@spin.cnr.it [SPIN-CNR, C.so Perrone 24, 16152 Genova (Italy); Ferretti, M. [SPIN-CNR, C.so Perrone 24, 16152 Genova (Italy); Universita degli Studi di Genova, Dipartimento di Chimica e Chimica Industriale, Via Dodecaneso 31, 16146 Genova (Italy); Cimberle, M.R. [IMEM-CNR, Via Dodecaneso 33, 16146, Genova (Italy); Ritter, C. [Institute Laue-Langevin, 6 rue Jules Horowitz, 38042 Grenoble Cedex 9 (France)

2012-12-15

The crystal and magnetic structures of (Tm{sub 0.50}Ca{sub 0.50})MnO{sub 3} and (Lu{sub 0.50}Ca{sub 0.50})MnO{sub 3} have been investigated between 5 K and 300 K by means of high resolution neutron powder diffraction followed by Rietveld refinement and dc magnetic measurements. During cooling orbital ordering at the Mn sub-lattice takes place at T{sub OO}{approx}280 K in both compounds, inducing an orthorhombic to monoclinic phase transition. As the temperature is further decreased an antiferromagnetic CE-type structure occurs in both compounds at T{sub N}{approx}105 K. The comparison with other (Ln{sub 0.50}Ca{sub 0.50})MnO{sub 3} compounds reveals that at room temperature the average Jahn-Teller distortion increases sharply with the decrease of the ionic radius for lanthanides heavier than Sm. The ordered magnetic moment progressively decreases as the lanthanide ionic radius decreases on account of the decreased values of the Mn-O-Mn bond angles. - Graphical abstract: Rietveld refinement plot for (Tm{sub 0.50}Ca{sub 0.50})MnO{sub 3} obtained from neutron powder diffraction data collected at 5 K; the inset shows the CE-type spin ordering taking place at the Mn sub-lattice. Highlights: Black-Right-Pointing-Pointer The crystal and magnetic structures of (Tm{sub 0.50}Ca{sub 0.50})MnO{sub 3} and (Lu{sub 0.50}Ca{sub 0.50})MnO{sub 3} were analyzed by neutron powder diffraction. Black-Right-Pointing-Pointer Orbital ordering takes place below T{sub OO}{approx}280 K in both compounds. Black-Right-Pointing-Pointer An antiferromagnetic CE-type structure occurs in both compounds below T{sub N}{approx}105 K. Black-Right-Pointing-Pointer A Comparison with other (Ln{sub 0.50}Ca{sub 0.50})MnO{sub 3} compounds is reported.

First principles density functional theory study of Pb doped α-MnO2 catalytic materials

Science.gov (United States)

Song, Zilin; Yan, Zhiguo; Yang, Xiaojun; Bai, Hang; Duan, Yuhua; Yang, Bin; Leng, Li

2018-03-01

The impact of Pb in the tunnels of manganese oxide octahedral molecular sieves on chemical state of Mn species and lattice oxygen were investigated utilizing density functional theory calculations. The results show that the Pb dopant in the tunnels of OMS-2 could reduce the average valence states of Mn. The lower energy required for bulk oxygen defects formation in Pb-OMS-2 validates the activation of lattice oxygen by inclusion of tunnel dopant. The inclusion of Pb promotes the catalytic oxidation activity of OMS-2 by reducing the energy required for the surface lattice oxygen migration during the Mars - van Krevelen oxidation process.

Large magnetoresistance in La-Ca-Mn-O films

International Nuclear Information System (INIS)

Chen, L.H.; Jin, S.; Tiefel, T.H.; Ramesh, R.; Schurig, D.

1995-01-01

A very large magnetoresistance value in excess of 10 6 % has been obtained at 110 K, H = 6 T in La-Ca-Mn-O thin films epitaxially grown on LaAlO 3 substrates by pulsed laser deposition. The as-deposited film exhibits a substantial magnetoresistance value of 39,000%, which is further improved by heat treatment. A strong dependence of the magnetoresistance on film thickness was observed, with the value reduced by orders of magnitude when the film is made thicker than ∼2,000 angstrom. This behavior is interpreted in terms of lattice strain in the La-Ca-Mn-O films

Thermoelectric properties of Ca1-xYxMnO3 and Ca0.9Y0.1-yFeyMnO3 perovskite compounds

DEFF Research Database (Denmark)

Thuy, Nguyen Thi; Minh, Dang Le; Van Nong, Ngo

2012-01-01

Polycrystalline Ca1-xYxMnO3 (x = 0.0; 0.1; 0.3; 0.5; 0.7) and Ca0.9Y0.1-yFeyMnO3 (y = 0.00; 0.01; 0.03; 0.05) compounds were prepared by solid-state reaction. X-ray diffraction (XRD) analysis revealed all XRD peaks of all the samples as identical to the orthorhombic structure. The thermoelectric ...

Far-infrared phonon spectroscopy of Pb1-xMn xTe layers grown by molecular beam epitaxy

International Nuclear Information System (INIS)

Romcevic, N.; Nadolny, A.J.; Romcevic, M.; Story, T.; Taliashvili, B.; Milutinovic, A.; Trajic, J.; Lusakowska, E.; Vasiljevic-Radovic, D.; Domukhovski, V.; Osinniy, V.; Hadzic, B.; Dziawa, P.

2007-01-01

In this paper we used far-infrared spectroscopy, reflection high energy electron diffraction (RHEED), X-ray diffraction and atomic force microscopy (AFM) to investigate structural and optical properties of Pb 1-x Mn x Te layers grown by molecular beam epitaxy (MBE). A numerical model for calculating the reflectivity coefficient for complex systems which include films, buffer layer and substrate has been applied. The infrared reflectivity spectra consist of Pb 1-x Mn x Te phonons, which exhibit intermediate one-two mode behavior, and MnTe phonons. A good agreement between calculated and experimental spectra is achieved. We registered the local distribution of Mn impurities depending on substrate type. For films growth on BaF 2 substrate we registered the orthorhombic local structure of MnTe clusters, while in the case of KCl substrate this structure is cubic. The Pb 1-x Mn x Te long wavelength optical phonons were described by the modified Genzel's model

Magnetic behaviour of hydrogenated La_0_._5Ca_0_._5MnO_3

International Nuclear Information System (INIS)

Lal, Ganesh; Punia, Khushboo; Kumar, Sudhish; Jyoti; Dolia, S.N.

2016-01-01

The half doped manganite La_0_._5Ca_0_._5MnO_3 have attracted considerable attention owing to its complex electrical and magnetic properties. This work is focused on the effects of hydrogenation on the magnetic behaviour of La_0_._5Ca_0_._5MnO_3. For hydrogenation the La_0_._5Ca_0_._5MnO_3 sample was annealed in a hydrogen atmosphere at 600°C for 6 hours in a reduction furnace and for reducing hydrogen the sample was heated in air at 600°C for 6 hours in a chamber furnace. Room temperature X-ray diffraction studies confirmed that the hydrogenation and annealing of the sample in air does not affect the single phase orthorhombic structure of La_0_._5Ca_0_._5MnO_3. These observations indicate that magnetic behaviour of La_0_._5Ca_0_._5MnO_3. can be tailored by hydrogenation

Calcium EXAFS establishes the Mn-Ca cluster in the oxygen-evolving complex of Photosystem II

Energy Technology Data Exchange (ETDEWEB)

Cinco, Roehl M.; McFarlane Holman, Karen L.; Robblee, John H.; Yano, Junko; Pizarro, Shelly A.; Bellacchio, Emanuele; Sauer, Kenneth; Yachandra, Vittal K.

2002-08-02

The proximity of Ca to the Mn cluster of the photosynthetic water-oxidation complex is demonstrated by X-ray absorption spectroscopy. We have collected EXAFS data at the Ca K-edge using active PS II membrane samples that contain approximately 2 Ca per 4 Mn. These samples are much less perturbed than previously investigated Sr-substituted samples, which were prepared subsequent to Ca depletion. The new Ca EXAFS clearly shows backscattering from Mn at 3.4 angstroms, a distance that agrees with that surmised from previously recorded Mn EXAFS. This result is also consistent with earlier related experiments at the Sr K-edge, using samples that contained functional Sr, that show Mn is {approx}; 3.5 angstroms distant from Sr. The totality of the evidence clearly advances the notion that the catalytic center of oxygen evolution is a Mn-Ca heteronuclear cluster.

Mn-Cr dating of Fe- and Ca-rich olivine from 'quenched' and 'plutonic' angrite meteorites using Secondary Ion Mass Spectrometry

Science.gov (United States)

McKibbin, Seann J.; Ireland, Trevor R.; Amelin, Yuri; Holden, Peter

2015-05-01

Angrite meteorites are suitable for Mn-Cr relative dating (53Mn decays to 53Cr with a half life of 3.7 Myr) using Secondary Ion Mass Spectrometry (SIMS) because they contain olivine and kirschsteinite with very high 55Mn/52Cr ratios arising from very low Cr concentrations. Discrepant Mn-Cr and U-Pb time intervals between the extrusive or 'quenched' angrite D'Orbigny and some slowly cooled or 'plutonic' angrites suggests that some have been affected by secondary disturbances, but this seems to have occurred in quenched rather than in slow-cooled plutonic angrites, where such disturbance or delay of isotopic closure might be expected. Using SIMS, we investigate the Mn-Cr systematics of quenched angrites to higher precision than previously achieved by this method and extend our investigation to non-quenched (plutonic or sub-volcanic) angrites. High values of 3.54 (±0.18) × 10-6 and 3.40 (±0.19) × 10-6 (2-sigma) are found for the initial 53Mn/55Mn of the quenched angrites D'Orbigny and Sahara 99555, which are preserved by Cr-poor olivine and kirschsteinite. The previously reported initial 53Mn/55Mn value of D'Orbigny obtained from bulk-rock and mineral separates is slightly lower and was probably controlled by Cr-rich olivine. Results can be interpreted in terms of the diffusivity of Cr in this mineral. Very low Cr concentrations in Ca-rich olivine and kirschsteinite are probably charge balanced by Al; this substitutes for Si and likely diffuses at a very slow rate because Si is the slowest-diffusing cation in olivine. Diffusion in Cr-rich Mg-Fe olivine is probably controlled by cation vacancies because of deficiency in charge-balancing Al and is therefore more prone to disturbance. The higher initial 53Mn/55Mn found by SIMS for extrusive angrites is more likely to reflect closure of Cr in kirschsteinite at the time of crystallisation, simultaneous with closure of U-Pb and Hf-W isotope systematics for these meteorites obtained from pyroxenes. For the younger

High-pressure compressibility and vibrational properties of (Ca,Mn)CO ₃

Energy Technology Data Exchange (ETDEWEB)

Liu, Jin; Caracas, Razvan; Fan, Dawei; Bobocioiu, Ema; Zhang, Dongzhou; Mao, Wendy L.

2016-12-01

Knowledge of potential carbon carriers such as carbonates is critical for our understanding of the deep-carbon cycle and related geological processes within the planet. Here we investigated the high-pressure behavior of (Ca,Mn)CO₃ up to 75 GPa by synchrotron single-crystal X-ray diffraction, laser Raman spectroscopy, and theoretical calculations. MnCO₃-rich carbonate underwent a structural phase transition from the CaCO₃-I structure into the CaCO₃-VI structure at 45–48 GPa, while CaCO₃-rich carbonate transformed into CaCO₃-III and CaCO₃-VI at approximately 2 and 15 GPa, respectively. The equation of state and vibrational properties of MnCO₃-rich and CaCO₃-rich carbonates changed dramatically across the phase transition. The CaCO₃-VI-structured CaCO₃-rich and MnCO₃-rich carbonates were stable at room temperature up to at least 53 and 75 GPa, respectively. The addition of smaller cations (e.g., Mn²⁺, Mg²⁺, and Fe²⁺) can enlarge the stability field of the CaCO₃-I phase as well as increase the pressure of the structural transition into the CaCO₃-VI phase.

Optical annealing of CaF2:Mn for cooled optically stimulated luminescence

International Nuclear Information System (INIS)

Miller, S.D.; Stahl, K.A.; Endres, G.W.R.; McDonald, J.C.

1989-01-01

Optical annealing of the cooled optically stimulated luminescence in CaF 2 :Mn at room temperature has been demonstrated. The laser of choice for optical annealing of CaF 2 : Mn is a 326 nm helium-cadmium ultraviolet laser. A complete cycle of readout and annealing of the CaF 2 :Mn cooled optically stimulated dosemeters can now be accomplished without heating the dosemeters above room temperature. This annealing work represents the next step toward creating a proton-recoil-based fast neutron dosimetry system based on the cooled optically stimulated luminescence technique. (author)

Electrical and magnetic behavior of La0.7Ca0.3MnO3/La0.7Sr0.2Ca0.1MnO3 composites

International Nuclear Information System (INIS)

Phong, P.T.; Dai, N.V.; Manh, D.H.; Thanh, T.D.; Khiem, N.V.; Hong, L.V.; Phuc, N.X.

2010-01-01

The electrical transport properties and the magnetoresistance of La 0.7 Ca 0.3 MnO 3 /La 0.7 Sr 0.2 Ca 0.1 MnO 3 composites are investigated as a function of sintering temperature. On the basis of an analysis by X-ray powder diffraction and scanning electron microscopy we suggest that raising the sintering temperature enhanced the interfacial reaction and creates interfacial phases at the boundaries of the La 0.7 Ca 0.3 MnO 3 and La 0.7 Sr 0.2 Ca 0.1 MnO 3 . Results also show that in 3 kOe, and at the Curie temperature, the magnetoresistance value of 14% was observed for the composite sintered at 1300 o C. Based on the phenomenological equation for conductivity under a percolation approach, which depends on the phase segregation of ferromagnetic metallic clusters and paramagnetic insulating regions, we fitted the experimental resistivity-temperature data from 50-300 K and find that the activation barrier decreases as temperature is increased.

Porous quasi three-dimensional nano-Mn3O4 + PbO2 composite as supercapacitor electrode material

International Nuclear Information System (INIS)

Dan Yuanyuan; Lin Haibo; Liu Xiaolei; Lu Haiyan; Zhao Jingzhe; Shi Zhan; Guo Yupeng

2012-01-01

Highlights: ► We prepare nano-PbO 2 + Mn 3 O 4 composite material by composite deposition method. ► The nano-PbO 2 + Mn 3 O 4 composite has porous quasi three-dimensional structure. ► Maximum electrochemically effective area (R F ) of the composite is 72. ► The composite shows high specific capacitance up to ∼340 F g −1 . ► A general knowledge of the pesudocapacitance behavior of the composite is acquired. - Abstract: Nano-Mn 3 O 4 + PbO 2 composite electrode materials with different compositions are prepared by anodic composite electrodeposition in Pb 2+ plating solution containing suspended nano-Mn 3 O 4 particles (40–60 nm). The particles are synthesized via one-step homogeneous precipitation at low temperature. The composite materials are characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and scanning electron microscopy (SEM) analyses. The results indicate that the composite composed of γ-Mn 3 O 4 and β-PbO 2 is porous and quasi three-dimensional (3D), and its maximum electrochemically effective area ratio (R F ) is 72. The capacitance performance of the composite is determined by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and charge–discharge test. The composite shows a high specific capacitance up to 338 F g −1 .

Thermoluminescence of CaCO3:Dy and CaCO3:Mn

International Nuclear Information System (INIS)

Bapat, V.N.; Nambi, K.S.V.

1976-01-01

CaCO 3 samples doped with Dy and Mn were prepared in the laboratory by co-precipitation techniques. Thermoluminescence and emission spectra of these phosphors were studied and were compared with those of the naturally occuring calcite and undoped CaCO 3 samples. Dy-doping seems to give a more efficient phosphor and indicates a possibility of getting a better phosphor by a judicious choice of a rare earth doping of CaCO 3 . Interesting result have been obtained on the TL glow curve variations of these phosphors with different temperature treatments prior to irradiation. (author)

Evolution of electrical properties and domain configuration of Mn modified Pb(In1/2Nb1/2)O3-PbTiO3 single crystals

Science.gov (United States)

Qiao, Huimin; He, Chao; Yuan, Feifei; Wang, Zujian; Li, Xiuzhi; Liu, Ying; Guo, Haiyan; Long, Xifa

2018-04-01

The acceptor doped relaxor-based ferroelectric materials are useful for high power applications such as probes in ultrasound-guided high intensity focused ultrasound therapy. In addition, a high Curie temperature is desired because of wider temperature usage and improved temperature stability. Previous investigations have focused on Pb(Mg1/3Nb2/3)O3-PbTiO3 and Pb(Zn1/3Nb2/3)O3-PbTiO3 systems, which have a ultrahigh piezoelectric coefficient and dielectric constant, but a relatively low Curie temperature. It is desirable to study the binary relaxor-based system with a high Curie temperature. Therefore, Pb(In1/2Nb1/2)O3-PbTiO3 (PINT) single crystals were chosen to study the Mn-doped influence on their electrical properties and domain configuration. The evolution of ferroelectric hysteresis loops for doped and virgin samples exhibit the pinning effect in Mn-doped PINT crystals. The relaxation behaviors of doped and virgin samples are studied by fit of the modified Curie-Weiss law and Volgel-Fucher relation. In addition, a short-range correlation length was fitted to study the behavior of polar nanoregions based on the domain configuration obtained by piezoresponse force microscopy. Complex domain structures and smaller short-range correlation lengths (100-150 nm for Mn-doped PINT and >400 nm for pure PINT) were obtained in the Mn-doped PINT single crystals.

Ca-site substitution induced a metal-insulator transition in manganite CaMnO3

International Nuclear Information System (INIS)

Sousa, D.; Nunes, M.R.; Silveira, C.; Matos, I.; Lopes, A.B.; Melo Jorge, M.E.

2008-01-01

A systematic study of the A-site doping in Mn(IV)-rich perovskite manganites Ca 1-x Ho x MnO 3 , over a large homogeneity range (0.1 ≤ x ≤ 0.4), has been performed. A significant increase in the lattice parameters indicated the presence of mixed valence state of Mn: Mn 3+ and Mn 4+ . The substitution of calcium by holmium also induces strong changes in the electrical properties. We found that small Ho concentration produces an important decrease in the electrical resistivity and induces an electrical transition, the temperature corresponding to the metal-insulator transition (T MI ) shifts with the holmium content. This electrical behavior is attributed to the Mn 3+ ions content and a charge order effect

Ultrasonic Investigations on Polonides of Ba, Ca, and Pb

Science.gov (United States)

Singh, Devraj; Bhalla, Vyoma; Bala, Jyoti; Wadhwa, Shikha

2017-10-01

The temperature-dependent mechanical and ultrasonic properties of barium, calcium, and lead polonides (BaPo, CaPo, and PbPo) were investigated in the temperature range 100-300 K. The second- and third-order elastic constants (SOECs and TOECs) were computed using Coulomb and Born-Mayer potential and these in turn have been used to estimate other secondary elastic properties such as strength, anisotropy, microhardness, etc. The theoretical approach followed the prediction that BaPo, CaPo, and PbPo are brittle in nature. PbPo is found to be the hardest amongst the chosen compounds. Further the SOECs and TOECs are applied to determine ultrasonic velocities, Debye temperature, and acoustic coupling constants along , , and orientations at room temperature. Additionally thermal conductivity has been computed using Morelli and Slack's approach along different crystallographic directions at room temperature. Finally ultrasonic attenuation due to phonon-phonon interaction and thermoelastic relaxation mechanisms has been computed for BaPo, CaPo, and PbPo. The behaviour of these compounds is similar to that of semi-metals with thermal relaxation time of the order 10-11 s. The present computation study is reasonably in agreement with the available theoretical data for the similar type of materials.

Local Structure of Mn in (La1-xHox)2/3Ca1/3MnO3 Studied by X-ray Absorption Fine Structure

International Nuclear Information System (INIS)

Pietnoczka, A.; Bacewicz, R.; Antonowicz, J.; Zalewski, W.; Pekala, M.; Drozd, V.; Fagnard, J.F.; Vanderbemden, P.

2010-01-01

Results of X-ray absorption fine structure measurements in manganites (La 1-x Ho x ) 2/3 Ca 1/3 MnO 3 with 0.15 3 is doped with a divalent element such as Ca 2+ , substituting for La 3+ , holes are induced in the filled Mn d orbitals. This leads to a strong ferromagnetic coupling between Mn sites. Ca ions in La 1-x Ca x MnO 3 introduce a distortion of the crystal lattice and mixed valence Mn ions (Mn 3+ and Mn 4+ ). On the other hand, in manganites (La 1-x Ho x ) 2/3 Ca 1/3 MnO 3 the substitution of La for Ho causes a lattice distortion and induces a disorder, which reduces a magnetic interaction. The ferromagnetic transition temperature and conductivity decrease very quickly with increasing x. The magnetic and transport properties of compounds depend on the local atomic structure around Mn ions. The information on the bond lengths and Debye-Waller factor are obtained from the extended X-ray absorption fine structure (EXAFS) data analysis. The charge state of Mn is determined from the position of the absorption edge in X-ray absorption near edge structure (XANES) data. XAFS results are in good agreement with magnetic characteristics of the studied materials. (authors)

Magnetotransport of CaCu3Mn4O12 complex perovskite derivatives

International Nuclear Information System (INIS)

Sanchez-Benitez, J.; Andres, A. de; Garcia-Hernandez, M.; Alonso, J.A.; Martinez-Lope, M.J.

2006-01-01

Neutron powder diffraction, magnetic and magnetotransport studies were carried out on new derivatives of the CaCu 3 Mn 4 O 12 (A'A 3 B 4 O 12 ) complex perovskite. The samples were prepared in polycrystalline form under moderate pressure conditions. Substitutions at A and A' sites of CaCu 3 Mn 4 O 12 , with only Mn 4+ and insulating behavior, imply electron doping that affects the magnetic and transport properties. X-ray Absorption Spectroscopy showed that Mn 3+ /Mn 4+ valence mixing occurs only at B site, progressively filling the e g band and providing the metallic character in these compounds, as we observe in most of these samples. A semiconducting behavior is observed in samples with 50% Mn 3+ at B site. This can be understood by the opening of a gap in the conduction band corresponding to the half filling of the e g states. This is the case of the tetravalent rare earth doped samples (Ce and Th at A' site) and of the appropriate A site doped Ca(CuMn 2 )Mn 4 O 12 sample. At the strongly distorted A positions, Mn 3+ , with localized e g electrons, act as magnetic impurities at very low temperatures (<40 K) giving rise to the observed upturn in the resistivity. The magnetic origin of this scattering is evidenced by its drastic reduction under a magnetic field

Pathways of Pb and Mn observed in a 5-year longitudinal investigation in young children and environmental measures from an urban setting

International Nuclear Information System (INIS)

Gulson, Brian; Mizon, Karen; Taylor, Alan; Korsch, Michael; Davis, J. Michael; Louie, Honway; Wu, Michael; Gomez, Laura; Antin, Luminita

2014-01-01

We monitored 108 children ≤5 years on a 6-month basis for up to 5 years in a major urban setting. Samples (n ∼ 7000) included blood, urine, handwipes (interior, and after exterior playing), 6-day duplicate diet, drinking water, interior house and day care dust-fall accumulation using petri dishes, exterior dust-fall accumulation, exterior dust sweepings, paint, soil and urban air. The geometric mean blood Pb (PbB) was 2.1 μg/dL and blood Mn (MnB) was 10.0 μg/L. Following a path modelling approach, mixed model analyses for a fully adjusted model showed the strongest associations for PbB were with interior house dust and soil; for MnB there were no significant associations with any predictors. Predictor variables only explained 9% of the variance for Pb and 0.7% for Mn. Relationships between environmental measures and PbB in children are not straightforward; soil and dust sweepings contribute only about 1/5th of the amounts to PbB found in other studies. - Highlights: • 5-year longitudinal study of young children in urban setting. • Samples analysed for Pb and Mn in blood and environmental samples. • Modified structural equation modelling. • Strongest associations for blood Pb with house dust and soil. • Soil and dust contribute very small amounts to blood Pb. - This study provides useful insights about the environmental pathways leading to Pb and Mn exposure in young children

Local structure in LaMnO3 and CaMnO3 perovskites: A quantitative structural refinement of Mn K-edge XANES data

International Nuclear Information System (INIS)

Monesi, C.; Meneghini, C.; Bardelli, F.; Benfatto, M.; Mobilio, S.; Manju, U.; Sarma, D.D.

2005-01-01

Hole-doped perovskites such as La 1-x Ca x MnO 3 present special magnetic and magnetotransport properties, and it is commonly accepted that the local atomic structure around Mn ions plays a crucial role in determining these peculiar features. Therefore experimental techniques directly probing the local atomic structure, like x-ray absorption spectroscopy (XAS), have been widely exploited to deeply understand the physics of these compounds. Quantitative XAS analysis usually concerns the extended region [extended x-ray absorption fine structure (EXAFS)] of the absorption spectra. The near-edge region [x-ray absorption near-edge spectroscopy (XANES)] of XAS spectra can provide detailed complementary information on the electronic structure and local atomic topology around the absorber. However, the complexity of the XANES analysis usually prevents a quantitative understanding of the data. This work exploits the recently developed MXAN code to achieve a quantitative structural refinement of the Mn K-edge XANES of LaMnO 3 and CaMnO 3 compounds; they are the end compounds of the doped manganite series La x Ca 1-x MnO 3 . The results derived from the EXAFS and XANES analyses are in good agreement, demonstrating that a quantitative picture of the local structure can be obtained from XANES in these crystalline compounds. Moreover, the quantitative XANES analysis provides topological information not directly achievable from EXAFS data analysis. This work demonstrates that combining the analysis of extended and near-edge regions of Mn K-edge XAS spectra could provide a complete and accurate description of Mn local atomic environment in these compounds

An experimental and thermodynamic equilibrium investigation of the Pb, Zn, Cr, Cu, Mn and Ni partitioning during sewage sludge incineration.

Science.gov (United States)

Liu, Jingyong; Fu, Jiewen; Ning, Xun'an; Sun, Shuiyu; Wang, Yujie; Xie, Wuming; Huang, Shaosong; Zhong, Sheng

2015-09-01

The effects of different chlorides and operational conditions on the distribution and speciation of six heavy metals (Pb, Zn, Cr, Cu, Mn and Ni) during sludge incineration were investigated using a simulated laboratory tubular-furnace reactor. A thermodynamic equilibrium investigation using the FactSage software was performed to compare the experimental results. The results indicate that the volatility of the target metals was enhanced as the chlorine concentration increased. Inorganic-Cl influenced the volatilization of heavy metals in the order of Pb>Zn>Cr>Cu>Mn>Ni. However, the effects of organic-Cl on the volatility of Mn, Pb and Cu were greater than the effects on Zn, Cr and Ni. With increasing combustion temperature, the presence of organic-Cl (PVC) and inorganic-Cl (NaCl) improved the transfer of Pb and Zn from bottom ash to fly ash or fuse gas. However, the presence of chloride had no obvious influence on Mn, Cu and Ni. Increased retention time could increase the volatilization rate of heavy metals; however, this effect was insignificant. During the incineration process, Pb readily formed PbSiO4 and remained in the bottom ash. Different Pb compounds, primarily the volatile PbCl2, were found in the gas phase after the addition of NaCl; the dominant Pb compounds in the gas phase after the addition of PVC were PbCl2, Pb(ClO4)2 and PbCl2O4. Copyright © 2015. Published by Elsevier B.V.

CaSO4:DY,Mn: A new and highly sensitive thermoluminescence phosphor for versatile dosimetry

Science.gov (United States)

Bahl, Shaila; Lochab, S. P.; Kumar, Pratik

2016-02-01

With the advent of newer techniques for dose reduction coupled with the development of more sensitive detectors, the radiation doses in radiological medical investigation are decreasing. Nevertheless, keeping the tenet in mind that all radiation doses could entail risk, there is a need to develop more sensitive dosimeters capable of measuring low doses. This paper gives the account of the development of a new and sensitive phosphor CaSO4:Dy,Mn and its characterization. The standard production procedure based on the recrystallization method was used to prepare CaSO4:Dy,Mn. The Thermoluminescence (TL) studies were carried out by exposing it with gamma radiation (Cs-137) from 10 μGy to 100 Gy. The theoretical studies to determine the number of peaks and kinetic parameters related to the TL glow peaks in CaSO4:Dy,Mn was performed using the Computerized Glow Curve Deconvolution (CGCD) method. Experiments were performed to determine optimum concentration of the dopants Dysprosium (Dy) and Mangnese (Mn) in the host CaSO4 so that maximum sensitivity of the phosphor may be achieved. The optimum dopant concentration turned out to be 0.1 mol%. As there were two dopants Dy and Mn their relative ratio were varied in steps of 0.025 keeping the concentration of total dopant (Dy and Mn) 0.1 mol% always. The maximum TL intensity was seen in the CaSO4:Dy(0.025),Mn(0.075) combination. The TL sensitivity of this phosphor was found to be about 2 and 1.8 times higher than that of popular phosphor CaSO4:Dy and LiF:Mg,Cu,P (TLD-700H) respectively. This new phosphor CaSO4:Dy,Mn showed fading of 11% which is similar to that of the standard phosphor CaSO4:Dy. The paper concludes that the new, highly sensitive TL phosphor CaSO4:Dy,Mn has shown higher sensitivity and hence the potential to replace commonly used CaSO4:Dy.

Remediation of a historically Pb contaminated soil using a model natural Mn oxide waste.

Science.gov (United States)

McCann, Clare M; Gray, Neil D; Tourney, Janette; Davenport, Russell J; Wade, Matthew; Finlay, Nina; Hudson-Edwards, Karen A; Johnson, Karen L

2015-11-01

A natural Mn oxide (NMO) waste was assessed as an in situ remediation amendment for Pb contaminated sites. The viability of this was investigated using a 10 month lysimeter trial, wherein a historically Pb contaminated soil was amended with a 10% by weight model NMO. The model NMO was found to have a large Pb adsorption capacity (qmax 346±14 mg g(-1)). However, due to the heterogeneous nature of the Pb contamination in the soils (3650.54-9299.79 mg kg(-1)), no treatment related difference in Pb via geochemistry could be detected. To overcome difficulties in traditional geochemical techniques due to pollutant heterogeneity we present a new method for unequivocally proving metal sorption to in situ remediation amendments. The method combines two spectroscopic techniques; namely electron probe microanalysis (EPMA) and X-ray photoelectron spectroscopy (XPS). Using this we showed Pb immobilisation on NMO, which were Pb free prior to their addition to the soils. Amendment of the soil with exogenous Mn oxide had no effect on microbial functioning, nor did it perturb the composition of the dominant phyla. We conclude that NMOs show excellent potential as remediation amendments. Copyright © 2015 The Authors. Published by Elsevier Ltd.. All rights reserved.

Metal-insulator transition and magnetic properties of La - (Ba/Ca) - Mn - O compounds

International Nuclear Information System (INIS)

Anbarasu, V.; Manigandan, A.; Sathiyakumar, S.; Jayabalan, K.; Kaliyaperumal, L.K.

2009-01-01

The manganite compounds La 2 BaMn (3+x) P y (where x = 0, 0.5 and 1) and La 2 CaMn 3 O y have been prepared for the importance in the field of magneto resistance materials through solid-state reaction technique. From the Powder XRD patterns it was confirmed that both compounds were in single phase and the refined crystal system matches with superconducting perovskite structure and the lattice parameters were calculated as a = 3.892( 6) A, b = 3.899(3) A and c = 11.619(8) A for La 2 BaMn 3 O y ; a = 3.851(3) A, b = 3.891(9) A and c = 11.542(7) A for La 2 CaMn 3 O y . The low temperature resistivity measurement reveals that the compound La 2 BaMn 3 O y exhibiting M - I transition and the transition temperature was found to be 270 K. The study on magnetization nature of the La 2 BaMn 3+x Oy (where x = 0, 0.5 and I) compounds through vibrating sample magnetometer confirms the superparamagnetic nature at room temperature condition where as La 2 CaMn 3 O y exhibits paramagnetic nature. The structural relations between the prepared manganite systems La 2 BaMn 3 O y and La 2 CaMn 3 O y with superconducting perovskite compound LaBa 2 Cu 3 O 7-y was studied with the technological application of magneto resistive property of the prepared compounds. (author)

Ultrasonic investigations on polonides of Ba, Ca, and Pb

Energy Technology Data Exchange (ETDEWEB)

Singh, Devraj; Bhalla, Vyoma [Amity School of Engineering and Technology, New Delhi (India). Dept. of Applied Physics; Bala, Jyoti [Amity School of Engineering and Technology, New Delhi (India). Dept. of Applied Physics; Guru Gobind Singh Indraprastha Univ., New Delhi (India). USICT; Wadhwa, Shikha [Amity Univ., Noida (India). Amity Inst. of Nanotechnology

2017-07-01

The temperature-dependent mechanical and ultrasonic properties of barium, calcium, and lead polonides (BaPo, CaPo, and PbPo) were investigated in the temperature range 100-300 K. The second- and third-order elastic constants (SOECs and TOECs) were computed using Coulomb and Born-Mayer potential and these in turn have been used to estimate other secondary elastic properties such as strength, anisotropy, microhardness, etc. The theoretical approach followed the prediction that BaPo, CaPo, and PbPo are brittle in nature. PbPo is found to be the hardest amongst the chosen compounds. Further the SOECs and TOECs are applied to determine ultrasonic velocities, Debye temperature, and acoustic coupling constants along left angle 100 right angle, left angle 110 right angle, and left angle 111 right angle orientations at room temperature. Additionally thermal conductivity has been computed using Morelli and Slack's approach along different crystallographic directions at room temperature. Finally ultrasonic attenuation due to phonon-phonon interaction and thermoelastic relaxation mechanisms has been computed for BaPo, CaPo, and PbPo. The behaviour of these compounds is similar to that of semi-metals with thermal relaxation time of the order 10{sup -11} s. The present computation study is reasonably in agreement with the available theoretical data for the similar type of materials.

Determination of Fe, Hg, Mn, and Pb in three-rings of poplar (Populus alba L.) by U-shaped DC arc

Science.gov (United States)

Marković, D. M.; Novović, I.; Vilotić, D.; Ignjatović, Lj.

2007-09-01

The U-shaped DC arc with aerosol supply was applied for the determination of Fe, Hg, Mn, and Pb in poplar (Populus alba L.) tree-rings. By optimization of the operating parameters and by selection of the most appropriate signal integration time (20 s for Fe, Mn, and Pb and 30 s for Hg), the obtained limits of detection for Fe, Hg, Mn, and Pb are 5.8, 2.6, 1.6, and 2.0 ng/ml, respectively. The detection limits achieved by this method for Fe, Hg, Mn, and Pb are comparable with the detection limits obtained for these elements by such methods as inductively coupled plasma-atomic emission spectrometry (ICP-AES), direct coupled plasmatomic emission spectrometry (DCP-AES), and microwave-induced plasma-atomic emission spectrometry (MIP-AES). We used the tree-rings of poplar from two different locations. The first one is in the area close to the power plant “Nikola Tesla” TENT A, Obrenovac, while the other one is in the urban area of Novi Sad. In almost all cases, samples from the location at Obrenovac registered elevated average concentrations of Fe, Hg, Mn, and Pb in the tree-rings of poplar.

Determination of Ca, Cu, Fe and Pb in sugarcane raw spirits by atomic absorption spectrophotometry

International Nuclear Information System (INIS)

Lorenzo, Magdalena; Reyes, Arlyn; Blanco, Idania; Vasallo, Maria C

2010-01-01

The determination of Ca, Cu, Fe and Pb in sugarcane raw spirits by atomic absorption spectrophotometry was carried out. For 20 μL injected sample, calibration within the 0,5-25,0 mg. L -1 Ca; 0,25-5,0 mg. L -1 Cu, Pb and Cu intervals were established using the ratios Cu, Ca, Fe and Pb absorbance versus analyte concentration, respectively. Typical linear correlations of r = 0,999 were obtained. The proposed method was applied for the direct determination of Ca, Cu, Fe and Pb in sugar cane spirits, and in samples. The results obtained were in accordance to those obtained at 95% confidence level

Postsynthetic Doping of MnCl2 Molecules into Preformed CsPbBr3 Perovskite Nanocrystals via a Halide Exchange-Driven Cation Exchange.

Science.gov (United States)

Huang, Guangguang; Wang, Chunlei; Xu, Shuhong; Zong, Shenfei; Lu, Ju; Wang, Zhuyuan; Lu, Changgui; Cui, Yiping

2017-08-01

Unlike widely used postsynthetic halide exchange for CsPbX 3 (X is halide) perovskite nanocrystals (NCs), cation exchange of Pb is of a great challenge due to the rigid nature of the Pb cationic sublattice. Actually, cation exchange has more potential for rendering NCs with peculiar properties. Herein, a novel halide exchange-driven cation exchange (HEDCE) strategy is developed to prepare dually emitting Mn-doped CsPb(Cl/Br) 3 NCs via postsynthetic replacement of partial Pb in preformed perovskite NCs. The basic idea for HEDCE is that the partial cation exchange of Pb by Mn has a large probability to occur as a concomitant result for opening the rigid halide octahedron structure around Pb during halide exchange. Compared to traditional ionic exchange, HEDCE is featured by proceeding of halide exchange and cation exchange at the same time and lattice site. The time and space requirements make only MnCl 2 molecules (rather than mixture of Mn and Cl ions) capable of doping into perovskite NCs. This special molecular doping nature results in a series of unusual phenomenon, including long reaction time, core-shell structured mid states with triple emission bands, and dopant molecules composition-dependent doping process. As-prepared dual-emitting Mn-doped CsPb(Cl/Br) 3 NCs are available for ratiometric temperature sensing. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Synthesis, microstructure and EPR of CaMnO{sub 3} and Eu{sub x}Ca{sub 1-x}MnO{sub 3} manganite, obtained by coprecipitation

Energy Technology Data Exchange (ETDEWEB)

Santiago T, M.; Hernandez C, L.; Legorreta G, F. [Universidad Autonoma del Estado de Hidalgo, AACTyM, Carretera Pachuca-Tulancingo Km 4.5, 42074 Pachuca, Hidalgo (Mexico); Montiel S, H. [UNAM, Centro de Ciencias Aplicadas y Desarrollo Tecnologico, Departamento de Tecnociencias, Ciudad Universitaria, 04510 Mexico D. F. (Mexico); Alvarez L, G. [IPN, Escuela Superior de Fisica y Matematicas, Departamento de Fisica, U. P. Adolfo Lopez Mateos, Edif. 9, Col. Lindavista, 07738 Mexico D. F. (Mexico); Flores G, M. A., E-mail: mar200878@hotmail.com [Universidad Politecnica de Pachuca, Laboratorio de Nanotecnologia y Bioelectromagnetismo Aplicado, Carretera Pachuca-Cd. Sahagun Km 20, Ex-Hacienda de Santa Barbara, 43830 Zempoala, Hidalgo (Mexico)

2011-07-01

The synthesis of CaMnO{sub 3} and Eu{sub x}Ca{sub 1-x}MnO{sub 3} obtained by coprecipitation method is showed. The synthesized samples were characterized by X-ray diffraction and scanning electronic microscopy, the powders showed orthorhombic structure and pnma space group. When it was doped with Europium, their morphology tendency was spherical. Measurements were carried out on electron paramagnetic resonance (EPR) with constant frequency = 9.4 GHz (band X) and dc magnetic field (H dc) 0-0.8 T, measurements were at 300 K and 77 K. EPR spectra showed significant differences between both samples, indicating that the substitution of divalent alkaline earth cations by trivalent rare earth ions, allowing the formation of a mixed valence state of manganese, Mn{sup 3+} and Mn{sup 4+}. A 77 K, the manganite of concentration x = 0.30 had a magnetic ordering, noted by the presence of hysteresis. (Author)

Piezoelectric properties and temperature stability of Mn-doped Pb(Mg1/3Nb2/3)-PbZrO3-PbTiO3 textured ceramics

Science.gov (United States)

Yan, Yongke; Cho, Kyung-Hoon; Priya, Shashank

2012-03-01

In this letter, we report the electromechanical properties of textured 0.4Pb(Mg1/3Nb2/3)O3-0.25PbZrO3-0.35PbTiO3 (PMN-PZT) composition which has relatively high rhombohedral to tetragonal (R-T) transition temperature (TR-T of 160 °C) and Curie temperature (TC of 234 °C) and explore the effect of Mn-doping on this composition. It was found that MnO2-doped textured PMN-PZT ceramics with 5 vol. % BaTiO3 template (T-5BT) exhibited inferior temperature stability. The coupling factor (k31) of T-5BT ceramic started to degrade from 75 °C while the random counterpart showed a very stable tendency up to 180 °C. This degradation was associated with the "interface region" formed in the vicinity of BT template. MnO2 doped PMN-PZT ceramics textured with 3 vol. % BT and subsequently poled at 140 °C (T-3BT140) exhibited very stable and high k31 (>0.53) in a wide temperature range from room temperature to 130 °C through reduction in the interface region volume. Further, the T-3BT140 ceramic exhibited excellent hard and soft combinatory piezoelectric properties of d33 = 720 pC/N, k31 = 0.53, Qm = 403, tan δ = 0.3% which are very promising for high power and magnetoelectric applications.

Synthesis and properties of a new quadruple perovskite: A-site ordered PbMn{sub 3}Mn{sub 4}O{sub 12}

Energy Technology Data Exchange (ETDEWEB)

Locherer, T.; Dinnebier, R.; Kremer, R.K. [Max Planck Institute for Solid State Research, Heisenbergstr. 1, D-70569 Stuttgart (Germany); Greenblatt, M., E-mail: martha@rutchem.rutgers.edu [Department of Chemistry and Chemical Biology, Rutgers University, Piscataway, NJ 08854 (United States); Jansen, M. [Max Planck Institute for Solid State Research, Heisenbergstr. 1, D-70569 Stuttgart (Germany)

2012-06-15

PbMn{sub 3}Mn{sub 4}O{sub 12} a quadruple perovskite was prepared by high pressure and high temperature synthesis. Powder X-ray diffraction (PXD) and differential scanning calorimetry reveal a structural phase transition at {approx}380 K. Rietveld refinement of the synchrotron room temperature data indicate rhombohedral symmetry (R-3) with a=6.43675(4) A and {alpha}=109.556(2) Degree-Sign . Similar 423 K PXD data refined in a body centered cubic cell (Im-3) with a=7.4283(9) A. The temperature variation of magnetization, shows a magnetic field dependent antiferromagnetic-like transition at 68 K, and dynamic fluctuations indicative of magnetic frustration. The semiconducting electrical behavior indicates a large decrease in the conductivity near 68 K. The temperature dependence of the real part of the dielectric constant, {epsilon}{sub real} increases dramatically at {approx}68 K, and shows relaxor-type ferroelectric behavior as a function of frequency. The intimate coupling of magnetic, electrical and dielectric properties at 68 K in PbMn{sub 3}Mn{sub 4}O{sub 12} suggests possible multiferroic behavior. - Graphical abstract: Resistance vs. temperature plot showing drastically increasing resistances at temperatures below 68 K (a). Formation of a frequency dependency of the dielectric constant between 68 K and ambient temperature (b). Sharp cusp in the magnetic susceptibility observed at 68 K which is suppressed with increasing magnetic field (c) indicates coupling of magnetic, electric and dielectric effects. Highlights: Black-Right-Pointing-Pointer PbMn{sub 3}Mn{sub 4}O{sub 12} a quadruple perovskite was prepared at high pressure. Black-Right-Pointing-Pointer A structural transition is seen at 380 K from space group R-3-to-Im-3. Black-Right-Pointing-Pointer An antiferromagnetic transition is observed at 68 K. Black-Right-Pointing-Pointer It is semiconducting with a large decrease in the conductivity near 68 K. Black-Right-Pointing-Pointer The temperature dependence

Pathways of Pb and Mn observed in a 5-year longitudinal investigation in young children and environmental measures from an urban setting.

Science.gov (United States)

Gulson, Brian; Mizon, Karen; Taylor, Alan; Korsch, Michael; Davis, J Michael; Louie, Honway; Wu, Michael; Gomez, Laura; Antin, Luminita

2014-08-01

We monitored 108 children ≤5 years on a 6-month basis for up to 5 years in a major urban setting. Samples (n ∼ 7000) included blood, urine, handwipes (interior, and after exterior playing), 6-day duplicate diet, drinking water, interior house and day care dust-fall accumulation using petri dishes, exterior dust-fall accumulation, exterior dust sweepings, paint, soil and urban air. The geometric mean blood Pb (PbB) was 2.1 μg/dL and blood Mn (MnB) was 10.0 μg/L. Following a path modelling approach, mixed model analyses for a fully adjusted model showed the strongest associations for PbB were with interior house dust and soil; for MnB there were no significant associations with any predictors. Predictor variables only explained 9% of the variance for Pb and 0.7% for Mn. Relationships between environmental measures and PbB in children are not straightforward; soil and dust sweepings contribute only about 1/5th of the amounts to PbB found in other studies. Copyright © 2014 Elsevier Ltd. All rights reserved.

Ferroelectricity-induced resistive switching in Pb(Zr0.52Ti0.48)O3/Pr0.7Ca0.3MnO3/Nb-doped SrTiO3 epitaxial heterostructure

Science.gov (United States)

Md. Sadaf, Sharif; Mostafa Bourim, El; Liu, Xinjun; Hasan Choudhury, Sakeb; Kim, Dong-Wook; Hwang, Hyunsang

2012-03-01

We investigated the effect of a ferroelectric Pb(Zr0.52Ti0.48)O3 (PZT) thin film on the generation of resistive switching in a stacked Pr0.7Ca0.3MnO3 (PCMO)/Nb-doped SrTiO3 (Nb:STO) heterostructure forming a p-n junction. To promote the ferroelectric effect, the thin PZT active layer was deposited on an epitaxially grown p-type PCMO film on a lattice-matched n-type Nb:STO single crystal. It was concluded that the observed resistive switching behavior in the all-perovskite Pt/PZT/PCMO/Nb:STO heterostructure was related to the modulation of PCMO/Nb:STO p-n junction's depletion width, which was caused either by the PZT ferroelectric polarization field effect, the electrochemical drift of oxygen ions under an electric field, or both simultaneously.

Formation of stable and metastable phases in reciprocal systems PbSe + MI2 = MSe + PbI2 (M = Hg, Mn, Sn)

International Nuclear Information System (INIS)

Odin, I.N.; Grin'ko, V.V.; Kozlovskij, V.F.; Safronov, E.V.; Gapanovich, M.V.

2004-01-01

Using data of differential thermal, X-ray phase and microstructural analyses, phase diagrams of reciprocal systems PbSe + MI 2 = MSe + PbI 2 (M=Hg (1), Mn (2), Sn (3)) were constructed. It was ascertained that the HgSe-PbI 2 diagonal in system 1 is stable. Transformations leading to crystallization of metastable ternary compound formed in the system PbSe-PbI 2 and metastable polytypes of lead iodide in systems 1 and 2 in the range of temperatures from 620 to 685 K were studied. New intermediate metastable phases in systems 1, 2 and 3 were prepared by melt quenching. Crystal lattice parameters of the phases crystallizing in the CdCl 2 structural type were defined [ru

Interrelation between domain structures and polarization switching in hybrid improper ferroelectric Ca3(Mn,Ti)2O7

Science.gov (United States)

Gao, Bin; Huang, Fei-Ting; Wang, Yazhong; Kim, Jae-Wook; Wang, Lihai; Lim, Seong-Joon; Cheong, Sang-Wook

2017-05-01

Ca3Mn2O7 and Ca3Ti2O7 have been proposed as the prototypical hybrid improper ferroelectrics (HIFs), and a significant magnetoelectric (ME) coupling in magnetic Ca3Mn2O7 is, in fact, reported theoretically and experimentally. Although the switchability of polarization is confirmed in Ca3Ti2O7 and other non-magnetic HIFs, there is no report of switchable polarization in the isostructural Ca3Mn2O7. We constructed the phase diagram of Ca3Mn2-xTixO7 through our systematic study of a series of single crystalline Ca3Mn2-xTixO7 (x = 0, 0.1, 1, 1.5, and 2). Using transmission electron microscopy, we have unveiled the unique domain structure of Ca3Mn2O7: the high-density 90° stacking of a- and b-domains along the c-axis due to the phase transition through an intermediate Acca phase and the in-plane irregular wavy ferroelastic twin domains. The interrelation between domain structures and physical properties is unprecedented: the stacking along the c-axis prevents the switching of polarization and causes the irregular in-plane ferroelastic domain pattern. In addition, we have determined the magnetic phase diagram and found complex magnetism of Ca3Mn2O7 with isotropic canted moments. These results lead to negligible observable ME coupling in Ca3Mn2O7 and guide us to explore multiferroics with large ME coupling.

Chemical abrasion-SIMS (CA-SIMS) U-Pb dating of zircon from the late Eocene Caetano caldera, Nevada

Science.gov (United States)

Watts, Kathryn E.; Coble, Matthew A.; Vazquez, Jorge A.; Henry, Christopher D.; Colgan, Joseph P.; John, David A.

2016-01-01

Zircon geochronology is a critical tool for establishing geologic ages and time scales of processes in the Earth's crust. However, for zircons compromised by open system behavior, achieving robust dates can be difficult. Chemical abrasion (CA) is a routine step prior to thermal ionization mass spectrometry (TIMS) dating of zircon to remove radiation-damaged parts of grains that may have experienced open system behavior and loss of radiogenic Pb. While this technique has been shown to improve the accuracy and precision of TIMS dating, its application to high-spatial resolution dating methods, such as secondary ion mass spectrometry (SIMS), is relatively uncommon. In our efforts to U-Pb date zircons from the late Eocene Caetano caldera by SIMS (SHRIMP-RG: sensitive high resolution ion microprobe, reverse geometry), some grains yielded anomalously young U-Pb ages that implicated Pb-loss and motivated us to investigate with a comparative CA and non-CA dating study. We present CA and non-CA 206Pb/238U ages and trace elements determined by SHRIMP-RG for zircons from three Caetano samples (Caetano Tuff, Redrock Canyon porphyry, and a silicic ring-fracture intrusion) and for R33 and TEMORA-2 reference zircons. We find that non-CA Caetano zircons have weighted mean or bimodal U-Pb ages that are 2–4% younger than CA zircons for the same samples. CA Caetano zircons have mean U-Pb ages that are 0.4–0.6 Myr older than the 40Ar/39Ar sanidine eruption age (34.00 ± 0.03 Ma; error-weighted mean, 2σ), whereas non-CA zircons have ages that are 0.7–1.3 Myr younger. U-Pb ages do not correlate with U (~ 100–800 ppm), Th (~ 50–300 ppm) or any other measured zircon trace elements (Y, Hf, REE), and CA and non-CA Caetano zircons define identical trace element ranges. No statistically significant difference in U-Pb age is observed for CA versus non-CA R33 or TEMORA-2 zircons. Optical profiler measurements of ion microprobe pits demonstrate consistent depths of ~ 1.6�

Thermal evolution of low-temperature manganese centers in X-irradiated CaF2:Mn

International Nuclear Information System (INIS)

Jahan, M.S.; Cooke, D.W.

1984-01-01

Thermal evolution of the radiation-induced defects in CaF 2 :Mn (0.1% by weight) are investigated by ESR techniques. The Mn + resonance is found to decay at 200 K with an activation energy of 0.44 eV and frequency factor 2.8 x 10 8 s -1 which agree with previous luminescence and optical absorption measurements. This activation energy and decay temperature also agree with that of the previously described H center. It is concluded that the luminescence in CaF 2 :Mn results from thermal release of holes at H centers with ultimate recombination at Mn + ions producing excited state Mn 2+ (*). Relaxation yields the observed 500 nm emission characteristic of Mn 2+ . A second defect which decays at 150 K is observed but not identified. (author)

The Properties of CaSO{sub 4}: Mn Thermoluminescence Dosimeters

Energy Technology Data Exchange (ETDEWEB)

Bjaerngard, Bengt

1963-06-15

The properties of the radio thermoluminescence of CaSO{sub 4}:Mn, used for dosimetry of gamma and roentgen radiation, have been investigated. The light yield of the luminophore has been determined to 1.5 percent for 1 MeV gamma radiation. The dependence of the thermoluminescence light sum on the exposure, the exposure rate, and the exposure time can qualitatively be described by the first order process model, modified by a broad energy distribution of the electron trap depths. Some applications are discussed. The cheapness of the dosimeters, the convenient read-out, and the broad range of measurable exposures suggest that CaSO{sub 4}:Mn can be a valuable complement to other dosimetry systems.

Capture reactions of 40Ca and 48Ca with targets of 197Au and 208Pb

International Nuclear Information System (INIS)

Stokstad, R.; Chan, Y.; Chavez, E.

1988-03-01

The reactions of 40 Ca and 48 Ca with targets of 197 Au and 208 Pb have been measured in the region from below the interaction barrier to about twice the barrier energy. The fission-like fragments were detected in a pair of position-sensitive, multi-wire proportional counters and were identified from measurements of position and time using two-body kinematics. In the region above the barrier the cross sections for capture are less than those given by the touching condition, indicating that an /open quotes/extra push/close quotes/ is required to induce capture. The observations for 40 Ca and 48 Ca show different fissilities for the onset of the extra push and indicate that charge equilibration may be an important factor governing capture reactions. Below the barrier the cross sections show an enhancement relative to the prediction for a one dimensional barrier. The enhancements are larger for 40 Ca than for 48 Ca (for both targets) and this is in qualitative agreement with predictions based on the coupling of the relative motion to low-lying collective states. Both above and below the barrier, we find that the change in the light partner, from 48 Ca to 40 Ca, has a larger effect on the cross sections than the change from 208 Pb to 197 Au, after correction for the change in the Coulomb barrier. 16 refs., 7 figs

Functionalization of biomass carbonaceous aerogels: selective preparation of MnO2@CA composites for supercapacitors.

Science.gov (United States)

Ren, Yumei; Xu, Qun; Zhang, Jianmin; Yang, Hongxia; Wang, Bo; Yang, Daoyuan; Hu, Junhua; Liu, Zhimin

2014-06-25

Functionalized porous carbon materials with hierarchical structure and developed porosity coming from natural and renewable biomass have been attracting tremendous attention recently. In this work, we present a facile and scalable method to synthesize MnO2 loaded carbonaceous aerogel (MnO2@CA) composites via the hydrothermal carbonaceous (HTC) process. We employ two reaction systems of the mixed metal ion precursors to study the optimal selective adsorption and further reaction of MnO2 precursor on CA. Our experimental results show that the system containing KMnO4 and Na2S2O3·5H2O exhibits better electrochemical properties compared with the reaction system of MnSO4·H2O and (NH4)2S2O8. For the former, the obtained MnO2@CA displays the specific capacitance of 123.5 F·g(-1). The enhanced supercapacitance of MnO2@CA nanocomposites could be ascribed to both electrochemical contributions of the loaded MnO2 nanoparticles and the porous structure of three-dimensional carbonaceous aerogels. This study not only indicates that it is vital for the reaction systems to match with porous carbonaceous materials, but also offers a new fabrication strategy to prepare lightweight and high-performance materials that can be used in energy storage devices.

Prediction of possible CaMnO3 modifications using an ab initio minimization data-mining approach.

Science.gov (United States)

Zagorac, Jelena; Zagorac, Dejan; Zarubica, Aleksandra; Schön, J Christian; Djuris, Katarina; Matovic, Branko

2014-10-01

We have performed a crystal structure prediction study of CaMnO3 focusing on structures generated by octahedral tilting according to group-subgroup relations from the ideal perovskite type (Pm\\overline 3 m), which is the aristotype of the experimentally known CaMnO3 compound in the Pnma space group. Furthermore, additional structure candidates have been obtained using data mining. For each of the structure candidates, a local optimization on the ab initio level using density-functional theory (LDA, hybrid B3LYP) and the Hartree--Fock (HF) method was performed, and we find that several of the modifications may be experimentally accessible. In the high-pressure regime, we identify a post-perovskite phase in the CaIrO3 type, not previously observed in CaMnO3. Similarly, calculations at effective negative pressure predict a phase transition from the orthorhombic perovskite to an ilmenite-type (FeTiO3) modification of CaMnO3.

Energy transfer of the quantum-cutter couple Pr{sup 3+}–Mn{sup 2+} in CaF{sub 2}:Pr{sup 3+}, Mn{sup 2+} nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Kuzmanoski, Ana [Karlsruhe Institute of Technology (KIT), Institute of Inorganic Chemistry, Engesserstraße 15, D-76131 Karlsruhe (Germany); Pankratov, Vladimir, E-mail: vpank@latnet.lv [Research Center of Molecular Materials, University of Oulu, PO Box 3000, 90014 Oulu (Finland); Feldmann, Claus, E-mail: claus.feldmann@kit.edu [Karlsruhe Institute of Technology (KIT), Institute of Inorganic Chemistry, Engesserstraße 15, D-76131 Karlsruhe (Germany)

2016-11-15

CaF{sub 2}:Pr (1 mol%), CaF{sub 2}:Mn (5 mol%) and CaF{sub 2}:Pr,Mn (1 mol%, 5 mol%) nanoparticles are prepared via a microwave-mediated synthesis in ionic liquids. The nanoparticles are highly crystalline and exhibit particle diameters <50 nm.In contrast to bulk-CaF{sub 2}:Pr,Mn,energy transfer between Pr{sup 3+}and Mn{sup 2+}under {sup 1}S{sub 0}→{sup 1}I{sub 6} relaxation on Pr{sup 3+} and {sup 4}G({sup 4}T{sub 1g})→{sup 6}S(A{sub 1g}) emission of Mn{sup 2+} is observed for the first time. Such energy transfer represents the essential first step of the quantum-cutting cascade via the Pr{sup 3+}–Mn{sup 2+} couple, which is most interesting as both expected photons – {sup 3}P{sub 0}→{sup 3}H{sub 4} emission of Pr{sup 3+}and {sup 4}G({sup 4}T{sub 1g})→{sup 6}S(A{sub 1g}) emission of Mn{sup 2+} – are emitted in the green spectral range. While bulk crystals were said not to show energy transfer due to prohibiting selection rules, vacuum ultraviolet (VUV) spectroscopy of CaF{sub 2}:Pr, Mn nanoparticles firstly proves efficient Pr{sup 3+}→Mn{sup 2+} energy transfer, which can be ascribed to the reduced site symmetry and considerable spin–orbit interaction in the nanocrystals.

Exchange bias in (La,Ca)MnO3 bilayers: influence of cooling process

International Nuclear Information System (INIS)

Restrepo-Parra, E; Agudelo, J D; Restrepo, J

2012-01-01

The exchange bias (EB) phenomenon in La 2/3 Ca 1/3 MnO 3 /La 1/3 Ca 2/3 MnO 3 bilayers was studied using Monte Carlo simulations combined with the Heisenberg model and the Metropolis algorithm. These simulations were carried out using the model proposed by Kiwi for an uncompensated interface. The Hamiltonian considered several terms corresponding to the nearest neighbor interaction, magnetocrystalline anisotropy and Zeeman effect. Several interactions in the ferromagnetic (FM), antiferromagnetic (AFM) and FM/AFM interface were considered, depending on the type of interacting ion (Mn 3+eg , Mn 3+eg′ or Mn 4+d3 ). The influence of field cooling and cooling temperature on the EB was analyzed and discussed. Regarding the field cooling, it caused an increase in the EB until a certain critical value was reached. After that, its effect was almost negligible. On the other hand, at low values of cooling temperature, not only the EB but also the coercive field were enhanced. (paper)

Luminescent properties and energy transfer of CaO:Ce3+, Mn2+ phosphors for white LED

International Nuclear Information System (INIS)

Liu, Qipeng; Yin, Huijun; Liu, Tao; Wang, CuiQing; Liu, Riqiang; Lü, Wei; You, Hongpeng

2016-01-01

We have synthesized yellow–orange CaO:Ce 3+ ,Mn 2+ phosphors by solid-state reaction. Photoluminescence properties and energy transfer mechanism from Ce 3+ to Mn 2+ ions have been investigated. The Ce 3+ activated phosphors exhibit strong absorption in the range of 250–490 nm and a yellow emission centered at 554 nm. When Mn 2+ ions were codoped, CaO:Ce 3+ ,Mn 2+ phosphors exhibit yellow emission band of Ce 3+ as well as orange emission band centered at 600 nm of Mn 2+ . We observed an efficient energy transfer from Ce 3+ to Mn 2+ ions in CaO:Ce 3+ ,Mn 2+ , which was verified from the lifetime decay curves and was discussed by Dexter's energy transfer theory. The critical distance of the energy transfer from Ce 3+ to Mn 2+ ions has also been calculated to be 12.3 Å by spectral overlap methods following Dexter's theory and by concentration quenching mechanism to be 15.2 Å. Moreover, by combining the synthesized phosphors and InGaN blue chip (460 nm), warm-white light has been created.

Direct determination of Cu, Mn, Pb, and Zn in beer by thermospray flame furnace atomic absorption spectrometry

International Nuclear Information System (INIS)

Nascentes, Clesia C.; Kamogawa, Marcos Y.; Fernandes, Kelly G.; Arruda, Marco A.Z.; Nogueira, Ana Rita A.; Nobrega, Joaquim A.

2005-01-01

In this work, thermospray flame furnace atomic absorption spectrometry (TS-FF-AAS) was employed for Cu, Mn, Pb, and Zn determination in beer without any sample digestion. The system was optimized and calibration was based on the analyte addition technique. A sample volume of 300 μl was introduced into the hot Ni tube at a flow-rate of 0.4 ml min -1 using 0.14 mol l -1 nitric acid solution or air as carrier. Different Brazilian beers were directly analyzed after ultrasonic degasification. Results were compared with those obtained by graphite furnace atomic absorption spectrometry (GFAAS). The detection limits obtained for Cu, Mn, Pb, and Zn in aqueous solution were 2.2, 18, 1.6, and 0.9 μg l -1 , respectively. The relative standard deviations varied from 2.7% to 7.3% (n=8) for solutions containing the analytes in the 25-50 μg l -1 range. The concentration ranges obtained for analytes in beer samples were: Cu: 38.0-155 μg l -1 ; Mn: 110-348 μg l -1 , Pb: 13.0-32.9 μg l -1 , and Zn: 52.7-226 μg l -1 . Results obtained by TS-FF-AAS and GFAAS were in agreement at a 95% confidence level. The proposed method is fast and simple, since sample digestion is not required and sensitivity can be improved without using expensive devices. The TS-FF-AAS presented suitable sensitivity for determination of Cu, Mn, Pb, and Zn in the quality control of a brewery

Exploring As-Cast PbCaSn-Mg Anodes for Improved Performance in Copper Electrowinning

Science.gov (United States)

Yuwono, Jodie A.; Clancy, Marie; Chen, Xiaobo; Birbilis, Nick

2018-06-01

Lead calcium tin (PbCaSn) alloys are the common anodes used in copper electrowinning (Cu EW). Given a large amount of energy consumed in Cu EW process, anodes with controlled oxygen evolution reaction (OER) kinetics and a lower OER overpotential are advantageous for reducing the energy consumption. To date, magnesium (Mg) has never been studied as an alloying element for EW anodes. As-cast PbCaSn anodes with the addition of Mg were examined herein, revealing an improved performance compared to that of the industrial standard PbCaSn anode. The alloy performances in the early stages of anode life and passivation were established from electrochemical studies which were designed to simulate industrial Cu EW process. The 24-hour polarization testing revealed that the Mg alloying depolarizes the anode potential up to 80 mV; thus, resulting in a higher Cu EW efficiency. In addition, scanning electron microscopy and X-ray photoelectron spectroscopy revealed that the alteration of the alloy microstructure and the corresponding interfacial reactions contribute to the changes of the anode electrochemical performances. The present study reveals for the first time the potency of Mg alloying in reducing the overpotential of PbCaSn anode.

Phase transition and multicolor luminescence of Eu2+/Mn2+-activated Ca3(PO4)2 phosphors

International Nuclear Information System (INIS)

Li, Kai; Chen, Daqin; Xu, Ju; Zhang, Rui; Yu, Yunlong; Wang, Yuansheng

2014-01-01

Graphical abstract: We have synthesized Eu 2+ doped and Eu 2+ /Mn 2+ co-doped Ca 3 (PO 4 ) 2 phosphors. The emitting color varies from blue to green with increasing of Eu 2+ content for the Eu 2+ -doped phosphor, and the quantum yield of the 0.05Eu 2+ : Ca 2.95 (PO 4 ) 2 sample reaches 56.7%. Interestingly, Mn 2+ co-doping into Eu 2+ : Ca 3 (PO 4 ) 2 leads to its phase transition from orthorhombic to rhombohedral, and subsequently generates tunable multi-color luminescence from green to red via Eu 2+ → Mn 2+ energy transfer. - Highlights: • A series of novel Eu 2+ : Ca 3 (PO 4 ) 2 phosphors were successfully synthesized. • Phase transition of Ca 3 (PO 4 ) 2 from orthorhombic to rhombohedral occurred when Mn 2+ ions were doped. • The phosphors exhibited tunable multi-color luminescence. • The quantum yield of 0.05Eu 2+ : Ca 2.95 (PO 4 ) 2 phosphor can reach 56.7%. • The analyses of phosphors were carried out by many measurements. - Abstract: Intense blue-green-emitting Eu 2+ : Ca 3 (PO 4 ) 2 and tunable multicolor-emitting Eu 2+ /Mn 2+ : Ca 3 (PO 4 ) 2 phosphors are prepared via a solid-state reaction route. Eu 2+ -doped orthorhombic Ca 3 (PO 4 ) 2 phosphor exhibits a broad emission band in the wavelength range of 400–700 nm with a maximum quantum yield of 56.7%, and the emission peak red-shifts gradually from 479 to 520 nm with increase of Eu 2+ doping content. Broad excitation spectrum (250–420 nm) of Eu 2+ : Ca 3 (PO 4 ) 2 matches well with the near-ultraviolet LED chip, indicating its potential applications as tri-color phosphors in white LEDs. Interestingly, Mn 2+ co-doping into Eu 2+ : Ca 3 (PO 4 ) 2 leads to its phase transition from orthorhombic to rhombohedral, and subsequently generates tunable multi-color luminescence from green to red via Eu 2+ → Mn 2+ energy transfer, under 365 nm UV lamp excitation

Position annihilation study on the (Bi,Pb)-Sr-Ca-Cu-(O,F) superconductor

International Nuclear Information System (INIS)

Wang Xiaogang; Gao Xiaohui; Wang Ruidan; Hu Pingya

1993-01-01

In this note, we report the results of positron lifetime measurements in heat-treated (Bi, Pb)-Sr-Ca-Cu-(O, F), and discuss the possible location of the doped fluorine in the (Bi, Pb)-system superconductors. (orig.)

Dielectric and piezoelectric properties of sol-gel derived Ca doped PbTiO3

International Nuclear Information System (INIS)

Chauhan, Arun Kumar Singh; Gupta, Vinay; Sreenivas, K.

2006-01-01

Synthesis of Ca doped PbTiO 3 powder by a chemically derived sol-gel process is described. Crystallization characteristics of different compositions Pb 1-x Ca x TiO 3 (PCT) with varying calcium (Ca) content in the range x = 0-0.45 has been investigated by DTA/TGA, X-ray diffraction and scanning electron microscopy. The crystallization temperature is found to decrease with increasing calcium content. X-ray diffraction reveals a tetragonal structure for PCT compositions with x ≤ 0.35, and a cubic structure for x = 0.45. Dielectric properties on sintered ceramics prepared with fine sol-gel derived powders have been measured. The dielectric constant is found to increase with increasing Ca content, and the dielectric loss decreases continuously. Sol-gel derived Pb 1-x Ca x TiO 3 ceramics with x = 0.45 after poling exhibit infinite electromechanical anisotropy (k t /k p ) with a high d 33 = 80 pC/N, ε' = 298 and low dielectric loss (tan δ = 0.0041)

Characterisation of Pb(Mn{sub 1/3}Nb{sub 2/3})O{sub 3} ceramics by SEM, XRD, XPS and dielectric permittivity tests

Energy Technology Data Exchange (ETDEWEB)

Molak, A. [Institute of Physics, University of Silesia, Ul. Uniwersytecka 4, PL-40-007 Katowice (Poland)]. E-mail: molak@us.edu.pl; Talik, E. [Institute of Physics, University of Silesia, Ul. Uniwersytecka 4, PL-40-007 Katowice (Poland); Kruczek, M. [Institute of Physics, University of Silesia, Ul. Uniwersytecka 4, PL-40-007 Katowice (Poland); Paluch, M. [Institute of Physics, University of Silesia, Ul. Uniwersytecka 4, PL-40-007 Katowice (Poland); Ratuszna, A. [Institute of Physics, University of Silesia, Ul. Uniwersytecka 4, PL-40-007 Katowice (Poland); Ujma, Z. [Institute of Physics, University of Silesia, Ul. Uniwersytecka 4, PL-40-007 Katowice (Poland)

2006-03-15

The Pb(Mn{sub 1/3}Nb{sub 2/3})O{sub 3} ceramics has been obtained from oxides by sintering in air, using a two-stage process with precursor columbite-like (Mn{sub 0.5}Nb)O{sub 3} phase. The PbO oxide was added in the second stage. Analysis of the X-ray diffraction pattern shows that the ceramics consist of 91% of major perovskite phase. A monoclinic distortion of the perovskite structure was found. The cell parameters are a = 12.193(3) A, b = 11.966(6) A, c 12.144(2) A, {beta} = 90{sup o}10.7'. The microanalysis made with SEM exhibited fluctuation in chemical composition of the perovskite phase. Precipitation of MnO{sub 2}, PbO and the Pb-Mn-Nb-O phase different from perovskite was found. The X-ray photoelectron spectroscopy was used to study the electronic structure of the Pb(Mn{sub 1/3}Nb{sub 2/3})O{sub 3} ceramics. The core levels of lead, manganese, niobium and oxygen were measured. The shape of valence band ridge is influenced by Mn 3d states. The real average chemical composition obtained from the XPS measurement is Pb{sub 0.99}(Mn{sub 0.42}Nb{sub 0.67})O{sub 2.92}. Broadband dielectric measurement was carried out in 10{sup -2} to 10{sup 6} Hz and within 80-700 K ranges. The dominant relaxation process exhibits characteristic times typical for ionic processes {tau} {sub 0,H} = 1 x 10{sup -11} s for the higher temperature range and, {tau} {sub 0,L} = 1 x 10{sup -9} s for lower temperatures. The activation energy of relaxation process, E {sub M,H} = 0.43 eV and E {sub M,L} = 0.34 eV corresponds to activation energy of electric conductivity. The dielectric relaxation is ascribed to dipoles created by oxygen vacancies and/or Mn-V {sub O} complexes.

Electrical and magnetic behavior of La{sub 0.7}Ca{sub 0.3}MnO{sub 3}/La{sub 0.7}Sr{sub 0.2}Ca{sub 0.1}MnO{sub 3} composites

Energy Technology Data Exchange (ETDEWEB)

Phong, P.T., E-mail: ptphong.nh@khanhhoa.edu.v [Nhatrang Pedagogic College, Khanhhoa (Viet Nam); Institute of Material Science, Vietnamese Academy of Science and Technology, Hanoi (Viet Nam); Dai, N.V.; Manh, D.H.; Thanh, T.D. [Institute of Material Science, Vietnamese Academy of Science and Technology, Hanoi (Viet Nam); Khiem, N.V. [Department of Natural Sciences, Hongduc University, Thanhhoa (Viet Nam); Hong, L.V.; Phuc, N.X. [Institute of Material Science, Vietnamese Academy of Science and Technology, Hanoi (Viet Nam)

2010-09-15

The electrical transport properties and the magnetoresistance of La{sub 0.7}Ca{sub 0.3}MnO{sub 3}/La{sub 0.7}Sr{sub 0.2}Ca{sub 0.1}MnO{sub 3} composites are investigated as a function of sintering temperature. On the basis of an analysis by X-ray powder diffraction and scanning electron microscopy we suggest that raising the sintering temperature enhanced the interfacial reaction and creates interfacial phases at the boundaries of the La{sub 0.7}Ca{sub 0.3}MnO{sub 3} and La{sub 0.7}Sr{sub 0.2}Ca{sub 0.1}MnO{sub 3}. Results also show that in 3 kOe, and at the Curie temperature, the magnetoresistance value of 14% was observed for the composite sintered at 1300 {sup o}C. Based on the phenomenological equation for conductivity under a percolation approach, which depends on the phase segregation of ferromagnetic metallic clusters and paramagnetic insulating regions, we fitted the experimental resistivity-temperature data from 50-300 K and find that the activation barrier decreases as temperature is increased.

Some studies about the NaCl:Ca2+ :Mn2+ and NaCl: Cd2+ :Mn2+ dosemeters

International Nuclear Information System (INIS)

Verdiguel G, H.; Flores J, C.; Camarillo G, E.; Espejel P, R.; Cabrera B, E.; Hernandez A, J.; Murrieta S, H.; Cruz Z, E.; Ramos B, S.; Negron, A.

2002-01-01

Nowadays, a great interest by counting with dosemeters of characteristics such as a high stability, of easy operation and easier production exists. Looking for a commitment with all these characteristics,a possibility to use the system NaCl: Ca 2+ :Mn 2+ and NaCl: Cd 2+ :Mn 2+ as dosemeters was studied. The studies were realized irradiating with gamma radiation from a 60 Co source. The crystals that were used as samples did not suffer any thermal treatment previous to irradiation. The supplied doses were 10, 30, 60, 100, 300, and 600 rads. 24 hours after irradiation the thermoluminescent response was obtained. In the case of the system NaCl: Ca 2+ :Mn 2+ several thermoluminescent bands were observed (BTL). Two concentrations of Mn 2+ with only one concentration of Ca 2+ (1%) were studied. For the case of the smaller concentration of Mn 2+ (0.1%) 4 BTL were observed, whereas for a greater concentration (0.3%) just 2 BTL were detected. The positions of the maximum of the BTL peaks differ for both concentrations, this possible due to what the nature of the traps for both cases differs by the type of precipitates present in the net. For the case of the system NaCl: Cd 2+ (1%) :Mn 2+ (0.1% and 0.5%) a similar situation to the previous was found, although in this case for both manganese concentrations just 2 BTL were observed; however all the peaks seem to be the superposition of several bands. Despite the apparent complexity of the thermoluminescent response, such response as function of the dose shows that both systems present a stable response to gamma radiation in the interval from 10 to 600 rads. In the case of calcium it is had a response of linear type of the Tl intensity depending on the dose, whereas for the cadmium system a supra linear response seems to exist. Nowadays, studies for determining the BTL origin being carried out. (Author)

The poisoning effect of PbO on Mn-Ce/TiO{sub 2} catalyst for selective catalytic reduction of NO with NH{sub 3} at low temperature

Energy Technology Data Exchange (ETDEWEB)

Zhou, Lingling [College of Environmental Science and Engineering, Hunan University, Changsha 410082 (China); Key Laboratory of Environmental Biology and Pollution Control (Hunan University), Ministry of Education, Changsha 410082 (China); Li, Caiting, E-mail: ctli@hnu.edu.cn [College of Environmental Science and Engineering, Hunan University, Changsha 410082 (China); Key Laboratory of Environmental Biology and Pollution Control (Hunan University), Ministry of Education, Changsha 410082 (China); Zhao, Lingkui; Zeng, Guangming; Gao, Lei; Wang, Yan; Yu, Ming’e [College of Environmental Science and Engineering, Hunan University, Changsha 410082 (China); Key Laboratory of Environmental Biology and Pollution Control (Hunan University), Ministry of Education, Changsha 410082 (China)

2016-12-15

Highlights: • The poisoning effects of PbO-doped Mn-Ce/TiO{sub 2} catalysts for low temperature NH{sub 3}-SCR were investigated. • Low concentration of Mn{sup 4+} and chemisorbed oxygen (O{sub b}) were not favorable for the generation of intermediates. • The decreased Ce{sup 3+} and less reducible of manganese oxides hindered the redox cycle (Mn{sup 3+} + Ce{sup 4+} ↔ Mn{sup 4+} + Ce{sup 3+}). • The doping of PbO not only altered acid sites but also inhibited ammonia adsorption as well as activation. • The poisoning of PbO resulted in the decrease of ad-NO{sub x} species (only a spot of bidentate nitrates remained). - Abstract: Lead oxide (PbO) as one of the typical heavy metals in flue gas from power plants has strong accumulation as well as poisoning effects on SCR catalysts. In this paper, a series of PbO-doped Mn-Ce/TiO{sub 2} catalysts were synthesized by impregnation method. The poisoning effects of PbO over Mn-Ce/TiO{sub 2} samples for selective catalytic reduction of NO by NH{sub 3} were investigated based on catalytic activity test and characterizations. The NO conversion of Mn-Ce/TiO{sub 2} was greatly decreased after the addition of PbO. It was obvious that the NO conversion efficiency of Mn-Ce/TiO{sub 2} catalyst declined from 96.75% to about 40% at 200 °C when Pb:Mn molar ratio reached 0.5. Brunauer-Emmett-Teller (BET), X-ray diffraction (XRD), Scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), Hydrogen temperature programmed reduction (H{sub 2}-TPR), Ammonia temperature programmed desorption (NH{sub 3}-TPD) and Fourier transform infrared spectroscopy (FT-IR) were carried out to study the deactivation reasons of PbO poisoned catalysts. Manganese oxides’ crystallization, less reducible of manganese and cerium oxides, the decreasing of surface area, Mn{sup 4+} as well as Ce{sup 3+} concentration and chemisorbed oxygen (O{sub b}) after the introduction of PbO, all of these resulted in a poor SCR performance

Manganite based hetero-junction structure of La_0_._7Sr_0_._7_−_xCa_xMnO_3 and CaMnO_3_−_δ for cross-point arrays

International Nuclear Information System (INIS)

Lee, Hong-Sub; Park, Hyung-Ho

2015-01-01

Resistive random access memory and the corresponding cross-point array (CPA) structure have received a great deal of attention for high-density next generation non-volatile memory. However, the cross-talk issue of CPA structure by sneak current should be overcome to realize the highest density integration. To accomplish this, the sneak current can be minimized by high, nonlinear characteristic behaviors of resistive switching (RS). Therefore this study fabricated pnp bipolar hetero-junction structure using the perovskite manganite family, such as La_0_._7Sr_0_._3_−_xCa_xMnO_3 (LSCMO) and CaMnO_3_−_δ (CMO), to obtain nonlinear RS behavior. The pnp structure not only shows nonlinear characteristics, but also a tunable characteristic with Ca substitution. (paper)

TXRF and XRF techniques for the determination of K, Ca, Cr, Mn, Fe, Ni, Cu, Zn, Br, Rb, Sr and Pb in some plant species and their infusion

Energy Technology Data Exchange (ETDEWEB)

Khuder, A [Atomic Energy Commission, Damascus (Syrian Arab Republic). Dept. of Chemistry

2009-02-15

The content of K, Ca, Ti, Cr, Mn, Fe, Ni, Cu, Zn, Br, Rb, and Sr elements in some medicinal plants, including: A. herba-alba, T. officinale, M. officinalis, T. syeriacus, T. vulgaris, A. officinalis, R. officinalis, M. piperita, M. aquatica, Zea mays, G. glabra, A. vulgare, U. urens, C. aronica, H. officinalis, M. aurea, C. cyminum, was determined using TXRF technique. Concentrations of Pb upper the detection limits of TXRF method was determined only in A. herba-alba leaves with a mean value of 3.6 ppm. The accuracy and the precision of TXRF method were verified using Apple leaves, Peach leaves, and Hay Powder Standard Reference Materials (SRM) for the analysis of plant samples. The previously mentioned elements were accurately determined by TXRF, except Br. Errors obtained by Br determination may be obtained by the partial losses of element content during evaporation of sample on quartz carrier proposed for TXRF measurements. TXRF results for Ca, Mn, and Sr elements agreed well with these obtained by XRF method with standard relative error (SR) better than 10 %, while, these obtained for rest elements, except Br, were with SR ranging between 11 %-20 %. Br was not included in the determination of elements by TXRF. Transfer of K, Ca, Mn, Fe, Cu, Zn, Br, Rb, and Sr from A. herba-alba, A. vulgare, Zea mays, M. aquatica, M. piperita, C. cyminum, G. glabra, M. officinalis, and R. officinalis plant materials to infusions at different temperatures were studied using XRF method. Data analyses were verified by Peach and Apple leaves of Standard Reference Materials. Potassium represented the dominant element in all studied plants, particularly, in roots of U. dioica plant with concentrations in the range of 59.3 g/Kg-90.8 g/Kg. Independently of brewing 5 temperature, potassium with a high ratio was transferred from plants to infusions. K transfer ratio was in a range from 57.2 % for A. vulgare leaves at 25 .C to 91 % for G. glabra at 55 .C. Although, Fe content in dry plant

TXRF and XRF techniques for the determination of K, Ca, Cr, Mn, Fe, Ni, Cu, Zn, Br, Rb, Sr and Pb in some plant species and their infusion

International Nuclear Information System (INIS)

Khuder, A.

2009-02-01

The content of K, Ca, Ti, Cr, Mn, Fe, Ni, Cu, Zn, Br, Rb, and Sr elements in some medicinal plants, including: A. herba-alba, T. officinale, M. officinalis, T. syeriacus, T. vulgaris, A. officinalis, R. officinalis, M. piperita, M. aquatica, Zea mays, G. glabra, A. vulgare, U. urens, C. aronica, H. officinalis, M. aurea, C. cyminum, was determined using TXRF technique. Concentrations of Pb upper the detection limits of TXRF method was determined only in A. herba-alba leaves with a mean value of 3.6 ppm. The accuracy and the precision of TXRF method were verified using Apple leaves, Peach leaves, and Hay Powder Standard Reference Materials (SRM) for the analysis of plant samples. The previously mentioned elements were accurately determined by TXRF, except Br. Errors obtained by Br determination may be obtained by the partial losses of element content during evaporation of sample on quartz carrier proposed for TXRF measurements. TXRF results for Ca, Mn, and Sr elements agreed well with these obtained by XRF method with standard relative error (SR) better than 10 %, while, these obtained for rest elements, except Br, were with SR ranging between 11 %-20 %. Br was not included in the determination of elements by TXRF. Transfer of K, Ca, Mn, Fe, Cu, Zn, Br, Rb, and Sr from A. herba-alba, A. vulgare, Zea mays, M. aquatica, M. piperita, C. cyminum, G. glabra, M. officinalis, and R. officinalis plant materials to infusions at different temperatures were studied using XRF method. Data analyses were verified by Peach and Apple leaves of Standard Reference Materials. Potassium represented the dominant element in all studied plants, particularly, in roots of U. dioica plant with concentrations in the range of 59.3 g/Kg-90.8 g/Kg. Independently of brewing 5 temperature, potassium with a high ratio was transferred from plants to infusions. K transfer ratio was in a range from 57.2 % for A. vulgare leaves at 25 .C to 91 % for G. glabra at 55 .C. Although, Fe content in dry plant

Effect of Sintering Time on Superconducting Wire Bi-Pb-Sr-Ca-Cu-O With Dopant MgO Sheated Ag Using Powder in Tube Method

Directory of Open Access Journals (Sweden)

Hariyati Lubis

2018-01-01

  DAFTAR PUSTAKA Abbas M.M., Abass L.K and Salman U., (2012, Influences of Sintering Time on the Tc of Bi2-xCuxPb0.3Sr2Ca2Cu3010+ High Temperature Superconductors, Energy Procedia 18, 215-224  Abbas, M.M., Abbas, L.K., Bahedh, H.S. 2015. Superconducting Properties of Bi2-SbxPb0,3Sr1,9Ba0,1Ca2Cu3O10+δ Compounds. Journal of Applied Science Research. 11. 22: 164-172 Darsono, N., Imaduddin, A., Raju, K., Yoon, D.H., (2015, Synthesis and Characterization of Bi1.6Pb0.4Sr2Ca2Cu3O7 Superconducting Oxide by High-Energy Milling, J Supercond Nov Magn. E. Chew,. (2010, Superconducting Transformer Design And Construction, University of Canterbury, Christchurch, New Zealand. March Hamadneh, I., Halim, S. A., dan Lee, C. K., (2006,  Characterization of Bi1.6Pb0.4Sr2Ca2Cu3Oy Ceramic Superconductor Prepared Via Coprecipitation Method at Different Sintering Time, J. Mater. Sci, 41: 5526-5530. Hermiz G.Y., Aljurani B.A., Beayaty M.A., (2014, Effect of Mn Substitution on the Superconducting Properties of Bi1.7Pb0,3Sr2Ca2-xMnxCu3O10+, International Journal Of Engineering and Advanced Technology (IJEAT. 3. 4: 213-217 John R Hull, (2003, Applications of high-temperature superconductors in power technology, Reports on Progress in Physics, Volume 66, Number 11 Lu, X.Y., Yi, D., Chen, H., Nagata, A. 2016. Effect of Sn, MgO and Ag2O mix-doping on the formation and superconducting properties of Bi-2223 Ag/tapes. Physics Procedia. 81: 129-132 Meretliev Sh., Sadykov K.B., Berkeliev A., (2000, Doping of High Temperature Superconductors, Turk J Phy.24: 39-48 Mohammed, N. H., Ramadhan A., Ali I. A., Ibrahim, I. H., dan Hassan, M. S, (2012, Optimizing the Preparation Conditions of Bi-2223 Superconducting Phase Using PbO and PbO2, Materials Sciences and Applications, 3: 224-233. Roumie, M., Marhaba, S., Awad R., Kork M., Hassan I., Mawassi R., (2014, Effect of Fe2O3 Nano-Oxide Addition on the Superconducting Properties of the (Bi,Pb-2223 Phase, Journal of Supercond Nov Magn, 27: 143-153 Serkan

Magnetic anisotropy in Pb_{1-x-y}Sn_{y}Mn_{x}Te studied by ferromagnetic resonance

NARCIS (Netherlands)

Eggenkamp, P.J.T.; Story, T.; Swüste, C.H.W.; Swagten, H.J.M.; Jonge, de W.J.M.

1993-01-01

Proceedings of the XXII International School of Semiconducting Compounds, Jaszowiec 1993 We will report on the anisotropy in (Pb)SnMnTe, studied by ferromagnetic resonance. We have found a cubic anisotropy with a = 73 × 10-4 cm-1 for Sn1-xMnxTe and a = 200 × 10-4 cm-1 for Pb0.28-xSn0.72MnxTe. We

Synthesis and Characterization of nanostructured Mn oxide in (Ca-OL-2) layers from ores of the Serra do Navio (Amapa) mine; Sintese e caracterizacao de oxido de Mn nanoestruturado em camada (Ca-Ol-2) a partir de minerios da antiga mina de Serra do Navio (Amapa)

Energy Technology Data Exchange (ETDEWEB)

Mar, I.C. do; Figueira, B.A.M., E-mail: brunoufopa@hotmail.com [Universidade Federal do Oeste do Para (UFOPA), Santarem, PA (Brazil). Instituto de Engenharia e Geociencias; Silva, L.N. da [Universidade Federal do Para (UFPA), Belem, PA (Brazil). Instituto de Geociencias; Mercury, J.M.R. [Instituto Federal do Maranhao (IFMA), Sao Luiz, MA (Brazil). Departamento de Quimica

2016-07-01

In this study, layered nanostructured Mn oxide, Ca-OL (octahedral layer), was obtained from Mn ores of Serra do Navio (Amapa, Brazil). The developed synthetic route used dissolution chemical processes, precipitation, ion exchange and hydrothermal treatment, respectively. The results showed the presence of DRX peaks in the position 12,5 and 25º (2 theta), confirming Mn oxide Na-birnessite-type structure (Na-OL-1) obtainment which transformed into Ca-buserite (Ca-OL-2) after Ca{sup 2+} ion exchange. Infrared spectroscopy (FTIR) bands of the MnO6 octahedrons Mn-O vibrational bond were identified in the range of 800 to 400 cm{sup -1} which confirmed the DRX data obtained. The Ca-OL-2 thermal behavior obtained by TG-DTA showed thermal stability above 850 deg C, thus exhibiting that products as ores can be transformed into Mn oxides nano layers with high thermal stability. (author)

Ca Mn exchange between grossular and MnCl2 solutions at 2 kbar and 600°°C: reaction mechanism and evidence for non-ideal mixing in spessartine-grossular garnets

Science.gov (United States)

Gavrieli, I.; Matthews, Alan; Holland, J. B.

1996-10-01

The hydrothermal reaction between grossular and 1 molar manganese chloride solution was studied at 2 kbar and 600 °C at various bulk Ca/(Ca+Mn) compositions: Ca3Al2Si3O12+3Mn2+(aq) ⇔ Mn3Al2Si3O12+3Ca2+(aq) The reaction products are garnets of the spessartine-grossular solid-solution series which discontinuously armour the dissolving grossular grains. The first garnet to crystallize is spessartine rich ( X gt Mn≥0.95), reflecting the high Mn content of the solution, but as the reaction proceeds more calcium-rich garnets progressively overgrow the initial products. The armouring product layer is detached from the dissolving grossular, which allows the progressive overgrowth to occur on both its external and internal surfaces and results in the development of a two directional Ca/(Ca+Mn) zoning pattern in the product grains. The compositional changes in the run products are consistent with attainment of heterogeneous equilibrium between the external rims of the spessartine-grossular garnets and the bulk solutions in runs of duration ≥24 hours. Plots of ln KD versus X gt Ca maxima show linear variations that are not consistent with the ideal mixing that has been proposed for spessartine-grossular garnets at temperatures of 900 to 1200 °C. The data rather fit a regular solution model with the parameters Δ G° (600 °C, 2 kbar)=-8.0±0.8 kJ/mol and w gt CaMn=2.6±2.0 kJ/mol. Existing solubility measurements and thermodynamic data from other Ca and Mn silicates support the calculated data. Grossular activities calculated using the w gt CaMn parameter indicate that even in manganese-rich metapelites pressure estimates calculated using the garnet-plagioclase-Al2SiO5-quartz barometer will not be increased by more than 0.2 kbar.

Valence band electronic structure of Ho-doped La0.67Ca0.33MnO3 using ultra-violet photoemission spectroscopy

Science.gov (United States)

Rout, S. K.; Mukharjee, R. N.; Mishra, D. K.; Roul, B. K.; Sekhar, B. R.; Dalai, M. K.

2017-05-01

In this manuscript we report the valence band electronic structure of Ho doped La0.67Ca0.33MnO3 using ultraviolet photoemission spectroscopy. We compared the density of states of La0.67Ca0.33MnO3, La0.67Ca0.3Ho0.03MnO3 and La0.64Ho0.03Ca0.33MnO3 near the Fermi level at various temperatures. Significant amount of changes have been observed at higher temperatures (220 K and 300 K) where the near Fermi level density of states increases with Ho doping into La0.67Ca0.33MnO3 indicating the enhancement of magnitude of change in metallicity (conductivity).

Structure and magnetic properties of La2/3Sr1/3MnO3/CaMnO3 multilayers

International Nuclear Information System (INIS)

Granada, Mara; Sirena, Martin; Steren, Laura B.; Leyva, Gabriela

2004-01-01

Structural and magnetic properties of manganite-based multilayers, La 2/3 Sr 1/3 MnO 3 /CaMnO 3 , composed of ferromagnetic metals and antiferromagnetic insulator barriers are investigated in this work. Compounds of similar lattice parameters were used to build the samples, so we expect an excellent stacking of the different layers along the structure. To get a first insight of this system, the crystalline structure of a series of samples, grown on (1 0 0) SrTiO 3 and (1 0 0) MgO single-crystalline substrates, has been studied. X-ray diffraction patterns show that the structure is strongly textured in the (1 0 0) direction when grown on SrTiO 3 , regardless the composition of the bottom layer. A different result is found on the same system grown on MgO: when the buffer layer is CaMnO 3 , the structure grows in the (1 1 0) orientation while it grows in the (1 0 0) direction when the bottom layer is La 2/3 Sr 1/3 MnO 3 . Magnetic coupling of the ferromagnetic layers across the antiferromagnetic spacer has been studied with magnetization measurements

Formation pathways in the synthesis and properties of (Tl0.5Pb0.5)(Sr0.9Ba0.1)2Ca2Cu3Oz and (Tl0.5Pb0.5)(Sr0.8Ba0.2)2Ca2Cu3Oz-1223 superconductors

International Nuclear Information System (INIS)

Auinger, M; Gritzner, G; Bertrand, Ch; Galez, Ph; Soubeyroux, J-L

2007-01-01

The formation pathway of (Tl 0.5 Pb 0.5 )(Sr 0.9 Ba 0.1 ) 2 Ca 2 Cu 3 O z and (Tl 0.5 Pb 0.5 )(Sr 0.8 Ba 0.2 ) 2 Ca 2 Cu 3 O z was studied by neutron and x-ray diffraction. The following reaction pathway was proposed: thallium oxide and lead oxide react with Sr-rich (Sr 1-x Ca x )CuO 2 and Ca-rich (Ca x Sr 1-x )O to form Sr 4 Tl 2 O 7 and (Ca x Sr 1-x )PbO 3 , respectively. The thallate and the plumbate compounds then form the (Tl 0.5 Pb 0.5 )-1212 phase starting at a temperature of 600 deg. C. Finally, between 850 and 900 deg. C, the 1223 phase is formed from (Tl 0.5 Pb 0.5 )-1212 (Ca x Sr 1-x ) 2 CuO 3 and CuO. Parallel experiments to fabricate the (Tl, Pb)-1223 superconductor resulted in specimens with critical temperatures of 117.5 K and 116 K, respectively, and transition widths of 2 K. Differences between the pathways for the formation of Pb-doped, Sr-rich and Pb-free, Ba-rich Tl-1223 superconductors are discussed

Investigations of small-gap semiconductors: HgTe, HgMnTe and PbMnTe in the far infrared region using Fourierspectroscopic methods

International Nuclear Information System (INIS)

Roschger, I.

1985-05-01

A special method was developed in the framework of this thesis to solve the inherent problem of dynamic range in Fourier spectrometry by using optical compensation. The so-called dual beam spectrometer consists of two coupled interferometers. This technique was adapted for measurements on small gap semiconductors. The investigated sample was n-HgTe, for which a resonant acceptor absorption in the conduction band was predicted. By alloying Mn-ions into the inverted gap-HgTe-crystal the band gap can be tuned to an open gap band structure. The mixed crystal exhibits additional structures in the phonon spectrum. The model of Barker and Verleur (including clustering) was applied. The substitution of Mn-ions in the IV-VI-compound PbTe leads to semimagnetic effects resolved by magneto-reflectivity measurements. The extrapolation in the fan-charts to zero-magnetic field suggests residual spin splitting either in the conduction and/or in the valence band. To evaluate the data an oscillator fit was applied to cyclotron absorption (Faraday- and Voigt-configuration) and was proved to be in agreement with the experimental data. Zero field splitting appears in PbMnTe in the valence band and indicates a weak ferromagnetism already observed in other measurements cited in the literature. Kramers-Kronig-data were in agreement with the theoretical results of the Barker-Verleur-model. The influence of clustering in the mixed crystal HgMnTe on the phonon spectra must be taken into account for Mn concentrations > 20%. The existence of the resonance acceptor state in HgTe was proved by optical transmission measurements. (Author, shortened by G.Q.)

Simultaneous efficient adsorption of Pb2+ and MnO4− ions by MCM-41 functionalized with amine and nitrilotriacetic acid anhydride

International Nuclear Information System (INIS)

Chen, Feiyun; Hong, Mingzhu; You, Weijie; Li, Chong; Yu, Yan

2015-01-01

Highlights: • MCM-41 was successfully modified with amine and nitrilotriacetic acid anhydride. • The adsorbent can simultaneously remove Pb 2+ and MnO 4 − by adjusting pH of the system. • The maximum adsorption capacities of Pb 2+ and MnO 4 − are 147 mg/g and 156 mg/g. • The absorbent exhibits good regeneration and reusability for 5 cycles use. - Abstract: A novel adsorbent NH 2 /MCM-41/NTAA, capable of simultaneous adsorption of cations and anions from aqueous solution, was prepared by immobilization of amine and nitrilotriacetic acid anhydride (NTAA) onto MCM-41. The structures and properties before and after surface modification were systematically investigated through X-ray diffraction (XRD), transmission electron microscope (TEM) and scanning electron microscope (SEM), nitrogen adsorption–desorption, and infrared spectroscopy (FTIR), thermogravimetry (TGA) and X-ray photoelectron spectroscopy (XPS). They together confirm that the amine and NTAA group were chemically bonded to the internal surface of the mesoporous. The NH 2 /MCM-41/NTAA were used to adsorb Pb 2+ and MnO 4 − in an aqueous solution in a batch system, and the maximum adsorption efficiency was found to occur at pH 5.0 and 3.0, respectively. NH 2 /MCM-41/NTAA exhibit preferable removal of Pb 2+ through electrostatic interactions and chelation, whereas it captures MnO 4 − by means of electrostatic interactions. The experimental data are fitted the Langmuir isotherm model reasonably well, with the maximum adsorption capacity of 147 mg/g for Pb 2+ and of 156 mg/g for MnO 4 − . The adsorption rates of both Pb 2+ and MnO 4 − are found to follow the pseudo-second order kinetics. Furthermore, the NH 2 /MCM-41/NTAA adsorbent performs good recyclability and reusability for 5 cycles use. This study indicates a potential applicability of NH 2 /MCM-41/NTAA as new absorbents for effective simultaneous adsorption of hazardous metal ions and anions from wastewater.

Dielectric and piezoelectric properties of sol-gel derived Ca doped PbTiO{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Chauhan, Arun Kumar Singh [Department of Physics and Astrophysics, University of Delhi, Delhi 110007 (India); Gupta, Vinay [Department of Physics and Astrophysics, University of Delhi, Delhi 110007 (India)]. E-mail: drvin_gupta@rediffmail.com; Sreenivas, K. [Department of Physics and Astrophysics, University of Delhi, Delhi 110007 (India)

2006-06-15

Synthesis of Ca doped PbTiO{sub 3} powder by a chemically derived sol-gel process is described. Crystallization characteristics of different compositions Pb{sub 1-x}Ca {sub x}TiO{sub 3} (PCT) with varying calcium (Ca) content in the range x = 0-0.45 has been investigated by DTA/TGA, X-ray diffraction and scanning electron microscopy. The crystallization temperature is found to decrease with increasing calcium content. X-ray diffraction reveals a tetragonal structure for PCT compositions with x {<=} 0.35, and a cubic structure for x = 0.45. Dielectric properties on sintered ceramics prepared with fine sol-gel derived powders have been measured. The dielectric constant is found to increase with increasing Ca content, and the dielectric loss decreases continuously. Sol-gel derived Pb{sub 1-x}Ca {sub x}TiO{sub 3} ceramics with x = 0.45 after poling exhibit infinite electromechanical anisotropy (k {sub t}/k {sub p}) with a high d {sub 33} = 80 pC/N, {epsilon}' = 298 and low dielectric loss (tan {delta} = 0.0041)

Improved performance of CdS/CdSe quantum dot-sensitized solar cells using Mn-doped PbS quantum dots as a catalyst in the counter electrode

International Nuclear Information System (INIS)

Kim, Byung-Man; Son, Min-Kyu; Kim, Soo-Kyoung; Hong, Na-Yeong; Park, Songyi; Jeong, Myeong-Soo; Seo, Hyunwoong; Prabakar, Kandasamy; Kim, Hee-Je

2014-01-01

Highlights: • PbS QDs synthesized using the SILAR method act not only as the electrochemical catalysts but as donors providing additional electrons under illumination. • The electrochemical and optical properties of the PbS QDs were enhanced considerably after Mn 2+ doping. • The electron supply from the counter electrode was significantly activated by Mn 2+ doping, improving the performance of QDSSC. - Abstract: This study reports the enhanced catalytic ability of Mn-doped PbS QDs synthesized using a successive ionic layer adsorption and reaction (SILAR) method for quantum dot-sensitized solar cells (QDSSCs). Electrochemical and optical analysis of each material showed that the catalytic ability of the PbS electrode was improved significantly by Mn 2+ doping. Two factors can explain this behavior. The first is that intentional impurities have an impact on the structure of the host material, such as increases in surface roughness. The other is that dopants create new energy states that delay the exciton recombination time and allow charge separation to be activated. As a result, the photoelectron supply from the counter electrode is accelerated, resulting in vigorous redox reactions at the polysulfide electrolyte. The performance of the CdS/CdSe QDSSC using a Mn-doped PbS counter electrode was compared with those using the Pt and PbS counter electrodes. Finally, a power conversion efficiency of 3.61% was achieved with the Mn-doped PbS counter electrode (V OC = 0.61 V, J SC = 11.67 mA cm −2 , FF = 0.51) under one sun illumination (100 mW cm −2 ), which is ∼40% higher than that of CdS/CdSe QDSSCs with the bare PbS counter electrode

Colossal Magnetoresistance in La-Y-Ca-Mn-O Films

NARCIS (Netherlands)

Chen, L.H.; Tiefel, T.H.; Jin, S.; Palstra, T.T.M.; Ramesh, R.; Kwon, C.

1996-01-01

Magnetoresistance behavior of La0.60Y0.07CaMnOx, thin films epitaxially grown on LaAlO3 has been investigated. The films exhibit colossal magnetoresistance with the MR ratio in excess of 10^8% at ~60K, H = 7T, which is the highest ever reported for thin film manganites. The partial substitution of

Graphite furnace analysis of a series of metals (Cu, Mn, Pb, Zn and Cd) in ox kidney

International Nuclear Information System (INIS)

Souza, Vivianne L.B. de; Nascimento, Rizia K. do; Paiva, Ana Claudia de; Silva, Josenilda M. da; Melo, Jessica V. de

2013-01-01

The aim of this study was to create a methodology for animal tissue analysis, with the use of flame atomic absorption spectrophotometry techniques and graphite furnace analysis to determining metal concentrations in ox kidney. The organ of this animal can be considered a great nutritional food, due to the high protein and micronutrient content beyond the ability to absorb and concentrate important metals such as Zn, Fe, Mn and Se. On the other hand, there is a risk when eating this food owing to the capacity to accumulate toxic metals such as Pb and Cd. In accordance with the laboratory analysis, Zn can be analyzed by flame atomic absorption spectrophotometry, but other metals such as Cu, Mn, Pb and Cd, could only be detected by graphite furnace analysis. The results showed that there is more Zn and Cu than other metals. Such metals follows an order reported by the literature (Zn > Cu > Cd > Pb > Mn). The results showed that kidney is actually a rich source of Zn and Cu. The Cd levels in the ox kidney did not exceed the values which cause toxic effects. The adequacy of the results indicates that the proposed methodology can be used for animal tissue analysis.(author)

Graphite furnace analysis of a series of metals (Cu, Mn, Pb, Zn and Cd) in ox kidney

Energy Technology Data Exchange (ETDEWEB)

Souza, Vivianne L.B. de; Nascimento, Rizia K. do; Paiva, Ana Claudia de; Silva, Josenilda M. da, E-mail: vlsouza@cnen.gov.br, E-mail: riziakelia@hotmail.com, E-mail: acpaiva@cnen.gov.br, E-mail: jmnilda@hotmail.com [Centro Regional de Ciencias Nucleares do Nordeste (CRCN-NE/CNEN-PE), Recife, PE (Brazil); Melo, Jessica V. de, E-mail: Jessica_clorofila@hotmail.com [Universidade de Pernambuco, Recife, PE (Brazil)

2013-07-01

The aim of this study was to create a methodology for animal tissue analysis, with the use of flame atomic absorption spectrophotometry techniques and graphite furnace analysis to determining metal concentrations in ox kidney. The organ of this animal can be considered a great nutritional food, due to the high protein and micronutrient content beyond the ability to absorb and concentrate important metals such as Zn, Fe, Mn and Se. On the other hand, there is a risk when eating this food owing to the capacity to accumulate toxic metals such as Pb and Cd. In accordance with the laboratory analysis, Zn can be analyzed by flame atomic absorption spectrophotometry, but other metals such as Cu, Mn, Pb and Cd, could only be detected by graphite furnace analysis. The results showed that there is more Zn and Cu than other metals. Such metals follows an order reported by the literature (Zn > Cu > Cd > Pb > Mn). The results showed that kidney is actually a rich source of Zn and Cu. The Cd levels in the ox kidney did not exceed the values which cause toxic effects. The adequacy of the results indicates that the proposed methodology can be used for animal tissue analysis.(author)

Punta Pitt Stable Isotope and Ion Data (delta 18O, delta 13C, Cd/Ca, Mn/Ca) for 1936 to 1982.5

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — File contains data presented by Shen et al. (1992a). Table includes d18O, d13C, Cd/Ca, Mn/Ca, and Ba/Ca data from a 2m coral head and, for comparison, SST records...

Effect of annealing and impurity concentration on the TL characteristics of nanocrystalline Mn-doped CaF2

International Nuclear Information System (INIS)

Sahare, P.D.; Singh, Manveer; Kumar, Pratik

2015-01-01

Nanocrystalline samples of Mn-doped CaF 2 were synthesized by chemical coprecipitation method. The impurity concentration was varied in the range of 0.5–4.0 mol%. The structure of the synthesized material was confirmed using powder XRD analysis. TEM images of the nanoparticles show their size occurring mostly in the range of 35–40 nm, with clusters of some impurity phases formed on annealing of the material at higher temperatures. Detailed studies on TL showed that the structures of glow curves depend on Mn concentrations and annealing temperatures. Optimization of the concentration and annealing temperature showed that the sample (doped with 3.0 mol% and annealed at 673 K) has almost a single dosimetric glow peak appearing at around 492 K. EPR and PL spectra were further studied to understand the reasons for changes in the glow curve structures. All detailed studies on TL, PL and EPR showed that the changes in glow curve structures are caused not only by the stress connected with the difference in ionic radii of host Ca 2+ and the guest impurity Mn 3+ /Mn 2+ , but are also governed by other reasons, like diffusion of atmospheric oxygen and formation of impurity aggregates, such as, MnO 2 , Mn 3 O 4 , etc. This is true not only for nanocrystalline CaF 2 :Mn but could also be so for the bulk CaF 2 :Mn (TLD-400) and would thus help in understanding complex glow curve structure, high fading and the loss of reusability on annealing beyond 673 K. - Highlights: • Nanocrystalline material CaF 2 :Mn is prepared by simple coprecipitation method. • The material is studied by XRD, TEM, ESR, TL and PL techniques. • High impurity concentrations give rise to clusters causing material instability. • Changes in ESR and PL and glow curve structures are studied and explained. • Better characteristics than the bulk make the nanophosphor useful for dosimetry

Long time relaxation of resistance in La0.8Sr0.2MnO3 ceramics and La0.65Ca0.35 MnO3 films on ferroelectric substrates

International Nuclear Information System (INIS)

Medvedev, Yu.V.; Mezin, N.I.; Nikolaenko, Yu.M.; Pigur, A.E.; Shishkova, N.V.; Ishchuk, V.M.; Chukanova, I.N.

2004-01-01

Galvanomagnetic properties of La 0.65 Ca 0.35 MnO 3 films with a thickness of 0.2 μm on Pb 2.9 Ba 0.05 Sr 0.05 (Zr 0.4 Ti 0.6 )O 3 ferroelectric ceramics substrates have been investigated. We have discovered the monotonic irreversible increase of the film resistance by 3-5 time of value during several hours after multiple inversion of substrate polarization. The long-time relaxation (LTR) of film resistance is explained by dielecrtrization of film intercrystallite boundaries as a result of oxygen redistribution under action of inhomogeneous mechanical stress. In addition, the LTR of resistance of La 0.8 Sr 0.2 MnO 3 and La 0.6 Sr 0.2 Mn 1.2 O 3 ceramic samples has been investigated under action of different kind of mechanical stress: stretch, compression and hydrostatic press. Time dependence of resistance is described by R 0 +ΔRexp(-t/τ). The magnitude of LTR is 5-10 time greater then fast variation of resistance under action of stress. The sign of ΔR is dependent on the kind of stress. The time constant (τ) has the value of 3-9 hours. (copyright 2004 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

The effect of Ca2+ ions and ionic strength on Mn(II) oxidation by spores of the marine Bacillus sp. SG-1

Science.gov (United States)

Toyoda, Kazuhiro; Tebo, Bradley M.

2013-01-01

Manganese(IV) oxides, believed to form primarily through microbial activities, are extremely important mineral phases in marine environments where they scavenge a variety of trace elements and thereby control their distributions. The presence of various ions common in seawater are known to influence Mn oxide mineralogy yet little is known about the effect of these ions on the kinetics of bacterial Mn(II) oxidation and Mn oxide formation. We examined factors affecting bacterial Mn(II) oxidation by spores of the marine Bacillus sp. strain SG-1 in natural and artificial seawater of varying ionic conditions. Ca2+ concentration dramatically affected Mn(II) oxidation, while Mg2+, Sr2+, K+, Na+ and NO3- ions had no effect. The rate of Mn(II) oxidation at 10 mM Ca2+ (seawater composition) was four or five times that without Ca2+. The relationship between Ca2+ content and oxidation rate demonstrates that the equilibrium constant is small (on the order of 0.1) and the binding coefficient is 0.5. The pH optimum for Mn(II) oxidation changed depending on the amount of Ca2+ present, suggesting that Ca2+ exerts a direct effect on the enzyme perhaps as a stabilizing bridge between polypeptide components. We also examined the effect of varying concentrations of NaCl or KNO3 (0-2000 mM) on the kinetics of Mn(II) oxidation in solutions containing 10 mM Ca2+. Mn(II) oxidation was unaffected by changes in ionic strength (I) below 0.2, but it was inhibited by increasing salt concentrations above this value. Our results suggest that the critical coagulation concentration is around 200 mM of salt (I = ca. 0.2), and that the ionic strength of seawater (I > 0.2) accelerates the precipitation of Mn oxides around the spores. Under these conditions, the aggregation of Mn oxides reduces the supply of dissolved O2 and/or Mn2+ and inhibits the Mn(II) → Mn(III) step controlling the enzymatic oxidation of Mn(II). Our results suggest that the hardness and ionic strength of the aquatic environment

Synthesis and Piezoelectric Properties of Li, Ca and Mn-codoped BaTiO3 by a Solvothermal Approach

International Nuclear Information System (INIS)

Kimura, T; Dong, Q; Yin, S; Sato, T; Hashimoto, T; Sasaki, A; Aisawa, S

2013-01-01

3 at.% Li-doped (Ba 1-x Ca x )(Ti 1-y Mn y )O 3 particles with the Ca 2+ mole fraction, x, of 0–0.09 and Mn mole fraction, y, of 0 and 0.0005 were synthesized by a solvothermal approach at 200°C. The products consisted of nanoparticles of 50–100 nm in diameter, and did not change very much depending on the amount of Li, Ca and Mn-codoping. The change in relative dielectric constant, Δε r , in around room temperature decreased by doping Ca 2+ , and the lowest Δε r (4.51%) could be realized at x value of 0.03. The mechanical quality factor, Q m , of 3 at.% Li-doped (Ba 0.97 Ca 0.03 )(Ti 0.9995 Mn 0.0005 )O 3 increased to 521, and Δε r decreased to 1.72%, while the piezoelectric constant, d 33 (234pC/N), and electromechanical coupling factor, k p (40.0%), did not change very much compared with 3 at.% Li-doped BaTiO 3

High pressure luminescence studies of localized excitations in ZnS doped with Pb2+ and Mn2+

International Nuclear Information System (INIS)

House, G.L.; Drickamer, H.G.

1977-01-01

High pressure luminescence measurements have been made on ZnS doped with Pb +2 and Mn +2 . The data include changes in peak energy and shape, integrated intensities, and lifetimes. These localized emissions are treated in terms of a single configuration coordinate model. For Pb +2 the emission peak shifted to lower energy by a moderate amount and narrowed. For excitation in the Pb +2 absorption the intensity was independent of pressure, which is consistent with the fact that the energy barrier for radiationless return to the ground state was high at all pressures. For excitation in the ZnS absorption edge the intensity decreased significantly with pressure above about 80 kbar. Data on shifts of the conduction band with pressure would indicate that one is approaching a transition from a direct to indirect transition at high pressure so that decrease in emission intensity may be associated with decreased absorption efficiency. The Mn+ 2 emission peak shifted strongly to lower energy with increasing pressure. The direction and magnitude of the shift were consistent with the predictions of ligand field theory. The intensity doubled in 100 kbar, while the lifetime decreased by roughly a factor of 2. These results could be described in terms of a model for a phonon assisted transition. In addition, peak location, intensity, and lifetime measurements were made on ZnS:Pb:Mn. There is clear evidence of energy transfer by exchange, but in addition there is a nonradiative process in the doubly doped crystal which affects both intensities and lifetimes

Study of the Cu, Mn, Pb and Zn dynamics in soil, plants and bee pollen from the region of Teresina (PI, Brazil

Directory of Open Access Journals (Sweden)

Aline S. Silva

2012-12-01

Full Text Available The purpose of this study is to characterize native bee plants regarding their capacity to extract and accumulate trace elements from the soil and its consequences to the sanity of the produced pollen. The trace elements Cu, Mn, Pb and Zn were analyzed in soil, plants and bee pollen from Teresina region (PI, Brazil, by flame atomic absorption spectrophotometer. Considering the studied plant species, Cu and Pb metals presented in the highest levels in the roots of B. platypetala with 47.35 and 32.71 μg.mL-1 and H. suaveolens with 39.69 and 17.06 μg.mL-1, respectively, while in the aerial parts Mn and Zn metals presented the highest levels in S. verticillata with 199.18 and 85.73 μg.mL-1. In the pollen, the levels of Cu, Mn, Pb and Zn vary from 5.44 to 11.75 μg.mL-1; 34.31 to 85.75 μg.mL-1; 13.98 to 18.19 μg.mL-1 and 50.19 to 90.35 μg.mL-1, respectively. These results indicate that in the apicultural pasture the translocation (from soil to pollen of Mn and Zn was more effective than in case of Cu and Pb, therefore, the bee pollen can be used as food supplement without causing risks to human health.O objetivo deste estudo é caracterizar plantas apícolas nativas, quanto a sua capacidade de extrair e acumular elementos-traço do solo e suas conseqüências na sanidade do pólen produzido. Os elementos-traço Cu, Mn, Pb e Zn foram analisados em solo, planta e pólen apícolas em Teresina (PI, Brasil, por espectrofotometria de absorção atômica com atomização em chama. Considerando as espécies de plantas estudadas, os metais Cu e Pb apresentaram nas raízes maiores teores de B. platypetala com 47,35 e 32,71 µg.mL-1 e H. suaveolens com 39,69 e 17,06 µg.mL-1, respectivamente, enquanto na parte aérea os metais Mn e Zn apresentaram os maiores teores, em S. verticillata com 199,18 e 85, 73 µg.mL-1. No pólen os teores de Cu, Mn, Pb e Zn varia de 5,44 a 11,75 µg.mL-1; 34,31 a 85,75 µg.mL-1; 13,98 a 18,19 µg.mL-1 e 50,19 a 90,35 µg.mL-1

Luminescent properties and energy transfer of CaO:Ce{sup 3+}, Mn{sup 2+} phosphors for white LED

Energy Technology Data Exchange (ETDEWEB)

Liu, Qipeng, E-mail: dadi0314@163.com [Lunan Institute of Coal Chemical Industry, Jining 272000, Shandong (China); Yin, Huijun; Liu, Tao; Wang, CuiQing; Liu, Riqiang [Lunan Institute of Coal Chemical Industry, Jining 272000, Shandong (China); Lü, Wei [State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); You, Hongpeng, E-mail: hpyou@ciac.ac.cn [State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China)

2016-09-15

We have synthesized yellow–orange CaO:Ce{sup 3+},Mn{sup 2+} phosphors by solid-state reaction. Photoluminescence properties and energy transfer mechanism from Ce{sup 3+} to Mn{sup 2+} ions have been investigated. The Ce{sup 3+} activated phosphors exhibit strong absorption in the range of 250–490 nm and a yellow emission centered at 554 nm. When Mn{sup 2+} ions were codoped, CaO:Ce{sup 3+},Mn{sup 2+} phosphors exhibit yellow emission band of Ce{sup 3+} as well as orange emission band centered at 600 nm of Mn{sup 2+}. We observed an efficient energy transfer from Ce{sup 3+} to Mn{sup 2+} ions in CaO:Ce{sup 3+},Mn{sup 2+}, which was verified from the lifetime decay curves and was discussed by Dexter's energy transfer theory. The critical distance of the energy transfer from Ce{sup 3+} to Mn{sup 2+} ions has also been calculated to be 12.3 Å by spectral overlap methods following Dexter's theory and by concentration quenching mechanism to be 15.2 Å. Moreover, by combining the synthesized phosphors and InGaN blue chip (460 nm), warm-white light has been created.

The accumulation of elements in plants growing spontaneously on small heaps left by the historical Zn-Pb ore mining.

Science.gov (United States)

Stefanowicz, Anna M; Stanek, Małgorzata; Woch, Marcin W; Kapusta, Paweł

2016-04-01

The study evaluated the levels of nine metals, namely Ca, Cd, Fe, K, Mg, Mn, Pb, Tl, and Zn, in soils and tissues of ten plant species growing spontaneously on heaps left by historical mining for Zn-Pb ores. The concentrations of Cd, Pb, Tl, and Zn in heap soils were much higher than in control soils. Plants growing on heaps accumulated excessive amounts of these elements in tissues, on average 1.3-52 mg Cd kg(-1), 9.4-254 mg Pb kg(-1), 0.06-23 mg Tl kg(-1) and 134-1479 mg Zn kg(-1) in comparison to 0.5-1.1 mg Cd kg(-1), 2.1-11 mg Pb kg(-1), 0.02-0.06 mg Tl kg(-1), and 23-124 mg Zn kg(-1) in control plants. The highest concentrations of Cd, Pb, and Zn were found in the roots of Euphorbia cyparissias, Fragaria vesca, and Potentilla arenaria, and Tl in Plantago lanceolata. Many species growing on heaps were enriched in K and Mg, and depleted in Ca, Fe, and Mn. The concentrations of all elements in plant tissues were dependent on species, organ (root vs. shoot), and species-organ interactions. Average concentrations of Ca, K, and Mg were generally higher in shoots than in roots or similar in the two organs, whereas Cd, Fe, Pb, Tl, and Zn were accumulated predominantly in the roots. Our results imply that heaps left by historical mining for Zn-Pb ores may pose a potential threat to the environment and human health.

Enhancement of Magnetocaloric Effect in ({ {La}}_{0.67}{ {Ca}}_{0.33}{ {MnO}}_{3})/({ {La}}_{0.7}{ {Ba}}_{0.3}{ {MnO}}_{3}) ( La 0.67 Ca 0.33 MnO 3 ) / ( La 0.7 Ba 0.3 MnO 3 ) Composite

Science.gov (United States)

Khelifi, J.; Dhahri, E.; Hlil, E. K.

2018-03-01

The composite (La_{0.67}Ca_{0.33}MnO3)/La_{0.7}Ba_{0.3}MnO3) sample was prepared using the conventional solid-state reaction method, and their crystallographic structure was achieved by X-ray diffraction pattern analysis. The magnetic and magnetocaloric effect has been studied by magnetization measurements. Based on the relation: χ ^{-1}(T)∝ (T-T_C^Rand )^{1-λ }, the inverse of susceptibility shows a downturn before T_C indicating the existence of Griffiths phase for the temperature range T_C^Randphase has been obtained from detailed magnetization studies. Furthermore, a large magnetic entropy change is observed in (La_{0.67}Ca_{0.33}MnO3)/(La_{0.7}Ba_{0.3}MnO3) composite which possesses a large MCE characterized by two Δ S_M(T) peaks. It has revealed that the combination of manganite materials with different Curie temperatures is a possible method for enhancement of magnetocaloric effect. To determine the field dependence of the experimental Δ S_M(T), a local exponent n( T, H) can be calculated from the logarithmic derivative of the magnetic entropy change versus field; it is shown that for a multiphase system n evolves with field both at the Curie temperature of the system and at the Curie temperatures of the constituent phases.

Macrocyclic receptor showing extremely high Sr(II)/Ca(II) and Pb(II)/Ca(II) selectivities with potential application in chelation treatment of metal intoxication.

Science.gov (United States)

Ferreirós-Martínez, Raquel; Esteban-Gómez, David; Tóth, Éva; de Blas, Andrés; Platas-Iglesias, Carlos; Rodríguez-Blas, Teresa

2011-04-18

Herein we report a detailed investigation of the complexation properties of the macrocyclic decadentate receptor N,N'-Bis[(6-carboxy-2-pyridil)methyl]-4,13-diaza-18-crown-6 (H(2)bp18c6) toward different divalent metal ions [Zn(II), Cd(II), Pb(II), Sr(II), and Ca(II)] in aqueous solution. We have found that this ligand is especially suited for the complexation of large metal ions such as Sr(II) and Pb(II), which results in very high Pb(II)/Ca(II) and Pb(II)/Zn(II) selectivities (in fact, higher than those found for ligands widely used for the treatment of lead poisoning such as ethylenediaminetetraacetic acid (edta)), as well as in the highest Sr(II)/Ca(II) selectivity reported so far. These results have been rationalized on the basis of the structure of the complexes. X-ray crystal diffraction, (1)H and (13)C NMR spectroscopy, as well as theoretical calculations at the density functional theory (B3LYP) level have been performed. Our results indicate that for large metal ions such as Pb(II) and Sr(II) the most stable conformation is Δ(δλδ)(δλδ), while for Ca(II) our calculations predict the Δ(λδλ)(λδλ) form being the most stable one. The selectivity that bp18c6(2-) shows for Sr(II) over Ca(II) can be attributed to a better fit between the large Sr(II) ions and the relatively large crown fragment of the ligand. The X-ray crystal structure of the Pb(II) complex shows that the Δ(δλδ)(δλδ) conformation observed in solution is also maintained in the solid state. The Pb(II) ion is endocyclically coordinated, being directly bound to the 10 donor atoms of the ligand. The bond distances to the donor atoms of the pendant arms (2.55-2.60 Å) are substantially shorter than those between the metal ion and the donor atoms of the crown moiety (2.92-3.04 Å). This is a typical situation observed for the so-called hemidirected compounds, in which the Pb(II) lone pair is stereochemically active. The X-ray structures of the Zn(II) and Cd(II) complexes show that

Crystal and magnetic study of the disordered perovskites Ca(Mn0.5Sb0.5)O3 and Ca(Fe0.5Sb0.5)O3

International Nuclear Information System (INIS)

Retuerto, M.; Martinez-Lope, M.J.; Garcia-Hernandez, M.; Munoz, A.; Fernandez-Diaz, M.T.; Alonso, J.A.

2010-01-01

We have investigated the double perovskites Ca 2 MSbO 6 (M = Mn, Fe) that have been prepared by solid-state reaction (M = Fe) and wet chemistry procedures (M = Mn). The crystal and magnetic structures have been studied from X-ray (XRD) and neutron powder diffraction (NPD) data. Rietveld refinements show that the crystal structures are orthorhombic (space group Pbnm) with complete disorder of M and Sb cations, so the formula should be rewritten as Ca(M 0.5 Sb 0.5 )O 3 . Due to this disorder no evidences of Jahn-Teller distortion can be observed in the MnO 6 octahedra of Ca(Mn 0.5 Sb 0.5 )O 3 , in contrast with the ordered double perovskite Sr 2 MnSbO 6 . Ca(Fe 0.5 Sb 0.5 )O 3 behaves as an antiferromagnet with an ordered magnetic moment for Fe 3+ of 1.53(4)μ B and a propagation vector k = 0, as investigated by low-temperature NPD. The antiferromagnetic ordering is a result of the high degree of Fe/Sb anti-site disorder of the sample, which originates the spontaneous formation of Fe-rich islands, characterized by the presence of strong Fe-O-Fe antiferromagnetic couplings with enough long-range coherence to produce a magnetic contribution perceptible by NPD. By contrast, the magnetic structure of Ca(Mn 0.5 Sb 0.5 )O 3 cannot be observed by low-temperature NPD because the magnitude of the ordered magnetic moments is below the detection threshold for neutrons.

[Effects of Low-Molecular-Weight Organic Acids on the Speciation of Pb in Purple Soil and Soil Solution].

Science.gov (United States)

Liu, Jiang; Jiang, Tao; Huang, Rong; Zhang, Jin-zhong; Chen, Hong

2016-04-15

Lead (Pb) in purple soil was selected as the research target, using one-step extraction method with 0.01 mol · L⁻¹ sodium nitrate as the background electrolyte to study the release effect of citric acid (CA), tartaric acid (TA) and acetic acid (AC) with different concentrations. Sequential extraction and geochemical model (Visual Minteq v3.0) were applied to analyze and predict the speciation of Pb in soil solid phase and soil solution phase. Then the ebvironmental implications and risks of low-molecule weight organic acid (LMWOA) on soil Pb were analyzed. The results indicated that all three types of LMWOA increased the desorption capacity of Pb in purple soil, and the effect followed the descending order of CA > TA > AC. After the action of LMWOAs, the exchangeable Pb increased; the carbonate-bound Pb and Fe-Mn oxide bound Pb dropped in soil solid phase. Organic bound Pb was the main speciation in soil solution phase, accounting for 45.16%-75.05%. The following speciation of Pb in soil solution was free Pb, accounting for 22.71%-50.25%. For CA and TA treatments, free Pb ions and inorganic bound Pb in soil solution increased with increasing LMWOAs concentration, while organic bound Pb suffered a decrease in this process. An opposite trend for AC treatment was observed compared with CA and TA treatments. Overall, LMWOAs boosted the bioavailability of Pb in purple soil and had a potential risk to contaminate underground water. Among the three LMWOAs in this study, CA had the largest potential to activate soil Pb.

Effect of Si, Mn, Sn on Tensile and Corrosion Properties of Mg-4Zn-0.5Ca Alloys for Biodegradable Implant Materials

Energy Technology Data Exchange (ETDEWEB)

Cho, Dae Hyun; Nam, Ji Hoon; Lee, Byeong Woo; Park, Ji Yong; Shin, Hyun Jung; Park, Ik Min [Pusan National University, Busan (Korea, Republic of)

2015-03-15

Effect of elements Si, Mn, Sn on tensile and corrosion properties of Mg-4Zn-0.5Ca alloys were investigated. The results of tensile properties show that the yield strength, ultimate tensile strength and elongation of Mg-4Zn-0.5Ca alloy increased significantly with the addition of 0.6 wt% Mn. This is considered the grain refinement effect due to addition of Mn. However addition of 0.6 wt% Si decreased yield strength, ultimate tensile strength and elongation. The bio-corrosion behavior of Mg-4Zn-0.5Ca-X alloys were investigated using immersion tests and potentiodynamic polarization test in Hank's solution. Immersion test showed that corrosion rate of Mg-4Zn-0.5Ca-0.6Mn alloy was the lowest rate and addition of 1.0 wt% Sn accelerated corrosion rate due to micro-galvanic effect in α-Mg/CaMgSn phases interface. And corrosion potential (E{sub c}orr) of Mg-4Zn-0.5Ca-0.6Mn alloy was the most noble among Mg-4Zn-0.5Ca-X alloys.

Study of the Cu, Mn, Pb and Zn dynamics in soil, plants and bee pollen from the region of Teresina (PI), Brazil.

Science.gov (United States)

Silva, Aline S; Araújo, Sebastião B; Souza, Darcet C; Silva, Fábio A Santos e

2012-12-01

The purpose of this study is to characterize native bee plants regarding their capacity to extract and accumulate trace elements from the soil and its consequences to the sanity of the produced pollen. The trace elements Cu, Mn, Pb and Zn were analyzed in soil, plants and bee pollen from Teresina region (PI), Brazil, by flame atomic absorption spectrophotometer. Considering the studied plant species, Cu and Pb metals presented in the highest levels in the roots of B. platypetala with 47.35 and 32.71 μg.mL(-1) and H. suaveolens with 39.69 and 17.06 μg.mL(-1), respectively, while in the aerial parts Mn and Zn metals presented the highest levels in S. verticillata with 199.18 and 85.73 μg.mL(-1). In the pollen, the levels of Cu, Mn, Pb and Zn vary from 5.44 to 11.75 μg.mL(-1); 34.31 to 85.75 μg.mL(-1); 13.98 to 18.19 μg.mL(-1) and 50.19 to 90.35 μg.mL(-1), respectively. These results indicate that in the apicultural pasture the translocation (from soil to pollen) of Mn and Zn was more effective than in case of Cu and Pb, therefore, the bee pollen can be used as food supplement without causing risks to human health.

Spin-polarized investigation of ferromagnetism on magnetic semiconductors Mn{sub x}Ca{sub 1−x}S in the rock-salt phase

Energy Technology Data Exchange (ETDEWEB)

Choutri, H.; Ghebouli, M.A. [LMSE Laboratory, University of Bachir Ibrahimi, 34265 Bordj-Bou-Arréridj (Algeria); Ghebouli, B. [Laboratory of Surface and Interface Studies of Solid Materials, Department of Physics, Faculty of Science, Setif University 1, Setif 19000 (Algeria); Bouarissa, N., E-mail: n_bouarissa@yahoo.fr [Department of Physics, Faculty of Science, University of M' sila, 28000 M' sila (Algeria); Uçgun, E.; Ocak, H.Y. [Department of Physics, Faculty of Arts and Sciences, Dumlupinar University, Kutahya (Turkey)

2014-12-15

The structural, elastic, electronic and magnetic properties of the diluted magnetic semiconductors Mn{sub x}Ca{sub 1−x}S in the rock-salt phase have been investigated using first-principles calculations with both LDA and LDA + U functional. Features such as lattice constant, bulk modulus, elastic constants, spin-polarized band structure, total and local densities of states have been computed. We predict the values of the exchange constants and the band edge spin splitting of the valence and conduction bands. The hybridization between S-3p and Mn-3d produces small local magnetic moment on the nonmagnetic Ca and S sites. The ferromagnetism is induced due to the exchange splitting of S-3p and Mn-3d hybridized bands. The total magnetic moment per Mn of Mn{sub x}Ca{sub 1−x}S is 4.4μ{sub B} and 4.5μ{sub B} for LDA and LDA + U functional and is independent of the Mn concentration. The unfilled Mn-3d levels reduce the local magnetic moment of Mn from its free space charge value of 5μ{sub B}–4.4μ{sub B} and4.5μ{sub B} for LDA and LDA + U functional due to 3p–3d hybridization. - Highlights: • Fundamental properties of magnetic semiconductors Mn{sub x}Ca{sub 1−x}S. • Rock-salt phase of Mn{sub x}Ca{sub 1−x}S. • Magnetic properties of the diluted magnetic semiconductors Mn{sub x}Ca{sub 1−x}S. • The use of LDA + U functionals.

Neutron investigation of Ru-doped Nd1/2Ca1/2MnO3. Comparison with Cr-doped Nd1/2Ca1/2MnO3

International Nuclear Information System (INIS)

Moritomo, Yutaka; Nonobe, Toshihiko; Machida, Akihiko; Ohoyama, Kenji

2002-01-01

Lattice and magnetic properties are investigated for 3% Ru- and Cr-doped Nd 1/2 Ca 1/2 MnO 3 . The parent Nd 1/2 Ca 1/2 MnO 3 is a charge-ordered insulator (T CO =250K). With decreasing temperature below ≅210K, these compounds are separated into two perovskite phases, that is, the long-c and short-c phases. The long-c region shows a ferromagnetic transition at T C ≅210K for the Ru-doped compound and ≅130K for the Cr-doped compound, while the short-c region shows antiferromagnetic transition at T N ≅150K for Ru and ≅110K for Cr. We discuss the origin of the enhanced T C for the Ru-doped compound in terms of the effective one-electron bandwidth W of the e g -band. (author)

Crystal structure, energy transfer and tunable luminescence properties of Ca8ZnCe(PO4)7:Eu2+,Mn2+ phosphor

Science.gov (United States)

Ding, Chong; Tang, Wanjun

2018-02-01

Single-phased Ca8ZnCe(PO4)7:Eu2+,Mn2+ phosphors with whitlockite-type structure have been prepared via the combustion-assisted synthesis technique. The XRD pattern show that the as-obtained phosphors crystallize in a trigonal phase with space group of R-3c (161). Ca8ZnCe(PO4)7 host is full of sensitizers (Ce3+) and the Ce3+ emission at different lattice sites has been discussed. The efficient energy transfers from Ce3+ ions to Eu2+/Mn2+ ions and from Eu2+ to Mn2+ have been validated. Under UV excitation, the emitting color of Ca8ZnCe(PO4)7:Eu2+/Mn2+ samples can be modulated from violet blue to green and from violet blue to red-orange by the energy transfers of Ce3+→Eu2+ and Ce3+→Mn2+, respectively. Additionally, white emission has been obtained through adjusting the relative concentrations of Eu2+ and Mn2+ ions in the Ca8ZnCe(PO4)7 host under UV excitation. These results indicate that as-prepared Ca8ZnCe(PO4)7:Eu2+,Mn2+ may be a potential candidate as color-tunable white light-emitting phosphors.

Distribution of P, K, Ca, Mg, Cd, Cu, Fe, Mn, Pb and Zn in wood and bark age classes of willows and poplars used for phytoextraction on soils contaminated by risk elements.

Science.gov (United States)

Zárubová, Pavla; Hejcman, Michal; Vondráčková, Stanislava; Mrnka, Libor; Száková, Jiřina; Tlustoš, Pavel

2015-12-01

Fast-growing clones of Salix and Populus have been studied for remediation of soils contaminated by risk elements (RE) using short-rotation coppice plantations. Our aim was to assess biomass yield and distributions of elements in wood and bark of highly productive willow (S1--[Salix schwerinii × Salix viminalis] × S. viminalis, S2--Salix × smithiana clone S-218) and poplar (P1--Populus maximowiczii × Populus nigra, P2--P. nigra) clones with respect to aging. The field experiment was established in April 2008 on moderately Cd-, Pb- and Zn- contaminated soil. Shoots were harvested after four seasons (February 2012) and separated into annual classes of wood and bark. All tested clones grew on contaminated soils, with highest biomass production and lowest mortality exhibited by P1 and S2. Concentrations of elements, with exception of Ca and Pb, decreased with age and were higher in bark than in wood. The Salix clones were characterised by higher removal of Cd, Mn and Zn compared to the Populus clones. Despite generally higher RE content in young shoots, partly due to lower wood/bark ratios and higher RE concentrations in bark, the overall removal of RE was higher in older wood classes due to higher biomass yield. Thus, longer rotations seem to be more effective when phytoextraction strategy is considered. Of the four selected clones, S1 exhibited the best removal of Cd and Zn and is a good candidate for phytoextraction.

Influence of Al and the heavy metals Fe, Mn, Zn, Cu, Pb, and Cd on development and efficacy of vesicular-arbuscular mycorrhiza in tropical and subtropical plants. Einfluss von Al und den Schwermetallen Fe, Mn, Zn, Cu, Pb und Cd auf die Effizienz der VA-Mykorrhiza bei tropischen und subtropischen Pflanzen

Energy Technology Data Exchange (ETDEWEB)

Fabig, B.

1982-07-08

In greenhouse experiments the influence of Al and the heavy metals Fe, Mn, Zn, Cu, Pb, and Cd on the efficacy of VA-mycorrhizal fungi was tested with special regard to several soil pH levels and soil water regimes in different combinations. The most important results were: The inoculation led to a significantly better growth of all test plants in the presence of Al, Fe, Mn, Zn, Cu, Pb, and Cd up to a specific amount of the soil-applied element; beyond this specific limit the efficacy of the mycorrhiza was more or less inhibited depending on the element. In correlation with the growth, the nearly always better P uptake of the inoculated plants was impaired only by the highest toxic amounts of the elements. In comparison with the uninoculated plants, all the inoculated plants showed higher P and Pb concentrations. The mycorrhizal plants generally had significantly higher concentrations of the elements Al, Mn, Zn, Cu, and Cd in the roots than the uninoculated plants. Generally even toxic levels of Fe in the soil did not lead to higher Fe concentrations in the plants. Even the highest amounts of Al, Fe, Mn, Zn, and Cu did not cause microscopically visible injuries to the development of the mycorrhiza and did not impede the infection. Only the toxic levels of Pb led to a decrease of the infection rate of about 50%. Pb and Cd were the reason for morphological changes of the different developmental phases of the fungus. High amounts of Pb induced an increased formation of vesicles. The highest amounts of Cd were accompanied by the crowded occurrence of arbuscules.

High Br- Content CsPb(Cl yBr1- y)3 Perovskite Nanocrystals with Strong Mn2+ Emission through Diverse Cation/Anion Exchange Engineering.

Science.gov (United States)

Li, Fei; Xia, Zhiguo; Pan, Caofeng; Gong, Yue; Gu, Lin; Liu, Quanlin; Zhang, Jin Z

2018-04-11

The unification of tunable band edge (BE) emission and strong Mn 2+ doping luminescence in all-inorganic cesium lead halide perovskite nanocrystals (NCs) CsPbX 3 (X = Cl and Br) is of fundamental importance in fine tuning their optical properties. Herein, we demonstrate that benefiting from the differentiation of the cation/anion exchange rate, ZnBr 2 and preformed CsPb 1- x Cl 3 : xMn 2+ NCs can be used to obtain high Br - content Cs(Pb 1- x- z Zn z )(Cl y Br 1- y ) 3 : xMn 2+ perovskite NCs with strong Mn 2+ emission, and the Mn 2+ substitution ratio can reach about 22%. More specifically, the fast anion exchange could be realized by the soluble halide precursors, leading to anion exchange within a few seconds as observed from the strong BE emission evolution, whereas the cation exchange instead generally required at least a few hours; moreover, their exchange mechanism and dynamics process have been evaluated. The Mn 2+ emission intensity could be further varied by controlling the replacement of Mn 2+ by Zn 2+ with prolonged ion exchange reaction time. White light emission of the doped perovskite NCs via this cation/anion synergistic exchange strategy has been realized, which was also successfully demonstrated in a prototype white light-emitting diode (LED) device based on a commercially available 365 nm LED chip.

Suppression of the long-range magnetic order in Pb{sub 3}(Mn{sub 1−x}Fe{sub x}){sub 7}O{sub 15} upon substitution of Fe for Mn

Energy Technology Data Exchange (ETDEWEB)

Volkov, N.V. [Kirensky Institute of Physics, Russian Academy of Sciences, Siberian Branch, Krasnoyarsk 660036 (Russian Federation); Eremin, E.V., E-mail: eev@iph.krasn.ru [Kirensky Institute of Physics, Russian Academy of Sciences, Siberian Branch, Krasnoyarsk 660036 (Russian Federation); Bayukov, O.A.; Sablina, K.A. [Kirensky Institute of Physics, Russian Academy of Sciences, Siberian Branch, Krasnoyarsk 660036 (Russian Federation); Solov’ev, L.A. [Institute of Chemistry and Chemical Technology, Russian Academy of Sciences, Siberian Branch, Krasnoyarsk 660049 (Russian Federation); Velikanov, D.A.; Mikhashenok, N.V.; Osetrov, E.I. [Kirensky Institute of Physics, Russian Academy of Sciences, Siberian Branch, Krasnoyarsk 660036 (Russian Federation); Schefer, J.; Keller, L. [Laboratory for Neutron Scattering, ETH Zurich and Paul Scherrer Institut, CH-5232 Villigen PSI (Switzerland); Boehm, M. [Institut Laue-Langevin, 6 rue Jules Horowitz, BP 156, 38042 Grenoble, Cedex 9 (France)

2013-09-15

Structure and magnetic properties of Pb{sub 3}(Mn{sub 1−x}Fe{sub x}){sub 7}O{sub 15} single crystals with x=0–0.2 grown by spontaneous crystallization from solution in melt have been investigated. All the crystals belong to the hexagonal space group P6{sub 3}/mcm. The magnetic properties appeared to be strongly dependent on the iron doping level. At small (x=0.05) dopant concentrations, the value of magnetization and Neel temperature T{sub N} decrease insignificantly (T{sub N}=70 K). With increasing x, the three-dimensional magnetic ordering does not occur and temperature dependences of magnetization at x≥0.1 exhibit spin-glass-like features in the low-temperature region. - Highlights: • In the first time the single crystals of Pb{sub 3}(Mn{sub 1−x}Fe{sub x}){sub 7}O{sub 15} were grown. • The valence and locations of iron ions in crystal were determined. • Suppression of the long-range magnetic order in Pb{sub 3}(Mn{sub 1−x}Fe{sub x}){sub 7}O{sub 15} was discovered.

Neutron diffraction and magnetic study of the Nd0.7Pb0.3Mn1-xFexO3 (0=

International Nuclear Information System (INIS)

Blanco, J.J.; Insausti, M.; Gil de Muro, I.; Lezama, L.; Rojo, T.

2006-01-01

The effect of Fe doping on the ferromagnetic Nd 0.7 Pb 0.3 Mn 1-x Fe x O 3 (x=0, 0.025, 0.05, 0.075, 0.1) phases has been studied in order to analyze the double-exchange interaction. The structural and magnetic study has been carried out by neutron powder diffraction and susceptibility measurements between 1.7 and 300K. The substitution of Fe at the Mn site results in reductions in both the Curie temperature T c and the magnetic moment per Mn ion without appreciable differences in the crystal structures. All the compounds crystallize in Pnma space group. The thermal evolution of the lattice parameters of the Nd 0.7 Pb 0.3 Mn 1-x Fe x O 3 (x=0.025, 0.05, 0.075) compounds shows discontinuities in volume and lattice parameters close to the magnetic transition temperature. Increasing amounts of Fe 3+ reduces the double exchange interactions and no magnetic contribution for x=0.1 is observed. The magnetic structures of Nd 0.7 Pb 0.3 Mn 1-x Fe x O 3 (x=0, 0.025, 0.05, 0.075) compounds show that the Nd and Mn ions are ferromagnetically ordered

Where Water is Oxidized to Dioxygen: Structure of the Photosynthetic Mn4Ca Cluster from X-ray Spectroscopy

Energy Technology Data Exchange (ETDEWEB)

Yano, Junko; Yano, Junko; Yachandra, Vittal K.

2007-10-24

Light-driven oxidation of water to dioxygen in plants, algae and cyanobacteria iscatalyzed within photosystem II (PS II) by a Mn4Ca cluster. Although the cluster has been studied by many different methods, the structure and the mechanism have remained elusive. X-ray absorption and emission spectroscopy and EXAFS studies have been particularly useful in probing the electronic and geometric structure, and the mechanism of the water oxidation reaction. Recent progress, reviewed here, includes polarized X-ray absorption spectroscopy measurements of PS II single crystals. Analysis of those results has constrained the Mn4Ca cluster geometry to a setof three similar high-resolution structures. The structure of the cluster from the present study is unlike either the 3.0 or 3.5 Angstrom-resolution X-ray structures or other previously proposed models. The differences between the models derived from X-rayspectroscopy and crystallography are predominantly because of damage to the Mn4Ca cluster by X-rays under the conditions used for structure determination by X-ray crystallography. X-ray spectroscopy studies are also used for studying the changes in the structure of the Mn4Ca catalytic center as it cycles through the five intermediate states known as the Si-states (i=0-4). The electronic structure of the Mn4Ca cluster has been studied more recently using resonant inelastic X-ray scattering spectroscopy (RIXS), in addition to the earlier X-ray absorption and emission spectroscopy methods. These studies are revealing that the assignment of formaloxidation states is overly simplistic. A more accurate description should consider the charge density on the Mn atoms that includes the covalency of the bonds and delocalization of the charge over the cluster. The geometric and electronic structure of the Mn4Ca cluster in the S-states derived from X-ray spectroscopy are leading to a detailed understanding of the mechanism of the O-O bond formation during the photosynthetic water

The effect of Fe, Mn, Ni and Pb Load on Soil and its enrichment factor ratios in different soil grain size fractions as an Indicator for soil pollution

International Nuclear Information System (INIS)

Rabie, F.H.; Abdel-Sabour, M.F.

2000-01-01

An industrial area north of greater Cairo was selected to investigate the impact of intensive industrial activities on soil characteristics and Fe, Mn, Ni and Pb total content. The studied area was divided to six sectors according to its source of irrigation water and/or probability of pollution. Sixteen soil profiles were dug and soil samples were taken, air dried, fractionated to different grain size fractions, then total heavy metals (Fe, Mn, Ni and Pb) were determined using ICP technique. The enrichment factor for each metal for each soil fraction/soil layer was estimated and discussed. The highest EF ratios in the clay fraction was mainly with Pb which indicated the industrial impact on the soil. In case of sand fraction, Mn was the highest always compared to other studied metals. Concerning silt fraction, a varied accumulation of Fe, Mn, and Pb was observed with soil depth and different soil profiles

Inhomogeneous ferrimagnetic-like behavior in Gd2/3Ca1/3MnO3 single crystals

International Nuclear Information System (INIS)

Haberkorn, N.; Larregola, S.; Franco, D.; Nieva, G.

2009-01-01

We present a study of the magnetic properties of Gd 2/3 Ca 1/3 MnO 3 single crystals at low temperatures, showing that this material behaves as an inhomogeneous ferrimagnet. In addition to small saturation magnetization at 5 K, we have found history dependent effects in the magnetization and the presence of exchange bias. These features are compatible with microscopic phase separation in the clean Gd 2/3 Ca 1/3 MnO 3 system studied

Magnetocaloric and magnetoresistive properties of La0.67Ca0.33-xSrxMnO3

DEFF Research Database (Denmark)

Dinesen, Anders Reves

This thesis presents results of an experimental investigation of magneto-caloric and magnetoresistive properties of a series of polycrystalline Ca- and Sr-doped lanthanum manganites, La0.67Ca0.33-xSrxMnO3 (0=x=0.33 ), with the perovskite structure. The samples consisted of sintered oxide powders...... prepared the glycine-nitrate combustion technique. The compounds were ferromagnetic and showed a Curie transition in the temperature range 267–370 K (TC increased with increasing x). An analysis of the structural properties was carried out by means of x-ray diffraction and the Rietveld technique...... and the Curie temperature. The Mn–O–Mn bonds mediate ferromagnetism and electrical transport in these materials via the double-exchange mechanism. The magnetocaloric effect of the La0.67Ca0.33-xSrxMnO3 samples was measured directly and indirectly (by means of magnetization measurements). All the samples showed...

Percolative nature of A-site disordered La0.75Ca0.25-xSrxMnO3 manganites

DEFF Research Database (Denmark)

Venkatesh, R.; Yadam, Sankararao; Venkateshwarlu, D.

2015-01-01

Magnetic, resistive, and magnetoresistance measurements were used to investigate the percolative nature of A-site disordered La0.75Ca0.25-xSrxMnO3(x = 0, 0.10) manganites. La0.75Ca0.15Sr0.10MnO3 has an orthorhombic structure and second order magnetic phase transition indicates the presence of two...

A -Site Ordered Double Perovskite CaMnTi ₂ O ₆ as a Multifunctional Piezoelectric and Ferroelectric–Photovoltaic Material

Energy Technology Data Exchange (ETDEWEB)

Gou, Gaoyang [Frontier Institute; Charles, Nenian [Department of Materials Science and Engineering, Drexel University, Philadelphia, Pennsylvania 19104, United States; Shi, Jing [MOE Key Laboratory; Rondinelli, James M. [Department; Materials Science Division, Argonne National Laboratory, Argonne, Illinois 60439, United States

2017-09-11

The double perovskite CaMnTi2O6, is a rare A site ordered perovskite oxide that exhibits a sizable ferroelectric polarization and relatively high Curie temperature. Using first-principles calculations combined with detailed symmetry analyses, we identify the origin of the ferroelectricity in CaMnTi2O6. We further explore the material properties of CaMnTi2O6, including its ferroelectric polarization, dielectric and piezoelectric responses, magnetic order, electronic structure, and optical absorption coefficient. It is found that CaMnTi2O6 exhibits room-temperature-stable ferroelectricity and moderate piezoelectric responses. Moreover, CaMnTi2O6 is predicted to have a semiconducting energy band gap similar to that of BiFeO3, and its band gap can further be tuned-via distortions of the planar Mn-O bond lengths. CaMnTi2O6 exemplifies a new class of single-phase semiconducting ferroelectric perovskites for potential applications in ferroelectric photovoltaic solar cells.

Modeling interactive effects of Pb contamination, Ca"2"+ and Mg"2"+ on passivity of alloy 800 in simulated crevice chemistries at high temperature

International Nuclear Information System (INIS)

Lu, Baotong

2015-01-01

Highlights: • The capability of Pb impurity degrading the passivity of alloy 800 in high temperature water is much stronger than those of dissolved Ca/Mg salts. • The interactive effects of Pb-impurities and Ca/Mg salts on the passivity are likely a result competitive adsorption. • A phenomenological model to interpret the interactive effect of Pb-impurities and Ca/Mg salts on the passivity. - Abstract: A phenomenological model is postulated to interpret the interactive impacts of dissolved Pb contamination, Ca"2"+ and Mg"2"+ on passivity of Alloy 800 in simulated crevice chemistries at 300 °C. Passivity degradation is characterized by the retarded dehydration during passivation and increased donor density in passive film. Ca"2"+ and Mg"2"+ can cause the passivity degradation in the Pb-free chemistries but, if the Pb-contamination concentration exceeds a critical value, would reduce the detrimental effect of Pb-contamination. This behavior may be related to the extremely strong adsorption capacity of Pb contamination. Finally, the applications in the water management strategy of nuclear power plants are discussed.

Determinación de Ca, Cu, Fe y Pb por espectrofotometría de absorción atómica en aguardientes de caña

OpenAIRE

Magdalena Lorenzo; Arlyn Reyes; Idania Blanco; María del Carmen Vasallo

2010-01-01

La determinación de Ca, Cu, Fe y Pb en aguardientes¸ se realizó por espectrofotometría de absorción atómica. El volumen de inyección fue 20 uL, la calibración se llevó a cabo en intervalos de 0,5-25,0 mg.L-1 de Ca; 0,25-5,0 mg.L-1 para el Cu, Pb y el Cu, y se utilizaron las absorbancias de Ca, Cu, Fe y Pb contra la concentración de los analitos, respectivamente. Las correlaciones lineales típicas de r = 0,99 en todos los casos. El método propuesto se aplicó para la determinación directa de C...

Application of atomic absorption spectrophotometry to determine Cd, Cu, Pb, Zn,...in vegetable samples in Dalat

Energy Technology Data Exchange (ETDEWEB)

Giang, Nguyen; Tam, Nguyen Thanh; Ngoc Trinh, Le Thi; Mai, Truong Phuong; Minh, Nguyen Van [Nuclear Research Institute, Dalat (Viet Nam)

2004-08-01

Nowadays atomic absorption spectrometry has become valuable method for trace element analysis because high specificity; low detection litmus, easy to use; easy sample preparation, low investment and running costs... atomic absorption spectrometry is generally accepted as one the most suitable method for single - element analysis of trace elements in various kinds of materiel. In 2003, we applied flame - atomic absorption spectrometry for analyzing Ca, Cd, Cu, Pb, Zn...in vegetables and their extracted juices were collected form 11 locations of Dalat, including two kinds of vegetables (goods and safety) in both the summer and winter. Average concentration of Ca = 240 mg/kg wet, Cd = 0.035 mg/kg wet, Cu = 0.67 mg/kg wet, Mg = 131 mg/kg wet, Fe = 8.1/kg wet, Mn = 3.1/kg wet, Na = 3266 mg/kg wet, Pb = 0.345 mg/kg wet and Zn = 3.3 mg wet. In their extracted juices: Ca = 89 mg/kg wet, Cd = 0.008 mg/kg wet, Cu = 0.19 mg/kg wet, Mg = 43 mg/kg wet, Fe = 2.3 mg/kg wet, Mn = 0.61 mg/kg wet, Na = 971 mg/kg wet, Pb = 0.107 mg/kg wet and Zn = 0.65 mg/kg wet. (author)

Application of atomic absorption spectrophotometry to determine Cd, Cu, Pb, Zn,...in vegetable samples in Dalat

International Nuclear Information System (INIS)

Nguyen Giang; Nguyen Thanh Tam; Le Thi Ngoc Trinh; Truong Phuong Mai; Nguyen Van Minh

2004-01-01

Nowadays atomic absorption spectrometry has become valuable method for trace element analysis because high specificity; low detection litmus, easy to use; easy sample preparation, low investment and running costs... atomic absorption spectrometry is generally accepted as one the most suitable method for single - element analysis of trace elements in various kinds of materiel. In 2003, we applied flame - atomic absorption spectrometry for analyzing Ca, Cd, Cu, Pb, Zn...in vegetables and their extracted juices were collected form 11 locations of Dalat, including two kinds of vegetables (goods and safety) in both the summer and winter. Average concentration of Ca = 240 mg/kg wet, Cd = 0.035 mg/kg wet, Cu = 0.67 mg/kg wet, Mg = 131 mg/kg wet, Fe = 8.1/kg wet, Mn = 3.1/kg wet, Na = 3266 mg/kg wet, Pb = 0.345 mg/kg wet and Zn = 3.3 mg wet. In their extracted juices: Ca = 89 mg/kg wet, Cd = 0.008 mg/kg wet, Cu = 0.19 mg/kg wet, Mg = 43 mg/kg wet, Fe = 2.3 mg/kg wet, Mn = 0.61 mg/kg wet, Na = 971 mg/kg wet, Pb = 0.107 mg/kg wet and Zn = 0.65 mg/kg wet. (author)

Adsorption and Desorption Characteristics of Cd2+ and Pb2+ by Micro and Nano-sized Biogenic CaCO3

Science.gov (United States)

Liu, Renlu; Guan, Yong; Chen, Liang; Lian, Bin

2018-01-01

The purpose of this study was to elucidate the characteristics and mechanisms of adsorption and desorption for heavy metals by micro and nano-sized biogenic CaCO3 induced by Bacillus subtilis, and the pH effect on adsorption was investigated. The results showed that the adsorption characteristics of Cd2+ and Pb2+ are well described by the Langmuir adsorption isothermal equation, and the maximum adsorption amounts for Cd2+ and Pb2+ were 94.340 and 416.667 mg/g, respectively. The maximum removal efficiencies were 97% for Cd2+, 100% for Pb2+, and the desorption rate was smaller than 3%. Further experiments revealed that the biogenic CaCO3 could maintain its high adsorption capability for heavy metals within wide pH ranges (3–8). The FTIR and XRD results showed that, after the biogenic CaCO3 adsorbed Cd2+ or Pb2+, it did not produce a new phase, which indicated that biogenic CaCO3 and heavy metal ions were governed by a physical adsorption process, and the high adsorptive capacity of biogenic CaCO3 for Cd2+ and Pb2+ were mainly attributed to its large total specific surface area. The findings could improve the state of knowledge about biogenic CaCO3 formation in the environment and its potential roles in the biogeochemical cycles of heavy metals. PMID:29434577

Distributions of dissolved trace metals (Cd, Cu, Mn, Pb, Ag in the southeastern Atlantic and the Southern Ocean

Directory of Open Access Journals (Sweden)

M. Boye

2012-08-01

Full Text Available Comprehensive synoptic datasets (surface water down to 4000 m of dissolved cadmium (Cd, copper (Cu, manganese (Mn, lead (Pb and silver (Ag are presented along a section between 34° S and 57° S in the southeastern Atlantic Ocean and the Southern Ocean to the south off South Africa. The vertical distributions of Cu and Ag display nutrient-like profiles similar to silicic acid, and of Cd similar to phosphate. The distribution of Mn shows a subsurface maximum in the oxygen minimum zone, whereas Pb concentrations are rather invariable with depth. Dry deposition of aerosols is thought to be an important source of Pb to surface waters close to South Africa, and dry deposition and snowfall may have been significant sources of Cu and Mn at the higher latitudes. Furthermore, the advection of water masses enriched in trace metals following contact with continental margins appeared to be an important source of trace elements to the surface, intermediate and deep waters in the southeastern Atlantic Ocean and the Antarctic Circumpolar Current. Hydrothermal inputs may have formed a source of trace metals to the deep waters over the Bouvet Triple Junction ridge crest, as suggested by relatively enhanced dissolved Mn concentrations. The biological utilization of Cu and Ag was proportional to that of silicic acid across the section, suggesting that diatoms formed an important control over the removal of Cu and Ag from surface waters. However, uptake by dino- and nano-flagellates may have influenced the distribution of Cu and Ag in the surface waters of the subtropical Atlantic domain. Cadmium correlated strongly with phosphate (P, yielding lower Cd / P ratios in the subtropical surface waters where phosphate concentrations were below 0.95 μM. The greater depletion of Cd relative to P observed in the Weddell Gyre compared to the Antarctic Circumpolar Current could be due to increase Cd uptake induced by iron-limiting conditions in these high

Tuning the magnetocaloric properties of La0.7Ca0.3MnO3 manganites through Ni-doping

Science.gov (United States)

Gómez, A.; Chavarriaga, E.; Supelano, I.; Parra, C. A.; Morán, O.

2018-04-01

The effect of Ni2+ doping on the magnetic and magnetocaloric properties of La0.7Ca0.3MnO3 manganites synthesized via the auto-combustion method is reported. The aim of studying Ni2+-substituted La0.7Ca0.3Mn1 - xNixO3 (x = 0 , 0.02 , 0.07, and 0.1) manganites was to explore the possibility of increasing the operating temperature range for the magnetocaloric effect through tuning of the magnetic transition temperature. X-ray diffraction analysis confirmed the phase purity of the synthesized samples. The substitution of Mn3+ ions by Ni2+ ions in the La0.7Ca0.3MnO3 lattice was also corroborated through this technique. The dependence of the magnetization on the temperature reveals that all the compositions exhibit a well-defined ferromagnetic to paramagnetic transition near the Curie temperature. A systematic decrease in the values of the Curie temperature is clearly observed upon Ni2+ doping. Probably the replacement of Mn3+ by Ni2+ ions in the La0.7Ca0.3MnO3 lattice weakens the Mn3+-O-Mn4+ double exchange interaction, which leads to a decrease in the transition temperature and the magnetic moment in the samples. By using Arrott plots, it was found that the phase transition from ferromagnetic to paramagnetic is second order. The maximum magnetic entropy changes observed for the x = 0 , 0.02 , 0.07, and 0.1 composites was 0.85, 0.77, 0.63, and 0.59 J/kg K, respectively, under a magnetic field of 1.5 T. In general, it was verified that the magnetic entropy change achieved for La0.7Ca0.3Mn1 - xNixO3 manganites synthesized via the auto-combustion method is higher than those reported for other manganites with comparable Ni2+-doping levels synthesized via standard solid state reaction. The addition of Ni2+ increases the value of the relative cooling power as compared to that of the parent compound. The highest value of this parameter (∼60 J/kg) is found for a Ni-doping level of 2% around 230 K in a field of 1.5 T.

Pecan nutshell as biosorbent to remove Cu(II), Mn(II) and Pb(II) from aqueous solutions.

Science.gov (United States)

Vaghetti, Julio C P; Lima, Eder C; Royer, Betina; da Cunha, Bruna M; Cardoso, Natali F; Brasil, Jorge L; Dias, Silvio L P

2009-02-15

In the present study we reported for the first time the feasibility of pecan nutshell (PNS, Carya illinoensis) as an alternative biosorbent to remove Cu(II), Mn(II) and Pb(II) metallic ions from aqueous solutions. The ability of PNS to remove the metallic ions was investigated by using batch biosorption procedure. The effects such as, pH, biosorbent dosage on the adsorption capacities of PNS were studied. Four kinetic models were tested, being the adsorption kinetics better fitted to fractionary-order kinetic model. Besides that, the kinetic data were also fitted to intra-particle diffusion model, presenting three linear regions, indicating that the kinetics of adsorption should follow multiple sorption rates. The equilibrium data were fitted to Langmuir, Freundlich, Sips and Redlich-Peterson isotherm models. Taking into account a statistical error function, the data were best fitted to Sips isotherm model. The maximum biosorption capacities of PNS were 1.35, 1.78 and 0.946mmolg(-1) for Cu(II), Mn(II) and Pb(II), respectively.

Phase diagram study for the PbO-ZnO-CaO-SiO_2 -“Fe_2O_3 ” system in air with CaO/SiO_2 in 1.1 and PbO/(CaO+SiO_2) in 2.4 weight ratios

International Nuclear Information System (INIS)

Lopez-Rodriguez, Josue; Romero-Serrano, Antonio; Hernandez-Ramirez, Aurelio; Cruz-Ramirez, Alejandro; Almaguer-Guzman, Isaias; Benavides-Perez, Ricardo; Flores-Favela, Manuel

2017-01-01

An experimental study on the phase equilibrium and the liquidus isotherms for the PbO-ZnO-CaO-SiO_2 -“Fe_2O_3 ” system with CaO/SiO_2 in 1.1 and PbO/(CaO+SiO_2) in 2.4 weight ratios, respectively, was carried out in the temperature range 1100-1300 deg C (1373-1573 K). High temperature phases were determined by the equilibrium-quenching method. Results are presented in the form of pseudo-ternary sections “Fe_2O_3 ”-ZnO-(PbO+CaO+SiO_2). X-Ray diffraction (XRD) and SEM-EDS results showed that the phase equilibria in this system are dominated by the high melting temperature spinel and zincite phases. It was observed that if the system is at a temperature below 1300 deg C and the total (Fe_2O_3 + ZnO) is greater than 20 wt%, spinel and/or zincite will be present in the slag system. As an application of the phase diagram, the liquid phase compositions below the liquidus surface were estimated, then their viscosities were calculated using FACTSage software. (author)

Quantitative trait loci controlling Cu, Ca, Zn, Mn and Fe content in ...

Indian Academy of Sciences (India)

of essential minerals (such as Fe, Zn etc), breeding mineral- efficient crops that produce .... and seven digenic interactions were identified for Cu, Ca,. Zn, Mn and Fe, .... Eva P. 1993 Cadmium, copper and lead in wild rice from central. Canada.

Growth of nucleation sites on Pb-doped Bi2Sr2Ca1Cu2O8+δ

International Nuclear Information System (INIS)

Finnemore, D.K.; Xu, M.; Kouzoudis, D.; Bloomer, T.; Kramer, M.J.; McKernan, S.; Balachandran, U.; Haldar, P.

1996-01-01

In the growth of Bi 2 Sr 2 Ca 2 Cu 3 O 10+δ from mixed powders of Pb-doped Bi 2 Sr 2 Ca 1 Cu 2 O 8+δ and other oxides, it has been discovered that a dense array of hillocks or mesas grow at the interface between a Ag overlay and Pb-doped Bi 2 Sr 2 Ca 1 Cu 2 O 8+δ grains during the ramp up to the reaction temperature. As viewed in an environmental scanning electron microscope, the Ag coated grains develop a texture that looks like open-quote open-quote chicken pox close-quote close-quote growing on the grains at about 700 degree C. These hillocks are about 100 nm across and are spaced at about 500 to 1000 nm. If there is no Ag, this texture does not develop. Preliminary measurements indicate that the hillocks are a recrystallization of (Bi,Pb) 2 Sr 2 Ca 1 Cu 2 O 8+δ , and are definitely not a Pb rich phase. copyright 1996 American Institute of Physics

On the “alpha-phase” of Ca{sub 2−x}Sr{sub x}MnO{sub 4} and extending the chemistry of Sr{sub 7−y}Ca{sub y}Mn{sub 4}O{sub 15} to y>1

Energy Technology Data Exchange (ETDEWEB)

Craddock, Sarah; Senn, Mark S.

2017-04-15

There has been renewed interest in the Ruddlesden-Popper phase (n=2) of composition Ca{sub n+1}Mn{sub n}O{sub 3} {sub n+1} in the light of recent research that has highlighted the nature of the improper ferroelectric ground state, which arises due to the couplings between specific combinations of MnO{sub 6} octahedral rotations and tilts. A fruitful route to control these octahedral degrees of freedom, and hence such desired physical properties, is through chemical substitution on the A–site cation i.e. Ca{sub 2−x}Sr{sub x}MnO{sub 4} for n =1, and in light of this, we have reinvestigated the chemistry of this solid solution. Here we focus on a common impurity phase observed during this synthesis which has been termed the “alpha-phase” in the literature. We show that this impurity phase is actually comprised mainly of a structure related to Sr{sub 7}Mn{sub 4}O{sub 15} but is found here with significantly higher Ca substitution than previously believed possible. Sr{sub 7}Mn{sub 4}O{sub 15} is an interesting structural type in its own right, but has been mainly overlooked to date, exhibiting interesting physics related to low dimensional magnetic ordering and dimer interactions, and we show here that the structural type is a likely candidate for exhibiting a multiferroic ground state. The prospect of being able to tune the lattice and the exchange interactions through further chemical substitution is likely to lead to a renewed interest in this material. - Graphical abstract: Extending the chemistry of Sr{sub 7−y}Ca{sub y}Mn{sub 4}O{sub 15} beyond y>1, revealing highly anisotropic cation ordering and tunable magnetic properties. - Highlights: • Chemistry of the unique structural type Sr{sub 7}Mn{sub 4}O{sub 15} is extended to high Ca concentrations. • Cation occupancy model is determined, showing highly anisotropic solubility of Ca on the 7 unique Sr crystallographic sites. • Anomalies in the magnetic susceptibility data are discussed with reference to

Synthesis and effect of Ce and Mn co-doping on photoluminescence characteristics of Ca6AlP5O20:Eu novel phosphors.

Science.gov (United States)

Shinde, K N; Dhoble, S J

2013-01-01

A series of Ca6AlP5O20 doped with rare earths (Eu and Ce) and co-doped (Eu, Ce and Eu,Mn) were prepared by combustion synthesis. Under Hg-free excitation, Ca6AlP5O20:Eu exhibited Eu(2+) (486 nm) emission in the blue region of the spectrum and under near Hg excitation (245 nm), Ca6AlP5O20:Ce phosphor exhibited Ce(3+) emission (357 nm) in the UV range. Photoluminescence (PL) peak intensity increased in Ca6AlP5O20:Eu,Ce and Ca6AlP5O20:Eu, Mn phosphors due to co-activators of Ce(3+) and Mn(2+) ions. As a result, these ions played an important role in PL emission in the present matrix. Ca6AlP5O20:Eu, Ce and Ca6AlP5O20:Eu, Mn phosphors provided energy transfer mechanisms via Ce(3+) → Eu(2+) and Eu(2+) → Mn(2+), respectively. Eu ions acted as activators and Ce ions acted as sensitizers. Ce emission energy was well matched with Eu excitation energy in the case of Ca6AlP5O20:Eu, Ce and Eu ions acted as activators and Mn ions acted as sensitizers in Ca6AlP5O20:Eu, Mn. This study included synthesis of new and efficient phosphate phosphors. The impact of doping and co-doping on photoluminescence properties and energy transfer mechanisms were investigated and we propose a feasible interpretation. Copyright © 2012 John Wiley & Sons, Ltd.

Atomic structure of CaF2/MnF2-Si(1 1 1) superlattices from X-ray diffraction

International Nuclear Information System (INIS)

Alcock, Simon G.; Nicklin, C.L.; Howes, P.B.; Norris, C.A.; Kyutt, R.N.; Sokolov, N.S.; Yakovlev, N.L.

2007-01-01

X-ray reflectivity and non-specular crystal truncation rod scans have been used to determine the three-dimensional atomic structure of the buried CaF 2 -Si(1 1 1) interface and ultrathin films of MnF 2 and CaF 2 within a superlattice. We show that ultrathin films of MnF 2 , below a critical thickness of approximately four monolayers, are crystalline, pseudomorphic, and adopt the fluorite structure of CaF 2 . High temperature deposition of the CaF 2 buffer layer produces a fully reacted, CaF 2 -Si(1 1 1) type-B interface. The mature, 'long' interface is shown to consist of a partially occupied layer of CaF bonded to the Si substrate, followed by a distorted CaF layer. Our atomistic, semi-kinematical scattering method extends the slab reflectivity method by providing in-plane structural information

Structure and magnetoresistance of La0.67Ca0.33MnO3 films grown coherently on (001)NdGaO3

International Nuclear Information System (INIS)

Bojkov, Yu.A.; Danilov, V.A.; Bojkov, A.Yu.

2003-01-01

The (001) La 0.67 Ca 0.33 MnO 3 films, 40-120 nm thick, grown through the method of the laser evaporation on the (001)NdGaO 3 , are studied. The crystalline lattice parameters, measured for the La 0.67 Ca 0.33 MnO 3 film in the substrate plane α parallel = 3.851 A and along the normal to its surface α perpendicular = 3.850 A practically coincide with the parameter of the pseudocubic elementary cell of the neodymium gallate. The elementary cell volume in the La 0.67 Ca 0.33 MnO 3 film was insignificantly lesser than the corresponding value for the stoichiometric voluminous samples. The position of the maximum on the specific resistance dependence on the temperature did not depend on the La 0.67 Ca 0.33 MnO 3 film thickness. The maximum values of the negative magnetoresistance (MR ≅ 0.25, H = 0.4 T) for the La 0.67 Ca 0.33 MnO 3 films were observed at the temperatures of 239-244 K [ru

Ion microprobe assessment of the heterogeneity of Mg/Ca, Sr/Ca and Mn/Ca ratios in Pecten maximus and Mytilus edulis (bivalvia shell calcite precipitated at constant temperature

Directory of Open Access Journals (Sweden)

P. S. Freitas

2009-07-01

Full Text Available Small-scale heterogeneity of biogenic carbonate elemental composition can be a significant source of error in the accurate use of element/Ca ratios as geochemical proxies. In this study ion microprobe (SIMS profiles showed significant small-scale variability of Mg/Ca, Sr/Ca and Mn/Ca ratios in new shell calcite of the marine bivalves Pecten maximus and Mytilus edulis that was precipitated during a constant-temperature culturing experiment. Elevated Mg/Ca, Sr/Ca and Mn/Ca ratios were found to be associated with the deposition of elaborate shell features, i.e. a shell surface stria in P. maximus and surface shell disturbance marks in both species, the latter a common occurrence in bivalve shells. In both species the observed small-scale elemental heterogeneity most likely was not controlled by variable transport of ions to the extra-pallial fluid, but by factors such as the influence of shell organic content and/or crystal size and orientation, the latter reflecting conditions at the shell crystal-solution interface. In the mid and innermost regions of the P. maximus shell the lack of significant small-scale variation of Mg/Ca ratios, which is consistent with growth at constant temperature, suggest a potential application as a palaeotemperature proxy. Cross-growth band element/Ca ratio profiles in the interior of bivalve shells may provide more promising palaeo-environmental tools than sampling from the outer region of bivalve shells.

Dissolved trace metals (Ni, Zn, Co, Cd, Pb, Al, and Mn) around the Crozet Islands, Southern Ocean

Science.gov (United States)

Castrillejo, Maxi; Statham, Peter J.; Fones, Gary R.; Planquette, Hélène; Idrus, Farah; Roberts, Keiron

2013-10-01

A phytoplankton bloom shown to be naturally iron (Fe) induced occurs north of the Crozet Islands (Southern Ocean) every year, providing an ideal opportunity to study dissolved trace metal distributions within an island system located in a high nutrient low chlorophyll (HNLC) region. We present water column profiles of dissolved nickel (Ni), zinc (Zn), cobalt (Co), cadmium (Cd), lead (Pb), aluminium (Al), and manganese (Mn) obtained as part of the NERC CROZEX program during austral summer (2004-2005). Two stations (M3 and M1) were sampled downstream (north) of Crozet in the bloom area and near the islands, along with a control station (M2) in the HNLC zone upstream (south) of the islands. The general range found was for Ni, 4.64-6.31 nM; Zn, 1.59-7.75 nM; Co, 24-49 pM; Cd, 135-673 pM; Pb, 6-22 pM; Al, 0.13-2.15 nM; and Mn, 0.07-0.64 nM. Vertical profiles indicate little island influence to the south with values in the range of other trace metal deprived regions of the Southern Ocean. Significant removal of Ni and Cd was observed in the bloom and Zn was moderately correlated with reactive silicate (Si) indicating diatom control over the internal cycling of this metal. Higher concentrations of Zn and Cd were observed near the islands. Pb, Al, and Mn distributions also suggest small but significant atmospheric dust supply particularly in the northern region.

EXAFS and EPR study of La0.6Sr0.2Ca0.2MnO3 and La0.6Sr0.2Ba0.2MnO3

International Nuclear Information System (INIS)

Yang, D.-K.Dong-Seok; Ulyanov, A.N.; Phan, Manh-Huong; Kim, Ikgyun; Ahn, Byong-Keun; Rhee, Jang Roh; Kim, Jung Sun; Nguyen, Chau; Yu, Seong-Cho

2003-01-01

Extended X-ray absorption fine structure (EXAFS) analysis and electron-paramagnetic resonance (EPR) have been used to examine the local structure and the internal dynamics of La 0.6 Sr 0.2 Ca 0.2 MnO 3 and La 0.6 Sr 0.2 Ba 0.2 MnO 3 lanthanum manganites. The Mn-O bond distance (∼1.94 Angst for both samples) and the Debye-Waller factors (0.36x10 -2 and 0.41x10 -2 Angst 2 for La 0.6 Sr 0.2 Ca 0.2 MnO 3 and for La 0.6 Sr 0.2 Ba 0.2 MnO 3 , respectively) were obtained from the EXAFS analysis. The dependence of the EPR line width on dopant kind (Ca or Ba) showed a decrease of the spin-lattice interaction with an increase of the Curie temperature. For both compositions, the EPR line intensity followed the exponential law I(T)=I 0 exp(E a /k B T), deduced on the basis of the adiabatic polaron hopping model

Pb(Zr,Ti)O3-Pb(Mn1/3Nb2/3)O3 piezoelectric thick films by aerosol deposition

International Nuclear Information System (INIS)

Ryu, Jungho; Choi, Jong-Jin; Hahn, Byung-Dong; Yoon, Woon-Ha; Lee, Byoung-Kuk; Choi, Joon Hwan; Park, Dong-Soo

2010-01-01

Piezoelectric thick films of Pb(Zr,Ti)O 3 -Pb(Mn 1/3 Nb 2/3 )O 3 (PZT-PMnN) with Zr:Ti ratios ranging from 0.45:0.55 to 0.60:0.40 were fabricated on a platinized silicon wafer by aerosol deposition (AD). All the films were deposited with a thickness of 10 μm with high density. By adding PMnN to 57:43 PZT, a dielectric constant as low as ∼660 was achieved while the effective piezoelectric constant was over 140 pC/N. PZT-PMnN with a Zr:Ti ratio of 57:43 thus showed a maximum piezoelectric voltage constant (g 33 ) of 23.8 x 10 -3 Vm/N and is a good candidate for high quality thick films for application to high-energy density or high sensitivity, piezoelectric energy harvesters and sensors.

A Structural Molar Volume Model for Oxide Melts Part I: Li2O-Na2O-K2O-MgO-CaO-MnO-PbO-Al2O3-SiO2 Melts—Binary Systems

Science.gov (United States)

Thibodeau, Eric; Gheribi, Aimen E.; Jung, In-Ho

2016-04-01

A structural molar volume model was developed to accurately reproduce the molar volume of molten oxides. As the non-linearity of molar volume is related to the change in structure of molten oxides, the silicate tetrahedral Q-species, calculated from the modified quasichemical model with an optimized thermodynamic database, were used as basic structural units in the present model. Experimental molar volume data for unary and binary melts in the Li2O-Na2O-K2O-MgO-CaO-MnO-PbO-Al2O3-SiO2 system were critically evaluated. The molar volumes of unary oxide components and binary Q-species, which are model parameters of the present structural model, were determined to accurately reproduce the experimental data across the entire binary composition in a wide range of temperatures. The non-linear behavior of molar volume and thermal expansivity of binary melt depending on SiO2 content are well reproduced by the present model.

Thermally activated demagnetization in (La0.97 Ca0.03)0.96Mn0.96 O3-δ

International Nuclear Information System (INIS)

Alonso, J.M.; Arroyo, A.; Cortes-Gil, R.; Garcia, M.A.; Gonzalez-Calbet, J.M.; Gonzalez, J.M.; Hernando, A.; Rojo, J.M.; Vallet-Regi, M.

2005-01-01

We report on the temperature dependence of the relaxation properties of a Mn perovskite with overall composition (La 0.97 Ca 0.03 ) 0.96 (Mn 4+ 0.07 Mn 3+ 0.93 ) 0.96 O 2.90 .Our data are correlated with the simultaneous occurrence in the sample of metallic double-exchange magnetically coupled, Mn 4+ clusters and of insulating superexchange coupled regions.

Spin texture of the surface state of three-dimensional Dirac material Ca3PbO

Science.gov (United States)

Kariyado, Toshikaze

2015-04-01

The bulk and surface electronic structures of a candidate three-dimensional Dirac material Ca3PbO and its family are discussed especially focusing on the spin texture on the surface states. We first explain the basic features of the bulk band structure of Ca3PbO, such as emergence of Dirac fermions near the Fermi energy, and compare it with the other known three-dimensional Dirac semimetals. Then, the surface bands and spin-texture on them are investigated in detail. It is shown that the surface bands exhibit strong momentum-spin locking, which may be useful in some application for spin manipulation, induced by a combination of the inversion symmetry breaking at the surface and the strong spin-orbit coupling of Pb atoms. The surface band structure and the spin-textures are sensitive to the surface types.

Spin texture of the surface state of three-dimensional Dirac material Ca3PbO

International Nuclear Information System (INIS)

Kariyado, Toshikaze

2015-01-01

The bulk and surface electronic structures of a candidate three-dimensional Dirac material Ca 3 PbO and its family are discussed especially focusing on the spin texture on the surface states. We first explain the basic features of the bulk band structure of Ca 3 PbO, such as emergence of Dirac fermions near the Fermi energy, and compare it with the other known three-dimensional Dirac semimetals. Then, the surface bands and spin-texture on them are investigated in detail. It is shown that the surface bands exhibit strong momentum-spin locking, which may be useful in some application for spin manipulation, induced by a combination of the inversion symmetry breaking at the surface and the strong spin-orbit coupling of Pb atoms. The surface band structure and the spin-textures are sensitive to the surface types. (paper)

Accumulation of Pb and Mn on Road Side Leaves, Analysis from Mauri Por to Hawks bay Road

International Nuclear Information System (INIS)

Salam, M.

2010-01-01

Accurate measurements of the heavy-metal contents in polluted areas are required to assess the potential ecological risks in these areas. Chemical and biological indicators are of interest when they provide information about the concentration and accumulation of heavy metals in the environment. These studies were conducted in order to investigate heavy-metal accumulation and the effect on Conocarpus (Conocarpus Erectus) on roadside trees. The total content of Pb and Mn was determined using atomic absorption spectrophotometry, AAS. The present results showed variations that indicate both the concerned species have the highest concentration in all the sampling areas near the road. According to the results present study, the average concentration of Pb and Mn are 10.576+3.482 micro g/gm and 91.977+ 30.030 micro g/gm respectively. The results showed that the plant demonstrated a physiological response to the heavy-metal pollution, which suggests that roadside plants are indicators of heavy-metal accumulation and the effect on the environment. (author)

Ag doped (Bi1.6Pb0.4Sr2CaCu2O8+δ textured rods

Directory of Open Access Journals (Sweden)

Díez, J. C.

2008-06-01

Full Text Available In this work, superconducting samples of (Bi1.6Pb0.4Sr2CaCu2O8+δ with Ag additions have been studied. (Bi1.6Pb0.4Sr2CaCu2O8+δ + x wt.% Ag (with x = 0, 1 and 3 powders were synthesized using a sol-gel method. The obtained powders were used as precursors to fabricate long textured cylindrical bars through a floating zone melting method. A drastic change on the microstructure has been found when comparing with undoped Bi2Sr2CaCu2O8+δ samples. The results showed that electrical resistivity at room temperature, critical current as well as flexural strength are improved when Ag is added to these Pb doped samples, while critical temperature does not change. On the other hand, it has been found that samples with composition (Bi1.6Pb0.4Sr2CaCu2O8+δ + Ag shown E-I curves with very high sharpness values on the zone of the superconducting to normal transition, reaching n-values (E∼In as high as 45 at 65K.Se han preparado polvos cerámicos de composición (Bi1.6Pb0.4Sr2CaCu2O8+δ + x % Ag en peso (con x = 0, 1 y 3 mediante un proceso sol-gel. Estos polvos se han utilizado para fabricar precursores que se texturaron por medio del método de fusión zonal flotante. Se ha encontrado un gran cambio en la microestructura cuando se compara con muestras de composición pura Bi2Sr2CaCu2O8+δ. Tanto la resistividad eléctrica a temperatura ambiente, como la corriente crítica, así como la resistencia a flexión se mejoran cuando la Ag se adiciona a estas muestras dopadas con Pb, mientras que no se observa cambio en la temperatura crítica. Por otra parte, se ha encontrado que las muestras de composición (Bi1.6Pb0.4Sr2CaCu2O8+δ + Ag presentan una gran pendiente de la curva E-I en la zona de transición entre el estado superconductor y el estado normal. Con estas composiciones, se han encontrado valores de n (E∼In de hasta 45 a 65K.

On the “alpha-phase” of Ca2−xSrxMnO4 and extending the chemistry of Sr7−yCayMn4O15 to y>1

International Nuclear Information System (INIS)

Craddock, Sarah; Senn, Mark S.

2017-01-01

There has been renewed interest in the Ruddlesden-Popper phase (n=2) of composition Ca n+1 Mn n O 3 n+1 in the light of recent research that has highlighted the nature of the improper ferroelectric ground state, which arises due to the couplings between specific combinations of MnO 6 octahedral rotations and tilts. A fruitful route to control these octahedral degrees of freedom, and hence such desired physical properties, is through chemical substitution on the A–site cation i.e. Ca 2−x Sr x MnO 4 for n =1, and in light of this, we have reinvestigated the chemistry of this solid solution. Here we focus on a common impurity phase observed during this synthesis which has been termed the “alpha-phase” in the literature. We show that this impurity phase is actually comprised mainly of a structure related to Sr 7 Mn 4 O 15 but is found here with significantly higher Ca substitution than previously believed possible. Sr 7 Mn 4 O 15 is an interesting structural type in its own right, but has been mainly overlooked to date, exhibiting interesting physics related to low dimensional magnetic ordering and dimer interactions, and we show here that the structural type is a likely candidate for exhibiting a multiferroic ground state. The prospect of being able to tune the lattice and the exchange interactions through further chemical substitution is likely to lead to a renewed interest in this material. - Graphical abstract: Extending the chemistry of Sr 7−y Ca y Mn 4 O 15 beyond y>1, revealing highly anisotropic cation ordering and tunable magnetic properties. - Highlights: • Chemistry of the unique structural type Sr 7 Mn 4 O 15 is extended to high Ca concentrations. • Cation occupancy model is determined, showing highly anisotropic solubility of Ca on the 7 unique Sr crystallographic sites. • Anomalies in the magnetic susceptibility data are discussed with reference to symmetry arguments pointing towards a possible novel multiferroic mechanism in this material.

Analytisch-chemische aspecten van de bepaling van As, Ca, Cd, Sb, Sn, Pb, Zn in MVS-filterdestruaten met ICP-MS

NARCIS (Netherlands)

Velde-Koerts T van der; Lesquillier AI; Ritsema R; LAC

1995-01-01

In dit onderzoek werd een ICP-MS-methode ontwikkeld voor de bepaling van Ca, Zn, As, Cd, Sb, Sn en Pb in filterdestruaten. De onderste analysegrens is 30 ng/l Sb, 60 ng/l Cd, 200 ng/l As, 300 ng/l Sn, 400 ng/l Pb, 4 mug/l Zn en 20 mug/l Ca ; de precisie is beter dan 7% RSD voor Ca, 4% RSD voor

Tunable multicolor and enhanced red emission of monodisperse CaF2:Yb3+/Ho3+ microspheres via Mn2+ doping

Science.gov (United States)

Wang, Rui; Yuan, Maohui; Zhang, Chaofan; Wang, Hongyan; Xu, Xiaojun

2018-05-01

Transition metal ions (e.g. Mn2+) and lanthanide co-doped upconversion (UC) materials have attracted wide attention in recent years due to their promising application in multicolor display. Here, we report the hydrothermal synthesis and characterization of Mn2+ doped monodisperse CaF2:Yb3+/Ho3+ microspheres. The results of X-ray diffraction (XRD) revealed that Mn2+ doping does not change the cubic phase of CaF2 material but will lead to diffraction peaks shifting slightly towards higher angle due to the substitution of larger Ca2+ by the relatively smaller Mn2+. Under the excitation of 980 nm continuous wave (CW) laser, these microspheres exhibit green-yellow-red tuning colors and remarkable enhancement of both red to green ratio (R/G) and red to blue ratio (R/B) when increasing Mn2+ concentration from 0 to 30 mol%. The energy migration process between Ho3+ and Mn2+ was proposed and supported by time-decay and power dependence measurements of Ho3+ UC emission. These upconversion materials may have potential applications in optical devices, color display, nanoscale lasers and biomedical imaging.

Optical non-linearity tuning in Ca{sub 8-x}Pb{sub x}MBi(VO{sub 4}){sub 7} whitlockite-type systems

Energy Technology Data Exchange (ETDEWEB)

Beskorovaynaya, Daria A., E-mail: darya.beskorovajnaya@list.ru [Chemistry Department, Moscow State University, 119991 Moscow (Russian Federation); Department of Physical and Colloid Chemistry, Gubkin Russian State University of Oil and Gas, 119991 Moscow (Russian Federation); Deyneko, Dina V. [Chemistry Department, Moscow State University, 119991 Moscow (Russian Federation); Shubnikov Institute of Crystallography RAS, 119333 Moscow (Russian Federation); Baryshnikova, Oksana V. [Chemistry Department, Moscow State University, 119991 Moscow (Russian Federation); Stefanovich, Sergey Yu. [Chemistry Department, Moscow State University, 119991 Moscow (Russian Federation); L.Ya. Karpov Institute of Physical Chemistry, 105064 Moscow (Russian Federation); Lazoryak, Bogdan I. [Chemistry Department, Moscow State University, 119991 Moscow (Russian Federation)

2016-07-25

Ca{sub 8-x}Pb{sub x}MBi(VO{sub 4}){sub 7}, M{sup 2+} = Mg{sup 2+}, Zn{sup 2+} (0 ≤ x ≤ 1.5) and M{sup 2+} = Ca{sup 2+}, Cd{sup 2+} (0 ≤ x ≤ 2) solid solutions with whitlockite-type structure have been prepared by solid state reactions in the form of powders and ceramics. Ferroelectric phase transitions (FPT) are revealed in the cause of dielectric, calorimetric and temperature second harmonic generation (SHG) investigations. It is found that ferroelectric Curie points in solid solutions decrease with x from 1000–1070 K to 730–800 K. The intensity of SHG firstly increases with x and then decreases, the highest SHG signal belongs to Ca{sub 7}PbCdBi(VO{sub 4}){sub 7} and Ca{sub 6.5}Pb{sub 1.5}CdBi(VO{sub 4}){sub 7}. Variation of Pb{sup 2+} concentration is shown to have a minor influence on the coherence length, therefore the SHG augmentation in solid solutions is attributed to optical nonlinear coefficient . The structure of Ca{sub 6.5}Pb{sub 1.5}MgBi(VO{sub 4}){sub 7} is resolved and crystal structure changes in solid solutions are analyzed. The results are interpreted in view of site occupancy by two- and trivalent cations and their influence on formation of spare space essential for Pb{sup 2+} and Bi{sup 3+} non-bonded electrons stereo-activity in whitlockite-type crystal structures. For the first time contribution to optical nonlinearity from VO{sub 4}{sup 3−} anionic groups in different positions is also discussed. - Highlights: • The Curie temperatures of ferroelectric Ca{sub 8-x}Pb{sub x}MBi(VO{sub 4}){sub 7} solid solutions are chemically controlled from 1070 down to 730–800 K. • Optical SHG non-linear coefficient in Ca{sub 8-x}Pb{sub x}MBi(VO{sub 4}) strongly increase up to 3.3 pm/V at an optimized Pb and Bi concentration. • Structure-property correlations in the whitlockites includes crystal site positions occupancy by two- and trivalent cations.

New members of the A2 M ‧ M2″ structure family (A=Ca, Sr, Yb, La; M ‧ = In , Sn , Pb; M ″ = Si , Ge)

Science.gov (United States)

Jehle, Michael; Dürr, Ines; Fink, Saskia; Lang, Britta; Langenmaier, Michael; Steckhan, Julia; Röhr, Caroline

2015-01-01

The new mixed tetrelides Sr2PbGe2 and Yb2SnGe2, several mixed Ca/Sr (AII) germanides A2II (Sn, Pb)Ge2 and two polymorphs of La2 InSi2 represent new members of the general structure family of ternary alkaline-earth/lanthanoid main group silicides/germanides A2 M ‧ M2″ (M ‧ = In , Sn , Pb ; M ″ = Si , Ge). All compounds were synthesized from melts of the elements and their crystal structures have been determined by means of single crystal X-ray diffraction. Sr2PbGe2 (Cmmm, a=402.36(11), b=1542.3(4), c=463.27(10) pm) crystallizes with the Mn2AlB2 -type structure. In exhibiting infinite planar Ge zig-zag chains, it represents one border of the compound series. The other borderline case, where only [Ge2 ] dumbbells are left as Ge building units, is represented by the Ca/Yb tin germanides Ca2SnGe2 and Yb2SnGe2 (Mo2FeB2 -type; P4/mbm, a=748.58(13)/740.27(7), c=445.59(8)/435.26(5) pm). In between these two border structures compounds with variable Si/Ge chain lengths could be obtained by varying the averaged size of the AII cations: Ca0.45Sr1.55PbGe2 (new structure type; Pbam, a=791.64(5), b=2311.2(2), c=458.53(3) pm) contains planar six-membered chain segments [Ge6 ]. Tetrameric pieces [Ge4 ] are the conspicuous structure elements in Ca1.16Sr0.84SnGe2 and La2 InSi2 (La2InNi2 -type; Pbam, a=781.01(2)/762.01(13), b=1477.95(3)/1494.38(6), c=457.004(9)/442.1(3) pm). The tetragonal form of 'La2 In Si2‧ (exact composition: La2In1.07Si1.93, P4/mbm, a=1309.11(12), c=443.32(4) pm) also crystallizes in a new structure type, containing only [Si3 ] trimers as cutouts of the planar chains. In all structures the Si/Ge zig-zag chains/chain segments are connected by In/Sn/Pb atoms to form planar M layers, which are separated by pure A layers. Band structure calculations within the FP-LAPW DFT approach together with the Zintl formalism, extended by the presence of hypervalent bonding of the heavier M ‧ elements, give insight into the chemical bonding of this series of p

Structural insights into the light-driven auto-assembly process of the water-oxidizing Mn4CaO5-cluster in photosystem II.

Science.gov (United States)

Zhang, Miao; Bommer, Martin; Chatterjee, Ruchira; Hussein, Rana; Yano, Junko; Dau, Holger; Kern, Jan; Dobbek, Holger; Zouni, Athina

2017-07-18

In plants, algae and cyanobacteria, Photosystem II (PSII) catalyzes the light-driven splitting of water at a protein-bound Mn 4 CaO 5 -cluster, the water-oxidizing complex (WOC). In the photosynthetic organisms, the light-driven formation of the WOC from dissolved metal ions is a key process because it is essential in both initial activation and continuous repair of PSII. Structural information is required for understanding of this chaperone-free metal-cluster assembly. For the first time, we obtained a structure of PSII from Thermosynechococcus elongatus without the Mn 4 CaO 5 -cluster. Surprisingly, cluster-removal leaves the positions of all coordinating amino acid residues and most nearby water molecules largely unaffected, resulting in a pre-organized ligand shell for kinetically competent and error-free photo-assembly of the Mn 4 CaO 5 -cluster. First experiments initiating (i) partial disassembly and (ii) partial re-assembly after complete depletion of the Mn 4 CaO 5 -cluster agree with a specific bi-manganese cluster, likely a di-µ-oxo bridged pair of Mn(III) ions, as an assembly intermediate.

Bio-corrosion characterization of Mg-Zn-X (X = Ca, Mn, Si) alloys for biomedical applications.

Science.gov (United States)

Rosalbino, F; De Negri, S; Saccone, A; Angelini, E; Delfino, S

2010-04-01

The successful applications of magnesium-based alloys as biodegradable orthopedic implants are mainly inhibited due to their high degradation rates in physiological environment. This study examines the bio-corrosion behaviour of Mg-2Zn-0.2X (X = Ca, Mn, Si) alloys in Ringer's physiological solution that simulates bodily fluids, and compares it with that of AZ91 magnesium alloy. Potentiodynamic polarization and electrochemical impedance spectroscopy results showed a better corrosion behaviour of AZ91 alloy with respect to Mg-2Zn-0.2Ca and Mg-2Zn-0.2Si alloys. On the contrary, enhanced corrosion resistance was observed for Mg-2Zn-0.2Mn alloy compared to the AZ91 one: Mg-2Zn-0.2Mn alloy exhibited a four-fold increase in the polarization resistance than AZ91 alloy after 168 h exposure to the Ringer's physiological solution. The improved corrosion behaviour of the Mg-2Zn-0.2Mn alloy with respect to the AZ91 one can be ascribed to enhanced protective properties of the Mg(OH)(2) surface layer. The present study suggests the Mg-2Zn-0.2Mn alloy as a promising candidate for its applications in degradable orthopedic implants, and is worthwhile to further investigate the in vivo corrosion behaviour as well as assessed the mechanical properties of this alloy.

High temperature superconductivity in Zn and Mn substituted (Tl,Cr)Sr2CaCu2O7

International Nuclear Information System (INIS)

Lo, S.V.; Abd Shukor, R.

1999-01-01

Samples with nominal starting composition (TICr 0 .15)Sr 2 (Ca 1-x M x )Cu 2 O 7 (TI-1212) for x=0 - 0.7 with M= Zn and Mn have been prepared and investigated by powder X-ray diffraction (XRD) and electrical resistance measurements. All sample showed a mixed phase of 1212 and 1201. Dominant 1212-phase was observed for x=0.0-0.5 and x=0.0-0.4, for Zn and Mn series, respectively. The superconducting transition temperature was suppressed when Zn and Mn are substituted at the Ca site. For the Zn series the normal state behavior is metallic throughout the doping range. For the Mn series the normal state behavior is metallic for 0.1≤x≥0.3 and semiconducting like x>0.3. The suppression of T c and formation of the TI-1212 phase are discussed in terms of the ionic radius and valence state of the substituted elements. (author)

Strain induced magnetism in La0.5Ca0.5MnO3 systems

Energy Technology Data Exchange (ETDEWEB)

Tietze, Thomas; Nolle, Daniela; Schuetz, Gisela; Goering, Eberhard [Max-Planck-Institut fuer Metallforschung, Stuttgart (Germany); Aydogdu, Guelguen; Habermeier, Hanns-Ulrich [Max-Planck-Institut fuer Festkoerperforschung, Stuttgart (Germany)

2009-07-01

The La{sub 1-x}Ca{sub x}MnO{sub 3} exhibits, besides the double exchange relate magneto resistive effects, many interesting properties as a function of the doping level. Depending on the doping level x the system may exhibit ferromagnetism, antiferromagnetism, orbital ordering, and charge ordering. Epitaxial tensile and compressive strains are very important for the fine tuning of the lattice degree of freedom and therefore for the magnetic nearest neighbor coupling. By *adjusting* tensile and compressive strain with corresponding substrates one can switch between FM and AFM coupling between the FM ordered ab-planes. In order to investigate the influence of different substrates and relaxation effects element specific XMCD measurements were performed on La{sub 0.5}Ca{sub 0.5}MnO{sub 3} systems.

Structure and magnetic properties of La{sub 2/3}Sr{sub 1/3}MnO{sub 3}/CaMnO{sub 3} multilayers

Energy Technology Data Exchange (ETDEWEB)

Granada, Mara [Centro Atomico Bariloche and Instituto Balseiro, CNEA-UNC, Av. Bustillo 9500, 8400 San Carlos de Bariloche (Argentina)]. E-mail: granadam@cab.cnea.gov.ar; Sirena, Martin [Centro Atomico Bariloche and Instituto Balseiro, CNEA-UNC, Av. Bustillo 9500, 8400 San Carlos de Bariloche (Argentina); Steren, Laura B. [Centro Atomico Bariloche and Instituto Balseiro, CNEA-UNC, Av. Bustillo 9500, 8400 San Carlos de Bariloche (Argentina); Leyva, Gabriela [Depto. de Fisica, Centro Atomico Constituyentes, CNEA, Av. Gral. Paz y Constituyentes, 1650 San Martin (Argentina)

2004-12-31

Structural and magnetic properties of manganite-based multilayers, La{sub 2/3}Sr{sub 1/3}MnO{sub 3}/CaMnO{sub 3}, composed of ferromagnetic metals and antiferromagnetic insulator barriers are investigated in this work. Compounds of similar lattice parameters were used to build the samples, so we expect an excellent stacking of the different layers along the structure. To get a first insight of this system, the crystalline structure of a series of samples, grown on (1 0 0) SrTiO{sub 3} and (1 0 0) MgO single-crystalline substrates, has been studied. X-ray diffraction patterns show that the structure is strongly textured in the (1 0 0) direction when grown on SrTiO{sub 3}, regardless the composition of the bottom layer. A different result is found on the same system grown on MgO: when the buffer layer is CaMnO{sub 3}, the structure grows in the (1 1 0) orientation while it grows in the (1 0 0) direction when the bottom layer is La{sub 2/3}Sr{sub 1/3}MnO{sub 3}. Magnetic coupling of the ferromagnetic layers across the antiferromagnetic spacer has been studied with magnetization measurements.

Bulk and nanocrystalline electron doped Gd0.15Ca0.85MnO3: Synthesis and magnetic characterization

Science.gov (United States)

Dhal, Lakshman; Chattarpal; Nirmala, R.; Santhosh, P. N.; Kumary, T. Geetha; Nigam, A. K.

2014-09-01

Polycrystalline Gd0.15Ca0.85MnO3 sample was prepared by solid state reaction method and nanocrystalline samples of different grain sizes of the same were prepared by sol-gel method. Phase purity and composition were verified by room temperature X-ray diffraction and SEM-EDAX analysis. Magnetization data of bulk Gd0.15Ca0.85MnO3 in 5 kOe field shows a peak at 119 K (TN) suggesting an antiferromagnetic transition. Nanocrystalline Gd0.15Ca0.85MnO3 sample ( 54 nm size) also shows a cusp at 107 K and a broad thermal hysteresis between field cooled cooling (FCC) and field cooled warming (FCW) data around this temperature. This thermal hysteresis suggests possible crystal structural transition. Field variation of magnetization of bulk Gd0.15Ca0.85MnO3 at 5 K shows a tendency to saturate, but yields a magnetic moment value of only 1.12 μB/f.u. in 70 kOe. The value of magnetization of nanocrystalline sample at 5 K in 70 kOe field is slightly larger and is 1.38 μB/f.u. which is probably due to the surface moments of the nanoparticle samples. Both the samples show Curie-Weiss-like behaviour in their paramagnetic state.

Possible origin of photoconductivity in La0.7Ca0.3MnO3

Science.gov (United States)

Sagdeo, P. R.; Choudhary, R. J.; Phase, D. M.

2010-01-01

The effect of photon energy on the density of states near Fermi level of pulsed laser deposited La0.7Ca0.3MnO3 thin film has been studied to investigate the possible origin of change in the conductivity of these manganites upon photon exposure. For this purpose the photoelectron spectroscopy measurements were carried out using CSR beamline (BL-2) on Indus-1 synchrotron radiation source. The valance band spectra were measured at room temperature with photon energy ranging from 40 to 60 eV. We could see huge change in the density of states near Fermi level and this change is observed to be highest at 56 eV which is due to the resonance between Mn 3p to Mn 3d level. Our results suggest that the probability of electron transfer from deep Mn 3p level to Mn 3d-eg level is higher than that of Mn 3d-t2g level. It appears that this transfer of electron from deep Mn level to Mn 3d-eg level not only modifies the density of state near Fermi level but also changes the mobility of electrons by modifying the electron lattice coupling due to presence of Mn+3 Jahn-Teller ion.

Structural and magnetic properties of layered perovskite manganite LaCaBiMn2O7

Directory of Open Access Journals (Sweden)

Oubla M.

2013-09-01

Full Text Available The layered perovskite oxide, LaCaBiMn2O7, has been prepared by the conventional aqueous solution precipitation method. The powder X-ray diffraction studies suggest that the phase crystallizes with tetragonal unit cell in the space group I4/mmm. The magnetic properties suggest that the ferromagnetic interactions are dominant and manganese ion in the phase is present in mixed valence states Mn3+and Mn4+. The thermomagnetization curve is found to obey the Bloch law. Spin wave stiffness constant D and the approximate value for JMnMnexchange interaction were estimated from the experimental results.

Evaluation of Ca3(Co,M2O6 (M=Co, Fe, Mn, Ni as new cathode materials for solid-oxide fuel cells

Directory of Open Access Journals (Sweden)

Fushao Li

2015-10-01

Full Text Available Series compounds Ca3(Co0.9M0.12O6 (M=Co, Fe, Mn, Ni with hexagonal crystal structure were prepared by sol–gel route as the cathode materials for solid oxide fuel cells (SOFCs. Effects of the varied atomic compositions on the structure, electrical conductivity, thermal expansion and electrochemical performance were systematically evaluated. Experimental results showed that the lattice parameters of Ca3(Co0.9Fe0.12O6 and Ca3(Co0.9Mn0.12O6 were both expanded to certain degree. Electron-doping and hole-doping effects were expected in Ca3(Co0.9Mn0.12O6 and Ca3(Co0.9Ni0.12O6 respectively according to the chemical states of constituent elements and thermal-activated behavior of electrical conductivity. Thermal expansion coefficients (TEC of Ca3(Co0.9M0.12O6 were measured to be distributed around 16×10−6 K−1, and compositional elements of Fe, Mn, and Ni were especially beneficial for alleviation of the thermal expansion problem of cathode materials. By using Ca3(Co0.9M0.12O6 as the cathodes operated at 800 °C, the interfacial area-specific resistance varied in the order of M=CoMn, and the over-potential increased in the order of M=Fe≈M=CoMnCa3(Co0.9Fe0.12O6 showed the best electrochemical performance and the power density as high as ca. 500 mW cm−2 at 800 °C achieved in the single cell with La0.8Sr0.2Ga0.83Mg0.17O2.815 as electrolyte and Ni–Ce0.8Sm0.2O1.9 as anode. Ca3(Co0.9M0.12O6 (M=Co, Fe, Mn, Ni can be used as the cost-effective cathode materials for SOFCs.

Crystalline behaviour and electrical properties of manganese perovskites substituted on A or B sites: ErMnO₃ modified by Ca and EuMnO₃ modified by Co

Directory of Open Access Journals (Sweden)

Tartaj, J.

2010-06-01

Full Text Available The structural and electrical features of the manganites solid solutions (Er,CaMnO₃ and Eu(Co,MnO₃, have been studied by X-ray diffraction and conductivity measurements. Powders were prepared by solid-state reaction between the component oxides and Calcium carbonate. Incorporation of Co²⁺ on the lattice in the B sites or the Ca²⁺ on the A sites leads to changes in the parameters and symmetry of the perovskite compound EuMnO₃ and hexagonal ErMnO₃ respectively. The phase transition depends on the amount of substituted Jahn-Teller Mn³⁺ cations. Solid solutions based on Eu(Mn,CoO₃ perovskite compound change from O’-type to O-type orthorhombic perovskite symmetry when the Mn³⁺ cation amount decreases, because of the progressive substitution by Co. This transition occurs for an amount of Co²⁺ as low as ~10 at% Co²⁺ cation. The (Er,CaMnO₃ based solid solutions showed a different behaviour. From x=0.25 there is a change in the symmetry of the solid solution from hexagonal to orthorhombic, O’-type perovskite. Steric influence seems to play a secondary role on the lattice distortion of manganites. Sintered samples of the perovskite solid solutions were measured for establishing their electrical properties. All the samples showed semiconducting behaviour.

Las características estructurales y eléctricas de las soluciones sólidas de manganitas (Er,CaMnO₃ y Eu(Co,MnO₃, han sido estudiadas por difracción de rayos X y medidas de la conductividad en continua. Los polvos fueron preparados por reacción en estado sólido entre los óxidos componentes y carbonato de calcio. La incorporación de Co²⁺ en la red en los sitios B o de Ca²⁺ en los sitios A conduce a cambios en los parámetros y la simetría de EuMnO₃ perovskita y ErMnO₃ hexagonal, respectivamente

Comment on 'Pressure-induced changes in transport properties of layered La1.2Ca1.8Mn2O7'

International Nuclear Information System (INIS)

Ganguly, R.; Siruguri, V.; Gopalakrishnan, I.K.; Yakhmi, J.V.

2000-01-01

We show that the compound La 1.2 Ca 1.8 Mn 2 O 7 does not form with layered Sr 3 Ti 2 O 7 -type structure as reported by Kamenev et al. [Phys. Rev. B 56, R12 688 (1997)]. Detailed analysis of the powder x-ray diffraction pattern of this compound (synthesized by using the solid-state method) by Rietveld method shows that it forms a multiphase mixture comprising hole-doped perovskite manganates (La 1-x Ca x MnO 3 ) as the majority phases and CaO as the minority phase

EMP and SIMS studies on Mn/Ca and Fe/Ca systematics in benthic foraminifera from the Peruvian OMZ: a contribution to the identification of potential redox proxies and the impact of cleaning protocols

OpenAIRE

Glock, N.; Eisenhauer, A.; Liebetrau, V.; Wiedenbeck, M.; Hensen, C.; Nehrke, G.

2012-01-01

In this study we present an initial dataset of Mn/Ca and Fe/Ca ratios in tests of benthic foraminifera from the Peruvian oxygen minimum zone (OMZ) determined with SIMS. These results are a contribution to a better understanding of the proxy potential of these elemental ratios for ambient redox conditions. Foraminiferal tests are often contaminated by diagenetic coatings, like Mn rich carbonate- or Fe and Mn rich (oxyhydr)oxide coatings. Thus, it is substantial to assure that...

Vapor-phase elemental mercury adsorption by Ca(OH){sub 2} impregnated with MnO{sub 2} and Ag in fixed-bed system

Energy Technology Data Exchange (ETDEWEB)

Y.J. Wang; Y.F. Duan; Z.J. Huang; S.L. Meng; L.G. Yang; C.S. Zhao [Southeast University, Nanjing (China). School of Energy and Environment

2010-05-15

The ability of three sorbents (untreated Ca(OH){sub 2}, MnO{sub 2}-impregnated Ca(OH){sub 2} and Ag-impregnated Ca(OH){sub 2}) removing the elemental mercury had been studied using a laboratory-scale fixed-bed reactor at 80{sup o}C under simulated fuel gas conditions. The adsorption performance of the three sorbents was compared by mercury removal efficiency and adsorption capacity. The effect of acid gases such as HCl and SO{sub 2} on the mercury removal was investigated and presented in this article. The results showed that the mercury removal by Ca(OH){sub 2} was mainly controlled by physical mechanisms. In the case of Ca(OH){sub 2}, the presence of both SO{sub 2} and HCl promoted the Hg{sup 0} removal, and compared HCl with SO{sub 2}, HCl had a higher mercury removal than SO{sub 2}. Ca(OH){sub 2} impregnated with MnO{sub 2} had a slightly higher mercury removal than the original Ca(OH){sub 2}, but it was beneficial for mercury speciation. The presence of both SO{sub 2} and HCl promotes the Hg0 removal greatly, which was adsorbed by Ca(OH){sub 2} impregnated with MnO{sub 2}. The Ca(OH){sub 2} impregnated with MnO{sub 2} adsorbed more than 50% total Hg due to the occurrence of chemisorptions. The mercury removal by Ca(OH){sub 2} impregnated with Ag was the highest. This may be because mercury integrated with silver easily that could produce silver amalgam alloy.

Enhancement of Low-field Magnetoresistance in Self-Assembled Epitaxial La0.67Ca0.33MnO3:NiO and La0.67Ca0.33MnO3:Co3O4 Composite Films via Polymer-Assisted Deposition.

Science.gov (United States)

Zhou, Meng; Li, Yuling; Jeon, Il; Yi, Qinghua; Zhu, Xuebin; Tang, Xianwu; Wang, Haiyan; Fei, Ling; Sun, Yuping; Deng, Shuguang; Matsuo, Yutaka; Luo, Hongmei; Zou, Guifu

2016-07-06

Polymer-assisted deposition method has been used to fabricate self-assembled epitaxial La0.67Ca0.33MnO3:NiO and La0.67Ca0.33MnO3:Co3O4 films on LaAlO3 substrates. Compared to pulsed-laser deposition method, polymer-assisted deposition provides a simpler and lower-cost approach to self-assembled composite films with enhanced low-field magnetoresistance effect. After the addition of NiO or Co3O4, triangular NiO and tetrahedral Co3O4 nanoparticles remain on the surface of La0.67Ca0.33MnO3 films. This results in a dramatic increase in resistivity of the films from 0.0061 Ω•cm to 0.59 Ω•cm and 1.07 Ω•cm, and a decrease in metal-insulator transition temperature from 270 K to 180 K and 172 K by the addition of 10%-NiO and 10%-Co3O4, respectively. Accordingly, the maximum absolute magnetoresistance value is improved from -44.6% to -59.1% and -52.7% by the addition of 10%-NiO and 10%-Co3O4, respectively. The enhanced low-field magnetoresistance property is ascribed to the introduced insulating phase at the grain boundaries. The magnetism is found to be more suppressed for the La0.67Ca0.33MnO3:Co3O4 composite films than the La0.67Ca0.33MnO3:NiO films, which can be attributed to the antiferromagnetic properties of the Co3O4 phase. The solution-processed composite films show enhanced low-field magnetoresistance effect which are crucial in practical applications. We expect our polymer-assisted deposited films paving the pathway in the field of hole-doped perovskites with their intrinsic colossal magnetoresistance.

Giant magnetostructural coupling in Gd{sub 2/3}Ca{sub 1/3}MnO{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Correa, V F; Nieva, G; Haberkorn, N [Comision Nacional de Energia Atomica, Centro Atomico Bariloche, 8400 S. C. de Bariloche (Argentina); Saenger, N [Fachbereich Physik, Universitaet Konstanz, D-78457 Konstanz (Germany); Jorge, G, E-mail: victor.correa@cab.cnea.gov.a [Departamento de Fisica, FCEyN, Universidad de Buenos Aires (Argentina)

2009-05-01

We report high magnetic field magnetostructural studies on Gd{sub 2/3}Ca{sub 1/3}MnO{sub 3} single crystals. A giant linear magnetostrictive effect is observed in a wide temperature range (T < 120 K). Above 25 K a large hysteresis is seen reflecting the Mn magnetic moments ordering. At lower temperature (T < 15 K), a rather complicated field dependence arising from the competition between the Mn and Gd magnetic sublattices is observed. The relevance of the Gd ions in the low temperature behavior is further corroborated by specific heat experiments.

Phase equilibria and homogeneity range of the high temperature superconducting compound (Bi,Pb)2+xSr2Ca2Cu3O10+δ

International Nuclear Information System (INIS)

Kaesche, S.

1995-01-01

For the superconducting cuprates (Bi,Pb) 2+x Sr 2 Ca 2 Cu 3 O 10+y phase equilibria, the homogeneity region, and the phase formation has been studied in the temperture range 800 to 890 C. Sintered samples were prepared by a solid state reaction starting from Bi 2 O 3 , PbO, CuO and carbonates CaCO 3 and SrCO 3 in a three-stage calcination process. For the phase identification polarization microscopy, X-ray diffraction and susceptibility measurements have been applied. Multi-phase regions were determined in the cross section of the quasi-ternary system (Bi,Pb) 2 O 3 -SrO-CaO-CuO with constant Bi/(Bi+Pb) ratio 0.84 taking into account the 2223-phase. The homogeneity region was determined as function of Sr, Ca, Bi and Pb concentration. Its maximum size was found at 850 C

Effect of Cu{sup 2+} and Ni{sup 2+} substitution at the Mn site in (La{sub 0.63}Ca{sub 0.37})MnO{sub 3}: A neutron powder diffraction investigation

Energy Technology Data Exchange (ETDEWEB)

Martinelli, A., E-mail: alberto.martinelli@spin.cnr.it [CNR-SPIN, C.so Perrone 24, 16152 Genova (Italy); Ferretti, M. [CNR-SPIN, C.so Perrone 24, 16152 Genova (Italy); Dipartimento di Chimica e Chimica Industriale, Università di Genova, Via Dodecaneso 31, 16146 Genova (Italy); Castellano, C. [Università degli Studi di Milano, Dipartimento di Chimica Strutturale e Stereochimica Inorganica, Via G. Venezian 21, 20133 Milano (Italy); Cimberle, M.R. [IMEM-CNR, Via Dodecaneso 33, 16146 Genova (Italy); Ritter, C. [Institute Laue—Langevin, 6 rue Jules Horowitz, 38042 Grenoble Cedex 9 (France)

2013-04-15

The crystal and magnetic structures of the (La{sub 0.63}Ca{sub 0.37})(Mn{sub 1−x}TM{sub x})O{sub 3} compounds (x=0.00, 0.03, 0.08; TM=Cu{sup 2+}, Ni{sup 2+}) were investigated between 5 K and 300 K by means of dc magnetic measurements and neutron powder diffraction analysis followed by Rietveld refinement. Both substituting cations lead to a reduction of the long range ferromagnetic ordering temperature; ferromagnetism is strongly suppressed in the 8% Cu-substituted sample, where long- and short-range FM magnetic orders coexist together with short-range A-type AFM order. This particular feature can be related to the Jahn–Teller character of Cu{sup 2+}, absent in Ni{sup 2+}, and suggests the occurrence of a quantum critical point in the (La{sub 0.63}Ca{sub 0.37})(Mn{sub 1−x}Cu{sub x})O{sub 3} system. - Graphical abstract: Rietveld refinement plot of (La{sub 0.63}Ca{sub 0.37})(Mn{sub 0.92}Cu{sub 0.08})O{sub 3} showing in the inset the coexistence of broad A-type AFM peaks with FM ones. Highlights: ► (La{sub 0.63}Ca{sub 0.37})MnO{sub 3} was substituted with Ni and Cu. ► Neutron powder diffraction and Rietveld refinement were carried out. ► A quantum critical point possibly occurs in the (La{sub 0.63}Ca{sub 0.37})(Mn{sub 1−x}Cu{sub x})O{sub 3} system.

Nonmonotonic and anisotropic magnetoresistance effect in antiferromagnet CaMn2Bi2

Science.gov (United States)

Kawaguchi, N.; Urata, T.; Hatano, T.; Iida, K.; Ikuta, H.

2018-04-01

We found a large and unique magnetoresistance (MR) effect for CaMn2Bi2 . When the magnetic field was applied along the crystallographic c axis at low temperatures, the resistivity increased with the magnetic field and the MR ratio reached several hundred percent, but then it decreased with further increasing the applied field. In addition, the angle dependence measurement revealed a strong anisotropy. This compound is an antiferromagnetic semiconductor with a narrow band gap, and Mn atoms form a corrugated honeycomb lattice. Therefore, a frustration among the magnetic moments is expected, and we propose that our observations can be understood by a nonmonotonic modulation of magnetic fluctuation under the magnetic field.

Verification of Ca F2:Mn type of dosemeters for personal dosimetry purposes

International Nuclear Information System (INIS)

Misovic, M.; Boskovic, Z.; Spasic-Jokic, V.

1995-01-01

Verification results of CaF2:Mn type of dosemeters for personal dosimetry purposes are presented in this paper. Tree types of irradiations are proceeded due to verification of relevant features of TLD. It is concluded that mentioned type of dosemeter can be used for purpose of personal dosimetry. (author)

Magnetic and structural properties of ferromagnetic Fe{sub 5}PB{sub 2} and Fe{sub 5}SiB{sub 2} and effects of Co and Mn substitutions

Energy Technology Data Exchange (ETDEWEB)

McGuire, Michael A., E-mail: McGuireMA@ornl.gov; Parker, David S. [Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831 (United States)

2015-10-28

Crystallographic and magnetic properties of Fe{sub 5}PB{sub 2}, Fe{sub 4}CoPB{sub 2}, Fe{sub 4}MnPB{sub 2}, Fe{sub 5}SiB{sub 2}, Fe{sub 4}CoSiB{sub 2}, and Fe{sub 4}MnSiB{sub 2} are reported. All adopt the tetragonal Cr{sub 5}B{sub 3} structure-type and are ferromagnetic at room temperature with easy axis of magnetization along the c-axis. The spin reorientation in Fe{sub 5}SiB{sub 2} is observed as an anomaly in the magnetization near 170 K and is suppressed by substitution of Co or Mn for Fe. The silicides are found to generally have larger magnetic moments than the phosphides, but the data suggest smaller magnetic anisotropy in the silicides. Cobalt substitution reduces the Curie temperatures by more than 100 K and ordered magnetic moments by 16%–20%, while manganese substitution has a much smaller effect. This suggests Mn moments align ferromagnetically with the Fe and that Co does not have an ordered moment in these structures. Anisotropic thermal expansion is observed in Fe{sub 5}PB{sub 2} and Fe{sub 5}SiB{sub 2}, with negative thermal expansion seen along the c-axis of Fe{sub 5}SiB{sub 2}. First principles calculations of the magnetic properties of Fe{sub 5}SiB{sub 2} and Fe{sub 4}MnSiB{sub 2} are reported. The results, including the magnetic moment and anisotropy, are in good agreement with experiment.

Effect of Mn-site vacancies on the magnetic entropy change and the Curie temperature of La0.67Ca0.33Mn1-xO3 perovskite

DEFF Research Database (Denmark)

Chen, Wei; Nie, L.Y.; Xu, Zhao

2006-01-01

Single-phase polycrystalline samples of La0.67Ca0.33Mn1-xO3 (x = 0.00, 0.02, 0.04, 0.06) have been prepared using the sol-gel method. The structure, magnetocaloric properties and the Curie temperature of the samples with different Mn vacancy concentrations have been investigated. The experimental...

Determination of Fe, Mn and Pb by GFAAS in red wine

International Nuclear Information System (INIS)

Ying Zhecong; Jin Hua; Su Yulan

2008-01-01

A method for determination of Fe, Mn and Pb in red wine samples was developed by the graphite furnace atomic absorption spectrometric. Several different matrix modifiers were necessary because of evident analyte losses that occurred immediately in sample incineration. Red wine samples were analyzed after microwave digestion using HNO 3 . Standard addition method was used, the calibration concentration was 1 ng · ml -1 , 3 ng · ml -1 , 5 ng · ml -1 which containing 580 μg/ml KNO 3 as matrix and 0.2% HNO 3 . The correlation coefficient of the calibration line was very good within the measurement area. The recovery with red wine sample was very good at the range from 95%-107.5%. (authors)

Paramagnetic fluctuations in Pr0.65Ca0.35MnO3 around the charge-ordering temperature

International Nuclear Information System (INIS)

Daoud-Aladine, A; Roessli, B; Gvasaliya, S N; Perca, C; Pinsard-Gaudart, L; Rodriguez-Carvajal, J; Revcolevschi, A

2006-01-01

We have studied the ferromagnetic and antiferromagnetic fluctuations in the charge-ordered Pr 0.65 Ca 0.35 MnO 3 antiferromagnet by triple-axis neutron spectrometry. Whereas ferromagnetic fluctuations are observed above and below the charge-ordering transition (T CO ), the antiferromagnetic fluctuations develop only below T CO . The dynamical exponent z of both ferromagnetic and antiferromagnetic fluctuations are determined. The ferromagnetic fluctuations are not completely suppressed below T CO and their correlation lengths are short-ranged at all temperatures. The results are discussed with respect to the Zener polaron model recently introduced to describe the charge-ordered state of Pr 0.6 Ca 0.40 MnO 3

Strain, size and field effects in (La,Ca)MnO3 thin films

NARCIS (Netherlands)

Beekman, Christianne

2010-01-01

Doped manganese oxides such as La0.67Ca0.33MnO3 (LCMO) are strongly correlated electron systems which display an insulator to metal transition upon cooling at a temperature T_MI. At low temperature the material is ferromagnetic. Above the transition the material is a paramagnetic insulator in which

Crystal and magnetic study of the disordered perovskites Ca(Mn{sub 0.5}Sb{sub 0.5})O{sub 3} and Ca(Fe{sub 0.5}Sb{sub 0.5})O{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Retuerto, M., E-mail: mretuerto@icmm.csic.es [Instituto de Ciencia de Materiales de Madrid, CSIC, Energia, Medio Ambiente y Tecnologias Sostenibles, Sor Juana Ines de la Cruz 3, Cantoblanco, E-28049 Madrid (Spain); Martinez-Lope, M.J.; Garcia-Hernandez, M. [Instituto de Ciencia de Materiales de Madrid, CSIC, Energia, Medio Ambiente y Tecnologias Sostenibles, Sor Juana Ines de la Cruz 3, Cantoblanco, E-28049 Madrid (Spain); Munoz, A. [Departamento de Fisica Aplicada, EPS, Universidad Carlos III, Avda. Universidad 30, E-28911 Leganes-Madrid (Spain); Fernandez-Diaz, M.T. [Institut Max Von Laue Paul Langevin, F-38042 Grenoble (France); Alonso, J.A. [Instituto de Ciencia de Materiales de Madrid, CSIC, Energia, Medio Ambiente y Tecnologias Sostenibles, Sor Juana Ines de la Cruz 3, Cantoblanco, E-28049 Madrid (Spain)

2010-10-15

We have investigated the double perovskites Ca{sub 2}MSbO{sub 6} (M = Mn, Fe) that have been prepared by solid-state reaction (M = Fe) and wet chemistry procedures (M = Mn). The crystal and magnetic structures have been studied from X-ray (XRD) and neutron powder diffraction (NPD) data. Rietveld refinements show that the crystal structures are orthorhombic (space group Pbnm) with complete disorder of M and Sb cations, so the formula should be rewritten as Ca(M{sub 0.5}Sb{sub 0.5})O{sub 3}. Due to this disorder no evidences of Jahn-Teller distortion can be observed in the MnO{sub 6} octahedra of Ca(Mn{sub 0.5}Sb{sub 0.5})O{sub 3}, in contrast with the ordered double perovskite Sr{sub 2}MnSbO{sub 6}. Ca(Fe{sub 0.5}Sb{sub 0.5})O{sub 3} behaves as an antiferromagnet with an ordered magnetic moment for Fe{sup 3+} of 1.53(4){mu}{sub B} and a propagation vector k = 0, as investigated by low-temperature NPD. The antiferromagnetic ordering is a result of the high degree of Fe/Sb anti-site disorder of the sample, which originates the spontaneous formation of Fe-rich islands, characterized by the presence of strong Fe-O-Fe antiferromagnetic couplings with enough long-range coherence to produce a magnetic contribution perceptible by NPD. By contrast, the magnetic structure of Ca(Mn{sub 0.5}Sb{sub 0.5})O{sub 3} cannot be observed by low-temperature NPD because the magnitude of the ordered magnetic moments is below the detection threshold for neutrons.

In-plain electric properties of [CaMnO3/REMO3] (RE=Bi, La M=Fe, Fe0.8Mn0.2) superlattices grown by pulsed laser deposition method

NARCIS (Netherlands)

Iwata, N.; Watabe, Y.; Oikawa, T.; Takase, K.; Huijben, Mark; Inaba, T.; Oshima, K.; Rijnders, Augustinus J.H.M.; Yamamoto, H.

2014-01-01

The [CaMnO3 (CMO)/REMO3] (RE = Bi, La M = Fe, Fe0.8Mn0.2) superlattices show semiconducting behavior with transition temperatures (TEg) of 71, 127, and 151 K in the [CMO/BiFe0.8Mn0.2O3], [CMO/BiFeO3], and [CMO/LaFeO3] superlattices. The formation of a magnetic polaron is expected in the CMO layer of

Survey of trace elements (Al, As, Cd, Cr, Co, Hg, Mn, Ni, Pb, Se, and Si) in retail samples of flavoured and bottled waters.

Science.gov (United States)

Barroso, M F; Ramos, S; Oliva-Teles, M T; Delerue-Matos, C; Sales, M G F; Oliveira, M B P P

2009-01-01

Concentrations of eleven trace elements (Al, As, Cd, Cr, Co, Hg, Mn, Ni, Pb, Se, and Si) were measured in 39 (natural and flavoured) water samples. Determinations were performed using graphite furnace electrothermetry for almost all elements (Al, As, Cd, Cr, Co, Mn, Ni, Pb, and Si). For Se determination hydride generation was used, and cold vapour generation for Hg. These techniques were coupled to atomic absorption spectrophotometry. The trace element content of still or sparkling natural waters changed from brand to brand. Significant differences between natural still and natural sparkling waters (p element was compared with the presence of flavours, preservatives, acidifying agents, fruit juice and/or sweeteners, according to the labelled composition. It was shown that flavoured waters generally increase the trace element content. The addition of preservatives and acidifying regulators had a significant influence on Mn, Co, As and Si contents (p < 0.05). Fruit juice can also be correlated to the increase of Co and As. Sweeteners did not provide any significant difference in Mn, Co, Se and Si content.

Biosynthesis of lipids in Chlorella vulgaris Beijer. under the action of Mn2+, Zn2+, Cu2+, and Pb2+

International Nuclear Information System (INIS)

Gorda, A.Yi.; Grubyinko, V.V.

2011-01-01

We study the influence of Mn 2+ , Zn 2+ , Cu 2+ , and Pb 2+ on the intensity of biosynthesis of lipids in unicellular algae Chlorella vulgaris Beijer. In all cases, there is a general tendency to the accumulation of triacylglycerols, dyacylglycerols, and nonesterified fatty acids, which participate in protecting the cages of algae from an unfavorable action, and to a decrease of the content of phospholipids. For the actions of Zn 2+ , Cu 2+ , and Pb 2+ , 14 C-acetate is maximally included in phospholipids, for the actions of Mn 2+ - in dyacylglycerols, and the synthesis of other classes of lipids is inhibited. The content of chlorophylls a and b grows substantially for the actions of ions of zinc and lead and diminishes for the actions of ions of copper and manganese. We discuss the regulatory role and the toxic influence of ions of metals on the lipid metabolism in chlorella.

Pembuatan La0,8Ca0,2MnO3 sebagai Katoda pada Solid Oxide Fuel Cell (SOFC dan Karakteristiknya

Directory of Open Access Journals (Sweden)

Riska Ekawati

2007-06-01

Full Text Available The making of La0,8Ca0,2MnO3 cathode material of solid oxide fuel cell from lanthanum oxide (La2O3, calcium oxide (CaO, and manganese carbonate hydrate (MnCO3.H2O has been done using tape casting method. Time of firing the La0,8Ca0,2MnO3 varied. The values of t = 30 minutes, 60 minutes and 120 minutes. Microstructure of these materials was analyzed and characterized by means of their electric conductivity, XRD (x ray diffraction and SEM (scanning electron microscope. It is found that formulated micro structure is orthorhombic. The result of measurement shows that density is in linear (positive correlation with increasing of holding time of firing, porosity and coefficient of thermal expansion is negatively correlated with density and electric conductivity is in linear (positive correlation with increase density.

Phase diagram study for the PbO-ZnO-CaO-SiO{sub 2} -“Fe{sub 2}O{sub 3} ” system in air with CaO/SiO{sub 2} in 1.1 and PbO/(CaO+SiO{sub 2}) in 2.4 weight ratios

Energy Technology Data Exchange (ETDEWEB)

Lopez-Rodriguez, Josue; Romero-Serrano, Antonio; Hernandez-Ramirez, Aurelio; Cruz-Ramirez, Alejandro, E-mail: romeroipn@hotmail.com [Instituto Politecnico Nacional-ESIQIE, Zacatenco, Mexico City (Mexico); Almaguer-Guzman, Isaias; Benavides-Perez, Ricardo; Flores-Favela, Manuel [Servicios Administrativos Penoles S.A de C.V., Torreon, Coahuila (Mexico)

2017-07-15

An experimental study on the phase equilibrium and the liquidus isotherms for the PbO-ZnO-CaO-SiO{sub 2} -“Fe{sub 2}O{sub 3} ” system with CaO/SiO{sub 2} in 1.1 and PbO/(CaO+SiO{sub 2}) in 2.4 weight ratios, respectively, was carried out in the temperature range 1100-1300 deg C (1373-1573 K). High temperature phases were determined by the equilibrium-quenching method. Results are presented in the form of pseudo-ternary sections “Fe{sub 2}O{sub 3} ”-ZnO-(PbO+CaO+SiO{sub 2}). X-Ray diffraction (XRD) and SEM-EDS results showed that the phase equilibria in this system are dominated by the high melting temperature spinel and zincite phases. It was observed that if the system is at a temperature below 1300 deg C and the total (Fe{sub 2}O{sub 3} + ZnO) is greater than 20 wt%, spinel and/or zincite will be present in the slag system. As an application of the phase diagram, the liquid phase compositions below the liquidus surface were estimated, then their viscosities were calculated using FACTSage software. (author)

Essential trace (Zn, Cu, Mn and toxic (Cd, Pb, Cr elements in the liver of birds from Eastern Poland

Directory of Open Access Journals (Sweden)

Komosa A.

2012-01-01

Full Text Available We have focused our study on the concentrations of essential heavy metals (Zn, Cu and Mn and non-essential trace metals (Pb, Cd and Cr in the livers of birds from Eastern Poland. The largest mean amount of Zn - as much as 279 mg/kg dry mass (d.m. - was found in mute swans. However, only in one of the analysed buzzard specimens the concentration of Zn, found to be 664 mg/kg d.m., exceeded the level indicative of poisoning for this element. Birds specializing in catching rodents accumulated Mn in their livers in a very narrow range of concentrations, around 5.0 mg/kg d.m. on average. The range of mean Mn concentrations (around 6.5 mg/kg d.m. was also found to be narrow for piscivorous birds. The highest mean levels of Pb were found in mute swans (2.7 mg/kg d.m., and the highest levels of Cd (2.0 mg/kg d.m. for rooks. Concentrations of total Cr above detection level were found in 22 specimens (53.7%, and concentration values were highest for rooks. Analyses showed that the concentrations of biogenic elements did not exceed the levels indicative of poisoning (except in one specimen. The study demonstrated that lead shots remain a hazard to water ecosystems. Pb, Cd and Cr levels in the livers of omnivorous and piscivorous species indicate the permanent presence of these elements in the environment and may confirm the thesis about the growing role of electronic waste, including metallic e-waste, in the emission of the total amount of contamination with these elements.

Specific heat (1-330K), magnetic susceptiblity and Meissner effect Bi-(Pb)-Sr-Ca-Cu-O samples

International Nuclear Information System (INIS)

Junod, A.; Eckert, D.; Triscone, G.; Brunner, O.; Muller, J.; Zhao, Z.

1989-01-01

Five samples in the Bi 2 - y Pb y Sr 2 CaCu 2 O 8 + x system selected for their sharp diamagnetic transitions are characterized with particular emphasis on the specific heat. The behavior of the magnetic susceptibility upon doping with holes (Pb) is similar to that of the La 1 - y Sr y CuO 4 system

The effect of disorder on electronic and magnetic properties of quaternary Heusler alloy CoFeMnSi with LiMgPbSb-type structure

International Nuclear Information System (INIS)

Feng, Yu; Chen, Hong; Yuan, Hongkuan; Zhou, Ying; Chen, Xiaorui

2015-01-01

Thin films based on Heusler alloy often lost their theoretical predicted ultra-high spin polarization owing to the appearance of disorder. Using the first-principles calculations within density functional theory (DFT), we investigate the effect of disorder including antisite and swap on electronic and magnetic properties of quaternary Heusler alloy CoFeMnSi with LiMgPbSb-type structure. Twelve kinds of antisites and six kinds of swap disorders are proposed and studied comprehensively. In our calculations, Co(Fe)-, Mn(Fe)-, Si(Mn)-antisite and Co–Fe swap disorders are most favorable due to their lowest formation energies. Moreover, the positive binding energies of Co–Fe, Co–Si, Fe–Si and Mn–Si swap disorders with respect to their corresponding antisite disorders indicate that these complex swap disorders are more stable compared with their corresponding isolated antisite disorders. The investigations on density of states (DOS) show that the spin down energy gap of disordered structures suffers contraction and their DOS entirely move towards lower zone. Besides, the 100% spin polarization is maintained in all structures with antisite and swap disorders except for those with Co(Mn)-, Co(Si)-antisite and Co–Mn, Co–Si swap disorders. Therefore, the half-metallicity of quaternary Heusler alloy CoFeMnSi is quite robust against interfering effects such as Si(Mn), Co(Fe) and Co–Fe disorders most possibly formed in the growth. - Highlights: • CoFeMnSi with LiMgPbSb-type structure is found to be a half-metallic ferromagnet. • Si(Mn), Co(Fe), Mn(Fe) antisites and Co–Fe swap disorders are most likely to form. • The half-metallicity of CoFeMnSi is robust against the most possible disorders. • The magnetic moments of the most possible disorders follow the Pauli-Slater rule

Role of metal mixtures (Ca, Cu and Pb) on Cd bioaccumulation and phytochelatin production by Chlamydomonas reinhardtii

International Nuclear Information System (INIS)

Abboud, Pauline; Wilkinson, Kevin J.

2013-01-01

The goal of the study was to determine whether metal uptake and biological effects could be predicted by free ion concentrations when organisms were exposed to Cd and a second metal. Bioaccumulation and algal phytochelatin (PC) concentrations were determined for Chlamydomonas reinhardtii following a 6-h exposure. Bioaccumulation results, after six hours of exposure, showed that Cd uptake decreased in the presence of relatively high concentrations of Ca, Cu and Pb, however, Cd bioaccumulation increased in the presence of ca. equimolar concentrations of Cu. A good correlation was observed between the production of PCs and the amount of metals bioaccumulated for the binary mixtures of Cd–Pb and Cd–Cu, but not the Cd–Ca mixture. Overall, the results suggested that, in the case of mixtures, bioaccumulated metal rather than free ion concentrations would be a better predictor of biological effect. -- Highlights: •Cd bioaccumulation and phytochelatin production were evaluated for metal mixtures. •Bioaccumulated metal rather than free ion was a better predictor of biological effect. •Calcium additions decreased Cd bioaccumulation but increased phytochelatin production. •Copper additions increased Cd bioaccumulation and phytochelatin production. •Lead additions had little effect on either Cd bioaccumulation or phytochelatin production. -- In metal mixtures containing Cd and Ca, Pb or Cu, bioaccumulated metal rather than free ion was a better predictor of biological effect

Structure and properties of electron-doped Ca1-xSmxMnO3 nanoparticles

International Nuclear Information System (INIS)

Sanmathi, C.S.; Retoux, R.; Singh, M.P.; Noudem, J.

2009-01-01

In this paper, we report the structural and magnetic properties of electron-doped Ca 1-x Sm x MnO 3 (CSM) nanoparticles. The samarium's composition 'x' was varied from 0 to 0.2 with the special attention up to 0.05. Spherical 60-70 nm polycrystalline CSM nanoparticles were synthesised by chemical co-precipitation technique. Doping of Sm 3+ in antiferromagnetic CaMnO 3 has drastically altered its magnetic behavior due to the formation of ferromagnetic clusters. For example, the CSM powder with x = 0.04 displays about 115 K magnetic Curie temperature and about 0.1 emu/mole saturation magnetization. Physical properties of our nano-CSM powders are also compared with identical bulk-samples. To understand the differences, we invoked the intra-grain and inter-grain magnetic coupling process that facilitates to enhance their ferromagnetic behaviors. Unlike the bulk samples, such magnetic couplings in nanoparticles are favored by the presence of low-level crystal and interfacial defects

Anisotropic strains and magnetoresistance of La0.7Ca0.3MnO3

International Nuclear Information System (INIS)

Koo, T.Y.; Park, S.H.; Lee, K.; Jeong, Y.H.

1997-01-01

Thin films of perovskite manganite La 0.7 Ca 0.3 MnO 3 were grown epitaxially on SrTiO 3 (100), MgO(100) and LaAlO 3 (100) substrates by the pulsed laser deposition method. Microscopic structures of these thin film samples as well as a bulk sample were fully determined by x-ray diffraction measurements. The unit cells of the three films have different shapes, i.e., contracted tetragonal, cubic, and elongated tetragonal for SrTiO 3 , MgO, and LaAlO 3 , respectively, while the unit cell of the bulk is cubic. It is found that the samples with a cubic unit cell show smaller peak magnetoresistance at low fields (approx-lt 1T) than the noncubic ones do. The present result demonstrates that the magnetoresistance of La 0.7 Ca 0.3 MnO 3 at low fields can be controlled by lattice distortion via externally imposed strains. copyright 1997 American Institute of Physics

Magnetocaloric properties in La{sub 1−x}Ca{sub x}MnO{sub 3} thin films: Monte Carlo simulations

Energy Technology Data Exchange (ETDEWEB)

Restrepo-Parra, E., E-mail: erestrepopa@unal.edu.co; Ramos-Rivera, L.; Londoño-Navarro, J.

2014-02-15

The magnetocaloric effect (MCE) of La{sub 1−x}Ca{sub x}MnO{sub 3} was analyzed when varying the stoichiometry (x=0.2, 0.33, 0.4 and 0.5) and the external applied magnetic field. Simulations were carried out using the Monte Carlo method having a configuration ascribed by the set S{sub z} of all-site spin projections, under the Metropolis algorithm. La{sub 1−x}Ca{sub x}MnO{sub 3} is characterized for three types of magnetic ions corresponding to Mn{sup 4+} (S=3/2), which are bonded to Ca{sup 2+}, and Mn{sup 3+}(e{sub g}) and Mn{sup 3+}(e{sub g′}, S=2), which are both bonded to La{sup 3+}. Different interactions must be considered depending on the type of interacting ions. The entropy change ΔS in an isothermal process as well as the temperature change ΔT in an adiabatic process was determined with this model. Both ΔS and ΔT show stoichiometry-dependent maximums near the paramagnetic–ferromagnetic transition temperature (T{sub C}), confirming the order–disorder change at this temperature. The strong dependence in La{sub 1−x}Ca{sub x}MnO{sub 3} of the MCE on the stoichiometry and the external magnetic field makes this phenomenon important for different technological applications, particularly in refrigeration. - Highlights: • Thermal behavior of entropy, susceptibility and isothermal entropy change is studied. • ΔS and ΔT present a transition at the critical temperature depending on the stoichiometry. • Semi-classical Heisenberg Hamiltonian allows simulation of magnetocaloric effect in LCMO. • External magnetic field produces changes in ΔS and ΔT observed in the shifting of T{sub C}.

Tunneling Evidence of Half-Metallic Ferromagnetism in La(0.7)Ca(0.3)MnO(3)

Science.gov (United States)

Wei, J. Y. T.; Yeh, N. C.; Vasquez, R. P.

1997-01-01

Direct experimental evidence of half-metallic density of states (DOS) is observed by scanning tunneling spectroscopy on ferromagnetic La(0.7)Ca(0.3)MnO(3) which exhibits colossal magnetoresistance (SMR).

Circadian rhythm in concentrations of Mg, K, Ca and Mn in Japanese morning glory during flowering process

International Nuclear Information System (INIS)

Ikeue, Natsuko; Tanoi, Keitaro; Furukawa, Jun; Yokota, Harumi; Okuni, Yoko; Nakanishi, Tomoko M.

2001-01-01

Concentrations of 4 trace elements, Mg, K, Ca and Mn, in each tissues of Japanese morning glory were analyzed during the flower development. To determine the element amount, neutron activation analysis with gamma-ray spectroscopy was performed. In this study, we focused on the movement of the trace elements especially with short-day treatment. Each element showed its specific distribution in the parts of a plant. The concentration of each element was changed rhythmically within a day. It was noted that, in the apical bud, concentrations of Mg, Ca and Mn were decreased from 5 h (2 h before light was on) to 7 h and increased again after 9 h. (author)

Circadian rhythm in concentrations of Mg, K, Ca and Mn in Japanese morning glory during flowering process

Energy Technology Data Exchange (ETDEWEB)

Ikeue, Natsuko; Tanoi, Keitaro; Furukawa, Jun; Yokota, Harumi; Okuni, Yoko; Nakanishi, Tomoko M. [Tokyo Univ. (Japan). Graduate School of Agricultural and Life Sciences

2001-06-01

Concentrations of 4 trace elements, Mg, K, Ca and Mn, in each tissues of Japanese morning glory were analyzed during the flower development. To determine the element amount, neutron activation analysis with gamma-ray spectroscopy was performed. In this study, we focused on the movement of the trace elements especially with short-day treatment. Each element showed its specific distribution in the parts of a plant. The concentration of each element was changed rhythmically within a day. It was noted that, in the apical bud, concentrations of Mg, Ca and Mn were decreased from 5 h (2 h before light was on) to 7 h and increased again after 9 h. (author)

The End of Monterey Submarine Canyon Incision and Potential River Source Areas-Os, Nd, and Pb Isotope Constraints from Hydrogenetic Fe-Mn Crusts

Science.gov (United States)

Conrad, T. A.; Nielsen, S.; Ehrenbrink, B. P. E.; Blusztajn, J.; Hein, J. R.; Paytan, A.

2015-12-01

The Monterey Canyon off central California is the largest submarine canyon off North America and is comparable in scale to the Grand Canyon. The age and history of the Monterey Canyon are poorly constrained due to thick sediment cover and sediment disruption from turbidity currents. To address this deficit we analyzed isotopic proxies (Os, Pb, Nd) from hydrogenetic ferromanganese (Fe-Mn) crusts, which grow over millions of years on elevated rock surfaces by precipitation of metals from seawater. Fe-Mn crusts were studied from Davidson Seamount near the base of the Monterey submarine fan, the Taney Seamount Chain, and from Hoss Seamount, which serves as a regional control (Fig.). Fe-Mn crusts were dated using Os isotope ratios compared to those that define the Cenozoic Os isotope seawater curve. Four Fe-Mn crust samples from Davidson and Taney Seamounts deviate from the Os isotopic seawater curve towards radiogenic values after 4.5±1 Ma. Osmium is well mixed in the global ocean and is not subject to significant diffusive reequilibration in Fe-Mn crusts. We therefore attribute deviations from the Os isotope seawater curve to large-scale terrestrial input that ended about 4.5±1 Ma. The two Davidson samples also show more radiogenic Nd isotope values from about 4.5±1 Ma. Lead isotopes in one Davidson Seamount crust, measured by LA-ICPMS, deviate from regional values after 4.5±1 Ma for about 500 ka towards terrestrial sources. The Taney Seamount Fe-Mn crust does not deviate from regional Nd nor Pb isotope values due to its greater distance from Monterey Canyon and the shorter marine residence times of Nd and Pb. Isotope plots of our crust data and compiled data for potential source rocks indicate that the river that carved Monterey Canyon carried sediment with values closer to the Sierra Nevada than to a Colorado Plateau source, with cessation of major riverine input occurring approximately 4.5±1 Ma, an age that we interpret as the end of the Monterey Canyon

Pb solubility of the high-temperature superconducting phase Bi2Sr2Ca2Cu3O10+d

International Nuclear Information System (INIS)

Kaesche, S.; Majewski, P.; Aldinger, F.

1994-01-01

For the nominal composition of Bi 2.27x Pb x Sr 2 Ca 2 Cu 3 O 10+d the lead content was varied from x=0.05 to 0.45. The compositions were examined between 830 degrees C and 890 degrees C which is supposed to be the temperature range over which the so-called 2223 phase (Bi 2 Sr 2 Ca 2 Cu 3 O 10+d ) is stable. Only compositions between x=0.18 to 0.36 could be synthesized in a single phase state. For x>0.36 a lead containing phase with a stoichiometry of Pb 4 (Sr,Ca) 5 CuO d is formed, for x 2 Sr 2 CaCu 2 O 8+d and cuprates are the equilibrium phases. The temperature range for the 2223 phase was found to be 830 degrees C to 890 degrees C but the 2223 phase has extremely varying cation ratios over this temperature range. Former single phase 2223 samples turn to multi phase samples when annealed at slightly higher or lower temperatures. A decrease in the Pb solubility with increasing temperature was found for the 2223 phase

Contamination assessment of heavy metals in the soils around Khouzestan Steel Company (Ni, Mn, Pb, Fe, Zn, Cr)

International Nuclear Information System (INIS)

Hormozi Nejad, F.; Rastmanesh, F.; Zarasvandi, A.

2016-01-01

The highest concentrations were found at soil samples 4 and 12. Comparison of heavy metals concentration with unpolluted soil standard indicated that, concentrations of Cr, Zn, Fe, Ni and Pb is higher than that of unpolluted soil standard. In general, Manganese, Chromium, Zinc and Lead are the most important elements that are found in emissions of steel plants. The soil samples near the steel plant and downwind direction have much higher pollution level. The results showed that Mn, Pb and Zn is related to human activity and Cr have geogenic source and Fe and Ni have both geogenic and anthropogenic source in the study area in the city of Ahwaz.

Simplified sample treatment for the determination of total concentrations and chemical fractionation forms of Ca, Fe, Mg and Mn in soluble coffees.

Science.gov (United States)

Pohl, Pawel; Stelmach, Ewelina; Szymczycha-Madeja, Anna

2014-11-15

A simpler, and faster than wet digestion, sample treatment was proposed prior to determination of total concentrations for selected macro- (Ca, Mg) and microelements (Fe, Mn) in soluble coffees by flame atomic absorption spectrometry. Samples were dissolved in water and acidified with HNO3. Precision was in the range 1-4% and accuracy was better than 2.5%. The method was used in analysis of 18 soluble coffees available on the Polish market. Chemical fractionation patterns for Ca, Fe, Mg and Mn in soluble coffees, as consumed, using a two-column solid-phase extraction method, determined Ca, Mg and Mn were present predominantly as cations (80-93% of total content). This suggests these elements are likely to be highly bioaccessible. Copyright © 2014 Elsevier Ltd. All rights reserved.

Comparison of the photoluminescence properties of Eu2+, Mn2+ co-doped M5(PO4)3Cl (M = Ca, Sr, Ba)

International Nuclear Information System (INIS)

Yang, Fengli; An, Wei; Wei, Heng-Wei; Chen, Guantong; Zhuang, Weidong; Jing, Xi-Ping

2014-01-01

Highlights: • Good size match between the doped and host cations narrows the emission band. • Low phonon energy of the hosts enhances the luminescence intensity. • “Inverse bottleneck effect” related to Eu/Mn lifetime mismatch causes quenching. • “Charge transfer process” in the Eu–Mn clusters causes quenching. -- Abstract: Eu 2+ and Mn 2+ singly doped or co-doped M 5 (PO 4 ) 3 Cl (M = Ca, Sr and Ba) phosphors were synthesized by conventional solid state reactions and characterized by X-ray diffraction (XRD), photoluminescence (PL) spectra, PL decay curves, energy dispersive spectra (EDS) and Raman spectra. The results show that a better size match between the doped cation and the host cation allows a wider solid solution range (e.g. Ca 2+ /Mn 2+ ) and a narrower emission band (e.g. Sr 2+ /Eu 2+ and Ca 2+ /Mn 2+ ). A lower phonon energy of the host (e.g. the Sr phase) reduces the non-radiation probability and enhances the PL efficiency. The PL performance of the Ba phase is exceptional possibly because of the large size difference between the doped cations and the host cations. The transfer efficiency (η) and the emission quantum efficiency (Q) were analyzed. In the studied phosphors, superficially Eu 2+ efficiently transferred its absorbed energy to Mn 2+ but the Q of the Mn 2+ emission was not as high as expected. Two loss mechanisms are proposed: an “inverse bottleneck effect” and “charge transfer” between Eu 2+ and Mn 2+

Size-driven magnetic transitions in La1/3Ca2/3MnO3 nanoparticles

Science.gov (United States)

Markovich, V.; Fita, I.; Wisniewski, A.; Mogilyansky, D.; Puzniak, R.; Titelman, L.; Gorodetsky, G.

2010-09-01

Magnetic properties of electron-doped La1/3Ca2/3MnO3 manganite nanoparticles with average particle size ranging from 12 to 42 nm, prepared by the glycine-nitrate method, have been investigated in temperature range 5-300 K and in magnetic fields up to 90 kOe. Reduction in the particle size suppresses antiferromagnetism and decreases the Néel temperature. In contrast to bulk crystals, the charge ordering does not occur in all studied nanoparticles, while a weak ferromagnetism appears above 200 K. Low temperature magnetic hysteresis loops indicate upon exchange bias effect displayed by horizontal and vertical shifts in field cooled processes. The spontaneous and remanent magnetization at low temperature shows a relatively complex variation with particle size. The size-induced structural/magnetic disorder drives the La1/3Ca2/3MnO3 nanoparticles to a pronounced glassy behavior for the smallest 12 nm particles, as evidenced by large difference between zero field cooled and field cooled magnetization, frequency dependent ac-susceptibility, as well as characteristic slowing down in the spin dynamics. Time evolution of magnetization recorded in magnetic fields after field cooling to low temperatures exhibits pronounced relaxation and a very noisy behavior that may be caused by formation of some collective states. Magnetic properties of the nanoparticle samples are compared with those of La0.2Ca0.8MnO3 nanoparticles. These results shed some light on the coupling between charges and spin degrees of freedom in antiferromagnetic manganite nanoparticles.

Resonant photoemission study on La0.7Ca0.3MnO3 using Indus-1 synchrotron source

International Nuclear Information System (INIS)

Sagdeo, P.R.; Choudhary, R.J.; Phase, D.M.

2008-01-01

The electronic valance band structure of pulsed laser deposited La 0.7 Ca 0.3 MnO 3 thin film has been investigated by resonant photoelectron spectroscopy using CSR beamline (BL-2) on Indus-1 synchrotron radiation source. The valance band spectra were measured at room temperature with the photon energy ranging from 40 eV to 60 eV. The contribution of Mn-3d to the valance band was determined using resonant photo-electron intensity near Mn3p-3d threshold. (author)

Role of metal mixtures (Ca, Cu and Pb) on Cd bioaccumulation and phytochelatin production by Chlamydomonas reinhardtii.

Science.gov (United States)

Abboud, Pauline; Wilkinson, Kevin J

2013-08-01

The goal of the study was to determine whether metal uptake and biological effects could be predicted by free ion concentrations when organisms were exposed to Cd and a second metal. Bioaccumulation and algal phytochelatin (PC) concentrations were determined for Chlamydomonas reinhardtii following a 6-h exposure. Bioaccumulation results, after six hours of exposure, showed that Cd uptake decreased in the presence of relatively high concentrations of Ca, Cu and Pb, however, Cd bioaccumulation increased in the presence of ca. equimolar concentrations of Cu. A good correlation was observed between the production of PCs and the amount of metals bioaccumulated for the binary mixtures of Cd-Pb and Cd-Cu, but not the Cd-Ca mixture. Overall, the results suggested that, in the case of mixtures, bioaccumulated metal rather than free ion concentrations would be a better predictor of biological effect. Copyright © 2013 Elsevier Ltd. All rights reserved.

Effect of Co substitution on magnetic ground state in Sm0.5Ca0.5MnO3

International Nuclear Information System (INIS)

Xu, Xiaolong; Li, Yu; Hou, Feifei; Cheng, Qian; Su, Runzhou

2015-01-01

Highlights: • Polycrystalline Sm 0.5 Ca 0.5 Mn 1−x Co x O 3 were prepared by standard solid-state reaction. • The orthorhombic deformation and normalized slope were calculated for each sample. • Critical slowing down model and dynamic scaling equation are applied in some samples. • Canted antiferromagnetic state via spin glass state, changes to ferrimagnetic state. - Abstract: The effect of cobalt doping on the structural and magnetic properties of polycrystalline Sm 0.5 Ca 0.5 Mn 1−x Co x O 3 (0 ⩽ x ⩽ 0.20) has been studied. Powder X-ray diffraction (XRD), dc magnetization and ac susceptibility measurements have been performed. The orthorhombic deformation caused by the Jahn–Teller (JT) effect can be counterbalanced by Co 3+ doping. Meanwhile, antiferromagnetic (AFM), spin glass (SG) and phase separation (PS) ferrimagnetic states appear, successively, with the increase of x. The critical slowing down model and the dynamic scaling equation were applied in some samples. The existence of two distinct length scales for SG and finite FM (ferromagnetic) order is the source of the progressive deviation which exists in the dynamic scaling fitting for x = 0.05. Moreover, the small peaks at ∼8 K in χ″(T) curves are believed to be induced by the canted moments of Mn ions as observed in Nd 2/3 Ca 1/3 MnO 3

Influence of the particle size reduction on magnetic properties of electron-doped Ca1-xYxMnO3

OpenAIRE

Alqat Aboalqasim; Gebrel Zohra; Spasojević Vojislav; Kusigerski Vladan; Bošković Snežana; Blanuša Jovan

2012-01-01

The electron-doped magnetic nanoparticles of Ca1-xYxMnO3 (x = 0, 0.05, 0.10, 0.15, 0.20, and 0.30) manganite with an average particle size of 50 nm are analyzed and discussed in relation to their bulk counterparts. Nanoparticle samples show dominant anti-ferromagnetic ordering with a significant increase of coercivity, with the maximum value of 0.9 T for x = 0. Particle size reduction in Ca1-xYxMnO3 retains the bulk-like magnetic behavior of samples having up to 15% of Y3+, with the sma...

210Pb geochronology and trace metal fluxes (Cd, Cu and Pb) in the Gulf of Tehuantepec, South Pacific of Mexico

International Nuclear Information System (INIS)

Ruiz-Fernandez, Ana Carolina; Paez-Osuna, Federico; Machain-Castillo, Maria Luisa; Arellano-Torres, Elsa

2004-01-01

Distributions of Al, Cd, Cu, Fe, Li, Mn and Pb were analyzed in a sediment core collected in the Gulf of Tehuantepec, an important fisheries region located in the South Pacific of Mexico, where data on metal accumulation and accretion rates were previously almost nonexistent. Depth profiles of metal concentrations were converted to time-based profiles by using a 210 Pb-derived vertical accretion rate, estimated to be 0.05 cm year -1 on the average. Sediments were dated up to 8 cm depth, corresponding to a layer of ca. 140 years old. The historical changes of metal accumulation along the sediment core have shown a moderate enrichment of Cd, Cu and Pb concentrations at present, of about threefold the corresponding background concentrations. Chronological trace metal records showed that metal fluxes have increased over the last 20 years, reaching the maximum values at present of 2.5, 22.5 and 45.8 (μg cm -2 year -1 ) for Cd, Pb and Cu, respectively. These increments in metal fluxes are likely influenced by the development of anthropogenic land-based activities since over this period of time oil production activities in the region have had a significant development

Divalent metal (Ca, Cd, Mn, Zn) uptake and interactions in the aquatic insect Hydropsyche sparna.

Science.gov (United States)

Poteat, Monica D; Díaz-Jaramillo, Mauricio; Buchwalter, David B

2012-05-01

Despite their ecological importance and prevalent use as ecological indicators, the trace element physiology of aquatic insects remains poorly studied. Understanding divalent metal transport processes at the water-insect interface is important because these metals may be essential (e.g. Ca), essential and potentially toxic (e.g. Zn) or non-essential and toxic (e.g. Cd). We measured accumulation kinetics of Zn and Cd across dissolved concentrations ranging 4 orders of magnitude and examined interactions with Ca and Mn in the caddisfly Hydropsyche sparna. Here, we provide evidence for at least two transport systems for both Zn and Cd, the first of which operates at concentrations below 0.8 μmol l(-1) (and is fully saturable for Zn). We observed no signs of saturation of a second lower affinity transport system at concentrations up to 8.9 μmol l(-1) Cd and 15.3 μmol l(-1) Zn. In competition studies at 0.6 μmol l(-1) Zn and Cd, the presence of Cd slowed Zn accumulation by 35% while Cd was unaffected by Zn. At extreme concentrations (listed above), Cd accumulation was unaffected by the presence of Zn whereas Zn accumulation rates were reduced by 58%. Increasing Ca from 31.1 μmol l(-1) to 1.35 mmol l(-1) resulted in only modest decreases in Cd and Zn uptake. Mn decreased adsorption of Cd and Zn to the integument but not internalization. The L-type Ca(2+) channel blockers verapamil and nifedipine and the plasma membrane Ca(2+)-ATPase inhibitor carboxyeosin had no influence on Ca, Cd or Zn accumulation rates, while Ruthenium Red, a Ca(2+)-ATPase inhibitor, significantly decreased the accumulation of all three in a concentration-dependent manner.

A polarised neutron scattering study of the excitations in the CMR manganite La0.7Ca0.3MnO3

International Nuclear Information System (INIS)

Hagen, M.; Dai, P.

2002-01-01

Full text: The magnetic excitations in the colossal magnetoresistance (CMR) materials A 1-x B x MnO 3 (A = La, Pr, Nd, B = Ca, Sr) near the optimum doping x = 1/3 show some remarkable features. In a recent unpolarised inelastic neutron scattering experiment on La 0.7 Ca 0.3 MnO 3 Dai et al. discovered that the magnetic excitations (spin waves) appeared to show considerable softening on approaching the Brillouin zone boundary. This softening appeared to occur when the spin wave dispersion relation crossed a number of flat optic phonon branches, and the possibility exists for interaction/hybridisation with the phonons. In order to separate the magnetic spin waves from the lattice dynamical phonons we have carried out an inelastic polarised neutron scattering study using the IN20 triple axis spectrometer at the Institut Laue Langevin, Grenoble, France. Because La 0.7 Ca 0.3 MnO 3 is a ferromagnet and our principle aim is to separate magnetic from lattice dynamical excitations we have been able to use a novel 'half-polarised' configuration for the spectrometer, originally developed by Holden and Stirling, which boosts the signal by a factor of ∼ 10x. The technique used and the results for La 0.7 Ca 0.3 MnO 3 will be described

Measurement of the mass attenuation coefficients and electron densities for BiPbSrCaCuO superconductor at different energies

Science.gov (United States)

Çevik, U.; Baltaş, H.

2007-03-01

The mass attenuation coefficients for Bi, Pb, Sr, Ca, Cu metals, Bi2O3, PbO, SrCO3, CaO, CuO compounds and solid-state forms of Bi1.7Pb0.3Sr2Ca2Cu3O10 superconductor were determined at 57.5, 65.2, 77.1, 87.3, 94.6, 122 and 136 keV energies. The samples were irradiated using a 57Co point source emitted 122 and 136 keV γ-ray energies. The X-ray energies were obtained using secondary targets such as Ta, Bi2O3 and (CH3COO)2UO22H2O. The γ- and X-rays were counted by a Si(Li) detector with a resolution of 0.16 keV at 5.9 keV. The effect of absorption edges on electron density, effective atomic numbers and their variation with photon energy in composite superconductor samples was discussed. Obtained values were compared with theoretical values.

The role of Si and Ca on new wrought Mg-Zn-Mn based alloy

International Nuclear Information System (INIS)

Ben-Hamu, G.; Eliezer, D.; Shin, K.S.

2007-01-01

The development of new wrought magnesium alloys for automotive industry has increased in recent years due to their high potential as structural materials for low density and high strength/weight ratio demands. However, the poor mechanical properties of the magnesium alloys have led to search a new kind of magnesium alloys for better strength and ductility. Magnesium alloys show strong susceptibility to localized corrosion in chlorides solutions due to their inhomogeneous microstructure. The existence of intermetallics in the microstructure of magnesium alloys might represent initiation sites for localized corrosion. This is due to the formation of galvanic couples between the intermetallics and the surrounding matrix. The main objective of this research is to investigate the corrosion behavior of new magnesium alloys; Mg-Zn-Mn-Si-Ca (ZSMX) alloys. The ZSM6X1 + YCa alloys were prepared by using hot extrusion method. AC and DC polarization tests were carried out on the extruded rods, which contain different amounts of silicon or calcium. The potential difference in air between different phases and the matrix was examined using scanning Kelvin probe force microscopy (SKPFM). The phases present in the alloys have been identified by optical microscopy and scanning electron microscopy/energy dispersive X-ray spectroscopy. Four different phases were found, i.e. intermetallics containing Si-Mn, Mg-Si, Mg-Zn and Mg-Si-Ca phase. All phases exhibited higher potential differences relative to magnesium matrix indicating a cathodic behavior. The potential difference revealed significant dependence on the chemical composition of the phases. Based on the results obtained from the scanning Kelvin probe force microscopy, the cathodic phases are effective sites for the initiation of localized corrosion in Mg-Zn-Mn-Si-Ca alloys

Anisotropic and excellent magnetocaloric properties of La0.7Ca0.3MnO3 single crystal with anomalous magnetization

International Nuclear Information System (INIS)

Debnath, J.C.; Zeng, R.; Kim, J.H.; Chen, D.P.; Dou, S.X.

2012-01-01

Highlights: ► ΔS M shows a very large reversibility value at low field. ► The single crystal exhibits anisotropy in the MCE. ► La 0.7 Ca 0.3 MnO 3 is weakly itinerant ferromagnetic. ► No hysteresis loss is observed. - Abstract: Magnetic properties and the magnetocaloric effect (MCE) have been investigated in La 0.7 Ca 0.3 MnO 3 single crystal with applied field along both the ab-plane and the c-direction. Due to the magnetocrystalline anisotropy, the crystal exhibits anisotropy in the MCE. Upon application of a 5 T field, the magnetic entropy changes (ΔS M ), reaching values of 7.668 J/(kg K) and 6.412 J/(kg K) for both the ab-plane and the c-direction, respectively. A magnetic entropy change of 3.3 J/(kg K) was achieved for a magnetic field change of 1.5 T at the Curie temperature, T C = 245 K. Due to the absence of grains in the single crystal, the ΔS M distribution here is much more uniform than for gadolinium (Gd) and other polycrystalline manganites, which is desirable for an Ericsson-cycle magnetic refrigerator. For a field change of 5 T, the relative cooling power, RCP, reached 358.17 J/kg, while the maximum adiabatic temperature change of 5.33 K and a magnetoresistance (MR) ratio of 507.88% at T C were observed. We analysed the magnetization of La 0.7 Ca 0.3 MnO 3 single crystal at T C and estimated several parameters of spin fluctuation on the basis of a self-consistent renormalization theory of spin fluctuations, with reciprocal susceptibility above T C . We found that the magnetic property of La 0.7 Ca 0.3 MnO 3 is weakly itinerant ferromagnetic. A large reversible MCE and no hysteresis loss with a considerable value of refrigerant capacity indicate that La 0.7 Ca 0.3 MnO 3 single crystal is a potential candidate as a magnetic refrigerant.

Structural, magnetic and thermal properties of CaMn0.9957Fe0.01O3-δ

International Nuclear Information System (INIS)

Przewoznik, J.; Chmist, J.; Kolwicz-Chodak, L.; Tarnawski, Z.; Kapusta, Cz.; Kolodziejczyk, A.

2007-01-01

The polycrystalline CaMn 0.99 57 Fe 0.01 O 3-δ compound was studied using powder X-ray diffraction, 57 Fe Moessbauer spectroscopy, ac susceptometry, dc magnetometry, specific heat and electrical resistivity measurements. X-ray diffraction measurements performed between 70 and 300 K show a thermal expansion anomaly at the Neel temperature. A weak ferromagnetic component and a spin-glass behaviour below Neel temperature are found in magnetic measurements. The Moessbauer spectroscopy measurements performed between 30 and 300 K provided the Neel temperature value of 118 K, the same as obtained from dc magnetisation and close to that derived from the specific heat (119 K). The temperature evolution of the Fe hyperfine field was analysed within a molecular field model and revealed equal strengths of the Fe-Mn and Mn-Mn exchange interactions in this compound

Theoretical study of EPR spectra in Cu2+ - and Mn2+ - doped CaCd(CH3COO)4.6H2O

International Nuclear Information System (INIS)

Zhou Yiyang; Zhao Minguang

1987-08-01

The EPR spectra of CaCd(CH 3 COO) 4 .6H 2 O doped with Cu 2+ and Mn 2+ have been studied theoretically. A comparison between the calculated results and the experimental data shows quantitatively that the Cu 2+ and Mn 2+ ions substitute for the Cd 2+ and Ca 2+ ions, respectively. This conclusion is consistent with the qualitative assumption given by previous authors. (author). 36 refs, 1 fig., 3 tabs

Typha latifolia L. Türünün Farklı Kısımlarındaki Ağır Metal ve Makro Element Miktarlarının Karşılaştırılması

Directory of Open Access Journals (Sweden)

Fatih KARAHASAN

2015-09-01

Full Text Available In this study, we determined the accumulation of heavy metals (Cu, Zn, Fe, Cd, Pb, Mn and the concentrations of macroelements (N, P, K, Ca, Mg, Na in root, steam, rhizome and leaf parts in Typha latifolia L. disturbed in Melet, Turnasuyu and Akçaova aquatic ecosystems in Ordu province. According to the analyzes, the amounts of heavy metal and macro elements of plant parts are N>P> K>N>Ca>Mg>Zn>Fe>Mn>Pb>Cd>Cu for the steam, N>P>K>Ca>Mg>Fe>Na>Mn> Zn>Pb>Cd>Cu for the root, N>P>K>Ca>Mg>Na>Mn>Zn>Fe>Pb>Cd>Cu for the leaves and N>P>K>Ca>Mg>Na>Fe>Zn>Mn>Pb>Cd>Cu for the rhizome. Our data is evaluated by using three-ways analysis of variance. According to variance analyses, we found significant statistical differences among overall average of factor levels for the elements Iron (Fe, Phosphorus (P and Magnesium (Mg (p<0.05 and/or p<0.01. While a triple interactions are found significant for Zinc (Zn and Nitrogen (N elements, various binary interactions are found for Copper (Cu, Cadmium (Cd, Lead (Pb, Manganese (Mn, Potassium (K, Calcium (Ca and Sodium (Na elements (p<0.05 and/or p<0.01

La 1-x Ca x MnO 3 semiconducting nanostructures: morphology and thermoelectric properties.

Science.gov (United States)

Culebras, Mario; Torán, Raquel; Gómez, Clara M; Cantarero, Andrés

2014-01-01

Semiconducting metallic oxides, especially perosvkite materials, are great candidates for thermoelectric applications due to several advantages over traditionally metallic alloys such as low production costs and high chemical stability at high temperatures. Nanostructuration can be the key to develop highly efficient thermoelectric materials. In this work, La 1-x Ca x MnO 3 perosvkite nanostructures with Ca as a dopant have been synthesized by the hydrothermal method to be used in thermoelectric applications at room temperature. Several heat treatments have been made in all samples, leading to a change in their morphology and thermoelectric properties. The best thermoelectric efficiency has been obtained for a Ca content of x=0.5. The electrical conductivity and Seebeck coefficient are strongly related to the calcium content.

Levels of Cd (II, Mn (II, Pb (II, Cu (II, and Zn (II in Common Buzzard (Buteo buteo from Sicily (Italy by Derivative Stripping Potentiometry

Directory of Open Access Journals (Sweden)

P. Licata

2010-01-01

Full Text Available The purpose of this study was to determine the concentrations of heavy metals (Cd, Pb, Cu, Mn, and Zn in different organs (liver, kidney, muscle, lung, skin, and feathers of buzzards (Buteo buteo, utilized as a “biological indicator” for environmental contamination, from different areas of Sicily and to investigate the relationships between birds sex, age, and weight and metal levels in these samples. All samples of common buzzards were collected at the “Recovery Center of Wild Fauna” of Palermo, through the Zooprophilactic Institute. Potentiometric stripping analysis (PSA was used to determine the content of Cd(II, Cu(II, Mn(II, Pb(II, and Zn(II in bird tissues. For toxic metals, the highest levels of Pb were in liver and those of Cd in lung; Zn levels were higher than Cu and Mn in all tissues analyzed. The concentrations in liver, lung, kidney, and muscle could be considered as an indicative of chronic exposure to metals while the presence of metals in skin could be consequential to storing and elimination processes. The found concentrations of metals in the studied matrices required a highly sensitive method for their determination and a simple sample preparation procedure, and the proposed method was well suited for this purpose.

An NMR study of Pr0.5Ca0.5Mn1-xGaxO3 (x = 0 and 0.03)

International Nuclear Information System (INIS)

Oates, C.J.; Sikora, M.; Zajac, D.; Rybicki, D.; Kapusta, Cz.; Riedi, P.C.; Martin, C.; Yaicle, M.; Maignan, A.

2004-01-01

An NMR study of polycrystalline Pr 0. 5Ca 0.5 Mn 1-x Ga x O 3 (x = 0 and 0.03) at 3 K is presented. Zero field spin echo spectra of the Ga doped compound consist of an overlapping 6: 9 ,71 Ga signal at 74 MHz (hyperfine field of 5.3 T), a 55 Mn double exchange line at 375 MHz (35.5 T) and a weak Mn 3+ signal between 400 and 550 MHz. Measurements in an applied field show a step-like increase in the double exchange line intensity, which corresponds to an increase in the amount of the ferromagnetic metallic phase. This coincides with a step-like feature in the bulk magnetization measurements. The effect is similar to that in the previous field dependent 55 Mn NMR measurements of Pr 0.67 Ca 0.33 MnO 3 . At the demagnetized and remanent state, a variation of spin-spin relaxation time T 2 , across the 55 Mn line, due to a Suhl-Nakamura interaction is observed, which suggests that the ferromagnetic metallic double exchange regions, at liquid helium temperatures, are at least 4 nm in size

Electronic and magnetic properties of R0.5A0.5MnO3 compounds (R=Gd, Dy, Ho, Er; A=Sr, Ca)

International Nuclear Information System (INIS)

Terai, T.; Sasaki, T.; Kakeshita, T.; Fukuda, T.; Saburi, T.; Kitagawa, H.; Kindo, K.; Honda, M.

2000-01-01

Electronic and magnetic properties of the perovskitelike compounds of R 0.5 A 0.5 MnO 3 (R=Gd, Dy, Ho, Er; A=Sr, Ca) have been studied by measuring lattice parameter, electrical resistivity, magnetic susceptibility, and magnetization. All the Sr-doped compounds show a transition from a paramagnetic insulator to a spin-glass-like insulator at T g , even though the manganite La 0.5 Ca 0.5 MnO 3 , with nearly the same tolerance factor t, have been shown by others, to have different transitions. On the other hand, all the Ca-doped compounds show a charge-ordering transition at T CO and show a transition from a paramagnetic insulator to a canted antiferromagnetic insulator and/or a spin-glass-like insulator at T CA below T CO . These transition temperatures decrease with decreasing t. In the compound of Gd 0.5 Ca 0.5 MnO 3 , the collapse of the charge ordering has been observed under a pulsed high magnetic field of 45 T at 4.2 K. On the other hand, in the compound of Gd 0.5 Sr 0.5 MnO 3 , the magnetization process depends on the strength of magnetic field. These electronic and magnetic properties depend not only on the tolerance factor but also the variance (second moment) of the A-site ion radii distribution

PbO-SiO_2及びPbO-SiO_2-K_2O-Na_2O系ガラス中のMn^<3+>イオンの光吸収スペクトル及びガラスの屈折率

OpenAIRE

小山田, 了三; 古賀, 秀人; 星野, 朝則

1985-01-01

PbO-SiO2系及びPbO-SiO2-K2O-Na2O系ガラス中のMn3+イオンの光吸収スペクトルとガラスの屈折率を測定し、ガラス組成と吸収ピーク波数及び屈折率の関係を調べた。PbO-SiO2系にMnO2を添加したガラス中のMn3+の吸収ピーク波数はMnO2添加量が増加するとともに低波数側へシフトした。屈折率はMnO2添加量が1.0mol%まではほぼ一定となった。PbO-SiO2-K2O-Na2O系ガラス中のMn3+の吸収ピーク波数は[K2O]/[K2O+Na2O]の値の増加とともに低波数側へシフトし、混合アルカリ効果ははっきりとは現れない。屈折率は[K2O]/[K2O+Na2O]の値の増加とともに直線的に減少し、混合アルカリ効果は明確には認められない。...

Radioactivity of β / γ and the Content of Ca, Fe, Mn, Mg, Na on the Spring of Ponorogo East Java Lime Area

International Nuclear Information System (INIS)

Sutjipto

2002-01-01

Radioactivity of β / γ and the content of Ca, Fe, Mn, Mg, Na on the source of Ponorogo East-Java lime area has been studied. This research was carried out to know radioactivity of β / γ and the content of Ca, Fe, Mn, Mg, Na on the spring of different three places were Ngebel-lake source, Ngembak source and Gonggang source. Samples taken, preparation and analysis based on the procedures of environmental radioactivity analysis and water sampling guidelines. The instrument used for the analysis radioactivity were low level β counter modified P3TM-BATAN Yogyakarta with detector GM and spectrometer γ with detector Ge(Li). Radioactivity of β (gross) from the source of different three places (β ≤ 1 Bq/L) are lower than the value of PPRI No. 20/1990. Radioactivity of γ comes from the natural radionuclides of Tl-208 and K-40 are lower than 1 Bq/L for the different of three places, respectively. The metals concentration of Ngebel-lake source were Ca ≤ 14.34 ppm; Fe ≤ 0.04 ppm; Mn ≤ 0.02 ppm; Mg ≤ 6.75 ppm; Na ≤ 14.63 ppm, Ngembak source were Ca ≤ 11.6 ppm; Fe ≤ 0.04 ppm; Mn ≤ 0.02 ppm; Mg ≤ 11.13 ppm; Na ≤ 16.75 ppm and Gonggang source were Ca ≤ 13.78 ppm; Fe ≤ 0.26 ppm; Mn ≤ 0.02 ppm; Mg ≤ 6.13 ppm; Na ≤ 15.00 ppm. The water of Ngebel-lake source, Ngembak source and Gonggang source can be classified as B category water based on radioactivity and the content of the metals concentration in its. (author)

Monte Carlo simulation of roughness effect on magnetic and magnetotransport behavior of La{sub 2/3}Ca{sub 1/3}MnO{sub 3}/La{sub 1/3}Ca{sub 2/3}MnO{sub 3} bilayers

Energy Technology Data Exchange (ETDEWEB)

Agudelo-Giraldo, J.D. [PCM Computational Applications, Universidad Nacional de Colombia-Sede Manizales, Km. 9 vía al aeropuerto, Manizales (Colombia); Restrepo-Parra, E., E-mail: erestrepopa@unal.edu.co [PCM Computational Applications, Universidad Nacional de Colombia-Sede Manizales, Km. 9 vía al aeropuerto, Manizales (Colombia); Restrepo, J. [Grupo de Magnetismo y Simulación, Instituto de Física, Universidad de Antioquia, A.A., 1226 Medellín (Colombia)

2014-02-01

In this work we address the study of the magnetic and magnetotransport properties of ferromagnetic (FM)/antiferromagnetic (AFM) La{sub 2/3}Ca{sub 1/3}MnO{sub 3}/La{sub 1/3}Ca{sub 2/3}MnO{sub 3} manganites bilayers by means of the standard Monte Carlo method. Simulations, implemented with a single spin flip Metropolis dynamics, were performed in the framework of a three-dimensional classical Heisenberg model. Four different superexchange interactions, with the two different types of ions Mn{sup 3+} and Mn{sup 4+} involved and the orbital differences accounting for the Mn{sup 3+} ions, were considered in the Hamiltonian. Likewise, terms dealing with magnetocrystalline anisotropy and the influence of an external applied magnetic field were also included. Samples were simulated having dimensions L×L×(d{sub FM}+d{sub AFM}) where L, measured in lattice parameter units, stands for the linear and lateral dimension along which periodic boundary conditions were implemented, whereas d{sub FM} and d{sub AFM} stand for the thicknesses of FM and AFM layers respectively with free boundary conditions. Different degrees of roughness at the interface were also simulated in order to analyze its influence on the magnetic and magnetotransport properties of the system. In particular, low-temperature results reveal a trend of the coercive field to increase with roughness contrary to the exchange bias field behavior, which tends to decrease. Both quantities are modulated by oscillations ascribed to the atomic disorder at the interface. Finally, the roughness effect upon the bilayer resistivity and on the metal–insulator temperature is also presented and discussed.

New Mn(II, Ni(II, Cd(II, Pb(II complexes with 2-methylbenzimidazole and other ligands. Synthesis, spectroscopic characterization, crystal structure, magnetic susceptibility and biological activity studies

Directory of Open Access Journals (Sweden)

Shayma A. Shaker

2016-11-01

Full Text Available Synthesis and characterization of Mn(II, Ni(II, Cd(II and Pb(II mixed ligand complexes of 2-methylbenzimidazole with other ligands have been reported. The structure of the ligands and their complexes was investigated using elemental analysis, IR, UV–Vis, (1H, 13C NMR spectroscopy, molar conductivity and magnetic susceptibility measurements. In all the studies of complexes, the 2-methylbenzimidazole behaves as a neutral monodentate ligand which is coordinated with the metal ions through the N atom. While benzotriazole behaves as a neutral bidentate ligand which is coordinated with the Ni(II ion through the two N atoms. Moreover, the N-acetylglycine behaves as a bidentate ligand which is coordinated with the Mn(II, Ni(II and Pb(II ions through the N atom and the terminal carboxyl oxygen atom. The magnetic and spectral data indicate the tetrahedral geometry for Mn(II complex, irregular tetrahedral geometry for Pb(II complex and octahedral geometry for Ni(II complex. The X-ray single crystal diffraction method was used to confirm a centrosymmetric dinuclear Cd(II complex as each two metal ions are linked by a pair of thiocyanate N = S bridge. Two 2-methylbenzimidazole N-atom donors and one terminal thiocyanate N atom complete a highly distorted square pyramid geometry around the Cd atom. Besides, different cell types were used to determine the inhibitory effect of Mn(II, Ni(II, Cd(II and Pb(II complexes on cell growth using MTT assay. Cd(II complex showed cytotoxic effect on various types of cancer cell lines with different EC50 values.

Bulk and nanocrystalline electron doped Gd{sub 0.15}Ca{sub 0.85}MnO{sub 3}: Synthesis and magnetic characterization

Energy Technology Data Exchange (ETDEWEB)

Dhal, Lakshman; Chattarpal [Department of Physics, Indian Institute of Technology Madras, Chennai 600 036 (India); Nirmala, R., E-mail: nirmala@iitm.ac.in [Department of Physics, Indian Institute of Technology Madras, Chennai 600 036 (India); Santhosh, P.N. [Department of Physics, Indian Institute of Technology Madras, Chennai 600 036 (India); Kumary, T. Geetha [CMPD, Materials Science Group, Indira Gandhi Centre for Atomic Research, Kalpakkam 603 102 (India); Nigam, A.K. [Tata Institute of Fundamental Research, Mumbai 400 005 (India)

2014-09-01

Polycrystalline Gd{sub 0.15}Ca{sub 0.85}MnO{sub 3} sample was prepared by solid state reaction method and nanocrystalline samples of different grain sizes of the same were prepared by sol–gel method. Phase purity and composition were verified by room temperature X-ray diffraction and SEM-EDAX analysis. Magnetization data of bulk Gd{sub 0.15}Ca{sub 0.85}MnO{sub 3} in 5 kOe field shows a peak at ∼119 K (T{sub N}) suggesting an antiferromagnetic transition. Nanocrystalline Gd{sub 0.15}Ca{sub 0.85}MnO{sub 3} sample (∼54 nm size) also shows a cusp at ∼107 K and a broad thermal hysteresis between field cooled cooling (FCC) and field cooled warming (FCW) data around this temperature. This thermal hysteresis suggests possible crystal structural transition. Field variation of magnetization of bulk Gd{sub 0.15}Ca{sub 0.85}MnO{sub 3} at 5 K shows a tendency to saturate, but yields a magnetic moment value of only ∼1.12 μ{sub B}/f.u. in 70 kOe. The value of magnetization of nanocrystalline sample at 5 K in 70 kOe field is slightly larger and is ∼1.38 μ{sub B}/f.u. which is probably due to the surface moments of the nanoparticle samples. Both the samples show Curie–Weiss-like behaviour in their paramagnetic state.

Rational assembly of Pb(II)/Cd(II)/Mn(II) coordination polymers based on flexible V-shaped dicarboxylate ligand: Syntheses, helical structures and properties

Energy Technology Data Exchange (ETDEWEB)

Yang, Gao-Shan [School of Environment and Chemical Engineering, Nanchang Hangkong University, Nanchang 330063 (China); Liu, Chong-Bo, E-mail: cbliu@nchu.edu.cn [School of Environment and Chemical Engineering, Nanchang Hangkong University, Nanchang 330063 (China); School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, GA 30332 (United States); Liu, Hong [School of Environment and Chemical Engineering, Nanchang Hangkong University, Nanchang 330063 (China); Robbins, Julianne; Zhang, Z. John [School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, GA 30332 (United States); Yin, Hong-Shan [School of Environment and Chemical Engineering, Nanchang Hangkong University, Nanchang 330063 (China); Wen, Hui-Liang [State Key Laboratory of Food Science and Technology, Nanchang University, Nanchang 330047 (China); Wang, Yu-Hua [School of Environment and Chemical Engineering, Nanchang Hangkong University, Nanchang 330063 (China)

2015-05-15

Six new coordination polymers, namely, [Pb(L)(H{sub 2}O)] (1), [Pb(L)(phen)] (2), [Pb{sub 2}(L){sub 2}(4,4′-bipy){sub 0.5}] (3), [Cd(L)(phen)] (4), [Cd(L)(4,4′-bipy)]·H{sub 2}O (5) and [Mn(L)(4,4′-bipy)]·H{sub 2}O (6) have been synthesized by the hydrothermal reaction of 2,2′-[hexafluoroisopropylidenebis(p-phenyleneoxy)]diacetic acid (H{sub 2}L) with Pb(II)/Cd(II)/Mn(II) in the presence of ancillary ligands 4,4′-bipyridine (4,4′-bipy) or 1,10-phenanthroline (phen). Complexes 1 and 4–6 exhibit 2-D structures, and complexes 2–3 display 3-D frameworks, of which L{sup 2−} ligands join metal ions to single-stranded helical chains of 1, 3–6 and double-stranded helical chains of 2. Complexes 2 and 3 also contain double-stranded Metal–O helices. Topology analysis reveals that complexes 1 and 4 both represent 4-connected sql net, 2 represents 6-connected pcu net, 3 exhibits a novel (3,12)-connected net, while 5 and 6 display (3,5)-connected gek1 net. The six complexes exhibit two kinds of inorganic–organic connectivities: I{sup 0}O{sup 2} for 1, 4–6, and I{sup 1}O{sup 2} for 2–3. The photoluminescent properties of 4–5 and the magnetic properties of 6 have been investigated. - Graphical abstract: Six new Pb(II)/Cd(II)/Mn(II) coordination polymers with helical structures based on flexible V-shaped dicarboxylate ligand have been synthesized and structurally characterized. Photoluminescent and magnetic properties have been investigated. - Highlights: • Six novel M(II) coordination polymers with 2,2′-[hexafluoroisopropylidenebis(p-phenyleneoxy)]diacetic acid and N-donor ligands. • Complexes 1–6 show diverse intriguing helical characters. • The luminescent properties of complexes 1–5 were investigated. • Complex 6 shows antiferromagnetic coupling.

Orientación de láminas delgadas de (Pb, CaTiO3

Directory of Open Access Journals (Sweden)

Mendiola, J.

1999-06-01

Full Text Available Calcium modified PbTiO3 thin films have been prepared on platinized Si, MgO and SrTiO3 substrates. The films were deposited from a sol-gel solution with a concentration of 0.3 M and with a 10% excess of PbO. Two deposits of this solution on the substrates were made by spin-coating, crystallizing each of them by a Rapid Thermal Processing. The resulting films present a single (Pb,CaTiO3 perovskite phase. All the films are textured, but the films deposited on MgO and SrTiO3 show a preferred orientation in the polar direction of the perovskite. As a result of this orientation, pyroelectric coefficients were measured, without any poling, for the films on MgO and SrTiO3. Pyroelectric measurements indicate the application of these films in infrarred sensors.Se han preparado láminas delgadas de PbTiO3 modificado con calcio sobre substratos de Si, MgO y SrTiO3 electrodados con Pt. Las películas se depositaron a partir de una solución sintetizada por sol-gel, con concentración 0.3 M y con un 10 % en exceso de PbO. En cada lámina se hicieron dos depósitos de la solución sobre el substrato mediante la técnica de “spin-coating”, cristalizando cada uno de ellos con un tratamiento térmico rápido. Todas las láminas resultantes presentaban como única fase cristalina la perovskita de (Pb,CaTiO3. Las láminas presentaron una cierta textura, observándose una orientación preferente en la dirección polar en el caso de las películas depositas sobre MgO y SrTiO3. Como resultado de esta orientación, se midieron coeficientes piroeléctricos, sin polarización previa, en las láminas sobre MgO y SrTiO3. Las medidas piroeléctricas de estos materiales evidencian su utilidad en dispositivos para sensores de infrarrojo.

Preparation and photoluminescence properties of Mn2+-activated M2Si5N8 (M = Ca, Sr, Ba) phosphors

NARCIS (Netherlands)

Duan, C.J.; Otten, W.M.; Delsing, A.C.A.; Hintzen, H.T.J.M.

2008-01-01

Mn2+-doped M2Si5N8 (M=Ca, Sr, Ba) phosphors have been prepared by a solid-state reaction method at high temperature and their photoluminescence properties were investigated. The Mn2+-activated M2Si5N8 phosphors exhibit narrow emission bands in the wavelength range of 500–700 nm with peak center at

Quantum mechanics/molecular mechanics simulation of the ligand vibrations of the water-oxidizing Mn4CaO5 cluster in photosystem II.

Science.gov (United States)

Nakamura, Shin; Noguchi, Takumi

2016-10-11

During photosynthesis, the light-driven oxidation of water performed by photosystem II (PSII) provides electrons necessary to fix CO 2 , in turn supporting life on Earth by liberating molecular oxygen. Recent high-resolution X-ray images of PSII show that the water-oxidizing center (WOC) is composed of an Mn 4 CaO 5 cluster with six carboxylate, one imidazole, and four water ligands. FTIR difference spectroscopy has shown significant structural changes of the WOC during the S-state cycle of water oxidation, especially within carboxylate groups. However, the roles that these carboxylate groups play in water oxidation as well as how they should be properly assigned in spectra are unresolved. In this study, we performed a normal mode analysis of the WOC using the quantum mechanics/molecular mechanics (QM/MM) method to simulate FTIR difference spectra on the S 1 to S 2 transition in the carboxylate stretching region. By evaluating WOC models with different oxidation and protonation states, we determined that models of high-oxidation states, Mn(III) 2 Mn(IV) 2 , satisfactorily reproduced experimental spectra from intact and Ca-depleted PSII compared with low-oxidation models. It is further suggested that the carboxylate groups bridging Ca and Mn ions within this center tune the reactivity of water ligands bound to Ca by shifting charge via their π conjugation.

Single component Mn-doped perovskite-related CsPb2ClxBr5-x nanoplatelets with a record white light quantum yield of 49%: a new single layer color conversion material for light-emitting diodes.

Science.gov (United States)

Wu, Hao; Xu, Shuhong; Shao, Haibao; Li, Lang; Cui, Yiping; Wang, Chunlei

2017-11-09

Single component nanocrystals (NCs) with white fluorescence are promising single layer color conversion media for white light-emitting diodes (LED) because the undesirable changes of chromaticity coordinates for the mixture of blue, green and red emitting NCs can be avoided. However, their practical applications have been hindered by the relative low photoluminescence (PL) quantum yield (QY) for traditional semiconductor NCs. Though Mn-doped perovskite nanocube is a potential candidate, it has been unable to realize a white-light emission to date. In this work, the synthesis of Mn-doped 2D perovskite-related CsPb 2 Cl x Br 5-x nanoplatelets with a pure white emission from a single component is reported. Unlike Mn-doped perovskite nanocubes with insufficient energy transfer efficiency, the current reported Mn-doped 2D perovskite-related CsPb 2 Cl x Br 5-x nanoplatelets show a 10 times higher energy transfer efficiency from perovskite to Mn impurities at the required emission wavelengths (about 450 nm for perovskite emission and 580 nm for Mn emission). As a result, the Mn/perovskite dual emission intensity ratio surprisingly elevates from less than 0.25 in case of Mn-doped nanocubes to 0.99 in the current Mn-doped CsPb 2 Cl x Br 5-x nanoplatelets, giving rise to a pure white light emission with Commission Internationale de l'Eclairage (CIE) color coordinates of (0.35, 0.32). More importantly, the highest PL QY for Mn-doped perovskite-related CsPb 2 Cl x Br 5-x nanoplatelets is up to 49%, which is a new record for white-emitting nanocrystals with single component. These highly luminescent nanoplatelets can be blended with polystyrene (PS) without changing the white light emission but dramatically improving perovskite stability. The perovskite-PS composites are available not only as a good solution processable coating material for assembling LED, but also as a superior conversion material for achieving white light LED with a single conversion layer.

Transport and ordering of polarons in CER manganites PrCaMnO

International Nuclear Information System (INIS)

Schramm, S; Hoffmann, J; Jooss, Ch

2008-01-01

The temperature-dependent resistivity and the colossal resistance effect induced by strong electric fields of the small-band Pr 1-x Ca x MnO 3 (PCMO) manganites are analysed with respect to the influence of the Ca doping, post-annealing, the prehistory of the electric stimulation, and the physical dimensions of the sample. Despite the phase separation between charge and orbital ordered and disordered phases, PCMO reveals the properties of a homogeneous medium with a conductivity governed by the hopping of small polarons if the electric field is not too strong. In contrast, high electric fields induce a structural transition which gives rise to a glassy behaviour in the transient regime. In the low resistance state the small activation energy of charge carrier hopping implies a transition to large polaron hopping

Hybrid improper ferroelectricity in Ruddlesden-Popper Ca{sub 3}(Ti,Mn){sub 2}O{sub 7} ceramics

Energy Technology Data Exchange (ETDEWEB)

Liu, X. Q., E-mail: xqliu@zju.edu.cn, E-mail: xmchen59@zju.edu.cn; Wu, J. W.; Shi, X. X.; Zhao, H. J.; Zhou, H. Y.; Chen, X. M., E-mail: xqliu@zju.edu.cn, E-mail: xmchen59@zju.edu.cn [Laboratory of Dielectric Materials, School of Materials Science and Engineering, Zhejiang University, 38 Zheda Road, Hangzhou 310027 (China); Qiu, R. H.; Zhang, W. Q. [Department of Physics, Shanghai University, 99 Shangda Road, Shanghai 200444 (China)

2015-05-18

The hybrid improper ferroelectricity (HIF) has been proposed as a promising way to create multiferroic materials with strong magnetoelectric coupling by the first-principle calculation, and the experimental evidences of HIF in Ruddlesden-Poper Ca{sub 3}(Ti{sub 1−x}Mn{sub x}){sub 2}O{sub 7} (x = 0, 0.05, 0.1, and 0.15) ceramics have been shown in the present work. The room temperature ferroelectric hysteresis loops are observed in these ceramics, and a polar orthorhombic structure with two oxygen tilting modes has been confirmed by the X-ray powder diffraction. A first-order phase transition around 1100 K in Ca{sub 3}Ti{sub 2}O{sub 7} was evidenced, and the temperatures of phase transitions decrease linearly with increasing of the contents of Mn{sup 4+} ions. Based on the result of first-principle calculations, the polarization should be reversed by switching through the mediated Amam phase in Ca{sub 3}Ti{sub 2}O{sub 7} ceramics.

Temperature dependent changes of the Mn 3d and 4p bands near $T_{c}$ in Colossal Magnetoresistance systems : a XANES study of $La_{1-x}Ca_{x}MnO_{3}$

NARCIS (Netherlands)

Bridges, F; Booth, C. H.; Kwei, G. H.; Neumeier, J. J.; Sawatzky, G. A.

2000-01-01

Abstract: We report high-resolution X-ray Absorption Near Edge Structure (XANES)measurements at the Mn K-edge as a function of temperature, forLa$_{1-x}$Ca$_x$MnO$_3$ samples, with a focus mainly on the pre-edge region.Small peaks labeled A$_1$-A$_3$ are observed which corresponds to

Preparation and Characteristics of Ultrasonic Transducers for High Temperature Using PbNb2O6

Science.gov (United States)

Soejima, Junichiro; Sato, Kokichi; Nagata, Kunihiro

2000-05-01

The substance PZT(Pb(Zr, Ti)O3) is chiefly used for piezoceramic transducers in many ultrasonic flow meters. It is difficult to use PZT transducers for flow meters for automobile exhaust gas at high temperatures over 350°C. Lead niobate (PbNb2O6) has a high Curie temperature of 540°C and a low mechanical quality factor, and is the most suitable as the sensor element in flow meters for automobile exhaust gas. However, it is difficult to fabricate dense PbNb2O6 ceramics that have good piezoelectric properties. In this study, ceramics with high density and a high piezoelectric effect were fabricated by adding various elements such as Mn and Ca to PbNb2O6 and by examining the sintering process. A Langevin transducer with a resonance frequency of 80 kHz was made for measuring automobile exhaust gas flow using PbNb2O6 ceramics.

Temperature dependence of colossal electro-resistance of Pr0.7Ca0.3MnO3 thin films

International Nuclear Information System (INIS)

Odagawa, A.; Kanno, T.; Adachi, H.; Sato, H.; Inoue, I.H.; Akoh, H.; Kawasaki, M.; Tokura, Y.

2005-01-01

The electronic conduction through a Pr 0.7 Ca 0.3 MnO 3 thin film is investigated by measurements using dc and pulsed bias. Pr 0.7 Ca 0.3 MnO 3 films sandwiched by electrodes exhibit two stable resistance states by means of applying voltage pulses. Both of the states show semiconducting behavior. The ratio of the two resistance states induces a colossal electro-resistance (CER) effect greater than 1000%. The CER behavior is seen in the temperature range of 300 K down to 150 K. The observed conduction characteristics exhibit the space-charge-limited-current effect, and the switching behavior can be ascribed to a carrier trapping/detrapping of the trap sites in the perovskite manganite

Magnetic field induced low temperature upturn of magnetization in highly Ca-doped La{sub 0.1875}Ca{sub 0.8125}MnO{sub 3} polycrystalline compound

Energy Technology Data Exchange (ETDEWEB)

Das, Kalipada, E-mail: kalipadadasphysics@gmail.com [Indian Association for the Cultivation of Science, 2A and 2B Raja S. C. Mullick Road, Jadavpur, Kolkata 700032 (India); Dasgupta, P.; Poddar, A. [CMP Division, Saha Institute of Nuclear Physics, 1/AF, Bidhannagar, Kolkata 700 064 (India)

2017-06-15

Highlights: • Magnetic field induced super paramagnetic nanoclusters formation. • Magnetic field dependent change of the curvature of the magnetization. • We report the training effect in polycrystalline La{sub 0.1875}Ca{sub 0.8125}MnO{sub 3} compound. - Abstract: In our present study we have reported the magnetic properties of highly Ca-doped polycrystalline compound La{sub 0.1875}Ca{sub 0.8125}MnO{sub 3}. Along with the conventional charge ordered antiferromagnetic ground state, a small ferromagnetic phase fraction is present at the low temperature. The effect of the external magnetic field markedly modifies the ground state of the compound. Our experimental results indicate that in addition to the ferromagnetic phase fraction, another field induced super paramagnetic phase grow at low temperature (T < 50 K) above H = 10 kOe magnetic field within the charge ordered antiferromagnetic matrix. The nature of the temperature dependent magnetization curves influenced by the external applied magnetic field was observed and analyzed using Langevin theory of super paramagnetism.

Magnetoresistance and magnetothermopower properties of Bi/Ca/Co/O and Bi(Pb)/Ca/Co/O misfit layer cobaltites

CERN Document Server

Maignan, A; Hervieu, M; Michel, C; Pelloquin, D; Khomskii, D

2003-01-01

Two new compounds of the Bi/Ca/Co/O and Bi(Pb)/Ca/Co/O systems have been prepared. Their structure is built up from the intergrowth of four rock-salt-type layers and one [CoO sub 2 ] hexagonal layer. Both cobaltites exhibit large thermopower values (S sub 3 sub 0 sub 0 sub K approx 140 mu V K sup - sup 1), low resistivity values (rho sub 3 sub 0 sub 0 sub K = 40-60 m OMEGA cm) and small thermal conductivities (kappa sub 3 sub 0 sub 0 sub K approx 1 W K sup - sup 1 m sup - sup 1). Furthermore, these compounds exhibit a negative magnetoresistance, (MR = rho sub H - rho sub H sub sub 0 /rho sub H sub = sub 0), reaching, at 2.5 K, - 85% in 7 T for the Bi/Ca/Co/O misfit cobaltite. A large negative magnetothermopower is also found for these cobaltites in the same temperature range. A qualitative explanation of the observed behaviour is proposed.

Radiation dosimetry by optically stimulated phosphorescence of CaF2:Mn

International Nuclear Information System (INIS)

Bernhardt, R.

1974-01-01

In addition to the light emission which occurs in TL, trapped electrons in CaF 2 :Mn can also be released by stimulation with visible and UV light. The measurement of stimulated light emission is disturbed by illumination. But there is an optically-stimulated phosphorescence, which permits to separate measurement of stimulated light emission and illumination. A theory is given. During illumination a part of the released electrons are captured by flat traps, which are emptied at room temperature. A dose dependent signal can be measured at a defined time after the stimulating pulse of visible light. Dosimeters (CaF 2 :Mn teflon disks) were illuminated by the light of a tungsten lamp. The dose response curve was found to be linear from 1 to 10 5 rads. The response curve obtained for optical stimulation was similar to the TL-response curve. Fading of the optically-stimulated signal was higher than TL-fading. Repeated readings of a single sample are possible. The number of readings is dependent on illumination conditions. Accuracy of sample to sample was about 3.5% (standard deviation). There are two background signals. (1) Post-irradiation phosphorescence occurs. Flat traps are also filled after 60 Co gamma excitation. The measurement of the signal is possible after decay of post-irradiation phosphorescence. (2) There is an optically-excited phosphorescence, which also occurs if all trapped electrons are released. The lower limit of dose measurements is given by deviations of optically-excited emission and the dark-current of the photomultiplier tube. (author)

A study of electron excitations in CaWO sub 4 and PbWO sub 4 single crystals

CERN Document Server

Muerk, V; Mihoková, E; Nitsch, K

1997-01-01

The excitation spectra of photo- and thermo-luminescence were compared in the VUV-UV spectral region in CaWO sub 4 and PbWO sub 4 scheelite tungstates. Temperature dependences of emission intensities and decay times were measured for PbWO sub 4 in the 80-300 K range and approximated by a simple phenomenological model. The energy level structure of the emission centre excited state and related kinetic processes are discussed for both tungstates. (author)

Magneto-caloric and magneto-resistive properties of La0.67Ca0.33-xSrxMnO3

International Nuclear Information System (INIS)

Reves Dinesen, Anders

2004-08-01

This thesis presents results of an experimental investigation of magneto-caloric and magneto-resistive properties of a series of polycrystalline Ca- and Sr-doped lanthanum manganites, La 0.67 Ca 0.33-x Sr x MnO 3 (0≤ x ≤ 0.33), with the perovskite structure. The samples consisted of sintered oxide powders prepared the glycine-nitrate combustion technique. The compounds were ferromagnetic and showed a Curie transition in the temperature range 267370 K (T C increased with increasing x). An analysis of the structural properties was carried out by means of x-ray diffraction and the Rietveld technique. The variation of the Ca/Sr ratio was found to cause a transition from orthorhombic to rhombohedral symmetry in the composition range 0.110 0.67 Ca 0.33-x Sr x MnO 3 samples was measured directly and indirectly (by means of magnetization measurements). All the samples showed a magnetocaloric effect in the vicinity of T C . A model for the mag-netocaloric effect based on Weiss mean field theory and classical theories for heat capacities was developed. The model provided reasonable predictions of the magneto-caloric properties of the samples. The compounds with low Sr content showed a magnetocaloric effect comparable to that of Gadolinium, the prototypical working material for magnetic refrigeration at room temperature. A less comprehensive part of the investigation regarded the magneto-resistive properties of the La 0.67 Ca 0.33-x Sr x MnO 3 system. It was found that th polycrystalline nature of the compounds played a decisive role for the magnetotransport properties. Characteristic grain boundary effects, such as a low-field magnetoresistance, which is absent in single-crystalline perovskites, were observed. The low-field effect is usually ascribed to spin-dependent scattering in grain boundaries. Qualitatively the results obtained for the La 0.67 Ca 0.33-x Sr x MnO 3 samples were consistent with this model. The resistivity contribution arising from the presence of

Electrical Transport and Magnetoresistance Properties of Tensile-Strained CaMnO3 Thin Films

Science.gov (United States)

Ullery, Dustin; Lawson, Bridget; Zimmerman, William; Neubauer, Samuel; Chaudhry, Adeel; Hart, Cacie; Yong, Grace; Smolyaninova, Vera; Kolagani, Rajeswari

We will present our studies of the electrical transport and magnetoresistance properties of tensile strained CaMnO3 thin films. We observe that the resistivity decreases significantly as the film thickness decreases which is opposite to what is observed in thin films of hole doped manganites. The decrease in resistivity is more pronounced in the films on (100) SrTiO3, with resistivity of the thinnest films being about 3 orders of magnitude lower than that of bulk CaMnO3. Structural changes accompanying resistivity changes cannot be fully explained as due to tensile strain, and indicate the presence of oxygen vacancies. These results also suggest a coupling between tensile strain and oxygen deficiency, consistent with predictions from models based on density functional theory calculations. We observe a change in resistance under the application of moderate magnetic field. Experiments are underway to understand the origin of the magnetoresistance and its possible relation to the tensile strain effects. We acknowledge support from: Towson Office of University Undergraduate Research, Fisher Endowment Grant and Undergraduate Research Grants from the Fisher College of Science and Mathematics, and Seed Funding Grant from the School of Emerging technologies.

Study of the analytic quality in the determinations of Cr, Fe, Mn, Cu, Zn, Pb and Hg through conventional and nuclear analytical techniques in mosses of the MATV; Estudio de la calidad analitica en las determinaciones de Cr, Fe, Mn, Cu, Zn, Pb y Hg a traves de tecnicas analiticas nucleares y convencionales en musgos de la ZMVT

Energy Technology Data Exchange (ETDEWEB)

Caballero S, B.

2013-07-01

To evaluate the environmental risks of air pollution and to facilitate the decision-making for control, is necessary to have the capacity to generate data with analytical quality. A comparison between nuclear (Neutron activation analysis and total reflection X-ray fluorescence spectrometry) and no nuclear analytical techniques (atomic absorption spectrometry and inductively coupled plasma optical emission spectrometry) for simultaneous determination of metal content (Cr, Cu, Fe, Hg, Mn, Pb and Zn) in mosses from Metropolitan Area of the Toluca Valley (MATV) was performed. Epiphytic mosses (Fabriona ciliaris and Leskea angustata) were sampled in two campaigns, 16 sites (urban, transition and natural) and were prepared for each technique. The biological certified reference materials were used for the quality control and to evaluate accuracy, precision, linearity, detection and quantification limits. Results show that nuclear analytical techniques and no nuclear applied in chemical analysis of Cr, Cu, Fe, Hg, Mn, Pb and Zn in moss from MATV are comparable and therefore all of these can potentially be used for this purpose. However, if its considered both, the performance parameters and economic/operational characteristics is widely recommended inductively coupled plasma optical emission spectrometry, conventional analytical technique, which showed the highest analytical grade quality. Also were observed spatial and temporal variations in the concentrations of Cr, Cu, Fe, Hg, Mn, Pb and Zn in mosses from MATV and was discussed its potential origin. The urban sites had the highest concentration of anthropogenic elements as Cr, Cu, Fe, Hg, Pb and Zn because are strongly impacted by roads with high vehicle traffic. (Author)

Magnetic phase diagram simulation of La{sub 1-x}Ca{sub x}MnO{sub 3} system by using Monte Carlo, Metropolis algorithm and Heisenberg model

Energy Technology Data Exchange (ETDEWEB)

Restrepo-Parra, E., E-mail: erestrepopa@unal.edu.c [Departamento de Fisica y Quimica, Universidad Nacional de Colombia-Sede Manizales, A.A. 127 Manizales (Colombia); Salazar-Enriquez, C.D.; Londono-Navarro, J.; Jurado, J.F. [Departamento de Fisica y Quimica, Universidad Nacional de Colombia-Sede Manizales, A.A. 127 Manizales (Colombia); Restrepo, J. [Grupo de Magnetismo y Simulacion, Instituto de Fisica. Universidad de Antioquia, A.A. 1226, Medellin (Colombia)

2011-06-15

This work presents a critical temperature study of La{sub 1-x}Ca{sub x}MnO{sub 3} manganites in bulk by means of Monte Carlo method thermal activated magnetic properties. The analysis was carried out for stoichiometries in the range of 0{<=}x{<=}1. The model is based on a three-dimensional classical Heisenberg-Hamiltonian involving the presence of Mn{sup 3+eg}, Mn{sup 3+eg'} and Mn{sup 4+} ions, and their nearest neighbor interaction. For this modeling, simple cubic lattice samples of size L{sup 3}, with L=6, 15 and 30 were used. The values of exchange parameters were determined by using LaMnO{sub 3} (x=0), La{sub 0.5}Ca{sub 0.5}MnO{sub 3} and CaMnO{sub 3} (x=1) phases. Relationships between exchange parameters and anisotropy constants for different hole densities were found. Results of transition temperatures for each phase showed good agreement with experimental reports, especially for L=30 and L{yields}{infinity}. - Research highlights: Stoichiometry influences the exchange interaction between magnetic ions. Charge and orbital ordering depend on the stoichiometry. LCMO magnetic phase diagram has a great variety of magnetic states.

Europium substitution effects on structural, magnetic and magnetocaloric properties in La0.5Ca0.5MnO3

Directory of Open Access Journals (Sweden)

Boujelben W.

2012-06-01

Full Text Available We have investigated structural, magnetic and magnetocaloric properties of polycrystalline samples La0.5-xEuxCa0.5MnO3 (x=0 and 0.1. Rietveld refinement of the X-ray diffraction patterns show that our samples are single phase and crystallize in the orthorhombic structure with Pnma space group. Magnetization measurements versus temperature at a magnetic applied field of 500 Oe indicate that La0.4Eu0.1Ca0.5MnO3 sample exhibits a paramagnetic to ferromagnetic transition with decreasing temperature. Magnetic measurements reveal strong magnetocaloric effect in the vicinity of the Curie temperature TC. The parent compound shows a negative magnetic entropy change of ∆SM=−1.13Jkg−1K−1 at 220K and a positive magnetocaloric effects ∆SM=1Jkg−1K−1 at 150K under a magnetic applied field of 2T. La0.4Eu0.1Ca0.5MnO3 exhibits a maximum value of magnetic entropy change ∆SM=−1.15Jkg−1K−1 at 130K under an applied field of 2T and a large relative cooling power RCP with a maximum value of 72 J/kg.

Structural, dielectric and magnetic properties of (Pb{sub 1−x}Ca{sub x})(Fe{sub 0.5}Nb{sub 0.5})O{sub 3} solid solution ceramics

Energy Technology Data Exchange (ETDEWEB)

Puri, Maalti; Bahel, Shalini [Guru Nanak Dev University, Punjab (India); Raevski, I.P. [Southern Federal University, Rostov-on-Don (Russian Federation); Narang, Sukhleen Bindra [Guru Nanak Dev University, Punjab (India)

2016-06-01

Ceramic samples of (Pb{sub 1−x}Ca{sub x})(Fe{sub 0.5}Nb{sub 0.5})O{sub 3} with x=0.0, 0.20, 0.40, 0.45, 0.50, 0.55, 0.60 and 1.0 were fabricated by columbite precursor method. All the synthesized samples have a perovskite structure and unit cell volume decreases with increasing Ca content. The substitution of Ca for Pb has been found to have a pronounced effect on structural, dielectric and magnetic properties. Saturated magnetic loops were observed at room temperature for compositions with x≥0.40. The observed maximal magnetization at room temperature is rather small and varies non-monotonically with increasing Ca contents. It is supposed that room-temperature magnetic properties of (Pb{sub 1−x}Ca{sub x})(Fe{sub 0.5}Nb{sub 0.5})O{sub 3} ceramics might be due to the presence of ferromagnetic impurity, presumably PbFe{sub 12}O{sub 19} and/or CaFe{sub 12}O{sub 19}. - Highlights: • Ceramic samples have been synthesized using columbite precursor method. • The substitution of Ca for Pb has a pronounced effect on various properties. • Low losses at high frequencies make these ceramics suitable for microwave applications. • M–H loops at room temperature are reported first time.

Broadening of the magnetic entropy change in La0.75Ca0.15Sr0.10MnO3

DEFF Research Database (Denmark)

Krishnan Venkatesh, Radha; Kuhn, Luise Theil; Pryds, Nini

2012-01-01

A broad table-like entropy change (ΔS) at room temperature has been observed in the ferromagnetic compound La0.75Ca0.15Sr0.10MnO3, which is analyzed in the concept of Landau theory and with critical exponent analysis obtained from the magnetization measurements. The change in entropy in La0.75Ca0...

Thermochromic effect at room temperature of Sm{sub 0.5}Ca{sub 0.5}MnO{sub 3} thin films

Energy Technology Data Exchange (ETDEWEB)

Boileau, A.; Capon, F.; Barrat, S.; Pierson, J. F. [Universite de Lorraine, Institut Jean Lamour, Departement CP2S, UMR CNRS 7198, Nancy, F-54042 (France); Laffez, P. [Groupe de Recherche Electronique, Materiaux, Acoustique, Nanoscience (GREMAN), Universite Francois Rabelais de Tours, UMR CNRS 7347, IUT de Blois, 15 rue de la Chocolaterie, Blois, F-41000 (France)

2012-06-01

Sm{sub 0.5}Ca{sub 0.5}MnO{sub 3} thermochromic thin films were synthesized using dc reactive magnetron co-sputtering and subsequent annealing in air. The film structure was studied by x-ray diffraction analysis. To validate the thermochromic potentiality of Sm{sub 0.5}Ca{sub 0.5}MnO{sub 3}, electrical resistivity and infrared transmittance spectra were recorded for temperatures ranging from 77 K to 420 K. The temperature dependence of the optical band gap was estimated in the near infrared range. Upon heating, the optical transmission decreases in the infrared domain showing a thermochromic effect over a wide wavelength range at room temperature.

Interface strain coupling and its impact on the transport and magnetic properties of LaMnO3 thin films grown on ferroelectrically active substrates

International Nuclear Information System (INIS)

Zheng, R.K.; Wang, Y.; Habermeier, H.-U.; Chan, H.L.W.; Li, X.M.; Luo, H.S.

2012-01-01

Highlights: ► Strong interface strain coupling in LaMnO 3 /PMN-PT heterostructure. ► In situ dynamic turning of the strain and lattice distortion of LaMnO 3 films. ► Coupling of electrons to lattice strain is crucial to understand the strain effect. - Abstract: Thin films of LaMnO 3 have been epitaxially grown on 〈0 0 1〉 oriented ferroelectric 0.67Pb(Mg 1/3 Nb 2/3 )O 3 -0.33PbTiO 3 (PMN-PT) single-crystal substrates. The poling of the PMN-PT crystal causes a decrease in the resistance and an increase in the magnetization and magnetoresistance of the LaMnO 3 film. In situ X-ray diffraction measurements revealed that these changes arise from the poling-induced strain in the PMN-PT substrate, which reduces the in-plane tensile strain and the Jahn–Teller (JT) distortion of MnO 6 octahedra of the LaMnO 3 film. Moreover, it was found that the transport properties of LaMnO 3 films are much more sensitive to the poling-induced strain than that of CaMnO 3 films for which there is no JT distortion, implying that the electron–lattice coupling is one of the most important ingredients in understanding the strain effect in LaMnO 3 films.

Comparative Effects of Biochar, Slag and Ferrous-Mn Ore on Lead and Cadmium Immobilization in Soil.

Science.gov (United States)

Mehmood, Sajid; Rizwan, Muhammad; Bashir, Saqib; Ditta, Allah; Aziz, Omar; Yong, Li Zhe; Dai, Zhihua; Akmal, Muhammad; Ahmed, Waqas; Adeel, Muhammad; Imtiaz, Muhammad; Tu, Shuxin

2018-02-01

A variety of remediation approaches have been applied to the heavy metals-contaminated soils, however, the immobilization of metals in co-contaminated soils still not cleared. Therefore, an incubation study was conducted to evaluate the instantaneous effects of different concentrations of biochar (BC), slag (SL) and Fe-Mn ore (FMO) on immobilization of Pb and Cd through the Toxicity Characteristic Leaching Procedure (TCLP) by following the the European Community Bureau of Reference (BCR), CaCl 2 and NH 4 NO 3 . The sequential extraction of BCR showed decrease in acid soluble fractions, while the residual proportions of Pb and Cd were enhanced with increasing concentrations of SL and BC. Addition of BC significantly lowered the extractable fractions of both metals by TCLP, NH 4 NO 3 and CaCl 2 as compared to SL and FMO. Among all amendments, BC incorporation into co-contaminated soil offered promising results for Pb and Cd immobilization. Overall, all amendments showed positive and long-term impact on the reclamation of co-contaminated soil with heavy metals and could deserve advance monitoring studies on a field scale.

Fluorescence and afterglow of Ca2Sn2Al2O9:Mn2+

Science.gov (United States)

Takemoto, Minoru; Iseki, Takahiro

2018-03-01

By using a polymerized complex method, we synthesized manganese (Mn)-doped Ca2Sn2Al2O9, which exhibits yellow fluorescence and afterglow at room temperature when excited by UV radiation. The material emits a broad, featureless fluorescence band centered at 564 nm, which we attribute to the presence of Mn2+ ions. The afterglow decay is well fit by a power-law function, rather than an exponential function. In addition, thermoluminescence analyses demonstrate that two different types of electron traps form in this material. Based on experimental results, we conclude that the fluorescence and afterglow both result from thermally assisted tunneling, in which trapped electrons are thermally excited to higher-level traps and subsequently tunnel to recombination centers.

Crystal structures and thermal decomposition of permanganates AE[MnO_4]_2 . n H_2O with the heavy alkaline earth elements (AE=Ca, Sr and Ba)

International Nuclear Information System (INIS)

Henning, Harald; Bauchert, Joerg M.; Conrad, Maurice; Schleid, Thomas

2017-01-01

Reexamination of the syntheses and crystal structures as well as studies of the thermal decomposition of the heavy alkaline earth metal permanganates Ca[MnO_4]_2 . 4 H_2O, Sr[MnO_4]_2 . 3 H_2O and Ba[MnO_4]_2 are the focus of this work. As an alternative to the very inelegant Muthmann method, established for the synthesis of Ba[MnO_4]_2 a long time ago, we employed a cation-exchange column loaded with Ba"2"+ cations and passed through an aqueous potassium-permanganate solution. We later used this alternative also with strontium- and calcium-loaded columns and all the compounds synthesized this way were indistinguishable from the products of the established methods. Ca[MnO_4]_2 . 4 H_2O exhibiting [CaO_8] polyhedra crystallizes in the orthorhombic space group Pccn with the lattice parameters a=1397.15(9), b=554.06(4) and c=1338.97(9) pm with Z=4, whereas Sr[MnO_4]_2 . 3 H_2O with [SrO_1_0] polyhedra adopts the cubic space group P2_13 with a=964.19(7) pm and Z=4. So the harder the AE"2"+ cation, the higher its demand for hydration in aqueous solution. Consequently, the crystal structure of Ba[MnO_4]_2 in the orthorhombic space group Fddd with a=742.36(5), b=1191.23(7) and c=1477.14(9) pm with Z=8 lacks any crystal water, but contains [BaO_1_2] polyhedra. During the thermal decomposition of Ca[MnO_4]_2 . 4 H_2O, the compound expels up to two water molecules of hydration, before the crystal structure collapses after the loss of the third H_2O molecule at 157 C. The crystal structure of Sr[MnO_4]_2 . 3 H_2O breaks down after the expulsion of the third water molecule as well, but this already occurs at 148 C. For both the calcium and the strontium permanganate samples, orthobixbyite-type α-Mn_2O_3 and the oxomanganates(III,IV) AEMn_3O_6 (AE=Ca and Sr) remain as final decomposition products at 800 C next to amorphous phases. On the other hand, the already anhydrous Ba[MnO_4]_2 thermally decomposes to hollandite-type BaMn_8O_1_6 and BaMnO_3 at 800 C.

Effect of doping Ca on polaron hopping in LaSr 2 Mn 2 O 7

Indian Academy of Sciences (India)

... Lecture Workshops · Refresher Courses · Symposia · Live Streaming. Home; Journals; Pramana – Journal of Physics; Volume 58; Issue 5-6. Effect of doping Ca on polaron hopping in LaSr2Mn2O7. S N Bhatia Osama A Yassin. Colossal Magnetoresistance & Other Materials Volume 58 Issue 5-6 May-June 2002 pp 1061- ...

Tunable magnetocaloric effect in Sr{sub 1-x}Ca{sub x}Mn{sub 0.5}Ti{sub 0.5}O{sub 3} perovskites

Energy Technology Data Exchange (ETDEWEB)

Shanmugapriya, K.; Palanivel, Balan [Pondicherry Engineering College, Department of Physics, Puducherry (India); Radheep, D.M.; Murugan, Ramaswamy [Pondicherry University, Department of Physics, Puducherry (India)

2017-07-15

Sr{sub 1-x}Ca{sub x}Mn{sub 0.5}Ti{sub 0.5}O{sub 3} (x = 0.25, 0.5 and 0.75) polycrystalline samples were synthesized by conventional solid-state reaction. Magnetic characterizations of Sr{sub 1-x}Ca{sub x}Mn{sub 0.5}Ti{sub 0.5}O{sub 3} revealed signature of antiferromagnetic ordering at temperatures (T{sub N}) ∝ 19, 25 and 29.5 K for x = 0.25, x = 0.5 and for x = 0.75, respectively. Sr{sub 1-x}Ca{sub x}Mn{sub 0.5}Ti{sub 0.5}O{sub 3} (x = 0.75) exhibits field-induced antiferromagnetic to ferromagnetic transition at ∝ 30 K with applied magnetic field of 4 and 5 T. Magnetocaloric change (ΔS{sub M}) increases from 3.5 to 19 J/kg K by increasing calcium concentration in the A-site. Those ΔS{sub M} values are relatively very high in these classes of antiferromagnetic perovskite systems and equal to the magnetisation values of the ferromagnetic perovskite manganites. This is the first report for the Sr{sub 1-x}Ca{sub x}Mn{sub 0.5}Ti{sub 0.5}O{sub 3} (x = 0.75) having large magnetic entropy changes induced by the low magnetic field. (orig.)

Site-occupancy, luminescent properties and energy transfer of a violet-to-red color-tunable phosphor Ca{sub 10}Li(PO{sub 4}){sub 7}: Ce{sup 3+}, Mn{sup 2+}

Energy Technology Data Exchange (ETDEWEB)

Zhang, Xinguo, E-mail: mpcc1@qq.com [Guangdong Provincial Key Laboratory of New Drug Screening, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou 510515 (China); Xu, Jungu [Guangxi Ministry-Province Jointly-Constructed Cultivation Base for State Key Laboratory of Processing for Nonferrous Metal and Featured Materials, MOE Key Laboratory of New Processing Technology for Nonferrous Metals and Materials, Guangxi Universities Key Laboratory of Non-ferrous Metal Oxide Electronic Functional Materials and Devices, College of Materials Science and Engineering, Guilin University of Technology, Guilin 541004 (China); Gong, Menglian [School of Chemistry, Sun Yat-Sen University, Guangzhou 510275 (China)

2017-03-15

A series of color-tunable phosphors Ca{sub 10}Li(PO{sub 4}){sub 7}: Ce{sup 3+}, Mn{sup 2+} were synthesized by high-temperature solid-state reaction. Site occupancy of Ce{sup 3+} and Mn{sup 2+} in Ca{sub 10}Li(PO{sub 4}){sub 7} and corresponding luminescent properties were systemically studied. Rietveld refinement results indicate that the Ce{sup 3+} ions are preferred to occupy 7-cooridnated M1 and M3 sites, and Mn{sup 2+} ions are mainly occupying distorted octahedral M5 sites, which results in Ce{sup 3+} violet emission at 370 nm and Mn{sup 2+} red emission at 640 nm. The intensity of Mn{sup 2+} red emission is greatly enhanced through efficient Ce{sup 3+}-Mn{sup 2+} energy transfer (η{sub ET}=94%). The critical distance and corresponding mechanism of Ce{sup 3+}-Mn{sup 2+} energy transfer was found to be ~11 Å and dipole-quadrupole interaction, respectively. The emitting colors of Ca{sub 10}Li(PO{sub 4}){sub 7}: Ce{sup 3+}, Mn{sup 2+} phosphors can be tuned from violet through pink to red by adjusting the Ce{sup 3+}/Mn{sup 2+} ratio. The composition-optimized red phosphor Ca{sub 10}Li(PO{sub 4}){sub 7}: 0.05Ce{sup 3+}, 0.09Mn{sup 2+} exhibits excellent thermal stability at high temperature (~100% at 160 °C).

Alkaline earth lead and tin compounds Ae2Pb, Ae2Sn, Ae = Ca, Sr, Ba, as thermoelectric materials

Science.gov (United States)

Parker, David; Singh, David J

2013-01-01

We present a detailed theoretical study of three alkaline earth compounds Ca2Pb, Sr2Pb and Ba2Pb, which have undergone little previous study, calculating electronic band structures and Boltzmann transport and bulk moduli using density functional theory. We also study the corresponding tin compounds Ca2Sn, Sr2Sn and Ba2Sn. We find that these are all narrow band gap semiconductors with an electronic structure favorable for thermoelectric performance, with substantial thermopowers for the lead compounds at temperature ranges from 300 to 800 K. For the lead compounds, we further find very low calculated bulk moduli—roughly half of the values for the lead chalcogenides, suggestive of soft phonons and hence low lattice thermal conductivity. All these facts indicate that these materials merit experimental investigation as potential high performance thermoelectrics. We find good potential for thermoelectric performance in the environmentally friendly stannide materials, particularly at high temperature. PMID:27877610

Alkaline earth lead and tin compounds Ae2Pb, Ae2Sn, Ae = Ca, Sr, Ba, as thermoelectric materials

Directory of Open Access Journals (Sweden)

David Parker and David J Singh

2013-01-01

Full Text Available We present a detailed theoretical study of three alkaline earth compounds Ca2Pb, Sr2Pb and Ba2Pb, which have undergone little previous study, calculating electronic band structures and Boltzmann transport and bulk moduli using density functional theory. We also study the corresponding tin compounds Ca2Sn, Sr2Sn and Ba2Sn. We find that these are all narrow band gap semiconductors with an electronic structure favorable for thermoelectric performance, with substantial thermopowers for the lead compounds at temperature ranges from 300 to 800 K. For the lead compounds, we further find very low calculated bulk moduli—roughly half of the values for the lead chalcogenides, suggestive of soft phonons and hence low lattice thermal conductivity. All these facts indicate that these materials merit experimental investigation as potential high performance thermoelectrics. We find good potential for thermoelectric performance in the environmentally friendly stannide materials, particularly at high temperature.

White LED based on CaAl2Si2O8:Eu2+ Mn2+ phosphor and CdS/ZnS quantum dots

Science.gov (United States)

Shen, Changyu; Zhong, Chuan; Hou, Qianglong; Li, Ke

2011-02-01

Core/shell CdS/ZnS quantum dots (QDs) with the emission wavelength of 610nm, was synthesized by thermal deposition using cadmium oxide and selenium as precursors in a hot lauric acid and hexadecylamine trioctylphosphine oxide hybrid. CaAl2Si2O8:Eu2+ Mn2+ phosphor was synthesized by high-temperature solid state reaction at 1290 °C for 2 hours under the H2 reducing atmosphere, and X-ray powder diffraction analysis confirmed the formation of it. It has two emission bands peaking at 420 nm and 580nm originated from the transition 5d to 4f of Eu2+ and 4T1-6A1 of Mn2+, respectively. Blends of CaAl2Si2O8:Eu2+,Mn2+ phosphor and CdS/ZnS QDs exhibited the prominent spectral evolution with an increasing content of QDs. A hybrid white LED, which combines a blue LED with the blend of CaAl2Si2O8:Eu2+ Mn2+ phosphor and QDs with a weight ratio of 2:1, with the CIE coordinate of (0.3183, 0.3036) and CRI of 85 was obtained.

Analysis of (Ba,Ca,Sr)3MgSi2O8:Eu2+, Mn2+ phosphors for application in solid state lighting

International Nuclear Information System (INIS)

Han, J.K.; Piqutte, A.; Hannah, M.E.; Hirata, G.A.; Talbot, J.B.; Mishra, K.C.; McKittrick, J.

2014-01-01

The luminescence properties of Eu 2+ and Mn 2+ co-activated (Ba,Ca,Sr) 3 MgSi 2 O 8 phosphors prepared by combustion synthesis were studied. Eu 2+ -activated (Ba,Ca,Sr) 3 MgSi 2 O 8 has a broad blue emission band centered at 450–485 nm and Eu 2+ –Mn 2+ -activated (Ba,Ca,Sr) 3 MgSi 2 O 8 exhibits a red emission around 620–703 nm, depending on the relative concentrations of Ba, Ca and Sr. The particle size of Eu 2+ and Mn 2+ co-activated (Ba,Ca) 3 MgSi 2 O 8 ranges from 300 nm to 1 μm depending on the metal ion and are agglomerated due to post-synthesis, high temperature annealing. The green emission of Ba 3 MgSi 2 O 8 originates from secondary phases (Ba 2 SiO 4 and BaMgSiO 4 ) confirmed by emission spectra and X-ray diffraction patterns. The secondary phases of Ba 3 MgSi 2 O 8 are removed by the addition of Sr. The quantum efficiencies range from 45% to 70% under 400 nm excitation and the lifetime of red emission of Ba 3 MgSi 2 O 8 decreases significantly with increasing temperature, which is 54% at 400 K of that at 80 K compared to that of blue emission (90% at 400 K of that at 80 K). -- highlights: • (Ba,Ca,Sr) 3 MgSi 2 O 8 :Eu 2+ , Mn 2+ phosphors were prepared by a combustion synthesis method. • The emission spectra consist of broad blue-emission band and red-emission band. • The quantum efficiencies range between 45% and 70%, depending on the relative concentrations of Ba, Ca and Sr. • The secondary phases were eliminated by additions of Sr. • Lifetime of the red-emission decreases with increasing temperature, suggesting that these phosphors are not useful for solid state lighting applications

Effect of cooling rate on the transition temperature in Bi-Pb-Sr-Ca-Cu-O system

International Nuclear Information System (INIS)

Wang Yugui; Wang Jinsong; Wang Nanlin; Jiao Xinping; Han Guchang; Chen Zhaojia; Wang Keqin; Wu Xiaoguang

1989-12-01

The resistance and a.c. susceptibility measurement show that cooling rate of the cast-annealing samples in heat treatment process has some effect on the 110K superconducting phase in Bi-Pb-Sr-Ca-Cu-O system. Rapid quenching of the sample in air from 845 deg C causes oxygen deficiency in lattice and brings about a trifling change of unit cell size along c-axis direction. The d.c. magnetization and specific heat anomaly Δc measurements demostrate that fast cooling rate can reduce the transition temperature of high-T c phase and the lower critical field, and weaken the pinning forces for vertex lines. The peak value of specific heat anomaly of the sample with nominal composition of Bi 1.7 Pb 0.3 Sr 2 Ca 2 Cu 4.5 O v is still small in comparison with YBa 2 Cu 3 O 7 . From the magnetization curve the authors estimate that the superconducting volume fraction is about 20%

Fabrication and Film Qualification of Sr Modified Pb(Ca) TiO3 Thin Films

International Nuclear Information System (INIS)

Naw Hla Myat San; Khin Aye Thwe; Than Than Win; Yin Maung Maung; Ko Ko Kyaw Soe

2011-12-01

Strontium and calcium - modified lead titanate (Pb0.7 Ca0.15 Sr0.15 ) TiO3 (PCST)thin films were prepared by using spin coating technique. Phase transition of PCST was interpreted by means of Er-T characteristics. Process temperature dependence on micro-structure of PCST film was studied. Charge conduction mechanism of PCST thin film was also investigated for film qualification.

Evaluation of the heavy metals Cr, Mn, Fe, Cu, Zn and Pb in water penny wort (Hydrocotyle ranunculoides) from the upper course of the Lerma River, Mexico; Evaluacion de los metales pesados Cr, Mn, Fe, Cu, Zn y Pb en sombrerillo de agua (Hydrocotyle ranunculoides) del curso alto del Rio Lerma, Mexico

Energy Technology Data Exchange (ETDEWEB)

Zarazua, G.; Avila P, P.; Tejeda, S. [ININ, Carretera Mexico-Toluca s/n, 52750 Ocoyoacac, Estado de Mexico (Mexico); Valdivia B, M.; Macedo M, G. [Instituto Tecnologico de Toluca, Av. Tecnologico s/n, Ex-Rancho La Virgen, 52140 Metepec, Estado de Mexico (Mexico); Zepeda G, C., E-mail: graciela.zarazua@inin.gob.mx [Universidad Autonoma del Estado de Mexico, Cerro de Coatepec s/n, Ciudad Universitaria, 50100 Toluca, Estado de Mexico (Mexico)

2013-07-01

The Lerma river is one of the most polluted water bodies in Mexico, it presents low biodiversity and lets grow up aquatic plants resistant to the pollution. The aim of this work was to evaluate the concentration and bioaccumulation factors of Cr, Mn, Fe, Cu, Zn and Pb in aerial and submerged structures of water penny wort (Hydrocotyle ranunculoides) from the upper course of the Lerma river. Inductively coupled plasma-optical emission spectrometry was used to determine the concentration of heavy metals in water and H. ranunculoides. Results show that the bioaccumulation factors of Fe and Zn were higher than those of Cu, Mn, Cr and Pb; with the exception of Zn, bioaccumulation factors were higher in the submerged structures of the plant, which shows low mobility of analyzed metals. As a result of this study H. ranunculoides can be considered as good indicator of metal pollution in water bodies. (Author)

Synthesis and structural studies on cerium substituted La0.4Ca0.6MnO3 as solid oxide fuel cell electrode material

Science.gov (United States)

Singh, Monika; Kumar, Dinesh; Singh, Akhilesh Kumar

2018-04-01

For solid oxide fuel cell electrode material, calcium doped lanthanum manganite La0.4Ca0.6MnO3 (LCMO) and cerium-incorporated on Ca-site with composition La0.40Ca0.55Ce0.05MnO3 (LCCMO) were synthesized using most feasible and efficient glycine-nitrate method. The formation of crystalline single phase was confirmed by x-ray diffraction (XRD). The Rietveld analysis reveals that both systems crystallize into orthorhombic crystal structure with Pnma space group. Additionally, 8 mole % Y2O3 stabilized ZrO2 (8YSZ) solid electrolyte was also synthesized using high energy ball mill to check the reaction with electrode materials. It was found that the substitution of Ce+4 cations in LCMO perovskite suppressed formation of undesired insulating CaZrO3 phase.

Citric acid improves lead (pb) phytoextraction in brassica napus L. by mitigating pb-induced morphological and biochemical damages.

Science.gov (United States)

Shakoor, Muhammad Bilal; Ali, Shafaqat; Hameed, Amjad; Farid, Mujahid; Hussain, Sabir; Yasmeen, Tahira; Najeeb, Ullah; Bharwana, Saima Aslam; Abbasi, Ghulam Hasan

2014-11-01

Phytoextraction is an environmentally friendly and a cost-effective strategy for remediation of heavy metal contaminated soils. However, lower bioavailability of some of the metals in polluted environments e.g. lead (Pb) is a major constraint of phytoextraction process that could be overcome by applying organic chelators. We conducted a glasshouse experiment to evaluate the role of citric acid (CA) in enhancing Pb phytoextraction. Brassica napus L. seedlings were grown in hydroponic media and exposed to various treatments of Pb (50 and 100 μM) as alone or in combination with CA (2.5mM) for six weeks. Pb-induced damage in B. napus toxicity was evident from elevated levels of malondialdehyde (MDA) and H2O2 that significantly inhibited plant growth, biomass accumulation, leaf chlorophyll contents and gas exchange parameters. Alternatively, CA application to Pb-stressed B. napus plants arrested lipid membrane damage by limiting MDA and H2O2 production and by improving antioxidant enzyme activities. In addition, CA significantly increased the Pb accumulation in B. napus plants. The study concludes that CA has a potential to improve Pb phytoextraction without damaging plant growth. Copyright © 2014 Elsevier Inc. All rights reserved.

Training-induced inversion of spontaneous exchange bias field on La{sub 1.5}Ca{sub 0.5}CoMnO{sub 6}

Energy Technology Data Exchange (ETDEWEB)

Bufaiçal, L., E-mail: lbufaical@ufg.br [Instituto de Física, Universidade Federal de Goiás, 74001-970 Goiânia, GO (Brazil); Finkler, R.; Coutrim, L.T. [Instituto de Física, Universidade Federal de Goiás, 74001-970 Goiânia, GO (Brazil); Pagliuso, P.G. [Instituto de Física “Gleb Wataghin”, UNICAMP, 13083-859 Campinas, SP (Brazil); Grossi, C.; Stavale, F.; Baggio-Saitovitch, E.; Bittar, E.M. [Centro Brasileiro de Pesquisas Físicas, Rua Dr. Xavier Sigaud 150, 22290-180 Rio de Janeiro, RJ (Brazil)

2017-07-01

Highlights: • La{sub 1.5}Ca{sub 0.5}CoMnO{sub 6} exhibits spontaneous exchange bias effect at low temperature. • For successive hysteresis cycles it inverts the shift sign from negative to positive. • For a field cooled hysteresis cycle, the exchange bias effect greatly enhances. • Our results are compared to those of the analogue compound La{sub 1.5}Sr{sub 0.5}CoMnO{sub 6}. - Abstract: In this work we report the synthesis and structural, electronic and magnetic properties of La{sub 1.5}Ca{sub 0.5}CoMnO{sub 6} double-perovskite. This is a re-entrant spin cluster material which exhibits a non-negligible negative exchange bias effect when it is cooled in zero magnetic field from an unmagnetized state down to low temperature. X-ray powder diffraction, X-ray photoelectron spectroscopy and magnetometry results indicate mixed valence state at Co site, leading to competing magnetic phases and uncompensated spins at the magnetic interfaces. We compare the results for this Ca-doped material with those reported for the resemblant compound La{sub 1.5}Sr{sub 0.5}CoMnO{sub 6}, and discuss the much smaller spontaneous exchange bias effect observed for the former in terms of its structural and magnetic particularities. For La{sub 1.5}Ca{sub 0.5}CoMnO{sub 6}, when successive magnetization loops are carried, the spontaneous exchange bias field inverts its sign from negative to positive from the first to the second measurement. We discuss this behavior based on the disorder at the magnetic interfaces, related to the presence of a glassy phase. This compound also exhibits a large conventional exchange bias, for which there is no sign inversion of the exchange bias field for consecutive cycles.

Double perovskite Ca2GdNbO6:Mn4+ deep red phosphor: Potential application for warm W-LEDs

Science.gov (United States)

Lu, Zuizhi; Huang, Tianjiao; Deng, Ruopeng; Wang, Huan; Wen, Lingling; Huang, Meixin; Zhou, Liya; Yao, Chunying

2018-05-01

A novel Mn4+-doped Ca2GdNbO6 (CGN) phosphor was prepared by high-temperature solid-state reaction. The crystal structure was investigated by X-ray diffraction patterns and unit cell structure. Mn4+ replaced the location of Nb5+ in the CGN lattice, and the value of energy gap (Egap) decreased from 2.16 eV to 1.13 eV, indicating that Mn4+ ions play a great influence on the absorption of CGN hosts. The broad excitation band from 250 nm to 550 nm matches well with commercial near-UV light emitting diodes, and the emission peak centered at 680 nm is due to 2E→4A2g transition in Mn4+ ions. The CIE chromaticity coordinates (0.698, 0.303) of CGN:Mn4+ phosphor was close to standard red color coordinates (0.666, 0.333). These investigations demonstrate CGN:Mn4+ phosphor as an efficient red phosphor for potential applications.

Measurements of Small Exposures of Gamma Radiation with CaSO{sub 4}:Mn Radiothermoluminescence

Energy Technology Data Exchange (ETDEWEB)

Bjaerngard, Bengt

1963-08-15

A system for measurements of small exposures of gamma radiation using CaSO{sub 4}:Mn thermoluminescence has been developed. The construction and performance of a read-out apparatus is described as well as the construction and characteristics of a simple dosimeter. The reproducibility of the method at various exposures is estimated. 20 {mu}R of 1 MeV gamma radiation can be measured with a reproducibility within {+-} 50 % (standard deviation)

Microstructure and mechanical properties of Mg-Al-Mn-Ca alloy sheet produced by twin roll casting and sequential warm rolling

International Nuclear Information System (INIS)

Wang Yinong; Kang, Suk Bong; Cho, Jaehyung

2011-01-01

Research highlights: → This work, taking AM30 + 0.2Ca alloy as experimental material, will provide some new information as follows: one is microstructural difference between twin roll cast and ingot cast AM31-0.2Ca alloy. The other is the comparison of tensile properties after warm rolling and annealing. Suggesting the possibility of the development of wrought magnesium alloy sheets by strip casting. - Abstract: Microstructural evolution and mechanical properties of twin roll cast (TRC) Mg-3.3 wt.%Al-0.8 wt.%Mn-0.2 wt.%Ca (AM31 + 0.2Ca) alloy strip during warm rolling and subsequent annealing were investigated in this paper. The as-TRC alloy strip shows columnar dendrites in surface and equiaxed dendrites in center regions, as well as finely dispersed primary Al 8 Mn 5 particles on interdendritic boundaries which result in the beneficial effect on microstructural refinement of strip casting. The warm rolled sheets show intensively deformed band or shear band structures, as well as finely and homogeneously dispersed Al-Mn particles. No evident dynamic recrystallization (DRX) takes place during warm rolling process, which is more likely attributed to the finely dispersed particle and high solid solution of Al and Mn atoms in α-Mg matrix. After annealing at 350 deg. C for 1 h, the warm rolled TRC sheets show fine equiaxed grains around 7.8 μm in average size. It has been shown that the present TRC alloy sheet has superior tensile strength and comparative elongation compared to commercial ingot cast (IC) one, suggesting the possibility of the development of wrought magnesium alloy sheets by twin roll strip casting processing. The microstructural evolution during warm rolling and subsequent annealing as well as the resulting tensile properties were analyzed and discussed.

Constraining 20th Century Pacific Trade-Wind Variability Using Coral Mn/Ca

Science.gov (United States)

Sayani, H. R.; Thompson, D. M.; Carilli, J.; Ireland, T. J.; Cobb, K. M.; Atwood, A. R.; Grothe, P. R.; Miller, S. J.; Hitt, N. T.; O'Connor, G.

2017-12-01

Global mean surface temperatures during the 20th century are characterized by multidecadal periods of either accelerated or reduced rates of warming that cannot be explained by external forcings alone. Both observations and modeling studies suggest that the reduced rate of global surface warming during the early-2000s can be largely explained by decadal climate variability in the tropical Pacific, specifically changes in trade-wind strength [e.g. Meehl et al., 2016]. However, the relationship between Pacific trade-wind strength and global surface warming is poorly constrained due to the lack of instrumental wind observations prior to the 1970s. Surface corals are now routinely used to generate records of past sea-surface temperature (SST) change, and have dramatically improved our understanding of oceanic variability in the tropical Pacific. Yet, there are few direct measurements of the atmospheric response to this SST variability. Skeletal Mn/Ca ratios in corals from Tarawa Atoll (1.3˚N, 173˚E) have been shown to track El Niño-related westerly wind events on interannual timescales [Shen et al., 1992], and the strength of Pacific trade winds on decadal timescales [Thompson et al., 2015]. Here, we investigate the utility of this novel wind proxy at Kiritimati Atoll (Christmas Island; 2˚N, 157.5˚W), a site that is hydrographically similar to Tarawa. We use a series of seawater samples collected across the 2015/16 El Niño to characterize and quantify the relationship between westerly wind events and seawater Mn variability around Kiritimati. Anchored by this modern-day calibration, we present a new reconstruction of westerly winds across the late-20thcentury from Kiritimati Atoll. We also assess the reproducibility of coral Mn/Ca across cores collected at varying distances from the lagoon, which represents the primary source of seawater Mn to the reef at our site. Lastly, we discuss the strengths and limitations of this novel proxy, as well as the potential for

The effect of CaNa{sub 2}EDTA on excretion of {sup 210}PB, {sup 210}Po and stable lead in cases of chronic lead intoxication

Energy Technology Data Exchange (ETDEWEB)

Knezevic, I.; Milacic, S.; Novak, Lj.; Uzelac, V.; Nesic, V

1998-07-01

The study describes the effect of CaNa{sub 2}EDTA on the excretion of the naturally occurring radionuclides {sup 210}Pb, {sup 210}Po and stable lead in workers' urine. The CaNa{sub 2}EDTA was administered intravenously to workers in the morning for five days. The results show that CaNa{sub 2}EDTA mobilises biologically active {sup 210}Pb, {sup 210}Po and stable lead, appreciably increasing their concentration in urine. (author)

Size effect on the structural, magnetic, and magnetotransport properties of electron doped manganite La0.15Ca0.85MnO3

Science.gov (United States)

Thomas, Rini; Das, Gangadhar; Mondal, Rajib; Pradheesh, R.; Mahato, R. N.; Geetha Kumary, T.; Nirmala, R.; Morozkin, A. V.; Lamsal, J.; Yelon, W. B.; Nigam, A. K.; Malik, S. K.

2012-04-01

Nanocrystalline La0.15Ca0.85MnO3 samples of various grain sizes ranging from ˜17 to 42 nm have been prepared by sol-gel technique. Phase purity and composition were verified by room temperature x-ray diffraction and SEM-EDAX analysis. The bulk La0.15Ca0.85MnO3 is known to order antiferromagnetically around 170 K and to undergo a simultaneous crystal structural transition. DC magnetization measurements on 17 nm size La0.15Ca0.85MnO3 show a peak at ˜130 K (TN) in zero-field-cooled (ZFC) state. Field-cooled magnetization bifurcates from ZFC data around 200 K hinting a weak ferromagnetic component near room temperature due to surface moments of the nanoparticle sample. Low temperature powder neutron diffraction experiments reveal that the incomplete structural transition from room temperature orthorhombic to low temperature orthorhombic-monoclinic state also occurs in the nanoparticle sample as in the bulk. Magnetization in the ordered state decreases as particle size increases, thus indicating the reduction of the competing ferromagnetic surface moments.

Multilevel Resistance Switching Memory in La2/3Ba1/3MnO3/0.7Pb(Mg1/3Nb2/3)O3-0.3PbTiO3 (011) Heterostructure by Combined Straintronics-Spintronics.

Science.gov (United States)

Zhou, Weiping; Xiong, Yuanqiang; Zhang, Zhengming; Wang, Dunhui; Tan, Weishi; Cao, Qingqi; Qian, Zhenghong; Du, Youwei

2016-03-02

We demonstrate a memory device with multifield switchable multilevel states at room temperature based on the integration of straintronics and spintronics in a La2/3Ba1/3MnO3/0.7Pb(Mg1/3Nb2/3)O3-0.3PbTiO3 (PMN-PT) (011) heterostructure. By precisely controlling the electric field applied on the PMN-PT substrate, multiple nonvolatile resistance states can be generated in La2/3Ba1/3MnO3 films, which can be ascribed to the strain-modulated metal-insulator transition and phase separation of Manganite. Furthermore, because of the strong coupling between spin and charge degrees of freedom, the resistance of the La2/3Ba1/3MnO3 film can be readily modulated by magnetic field over a broad temperature range. Therefore, by combining electroresistance and magnetoresistance effects, multilevel resistance states with excellent retention and endurance properties can be achieved at room temperature with the coactions of electric and magnetic fields. The incorporation of ferroelastic strain and magnetic and resistive properties in memory cells suggests a promising approach for multistate, high-density, and low-power consumption electronic memory devices.

Pressure-induced suppression of ferromagnetic phase and conduction in CaMn1-xRuxO3

International Nuclear Information System (INIS)

Markovich, V.; Fita, I.; Puzniak, R.; Rozenberg, E.; Martin, C.; Wisniewski, A.; Maignan, A.; Raveau, B.; Yuzhelevskii, Y.; Gorodetsky, G.

2005-01-01

Magnetic and transport properties of polycrystalline CaMn 1-x Ru x O 3 (x=0-0.4) perovskites were investigated under pressures up to 12kbar. It was found that an applied pressure suppresses ferromagnetism and increases resistivity. The results are discussed in the context of phase separation and valence effects

The crystal structure and electrical properties of K{sub 2}NiF{sub 4}-type (Ca{sub 2−x}Sm{sub x})MnO{sub 4}

Energy Technology Data Exchange (ETDEWEB)

Taguchi, Hideki, E-mail: htaguchi@cc.okayama-u.ac.jp [The Graduate School of Natural Science and Technology (Science), Okayama University, 3-1-1 Tsushima-Naka, Kita-Ku, Okayama 700-8530 (Japan); Kido, Hiroyasu [Osaka Municipal Technical Research Institute, 1-6-50 Morinomiya, Jyoto-Ku, Osaka 536-8553 (Japan); Kato, Masaki; Hirota, Ken [Department of Molecular Chemistry and Biochemistry, Faculty of Science and Engineering, Doshisha University, Kyo-Tanabe 610-0321 (Japan)

2015-04-15

Graphical abstract: The relationship between log ρ of K{sub 2}NiF{sub 4}-type (Ca{sub 2−x}Sm{sub x})MnO{sub 4} and 1000/T. - Highlights: • K{sub 2}NiF{sub 4}-type (Ca{sub 2−x}Sm{sub x})MnO{sub 4} was synthesized using a polymerized complex route. • The semiconductive samples had minimum values of ρ and E{sub a} at x = 0.1. • The log ρ–1/T curve of x = 0.3 consisted of two different lines at 315 K. • The 1/χ − T curve of x = 0.3 had a peak at 325 K. • These results indicated the presence of a charge-ordering transition at x = 0.3. - Abstract: K{sub 2}NiF{sub 4}-type (Ca{sub 2−x}Sm{sub x})MnO{sub 4} (0.02 ≤ x ≤ 0.3) was synthesized using a polymerized complex route. The crystal structure changed from tetragonal to orthorhombic at x = 0.3. A variation in the lattice parameters was explained by the Mn–O(2) distance, the Mn−O(2)−Mn angle, and the (Ca,Sm)–(Ca,Sm) distance. The samples were n-type semiconductors, and the minimum values of electrical resistivity (ρ) and an energy gap (E{sub g}) at x = 0.1 were accounted by electron transfer through an Mn−O(2)−Mn path and overlap between the Mnt{sub 2g} and Op{sub π} orbitals. In the sample (x = 0.3), the log ρ–1000/T curve consisted of two different lines that intersected at ca. 325 K, and a peak was observed at ca. 315 K in the magnetic susceptibility–temperature curve. These results indicated the presence of a charge-ordering (CO) transition at 315–325 K.

Enhanced electrical and magnetic properties in La0.7Sr0.3MnO3 thin films deposited on CaTiO3-buffered silicon substrates

Directory of Open Access Journals (Sweden)

C. Adamo

2015-06-01

Full Text Available We investigate the suitability of an epitaxial CaTiO3 buffer layer deposited onto (100 Si by reactive molecular-beam epitaxy (MBE for the epitaxial integration of the colossal magnetoresistive material La0.7Sr0.3MnO3 with silicon. The magnetic and electrical properties of La0.7Sr0.3MnO3 films deposited by MBE on CaTiO3-buffered silicon (CaTiO3/Si are compared with those deposited on SrTiO3-buffered silicon (SrTiO3/Si. In addition to possessing a higher Curie temperature and a higher metal-to-insulator transition temperature, the electrical resistivity and 1/f noise level at 300 K are reduced by a factor of two in the heterostructure with the CaTiO3 buffer layer. These results are relevant to device applications of La0.7Sr0.3MnO3 thin films on silicon substrates.

Evolution of the structural and multiferroic properties of PbFe{sub 2/3}W{sub 1/3}O{sub 3} ceramics upon Mn-doping

Energy Technology Data Exchange (ETDEWEB)

Ivanov, S.A. [Center of Materials Science, Karpov' Institute of Physical Chemistry, Vorontsovo Pole 10, Moscow, 105064 (Russian Federation); Department of Engineering Sciences, Uppsala University, Box 534, 751 21, Uppsala (Sweden); Bush, A.A. [Moscow State University of Information Technologies, RadioEngineering and Electronics, pr.Vernadskogo 78, Moscow, 119454 (Russian Federation); Ritter, C. [Institute Laue-Langevin, BP 156, F-38042, Grenoble (France); Behtin, M.A. [Moscow State University of Information Technologies, RadioEngineering and Electronics, pr.Vernadskogo 78, Moscow, 119454 (Russian Federation); Cherepanov, V.M. [National Research Centre Kurchatov Institute, pl. Kurchatova 1, Moscow, 123182 (Russian Federation); Autieri, C.; Kvashnin, Y.O.; Di Marco, I.; Sanyal, B.; Eriksson, O. [Department of Physics and Astronomy, Uppsala University, Box 516, 751 20, Uppsala (Sweden); Kumar, P. Anil; Nordblad, P. [Department of Engineering Sciences, Uppsala University, Box 534, 751 21, Uppsala (Sweden); Mathieu, R., E-mail: roland.mathieu@angstrom.uu.se [Department of Engineering Sciences, Uppsala University, Box 534, 751 21, Uppsala (Sweden)

2017-02-01

The perovskite system Pb(Fe{sub 1-x}Mn{sub x}){sub 2/3}W{sub 1/3}O{sub 3} (0 ≤ x ≤ 1, PFMWO) has been prepared by conventional solid-state reaction under different sintering conditions. Structures and phase composition as well as thermal, magnetic and dielectric properties of the compounds have been systematically investigated experimentally and by first-principles density functional calculations. A clean perovskite phase is established at room temperature for compositions 0 ≤ x ≤ 0.4. Rietveld refinements of X-ray and neutron powder diffraction patterns demonstrate that the compounds crystallize in space group Pm-3m (0 ≤ x ≤ 0.4). The degree of ordering of the Fe and W/Mn cations was found to depend on the concentration of Mn. First-principles calculations suggest that the structural properties of PFMWO are strongly influenced by the Jahn-Teller effect. The PFMWO compounds behave as relaxor ferroelectrics at weak Mn-doping with a dielectric constant that rapidly decreases with increasing Mn content. A low temperature antiferromagnetic G-type order with propagation vector k = (1/2,1/2,1/2) is derived from neutron powder diffraction data for the samples with x ≤ 0.4. However with increasing doping concentration, the magnetic order is perturbed. First-principles calculations show that the dominant exchange coupling is antiferromagnetic and occurs between nearest neighbor Fe atoms. When the system is doped with Mn, a relatively weak ferromagnetic (FM) interaction between Fe and Mn atoms emerges. However, due to the presence of this FM interaction, the correlation length of the magnetic order is greatly shortened already at rather low doping levels. - Highlights: • The perovskite system Pb(Fe{sub 1−x}Mn{sub x}){sub 2/3}W{sub 1/3}O{sub 3} (0 ≤ x ≤ 1, PFMWO) has been synthesized. • The structural, magnetic, and dielectric properties of PFMWO have been investigated. • The degree of ordering of the Fe and W/Mn cations was found to depend on x. �

Emergence of Griffiths phase and glassy mixed phase in Sm0.5Ca0.5MnO3 nanomanganites

International Nuclear Information System (INIS)

Giri, S.K.; Yusuf, S.M.; Mukadam, M.D.; Nath, T.K.

2014-01-01

Graphical abstract: A detailed investigation on the effect of grain size on formation of Griffiths phase, and glassy mixed phase in CE-type antiferromagnetic Sm 0.5 Ca 0.5 MnO 3 manganite are carried out. A rigorous measurement of linear and non-linear ac magnetic susceptibilities, time dependent relaxation and aging phenomena in Sm 0.5 Ca 0.5 MnO 3 nanomanganite confirm the existence of a glassy mixed phase in the low temperature regime. The signature of Griffiths phase in nanosized manganite has been confirmed from the detailed ac and dc magnetization studies. The existence of Griffiths phase is verified through the anomalous behavior of the low field temperature dependent an inverse ac and dc magnetic susceptibility. Based on experimental results, the glassy phase of nanomanganites has been attributed to the phase separation effect and interaction between the ferromagnetic clusters. A phenomenological core/shell model has also been proposed based on the surface disorder to explain the observed Griffiths phase in these nanosized manganites. Fig. 1: (Left) The plot of inverse of ac susceptibility χ ac -1 measured at f = 1 Hz and H ac = 2 Oe as a function of temperature for S750 sample. Inset shows the same for S550 sample. (Right) A schematic of the proposed model to describe the magnetic state of the Sm 0.5 Ca 0.5 MnO 3 system at different average sizes. Highlights: • Effect of grain size on Griffiths phase and glassy mixed phase is discussed. • GP is confirmed by dc, linear and non-linear ac magnetization in nanomanganites. • Glassy mixed phase is discussed by time dependent relaxation and aging phenomena. • The existence of GP is verified through an inverse ac and dc magnetic susceptibility. • A phenomenological core/shell model has been proposed based on surface disorder. -- Abstract: A detailed investigation on the effect of grain size on formation of Griffiths phase (GP), and glassy mixed phase in CE-type antiferromagnetic Sm 0.5 Ca 0.5 MnO 3

High-density Bi-Pb-Sr-Ca-Cu-O superconductor prepared by rapid thermal melt processing

Science.gov (United States)

Moon, B. M.; Lalevic, B.; Kear, B. H.; McCandlish, L. E.; Safari, A.; Meskoob, M.

1989-10-01

A high quality, dense Bi-Pb-Sr-Ca-Cu-O superconductor has been successfully synthesized by rapid thermal melt processing. Conventionally sintered pellets were melted at 1200 °C, cooled rapidly, and then annealed. As-melted samples exhibited semiconductor behavior, which upon annealing became superconducting at 115 K [Tc(zero)=105 K]. A detailed study of various processing techniques has been carried out.

Growth and characterization of La2CoMnO6 crystals doped with Pb

International Nuclear Information System (INIS)

Milenov, T.I.; Rafailov, P.M.; Abrashev, M.V.; Nikolova, R.P.; Nakatsuka, A.; Avdeev, G.V.; Veleva, M.N.; Dobreva, S.; Yankova, L.; Gospodinov, M.M.

2010-01-01

Crystals of La 2 CoMnO 6 doped with Pb were grown by the high temperature solution growth method. Several crystals were examined by scanning electron microscopy (SEM), energy-dispersive X-ray analysis (EDAX), X-ray single-crystal diffractometry and polarized Raman spectroscopy. Some variations in the composition of different crystals are observed, however, within the volume of each distinct crystal the composition is found to be fairly constant. Crystals with lateral dimensions larger than 2 mm and thicker than 1 mm contain structural defects as twin lamellae and surface roughness. The results from the characterization of the grown crystals with X-ray diffraction and Raman spectroscopy are consistent with an assumption for a coexistence of an ordered monoclinic and a disordered orthorhombic phase.

Microstructure, mechanical properties and bio-corrosion properties of Mg-Zn-Mn-Ca alloy for biomedical application

International Nuclear Information System (INIS)

Zhang Erlin; Yang Lei

2008-01-01

Microstructure, mechanical properties and bio-corrosion properties of as-cast Mg-Zn-Mn-Ca alloys were investigated for biomedical application in detail by optical microscopy, scanning electronic microscopy (SEM), mechanical properties testing and electrochemical measurement. SEM and optical microscopy observation indicated that the grain size of the as-cast alloys significantly decreased with the increasing of Ca content up to 0.5 wt.%. Further increasing of Ca content did not refine the grain more. The phase constitute was mainly controlled by the atomic ratio of Zn to Ca. When the ratio was more than 1.0-1.2, the alloy was mainly composed of primary Mg and lamellar eutectic (α-Mg + Ca 2 Mg 6 Zn 3 ), while the alloy was composed of primary Mg and divorced eutectic (α-Mg + Mg 2 Ca + Ca 2 Mg 6 Zn 3 ) when the atomic ratio was less than 1.0-1.2. The yield strength of the as-cast alloy increased but the elongation and the tensile strength increased first and then decreased with the increasing of Ca content. It was thought that Mg 2 Ca phase deteriorated the tensile strength and ductility. Electrochemical measurements indicated that Mg 2 Ca phase improved the corrosion resistance of the as-cast alloy

Determination of Mn, Fe, Ni, Cu, Zn and Pb contents in samples in samples of apple trees by radionuclide X-ray fluorescence analysis

International Nuclear Information System (INIS)

Bumbalova, A.; Havranek, E.; Harangozo, M.

1982-01-01

The applicability of the radionuclide X-ray fluorescence analysis (RXFA) for qualitative and quantitative evaluation of environmental plant samples is discussed and examples of determination of Mn, Fe, Ni, Cu, Zn, Pb in samples of apple trees are given. The instrumentation, the standard and sample preparation are also presented. (author)

Computational study of electronic, optical and thermoelectric properties of X3PbO (X = Ca, Sr, Ba) anti-perovskites

Science.gov (United States)

Hassan, M.; Arshad, I.; Mahmood, Q.

2017-11-01

We report the structural, electronic, optical and thermoelectric (TE) properties of X3PbO (X = Ca, Sr, Ba) anti-perovskites as a function of X cations belonging to the group IIA. The computations are done by using the most recently introduced modified Becke-Johnson potential. It has been observed that the cubic lattice constant increases as the cations change from Ca to Ba, consequently, the bulk modulus reduces. The bottom of conduction band shows strong hybridization between Pb-6p, O-2p and X-s states, in contrast, valence band maxima are mainly manufactured by Pb-6p states. The anti-perovskites exhibit narrow direct band gap that show an inverse relation to the static real dielectric constants that verifies Penn’s model. In addition, the X cations induced tuning of the absorption edge in the visible and the ultraviolet energy suggest optical device applications. The computed TE parameters have been found sensitive to the X cations and have been demonstrated to be best suited for the TE devices operating at high temperatures.

Sem-EDAX'S Application For Characterization Of Superconductor Material Of (Bi,Pb)-Sr-Ca-Cu-O

International Nuclear Information System (INIS)

Handayani, Ari; Wuryanto; Prambudi, Bambang

1996-01-01

The microstructure and composition analysis of superconductor material of (Bi,Pb)-Sr-Ca-Cu-O which were synthesized by two different processes (CA and CD Process) by varying the sintering time, i.e. 20,60 and 100 hours were done by using SEM-EDAX method. The standard sample of superconductor material of Bi-Sr-Ca-Cu-O with 1112, 2212 and 2223 phase from Stream has been used for comparison, At 25 kV, the composition analysis showed that, at 20 and 60 hours of sintering, a mixture of phases existed while 100 hours of sintering resulted in a phase close to phase 2223. The result of microstructure observation showed significant differences. At synthesized CA process, 100 hours of sintering gives bigger and clearer platelet microstructure shape than that given by 20 and 60 hours of sintering. Also from the synthesized CD process, the 60 and 100 hours of sintering gives bigger and clearer platelet microstructure shape than that given by the 20 hours of sintering

Effect of Pb and Ag additions on electrical properties Bi2Sr2Ca2Cu3Ox superconductive ceramics

International Nuclear Information System (INIS)

Reddi, B.V.; Uskov, E.M.

1990-01-01

The influence of Pb and Ag additions on the electrical properties of Bi 2 Sr 2 Ca 2 Cu 3 O x superconducting ceramics has been studied by Hall method. It was found that the Pb additions has more influence on the sample characteristics than Ag. It was found, that Hall EMF at 77 K equal to zero in the samples having some residue resistance

Impacts of MnZn doping on the structural and magnetic properties of M-type SrCaLa hexaferrites

Energy Technology Data Exchange (ETDEWEB)

Yang, Yujie; Shao, Juxiang; Wang, Fanhou; Huang, Duohui [Yibin University, Computational Physics Key Laboratory of Sichuan Province, School of Physics and Electronic Engineering, Yibin (China); Liu, Xiansong [Anhui University, Engineering Technology Research Center of Magnetic Materials, Anhui Province, School of Physics and Materials Science, Hefei (China)

2017-05-15

M-type hexaferrites with chemical compositions of Sr{sub 0.5}Ca{sub 0.2}La{sub 0.3}Fe{sub 12.0-2x} (MnZn){sub x} O{sub 19} (0.0 ≤ x ≤ 0.5) were synthesized by the traditional ceramic method. The crystal structure of M-type hexaferrite samples was examined by X-ray diffraction. The structural analyses reveal that all samples are in single M-type hexagonal phase and no secondary phase is present. A physical property measurement system-vibrating sample magnetometer was used to measure the magnetic properties of M-type hexaferrite samples. The saturation magnetization (M{sub s}), remanent magnetization (M{sub r}) and coercivity (H{sub c}) were calculated from magnetic hysteresis loops. M{sub s} first increases with MnZn content (x) from 0.0 to 0.1, and then decreases with MnZn content (x) from 0.1 to 0.5. While, M{sub r} decreases with MnZn content (x) from 0.0 to 0.2, and then increases with MnZn content (x) from 0.2 to 0.5. H{sub c} first decreases with MnZn content (x) from 0.0 to 0.2, and then increase with MnZn content (x) from 0.2 to 0.5. (orig.)

The suitability of annual tree growth rings as environmental archives: Evidence from Sr, Nd, Pb and Ca isotopes in spruce growth rings from the Strengbach watershed

Science.gov (United States)

Stille, Peter; Schmitt, Anne-Désirée; Labolle, François; Pierret, Marie-Claire; Gangloff, Sophie; Cobert, Florian; Lucot, Eric; Guéguen, Florence; Brioschi, Laure; Steinmann, Marc; Chabaux, François

2012-05-01

The combination of the Sr, Nd and Pb isotope systems, recognized as tracers of sources, with the Ca isotope system, known to reveal biology-related fractionations, allowed us to test the reliability of spruce (Picea abies) growth rings as environmental archives through time (from 1916 to 1983) in a forest ecosystem affected by acid atmospheric deposition. Sr and Pb isotopes have already been applied in former tree-ring studies, whereas the suitability of Nd and Ca isotope systems is checked in the present article. Our Sr and Nd isotope data indicate an evolution in the cation origin with a geogenic origin for the oldest rings and an atmospheric origin for the youngest rings. Ca isotopes show, for their part, an isotopic homogeneity which could be linked to the very low weathering flux of Ca. Since this flux is weak the spruces' root systems have pumped the Ca mainly from the organic matter-rich top-soil over the past century. In contrast, the annual growth rings studied are not reliable and suitable archives of past Pb pollution.

Study of the analytic quality in the determinations of Cr, Fe, Mn, Cu, Zn, Pb and Hg through conventional and nuclear analytical techniques in mosses of the MATV

International Nuclear Information System (INIS)

Caballero S, B.

2013-01-01

To evaluate the environmental risks of air pollution and to facilitate the decision-making for control, is necessary to have the capacity to generate data with analytical quality. A comparison between nuclear (Neutron activation analysis and total reflection X-ray fluorescence spectrometry) and no nuclear analytical techniques (atomic absorption spectrometry and inductively coupled plasma optical emission spectrometry) for simultaneous determination of metal content (Cr, Cu, Fe, Hg, Mn, Pb and Zn) in mosses from Metropolitan Area of the Toluca Valley (MATV) was performed. Epiphytic mosses (Fabriona ciliaris and Leskea angustata) were sampled in two campaigns, 16 sites (urban, transition and natural) and were prepared for each technique. The biological certified reference materials were used for the quality control and to evaluate accuracy, precision, linearity, detection and quantification limits. Results show that nuclear analytical techniques and no nuclear applied in chemical analysis of Cr, Cu, Fe, Hg, Mn, Pb and Zn in moss from MATV are comparable and therefore all of these can potentially be used for this purpose. However, if its considered both, the performance parameters and economic/operational characteristics is widely recommended inductively coupled plasma optical emission spectrometry, conventional analytical technique, which showed the highest analytical grade quality. Also were observed spatial and temporal variations in the concentrations of Cr, Cu, Fe, Hg, Mn, Pb and Zn in mosses from MATV and was discussed its potential origin. The urban sites had the highest concentration of anthropogenic elements as Cr, Cu, Fe, Hg, Pb and Zn because are strongly impacted by roads with high vehicle traffic. (Author)

The Nd-Mn exchange interaction, low temperature specific heat and magnetism of Nd{sub 2/3}Ca{sub 1/3}MnO{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Beznosov, Anatoly [B. Verkin Institute for Low Temperature Physics and Engineering NASU, 47 Lenin Avenue, Kharkov 61103 (Ukraine); Fertman, Elena, E-mail: fertman@ilt.kharkov.ua [B. Verkin Institute for Low Temperature Physics and Engineering NASU, 47 Lenin Avenue, Kharkov 61103 (Ukraine); Desnenko, Vladimir [B. Verkin Institute for Low Temperature Physics and Engineering NASU, 47 Lenin Avenue, Kharkov 61103 (Ukraine); Kajnakova, Marcela; Feher, Alexander [Centre of Low Temperature Physics of the Faculty of Science UPJS and IEP SAS, Park Angelinum 9, 04154 Kosice (Slovakia)

2011-10-15

The low temperature specific heat and magnetic characteristics of Nd{sub 2/3}Ca{sub 1/3}MnO{sub 3} perovskite are studied in a wide range of magnetic fields (up to 9 T). Temperature dependent specific heat data show a broadened Schottky-like anomaly below 20 K caused by splitting of the Nd{sup 3+} ions ground-state doublet in the effective molecular field H{sub ex}, determined by exchange interaction between Nd and Mn spin systems supplemented by an applied external magnetic field. Existence of the splitting at zero magnetic field and expressed field dependence is the evidence of a strong exchange coupling between Nd and Mn magnetic subsystems. The Nd-ions magnetic ordering leads to an additional contribution to the magnetic moment of the system below 30 K, producing anomalies of the magnetic loss and field-cooled and zero-field-cooled magnetizations. The observed broadened Schottky-like anomalies are fitted for each applied magnetic field by the sum of three Schottky functions. Applied magnetic field extends the anomaly region and shifts it to higher temperatures. Splitting of the higher crystal field Kramers doublets gives an additional contribution to the heat capacity in magnetic fields. The ground state doublet g-factors g{sub ||} and g{sub perpendicular} were estimated to be 3.4 and 2.2, respectively, and H{sub ex} was estimated to be 9 T. The Nd{sup 3+} ions magnetic moment estimated from the magnetization data agrees with the value obtained from the specific heat data. - Highlights: > Low temperature specific heat of Nd{sub 2/3}Ca{sub 1/3}MnO{sub 3} has been measured in magnetic fields up to 9 T. > Schottky-like anomalies are fitted for each magnetic field by a sum of three Schottky functions. > An effective magnetic field of the Mn spin system on Nd ion has been estimated as H{sub ex}=9 T. > Nd{sup 3+} ground-state g-factors have been estimated as g{sub ||}=3.4 and g{sub perpendicular} =2.2. > Magnetic ordering of the Nd subsystem has been revealed below

Crystal-field and Nd-Mn exchange interaction in Nd{sub 2/3}Ca{sub 1/3}MnO{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Beznosov, A; Fertman, E; Desnenko, V; Loginov, A [B Verkin Institute for Low Temperature Physics and Engineering, NASU, 47 Lenin Ave., 61103 Kharkov (Ukraine); Feher, A; Kajnakova, M, E-mail: fertman@ilt.kharkov.u [Centre of Low Temperature Physics of the Faculty of Science of P.J. Safarik University and IEP SAS, Park Angelinum 9, SK-04154 Kotice (Slovakia)

2010-01-01

A study of the low field magnetization and specific heat in magnetic fields up to 9 T of Nd{sub 2/3}Ca{sub 1/3}MnO{sub 3} perovskite in the 2-30 K temperature range has been done. All the specific heat data show broadened Schottky-like anomaly below 20 K. We suppose that such a behavior originates from the Nd magnetic ordering caused by the splitting of the Nd{sup 3+} ions ground-state doublet (GSD) in the effective molecular field H{sub ex} of Mn spin system supplemented by an applied external magnetic field. The zero field GSD splitting is an evidence of a strong exchange coupling between Nd and Mn magnetic subsystems. The Nd-ions magnetic ordering introduces an additional contribution to the ferromagnetic moment producing anomalies of the field-cooled and zero-field-cooled magnetizations of the system below 28 K. The broadened Schottky-like anomalies found are fitted for every field by a set of three Schottky functions. Applied magnetic field extends the anomaly region and shifts it to the higher temperatures. Splitting of the higher crystal field Kramers doublets gives an additional contribution to the heat capacity under magnetic fields. The GSD g-factors g{sub ||} and g{sub p}erpendicular was estimated as 3.4 and 2.2, respectively, and H{sub ex} as 9 T.

Structural and electrical characterization of La{sub 0.72}Ca{sub 0.28}MnO{sub 3} ceramic and thin films

Energy Technology Data Exchange (ETDEWEB)

Ma Ji [Faculty of Materials Science and Engineering, Kunming University of Science and Technology, Kunming 650093 (China); Theingi, Mya [Faculty of Materials Science and Engineering, Kunming University of Science and Technology, Kunming 650093 (China); Department of Chemistry, University of Yangon, Yangon 11181 (Myanmar); Zhang Hui; Ding Xuan [Faculty of Materials Science and Engineering, Kunming University of Science and Technology, Kunming 650093 (China); Chen Qingming, E-mail: chqm99@yahoo.com [Faculty of Materials Science and Engineering, Kunming University of Science and Technology, Kunming 650093 (China)

2013-01-01

Highlights: Black-Right-Pointing-Pointer La{sub 0.72}Ca{sub 0.28}MnO{sub 3} films were prepared on flat and 15 Degree-Sign vicinal cut LaAlO{sub 3} substrate by pulsed laser deposition method. Black-Right-Pointing-Pointer The target used was fabricated with powders synthesized through sol-gel process. Black-Right-Pointing-Pointer Rocking curve and atomic force microscope images demonstrate the high crystalline quality. Black-Right-Pointing-Pointer The film deposited on tilted substrate shows a more uniform grain size. Black-Right-Pointing-Pointer The film deposited on tilted substrate shows a larger temperature coefficient of resistance value (11.3%). - Abstract: La{sub 1-x}Ca{sub x}MnO{sub 3} bulk ceramic with Ca content of 0.28 was sintered from nano-powders synthesized by sol-gel method. Epitaxial thin films of La{sub 0.72}Ca{sub 0.28}MnO{sub 3} have been prepared on both untilted and 15 Degree-Sign vicinal cut LaAlO{sub 3} (0 0 1) substrates by pulsed laser deposition technique. The structure and surface morphology of LCMO samples (powders, target and films) were investigated by X-ray diffraction, scanning electron microscope and atom force microscope. The temperature dependence of the resistance was also studied. Large temperature coefficient of resistance value of 11.3% at 234.1 K was obtained for the film grown on titled substrate.

Evaluation of the magnetocaloric response of nano-sized La0.7Ca0.3Mn1-xNixO3 manganites synthesized by auto-combustion method

Science.gov (United States)

Gómez, Adrián; Chavarriaga, Edgar; Supelano, Iván; Parra, Carlos Arturo; Morán, Oswaldo

2018-05-01

A systematic study of the dependence of the magnetization on the magnetic field around the ferromagnetic-paramagnetic phase transition temperature is carried out on La0.7Ca0.3Mn1-xNixO3 (x=0, 0.02, 0.07, and 1) samples synthesized by auto-combustion method. The successful substitution of Mn3+ ions by Ni2+ ions in the La0.7Ca0.3MnO3 lattice is corroborated by X-ray diffraction technique. Banerjees criteria, Arrott plots, and the scaling hypothesis are used to analyze the experimental data. It is verified that the Ni-doping increases the operating temperature range for magnetocaloric effect through tuning of the magnetic transition temperature. Probably, the replacement of Mn3+ by Ni2+ ions in the La0.7Ca0.3MnO3 lattice weakens the Mn3+-O-Mn4+ double exchange interaction, which leads to a decrease in the transition temperature and magnetic moment in the samples. The Arrott plots suggest that the phase transition from ferromagnetic to paramagnetic in the nano-sized manganite is of second order. The analysis of the magnetization results show that the maximum magnetic entropy changes observed for x=0, 0.02, 0.07, and 0.1 compositions are 0.85, 0.77, 0.63, and 0.59 J/kg K, under a magnetic field of 1.5 T. These values indicate that the magnetic entropy change achieved for La0.7Ca0.3Mn1-xNixO3 manganites synthesized by auto-combustion method is higher than those reported for other manganites with comparable Ni-doping levels but synthesized by standard solid state reaction. It is also observed that the addition of Ni2+ increases the value of the relative cooling power as compared to that of the parent compound. The highest value of this parameter (˜60 J/kg) is found for a Ni-doping level of 2 % around 230 K in a field of 1.5 T.

Polarization fatigue resistance of Ca-doped Pb(Zr0.52Ti0.48)O3 thin films prepared by the sol-gel method

International Nuclear Information System (INIS)

Wei, T.; Wang, Y.; Zhu, C.; Dong, X.W.; Xia, Y.D.; Zhu, J.S.; Liu, J.-M.

2008-01-01

The ferroelectric and polarization fatigue characteristics of Pb 1-x Ca x (Zr 0.52 Ti 0.48 )O 3 (PCZT) thin films prepared using the sol-gel method were studied. The Ca-doping slightly suppresses the ferroelectricity of Pb(Zr 0.52 Ti 0.48 )O 3 (PZT) because of the quantum paraelectric behavior of CaTiO 3 . Compared with PZT thin films, the PCZT (x=0.2) thin films show enhanced fatigue resistance at room temperature, further emphasized by the almost fatigue-free behavior at 100 K. The temperature-dependent dc-conductivity suggests a decrease of the oxygen vacancy density by almost 20 times and a slightly declined activation energy U for oxygen vacancies, upon increasing of the Ca-doping content from 0.0 to 0.2. It is argued that the improved fatigue endurance is ascribed to the decreasing density of oxygen vacancies due to the Ca-doping, although the lowered activation energy of oxygen vacancies is unfavorable. (orig.)

Rapid formation of the 110 K phase in Bi-Pb-Sr-Ca-Cu-O through freeze-drying powder processing

International Nuclear Information System (INIS)

Song, K.H.; Liu, H.K.; Dou, S.X.; Sorrell, C.C.

1990-01-01

This paper reports three techniques for processing Bi-Pb-Sr-Ca-Cu-O (BPSCCO) powders investigated: dry-mixing, sol-gel formation, and freeze-drying. It was found that sintering for 120 h at 850 degrees C is required to form nearly single-phase (Bi,Pb) 2 Sr 2 Ca 2 Cu 3 O 10-y by dry-mixing, whereas sintering for 30 h at 840 degrees C was sufficient to form the 110 K (2223) phase when freeze-drying was used. The sol-gel route was found to be intermediate in efficiency between these two techniques. Freeze-drying provided highly reactive, intimately mixed, and carbon-free precursors. The presence of carbonates in the uncalcined powders was the major cause of phase segregation and sluggishness of the 110 K phase formation

Picosecond energy relaxation in La0.67Ca0.33MnO3

International Nuclear Information System (INIS)

Dorosinets, Vladimir; Richter, Pablo; Mohler, Ernst; Roskos, Hartmut G.; Jakob, Gerhard

2005-01-01

Investigating the reflectance response dynamics of La 0.67 Ca 0.33 MnO 3 thin films after excitation by femtosecond laser pulses, we identify for the first time a picosecond relaxation step which only exists below the Curie temperature T C . The relaxation time increases from zero at T C to several picoseconds at low temperatures. The data can be explained with the existence of a magnetization-related effective energy gap, and assuming relaxation between these states to be mediated by a Frohlich-type electron-lattice interaction

Substrate-induced strain effects on Pr0.6Ca0.4MnO3 films

International Nuclear Information System (INIS)

Nelson, C S; Hill, J P; Gibbs, Doon; Rajeswari, M; Biswas, A; Shinde, S; Greene, R L; Venkatesan, T; Millis, A J; Yokaichiya, F; Giles, C; Casa, D; Venkataraman, C T; Gog, T

2004-01-01

We report the characterization of the crystal structure, low-temperature charge and orbital ordering, transport and magnetization of Pr 0.6 Ca 0.4 MnO 3 films grown on LaAlO 3 , NdGaO 3 and SrTiO 3 substrates, which provide compressive (LaAlO 3 ) and tensile (NdGaO 3 and SrTiO 3 ) strain. The films are observed to exhibit different crystallographic symmetries from the bulk material and the low-temperature ordering is found to be more robust under compressive as opposed to tensile strain. In fact, bulk-like charge and orbital ordering is not observed in the film grown on NdGaO 3 , which is the substrate that provides the least amount of measured, but tensile, strain. This result suggests the importance of the role played by the Mn-O--Mn bond angles in the formation of charge and orbital ordering at low temperatures. Finally, in the film grown on LaAlO 3 , a connection between the lattice distortion associated with orbital ordering and the magnetization is reported

Interpretation of anomalous optical conductivity in the ferromagnetic metallic state of La0.7Ca0.3MnO3 manganites

International Nuclear Information System (INIS)

Varshney, Dinesh; Kaurav, N.; Singh, R.K.

2006-01-01

Observed frequency dependent optical response of La 0.7 Ca 0.3 MnO 3 has been analysed within the two- component scheme. One is the coherent free carrier excitations and the other is incoherent motion of carriers from one site to other leading to a polaron formation. The frequency dependent relaxation rates are expressed in terms of memory functions and the coherent carriers leads to a sharp peak at zero frequency and a long tail in the infrared region. The hopping of carriers from Mn to Mn and Mn to O site yields peak values around 0.4 and 4.0 e V in the optical conductivity centred at mid-infrared region. (author)

Mn-Doped CaBi4Ti4O15/Pb(Zr,TiO3 Ultrasonic Transducers for Continuous Monitoring at Elevated Temperatures

Directory of Open Access Journals (Sweden)

Makiko Kobayashi

2017-11-01

Full Text Available Continuous ultrasonic in-situ monitoring for industrial applications is difficult owing to the high operating temperatures in industrial fields. It is expected that ultrasonic transducers consisting of a CaBi4Ti4O15(CBT/Pb(Zr,TiO3(PZT sol-gel composite could be one solution for ultrasonic nondestructive testing (NDT above 500 °C because no couplant is required and CBT has a high Curie temperature. To verify the high temperature durability, CBT/PZT sol-gel composite films were fabricated on titanium substrates by spray coating, and the CBT/PZT samples were tested in a furnace at various temperatures. Reflected echoes with a high signal-to-noise ratio were observed up to 600 °C. A thermal cycle test was conducted from room temperature to 600 °C, and no significant deterioration was found after the second thermal cycle. To investigate the long-term high-temperature durability, a CBT/PZT ultrasonic transducer was tested in the furnace at 600 °C for 36 h. Ultrasonic responses were recorded every 3 h, and the sensitivity and signal-to-noise ratio were stable throughout the experiment.

Geology, S-Pb isotopes, and 40Ar/39Ar geochronology of the Zhaxikang Sb-Pb-Zn-Ag deposit in Southern Tibet: implications for multiple mineralization events at Zhaxikang

Science.gov (United States)

Sun, Xiang; Zheng, Youye; Pirajno, Franco; McCuaig, T. Campbell; Yu, Miao; Xia, Shenlan; Song, Qingjie; Chang, Huifang

2018-03-01

Several Au, Sb, Sb-Au, Pb-Zn, and Sb-Pb-Zn-Ag deposits are present throughout the North Himalaya in southern Tibet, China. The largest Sb-Pb-Zn-Ag deposit is Zhaxikang (18 Mt at 0.6 wt% Sb, 2.0 wt% Pb, 3.5 wt% Zn, and 78 g/t Ag). Zhaxikang veins are hosted within N-S trending faults, which crosscut the Early-Middle Jurassic Ridang Formation consisting of shale interbedded with sandstone and limestone deposited on a passive continental margin. Ore paragenesis indicates that Zhaxikang mineralization occurred in two main phases composed of six total stages. The initial phase was characterized by assemblages of fine-grained Mn-Fe carbonate + arsenopyrite + pyrite + sphalerite (stage 1), followed by relatively coarse-grained Mn-Fe carbonate + Fe-rich sphalerite + galena + pyrite (stage 2). The second phase was marked by assemblages of quartz + pyrite + Fe-poor sphalerite and Ag-rich galena + tetrahedrite + sericite (stage 3), quartz + Sb-Pb sulfosalt minerals mainly composed of boulangerite and jamesonite (stage 4), quartz + stibnite ± cinnabar (stage 5), and quartz ± calcite (stage 6). Sulfides of stage 2 have δ34SV-CDT of 8.4-12.0‰, 206Pb/204Pb ratios of 19.648 to 19.659, 207Pb/204Pb ratios of 15.788 to 15.812, and 208Pb/204Pb ratios of 40.035 to 40.153. Sulfides of stage 3 have similar δ34SV-CDT of 6.1-11.2‰ and relatively more radiogenic lead isotopes (206Pb/204Pb = 19.683-19.792). Stage 4 Sb-Pb sulfosalt minerals have δ34SV-CDT of 5.0-7.2‰ and even more radiogenic lead (206Pb/204Pb = 19.811-19.981). By contrast, stibnite of stage 5 has δ34SV-CDT of 4.5-7.8‰ and less radiogenic lead (206Pb/204Pb = 18.880-18.974). Taken together with the geological observations that the Pb-Zn-bearing Mn-Fe carbonate veins were crosscut by various types of quartz veins, sphalerite and galena of stage 2 underwent dissolution and remobilization, and that Sb-Pb(-Fe) sulfosalts formed at the expense of Pb from stage 2 galena and of Fe from stage 2 sphalerite, we argue that

Effects of Ba doping on physical properties of La-Ca-Mn-O thin films

CERN Document Server

Hong, N H; Sakai, J; Iwasaki, H

2003-01-01

Transport and magnetic properties of La-Ba-Ca-Mn-O thin films fabricated by the pulsed laser deposition technique had been investigated systematically to see the effects of substitution of the small atom Ca by Ba which is much bigger. The induced insulator-to-metal (IM) transition was obtained not only in compositions near 0.5 and 0.18 which are boundaries between metallic and insulating phases but also in the heavily doped region. In the region of x > 0.5, the Ba doping causes an anomalous response of the system to the magnetic field and a positive magnetoresistance was observed. Besides, our results concerning the vicinity of 0.5 imply the existence of phase separation. As for x < 0.5, the doping enhances remarkably the paramagnetism-ferromagnetism transition and the IM transition temperatures.

Magnetic, transport, and optical properties of Ca0.85Eu0.15MnO3 single crystal

International Nuclear Information System (INIS)

Naumov, S.V.; Loshkareva, N.N.; Mostovshchikova, E.V.; Solin, N.I.; Korolev, A.V.; Arbuzova, T.I.; Telegin, S.V.; Patrakov, E.I.

2013-01-01

Magnetic, transport and optical properties of the Ca 0.85 Eu 0.15 MnO 3 single crystal are studied and discussed in comparison with the properties of polycrystalline sample. The magnetic data show existence the two magnetic phase transitions under cooling: the transition near 150 K occurs from the paramagnetic orthorhombic to C-type antiferromagnetic monoclinic phase with the charge/orbital ordering in some part of the crystal; and at 90 K the transition from the paramagnetic to G-type antiferromagnetic phase takes place in another part of the crystal with the orthorhombic structure. The magnetoresistance of the Ca 0.85 Eu 0.15 MnO 3 single crystal has features at temperatures of these phase transitions. Differences in the properties of single crystal and polycrystalline sample with the same content of Eu are associated with the ordering of oxygen vacancies that appear under the crystal growth. The reflection spectra in infrared range confirm the existence of the electron conductivity in a narrow band at room temperature.

Optical properties of white organic light-emitting devices fabricated utilizing a mixed CaAl12O19:Mn4+ and Y3Al5O12:Ce3+ color conversion layer.

Science.gov (United States)

Jeong, H S; Kim, S H; Lee, K S; Jeong, J M; Yoo, T W; Kwon, M S; Yoo, K H; Kim, T W

2013-06-01

White organic light-emitting devices (OLEDs) were fabricated by combining a blue OLED with a color conversion layer made of mixed Y3Al5O12:Ce3+ green and Ca2AlO19:Mn4+ red phosphors. The X-ray diffraction patterns showed that Ce3+ ions in the Y3Al5O12:Ce3+ phosphors completely substituted for the Y3+ ions and the Mn4+ ions in the CaAl12O19:Mn4+ phosphors completely substituted for the Ca2+ ions. Electroluminescence spectra at 11 V for the OLEDs fabricated utilizing a color conversion layer showed that the Commission Internationale de l'Eclairage coordinates for the Y3Al5O12:Ce3+ and CaAl12O19:Mn4+ phosphors mixed at the ratio of 1:5 and 1:10 were (0.31, 0.34) and (0.32, 0.37), respectively, indicative of a good white color.

Influence of Fe doped on the magnetocaloric behavior of La_{{2}/{3}} Ca_{{1}/{3}} Mn1-x Fe x O3 compounds: a Monte Carlo simulation

Science.gov (United States)

Alzate-Cardona, J. D.; Barco-Rios, H.; Restrepo-Parra, E.

2018-02-01

The magnetocaloric behavior of La{2/{3}} Ca{1/{3}} Mn1-x Fe x O3 for x  =  0.00, 0.02, 0.03, 0.05, 0.07, 0.08 and 0.10 under the influence of an external magnetic field was simulated and analyzed. Simulations were carried out using the Monte Carlo method and the classical Heisenberg model under the Metropolis algorithm. These mixed valence manganites are characterized by having three types of magnetic ions corresponding to Mn4+≤ft(S=\\frac{3}{2}\\right) , which are bonded with Ca2+ , and Mneg3+ and Mneg\\prime3+ (S=2) , related to La3+ . The Fe ions were randomly included, replacing Mn ions. With this model, the magnetic entropy change, Δ S , in an isothermal process was determined. -Δ Sm showed maximum peaks around the paramagnetic-ferromagnetic transition temperature, which depends on Fe doping. Relative cooling power was computed for different Fe concentrations varying the magnetic applied field. Our model and results show that the Fe doping decreases the magnetocaloric effect in the La{2/{3}} Ca{1/{3}} Mn1-x Fe x O3, making this a bad candidate for magnetic refrigeration. The strong dependence of the magnetocaloric behavior on Fe doping and the external magnetic field in La{2/{3}} Ca{1/{3}} Mn1-x Fe x O3 can boost these materials for the future technological applications.

Microstructure of laser floating zone (LFZ) textured (Bi,Pb)-Sr-Ca-Cu-O superconductor composites

International Nuclear Information System (INIS)

Fuente, G.F. de la; Ruiz, M.T.; Sotelo, A.; Larrea, A.; Navarro, R.

1993-01-01

Directionally solidified high temperature superconducting (Bi,Pb)-Sr-Ca-Cu-O pure ceramics and composites were obtained using a laser floating zone (LFZ) apparatus. The presence of secondary non-superconducting and metallic phases as well as their solidification habit have been analysed. The influence of the LFZ growth conditions and the precursor composition on the microstructure of the final products was studied using optical and electron microscopies. (orig.)

Monte Carlo study of the critical behavior and magnetic properties of La{sub 2/3}Ca{sub 1/3}MnO{sub 3} thin films

Energy Technology Data Exchange (ETDEWEB)

Restrepo-Parra, E., E-mail: erestrepopa@unal.edu.c [Departamento de Fisica y Quimica, Universidad Nacional de Colombia-Sede Manizales, A.A. 127 Manizales (Colombia); Bedoya-Hincapie, C.M.; Jurado, F.J.; Riano-Rojas, J.C. [Departamento de Fisica y Quimica, Universidad Nacional de Colombia-Sede Manizales, A.A. 127 Manizales (Colombia); Restrepo, J. [Grupo de Magnetismo y Simulacion G, Instituto de Fisica, Universidad de Antioquia, A.A. 1226 Medellin (Colombia)

2010-11-15

Critical exponents offer important information concerning the interaction mechanisms near the paramagnetic to ferromagnetic transition. In this work a Monte Carlo-Metropolis simulation of the critical behavior in La{sub 2/3}Ca{sub 1/3}MnO{sub 3} thin films is addressed. Canonical ensemble averages for magnetization per site, magnetic susceptibility and specific heat of stoichiometric manganite within a three-dimensional classical Heisenberg model with nearest magnetic neighbor interactions are computed. The La{sub 2/3}Ca{sub 1/3}MnO{sub 3} thin films were simulated addressing the thickness influence and thermal dependence. In the model, Mn magnetic ions are distributed on a simple cubic lattice according to the perovskite structure of this manganite. Ferromagnetic coupling for the bonds Mn{sup 3+}-Mn{sup 3+}(e{sub g}-e{sub g}'), Mn{sup 3+}-Mn{sup 4+}(e{sub g}-d{sup 3}) and Mn{sup 3+}-Mn{sup 4+}(e{sub g}'-d{sup 3}) were taken into account. On the basis of finite-size scaling theory, our best estimates of critical exponents, linked to the ferromagnetic to paramagnetic transition, for the correlation length, specific heat, magnetization and susceptibility are, respectively: v=0.56{+-}0.01, {alpha}=0.16{+-}0.03, {beta}=0.34{+-}0.04{gamma} and {gamma}=1.17{+-}0.05. These theoretical results are consistent with the Rushbrooke equalitiy {alpha}+2{beta}+{gamma}=2.

Manganese in the shell of the bivalve Mytilus edulis: Seawater Mn or physiological control?

Science.gov (United States)

Freitas, Pedro S.; Clarke, Leon J.; Kennedy, Hilary; Richardson, Christopher A.

2016-12-01

Manganese in the shell calcite of marine bivalves has been suggested to reflect ambient seawater Mn concentrations, thus providing a high-resolution archive of past seawater Mn concentrations. However, a quantitative relationship between seawater Mn and shell Mn/Ca ratios, as well as clear understanding of which process(es) control(s) shell Mn/Ca, are still lacking. Blue mussels, Mytilus edulis, were grown in a one-year duration field experiment in the Menai Strait, U.K., to study the relationship between seawater particulate and dissolved Mn2+ concentrations and shell calcite Mn/Ca ratios. Shell Mn/Ca showed a well-defined intra-annual double-peak, with maximum values during early spring and early summer and low values during autumn and winter. Seawater particulate Mn peaked during winter and autumn, with a series of smaller peaks during spring and summer, whereas dissolved Mn2+ exhibited a marked single maximum during late-spring to early-summer, being low during the remainder of the year. Consequently, neither seawater particulate Mn nor dissolved Mn2+ concentrations explain the intra-annual variation of shell Mn/Ca ratios. A physiological control on shell Mn/Ca ratios is evident from the strong similarity and timing of the double-peaked intra-annual variations of Mn/Ca and shell growth rate (SGR), the latter corresponding to periods of increased metabolic activity (as indicated by respiration rate). It is thus likely that in M. edulis SGR influences shell Mn/Ca by altering the concentration or activity of Mn2+ within the extra-pallial fluid (EPF), by changing the flux of Mn into or the proportion of protein bound Mn within the EPF. By linking shell Mn/Ca ratios to the endogenous and environmental factors that determine growth and metabolic activity, this study helps to explain the lack of a consistent relationship between shell Mn/Ca in marine bivalve shell calcite and seawater particulate and dissolved Mn2+ concentrations. The use of Mn content from M. edulis

Influence of conditions of preparation on quality of superconductors Bi(Pb)SrCaCuO with boron

International Nuclear Information System (INIS)

Sykorova, D.; Smrckova, O.; Ptrydes, D.; Vasek, P.

1999-01-01

The aim of this work was to verify influence of B 2 O 3 on formation of the phase Bi-2223 of samples with nominal composition Bi 1.8 (Pb 0.26 )Sr 2 Ca 2 Cu 3 O 8+x . Conditions of preparation of superconductors as well as their properties are described

Atomic absorption spectrophotometric determination of microgram levels of Co, Ni, Cu, Pb, and Zn in soil and sediment extracts containing large amounts of Mn and Fe

Science.gov (United States)

Chao, T.T.; Sanzolone, R.F.

1973-01-01

An atomic absorption spectrophotometric method has been developed for the determination of seven metal ions in the hydroxylamine extract of soils and sediments. Mn, Fe, and Zn are directly determined in the aqueous extract upon dilution. Co, Ni, Cu, and Pb in a separate aliquot of the extract are chelated with APDC (ammonium pyrrolidine dithiocarbamate) and extracted into MIBK (methyl isobutyl ketone) before determination. Data are presented to show the quantitative recovery of microgram levels of Co, Ni, Cu, and Pb by APDC-MIBK chelation-extraction from synthetic solutions containing as much as 2,000 ug/ml (micrograms per milliliter) Mn or 50 ug/ml Fe. Recovery of known amounts of the metal ions from sample solutions is equally satisfactory. Reproducible results are obtained by replicate analyses of two sediment samples for the seven metals.

Antiferromagnetism at the YBa2Cu3O7/La2/3Ca1/3MnO3 interface

International Nuclear Information System (INIS)

Haberkorn, N.; Guimpel, J.; Sirena, M.; Steren, L.B.; Saldarriaga, W.; Baca, E.; Gomez, M.E.

2004-01-01

The magnetic properties of a series of YBa 2 Cu 3 O 7-x /La 2/3 Ca 1/3 MnO 3 (YBCO/LC 1/3 MO) superlattices grown by dc sputtering at high oxygen pressures (3.5 mbar) show the expected ferromagnetic behavior. However, field-cooled hysteresis loops at a low temperatures show the unexpected existence of exchange bias effect associated with the existence of ferromagnetic/antiferromagnetic (AF) interfaces. The blocking temperature (T B ) is found to be thickness dependent and the exchange bias field (H EB ) is found to be inversely proportional to the ferromagnetic layer thickness, as expected. The presence of an AF material is probably associated with interface disorder and Mn valence shift toward Mn 4+

Thickness dependence of La0.7Sr0.3MnO3/PbZr0.2Ti0.8O3 magnetoelectric interfaces

Science.gov (United States)

Zhou, Jinling; Tra, Vu Thanh; Dong, Shuai; Trappen, Robbyn; Marcus, Matthew A.; Jenkins, Catherine; Frye, Charles; Wolfe, Evan; White, Ryan; Polisetty, Srinivas; Lin, Jiunn-Yuan; LeBeau, James M.; Chu, Ying-Hao; Holcomb, Mikel Barry

2015-10-01

Magnetoelectric materials have great potential to revolutionize electronic devices due to the coupling of their electric and magnetic properties. Thickness varying La0.7Sr0.3MnO3 (LSMO)/PbZr0.2Ti0.8O3 (PZT) heterostructures were built and measured in this article by valence sensitive x-ray absorption spectroscopy. The sizing effects of the heterostructures on the LSMO/PZT magnetoelectric interfaces were investigated through the behavior of Mn valence, a property associated with the LSMO magnetization. We found that Mn valence increases with both LSMO and PZT thickness. Piezoresponse force microscopy revealed a transition from monodomain to polydomain structure along the PZT thickness gradient. The ferroelectric surface charge may change with domain structure and its effects on Mn valence were simulated using a two-orbital double-exchange model. The screening of ferroelectric surface charge increases the electron charges in the interface region, and greatly changes the interfacial Mn valence, which likely plays a leading role in the interfacial magnetoelectric coupling. The LSMO thickness dependence was examined through the combination of two detection modes with drastically different attenuation depths. The different length scales of these techniques' sensitivity to the atomic valence were used to estimate the depth dependence Mn valence. A smaller interfacial Mn valence than the bulk was found by globally fitting the experimental results.

Valence state of Mn in Ca-doped LaMnO3 studied by high-resolution Mn K ß emission spectroscopy

NARCIS (Netherlands)

Tyson, T.A.; Qian, Q.; Kao, C.-C.; Rueff, J.-P.; Groot, F.M.F. de; Croft, M.; Cheong, S.-W.; Greenblatt, M.; Subramanian, M.A.

1999-01-01

Mn K ß x-ray emission spectra provide a direct method to probe the effective spin state and charge density on the Mn atom and is used in an experimental study of a class of Mn oxides. Specifically, the Mn K ß line positions and detailed spectral shapes depend on the oxidation and the spin state of

MnO - induced crystallization and optical characteristics of PbO-Sb{sub 2}O{sub 3}-B{sub 2}O{sub 3} glass system

Energy Technology Data Exchange (ETDEWEB)

Satyanarayana, T; Nagarjuna, G; Veeraiah, N [Department of Physics, Acharya Nagarjuna University-Nuzvid Campus, Nuzvid - 521 201, A.P (India); Raghavaiah, B V [St. Ann' s College of Engineering and Technology, Chirala-523 187, A.P (India); Mohan, N Krishna, E-mail: nvr8@rediffmail.com [Department of Physics, Akkineni Nageswara Rao College, Gudivada-521 301, A.P (India)

2009-07-15

PbO-Sb{sub 2}O{sub 3}-B{sub 2}O{sub 3} glasses mixed with different concentrations of MnO (ranging from 0 to 3.0 mol %) were crystallized. The samples were characterized by X-ray diffraction, scanning electron microscopy and EDS techniques. A number of studies viz., optical absorption, ESR, IR, magnetic susceptibility and luminescence of these glass ceramics have been carried out. The X-ray diffraction spectra revealed the presence of lead antimony oxide and manganese antimony oxide crystalline phases in these samples. The variations observed as the function of the crystallizing agent in all the properties have been analyzed in the light of different oxidation states (Mn{sup 2+} and Mn{sup 3+}) and environment of manganese ions in the glass ceramic network.

Comparison of the photoluminescence properties of Eu{sup 2+}, Mn{sup 2+} co-doped M{sub 5}(PO{sub 4}){sub 3}Cl (M = Ca, Sr, Ba)

Energy Technology Data Exchange (ETDEWEB)

Yang, Fengli [National Engineering Research Center for Rare Earth Materials, General Research Institute for Nonferrous Metals, and Grirem Advanced Materials Co., Ltd., Beijing 100088 (China); State Key Laboratory of Rare Earth Materials and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China); School of Metallurgy and Chemical Engineering, Jiangxi University of Science and Technology, Ganzhou, Jiangxi 341000 (China); An, Wei [School of Physics, Peking University, Beijing 100871 (China); Wei, Heng-Wei [State Key Laboratory of Rare Earth Materials and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China); Chen, Guantong [National Engineering Research Center for Rare Earth Materials, General Research Institute for Nonferrous Metals, and Grirem Advanced Materials Co., Ltd., Beijing 100088 (China); Zhuang, Weidong, E-mail: wdzhuang@126.com [National Engineering Research Center for Rare Earth Materials, General Research Institute for Nonferrous Metals, and Grirem Advanced Materials Co., Ltd., Beijing 100088 (China); Jing, Xi-Ping, E-mail: xpjing@pku.edu.cn [State Key Laboratory of Rare Earth Materials and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China)

2014-03-25

Highlights: • Good size match between the doped and host cations narrows the emission band. • Low phonon energy of the hosts enhances the luminescence intensity. • “Inverse bottleneck effect” related to Eu/Mn lifetime mismatch causes quenching. • “Charge transfer process” in the Eu–Mn clusters causes quenching. -- Abstract: Eu{sup 2+} and Mn{sup 2+} singly doped or co-doped M{sub 5}(PO{sub 4}){sub 3}Cl (M = Ca, Sr and Ba) phosphors were synthesized by conventional solid state reactions and characterized by X-ray diffraction (XRD), photoluminescence (PL) spectra, PL decay curves, energy dispersive spectra (EDS) and Raman spectra. The results show that a better size match between the doped cation and the host cation allows a wider solid solution range (e.g. Ca{sup 2+}/Mn{sup 2+}) and a narrower emission band (e.g. Sr{sup 2+}/Eu{sup 2+} and Ca{sup 2+}/Mn{sup 2+}). A lower phonon energy of the host (e.g. the Sr phase) reduces the non-radiation probability and enhances the PL efficiency. The PL performance of the Ba phase is exceptional possibly because of the large size difference between the doped cations and the host cations. The transfer efficiency (η) and the emission quantum efficiency (Q) were analyzed. In the studied phosphors, superficially Eu{sup 2+} efficiently transferred its absorbed energy to Mn{sup 2+} but the Q of the Mn{sup 2+} emission was not as high as expected. Two loss mechanisms are proposed: an “inverse bottleneck effect” and “charge transfer” between Eu{sup 2+} and Mn{sup 2+}.

Fine scale distributions of porosity and particulate excess 210Pb, organic carbon and CaCO3 in surface sediments of the deep equatorial Pacific

International Nuclear Information System (INIS)

Jahnke, R.A.; Emerson, S.R.; Cochran, J.K.; Hirschberg, D.J.

1986-01-01

Sediment samples were recovered from the central equatorial Pacific Ocean, sectioned at 1-mm intervals, and analyzed for porosity, organic carbon, excess 210 Pb and CaCO 3 . Steep porosity gradients were measured in the upper 1 cm of the sediment column with extremely high values observed near the sediment surface. Similarly, particulate organic carbon contents are highest at the sediment surface, decrease sharply in the upper 1 cm, and are relatively constant between 1 and 5 cm. CaCO 3 values, on the other hand, are lowest at the sediment surface and increase to a constant value below 5-10 mm depth. At the carbonate ooze sites, excess 210 Pb is present throughout the upper 5 cm of the sediments suggesting relatively rapid particle mixing rates. However, extremely high excess 210 Pb activities (> 100 dpm/g) are observed at the sediment surface with sharp gradients present in the upper 1 cm which would suggest slow rates of mixing. This apparent contradiction along with the major features of the CaCO 3 and particulate organic carbon profiles can be explained by a particle-selective feeding mechanism in which organic carbon, excess 210 Pb-enriched particles are preferentially maintained at the sediment surface via ingestion and defecation by benthic organisms. (orig.)

Radiative muon capture on Al, Si, Ca, Mo, Sn, and Pb

International Nuclear Information System (INIS)

Armstrong, D.S.; Serna-Angel, A.; Ahamad, S.

1992-08-01

The branching ratio for radiative muon capture relative to the non-radiative process, is sensitive to g p , the induced pseudoscalar coupling constant of the weak hadronic current. The photon energy spectra from RMC on 27 Al, 28 Si, 40 Ca, nat Mo, nat Sn, and nat Pb have been measured using a high-acceptance pair spectrometer. The measured partial branching ratios, R γ , for photons of E γ > 57 MeV are 1.43 ± 0.13, 1.93 ± 0.18, 2.09 ± 0.19, 1.11 ± 0.11, 0.98 ± 0.09 and 0.60 ± 0.07 respectively, in units of 10 -5 . The results confirm the previously observed suppression of R γ with increasing Z for Z > 20. For 40 Ca the present result is in good agreement with previous measurements. For the heavier nuclei, the results are compared with two recent calculations performed in the Fermi-gas model. In one case the data indicate a complete quenching of g p , but the more recent calculation does not reproduce the data for any value of g p . 50 refs., 9 figs., 8 tabs

Radiative muon capture on Al, Si, Ca, Mo, Sn, and Pb

International Nuclear Information System (INIS)

Armstrong, D.S.; Serna-Angel, A.; Ahmad, S.; Azuelos, G.; Bertl, W.; Blecher, M.; Chen, C.Q.; Depommier, P.; von Egidy, T.; Gorringe, T.P.; Hasinoff, M.D.; Henderson, R.S.; Larabee, A.J.; Macdonald, J.A.; McDonald, S.C.; Poutissou, J.; Poutissou, R.; Robertson, B.C.; Sample, D.G.; Taylor, G.N.; Wright, D.H.; Zhang, N.S.

1992-01-01

The branching ratio for radiative muon capture (RMC), relative to the nonradiative process, is sensitive to g p , the induced pseudoscalar coupling constant of the weak hadronic current. The photon energy spectra from RMC on 27 Al, 28 Si, 40 Ca, nat Mo, nat Sn, and nat Pb have been measured using a high-acceptance pair spectrometer. The measured partial branching ratios, R γ , for photons of E γ >57 MeV are 1.43±0.13, 1.93±0.18, 2.09±0.19, 1.11±0.11, 0.98±0.09, and 0.60±0.07 respectively, in units of 10 -5 . The results confirm the previously observed suppression of R γ with increasing Z for Z>20. For 40 Ca the present result is in good agreement with previous measurements. For the heavier nuclei, the results are compared with two recent calculations performed in the Fermi-gas model. In one case the data indicate a complete quenching of g p , but the more recent calculation does not reproduce the data for any value of g p

Toxic Metals (Pb and Cd and Their Respective Antagonists (Ca and Zn in Infant Formulas and Milk Marketed in Brasilia, Brazil

Directory of Open Access Journals (Sweden)

José G. Dórea

2010-11-01

Full Text Available In non-ideal scenarios involving partial or non-breastfeeding, cow’s milk-based dairy products are mainstream in infant feeding. Therefore, it is important to study the concentrations of potentially neurotoxic contaminants (Pb and Cd and their respective counteracting elements (Ca and Zn in infant dairy products. Fifty-five brands of infant formulas and milk sold in Brasilia, Brazil were analyzed. The dairy products came from areas in the central-west (26%, southeast (29% and south of Brazil (36% extending as far as Argentina (7% and the Netherlands (2%. For toxic Pb and Cd, median concentrations in powdered samples were 0.109 mg/kg and 0.033 mg/kg, respectively; in fluid samples median Pb concentration was 0.084 mg/kg, but median Cd concentration was below the limit of detection and overall values were below reference safety levels. However, 62% of these samples presented higher Pb concentration values than those established by FAO/WHO. Although the inverse correlation between Cd and Zn (Spearman r = −0.116; P = 0.590 was not statistically significant, the positive correlation between Ca and Pb was (Spearman r = 0.619; P < 0.0001. Additionally, there was a significant correlation between Pb and Cd. Furthermore, the study also revealed that provision of the essential trace element Zn in infant formulas can provide adequate amounts of the recommended daily requirements. Infant formulas and milk sold for consumption by infants and children can be an efficient tool to monitor neurotoxic metal risk exposure among young children.

Magneto-caloric and magneto-resistive properties of La{sub 0.67}Ca{sub 0.33-x}Sr{sub x}MnO{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Reves Dinesen, Anders

2004-08-01

This thesis presents results of an experimental investigation of magneto-caloric and magneto-resistive properties of a series of polycrystalline Ca- and Sr-doped lanthanum manganites, La{sub 0.67}Ca{sub 0.33-x}Sr{sub x}MnO{sub 3} (0{<=} x {<=} 0.33), with the perovskite structure. The samples consisted of sintered oxide powders prepared the glycine-nitrate combustion technique. The compounds were ferromagnetic and showed a Curie transition in the temperature range 267370 K (T{sub C} increased with increasing x). An analysis of the structural properties was carried out by means of x-ray diffraction and the Rietveld technique. The variation of the Ca/Sr ratio was found to cause a transition from orthorhombic to rhombohedral symmetry in the composition range 0.110 < x < 0.165. The analysis suggested a strong correlation between structural properties and magnetism, for instance a relationship between the mean MnOMn bond angle and the Curie temperature. The MnOMn bonds mediate ferromagnetism and electrical transport in these materials via the double-exchange mechanism. The magnetocaloric effect of the La{sub 0.67}Ca{sub 0.33-x}Sr{sub x}MnO{sub 3} samples was measured directly and indirectly (by means of magnetization measurements). All the samples showed a magnetocaloric effect in the vicinity of T{sub C}. A model for the mag-netocaloric effect based on Weiss mean field theory and classical theories for heat capacities was developed. The model provided reasonable predictions of the magneto-caloric properties of the samples. The compounds with low Sr content showed a magnetocaloric effect comparable to that of Gadolinium, the prototypical working material for magnetic refrigeration at room temperature. A less comprehensive part of the investigation regarded the magneto-resistive properties of the La{sub 0.67}Ca{sub 0.33-x}Sr{sub x}MnO{sub 3} system. It was found that th polycrystalline nature of the compounds played a decisive role for the magnetotransport properties

Direct evidence for double-exchange coupling in Ru- substituted La0.7Pb0.3Mn 1 - x Ru x O3, 0.0 <= x <= 0.4

Science.gov (United States)

Sundar Manoharan, S.; Sahu, R. K.; Rao, M. L.; Elefant, D.; Schneider, C. M.

2002-08-01

The La0.7Pb0.3Mn 1 - x Ru x O3 (0.0 innate relationship between Mn and Ru ions by a unique double-exchange mediated transport behavior. This is exonerated by the coexistence of Tp and Tc (range 330 K 245 K for 0.0 30%, the hole carrier mass influences the transport property. X-ray absorption spectra suggest that the Tc-Tp match is due to the transport mediated by the Mn3+/Mn4+ leftrightarrow Ru4+/Ru5+ redox pair and also due to the broad low-spin Ru:4d conduction band. For x > 0.2, T < 0.5Tc obeys a modified variable-range hopping model, where kT0 propto (M/Ms)2, suggesting a random magnetic potential which localizes the charge carriers.

Radionuclide X-ray fluorescence determination of Mn, Fe, Cu, Zn and Pb in wastewaters and sludges from wastewater treatment plants in Bratislava (SR)

International Nuclear Information System (INIS)

Harangozo, M.; Toelgyessy, J.

1997-01-01

Radiometric X-ray fluorescence analysis was used for the determination of Mn, Fe, Cu, Zn and Pb in wastewater and sludges from three wastewater treatment plants in Bratislava (SR). Metals were determined in wastewaters after preconcentration by 8-hydroxyquinoline and in sludges by drying and pressing to pellets. 238 Pu and 109 Cd was used for excitation of fluorescence radiation. (author)

Structural study of CaMn_1_−_xMo_xO_3 (0.08 ≤ x ≤ 0.12) system by neutron powder diffraction

International Nuclear Information System (INIS)

Supelano, G.I.; Parra Vargas, C.A.; Barón-González, A.J.; Sarmiento Santos, A.; Frontera, C.

2016-01-01

Neutron powder diffraction experiments and magnetic measurements in polycrystalline CaMn_1_−_xMo_xO_3 (x = 0.08, 0.10, 0.12) point towards a possible charge and orbital order in this system. The analysis of structural and magnetic data show that the samples present structural phase transformation from Pnma to P2_1/m space group and the system has a C-type antiferromagnetic configuration at low temperature. A detailed analysis of the bond distances signals a small Jahn-Teller distortion of only one (x = 0.08) or of the two Mn ions (x = 0.10, 0.12). We identify the partially occupied e_g orbitals and this explains the C-type magnetic structure. - Highlights: • CaMn_1_−_xMo_xO_3 (x = 0.08, 0.10, 0.12) is investigated by neutron powder diffraction. • Analysis of individual Mn-O distances demonstrates the apparition of orbital order. • By symmetry analysis, we find that the low temperature magnetic structure is C-type. • Magnetic interactions foreseen by the orbital order explain the magnetic structure.

Evaluación de la corrosión de una aleación Pb-Ca-Sn por medio de técnicas electroquímicas

Directory of Open Access Journals (Sweden)

Hugo A. Estupiñán Duran

2014-06-01

Full Text Available In this paper, the influence of increasing temperature on the corrosion rate of Pb-Ca-Sn alloy, the primary component of the negative grid of a starter battery car, was evaluated by electrochemical techniques: RPL, potentiodynamic curves, Tafel and EIS. By optical microscopy, SEM -EDS and XRD, the compounds formed on the grids were characterized during testing. The passive layer formed on the grids used as cathode and anode in lead-acid batteries allows the anchor in grid-PAM interface (Positive Active Material or NAM (Negative Active Material. A bad process of to form this layer produces the detachment of PAM/NAM, leading to premature failure. The temperature directly affects the kinetics and thermodynamics degradation of the redox reactions taking place in the system grid-PAM/NAM. An increase in temperature causes variations in the chemical composition, favoring the formation of oxides and sulphates mixtures in grid-PAM/NAM interface, its volume and porous structure make it susceptible to failure by tri-axial stress on the interface, producing cracks and detachment of PAM or NAM and reducing the lifetime of the battery. It was found that the Pb-Ca-Sn alloys in 0.5M H2SO4 solution form a multilayer system, verified by the results of EIS and SEM, in which a compact layer of PbO2 and porous layer by PbSO4. Porous layer of PbSO4 was obtained, when the temperature was increased implying greater corrosion kinetics of Pb-Ca-Sn alloy were detected.

Assessment of Pb, Cd and Hg soil contamination and its potential to cause cytotoxic and genotoxic effects in human cell lines (CaCo-2 and HaCaT).

Science.gov (United States)

Sljivic Husejnovic, Maida; Bergant, Martina; Jankovic, Sasa; Zizek, Suzana; Smajlovic, Aida; Softic, Adaleta; Music, Omer; Antonijevic, Biljana

2018-01-23

Soil contamination by heavy metals is a serious global environmental problem, especially for developing countries. A large number of industrial plants, which continually pollute the environment, characterize Tuzla Canton, Bosnia and Herzegovina. The aim of this study was to assess the level of soil pollution by heavy metals and to estimate cytotoxicity and genotoxicity of soil leachates from this area. Lead (Pb), cadmium (Cd) and mercury (Hg) were analyzed by ICP-AES and AAS. Soil contamination was assessed using contamination factor, degree of contamination, geoaccumulation index and pollution load index. To determine the connection of variables and understanding their origin in soils, principal component analysis (PCA) and cluster analysis (CA) were used. The results indicate that Cd and Hg originated from natural and anthropogenic activities, while Pb is of anthropogenic origin. For toxicity evaluation, CaCo-2 and HaCaT cells were used. PrestoBlue assay was used for cytotoxicity testing, and γH2A.X for genotoxicity evaluation. Concerning cytotoxicity, Cd and Hg had a positive correlation with cytotoxicity in HaCaT cells, but only Hg induced cytotoxicity in CaCo-2 cells. We also demonstrate that soil leachates contaminated by heavy metals can induce genotoxicity in both used cell lines. According to these results, combining bioassays with standard physicochemical analysis can be useful for evaluating environmental and health risks more accurately. These results are important for developing proper management strategies to decrease pollution. This is one of the first studies from this area and an important indication of soil quality in Southeast Europe.

Pb solubility of the high-temperature superconducting phase Bi{sub 2}Sr{sub 2}Ca{sub 2}Cu{sub 3}O{sub 10+d}

Energy Technology Data Exchange (ETDEWEB)

Kaesche, S.; Majewski, P.; Aldinger, F. [Max-Planck-Institut fuer Metallforschung, Stuttgart (Germany)] [and others

1994-12-31

For the nominal composition of Bi{sub 2.27x}Pb{sub x}Sr{sub 2}Ca{sub 2}Cu{sub 3}O{sub 10+d} the lead content was varied from x=0.05 to 0.45. The compositions were examined between 830{degrees}C and 890{degrees}C which is supposed to be the temperature range over which the so-called 2223 phase (Bi{sub 2}Sr{sub 2}Ca{sub 2}Cu{sub 3}O{sub 10+d}) is stable. Only compositions between x=0.18 to 0.36 could be synthesized in a single phase state. For x>0.36 a lead containing phase with a stoichiometry of Pb{sub 4}(Sr,Ca){sub 5}CuO{sub d} is formed, for x<0.18 mainly Bi{sub 2}Sr{sub 2}CaCu{sub 2}O{sub 8+d} and cuprates are the equilibrium phases. The temperature range for the 2223 phase was found to be 830{degrees}C to 890{degrees}C but the 2223 phase has extremely varying cation ratios over this temperature range. Former single phase 2223 samples turn to multi phase samples when annealed at slightly higher or lower temperatures. A decrease in the Pb solubility with increasing temperature was found for the 2223 phase.

Development of Pb-rich (Bi, Pb) sub 3 Sr sub 2 Ca sub 2 Cu sub 1 O sub x phase during reformation of lead doped 2223 superconducting phase from melt quenched glass. [BiPbSrCaCuO

Energy Technology Data Exchange (ETDEWEB)

Oezkan, N; Glowacki, B A [IRC in Superconductivity, Univ. of Cambridge (United Kingdom)

1992-05-01

The reformation process of the lead doped superconducting 2223 phase from the melt quenched glass was investigated. It was shown that during the crystallisation of the glass a new lead rich phase, Bi{sub 0.5}Pb{sub 3}Sr{sub 2}Ca{sub 2}Cu{sub 1}O{sub x}, was formed and severe copper segregation was observed. The volume fraction of the high Tc 2223 phase increased with annealing time for an annealing temperature of 840degC. A glass sample annealed at 840degC for 150 h showed two superconducting transitions Tc = 107 K and Tc = 70 K. (orig.).

Analysis of whole human blood for Pb, Cd, Hg, Se, and Mn by ICP-DRC-MS for biomonitoring and acute exposures.

Science.gov (United States)

Jones, Deanna R; Jarrett, Jeffery M; Tevis, Denise S; Franklin, Melanie; Mullinix, Neva J; Wallon, Kristen L; Derrick Quarles, C; Caldwell, Kathleen L; Jones, Robert L

2017-01-01

We improved our inductively coupled plasma mass spectrometry (ICP-MS) whole blood method [1] for determination of lead (Pb), cadmium (Cd), and mercury (Hg) by including manganese (Mn) and selenium (Se), and expanding the calibration range of all analytes. The method is validated on a PerkinElmer (PE) ELAN® DRC II ICP-MS (ICP-DRC-MS) and uses the Dynamic Reaction Cell (DRC) technology to attenuate interfering background ion signals via ion-molecule reactions. Methane gas (CH 4 ) eliminates background signal from 40 Ar 2 + to permit determination of 80 Se + , and oxygen gas (O 2 ) eliminates several polyatomic interferences (e.g. 40 Ar 15 N + , 54 Fe 1 H + ) on 55 Mn + . Hg sensitivity in DRC mode is a factor of two higher than vented mode when measured under the same DRC conditions as Mn due to collisional focusing of the ion beam. To compensate for the expanded method's longer analysis time (due to DRC mode pause delays), we implemented an SC4-FAST autosampler (ESI Scientific, Omaha, NE), which vacuum loads the sample onto a loop, to keep the sample-to-sample measurement time to less than 5min, allowing for preparation and analysis of 60 samples in an 8-h work shift. The longer analysis time also resulted in faster breakdown of the hydrocarbon oil in the interface roughing pump. The replacement of the standard roughing pump with a pump using a fluorinated lubricant, Fomblin®, extended the time between pump maintenance. We optimized the diluent and rinse solution components to reduce carryover from high concentration samples and prevent the formation of precipitates. We performed a robust calculation to determine the following limits of detection (LOD) in whole blood: 0.07µgdL -1 for Pb, 0.10µgL -1 for Cd, 0.28μgL -1 for Hg, 0.99µgL -1 for Mn, and 24.5µgL -1 for Se. Published by Elsevier B.V.

139La NMR evidence for sensitivity of local structure to magnetic field in La0.5Ca0.5MnO3

International Nuclear Information System (INIS)

Yoshinari, Y.; Hammel, P.C.; Thompson, J.D.; Cheong, S.

1999-01-01

We report 139 La nuclear-magnetic-resonance measurements on La 0.5 Ca 0.5 MnO 3 . Two resonance peaks observed in zero applied field are identified as ferromagnetic (FM) resonances arising from FM domains with eight nearest Mn moments almost fully polarized. The two La sites are distinguished by experiencing different covalent configurations with respect to the nearest Mn ions, likely caused by the charge/orbital ordering. The two sites collapse into one in the presence of a strong magnetic field, indicating the close relationship between magnetism and the lattice deformation. copyright 1999 The American Physical Society

Evaluation of the heavy metals Cr, Mn, Fe, Cu, Zn and Pb in water penny wort (Hydrocotyle ranunculoides) from the upper course of the Lerma River, Mexico

International Nuclear Information System (INIS)

Zarazua, G.; Avila P, P.; Tejeda, S.; Valdivia B, M.; Macedo M, G.; Zepeda G, C.

2013-01-01

The Lerma river is one of the most polluted water bodies in Mexico, it presents low biodiversity and lets grow up aquatic plants resistant to the pollution. The aim of this work was to evaluate the concentration and bioaccumulation factors of Cr, Mn, Fe, Cu, Zn and Pb in aerial and submerged structures of water penny wort (Hydrocotyle ranunculoides) from the upper course of the Lerma river. Inductively coupled plasma-optical emission spectrometry was used to determine the concentration of heavy metals in water and H. ranunculoides. Results show that the bioaccumulation factors of Fe and Zn were higher than those of Cu, Mn, Cr and Pb; with the exception of Zn, bioaccumulation factors were higher in the submerged structures of the plant, which shows low mobility of analyzed metals. As a result of this study H. ranunculoides can be considered as good indicator of metal pollution in water bodies. (Author)

Pressure-induced electrical and magnetic property changes in CaCuMn6O12

International Nuclear Information System (INIS)

Zhang, W.; Yao, L.D.; Yang, L.X.; Li, F.Y.; Liu, Z.X.; Jin, C.Q.; Yu, R.C.

2006-01-01

CaCuMn 6 O 12 was prepared by using a traditional solid-state reaction method. It is a highly correlated electron system with a small gap appearing at E F and cluster glass state at low temperature, whereas temperature dependence of resistivity suggests that it is related to thermally activated nearest-neighbor hopping in paramagnetism state in higher temperature range. The resistivity decreases with increasing pressure until 11 kbar, and then increases with further increasing pressure. The blocking temperature T b goes down under pressure, indicating the suppression of cluster glass state under pressure

Effects of Nb doping level on the electronic transport, photoelectric effect and magnetoresistance across La0.5Ca0.5MnO3/Nb:SrTiO3 junctions

Science.gov (United States)

Wang, J. F.; Jiang, Y. C.; Chen, M. G.; Gao, J.

2013-12-01

Heterojunctions composed of La0.5Ca0.5MnO3 and Nb doped SrTiO3 were fabricated, and the effects of the Nb doping level on their electronic transport, photoelectric effect, and magnetoresistance were investigated. A lower doping concentration of Nb led to better rectifying properties and higher open circuit voltages. The I-V curves for La0.5Ca0.5MnO3/0.7 wt. % Nb-SrTiO3 showed a negligible response to magnetic fields for all temperatures, whereas La0.5Ca0.5MnO3/0.05 wt. % Nb-SrTiO3 exhibited distinct magnetoresistance, which depended on both the bias voltage and temperature. These results are discussed with the assistance of conventional semiconductor theories.

Biosorption of Cd, Cr, Mn, and Pb from aqueous solutions by Bacillus sp strains isolated from industrial waste activate sludge

OpenAIRE

Rocío García; Juan Campos; Julio Alfonso Cruz; Ma. Elena Calderón; Ma. Elena Rayna; Germán Buitrón

2016-01-01

Los microorganismos tienen capacidad de acumular metales pesados como agentes bioadsorbentes ofreciendo una alternativa para la remoción de metales tóxicos en aguas de efluentes industriales. El objetivo del presente trabajo fue aislar e identificar bacterias tolerantes a los metales pesados (Cd, Cr, Mn y Pb) de lodos activados provenientes de la planta de tratamiento de agua del Municipio de Santa Rosa Jáuregui, Querétaro. Para seleccionar las bacterias que son tolerantes a los metales se ai...

Effect of Homogenization on Microstructure Characteristics, Corrosion and Biocompatibility of Mg-Zn-Mn-xCa Alloys

Science.gov (United States)

Li, Jingyuan; Lai, Huiying; Xu, Yuzhao

2018-01-01

The corrosion behaviors of Mg-2Zn-0.2Mn-xCa (denoted as MZM-xCa alloys) in homogenization state have been investigated by immersion test and electrochemical techniques in a simulated physiological condition. The microstructure features were characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), transmission electron microscopy (TEM) and electron probe microanalysis (EPMA), and the corrosion mechanism was illustrated using atomic force microscope (AFM), X-ray photoelectron spectroscopy (XPS) and confocal laser scanning microscopy (CLSM). The electrochemical and immersion test verify the MZM-0.38% Ca owns the best corrosion performance with the corrosion rate of 6.27 mm/year. Furthermore, the film layer of MZM-0.38% Ca is more compact and denser than that of others. This improvement could be associated with the combined effects of the suitable content of Zn/Ca dissolving into the α-Mg matrix and the modification of Ca-containing compounds by heat-treatment. However, the morphologies were transformed from uniform corrosion to localized pitting corrosion with Ca further addition. It could be explained that the excessive Ca addition can strengthen the nucleation driving force for the second phase formation, and the large volumes fraction of micro-galvanic present interface sites accelerate the nucleation driving force for corrosion propagation. In addition, in vitro biocompatibility tests also show the MZM-0.38% Ca was safe to bone mesenchymal stem cells (BMSCs) and was promising to be utilized as implant materials. PMID:29389894

Effect of Homogenization on Microstructure Characteristics, Corrosion and Biocompatibility of Mg-Zn-Mn-xCa Alloys

Directory of Open Access Journals (Sweden)

Yuan Zhang

2018-02-01

Full Text Available The corrosion behaviors of Mg-2Zn-0.2Mn-xCa (denoted as MZM-xCa alloys in homogenization state have been investigated by immersion test and electrochemical techniques in a simulated physiological condition. The microstructure features were characterized using scanning electron microscopy (SEM, X-ray diffraction (XRD, transmission electron microscopy (TEM and electron probe microanalysis (EPMA, and the corrosion mechanism was illustrated using atomic force microscope (AFM, X-ray photoelectron spectroscopy (XPS and confocal laser scanning microscopy (CLSM. The electrochemical and immersion test verify the MZM-0.38% Ca owns the best corrosion performance with the corrosion rate of 6.27 mm/year. Furthermore, the film layer of MZM-0.38% Ca is more compact and denser than that of others. This improvement could be associated with the combined effects of the suitable content of Zn/Ca dissolving into the α-Mg matrix and the modification of Ca-containing compounds by heat-treatment. However, the morphologies were transformed from uniform corrosion to localized pitting corrosion with Ca further addition. It could be explained that the excessive Ca addition can strengthen the nucleation driving force for the second phase formation, and the large volumes fraction of micro-galvanic present interface sites accelerate the nucleation driving force for corrosion propagation. In addition, in vitro biocompatibility tests also show the MZM-0.38% Ca was safe to bone mesenchymal stem cells (BMSCs and was promising to be utilized as implant materials.

The analysis of strain of giant magnetoresistive Pr0.7Sr0.3MnO3/La0.5Ca0.5MnO3/Pr0.7Sr0.3MnO-3 trilayers

International Nuclear Information System (INIS)

Wang Haiou; Liu Hao; Dai Ping; Tan Weishi; Wu Xiaoshan; Jia Quanjie; Li Xiaolong

2012-01-01

Pr 0.7 Sr 0.3 MnO 3 /La 0.5 Ca 0.5 MnO 3 /Pr 0.7 Sr 0.3 MnO 3 (PSMO/LCMO/PSMO) trilayers were deposited on (001)-oriented single crystal MgO by pulsed laser deposition. The thickness of both PSMO layers was 36 nm while the thickness of LCMO layer was 6, 12, 18, 24, 30 and 36 nm, respectively. Out-of-plane and in-plane lattice parameters of trilayers were obtained by using symmetric scanning and asymmetric scanning mode of high resolution X-ray diffraction. Strain states of trilayers have been studied. The results showed that strain relaxation states of trilayers were decided by bulk strain and Jahn-Teller (JT) strain together: The mechanism for strain relaxation in trilayers is different from that for tetragonal distortion. The competition between bulk strain and Jahn-Teller (JT) strain played an important role in the magnetotransport and magnetic properties of trilayers. (authors)

Investigation of the charge-orbital ordering mechanism in single-layered Pr0.5Ca1.5MnO4

Science.gov (United States)

Rangkuti, C. N.; Majidi, M. A.

2018-04-01

Motivated by the experimental study of half-doped single-layered Pr0.5Ca1.5MnO4 showing charge, orbital, and spin orderings [1], we propose a model to theoretically study the system to explain such ordering phenomena. The ground state electron configuration reveals that the charges form a checkerboard pattern with alternating Mn3+/Mn4+ sites, while the orbitals are aligned in zigzag chains [1, 2]. We calculate the ground state energy of this system to find the most preferable configuration by comparing three types of configurations (charge-unordered, charge-ordered, and charge-orbital-ordered states). The calculations are based on a tight-binding model representing effective electron hoppings among Mn ions in MnO2-plane. We take into account the horizontally- and vertically-oriented orbital and spin degrees of freedom at Mn sites. We assume that the hopping integral values depend on the relative orientation between the corresponding orbitals of adjacent Mn ions. The interaction terms we incorporate into our effective Hamiltonian include inter-orbital, intra-orbital Hubbard repulsions, and Jahn-Teller distortion [2]. We absorb the exchange interaction between spins into local self-energy that we calculate within dynamical mean field algorithm [2]. Within our model we show a circumstance in which the charge-orbital ordered configuration has the lowest energy, consistent with the ground state ordering revealed by the experimental data.

Structural studies of five layer Aurivillius oxides: A2Bi4Ti5O18 (A=Ca, Sr, Ba and Pb)

International Nuclear Information System (INIS)

Ismunandar; Kamiyama, T.; Hoshikawa, A.; Zhou, Q.; Kennedy, B.J.; Kubota, Y.; Kato, K.

2004-01-01

The room temperature structures of the five layer Aurivillius phases A 2 Bi 4 Ti 5 O 18 , (A=Ca, Sr, Ba and Pb) have been refined from powder neutron diffraction data using the Rietveld method. The structures consist of [Bi 2 O 2 ] 2+ layers interleaved with perovskite-like [A 2 Bi 2 Ti 5 O 16 ] 2- blocks. The structures were refined in the orthorhombic space group B2eb (SG. No. 41), Z=4, and the unit cell parameters of the oxides are a=5.4251(2), b=5.4034(1), c=48.486(1); a=5.4650(2), b=5.4625(3), c=48.852(1); a=5.4988(3), b=5.4980(4), c=50.352(1); a=5.4701(2), b=5.4577(2), c=49.643(1) for A=Ca, Sr, Ba and Pb, respectively. The structural features of the compounds were found similar to n=2-4 layers bismuth oxides. The strain caused by mismatch of cell parameter requirements for the [Bi 2 O 2 ] 2+ layers and perovskite-like [A 2 Bi 2 Ti 5 O 16 ] 2- blocks were relieved by tilting of the TiO 6 octahedra. Variable temperature synchrotron X-ray studies for Ca and Pb compounds showed that the orthorhombic structure persisted up to 675 and 475K, respectively. Raman spectra of the compounds are also presented

Efeito da adição de fontes de matéria orgânica como amenizantes do efeito tóxico de B, Zn, Cu, Mn e Pb no cultivo de Brassica juncea Effect of sources of organic matter in the alleviation of the toxic effects of B, Zn, Cu, Mn and Pb to Brassica Juncea

Directory of Open Access Journals (Sweden)

Glaucia Cecília Grabrielli dos Santos

2007-08-01

Full Text Available Atividades humanas como mineração, siderurgia e aplicação de fertilizantes tornam a poluição por metais sério problema ambiental na atualidade. A fitorremediação - uso de plantas e da microbiota, associada ou não a adições de amenizantes de solo, para extrair, seqüestrar e, ou, reduzir a toxicidade dos poluentes - tem sido descrita como uma tecnologia efetiva, não-destrutiva, econômica e socialmente aceita para remediar solos poluídos. O objetivo deste trabalho foi avaliar a eficiência da mostarda na remoção de Zn, Cu, Mn, Pb e B de um solo contaminado e o efeito da adição de materiais orgânicos na redução da disponibilidade de metais pesados e B para essa planta. O trabalho foi realizado em casa de vegetação, com delineamento inteiramente casualizado em esquema fatorial 3 x 5 com quatro repetições, utilizando 0, 7, 14, 21 e 28 g kg-1 de C no solo. Os materiais orgânicos utilizados foram: solomax, turfa e concentrado húmico mineral (CHM. A adição de turfa e concentrado húmico mineral reduziu os teores de Zn, Cu, Pb e B extraíveis do solo e na parte aérea da mostarda; contudo, essa redução não foi suficiente para impedir os efeitos fitotóxicos dos elementos. A adição dos materiais orgânicos promoveu aumento nos teores de Mn no solo, entretanto apenas o solomax proporcionou aumento na concentração do elemento na parte aérea das plantas. Os efeitos da turfa e do CHM sobre a disponibilidade de Zn, Cu, Mn, Pb e B no solo, a concentração na parte aérea e o crescimento das plantas indicaram o potencial desses materiais como agentes amenizantes de toxicidade e do solomax como auxiliar em programas de fitoextração induzida.As a result of anthropogenic activities such as mining, metal industry and agricultural fertilizer application, metal pollution has become one of the most serious environmental problems of today. Phytoremediation denotes the use of plants and micro-biota, together or without soil

Kinetics of electrodialytic extraction of Pb and soil cations from a slurry of contaminated soil fines

DEFF Research Database (Denmark)

Jensen, Pernille Erland; Ottosen, Lisbeth M.; Ferreira, Célia

2006-01-01

-removal was obtained. During the first phase dissolution of carbonates was the prevailing process, resulting in a corresponding loss of soil-mass. During this phase, the investigated ions accounted for the major current transfer, while, as remediation proceeded hydrogen-ions increasingly dominated the transfer. During......The objective of this work was to investigate the kinetics of Pb removal from soil-fines during electrodialytic remediation in suspension, and study the simultaneous dissolution of common soil cations (Al, Ca, Fe, Mg, Mn, Na and K). This was done to evaluate the possibilities within control...

Reentrant Superspin Glass Phase in a La_{0.82}Ca_{0.18}MnO_{3} Ferromagnetic Insulator

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P. Anil Kumar

2014-03-01

Full Text Available We report results of the magnetization and ac susceptibility measurements down to very low fields on a single crystal of the perovskite manganite, La_{0.82}Ca_{0.18}MnO_{3}. This composition falls in the intriguing ferromagnetic insulator region of the manganite phase diagram. In contrast to earlier beliefs, our investigations reveal that magnetically (and in every other sense, this is a single-phase system with a ferromagnetic ordering temperature of around 170 K. However, this ferromagnetic state is magnetically frustrated, and the system exhibits pronounced glassy dynamics below 90 K. Based on measured dynamical properties, we propose that this quasi-long-ranged ferromagnetic phase, and the associated superspin glass behavior, is the true magnetic state of the system, rather than being a macroscopic mixture of ferromagnetic and antiferromagnetic phases, as often suggested. Our results provide an understanding of the quantum phase transition from an antiferromagnetic insulator to a ferromagnetic metal via this ferromagnetic insulating state as a function of x in La_{1−x}Ca_{x}MnO_{3}, in terms of the possible formation of magnetic polarons.

Conductivity and superconductivity of (Bi,Pb)-Sr-Ca-Cu-O

International Nuclear Information System (INIS)

Gazda, M.; Kusz, B.; Klimczuk, T.; Natali, R.; Stizza, S.

2007-01-01

The (Bi,Pb)-Sr-Ca-Cu-O glass-ceramics may be considered as disordered metal and superconductor. Depending on the heat treatment conditions the materials are either composed of the oval grains of the 2212 or 2201 phases embedded in the insulating matrix or they mainly contain the 2212 plate-like crystallites weakly connected one with another. The materials have large resistivity and usually large negative temperature coefficient of resistivity (TCR). The granular and disordered character of the materials is also reflected in their superconducting properties. Both the normal-state and superconducting properties correlate one with another. The glass-ceramic samples were obtained by annealing the amorphous solid at temperatures between 840 and 860 deg. C. The measurements of the temperature dependence of resistivity in annealed samples were carried out with the conventional four-terminal method in a temperature range from 3 to 300 K

Chemical deposition of La0.7Ca0.3MnO3±δ films on ceramic substrates

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Cássio Morilla-Santos

2011-01-01

Full Text Available In this paper, it is reported the growth of La0.7Ca0.3MnO3±δ films using a chemical solution deposition method (CSD by the spin-coating technique. Such solution was prepared through a route based on modified polymeric precursor method. Spin-coating deposition on different ceramic substrates was performed and analyzed by X-ray diffraction (XRD, scanning electron microscopy (SEM and X-ray photoelectron spectroscopy (XPS. The magnetic response of the prepared specimens was studied using a SQUID magnetometer. The obtained results indicated uniform deposition on SrTiO3 and LaAlO3 substrates with similar characteristics. Furthermore, significant differences were detected in the Mn3+/Mn4+ valence ratio and a corresponding diverse magnetic response was observed. The sample prepared on SrTiO3 and LaAlO3 presented a critical temperature around 270 K as expected.

Manipulating the magnetism and resistance state of Mn:ZnO/Pb(Zr0.52Ti0.48)O3 heterostructured films through electric fields

Science.gov (United States)

Li, Yong-Chao; Wu, Jun; Pan, Hai-Yang; Wang, Jue; Wang, Guang-Hou; Liu, Jun-Ming; Wan, Jian-Guo

2018-05-01

Mn:ZnO/Pb(Zr0.52Ti0.48)O3 (PZT) heterostructured films have been prepared on Pt/Ti/SiO2/Si wafers by a sol-gel process. Nonvolatile and reversible manipulation of the magnetism and resistance by electric fields has been realized. Compared with the saturation magnetic moment (Ms) in the +3.0 V case, the modulation gain of Ms can reach 270% in the -3.0 V case at room temperature. The resistance change is attributed to the interfacial potential barrier height variation and the formation of an accumulation (or depletion) layer at the Mn:ZnO/PZT interface, which can be regulated by the ferroelectric polarization direction. The magnetism of Mn:ZnO originates from bound magnetic polarons. The mobile carrier variation in Mn:ZnO, owing to interfacial polarization coupling and the ferroelectric field effect, enables the electric manipulation of the magnetism in the Mn:ZnO/PZT heterostructured films. This work presents an effective method for modulating the magnetism of magnetic semiconductors and provides a promising avenue for multifunctional devices with both electric and magnetic functionalities.

Synthesis of the phase with T sub c =110 K in Bi(Pb)-Sr-Ca-Cu-O superconducting ceramics. Sintez fazy T sub c =110 K sverkhprovodyashchej keramiki sostava Bi(Pb)-Sr-Ca-Cu-O

Energy Technology Data Exchange (ETDEWEB)

Dubovitskij, A V; Makarov, E F; Makova, M K; Merzhanov, V A; Topnikov, V N [AN SSSR, Moscow (USSR). Inst. Khimicheskoj Fiziki

1991-05-01

Synthesis of 110 K single-phase bismuth ceramics (BiPb){sub 2}Sr{sub 2}Ca{sub n-1}Cu{sub n}O{sub x} was conducted in narrow temperature and time range. Diffusion of bismuth ions is proposed to be the decisive factor of synthesis of bismuth ceramics. The diffusion depends on prehistory of basic burden preparation and on its dispersivity and homogeneity in particluar. Optimal time of synthesis for lead doped ceramics of 2223 composition, synthesized from initial nitrate components, is equal to 65 h at 850 deg C. The role of Pb{sup 2+} ions is probably reduced to decrease of diffusion mobility of Bi{sup 3+} ions over the bismuth sublattice. Ceramics doping with CdO and CdCl{sub 2} compounds instead of lead stabilizes superconductivity in bismuth ceramics, but with worth superconducting parameters.

Langmuir probe measurements and mass spectrometry of plasma plumes generated by laser ablation of La0.4Ca0.6MnO3

Science.gov (United States)

Chen, Jikun; Lunney, James G.; Lippert, Thomas; Ojeda-G-P, Alejandro; Stender, Dieter; Schneider, Christof W.; Wokaun, Alexander

2014-08-01

The plasma formed in vacuum by UV nanosecond laser ablation of La0.4Ca0.6MnO3 in the fluence range of 0.8 to 1.9 J cm-2 using both Langmuir probe analysis and energy-resolved mass spectrometry has been studied. Mass spectrometry shows that the main positive ion species are Ca+, Mn+, La+, and LaO+. The Ca+ and Mn+ energy distributions are quite broad and lie in the 0-100 eV region, with the average energies increasing with laser fluence. In contrast, the La+ and LaO+ distributions are strongly peaked around 10 eV. The net time-of-arrival signal derived from the measured positive ion energy distributions is broadly consistent with the positive ion signal measured by the Langmuir probe. We also detected a significant number of O- ions with energies in the range of 0 to 10 eV. The Langmuir probe was also used to measure the temporal variation of the electron density and temperature at 6 cm from the ablation target. In the period when O- ions are found at this position, the plasma conditions are consistent with those required for significant negative oxygen ion formation, as revealed by studies on radio frequency excited oxygen plasma.

Frequency effects on charge ordering in Y{sub 0.5}Ca{sub 0.5}MnO{sub 3} by impedance spectroscopy

Energy Technology Data Exchange (ETDEWEB)

Sarwar, Tuba, E-mail: sarwartuba@gmail.com [EMMG, Physics Division, PINSTECH, P. O. Nilore, Islamabad (Pakistan); DPAM, PIEAS, P. O. Nilore, Islamabad (Pakistan); Qamar, Afzaal [Queensland Micro-Nanotechnology Centre, Griffith University, Nathan, QLD 4111 (Australia); Nadeem, Muhammad [EMMG, Physics Division, PINSTECH, P. O. Nilore, Islamabad (Pakistan)

2015-02-01

In this work, structural and electrical properties of Y{sub 0.5}Ca{sub 0.5}MnO{sub 3} are investigated by employing X-ray diffraction and impedance spectroscopy, respectively. Applied ac electric field showed the charge ordering transition temperature around 265 K and below this temperature the heteromorphic behavior of the sample is discussed in the proximity of T{sub CO}. With frequency effects the volume of robust charge orbital ordering (COO) domains diminishes due to different competing phases along with Jahn Teller distortions. Comprehensive melting and collapse of charge orbital ordering occurs below T{sub N}(125 K), where a colossal drop in the value of impedance is observed. The change in profile of modulus plane plots determines the spreading of relaxation time of intermingled phases. Hopping mechanism is elaborated in terms of strong electron phonon coupling. Variable range hopping model and Arrhenius model are used to discuss the short and long range hopping between Mn{sup 3+} and Mn{sup 4+} channels assessing the activation energy E{sub a}. - Highlights: • Present study contains a detailed investigation over the electrical and structural properties of Y{sub 0.5}Ca{sub 0.5}MnO{sub 3} especially its behavior across the charge ordering transition. • Impedance measurements illustrate the comprehensive melting and collapse of robust charge orbital ordering with colossal drop in impedance. • In T{sub N}Mn{sup 3+} and Mn{sup 4+} channels assessing the activation energy E{sub a}.

Thermal expansion analysis and structural characteristics of the (Pb, Ca)TiO{sub 3} solid solutions from 150 to 570 K; Analise da expansao termica volumetrica e das caracteristicas estruturais de solucoes solidas de (Pb, Ca)TiO{sub 3} entre 150 e 570 K

Energy Technology Data Exchange (ETDEWEB)

Estrada, F.R.; Eiras, J.A.; Garcia, D., E-mail: frestrada@df.ufscar.br, E-mail: eiras@df.ufscar.br, E-mail: ducinei@df.ufscar.br [Universidade Federal de Sao Carlos (UFSCar), SP (Brazil). Departamento de Fisica. Grupo de Materiais Ferroicos

2017-01-15

Ceramic samples of lead modified calcium titanate (Pb{sub 1-x}Ca{sub x} TiO{sub 3}) with calcium concentration between 0.24≤x≤0.55 were prepared and analyzed in order to determine the structural origin of the negative thermal expansion observed in this ferroelectric system. The Rietveld structural refinement method was used to assess the thermal evolution of the structural parameters using powder X-ray diffraction data collected between 150 and 570 K. Since the Pb{sub 1-x}Ca{sub x} TiO{sub 3} phase diagram and space groups are still unknown for the temperature range investigated, the structural analyses were based on adjustments of the refinement protocol. The results revealed the existence of a correlation between symmetry transitions and anomalies in the thermal expansion of the unit cell, being such transitions not necessarily of the ferroelectric-paraelectric nature. (author)

Use of response surface methodology to evaluate the effect of metal ions (Ca2+, Ni2+, Mn2+, Cu2+) on production of antifungal compounds by Paenibacillus polymyxa.

Science.gov (United States)

Raza, Waseem; Hongsheng, Wu; Qirong, Shen

2010-03-01

The effects of four metal ions (Ca(2+), Ni(2+), Mn(2+) and Cu(2+)) were evaluated on growth and production of antifungal compounds by Paenibacillus polymyxa SQR-21 and a quadratic predictive model was developed using response surface methodology (RSM). The results revealed, Mn(2+) and Ni(2+) showed most positive synergistic interactive affect on production of antifungal compounds followed by the positive interactive synergistic affect of Cu(2+) and Ni(2+) and then Mn(2+) and Cu(2+). While the interactive effect of Ca(2+) with all other three metals inhibited the production of antifungal compounds. The Mn(2+) (P=0.0384), Ni(2+) (P=0.0004) and Cu(2+) (P=0.0117) significantly affected the production of antifungal compounds while the effect of Ca(2+) (P=0.1851) was less significant. The maximum growth (OD(600)=1.55) was obtained at 500 (0), 125 (0), 100 (-2) and 37.5 (0) microM levels and the maximum size of inhibition zone (31 mm) was measured at 400 (-1), 150 (1), 400 (1) and 25 microM (-1) levels of Ca(2+), Mn(2+), Ni(2+) and Cu(2+), respectively. The RSM model provided an easy and effective way to determine the interactive effect of metal ions on production of antifungal compounds by P. polymyxa SQR-21 so that optimum media recipes can be developed to produce maximum amounts of antifungal compounds under laboratory and commercial fermentation conditions. Copyright (c) 2009 Elsevier Ltd. All rights reserved.

Crystal structures and thermal decomposition of permanganates AE[MnO{sub 4}]{sub 2} . n H{sub 2}O with the heavy alkaline earth elements (AE=Ca, Sr and Ba)

Energy Technology Data Exchange (ETDEWEB)

Henning, Harald; Bauchert, Joerg M.; Conrad, Maurice; Schleid, Thomas [Stuttgart Univ. (Germany). Inst. fuer Anorganische Chemie

2017-10-01

Reexamination of the syntheses and crystal structures as well as studies of the thermal decomposition of the heavy alkaline earth metal permanganates Ca[MnO{sub 4}]{sub 2} . 4 H{sub 2}O, Sr[MnO{sub 4}]{sub 2} . 3 H{sub 2}O and Ba[MnO{sub 4}]{sub 2} are the focus of this work. As an alternative to the very inelegant Muthmann method, established for the synthesis of Ba[MnO{sub 4}]{sub 2} a long time ago, we employed a cation-exchange column loaded with Ba{sup 2+} cations and passed through an aqueous potassium-permanganate solution. We later used this alternative also with strontium- and calcium-loaded columns and all the compounds synthesized this way were indistinguishable from the products of the established methods. Ca[MnO{sub 4}]{sub 2} . 4 H{sub 2}O exhibiting [CaO{sub 8}] polyhedra crystallizes in the orthorhombic space group Pccn with the lattice parameters a=1397.15(9), b=554.06(4) and c=1338.97(9) pm with Z=4, whereas Sr[MnO{sub 4}]{sub 2} . 3 H{sub 2}O with [SrO{sub 10}] polyhedra adopts the cubic space group P2{sub 1}3 with a=964.19(7) pm and Z=4. So the harder the AE{sup 2+} cation, the higher its demand for hydration in aqueous solution. Consequently, the crystal structure of Ba[MnO{sub 4}]{sub 2} in the orthorhombic space group Fddd with a=742.36(5), b=1191.23(7) and c=1477.14(9) pm with Z=8 lacks any crystal water, but contains [BaO{sub 12}] polyhedra. During the thermal decomposition of Ca[MnO{sub 4}]{sub 2} . 4 H{sub 2}O, the compound expels up to two water molecules of hydration, before the crystal structure collapses after the loss of the third H{sub 2}O molecule at 157 C. The crystal structure of Sr[MnO{sub 4}]{sub 2} . 3 H{sub 2}O breaks down after the expulsion of the third water molecule as well, but this already occurs at 148 C. For both the calcium and the strontium permanganate samples, orthobixbyite-type α-Mn{sub 2}O{sub 3} and the oxomanganates(III,IV) AEMn{sub 3}O{sub 6} (AE=Ca and Sr) remain as final decomposition products at 800 C

Phase separation over an extended compositional range: Studies of the Ca1-xBixMnO3 (x≤0.25) phase diagram

International Nuclear Information System (INIS)

Santhosh, P. N.; Goldberger, J.; Woodward, P. M.; Vogt, T.; Lee, W. P.; Epstein, A. J.

2000-01-01

Phase transitions on the electron-doped side of the Ca 1-x Bi x MnO 3 system (x≤0.25) have been investigated using high-resolution synchrotron x-ray and neutron powder-diffraction techniques, electrical transport and magnetic susceptibility measurements. At room temperature all samples investigated were single phase, paramagnetic conductors (ρ 3 (space group Pnma). The Mn-O-Mn angles remain nearly constant from x=0 to x=0.25, while the Mn-O distances steadily increase with the Mn 3+ content. Three distinct phases are observed at 25 K. The first one, observed from 0.15≥x≥0.03, is characterized by the absence of charge and orbital ordering, a canted G-type antiferromagnetic spin structure, and delocalized electron transport. The second phase, observed from 0.25≥x≥0.12 (single phase at x=0.18), is characterized by pronounced orbital ordering, a C-type antiferromagnetic spin structure, and insulating behavior. The third low-temperature phase, observed for x≥0.20, is characterized by orbital and magnetic ordering similar to the Wigner crystal structure previously observed for Ca 0.67 La 0.33 MnO 3 , but with a 4axbx2c unit cell. The most striking feature of the phase diagram is the wide compositional range over which low-temperature phase separation is observed. Only those samples with x<0.12 and x=0.18 did not undergo phase separation upon cooling. We show that this behavior cannot be attributed to compositional variations, and therefore, propose that anisotropic strain interactions between crystallites may be partially responsible for this behavior

Certification of the contents (mass fractions) of Cd, Pb, Se, Cu, Zn, Fe and Mn in wholemeal flour and lyophilized brown bread reference materials. Wholemeal flour - CRM no. 189; brown bread - CRM no. 191

Energy Technology Data Exchange (ETDEWEB)

Wagstaffe, P J; Griepink, B; Muntau, H; Schramel, P

1987-01-01

The report describes the preparation and certification of a wholemeal flour (CRM 189) and a lyophilised brown breas (CRM 191) for their contents (mass fractions) of elements of toxicological and nutritional importance: Cd, Pb, Se, Cu, Zn, Fe and Mn. Indicative values are also given for As, Ca, Cl, Cr, Hg, Mg, Na, Ni, P and K. Details are given of a preliminary intercomparison of methods for these elements in a wholemeal flour sample, homogeneity and stability studies on the two reference materials and the results and evaluation of the certification exercise which involved 21 European Laboratories. Summaries of the certification methods are also presented. The report concludes with a discussion of the most common sources of error in determining the elements of interest and the steps to be taken to control them. With 7 figs., 28 tabs.

AC losses in (Bi,Pb) 2Sr 2Ca 2Cu 3O x tapes

Science.gov (United States)

D'Anna, G.; Indenbom, M. V.; André, M.-O.; Benoit, W.; Grivel, J.-C.; Hensel, B.; Flükiger, R.

1994-05-01

A double peak structure is observed in the AC losses of (Bi,Pb) 2Sr 2Ca 2Cu 3O x silver-sheathed tapes using a torsion-pendulum oscillator. The low-temperature peak is associated to the intragrain flux expulsion, while the high-temperature peak results from a macroscopic current path around the whole sample due to a well-coupled fraction of the grains. The flux pinning by the dislocations forming small-angle grain boundaries is suggested to control the transport current.

Structural characterization of PbTi03, Sm0.6Nd0.4NiO3 and NdMnO3 multifunctional Perovskite thin films

Directory of Open Access Journals (Sweden)

Rapenne L.

2012-06-01

Full Text Available Different multifunctional (PbTiO3, Sm0.6Nd0.4NiO3, NdMnO3 thin films were grown by metalorganic chemical vapor deposition (MOCVD technique on SrTiO3 and LaAlO3 substrates. TEM and X-ray diffraction measurements reveal that almost single crystalline thin films can be epitaxially grown on the top of substrates. The relationship between the crystallographic orientation of the films and those of the substrates were determined by reciprocal space mapping and TEM analyses. PbTi03 thin films appear to be under tensile or compressive strain according to the different mismatch of their cell parameter with those of the substrate. Relaxation mechanism as a function of the film thickness arises from coexistence of different type of domains and size and strain effect are analyzed. SmNiO3 thin films present diffuse scattering strikes and are less well organized when compared to PbTi03 thin films. Different domains are observed as well as an additional parasitic phase close to NiO. Its regular distribution can be associated to reduced transport properties. Preliminary observations on NdMnO3 thin films show that an amorphous phase is obtained during MOCVD that can be transformed in a single crystalline film by annealing. The films are under tensile or compressive strain according to the different mismatch of their cell parameter with those of the substrate. Magnetic properties are investigated.

Determination of Na, Cl, Ca, Mg, Mn and K in milk samples by activation analysis

International Nuclear Information System (INIS)

Kira, Carmen S.; Maihara, Vera A.

2000-01-01

In the present work cow milk samples distributed for Sao Paulo government institutions, by means of the 'Viva leite' programme, have been monitored. The concentrations of Ca, Cl, K, Mg, Mn and Na were determined in five milk samples and in three different kinds of commercial powder milk, by instrumental neutron activation. For quality control, the reference materials NIST whole milk powder and non fat milk powder were analysed. The results obtained are in the range of the concentrations mentioned in the literature for these elements. (author)

The manifestation of spin-phonon coupling in CaMnO{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Goian, V., E-mail: goian@fzu.cz; Kamba, S.; Borodavka, F.; Nuzhnyy, D.; Savinov, M. [Institute of Physics, The Czech Academy of Sciences, Na Slovance 2, 182 21 Prague (Czech Republic); Belik, A. A. [International Center for Materials Nanoarchitectonics (WPI-MANA), National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki 305-0044 (Japan)

2015-04-28

Recently predicted presence of spin-phonon coupling in the CaMnO{sub 3} is experimentally confirmed in infrared (IR), Raman and time-domain THz spectra. Most of phonon frequencies seen below 350 cm{sup −1} exhibit significant shifts on cooling below antiferromagnetic phase transition at T{sub N} ≅ 120 K. Moreover, several new modes activate in the IR and Raman spectra on cooling below T{sub N}. Sum of phonon contributions to static permittivity exhibits small but reliable anomaly at T{sub N}. On the other hand, the spin-phonon coupling is not manifested in temperature dependence of radio-frequency permittivity, because intrinsic permittivity is screened by extrinsic contribution from conductivity, which enhances the permittivity to giant values.

Tunable white light of a Ce3+,Tb3+,Mn2+ triply doped Na2Ca3Si2O8 phosphor for high colour-rendering white LED applications: tunable luminescence and energy transfer.

Science.gov (United States)

Lü, Wei; Xu, Huawei; Huo, Jiansheng; Shao, Baiqi; Feng, Yang; Zhao, Shuang; You, Hongpeng

2017-07-18

A tunable white light emitting Na 2 Ca 3 Si 2 O 8 :Ce 3+ ,Tb 3+ ,Mn 2+ phosphor with a high color rendering index (CRI) has been prepared. Under UV excitation, Na 2 Ca 3 Si 2 O 8 :Ce 3+ phosphors present blue luminescence and exhibit a broad excitation ranging from 250 to 400 nm. When codoping Tb 3+ /Mn 2+ ions into Na 2 Ca 3 Si 2 O 8 , energy transfer from Ce 3+ to Tb 3+ and Ce 3+ to Mn 2+ ions is observed from the spectral overlap between Ce 3+ emission and Tb 3+ /Mn 2+ excitation spectra. The energy-transfer efficiencies and corresponding mechanisms are discussed in detail. The mechanism of energy transfer from Ce 3+ to Tb 3+ is demonstrated to be a dipole-quadrupole mechanism by the Inokuti-Hirayama model. The wavelength-tunable white light can be realized by coupling the emission bands centered at 440, 550 and 590 nm ascribed to the contribution from Ce 3+ , Tb 3+ and Mn 2+ , respectively. The commission on illumination value of color tunable emission can be tuned by controlling the content of Ce 3+ , Tb 3+ and Mn 2+ . Temperature-dependent luminescence spectra proved the good thermal stability of the as-prepared phosphor. White LEDs with CRI = 93.5 are finally fabricated using a 365 nm UV chip and the as-prepared Na 2 Ca 3 Si 2 O 8 :Ce 3+ ,Tb 3+ ,Mn 2+ phosphor. All the results suggest that Na 2 Ca 3 Si 2 O 8 :Ce 3+ ,Tb 3+ ,Mn 2+ can act as potential color-tunable and single-phase white emission phosphors for possible applications in UV based white LEDs.

Biosorption of Cd, Cr, Mn, and Pb from aqueous solutions by Bacillus sp strains isolated from industrial waste activate sludge

Directory of Open Access Journals (Sweden)

Rocío García

2016-01-01

Full Text Available Los microorganismos tienen capacidad de acumular metales pesados como agentes bioadsorbentes ofreciendo una alternativa para la remoción de metales tóxicos en aguas de efluentes industriales. El objetivo del presente trabajo fue aislar e identificar bacterias tolerantes a los metales pesados (Cd, Cr, Mn y Pb de lodos activados provenientes de la planta de tratamiento de agua del Municipio de Santa Rosa Jáuregui, Querétaro. Para seleccionar las bacterias que son tolerantes a los metales se aislaron 37 cepas bacterianas de las cuales se seleccionaron la Cepa-13 y Cepa-16 (C-13 y C-16, que presentaron una máxima capacidad de adsorción para los metales estudiados. En este artículo, el término biosorción describe la remoción de contaminantes y la utilización de biomasas (muerta mediante mecanismos fisicoquímicos como el proceso de adsorción o de intercambio iónico. Para obtener las condiciones de máxima adsorción se aplicó un tratamiento alcalino y uno ácido. La capacidad de adsorción fue menor en medio ácido que el bioadsorbente con tratamiento alcalino. Una segunda etapa del estudio fue la biosorción de metales pesados (Cd, Cr, Mn, y Pb utilizando las biomasas muertas de Bacillus sp (cepa C13 y C16 aisladas de los lodos activados de la primera etapa.

Phase Identification and Dielectric Properties of Pb0.94 Ca0.06 TiO3 Ceramics

International Nuclear Information System (INIS)

Khin Thida; Tin Tin Aye; Aye Aye Phyu; Moe Moe Myint; Ko Ko Kyaw Soe

2008-03-01

The ferroelectric materials of Ca (6 mol %) doped PbTiO3 (abbreviated to PCT6) ceamics were prepared by using conventional solid solution method. Phase assignment is identified by XRD technique. The change in capacitance, the variation of dielectric constant and dielectric loss as a function of applied frequency modes (1 kHz-10 kHz)at zero bias voltage of PCT6 ceramics by using Cu and Ag electrodes were investigated.

Frequency effects on charge ordering in Y0.5Ca0.5MnO3 by impedance spectroscopy

Science.gov (United States)

Sarwar, Tuba; Qamar, Afzaal; Nadeem, Muhammad

2015-02-01

In this work, structural and electrical properties of Y0.5Ca0.5MnO3 are investigated by employing X-ray diffraction and impedance spectroscopy, respectively. Applied ac electric field showed the charge ordering transition temperature around 265 K and below this temperature the heteromorphic behavior of the sample is discussed in the proximity of TCO. With frequency effects the volume of robust charge orbital ordering (COO) domains diminishes due to different competing phases along with Jahn Teller distortions. Comprehensive melting and collapse of charge orbital ordering occurs below TN(125 K), where a colossal drop in the value of impedance is observed. The change in profile of modulus plane plots determines the spreading of relaxation time of intermingled phases. Hopping mechanism is elaborated in terms of strong electron phonon coupling. Variable range hopping model and Arrhenius model are used to discuss the short and long range hopping between Mn3+ and Mn4+ channels assessing the activation energy Ea.

La{sub 0.67}Pb{sub 0.33-x}K{sub x}MnO{sub 3} perovskites synthesized by sol-gel method: the effect of potassium substitution on the magnetic and electrical properties

Energy Technology Data Exchange (ETDEWEB)

Zaidi, Asma; Dhahri, J. [University of Monastir, Physics Laboratory of the Condensed Material and the Nanoscience' s, Faculty of Science, Monastir (Tunisia); Alharbi, T.; Alzobaidi, S.; Zaidi, M.A. [Majmaah University, College of Science of Zulfi, Riyadh (Saudi Arabia); Hlil, E.K. [CNRS-Universite J. Fourier, Institut Neel, BP 166, Gronoble (France)

2017-01-15

The influence of the potassium substitution for Pb ions in the mixed valence perovskites La{sub 0.67}Pb{sub 0.33-x}K{sub x}MnO{sub 3} (0 ≤ x ≤ 0.15) was investigated by X-ray diffraction, magnetic and electric transport measurements. All the compositions were synthesized using the sol-gel technique. X-ray diffraction and structure refinement showed that they crystallize in the rhombohedral structure with R anti 3c space group. Upon K doping on Pb sites, the lattice parameters, unit cell volume, and the Mn-O-Mn bond angle were reduced. All the samples exhibited a ferromagnetic-paramagnetic transition and metallic-semiconductor one with increasing temperature. The analysis of the electrical resistivity data concluded that the metallic (ferromagnetic) part of the resistivity (below T{sub M-Sc}) can be explained by the following equation ρ(T) = ρ{sub 0} + ρ{sub 2}T{sup 2} + ρ{sub 4.5}T{sup 4.5}, signifying the importance of the domain boundary/grain, combination of electron-magnon, electron-electron and electron-phonon scattering processes. At higher-temperature (T > T{sub M-Sc}) paramagnetic semiconducting regime, the adiabatic small polarons hopping mechanism (ASPH) was found to fit well. (orig.)

Tracing anthropogenic Hg and Pb input using stable Hg and Pb isotope ratios in sediments of the central Portuguese Margin

NARCIS (Netherlands)

Mil-Holmens, M.; Blum, J.; Canário, J.; Caetano, M.; Costa, A.M.; Lebreiro, S.M.; Trancoso, M.; Richter, T.O.; de Stigter, H.; Johnson, M.; Branco, V.; Cesário, R.; Mouro, F.; Mateus, M.; Boer, W.; Melo, Z.

2013-01-01

Three short marine sediment cores from the Cascais Submarine Canyon (CSC; cores 252-32 and 252-35) and the Estremadura Spur (core 252-16) on the central Portuguese Margin were analysed for Hg, Pb, Al, and Mn concentrations, and both Pb and Hg stable isotope compositions, in order to reconstruct

Growth and electrical properties of (Mn,F) co-doped 0.92Pb(Zn 1/3Nb 2/3)O 3-0.08PbTiO 3 single crystal

Science.gov (United States)

Zhang, Shujun; Lebrun, Laurent; Randall, Clive A.; Shrout, Thomas R.

2004-06-01

The growth and characterization of (Mn,F) doped Pb(Zn 1/3Nb 2/3)O 3-PbTiO 3 (PZNT) single crystals are reported in this paper. The typical single crystal obtained is up to 30 mm size with dark brown color. The crystal lattice parameters of doped PZNT crystal are slightly decreased compared to the pure one. The room temperature dielectric permittivity along direction is about 6000, which is lower than that of the pure PZNT8 because of the dopants. The Curie temperature of the doped crystal is about 180°C while the ferroelectric phase transition temperature is around 100°C, which are higher than those of the pure PZNT8 single crystal. The remnant polarization and coercive field of oriented doped crystal measured at 1 Hz and 10 kV/cm field are about 27 μC/cm 2 and 4.2 kV/cm, respectively. The room temperature mechanical quality factor is ˜300. Piezoelectric coefficient of oriented doped crystal is higher than 3500 pC/N and the longitudinal electromechanical coupling factor is larger than 93%. The piezoelectric properties of doped PZNT single crystal with temperature and orientations are also reported in this paper. The valence state of the manganese dopant was determined by electron spin resonance, indicating no Mn 4+ in the crystals, suggesting the valence of manganese ions in PZNT crystals may be 2+, which acts as a hardener, stabilizes the domain wall and pins the domain wall motion, on the other hand, the dopant will enter Ti 4+ position, shifting the crystal composition to higher PT content.

High-Resolution Zircon U-Pb CA-TIMS Dating of the Carboniferous—Permian Successions, Paraná Basin, Brazil

Science.gov (United States)

Griffis, N. P.; Mundil, R.; Montanez, I. P.; Isbell, J.; Fedorchuk, N.; Lopes, R.; Vesely, F.; Iannuzzi, R.

2015-12-01

The late Paleozoic Ice Age (LPIA) is Earth's only record of a CO2-forced climatic transition from an icehouse to greenhouse state in a vegetated world. Despite a refined framework of Gondwanan ice distribution, questions remain about the timing, volume, and synchronicity of high-latitude continental ice and the subsequent deglaciation. These questions ultimately preclude our understanding of linkages between ice volume, sea level, and high- and low-latitude climate. Poor constraints on the timing and synchronicity of glacial and interglacial transitions reflect a lack of high-resolution radioisotopic dates from high-latitude, ice-proximal Carboniferous-Permian successions. The Rio Bonito Fm in Rio Grande do Sul State of southern Brazil hosts the oldest non-glaciogenic Carboniferous- Permian deposits of the Paraná Basin, thus recording the icehouse-to-greenhouse transition. Despite a widespread effort over the last two decades to constrain these deposits in time by means of U-Pb zircon geochronology, published data sets of the Candiota and Faxinal coals of the Rio Bonito Fm host discrepancies that may reflect post- eruptive open system behavior of zircon and analytical artifacts. These discrepancies have hindered the correlation of the Candiota and Faxinal sediments within the larger Gondwanan framework. Here we present the first U-Pb ages on closed system single zircons using CA-TIMS techniques on Permo-Carboniferous ash deposits of the Paraná Basin. Preliminary results indicate two major and distinct coal-forming periods that are separated by ca 10 Ma. Our results and conclusions are not in agreement with multi- crystal U-Pb TIMS and SIMS ages that suggest coeval deposition of the Candiota and Faxinal coals. CA-TIMS analyses applied to zircons from additional ash deposits are aimed at constructing a robust chronostratigraphic framework for the Carboniferous- Permian succession of the Paraná Basin, which will facilitate a better understanding of the timing and

Photoluminescence properties of whitlockite-type Ca{sub 9}MgK(PO{sub 4}){sub 7}:Eu{sup 2+},Mn{sup 2+} phosphor

Energy Technology Data Exchange (ETDEWEB)

Guo, Ning, E-mail: guoning@usst.edu.cn [Department of Chemistry, University of Shanghai for Science and Technology, Shanghai 200093 (China); Li, Shuo; Chen, Jishen; Li, Jing; Zhao, Yuefeng; Wang, Lu; Jia, Chengzheng; Ouyang, Ruizhuo [Department of Chemistry, University of Shanghai for Science and Technology, Shanghai 200093 (China); Lü, Wei [State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China)

2016-11-15

Novel single-phased Eu{sup 2+}/Mn{sup 2+}-coactivated whitlockite-type Ca{sub 9}MgK(PO{sub 4}){sub 7} phosphors which can emit white light upon UV light excitation, are prepared by the solid-state method, and their luminescence properties are systematically investigated via a combination of X-ray powder diffraction and spectroscopy measurements. For Eu{sup 2+}–Mn{sup 2+} codoped samples, an efficient energy transfer process can takes place and its mechanism is a resonant type via a dipole-quadrupole interaction which can be elucidated by DexterГ—Віs theoretical model. Following the principle of energy transfer, myriad luminescence colors with a large gamut from blue to purplish red and across white zone in a line in the chromaticity diagram of the CIE can be obtained by simply adjusting the concentration ratio of Eu{sup 2+} to Mn{sup 2+}. Photoluminescence spectra reveal that the white color emission is originated from the combination of two emission bands of Eu{sup 2+} and Mn{sup 2+} ions. Additionally, their CIE chromaticity coordinates and correlated color temperatures (CCT) have been calculated and discussed in detail. The luminescence suggest that whitlockite-type phosphor, Ca{sub 9}MgK(PO{sub 4}){sub 7}, co-activated with europium and manganese, is a promising single-phased white-emitting candidate for use in ultraviolet-chip-based white LEDs.

Highly polarized single-c-domain single-crystal Pb(Mn,Nb)O(3)-PZT thin films.

Science.gov (United States)

Wasa, Kiyotaka; Adachi, Hideaki; Nishida, Ken; Yamamoto, Takashi; Matsushima, Tomoaki; Kanno, Isaku; Kotera, Hidetoshi

2012-01-01

In-plane unstrained single-c-domain/single-crystal thin films of PZT-based ternary ferroelectric perovskite, ξPb(Mn,Nb)O3-(1 - ξ)PZT, were grown on SrRuO(3)/Pt/MgO substrates using magnetron sputtering followed by quenching. The sputtered unstrained thin films exhibit unique ferroelectric properties: high coercive field, Ec > 180 kV/cm, large remanent polarization, P(r) = 100 μC/cm(2), small relative dielectric constants, ε* = 100 to 150, high Curie temperature, Tc = ~600 °C, and bulk-like large transverse piezoelectric constants, e31,f = -12.0 C/m(2) for PZT(48/52) at ξ = 0.06. The unstrained thin films are an ideal structure to extract the bulk ferroelectric properties. Their micro-structures and ferroelectric properties are discussed in relation to the potential applications for piezoelectric MEMS. © 2012 IEEE

Statistical analysis of trace metals in the plasma of cancer patients versus controls

International Nuclear Information System (INIS)

Pasha, Qaisara; Malik, Salman A.; Shah, Munir H.

2008-01-01

The plasma of cancer patients (n = 112) and controls (n = 118) were analysed for selected trace metals (Al, Ca, Cd, Co, Cr, Cu, Fe, K, Li, Mg, Mn, Mo, Na, Ni, Pb, Sb, Sr and Zn) by flame atomic absorption spectroscopy. In the plasma of cancer patients, mean concentrations of macronutrients/essential metals, Na, K, Ca, Mg, Fe and Zn were 3971, 178, 44.1, 7.59, 4.38 and 3.90 ppm, respectively, while the mean metal levels in the plasma of controls were 3844, 151, 74.2, 18.0, 6.60 and 2.50 ppm, respectively. Average concentrations of Cd, Cr, Cu, Mn, Mo, Ni, Pb, Sb, Sr and Zn were noted to be significantly higher in the plasma of cancer patients compared with controls. Very strong mutual correlations (r > 0.70) in the plasma of cancer patients were observed between Fe-Mn, Ca-Mn, Ca-Ni, Ca-Co, Cd-Pb, Co-Ni, Mn-Ni, Mn-Zn, Cr-Li, Ca-Zn and Fe-Ni, whereas, Ca-Mn, Ca-Mg, Fe-Zn, Ca-Zn, Mg-Mn, Mg-Zn, Cd-Sb, Cd-Co, Cd-Zn, Co-Sb and Sb-Zn exhibited strong relationships (r > 0.50) in the plasma of controls, all were significant at p < 0.01. Principal component analysis (PCA) of the data extracted five PCs, both for cancer patients and controls, but with considerably different loadings. The average metals levels in male and female donors of the two groups were also evaluated and in addition, the general role of trace metals in the carcinogenesis was discussed. The study indicated appreciably different pattern of metal distribution and mutual relationships in the plasma of cancer patients in comparison with controls

Statistical analysis of trace metals in the plasma of cancer patients versus controls

Energy Technology Data Exchange (ETDEWEB)

Pasha, Qaisara; Malik, Salman A. [Department of Biochemistry, Quaid-i-Azam University, Islamabad 45320 (Pakistan); Shah, Munir H. [Department of Chemistry, Quaid-i-Azam University, Islamabad 45320 (Pakistan)], E-mail: munir_qau@yahoo.com

2008-05-30

The plasma of cancer patients (n = 112) and controls (n = 118) were analysed for selected trace metals (Al, Ca, Cd, Co, Cr, Cu, Fe, K, Li, Mg, Mn, Mo, Na, Ni, Pb, Sb, Sr and Zn) by flame atomic absorption spectroscopy. In the plasma of cancer patients, mean concentrations of macronutrients/essential metals, Na, K, Ca, Mg, Fe and Zn were 3971, 178, 44.1, 7.59, 4.38 and 3.90 ppm, respectively, while the mean metal levels in the plasma of controls were 3844, 151, 74.2, 18.0, 6.60 and 2.50 ppm, respectively. Average concentrations of Cd, Cr, Cu, Mn, Mo, Ni, Pb, Sb, Sr and Zn were noted to be significantly higher in the plasma of cancer patients compared with controls. Very strong mutual correlations (r > 0.70) in the plasma of cancer patients were observed between Fe-Mn, Ca-Mn, Ca-Ni, Ca-Co, Cd-Pb, Co-Ni, Mn-Ni, Mn-Zn, Cr-Li, Ca-Zn and Fe-Ni, whereas, Ca-Mn, Ca-Mg, Fe-Zn, Ca-Zn, Mg-Mn, Mg-Zn, Cd-Sb, Cd-Co, Cd-Zn, Co-Sb and Sb-Zn exhibited strong relationships (r > 0.50) in the plasma of controls, all were significant at p < 0.01. Principal component analysis (PCA) of the data extracted five PCs, both for cancer patients and controls, but with considerably different loadings. The average metals levels in male and female donors of the two groups were also evaluated and in addition, the general role of trace metals in the carcinogenesis was discussed. The study indicated appreciably different pattern of metal distribution and mutual relationships in the plasma of cancer patients in comparison with controls.

Large anisotropy in colossal magnetoresistance of charge orbital ordered epitaxial Sm0.5Ca0.5MnO3 films

DEFF Research Database (Denmark)

Chen, Yunzhong; Sun, J.R.; Zhao, J.L.

2009-01-01

We investigated the structure and magnetotransport properties of Sm0.5Ca0.5MnO3 (SCMO) films epitaxially grown on (011)-oriented SrTiO3 substrates, which exhibited clear charge/orbital ordering transition. A significant anisotropy of ~1000 in the colossal magnetoresistance (CMR) effect was observ...

Tracing the origin of Pb using stable Pb isotopes in surface sediments along the Korean Yellow Sea coast

Science.gov (United States)

Park, Jong-Kyu; Choi, Man-Sik; Song, Yunho; Lim, Dhong-Il

2017-06-01

To investigate the factors controlling lead (Pb) concentration and identify the sources of Pb in Yellow Sea sediments along the Korean coast, the concentration of Pb and Pb isotopes in 87 surface and 6 core sediment samples were analyzed. The 1 M HCl leached Pb concentrations had a similar geographic distribution to those of fine-grained sediments, while the distribution of residual Pb concentrations resembled that of coarse-grained sediments. Leached Pb was presumed to be associated with manganese (Mn) oxide and iron (Fe) oxy/hydroxide, while residual Pb was associated with potassium (K)-feldspar, based on good linear relationships between the leached Pb and the Fe/Mn concentrations, and the residual Pb and K concentrations. Based on a ratio-ratio plot with three isotopes (207Pb/206Pb and 208Pb/206Pb) and the geographic location of each sediment, sediments were categorized into two groups of samples as group1 and group2. Group 1 sediments, which were distributed in Gyeonggi Bay and offshore (north of 36.5°N), were determined to be a mixture of anthropogenic and natural Pb originating from the Han River, based on a 208Pb/206Pb against a Cs/Pbleached mixing plot of core and surface sediments. Group 2 sediments, which were distributed in the south of 36.5°N, also showed a two endmembers mixing relationship between materials from the Geum River and offshore materials, which had very different Pb concentrations and isotope ratios. Based on the isotopes and their concentrations in core and surface sediments, this mixing relationship was interpreted as materials from two geographically different origins being mixed, rather than anthropogenic or natural mixing of materials with the same origin. Therefore, the relative percentage of materials supplied from the Geum River was calculated using a two endmembers mixing model and estimated to be as much as about 50% at 35°N. The spatial distribution of materials derived from the Geum River represented that of fine

Role of a Water Network around the Mn4CaO5 Cluster in Photosynthetic Water Oxidation: A Fourier Transform Infrared Spectroscopy and Quantum Mechanics/Molecular Mechanics Calculation Study.

Science.gov (United States)

Nakamura, Shin; Ota, Kai; Shibuya, Yuichi; Noguchi, Takumi

2016-01-26

Photosynthetic water oxidation takes place at the Mn4CaO5 cluster in photosystem II. Around the Mn4CaO5 cluster, a hydrogen bond network is formed by several water molecules, including four water ligands. To clarify the role of this water network in the mechanism of water oxidation, we investigated the effects of the removal of Ca(2+) and substitution with metal ions on the vibrations of water molecules coupled to the Mn4CaO5 cluster by means of Fourier transform infrared (FTIR) difference spectroscopy and quantum mechanics/molecular mechanics (QM/MM) calculations. The OH stretching vibrations of nine water molecules forming a network between D1-D61 and YZ were calculated using the QM/MM method. On the the calculated normal modes, a broad positive feature at 3200-2500 cm(-1) in an S2-minus-S1 FTIR spectrum was attributed to the vibrations of strongly hydrogen-bonded OH bonds of water involving the vibrations of water ligands to a Mn ion and the in-phase coupled vibration of a water network connected to YZ, while bands in the 3700-3500 cm(-1) region were assigned to the coupled vibrations of weakly hydrogen-bonded OH bonds of water. All the water bands were lost upon Ca(2+) depletion and Ba(2+) substitution, which inhibit the S2 → S3 transition, indicating that a solid water network was broken by these treatments. By contrast, Sr(2+) substitution slightly altered the water bands around 3600 cm(-1), reflecting minor modification in water interactions, consistent with the retention of water oxidation activity with a decreased efficiency. These results suggest that the water network around the Mn4CaO5 cluster plays an essential role in the water oxidation mechanism particularly in a concerted process of proton transfer and water insertion during the S2 → S3 transition.

Thermal conductivity in Pr{sub 1-x}Ca{sub x}MnO{sub 3} and SrTiO{sub 3} thin film systems

Energy Technology Data Exchange (ETDEWEB)

Wiedigen, Stefanie; Kramer, Thilo; Mangipudi, Kodanda R.; Hoffmann, Joerg; Volkert, Cynthia A.; Jooss, Christian [Institute for Materials Physics, University of Goettingen (Germany); Feuchter, Manuel; Kamlah, Marc [Institute for Applied Materials, Karlsruhe Institute of Technology (Germany)

2012-07-01

Epitaxial multilayers and superlattices are one recent approach for the design of efficient thermoelectrics. To study the effect of phonon blocking and scattering on thermal conductivity of oxide multilayers, a combination of two perovskites with promising thermoelectric properties is selected: the orthorhombic Pr{sub 1-x}Ca{sub x}MnO{sub 3} and the cubic SrTiO{sub 3}. In order to investigate the effect of microstructure, interfaces and acoustic impedance mismatch on thermal conductivity {kappa} high preparation quality is needed. Our thin films were prepared by ion-beam and magnetron sputtering. Structural analysis is done by XRD and TEM and is presented in combination with thermal conductivity measurements using the 3{omega} method. Single layers of Pr{sub 1-x}Ca{sub x}MnO{sub 3} show low {kappa} values and no significant increase of thermal conductivity with increasing doping. In homoepitaxial single layers of SrTiO{sub 3} preparation conditions have a high impact on {kappa}, most probably due to different concentrations of point defects. Pr{sub 1-x}Ca{sub x}MnO{sub 3}/SrTiO{sub 3} multilayers show a {kappa} decreases systematically with increasing number of double layers. The results are discussed in the light of the theoretically calculated phonon dispersion and the experimentally observed microstructure.

Size effect on the magnetic properties of antiferromagnetic La0.2Ca0.8MnO3 nanoparticles

Science.gov (United States)

Markovich, V.; Fita, I.; Wisniewski, A.; Mogilyansky, D.; Puzniak, R.; Titelman, L.; Martin, C.; Gorodetsky, G.

2010-03-01

Magnetic properties of electron-doped La0.2Ca0.8MnO3 manganite nanoparticles with average particle size ranging from 15 to 37 nm, prepared by the glycine-nitrate method, have been investigated in temperature range 5-300 K and in magnetic fields up to 90 kOe. A monotonous enhancement of weak ferromagnetism linked to the reduction in the particle size was observed for all nanoparticles. Magnetic hysteresis loops also indicate size-dependent exchange bias effect displayed by horizontal and vertical shifts in field-cooled processes. The magnetization data reveal two ferromagnetic components: first one appears at T˜200K and may be attributed to surface magnetization and second one appears as a result of spin canting of antiferromagnetic core or is developed at some interfaces inside nanoparticles. Time evolution of magnetization recorded in magnetic fields after the field cooling to low temperatures exhibits a very noisy behavior that may be caused by formation of collective state of nanoparticles with no clear tendency to reach equilibrium state. Magnetic properties of the nanoparticle samples are compared with those of the bulk La0.2Ca0.8MnO3 .

High-Temperature Photovoltaic Effect in La.Ca.MnO/SiO/Si Heterojunction

Directory of Open Access Journals (Sweden)

Hao Ni

2012-01-01

Full Text Available We fabricated a heterojunction of La0.4Ca0.6MnO3/SiO/n-Si and investigated its electronic transport and ultraviolet photovoltaic properties at higher temperature up to 673 K. The rectifying behaviors vanished with the energy-band structure evolvement from 300 to 673 K. Under irradiation of a 248 nm pulse laser, the peak values of open-circuit photovoltage and short-circuit photocurrent decreased drastically. This understanding of the temperature-related current-voltage behavior and ultraviolet photodetection of oxide heterostructures should open a route for devising future microelectronic devices working at high temperature. PACS: 73.40.Lq, 71.27.+ a, 73.50.Pz.

Structural phase transition and multiferroic properties of Bi0.8A0.2Fe0.8Mn0.2O3 (A = Ca, Sr)

Science.gov (United States)

Rout, Jyoshna; Choudhary, R. N. P.

2018-05-01

The multiferroic BiFeO3 and Bi0.8A0.2Fe0.8Mn0.2O3 (A = Ca, Sr) have been synthesized using direct mechanosynthesis. Detailed investigations were made on the influence of Ca-Mn and Sr-Mn co-substitutions on the structure change, electric and magnetic properties of the BFO. Rietveld refinement on the XRD pattern of the modified samples clarifies the structural transition from R3c:H (parent BiFeO3) to the biphasic structure (R3c: H + Pnma). Scanning electron micrographs confirmed the polycrystalline nature of the materials and each of the microstructure comprised of uniformly distributed grains with less porosity. The dielectric measurements reveal that enhancement in dielectric properties due to the reduction of oxygen vacancies by substitutional ions. Studies of frequency-dependence of impedance and related parameters exhibit that the electrical properties of the materials are strongly dependent on temperature, and bear a good correlation with its microstructure. The bulk resistance (evaluated from impedance studies) is found to decrease with increasing temperature for all the samples. The alternating current (ac) conductivity spectra show a typical signature of an ionic conducting system, and are found to obey Jonscher's universal power law. Preliminary studies of magnetic characteristics of the samples reveal enhanced magnetization for Ca-Mn co-substituted sample. The magnetoelectric coefficient as the function of applied dc magnetizing field under fixed ac magnetic field 15.368 Oe is measured and this ME coefficient αME corresponds to induction of polarization by a magnetic field.

Chemical disorder influence on magnetic state of optimally-doped La0.7Ca0.3MnO3

Science.gov (United States)

Rozenberg, E.; Auslender, M.; Shames, A. I.; Jung, G.; Felner, I.; Tsindlekht, M. I.; Mogilyansky, D.; Sominski, E.; Gedanken, A.; Mukovskii, Ya. M.; Gorodetsky, G.

2011-10-01

X-band electron magnetic resonance and dc/ac magnetic measurements have been employed to study the effects of chemical disorder on magnetic ordering in bulk and nanometer-sized single crystals and bulk ceramics of optimally-doped La0.7Ca0.3MnO3 manganite. The magnetic ground state of bulk samples appeared to be ferromagnetic with the lower Curie temperature and higher magnetic homogeneity in the vicinity of the ferromagnetic-paramagnetic phase transition in the crystal, as compared with those characteristics in the ceramics. The influence of technological driven "macroscopic" fluctuations of Ca-dopant level in crystal and "mesoscopic" disorder within grain boundary regions in ceramics was proposed to be responsible for these effects. Surface spin disorder together with pronounced inter-particle interactions within agglomerated nano-sample results in well defined core/shell spin configuration in La0.7Ca0.3MnO3 nano-crystals. The analysis of the electron paramagnetic resonance data enlightened the reasons for the observed difference in the magnetic order. Lattice effects dominate the first-order nature of magnetic phase transition in bulk samples. However, mesoscale chemical disorder seems to be responsible for the appearance of small ferromagnetic polarons in the paramagnetic state of bulk ceramics. The experimental results and their analysis indicate that a chemical/magnetic disorder has a strong impact on the magnetic state even in the case of mostly stable optimally hole-doped manganites.

Calcium availability but not its content modulates metal toxicity in Scenedesmus quadricauda.

Science.gov (United States)

Kováčik, Jozef; Dresler, Sławomir

2018-01-01

Impact of calcium nutrition (pre-culture on solid medium with standard or elevated Ca dose, i. e. 0.17 and 4.40mM marked as low and high Ca) on acute metal toxicity (Cd, Mn and Pb, 24h of exposure to 10µM) in freshwater green alga Scenedesmus quadricauda was studied. Surprisingly, Ca content differed only slightly between low and high Ca samples and applied metals rather suppressed its amount. Na content was higher in metal-exposed high Ca samples, indicating that Ca/Na ratio may affect accumulation of metals. Content of heavy metals increased in order Cd < Mn < Pb and high Ca samples contained less metal than low Ca samples at least in absorbed fraction. Accumulation of ascorbic acid and thiols (GSH - glutathione and PC2 - phytochelatin 2) was affected mainly by Cd, GSH also by Mn and PC2 by Pb with often significant differences between low Ca and high Ca samples. Calcium nutrition also affected responses of algae to metals at the level of antioxidative enzyme activities (SOD, APX, and CAT) and elevated values were typically found in high Ca samples while ROS (hydrogen peroxide and superoxide radical) were mainly depleted in Mn treatment. These data confirm that Ca nutrition affects accumulation of metals in algae and metabolic parameters as observed in vascular plants but, unlike them, rather Ca/Na ratio than absolute Ca content seems to regulate the uptake of metals. Copyright © 2017 Elsevier Inc. All rights reserved.

Ca8NaY(PO4)6F2:Eu2+,Mn2+: a potential color-tunable phosphor for white LEDs applications

International Nuclear Information System (INIS)

Fen, Zhang; Wanjun, Tang

2015-01-01

Eu 2+ - and/or Mn 2+ -activated Ca 8 NaY(PO 4 ) 6 F 2 phosphors have been prepared via a combustion-assisted synthesis route. The powder X-ray diffraction measurement revealed that Ca 8 NaY(PO 4 ) 6 F 2 crystallized in a hexagonal crystal system with the space group P6 3 /m (176). The photoluminescence spectrum of the Eu 2+ single-doped phosphor shows a broad blue emission band peaking at 451 nm under the excitation of UV irradiation. The Eu 2+ -/Mn 2+ -codoped phosphors show a blue emission band and an orange emission band, and the corresponding CIE coordinates intuitively indicate the tunable colors from blue to yellow area. The energy transfer from the Eu 2+ to Mn 2+ ions is demonstrated to be a quadrupole-quadrupole mechanism in terms of the experimental results and analysis of PL spectra and decay curves of the phosphors. The developed phosphors can be efficiently excited in the UV region and exhibit a tunable white-light emission, making them attractive as single-component white-light-emitting conversion phosphors for UV-based white LEDs. (orig.)

Spin-phonon and magnetostriction phenomena in CaMn7O12 helimagnet probed by Raman spectroscopy

International Nuclear Information System (INIS)

Nonato, A.; Araujo, B. S.; Ayala, A. P.; Maciel, A. P.; Yanez-Vilar, S.; Sanchez-Andujar, M.; Senaris-Rodriguez, M. A.; Paschoal, C. W. A.

2014-01-01

In this letter, we investigated the temperature-dependent Raman spectra of CaMn 7 O 12 helimagnet from room temperature down to 10 K. The temperature dependence of the Raman mode parameters shows remarkable anomalies for both antiferromagnetic and incommensurate transitions that this compound undergoes at low temperatures. The anomalies observed at the magnetic ordering transition indicate a spin-phonon coupling at higher-temperature magnetic transition in this material, while a magnetostriction effect at the lower-temperature magnetic transition

Magnetic properties of Nd-deficient manganites Nd0.9-xCaxMnOy

International Nuclear Information System (INIS)

Troyanchuk, I.O.; Khomchenko, V.A.; Pastushonok, S.N.; Novitsky, O.A.; Pavlov, V.I.; Szymczak, H.

2006-01-01

X-ray diffraction and magnetic studies of neodymium deficient Nd 0.9-x Ca x MnO y (0= 0.9 MnO y samples have been prepared in the 2.85= g -orbitals of manganese ions. Composition with y=2.85 is antiferromagnet with T N =85K, whereas for more oxidized Nd 0.9 MnO y samples a coexistence of antiferromagnetic and ferromagnetic phases is suggested. Low-temperature magnetic phase transition which is accompanied by a negative magnetization appearance has been found in the Nd 0.9 MnO 2.90 compound. Magnetic behavior of Nd 0.9-x Ca x MnO y (0.1= 1-x Ca x MnO 3 series. Properties of the Nd 0.9-x Ca x MnO y (0=< x=<0.4) solid solutions are in agreement with a hypothesis according to which a part of Nd ions can be substituted by Mn ions

Propiedades dieléctricas de láminas delgadas de (Pb,CaTiO3 con alto contenido de Ca

Directory of Open Access Journals (Sweden)

Calzada, M. L.

2004-04-01

Full Text Available Lead titanate thin films modified with calcium, Pb1-xCaxTiO3, with x>35%, have been deposited onto Pt/TiO2/SiO2/(100Si y Pt/(100MgO substrates, by the sol-gel method and a rapid thermal processing (RTP. Properties similar to the counterpart bulk ceramics are planned, such as the decrease of the phase transition temperature and the increase of permittivity at room temperature. Films with Ca content close to 40 % and 50% exhibit at room temperature, high enough permittivity with reduced temperature dependence and a C-V behaviour that make them of interest for DRAM and high frequency devices.Se han preparado láminas delgadas de titanato de plomo modificado con calcio, Pb1-xCaxTiO3, (PTCa con x>35%, depositadas sobre substratos de Pt/TiO2/SiO2/(100Si y Pt/(100MgO, empleando la técnica de sol-gel y un horno rápido de procesado (RTP. Se intenta obtener propiedades cercanas al material cerámico masivo, como son la bajada de la temperatura de la transición ferro-paraeléctrica y el aumento de la permitividad, ε´ a temperatura ambiente. Así, se consiguen láminas de contenido de Ca próximas al 40% y 50% con valores altos de permitividad, poco dependientes de la temperatura, que presentan un alto carácter difuso en la transición para temperaturas próxima a ambiente y un comportamiento de la capacidad con el voltaje, C-V,que las hacen de interés en la fabricación de DRAM y dispositivos para alta frecuencia.

Internal background build-up measurements in CaF2:Mn thermoluminescent dosimeters

International Nuclear Information System (INIS)

Balasybrahmanyam, V.; Measures, M.P.

1977-01-01

Some problems associated with the internal background build-up (IBB) of CaF 2 :Mn thermoluminescent dosimeters are reported. As a result of an investigation of batches of the EG and G model 15 dosimeter it is considered that measurements using this type of dosimeter are accurate and reproducible once the IBB has been determined. However, the use of the Manufacturer's claimed average of 0.064 mR/day can lead to erroneous results when determining environmental background dose rates. The authors therefore urge a rigid quality control program by the manufacturer and suggest that purchasers should be supplied with IBB information of each batch of dosimeters. Meanwhile each user should be aware of the IBB problem and be extremely cautious when using these dosimeters for environmental monitoring purposes. (U.K.)

New insights into organic-inorganic hybrid perovskite CH₃NH₃PbI₃ nanoparticles. An experimental and theoretical study of doping in Pb²⁺ sites with Sn²⁺, Sr²⁺, Cd²⁺ and Ca²⁺.

Science.gov (United States)

Navas, Javier; Sánchez-Coronilla, Antonio; Gallardo, Juan Jesús; Hernández, Norge Cruz; Piñero, Jose Carlos; Alcántara, Rodrigo; Fernández-Lorenzo, Concha; De los Santos, Desireé M; Aguilar, Teresa; Martín-Calleja, Joaquín

2015-04-14

This paper presents the synthesis of the organic-inorganic hybrid perovskite, CH3NH3PbI3, doped in the Pb(2+) position with Sn(2+), Sr(2+), Cd(2+) and Ca(2+). The incorporation of the dopants into the crystalline structure was analysed, observing how the characteristics of the dopant affected properties such as the crystalline phase, emission and optical properties. XRD showed how doping with Sn(2+), Sr(2+) and Cd(2+) did not modify the normal tetragonal phase. When doping with Ca(2+), the cubic phase was obtained. Moreover, DR-UV-Vis spectroscopy showed how the band gap decreased with the dopants, the values following the trend Sr(2+) Ca(2+) Cd(2+) > Sr(2+) for the tetragonal structure and Pb(2+) > Ca(2+) for the cubic phase. The electron localization function (ELF) analysis showed similar electron localizations for undoped and Sn(2+)-doped tetragonal structures, which were different from those doped with Sr(2+) and Cd(2+). Furthermore, when Cd(2+) was incorporated, the Cd-I interaction was strengthened. For Ca(2+) doping, the Ca-I interaction had a greater ionic nature than Cd-I. Finally, an analysis based on the non-covalent interaction (NCI) index is presented to determine the weak-type interactions of the CH3NH3 groups with the dopant and I atoms. To our knowledge, this kind of analysis with these hybrid systems has not been performed previously.

Effect of B-doping on the structural, magnetotransport and magnetocaloric properties of La0.67Ca0.33MnO3 compounds

International Nuclear Information System (INIS)

Kolat, V.S.; Gencer, H.; Gunes, M.; Atalay, S.

2007-01-01

In this study, the effect of Mn site substitution of B on the structural, electrical and magnetocaloric properties of manganites was investigated. Polycrystalline manganites with the chemical composition La 0.67 Ca 0.33 Mn 1-x B x O 3 (x = 0, 0.1, 0.2 and 0.3) were prepared by the standard solid-state process. It was found that the magnetisation, the Curie temperature and the maximum value of the magnetic entropy change |ΔS m | decrease with increasing concentration of B

Soft antiphase tilt of oxygen octahedra in the hybrid improper multiferroic Ca3Mn1.9Ti0.1O7

Science.gov (United States)

Ye, Feng; Wang, Jinchen; Sheng, Jieming; Hoffmann, C.; Gu, T.; Xiang, H. J.; Tian, Wei; Molaison, J. J.; dos Santos, A. M.; Matsuda, M.; Chakoumakos, B. C.; Fernandez-Baca, J. A.; Tong, X.; Gao, Bin; Kim, Jae Wook; Cheong, S.-W.

2018-01-01

We report a single crystal neutron and x-ray diffraction study of the hybrid improper multiferroic Ca3Mn1.9Ti0.1O7 (CMTO), a prototypical system where the electric polarization arises from the condensation of two lattice distortion modes. With increasing temperature (T ), the out-of-plane, antiphase tilt of MnO6 decreases in amplitude while the in-plane, in-phase rotation remains robust and experiences abrupt changes across the first-order structural transition. Application of hydrostatic pressure (P ) to CMTO at room temperature shows a similar effect. The consistent behavior under both T and P reveals the softness of antiphase tilt and highlights the role of the partially occupied d orbital of the transition-metal ions in determining the stability of the octahedral distortion. Polarized neutron analysis indicates the symmetry-allowed canted ferromagnetic moment is less than the 0.04 μB/Mn site, despite a substantial out-of-plane tilt of the MnO6 octahedra.

Magnetocaloric response of La 0.70 Ca 0.1 Sr 0.2 Fe 0.1 Mn 0.9 O 3 ...

Indian Academy of Sciences (India)

Home; Journals; Bulletin of Materials Science; Volume 38; Issue 1. Magnetocaloric response of La0.70Ca0.1Sr0.2Fe0.1Mn0.9O3 pervoskite for magnetic refrigeration. M S Anwar Faheem Ahmed Bon Heun Koo. Volume 38 Issue 1 February 2015 pp 101-104 ...

Phase equilibria melt-solid in the systems Pb-InSb-CaSb and Pb-InCs-GaAs

International Nuclear Information System (INIS)

Grebenyuk, A.M.; Charykov, N.A.; Puchkov, L.V.

1992-01-01

Results of experimental investigation and thermodynamic calculation of fusibility curves of Pb-InSb-GaSb and Pb-InAs-GaAs thernary systems, which haven't been investigated earlier, are presented. Fusibility curves of Pb-InSb-GaSb and Pb-InAs-GaAs systems contain two crystallization fields: solid solutions of In x Ga 1-x Sb and Pb, In x Ga 1-x As and Pb. The latter fields are retained against Pb figurative point and conform to 582 K < T < 593 K crystallization temperatures

CaMn(1-x)Nb(x)O3 (x < or = 0.08) perovskite-type phases as promising new high-temperature n-type thermoelectric materials.

Science.gov (United States)

Bocher, L; Aguirre, M H; Logvinovich, D; Shkabko, A; Robert, R; Trottmann, M; Weidenkaff, A

2008-09-15

Perovskite-type CaMn(1-x)Nb(x)O(3+/-delta) (x = 0.02, 0.05, and 0.08) compounds were synthesized by applying both a "chimie douce" (SC) synthesis and a classical solid state reaction (SSR) method. The crystallographic parameters of the resulting phases were determined from X-ray, electron, and neutron diffraction data. The manganese oxidations states (Mn(4+)/Mn(3+)) were investigated by X-ray photoemission spectroscopy. The orthorhombic CaMn(1-x)Nb(x)O(3+/-delta) (x = 0.02, 0.05, and 0.08) phases were studied in terms of their high-temperature thermoelectric properties (Seebeck coefficient, electrical resistivity, and thermal conductivity). Differences in electrical transport and thermal properties can be correlated with different microstructures obtained by the two synthesis methods. In the high-temperature range, the electron-doped manganate phases exhibit large absolute Seebeck coefficient and low electrical resistivity values, resulting in a high power factor, PF (e.g., for x = 0.05, S(1000K) = -180 microV K(-1), rho(1000K) = 16.8 mohms cm, and PF > 1.90 x 10(-4) W m(-1) K(-2) for 450 K 0.3) make these phases the best perovskitic candidates as n-type polycrystalline thermoelectric materials operating in air at high temperatures.

Magnetoresistive memory in phase-separated La0.5Ca0.5MnO3

Energy Technology Data Exchange (ETDEWEB)

Sacanell, J. [Departamento de Fisica, Unidad de Actividad Fisica-Centro Atomico de Constituyentes, CNEA, Av. Gral. Paz 1499, San Martin 1650, Pcia. de Buenos Aires (Argentina)]. E-mail: sacanell@cnea.gov.ar; Parisi, F. [Departamento de Fisica, Unidad de Actividad Fisica-Centro Atomico de Constituyentes, CNEA, Av. Gral. Paz 1499, San Martin 1650, Pcia. de Buenos Aires (Argentina); Levy, P. [Departamento de Fisica, Unidad de Actividad Fisica-Centro Atomico de Constituyentes, CNEA, Av. Gral. Paz 1499, San Martin 1650, Pcia. de Buenos Aires (Argentina); Ghivelder, L. [Instituto de Fisica, UFRJ, Rio de Janeiro (Brazil)

2004-12-31

We have studied a non-volatile memory effect in the mixed valent compound La0.5Ca0.5MnO3 induced by magnetic field (H). In a previous work (Phys. Rev. B 65 (2002) 104403), it has been shown that the response of this system upon application of H strongly depends on the temperature range, related to three well-differentiated regimes of phase separation occurring below 220K. In this work we compare memory capabilities of the compound, determined following two different experimental procedures for applying H, namely zero-field cooling and field cooling the sample. These results are analyzed and discussed within the scenario of phase separation.

Magnetoresistive memory in phase-separated La0.5Ca0.5MnO3

International Nuclear Information System (INIS)

Sacanell, J.; Parisi, F.; Levy, P.; Ghivelder, L.

2004-01-01

We have studied a non-volatile memory effect in the mixed valent compound La0.5Ca0.5MnO3 induced by magnetic field (H). In a previous work (Phys. Rev. B 65 (2002) 104403), it has been shown that the response of this system upon application of H strongly depends on the temperature range, related to three well-differentiated regimes of phase separation occurring below 220K. In this work we compare memory capabilities of the compound, determined following two different experimental procedures for applying H, namely zero-field cooling and field cooling the sample. These results are analyzed and discussed within the scenario of phase separation

Anomalous aging and strain induced time dependent phenomena in ultra-thin La0.65Ca0.35MnO3 films

International Nuclear Information System (INIS)

Egilmez, M.; Saber, M.M.; Abdelhadi, M.; Chow, K.H.; Jung, J.

2011-01-01

We have shown that ultra-thin La 0.65 Ca 0.35 MnO 3 films exhibit strong metastable behavior. The resistance can vary with time significantly, suggesting that a state of dynamic phase separation exists whereby one phase grows at the expense of another. Physical properties associated with the metastable behavior have been investigated on the films grown on different substrates. We have found that ultra-thin films age much faster than the thicker counterparts and more interestingly the metastability in the resistance of these films enhanced when aged. -- Highlights: → Ultra-thin La 0.67 Ca 0.33 MnO 3 films exhibit metastable behavior. → Physical properties associated with metastable behavior have been investigated. → The metastability in resistance of the films enhanced when films are aged. → Relaxation rates were used as a relative measure the metastability. → The metastable behavior is sensitive to the strain state of the film.

Oyonite, Ag3Mn2Pb4Sb7As4S24, a New Member of the Lillianite Homologous Series from the Uchucchacua Base-Metal Deposit, Oyon District, Peru

Directory of Open Access Journals (Sweden)

Luca Bindi

2018-05-01

Full Text Available The new mineral species oyonite, ideally Ag3Mn2Pb4Sb7As4S24, has been discovered in the Uchucchacua base-metal deposit, Oyon district, Catajambo, Lima Department, Peru, as very rare black metallic subhedral to anhedral crystals, up to 100 μm in length, associated with orpiment, tennantite/tetrahedrite, menchettiite, and other unnamed minerals of the system Pb-Ag-Sb-Mn-As-S, in calcite matrix. Its Vickers hardness (VHN100 is 137 kg/mm2 (range 132–147. In reflected light, oyonite is weakly to moderately bireflectant and weakly pleochroic from dark grey to a dark green. Internal reflections are absent. Reflectance values for the four COM wavelengths [Rmin, Rmax (% (λ in nm] are: 33.9, 40.2 (471.1; 32.5, 38.9 (548.3, 31.6, 38.0 (586.6; and 29.8, 36.5 (652.3. Electron microprobe analysis gave (in wt %, average of 5 spot analyses: Cu 0.76 (2, Ag 8.39 (10, Mn 3.02 (7, Pb 24.70 (25, As 9.54 (12, Sb 28.87 (21, S 24.30 (18, total 99.58 (23. Based on 20 cations per formula unit, the chemical formula of oyonite is Cu0.38Ag2.48Mn1.75Pb3.79Sb7.55As4.05S24.12. The main diffraction lines are (d in Å, hkl and relative intensity: 3.34 (−312; 40, 3.29 (−520; 100, 2.920 (−132; 40, 2.821 (−232; 70, 2.045 (004; 50. The crystal structure study revealed oyonite to be monoclinic, space group P21/n, with unit-cell parameters a = 19.1806 (18, b = 12.7755 (14, c = 8.1789 (10 Å, β = 90.471 (11°, V = 2004.1 (4 Å3, Z = 2. The crystal structure was refined to a final R1 = 0.032 for 6272 independent reflections. Oyonite belongs to the Sb-rich members of the andorite homeotypic sub-series within the lillianite homologous series. The name oyonite is after the Oyon district, Lima Department, Peru, the district where the type locality (Uchucchacua mine is located.

Antisite-disorder driven large exchange bias effect in phase separated La{sub 1.5}Ca{sub 0.5}CoMnO{sub 6} double perovskite

Energy Technology Data Exchange (ETDEWEB)

Sahoo, R.C.; Paladhi, D. [Department of Physics, Indian Institute of Technology Kharagpur, West Bengal 721302 (India); Dasgupta, Papri; Poddar, A. [Experimental Condensed Matter Physics Division, Saha Institute of Nuclear Physics, West Bengal (India); Singh, Ripandeep; Das, A. [Solid State Physics Division, Bhabha Atomic Research Centre, Mumbai 400085 (India); Nath, T.K., E-mail: tnath@phy.iitkgp.ernet.in [Department of Physics, Indian Institute of Technology Kharagpur, West Bengal 721302 (India)

2017-04-15

Investigations of structural and magnetic properties of polycrystalline hole doped double perovskite La{sub 1.5}Ca{sub 0.5}CoMnO{sub 6} has clearly revealed the existence of structural antisite-disorder (either, Co–O–Co or Mn–O–Mn) in the system. The ordering of Co{sup 2+} and Mn{sup 4+} gives rise to a ferromagnetic transition around 157 K. A spin-canted antiferromagnetic transition is found in this material at T{sub CAFM} ~9 K. The effect of antisite-disorder in the double perovskite structure is most likely the prime reason for antiferromagnetic interaction. The temperature dependent inverse susceptibility exhibits Curie-Weiss like behaviour and it yields an effective paramagnetic moment of 6.49 μ{sub B}. At very low temperature (TCa{sub 0.5}CoMnO{sub 6} mainly on the basis of uncompensated interface spins. - Highlights: • Large exchange bias (EB) effect has been observed in 25% Ca doped La{sub 2}CoMnO{sub 6} antisite-disordered system. • Neutron powder diffraction analysis clearly suggested canted antiferromagnetic spin ordering at low temperature in our phase separated system. • A phenomenological model has been proposed for experimental results. • The results may be useful to acquire enough information about exchange biased interfaces for various magnetic device applications.

Magnetic properties of CaCu{sub 5}-type RNi{sub 3}TSi (R=Gd and Tb, T=Mn, Fe, Co and Cu) compounds

Energy Technology Data Exchange (ETDEWEB)

Morozkin, A.V., E-mail: morozkin@tech.chem.msu.ru [Department of Chemistry, Moscow State University, Leninskie Gory, House 1, Building 3, GSP-2, Moscow 119992 (Russian Federation); Knotko, A.V. [Department of Chemistry, Moscow State University, Leninskie Gory, House 1, Building 3, GSP-2, Moscow 119992 (Russian Federation); Yapaskurt, V.O. [Department of Petrology, Geological Faculty, Moscow State University, Leninskie Gory, Moscow 119992 (Russian Federation); Yao, Jinlei [Research Center for Solid State Physics and Materials, School of Mathematics and Physics, Suzhou University of Science and Technology, Suzhou 215009 (China); Yuan, Fang; Mozharivskyj, Y. [Department of Chemistry and Chemical Biology, McMaster University, 1280 Main Street West, Hamilton, Ontario, Canada L8S 4M1 (Canada); Nirmala, R. [Indian Institute of Technology Madras, Chennai 600036 (India); Quezado, S.; Malik, S.K. [Departamento de Física Teórica e Experimental, Universidade Federal do Rio Grande do Norte, Natal 59082-970 (Brazil)

2015-12-15

Magnetic properties and magnetocaloric effect of CaCu{sub 5}-type RNi{sub 3}TSi (R=Gd and Tb, T=Mn, Fe, Co and Cu) compounds have been investigated. Magnetic measurements of RNi{sub 3}TSi display the increasing of Curie temperature and the decreasing of magnetocaloric effect and saturated magnetic moment in the row of ‘RNi{sub 3}CuSi–RNi{sub 3}NiSi–RNi{sub 3}CoSi–RNi{sub 3}MnSi–RNi{sub 3}FeSi’. In contrast to GdNi{sub 3}{Mn, Fe, Co}Si, TbNi{sub 3}{Mn, Fe, Co}Si exhibit significant magnetic hysteresis. The coercive field increases from TbNi{sub 4}Si (~0.5 kOe) to TbNi{sub 3}CoSi (4 kOe), TbNi{sub 3}MnSi (13 kOe) and TbNi{sub 3}FeSi (16 kOe) in field of 50 kOe at 5 K, whereas TbNi{sub 3}CuSi exhibits a negligible coercive field. - Graphical abstract: Magnetic measurements of RNi{sub 3}TSi show the increasing of Curie temperature and the decreasing of magnetocaloric effect and saturated magnetic moment in the row of 'RNi{sub 3}CuSi–RNi{sub 3}NiSi–RNi{sub 3}CoSi–RNi{sub 3}MnSi–RNi{sub 3}FeSi'. In contrast to GdNi{sub 3}{Mn, Fe, Co}Si, TbNi{sub 3}{Mn, Fe, Co}Si exhibit significant magnetic hysteresis. The coercive field increases from TbNi{sub 4}Si (~0.5 kOe) to TbNi{sub 3}CoSi (4 kOe), TbNi{sub 3}MnSi (13 kOe) and TbNi{sub 3}FeSi (16 kOe) in field of 50 kOe at 5 K, whereas TbNi{sub 3}CuSi exhibits a negligible coercive field. - Highlights: • CaCu{sub 5}-type RNi{sub 3}TSi show ferromagnetic ordering (R=Gd, Tb, T=Mn–Co, Cu). • Curie point increases in ‘RNi{sub 3}CuSi–RNi{sub 3}NiSi–RNi{sub 3}CoSi–RNi{sub 3}MnSi–RNi{sub 3}FeSi’ row. • MCE decreases in ‘RNi{sub 3}CuSi–RNi{sub 3}NiSi–RNi{sub 3}CoSi–RNi{sub 3}MnSi–RNi{sub 3}FeSi’ row. • TbNi{sub 3}{Mn, Fe, Co}Si exhibit significant magnetic hysteresis. • The coercive field of TbNi{sub 3}MnSi and TbNi{sub 3}FeSi reach 13 kOe and 16 kOe at 5 K.

Stress relaxation of La1/2Sr1/2MnO3 and La2/3Ca1/3MnO3 at solid oxide fuel cell interfaces

International Nuclear Information System (INIS)

Lussier, A.; Dvorak, J.; Stadler, S.; Holroyd, J.; Liberati, M.; Arenholz, E.; Ogale, S.B.; Wu, T.; Venkatesan, T.; Idzerda, Y.U.

2008-01-01

Interfacial stress is thought to have significant effects on electrical and oxygen transport properties in thin films of importance in solid oxide fuel cell applications. We investigate how in-plane biaxial stress modifies the electronic structure of La 2/3 Ca 1/3 MnO 3 and La 1/2 Sr 1/2 MnO 3 thin films prepared by pulsed laser deposition on three different substrates to vary the in-plane stress from tensile to compressive. The electronic structure was probed by X-ray absorption spectroscopy of the Mn L 2,3 -edge to characterize the interfacial disruption in this region in an element-specific, site-specific manner. The compressive or tensile interfacial strain modifies the relative concentrations of La and Sr in the interfacial region in order to achieve a better lattice match to the contact material. This atomic migration generates an interfacial region dominated by a compound with a single valency for the transition metal ion, resulting in a severe barrier to oxygen and electron transport through this region

On the novel double perovskites A2Fe(Mn0.5W0.5)O6 (A= Ca, Sr, Ba). Structural evolution and magnetism from neutron diffraction data

Science.gov (United States)

García-Ramos, Crisanto A.; Larrégola, Sebastián; Retuerto, María; Fernández-Díaz, María Teresa; Krezhov, Kiril; Alonso, José Antonio

2018-06-01

New A2Fe(Mn0.5W0.5)O6 (A = Ca, Sr, Ba) double perovskite oxides have been prepared by ceramic techniques. X-ray diffraction (XRD) complemented with neutron powder diffraction (NPD) indicate a structural evolution from monoclinic (space group P21/n) for A = Ca to cubic (Fm-3m) for A = Sr and finally to hexagonal (P63/mmc) for A = Ba as the perovskite tolerance factor increases with the A2+ ionic size. The three oxides present different tilting schemes of the FeO6 and (Mn,W)O6 octahedra. NPD data also show evidence in all cases of a considerable anti-site disordering, involving the partial occupancy of Fe positions by Mn atoms, and vice-versa. Magnetic susceptibility data show magnetic transitions below 50 K characterized by a strong irreversibility between ZFC and FC susceptibility curves. The A = Ca perovskite shows a G-type magnetic structure, with weak ordered magnetic moments due to the mentioned antisite disordering. Interesting magnetostrictive effects are observed for the Sr perovskite below 10 K.

Cation Effects on the Layer Structure of Biogenic Mn-Oxides

Energy Technology Data Exchange (ETDEWEB)

Zhu, M.; Ginder-Vogel, M; Parikh, S; Feng, X; Sparks, D

2010-01-01

Biologically catalyzed Mn(II) oxidation produces biogenic Mn-oxides (BioMnO{sub x}) and may serve as one of the major formation pathways for layered Mn-oxides in soils and sediments. The structure of Mn octahedral layers in layered Mn-oxides controls its metal sequestration properties, photochemistry, oxidizing ability, and topotactic transformation to tunneled structures. This study investigates the impacts of cations (H{sup +}, Ni(II), Na{sup +}, and Ca{sup 2+}) during biotic Mn(II) oxidation on the structure of Mn octahedral layers of BioMnO{sub x} using solution chemistry and synchrotron X-ray techniques. Results demonstrate that Mn octahedral layer symmetry and composition are sensitive to previous cations during BioMnO{sub x} formation. Specifically, H{sup +} and Ni(II) enhance vacant site formation, whereas Na{sup +} and Ca{sup 2+} favor formation of Mn(III) and its ordered distribution in Mn octahedral layers. This study emphasizes the importance of the abiotic reaction between Mn(II) and BioMnO{sub x} and dependence of the crystal structure of BioMnO{sub x} on solution chemistry.

Magnetoelastic effects in La{sub 0.7}Sr{sub 0.3−x}Ca{sub x}MnO{sub 3} nanocrystalline perovskites

Energy Technology Data Exchange (ETDEWEB)

Tabatabai Yazdi, Sh., E-mail: sh_tabatabai3@yahoo.com [Department of Physics, Faculty of Sciences, Ferdowsi University of Mashhad, Mashhad 91755-1436 (Iran, Islamic Republic of); Iranmanesh, P. [Department of Physics, Vali-e-Asr University of Rafsanjan, 77139-36417 Rafsanjan (Iran, Islamic Republic of)

2014-09-01

La{sub 0.7}Sr{sub 0.3−x}Ca{sub x}MnO{sub 3} (x=0, 0.1, 0.2 and 0.3) nanoparticles, prepared by sol–gel method, were studied by means of X-ray diffraction, transmission electron microscopy, thermal expansion and magnetostriction measurements. It was revealed that samples of low Ca concentration (x≤0.1) crystallize in rhombohedral perovskite structure with R-3c space group, and by increasing x, smaller Ca radius causes the lattice to convert to orthorhombic structure (space group of Pbnm). The results exhibit an anomalous behavior in the thermal expansion behavior of all samples, as well as temperature dependence of their volume magnetostriction being related to the presence of a conductive magnetic two-phase state at temperatures higher than T{sub C}. Moreover, the magnitude of this magnetovolume effect increases with x due to smaller Ca size, which softens the crystal lattice. The results show that Ca substitution results in weakening the double-exchange interaction and consequently reducing T{sub C}, as well as decreasing the magnetic anisotropy. Furthermore, our nanocrystalline samples have a relatively lower T{sub C}, compared with the reported values for similar compounds with larger particle size. Among them, the sample with x=0.2 possess T{sub C} value of about room temperature; to say by partial substitution of Ca for Sr we succeeded in adjusting the transition temperature of this series of manganites which was a main motivation for this research. - Highlights: • Magnetoelastic properties of La{sub 0.7}Sr{sub 0.3−x}Ca{sub x}MnO{sub 3} nanocrystalline samples are investigated. • Substitution of Sr by Ca causes structure to convert from rhombohedral to orthorhombic perovskite. • Considerable magnetovolume anomalies are revealed due to presence of conductive MTPS above T{sub C}. • Ca softens the crystal lattice and intensifies the magnetovolume effects. • Ca reduces T{sub C} and magnetic anisotropy of compounds by weakening DE interactions.

Pb-Pb dating of individual chondrules from the CB_a chondrite Gujba

DEFF Research Database (Denmark)

Bollard, Jean Francois André; Connelly, James; Bizzarro, Martin

2015-01-01

-stage impact origin. Here, we report high-precision internal isochrons for four individual chondrules of the Gujba chondrite to probe the formation history of CB chondrites and evaluate the concordancy of relevant short-lived radionuclide chronometers. All four chondrules define a brief formation interval......-behaved Pb-Pb systematics of all four chondrules, a precise formation age and the concordancy of the Mn-Cr, Hf-W, and I-Xe short-lived radionuclide relative chronometers, we propose that Gujba may serve as a suitable time anchor for these systems....

Magnetic, transport, and optical properties of Ca{sub 0.85}Eu{sub 0.15}MnO{sub 3} single crystal

Energy Technology Data Exchange (ETDEWEB)

Naumov, S.V., E-mail: naumov@imp.uran.ru [Institute of Metal Physics, Ural Branch of RAS, Kovalevskaya Street 18, Ekaterinburg 620990 (Russian Federation); Loshkareva, N.N.; Mostovshchikova, E.V.; Solin, N.I.; Korolev, A.V.; Arbuzova, T.I.; Telegin, S.V.; Patrakov, E.I. [Institute of Metal Physics, Ural Branch of RAS, Kovalevskaya Street 18, Ekaterinburg 620990 (Russian Federation)

2013-01-01

Magnetic, transport and optical properties of the Ca{sub 0.85}Eu{sub 0.15}MnO{sub 3} single crystal are studied and discussed in comparison with the properties of polycrystalline sample. The magnetic data show existence the two magnetic phase transitions under cooling: the transition near 150 K occurs from the paramagnetic orthorhombic to C-type antiferromagnetic monoclinic phase with the charge/orbital ordering in some part of the crystal; and at 90 K the transition from the paramagnetic to G-type antiferromagnetic phase takes place in another part of the crystal with the orthorhombic structure. The magnetoresistance of the Ca{sub 0.85}Eu{sub 0.15}MnO{sub 3} single crystal has features at temperatures of these phase transitions. Differences in the properties of single crystal and polycrystalline sample with the same content of Eu are associated with the ordering of oxygen vacancies that appear under the crystal growth. The reflection spectra in infrared range confirm the existence of the electron conductivity in a narrow band at room temperature.

Magnetic and magnetocaloric properties of La{sub 0.7}Ca{sub 0.3}Mn{sub 1−x}Zn{sub x}O{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Ho, T.A. [Department of Materials Science and Engineering, Korea University, Seoul 02841 (Korea, Republic of); Lim, S.H., E-mail: sangholim@korea.ac.kr [Department of Materials Science and Engineering, Korea University, Seoul 02841 (Korea, Republic of); Tho, P.T.; Phan, T.L. [Department of Physics and Oxide Research Center, Hankuk University of Foreign Studies, Yongin 17035 (Korea, Republic of); Yu, S.C. [Department of Physics, Chungbuk National University, Cheongju 28644 (Korea, Republic of)

2017-03-15

The magnetic Mn{sup 3+} ions in La{sub 0.7}Ca{sub 0.3}MnO{sub 3} are partially replaced by nonmagnetic Zn{sup 2+} ions to form La{sub 0.7}Ca{sub 0.3}Mn{sub 1−x}Zn{sub x}O{sub 3} compounds (x=0.0, 0.06, 0.08, and 0.1), and their magnetic and magnetocaloric properties are investigated. The Curie temperature decreases drastically from 245 to 70 K as x increases from 0 to 0.1. An analysis using the Banerjee's criterion of the experimental results for magnetization as a function of temperature and magnetic field indicates that the first-to-second order magnetic phase transformation occurs at a threshold composition of x=0.06, which is further supported by the universal curves of the normalized entropy change versus reduced temperature. The maximum magnetic entropy change measured at a magnetic field span of 50 kOe, which occurs near the Curie temperature, decreases from 10.30 to 2.15 J/kg K with the increase of x from 0.0 to 0.1. However, the relative cooling power, an important parameter for practical applications, shows a maximum value of 404 J/kg at x=0.08, which is 1.5 times greater than that observed for the undoped sample. - Highlights: • Magnetic and MCE of La{sub 0.7}Ca{sub 0.3}Mn{sub 1−x}Zn{sub x}O{sub 3} are investigated. • Order of magnetic phase transition is dependent on the Zn doping concentration. • Although the |∆S{sub max}| decreases with increasing x, RCP increase remarkably.

Analysis of (Ba,Ca,Sr){sub 3}MgSi{sub 2}O{sub 8}:Eu{sup 2+}, Mn{sup 2+} phosphors for application in solid state lighting

Energy Technology Data Exchange (ETDEWEB)

Han, J.K. [University of California, San Diego, Materials Science and Engineering Program, La Jolla, CA 92093 (United States); Piqutte, A.; Hannah, M.E. [OSRAM SYLVANIA Central Research, 71 Cherry Hill Drive Beverly, MA 01915 (United States); Hirata, G.A. [Centro de Nanociencias y Nanotecnolgía, Universidad Nacional Autónoma de México, Km. 107 Carretera Tijuana-Ensenada Apdo, Ensenada MX CP 22860 (Mexico); Talbot, J.B. [University of California, San Diego, Materials Science and Engineering Program, La Jolla, CA 92093 (United States); University of California, San Diego, Department of Nanoengineering, La Jolla, CA 92093 (United States); Mishra, K.C. [OSRAM SYLVANIA Central Research, 71 Cherry Hill Drive Beverly, MA 01915 (United States); McKittrick, J., E-mail: jmckittrick@ucsd.edu [University of California, San Diego, Materials Science and Engineering Program, La Jolla, CA 92093 (United States); University of California, San Diego, Department of Mechanical and Aerospace Engineering, La Jolla, CA 92093 (United States)

2014-04-15

The luminescence properties of Eu{sup 2+} and Mn{sup 2+} co-activated (Ba,Ca,Sr){sub 3}MgSi{sub 2}O{sub 8} phosphors prepared by combustion synthesis were studied. Eu{sup 2+}-activated (Ba,Ca,Sr){sub 3}MgSi{sub 2}O{sub 8} has a broad blue emission band centered at 450–485 nm and Eu{sup 2+}–Mn{sup 2+}-activated (Ba,Ca,Sr){sub 3}MgSi{sub 2}O{sub 8} exhibits a red emission around 620–703 nm, depending on the relative concentrations of Ba, Ca and Sr. The particle size of Eu{sup 2+} and Mn{sup 2+} co-activated (Ba,Ca){sub 3}MgSi{sub 2}O{sub 8} ranges from 300 nm to 1 μm depending on the metal ion and are agglomerated due to post-synthesis, high temperature annealing. The green emission of Ba{sub 3}MgSi{sub 2}O{sub 8} originates from secondary phases (Ba{sub 2}SiO{sub 4} and BaMgSiO{sub 4}) confirmed by emission spectra and X-ray diffraction patterns. The secondary phases of Ba{sub 3}MgSi{sub 2}O{sub 8} are removed by the addition of Sr. The quantum efficiencies range from 45% to 70% under 400 nm excitation and the lifetime of red emission of Ba{sub 3}MgSi{sub 2}O{sub 8} decreases significantly with increasing temperature, which is 54% at 400 K of that at 80 K compared to that of blue emission (90% at 400 K of that at 80 K). -- highlights: • (Ba,Ca,Sr){sub 3}MgSi{sub 2}O{sub 8}:Eu{sup 2+}, Mn{sup 2+} phosphors were prepared by a combustion synthesis method. • The emission spectra consist of broad blue-emission band and red-emission band. • The quantum efficiencies range between 45% and 70%, depending on the relative concentrations of Ba, Ca and Sr. • The secondary phases were eliminated by additions of Sr. • Lifetime of the red-emission decreases with increasing temperature, suggesting that these phosphors are not useful for solid state lighting applications.

Magnetic, electronic, dielectric and optical properties of Pr(Ca:Sr)MnO 3

Science.gov (United States)

Sichelschmidt, J.; Paraskevopoulos, M.; Brando, M.; Wehn, R.; Ivannikov, D.; Mayr, F.; Pucher, K.; Hemberger, J.; Pimenov, A.; Krug von Nidda, H.-A.; Lunkenheimer, P.; Ivanov, V. Yu.; Mukhin, A. A.; Balbashov, A. M.; Loidl, A.

2001-03-01

The charge-ordered perovskite Pr0.65Ca0.28Sr0.07MnO3 was investigated by means of magnetic susceptibility, specific heat, dielectric and optical spectroscopy and electron-spin resonance techniques. Under moderate magnetic fields, the charge order melts yielding colossal magnetoresistance effects with changes of the resistivity over eleven orders of magnitude. The optical conductivity is studied from audio frequencies far into the visible spectral regime. Below the phonon modes hopping conductivity is detected. Beyond the phonon modes the optical conductivity is explained by polaronic excitations out of a bound state. ESR techniques yield detailed informations on the (H,T ) phase diagram and reveal a broadening of the linewidth which can be modeled in terms of activated polaron hopping.