Crystal structure of 5,7,12,14-tetrahydro-5,14:7,12-bis([1,2]benzenopentacene-6,13-dione

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Mohammad Nozari

2016-12-01

Full Text Available The lattice of 5,7,12,14-tetrahydro-5,14:7,12-bis([1,2]benzenopentacene-6,13-dione, C34H20O2, at 173 K has triclinic (P-1 symmetry and crystallizes with four independent half-molecules in the asymmetric unit. Each molecule is generated from a C17H10O substructure through an inversion center at the centroid of the central quinone ring, generating a wide H-shaped molecule, with a dihedral angle between the mean planes of the terminal benzene rings in each of the two symmetry-related pairs over the four molecules of 68.6 (1 (A, 65.5 (4 (B, 62.3 (9 (C, and 65.8 (8° (D, an average of 65.6 (1°. This compound has applications in gas-separation membranes constructed from polymers of intrinsic microporosity (PIM. The title compound is a product of a double Diels–Alder reaction between anthracene and p-benzoquinone followed by dehydrogenation. It has also been characterized by cyclic voltammetry and rotating disc electrode polarography, FT–IR, high resolution mass spectrometry, elemental analysis, and 1H NMR.

Optical, ferroelectric and magnetic properties of multiferroelectric BiFeO3-(K0.5Na0.5)0.4(Sr 0.6Ba0.4)0.8Nb2O6 thin films

KAUST Repository

Yao, Yingbang

2014-02-01

Multiferroic BiFeO3-(K0.5Na0.5) 0.4(Sr0.6Ba0.4)0.8Nb 2O6 (BFO-KNSBN) trilayer thin films, were epitaxially grown on MgO(0 0 1) and SrTiO3(0 0 1) by using pulsed laser deposition (PLD). Their ferroelectric, magnetic, dielectric and optical properties were investigated. It was found that both ferroelectric polarization and dielectric constant of the films were enhanced by introducing KNSBN as a barrier layer. Meanwhile, ferromagnetism of BFO was maintained. More interestingly, a double hysteresis magnetic loop was observed in the KNSBN-BFO-KNSBN trilayer films, where exchange bias and secondary phase in the BFO layer played crucial roles. Interactions between adjacent layers were revealed by temperature-dependent Raman spectroscopic measurements. © 2013 Elsevier B.V. All rights reserved.

6-[N,S-dimethyl-N'-cyanothioureidomethyl]-6,11-dihydro-5H- dibenz[b,e]azepine hydrochloride (Fran 12): a histamine and 5-hydroxytryptamine antagonist with pressor properties.

Science.gov (United States)

Law, S C; Guyett, F J; King, R G; Boura, A L; Jackson, W R; Hodgson, W C

1992-01-01

We have synthesized and examined some of the pharmacological properties of 6-[N,S-dimethyl-N'-cyanoisothioureidomethyl]-6,11-dihydro-5H- dibenz(b,e)azepine hydrochloride (Fran 12), a derivative of 6-methylaminomethyl-6,11-dihydro-5H- dibenz[b,e,]azepine. In the guinea-pig isolated ileum, Fran 12 (10(-7)-10(-5) M) caused parallel rightward shifts of the concentration-response curves to histamine. A Schild plot gave a pA2 of 7.48, with a slope not significantly different from -1.0. In the rat stomach fundus strip and in endothelium-denuded aortic rings, Fran 12 inhibited contractile responses to 5-hydroxytryptamine in a non-competitive manner. In both chloralose-anaesthetized and pithed rats, it inhibited pressor responses to 5-hydroxytryptamine. It had no effect on depressor responses to 5-hydroxytryptamine in anaesthetized rats. In pithed rats, Fran 12 (0.25-2 mg/kg, i.v.) produced dose-dependent increases in blood pressure. These were not inhibited by i.v. phentolamine, prazosin, yohimbine, propranolol, methysergide, pentolinium or atropine but were inhibited by verapamil. These results indicate that Fran 12 is a histamine and 5-hydroxytryptamine antagonist which also exerts pressor effects via a peripheral action. The pressor action does not appear to be mediated via effects on alpha 1- or alpha 2-adrenoceptors, muscarinic or nicotinic cholinoceptors or 5-hydroxytryptamine receptors, although calcium channel activation may play a role.

Magnetoelectric effect of (1-x) Ba0.5Sr0.5Zr0.5Ti0.5O3+(x) Ni0.12Mg0.18Cu0.2Zn0.5Fe2O4 composites

Science.gov (United States)

Rahaman, Md. D.; Saha, S. K.; Ahmed, T. N.; Saha, D. K.; Hossain, A. K. M. Akther

2014-12-01

The magnetoelectric composites with chemical compositions (1-x) Ba0.5Sr0.5Zr0.5Ti0.5O3+(x) Ni0.12Mg0.18Cu0.2Zn0.5Fe2O4 (x=20, 40, 60 and 80 wt%) was prepared by the conventional solid state reaction method. The presence of a biphase composition was confirmed by X-ray diffraction while the microstructure of the composites was studied by scanning electron microscopy revealing a good mixing of the two phases and a good densification of the bulk ceramics. The dielectric dispersion is observed at lower frequencies due to interfacial polarization arising from the interface of the two phases. At higher frequencies, the dielectric constant is almost constant due to the inability of electric dipoles to follow the first variation of the alternating applied electric field. The dielectric loss shows maxima which are attributed when the hopping frequency of electrons between different ionic sites becomes nearly equal to the frequency of the applied field. The linearity in the log(σAC) vs. log(ω2) plots confirmed the small polaron hopping type of conduction mechanism. The composite materials are found to exhibit an excellent frequency dependence of magnetic properties. In the high frequency range, with increasing ferrite concentration the initial permeability increases and cut-off frequency decreases. An optimal magnetoelectric coupling responding voltage of about 600 μV cm-1 Oe-1 is obtained for x=20 wt% at room temperature.

5 CFR 2429.12 - Service of process and papers by the Authority.

Science.gov (United States)

2010-01-01

... 5 Administrative Personnel 3 2010-01-01 2010-01-01 false Service of process and papers by the... REQUIREMENTS Miscellaneous § 2429.12 Service of process and papers by the Authority. (a) Methods of service... COUNSEL OF THE FEDERAL LABOR RELATIONS AUTHORITY AND FEDERAL SERVICE IMPASSES PANEL FEDERAL LABOR...

Photoluminescence and scintillation properties of Ce-doped Sr2(Gd1-xLux)8(SiO4)6O2 (x = 0.1, 0.2, 0.4, 0.5, 0.6) crystals

Science.gov (United States)

Igashira, Takuya; Kawano, Naoki; Okada, Go; Kawaguchi, Noriaki; Yanagida, Takayuki

2018-05-01

Apatite crystals with chemical compositions of 0.5% Ce-doped Sr2(Gd1-xLux)8(SiO4)6O2 (x = 0.1, 0.2, 0.4, 0.5, 0.6) were synthesized by the Floating Zone method, and then we evaluated their photoluminescence (PL) and scintillation properties. All the Ce-doped samples exhibited PL and scintillation with an intense broad emission in 400-550 nm in which the origin was attributed to the 5d-4f transition of Ce3+, and the emission peak became broader with increasing the concentration of Lu3+. Both PL and scintillation decay time profiles were best-approximated by a sum of two exponential decay functions, and the origin of slower component was attributed to the 5d-4f transition of Ce3+. In the X-ray induced afterglow measurements, the Ce-doped Sr2(Gd0.4Lu0.6)8(SiO4)6O2 sample exhibited the lowest afterglow level. Furthermore, the Ce-doped Sr2(Gd0.5Lu0.5)8(SiO4)6O2 and Sr2(Gd0.4Lu0.6)8(SiO4)6O2 samples showed a clear full energy deposited peak under 5.5 MeV 241Am α-ray irradiation, and the estimated absolute scintillation light yields were around 290 and 1300 ph/5.5 MeV-α, respectively.

Bimatoprost 0.03%/timolol 0.5% preservative-free ophthalmic solution versus bimatoprost 0.03%/timolol 0.5% ophthalmic solution (Ganfort) for glaucoma or ocular hypertension: a 12-week randomised controlled trial

Science.gov (United States)

Goldberg, Ivan; Gil Pina, Rafael; Lanzagorta-Aresti, Aitor; Schiffman, Rhett M; Liu, Charlie; Bejanian, Marina

2014-01-01

Aim To compare the efficacy and safety of single-dose bimatoprost 0.03%/timolol 0.5% preservative-free (PF) ophthalmic solution with bimatoprost 0.03%/timolol 0.5% ophthalmic solution in patients with open-angle glaucoma or ocular hypertension. Methods In this multicentre, randomised, parallel-group study, patients were randomised to bimatoprost/timolol PF or bimatoprost/timolol once daily in the morning for 12 weeks. Primary efficacy endpoints, reflecting differing regional regulatory requirements, included change from baseline in worse eye intraocular pressure (IOP) in the per-protocol population at week 12, and the average eye IOP at weeks 2, 6 and 12 in the intent-to-treat population. Results 561 patients were randomised (278 to bimatoprost/timolol PF; 283 to bimatoprost/timolol); 96.3% completed the study. Both treatment groups showed statistically and clinically significant mean decreases from baseline in worse eye IOP and in average eye IOP at all follow-up time points (p<0.001). Bimatoprost/timolol PF met all pre-established criteria for non-inferiority and equivalence to bimatoprost/timolol. Ocular adverse events were similar between treatment groups, with conjunctival hyperaemia being the most frequent. Most were mild or moderate in severity. Conclusions Bimatoprost/timolol PF demonstrated non-inferiority and equivalence in IOP lowering compared with bimatoprost/timolol, with no significant differences in safety and tolerability. Trial registration number NCT01177098. PMID:24667994

Assessment of ocular hypotensive effect and safety 12 months after changing from an unfixed combination to a latanoprost 0.005% + timolol maleate 0.5% fixed combination.

Science.gov (United States)

Inoue, Kenji; Okayama, Ryoko; Higa, Risako; Wakakura, Masato; Tomita, Goji

2012-01-01

Latanoprost 0.005% + timolol maleate 0.5% combined eyedrops were recently made available in Japan. We prospectively investigated the intraocular pressure (IOP)-lowering effect, visual preservation effect, and adverse reactions of a one-year administration of this fixed combination. The subjects included 162 eyes from 162 patients diagnosed with either primary open-angle glaucoma or ocular hypertension and using an unfixed combination of latanoprost 0.005% and timolol maleate 0.5%. The unfixed combination was discontinued and replaced with the latanoprost 0.005% + timolol maleate 0.5% fixed combination with no washout period. IOP was measured before (baseline) and 3, 6, 9, and 12 months after the change. The mean deviation value of Humphrey field analysis was compared. Adverse reactions were examined at every follow-up. No significant differences were found between mean IOP values obtained at baseline (mean ± standard deviation, 15.2 ± 3.3 mmHg) 3 months (15.1 ± 3.2 mmHg), 6 months (15.3 ± 3.1 mmHg), 9 months (15.3 ± 3.1 mmHg), and 12 months (15.1 ± 3.2 mmHg) after the change from the unfixed to the fixed combination of eyedrops (P = 0.212). In addition, no significant differences were observed between mean deviation values obtained at baseline (-9.11 ± 6.94 dB) and 12 months (-10.08 ± 7.24 dB) after the change (P = 0.114). Thirty-one patients discontinued the fixed combination within 12 months of replacement, due to an insufficient IOP decrease (20 patients, 12.3%) and adverse reactions (11 patients, 6.8%). Following replacement of two eyedrop medications (latanoprost 0.005% and timolol maleate 0.5%) by one fixed combination (latanoprost 0.005% + timolol maleate 0.5%), IOP and visual field were preserved. However, 20% of the patients discontinued the new treatment because of an insufficient IOP decrease and complaints of adverse reactions.

Perovskites A/sub 2/sup(II)Bsub(0. 5)sup(I)Bsub(0. 5)sup(III)Wsup(VI)O/sub 6/

Energy Technology Data Exchange (ETDEWEB)

Roller, H; Kemmler-Sack, S [Tuebingen Univ. (Germany, F.R.). Inst. fuer Chemie

1978-05-01

Compounds of type A/sub 2/sup(II)Bsub(0.5)sup(I)Bsub(0.5)sup(III)Wsup(VI)O/sub 6/ can be obtained with Asup(II) = Ba; Bsup(I) = Li, Na and Bsup(III) = La, Nd, Sm, Gd, Y, In, Sc just as with Asup(II) = Sr; Bsup(I) = Li and Bsup(III) = La, Nd, Sm, Gd, Y, In (all cubic ordered perovskites). For the cubic perovskites Sr/sub 2/Nasub(0.5)Lasub(0.5)WO/sub 6/ and Sr/sub 2/Nasub(0.5)Ndsub(0.5)WO/sub 6/ additional superlattice reflections are observed (a approximately equal to 16.4 A). The compounds Sr/sub 2/Nasub(0.5)Bsub(0.5)sup(III)WO/sub 6/ crystallize with Bsup(III) = Sm, Gd in a monoclinic and with Bsup(III) = Y, In in a rhombic distorted perovskite lattice. For the perovskites with A = Sr - dependent on ionic radii of the B ions - two different lattice types are present.

Synthesis and electrochemical properties of LiNi0.4Mn1.5Cr0.1O4 and Li4Ti5O12

CSIR Research Space (South Africa)

Liu, GQ

2011-08-01

Full Text Available Spinel compound LiNi0.4Mn1.5Cr0.1O4 (LNMCO) and Li4Ti5O12 (LTO) were synthesized by the sol-gel method and the solid-state method, respectively. The particle sizes of the products LiNi0.4Mn1.5Cr0.1O4 and Li4Ti5O12 were 0.5 to 2 um and 0.5 to 0.8 um...

Various properties of the 0.6BaTiO3–0.4Ni0.5Zn0.5Fe2O4 ...

Indian Academy of Sciences (India)

2016-09-06

Sep 6, 2016 ... This property pro- motes the magnetoelectric energy conversion and thus ... Wet mixing was done with ethanol to obtain a homogeneous powder mix- ... rite was prepared by mixing NiO, ZnO and Fe2O3 in. 0.5:0.5:1 molar ...

Bimatoprost 0.03%/timolol 0.5% preservative-free ophthalmic solution versus bimatoprost 0.03%/timolol 0.5% ophthalmic solution (Ganfort) for glaucoma or ocular hypertension: a 12-week randomised controlled trial.

Science.gov (United States)

Goldberg, Ivan; Gil Pina, Rafael; Lanzagorta-Aresti, Aitor; Schiffman, Rhett M; Liu, Charlie; Bejanian, Marina

2014-07-01

To compare the efficacy and safety of single-dose bimatoprost 0.03%/timolol 0.5% preservative-free (PF) ophthalmic solution with bimatoprost 0.03%/timolol 0.5% ophthalmic solution in patients with open-angle glaucoma or ocular hypertension. In this multicentre, randomised, parallel-group study, patients were randomised to bimatoprost/timolol PF or bimatoprost/timolol once daily in the morning for 12 weeks. Primary efficacy endpoints, reflecting differing regional regulatory requirements, included change from baseline in worse eye intraocular pressure (IOP) in the per-protocol population at week 12, and the average eye IOP at weeks 2, 6 and 12 in the intent-to-treat population. 561 patients were randomised (278 to bimatoprost/timolol PF; 283 to bimatoprost/timolol); 96.3% completed the study. Both treatment groups showed statistically and clinically significant mean decreases from baseline in worse eye IOP and in average eye IOP at all follow-up time points (p<0.001). Bimatoprost/timolol PF met all pre-established criteria for non-inferiority and equivalence to bimatoprost/timolol. Ocular adverse events were similar between treatment groups, with conjunctival hyperaemia being the most frequent. Most were mild or moderate in severity. Bimatoprost/timolol PF demonstrated non-inferiority and equivalence in IOP lowering compared with bimatoprost/timolol, with no significant differences in safety and tolerability. NCT01177098. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.

TRMM Microwave Imager (TMI) Level 3 Monthly 0.5 degree x 0.5 degree Profiling V7 (3A12) at GES DISC V7

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National Aeronautics and Space Administration — This document provides basic information on 3A12, TMI Monthly 0.5 deg. x 0.5 deg. Profiling. Algorithm 3A12 produces global 0.5 deg. x 0.5 deg. monthly gridded means...

A new silver metaniobate semiconductor of Ag0.5La0.5Nb2O6 with defect-perovskite structure

Science.gov (United States)

Mi, Longqing; Feng, Yongyi; Cao, Lei; Xue, Mingqiang; Huang, Yanlin; Qin, Lin; Seo, Hyo Jin

2018-03-01

Silver-containing lanthanum metaniobate Ag0.5La0.5Nb2O6 nanoparticles were synthesized by sol-gel polymerized complex method. A typical defect-perovskite structure was confirmed by XRD Rietveld refinements. The surface characteristics of the sample were tested by SEM, TEM and EDS measurements. SEM and TEM show that the sample presents ball-like particles with the diameters of 100 nm to 400 nm. The sample shows both self-activated luminescence and photocatalytic activities. Ag0.5La0.5Nb2O6 has a direct transition with band energy of 2.85 eV. The Ag4d-O2p hybridization in the valence band contributes to the narrowed band gap. The luminescence properties of Ag0.5La0.5Nb2O6 have been investigated for the first time. The luminescence is characterized by two emission centers with maximum wavelength near 460 and 530 nm. The emission and excitation spectra, decay curves and the thermal quenching mechanism were discussed. Ag0.5La0.5Nb2O6 shows the efficient photocatalytic activities and the photodegradation rate for methylene blue dye (MB) can reach about 95% under visible light (> 420 nm) irradiation in 5 h. The trapped experiments for the active species were tested and discussed, which verified that rad OH radicals could be the major active species in photocatalysis.

Comparative investigation of the solution species [U(CO3)5]6- and the crystal structure of Na6[U(CO3)5].12H2O.

Science.gov (United States)

Hennig, Christoph; Ikeda-Ohno, Atsushi; Emmerling, Fanziska; Kraus, Werner; Bernhard, Gert

2010-04-21

The limiting U(IV) carbonate species in aqueous solution was investigated by comparing its structure parameters with those of the complex preserved in a crystal structure. The solution species prevails in aqueous solution of 0.05 M U(IV) and 1 M NaHCO(3) at pH 8.3. Single crystals of Na(6)[U(CO(3))(5)].12H(2)O were obtained directly from this mother solution. The U(IV) carbonate complex in the crystal structure was identified as a monomeric [U(CO(3))(5)](6-) anionic complex. The interatomic distances around the U(IV) coordination polyhedron show average distances of U-O = 2.461(8) A, U-C = 2.912(4) A and U-O(dist) = 4.164(6) A. U L(3)-edge EXAFS spectra were collected from the solid Na(6)[U(CO(3))(5)].12H(2)O and the corresponding solution. The first shell of the Fourier transforms (FTs) revealed, in both samples, a coordination of ten oxygen atoms at an average U-O distance of 2.45 +/- 0.02 A, the second shell originates from five carbon atoms with a U-C distance of 2.91 +/- 0.02 A, and the third shell was fit with single and multiple scattering paths of the distal oxygen at 4.17 +/- 0.02 A. These data indicate the identity of the [U(CO(3))(5)](6-) complex in solid and solution state. The high negative charge of the [U(CO(3))(5)](6-) anion is compensated by Na(+) cations. In solid state the Na(+) cations form a bridging network between the [U(CO(3))(5)](6-) units, while in liquid state the Na(+) cations seem to be located close to the anionic complex. The average metal-oxygen distances of the coordination polyhedron show a linear correlation to the radius contraction of the neighbouring actinide(IV) ions and indicate the equivalence of the [An(CO(3))(5)](6-) coordination within the series of thorium, uranium, neptunium and plutonium.

The H_6_0Si_6C_5_4 heterofullerene as high-capacity hydrogen storage medium

International Nuclear Information System (INIS)

Yong, Yongliang; Zhou, Qingxiao; Li, Xiaohong; Lv, Shijie

2016-01-01

With the great success in Si atoms doped C_6_0 fullerene and the well-established methods for synthesis of hydrogenated carbon fullerenes, this leads naturally to wonder whether Si-doped fullerenes are possible for special applications such as hydrogen storage. Here by using first-principles calculations, we design a novel high-capacity hydrogen storage material, H_6_0Si_6C_5_4 heterofullerene, and confirm its geometric stability. It is found that the H_6_0Si_6C_5_4 heterofullerene has a large HOMO-LUMO gap and a high symmetry, indicating it is high chemically stable. Further, our finite temperature simulations indicate that the H_6_0Si_6C_5_4 heterofullerene is thermally stable at 300 K. H_2 molecules would enter into the cage from the Si-hexagon ring because of lower energy barrier. Through our calculation, a maximum of 21 H_2 molecules can be stored inside the H_6_0Si_6C_5_4 cage in molecular form, leading to a gravimetric density of 11.11 wt% for 21H_2@H_6_0Si_6C_5_4 system, which suggests that the hydrogenated Si_6C_5_4 heterofullerene could be suitable as a high-capacity hydrogen storage material.

FTIR spectra of the solid solutions (Na0.88K0.12)VO3, (Na0.5K0.5)VO3, and Na(V0.66P0.34)O3

Science.gov (United States)

de Waal, D.; Heyns, A. M.

1992-03-01

It is known that three different solid solutions, (Na0.88K0.12)VO3, (Na0.5K0.5)VO3 and Na(V0.66P0.34)O3, form in the (Na,K)(V,P)O3 system. These compounds all have monoclinic crystal structures similar to the pure alkali metal metavanadates containing small cations, e.g. Li+ and Na+ (Space group C2/c). Metavanadates with large cations like K+, Rb+, C+s and NH+4 form orthorhombic crystals, space group Pbcm. All those are structurally related to the silicate pyroxenes. Na(V0.66P0.34)O3 and (Na0.88K0.12)VO3 have the same modified diopside structure as (alpha) - NaVO3 while (Na0.5K0.5)VO3 adopts the true diopside structure. The infrared spectra of the three solid solutions are reported here in comparison with those of (alpha) -NaVO3 and KVO3. The results are also correlated with those obtained in two independent high pressure Raman studies of NH4VO3 and RbVO3 as the introduction of a larger cation like K+ should increase the pressure in the structure.

Polarisation parameter measurement in the proton-proton elastic scattering from 0.5 to 1.2 GeV

International Nuclear Information System (INIS)

Ducros, Yves

1970-01-01

The angular distribution of the polarisation parameter was measured in the proton-proton elastic - scattering at seven energies between 0.5 and 1.2 GeV. A polarized proton target was used. The results show a maximum of the polarisation parameter of 0.6, at 0.73 GeV. This maximum is due to the important increase of the total cross section between 0.6 and 0.73 GeV. At 1.2 GeV the angular distribution of the polarisation shows a minimum for a momentum transfer value of -1 (GeV/c) 2 . A phase shift analysis was done at 0.66 GeV, using all available experimental data at this energy. There is no evidence of a di-baryonic resonance in the 1 D 2 phase. (author) [fr

Combustion Synthesis of Sm0.5Sr0.5CoO3-x and La0.6Sr0.4CoO3-x Nanopowders for Solid Oxide Fuel Cell Cathodes

Science.gov (United States)

Bansal, Narottam P.; Zhong, zhimin

2005-01-01

Nanopowders of Sm0.5Sr0.5CoO(3-x) (SSC) and La0.6Sr0.4CoO(3-x) (LSC) compositions, which are being investigated as cathode materials for intermediate temperature solid oxide fuel cells, were synthesized by a solution-combustion method using metal nitrates and glycine as fuel. Development of crystalline phases in the as-synthesized powders after heat treatments at various temperatures was monitored by x-ray diffraction. Perovskite phase in LSC formed more readily than in SSC. Single phase perovskites were obtained after heat treatment of the combustion synthesized LSC and SSC powders at 1000 and 1200 C, respectively. The as-synthesized powders had an average particle size of 12 nm as determined from x-ray line broadening analysis using the Scherrer equation. Average grain size of the powders increased with increase in calcination temperature. Morphological analysis of the powders calcined at various temperatures was done by scanning electron microscopy.

Detailed investigation of thermal and electron transport properties in strongly correlated compound Ce6Pd12In5 and its nonmagnetic analog La6Pd12In5

Science.gov (United States)

Falkowski, M.; Krychowski, D.; Strydom, A. M.

2016-11-01

An in-depth study of thermal and electron transport properties including thermal conductivity κ(T), thermoelectric power S(T), and electrical resistivity ρ(T) of the heavy fermion Kondo lattice Ce6Pd12In5 and its nonmagnetic reference compound La6Pd12In5 is presented. The absolute κ(T) value of Ce6Pd12In5 is smaller that than of La6Pd12In5, which indicates that conduction electron-4f electron scattering has a large impact on the reduction of thermal conductivity. The isolated 4f electron contributions to the electrical resistivity ρ 4 f (T), electronic thermal resistivity displayed in the form W e l , 4 f (T) .T, and thermoelectric power S 4 f (T) reveal a low- and high-temperature -lnT behaviour characteristic of Kondo systems with strong crystal-electric field (CEF) interactions. The analysis of phonon scattering processes of lattice thermal conductivity κph(T) in (Ce, La)6Pd12In5 was performed over the whole accessible temperature range according to the Callaway model. In the scope of a theoretical approach based on the perturbation type calculation, we were able to describe our experimental data of ρ 4 f (T) and W e l , 4 f (T) .T by using the model incorporating simultaneously the Kondo effect in the presence of the CEF splitting, as it is foreseen in the framework of the Cornut-Coqblin and Bhattacharjee-Coqblin theory. Considering the fact that there are not many cases of similar studies at all, we also show the numerical calculations of temperature-dependent behaviour of spin-disorder resistivity ρs(T), magnetic resistivity ρ 4 f (T), and occupation number ⟨ N i ⟩ due to the various types of degeneracy of the ground state multiplet of Ce 3 + (J = 5/2).

Microstructural analysis nanoferritas Mn_0_,_5Zn_0_,_5Fe_2O_4 e Mn_0_,_6_5Zn_0_,_3_5Fe_2O_4 synthesized by combustion reaction

International Nuclear Information System (INIS)

Diniz, V.C.S.; Figueiredo, A.R.; Costa Junior, A.D.S.; Diniz, H.M.; Vieira, D.A.; Costa, A.C.F.M.

2014-01-01

The MnZn ferrites are ferrimagnetic materials that have been studied and used in various technological fields. In this work investigated the microstructural characteristics of ferrites and Mn_0_,_5Zn_0_,_5Fe_2O_4 Mn_0_,_6_5Zn_0_,_3_5Fe_2O_4 synthesized by combustion reaction in 200g scale production. The samples were characterized by XRD, crystallinity, crystallite size, X-ray fluorescence and scanning electron microscopy. Given the results it was observed that for both samples the synthesis combustion reaction was efficient for the production of single-phase ferrites with high crystallinity. With respect to the analysis of X-ray fluorescence was noted that the experimental values composition were consistent with the theoretical values calculated for both samples. Regarding morphology for both samples, the formation of the porous powders with feature consisting of dense clumps in the form of irregular foam was observed. (author)

Poly[[aqua(μ5-3,4,5,6-tetracarboxycyclohexane-1,2-dicarboxylatostrontium] monohydrate

Directory of Open Access Journals (Sweden)

Pei-Chi Cheng

2011-12-01

Full Text Available In the title compound, {[Sr(C12H10O12(H2O]·H2O}n, the SrII ion is coordinated by six O atoms of five symmetry-related 3,4,5,6-tetracarboxycyclohexane-1,2-dicarboxylate ligands and one water molecule in a slightly distorted monocapped trigonal–prismatic environment. The ligands bridge the SrII ions, forming a two-dimensional structure. In the crystal, O—H...O hydrogen bonds further connect the structure into a three-dimensional network. The H atoms of two of the carboxyl groups were refined as half-occupancy.

Oxygen vacancy as fatigue evidence of La0.5Sr0.5CoO3/PbZr0.4Ti0.6O3/La0.5Sr0.5CoO3 capacitors

Science.gov (United States)

Liu, B. T.; Chen, J. E.; Sun, J.; Wei, D. Y.; Chen, J. H.; Li, X. H.; Bian, F.; Zhou, Y.; Guo, J. X.; Zhao, Q. X.; Guan, L.; Wang, Y. L.; Guo, Q. L.; Ma, L. X.

2010-09-01

La0.5Sr0.5CoO3 (LSCO) films grown on SrTiO3 substrates, cooled at reduced oxygen pressures, ranging from 8×104 to 1×10-4 Pa, from the depostion temperature, are used as the bottom electrodes of PbZr0.4Ti0.6O3 (PZT) capacitors to study the impact of oxygen stoichiometry of the LSCO bottom electrodes on the structural and physical properties of LSCO/PZT/LSCO capacitors. It is found that the tetragonality, polarization and fatigue-resistance of PZT films decrease with the decrease of the cooling oxygen pressure. Almost 60% polarization degradation occurs for the PZT capacitor with the LSCO bottom electrode cooled in 1×10-4 Pa oxygen up to 1010 switching cycles, indicating that the oxygen vacancy of the bottom electrode can result in fatigue of the LSCO/PZT/LSCO capacitor.

Study on magnetic properties of (Nd{sub 0.8}Ce{sub 0.2}){sub 2−x}Fe{sub 12}Co{sub 2}B (x = 0–0.6) alloys

Energy Technology Data Exchange (ETDEWEB)

Tan, G.S.; Xu, H., E-mail: huixu8888@shu.edu.cn; Yu, L.Y.; Tan, X.H.; Zhang, Q.; Gu, Y.; Hou, X.L.

2017-09-01

Highlights: • (Nd{sub 0.8}Ce{sub 0.2}){sub 2−x}Fe{sub 12}Co{sub 2}B alloys are prepared by melt-spinning method with simultaneously decreasing of Nd, Ce concentration. • The magnetic properties B{sub r}, (BH){sub max} and squareness are all improved with an appropriate reduction of Nd, Ce concentration. • Magnetic field heat treatment offers a significant improvement in B{sub r}, (BH){sub max} and squareness. - Abstract: In the present work, (Nd{sub 0.8}Ce{sub 0.2}){sub 2−x}Fe{sub 12}Co{sub 2}B (x = 0–0.6) permanent alloys are prepared by melt-spinning method. The hard magnetic properties of (Nd{sub 0.8}Ce{sub 0.2}){sub 2−x}Fe{sub 12}Co{sub 2}B (x = 0–0.6) alloys annealed at optimum temperatures have been investigated systematically. Depending on the Nd, Ce concentration, the maximum energy product ((BH){sub max}) and remanence (B{sub r}) increase gradually with x in the range of 0 ≤ x ≤ 0.4, whereas decrease gradually in the alloys with 0.4 < x ≤ 0.6. It is found that the optimum magnetic properties are obtained at x = 0.4: H{sub ci} = 4.9 kOe, B{sub r} = 10.1 kG, (BH){sub max} = 13.7 MGOe. Specifically, magnetic field heat treatment below the Curie temperature is applied for (Nd{sub 0.8}Ce{sub 0.2}){sub 1.6}Fe{sub 12}Co{sub 2}B (x = 0.4) annealed ribbons. The magnetic properties B{sub r}, (BH){sub max} and squareness are all enhanced after the magnetic field heat treatment. The (BH){sub max} shows a substantial increase from 13.7 MGOe to 16.0 MGOe after the heat treatment at 623 K with a magnetic field of 1 T, which gets 17% improvement compared with that of the sample without a magnetic field heat treatment. We demonstrate that the magnetic field heat treatment plays a certain role in the magnetization reversal behavior and can improve the microstructure of (Nd{sub 0.8}Ce{sub 0.2}){sub 1.6}Fe{sub 12}Co{sub 2}B alloy.

Cs0.49NbPS6

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Hoseop Yun

2011-01-01

Full Text Available The quaternary thiophosphate, Cs0.49NbPS6, caesium hexathioniobiophosphate(V, has been synthesized by the reactive halide flux method. The title compound is isotypic with Rb0.46TaPS6 and is made up of a bicapped trigonal–biprismatic [Nb2S12] unit and a tetrahedral [PS4] group. The [Nb2S12] units linked by the [PS4] tetrahedra form infinite chains, yielding a three-dimensional network with rather large van der Waals gaps along the c axis in which the disordered Cs+ ions reside. The electrons released by the Cs atoms are transferred to the pairwise niobium metal site and there are substantial intermetallic Nb—Nb bonding interactions. This leads to a significant decrease of the intermetallic distance in the title compound compared to that in TaPS6. The classical charge balance of the title compound may be represented as [Cs+]0.49[Nb4.51+][P5+][S2−]4[S22−].

A 6-week, multicenter, randomized, double-masked, parallel-group study comparing travoprost 0.004% to latanoprost 0.005% followed by 6-week, open-label treatment with travoprost 0.004%.

Science.gov (United States)

Maul, Eugenio; Carrasco, Félix Gil; Costa, Vital Paulino; Casiraghi, Javier F; Vargas, Enrique; Sarmina, Judith S; Mayol, Renato

2007-09-01

The aim of this study was to compare the tolerability and efficacy of once-daily travoprost 0.004% versus latanoprost 0.005% for 6 weeks followed by 6 weeks of once-daily travoprost 0.004% in decreasing intraocular pressure (IOP) in patients with open-angle glaucoma (OAG) or ocular hypertension (OH). This multicenter, randomized, doublemasked, active-controlled, parallel-group trial was conducted at 32 centers across Latin America. Patients aged > or =18 years with OAG or OH were randomly assigned to receive topical travoprost 0.004% or latanoprost 0.005% 1 drop QD (9 PM) for 6 weeks (masked phase). At 6 weeks, all patients were assigned to receive open-label travoprost 0.004% 1 drop QD (9 PM) for 6 additional weeks (open-label phase). Study visits were scheduled at weeks 1, 2, 4, 6, 8, and 12. At each study visit, IOP was measured at 5 PM (+/-1 hour; approximately 20 hours after study drug administration). IOP changes from baseline were combined (pooled) from the 1-, 2-, 4-, and 6-week data to provide a comparison between the 2 treatment groups. Ocular adverse events (AEs) were monitored using slit-lamp examination. A total of 302 patients were enrolled (travoprost group, 155 patients; latanoprost group, 147 patients). The mean (SD) age of the travoprost group was 61.9 (10.6) years; 60.6% were female; and 47.1% were white. The mean (SD) age of the latanoprost group was 60.5 (12.4) years; 62.6% were female; and 49.0% were white. Mean IOP values were not significantly different between the travoprost and latanoprost groups at baseline (24.7 vs 24.2 mm Hg) or 6 weeks; however, the between-group difference in reductions from baseline in pooled IOP during the masked phase of the study was statistically significant (-8.3 vs -7.5 mm Hg; P = 0.009). At weeks 6 and 12, mean lOP levels were 16.1 and 16.2 mm Hg, respectively, in the travoprost group and 16.4 and 16.1 mm Hg in the group that was switched from latanoprost to travoprost (all, P = NS). The most common ocular AEs

The effect of texture in (Bi3.5Nd0.5)(Ti2.97Nb0.03)O12 ceramics

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Cao, Ziping; Ding, Aili; Zheng, Xinsen; Qiu, Pingsun; Cheng, Wenxiu

2004-11-01

(Bi3.5Nd0.5) (Ti2.97Nb0.03)O12 ferroelectric ceramics was successfully prepared by a hot-pressing method. XRD diffraction confirms that the samples hold different texture in the sliced planes parallel and perpendicular to the hot-pressing axis, respectively. The anisotropy of ferroelectric, dielectric and piezoelectric properties were all observed in the textured ceramics. Due to the great improvement of ferroelectric and piezoelectric properties, the sample which was sliced along the direction parallel to the hot-pressing axis can be considered as a good candidate of high temperature piezoelectric materials.

Supplementing lactating dairy cows with a vitamin B12 precursor, 5,6-dimethylbenzimidazole, increases the apparent ruminal synthesis of vitamin B12.

Science.gov (United States)

Brito, A; Chiquette, J; Stabler, S P; Allen, R H; Girard, C L

2015-01-01

Cobalamin (CBL), the biologically active form of vitamin B12, and its analogs, are produced by bacteria only if cobalt supply is adequate. The analogs differ generally by the nucleotide moiety of the molecule. In CBL, 5,6-dimethylbenzimidazole (5,6-DMB) is the base in the nucleotide moiety. The present study aimed to determine if a supplement of 5,6-DMB could increase utilization of dietary cobalt for synthesis of CBL and change ruminal fermentation, nutrient digestibility, omasal flow of nutrients and ruminal protozoa counts. Eight ruminally cannulated multiparous Holstein cows (mean±standard deviation=238±21 days in milk and 736±47 kg of BW) were used in a crossover design. Cows were randomly assigned to a daily supplement of a gelatin capsule containing 1.5 g of 5,6-DMB via the rumen cannula or no supplement. Each period lasted 29 days and consisted of 21 days for treatment adaptation and 8 days for data and samples collection. Five corrinoids, CBL and four cobamides were detected in the total mixed ration and the omasal digesta from both treatments. The dietary supplement of 5,6-DMB increased (P=0.02) apparent ruminal synthesis of CBL from 14.6 to 19.6 (s.e.m. 0.8) mg/day but had no effect (P>0.1) on apparent ruminal synthesis of the four analogs. The supplement of 5,6-DMB had no effect (P>0.1) on milk production and composition, or on protozoal count, ruminal pH and concentrations of volatile fatty acids and ammonia nitrogen in rumen content. The supplement had also no effect (P>0.1) on intake, omasal flow and apparent ruminal digestibility of dry matter, organic matter, NDF, ADF and nitrogenous fractions. Plasma concentration of CBL was not affected by treatments (P=0.98). Providing a preformed part of the CBL molecule, that is, 5,6-DMB, increased by 34% the apparent ruminal synthesis of CBL by ruminal bacteria but had no effect on ruminal fermentation or protozoa count and it was not sufficient to increase plasma concentrations of the vitamin. Even though

Oxygen permeation and stability of La 0.4Ca 0.6Fe 1-xCo xO 3-δ ( x = 0, 0.25, 0.5) membranes

Science.gov (United States)

Diethelm, S.; Van herle, J.; Middleton, P. H.; Favrat, D.

Three perovskite-type compounds of composition La 0.4Ca 0.6Fe 1- xCo xO 3- δ ( x=0, 0.25 and 0.5) were investigated for use as oxygen separation membranes for the partial oxidation (POX) of methane to syngas. Special attention was given to the question of their stability in real operating conditions. A permeation set-up was specially designed to measure oxygen fluxes through these materials when placed in a strong pO 2 gradient. It also facilitated testing the long-term stability of the specimen. Permeation measurements performed in an air/argon gradient between 800 and 1000 °C showed that the highest fluxes were obtained with the highest content of cobalt (La 0.4Ca 0.6Fe 0.5Co 0.5O 3- δ ≅ La 0.4Ca 0.6Fe 0.75Co 0.25O 3- δ > La 0.4Ca 0.6FeO 3- δ). In addition, comparison between the fluxes of samples of different thickness gave clear evidence of surface limitations in the oxygen transport. The long-term stability test showed opposite trends: only the two lowest Co containing compounds ( x=0 and 0.25) sustained an air/(Ar+H 2) gradient over more than 600 h. The other ( x=0.5) broke shortly after the introduction of H 2. In the presence of H 2, the oxygen flux was increased by a factor 10 compared to Ar and reached 0.83 μmol/cm 2 s for La 0.4Ca 0.6Fe 0.75Co 0.25O 3- δ at 900 °C. Post-operation SEM examination of the cross-section and both surfaces revealed that the surface exposed to H 2 had started to decompose resulting in the formation of a thin porous layer but the bulk of the material remained unchanged.

Synthesis of novel 4,6-di(substituted)amino-1,2-dihydro-1,3,5-triazine derivatives as topical antiseptic agents.

Science.gov (United States)

Maeda, Shirou; Kita, Toshiko; Meguro, Kanji

2009-02-12

A series of novel 4,6-di(substituted)amino-1,2-dihydro-1,3,5-triazine derivatives designed to have ClogP of 5.1-7.5 was synthesized and evaluated for their antiseptic properties by MIC and MBC tests against Gram-positive and Gram-negative bacteria, including MRSA, VRE, and P. aeruginosa. Among these compounds, 4-alkyl-6-aralkyl derivatives having ClogP of 6.6-7.1 and 4-alkyl-6-aryl or 4,6-dialkyl derivatives with ClogP of 6.0-6.4 showed pronounced antibacterial activities in both tests.

The effect of texture in (Bi3.5Nd0.5)(Ti2.97Nb0.03)O12 ceramics

International Nuclear Information System (INIS)

Cao, Ziping; Ding, Aili; Zheng, Xinsen; Qiu, Pingsun; Cheng, Wenxiu

2004-01-01

(Bi 3.5 Nd 0.5 ) (Ti 2.97 Nb 0.03 )O 12 ferroelectric ceramics was successfully prepared by a hot-pressing method. XRD diffraction confirms that the samples hold different texture in the sliced planes parallel and perpendicular to the hot-pressing axis, respectively. The anisotropy of ferroelectric, dielectric and piezoelectric properties were all observed in the textured ceramics. Due to the great improvement of ferroelectric and piezoelectric properties, the sample which was sliced along the direction parallel to the hot-pressing axis can be considered as a good candidate of high temperature piezoelectric materials. (copyright 2004 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

Microstructure and Mechanical Properties of Mg-11Li-6Zn-0.6Zr-0.4Ag-0.2Ca-x Y Alloys.

Science.gov (United States)

Kim, Yong-Ho; Yoo, Hyo-Sang; Son, Hyeon-Taek

2018-09-01

Magnesium and its alloys are potential candidates for many automotive and aerospace applications due to their low density and high specific strength. However, the use of magnesium as wrought products is limited because of its poor workability at ambient temperatures. Mg-Li alloys containing 5-11 wt.% Li exhibit a two-phase structure consisting of a α (hcp) Mg-rich phase and a β (bcc) Li-rich phase. Mg-Li alloys with Li content greater than 11 wt.% exhibit a single-phase structure consisting of only the β phase. In the present study, we studied the effects of Y addition on the microstructure and mechanical properties of Mg-11Li-6Zn-0.6Zr-0.4Ag-0.2Ca based alloys. The melt was maintained at 720 °C for 20 min and poured into a mold. Then, the as-cast Mg alloys were homogenized at 350 °C for 4 h and were hot-extruded onto a 4-mm-thick plate with a reduction ratio of 14:1. The as-cast Mg-11Li-6Zn-0.6Zr-0.4Ag-0.2Ca-xY (x 0, 1, 3, and 5 wt.%) alloys were composed of α-Mg, β-Li, γ-Mg2Zn3Li, I-Mg3YZn6, W-Mg3Y2Zn3, and X-Mg12YZn phases. By increasing the Y content from 0 to 5 wt.%, the composition of the W-Mg3Y2Zn3 phase increased. With increasing Y content, from 0 to 1, 3, and 5 wt.%, the average grain size and ultimate tensile of the as-extruded Mg alloys decreased slightly, from 8.4, to 3.62, 3.56, and 3.44 μm and from 228.92 to 215.57, 187.47, and 161.04 MPa, respectively, at room temperature.

Particle morphology and magnetic properties of Ba{sub 0.5}Sr{sub 0.5}Fe{sub 12}O{sub 19} powder calcined conventionally and by microwave heating

Energy Technology Data Exchange (ETDEWEB)

Kanagesan, S., E-mail: kanagu1980@gmail.com [Materials Synthesis and Characterization Laboratory (MSCL), Institute of Advanced Technology (ITMA), Universiti Putra Malaysia, Serdang 43400, Selangor (Malaysia); Hashim, M. [Materials Synthesis and Characterization Laboratory (MSCL), Institute of Advanced Technology (ITMA), Universiti Putra Malaysia, Serdang 43400, Selangor (Malaysia); Physics Department, Faculty of Science, Universiti Putra Malaysia, Serdang 43400, Selangor (Malaysia); Jesurani, S. [Department of Physics, Jeyaraj Annapackium College for Women, Periyakulam 625601, Tamil Nadu (India); Kalaivani, T. [Center for material science and Nano Devices, Department of Physics, SRM University, Kattankulathur 603203, Tamil Nadu (India); Ismail, I.; Shafie, M.S.E. [Materials Synthesis and Characterization Laboratory (MSCL), Institute of Advanced Technology (ITMA), Universiti Putra Malaysia, Serdang 43400, Selangor (Malaysia)

2012-12-05

Highlights: Black-Right-Pointing-Pointer Synthesis of Ba{sub 0.5}Sr{sub 0.5}Fe{sub 12}O{sub 19} by sol-gel technique. Black-Right-Pointing-Pointer Crystallization temperature is reduced to 900 Degree-Sign C due to the addition of D-Fructose. Black-Right-Pointing-Pointer Results of conventional and microwave calcined samples are reported. - Abstract: Barium strontium hexaferrite (Ba{sub 0.5}Sr{sub 0.5}Fe{sub 12}O{sub 19}-BSF) has been prepared by sol-gel process involving use of D-Fructose as a fuel. The prepared precursor was calcined in two different calcinations techniques conventional and microwave furnace. X-ray powder diffraction studies confirmed the formation of single phase Ba{sub 0.5}Sr{sub 0.5}Fe{sub 12}O{sub 19}. HR-SEM results show the morphology of the particles is hexagonal structures in platelet form. The average particle size of conventionally calcined BSF powder is 100-250 nm and that of microwave calcined powder is 30-100 nm. The broad hysteresis loop reveals that powder is well crystallized and exhibits hard magnetic properties.

Efficacy and safety of fixed-combination travoprost 0.004%/timolol 0.5% in patients transitioning from bimatoprost 0.03%/timolol 0.5% combination therapy

Directory of Open Access Journals (Sweden)

Schnober D

2015-05-01

Full Text Available Dietmar Schnober,1 Douglas A Hubatsch,2 Maria-Luise Scherzer3 1Private Ophthalmology Practice, Werdohl, Germany; 2Alcon Laboratories, Inc., Fort Worth, TX, USA; 3Private Ophthalmology Practice, Regenstauf, Germany Purpose: To determine the efficacy and safety of fixed-combination travoprost 0.004%/timolol 0.5% preserved with polyquaternium-1 in patients with insufficient response to bimatoprost 0.03%/timolol 0.5% preserved with benzalkonium chloride.Patients and methods: In this open-label nonrandomized study conducted at 13 European sites, patients with primary open-angle glaucoma or ocular hypertension with insufficient intraocular pressure (IOP reduction during bimatoprost/timolol therapy were transitioned to travoprost/timolol (DuoTrav® administered every evening for 12 weeks. Change in IOP from baseline to week 12 was assessed in patients who transitioned from fixed-combination bimatoprost/timolol (n=57, primary endpoint. Secondary assessments included change in IOP at week 4, percentage of patients with IOP ≤18 mmHg at weeks 4 and 12, change in Ocular Surface Disease Index and ocular hyperemia scores at week 12, and patient preference. Adverse events were also reported.Results: IOP change (mean ± SD from baseline to week 12 was –3.8±1.9 mmHg (P<0.001; results were similar at week 4. Most patients had IOP ≤18 mmHg at weeks 4 and 12 (78.6% and 85.5%, respectively. Mean Ocular Surface Disease Index score was significantly reduced (P<0.001; no significant change in ocular hyperemia score was observed (P=0.197. Treatment-related adverse events included dysgeusia, nausea, paresthesia, myalgia, headache, and eye irritation (n=1 each. Most patients (74.5% preferred travoprost/timolol over bimatoprost/timolol.Conclusion: Transition to travoprost/timolol significantly reduced IOP and was well tolerated in patients who had elevated IOP despite bimatoprost/timolol therapy. Polyquaternium-1–preserved travoprost/timolol was preferred over

Hyperfine interactions and electric dipole moments in the [16.0]1.5(v = 6), [16.0]3.5(v = 7), and X2Δ(5/2) states of iridium monosilicide, IrSi.

Science.gov (United States)

Le, Anh; Steimle, Timothy C; Morse, Michael D; Garcia, Maria A; Cheng, Lan; Stanton, John F

2013-12-19

The (6,0)[16.0]1.5-X(2)Δ(5/2) and (7,0)[16.0]3.5-X(2)Δ(5/2) bands of IrSi have been recorded using high-resolution laser-induced fluorescence spectroscopy. The field-free spectra of the (191)IrSi and (193)IrSi isotopologues were modeled to generate a set of fine, magnetic hyperfine, and nuclear quadrupole hyperfine parameters for the X(2)Δ(5/2)(v = 0), [16.0]1.5(v = 6), and [16.0]3.5 (v = 7) states. The observed optical Stark shifts for the (193)IrSi and (191)IrSi isotopologues were analyzed to produce the permanent electric dipole moments, μ(el), of -0.414(6) D and 0.782(6) D for the X(2)Δ(5/2) and [16.0]1.5 (v = 6) states, respectively. Properties of the X(2)Δ(5/2) state computed using relativistic coupled-cluster methods clearly indicate that electron correlation plays an essential role. Specifically, inclusion of correlation changes the sign of the dipole moment and is essential for achieving good accuracy for the nuclear quadrupole coupling parameter eQq0.

Low cycle fatigue behaviour of Ti-6Al-5Zr-0.5Mo-0.25Si alloy at room temperature

International Nuclear Information System (INIS)

Nag, Anil Kumar; Praveen, K.V.U.; Singh, Vakil

2006-01-01

Low cycle fatigue (LCF) behaviour of the near α titanium alloy, Ti-6Al-5Zr-0.5Mo-0.25Si (LT26A), was investigated in the (α+ β) as well as β treated conditions at room temperature. LCF tests were carried out under total strain controlled mode in the range of Δε t /2: from ± 0.60% to ± 1.40%. The alloy shows cyclic softening in both the conditions. Also it exhibits dual slope Coffin-Manson (C-M) relationship in both the treated conditions. (author)

Crystal and molecular structures of benzo[4,5]imidazo[1,2-c]quinazolin-6-one and 10-carboxybenzo[4,5]imidazo[1,2-c]quinazolin-6-one: A quantum-chemical study of their tautomerism

International Nuclear Information System (INIS)

Koval’chukova, O. V.; Stash, A. I.; Strashnov, P. V.; Neborak, E. V.; Strashnova, S. B.; Zaitsev, B. E.

2011-01-01

Benzo[4,5]imidazo[1,2-c]quinazolin-6-one and 10-carboxybenzo[4,5]imidazo[1,2-c]quinazolin-6-one were isolated in the crystalline state and studied by X-ray diffraction. The crystal and molecular structures of these compounds were determined by X-ray diffraction. The energy characteristics of the tautomeric and ionic forms were calculated by the quantum-chemical PM3 method.

C_6_0"3"- versus C_6_0"4"- /C_6_0"2"- - synthesis and characterization of five salts containing discrete fullerene anions

International Nuclear Information System (INIS)

Boeddinghaus, M. Bele; Klein, Wilhelm; Wahl, Bernhard; Faessler, Thomas F.; Jakes, Peter; Eichel, Ruediger A.

2014-01-01

Five new compounds, [Rb(18crown-6)]_3[C_6_0] (1), [Rb(18crown-6)]_6[C_6_0]_2(C_3H_7NO)_2(C_4H_8O)_2 (2), [Rb(benzo18crown-6)]_6[C_6_0]_2(C_2H_8N_2)_5 (3), [Cs(benzo18crown-6)]_3C_6_0(C_2H_8N_2)_2 (4), and [Cs_3(benzo18crown-6)_5]C_6_0(C_2H_8N_2)_(_4_._5_+_x_) (5) were synthesized and characterized by single-crystal X-ray structure determination. All compounds contain discrete C_6_0 anions, which are ordered in 1, 2, and 4, where direct cation-anion contacts occur. The unit cells of 1 and 2 contain two independent fullerides, which coordinate to the rubidium atoms either of two or of four [Rb(18crown-6)] units. Owing to the presence of differently coordinated fullerene units in compounds 1 and 2, a possible disproportionation of C_6_0"3"- into C_6_0"2"- and C_6_0"4"- anions is discussed. In 3 and 4 the C_6_0 anions are coordinated by three Rb and Cs atoms, respectively. In all compounds the average charge of the anion is -3. Magnetic data reveal a doublet spin state for 3. The EPR spectra are discussed for compounds 3 and 5. The role of a dynamic Jahn-Teller distortion is discussed, and we report the first IR spectroscopic data of fullerene trianions, which have been obtained in solution. (Copyright copyright 2014 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Energy-Transfer Kinetics for Xe (6p[1/2]0) Atoms in Kr, Ar, Ne, and He.

Science.gov (United States)

He, Shan; Liu, Dong; Li, Xueyang; Chu, Junzhi; Guo, Jingwei; Liu, Jinbo; Hu, Shu; Sang, Fengting; Jin, Yuqi

2018-06-11

The kinetic processes for the Xe (6p[1/2] 0 ) atoms in Kr, Ar, Ne, and He buffer gases were studied. We found that Kr, Ar, and Ne atoms can be used to switch the amplified spontaneous emission (ASE) channel from 3408 nm (6p[1/2] 0 -6s'[1/2] 1 ) to 3680 nm (5d[1/2] 1 -6p[1/2] 1 ), while Xe and He atoms do not show such a phenomenon. This ASE channel switch is mainly ascribed to the fast transfer of 6p[1/2] 0 → 5d[1/2] 1 . On the basis of the rate equations for two-state coupling (energy-transfer processes between the two states are very rapid), the reason why the ASE channel switch effect normally coincides with a double exponential decay of the spontaneous emission at 828 nm (6p[1/2] 0 -6s[3/2] 1 ) is explained. The actual situations in Xe, Ar, Ne, and He follow this rule. However, the strictly single exponential decay of the spontaneous emission at 828 nm and strong ASE channel switch effect simultaneously emerge in Kr. This indicates that the transfer of 6p[1/2] 0 → 5d[1/2] 1 in Kr does not occur via two-state coupling, but via two steps of near-resonance collision through the 5s[3/2] 2 (Kr) state as the intermediate state (6p[1/2] 0 → 5s[3/2] 2 (Kr) → 5d[1/2] 1 ). In addition, we found Xe (6p[1/2] 0 ) atoms strongly tend to reach the 6p[3/2] 2 , 6p[3/2] 1 , and 6p[5/2] 2 states through the 5s[3/2] 2 (Kr) state as the intermediate state in Kr. The 5s[3/2] 2 (Kr) state plays a very important role in the energy-transfer kinetics for the Xe (6p[1/2] 0 ) atoms. Kr is probably an excellent buffer gas for laser systems based on Xe.

π0 decay branching ratios of 5ΛHe and 12ΛC hypernuclei

International Nuclear Information System (INIS)

Okada, S.; Ajimura, S.; Aoki, K.; Banu, A.; Bhang, H.C.; Fukuda, T.; Hashimoto, O.; Hwang, J.I.; Kameoka, S.; Kang, B.H.; Kim, E.H.; Kim, J.H.; Kim, M.J.; Maruta, T.; Miura, Y.; Miyake, Y.; Nagae, T.; Nakamura, M.; Nakamura, S.N.; Noumi, H.; Okayasu, Y.; Outa, H.; Park, H.; Saha, P.K.; Sato, Y.; Sekimoto, M.; Takahashi, T.; Tamura, H.; Tanida, K.; Toyoda, A.; Tsukada, K.; Watanabe, T.; Yim, H.J.

2005-01-01

We precisely measured π0 branching ratios of 5 Λ He and 12 Λ C hypernuclei produced via the (π+,K+) reaction. Using these π0 branching ratios with the π- branching ratios and lifetimes, we obtained the π0 decay widths and the non-mesonic weak decay widths with an accuracy of ∼5% (stat) for both hypernuclei

Magnetoelectric effect of (1−x) Ba{sub 0.5}Sr{sub 0.5}Zr{sub 0.5}Ti{sub 0.5}O{sub 3}+(x) Ni{sub 0.12}Mg{sub 0.18}Cu{sub 0.2}Zn{sub 0.5}Fe{sub 2}O{sub 4} composites

Energy Technology Data Exchange (ETDEWEB)

Rahaman, Md. D., E-mail: dalilurrahaman1976@gmail.com [Department of Physics, University of Dhaka, Dhaka-1000 (Bangladesh); Saha, S.K.; Ahmed, T.N. [Department of Physics, University of Dhaka, Dhaka-1000 (Bangladesh); Department of Physics, Bangladesh University of Engineering and Technology, Dhaka 1000 (Bangladesh); Saha, D.K. [Materials Science Division, Atomic Energy Centre, PO Box 164, Dhaka 1000 (Bangladesh); Hossain, A.K.M. Akther [Department of Physics, Bangladesh University of Engineering and Technology, Dhaka 1000 (Bangladesh)

2014-12-15

The magnetoelectric composites with chemical compositions (1−x) Ba{sub 0.5}Sr{sub 0.5}Zr{sub 0.5}Ti{sub 0.5}O{sub 3}+(x) Ni{sub 0.12}Mg{sub 0.18}Cu{sub 0.2}Zn{sub 0.5}Fe{sub 2}O{sub 4} (x=20, 40, 60 and 80 wt%) was prepared by the conventional solid state reaction method. The presence of a biphase composition was confirmed by X-ray diffraction while the microstructure of the composites was studied by scanning electron microscopy revealing a good mixing of the two phases and a good densification of the bulk ceramics. The dielectric dispersion is observed at lower frequencies due to interfacial polarization arising from the interface of the two phases. At higher frequencies, the dielectric constant is almost constant due to the inability of electric dipoles to follow the first variation of the alternating applied electric field. The dielectric loss shows maxima which are attributed when the hopping frequency of electrons between different ionic sites becomes nearly equal to the frequency of the applied field. The linearity in the log(σ{sub AC}) vs. log(ω{sup 2}) plots confirmed the small polaron hopping type of conduction mechanism. The composite materials are found to exhibit an excellent frequency dependence of magnetic properties. In the high frequency range, with increasing ferrite concentration the initial permeability increases and cut-off frequency decreases. An optimal magnetoelectric coupling responding voltage of about 600 μV cm{sup −1} Oe{sup −1} is obtained for x=20 wt% at room temperature. - Highlights: • XRD patterns confirmed the coexistence of ferroelectric and ferrimagnetic phases. • Dielectric dispersion observed at low frequencies due to interfacial polarization. • Linearity in logσ{sub ac} vs. logω{sup 2} is due to small polaron hopping mechanism. • Maximum ME voltage coefficient 600 μV cm{sup −1} Oe{sup −1} observed for 20% of ferrite.

Controlled synthesis of lithium-rich layered Li1.2Mn0.56Ni0.12Co0.12O2 oxide with tunable morphology and structure as cathode material for lithium-ion batteries by solvo/hydrothermal methods

International Nuclear Information System (INIS)

Fu, Fang; Huang, Yiyin; Wu, Peng; Bu, Yakun; Wang, Yaobing; Yao, Jiannian

2015-01-01

Highlights: • Li 1.2 Mn 0.56 Ni 0.12 Co 0.12 O 2 with different shapes was successfully prepared. • The solvent plays a key role in the formation of the product with various shapes. • The sample prepared by solvothermal method exhibits higher discharge capacity. • Its reversible capacity is approximately 306.9 mA h g −1 at 0.2 C. - Abstract: A Li-rich layered cathode material Li 1.2 Mn 0.56 Ni 0.12 Co 0.12 O 2 (0.5Li 2 MnO 3 ⋅0.5Li 1.2 Mn 0.4 Ni 0.3 Co 0.3 O 2 ) with different morphologies has been successfully prepared by solvothermal and hydrothermal methods. The result demonstrates that the solvent plays a crucial role in the formation of the precursor and final product with various shapes and sizes. When tested as the cathode material for lithium ion batteries, the sample prepared by solvothermal method exhibits higher discharge capacity, better cycling performance, and more excellent rate capacity. It delivers a discharge capacity of 306.9 mA h g −1 at 0.2 C and 118.6 mA h g −1 even at a high rate of 5.0 C. The outstanding performance of the sample prepared by solvothermal method can be attributed to the well-ordered structure and well-defined morphology with smaller particle size and uniform distribution. The current study paves a new concept and applicable way to prepare high performance Li-rich layered cathode material for LIBs

Bromine-rich Zinc Bromides: Zn6Br12(18-crown-6)2×(Br2)5, Zn4Br8(18-crown-6)2×(Br2)3, and Zn6Br12(18-crown-6)2×(Br2)2.

Science.gov (United States)

Hausmann, David; Feldmann, Claus

2016-06-20

The bromine-rich zinc bromides Zn6Br12(18-crown-6)2×(Br2)5 (1), Zn4Br8(18-crown-6)2×(Br2)3 (2), and Zn6Br12(18-crown-6)2×(Br2)2 (3) are prepared by reaction of ZnBr2, 18-crown-6, and elemental bromine in the ionic liquid [MeBu3N][N(Tf)2] (N(Tf)2 = bis(trifluoromethylsulfonyl)amide). Zn6Br12(18-crown-6)2×(Br2)5 (1) is formed instantaneously by the reaction. Even at room temperature, compound 1 releases bromine, which was confirmed by thermogravimetry (TG) and mass spectrometry (MS). The release of Br2 can also be directly followed by the color and density of the title compounds. With controlled conditions (2 weeks, 25 °C, absence of excess Br2) Zn6Br12(18-crown-6)2×(Br2)5 (1) slowly releases bromine with conconcurrent generation of Zn4Br8(18-crown-6)2×(Br2)3 (2) (in ionic liquid) and Zn6Br12(18-crown-6)2×(Br2)2 (3) (in inert oil). All bromine-rich zinc bromides contain voluminous uncharged (e.g., Zn3Br6(18-crown-6), Zn2Br4(18-crown-6)) or ionic (e.g., [Zn2Br3(18-crown-6)](+), [(Zn2Br6)×(Br2)2](2-)) building units with dibromine molecules between the Zn oligomers and partially interconnecting the Zn-containing building units. Due to the structural similarity, the bromine release is possible via crystal-to-crystal transformation with retention of the crystal shape.

Performance improvement of charge-trap memory by using a stacked Zr_0_._4_6Si_0_._5_4O_2/Al_2O_3 charge-trapping layer

International Nuclear Information System (INIS)

Tang, Zhenjie; Hu, Dan; Zhang, Xiwei; Zhao, Yage; Li, Rong

2016-01-01

The postdeposition annealing (PDA)-treated charge-trap flash memory capacitor with stacked Zr_0_._4_6Si_0_._5_4O_2/Al_2O_3 charge-trapping layer flanked by a SiO_2 tunneling oxide and an Al_2O_3 blocking oxide was fabricated and investigated. It is observed that the memory capacitor exhibits prominent memory characteristics with large memory windows 12.8 V in a ±10 V gate sweeping voltage range, faster program/erase speed, and good data-retention characteristics even at 125 C compared to a single charge-trapping layer (Zr_0_._4_6Si_0_._5_4O_2, Zr_0_._7_9Si_0_._2_1O_2, and Zr_0_._4_6Al_1_._0_8O_2_._5_4). The quantum wells and introduced interfacial traps of the stacked trapping layer regulate the storage and loss behavior of charges, and jointly contribute to the improved memory characteristics. Hence, the memory capacitor with a stacked trapping layer is a promising candidate in future nonvolatile charge-trap memory device design and application. (copyright 2016 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Effects of flux additives on the characteristics of Y2.95Al5O12:0.05Ce3+ phosphor: Particle growth mechanism and luminescence

International Nuclear Information System (INIS)

Chiang, Chung-Hao; Liu, Te-Hsing; Lin, Han-Yu; Kuo, Hung-Yi; Chu, Sheng-Yuan

2013-01-01

The dependence of the amount of the BaF 2 flux additive on the luminescence of Y 2.95 Al 5 O 12 :0.05Ce 3+ phosphors was investigated. The integrated emission intensity of Y 2.95 Al 5 O 12 :0.05Ce 3+ prepared without the flux was enhanced by 29% with the addition of BaF 2 flux at the optimum amount of 6 wt. %. Such an enhancement can be attributed to the purer phase of Y 3 Al 5 O 12 and the morphology change from the irregular shape to spherical shape with the smoother surface due to the flux. The morphology and luminescence of Y 2.95 Al 5 O 12 :0.05Ce 3+ prepared with the 6 wt. % BaF 2 flux additive (Sample II) were further compared with those of Y 2.95 Al 5 O 12 :0.05Ce 3+ prepared with the 7 wt. % H 3 BO 3 flux additive (Sample I). The particle size, particle shape, and integrated emission intensity (λ ex  = 450 nm) of the former were found to be larger, more regular, and 6% higher than those of the latter. The difference in the morphology of Samples I and II, which led to the difference in the emission intensity and the external quantum efficiency, were well explained by the particle growth mechanism

[C II] and {sup 12}CO(1-0) emission maps in HLSJ091828.6+514223: A strongly lensed interacting system at z = 5.24

Energy Technology Data Exchange (ETDEWEB)

Rawle, T. D.; Altieri, B. [ESAC, ESA, P.O. Box 78, Villanueva de la Cañada, E-28691 Madrid (Spain); Egami, E.; Rex, M.; Clement, B. [Steward Observatory, University of Arizona, 933 N. Cherry Ave., Tucson, AZ 85721 (United States); Bussmann, R. S.; Gurwell, M.; Fazio, G. G. [Harvard-Smithsonian Center for Astrophysics, 60 Garden Street, Cambridge, MA 02138 (United States); Ivison, R. J. [Institute for Astronomy, University of Edinburgh, Royal Observatory, Blackford Hill, Edinburgh EH9 3HJ (United Kingdom); Boone, F. [Université de Toulouse, UPS-OMP, CNRS, IRAP, 9 Av. Colonel Roche, BP 44346, F-31028 Toulouse Cedex 4 (France); Combes, F. [Observatoire de Paris, LERMA, CNRS, 61 Av. de l' Observatoire, F-75014 Paris (France); Danielson, A. L. R.; Smail, I.; Swinbank, A. M.; Edge, A. C. [Institute for Computational Cosmology, Durham University, South Road, Durham DH1 3LE (United Kingdom); Richard, J. [CRAL, Université Lyon-1, 9 Av. Charles Andr, F-69561 St Genis Laval (France); Blain, A. W. [Department of Physics and Astronomy, University of Leicester, University Road, Leicester LE1 7RH (United Kingdom); Dessauges-Zavadsky, M. [Observatoire de Genève, Université de Genève, 51 Ch. des Maillettes, 1290, Sauverny (Switzerland); Jones, T. [Department of Physics, University of California, Santa Barbara, CA 93106 (United States); Kneib, J.-P., E-mail: tim.rawle@sciops.esa.int [Laboratoire d' Astrophysique EPFL, Observatoire de Sauverny, Versoix 1290 (Switzerland); and others

2014-03-01

We present Submillimeter Array [C II] 158 μm and Karl G. Jansky Very Large Array {sup 12}CO(1-0) line emission maps for the bright, lensed, submillimeter source at z = 5.2430 behind A 773: HLSJ091828.6+514223 (HLS0918). We combine these measurements with previously reported line profiles, including multiple {sup 12}CO rotational transitions, [C I], water, and [N II], providing some of the best constraints on the properties of the interstellar medium in a galaxy at z > 5. HLS0918 has a total far-infrared (FIR) luminosity L {sub FIR(8–1000} {sub μm)} = (1.6 ± 0.1) × 10{sup 14} L {sub ☉} μ{sup –1}, where the total magnification μ{sub total} = 8.9 ± 1.9, via a new lens model from the [C II] and continuum maps. Despite a HyLIRG luminosity, the FIR continuum shape resembles that of a local LIRG. We simultaneously fit all of the observed spectral line profiles, finding four components that correspond cleanly to discrete spatial structures identified in the maps. The two most redshifted spectral components occupy the nucleus of a massive galaxy, with a source-plane separation <1 kpc. The reddest dominates the continuum map (demagnified L {sub FIR,} {sub component} = (1.1 ± 0.2) × 10{sup 13} L {sub ☉}) and excites strong water emission in both nuclear components via a powerful FIR radiation field from the intense star formation. A third star-forming component is most likely a region of a merging companion (ΔV ∼ 500 km s{sup –1}) exhibiting generally similar gas properties. The bluest component originates from a spatially distinct region and photodissociation region analysis suggests that it is lower density, cooler, and forming stars less vigorously than the other components. Strikingly, it has very strong [N II] emission, which may suggest an ionized, molecular outflow. This comprehensive view of gas properties and morphology in HLS0918 previews the science possible for a large sample of high-redshift galaxies once ALMA attains full sensitivity.

Crystal structure and magnetic properties of La2−x(Sr0.5Ca0.5)1+xMn2O7 (x=0.6, 0.8 and 1.0) Ruddlesden–Popper manganites

International Nuclear Information System (INIS)

Raju, K.; Song, M.S.; Lee, J.Y.

2014-01-01

Double layer perovskite (Ruddlesden–Popper) manganites with the nominal composition of La 2−x (Sr 0.5 Ca 0.5 ) 1+x Mn 2 O 7 (x=0.6, 0.8 and 1.0) were synthesized via a solid state reaction route. X-ray and neutron diffraction were performed at room temperature and the crystal structure was refined using the Rietveld method based on the space group, I4/mmm. The temperature variation of the susceptibility revealed a spin glass transition at 28 K for x=0.6, a charge ordering transition at 245 K and a Neel transition at 170 K for x=1.0. - Highlights: • Lanthanum based double layered manganites were prepared by doping with the same amounts of Sr and Ca. • X-ray and neutron diffraction were performed and the crystal structure was refined using the Rietveld method. • Different magnetic transitions were observed depending upon the doping concentration. • Qualitative explanation for the various observed phenomena was given

Effect of fluorination treatment on electrochemical properties of M1Ni{sub 3.5}Co{sub 0.6}Mn{sub 0.4}Al{sub 0.5} hydrogen storage alloy

Energy Technology Data Exchange (ETDEWEB)

Huang, Hongxia, E-mail: hhxhunan@yahoo.com.cn [College of Chemistry and Bioengineering, Guilin University of Technology, Guilin (China); Huang, Kelong [College of Chemistry and Chemical Engineering, Central South University (China)

2012-05-15

The influence of surface treatment by solutions of NH{sub 4}F, LiF and LiF containing KBH{sub 4} on the structure and electrochemical properties of the M1Ni{sub 3.5}Co{sub 0.6}Mn{sub 0.4}Al{sub 0.5} hydrogen storage alloy (in which M1 denotes mischmetal) is investigated. The fluorination treatment improves the electrochemical performances of the M1Ni{sub 3.5}Co{sub 0.6}Mn{sub 0.4}Al{sub 0.5} alloy. The maximum discharge capacity (C{sub max}) increases from 314.8 to 325.7 (NH{sub 4}F), 326.5 (LiF) and 316.4 mAh g{sup -1} (LiF+KBH{sub 4}). After 60 cycles, the capacity retention rate increases from 83.5 to 84.8% (NH{sub 4}F), 89.5% (LiF) and 93.9% (LiF+KBH{sub 4}). The results of the linear polarization and anodic polarization reveal that the exchange current density (I{sub 0}) and the limiting current density (I{sub L}) increase after fluorination treatment, indicating an improvement of the kinetics of the hydrogen absorption/desorption. (author)

Chromosomal aberrations induced by 12C6+ ions and 6Co γ-rays in mouse immature oocytes

International Nuclear Information System (INIS)

Zhang Hong; Duan Xin; Yuan Zhigang; Li Wenjian; Zhou Guangming; Zhou Qingming; Bing Liu; Min Fengling; Li Xiaoda; Xie Yi

2006-01-01

The ovaries of Kun-Ming strain mice (3 weeks) were irradiated with different doses of 12 C 6+ ion or 6 Co γ-ray. Chromosomal aberrations were analyzed in metaphase II oocytes at 7 weeks after irradiation. The relative biological effectiveness (RBE) of 12 C 6+ ion was calculated with respect to 6 Co γ-ray for the induction of chromosomal aberrations. The 12 C 6+ ion and 6 Co γ-ray dose-response relationships for chromosomal aberrations were plotted by linear quadratic models. The data showed that there was a dose-related increase in frequency of chromosomal aberrations in all the treated groups compared to controls. The RBE values for 12 C 6+ ions relative to 6 Co γ-rays were 2.49, 2.29, 1.57, 1.42 or 1.32 for the doses of 0.5, 1.0, 2.0, 4.0 or 6.0 Gy, respectively. Moreover, a different distribution of the various types of aberrations has been found for 12 C 6+ ion and 6 Co γ-ray irradiations. The dose-response relationships for 12 C 6+ ion and 6 Co γ-ray exhibited positive correlations. The results from the present study may be helpful for assessing genetic damage following exposure of immature oocytes to ionizing radiation

Scalable synthesis of 5,11-diethynylated indeno[1,2-b]fluorene-6,12-diones and exploration of their solid state packing

Directory of Open Access Journals (Sweden)

Bradley D. Rose

2014-09-01

Full Text Available We report a new synthetic route to 5,11-disubstituted indeno[1,2-b]fluorene-6,12-diones that is amenable to larger scale reactions, allowing for the preparation of gram amounts of material. With this new methodology, we explored the effects on crystal packing morphology for the indeno[1,2-b]fluorene-6,12-diones by varying the substituents on the silylethynyl groups.

Atmospheric histories and growth trends of C4F10, C5F12, C6F14, C7F16 and C8F18

Directory of Open Access Journals (Sweden)

R. F. Weiss

2012-05-01

Full Text Available Atmospheric observations and trends are presented for the high molecular weight perfluorocarbons (PFCs: decafluorobutane (C4F10, dodecafluoropentane (C5F12, tetradecafluorohexane (C6F14, hexadecafluoroheptane (C7F16 and octadecafluorooctane (C8F18. Their atmospheric histories are based on measurements of 36 Northern Hemisphere and 46 Southern Hemisphere archived air samples collected between 1973 to 2011 using the Advanced Global Atmospheric Gases Experiment (AGAGE "Medusa" preconcentration gas chromatography-mass spectrometry systems. A new calibration scale was prepared for each PFC, with estimated accuracies of 6.8% for C4F10, 7.8% for C5F12, 4.0% for C6F14, 6.6% for C7F16 and 7.9% for C8F18. Based on our observations the 2011 globally averaged dry air mole fractions of these heavy PFCs are: 0.17 parts-per-trillion (ppt, i.e., parts per 1012 for C4F10, 0.12 ppt for C5F12, 0.27 ppt for C6F14, 0.12 ppt for C7F16 and 0.09 ppt for C8F18. These atmospheric mole fractions combine to contribute to a global average radiative forcing of 0.35 mW m−2, which is 6% of the total anthropogenic PFC radiative forcing (Montzka and Reimann, 2011; Oram et al., 2012. The growth rates of the heavy perfluorocarbons were largest in the late 1990s peaking at 6.2 parts per quadrillion (ppq, i.e., parts per 1015 per year (yr for C4F10, at 5.0 ppq yr−1 for C5F12 and 16.6 ppq yr−1 for C6F14 and in the early 1990s for C7F16 at 4.7 ppq yr−1 and in the mid 1990s for C8F18 at 4.8 ppq yr−1. The 2011 globally averaged mean atmospheric growth rates of these PFCs are subsequently lower at 2.2 ppq yr−1 for C4F10, 1.4 ppq yr−1 for C5F12, 5.0 ppq yr−1 for C6F14, 3.4 ppq yr−1 for C7F16 and 0.9 ppq yr−1 for C8F18. The more recent slowdown in the growth rates suggests that emissions are declining as compared to the 1980s and 1990s.

Comparison of evening and morning dosing of travoprost 0.004%/timolol 0.5% fixed combination in 6 month period.

Science.gov (United States)

Suić, Smiljka Popović; Laus, Katia Novak; Dosen, Vukosava Maricic; Ekert, Miroslav; Mandić, Zdravko; Bojić, Lovro

2010-09-01

An open label, multi-center, 6 months observational study of new fixed combination (travoprost 0.004%/timolol 0.5%), in order to evaluate both efficacy (intraocular pressure lowering) and tolerability (patient and investigator satisfaction) of two dosing regimens--evening (PM) and morning (AM). After screening for enrollment, to 40 patients (79 eyes with primary open angle glaucoma or ocular hypertension), new fixed combination travoprost 0.004%/timolol 0.5% was prescribed once a day in the evening (PM). Patients were enrolled according to each investigator decision on indication for travoprost 0.004%/timolol 0.5% fixed combination once a day, without washout period after previous medication. Intraocular pressure was measured at 9 AM at all time control points: at baseline, after 1 month, after 3 months and after 6 month. After 1 month, screening for nonresponders (criteria: 20% intraocular pressure lowering) and subjects with major side effects was performed. At second control visit, after 3 months PM dosing, intraocular pressure was measured and patients were instructed to continue once a day the same medication, but in the morning (AM) for consequent 3 months. After 1 month, reduction in mean intraocular pressure value was 21.66%. At the visit after 3 month, the mean intraocular pressure was 15.67 +/- 2.17 mm Hg (reduction 21.14%). 3 month after dosing regimen changed to AM (6 month after beginning of travoprost 0.004%/timolol 0.5% combination therapy), reduction in intraocular pressure value was 19.86%. The differences (mean +/- standard deviation) in intraocular pressure values after 1, 3 and 6 month were all highly statistically significant compared to baseline values. The tolerability was evaluated in five steps (Likert scale) ranging from unsatisfactory to excellent by both patient and investigator--taken at 3 and 6 month control visit. 95% of patients and 100% of investigators were satisfied with the possibility of choosing dosing regimen for travoprost 0

Sol-Gel Synthesis of La(0.6)Sr(0.4)CoO(3-x) and Sm(0.5)Sr(0.5)CoO(3-x) Cathode Nanopowders for Solid Oxide Fuel Cells

Science.gov (United States)

Bansal, Narottam P.; Wise, Brent

2011-01-01

Nanopowders of La(0.6)Sr(0.4)CoO(3-x) (LSC) and Sm(0.5)Sr(0.5)CoO(3-x) (SSC) compositions, which are being investigated as cathode materials for intermediate temperature solid oxide fuel cells (IT-SOFC) with La(Sr)Ga(Mg)O(3-x) (LSGM) as the electrolyte, were synthesized by low-temperature sol-gel method using metal nitrates and citric acid. Thermal decomposition of the citrate gels was followed by simultaneous DSC/TGA methods. Development of phases in the gels, on heat treatments at various temperatures, was monitored by x-ray diffraction. Solgel powders calcined at 550 to 1000 C consisted of a number of phases. Single perovskite phase La(0.6)Sr(0.4)CoO(3-x) or Sm(0.5)Sr(0.5)CoO(3-x) powders were obtained at 1200 and 1300 C, respectively. Morphological analysis of the powders calcined at various temperatures was done by scanning electron microscopy. The average particle size of the powders was approx.15 nm after 700 C calcinations and slowly increased to 70 to 100 nm after heat treatments at 1300 to 1400 C.

The synthesis, structure, and properties of 5,6,11,12-tetraarylindeno[1,2-b]fluorenes and their applications as donors for organic photovoltaic devices

KAUST Repository

Lo, Yuan-Chih; Ting, Hao-Chun; Li, Ya-Ze; Li, Yi-Hua; Liu, Shun-Wei; Huang, Kuo-Wei; Wong, Ken-Tsung

2016-01-01

The synthesis, structure, and properties of three new 5,6,11,12-tetraarylindeno[1,2-b]fluorenes are reported. The highly twisted conformations between an indeno[1,2-b]fluorene core and peripheral aryl substitutions endow these indeno[1,2-b]fluorene derivatives with good photostability for use as electron donors for vacuum-deposited photovoltaic devices. The optimized device based on a TAInF2 donor blended with C70 as an electron acceptor produces a high open-circuit voltage (>0.9 V) and a power conversion efficiency of 2.91%. This work demonstrates the first application of an indenofluorene derivative as an electron donor in organic solar cells.

The synthesis, structure, and properties of 5,6,11,12-tetraarylindeno[1,2-b]fluorenes and their applications as donors for organic photovoltaic devices

KAUST Repository

Lo, Yuan-Chih

2016-12-01

The synthesis, structure, and properties of three new 5,6,11,12-tetraarylindeno[1,2-b]fluorenes are reported. The highly twisted conformations between an indeno[1,2-b]fluorene core and peripheral aryl substitutions endow these indeno[1,2-b]fluorene derivatives with good photostability for use as electron donors for vacuum-deposited photovoltaic devices. The optimized device based on a TAInF2 donor blended with C70 as an electron acceptor produces a high open-circuit voltage (>0.9 V) and a power conversion efficiency of 2.91%. This work demonstrates the first application of an indenofluorene derivative as an electron donor in organic solar cells.

A new, high energy rechargeable lithium ion battery with a surface-treated Li1.2Mn0.54Ni0.13Co0.13O2 cathode and a nano-structured Li4Ti5O12 anode

International Nuclear Information System (INIS)

Liu, Xiaoyu; Huang, Tao; Yu, Aishui

2015-01-01

Through elaborate design, a new rechargeable lithium ion battery has been developed by comprising a surface-treated Li 1.2 Mn 0.54 Ni 0.13 Co 0.13 O 2 cathode and a nano-structured Li 4 Ti 5 O 12 anode. After precondition Na 2 S 2 O 8 treatment, the initial coulombic efficiency of Li 1.2 Mn 0.54 Ni 0.13 Co 0.13 O 2 cathode has been significantly increased and can be compatible with that of the nano-structured Li 4 Ti 5 O 12 anode. The optimization of structure and morphology for both active electrode materials result in their remarkable electrochemical performances in respective lithium half-cells. Ultimately, the rechargeable lithium ion full battery consisting of both electrodes delivers a specific capacity of 99.0 mAh g −1 and a practical energy density of 201 Wh kg −1 , based on the total weight of both active electrode materials. Furthermore, as a promising candidate in the lithium ion battery field, this full battery also achieves highly attractive electrochemical performance with high coulombic efficiency, excellent cycling stability and outstanding rate capability. Thus the proposed battery displays broad practical application prospects for next generation of high-energy lithium ion battery. - Highlights: • The Li 1.2 Mn 0.54 Ni 0.13 Co 0.13 O 2 cathode is surface-treated by Na 2 S 2 O 8 . • The nano-sized Li 4 Ti 5 O 12 anode is obtained by a solid-state method. • A new Li 1.2 Mn 0.54 Ni 0.13 Co 0.13 O 2 /Li 4 Ti 5 O 12 lithium ion battery is developed. • The battery shows high coulombic efficiency, specific capacity and energy density. • The battery shows high capacity retention rate and good high-rate capability

5 CFR 2430.12 - Administrative Law Judge's decision; contents; service; transfer of case to the Authority...

Science.gov (United States)

2010-01-01

... Administrative Law Judge's decision and of the order transferring the case to the Board shall be complete upon... 5 Administrative Personnel 3 2010-01-01 2010-01-01 false Administrative Law Judge's decision; contents; service; transfer of case to the Authority; contents of record in case. 2430.12 Section 2430.12...

Investigation of the crystal structure of a basic bismuth(III) nitrate with the composition [Bi6O4(OH)(4)](0.54(1))[Bi6O5(OH)(3)](0.46(1))(NO3)(5.54(1))

DEFF Research Database (Denmark)

Christensen, Axel Norlund; Lebech, Bente

2012-01-01

A basic bismuth(III) nitrate with the composition [Bi6O4(OH)(4)](0.5)[Bi6O5(OH)(3)](0.5)(NO3)(5.5) formed in a slow crystal growth mode has an ordered crystal structure with the monoclinic space group P2(1) and lattice parameters a = 15.850(3), b = 14.986(3), c = 18.230(4) angstrom, beta = 107...... a trigonal R (3) over bar cell with a = 15.1865(1) and c = 15.8416(1) angstrom (hexagonal setting). In a Rietveld type structure model refinement with a total of 28 atom sites (4 Bi, 3 N, 15 O and 6 H), the composition of this sample is determined to be [Bi6O4(OH)(4)](0.54(1))[Bi6O5(OH)(3)](0.46(1))(NO3)(5.54(1))....

7 CFR 371.6 - Wildlife Services.

Science.gov (United States)

2010-01-01

... 7 Agriculture 5 2010-01-01 2010-01-01 false Wildlife Services. 371.6 Section 371.6 Agriculture..., DEPARTMENT OF AGRICULTURE ORGANIZATION, FUNCTIONS, AND DELEGATIONS OF AUTHORITY § 371.6 Wildlife Services. (a) General statement. Wildlife Services (WS) manages problems caused by wildlife. (b) Deputy Administrator of...

Synthesis and Spectral Analysis of 3,4,5-trichloro-6-(dibenzo[d,f][1,3]diazepin-5-yl-[1,2]-benzoquinones

Directory of Open Access Journals (Sweden)

Mohsen A. M. Gomaa

2011-01-01

Full Text Available Reaction of N1,N2-di-(4-methoxyphenyl- or N1,N2-di-(4-hydroxyphenyl -amidines (1a-d with 3,4,5,6-tetrachloro-1,2-benzoquinone (2 in ethyl acetate at room temperature led to formation of new 3,4,5-trichloro-6-(2-hydroxy-6-methyldibenzo[d,f][1,3]diazepin-5-yl[1,2]-benzoquinones (3a-d in addition to N-aryl-N'-(6,7,8,9-tetrachloro-4-hydroxydibenzo-[1,4]dioxin-2-ylacetamidines (4a,b. The rational of formation of products 3a-d and 4a,b was discussed and structures were confirmed on the basis of elemental analysis and spectral data.

Large low field room temperature magneto-dielectric response from (Sr_0_._5Ba_0_._5)Nb_2O_6/Co(Cr_0_._4Fe_1_._6)O_4 bulk 3-0 composites

International Nuclear Information System (INIS)

Rathore, Satyapal Singh; Vitta, Satish

2016-01-01

Highlights: • The essential highlights of this work are;. • Bulk composite with varying amounts of relaxor and ferromagnetic phases has been synthesized by simple steps. • Processing yields an optimal structure with 30% ferromagnetic phase to couple the two ferroic orders. • Magneto dielectric constant shows large changes, 3.2%, at room temperature in moderate magnetic fields. • Large changes in dielectric constant are due to configurational arrangement of the two phases. - Abstract: Bulk magneto-dielectric composites with a 3-0 configuration comprised of ferroelectric-magnetostrictive phases have been synthesized using (Sr_0_._5Ba_0_._5)Nb_2O_6–Co(Cr_0_._4Fe_1_._6)O_4 as the two constituents, respectively. The ferroelectric phase made by a dual stage sintering process has a uniform grain size of 15 μm while the magnetostrictive phase has a grain size of 2–3 μm. Composites synthesized by conventional solid state processing using these two constituents exhibit large magneto-dielectric coupling at room temperature which increases with increasing magnetic field. The composite with 30% magnetostrictive phase distributed uniformly in the ferroelectric phase has the most desirable microstructure and exhibits a large coupling with 3.2% change in the dielectric constant at 1 kHz and 8 kOe magnetic field. This change in dielectric constant was found to be a maximum with respect to variation of the fraction of magnetostrictive phase, indicating that 30% is the optimal value to realize large coupling between the two phases. The decrease in magneto-dielectric constant upon application of an external magnetic field is possibly due to the inherent magnetoresistance of the magnetic component. The resistivity of the magnetic component decreases in an external magnetic field leading to the formation of 3D percolating conducting paths. This causes the coupling to decrease in composites with >30% magnetostrictive phase.

12 CFR 600.10 - Service of Process.

Science.gov (United States)

2010-01-01

... 12 Banks and Banking 6 2010-01-01 2010-01-01 false Service of Process. 600.10 Section 600.10 Banks... Procedures for Service Upon the Farm Credit Administration § 600.10 Service of Process. (a) Except as... Administration Board, 1501 Farm Credit Drive, McLean, Virginia 22102-5090. (b) Service of process upon the...

Effect of cerium addition on the microstructure, electrical and relaxor behavior of Sr{sub 0.5}Ba{sub 0.5}Nb{sub 2}O{sub 6} ceramics

Energy Technology Data Exchange (ETDEWEB)

Velayutham, T.S., E-mail: t_selvi@um.edu.my; Salim, N.I.F.; Gan, W.C.; Abd Majid, W.H.

2016-05-05

Sr{sub 0.5}Ba{sub 0.5}Nb{sub 2}O{sub 6} (SBN50) ceramic doped with different concentrations of Cerium (Ce) according to the stoichiometry formulation of Sr{sub 0.5-3y/2}Ba{sub 0.5}Ce{sub y}Nb{sub 2}O{sub 6} (Ce-SBN) with y = 0, 0.01, 0.02, 0.03, 0.04 and 0.05 was prepared using the conventional solid state reaction method. The morphology, structure, and electrical properties of the samples were studied using field emission scanning electron microscope (FESEM), X-ray diffraction (XRD), ferroelectric and dielectric spectroscopy, respectively. The FESEM images reveal a strong influence of cerium on the SBN microstructure. The X-ray diffraction patterns show that all compositions of SBN ceramic exhibit tetragonal tungsten bronze structure. As the dopant concentration, y increased, both unit cell volume and axial ratio c/a decreased gradually. In addition, dopant incorporation lowers the phase transition temperature, T{sub m}. As a result, all practical parameters are sufficiently increased, i.e. the dielectric constant and remnant polarization. SBN50 doped with a 3% Ce sample is most attractive for practical applications due to its high remnant polarization, P{sub r} = 58.6 μC/cm{sup 2} and dielectric constant, ε’ ≈ 8000 (10 kHz) at room temperature, respectively. - Highlights: • Sr{sub 0.5-3y/2}Ba{sub 0.5}Ce{sub y}Nb{sub 2}O{sub 6} synthesized using solid-state reaction method. • Cerium dopant improved the overall properties of SBN. • Dopant incorporation lowers the phase transition temperature, T{sub m}. • 3% Ce dopant exhibits best functional properties among the rest of the composition. • The P{sub r} of 3%Ce-doped SBN is 58.6 μC/cm{sup 2} and ε’ ≈ 8000 (10 kHz) at room temperature.

[Socioeconomic inequalities in oral health service utilization any time in their lives for Mexican schoolchildren from 6 to 12 years old].

Science.gov (United States)

Jiménez-Gayosso, Sandra Isabel; Medina-Solís, Carlo Eduardo; Lara-Carrillo, Edith; Scougal-Vilchis, Rogelio José; de la Rosa-Santillana, Rubén; Márquez-Rodríguez, Sonia; Mendoza-Rodríguez, Martha; Navarrete-Hernández, José de Jesús

2015-01-01

To determine the prevalence and the existence of socioeconomic inequalities in dental health service utilization (DHSU) any time in the life of Mexican schoolchildren aged 6-12 years of Pachuca Hidalgo, Mexico. We performed a cross-sectional study in 1,404 school children 6-12 years of age from 14 public schools in the city of Pachuca, Hidalgo, Mexico. Questionnaires were distributed to determine socioeconomic position variables (SEP). The dependent variable was DHSU once in life (0 = No, 1 = Yes). The analysis was performed in Stata 9 using chi-square tests. The mean age was 8.97 ± 1.99 years, 50.1% were boys. The prevalence of DHSU any time in life was 71.4%. The DHSU percentage increased according increasing age (p insurance, car ownership in the home, dwelling and household characteristics, a better level of SEP increased prevalence of DHSU. Although in the mother's schooling no differences were observed (p > 0.05), father's schooling was associated (p < 0.05) inversely to expectations. The findings of this study demonstrate that the prevalence of DHSU was not 100%; 28.6% of children have never had contact with a dentist. We identified certain indicator variables of SEP associated with DHSU, indicating the existence of inequalities in this oral health indicator.

Conceptos de ataque frente a variantes defensivas 6:0 y 5:1 [Concepts of attacks against the variants defensive 6:0 and 5:1

Directory of Open Access Journals (Sweden)

Juan de Dios Román Seco

2009-12-01

Full Text Available Resumen: La filosofía del juego de ataque contra diferentes Sistemas Defensivos tiene una raíz basada en los Principios Tácticos Colectivos del Ataque que se orienta y apoya a nivel práctico en los medios tácticos colectivos. Las diferentes estructuras colectivas en defensa exigen cumplir aquellos y saber elegir los medios tácticos adecuados. En síntesis, no existen "recetas" para resolver problemas sino la utilización de los medios tácticos adecuados. La estrategia tiene su fundamento y lleva al éxito siempre que se defina a partir de buenas bases tácticas. Palabras clave: Ataque, Defensa 6:0, Defensa 5.1 Abstract: The philosophy of the attack game against different Defensive Systems has a root based on the Principles Tactical Communities of the Attack that it is guided and it supports at practical level in the collective tactical means. The different collective structures in defense demand to complete those and to know how to choose the appropriate tactical means. In synthesis, recipes don't exist to solve problems but the use of the appropriate tactical means. The strategy has its foundation and it takes to the success whenever he/she is defined starting from good tactical bases. Key words: Attacks, variant defensive 6:0, variant defensive 5:1.

Women and men in education services: comparison of gender representation in Italian pre-school (0-6 services.

Directory of Open Access Journals (Sweden)

Rosy Nardone

2014-12-01

Full Text Available This contribution presents a part of the results of the research project entitled “Stereotipi di genere, relazioni educative e infanzie” (“Gender stereotypes, educational relationships and childhood" conducted between 2010 and 2012 by a group of researchers from the CSGE (Gender and Education Study Centre of the University of Bologna, funded by the Emilia-Romagna Region. The research aimed to measure the ideas and representations of gender and the gender relations among adults who are educationally significant for preschool children (0-6 years, and to develop widespread reflection on the issue of the stereotyped images of female and male identity that still exist and are transmitted from a very early age. This article particularly focuses on the analysis developed on gender representations in educational services 0-6 years by the professionals working in the centres involved, relating quantitative data with the considerations that emerged from the focus groups, about the female and male in education.

39 CFR 6.5 - Minutes of meetings.

Science.gov (United States)

2010-07-01

... 39 Postal Service 1 2010-07-01 2010-07-01 false Minutes of meetings. 6.5 Section 6.5 Postal Service UNITED STATES POSTAL SERVICE THE BOARD OF GOVERNORS OF THE U.S. POSTAL SERVICE MEETINGS (ARTICLE...) or 39 U.S.C. 410(c). ...

Magneto-optical properties BaBi{sub x}La{sub x}Fe{sub 12−2x}O{sub 19} (0.0≤x≤0.5) hexaferrites

Energy Technology Data Exchange (ETDEWEB)

Auwal, I.A. [Department of Chemistry, Fatih University, 34500 B.Çekmece, İstanbul (Turkey); Baykal, A., E-mail: hbaykal@fatih.edu.tr [Department of Chemistry, Fatih University, 34500 B.Çekmece, İstanbul (Turkey); Güner, S. [Department of Physics, Fatih University, 34500 B.Çekmece, İstanbul (Turkey); Sertkol, M. [Department of Physics Engineering, Istanbul Technical University, 34469 Maslak, Istanbul (Turkey); Sözeri, H. [TUBITAK-UME, National Metrology Institute, P.O. Box 54, 41470 Gebze, Kocaeli (Turkey)

2016-07-01

BaBi{sub x}La{sub x}Fe{sub (12−2x)}O{sub 19} (0.0≤x≤0.5) hexaferrites were synthesized by solid state synthesis route and the effects of Bi, La substitutions on structural, magnetic and optical properties were investigated. X-ray powder diffraction, Scanning electron microscopy, Vibrating sample magnetometer, and Percent diffuse reflectance spectroscopy were used to study the physical properties. Room temperature specific magnetization (M–H) curves revealed the ferromagnetic nature of all products. The increasing Bi, La compositions increased the magnetic properties at different magnitudes with respect to undoped BaFe{sub 12}O{sub 19} sample. The maximum values of remnant specific magnetization (M{sub r}=30.3 emu/g), extrapolated specific saturation magnetization (M{sub s}=62.12 emu/g), and magneton number (n{sub B}=16.27) were recorded from BaBi{sub 0.2}La{sub 0.2}Fe{sub 11.4}O{sub 19} hexaferrite. The average crystallite size varies in a range of (37.35–51.36) nm. The coercive field (H{sub c}) of undoped hexaferrites is 1180 Oe and increased to maximum 2320 Oe belonging to BaBi{sub 0.4}La{sub 0.4}Fe{sub 11.2}O{sub 19}. Magnetic anisotropy was confirmed as uniaxial and calculated effective anisotropy constants (K{sub eff}) are between 4.27×10{sup 5} Ergs/g and 5.05×10{sup 5} Ergs/g. The high magnitudes of magnetocrystalline anisotropy (H{sub a}) above than 16,200 Oe revealed that all samples are magnetically hard materials. The Tauc plots were drawn to extrapolate the direct optical energy band gap (E{sub g}) of hexaferrites. The E{sub g} values decreased from 1.76 eV to 1.47 eV with increasing Bi, La compositions. - Highlights: • BaBi{sub x}La{sub x}Fe{sub (12−2x)}O{sub 19} (0.0≤x≤0.5) hexaferrites were synthesized by solid state synthesis route. • The E{sub g} values decreased from 1.76 eV to 1.47 eV with increasing Bi, La compositions. • BaBi{sub xx}La{sub xx}Fe{sub 12-2x}O{sub 19} hexaferrites good candidate for potential applications

12 CFR 561.45 - Service corporation.

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2010-01-01

... 12 Banks and Banking 5 2010-01-01 2010-01-01 false Service corporation. 561.45 Section 561.45... AFFECTING ALL SAVINGS ASSOCIATIONS § 561.45 Service corporation. The term service corporation means any corporation, the majority of the capital stock of which is owned by one or more savings associations and which...

Dipropyl 3,6-diphenyl-1,2-dihydro-1,2,4,5-tetrazine-1,2-dicarboxylate.

Science.gov (United States)

Rao, Guo-Wu; Hu, Wei-Xiao

2003-05-01

The title compound, C(22)H(24)N(4)O(4), was prepared from propyl chloroformate and 3,6-diphenyl-1,2-dihydro-s-tetrazine. This reaction yields the title compound rather than dipropyl 3,6-diphenyl-1,4-dihydro-s-tetrazine-1,4-dicarboxylate. The 2,3-diazabutadiene group in the central six-membered ring is not planar; the C=N double-bond length is 1.285 (2) A, and the average N-N single-bond length is 1.401 (3) A, indicating a lack of conjugation. The ring has a twist conformation, in which adjacent N atoms lie +/- 0.3268 (17) A from the plane of the ring. The molecule has twofold crystallographic symmetry.

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.

12 CFR 618.8010 - Related services authorization process.

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2010-01-01

... 12 Banks and Banking 6 2010-01-01 2010-01-01 false Related services authorization process. 618... PROVISIONS Related Services § 618.8010 Related services authorization process. (a) Authorities. System banks and associations may only offer related services that meet the criteria specified in this regulation...

Experimental and theoretical studies of the C{sub 6}H{sub 5} + C{sub 6}H{sub 6} reaction

Energy Technology Data Exchange (ETDEWEB)

Park, J.; Burova, S.; Rodgers, A.S.; Lin, M.C.

1999-11-11

The absolute rate constants for the C{sub 6}H{sub 5} + C{sub 6}H{sub 6} and C{sub 6}D{sub 6} reactions have been measured by cavity ringdown spectrometry at temperatures between 298 and 495 K at a constant 40 Torr Ar pressure. The new results, which reveal no detectable kinetic isotopic effect, can be represented by the Arrhenius equation, {kappa}{sub 1} = 10{sup (11.91{+-}0.13)} exp[{minus}(2,102 {+-} 106)/T] cm{sup 3}/(mol s). Low-temperature data for the addition/stabilization process, C{sub 6}H{sub 5} + C{sub 6}H{sub 6} {r{underscore}arrow} C{sub 12}H{sub 11}, can be correlated with those obtained in a low-pressure, high-temperature Knudsen cell study for the addition/displacement reaction, C{sub 6}H{sub 5} + C{sub 6}H{sub 6} {r{underscore}arrow} C{sub 12}H{sub 10} + H, by the RRKM theory using the molecular and transition-state parameters computed at the B3LYP/6-311G(d,p) level of theory. Combination of these two sets of data gives {kappa}{sub 1} = 10{sup (11.98{+-}0.03)} exp[{minus}(2168 {+-} 34)/T] cm{sup 3}/(mol s) covering the temperature range 298--1,330 K. The RRKM theory also correlates satisfactorily the forward reaction data with the high-temperature shock-tube result for the reverse H-for-C{sub 6}H{sub 5} substitution process with 2.7 and 4.7 kcal/mol barriers for the entrance (C{sub 6}H{sub 5} + C{sub 6}H{sub 6}) and reverse (H + C{sub 12}H{sub 10}) reactions, respectively. For modeling applications, the authors have calculated the forward reaction rate constants for the formation of the two competing products, H + C{sub 12}H{sub 10} and C{sub 12}H{sub 11}, at several pressures covering 300 K {lt} T {lt} 2,500 K.

An Expeditious Synthesis of [1,2]Isoxazolidin-5-ones and [1,2]Oxazin-6-ones from Functional Allyl Bromide Derivatives

Directory of Open Access Journals (Sweden)

Imen Beltaïef

2010-06-01

Full Text Available Reaction of allyl bromide (Z-1 and (Z-2 with N-substituted hydroxylamine hydrochlorides in presence of tert-butoxide in tert-butanol at reflux provides a short and effective route to [1,2]isoxazolidin-5-ones 3 and [1,2]oxazin-6-ones 4.

Charge-ordering, magnetic and electric-transport properties of Bi0.6-xEuxCa0.4MnO3 (0.0≤x≤0.6)

International Nuclear Information System (INIS)

Yadava, Kamlesh; Varma, G.D.; Singh, M.P.; Razavi, F.S.

2012-01-01

We have studied structure, magnetic and transport properties of polycrystalline Bi 0.6-x Eu x Ca 0.4 MnO 3 (x=0.0, 0.1, 0.2, 0.3, 0.4, 0.5 and 0.6) perovskite manganites. Magnetic measurements show that the charge-ordering temperature (T CO ) decreases with increasing x up to x=0.4 and then slightly increases with further increasing x up to x=0.6. Further, the antiferromagnetic (AFM) ordering temperature (T N ) decreases with increasing x. At T N a transition to metamagnetic glass like state is also seen. Eu doping also leads to enhancement in the magnetic moment and a concomitant decrease in resistivity up to x=0.2 and then an increase in resistivity up to x=0.5. We propose that the local lattice distortion induced by the size mismatch between the A-site cations and 6s 2 character of Bi 3+ lone pair electron are responsible for the observed variation in physical properties. (author)

5,11-Ditosyl-5H,11H-dibenzo[b,f][1,5]diazocine-6,12-dione acetic acid hemisolvate

Directory of Open Access Journals (Sweden)

Najat Abbassi

2013-04-01

Full Text Available The molecular structure of the title compound, C28H22N2O6S2·0.5CH3COOH, is built up from three fused rings, two six and one eight membered. The eight-membered ring shows a boat conformation and the dihedral angle between the two benzene groups attached thereto is 66.43 (11°, resulting in a V-shaped geometry. Two tosyl substituents are bound to the N atoms. The planes through the tolyl rings are roughly perpendicular, as indicated by the dihedral angle of 82.44 (12°. In the crystal, the molecule and its inversion-related symmetry-equivalent are linked to the acetic acid solvent molecule by non-classical O—H...O and C—H...O hydrogen bonds. Two half-occupied acetic acid solvent molecules are disordered at the same site and linked by a center of symmetry.

Suitability of Sr{sub 0.5}Ba{sub 0.5-x}Ce{sub x}Fe{sub 12-y}Ni{sub y}O{sub 19} co-precipitated nanomaterials for inductor applications

Energy Technology Data Exchange (ETDEWEB)

Iqbal, Muhammad Javed, E-mail: mjiqauchem@yahoo.co [Surface and Solid State Chemistry Laboratory, Department of Chemistry, Quaid-i-Azam University, Islamabad 45320 (Pakistan); Farooq, Saima [Surface and Solid State Chemistry Laboratory, Department of Chemistry, Quaid-i-Azam University, Islamabad 45320 (Pakistan)

2010-03-18

The present investigation deals with the synthesis and characterization of Ce-Ni ions substituted nanocrystalline strontium-barium hexaferrites (Sr{sub 0.5}Ba{sub 0.5}Fe{sub 12}O{sub 19}) by the chemical co-precipitation method, with focus on the optimization of annealing temperature for the hexagonal phase development. The synthesis involves co-precipitation of aqueous solutions of water-soluble salts of strontium, barium and iron, at pH 9 using an ammonium hydroxide solution as a precipitating agent. The optimum temperature of annealing, necessary for the hexagonal phase development, is determined on the basis of thermo-gravimetric analysis (TGA). The co-precipitate is annealed at a temperature of 1323 K for 6 h, to produce a single magnetoplumbite phase of Sr-Ba hexaferrites, with the corresponding average crystallite size ranging from 36 to 48 nm. Observed changes in the lattice structure determined by the powder X-ray diffraction (XRD) studies are not in contradiction with the results of TGA. DC-electrical resistivity increases from 1.8 x 10{sup 10} to 12.5 x 10{sup 10} {Omega} cm, whereas the drift mobility, dielectric constant and dielectric loss tangent decrease with increasing the Ce-Ni content of the samples. Material of above-mentioned characteristics is considered to be suitable for applications in the microwave and surface mount devices (SMD) for fabricating the multilayer chip inductors (MLCI).

Magnetic and charge ordering properties of Bi0.6−xEuxCa0.4MnO3 (0.0≤x≤0.6)

International Nuclear Information System (INIS)

Yadav, Kamlesh; Singh, M.P.; Razavi, F.S.; Varma, G.D.

2012-01-01

We have studied structure, magnetic and transport properties of polycrystalline Bi 0.6−x Eu x Ca 0.4 MnO 3 (x=0.0, 0.1, 0.2, 0.3, 0.4, 0.5 and 0.6) perovskite manganites. Magnetic measurements show that the charge-ordering temperature (T CO ) decreases with increasing x up to x=0.4 and then slightly increases with further increasing x up to x=0.6. Further, the antiferromagnetic (AFM) ordering temperature (T N ) decreases with increasing x. At T N a transition to metamagnetic glass like state is also seen. Eu doping also leads to enhancement in the magnetic moment and a concomitant decrease in resistivity up to x=0.2 and then an increase in resistivity up to x=0.5. We propose that the local lattice distortion induced by the size mismatch between the A-site cations and 6s 2 character of Bi 3+ lone pair electron are responsible for the observed variation in physical properties. - Highlights: ► We have studied structure, magnetic and transport properties of Bi 0.6−x Eu x Ca 0.4 MnO 3 (0.0≤x≤0.6). ► Substitution of Eu at Bi-site induces a strong interplay between the magnetic and charge-ordering properties. ► T CO decreases with increasing x up to x=0.4 and then slightly increases with further increasing x up to x=0.6. ► The antiferromagnetic ordering temperature (T N ) decreases with increasing x. ► The A-site cations size mismatch and 6s 2 character of Bi 3+ lone pair electron explain variation in physical properties.

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

Composition and phase analysis of nanocrystalline Ba{sub x}Sr{sub 1-x}Fe{sub 12}O{sub 19} (x = 1.0; 0.6; and 0.4) by using general structure analysis system

Energy Technology Data Exchange (ETDEWEB)

Gunanto, Y. E., E-mail: yohanes.gunanto@uph.edu [Departement of Biology Education, Pelita Harapan University, Karawaci, Tangerang, 15811 (Indonesia); Jobiliong, E., E-mail: eric.jobiliong@uph.edu [Departement of Industrial Engineering, Pelita Harapan University, Karawaci, Tangerang, 15811 (Indonesia); Adi, Wisnu Ari, E-mail: dwisnuaa@batan.go.id [Centre for Sci. and Tech. of Adv. Materials, BATAN, Serpong, Tangerang Selatan, 15314 (Indonesia)

2016-03-11

Single phase of nanocrystalline Ba{sub x}Sr{sub 1-x}Fe{sub 12}O{sub 19} (x = 1.0; 0.6; and 0.4) was successfully synthesized by mechanical milling method and thermal process. Stoichiometric quantities of analytical-grade SrCO{sub 3}, BaCO{sub 3}, and Fe{sub 2}O{sub 3}, were mixed and milled using a high-energy milling. The mixture of all precursors was sintered at a temperature of 1000 °C for 10 hours. The refinement of x-ray diffraction trace for all samples confirmed a single phase material with a hexagonal structure. The increase of the amount of strontium content in the barium atoms in the Ba{sub x}Sr{sub 1-x}Fe{sub 12}O{sub 19} system can decrease the lattice parameter which have been successfully substituted into the barium atoms. The calculation result of cationic distribution showed that the Ba{sub x}Sr{sub 1-x}Fe{sub 12}O{sub 19} (x = 0.6) and (x = 0.4) samples have nominal composition of Ba{sub 0,61}Sr{sub 0,39}Fe{sub 12}O{sub 19} and Ba{sub 0,37}Sr{sub 0,63}Fe{sub 12}O{sub 19}, respectively. Results of the mean of crystallite size evaluation for respective powder materials showed that the Ba{sub x}Sr{sub 1-x}Fe{sub 12}O{sub 19} (x = 1.0; 0.6; and 0.4) samples have the crystallite size of 22 nm, 25 nm and 34 nm, respectively. We concluded that the cationic distribution of barium atoms was successfully substituted by strontium atoms approaching the nominal stoichiometric composition.

Laser spectroscopy of the 5P3/2 → 6Pj (j = 1/2 and 3/2) electric dipole forbidden transitions in atomic rubidium

Science.gov (United States)

Ponciano-Ojeda, F.; Hernández-Gómez, S.; Mojica-Casique, C.; Hoyos, L. M.; Flores-Mijangos, J.; Ramírez-Martínez, F.; Sahagún, D.; Jáuregui, R.; Jiménez-Mier, J.

2018-04-01

Doppler-free optical double-resonance spectroscopy is used to study the 5S1/2 → 5P3/2 → 6Pj (j = 3/2,1/2) excitation sequence in room-temperature rubidium atoms. This involves a 5S1/2 → 5P3/2 electric dipole preparation step followed by the 5P3/2 → 6Pj electric quadrupole excitation. The electric dipole forbidden transitions occur at 911.0 nm (j = 3/2) and 917.5 nm (j = 1/2). Production of atoms in the 6Pj states is detected by observing their direct decay to the ground state through emission of blue photons (λ ≈ 420 nm). A detailed experimental and theoretical study of the dependence on the relative linear polarizations of excitation beams is made. It is shown that specific electric quadrupole selection rules over magnetic quantum numbers are directly related to the relative orientation of the linear polarization of the excitation beams.

12 CFR 510.4 - Service of process.

Science.gov (United States)

2010-01-01

... 12 Banks and Banking 5 2010-01-01 2010-01-01 false Service of process. 510.4 Section 510.4 Banks and Banking OFFICE OF THRIFT SUPERVISION, DEPARTMENT OF THE TREASURY MISCELLANEOUS ORGANIZATIONAL REGULATIONS § 510.4 Service of process. (a) Service of Process. Service of process may be made upon the Office...

Isochrones for old (>5 Gyr) stars and stellar populations. I. Models for –2.4 ≤ [Fe/H] ≤+0.6, 0.25 ≤ Y ≤ 0.33, and –0.4 ≤ [α/Fe] ≤+0.4

Energy Technology Data Exchange (ETDEWEB)

VandenBerg, Don A. [Department of Physics and Astronomy, University of Victoria, P.O. Box 1700 STN CSC, Victoria, B.C., V8W 2Y2 (Canada); Bergbusch, Peter A. [Department of Physics, University of Regina, Regina, Saskatchewan, S4S 0A2 (Canada); Ferguson, Jason W. [Department of Physics, Wichita State University, Wichita, KS 67260-0032 (United States); Edvardsson, Bengt, E-mail: vandenbe@uvic.ca, E-mail: pbergbusch@accesscomm.ca, E-mail: Jason.Ferguson@wichita.edu, E-mail: Bengt.Edvardsson@physics.uu.se [Theoretical Astrophysics, Department of Physics and Astronomy, Uppsala University, Box 516, SE-751 20 Uppsala (Sweden)

2014-10-10

Canonical grids of stellar evolutionary sequences have been computed for the helium mass-fraction abundances Y = 0.25, 0.29, and 0.33, and for iron abundances that vary from –2.4 to +0.4 (in 0.2 dex increments) when [α/Fe] =+0.4, or for the ranges –2.0 ≤ [Fe/H] ≤+0.6, –1.8 ≤ [Fe/H] ≤+0.6 when [α/Fe] =0.0 and –0.4, respectively. The grids, which consist of tracks for masses from 0.12 M{sub ⊙} to 1.1-1.5 M{sub ⊙} (depending on the metallicity) are based on up-to-date physics, including the gravitational settling of helium (but not metals diffusion). Interpolation software is provided to generate isochrones for arbitrary ages between ≈5 and 15 Gyr and any values of Y, [α/Fe], and [Fe/H] within the aformentioned ranges. Comparisons of isochrones with published color-magnitude diagrams (CMDs) for the open clusters M67 ([Fe/H] ≈0.0) and NGC 6791 ([Fe/H] ≈0.3) and for four of the metal-poor globular clusters (47 Tuc, M3, M5, and M92) indicate that the models for the observed metallicities do a reasonably good job of reproducing the locations and slopes of the cluster main sequences and giant branches. The same conclusion is reached from a consideration of plots of nearby subdwarfs that have accurate Hipparcos parallaxes and metallicities in the range –2.0 ≲ [Fe/H] ≲ –1.0 on various CMDs and on the (log T {sub eff}, M{sub V} ) diagram. A relatively hot temperature scale similar to that derived in recent calibrations of the infrared flux method is favored by both the isochrones and the adopted color transformations, which are based on the latest MARCS model atmospheres.

Evaluation of 5P12-RANTES analogue expression in Nicotiana benthamiana

CSIR Research Space (South Africa)

Mawela, KG

2012-10-10

Full Text Available 100 200 300 400 500 600 700 Apoplast Cytosol pICH11599 (-ve control) 5P 12 (? g /k g F W ) 3 dpi 6 dpi 9 dpi (B) Bacterial vector system 0 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 Cytosol ER Chloroplast pICH11599 (-ve... MTS tetrazolium compound, {3-(4,5-dimethyl-2-yl)-5-(3- carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium} Efficacy testing Table 1 Summary of IC50 values of the HIV-1 pseudovirions screened. Sample identification ZM53 (targets CCR5) IC50 (?g...

12 CFR 608.813 - Contracting for collection services.

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2010-01-01

... 12 Banks and Banking 6 2010-01-01 2010-01-01 false Contracting for collection services. 608.813 Section 608.813 Banks and Banking FARM CREDIT ADMINISTRATION ADMINISTRATIVE PROVISIONS COLLECTION OF... services. The Chairman, or designee of the Chairman, may contract for collection services in accordance...

Magnetodielectric effect in (1 - x)(Ba0.88Ca0.12)(Ti0.88Zr0.12)O3 - xCoFe2O4

Science.gov (United States)

Pan, Pengfei; Tao, Jin; Ma, Fusheng; Zhang, Ning

2018-05-01

Magnetodielectric (MD) materials have attracted considerable attention due to their intriguing physics and potential future applications. In this work, polycrystalline (1 - x)(Ba0.88Ca0.12)(Ti0.88Zr0.12)O3 - xCoFe2O4 (x = 0.10, 0.20, 0.30, 0.40) ceramic have been prepared via sol-gel method. The room temperature magnetic and ferroelectric behaviors of the synthesized composites were investigated. For the composite with x = 0.40, a MD ratio of 5.37% was achieved under a magnetic field of 1.5 T at f = 1 kHz. The measured "butterfly hysteresis" MD curves exhibit an obvious dielectric anomaly. Theoretical analysis suggests that the observed magnetodielectric effect is attributed to the magnetoresistance effect and magnetoelectric coupling.

XMCD study of the Ruddlesden-Popper phase La1.2Nd0.2Sr1.6Mn2O7

International Nuclear Information System (INIS)

Weigand, F.; Goering, E.; Geissler, J.; Justen, M.; Ruck, K.; Schuetz, G.; Doerr, K.

2001-01-01

X-ray Magnetic Circular Dichroism (XMCD) measurements of the Ruddlesden-Popper Phase La 1.2 Nd 0.2 Sr 1.6 Mn 2 O 7 are reported. The Mn K, La and Nd L 2 , 3 edges have been measured on a powder sample at two different magnetic fields at low temperature. The analysis of the spectra at B = 1T indicates a large orbital moment of the Nd 5d-states and a significant spin-polarization of the La 5d-band. Furthermore at the Mn Κ-edge a XMCD-signal is observed, showing a polarization of the Mn 4p-band. At lower field (0.2T) all XMCD-signals are about two times smaller corresponding to the lower total magnetization. The signal at the Nd L 2 edge vanishes completely at 0.2T. (au)

12 CFR 563e.24 - Service test.

Science.gov (United States)

2010-01-01

... 12 Banks and Banking 5 2010-01-01 2010-01-01 false Service test. 563e.24 Section 563e.24 Banks and... Assessing Performance § 563e.24 Service test. (a) Scope of test. The service test evaluates a savings... performance, a community development service provided by an affiliate of the savings association, if the...

Prevalence of Dental Caries in 5 – 6 Years and 12 – 13 Years Age Group of School Children of Kathmandu Valley

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B Subedi

2011-12-01

Full Text Available Introduction: Dental caries is one of the most common conditions affecting the general health of children. The present study was carried out among school children of Kathmandu valley to determine the prevalence of dental caries in two age groups. Methods: The study was conducted from December 2007 to May 2008. The age of the school children of the study was divided into two group: 5 - 6 years and 12 - 13 years. A stratifi ed cluster sampling with proportional allocation was used while grouping the subjects. The dental status examination was done with the help of trained dentists. Decayed, missed and fi lled teeth index and decayed, missed and fi lled surfaces index (dmft for primary dentition and DMFT for permanent dentition were used as the standard tools for the determination of prevalence. Results: A total of 638 students (325 of age group 12 - 13 years and 313 of age group 5 - 6 years from 30 different schools of the Kathmandu valley were included in the study. The caries status was found higher in the age group of 5 - 6 years than in the 12 - 13 years and it was found to be statistically signifi cant (p < 0.001. The dmfs and caries percentage of the age group 5 - 6 years and the DMFS and caries percent of the 12 - 13 years was found to be 3.79, 69 % and 1.6, 53.23 % respectively. The dmft/dmfs value was found to be signifi cant according to the districts in the 5 - 6 years age group whereas the DMFS was found statistically signifi cant among the sexes of the 12 - 13 years age group. Conclusions: The caries percentage was found to be above the recommended level of the World Health Organization. However, the DMFS and DMFT values were within the WHO level. Keywords: Children, dental caries, DMF index.

Tris[2,2,6,6-tetramethyl-8-(trimethylsilylbenzo[1,2-d;4,5-d′]bis(1,3-dithiol-4-yl]methanol diethyl ether monosolvate

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Nico Fleck

2018-04-01

Full Text Available The title compound, a triarylmethanol, C46H64OS12Si3 1, was synthesized via lithiation of tris-2,2,6,6-tetramethylbenzo[1,2-d;4,5-d′]bis[1,3]dithiol-4-yl-methanol, 2, and electrophilic quenching with trimethylsilyl chloride. The current crystal structure reveals information about the reactivity of this compound and compares well with the structure reported for the unsubstituted parent compound 2 [Driesschaert et al. (2012. Eur. J. Org. Chem. 33, 6517–6525]. The title compound 1 forms molecular propellers and crystallizes in P\\overline{1}, featuring an unusually long Si—Car bond of 1.910 (3 Å. Moreover, the geometry at the central quaternary carbon is rather trigonal-pyramidal than tetrahedral due to vast intramolecular stress. One trimethylsilyl group is disordered over two positions in a 0.504 (4:0.496 (4 ratio and one S atom is disordered over two positions in a 0.509 (7:0.491 (7 ratio. The contribution of disordered diethyl ether solvent molecule(s was removed using the PLATON SQUEEZE (Spek, 2015 solvent masking procedure. These solvent molecules are not considered in the given chemical formula and other crystal data.

Structural study of the semimagnetic semiconductor Zn{sub 0.5}Mn{sub 0.5}In{sub 2}Te{sub 4}

Energy Technology Data Exchange (ETDEWEB)

Delgado, G.E. [Laboratorio de Cristalografia, Departamento de Quimica, Facultad de Ciencias, Universidad de Los Andes, Merida (Venezuela); Sagredo, V. [Laboratorio de Magnetismo en Solidos, Departamento de Quimica, Facultad de Ciencias, Universidad de Los Andes, Merida (Venezuela)

2009-02-15

The semimagnetic semiconductor alloy Zn{sub 0.5}Mn{sub 0.5}In{sub 2}Te{sub 4} was refined from an X-ray powder diffraction pattern using the Rietveld method. This compound crystallizes in the space group I anti 42m (N {sup circle} 121), Z=2, with unit cell parameters a=6.1738(1)A, c=12.3572(4)A, V=471.00(2)A3, c/a=2.00. This material crystallizes in a stannite-type structure. (copyright 2009 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

Microstructures and mechanical properties of squeeze cast Al–5.0Cu–0.6Mn alloys with different Fe content

International Nuclear Information System (INIS)

Zhang, WeiWen; Lin, Bo; Zhang, DaTong; Li, YuanYuan

2013-01-01

Highlights: • The effect of Fe-rich phases on squeeze cast Al–Cu alloys with high Fe content. • Four kinds of Fe-rich phases may present in Al–Cu alloys. • There is great tolerance to Fe impurities in squeeze cast Al–Cu alloys. - Abstract: The microstructures and mechanical properties of gravity die cast and squeeze cast Al–5.0 wt% Cu–0.6 wt% Mn alloys with different Fe content have been studied using tensile test, optical microscope, scanning electron microscope, electron probe micro-analyzer and image analysis. The results show that four kinds of Fe-rich intermetallics may present in the final microstructures of the alloys: Chinese script α-Fe (Al 15 (FeMn) 3 (CuSi) 2 ) and Al 6 (FeMn), needle-like β-Fe(Al 7 Cu 2 Fe) and Al 3 (FeMn) when the Fe content increases from 0.1 wt% to 1.5 wt%. In the gravity die cast alloy with 0.5 wt% Fe, the Chinese script α-Fe presents as the main Fe-rich intermetallics, and a few needle-like β-Fe also exist. When the Fe content increases to 1.0 wt%, the main Fe-rich intermetallics change to needle-like Al 3 (FeMn) and Chinese-script Al 6 (FeMn). The needle-like β-Fe disappears when the Fe content is 0.5 wt% in the squeeze cast alloy with an applied pressure of 75 MPa. Furthermore, the secondary dendritic arm spacing of α(Al), the percentage of porosity and the volume fraction of the second intermetallics decrease distinctly in the squeeze cast alloy compared to the gravity die cast alloy. There is a peak value of ultimate strength and yield strength for the alloy with 0.5 wt% Fe. The elongations of the alloys decrease gradually with increasing Fe content and the elongation of the squeeze cast alloys is two times more than that of the gravity die cast alloys

Synthesis and photoluminescence properties of red-emitting Y{sub 6}WO{sub 12}:Eu{sup 3+} phosphors

Energy Technology Data Exchange (ETDEWEB)

Chien, Tzu-Chin; Yang, Ji-Chun; Hwang, Chii-Shyang, E-mail: cshwang@mail.ncku.edu.tw; Yoshimura, Masahiro

2016-08-15

For a system of white-light-emitting diodes (WLEDs) fabricated using near-ultraviolet (UV) LED chips coated with RGB tri-color phosphors, the most important issue is enhancing the efficiency of the red phosphor. Y{sub 6}WO{sub 12}:Eu{sup 3+} phosphor is a potential material that can emit red color under near-UV excitation. This work investigated the luminescence properties of Y{sub 6}WO{sub 12}:Eu{sup 3+} under UV light excitation. The photoluminescence (PL) emission intensity of Eu{sub x}Y{sub 6–x}WO{sub 12} (x = 0.1–1.0) phosphor from the {sup 5}D{sub 0}→{sup 7}F{sub 2} transition increased with Eu{sup 3+} content until x = 0.9. For x > 0.9, the PL emission intensity decreased due to concentration quenching. The decay time of Eu{sub x}Y{sub 6–x}WO{sub 12} (x = 0.1–1.0) phosphor for the {sup 5}D{sub 0}→{sup 7}F{sub 2} transition was about 0.6–0.7 ms and did not decrease obviously, which means that there was no nonradiative energy transfer in the phosphor. The asymmetry ratio ({sup 5}D{sub 0} → {sup 7}F{sub 2}/{sup 5}D{sub 0} → {sup 7}F{sub 1}) of Eu{sub x}Y{sub 6–x}WO{sub 12} (x = 0.1–1.0) was about 2, which caused the PL emission intensity of Eu{sub x}Y{sub 6–x}WO{sub 12} (x = 0.1–1.0) phosphor from the {sup 5}D{sub 0}→{sup 7}F{sub 2} transition to be higher than that from the {sup 5}D{sub 0}→{sup 7}F{sub 1} transition. The chromaticity coordinates of the Eu{sub x}Y{sub 6–x}WO{sub 12} (x = 0.1–1.0) phosphor were close to the chromaticity coordinates of the standard red color. The Eu{sub x}Y{sub 6–x}WO{sub 12} (x = 0.9) phosphor showed the highest quantum efficiency. - Highlights: • Eu{sub x}Y{sub 6–x}WO{sub 12} (x = 0.1–1.0) phosphors were synthesized via a solid-state reaction. • Strongest excitation peaks observed at 392 nm (near UV) and 463 nm (blue). • The major emission peak of the red phosphor excited by 392 nm was at 605 nm. • The quantum efficiency of Eu{sub x}Y{sub 6–x}WO{sub 12} (x = 0.1–1.0) phosphors

Crystal structure of tetraethylammonium chloride 3,4,5,6-tetrafluoro-1,2-diiodobenzene

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Jasmine Viger-Gravel

2015-05-01

Full Text Available Equimolar quantities of tetraethylammonium chloride (Et4NCl and 3,4,5,6-tetrafluoro-1,2-diiodobenzene (o-DITFB or o-C6F4I2 have been co-crystallized in a solution of dichloromethane yielding a pure halogen-bonded compound, 3,4,5,6-tetrafluoro-1,2-diiodobenzene–tetraethyl ammonium chloride (2/1, Et4N+·Cl−·2C6F4I2, in the form of translucent needles. [(Et4NCl(o-C6F4I22] packs in the C2/c space group. The asymmetric unit includes one molecule of DITFB, one Et4N+ cation located on a twofold rotation axis, and one chloride anion also located on a twofold rotation symmetry axis. This compound has an interesting halogen-bonding environment surrounding the halide. Here, the chloride anion acts as a tetradentate halogen bond acceptor and forms a distorted square-pyramidal geometry, with I...Cl−...I angles of 80.891 (6 and 78.811 (11°, where two crystallographically distinct iodine atoms form halogen bonds with the chloride anion. Resulting from that square-pyramidal geometry are short contacts between some of the adjacent F atoms. Along the b axis, the halogen-bonding interaction results in a polymeric network, producing a sheet in which the two closest chloride ions are 7.8931 (6 Å apart. The Et4N+ cation alternates in columns with the halide ion. The expected short contacts (shorter than the sum of their van der Waals radii are observed for the halogen bonds [3.2191 (2 and 3.2968 (2 Å], as well as almost linear angles [170.953 (6 and 173.529 (6°].

Effect of oxygen content on the electrical transport and superconducting properties of Pb0.5Sr2.5Y0.6Ca0.4Cu2O7-y

International Nuclear Information System (INIS)

Ruan, K.Q.; China Univ. of Science and Technology, Hefei, AH; Jin, H.; China Univ. of Science and Technology, Hefei, AH; Feng, Y.; China Univ. of Science and Technology, Hefei, AH; Zhou, Y.Q.; China Univ. of Science and Technology, Hefei, AH; Chui, X.D.; China Univ. of Science and Technology, Hefei, AH; Wang, C.Y.; China Univ. of Science and Technology, Hefei, AH; Cao, L.Z.; China Univ. of Science and Technology, Hefei, AH; Wang, L.B.; Zhang, Y.H.

1997-01-01

Two kinds of methods have been used to synthesize Pb 0.5 Sr 2.5 Y 0.6 Ca 0.4 Cu 2 O 7-y samples. The synthesized sample using the first method shows superconductivity, while that using the second method exhibits a localized behavior at low temperatures Thermogravimetric analysis (TGA) and electrical transport measurements have been carried out on superconducting and nonsuperconducting samples grown under the two kinds of synthesis conditions and the effect of oxygen content on the transport and superconducting properties is discussed briefly. (orig.)

Synthesis and piezoelectric properties of (1 - x)Bi0.5(Na0.8K0.2)0.5TiO3-xSr2ZrTiO6 ceramics

Science.gov (United States)

Onishi, Ryo; Ogawa, Hirotaka; Iida, Daiki; Kan, Akinori

2017-10-01

The effects of Sr2ZrTiO6 (SZT) addition on the piezoelectric properties of (1 - x)Bi0.5(Na0.8K0.2)0.5TiO3 (BNKT)-xSZT ceramics were characterized in this study. The X-ray powder diffraction (XRPD) profiles and Raman spectra of the ceramics in the composition range of 0-0.02 implies the presence of morphotropic phase boundary (MPB) which consists of the rhombohedral and tetragonal phases. Moreover, the temperature dependence of dielectric loss indicated a presence of the ferroelectric-relaxor transition temperature (T F-R) of around 75 °C for x = 0.005 and the temperature dependence shifted to a lower temperature at x = 0.01. The temperature dependence of the P-E hysteresis loop of the ceramics at the compositions of x = 0.005-0.02 showed pinched hysteresis loops above T F-R. Regarding the piezoelectric constant (d 33), it was increased by SZT addition in the MPB region (x = 0-0.01) and the highest d 33 of 202 pC/N was obtained at the composition of x = 0.0025. The S-E unipolar loop was also evaluated, the strain of the ceramic increased up to x = 0.02; and the highest d33* = 436 pm/V was obtained at the composition of x = 0.02.

The microstructures and electrochemical performances of La0.6Gd0.2Mg0.2Ni3.0Co0.5-xAlx (x=0-0.5) hydrogen storage alloys as negative electrodes for nickel/metal hydride secondary batteries

Science.gov (United States)

Li, Rongfeng; Xu, Peizhen; Zhao, Yamin; Wan, Jing; Liu, Xiaofang; Yu, Ronghai

2014-12-01

La0.6Gd0.2Mg0.2Ni3.0Co0.5-xAlx (x = 0-0.5) hydrogen storage alloys were prepared by induction melting followed by annealing treatment at 1173 K for 8 h. The effects of substitution Al for Co on the microstructures and electrochemical performances were studied systematically. The structure analyses show that all alloys consist of multiphase structures such as (La, Mg)2Ni7 phase, (La, Mg) Ni3 phase and LaNi5 phase. The abundance of (La, Mg)2Ni7 phase decreases while the abundance of LaNi5 phase and (La, Mg)Ni3 phase increases directly as the Al content increasing. The electrochemical tests show that the maximum discharge capacity of alloy electrodes are almost unchanged when x ≤ 0.2 while the cyclic stability of the alloy electrode are improved significantly after proper amount of Al substitution for Co. The alloy electrode with x = 0.1 exhibits the better balance between discharge capacity and cycling life than any others. Moreover, at the discharge current density of 900 mA g-1, the high rate dischargeability (HRD) of the alloy electrodes decreases with increasing Al substitution and the relative analyses reveal that the charge transfer on alloy surface is more important than the hydrogen diffusion in alloy bulk for the kinetic properties of the alloy electrodes.

Synthesis and study of NH4[HSiUO6]·0.5H2O

International Nuclear Information System (INIS)

Chernorukov, N.G.; Kortikov, V.E.

2000-01-01

Previously unknown ammonium uranosilicate of NH 4 [HSiUO 6 ]·0.5H 2 O composition is synthesised by precipitation from aqueous solution containing ammonium chloride, uranyl nitrate and quartz glass with the size of granules ≤ 2. On evidence of X-ray diffraction ammonium uranosilicate is a full crystallographic analog of proper lithium and potassium derivatives with approaching parameters of crystal lattices: a= 7.01(2), b=7.03(8), c=6.65(9) A, β=105.6(0) Deg. Functional composition and peculiarity of ammonium uranosilicate structure are detected by IR spectroscopic study. Scheme of thermal decomposition of ammonium uranosilicate is demonstrated based on thermal gravimetric and X-ray diffraction measurements. NH 4 [HSiUO 6 ]·0.5H 2 O is among of morphotropic raw of A 1/k k HSiUO 6 ·nH 2 O [ru

Efficient bright white organic light-emitting diode based on non-doped ultrathin 5,6,11,12-tetraphenylnaphthacene layer

International Nuclear Information System (INIS)

Li Lu; Yu Junsheng; Tang Xiaoqing; Wang Tao; Li Wei; Jiang Yadong

2008-01-01

High-performance undoped white organic light-emitting diode (OLED) has been fabricated using an ultrathin yellow-emitting layer of 5,6,11,12-tetraphenylnaphthacene (rubrene) inserted at two sides of interface between two N,N'-bis-(1-naphthyl)-N,N'- biphenyl-1,1'-biphenyl-4,4'- diamine (NPB) layers as a hole transporting and blue emissive layer, respectively. The results showed that a maximum luminance of the device reached to as high as 21,500 cd/m 2 at 15 V. The power efficiencies of 2.5 and 1.6 lm/W at a luminance of 1000 and 10000 cd/m 2 , respectively, were obtained. The peaks of electroluminescent (EL) spectra locate at 429 and 560 nm corresponding to the Commissions Internationale De L'Eclairage (CIE) coordinates of (0.32, 0.33), which is independent of bias voltage. The performance enhancement of the device may result from direct charge carrier trapping in rubrene. Energy transfer mechanism was also found in the EL process

High-pressure synthesis and magnetic behavior of A-site columnar-ordered double perovskites, LnMn(Ga{sub 0.5}Ti{sub 0.5}){sub 2}O{sub 6} (Ln = Sm, Gd)

Energy Technology Data Exchange (ETDEWEB)

Shimura, Gen; Niwa, Ken; Shirako, Yuichi; Hasegawa, Masashi [Department of Crystalline Materials Science, Nagoya University, 464-8601, Nagoya (Japan)

2017-01-26

A-site columnar-ordered double perovskites, LnMn(Ga{sub 0.5}Ti{sub 0.5}){sub 2}O{sub 6} (Ln = Sm, Gd), were successfully synthesized under high pressure and high temperature (6 GPa, 1375 K). From the synchrotron powder X-ray diffraction patterns, all of the diffraction peaks can be indexed by the P4{sub 2}/nmc space group with lattice parameters a, c ∼ 2a{sub p} (a{sub p}: primitive cubic perovskite lattice) and no ordering of the B-site cations. Rietveld analysis of the synchrotron powder X-ray diffraction patterns and Curie-Weiss fitting of their magnetizations reveal that the ionic formulae of these perovskites are Ln{sup 3+}Mn{sup 2+}(Ga{sup 3+}{sub 0.5}Ti{sup 4+}{sub 0.5}){sub 2}O{sup 2-}{sub 6}. SmMn(Ga{sub 0.5}Ti{sub 0.5}){sub 2}O{sub 6} shows canted-antiferromagnetic behavior, whereas GdMn(Ga{sub 0.5}Ti{sub 0.5}){sub 2}O{sub 6} exhibits two different magnetic states at low temperature depending on the applied magnetic field and shows an unusual magnetization curve. These magnetic behaviors originate by decreasing the antiferromagnetic interaction by substituting Ga{sup 3+}(d{sup 10}) for Ti{sup 4+}(d{sup 0}) and by decreasing the ferromagnetic interaction between columnar-ordered Ln{sup 3+} and Mn{sup 2+}. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

12 CFR 760.10 - Notice of servicer's identity.

Science.gov (United States)

2010-01-01

... 12 Banks and Banking 6 2010-01-01 2010-01-01 false Notice of servicer's identity. 760.10 Section... LOANS IN AREAS HAVING SPECIAL FLOOD HAZARDS § 760.10 Notice of servicer's identity. (a) Notice... notify the Director of FEMA (or the Director's designee) in writing of the identity of the servicer of...

12 CFR 614.4960 - Notice of servicer's identity.

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2010-01-01

... 12 Banks and Banking 6 2010-01-01 2010-01-01 false Notice of servicer's identity. 614.4960 Section... Flood Insurance Requirements § 614.4960 Notice of servicer's identity. (a) Notice requirement. When a... Director of FEMA (or the Director's designee) in writing of the identity of the servicer of the loan. The...

KARAKTERISTIK MIKROSTRUKTUR DAN FASA PADUAN Zr- 0,3%Nb-0,5%Fe-0,5%Cr PASCA PERLAKUAN PANAS DAN PENGEROLAN DINGIN

Directory of Open Access Journals (Sweden)

Sungkono Sungkono

2015-07-01

Full Text Available KARAKTERISTIK MIKROSTRUKTUR DAN FASA PADUAN Zr-0,3%Nb-0,5%Fe-0,5%Cr PASCA PERLAKUAN PANAS DAN PENGEROLAN DINGIN. Logam paduan Zr-Nb-Fe-Cr dikembangkan sebagai material kelongsong elemen bakar dengan fraksi bakar tinggi untuk reaktor daya maju. Dalam penelitian ini telah dibuat paduan Zr-0,3%Nb-0,5%Fe-0,5%Cr yang mendapat perlakuan panas pada temperatur 650 dan 750°C dengan waktu penahanan 1–2 jam. Tujuan penelitian adalah mendapatkan karakter paduan Zr-0,3%Nb-0,5%Fe-0,5%Cr pasca perlakuan panas dan pengerolan dingin yaitu mikrostruktur, struktur kristal dan fasa-fasa yang ada dalam paduan. Hasil penelitian menunjukkan bahwa paduan Zr-0,3%Nb-0,5%Fe-0,5%Cr pasca perlakuan panas (650ºC, 1-2 jam mempunyai struktur butir ekuiaksial dengan ukuran butir bertambah besar seiring dengan bertambahnya waktu penahanan. Sementara itu, pasca perlakuan panas (750ºC, 1-2 jam terjadi perubahan mikrostruktur paduan dari butir ekuiaksial dan kolumnar menjadi butir ekuiaksial lebih besar. Paduan Zr-0,3%Nb-0,5%Fe-0,5%Cr pasca perlakuan panas (650°C, 1 jam dan (750°C, 1 jam tidak dapat dirol dingin dengan reduksi tebal 5 – 10%, sedangkan pasca perlakuan panas (650ºC, 2 jam dan (750°C, 1.5-2 jam mampu menerima deformasi dingin dengan reduksi ketebalan 5-10% tanpa mengalami keretakan. Senyawa Zr2Fe, ZrCr2 dan FeCr teridentifikai dari hasil uji kristalografi paduan Zr-0,3%Nb-0,5%Fe-0,5%Cr.   MICROSTRUCTURE AND PHASE CHARACTERISTICSOF Zr-0.3%Nb-0.5%Fe-0.5%Cr ALLOY POST HEAT TREATMENT AND COLD ROLLING. Zr-Nb-Fe-Cr alloys was developed as fuel elements cladding with high burn up for advanced power reactors. In this research has been made of Zr-0.3% Nb-0.5% Fe-0.5% Cr alloy were heat treated with varying temperatures at650 and 750°C for 1 until 2 hours. The objectives of this research was to obtain the character of Zr-0.3% Nb-0.5% Fe-0.5% Cr alloy post heat treatment and cold rolling, microstructure nomenclature, crystal structure and phases that presents in the

Electrical properties and x-ray photoelectron spectroscopy studies of Bi(Zn0.5Ti0.5)O3 doped Pb(Zr0.4Ti0.6)O3 thin films

Science.gov (United States)

Tang, M. H.; Zhang, J.; Xu, X. L.; Funakubo, H.; Sugiyama, Y.; Ishiwara, H.; Li, J.

2010-10-01

(1-x)Pb(Zr0.4,Ti0.6)O3-(x)Bi(Zn0.5,Ti0.5)O3 (PZT-BZT) (x =0, 0.03, 0.05, 0.08, and 0.1) films were deposited on Pt(111)/Ti/SiO2/Si(100) substrates by chemical solution deposition using spin-coating. All samples showed highly (111) oriented perovskite phase and no other phase was observed. The ferroelectric properties of PZT-BZT films were systematically investigated as a function of the content x of the BZT solution. It is found that BZT doping in PZT films could greatly enhance the remnant polarization (Pr), as well as improve the fatigue property. In a 3 wt % BZT-doped PZT film, the 2Pr and the coercive field (Ec) are 90 μC/cm2 and 95 kV/cm at 10 kHz, respectively, at an electric field of 500 kV/cm, and the leakage current density is less than 1×10-7 A/cm2. The impact of BZT doping on the structure of PZT has been investigated by x-ray photoelectron spectroscopy.

Structural phase transitions in Bi[sub 2]V[sub 1[minus]x]Ge[sub x]O[sub 5. 5[minus]x/2] (x = 0. 2, 0. 4, and 0. 6) single crystals: X-ray crystallographic study

Energy Technology Data Exchange (ETDEWEB)

Sooryanarayana, K.; Guru Row, T.N.; Varma, K.B.R. (Indian Inst. of Science, Bangalore (India))

1999-02-01

Single crystals of Bi[sub 2]V[sub 1[minus]x]Ge[sub x]O[sub 5.5[minus]x/2] (x = 0.2, 0.4, and 0.6) were grown by slow cooling of melts. Bismuth vanadate transforms from an orthorhombic to a tetragonal structure and subsequently to an orthorhombic system when the Ge[sup 4+] concentration was varied from x = 0.2 to x = 0.6. All of these compositions crystallized in polar space groups (Aba2, F4mm, and Fmm2 for x = 0.2, 0.4, and 0.6, respectively). The structures were fully determined by single crystal X-ray diffraction studies.

ANC of 6.92 MeV (2"+) and 7.12 MeV (1"-) states from sub-Coulomb "1"2C("6Li,d) data

International Nuclear Information System (INIS)

Mondal, Ashok; Basu, C.; Adhikari, S.

2016-01-01

The determination of the astrophysical S-factor of the "1"2C(α,γ) reaction at 300 keV requires a R-matrix extrapolation. This is because a direct measurement of this reaction at 300 keV is almost impossible due to the very small cross-section. The R-matrix extrapolation requires as input the asymptotic normalization constant (ANC) of mainly two "1"6O states states viz. 6.92 MeV and 7.12 MeV on which the fit is most sensitive. The ANC of these two states have been determined from indirect measurements, mainly from "1"2C("6Li,d) and "1"2C("7Li,t) alpha transfer reactions. Most of these measurements are done at above barrier energies as cross-sections are larger. In this work, we determine the ANC of the 6.92 MeV and 7.12 MeV states of "1"6O using the "1"2C("6Li,d) data of Heikkinen et al measured at 4.5 to 5.0 MeV incident energies. The data spans over a larger angular span in comparison to Avila though the former data do not cover the very backward angles as in the Avila data. As the Heikkinen data has never been analyzed to extract the ANC we report the results of our analysis of the data

Electronic structures and abnormal phonon behaviors of cobalt-modified Na0.5Bi0.5TiO3-6%BaTiO3 single crystals

Science.gov (United States)

Huang, T.; Zhang, P.; Xu, L. P.; Chen, C.; Zhang, J. Z.; Hu, Z. G.; Luo, H. S.; Chu, J. H.

2016-10-01

Optical properties, electronic structures, and structural variations of x wt% cobalt (Co) doped Na0.5Bi0.5TiO3-6%BaTiO3 (x=0%, 0.5%, 0.8%) single crystals have been studied by temperature-dependent optical ellipsometry and Raman spectra from 250 to 650 K. Based on the temperature evolution of electronic transitions (Ecp1 and Ecp2) and the phonon modes involving Ti-O vibrations, two critical temperature points exhibit an increasing trend with Co dopants, which are related to structural variations for ferroelectric to anti-ferroelectric, and anti-ferroelectric to paraelectric transition, respectively. Additionally, distinguishing abnormal phonon behaviors can be observed from Raman spectra for the crystal of x=0.5% and 0.8%, which show reverse frequency shift of the modes involving Ti-O vibration. It can be ascribed to different relative concentration of Co2+ and Co3+ in the crystals, which has been confirmed by X-ray Photoelectron Spectroscopy data.

Electronic structures and abnormal phonon behaviors of cobalt-modified Na0.5Bi0.5TiO3-6%BaTiO3 single crystals

Directory of Open Access Journals (Sweden)

T. Huang

2016-10-01

Full Text Available Optical properties, electronic structures, and structural variations of x wt% cobalt (Co doped Na0.5Bi0.5TiO3-6%BaTiO3 (x=0%, 0.5%, 0.8% single crystals have been studied by temperature-dependent optical ellipsometry and Raman spectra from 250 to 650 K. Based on the temperature evolution of electronic transitions (Ecp1 and Ecp2 and the phonon modes involving Ti-O vibrations, two critical temperature points exhibit an increasing trend with Co dopants, which are related to structural variations for ferroelectric to anti-ferroelectric, and anti-ferroelectric to paraelectric transition, respectively. Additionally, distinguishing abnormal phonon behaviors can be observed from Raman spectra for the crystal of x=0.5% and 0.8%, which show reverse frequency shift of the modes involving Ti-O vibration. It can be ascribed to different relative concentration of Co2+ and Co3+ in the crystals, which has been confirmed by X-ray Photoelectron Spectroscopy data.

12 CFR 747.11 - Service of papers.

Science.gov (United States)

2010-01-01

... 12 Banks and Banking 6 2010-01-01 2010-01-01 false Service of papers. 747.11 Section 747.11 Banks... Practice and Procedure § 747.11 Service of papers. (a) By the parties. Except as otherwise provided, a party filing papers shall serve a copy upon the counsel of record for all other parties to the...

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)

Ethyl 13-(4-chlorophenyl-11-methyl-6-oxo-5-phenyl-8-thia-3,4,5,10-tetraazatricyclo[7.4.0.02,7]trideca-1(9,2(7,3,10,12-pentaene-12-carboxylate

Directory of Open Access Journals (Sweden)

Elham A. Al-Taifi

2016-05-01

Full Text Available In the title molecule, C24H17ClN4O3S, the central tricyclic moiety is twisted slightly, as indicated by the dihedral angles of 4.86 (5 and 0.97 (6°, respectively, between the five-membered ring and the C3N3 and pyridyl rings. Additionally, the chlorobenzene ring makes a dihedral angle of 65.80 (5° with the pyridyl ring. Weak C—H...O, C—Cl...N [3.0239 (13 Å] and π–π stacking interactions [inter-centroid distance between thienyl rings = 3.6994 (8 Å, and between thienyl and pyridyl rings = 3.7074 (8 Å] contribute to the molecular packing. The ethyl group in the ester moiety is disordered over two sets of sites, with the major component having an occupancy of 0.567 (11.

5,11-Ditosyl-5H,11H-dibenzo[b,f][1,5]diazo-cine-6,12-dione acetic acid hemisolvate.

Science.gov (United States)

Abbassi, Najat; Bassou, Oulemda; Rakib, El Mostapha; Saadi, Mohamed; El Ammari, Lahcen

2013-04-01

The mol-ecular structure of the title compound, C28H22N2O6S2·0.5CH3COOH, is built up from three fused rings, two six and one eight membered. The eight-membered ring shows a boat conformation and the dihedral angle between the two benzene groups attached thereto is 66.43 (11)°, resulting in a V-shaped geometry. Two tosyl substituents are bound to the N atoms. The planes through the tolyl rings are roughly perpendicular, as indicated by the dihedral angle of 82.44 (12)°. In the crystal, the mol-ecule and its inversion-related symmetry-equivalent are linked to the acetic acid solvent mol-ecule by non-classical O-H⋯O and C-H⋯O hydrogen bonds. Two half-occupied acetic acid solvent mol-ecules are disordered at the same site and linked by a center of symmetry.

Fabrication of Zr2WP2O12/ZrV0.6P1.4O7 composite with a nearly zero-thermal-expansion property.

Science.gov (United States)

Yanase, Ikuo; Sakai, Hiroshi; Kobayashi, Hidehiko

2017-11-15

Sintered bodies of Zr 2 WP 2 O 12 (ZWP) and ZrV 0.6 P 1.4 O 7 (ZVP) were fabricated, and their linear thermal expansion coefficients (TEC) were found to be -2.92 × 10 -6 and 3.27 × 10 -6  °C -1 , respectively, in the range 25-500 °C. In an attempt to fabricate composites with a zero-thermal-expansion property, sintered ZWP/ZVP composites with ZVP/ZWP volume ratios of 0.5/0.5, 0.53/0.47, 0.55/0.45, and 0.6/0.4 were fabricated. Scanning electron microscopy revealed that sintering of ZVP/ZWP composites progressed well compared with that of ZWP. A porous ZVP/ZWP composite with a relative density of ca. 83% was fabricated at a ZVP/ZWP volume ratio of 0.53/0.47. X-ray diffractometry and energy dispersive X-ray spectrometry clarified that the ZVP/ZWP composite mainly consisted of ZWP and ZVP grains. Thermomechanical analysis confirmed that the ZVP/ZWP composite exhibited very low thermal expansion with a slight hysteresis with a TEC of -0.29 × 10 -7  °C -1 in the range 25-500 °C.

Synthesis, characterization and mechanoluminescence of europium doped ZnxBa(1−x)Al2O4 (x=0, 0.4, 0.5, 0.6, 0.8, 1.0) phosphor

International Nuclear Information System (INIS)

Sajan, S.J.; Gopakumar, N.; Anjana, P.S.; Madhukumar, K.

2016-01-01

The samples of Zn x Ba (1−x) Al 2 O 4 :0.1%Eu (x=0, 0.4, 0.5, 0.6, 0.8, 1.0) were prepared via high temperature solid state reaction method. The phase formation of the powder samples were confirmed by taking X-ray diffraction analysis. The mechanoluminescence (ML) property of the samples by impact method was studied by using ML measuring apparatus. The variations in the ML peak intensity due to the impact velocity of a load falling from different heights and due to the variation of composition were investigated. The photoluminescence studies of the samples were also conducted.

Temporal Differential Gene Expression in Explanted Human Retinal Pigment Epithelial Cells at 0.5, 1.0, 3.0, 6.0, 12 and 24 Hours Post-Exposure to 1064 nm, 3.6 ns Pulsed Laser Light

Science.gov (United States)

2005-05-01

regulated 10-fold at 1-3 hrs and -5-fold at 12 hrs. Roughly the same can be said for xeroderma pigmentosum group CC repair complementing protein p58 (C08n...Staudt L M, Hudson J, Boguski MS, Lashkari D, Shalon D, Botstein D and Brown PO : The Transcriptional Program in the Response of Human Fibroblasts to...467-470. Schena M, Shalon D, Heller R, Chai A, Brown PO , Davis R: Parallel human genome analysis: Microarray-based expression monitoring of 1000 genes

Phase transitions and electrical characterizations of (K 0.5Na 0.5) 2x(Sr 0.6Ba 0.4) 5-xNb 10O 30 (KNSBN) ceramics with 'unfilled' and 'filled' tetragonal tungsten-bronze (TTB) crystal structure

KAUST Repository

Yao, Yingbang

2012-12-01

Alkali-doped strontium barium niobate (K 0.5Na 0.5) 2x(Sr 0.6Ba 0.4) 5-xNb 10O 30 (KNSBN) ceramics has been prepared by a conventional solid-state reaction method. The alkali-dopant concentration x has been varied from 0.24 to 1.15 so that the crystal structure was transformed from \\'unfilled\\' to \\'filled\\' tetragonal tungsten-bronze (TTB) structure. Apart from the change in the structural properties, the effects of the alkali-dopants on the phase transition as well as ferroelectric, piezoelectric and pyroelectric properties have also been investigated. Phase transitions have been studied in the temperature range of -200°C to 350°C. The origins of these phase transitions are discussed. The addition of the alkali-dopants enhances the ferroelectric, piezoelectric and pyroelectric properties of the KNSBN ceramics. Alkali-doping also favors abnormal grain growth and thus results in a porous microstructure, which might contribute to the enhancement of the pyroelectric performance. © 2012 Elsevier Ltd.

Phase transitions and electrical characterizations of (K 0.5Na 0.5) 2x(Sr 0.6Ba 0.4) 5-xNb 10O 30 (KNSBN) ceramics with 'unfilled' and 'filled' tetragonal tungsten-bronze (TTB) crystal structure

KAUST Repository

Yao, Yingbang; Mak, C. L.; Ploss, Bernd

2012-01-01

Alkali-doped strontium barium niobate (K 0.5Na 0.5) 2x(Sr 0.6Ba 0.4) 5-xNb 10O 30 (KNSBN) ceramics has been prepared by a conventional solid-state reaction method. The alkali-dopant concentration x has been varied from 0.24 to 1.15 so that the crystal structure was transformed from 'unfilled' to 'filled' tetragonal tungsten-bronze (TTB) structure. Apart from the change in the structural properties, the effects of the alkali-dopants on the phase transition as well as ferroelectric, piezoelectric and pyroelectric properties have also been investigated. Phase transitions have been studied in the temperature range of -200°C to 350°C. The origins of these phase transitions are discussed. The addition of the alkali-dopants enhances the ferroelectric, piezoelectric and pyroelectric properties of the KNSBN ceramics. Alkali-doping also favors abnormal grain growth and thus results in a porous microstructure, which might contribute to the enhancement of the pyroelectric performance. © 2012 Elsevier Ltd.

Electrochemical Characteristics and Li+ Ion Intercalation Kinetics of Dual-phase Li4Ti5O12/Li2TiO3 Composite in Voltage Range of 0−3 V

KAUST Repository

Bhatti, Humaira S

2016-04-20

Li4Ti5O12, Li2TiO3 and dual-phase Li4Ti5O12/Li2TiO3 composite were prepared by sol-gel method with average particle size of 1 µm, 0.3 µm and 0.4 µm, respectively. Though Li2TiO3 is electrochemically inactive, the rate capability of Li4Ti5O12/Li2TiO3 is comparable to Li4Ti5O12 at different current rates. Li4Ti5O12/Li2TiO3 also shows good rate performance of 90 mA h g-1 at high rate of 10 C in voltage range of 1−3 V, attributable to increased interfaces in the composite. While Li4Ti5O12 delivers capacity retention of 88.6 % at 0.2 C over 50 cycles, Li4Ti5O12/Li2TiO3 exhibits no capacity fading at 0.2 C (40 cycles) and capacity retention of 98.45 % at 0.5 C (50 cycles). This highly stable cycling performance is attributed to the contribution of Li2TiO3 in preventing undesirable reaction of Li4Ti5O12 with the electrolyte during cycling. CV curves of Li4Ti5O12/Li2TiO3 in 0−3 V range exhibit two anodic peaks at 1.51 V and 0.7−0.0 V, indicating two modes of lithium intercalation into the lattice sites of active material. Owing to enhanced intercalation/de-intercalation kinetics in 0−3 V, composite electrode delivers superior rate performance of 203 mAh/g at 2.85 C and 140 mAh/g at 5.7 C with good reversible capacity retention over 100 cycles.

Electrochemical Characteristics and Li+ Ion Intercalation Kinetics of Dual-phase Li4Ti5O12/Li2TiO3 Composite in Voltage Range of 0−3 V

KAUST Repository

Bhatti, Humaira S; Anjum, Dalaver H.; Ullah, Shafiq; Ahmed, Bilal; Habib, Amir; Karim, Altaf; Hasanain, Syed Khurshid

2016-01-01

Li4Ti5O12, Li2TiO3 and dual-phase Li4Ti5O12/Li2TiO3 composite were prepared by sol-gel method with average particle size of 1 µm, 0.3 µm and 0.4 µm, respectively. Though Li2TiO3 is electrochemically inactive, the rate capability of Li4Ti5O12/Li2TiO3 is comparable to Li4Ti5O12 at different current rates. Li4Ti5O12/Li2TiO3 also shows good rate performance of 90 mA h g-1 at high rate of 10 C in voltage range of 1−3 V, attributable to increased interfaces in the composite. While Li4Ti5O12 delivers capacity retention of 88.6 % at 0.2 C over 50 cycles, Li4Ti5O12/Li2TiO3 exhibits no capacity fading at 0.2 C (40 cycles) and capacity retention of 98.45 % at 0.5 C (50 cycles). This highly stable cycling performance is attributed to the contribution of Li2TiO3 in preventing undesirable reaction of Li4Ti5O12 with the electrolyte during cycling. CV curves of Li4Ti5O12/Li2TiO3 in 0−3 V range exhibit two anodic peaks at 1.51 V and 0.7−0.0 V, indicating two modes of lithium intercalation into the lattice sites of active material. Owing to enhanced intercalation/de-intercalation kinetics in 0−3 V, composite electrode delivers superior rate performance of 203 mAh/g at 2.85 C and 140 mAh/g at 5.7 C with good reversible capacity retention over 100 cycles.

High performance Bi0.5Na0.5TiO3-BiAlO3-K0.5Na0.5NbO3 lead-free pyroelectric ceramics for thermal detectors

Science.gov (United States)

Liu, Zhen; Ren, Weijun; Peng, Ping; Guo, Shaobo; Lu, Teng; Liu, Yun; Dong, Xianlin; Wang, Genshui

2018-04-01

Both high pyroelectric properties and good temperature stability of ferroelectric materials are desirable when used for applications in infrared thermal detectors. In this work, we report lead-free ternary 0.97(0.99Bi0.5Na0.5TiO3-0.01BiAlO3)-0.03K0.5Na0.5NbO3 (BNT-BA-KNN) ceramics, which not only exhibits a large pyroelectric coefficient (p ˜ 3.7 × 10-8 C cm-2 K-1) and figures of merit (Fi, Fv, and Fd) but also shows excellent thermal stable properties. At room temperature, Fi, Fv, and Fd are determined as high as 1.32 × 10-10 m/V, 2.89 × 10-2 m2/C, and 1.15 × 10-5 Pa-1/2 at 1 kHz and 1.32 × 10-10 m/V, 2.70 × 10-2 m2/C, and 1.09 × 10-5 Pa-1/2 at 20 Hz, respectively. During the temperature range of RT to 85 °C, the achieved p, Fi, Fv, and Fd do not vary too much. The high depolarization temperature and the undispersed ferroelectric-ergodic relaxor phase transition with a sharp pyroelectric coefficient peak value of ˜400 × 10-8 C cm-2 K-1 are suggested to be responsible for this thermal stability, which ensures reliable actual operation. The results reveal the BNT-BA-KNN ceramics as promising lead-free candidates for infrared thermal detector applications.

Synthetic Swan band profile of (1,0) of 12C12C and (0,0) of 12C12C and 12C13C in comets

International Nuclear Information System (INIS)

Swamy, K.S.K.

1987-01-01

The statistical equilibrium calculations of the 12 C 13 C molecule based on the resonance fluorescence process give similar results to those of the normal molecule. Therefore the assumption that the observed intensities of bands of the normal and the isotopic molecule differ only by their abundance ratio is reasonable. The synthetic profile of the (1,0) Swan band of 12 C 13 C (0,0) band of 12 C 12 C and 12 C 13 C have been calculated. The relative merits of using the rotational structure of the (1,0) or (0,0) band for the determination of the isotopic ratio 12 C/ 13 C is discussed briefly. (author)

Bi1−xNbxO1.5+x (x=0.0625, 0.12) fast ion conductors: Structures, stability and oxide ion migration pathways

International Nuclear Information System (INIS)

Tate, Matthew L.; Hack, Jennifer; Kuang, Xiaojun; McIntyre, Garry J.; Withers, Ray L.; Johnson, Mark R.; Radosavljevic Evans, Ivana

2015-01-01

A combined experimental and computational study of Bi 1−x Nb x O 1.5+x (x=0.0625 and 0.12) has been carried out using laboratory X-ray, neutron and electron diffraction, impedance measurements and ab-initio molecular dynamics. We demonstrate that Bi 0.9375 Nb 0.0625 O 1.5625 , previously reported to adopt a cubic fluorite-type superstructure, can form two different polymorphs depending on the synthetic method: a metastable cubic phase is produced by quenching; while slower cooling yields a stable material with a tetragonal √2×√2×1 superstructure, which undergoes a reversible phase transition into the cubic form at ~680 °C on subsequent reheating. Neutron diffraction reveals that the tetragonal superstructure arises mainly from ordering in the oxygen sublattice, with Bi and Nb remaining disordered, although structured diffuse scattering observed in the electron diffraction patterns suggests a degree of short-range ordering. Both materials are oxide ion conductors. On thermal cycling, Bi 0.88 Nb 0.12 O 1.62 exhibits a decrease in conductivity of approximately an order of magnitude due to partial transformation into the tetragonal phase, but still exhibits conductivity comparable to yttria-stabilised zirconia (YSZ). Ab-initio molecular dynamics simulations performed on Bi 0.9375 Nb 0.0625 O 1.5625 show that oxide ion diffusion occurs by O 2− jumps between edge- and corner-sharing OM 4 groups (M=Bi, Nb) via tetrahedral □M 4 and octahedral □M 6 vacancies. - Graphical abstract: Oxide ion migration in tetragonal Bi 0.9375 Nb 0.0625 O 1.5625 occurs by O 2− jumps between edge- and corner-sharing OM 4 groups (M=Bi, Nb) via tetrahedral M 4 and octahedral M 6 vacancies. - Highlights: • Bi 0.9375 Nb 0.0625 O 1.5625 adopts a tetragonal √2×√2×1 fluorite superstructure. • Superstructure is due to ordering in the O-sublattice, with Bi/Nb disordered. • Bi 0.9375 Nb 0.0625 O 1.5625 is a good oxide ion conductor. • O 2− jump between OM 4 groups (M

CLIPS 6.0 - C LANGUAGE INTEGRATED PRODUCTION SYSTEM, VERSION 6.0 (UNIX VERSION)

Science.gov (United States)

Donnell, B.

1994-01-01

command line version. For the UNIX version of CLIPS 6.0, the command line interface has been successfully implemented on a Sun4 running SunOS, a DECstation running DEC RISC ULTRIX, an SGI Indigo Elan running IRIX, a DEC Alpha AXP running OSF/1, and an IBM RS/6000 running AIX. Command line interface executables are included for Sun4 computers running SunOS 4.1.1 or later and for the DEC RISC ULTRIX platform. The makefiles may have to be modified slightly to be used on other UNIX platforms. The UNIX, Macintosh, and IBM PC versions of CLIPS 6.0 each have a platform specific interface. Source code, a makefile, and an executable for the Windows 3.1 interface version of CLIPS 6.0 are provided only on the IBM PC distribution diskettes. Source code, a makefile, and an executable for the Macintosh interface version of CLIPS 6.0 are provided only on the Macintosh distribution diskettes. Likewise, for the UNIX version of CLIPS 6.0, only source code and a makefile for an X-Windows interface are provided. The X-Windows interface requires MIT's X Window System, Version 11, Release 4 (X11R4), the Athena Widget Set, and the Xmu library. The source code for the Athena Widget Set is provided on the distribution medium. The X-Windows interface has been successfully implemented on a Sun4 running SunOS 4.1.2 with the MIT distribution of X11R4 (not OpenWindows), an SGI Indigo Elan running IRIX 4.0.5, and a DEC Alpha AXP running OSF/1 1.2. The VAX version of CLIPS 6.0 comes only with the generic command line interface. ASCII makefiles for the command line version of CLIPS are provided on all the distribution media for UNIX, VMS, and DOS. Four executables are provided with the IBM PC version: a windowed interface executable for Windows 3.1 built using Borland C++ v3.1, an editor for use with the windowed interface, a command line version of CLIPS for Windows 3.1, and a 386 command line executable for DOS built using Zortech C++ v3.1. All four executables are capable of utilizing extended memory

CLIPS 6.0 - C LANGUAGE INTEGRATED PRODUCTION SYSTEM, VERSION 6.0 (MACINTOSH VERSION)

Science.gov (United States)

Riley, G.

1994-01-01

command line version. For the UNIX version of CLIPS 6.0, the command line interface has been successfully implemented on a Sun4 running SunOS, a DECstation running DEC RISC ULTRIX, an SGI Indigo Elan running IRIX, a DEC Alpha AXP running OSF/1, and an IBM RS/6000 running AIX. Command line interface executables are included for Sun4 computers running SunOS 4.1.1 or later and for the DEC RISC ULTRIX platform. The makefiles may have to be modified slightly to be used on other UNIX platforms. The UNIX, Macintosh, and IBM PC versions of CLIPS 6.0 each have a platform specific interface. Source code, a makefile, and an executable for the Windows 3.1 interface version of CLIPS 6.0 are provided only on the IBM PC distribution diskettes. Source code, a makefile, and an executable for the Macintosh interface version of CLIPS 6.0 are provided only on the Macintosh distribution diskettes. Likewise, for the UNIX version of CLIPS 6.0, only source code and a makefile for an X-Windows interface are provided. The X-Windows interface requires MIT's X Window System, Version 11, Release 4 (X11R4), the Athena Widget Set, and the Xmu library. The source code for the Athena Widget Set is provided on the distribution medium. The X-Windows interface has been successfully implemented on a Sun4 running SunOS 4.1.2 with the MIT distribution of X11R4 (not OpenWindows), an SGI Indigo Elan running IRIX 4.0.5, and a DEC Alpha AXP running OSF/1 1.2. The VAX version of CLIPS 6.0 comes only with the generic command line interface. ASCII makefiles for the command line version of CLIPS are provided on all the distribution media for UNIX, VMS, and DOS. Four executables are provided with the IBM PC version: a windowed interface executable for Windows 3.1 built using Borland C++ v3.1, an editor for use with the windowed interface, a command line version of CLIPS for Windows 3.1, and a 386 command line executable for DOS built using Zortech C++ v3.1. All four executables are capable of utilizing extended memory

Crystal structure and magnetic properties of La{sub 2−x}(Sr{sub 0.5}Ca{sub 0.5}){sub 1+x}Mn{sub 2}O{sub 7} (x=0.6, 0.8 and 1.0) Ruddlesden–Popper manganites

Energy Technology Data Exchange (ETDEWEB)

Raju, K.; Song, M.S.; Lee, J.Y., E-mail: jylee@yu.ac.kr

2014-05-01

Double layer perovskite (Ruddlesden–Popper) manganites with the nominal composition of La{sub 2−x}(Sr{sub 0.5}Ca{sub 0.5}){sub 1+x}Mn{sub 2}O{sub 7} (x=0.6, 0.8 and 1.0) were synthesized via a solid state reaction route. X-ray and neutron diffraction were performed at room temperature and the crystal structure was refined using the Rietveld method based on the space group, I4/mmm. The temperature variation of the susceptibility revealed a spin glass transition at 28 K for x=0.6, a charge ordering transition at 245 K and a Neel transition at 170 K for x=1.0. - Highlights: • Lanthanum based double layered manganites were prepared by doping with the same amounts of Sr and Ca. • X-ray and neutron diffraction were performed and the crystal structure was refined using the Rietveld method. • Different magnetic transitions were observed depending upon the doping concentration. • Qualitative explanation for the various observed phenomena was given.

Efficient bright white organic light-emitting diode based on non-doped ultrathin 5,6,11,12-tetraphenylnaphthacene layer

Energy Technology Data Exchange (ETDEWEB)

Li Lu [State Key Laboratory of Electronic Thin Films and Integrated Devices, School of Optoelectronic Information, University of Electronic Science and Technology of China (UESTC), Chengdu 610054 (China); Yu Junsheng [State Key Laboratory of Electronic Thin Films and Integrated Devices, School of Optoelectronic Information, University of Electronic Science and Technology of China (UESTC), Chengdu 610054 (China)], E-mail: jsyu@uestc.edu.cn; Tang Xiaoqing; Wang Tao; Li Wei; Jiang Yadong [State Key Laboratory of Electronic Thin Films and Integrated Devices, School of Optoelectronic Information, University of Electronic Science and Technology of China (UESTC), Chengdu 610054 (China)

2008-11-15

High-performance undoped white organic light-emitting diode (OLED) has been fabricated using an ultrathin yellow-emitting layer of 5,6,11,12-tetraphenylnaphthacene (rubrene) inserted at two sides of interface between two N,N'-bis-(1-naphthyl)-N,N'- biphenyl-1,1'-biphenyl-4,4'- diamine (NPB) layers as a hole transporting and blue emissive layer, respectively. The results showed that a maximum luminance of the device reached to as high as 21,500 cd/m{sup 2} at 15 V. The power efficiencies of 2.5 and 1.6 lm/W at a luminance of 1000 and 10000 cd/m{sup 2}, respectively, were obtained. The peaks of electroluminescent (EL) spectra locate at 429 and 560 nm corresponding to the Commissions Internationale De L'Eclairage (CIE) coordinates of (0.32, 0.33), which is independent of bias voltage. The performance enhancement of the device may result from direct charge carrier trapping in rubrene. Energy transfer mechanism was also found in the EL process.

Pressure Effects on the Magnetic Phase Transition of Mn3SnC1−xNx (x = 0, 0.5)

International Nuclear Information System (INIS)

Hu Jing-Yu; Zhao Qing; Wen Yong-Chun; Wang Cong; Yao Yuan; Jin Chang-Qing; Yu Ri-Cheng

2012-01-01

The electronic transport properties of Mn 3 SnC and Mn 3 SnC 0.5 N 0.5 were measured under pressures up to 1.8 GPa. At ambient pressure, an abrupt increase of resistance occurs around the temperature of magnetic phase transition in both samples. The transition temperature Tc from paramagnetic to ferrimagnetic state decreases linearly at rates of 12.6 and 6.3K/GPa with pressure for Mn 3 SnC and Mn 3 SnC 0.5 N 0.5 , respectively. This phenomenon could be understood by the Labbe-Jardin tight binding approximation model. (condensed matter: structure, mechanical and thermal properties)

Beam-foil lifetime measurements for some 5d10 nl and 5d96s6p levels of Pb IV

International Nuclear Information System (INIS)

Pinnington, E.H.; Ansbacher, W.; Tauheed, A.; Kernahan, J.A.

1991-01-01

The beam-foil technique was used to measure the lifetimes of the 5d 10 5f, 5g, 6d, 6h, 7p, 7d, 8s and 5d 9 6s6p (2) 0 , (3) 0 , (6) 0 , (14) 0 , (17) 0 levels of Pb IV. Correlated decay-curve analyses were used to correct for the effects of cascading in the case of the 5d 10 5f, 5g, 6d, and 7p levels. The numerical Coulomb approximation was used to calculate comparison values for the 5d 10 nl levels. The need for a more rigorous calculation for specific levels is discussed. (12 refs., fig., tab.)

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.

12 CFR 618.8030 - Out-of-territory related services.

Science.gov (United States)

2010-01-01

... 12 Banks and Banking 6 2010-01-01 2010-01-01 false Out-of-territory related services. 618.8030 Section 618.8030 Banks and Banking FARM CREDIT ADMINISTRATION FARM CREDIT SYSTEM GENERAL PROVISIONS Related Services § 618.8030 Out-of-territory related services. (a) System banks and associations may offer...

12 CFR 614.4356 - Farm Credit Leasing Services Corporation.

Science.gov (United States)

2010-01-01

... 12 Banks and Banking 6 2010-01-01 2010-01-01 false Farm Credit Leasing Services Corporation. 614... OPERATIONS Lending and Leasing Limits § 614.4356 Farm Credit Leasing Services Corporation. The Farm Credit Leasing Services Corporation may enter into a lease agreement with a lessee if the consolidated amount of...

Electrochemical hydrogen-storage properties of La{sub 0.78}Mg{sub 0.22}Ni{sub 2.67}Mn{sub 0.11}Al{sub 0.11}Co{sub 0.52}-M1Ni{sub 3.5}Co{sub 0.6}Mn{sub 0.4}Al{sub 0.}-5 composites

Energy Technology Data Exchange (ETDEWEB)

Huang, Hongxia, E-mail: hhxhunan@126.com [Key Lab of New Processing Technology for Nonferrous Metals and Materials Ministry of Education, Guilin University of Technology, Guilin (China); Li, Guohui [Guangxi Scientific Experiment Center of Mining, Metallurgy and Environment, College of Chemistry and Bioengineering, Guilin University of Technology, Guilin (China); Zhuang, Shuxin [School of Material Science and engineering, Xiamen University of Technology, Xiamen (China)

2013-07-15

For improving the electrochemical properties of nonstoichiometric AB{sub 3} -type La{sub 0.7}8Mg{sub 0.22}Ni{sub 2.67}Mn{sub 0.11}Al{sub 0.11}Co{sub 0.52} alloy as negative electrode of Ni-MH battery, its related composites La{sub 0.78}Mg{sub 0.22}Ni{sub 2.67}Mn{sub 0.11}Al{sub 0.11}Co{sub 0.52}-x wt.% M1Ni{sub 3.5}Co{sub 0.6}Mn{sub 0.4}Al{sub 0.5} (x = 0, 10, 20, 30) were prepared. Analysis by X-ray diffractometry (XRD) revealed that the composites consist mainly of LaNi{sub 5} and La{sub 2}Ni{sub 7} phases. Despite the small decrease in the maximum discharge capacity, the cycle performance was significantly enhanced. Linear polarization (LP), anodic polarization (AP) and potential step discharge experiments revealed that the electrochemical kinetics increases first and then decreases with increasing x. (author)

Evidence for a narrow peak in K0sub(s)π+-π+π- at 2.6 GeV in 12 GeV/c anti pp interactions

International Nuclear Information System (INIS)

Apostolakis, A.; Casali, R.; Caso, C.; Goldschmidt-Clermont, Y.; Pape, L.; Porte, J.P.; Stergiou, A.; Tallini, B.; Vassiliadis, G.; Wenninger, H.; Grard, G.; Henri, V.P.; Herquet, P.; Kesteman, J.; Banerjee, S.; Barnham, K.W.J.; Beuselinck, R.; Butterworth, I.; Campbell, J.R.; Chaff, J.; Mermikides, M.E.; Miller, D.B.; Bertrand, D.; Johnson, D.; Lemonne, J.; Renton, P.; Wickens, J.; Bogaert, F. van den; Daugeras, B.; Jacholkowska, A.

1977-01-01

The evidence is reported for a narrow charged peak (5.5 s.d.), which the authors suggest calling the I, in the 6-prong-V 0 topology of anti pp interactions at 12 GeV/c. The mass, width and the product of cross section sigmasub(I) times the branching ratio BR into the final state (K 0 sub(s)π +- π + π - ) are found to be: Msub(I)=2.60+-0.01 GeV/c 2 , GAMMAsub(I) 2 , sigmasub(I).BR approximately 20 μbarn. (Auth.)

Strong piezoelectricity in (1 - x)(K0.4Na0.6)(Nb0.96Sb0.04)O3-xBi0.5K0.5Zr1-ySnyO3 lead-free binary system: identification and role of multiphase coexistence.

Science.gov (United States)

Zheng, Ting; Wu, Jiagang; Xiao, Dingquan; Zhu, Jianguo; Wang, Xiangjian; Xin, Lipeng; Lou, Xiaojie

2015-03-18

Here we report a strong piezoelectric activity in (1 - x)(K0.4Na0.6)(Nb0.96Sb0.04)O3-xBi0.5K0.5Zr1-ySnyO3 lead-free ceramics by designing different phase boundaries. The phase boundaries concerning rhombohedral-orthorhombic-tetragonal (R-O-T) and rhombohedral-tetragonal (R-T) multiphase coexistence were attained by changing BKZS and Sn contents and then were identified by the X-ray diffraction patterns as well as temperature-dependent permittivity and ν1 Raman modes associated with BO6 perovskite octahedron. A high strain (strain = 0.21-0.28% and d33* = 707-880 pm/V) and a strong piezoelectric coefficient (d33 = 415-460 pC/N) were shown in the ceramics located at the multiphase coexistence region. The reported results of this work are superior to that (d33* ∼ 570 pm/V and d33 ∼ 416 pC/N) of the textured (K,Na,Li)(Nb,Ta,Sb)O3 ceramics [Nature 2004, 432, 84]. We believe that the material system of this work will become one of the most promising candidates for piezoelectric actuators.

12 CFR 572.10 - Notice of servicer's identity.

Science.gov (United States)

2010-01-01

... 12 Banks and Banking 5 2010-01-01 2010-01-01 false Notice of servicer's identity. 572.10 Section... HAVING SPECIAL FLOOD HAZARDS § 572.10 Notice of servicer's identity. (a) Notice requirement. When a... the Director of FEMA (or the Director's designee) in writing of the identity of the servicer of the...

Crystal structure of tetrabutylammonium bromide–1,2-diiodo-3,4,5,6-tetrafluorobenzene–dichloromethane (2/2/1

Directory of Open Access Journals (Sweden)

Jasmine Viger-Gravel

2015-05-01

Full Text Available The crystallization of a 1:1 molar solution of 1,2-diiodo-3,4,5,6-tetrafluorobenzene (o-DITFB and tetrabutylammonium bromide (n-Bu4NBr from dichloromethane yielded pure white crystals of a halogen-bonded compound, C16H36N+·Br−·C6F4I2·0.5CH2Cl2 or [(n-Bu4NBr(o-DITFB]·0.5CH2Cl2. The compound may be described as a quaternary system and may be classified as a salt–cocrystal solvate. The asymmetric unit contains one molecule of solvent, two o-DITFB molecules, two cations (n-Bu4N+ and two crystallographically distinct bromide ions [θI...Br-...I = 144.18 (1 and 135.35 (1°]. The bromide ion is a bidentate halogen-bond acceptor which interacts with two covalently bonded iodines (i.e. halogen-bond donors, resulting in a one-dimensional polymeric zigzag chain network approximately along the a axis. The observed short contacts and angles are characteristic of the non-covalent interaction [dC—I...Br = 3.1593 (4–3.2590 (5 Å; θC—I...Br = 174.89 (7 and 178.16 (7°]. It is noted that iodine acts as both a halogen-bond donor and a weak CH hydrogen-bond acceptor, while the bromide ions act as acceptors for weak CH hydrogen bonds and halogen bonds.

Electrical analysis of inter-growth structured Bi4Ti3O12-Na0.5Bi4.5Ti4O15 ceramics

Science.gov (United States)

Jiang, Xiangping; Jiang, Yalin; Jiang, Xingan; Chen, Chao; Tu, Na; Chen, Yunjing

2017-06-01

Inter-growth bismuth layer-structured ferroelectrics (BLSFs), Bi4Ti3O12-Na0.5Bi4.5Ti4O15 (BIT-NBT), were successfully synthesized using the traditional solid-state reaction method. X-ray diffraction (XRD) Rietveld refinements were conducted using GSAS software. Good agreement and low residual are obtained. The XRD diffraction peaks can be well indexed into I2cm space group. The inter-growth structure was further observed in the high-resolution TEM image. Dielectric and impedance properties were measured and systematically analyzed. At the temperature range 763-923 K (below {T}{{c}}), doubly ionized oxygen vacancies (OVs) are localized and the short-range hopping leads to the relaxation processes with an activation energy of 0.79-1.01 eV. Above {T}{{c}}, the doubly charged OVs are delocalized and become free ones, which contribute to the long-range dc conduction. The reduction in relaxation species gives rise to a higher relaxation activation energy ˜1.6  eV. Project supported by the National Natural Science Foundation of China (Grant Nos. 51562014, 51262009, and 51602135).

5,11-Ditosyl-5H,11H-dibenzo[b,f][1,5]diazo­cine-6,12-dione acetic acid hemisolvate

Science.gov (United States)

Abbassi, Najat; Bassou, Oulemda; Rakib, El Mostapha; Saadi, Mohamed; El Ammari, Lahcen

2013-01-01

The mol­ecular structure of the title compound, C28H22N2O6S2·0.5CH3COOH, is built up from three fused rings, two six and one eight membered. The eight-membered ring shows a boat conformation and the dihedral angle between the two benzene groups attached thereto is 66.43 (11)°, resulting in a V-shaped geometry. Two tosyl substituents are bound to the N atoms. The planes through the tolyl rings are roughly perpendicular, as indicated by the dihedral angle of 82.44 (12)°. In the crystal, the mol­ecule and its inversion-related symmetry-equivalent are linked to the acetic acid solvent mol­ecule by non-classical O—H⋯O and C—H⋯O hydrogen bonds. Two half-occupied acetic acid solvent mol­ecules are disordered at the same site and linked by a center of symmetry. PMID:23634138

Electronic structure of bismuth in high-temperature superconductor Bi1.6Pb0.4Sr2Ca2.5Cu3.5Oσ

International Nuclear Information System (INIS)

Band, I.M.; Egorovm, A.I.; Karazhanova, G.I.

1990-01-01

The shifts of K α1 X-ray of bismuth in the HTS-ceramic Bi 1.6 Pb 0.4 Sr 2 Ca 2.5 Cu 5 O σ and Bi 2 O 3 are measured experimentally. It is shown that bismuth is threevalent in the HTS-ceramic. From comparison of the experimental values of shifts with theoretical values calculated within the framework of different modifications of Hartree-Fock method the effective charge at the bismuth atoms in these compounds is determined: q(Bi 2 O 3 )=1.5+2.0, q(Bi 1.6 Pb 0.4 Sr 2 Ca 2.5 Cu 3.5 O σ )= 1.6+2.1. It was suggested, That the Bi significant covalence degree in HTS-ceramic may be a cause of noticeable contribution of the Bi 6p-states in the density of states at Fermi-level. 13 refs.; 1 fig.; 2 tabs

12 CFR 509.11 - Service of papers.

Science.gov (United States)

2010-01-01

... 12 Banks and Banking 5 2010-01-01 2010-01-01 false Service of papers. 509.11 Section 509.11 Banks... IN ADJUDICATORY PROCEEDINGS Uniform Rules of Practice and Procedure § 509.11 Service of papers. (a) By the parties. Except as otherwise provided, a party filing papers shall serve a copy upon the...

Aquaporins 6-12 in the human eye

DEFF Research Database (Denmark)

Tran, Thuy Linh; Bek, Toke; Holm, Lars

2012-01-01

Purpose: Aquaporins (AQPs) are widely expressed and have diverse distribution patterns in the eye. AQPs 0-5 have been localized at the cellular level in human eyes. We investigated the presence of the more recently discovered AQPs 6-12 in the human eye. Methods: RT-PCR was performed on fresh tissue...... from two human eyes divided into the cornea, corneal limbus, ciliary body and iris, lens, choroid, optic nerve, retina and sclera. Each structure was examined to detect the mRNA of AQPs 6-12. Twenty-one human eyes were examined using immunohistochemical and immunofluorescence techniques to determine...... was detected in the corneal epithelium, corneal endothelium, trabecular meshwork endothelium, ciliary epithelia, lens epithelium, the inner and outer limiting membrane of the retina, the retinal pigment epithelium and the capillary endothelium of all parts of the eye. AQP9 immunolabelling was detected...

Structure analysis of mutually incommensurate composite crystal (Ca0.5Y0.5)0.8CuO2

International Nuclear Information System (INIS)

Gotoh, Y.; Yamaguchi, I.; Takeya, S.; Fujihisa, H.; Honda, K.; Ito, T.; Oka, K.; Yamaguchi, H.

2006-01-01

Single-crystal X-ray structure analysis of mutually incommensurate (Ca 0.5 Y 0.5 ) 0.8 CuO 2 , 'Ca 2 Y 2 Cu 5 O 1 ' has been performed by the composite approach which leads to average substructures and their relative arrangement. The composite crystal structure of (Ca 0.5 Y 0.5 ) 0.8 CuO 2 has the CuO 2 substructure and the Ca 0.5 Y 0.5 substructure. The CuO 2 substructure with a 1 = 10.598(2) A, b = 6.189(2) A, c 1 = 2.825(2) A, β 1 = 90.19(4) o , V 1 = 185.4(1) A 3 , Z = 4 and space group F2/m has the plane of edge-shared one-dimensional CuO 2 chains along the c-axis. The Ca 0.5 Y 0.5 substructure with a 2 = 10.629(2) A, b = 6.189(2) A, c 2 3.517(1) A, β 2 = 94.36(3) o , V 2 = 230.7(1) A 3 , Z = 4 and space group F2/m forms the sheet of (Ca, Y) atoms in the ac-plane. By considering (3 + 1)-dimensional superspace group symmetry, it is concluded that the incommensurate composite crystal structure of (Ca 0.5 Y 0.5 ) 0.8 CuO 2 should be described by the combination of F2/m for the CuO 2 substructure and F2/c for the Ca 0.5 Y 0.5 substructure. The composite approach has made clear that the plane of CuO 2 chains and the sheet of (Ca, Y) atoms stack alternately to form a mutually incommensurate composite crystal with layered substructures

Antioxidant Properties and PC12 Cell Protective Effects of a Novel Curcumin Analogue (2E,6E-2,6-Bis(3,5- dimethoxybenzylidenecyclohexanone (MCH

Directory of Open Access Journals (Sweden)

Gui-Zhen Ao

2014-03-01

Full Text Available The antioxidative properties of a novel curcumin analogue (2E,6E-2,6-bis(3,5-dimethoxybenzylidenecyclohexanone (MCH were assessed by several in vitro models, including superoxide anion, hydroxyl radical and 1,1-diphenyl-2-picrylhydrazyl (DPPH radical scavenging and PC12 cell protection from H2O2 damage. MCH displayed superior O2•− quenching abilities compared to curcumin and vitamin C. In vitro stability of MCH was also improved compared with curcumin. Exposure of PC12 cells to 150 µM H2O2 caused a decrease of antioxidant enzyme activities, glutathione (GSH loss, an increase in malondialdehyde (MDA level, and leakage of lactate dehydrogenase (LDH, cell apoptosis and reduction in cell viability. Pretreatment of the cells with MCH at 0.63–5.00 µM before H2O2 exposure significantly attenuated those changes in a dose-dependent manner. MCH enhanced cellular expression of transcription factor NF-E2-related factor 2 (Nrf2 at the transcriptional level. Moreover, MCH could mitigate intracellular accumulation of reactive oxygen species (ROS, the loss of mitochondrial membrane potential (MMP, and the increase of cleaved caspase-3 activity induced by H2O2. These results show that MCH protects PC12 cells from H2O2 injury by modulating endogenous antioxidant enzymes, scavenging ROS, activating the Nrf2 cytoprotective pathway and prevention of apoptosis.

Crystal structure and optical absorption spectra of Ga0.5Fe0.5InS3 and Ga0.5Fe0.25In1.25S3 crystals

International Nuclear Information System (INIS)

Gusejnov, G.G.; Musaeva, N.N.; Kyazumov, M.G.; Asadova, I.B.; Aliev, O.M.

2003-01-01

Single crystals of Ga 0.5 Fe 0.5 InS 3 are grown by the method of chemical gas-transport reactions and those of Ga 0.5 Fe 0.25 In 1.25 S 3 - by Bridgman method. X-ray diffraction studies reveal that they crystallize in trigonal and rhombohedral systems with lattice parameters of a = 3.796 x 2 A, c = 12.210 A, P3m1; a = 3.786 x 2 A, c = 36.606 A, R3m, respectively. An optical absorption edge in a wide range of photon energy and an energy gap width are determined: E g = 1.885 eV for Ga 0.5 Fe 0.5 InS 3 and E g 1.843 eV for Ga 0.5 Fe 0.25 In 1.25 S 3 [ru

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.

Evidence for a narrow peak in $K0_{S}\\pi \\pm \\pi^{+}pi^{-}$ at 2.6 GeV in 12 GeV/c $\\overline{p}$p interactions

CERN Document Server

Apostolakis, Alcibiades J; Caso, Carlo; Goldschmidt-Clermont, Yves; Pape, L; Porte, J P; Stergiou, Athanase; Tallini, Bruno; Vasileiadis, G; Wenninger, Horst; Grard, G; Henri, V P; Herquet, P; Kesteman, J; Banerjee, S; Barnham, Keith W J; Beuselinck, R; Butterworth, Ian; Campbell, J Ronald; Chaff, J A; Mermikides, Michael E; Miller, D B; Bertrand, D; Johnson, D; Lemonne, J; Renton, P B; Wickens, J H; Van den Bogaert, F; Daugeras, B Y; Jacholkowska, A

1977-01-01

The authors report the evidence for a narrow charged peak (5.5 s.d.), which they suggest calling the I, in the 6-prong-V/sup 0/ topology of pp interactions at 12 GeV/c. The mass, width and the product of cross section sigma /sub I/ times the branching ratio BR into the final state (K/sub s//sup 0/ pi /sup +or-/ pi /sup +/ pi /sup -/) are found to be: M/sub I/=2.60+or-0.01 GeV/c/sup 2/, Gamma /sub I/0.018 GeV /c/sup 2/, sigma /sub I/.BR approximately=20 mu barn. (5 refs).

0 + 5 Vascular Surgery Residents' Operative Experience in General Surgery: An Analysis of Operative Logs from 12 Integrated Programs.

Science.gov (United States)

Smith, Brigitte K; Kang, P Chulhi; McAninch, Chris; Leverson, Glen; Sullivan, Sarah; Mitchell, Erica L

2016-01-01

Integrated (0 + 5) vascular surgery (VS) residency programs must include 24 months of training in core general surgery. The Accreditation Council for Graduate Medical Education currently does not require specific case numbers in general surgery for 0 + 5 trainees; however, program directors have structured this time to optimize operative experience. The aim of this study is to determine the case volume and type of cases that VS residents are exposed to during their core surgery training. Accreditation council for graduate medical education operative logs for current 0 + 5 VS residents were obtained and retrospectively reviewed to determine general surgery case volume and distribution between open and laparoscopic cases performed. Standard statistical methods were applied. A total of 12 integrated VS residency programs provided operative case logs for current residents. A total of 41 integrated VS residents in clinical years 2 through 5. During the postgraduate year-1 training year, residents participated in significantly more open than laparoscopic general surgery cases (p surgery cases are hernia repair (20%), skin and soft tissue (7.4%), and breast (6.3%). Residents in programs with core surgery over 3 years participated in significantly more general surgery operations compared with residents in programs with core surgery spread out over 4 years (p = 0.035). 0 + 5 VS residents perform significantly more open operations than laparoscopic operations during their core surgery training. The majority of these operations are minor, nonabdominal procedures. The 0 + 5 VS residency program general surgery operative training requirements should be reevaluated and case minimums defined. The general surgery training component of 0 + 5 VS residencies may need to be restructured to meet the needs of current and future trainees. Copyright © 2016 Association of Program Directors in Surgery. Published by Elsevier Inc. All rights reserved.

CLIPS 6.0 - C LANGUAGE INTEGRATED PRODUCTION SYSTEM, VERSION 6.0 (IBM PC VERSION)

Science.gov (United States)

Donnell, B.

1994-01-01

command line version. For the UNIX version of CLIPS 6.0, the command line interface has been successfully implemented on a Sun4 running SunOS, a DECstation running DEC RISC ULTRIX, an SGI Indigo Elan running IRIX, a DEC Alpha AXP running OSF/1, and an IBM RS/6000 running AIX. Command line interface executables are included for Sun4 computers running SunOS 4.1.1 or later and for the DEC RISC ULTRIX platform. The makefiles may have to be modified slightly to be used on other UNIX platforms. The UNIX, Macintosh, and IBM PC versions of CLIPS 6.0 each have a platform specific interface. Source code, a makefile, and an executable for the Windows 3.1 interface version of CLIPS 6.0 are provided only on the IBM PC distribution diskettes. Source code, a makefile, and an executable for the Macintosh interface version of CLIPS 6.0 are provided only on the Macintosh distribution diskettes. Likewise, for the UNIX version of CLIPS 6.0, only source code and a makefile for an X-Windows interface are provided. The X-Windows interface requires MIT's X Window System, Version 11, Release 4 (X11R4), the Athena Widget Set, and the Xmu library. The source code for the Athena Widget Set is provided on the distribution medium. The X-Windows interface has been successfully implemented on a Sun4 running SunOS 4.1.2 with the MIT distribution of X11R4 (not OpenWindows), an SGI Indigo Elan running IRIX 4.0.5, and a DEC Alpha AXP running OSF/1 1.2. The VAX version of CLIPS 6.0 comes only with the generic command line interface. ASCII makefiles for the command line version of CLIPS are provided on all the distribution media for UNIX, VMS, and DOS. Four executables are provided with the IBM PC version: a windowed interface executable for Windows 3.1 built using Borland C++ v3.1, an editor for use with the windowed interface, a command line version of CLIPS for Windows 3.1, and a 386 command line executable for DOS built using Zortech C++ v3.1. All four executables are capable of utilizing extended memory

Prognosis at 6 and 12months after self-attempted hanging.

Science.gov (United States)

Gantois, Guillaume; Parmentier-Decrucq, Erika; Duburcq, Thibault; Favory, Raphaël; Mathieu, Daniel; Poissy, Julien

2017-11-01

Patients surviving a self-attempted hanging have a total neurological recovery in 57-77% of cases at hospital discharge, but no long-term data are available. In this observational study, all patients hospitalized post-self-attempted hanging in the intensive care unit (ICU) in a 5-year period were included. Neurological evaluations at 6 and 12months were performed according to Cerebral Performance Category (CPC) scores. Factors associated with neurological recovery were determined by comparing CPC2+3+4 (bad recovery) vs. CPC1 (good recovery). Of 231 patients included, 104 (47%) were found to have cardiac arrest (CA). Ninety-five (41%) patients died in the ICU: 93 (89%) in the CA group and 2 (1.6%) in the group without CA. Neurological evaluations at 6 and 12months were obtained in 97 of the 136 surviving patients. At 6months, in the CA group (n=9), the CPC score was 1 for 6 patients, 2 for 2, and 4 for 1 patient. In the group without CA (n=88), 79 patients had normal neurological status at 6months and 78 at 12months. Among these patients, 96% returned home, 77% returned to work, 16 (18%) patients re-attempted suicide within the year. Risk factors of neurological sequelae at 6months were a CA at the hanging site (P=0.045), an elevated diastolic blood pressure (87 vs. 70 mm Hg; P=0.04), a lower initial Glasgow score (4 vs. 5; P=0.04), and an elevated blood glucose level (139 vs. 113 mg/dL; Pgood neurological outcome. The rate of suicidal recidivism is particularly important, which justifies joint work with psychiatrists. Copyright © 2017 Elsevier Inc. All rights reserved.

Energy distributions study of spallation neutrons produced at 0 deg. by proton beams (0.8 GeV and 1.6 GeV) and deuteron beams (1.2 and 1.6 GeV)

International Nuclear Information System (INIS)

Martinez, Eugenie

1997-01-01

We are studying the energy distributions of spallation neutrons produced at 0 deg. by protons of 0.8 GeV up to 1.6 GeV and deuterons of 1.2 and 1.6 GeV with two complementary experimental techniques: the time of flight measurement with tagged incident protons for low energy neutrons (3-400 MeV) and the use of a magnetic spectrometer at high energy (E ≥ 200 MeV). These measurements enable us to measure for the first time the neutron spectra for incident energies higher than 800 MeV. We have compared the double differential cross sections produced with 1.2 GeV protons on several thin targets (Al, Fe, Zr, W, Pb and Th). The neutron production obtained for a lead target is also studied for various energies (0.8 up to 1.6 GeV) and incident particles (p, d). Data are compared with theoretical simulations carried out using the TIERCE system and the intranuclear cascade model of J. Cugnon associated to the decay code of D. Durand. The neutron spectra calculated by using the HETC and MCNP codes, included in TIERCE, are significantly higher than the measured distributions. A better agreement is observed with the results of the Cugnon's cascade model. (author) [fr

STRUCTURAL AND DIELECTRIC STUDIES ON Sr0.5-3y/2LayBa0.5Nb2O6 CERAMIC SYSTEMS WITH VARIED SINTERING TIME AND La CONCENTRATION

Directory of Open Access Journals (Sweden)

Zahariman S. R.

2013-12-01

Full Text Available Sr0.5Ba0.5Nb2O6 (SBN50 ceramic doped with different concentration of Lanthanum, La according to stoichiometric formulation of Sr0.5-3y/2LayBa0.5Nb2O6 (LSBN with y = 0.01, 0.03, 0.05 and 0.07 prepared using traditional ceramic method at the calcination temperature of 1200°C and sintered at 1300°C at varied sintering time. The effects of the sintering time and La3+ substitution on the morphological, compositional, structural and electrical properties of the LSBN is presented using scanning electronic microscopy (SEM, energy dispersive spectroscopy (EDS, X-ray diffraction (XRD and dielectric analysis. The XRD spectra confirm the presence of TTB structure in the ceramics. The Curie temperature (Tc of the ceramic identified from the dielectric studies performed in the temperature range of 28°C to 300°C. The temperature dependent dielectric exhibits broad peaks indicating a diffuse phase transition and relaxor behavior of the ceramic. The measured density of the samples is proportional to the sintering time and inversely proportional to the amount of the La3+ substitution. The solubility limit of La3+ ions in the SBN solid solution is at y ~ 0.05. This observation is also supported by the dielectric results where the dielectric properties of the ceramic deteriorate for y > 0.05 La substitution.

Laser shock peening of steam turbine blade for enhanced service life

Indian Academy of Sciences (India)

2014-02-13

Feb 13, 2014 ... study to develop indigenous LSP process for enhanced service life ... DINX10Cr- 0.08–0.13 11.5–12.5 2.2–2.8 0.1–0.5 1.6–1.8 0.6–0.9 0.25–0.4 Balance ... LSP is done by scanning the taped surface of the work piece with a ...

Hierarchically porous micro-rod lithium-rich cathode material Li1.2Ni0.13Mn0.54Co0.13O2 for high performance lithium-ion batteries

International Nuclear Information System (INIS)

Zhang, Linjing; Borong, Wu.; Ning, Li.; Feng, Wu.

2014-01-01

Graphical abstract: - Highlights: • The hierarchically porous micro-rod Li 1.2 Ni 0.13 Mn 0.54 Co 0.13 O 2 material is prepared by a facile hydrothermal method. • This material exhibits good cycling performance. • It delivers discharge capacities of 280.7, 254.8, 232.3, 225.6, 201.7 and 172.7 mAh g −1 at 0.1 C, 0.2 C, 0.5 C, 1 C, 2 C and 5 C rates, respectively. • Excellent rate capability and cycleability are obtained attributed to the hierarchically porous micro-rod structure. - Abstract: Lithium-rich cathode material Li 1.2 Ni 0.13 Mn 0.54 Co 0.13 O 2 with hierarchically porous micro-rod structures has been synthesized using a facile hydrothermal method. The morphology and XRD patterns explain the formation mechanism of the sample. Micro-rod oxalates precursor with rough surface is formed during the hydrothermal reaction, and then the product with hierarchically porous structures constructed of nanoparticles is synthesized during the sintering process at high temperatures. The electrochemical performance results show that the as-prepared sample exhibits high capacities, good cycleability and outstanding rate capability. It delivers discharge capacities of 280.7, 254.8, 232.3, 225.6, 201.7 and 172.7 mAh g −1 at 0.1 C, 0.2 C, 0.5 C, 1 C, 2 C and 5 C rates, respectively. The cycle voltammograms indicate the good reversibility of the as-prepared Li 1.2 Ni 0.13 Mn 0.54 Co 0.13 O 2 material. The high onset temperature of the exothermal peak in the differential scanning calorimetry curve implies its good thermal stability. The good performance of the as-prepared material is endowed by its hierarchically porous structures

Service use in children aged 6-8 years with attention deficit hyperactivity disorder.

Science.gov (United States)

Efron, Daryl; Moisuc, Olga; McKenzie, Vicki; Sciberras, Emma

2016-02-01

This study investigated prevalence, types and predictors of professional service use in families of children identified with attention deficit hyperactivity disorder (ADHD) in the community. children with ADHD were identified through 43 schools using parent and teacher screening questionnaires (Conners 3 ADHD Index) followed by case confirmation using the Diagnostic Interview Schedule for Children Version IV. Parents completed a survey about professional service use in the last 12 months. data on variables potentially associated with service use were collected from parents (interview and questionnaires), teachers (questionnaires) and children (direct assessment). Logistic regression was used to examine predictors of service use in univariate and multivariable analyses. The sample comprised 179 children aged 6-8 years with ADHD. Over one-third (37%) had not received professional services in the last 12 months. The strongest predictors of service use were older child age (adjusted OR=3.0, 95% CI 1.0 to 8.9, p=0.05), and the degree to which the child's behaviour impacted on the family (adjusted OR=2.0, 95% CI 1.3 to 3.3, p=0.007), after controlling for ADHD subtype and severity, externalising comorbidities, academic achievement and parent-reported impairment. A substantial proportion of children with ADHD are not accessing professional services. Our findings suggest that the child's age and the impact of the child's behaviour on the family are the strongest predictors of service use. Given the demonstrated benefits from various interventions in ADHD, there is a need to improve case identification and referral for services. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/

Investigation into self-pumped and mutually pumped phase conjugation with beams entering the negative c face of doped (K0.5Na0.5)0.2(Sr0.75 Ba0.25)0.9Nb2O6 crystals

International Nuclear Information System (INIS)

Zhang, J.; Liu, H.; Jia, W.

1997-01-01

We investigated some novel geometries of self-pumped phase conjugation (SPPC) and mutually pumped phase conjugation (MPPC), relying on total internal reflection both from the a face and from corners, with beams entering the negative c face of doped (K 0.5 Na 0.5 ) 0.2 (Sr 0.75 Ba 0.25 ) 0.9 Nb 2 O 6 crystals. The different situations for internal light paths and their direct transformation at the same incident wavelength were observed. Similarities and differences between SPPC and MPPC are discussed. The dynamic features of SPPC and MPPC in different situations were also observed. Three or more four-wave-mixing interaction regions were clearly observed inside the phase conjugators. The multistep interaction and its influence on the response rate and conjugation fidelity are analyzed. The large size of the samples seems necessary to ensure an optical path that is long enough for multistep bifurcation. The stability of the light channels is discussed based on the fanning effect. copyright 1997 Optical Society of America

Thermally assisted interlayer magnetic coupling through Ba_0_._0_5Sr_0_._9_5TiO_3 barriers

International Nuclear Information System (INIS)

Carreira, Santiago J.; Steren, Laura B.; Avilés Félix, Luis; Alejandro, Gabriela; Sirena, Martín

2016-01-01

We report on the interlayer exchange coupling across insulating barriers observed on Ni_8_0Fe_2_0/Ba_0_._0_5Sr_0_._9_5TiO_3/La_0_._6_6Sr_0_._3_3MnO_3 (Py/BST_0_._0_5/LSMO) trilayers. The coupling mechanism has been analyzed in terms of the barrier thickness, samples' substrate, and temperature. We examined the effect of MgO (MGO) and SrTiO_3 (STO) (001) single-crystalline substrates on the magnetic coupling and also on the magnetic anisotropies of the samples in order to get a deeper understanding of the magnetism of the structures. We measured a weak coupling mediated by spin-dependent tunneling phenomena whose sign and strength depend on barrier thickness and substrate. An antiferromagnetic (AF) exchange prevails for most of the samples and smoothly increases with the barrier thicknesses as a consequence of the screening effects of the BST_0_._0_5. The coupling monotonically increases with temperature in all the samples and this behavior is attributed to thermally assisted mechanisms. The magnetic anisotropy of both magnetic components has a cubic symmetry that in the case of permalloy is added to a small uniaxial component.

The Magnetoelectric Effect of a Ni0.3Zn0.62Cu0.08Fe2O4 - PbFe0.5Nb0.5O3 Multilayer Composite

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Guzdek P.

2014-10-01

Full Text Available The magnetoelectric effect in multiferroic materials has been widely studied for its fundamental interest and practical applications. The magnetoelectric effect observed for single phase materials like Cr2O3, BiFeO3, and Pb(Fe0.5Nb0.5O3 is usually small. A much larger effect can be obtained in composites consisting of magnetostrictive and piezoelectric phases. This paper investigates the magnetoelectric effect of a multilayer (laminated structure consisting of 6 nickel ferrite and 7 PFN relaxor layers. It describes the synthesis and tape casting process for Ni0.3Zn0.62Cu0.08Fe2O4 ferrite and relaxor PbFe0.5Nb0.5O3 (PFN. Magnetic hysteresis, ZFC - FC curves and dependencies of magnetization versus temperature for PFN relaxor and magnetoelectric composite were measured with a vibrating sample magnetometer (VSM in an applied magnetic field up to 85 kOe at a temperature range of 10 – 400 K. Magnetoelectric effect at room temperature was investigated as a function of a static magnetic field (0.3 - 6.5 kOe and the frequency of sinusoidal magnetic field (0.01 - 6.5 kHz. At lower magnetic field, the magnetoelectric coefficient increases slightly before reaching a maximum and then decreases. The magnetoelectric coefficient aME increases continuously as the frequency is raised, although this increase is less pronounced in the 1-6.5 kHz range. Maximum values of the magnetoelectric coefficient attained for the layered composites exceed about 50 mV/(Oe cm.

Enthalpies of formation of 5,6-dihydro-5-methyluracil and 5,6-dihydro-6-methyluracil

International Nuclear Information System (INIS)

Amaral, Luísa M.P.F.; Szterner, Piotr; Ribeiro da Silva, Manuel A.V.

2013-01-01

Highlights: • Δ c H m ° of two methyl-5,6-dihydrouracils have been determined by combustion calorimetry. • Vapor pressures were measured by the Knudsen effusion technique. • Gas phase enthalpies of formation of methyl-5,6-dihydrouracils, have been derived. -- Abstract: The standard (p° = 0.1 MPa) molar enthalpy of combustion, Δ c H m ° , of two crystalline compounds, 5,6-dihydro-5-methyluracil and 5,6-dihydro-6-methyluracil, were determined, at T = 298.15 K, using a static bomb combustion calorimeter. The vapor pressures as a function of the temperature were measured for those compounds, by the Knudsen effusion technique, and the standard molar enthalpies of sublimation at the mean temperature of the vapor pressure measurements were derived from the Clausius–Clapeyron equation, and corrected to T = 298.15 K using an estimated value for Δ cr g C p,m ° . These values were used to derive the standard molar enthalpies of formation of the two compounds studied, in the condensed and gaseous phases. Some considerations about the relative stability of the two isomers were made and compared with similar compounds

12 CFR 505.5 - Delivery of process.

Science.gov (United States)

2010-01-01

... 12 Banks and Banking 5 2010-01-01 2010-01-01 false Delivery of process. 505.5 Section 505.5 Banks and Banking OFFICE OF THRIFT SUPERVISION, DEPARTMENT OF THE TREASURY FREEDOM OF INFORMATION ACT § 505.5 Delivery of process. Service of process will be received as set forth in § 510.4 of this chapter...

Diaqua{6,6′-dimethoxy-2,2′-[ethane-1,2-diylbis(nitrilomethylidyne]diphenolato-κ2O,N,N′,O′}manganese(III perchlorate 18-crown-6 hemisolvate monohydrate

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Ming-Ming Yu

2009-02-01

Full Text Available In the cation of the title compound, [Mn(C18H18N2O4(H2O2]ClO4·0.5C12H24O6·H2O, the MnIII ion is coordinated by two water O atoms, and two O atoms and two N atoms from the tetradentate 6,6′-dimethoxy-2,2′-[ethane-1,2-diylbis(nitrilomethylidyne]diphenolate ligand, completing a distorted octahedral geometry. One O atom of the 18-crown-6-ether is disordered over two positions with occupancies of 0.70 (2 and 0.30 (2.

New representatives of the Raddlesden-Popper homologous series: anion-deficient oxides Sr3Co2-xZnxO6+δ (x=0.5, 0.7)

International Nuclear Information System (INIS)

Chupakhina, T.I.; Zajtseva, N.A.; Melkozerova, M.A.; Bazuev, G.V.

2006-01-01

New complex oxides Sr 3 Co 2-x Zn x O 6+δ (x=0.5, 0.7) of the Raddlesden-Popper homologous series are synthesized; structural characteristics and magnetic properties are investigated. Lattice parameters are determined. It is established that Sr 3 Co 1.5 Zn 0.5 O 6.25 magnetic susceptibility dependence on temperature follows Curie-Weiss law only within 250-300 K temperature range. In low temperature range the compound has spin glass properties with characteristic phenomena of magnetic and temperature hysteresis [ru

Synthetic Cu 0.507(5)Pb 8.73(9)Sb 8.15(8)I 1.6S 20.0(2) nanowires

Science.gov (United States)

Kryukova, Galina N.; Heuer, Matthias; Wagner, Gerald; Doering, Thomas; Bente, Klaus

2005-01-01

Nanowires of an iodine containing Pb-Sb-sulfosalt have been synthesized by chemical vapor transport. Their structure was studied using high-resolution transmission electron microscopy and X-ray powder diffraction. The lattice parameters show values equal to a=4.9801(4) nm, b=0.41132(8) nm (with two-fold superstructure), c=2.1989(1) nm and β=99.918(6)°. These parameters and the results of a multislice simulation are in good agreement with the mineral pillaite, Cu 0.10Pb 9.16Sb 9.84S 22.94Cl 1.06O 0.5 (space group C2/m, a=4.949(1) nm, b=0.41259(8) nm, c=2.1828(4) nm, and β=99.62(3)°). Microprobe and EDX analyses yielded a chemical composition of Cu 0.507(5)Pb 8.73(9)Sb 8.15(8)I 1.6S 20.0(2) which is close to natural pillaite but contains no oxygen and iodine instead of chlorine. The structure of the investigated material is based on chains of M-S polyhedra ( M=Pb or Sb) typical for the architecture of sulfosalts implying iodine atoms in trigonal prismatic coordination with Pb atoms from the M-S polyhedra of neighboring chains. The [010] superstructure of the specimen was found to be unstable under electron beam irradiation with a rapid decrease of the b lattice parameter from 0.8 to 0.4 nm within 5 min.

Synthetic Cu0.507(5)Pb8.73(9)Sb8.15(8)I1.6S20.0(2) nanowires

International Nuclear Information System (INIS)

Kryukova, Galina N.; Heuer, Matthias; Wagner, Gerald; Doering, Thomas; Bente, Klaus

2005-01-01

Nanowires of an iodine containing Pb-Sb-sulfosalt have been synthesized by chemical vapor transport. Their structure was studied using high-resolution transmission electron microscopy and X-ray powder diffraction. The lattice parameters show values equal to a=4.9801(4)nm, b=0.41132(8)nm (with two-fold superstructure), c=2.1989(1)nm and β=99.918(6) o . These parameters and the results of a multislice simulation are in good agreement with the mineral pillaite, Cu 0.10 Pb 9.16 Sb 9.84 S 22.94 Cl 1.06 O 0.5 (space group C2/m, a=4.949(1)nm, b=0.41259(8)nm, c=2.1828(4)nm, and β=99.62(3) o ). Microprobe and EDX analyses yielded a chemical composition of Cu 0.507(5) Pb 8.73(9) Sb 8.15(8) I 1.6 S 20.0(2) which is close to natural pillaite but contains no oxygen and iodine instead of chlorine. The structure of the investigated material is based on chains of M-S polyhedra (M=Pb or Sb) typical for the architecture of sulfosalts implying iodine atoms in trigonal prismatic coordination with Pb atoms from the M-S polyhedra of neighboring chains. The [010] superstructure of the specimen was found to be unstable under electron beam irradiation with a rapid decrease of the b lattice parameter from 0.8 to 0.4nm within 5min

Crystallographic alignment evolution and magnetic properties of anisotropic Sm{sub 0.6}Pr{sub 0.4}Co{sub 5} nanoflakes prepared by surfactant-assisted ball milling

Energy Technology Data Exchange (ETDEWEB)

Xu, M.L.; Wu, Q.; Li, Y.Q.; Liu, W.Q.; Lu, Q.M.; Yue, M., E-mail: yueming@bjut.edu.cn

2015-08-01

The microstructure, crystal structure and magnetic properties were studied for Sm{sub 0.6}Pr{sub 0.4}Co{sub 5} nanoflakes prepared by surfactant-assisted high-energy ball milling (SAHEBM). Effect of ball-milling time on the c-axis crystallographic alignment, morphology and magnetic properties of Sm{sub 0.6}Pr{sub 0.4}Co{sub 5} nanoflakes was systematically investigated. With increasing milling time from 1 h to 7 h, the intensity ratio between (002) and (111) reflection peaks indicating degree of c-axis crystal texture of the (Sm, Pr)Co{sub 5} phase increases first, peaks at 3 h, then drops again, revealing that the strongest c-axis crystal texture was obtained in the nanoflakes milled for 3 h. On the other hand, the coercivity (H{sub ci}) of the flakes increases gradually from 1.71 to 14.65 kOe with the increase of ball milling time. As a result, an optimal magnetic properties of M{sub r} of 10.23 kGs, H{sub ci} of 11.45 kOe and (BH){sub max} of 24.40 MGOe was obtained in Sm{sub 0.6}Pr{sub 0.4}Co{sub 5} nanoflakes milled for 3 h, which also displayed a high aspect ratio, small in-plane size, pronounced (001) out-of-plane texture. - Highlights: • Anisotropic Sm{sub 0.6}Pr{sub 0.4}Co{sub 5} nanoflakes with strong c-axis texture were prepared. • Effects of ball-milling time on structure and magnetic properties were studied. • (BH){sub max} value of Sm{sub 0.6}Pr{sub 0.4}Co{sub 5} nanoflakes is larger than that of SmCo{sub 5} nanoflakes.

Efficacy and safety of 0.5% levobupivacaine versus 0.5% bupivacaine for peribulbar anesthesia

Directory of Open Access Journals (Sweden)

Pacella E

2013-05-01

Full Text Available Elena Pacella,1 Fernanda Pacella,1 Fabiana Troisi,2 Domenico Dell'Edera,3 Paolo Tuchetti,4 Tommaso Lenzi,1 Saul Collini21Department of Sense Organs, Faculty of Medicine and Dentistry, Rome, 2Department of Medical Surgical Sciences and Translational Medicine Sapienza, Faculty of Medicine and Psychology, Roma, University of Rome, Rome, 3Unit of Cytogenetic and Molecular Genetics, Madonna delle Grazie Hospital, Matera, 4National Institute for Health, Migration and Poverty, Rome, ItalyBackground: This randomized double-blind study examined the use of a new anesthetic agent, levobupivacaine 0.5%, which is the S(−-enantiomer of a racemic mixture of bupivacaine, for peribulbar anesthesia and compared it with racemic bupivacaine 0.5% alone or in combination with hyaluronidase 10 IU/mL.Methods: A total of 160 patients undergoing ophthalmic surgery were randomized into four groups (n = 40 each to receive inferotemporal peribulbar injection of levobupivacaine 0.5% (group L, racemic bupivacaine 0.5% (group B, levobupivacaine + hyaluronidase 10 IU/mL (group LH, or racemic bupivacaine + hyaluronidase 10 IU/mL (group BH by two anesthetists and two ophthalmologists in a ratio of 25% each. Ocular akinesia and orbicularis oculi function were evaluated using a three-point scale; a value < 5 points was considered as requiring surgery, and movements were re-evaluated the day following surgery to confirm regression of the block.Results: The time to onset (12 ± 2.6 minutes versus 13 ± 2.8 minutes and duration of anesthesia (185 ± 33.2 minutes versus 188 ± 35.7 minutes were similar between groups L and B. Complete akinesia (score 0 was obtained more frequently when hyaluronidase was used in addition to the anesthetic, with occurrences of 72.5% versus 57.5% in group LH versus L, respectively, and 67.5% versus 45% in group BH versus B. Moderate hypotension (<30% of baseline was observed in four patients (10% in group L, two (5.0% in group B, one (2.5% in group LH

Optical conductivity of Ni1 − xPtx alloys (00.25 from 0.76 to 6.6 eV

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Lina S. Abdallah

2014-01-01

Full Text Available Using spectroscopic ellipsometry and Drude-Lorentz oscillator fitting, we determined the dielectric function and optical conductivity versus photon energy from 0.76 to 6.6 eV of 10 nm thick Ni1 − xPtx alloy (00.25 films deposited on thick thermal oxides. We find absorption peaks near 1.6 and 5.0 eV due to interband optical transitions. There is a significant broadening of the UV peak with increasing Pt content, since the bandwidth of the 3d electrons in Ni is smaller than that of the 5d bands in Pt. Our experimental observation is consistent with ab initio calculations of the density of states for Ni, Pt, and the Ni3Pt compound. Annealing the metals at 500°C for 30 s increases the optical conductivity.

13b,13c-Di-2-pyridyl-5,7,12,13b,13c,14-hexahydro-6H,13H-5a,6a,12a,13a-tetraazabenz[5,6]azuleno[2,1,8-ija]benz[f]azulene-6,13-dione methanol hemisolvate

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Lin Li

2008-01-01

Full Text Available The title compound, C30H24N6O2·0.5CH3OH, a glycoluril derivative with two pyridine substituents on the convex face of the glycoluril system, is an important intermediate for the synthesis of more complex glycoluril derivatives. The compound crystallizes with two independent molecules in the asymmetric unit, one of which exhibits disorder of one benzene ring over two orientations with refined site occupancy factors 0.65 (4:0.35 (4. The crystal structure contains several short C—H...O contacts, and the methanol molecule forms an O—H...O hydrogen bond to one of the glycoluril molecules.

The Impact of Polymorphic Variations in the 5p15, 6p12, 6p21 and 15q25 Loci on the Risk and Prognosis of Portuguese Patients with Non-Small Cell Lung Cancer

Science.gov (United States)

de Mello, Ramon Andrade; Ferreira, Mónica; Soares-Pires, Filipa; Costa, Sandra; Cunha, João; Oliveira, Pedro; Hespanhol, Venceslau; Reis, Rui Manuel

2013-01-01

Introduction Polymorphic variants in the 5p15, 6p12, 6p21, and 15q25 loci were demonstrated to potentially contribute to lung cancer carcinogenesis. Therefore, this study was performed to assess the role of those variants in non-small cell lung cancer (NSCLC) risk and prognosis in a Portuguese population. Materials and Methods Blood from patients with NSCLC was prospectively collected. To perform an association study, DNA from these patients and healthy controls were genotyped for a panel of 19 SNPs using a Sequenom® MassARRAY platform. Kaplan-Meier curves were used to assess the overall survival (OS) and progression-free survival (PFS). Results One hundred and forty-four patients with NSCLC were successfully consecutively genotyped for the 19 SNPs. One SNP was associated with NSCLC risk: rs9295740 G/A. Two SNPs were associated with non-squamous histology: rs3024994 (VEGF intron 2) T/C and rs401681 C/T. Three SNPs were associated with response rate: rs3025035 (VEGF intron 7) C/T, rs833061 (VEGF –460) C/T and rs9295740 G/A. One SNP demonstrated an influence on PFS: rs401681 C/T at 5p15, p = 0.021. Four SNPs demonstrated an influence on OS: rs2010963 (VEGF +405 G/C), p = 0.042; rs3025010 (VEGF intron 5 C/T), p = 0.047; rs401681 C/T at 5p15, p = 0.046; and rs31489 C/A at 5p15, p = 0.029. Conclusions Our study suggests that SNPs in the 6p12, 6p21, and 5p15 loci may serve as risk, predictive and prognostic NSCLC biomarkers. In the future, SNPs identified in the genomes of patients may improve NSCLC screening strategies and therapeutic management as well. PMID:24039754

The LiyNi0.2Mn0.2Co0.6O2 electrode materials: A structural and magnetic study

International Nuclear Information System (INIS)

Labrini, Mohamed; Saadoune, Ismael; Almaggoussi, Abdelmajid; Elhaskouri, Jamal; Amoros, Pedro

2012-01-01

Graphical abstract: EPR signal of the Li 0.6 Co 0.6 Ni 0.2 Mn 0.2 O 2 composition showing that Mn 4+ ions are the solely paramagnetic ions in the structure. Highlights: ► LiCo 0.6 Ni 0.2 Mn 0.2 O 2 was prepared by the combustion method with sucrose as a fuel. ► Chemical delithiaition was performed by using NO 2 BF 4 oxidizing agent. ► The rhombohedral symmetry was preserved upon lithium removal. ► Lithium extraction leads to Ni 2+ oxidation to Ni 4+ followed by Co 3+ oxidation. ► The EPR narrow signal of Li 0.6 Co 0.6 Ni 0.2 Mn 0.2 O 2 is due to the only active Mn 4+ ions. -- Abstract: Layered LiNi 0.2 Mn 0.2 Co 0.6 O 2 phase, belonging to a solid solution between LiNi 1/2 Mn 1/2 O 2 and LiCoO 2 most commercialized cathodes, was prepared via the combustion method at 900 °C for a short time (1 h). Structural and magnetic properties of this material during chemical extraction were investigated. The powders adopted the α-NaFeO 2 structure with almost none of the well-known Li/Ni cation disorder. The analysis of the magnetic properties in the paramagnetic domain agrees with the combination of Ni 2+ (S = 1), Co 3+ (S = 0) and Mn 4+ (S = 3/2) spin-only values. X-ray analysis of the chemically delithiated Li y Ni 0.2 Mn 0.2 Co 0.6 O 2 reveals no structural transition. The process of lithium extraction from and insertion into LiNi 0.2 Mn 0.2 Co 0.6 O 2 was discussed on the basis of ex situ EPR experiments and magnetic susceptibility. Oxidation of Ni 2+ (S = 1) to Ni 3+ (S = 1/2) and to Ni 4+ (S = 0) was observed upon lithium removal.

CLIPS 6.0 - C LANGUAGE INTEGRATED PRODUCTION SYSTEM, VERSION 6.0 (DEC VAX VMS VERSION)

Science.gov (United States)

Donnell, B.

1994-01-01

command line version. For the UNIX version of CLIPS 6.0, the command line interface has been successfully implemented on a Sun4 running SunOS, a DECstation running DEC RISC ULTRIX, an SGI Indigo Elan running IRIX, a DEC Alpha AXP running OSF/1, and an IBM RS/6000 running AIX. Command line interface executables are included for Sun4 computers running SunOS 4.1.1 or later and for the DEC RISC ULTRIX platform. The makefiles may have to be modified slightly to be used on other UNIX platforms. The UNIX, Macintosh, and IBM PC versions of CLIPS 6.0 each have a platform specific interface. Source code, a makefile, and an executable for the Windows 3.1 interface version of CLIPS 6.0 are provided only on the IBM PC distribution diskettes. Source code, a makefile, and an executable for the Macintosh interface version of CLIPS 6.0 are provided only on the Macintosh distribution diskettes. Likewise, for the UNIX version of CLIPS 6.0, only source code and a makefile for an X-Windows interface are provided. The X-Windows interface requires MIT's X Window System, Version 11, Release 4 (X11R4), the Athena Widget Set, and the Xmu library. The source code for the Athena Widget Set is provided on the distribution medium. The X-Windows interface has been successfully implemented on a Sun4 running SunOS 4.1.2 with the MIT distribution of X11R4 (not OpenWindows), an SGI Indigo Elan running IRIX 4.0.5, and a DEC Alpha AXP running OSF/1 1.2. The VAX version of CLIPS 6.0 comes only with the generic command line interface. ASCII makefiles for the command line version of CLIPS are provided on all the distribution media for UNIX, VMS, and DOS. Four executables are provided with the IBM PC version: a windowed interface executable for Windows 3.1 built using Borland C++ v3.1, an editor for use with the windowed interface, a command line version of CLIPS for Windows 3.1, and a 386 command line executable for DOS built using Zortech C++ v3.1. All four executables are capable of utilizing extended memory

Metabolism of 5,6-epoxyeicosatrienoic acid by the human platelet. Formation of novel thromboxane analogs.

Science.gov (United States)

Balazy, M

1991-12-15

Radiolabeled cis-(+-)-5,6-epoxyeicosatrienoic acid (5(6)-EpETrE) was incubated with a suspension of isolated human platelets in order to study its metabolic fate. The epoxide slowly disappeared from the suspension and was completely metabolized within 30 min. After extraction and analysis by reverse-phase high performance liquid chromatography, seven metabolites were found. Addition of either indomethacin (0.01 mM, cyclooxygenase inhibitor) or BW755C (0.1 mM, cyclooxygenase/lipoxygenase inhibitor) to the incubations blocked the formation of four and six metabolites, respectively, 1,2-Epoxy-3,3,3-trichloropropane (inhibitor of microsomal epoxide hydrolase) failed to inhibit the formation of 5,6-dihydroxyeicosatrienoic acid (5,6-DiHETrE), a hydrolysis product of the precursor 5(6)-EpETrE. The metabolites were characterized by UV spectroscopy, negative ion chemical ionization liquid chromatography/mass spectrometry, gas chromatography/mass spectrometry and, in one instance, coelution with synthetic standard. Three primary platelet metabolites were structurally determined to be 5,6-epoxy-12-hydroxyeicosatrienoic acid, 5,6-epoxy-12-hydroxyheptadecadienoic acid, and a unique bicyclic metabolite, 5-hydroxy-6,9-epoxy-thromboxane B1, which originated from intramolecular hydrolysis of 5,6-epoxythromboxane-B1. This thromboxane analog was partially separated into stereoisomers and coeluted with the racemic synthetic standard in gas chromatography/mass spectrometry and liquid chromatography/mass spectrometry. Three other metabolites were characterized as 5,6,12-trihydroxyeicosatrienoic acid, 5,6,12-trihydroxyheptadecadienoic acid, and 5,6-dihydroxythromboxane-B1, and resulted from the hydrolysis of the corresponding epoxides rather than from the metabolism of 5,6-DiHETrE. The latter was not metabolized by platelet cyclooxygenase or lipoxygenase. The biosynthesis of two cyclooxygenase metabolites indicated the formation of unstable 5,6-epoxythromboxane-A1 as an intermediate

The structure of carbon nanotubes formed of graphene layers L4-8, L5-7, L3-12, L4-6-12

Science.gov (United States)

Shapovalova, K. E.; Belenkov, E. A.

2017-11-01

We geometrically calculate the optimized structure of nanotubes based on the graphene layers, using the method of molecular mechanics MM+. It was found that only the nanotubes, based on the graphene layers L4-8, L5-7, L3-12, L4-6-12, have a cylindrical form. Calculations of the sublimation energy, carried out using the semi-empirical quantum-mechanic method PM3, show that energy increases with the increase of nanotube diameters.

Performance of ultra-small silicon photomultiplier array with active area of 0.12 mm×0.12 mm

Energy Technology Data Exchange (ETDEWEB)

Yue, Wang; Zongde, Chen; Chenhui, Li; Ran, He; Shenyuan, Wang; Baicheng, Li; Ruiheng, Wang; Kun, Liang, E-mail: lk@bnu.edu.cn; Ru, Yang; Dejun, Han

2015-07-01

We report the performance of an ultra-small silicon photomultiplier (SiPM) line array with 7 elements of 0.12×0.12 mm{sup 2} in active area, 0.2 mm in pitch and 120 micro cells in one element. The device features an epitaxial bulk quenching resistor concept, demonstrated high geometrical fill factor of 41% and photon detection efficiency (PDE) of 25.4% in the wavelength region between 430 nm and 480 nm while retaining high micro cell density around 10 000 mm{sup −2} and ~3 ns FWHM of dark pulses width; it also demonstrated dark count rate of less than 28.7 kHz, optical crosstalk of the order of 2% to 4%, and excellent photon number discrimination. A 0.15 mm×1.6 mm×1.6 mm lutetium yttrium oxyorthosilicate (LYSO) crystal, corresponding to the width, length and height respectively, was successfully coupled to the 1×7 SiPM array for possible ultra-highly resolved positron emission tomography (PET) applications. This novel type of device has advantages particularly for small active area since the performances, such as PDE and response speed is one of the best among SiPMs with similarly high density of micro cells. It may pave a way for this type of SiPM as a promising pixel position sensitive device in imaging sensor applications. - Highlights: • The ultra-small SiPM line array with active area of 0.12 mm×0.12 mm was presented. • The ultra-small SiPM employs the bulk silicon structure as quenching resistor. • A considerable dynamic range and PDE over 25.4% @ 430 nm to 480 nm were characterized.

Dielectric properties of (K0.5Na0.5)NbO3-(Bi0.5Li0.5)ZrO3 lead-free ceramics as high-temperature ceramic capacitors

Science.gov (United States)

Yan, Tianxiang; Han, Feifei; Ren, Shaokai; Ma, Xing; Fang, Liang; Liu, Laijun; Kuang, Xiaojun; Elouadi, Brahim

2018-04-01

(1 - x)K0.5Na0.5NbO3- x(Bi0.5Li0.5)ZrO3 (labeled as (1 - x)KNN- xBLZ) lead-free ceramics were fabricated by a solid-state reaction method. A research was conducted on the effects of BLZ content on structure, dielectric properties and relaxation behavior of KNN ceramics. By combining the X-ray diffraction patterns with the temperature dependence of dielectric properties, an orthorhombic-tetragonal phase coexistence was identified for x = 0.03, a tetragonal phase was determined for x = 0.05, and a single rhombohedral structure occurred at x = 0.08. The 0.92KNN-0.08BLZ ceramic exhibits a high and stable permittivity ( 1317, ± 15% variation) from 55 to 445 °C and low dielectric loss (≤ 6%) from 120 to 400 °C, which is hugely attractive for high-temperature capacitors. Activation energies of both high-temperature dielectric relaxation and dc conductivity first increase and then decline with the increase of BLZ, which might be attributed to the lattice distortion and concentration of oxygen vacancies.

Analysis of the U.S. Navy Food Service Recruiting Program. Part 1. Attitudes and Reenlistment Plans of Food Service Enlistees

Science.gov (United States)

1984-05-01

the Navy? (PLEASE CHECK ALL THAT APPLY TO WHERE YOU WORKED) FAST FOOD FRANCHISE CAFETERIA • BAKERY DELICATESSEN _ARANT NONE COFFEE SHOP 26. Was any...service equipment (item 20), working conditions in the galley and bakery (item 17), the quality of an MS’s co-workers (item 12), the chances for MS’s to... bakery 4.5 14.3 6.0 79.7 18. Food service work is routine and boring 3.7 5.6 16.3 78.1 19. You’d have lots of adventure 5.0 66.9 1.3 31.8 20. Food

A new, high energy rechargeable lithium ion battery with a surface-treated Li{sub 1.2}Mn{sub 0.54}Ni{sub 0.13}Co{sub 0.13}O{sub 2} cathode and a nano-structured Li{sub 4}Ti{sub 5}O{sub 12} anode

Energy Technology Data Exchange (ETDEWEB)

Liu, Xiaoyu; Huang, Tao; Yu, Aishui, E-mail: asyu@fudan.edu.cn

2015-11-05

Through elaborate design, a new rechargeable lithium ion battery has been developed by comprising a surface-treated Li{sub 1.2}Mn{sub 0.54}Ni{sub 0.13}Co{sub 0.13}O{sub 2} cathode and a nano-structured Li{sub 4}Ti{sub 5}O{sub 12} anode. After precondition Na{sub 2}S{sub 2}O{sub 8} treatment, the initial coulombic efficiency of Li{sub 1.2}Mn{sub 0.54}Ni{sub 0.13}Co{sub 0.13}O{sub 2} cathode has been significantly increased and can be compatible with that of the nano-structured Li{sub 4}Ti{sub 5}O{sub 12} anode. The optimization of structure and morphology for both active electrode materials result in their remarkable electrochemical performances in respective lithium half-cells. Ultimately, the rechargeable lithium ion full battery consisting of both electrodes delivers a specific capacity of 99.0 mAh g{sup −1} and a practical energy density of 201 Wh kg{sup −1}, based on the total weight of both active electrode materials. Furthermore, as a promising candidate in the lithium ion battery field, this full battery also achieves highly attractive electrochemical performance with high coulombic efficiency, excellent cycling stability and outstanding rate capability. Thus the proposed battery displays broad practical application prospects for next generation of high-energy lithium ion battery. - Highlights: • The Li{sub 1.2}Mn{sub 0.54}Ni{sub 0.13}Co{sub 0.13}O{sub 2} cathode is surface-treated by Na{sub 2}S{sub 2}O{sub 8}. • The nano-sized Li{sub 4}Ti{sub 5}O{sub 12} anode is obtained by a solid-state method. • A new Li{sub 1.2}Mn{sub 0.54}Ni{sub 0.13}Co{sub 0.13}O{sub 2}/Li{sub 4}Ti{sub 5}O{sub 12} lithium ion battery is developed. • The battery shows high coulombic efficiency, specific capacity and energy density. • The battery shows high capacity retention rate and good high-rate capability.

Validation and comparison of EuroQoL-5 dimension (EQ-5D) and Short Form-6 dimension (SF-6D) among stable angina patients.

Science.gov (United States)

Wu, Jing; Han, Yuerong; Zhao, Fei-Li; Zhou, Jin; Chen, Zhijun; Sun, He

2014-10-25

Several preference-based health-related quality of life (HRQoL) instruments have been published and widely used in different populations. However no consensus has emerged regarding the most appropriate instrument in therapeutic area of stable angina. This study compared and validated the psychometric properties of two generic preference-based instruments, the EQ-5D and SF-6D, among Chinese stable angina patients. Convergent validity of the EQ-5D and SF-6D was examined with eight a priori hypotheses from stable angina patients in conjunction with Seattle Angina Questionnaire (SAQ). Responsiveness was compared using the effect size (ES), relative efficiency (RE) and receiver operating characteristic (ROC) curves. Agreement between the EQ-5D and SF-6D was tested using intra-class correlation coefficient (ICC) and Bland-Altman plot. Factors affecting utility difference were explored with multiple linear regression analysis. In 411 patients (mean age 68.08 ± 11.35), mean utility scores (SD) were 0.78 (0.15) for the EQ-5D and 0.68 (0.12) for the SF-6D. Validity was demonstrated by the moderate to strong correlation coefficients (Range: 0.368-0.594, Pstable-angina-specific health status than the EQ-5D (ES: 0.426 to 1.126). RE suggested that the SF-6D (RE: 44.8 to 177.8%) was more efficient than the EQ-5D except for physical function. Poor agreement between them was observed with ICC (0.448, Pstable angina patients. The SF-6D may be a more effective tool with lower ceiling effect and greater sensitivity. Further study is needed to compare other properties, such as reliability and longitudinal response.

Synthesis, properties, crystal structures, and semiconductor characteristics of naphtho[1,2-b:5,6-b']dithiophene and -diselenophene derivatives.

Science.gov (United States)

Shinamura, Shoji; Miyazaki, Eigo; Takimiya, Kazuo

2010-02-19

In this paper we present the synthesis, structures, characterization, and applications to field-effect transistors (FETs) of naphtho[1,2-b:5,6-b']dithiophene (NDT) and -diselenophene (NDS) derivatives. Treatment of 1,5-dichloro-2,6-diethynylnaphthalenes, easily derived from commercially available 2,6-dihydroxynaphthalene, with sodium chalcogenide afforded a straightforward access to NDTs and NDSs including the parent and dioctyl and diphenyl derivatives. Physicochemical evaluations of NDT and NDS derivatives showed that these heteroarenes have a similar electronic structure with isomeric [1]benzothieno[2,3-b][1]benzothiophene (BTBT) and [1]benzoselenopheneno[2,3-b][1]benzoselenophene (BSBS) derivatives, respectively. Although attempts to fabricate solution-processed field-effect transistors (FETs) with soluble dioctyl-NDT (C(8)-NDT) and -NDS (C(8)-NDS) failed, diphenyl derivatives (DPh-NDT and DPh-NDS) afforded vapor-processed FETs showing field-effect mobility as high as 0.7 cm(2) V(-1) s(-1). These results indicated that NDT and NDS are new potential heteroarene core structures for organic semiconducting materials.

Freeze drying synthesis of LiNi0.5Mn0.5O2 cathode materials

International Nuclear Information System (INIS)

Shlyakhtin, O.A.; Yoon, Young Soo; Choi, Sun Hee; Oh, Young-Jei

2004-01-01

The influence of several processing conditions on the phase formation and electrochemical performance of LiNi 0.5 Mn 0.5 O 2 powders, obtained by freeze drying method, is studied. Thermal processing in pellets at maximum heating rate promotes better crystallographic ordering of hexagonal LiNi 0.5 Mn 0.5 O 2 and maximum capacity values irrespectively of chemical composition of the precursor. Instead, intense mechanical processing of precursors exerts considerable negative effect on the electrochemical performance. Cathode materials containing superstoichiometric amount of lithium (Li 1.3 Mn 0.5 Ni 0.5 O 2+δ ) demonstrate reversible capacity values up to 190 mAh/g between 2.5 and 4.6 V

[Suicide attempts of 48 children aged 6-12 years].

Science.gov (United States)

Berthod, C; Giraud, C; Gansel, Y; Fourneret, P; Desombre, H

2013-12-01

Research is limited on suicide attempts in children under 13 years of age. The objective of this study was to provide an in-depth description of this population. The present study is both retrospective and descriptive. Data were collected retrospectively from a file containing the causes for hospitalization of each child admitted into the Department of Child Psychiatry at the hôpital Femme-Mère-Enfant (hospices civils de Lyon). We included all patients under 13 years of age who were hospitalized for a suicide attempt between 2008 and 2011. The methods used to collect the medical records consisted in using a form made up of four major parts: suicide attempts, social environment, medical history, and therapy. The 26 girls and 22 boys included had a mean age of 11.52 years. The boys were younger than the girls (P=0.047) and their parents were usually separated (P=0.034). The boys used more violent means to commit suicide in comparison to the girls (P=0.048). On average, children using violent means were younger (P=0.013). Boys underwent more psychotherapy (P=0.027) and were prescribed more psychotropic medication in comparison to girls (P=0.051). Adjustment disorders (37.5%) and depression (27%) were the two main diagnoses for hospitalization. They were hospitalized on average (±standard deviation) 9.6 days (±10 days). Psychotherapy was organized when leaving the hospital (98%) with legal measures (8.3%), change of residence (12.5%), and prescription of psychotropic drugs (37.5%). None had physical complications. In children under 13 years of age, attempted suicide was more frequent in girls than boys. However, the sample included 18 girls and nine boys who were 12 years old (sex ratio of 12-year-olds, 0.5). There were more boys (16 boys/eight girls) in the children under 12 (sex ratio of 8- to 11-year-olds, 1.6). Children under 11 used more violent means (P=0.01). The literature also reports that more violent means lead to a greater risk of death by suicide

A screen-printed Ce 0.8Sm 0.2O 1.9 film solid oxide fuel cell with a Ba 0.5Sr 0.5Co 0.8Fe 0.2O 3- δ cathode

Science.gov (United States)

Zhang, Yaohui; Huang, Xiqiang; Lu, Zhe; Liu, Zhiguo; Ge, Xiaodong; Xu, Jiahuan; Xin, Xianshuang; Sha, Xueqing; Su, Wenhui

Screen-printing technology was developed to fabricate Ce 0.8Sm 0.2O 1.9 (SDC) electrolyte films onto porous NiO-SDC green anode substrates. After sintering at 1400 °C for 4 h, a gas-tight SDC film with a thickness of 12 μm was obtained. A novel cathode material of Ba 0.5Sr 0.5Co 0.8Fe 0.2O 3- δ was subsequently applied onto the sintered SDC electrolyte film also by screen-printing and sintered at 970 °C for 3 h to get a single cell. A fuel cell of Ni-SDC/SDC (12 μm)/Ba 0.5Sr 0.5Co 0.8Fe 0.2O 3- δ provides the maximum power densities of 1280, 1080, 670, 370, 180 and 73 mW cm -2 at 650, 600, 555, 505, 455 and 405 °C, respectively, using hydrogen as fuel and stationary air as oxidant. When dry methane was used as fuel, the maximum power densities are 876, 568, 346 and 114 mW cm -2 at 650, 600, 555 and 505 °C, respectively. The present fuel cell shows excellent performance at lowered temperatures.

Crystallization of Sr0.5Ba0.5Nb2O6 Thin Films on LaNiO3 Electrodes by RF Magnetron Reactive Sputtering

Science.gov (United States)

Jong, Chao-An; Gan, Jon-Yiew

2000-02-01

Strontium barium niobium (Sr0.5Ba0.5Nb2O6) (SBN) thin films are prepared on conductive-oxide LNO (LaNiO3) electrodes by the rf magnetron sputtering system. Instead of conventional furnace annealing, SBN thin films are crystallized by rapid thermal annealing (RTA) above 700°C for 5 min. The textured SBN films are crystallized with two orientations: one is the (001) or (310) direction, and the other is the (002) or (620) direction. Films compositions measured by the electron spectroscopy of chemical analysis (ESCA) quantitative analysis method show nearly the same stoichiometric ratio as the target. The depth profiles of SBN films and the target are examined by secondary ion mass spectrometer (SIMS). The concentrations of the films are quite uniform. After being heat treated at 800°C for 5 min by RTA, La and Ni diffuse into the SBN film. The diffusion coefficient of La in SBN films is also calculated.

XRD and DSC study of the formation and the melting of a new zeolite like borosilicate CsBSi5O12 and (Cs,Rb)BSi5O12 solid solutions

International Nuclear Information System (INIS)

Bubnova, R.S.; Ugolkov, V.L.; Krzhizhanovskaya, M.G.; Filatov, S.K.; Paufler, P.

2007-01-01

Polycrystalline CsBSi 5 O 12 was prepared from a stoichiometric mixture by solid-state reaction above 1000 C. The solid solutions Cs 1-x Rb x BSi 5 O 12 were obtained at 1000 C during a long heat treatment of polycrystalline Cs 1-x Rb x BSi 2 O 6 boropollucites (x Rb = 0, 0.05, 0.2, 0.4). A new borosilicate compound and its solid solutions were studied using X-ray powder diffraction (XRD), annealing, differential scanning calorimetry (DSC), and thermogravimetry (TG). For Cs,Rb-boropollucites the new phase formation is accompanied by significant mass losses detected by DSC and TG. The following mechanism of phase transformations is assumed: (Cs,Rb)BSi 2 O 6 → (Cs,Rb)BSi 5 O 12 + (Cs,Rb)BO 2 ↑. The zeolite phase forms as a result of the boropollucite decomposition over 1000 C. Zeolite decomposes also on further heating and the SiO 2 reflections are observed in the XRD pattern only. Thus above 1000 C both boropollucite and zeolite phases are unstable presumably due to the ability of the alkali cations to leave the structure. Using XRD the unit cell parameters of CsBSi 5 O 12 have been determined in the orthorhombic crystal system: a = 16.242(4) A, b = 13.360(4) A, c = 4.874(1) A. The compound is isostructural with the zeolite compound CsAlSi 5 O 12 . In the crystal structure of Cs 1-x Rb x BSi 5 O 12 solid solutions the changes of cell parameters are insignificant under the substitution of Cs by Rb atoms that indicates a very limited substitution range. (orig.)

Improved electrochemical properties of Li{sub 4}Ti{sub 5}O{sub 12}–Li{sub 0.33}La{sub 0.56}TiO{sub 3} composite anodes prepared by a solid-state synthesis

Energy Technology Data Exchange (ETDEWEB)

Zhu, Yan-Rong; Yuan, Jing; Zhu, Min [School of Chemistry and Chemical Engineering, Anhui University of Technology, Maanshan, Anhui 243002 (China); Hao, Guodong [College of Chemistry and Chemical Engineering, Mudanjiang Normal University, Mudanjiang, Heilongjiang 157012 (China); Yi, Ting-Feng, E-mail: tfyihit@163.com [School of Chemistry and Chemical Engineering, Anhui University of Technology, Maanshan, Anhui 243002 (China); Xie, Ying, E-mail: xieying@hlju.edu.cn [Key Laboratory of Functional Inorganic Material Chemistry, Ministry of Education, School of Chemistry and Materials Science, Heilongjiang University, Harbin, Heilongjiang 150080 (China)

2015-10-15

Li{sub 4}Ti{sub 5}O{sub 12}–Li{sub 0.33}La{sub 0.56}TiO{sub 3} composite anodes are successfully prepared by a facile solid state route. The structure, morphology and electrochemical performance of all samples are characterized by X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscope (SEM), cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and charge–discharge tests, respectively. XRD reveals that the little La{sup 3+} ions enter into the lattice, and then make the crystal lattice of Li{sub 4}Ti{sub 5}O{sub 12} expand. SEM shows that all samples are composed of 1–2 μm primary particles with irregular shapes. CV and EIS imply that Li{sub 4}Ti{sub 5}O{sub 12}–Li{sub 0.33}La{sub 0.56}TiO{sub 3} composites have lower polarization, larger lithium-ion diffusion coefficient and smaller charge transfer resistance corresponding to a much higher conductivity than those of Li{sub 4}Ti{sub 5}O{sub 12} corresponding to the extraction of Li{sup +} ions. The improved electrochemical performance of Li{sub 4}Ti{sub 5}O{sub 12}–Li{sub 0.33}La{sub 0.56}TiO{sub 3} composites can be attributed to the enhanced transfer kinetics of both the lithium ions and electrons. Particularly, Li{sub 4}Ti{sub 5}O{sub 12}–Li{sub 0.33}La{sub 0.56}TiO{sub 3} (5 wt.%) composite shows a excellent high-rate capability and cycling stability. Therefore, the present Li{sub 4}Ti{sub 5}O{sub 12}–Li{sub 0.33}La{sub 0.56}TiO{sub 3} (5 wt.%) composite anode is capable of large-scale applications, such as electric vehicles and hybrid electric vehicles, requiring high energy, long life and excellent safety. - Highlights: • The electrochemical property of Li{sub 4}Ti{sub 5}O{sub 12}–Li{sub 0.33}La{sub 0.56}TiO{sub 3} down to 0 V is first reported. • Li{sub 0.33}La{sub 0.56}TiO{sub 3} modifying results in fast lithium insertion/extraction kinetics. • Li{sub 4}Ti{sub 5}O{sub 12}–Li{sub 0.33}La{sub 0.56}TiO{sub 3} (5 wt.%) exhibits a good fast charge

The study of sup 1 sup 0 sup 5 Pd(n,gamma) sup 1 sup 0 sup 6 Pd reaction with thermal neutrons

CERN Document Server

Miah, M M H; Harada, H; Nakamura, S

2002-01-01

This is a report about the study of sup 1 sup 0 sup 5 Pd(n,gamma) sup 1 sup 0 sup 6 Pd reaction with thermal neutrons performed by Dr. M.M.H.Miah, who was engaged in the investigation as a visiting research associate of Japan Nuclear Cycle Development Institute (JNC) under the STA fellowship program for the periods ranging from January 2001 to July 2002, together with members belong to System Design Analysis Group of JNC. The investigation of sup 1 sup 0 sup 5 Pd(n,gamma) sup 1 sup 0 sup 6 Pd reaction has been performed by using the prompt gamma-ray spectroscopic technique to supply basic data for the nuclear transmutation. Samples of natural Pd and enriched sup 1 sup 0 sup 5 Pd were irradiated separately with the B-4 thermal neutron guide facilities at Kyoto University Research Reactor Institute (KURRI). Capture prompt gamma-rays were detected in both singles and coincidence modes by using two high purity Ge detectors. By analyzing gamma-gamma coincidence data, 42 cascading gamma-transitions were identified ...

Residual thermal desorption studies of Ga adatoms on trenched Si(5 5 12) surface

International Nuclear Information System (INIS)

Kumar, Praveen; Kumar, Mahesh; Shivaprasad, S.M.

2013-01-01

We present here the thermal stability studies of the room temperature adsorbed Ga/Si(5 5 12) interfaces in the monolayer coverage regime, using AES and LEED as in-situ UHV characterization probes. Ga grows in Stranski–Krastanov growth mode at RT on the 2 × 1 reconstructed Si(5 5 12) surface where islands form on top of 2 ML of flat pseudomorphic Ga, yielding a (1 × 1) LEED pattern for coverages of 1.2 ML and above. When this RT adsorbed Ga/Si(5 5 12) interface is annealed at different temperatures, initially the strained Ga adlayers relax by agglomerating into 3D islands on top of a single Ga monolayer with an activation energy of 0.19 eV in the temperature range of 200–300 °C. The remnant Ga monolayer with a sharp (1 × 1) LEED pattern desorbs at temperature >400 °C, yielding the (1 1 2)–6 × 1 and 2 × (3 3 7) sub-monolayer superstructural. Finally at 720 °C Ga completely desorbs from the surface and leaves the clean 2 × 1 reconstructed Si(5 5 12) surface. The studies demonstrate the richness of the atomically trenched high index Si(5 5 12) surface, in obtaining several anisotropic features that can be used as templates to grow self-assembled nanostructures.

Residual thermal desorption studies of Ga adatoms on trenched Si(5 5 12) surface

Energy Technology Data Exchange (ETDEWEB)

Kumar, Praveen [Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore 560064 (India); ISOM, Universidad Politecnia de Madrid, 28040 (Spain); Kumar, Mahesh [Physics and Energy Harvesting Group, National Physical Laboratory, New Delhi 110012 (India); Shivaprasad, S.M., E-mail: smsprasad@jncasr.ac.in [Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore 560064 (India)

2013-10-01

We present here the thermal stability studies of the room temperature adsorbed Ga/Si(5 5 12) interfaces in the monolayer coverage regime, using AES and LEED as in-situ UHV characterization probes. Ga grows in Stranski–Krastanov growth mode at RT on the 2 × 1 reconstructed Si(5 5 12) surface where islands form on top of 2 ML of flat pseudomorphic Ga, yielding a (1 × 1) LEED pattern for coverages of 1.2 ML and above. When this RT adsorbed Ga/Si(5 5 12) interface is annealed at different temperatures, initially the strained Ga adlayers relax by agglomerating into 3D islands on top of a single Ga monolayer with an activation energy of 0.19 eV in the temperature range of 200–300 °C. The remnant Ga monolayer with a sharp (1 × 1) LEED pattern desorbs at temperature >400 °C, yielding the (1 1 2)–6 × 1 and 2 × (3 3 7) sub-monolayer superstructural. Finally at 720 °C Ga completely desorbs from the surface and leaves the clean 2 × 1 reconstructed Si(5 5 12) surface. The studies demonstrate the richness of the atomically trenched high index Si(5 5 12) surface, in obtaining several anisotropic features that can be used as templates to grow self-assembled nanostructures.

Electronic, Structural, and Electrochemical Properties of LiNixCuyMn2-x-yO4 (0 < x < 0.5, 0 < y < 0.5) High-Voltage Spinel Materials

International Nuclear Information System (INIS)

Yang, Ming-Che; Xu, Bo; Cheng, Ju-Hsiang; Pan, Chun-Jern; Hwang, Bing-Joe; Meng, Ying S.

2011-01-01

First principles computation is carried out for investigating the electronic, structural, and electrochemical properties of LiM 1/2 Mn 3/2 O 4 (M = Ti, V, Cr, Fe, Co, Ni, and Cu). The computation results suggest that doping with Co or Cu can potentially lower Li diffusion barrier as compared to Ni doping. Our experimental research has focused on LiNi x Cu y Mn 2-x-y O 4 (0 x Cu y Mn 2-x-6 O 4 (0 0.25 Cu 0.25 Mn 1.50 O 4 , the proposed explanation of the voltage profile by the first principles computation was proven, a second plateau at 4.2 V originates from the oxidation of Cu 2+ to Cu 3+ , and the plateau at 4.95 V may originate from extra electrons provided by oxygen ions. Although the reversible discharge capacity decreases with increasing Cu amount, optimized composition such as LiCu 0.25 Ni 0.25 Mn 1.5 O 4 exhibits high capacities at high rates.

Crystal structure of 2-amino-1,3-dibromo-6-oxo-5,6-dihydropyrido[1,2-a]quinoxalin-11-ium bromide monohydrate

Directory of Open Access Journals (Sweden)

Md. Serajul Haque Faizi

2015-11-01

Full Text Available In the title hydrated salt, C12H8Br2N3O+·Br−·H2O, which was synthesized by the reaction of the pyridine derivative Schiff base N1,N4-bis(pyridine-2-ylmethylenebenzene-1,4-diamine with bromine, the asymmetric unit contains a 2-amino-1,3-dibromo-6-oxo-5,6-dihydropyrido[1,2-a]quinoxalin-11-ium cation, with a protonated pyridine moiety, a bromide anion and a water molecule of solvation. The cation is non-planar with the dibromo-substituted benzene ring, forming dihedral angles of 24.3 (4 and 11.5 (4° with the fused pyridine and pyrazine ring moieties, respectively. In the crystal, the cations are linked through a centrosymmetric hydrogen-bonded cyclic R42(8 Br2(H2O2 unit by N—H...Br, N—H...O and O—H...Br hydrogen bonds, forming one-dimensional ribbons extending along b, with the planes of the cations lying parallel to (100.

12 CFR 704.5 - Investments.

Science.gov (United States)

2010-01-01

... 12 Banks and Banking 6 2010-01-01 2010-01-01 false Investments. 704.5 Section 704.5 Banks and... § 704.5 Investments. (a) Policies. A corporate credit union must operate according to an investment... must address, at a minimum: (1) Appropriate tests and criteria for evaluating investments and...

Metamagnetic behaviour of La1-xGdxFe12B6 compounds

International Nuclear Information System (INIS)

Li, Q.A.; Groot, C.H. de; Boer, F.R. de; Buschow, K.H.J.

1997-01-01

The magnetic properties of compounds of the type La 1-x Gd x Fe 12 B 6 have been studied in high magnetic fields at 4.2 K. LaFe 12 B 6 is a compound with Fe moments close to magnetic instability and values not larger than about 0.5 μ B . Substitution of Gd for part of the La and application of high magnetic fields enhance the Fe moments to values in excess of 2 μ B . The high-moment state in LaFe 12 B 6 is reached via a metamagnetic transition. This first-order transition is associated with an extremely large hysteresis of nearly 7 T at 4.2 K. (orig.)

Microstructures and mechanical properties of heat-treated Al–5.0Cu–0.5Fe squeeze cast alloys with different Mn/Fe ratio

Energy Technology Data Exchange (ETDEWEB)

Zhang, Weiwen, E-mail: mewzhang@scut.edu.cn; Lin, Bo; Fan, Jianlei; Zhang, Datong; Li, Yuanyuan

2013-12-20

The Al–5.0 wt% Cu–0.5 wt% Fe alloys with different Mn/Fe ratio were prepared by squeeze casting. Various test techniques, including tensile test, image analysis, scanning electron microscope (SEM), X-ray diffraction (XRD), electron probe micro-analyzer (EPMA) and transmission electron microscopy (TEM) were used to examine the microstructures and mechanical properties of the alloys in T5 heat-treated condition. The results show that the β-Fe (Al{sub 7}Cu{sub 2}Fe) is stable and its needle-like morphology is maintained after T5 heat treatment. However, the Chinese script Al{sub m}Fe, α-Fe or Al{sub 6}(FeMn) partially transform to a new Chinese script Cu-rich α(CuFe) (Al{sub 7}Cu{sub 2}Fe or Al{sub 7}Cu{sub 2}(FeMn)), which is harmful to the mechanical properties of the alloys due to the decrease of the Cu content in α(Al) matrix. The optimal Mn/Fe ratio is determined by the morphology of Fe-rich intermetallics, volume fraction of θ′ and T (Al{sub 20}Cu{sub 2}Mn{sub 3}), size of α(Al) dendrite and porosity. Excessive Mn/Fe ratio will deteriorate the mechanical properties of the alloys due to the increase of the total amount of porosity and the Fe-rich intermetallics. When the Mn/Fe ratio is 1.6 and 1.2 for the applied pressure of 0 MPa and 75 MPa, respectively, the needle-like β-Fe phase is completely converted to the Chinese script Fe-rich intermetallics. The ultimate tensile strength, yield strength and elongation of the T5 heat-treated alloy with the Mn/Fe ratio of 1.2 and applied pressure of 75 MPa reach 395 MPa, 335 MPa and 14%, respectively.

Microstructures and mechanical properties of heat-treated Al–5.0Cu–0.5Fe squeeze cast alloys with different Mn/Fe ratio

International Nuclear Information System (INIS)

Zhang, Weiwen; Lin, Bo; Fan, Jianlei; Zhang, Datong; Li, Yuanyuan

2013-01-01

The Al–5.0 wt% Cu–0.5 wt% Fe alloys with different Mn/Fe ratio were prepared by squeeze casting. Various test techniques, including tensile test, image analysis, scanning electron microscope (SEM), X-ray diffraction (XRD), electron probe micro-analyzer (EPMA) and transmission electron microscopy (TEM) were used to examine the microstructures and mechanical properties of the alloys in T5 heat-treated condition. The results show that the β-Fe (Al 7 Cu 2 Fe) is stable and its needle-like morphology is maintained after T5 heat treatment. However, the Chinese script Al m Fe, α-Fe or Al 6 (FeMn) partially transform to a new Chinese script Cu-rich α(CuFe) (Al 7 Cu 2 Fe or Al 7 Cu 2 (FeMn)), which is harmful to the mechanical properties of the alloys due to the decrease of the Cu content in α(Al) matrix. The optimal Mn/Fe ratio is determined by the morphology of Fe-rich intermetallics, volume fraction of θ′ and T (Al 20 Cu 2 Mn 3 ), size of α(Al) dendrite and porosity. Excessive Mn/Fe ratio will deteriorate the mechanical properties of the alloys due to the increase of the total amount of porosity and the Fe-rich intermetallics. When the Mn/Fe ratio is 1.6 and 1.2 for the applied pressure of 0 MPa and 75 MPa, respectively, the needle-like β-Fe phase is completely converted to the Chinese script Fe-rich intermetallics. The ultimate tensile strength, yield strength and elongation of the T5 heat-treated alloy with the Mn/Fe ratio of 1.2 and applied pressure of 75 MPa reach 395 MPa, 335 MPa and 14%, respectively

Thermo-physical characterization of the Fe_6_7Mo_6Ni_3_._5Cr_3_._5P_1_2C_5_._5B_2_._5 bulk metallic glass forming alloy

International Nuclear Information System (INIS)

Bochtler, Benedikt; Gross, Oliver; Gallino, Isabella; Busch, Ralf

2016-01-01

The iron-phosphorus based bulk metallic glass forming alloy Fe_6_7Mo_6Ni_3_._5Cr_3_._5P_1_2C_5_._5B_2_._5 is characterized with respect to its thermophysical properties, crystallization and relaxation behavior, as well as its viscosity. The alloy provides a high critical casting thickness of 13 mm, thus allowing for the casting of amorphous parts with a considerable size. Calorimetric measurements reveal the characteristic transformation temperatures, transformation enthalpies, and the specific heat capacity. The analyses show that no stable supercooled liquid region exists upon heating. The specific heat capacity data are used to calculate the enthalpy, entropy, and Gibbs free energy differences between the crystalline and the supercooled liquid state. The crystallization behavior of amorphous samples upon heating is analyzed by differential scanning calorimetry and X-ray diffraction, and a time-temperature-transformation diagram is constructed. Dilatometry is used to determine the thermal expansion behavior. The equilibrium viscosity below the glass transition as well as volume relaxation behavior are measured by three-point beam bending and dilatometry, respectively, to assess the kinetic fragility. With a kinetic fragility parameter of D* = 21.3, the alloy displays a rather strong liquid behavior. Viscosity above the melting point is determined using electromagnetic levitation in microgravity on a reduced gravity aircraft in cooperation with the German Aerospace Center (DLR). These high-temperature viscosity data are compared with the low-temperature three-point beam bending measurements. The alloy displays a strong liquid behavior at low temperatures and a fragile behavior at high temperatures. These results are analogous to the ones observed in several Zr-based bulk metallic glass forming liquids, indicating a strong to fragile liquid-liquid transition in the undercooled liquid, which is obscured by crystallization.

Home Economics/Health Grades 6-12. Program Evaluation.

Science.gov (United States)

Des Moines Public Schools, IA. Teaching and Learning Div.

Home economics programs are offered to students in grades 6-12 in the Des Moines INdependent Community School District (Iowa). Programs at the middle school level are exploratory, leading to occupational training in family and consumer science, child care, food service, and textile and fashion arts at the high school level. Health education…

Enhanced elevated-temperature performance of LiAl_xSi_0_._0_5Mg_0_._0_5Mn_1_._9_0_-_xO_4 (0≤x≤0.08) cathode materials for high-performance lithium-ion batteries

International Nuclear Information System (INIS)

Zhao, Hongyuan; Liu, Shanshan; Wang, Zhenwei; Cai, Yu; Tan, Ming; Liu, Xingquan

2016-01-01

In order to significantly enhance the elevated-temperature performance of LiSi_0_._0_5Mg_0_._0_5Mn_1_._9_0O_4, the LiAl_xSi_0_._0_5Mg_0_._0_5Mn_1_._9_0_-_xO_4 (0 ≤ x ≤ 0.08) samples were firstly prepared via sol-gel technique. All the obtained samples showed the intrinsic spinel structure without any other detectable impurity phases. Among these samples, the LiAl_0_._0_5Si_0_._0_5Mg_0_._0_5Mn_1_._8_5O_4 sample was found to be optimal possessing regular crystal morphology with clean surfaces and presented much better elevated-temperature cycling stability and rate capability. When carried out at 55 °C, the LiAl_0_._0_5Si_0_._0_5Mg_0_._0_5Mn_1_._8_5O_4 sample exhibited the initial discharge capacity of 123.6 mAh g"−"1 at 0.5C between 3.20 and 4.35 V. After 100 cycles, the discharge capacity could still reach up to 115.9 mAh g"−"1 with capacity retention of 93.8%, which was much higher than that of LiSi_0_._0_5Mg_0_._0_5Mn_1_._9_0O_4. At the higher discharge rate of 10C, a high discharge capacity of 82.5 mAh g"−"1 could be obtained with capacity retention of 95.6% after 50 cycles at 55 °C. By contrast, the LiSi_0_._0_5Mg_0_._0_5Mn_1_._9_0O_4 sample only exhibited 43.7 mAh g"−"1 with lower capacity retention of 61.8%. These results indicate that the introduction of appropriate amount of aluminium ions in the magnesium and silicon co-doped spinel can make up for the shortage of co-doping with magnesium and silicon ions in term of the elevated-temperature performance.

Enthalpies of formation of layered LiNixMnxCo1-2xO2 (0 ≤ x ≤ 0.5) compounds as lithium ion battery cathode materials

International Nuclear Information System (INIS)

Masoumi, Maryam; Cupid, Damian M.; Reichmann, Thomas L.; Seifert, Hans J.; Chang, Keke; Music, Denis; Schneider, Jochen M.

2017-01-01

Layer-structured mixed transition metal oxides with the formula LiNi x Mn x Co 1-2x O 2 (0 ≤ x ≤ 0.5) are considered as important cathode materials for lithium-ion batteries. In an effort to evaluate the relative thermodynamic stabilities of individual compositions in this series, the enthalpies of formation of selected stoichiometries are determined by high temperature oxide melt drop solution calorimetry and verified by ab-initio calculations. The measured and calculated data are in good agreement with each other, and the results show that LiCoO 2 -LiNi 0.5 Mn 0.5 O 2 solid solution approaches ideal behavior. By increasing x, i.e. by equimolar substitution of Mn 4+ and Ni 2+ for Co 3+ , the enthalpy of formation of LiNi x Mn x Co 1-2x O 2 from the elements becomes more exothermic, implying increased energetic stability. This conclusion is in agreement with the literature results showing improved structural stability and cycling performance of Ni/Mn-rich LiNi x Mn x Co 1-2x O 2 compounds cycled to higher cut-off voltages.

12 CFR 810.5 - Taxation.

Science.gov (United States)

2010-01-01

... 12 Banks and Banking 6 2010-01-01 2010-01-01 false Taxation. 810.5 Section 810.5 Banks and Banking FEDERAL FINANCING BANK FEDERAL FINANCING BANK BILLS § 810.5 Taxation. All FFB bills shall be subject to Federal taxation to the same extent as obligations of private corporations are taxed. ...

Crystal structure and optical absorption spectra of Ga{sub 0.5}Fe{sub 0.5}InS{sub 3} and Ga{sub 0.5}Fe{sub 0.25}In{sub 1.25}S{sub 3} crystals; Struktura i opticheskoe pogloshchenie kristallov Ga{sub 0.5}Fe{sub 0.5}InS{sub 3} i Ga{sub 0.5}Fe{sub 0.25}In{sub 1.25}S{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Gusejnov, G G; Musaeva, N N; Kyazumov, M G [NAN Azerbajdzhana, Inst. Fiziki, Baku (Azerbaijan); Asadova, I B; Aliev, O M [NAN Azerbajdzhana, Inst. Neorganicheskoj i Fizicheskoj Khimii, Baku (Azerbaijan)

2003-09-01

Single crystals of Ga{sub 0.5}Fe{sub 0.5}InS{sub 3} are grown by the method of chemical gas-transport reactions and those of Ga{sub 0.5}Fe{sub 0.25}In{sub 1.25}S{sub 3} - by Bridgman method. X-ray diffraction studies reveal that they crystallize in trigonal and rhombohedral systems with lattice parameters of a = 3.796 x 2 A, c = 12.210 A, P3m1; a = 3.786 x 2 A, c = 36.606 A, R3m, respectively. An optical absorption edge in a wide range of photon energy and an energy gap width are determined: E{sub g} = 1.885 eV for Ga{sub 0.5}Fe{sub 0.5}InS{sub 3} and E{sub g} 1.843 eV for Ga{sub 0.5}Fe{sub 0.25}In{sub 1.25}S{sub 3}.

Hierarchical Li1.2 Ni0.2 Mn0.6 O2 nanoplates with exposed {010} planes as high-performance cathode material for lithium-ion batteries.

Science.gov (United States)

Chen, Lai; Su, Yuefeng; Chen, Shi; Li, Ning; Bao, Liying; Li, Weikang; Wang, Zhao; Wang, Meng; Wu, Feng

2014-10-22

Hierarchical Li1.2 Ni0.2 Mn0.6 O2 nanoplates with exposed {010} planes are designed and synthesized. In combination with the advantages from the hierarchical archi-tecture and the exposed electrochemically active {010} planes of layered materials, this material satisfies both efficient ion and electron transport and thus shows superior rate capability and excellent cycling stability. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

An ultrasonic therapeutic transducers using lead-free Na0.5K0.5NbO3-CuNb2O6 ceramics

International Nuclear Information System (INIS)

Yang, Ming-Ru; Chu, Sheng-Yuan; Tsai, Cheng-Che

2010-01-01

Research highlights: → In this paper, CN was added to NKN ceramics to decrease the sintering temperature and to improve the density and piezoelectric characteristics. The influence of CuNb 2 O 6 (CN) content on the microstructure, electrical properties, temperature stability, and mechanical properties of the synthesized samples was investigated. Results show that the samples synthesized with CN-doped not only improved the density but also exhibited superior piezoelectric characteristic, temperature stability of resonance frequency (TCF), and elastic stiffness coefficient than those of pure NKN piezoelectric ceramics. → The bulk density (4.47 g/cm 3 ), k p (40%), k t (45%), Q m (1642), C 33 D (19.64 x 10 10 N/m 2 ), TCF (-0.011%/ o C) and TCC (0.135%/ o C) values for NKN-01CN ceramics obtained from experiments show excellent 'hard' piezoelectric properties. Furthermore, a lead-free NKN-01CN ultrasonic therapeutic transducer was successfully driven by a self-tuning circuit. - Abstract: In this work, we reports on the CuNb 2 O 6 (CN) modified lead-free Na 0.5 K 0.5 NbO 3 (NKN) based piezoelectric ceramics were synthesized by solid-state reaction methods and sintered at 1075 o C for 3 h. A secondary phase of K 4 CuNb 8 O 23 was found in the XRD pattern of NKN-based ceramics as the CN dopants is 1 mol%. Microstructural analyses of un-doped and CN-doped ceramics were performed in a scanning electron microscope. The influence of CN content on the microstructure, electrical properties, temperature stability, and mechanical properties of the synthesized ceramics was investigated. The results show that the synthesized ceramics with CN-doped not only had improved density but also exhibited superior piezoelectric characteristics, temperature stability of resonance frequency (TCF), and a better elastic stiffness coefficient than those of pure NKN piezoelectric ceramics. The bulk density (4.47 g/cm 3 ), k p (40%), k t (45%), Q m (1642), C 33 D (19.64 x 10 10 N/m 2 ), TCF (-0

A Simple and Efficient Approach to the Synthesis of Endo and Exo Bicyclo[6.1.0]nona-3,5-diene-9-carboxaldehyde

Directory of Open Access Journals (Sweden)

Gholamreza Mashayekhi

2007-10-01

Full Text Available Monobromination of 1,5-cyclooctadiene, followed by cyclopropanation with ethyl diazoacetate, led to the formation of endo and exo ethyl 4,5-dibromobicyclo[6.1.0]nonane-9-carboxylates 3a and 3b. Bis-dehydrobromination of 3a and 3b using 1,8-diazabicyclo[5,4,0]undec-7-ene (DBU afforded the endo and exo ethyl bicyclo[6.1.0]nona-3,5-diene-9-carboxylates 4a and 4b. Reduction of these compounds to the corresponding alcohols 5a and 5b and subsequent oxidation with pyridinium chlorochromate (PCC resulted in the formation of the target compounds endo and exo bicyclo[6.1.0]nona-3,5-diene-9-carboxaldehydes 6a and 6b.

Luminescence of Eu:Y3Al5O12, Eu:Lu3Al5O12, and Eu:GdAlO3 Nanocrystals Synthesized by Solution Combustion

Science.gov (United States)

Vilejshikova, E. V.; Khort, A. A.; Podbolotov, K. B.; Loiko, P. A.; Shimanski, V. I.; Shashkov, S. N.; Yumashev, K. V.

2017-11-01

Nanocrystals of rare-earth garnets Y3Al5O12 and Lu3Al5O12 and perovskite GdAlO3 highly doped (10-20 at%) with Eu3+ are synthesized by the solution combustion technique and subsequent annealing in air at 800 and 1300oC. Their structure, morphology, and phase composition are studied. These materials exhibit intense red luminescence under UV excitation. Eu:GdAlO3 luminescence has CIE 1931 color coordinates (0.632, 0.368); dominant wavelength, 599.6 nm; and color purity, >99%. Judd-Ofelt parameters, luminescence branching ratios, and lifetimes of the Eu3+ 5D0 state are determined. The luminescence quantum yield for Eu:GdAlO3 (10 at%) reaches 74% with a lifetime of 1.4 ms for the 5D0 state. The synthesized materials are promising for red ceramic phosphors.

Efficiency, safety, and patient preference of switching from dorzolamide 1%/timolol 0.5% to brinzolamide 1%/timolol 0.5% while maintaining the prostaglandin F2α analog.

Science.gov (United States)

Shimizu, Yoshie; Nakakura, Shunsuke; Nishiyama, Makiko; Tabuchi, Hitoshi; Kiuchi, Yoshiaki

2015-01-01

We investigated the efficiency, safety and patient preference of switching from dorzolamide 1%/timolol 0.5% to brinzolamide 1%/timolol 0.5% while maintaining the prostaglandin F2α analog. We initially enrolled 44 eyes from 44 primary open angle glaucoma patients, and a total of 42 patients completed the study. All patients were under treatment with various prostaglandin F2α analogs and dorzolamide 1%/timolol 0.5%. While maintaining the prostaglandin F2α analog, dorzolamide 1%/timolol 0.5% was switched to brinzolamide 1%/timolol 0.5%. Conjunctival hyperemia, superficial punctate keratopathy, and intraocular pressure (IOP) were evaluated at baseline and at 4, 12, and 24 weeks. Adverse events and patient preferences, measured using a questionnaire at study initiation and at 24 weeks, were also noted. The IOP was 17.7±1.7, 16.8±2.6, 16.7±2.2, and 16.7±2.4 mmHg at baseline and at 4, 12, and 24 weeks, respectively, with no significant differences in IOP values at any time point (P=0.117, one-way analysis of variance). In addition, no significant differences were found in the incidence of conjunctival hyperemia or SPK score at any time point (all P>0.5, by Kruskal-Wallis test). Based on the evaluation of side effects using the questionnaire, stinging/burning was less common (P=0.042), while blurred vision was more common (P=0.003), after switching to brinzolamide 1%/timolol 0.5%. Regarding patient preferences, 13 patients (31%) preferred dorzolamide 1%/timolol 0.5%, 12 patients (29%) preferred brinzolamide 1%/timolol 0.5%, and 17 patients (40%) preferred neither. When switching from dorzolamide 1%/timolol 0.5% to brinzolamide 1%/timolol 0.5%, the IOP values and incidence of superficial punctate keratopathy and conjunctival hyperemia were sustained throughout the 24-week observation period, and the patient preferences were similar for the two regimens. However, differences were observed in the ocular sensations of stinging/burning with dorzolamide 1%/timolol 0.5

Hydrogen storage properties in the Mg_0_._7_5Ta_0_._2_5 system prepared by mechanical milling

International Nuclear Information System (INIS)

Ramirez G, J. A.

2016-01-01

Magnesium and most of its mixtures have slow sorption-desorption kinetics of hydrogen, which limits their technological application and their viability from the economic view point. Recently, has been observed that by the synthesis of advanced materials, using the mechanical milling technique, positive changes in the kinetics are introduced. In order to improve the sorption-desorption hydrogen properties, in the present work a mixture consisting of Mg_0_._7_5Ta_0_._2_5 was prepared using methanol as process control agent. To this end, the first methodological step was to carry out, by means of the mechanical milling technique, the synthesis of the mixture Mg_0_._7_5Ta_0_._2_5 in a Spex type vibratory mill at times of 6, 12, 18 and 24 h. Subsequently, the material was characterized by different analytical techniques such as scanning electron microscopy with elemental analysis, X-ray diffraction and N_2 physisorption analysis. Subsequently, hydrogen sorption experiments were carried out in a Parr reactor to evaluate the hydrogen storage capacity of the mixture, varying temperature parameters, pressure and time, in order to determine the optimal parameters of hydrogen sorption. The characterization of the hydrogen storage capacity was analyzed by the thermogravimetric analysis/differential scanning calorimetry technique coupled to a mass spectrometer. X ray diffraction analysis reveals that there is a mixture between the starting compounds, with an important refinement of the microstructure as a consequence of the mechanical milling process. The results of the hydrogen sorption tests at 1, 5 and 10 cycles showed that the storage of hydrogen in the Mg_0_._7_5Ta_0_._2_5 mixture can be carried out at a temperature of 25 degrees Celsius with a pressure of 2 atm and a contact time of 1 h. (Author)

A 6.2 mW 0.024 mm2 fully-passive RF downconverter with 12 dB gain enhancement using MOS parametric amplification

DEFF Research Database (Denmark)

Custódio, J. R.; Bastos, I.; Oliveira, L. B.

2013-01-01

This paper describes a fully-passive discrete-time switched-capacitor RF downconverter with an on-chip oscillator, that combines quadrature mixing and harmonic rejection, designed in a 130 nm digital CMOS technology. By using MOS capacitors (varactors) to perform parametric amplification, it is p......, it is possible to achieve a measured gain enhancement of about 12 dB, together with 21 dB noise figure and more than 5 dBm IIP3. Operating in the VHF-III band, the downconverter core dissipates 6.2 mW and occupies 0.024 mm2....

3.5% urea-linked gelatin is as effective as 6% HES 200/0.5 for volume management in cardiac surgery patients

NARCIS (Netherlands)

van der Linden, Philippe J.; de Hert, Stefan G.; Daper, Anne; Trenchant, Anne; Schmartz, Denis; Defrance, Pierre; Kimbimbi, Pierre

2004-01-01

PURPOSE: To compare the efficacy of volume expansion with 3.5% gelatin and 6% hydroxyethyl starch 200/0.5 in patients undergoing cardiac surgery. The second objective was to compare the two colloids in terms of blood losses and allogeneic blood transfusion exposure rate. METHODS: In this open-label

Criticality safety review of 2 1/2-, 10-, and 14-ton UF6 cylinders

International Nuclear Information System (INIS)

Broadhead, B.L.

1991-10-01

Currently, UF 6 cylinders designed to contain 2 1/2 tons of UF 6 are classified as Fissile Class 2 packages with a transport index (TI) of 5 for the purpose of transportation. The 10-ton UF 6 cylinders are classified as Fissile Class 1 with no TI assigned for transportation. The 14-ton cylinders, although not certified for transport with enrichments greater than 1 wt % because they have no approved overpack, can be used in on-site operations for enrichments greater than 1 wt %. The maximum 235 U enrichments for these cylinders are 5.0 wt % for the 2 1/2-ton cylinder and 4.5 wt % for the 10- and 14-ton cylinders. This work reviews the suitability for reclassification of the 2 1/2-ton UF 6 packages as Fissile Class 1 with a maximum 235 U enrichment of 5 wt %. Additionally, the 10- and 14-ton cylinders are reviewed to address a change in maximum 235 U enrichment from 4.5 to 5 wt %. Based on this evaluation, the 2 1/2-ton UF 6 cylinders meet the 10 CFR.71 criteria for Fissile Class 1 packages, and no TI is needed for criticality safety purposes; however, a TI may be required based on radiation from the packages. Similarly, the 10- and 14-ton UF 6 packages appear acceptable for a maximum enrichment rating change to 5 wt % 235 U. 11 refs., 13 figs., 7 tabs

Crystal and molecular structure of 6,9-bis(trimethylamine)-nido-decarborane(12) B10H12[N(CH3)3]2

International Nuclear Information System (INIS)

Polyanskaya, T.M.; Volkov, V.V.

1989-01-01

The spatial structure of 6.9-bis(trimethylamine)-nido-decarborane (12) is established on the basis of X-ray diffraction analysis. Crystals are rhombic, a = 12.619, b = 11.804, c = 11.058A, Z=4, sp. gr. P na 2 1 . The structure is of molecular type. Main geometrical parameters of the molecule are: symmetry - C1, interatomic distances - B-B 1.66-1.90, B-N 1.61, N-C 1.50 A, angles - BBB 55.0-66.5, CNC 108, BBN 119.5 deg. The (B 10 H 12 ) cluster size between B(6) and B(9) is 3.30 A. Increase approximately by 0.1 A of lengths of external bonds B-B in comparison with internal ones and tightening approximately by 3 deg of valent angles BBB at external atoms of boron also in comparison with internal ones are observed

The quinternary thiophosphate Cs0.5Ag0.5Nb2PS10

Directory of Open Access Journals (Sweden)

Sojeong Park

2010-07-01

Full Text Available The quinternary thiophosphate Cs0.5Ag0.5Nb2PS10, cesium silver tris(disulfido[tetrathiophosphato(V]diniobate(IV, has been prepared from the elements using a CsCl flux. The crystal structure is made up of ∞1[Nb2PS10] chains expanding along [010]. These chains are built up from bicapped trigonal-prismatic [Nb2S12] units and tetrahedral [PS4] groups and are linked through a linear S—Ag—S bridge, forming a two-dimensional layer. These layers then stack on top of each other, completing the three-dimensional structure with an undulating van der Waals gap. The disordered Cs+ ions reside on sites with half-occupation in the voids of this arrangement. Short [2.8843 (5 Å] and long [3.7316 (4 Å] Nb—Nb distances alternate along the chains, and anionic S22− and S2− species are observed. The charge balance of the compound can be represented by the formula [Cs+]0.5[Ag+]0.5[Nb4+]2[PS43−][S22−]3.

Resveratrol Protects PC12 Cell against 6-OHDA Damage via CXCR4 Signaling Pathway

Directory of Open Access Journals (Sweden)

Jing Zhang

2015-01-01

Full Text Available Resveratrol, herbal nonflavonoid polyphenolic compound naturally derived from grapes, has long been acknowledged to possess extensive biological and pharmacological properties including antioxidant and anti-inflammatory ones and may exert a neuroprotective effect on neuronal damage in neurodegenerative diseases. However, the underlying molecular mechanisms remain undefined. In the present study, we intended to investigate the neuroprotective effects of resveratrol against 6-OHDA-induced neurotoxicity of PC12 cells and further explore the possible mechanisms involved. For this purpose, PC12 cells were exposed to 6-OHDA in the presence of resveratrol (0, 12.5, 25, and 50 μM. The results showed that resveratrol increased cell viability, alleviated the MMP reduction, and reduced the number of apoptotic cells as measured by MTT assay, JC-1 staining, and Hoechst/PI double staining (all p<0.01. Immunofluorescent staining and Western blotting revealed that resveratrol averts 6-OHDA induced CXCR4 upregulation (p<0.01. Our results demonstrated that resveratrol could effectively protect PC12 cells from 6-OHDA-induced oxidative stress and apoptosis via CXCR4 signaling pathway.

PHASE EVOLUTION AND MICROWAVE DIELECTRIC PROPERTIES OF (Li0.5Bi0.5)(W1-xMox)O4(0.0 ≤ x ≤ 1.0) CERAMICS WITH ULTRA-LOW SINTERING TEMPERATURES

Science.gov (United States)

Zhou, Di; Guo, Jing; Yao, Xi; Pang, Li-Xia; Qi, Ze-Ming; Shao, Tao

2012-11-01

The (Li0.5Bi0.5)(W1-xMox)O4(0.0 ≤ x ≤ 1.0) ceramics were prepared via the solid state reaction method. The sintering temperature decreased almost linearly from 755°C for (Li0.5Bi0.5)WO4 to 560°C for (Li0.5Bi0.5)MoO4. When the x≤0.3, a wolframite solid solution can be formed. For x = 0.4 and x = 0.6 compositions, both the wolframite and scheelite phases can be formed from the X-ray diffraction analysis, while two different kinds of grains can be revealed from the scanning electron microscopy and energy-dispersive X-ray spectrometer results. High performance of microwave dielectric properties were obtained in the (Li0.5Bi0.5)(W0.6Mo0.4)O4 ceramic sintered at 620°C with a relative permittivity of 31.5, a Qf value of 8500 GHz (at 8.2 GHz), and a temperature coefficient value of +20 ppm/°C. Complex dielectric spectra of pure (Li0.5Bi0.5)WO4 ceramic gained from the infrared spectra were extrapolated down to microwave range, and they were in good agreement with the measured values. The (Li0.5Bi0.5)(W1-xMox)O4(0.0 ≤ x ≤ 1.0) ceramics might be promising for low temperature co-fired ceramic technology.

Conducting, magnetic polyaniline/Ba0.25Sr0.75 Fe11(Ni0.5Mn0.5)O19 nanocomposite: Fabrication, characterization and application

International Nuclear Information System (INIS)

Ezzati, S. Noushin; Rabbani, Mahboubeh; Leblanc, Roger M.; Asadi, Ebadullah; Ezzati, S. Mohammad H.; Rahimi, Rahmatollah; Azodi-Deilami, Saman

2015-01-01

In this contribution, Ni/Mn doped Barium Strontium Ferrite nanoparticles (Ba 0.25 Sr 0.75 Fe 11 (Ni 0.5 Mn 0.5 )O 19 ) and conducting polyaniline/Ba 0.25 Sr 0.75 Fe 11 (Ni 0.5 Mn 0.5 )O 19 nanocomposite were fabricated successfully through sol–gel method and in-situ polymerization technique, respectively. Field emission scanning electron microscope (FESEM), Energy-dispersive X-ray spectroscopy analysis (EDX), X-ray powder diffraction (XRD), Mössbauer spectroscopic measurements and Fourier transform infrared spectroscope (FT-IR) analyses were adopted to confirm the composition, morphology and structure of materials. The obtained results revealed the formation of hexagonal M-type rod-shape ferrite with average particle size of about 45 nm (according to XRD data, using Debye–Scherre formula). The saturation magnetization of ferrite nanoparticles and PANI/Ferrite nanocomposite reported 44.03 and 9.85 emu/g, respectively, using vibrant sample magnetometer (VSM). Standard four-point-probe technique was employed to measure the conductivity of samples. Also optical characteristic of samples was examined by means of UV–Vis and Diffuse Reflectance Spectra (DRS) techniques which proved the formation of conducting coating of emeraldine on the surface of magnetic nanoparticles. Also the UV–vis studies indicated that the ferrite nanoparticles have an optical band gap of 1.8 eV while the values of 1.65 and 2.66 eV obtained for PANI/Ferrite nanocomposite. Finally, the microwave absorption properties of prepared nanoferrite and nanocomposite at different thicknesses (2, 3 and 4 mm) were determined at the X-band (8–12 GHz) using vector network analyzer (VNA). In this study, minimum reflection loss of −21.68 dB and maximum available bandwidth of 4.8 GHz were obtained for PANI/Ferrite (20 wt% ferrite) at the frequency of 10.6 GHz. The results suggested the fabricated nanocomposite could be a suitable candidate for decreasing radar signature. - Highlights: • Polyaniline

Combustion synthesis and characterization of MV0.5P0.5O4: Sm3+, Tm3+ (M = Gd, La, Y)

Science.gov (United States)

Motloung, Selepe J.; Lephoto, Mantwa A.; Tshabalala, Kamohelo G.; Ntwaeaborwa, Odireleng M.

2018-04-01

In this paper, GdV0.5P0.5O4: Sm3+, Tm3+, LaV0.5P0.5O4: Sm3+, Tm3+ and YV0.5P0.5O4: Sm3+, Tm3+ phosphor powders were prepared by solution combustion method using urea as a fuel. The phase purity, surface morphology, optical and photoluminescence properties were investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), UV-vis spectroscopy and photoluminescence spectroscopy. The XRD results indicated that the prepared powders are of a single phase and crystallized in tetragonal structure for Gd and Y systems while monoclinic phase was observed for La system. SEM showed that the samples consisted of mixed structures. The estimated band gaps were 2.2, 2.4 and 2.3 eV for Y, Gd and La systems respectively. The photoluminescence results showed four emission peaks. One peak is assigned to 1G4 - 3H6 transition of Tm3+, and three other emission peaks are attributed to 6G5/2 - 6H5/2, 6G5/2 - 6H7/2 and 6G5/2 - 6H9/2 transitions of Sm3+. The photoluminescent intensity was the highest in the gadolinium system.

12 CFR 613.3020 - Financing for farm-related service businesses.

Science.gov (United States)

2010-01-01

... 12 Banks and Banking 6 2010-01-01 2010-01-01 false Financing for farm-related service businesses... AND SCOPE OF FINANCING Financing Under Titles I and II of the Farm Credit Act § 613.3020 Financing for farm-related service businesses. (a) Eligibility. An individual or legal entity that furnishes farm...

1,2-Bis(2-methoxy-6-formylphenoxyethane

Directory of Open Access Journals (Sweden)

Hongqi Li

2011-02-01

Full Text Available In the title compound [systematic name: 3,3′-dimethoxy-2,2′-(ethane-1,2-diyldioxydibenzaldehyde], C18H18O6, prepared from 1,2-dibromoethane and ortho-vanillin in the presence of sodium carbonate, the two vanillin units are linked via a CH2–CH2 bridge. The two benzene rings are inclined at a dihedral angle of 41.6 (5°.

Crystal growth, spectroscopic and CW laser properties of Nd0.03Lu2.871Gd0.099Al5O12 crystal

Science.gov (United States)

Di, J. Q.; Xu, X. D.; Cheng, S. S.; Li, D. Z.; Zhou, D. H.; Wu, F.; Zhao, Z. W.; Xu, J.

2011-11-01

Nd0.03Lu2.871Gd0.099Al5O12 (Nd:LuGdAG) crystal was grown by the Czochralski method. The absorption, fluorescence spectra and fluorescence lifetime of Nd:LuGdAG crystal at room temperature were investigated for the first time. We reported the continuous-wave (CW) Nd:LuGdAG laser operation under diode pumping. Output power of 1.43 W at 1064 nm was achieved with a slope efficiency of 34.1%. All the results show that Nd:LuGdAG crystal is a promising laser material.

Non-stoichiometry in the KMo2P3O12-tunnel structure: The oxide K0.75MoNbP3O12

International Nuclear Information System (INIS)

Leclaire, A.; Borel, M.M.; Grandin, A.; Raveau, B.

1990-01-01

K 0.75 MoNbP 3 O 12 , M r =503.009, orthorhombic, Pbcm, a=8.8518 (5), b=9.1453 (11), c=12.5174 (11) A, V=1013.3 (3) A 3 , Z=4, D x =3.300 Mg m -3 , λ(Mo Kα)=0.71073 A, μ=3.13 mm -1 , F(000)=953, T=294 K, R=0.029, wR=0.033 for 1235 observed reflections. This compound is isostructural with KMo 2 P 3 O 12 -type oxides. Its framework is built up from MoO 6 octahedra and PO 4 tetrahedra which delimit tunnels running along b. Different from KMo 2 P 3 O 12 , the tunnels are partly occupied by the potassium ions which are distributed at random. (orig.)

Myeloid Neoplasms with t(5;12 and ETV6-ACSL6 Gene Fusion, Potential Mimickers of Myeloid Neoplasm with PDGFRB Rearrangement: Case Report with Imatinib Therapy and Review of the Literature

Directory of Open Access Journals (Sweden)

Javier De Luca-Johnson

2016-01-01

Full Text Available We report the second case of ETV6-ACSL6 associated myeloproliferative neoplasm that has received a full course of imatinib therapy. The patient was a 51-year-old previously healthy man who presented with three months of worsening dyspnea and was found to have a white count of 216,000/cmm, of which 84% were eosinophil lineage. Cytogenetic analysis revealed a t(5;12(q31~33;p13. FISH was negative for PDGFRB rearrangement but additional FISH testing demonstrated an ACSL6 rearrangement. ETV6-ACSL6 gene fusion is a rare abnormality that most often presents as a myeloproliferative-type disorder with prominent eosinophilia or basophilia. Review of the literature yielded a total of 11 previous cases. This gene fusion results in a t(5;12(q31~33;p13 that mimics the t(5;12 found in ETV6-PDGFRB neoplasms. Identification of the fusion genes involved in t(5;12 in eosinophilia-associated myeloproliferative disorders is crucial to direct an effective treatment plan. In particular, while tyrosine kinase inhibitor therapy is effective in patients with PDGFRB rearrangement, there is little information on imatinib efficacy in patients with ETV6-ACSL6 gene fusion. Our patient was found to be nonresponsive to imatinib therapy.

Mechanical bending strength of (Bi0.5Na0.5 TiO3-based lead-Free piezoelectric ceramics

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Hiroaki Takahashi

2017-09-01

Full Text Available (Bi0.5Na0.5TiO3 [BNT] is expected as one of candidate lead-free materials because these ceramics show relatively good high-power piezoelectric properties. In this study, we tried to understand the bending strength and fracture behavior of the BNT-based ceramics. To measure the bending strength, a three-point bending test on the basis of JIS was conducted using 12.0 × 4.0 × 1.0 mm3 specimens. An average bending strength, σA, of pure BNT ceramics sintered at 1100 °C for 2, 12 and 24 h were 217, 195 and 187 MPa, respectively. It is cleared that the σA increased with decreasing the sintering time, (grain size and pore size. We also investigated the bending strength of Nb2O5 doped BNT ceramics [BNT-Nb x, x = 0.05 ∼ 1.5 wt%] and MnCO3 doped BNT ceramics [BNT-Mn x, x = 0.5 and 1.0 wt%]. Values of the σA of BNT-Nb 0.5 and BNT-Mn 0.5 were 222, and 188 MPa, respectively. It is clarified that soft dopants (Nb can improve the bending strength of BNT-based ceramics. Additionally, hot-pressed BNT [HP-BNT] were sintered at 1050 °C for 5 h, and the σA of HP-BNT was 245 MPa.

Effect of Natural Aging and Cold Working on Microstructures and Mechanical Properties of Al-4.6Cu-0.5Mg-0.5Ag alloy

Science.gov (United States)

Chen, Yu-Te; Lee, Sheng-Long; Bor, Hui-Yun; Lin, Jing-Chie

2013-06-01

This research investigates the effects of natural aging and cold working prior to artificial aging on microstructures and mechanical properties of Al-4.6Cu-0.5Mg-0.5Ag alloy. Mechanical properties relative to microstructure variations were elucidated by the observations of the optical microscope (OM), differential scanning calorimeter (DSC), electrical conductivity meter (pct IACS), and transmission electron microscopy (TEM). The results showed that natural aging treatment has little noticeable benefit on the quantity of precipitation strengthening phases and mechanical properties, but it increases the precipitation strengthening rate at the initial stage of artificial aging. Cold working brings more lattice defects which suppress Al-Cu (GP zone) and Mg-Ag clustering, and therefore the precipitation of Ω phase decreases. Furthermore, more dislocations are formed, leading to precipitate the more heterogeneous nucleation of θ' phase. The above-mentioned precipitation phenomena and strain hardening effect are more obvious with higher degrees of cold working.

Structure and electrical properties of (1 − x) (Na0.5Bi0.5)0.94Ba0.06TiO3–x BiAlO3 lead-free piezoelectric ceramics

International Nuclear Information System (INIS)

Fu, Peng; Xu, Zhijun; Chu, Ruiqing; Wu, Xueyan; Li, Wei; Li, Xiaodong

2013-01-01

Highlights: ► (1 − x) BNBT6–x BA ceramics were prepared by solid-state reaction method. ► Electrical properties of BNBT6 ceramics are improved by the addition of BA. ► (1 − x) BNBT6 - x BA ceramics at x = 0.0225 have the best electrical properties. - Abstract: (1 − x) (Na 0.5 Bi 0.5 ) 0.94 Ba 0.06 TiO 3 –x BiAlO 3 ((1 − x) BNBT6–x BA) lead-free piezoelectric ceramics were synthesized by conventional solid-state processes. Effects of BiAlO 3 (BA) on the structure and electrical properties of (Na 0.5 Bi 0.5 ) 0.94 Ba 0.06 TiO 3 (BNBT6) ceramics were investigated. X-ray diffraction (XRD) data shows that (1 − x) BNBT6–x BA ceramics form the pure perovskite phases, and the ceramics have the morphotropic phase boundary (MPB) when x r = 42.5 μC/cm 2 ), the highest piezoelectric coefficient (d 33 = 204 pC/N), the highest planar coupling factor (k p = 0.3292), the highest dielectric constant (ε r = 1687) and higher mechanical quality factor (Q m = 112)

ZnO nanorods/ZnS.(1,6-hexanediamine)0.5 hybrid nanoplates hierarchical heteroarchitecture with improved electrochemical catalytic properties for hydrazine

Science.gov (United States)

Wu, Zhengcui; Wu, Yaqin; Pei, Tonghui; Wang, Huan; Geng, Baoyou

2014-02-01

Novel hierarchical heteronanostructures of ZnO nanorods/ZnS.(HDA)0.5 (HDA = 1,6-hexanediamine) hybrid nanoplates on a zinc substrate are successfully synthesized on a large scale by combining hydrothermal growth (for ZnO nanorods) and liquid chemical conversion (for ZnS.(HDA)0.5 nanoplates) techniques. The formation of ZnS.(HDA)0.5 hybrid nanoplates branches takes advantage of the preferential binding of 1,6-hexanediamine on specific facets of ZnS, which makes the thickening rate much lower than the lateral growth rate. The ZnS.(HDA)0.5 hybrid nanoplates have a layered structure with 1,6-hexanediamine inserted into interlayers of wurtzite ZnS through the bonding of nitrogen. The number density and thickness of the secondary ZnS.(HDA)0.5 nanoplates can be conveniently engineered by variation of the sulfur source and straightforward adjustment of reactant concentrations such as 1,6-hexanediamine and the sulfur source. The fabricated ZnO/ZnS.(HDA)0.5 heteronanostructures show improved electrochemical catalytic properties for hydrazine compared with the primary ZnO nanorods. Due to its simplicity and efficiency, this approach could be similarly used to fabricate varieties of hybrid heterostructures made of materials with an intrinsic large lattice mismatch.Novel hierarchical heteronanostructures of ZnO nanorods/ZnS.(HDA)0.5 (HDA = 1,6-hexanediamine) hybrid nanoplates on a zinc substrate are successfully synthesized on a large scale by combining hydrothermal growth (for ZnO nanorods) and liquid chemical conversion (for ZnS.(HDA)0.5 nanoplates) techniques. The formation of ZnS.(HDA)0.5 hybrid nanoplates branches takes advantage of the preferential binding of 1,6-hexanediamine on specific facets of ZnS, which makes the thickening rate much lower than the lateral growth rate. The ZnS.(HDA)0.5 hybrid nanoplates have a layered structure with 1,6-hexanediamine inserted into interlayers of wurtzite ZnS through the bonding of nitrogen. The number density and thickness of the

Polarization properties of La0.6Sr0.4Co0.2Fe0.8O3-based double layer-type oxygen electrodes for reversible SOFCs

International Nuclear Information System (INIS)

Tao, Y.; Nishino, H.; Ashidate, S.; Kokubo, H.; Watanabe, M.; Uchida, H.

2009-01-01

We have developed double layer-type (catalyst layer/current collecting layer) oxygen electrodes (DLE) for reversible SOFCs. As the catalyst layer (cathode for SOFC and anode for steam electrolysis) interfaced with a samaria-doped ceria [(CeO 2 ) 0.8 (SmO 1.5 ) 0.2 , SDC] interlayer/YSZ solid electrolyte, mixed conducting La 0.6 Sr 0.4 Co 0.2 Fe 0.8 O 3 (LSCF) and SDC particles were employed. The current collecting porous LSCF layer was formed on the catalyst layer. By controlling the SDC content, as well as the thickness and porosity of the catalyst layer, the gas diffusion rate and the conduction networks for electrons and oxide ions were optimized, resulting in a marked reduction of the overpotential. The LSCF + SDC/LSCF DLE exhibited higher performance than single-layer electrodes of LSCF + SDC or LSCF; the IR-free anode potential vs. an air reference electrode was 0.12 V (corresponding to an overpotential of 0.08 V) at 0.5 A cm -2 and 900 deg. C under an atmosphere of O 2 (1 atm)

A pragmatic implementation of a 6-day physiotherapy service in a mixed inpatient rehabilitation unit.

Science.gov (United States)

Caruana, Erin L; Kuys, Suzanne S; Clarke, Jane; Bauer, Sandra G

2017-08-01

This study determined the impact of a pragmatic 6-day physiotherapy service on length of stay, functional independence, gait and balance in people undergoing inpatient rehabilitation, compared to a 5-day service. A prospective cohort study with historical comparison was undertaken in a mixed inpatient rehabilitation unit. Intervention period participants (2011) meeting inclusion criteria were eligible for a 6-day physiotherapy service. All other participants, including the historical cohort (2010) received usual care (5-day physiotherapy). Length of stay, functional independence, gait and balance performance were measured. A total of 536 individuals participated in this study; 270 in 2011 (60% received 6-day physiotherapy) and 266 in 2010. Participants in 2011 showed a trend for reduced length of stay (1.7 days, 95%CI -0.53 to 3.92) compared to 2010. Other measures showed no significant differences between cohorts. In 2011, those receiving 6-day physiotherapy were more dependent, but showed significantly improved functional independence and balance compared to those receiving 5-day physiotherapy (p physiotherapy service in a "real-world" rehabilitation setting demonstrated a trend towards reduced length of stay, and improved functional gains. This service could lead to cost-savings for hospitals and improved patient flow. Implications for Rehabilitation "Real-world" implementation of a 6-day physiotherapy service in rehabilitation shows a trend for reducing length of stay. This reduction in length of stay may lead to cost-savings for the hospital system, and improve patient flow into rehabilitation. Patients receiving 6-day physiotherapy made significant gains in balance and functional independence compared to patients receiving 5-day physiotherapy services in the rehabilitation setting.

Thermoelectric power measurements in Fe doped La sub 0 sub . sub 6 sub 5 Ca sub 0 sub . sub 3 sub 5 MnO sub 3

CERN Document Server

Aslam, A; Zubair, M; Akhtar, M J; Nadeem, M

2002-01-01

We report measurements of the thermoelectric power (TEP) on the La sub 0 sub . sub 6 sub 5 Ca sub 0 sub . sub 3 sub 5 Mn sub 1 sub - sub x Fe sub x O sub 3 system for 0.00 <= x <= 0.07. The ferromagnetic and metallic transition temperatures are lowered and the TEP shows an increasingly positive trend with the addition of Fe. We also observe a clear magnetic contribution that manifests itself as a peak in the TEP close to the critical temperature. The activation energies determined from the TEP are seen to be insensitive to the Fe content. The data are interpreted firstly as showing a decrease in the density of active holes, i.e. holes that can participate in the hopping process, with increasing Fe content. Secondly the data suggest the role of magnetic scattering due to the clusters formed by the antiferromagnetically coupled Fe. Abrupt changes in the variation of the TEP are observed at the concentration region x approx 0.04 consistent with the hole density variation and with previously reported transp...

Synthesis and characterization of superionic (LiBr)_0_._5(AlSiO)_0_._5

International Nuclear Information System (INIS)

Aziz K Jahja; Safei Purnama

2010-01-01

Materials of LiBr silicate aluminum ionic conductor have been prepared by powder metallurgy method in which 0.5 mole of LiBr powder is mixed with about 0.5 mole silicate aluminum in liquid medium of aquadest. After mixing and homogenization, the samples are dried, compacted and heated at 600 °C for 1 hour. Characterization of materials structure was carried out by X-Ray diffraction, ionic conductivity was measured by LCR meter with frequency range of 10"-"1 to 10"5 Hz at room temperature. Results of measurement show the (LiBr)_0_._5(AlSiO)_0_._5 conductor has the structure of both LiBr and of silicate aluminum. (LiBr)_0_._5(AlSiO)_0_._5 has the highest ionic conductivity in the order of 10"-"3 S.cm"-"1 while the ionic conductivity of LiBr is found to be about 10"-"4 S.cm"-"1 and that of silicate aluminum is about 10"-"6 S.cm"-"1, all measured at room temperature. (author)

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.

The U5.0 Undulator for the ALS

International Nuclear Information System (INIS)

Hoyer, E.; Chin, J.; Halbach, K.; Hassenzahl, W.V.; Humphries, D.; Kincaid, B.; Lancaster, H.; Plate, D.

1991-05-01

The U5.0 Undulator, an 89 period, 5 cm period length, 4.6 m long insertion device has been designed and is in fabrication. This undulator will be the first high brightness source, in the 50 to 1500 eV range, for the Advanced Light Source (ALS) and is scheduled for completion in 1992. A modular hybrid configuration utilizing Nd-Fe-B permanent magnet material and vanadium permendur is used that achieves 0.837 Tesla effective peak field. Correction of the vertical field integral is with permanent magnet rotors at the ends. Gap adjustment is with an arrangement of roller screws, chains drives, a gear reduction unit and a stepper motor driven by a closed loop control system. The vacuum chamber design is a two-piece, machined and welded 5083-H321 aluminum construction of 5.1 m length. Magnetic design, subsystem design and fabrication progress are presented. 12 refs., 4 figs., 2 tabs

Specific heat measurements of TiB2 and 6LiF from 0.5 to 30 K

International Nuclear Information System (INIS)

Lang, Brian E.; Donaldson, Marcus H.; Woodfield, Brian F.; Burger, Arnold; Roy, Utupal N.; Lamberti, Vincent; Bell, Zane W.

2005-01-01

The specific heats of TiB 2 and 6 LiF have been measured from 0.5 to 30 K as part of a larger project in the construction of a neutron spectrometer. For this application, the measured specific heats were used to extrapolate the specific heats down to 0.1 K with lattice, electronic, and Schottky equations for the respective samples. The resultant specific heat values at 0.1 K for TiB 2 and 6 LiF are 4.08 x 10 -4 ± 0.27 x 10 -4 J/K/mol and 9.19 x 10 -9 ± 0.15 x 10 -9 J/K/mol, respectively

A giant enhancement of CMR in Eu{sub 0.6}Ca{sub 0.4}B{sub 6}

Energy Technology Data Exchange (ETDEWEB)

Glushkov, V V; Bogach, A V; Demishev, S V; Sluchanko, N E [A.M.Prokhorov General Physics Institute of RAS, 38, Vavilov str., Moscow 119991 (Russian Federation); Anisimov, M A [Moscow Institute of Physics and Technology, 9, Institutskii per., Dolgoprudny, Moscow Region 141700 (Russian Federation); Churkin, O A; Kuznetsov, A V [Moscow Engineering Physics Institute, 31, Kashirskoe Shosse, Moscow 115409 (Russian Federation); Filipov, V B; Levchenko, A V; Shitsevalova, N Yu [I. Frantsevich Institute for Problems of Materials Science NAS, 3, Krzhyzhanovsky str., Kiev 03680 (Ukraine); Flachbart, K, E-mail: glushkov@lt.gpi.r [Centre of Low Temperature Physics, IEP SAS and IPS FS UPJS, Kosice SK-04001 (Slovakia)

2010-01-15

The transport and magnetic properties of Eu{sub 0.6}Ca{sub 0.4}B{sub 6} single crystals have been studied at temperatures 1.8-300 K in magnetic fields up to 80 kOe. It was found that lowering of temperature results in a drastic increase of magnetoresistance up to the values of {rho}(0)/{rho}(H){approx}7{center_dot}10{sup 5} detected below 6K. The Hall and Seebeck effect measurements showed that colossal magnetoresistance (CMR) observed in Eu{sub 0.6}Ca{sub 0.4}B{sub 6} is accompanied by a crossover from hole-like to electron-like regime of charge transport induced by applied magnetic field. Hall mobility values {mu}{sub H{approx}}200-350 cm{sup 2}/(Vs) estimated for the high conductive state of Eu{sub 0.6}Ca{sub 0.4}B{sub 6} in the presence of strong substitutional disorder were proved to be comparable with these ones measured for undoped EuB{sub 6}. The anomalous behaviour of transport and magnetic parameters is discussed in terms of metal-insulator transition earlier predicted for this low carrier density system within double exchange model by V M Pereira et al., Phys. Rev. Lett. 93 147202 (2004).

Efficiency, safety, and patient preference of switching from dorzolamide 1%/timolol 0.5% to brinzolamide 1%/timolol 0.5% while maintaining the prostaglandin F2α analog

Directory of Open Access Journals (Sweden)

Shimizu Y

2015-03-01

Full Text Available Yoshie Shimizu,1 Shunsuke Nakakura,1 Makiko Nishiyama,1 Hitoshi Tabuchi,1 Yoshiaki Kiuchi2 1Department of Ophthalmology, Saneikai Tsukazaki Hospital, Himeji, 2Department of Ophthalmology and Visual Sciences, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan Background: We investigated the efficiency, safety and patient preference of switching from dorzolamide 1%/timolol 0.5% to brinzolamide 1%/timolol 0.5% while maintaining the prostaglandin F2α analog.Methods: We initially enrolled 44 eyes from 44 primary open angle glaucoma patients, and a total of 42 patients completed the study. All patients were under treatment with various prostaglandin F2α analogs and dorzolamide 1%/timolol 0.5%. While maintaining the prostaglandin F2α analog, dorzolamide 1%/timolol 0.5% was switched to brinzolamide 1%/timolol 0.5%. Conjunctival hyperemia, superficial punctate keratopathy, and intraocular pressure (IOP were evaluated at baseline and at 4, 12, and 24 weeks. Adverse events and patient preferences, measured using a questionnaire at study initiation and at 24 weeks, were also noted.Results: The IOP was 17.7±1.7, 16.8±2.6, 16.7±2.2, and 16.7±2.4 mmHg at baseline and at 4, 12, and 24 weeks, respectively, with no significant differences in IOP values at any time point (P=0.117, one-way analysis of variance. In addition, no significant differences were found in the incidence of conjunctival hyperemia or SPK score at any time point (all P>0.5, by Kruskal–Wallis test. Based on the evaluation of side effects using the questionnaire, stinging/burning was less common (P=0.042, while blurred vision was more common (P=0.003, after switching to brinzolamide 1%/timolol 0.5%. Regarding patient preferences, 13 patients (31% preferred dorzolamide 1%/timolol 0.5%, 12 patients (29% preferred brinzolamide 1%/timolol 0.5%, and 17 patients (40% preferred neither.Conclusion: When switching from dorzolamide 1%/timolol 0.5% to brinzolamide 1

Analysis of glow curve of GaS{sub 0.5}Se{sub 0.5} single crystals

Energy Technology Data Exchange (ETDEWEB)

Isik, Mehmet, E-mail: mehmet.isik@atilim.edu.tr [Department of Electrical and Electronics Engineering, Atilim University, 06836 Ankara (Turkey); Delice, Serdar [Department of Physics, Middle East Technical University, 06800 Ankara (Turkey); Gasanly, Nizami [Department of Physics, Middle East Technical University, 06800 Ankara (Turkey); Virtual International Scientific Research Centre, Baku State University, 1148 Baku (Azerbaijan)

2015-12-15

Characterization of shallow trapping centers in GaS{sub 0.5}Se{sub 0.5} crystals grown by a Bridgman method was carried out in the present work using thermoluminescence (TL) measurements performed in the low temperature range of 10–300 K. The activation energies of the trapping centers were obtained under the light of results of various analysis methods. The presence of three trapping centers located at 6, 30 and 72 meV was revealed. The analysis of the experimental glow curve gave reasonable results under the model that assumes slow retrapping which states the order of kinetics as b=1. Heating rate dependence of the observed TL peaks was studied for the rates between 0.4 and 1.0 K/s. Distribution of the traps was also investigated using an experimental technique based on the thermal cleaning of centers giving emission at lower temperatures. The distributed levels with activation energies increasing from 6 to 136 meV were revealed by increasing the stopping temperature from 10 to 52 K. - Highlights: • TL measurements were performed in the 10–300 K range on GaS{sub 0.5}Se{sub 0.5} crystals. • Atomic composition ratio of the elements was found. • Three trapping centers located at 6, 30 and 72 meV were revealed. • Distribution of trapping centers was studied on as-grown crystal.

Exploring Pre-Service Teachers' Beliefs about Using Web 2.0 Technologies in K-12 Classroom

Science.gov (United States)

Sadaf, Ayesha; Newby, Timothy J.; Ertmer, Peggy A.

2012-01-01

This qualitative study explored pre-service teachers' behavioral, normative, and control beliefs regarding their intentions to use Web 2.0 technologies in their future classrooms. The Theory of Planned Behavior (TPB) was used as the theoretical framework (Ajzen, 1991) to understand these beliefs and pre-service teachers' intentions for why they…

Rights of patients required in a public service ombudsman

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Maristela Santini Martins

2015-07-01

Full Text Available Objective: analyzing the rights of patients required in a public service ombudsmen. Methods: an exploratory, descriptive study of documentary research. 109 complaint forms coming from the basic network were analyzed, related to 12 Basic Health Units located within the Southern Health Technical Supervision. Results: grouped into four categories of required rights: access to goods and services (62.4% being, access to specialized exams (28.7%, access to consultations (16.6%, referral to a specialist (5.7%, referral for urgent/emergency cases (1.3%, monitoring through home visits (7.6%, guaranteed medications (2.5%. Quality of health services (36.9% divided into: decent, considerate and respectful care (26.8%, guidance/clarification (9.6%, and public disclosure of government programs (0.6% and adequate infrastructure (0.6%. Conclusion: the rights that patients required are related to access, quality, treatment and adequate infrastructure.

Magnetic properties and magnetocaloric effect of MnFeP0.5Ge0.5-xSix compounds

International Nuclear Information System (INIS)

Song, L.; Wang, G.F.; Ou, Z.Q.; Haschaolu, O.; Tegus, O.; Brueck, E.; Buschow, K.H.J.

2009-01-01

We have studied the magnetic properties and magnetic-entropy changes of the MnFeP 0.5 Ge 0.5-x Si x compounds with x = 0.1, 0.2, 0.3, 0.4 and 0.45. X-ray diffraction shows that the compounds crystallize in the Fe 2 P-type hexagonal structure. The lattice parameter a and the Curie temperature decreases with increasing x. The maximal magnetic-entropy changes for x = 0.4 and 0.45 derived from the magnetization data are about 6.0 J/kg K and 5.8 J/kg K, respectively, for a field change from 0 to 1.5 T

12 CFR 563g.6 - Effective date.

Science.gov (United States)

2010-01-01

... 12 Banks and Banking 5 2010-01-01 2010-01-01 false Effective date. 563g.6 Section 563g.6 Banks and Banking OFFICE OF THRIFT SUPERVISION, DEPARTMENT OF THE TREASURY SECURITIES OFFERINGS § 563g.6 Effective date. (a) Except as provided for in paragraph (d) of this section, an offering circular filed by a...

12 CFR 528.6 - Loan application register.

Science.gov (United States)

2010-01-01

... 12 Banks and Banking 5 2010-01-01 2010-01-01 false Loan application register. 528.6 Section 528.6 Banks and Banking OFFICE OF THRIFT SUPERVISION, DEPARTMENT OF THE TREASURY NONDISCRIMINATION... Mortgage Disclosure Act Loan Application Registers with the Office of Thrift Supervision in accordance with...

Total and inclusive hadron production by e+e- annihilation at √S = 5.2, 6.5 and 29.0 GeV

International Nuclear Information System (INIS)

Patrick, J.F.

1982-07-01

Measurements are presented of R, the ratio of the total hadronic cross section to the cross section for mu pair production, and of the inclusive charged particle momentum distribution so sigma/dx for e + e - annihilation at center of mass energies of 5.2, 6.5, and 29.0 GeV. The ratio R is found to be approximately 3.9, consistent with quark-parton model expectations, at each of the three energies with an estimated systematic uncertainty of 6%. The inclusive cross sections show significant deviation from the scaling behavior predicted by the quark-parton model

Effect of 3 years of treatment with a dorzolamide/timolol (1%/0.5% combination on intraocular pressure

Directory of Open Access Journals (Sweden)

Takeda S

2014-09-01

Full Text Available Sakurako Takeda,1,2 Tatsuya Mimura,1 Masao Matsubara1,2 1Department of Ophthalmology, Tokyo Women’s Medical University Medical Center East, Tokyo, Japan; 2Department of Ophthalmology, Nippori Clinic, Medical Center East, Tokyo Women’s Medical University, Tokyo, Japan Purpose: We aimed to evaluate the effect on the intraocular pressure (IOP of a dorzolamide/timolol (1%/0.5% fixed combination (DTFC ophthalmic agent for 3 years.Participants: A total of 19 consecutive patients who had previously been treated with monotherapy or any combination of a beta-blocker, carbonic anhydrase inhibitor, or prostaglandin analog, for primary open-angle glaucoma (POAG (n=5 or normal tension glaucoma (N=14 were enrolled.Methods: Patients were switched to DTFC from their prior glaucoma therapy. The IOP was measured at intervals of 4–6 weeks for 3 years. Treatment failure was defined as an increase of IOP by ≥10% from baseline after switching to DTFC.Results: The average IOP decreased significantly from 14.1±2.9 mmHg at baseline to 12.2±2.2, 11.8±2.4, 12.1±2.5, 11.6±1.8, and 12.1±2.7 mmHg at 3, 6, 12, 24, and 36 months, respectively, after switching therapy (all P<0.05. The mean percent decrease of IOP was 12.0%±13.0%, 14.5%±14.2%, 12.2%±18.7%, 16.0%±12.8%, and 12.8%±15.2% at 3, 6, 12, 24, and 36 months, respectively, after switching. Univariate or multivariate analysis revealed the percent decrease of IOP was associated with the type of glaucoma (POAG at 3 and 12 months, and with the baseline IOP at 3, 12, 24, and 36 months. Kaplan–Meier analysis demonstrated that the percentage of patients who remained on treatment with DTFC was 94.7%, 94.7%, 84.2%, 78.9%, and 78.9% at 3, 6, 12, 24, and 36 months, respectively. Cox proportional hazards analysis showed that the type of glaucoma (POAG was associated with an increased risk of failure to control the IOP.Conclusion: The IOP-lowering effect of DTFC was demonstrated for 3 years in this

Lithium ion diffusion measurements on a garnet-type solid conductor Li6.6La3Zr1.6Ta0.4O12 by using a pulsed-gradient spin-echo NMR method.

Science.gov (United States)

Hayamizu, Kikuko; Matsuda, Yasuaki; Matsui, Masaki; Imanishi, Nobuyuki

2015-09-01

The garnet-type solid conductor Li7-xLa3Zr2-xTaxO12 is known to have high ionic conductivity. We synthesized a series of compositions of this conductor and found that cubic Li6.6La3Zr1.6Ta0.4O12 (LLZO-Ta) has a high ionic conductivity of 3.7×10(-4)Scm(-1) at room temperature. The (7)Li NMR spectrum of LLZO-Ta was composed of narrow and broad components, and the linewidth of the narrow component varied from 0.69kHz (300K) to 0.32kHz (400K). We carried out lithium ion diffusion measurements using pulsed-field spin-echo (PGSE) NMR spectroscopy and found that echo signals were observed at T≥313K with reasonable sensitivity. The lithium diffusion behavior was measured by varying the observation time and pulsed-field gradient (PFG) strength between 313 and 384K. We found that lithium diffusion depended significantly on the observation time and strength of the PFG, which is quite different from lithium ion diffusion in liquids. It was shown that lithium ion migration in the solid conductor was distributed widely in both time and space. Copyright © 2015 Elsevier Inc. All rights reserved.

Disk-type piezoelectric transformer of a Na0.5K0.5NbO3–CuNb2O6 lead-free ceramic for driving T5 fluorescent lamp

International Nuclear Information System (INIS)

Yang, Ming-Ru; Chu, Sheng-Yuan; Chan, I.-Hao; Yang, Song-Ling

2012-01-01

Highlights: ► CuNb 2 O 6 dopants were doped into NKN ceramics not only improved the density but also exhibited superior piezoelectric characteristic, temperature stability of resonance frequency. ► Lead-free NKN-01CN piezoelectric transformer was simplified as an equivalent circuit and analyzed using MATLAB. ► An 8W T5 fluorescent lamp was successfully driven by the NKN-01CN piezoelectric transformer. - Abstract: Lead-free (Na 0.5 K 0.5 )NbO 3 (NKN) ceramics doped with 1 mol% CuNb 2 O 6 (CN) ceramics were prepared using the conventional mixed oxide method, with a sintering temperature of 1075 °C. Microstructural analyses of the NKN–01CN ceramics were carried out and compared, using X-ray diffraction (XRD). NKN–01CN ceramics sintered at 1075 °C not only exhibited excellent ‘hard’ piezoelectric properties of k p = 40%, k t = 45%, k 33 = 57%, a ferroelectric property of E c = 23 kV/cm, and an extraordinarily high mechanical quality factor (Q m ) of 1933 but also showed excellent stability with temperature (TCF = −154 ppm/°C). The piezoelectric transformer was simplified, using an equivalent circuit, and analyzed, using MATLAB; the simulation data agreed well with the experimental results. An efficiency of 95.7% was achieved for the NKN–01CN piezoelectric transformer with load resistance of 20 kΩ. An 8 W T5 fluorescent lamp was successfully driven by the NKN–01CN piezoelectric transformer.

Stability and oxygen transport property of La0.8Sr0.2Cr0.5Fe0.5O3 -δ

DEFF Research Database (Denmark)

He, Wei; Huang, Hua; Chen, Ming

2014-01-01

vacancies in the lattice. LSCrF powder exposed to flowing concentrated hydrogen for 30 h was found to decompose partially. The decomposition oxygen partial pressure of LSCrF at 950 °C was estimated to be 6.3 × 10- 28 atm from thermodynamic calculations. The stability of LSCrF under an oxygen chemical......The stability of La0.8Sr0.2Cr0.5Fe 0.5O3 -δ (LSCrF) in reducing atmosphere was investigated by examining the extent of its reaction with hydrogen at elevated temperature. LSCrF powder exposed to diluted hydrogen was found to loss a weight of only ~ 0.5%, corresponding to the formation of oxygen...... potential gradient was also examined by exposing a disk-shaped dense sample to air at one side and to reducing atmosphere (CO) at the other side at elevated temperatures. A thin, porous layer was found to form on the CO side surface. An oxygen permeation flux of 2.5 × 10- 7 mol cm- 2 s- 1 was observed...

ZnO nanorods/ZnS·(1,6-hexanediamine)(0.5) hybrid nanoplates hierarchical heteroarchitecture with improved electrochemical catalytic properties for hydrazine.

Science.gov (United States)

Wu, Zhengcui; Wu, Yaqin; Pei, Tonghui; Wang, Huan; Geng, Baoyou

2014-03-07

Novel hierarchical heteronanostructures of ZnO nanorods/ZnS·(HDA)0.5 (HDA = 1,6-hexanediamine) hybrid nanoplates on a zinc substrate are successfully synthesized on a large scale by combining hydrothermal growth (for ZnO nanorods) and liquid chemical conversion (for ZnS·(HDA)0.5 nanoplates) techniques. The formation of ZnS·(HDA)0.5 hybrid nanoplates branches takes advantage of the preferential binding of 1,6-hexanediamine on specific facets of ZnS, which makes the thickening rate much lower than the lateral growth rate. The ZnS·(HDA)0.5 hybrid nanoplates have a layered structure with 1,6-hexanediamine inserted into interlayers of wurtzite ZnS through the bonding of nitrogen. The number density and thickness of the secondary ZnS·(HDA)0.5 nanoplates can be conveniently engineered by variation of the sulfur source and straightforward adjustment of reactant concentrations such as 1,6-hexanediamine and the sulfur source. The fabricated ZnO/ZnS·(HDA)0.5 heteronanostructures show improved electrochemical catalytic properties for hydrazine compared with the primary ZnO nanorods. Due to its simplicity and efficiency, this approach could be similarly used to fabricate varieties of hybrid heterostructures made of materials with an intrinsic large lattice mismatch.

Solvothermal synthesis and characterisation of new one-dimensional indium and gallium sulphides: [C1N4H26]0.5[InS2] and [C1N4H26]0.5[GaS2

International Nuclear Information System (INIS)

Vaqueiro, Paz

2006-01-01

Two new main group metal sulphides, [C 1 N 4 H 26 ] 0.5 [InS 2 ] (1) and [C 1 N 4 H 26 ] 0.5 [GaS 2 ] (2) have been prepared solvothermally in the presence of 1,4-bis(3-aminopropyl)piperazine and their crystal structures determined by single-crystal X-ray diffraction. Both compounds are isostructural and crystallise in the monoclinic space group P2 1 /n (Z=4), with a=6.5628(5), b=11.2008(9), c=12.6611(9) A and β=94.410(4) o (wR=0.035) for compound (1) and a=6.1094(5), b=11.2469(9), c=12.7064(10) A and β=94.313(4) o (wR=0.021) for compound (2). The structure of [C 1 N 4 H 26 ] 0.5 [MS 2 ] (M=In,Ga) consists of one-dimensional [MS 2 ] - chains which run parallel to the crystallographic a axis and are separated by diprotonated amine molecules. These materials represent the first example of solvothermally prepared one-dimensional gallium and indium sulphides. -- Graphical abstract: [C 1 N 4 H 26 ] 0.5 [InS 2 ] and [C 1 N 4 H 26 ] 0.5 [GaS 2 ], prepared under solvothermal conditions, consist of one-dimensional [MS 2 ] - chains separated by diprotonated 1,4-bis(3-aminopropyl)piperazine molecules

12 CFR 528.2 - Nondiscrimination in lending and other services.

Science.gov (United States)

2010-01-01

... 12 Banks and Banking 5 2010-01-01 2010-01-01 false Nondiscrimination in lending and other services. 528.2 Section 528.2 Banks and Banking OFFICE OF THRIFT SUPERVISION, DEPARTMENT OF THE TREASURY NONDISCRIMINATION REQUIREMENTS § 528.2 Nondiscrimination in lending and other services. (a) No savings association...

Interplay between charge and antiferromagnetic ordering in Bi0.6-xPrxCa0.4MnO3 (0≤x≤0.6) perovskite manganite

International Nuclear Information System (INIS)

Yadav, Kamlesh; Singh, H.K.; Varma, G.D.

2012-01-01

Structure, magnetic and transport properties of polycrystalline Bi 0.6-x Pr x Ca 0.4 MnO 3 (x=0.0, 0.1, 0.2, 0.3, 0.4, 0.5 and 0.6) have been studied. Systematic substitution of Pr at Bi site induces an interesting interplay between the charge ordering and antiferromagnetism. The charge ordering temperature (T CO ) decreases with increasing x. The antiferromagnetic (AFM) ordering temperature (T N ) increases sharply at both the extremes but remains nearly constant from x=0.2 to 0.4. At temperatures lower than T N a transition to the glassy state is observed. The nature of this glass like state appears to be controlled by the Pr content, and at lower values of x this is akin to a spin glass, while at higher x it has a characteristic of cluster glass. The Pr doping also leads to enhancement in the magnetic moment. In the present work it has been proposed that the local lattice distortion induced due to size mismatch between the A-site cations and 6s 2 character of Bi 3+ lone pair electron is responsible for the observed magnetic and electrical properties.

μSR in oxygen deficient YBa2Cu3Ox (6.5≤x≤7.0)

International Nuclear Information System (INIS)

Puempin, B.; Keller, H.; Kuendig, W.; Savic, I.M.; Schneider, J.W.; Simmler, H.; Zimmermann, P.; Kaldis, E.; Rusiecki, S.; Rossel, C.

1991-01-01

A systematic μSR study of the local magnetic field distribution in a series of oxygen deficient YBa 2 Cu 3 O x samples with 6.5≤x≤7.0 is reported. Special attention was given to perform the experiments under the same conditions, so that the oxygen content of the measured samples was the only parameter varied. The behavior of the depolarization rate σ as a function of the oxygen content x was found to have strong similarities with the behavior of the critical temperature Tc as a function of x. In particular, two step-like increases of σ were observed above x=6.7 and 6.9. The temperature dependence of the normalized depolarization rate σ(T)/σ(0) is well described by the two-fluid model for x≥6.781(1) and clearly deviates from this behavior for x≤6.704(1). Our results are compared to those obtained by other groups. (orig.)

12 CFR 725.5 - Capital stock.

Science.gov (United States)

2010-01-01

... 12 Banks and Banking 6 2010-01-01 2010-01-01 false Capital stock. 725.5 Section 725.5 Banks and Banking NATIONAL CREDIT UNION ADMINISTRATION REGULATIONS AFFECTING CREDIT UNIONS NATIONAL CREDIT UNION ADMINISTRATION CENTRAL LIQUIDITY FACILITY § 725.5 Capital stock. (a) The capital stock of the Facility is divided...

Photoassociation spectroscopy of 87Rb2 (5s1/2+5p1/2)0u+ long-range molecular states: Coupling with the (5s1/2+5p3/2)0u+ series analyzed using the Lu-Fano approach

International Nuclear Information System (INIS)

Jelassi, H.; Viaris de Lesegno, B.; Pruvost, L.

2006-01-01

We report on photoassociation of cold 87 Rb atoms providing the spectroscopy of (5s 1/2 +5p 1/2 )0 u + long-range molecular states, in the energy range of [-12.5, -0.7 cm -1 ] below the dissociation limit. A Lu-Fano approach coupled to the LeRoy-Bernstein formula is used to analyze the data. The Lu-Fano graph exhibits the coupling of the molecular series with the (5s 1/2 +5p 3/2 )0 u + one, which is due to spin effects in the molecule. A two-channel model involving an improved LeRoy-Bernstein formula allows us to characterize the molecular series, to localize (5s 1/2 +5p 3/2 )0 u + levels, to evaluate the coupling, and to predict the energy and width of the first predissociated level of (5s 1/2 +5p 3/2 )0 u + series. An experimental spectrum confirms the prediction

Microstructure, mechanical property and in vitro biocorrosion behavior of single-phase biodegradable Mg–1.5Zn–0.6Zr alloy

Directory of Open Access Journals (Sweden)

Tao Li

2014-06-01

Full Text Available The microstructure, mechanical property, and in vitro biocorrosion behavior of as-cast single-phase biodegradable Mg–1.5Zn–0.6Zr alloy were investigated and compared with a commercial as-cast AZ91D alloy. The results show that the Mg–1.5Zn–0.6Zr alloy had a single-phase solid solution structure, with an average grain size of 34.7 ± 13.1 μm. The alloy exhibited ultimate tensile strength of 168 ± 2.0 MPa, yield strength of 83 ± 0.6 MPa, and elongation of 9.1 ± 0.6%. Immersion tests and electrochemical measurements reveal that the alloy displayed lower biocorrosion rate and more uniform corrosion mode than AZ91D in Hank's solution. The elimination of intensive galvanic corrosion reactions and the formation of a much more compact and uniform corrosion film mainly account for the better biocorrosion properties of the Mg–1.5Zn–0.6Zr alloy than AZ91D.

Hadron masses and decay constants with Wilson quarks at β=5.85 and 6.0

International Nuclear Information System (INIS)

Anon.

1996-01-01

We present results of a high statistics calculation of hadron masses and meson decay constants in the quenched approximation to lattice QCD with Wilson quarks at β= 5.85 and 6.0 on 24 3 x54 lattices. We analyze the data paying attention in particular to the systematic errors due to the choice of fitting range and due to the contamination from excited states. We find that the systematic errors for the hadron masses with quarks lighter than the strange quark amount to 1 to 2 times the statistical errors. When the lattice scale is fixed from the ρ meson mass, the masses of the Ω - baryon and the φ meson at two β close-quote s agree with experiment within about one standard deviation. On the other hand, the central value of the nucleon mass at β=6.0 (5.85) is larger than its experimental value by about 15% (20%) and that of the Δ mass by about 15% (4%): Even when the systematic errors are included, the baryon masses at β=6.0 do not agree with experiment. Vector meson decay constants at two values of β agree well with each other and are consistent with experiment for a wide range of the quark mass, when we use current renormalization constants determined nonperturbatively by numerical simulations. The pion decay constant agrees with experiment albeit with large errors. Results for the masses of excited states of the ρ meson and the nucleon are also presented. copyright 1996 The American Physical Society

Enhancement in electrical and magnetic properties with Ti-doping in Bi0.5La0.5Fe0.5Mn0.5O3

Science.gov (United States)

Singh, Rahul; Gupta, Prince Kumar; Kumar, Shiv; Joshi, Amish G.; Ghosh, A. K.; Patil, S.; Chatterjee, Sandip

2017-04-01

In this investigation, we have synthesized Bi0.5La0.5Fe0.5Mn0.5-xTixO3 (where x = 0 and 0.05) samples. The Rietveld refinement of X-ray diffraction (XRD) patterns shows that the systems crystallize in the orthorhombic phase with the Pnma space group. The observed Raman modes support the XRD results. The appearance of prominent A1-3 and weak E-2 modes in Bi0.5La0.5Fe0.5Mn0.45Ti0.05O3 indicates the presence of chemically more active Bi-O covalent bonds. Ferromagnetism of Bi0.5La0.5Fe0.5Mn0.5O3 is enhanced by Ti doping at the Mn-site, indicating that these particular samples might be interesting for device applications.

Microstructure, mechanical property and in vitro biocorrosion behavior of single-phase biodegradable Mg–1.5Zn–0.6Zr alloy

OpenAIRE

Tao Li; Yong He; Hailong Zhang; Xitao Wang

2014-01-01

The microstructure, mechanical property, and in vitro biocorrosion behavior of as-cast single-phase biodegradable Mg–1.5Zn–0.6Zr alloy were investigated and compared with a commercial as-cast AZ91D alloy. The results show that the Mg–1.5Zn–0.6Zr alloy had a single-phase solid solution structure, with an average grain size of 34.7 ± 13.1 μm. The alloy exhibited ultimate tensile strength of 168 ± 2.0 MPa, yield strength of 83 ± 0.6 MPa, and elongation of 9.1 ± 0.6%. Immersion tests and electroc...

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

4-Nitrophenol–2,4,6-triamino-1,3,5-triazine–water (2/1/1

Directory of Open Access Journals (Sweden)

N. Kanagathara

2012-07-01

Full Text Available In the title adduct, 2C6H5NO3·C3H6N6·H2O, the melamine and the two independent nitrophenol molecules are essentially planar, with maximum deviations of 0.0294 (10, 0.0706 (12 and 0.0742 (12 Å, respectively. In the crystal, N—H...N, O—H...N, N—H...O and O—H...O hydrogen bonds link the components into a three-dimensional network. In addition, weak π–π interactions [centroid–centroid distances = 3.728 (3 and 3.749 (3 Å] are observed.

12 CFR 5.65 - Restrictions on undercapitalized institutions.

Science.gov (United States)

2010-01-01

... 12 Banks and Banking 1 2010-01-01 2010-01-01 false Restrictions on undercapitalized institutions. 5.65 Section 5.65 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY RULES... defined in 12 CFR part 6. ...

Synthesis and luminescent properties of Sr{sub 2}Gd{sub 6.8}Eu{sub 1.2}Si{sub 6(1−x)}P{sub 6x}O{sub 26} oxyapatites

Energy Technology Data Exchange (ETDEWEB)

Ishchenko, A.V., E-mail: a-v-i@mail.ru [Ural Federal University, 620002 Ekaterinburg (Russian Federation); Zuev, M.G. [Ural Federal University, 620002 Ekaterinburg (Russian Federation); Institute of Solid State Chemistry, Ural Branch of the Russian Academy of Sciences, 620990 Ekaterinburg (Russian Federation); Vasin, A.A. [Institute of Solid State Chemistry, Ural Branch of the Russian Academy of Sciences, 620990 Ekaterinburg (Russian Federation); Yagodin, V.V.; Viktorov, L.V.; Shulgin, B.V. [Ural Federal University, 620002 Ekaterinburg (Russian Federation)

2016-01-15

The solid solutions Sr{sub 2}Gd{sub 6.8}Eu{sub 1.2}Si{sub 6(1−x)}P{sub 6x}O{sub 26−δ} (where x=0–0.15 and δ is oxygen nonstoichiometry) were synthesized. The structural properties of the crystal lattice of the solid solutions and the peculiarities of Eu{sup 3+} and P{sup 5+} dopants substitution for matrix ions have been considered. The photo-, X-ray and pulsed cathode luminescence properties have been studied. It has been found that substitution of (SiO{sub 4}){sup 4−} by (PO{sub 4}){sup 3−} tetrahedron in Eu{sup 3+}-doped oxyapatites does not bring significant changes to bands structure Eu{sup 3+} in luminescence spectra under different excitation (UV, X-ray, pulse cathode beam). However, the increase of P{sup 5+} concentration in Sr{sub 2}Gd{sub 6.8}Eu{sub 1.2}Si{sub 6(1−x)}P{sub 6x}O{sub 26–δ} compounds leads to a decrease of integral intensity of Eu{sup 3+} luminescence bands due to local environment symmetry modifications and covalency degree changes. Two nonequivalent optical Eu{sup 3+} centers have been found. These compounds are of interest for efficient X-ray phosphors, display devices and LED engineering material creation. - Highlights: • The luminescence properties were studied upon UV, X-ray and pulse cathode beam. • P{sup 5+} doping of Sr{sub 2}Gd{sub 6.8}Eu{sub 1.2}Si{sub 6}O{sub 26} leads to luminescence intensity reduction. • At least two types of optical centers formed by Eu{sup 3+} ions were found. • The structural features of Sr{sub 2}Gd{sub 6.8}Eu{sub 1.2}Si{sub 6(1−x)}P{sub 6x}O{sub 26} were reported. • Partial replacement of Si by P does not change the Sr{sub 2}Gd{sub 6.8}Eu{sub 1.2}Si{sub 6}O{sub 26} structure.

12 CFR 564.6 - Professional association membership; competency.

Science.gov (United States)

2010-01-01

... 12 Banks and Banking 5 2010-01-01 2010-01-01 false Professional association membership; competency. 564.6 Section 564.6 Banks and Banking OFFICE OF THRIFT SUPERVISION, DEPARTMENT OF THE TREASURY APPRAISALS § 564.6 Professional association membership; competency. (a) Membership in appraisal organizations...

Total photoabsorption cross section on nuclei measured in energy range 0.5-2.6 GeV

International Nuclear Information System (INIS)

Mirazita, M.

1998-03-01

The total photoabsorption cross section on several nuclei has been measured in the energy range 0.5 - 2.6 GeV. Nuclear data show a significant reduction of the absorption strength with respect to the free nucleon case suggesting a shadowing effect at low energies

Measurement of the /sup 12/C(n,γ0)/sup 13/C cross section in the giant dipole resonance region

International Nuclear Information System (INIS)

August, R.A.; Weller, H.R.; Tilley, D.R.

1987-01-01

The /sup 12/C(n,γ 0 ) /sup 13/C excitation function at 90 0 has been measured for neutron energies from 6.5 to 18.5 MeV. Whereas previous measurements disagreed at the lower energies with a direct-semidirect capture calculation based on /sup 12/C(p,γ 0 ) /sup 13/N data, the present results, especially when the uncertainty in absolute cross section is considered, indicate reasonable qualitative agreement with the calculation

Piezoelectric properties of lead-free submicron-structured (Bi0.5Na0.5)0.94Ba0.06TiO3 ceramics from nanopowders

International Nuclear Information System (INIS)

Pardo, Lorena; García, Alvaro; Brebøl, Klaus; Mercadelli, Elisa; Galassi, Carmen

2010-01-01

Submicron-structured (Bi 0.5 Na 0.5 ) 0.94 Ba 0.06 TiO 3 (BNBT6) ceramics were obtained from nanometric powder synthesized by sol–gel auto-combustion at 500 °C. Hot-pressing at low temperatures and a combination of this with recrystallization, still moderate in order to reduce the loss of volatile elements, have been tested. Material properties, including all losses, were determined at the resonances of thin discs using Alemany et al software. Ceramics hot-pressed at 700–800 °C for 2 h have a pseudo-cubic structure, a grain size of a few hundred nanometers and are homogeneous. Both their crystal structure and the lack of sintering prevent their poling. For ceramics hot-pressed at 950 °C for 3 h, Bi or Bi 0.5 Na 0.5 loss, together with low piezoelectric properties (d 33 = 60 pC N −1 , k p = 8.3% and k t = 9.5%), was observed. Recrystallization at 1000 °C-1 h of ceramics hot-pressed at 700 and 800 °C for 2 h keeps the submicron structure, reduces porosity and prevents off-stoichiometry. Mechanical and piezoelectric losses are also reduced and coupling factors increased (k p = 24.6%, k t = 36.4%). The best piezoelectric coefficient obtained in these ceramics (d 33 = 143 pC N −1 ) is comparable with those reported for coarse-grained ceramics

RELATIVISTIC (E > 0.6, > 2.0, AND > 4.0 MeV) ELECTRON ACCELERATION AT GEOSYNCHRONOUS ORBIT DURING HIGH-INTENSITY, LONG-DURATION, CONTINUOUS AE ACTIVITY (HILDCAA) EVENTS

International Nuclear Information System (INIS)

Hajra, Rajkumar; Echer, Ezequiel; Gonzalez, Walter D.; Tsurutani, Bruce T.; Santolik, Ondrej

2015-01-01

Radiation-belt relativistic (E > 0.6, > 2.0, and > 4.0 MeV) electron acceleration is studied for solar cycle 23 (1995-2008). High-intensity, long-duration, continuous AE activity (HILDCAA) events are considered as the basis of the analyses. All of the 35 HILDCAA events under study were found to be characterized by flux enhancements of magnetospheric relativistic electrons of all three energies compared to the pre-event flux levels. For the E > 2.0 MeV electron fluxes, enhancement of >50% occurred during 100% of HILDCAAs. Cluster-4 passes were examined for electromagnetic chorus waves in the 5 < L < 10 and 0 < MLT < 12 region when wave data were available. Fully 100% of these HILDCAA cases were associated with enhanced whistler-mode chorus waves. The enhancements of E > 0.6, > 2.0, and > 4.0 MeV electrons occurred ∼1.0 day, ∼1.5 days, and ∼2.5 days after the statistical HILDCAA onset, respectively. The statistical acceleration rates for the three energy ranges were ∼1.8 × 10 5 , 2.2 × 10 3 , and 1.0 × 10 1 cm –2 s –1 sr –1 d –1 , respectively. The relativistic electron-decay timescales were determined to be ∼7.7, 5.5, and 4.0 days for the three energy ranges, respectively. The HILDCAAs were divided into short-duration (D ≤ 3 days) and long-duration (D > 3 days) events to study the dependence of relativistic electron variation on HILDCAA duration. For long-duration events, the flux enhancements during HILDCAAs with respect to pre-event fluxes were ∼290%, 520%, and 82% for E > 0.6, > 2.0, and > 4.0 MeV electrons, respectively. The enhancements were ∼250%, 400%, and 27% respectively, for short-duration events. The results are discussed with respect to the current understanding of radiation-belt dynamics

Dielectric and Ferroelectric Properties of SrTiO3-Bi0.5Na0.5TiO3-BaAl0.5Nb0.5O3 Lead-Free Ceramics for High-Energy-Storage Applications.

Science.gov (United States)

Yan, Fei; Yang, Haibo; Lin, Ying; Wang, Tong

2017-11-06

Pulsed capacitors require high-recoverable energy-storage density (W rec ) and high energy-storage efficiency (η), which can be realized through the selection and adjustment of the composition. In this work, (1 - x)SrTiO 3 -x(0.95Bi 0.5 Na 0.5 TiO 3 -0.05BaAl 0.5 Nb 0.5 O 3 ) [(1 - x)ST-x(BNT-BAN)] ceramics were successfully prepared via the pressureless solid-state reaction method. The dielectric constant increases gradually with the introduction of BNT-BAN and obtains a maximum value of 3430 with the composition of 0.4ST-0.6(BNT-BAN) at 100 Hz, which is 10.39 times higher than that of the pure ST sample (∼330). Dispersive relaxor behaviors and ferroelectric performances can be enhanced with the introduction of BNT-BAN. The composition of 0.5ST-0.5(BNT-BAN) exhibits a high W rec of 1.89 J/cm 3 as well as a high η of 77%. Therefore, the (1 - x)ST-x(BNT-BAN) systems are candidate materials for pulsed capacitor applications.

Reticular V2O5·0.6H2O Xerogel as Cathode for Rechargeable Potassium Ion Batteries.

Science.gov (United States)

Tian, Bingbing; Tang, Wei; Su, Chenliang; Li, Ying

2018-01-10

Potassium ion batteries (KIBs), because of their low price, may exhibit advantages over lithium ion batteries as potential candidates for large-scale energy storage systems. However, owing to the large ionic radii of K-ions, it is challenging to find a suitable intercalation host for KIBs and thus the rechargeable KIB electrode materials are still largely unexplored. In this work, a reticular V 2 O 5 ·0.6H 2 O xerogel was synthesized via a hydrothermal process as a cathode material for rechargeable KIBs. Compared with the orthorhombic crystalline V 2 O 5 , the hydrated vanadium pentoxide (V 2 O 5 ·0.6H 2 O) exhibits the ability of accommodating larger alkali metal ions of K + because of the enlarged layer space by hosting structural H 2 O molecules in the interlayer. By intercalation of H 2 O into the V 2 O 5 layers, its potassium electrochemical activity is significantly improved. It exhibits an initial discharge capacity of ∼224.4 mA h g -1 and a discharge capacity of ∼103.5 mA h g -1 even after 500 discharge/charge cycles at a current density of 50 mA g -1 , which is much higher than that of the V 2 O 5 electrode without structural water. Meanwhile, X-ray diffraction and X-ray photoelectron spectroscopy combined with energy dispersive spectroscopy techniques are carried out to investigate the potassiation/depotassiation process of the V 2 O 5 ·0.6H 2 O electrodes, which confirmed the potassium intercalation storage mechanisms of this hydrated material. The results demonstrate that the interlayer-spacing-enlarged V 2 O 5 ·0.6H 2 O is a promising cathode candidate for KIBs.

Bi{sub 1−x}Nb{sub x}O{sub 1.5+x} (x=0.0625, 0.12) fast ion conductors: Structures, stability and oxide ion migration pathways

Energy Technology Data Exchange (ETDEWEB)

Tate, Matthew L. [Department of Chemistry, Durham University, Science Site, South Road, Durham DH1 3LE (United Kingdom); Australian Nuclear Science and Technology Organisation, Lucas Heights 2234, NSW (Australia); Hack, Jennifer [Department of Chemistry, Durham University, Science Site, South Road, Durham DH1 3LE (United Kingdom); Institut Laue-Langevin, Grenoble (France); Kuang, Xiaojun [Department of Chemistry, Durham University, Science Site, South Road, Durham DH1 3LE (United Kingdom); McIntyre, Garry J. [Australian Nuclear Science and Technology Organisation, Lucas Heights 2234, NSW (Australia); Withers, Ray L. [Research School of Chemistry, Australian National University, Canberra, ACT (Australia); Johnson, Mark R. [Institut Laue-Langevin, Grenoble (France); Radosavljevic Evans, Ivana, E-mail: ivana.radosavljevic@durham.ac.uk [Department of Chemistry, Durham University, Science Site, South Road, Durham DH1 3LE (United Kingdom); Australian Nuclear Science and Technology Organisation, Lucas Heights 2234, NSW (Australia)

2015-05-15

A combined experimental and computational study of Bi{sub 1−x}Nb{sub x}O{sub 1.5+x} (x=0.0625 and 0.12) has been carried out using laboratory X-ray, neutron and electron diffraction, impedance measurements and ab-initio molecular dynamics. We demonstrate that Bi{sub 0.9375}Nb{sub 0.0625}O{sub 1.5625}, previously reported to adopt a cubic fluorite-type superstructure, can form two different polymorphs depending on the synthetic method: a metastable cubic phase is produced by quenching; while slower cooling yields a stable material with a tetragonal √2×√2×1 superstructure, which undergoes a reversible phase transition into the cubic form at ~680 °C on subsequent reheating. Neutron diffraction reveals that the tetragonal superstructure arises mainly from ordering in the oxygen sublattice, with Bi and Nb remaining disordered, although structured diffuse scattering observed in the electron diffraction patterns suggests a degree of short-range ordering. Both materials are oxide ion conductors. On thermal cycling, Bi{sub 0.88}Nb{sub 0.12}O{sub 1.62} exhibits a decrease in conductivity of approximately an order of magnitude due to partial transformation into the tetragonal phase, but still exhibits conductivity comparable to yttria-stabilised zirconia (YSZ). Ab-initio molecular dynamics simulations performed on Bi{sub 0.9375}Nb{sub 0.0625}O{sub 1.5625} show that oxide ion diffusion occurs by O{sup 2−} jumps between edge- and corner-sharing OM{sub 4} groups (M=Bi, Nb) via tetrahedral □M{sub 4} and octahedral □M{sub 6} vacancies. - Graphical abstract: Oxide ion migration in tetragonal Bi{sub 0.9375}Nb{sub 0.0625}O{sub 1.5625} occurs by O{sup 2−} jumps between edge- and corner-sharing OM{sub 4} groups (M=Bi, Nb) via tetrahedral M{sub 4} and octahedral M{sub 6} vacancies. - Highlights: • Bi{sub 0.9375}Nb{sub 0.0625}O{sub 1.5625} adopts a tetragonal √2×√2×1 fluorite superstructure. • Superstructure is due to ordering in the O-sublattice, with Bi

Total photoabsorption cross section on nuclei measured in energy range 0.5-2.6 GeV; Misura della sezione d`urto di fotoassorbimento tra 0.5 e 2.6 GeV su nuclei ed analisi dei dati

Energy Technology Data Exchange (ETDEWEB)

Mirazita, M. [INFN, Laboratori Nazionali di Frascati, Rome (Italy)

1998-03-01

The total photoabsorption cross section on several nuclei has been measured in the energy range 0.5 - 2.6 GeV. Nuclear data show a significant reduction of the absorption strength with respect to the free nucleon case suggesting a shadowing effect at low energies.

12 CFR 563f.6 - General exemption.

Science.gov (United States)

2010-01-01

... 12 Banks and Banking 5 2010-01-01 2010-01-01 false General exemption. 563f.6 Section 563f.6 Banks and Banking OFFICE OF THRIFT SUPERVISION, DEPARTMENT OF THE TREASURY MANAGEMENT OFFICIAL INTERLOCKS... controlled or managed by persons who are members of a minority group, or women; (3) Is a depository...

Service life of 1-W, 0.985-μm solitary heterolasers

International Nuclear Information System (INIS)

Kochetkov, A A; Konyaev, V P

2001-01-01

The service life of solitary heterolasers at a temperature of 50 0 C (P = 1W, λ = 0.98 - 0.99 μm) is studied. The maximum service life of heterolasers under such working conditions is 60000 hours for an average pumping current 1.5 A. (lasers and amplifiers)

12 CFR 722.5 - Appraiser independence.

Science.gov (United States)

2010-01-01

... 12 Banks and Banking 6 2010-01-01 2010-01-01 false Appraiser independence. 722.5 Section 722.5 Banks and Banking NATIONAL CREDIT UNION ADMINISTRATION REGULATIONS AFFECTING CREDIT UNIONS APPRAISALS... interest, financial or otherwise, in the property. If the only qualified persons available to perform an...

Phobos - Spectrophotometry between 0.3 and 0.6 micron and IR-radiometry

Science.gov (United States)

Ksanfomality, L.; Murchie, S.; Britt, D.; Fisher, P.; Duxbury, T.

1991-01-01

A 0.3 - 0.6 micron UV-visible spectrophotometer and a 5 - 50 micron radiometer in the KRFM experiment on Phobos 2 measured two groundtracks in the equatorial region of Phobos. Preliminary results indicate that three surface units can be recognized on the basis of differing UV-visible spectral reflectance properties. One of the units is most comparable spectrally to optically darkened mafic material, and a second is comparable either to anhydrous carbonaceous chondrite or to blackened mafic material. Spectral properties of the third unit do not resemble those of known meteorite types. Brightness temperatures measured by the radiometer are consistent with a typical surface thermal inertia of 1 - 3 x 10 to the -3 cal/(sq cm deg s exp 1/2), as suggested by previous investigations, implying a lunar-like regolith texture. At least one area of possibly higher thermal inertia has been tentatively identified, where a large degraded crater is crossed by several grooves. These results indicate significant lateral heterogeneity in the optical and textural properties of Phobos' surface.

The valence state of uranium in K{sub 6}Cu{sub 12}U{sub 2}S{sub 15}

Energy Technology Data Exchange (ETDEWEB)

Schilder, H; Speldrich, M; Lueken, H; Sutorik, A C; Kanatzidis, M G

2004-07-14

The paramagnetic behaviour of K{sub 6}Cu{sub 12}U{sub 2}S{sub 15} has been analysed, regarding copper as diamagnetic (Cu{sup +}), sulfur as mixed-valent S{sup 2-}/S{sup -} with magnetically silent delocalized S{sup -} holes in the valence band, and the actinide as either U{sup 5+}[5f{sup 1}] or U{sup 4+}[5f{sup 2}] in trigonally distorted octahedral surrounding (pseudosymmetry 3-bar) of sulfur. Fitting procedures have been carried out, accounting for spin-orbit coupling, ligand-field potential (parameters B{sup k}{sub q}), interelectronic repulsion (for U{sup 4+}[5f{sup 2}]), cooperative magnetic effects (molecular field parameter {lambda}), and applied magnetic field. Keeping the ratios B{sup 4}{sub 3}/B{sup 4}{sub 0}, B{sup 6}{sub 3}/B{sup 6}{sub 0}, B{sup 6}{sub 6}/B{sup 6}{sub 0} on their point charge electrostatic values with respect to the sulfur ligands, the three axial parameters B{sup k}{sub 0} (k=2,4,6) and {lambda} were refined. Agreement between measured and calculated susceptibility data was obtained for U{sup 5+} with B{sup k}{sub 0} values expected for octahedral surrounding and {lambda}<0 speaking for antiferromagnetic interactions. The U{sup 4+} model does yield a fit of comparable quality, but gives B{sup k}{sub 0} values that are unreasonable with respect to sign and magnitude. To conclude, on the basis of the magnetic properties the title compound is a 5f{sup 1} system corresponding to the elements formal charges (K{sup +}){sub 6}(Cu{sup +}){sub 12}(U{sup 5+}){sub 2}(S{sup 2-}){sub 13}(S{sup -}){sub 2}.

Comparative study on microstructures and mechanical properties of the heat-treated Al–5.0Cu–0.6Mn–xFe alloys prepared by gravity die casting and squeeze casting

International Nuclear Information System (INIS)

Lin, Bo; Zhang, WeiWen; Lou, ZhaoHui; Zhang, DaTong; Li, YuanYuan

2014-01-01

Highlights: • Only two kind Fe-rich intermetallics are found in the heat-treated Al–5.0Cu–0.6Mn–xFe alloys. • Squeeze cast Al–5.0Cu–0.6Mn alloys containing 1.5% Fe have desirable mechanical properties. • The difference between gravity die cast and squeeze cast Al–5.0Cu–0.6Mn–xFe alloys. - Abstract: The Al–5.0 wt% Cu–0.6 wt% Mn alloys with different Fe contents were prepared by gravity die casting and squeeze casting. The difference in microstructures and mechanical properties of the T5 heat-treated alloys was examined by tensile test, optical microscopy, deep etching technique, scanning electron microscope and electron probe micro-analyzer. The results show that both β-Fe and α (CuFe) are observed in T5 heat-treated gravity die cast alloy and only α (CuFe) appears in the squeeze cast alloy when the Fe content is 0.5 wt%. When the Fe content is more than 1.0 wt%, the main Fe-rich intermetallics is α (CuFe) in both squeeze cast and gravity die cast alloys. The mechanical properties of both the gravity die cast and squeeze cast alloys decrease gradually with the increase of Fe content due to the decreased volume fraction of precipitation particles, the increased volume fraction of Fe-rich intermetallics and the increased size of α (Al) dendrites. The squeeze cast alloys with different Fe contents have superior mechanical properties compared to the gravity die cast alloys, which is mainly attributed to the reduction of porosity and refinement of Fe-rich intermetallics and α (Al) dendrite. In particularly, the elongation of the squeeze cast alloys is less sensitive to the Fe content than that of the gravity die cast alloys. An elongation level of 13.7% is obtained in squeeze cast alloy even when the Fe content is as high as 1.5%, while that of the gravity die cast alloy is only 5.3%

High temperature drop calorimetric studies on La6UO12 and Nd6UO12

International Nuclear Information System (INIS)

Babu, R.; Senapati, A.; Rao, G.J.; Venkata Krishnan, R.; Ananthasivan, K.; Nagarajan, K.

2014-01-01

Rare earth elements produced in the reactor during irradiation can interact with the fuel. Under transient conditions, compounds of formula, RE 6 UO 12 with rhombohedral crystal structure are expected to be formed. Hence, thermodynamic properties of these compounds are useful in interpreting the behaviour of fuels during irradiation. Thermal expansion and heat capacities by DSC have been reported for La 6 UO 12 and Nd 6 UO 12 . There are no experimentally measured values of enthalpy. Hence, measurements on enthalpy increments of La 6 UO 12 and Nd 6 UO 12 were carried out for the first time by inverse drop calorimetry in the temperature range 534-1738 K and computed the thermodynamic functions

Electromagnetic attenuation analysis of Ni{sub 0.4}Zn{sub 0.6}Fe{sub 2O4} obtained by citrate precursor method; Analise da atenuacao de radiacao eletromagnetica de Ni{sub 0.4}Zn{sub 0.6}Fe{sub 2O4} obtido pelo metodo de citrato precursor

Energy Technology Data Exchange (ETDEWEB)

Hwang, K. [Centro Tecnico Aeroespacial (CTA-IAE), Sao Jose dos Campos, SP (Brazil). Inst. de Atividades Espaciais. Div. Materiais; Moura, A.E.G.; Nasar, R.S.; Nasar, M.C. [Universidade Federal do Rio Grande do Norte (UFRN), Natal (Brazil). Dept. de Quimica; Pereira, J.J. [Universidade de Taubate, SP (Brazil)

2010-07-01

In this work, two types of synthesized Ni{sub 0,4}Zn{sub 0,6}Fe{sub 2}O{sub 4} by citrate precursor method. The first type was calcined at 350 deg C for 3.5 h, and the second, after calcination, it was subjected to heat treatment at 600 deg C for 2h in argon atmosphere. Both types were analyzed by X-ray diffraction (XRD) and equipment waveguide. The data were investigated by Rietveld refinement method and showed the NiZn ferrite phase with crystallite size of 12.2 +- 0.1 nm (350 deg C) and 166.7 +- 3.6 nm (600 deg C). The heat treatment also influenced the values of electric permittivity and magnetic permeability, and attenuation of electromagnetic radiation in the frequency range in microwave (8-12 GHz). The sample treated attenuates more and allows its application with thinner, making it attractive its use as absorber material in this frequency range. (author)

Inhibition of mild steel corrosion by 1,4,6-trimethyl-2-oxo-1,2-dihydropyridine-3-carbonitrile and synergistic effect of halide ion in 0.5 M H{sub 2}SO{sub 4}

Energy Technology Data Exchange (ETDEWEB)

Mourya, Punita, E-mail: mouryapunita025@gmail.com [Department of Chemistry, Indian Institute of Technology (Banaras Hindu University), Varanasi 221005 (India); Singh, Praveen [Department of Chemistry, Banaras Hindu University, Varanasi 221005 (India); Rastogi, R.B.; Singh, M.M. [Department of Chemistry, Indian Institute of Technology (Banaras Hindu University), Varanasi 221005 (India)

2016-09-01

Highlights: • TODPCN is a good corrosion inhibitor for mild steel in 0.5 M H{sub 2}SO{sub 4} solution. • Addition of iodide ion increases the inhibition efficiency of the studied nitrile derivative. • Inhibition efficiency successively increases with concentration. • XPS study has revealed the chemical composition of the protective film. - Abstract: The effect of iodide ions on inhibitive performance of 1,4,6-trimethyl-2-oxo-1,2-dihydropyridine-3-carbonitrile (TODPCN) on mild steel (MS) corrosion in 0.5 M H{sub 2}SO{sub 4} was studied using gravimetric and electrochemical measurements. TODPCN inhibits the corrosion of MS to the extent of 62.3% at its lowest concentration (0.5 mM) and its inhibition efficiency (η) further increases on increasing concentration at 298 K. The adsorption of TODPCN on MS was found to follow the Langmuir adsorption isotherm. The value of η increased on the addition of 2.0 mM KI. The value of synergism parameter being more than unity indicates that the enhanced η value in the presence of iodide ions is only due to synergism. Thus, a cooperative mechanism of inhibition exists between the iodide anion and TODPCN cations. The increase in surface coverage in the presence of KI indicates that iodide ions enhance the adsorption of TODPCN. The surface morphology of corroded/inhibited MS was studied by atomic force microscopy. X-ray photoelectron spectroscopy of inhibited MS surface was carried out to determine the composition of the adsorbed film. Some quantum chemical parameters and the Mulliken charge densities for TODPCN calculated by density functional theory provided further insight into the mechanism of inhibition.

High temperature study on the thermal properties of few-layer Mo0.5W0.5S2 and effects of capping layers

Directory of Open Access Journals (Sweden)

Hong Gu

Full Text Available We investigated the thermal properties of few-layer Mo0.5W0.5S2 using a series of samples with different kinds of capping layers. Temperature-dependent Raman measurements were conducted in the range of 300–500 K, with power-dependent measurements also carried out. It indicated, for the few-layer Mo0.5W0.5S2, the temperature coefficients of the WS2-like E12g mode, MoS2-like E12g mode and A1g mode were −0.0155 cm−1/K, −0.0146 cm−1/K, and −0.0130 cm−1/K, respectively. And the thermal conductivity was estimated to be 44.8 W/mK. Moreover, the Mo0.5W0.5S2 samples coated with capping layers (ZrO2, HfO2 both showed a better thermal stability and a larger thermal conductivity than the one without. The results revealed that the capping layer should be an important factor in the thermal property. Keywords: Mo0.5W0.5S2, TMDs, Thermal properties, High temperature, Capping layers, Raman

Spin 1/2 Delafossite Honeycomb Compound Cu5SbO6

DEFF Research Database (Denmark)

Climent-Pascual, E.; Norby, Poul; Andersen, Niels Hessel

2012-01-01

Cu5SbO6 is found to have a monoclinic, Delafossite-derived structure consisting of alternating layers of O–Cu(I)–O sticks and magnetic layers of Jahn–Teller distorted Cu(II)O6 octahedra in an edge sharing honeycomb arrangement with Sb(V)O6 octahedra. This yields the structural formula Cu(I)3Cu(II...

Areva at September 30, 2012: Backlog at a record level of euros 47 bn (+10.1% year on year). Revenue up sharply to euros 6.542 bn (+10.0% compared with September 2011, +8.5% like for like)

International Nuclear Information System (INIS)

Marie, Patricia; Briand, Pauline; Thebault, Alexandre; Rosso, Jerome; Scorbiac, Marie de; Repaire, Philippine du

2012-01-01

AREVA generated consolidated revenue of 6.542 billion euros over the first nine months of 2012, representing growth of 10.0% (+8.5% growth like for like) compared with the same period in 2011. Revenue growth was fueled by a 7.0% increase in recurring business (+5.6% like for like) and ramp-up of the renewable business. Revenue from nuclear operations was 6.035 billion euros over the first nine months of 2012, compared with 5.731 billion euros for the first nine months of 2011, representing a 5.3% increase (+3.9% like for like). Like for like, revenue was led by the Mining BG (+28.0%), the Reactors and Services BG (+2.1%) and the Back End BG (+11.8%), offsetting the downturn in business in the Front End BG (-12.1%). Revenue was up 272% like for like in renewable energies. Foreign exchange had a positive impact of 130 million euros over the period. The change in consolidation scope had a negative impact of 52 million euros. Revenue growth was balanced between France and internationally, reflecting AREVA's ability to capture market opportunities while capitalizing on long-standing relations with its customers. Sales revenue for the third quarter of 2012 was 2.214 billion euros, an increase of 13.4% (+12.4% like for like) compared with the third quarter of 2011. Foreign exchange had a positive impact of 52 million euros over the period, while the change in consolidation scope had a negative impact of 34 million euros. At September 30, 2012, the consolidated backlog for the nuclear and renewable energy businesses was the highest since the Group was established, at a total of 47 billion euros. This represents an increase of 10.1% in relation to September 30, 2011 (42.7 billion euros) and an increase of 4.1% in relation to June 30, 2012 (45.2 billion euros). The increase is attributable mainly to the Mining, Front End and Reactors and Services BGs. Order intakes over the first nine months of the year were up 87% compared with first nine months of 2011. Order cancellations

Effect of Nb and F Co-doping on Li1.2Mn0.54Ni0.13Co0.13O2 Cathode Material for High-Performance Lithium-Ion Batteries

Directory of Open Access Journals (Sweden)

Lei Ming

2018-04-01

Full Text Available The Li1.2Mn0.54−xNbxCo0.13Ni0.13O2−6xF6x (x = 0, 0.01, 0.03, 0.05 is prepared by traditional solid-phase method, and the Nb and F ions are successfully doped into Mn and O sites of layered materials Li1.2Mn0.54Co0.13Ni0.13O2, respectively. The incorporating Nb ion in Mn site can effectively restrain the migration of transition metal ions during long-term cycling, and keep the stability of the crystal structure. The Li1.2Mn0.54−xNbxCo0.13Ni0.13O2−6xF6x shows suppressed voltage fade and higher capacity retention of 98.1% after 200 cycles at rate of 1 C. The replacement of O2− by the strongly electronegative F− is beneficial for suppressed the structure change of Li2MnO3 from the eliminating of oxygen in initial charge process. Therefore, the initial coulombic efficiency of doped Li1.2Mn0.54−xNbxCo0.13Ni0.13O2−6xF6x gets improved, which is higher than that of pure Li1.2Mn0.54Co0.13Ni0.13O2. In addition, the Nb and F co-doping can effectively enhance the transfer of lithium-ion and electrons, and thus improving rate performance.

Flood-inundation maps for a 12.5-mile reach of Big Papillion Creek at Omaha, Nebraska

Science.gov (United States)

Strauch, Kellan R.; Dietsch, Benjamin J.; Anderson, Kayla J.

2016-03-22

Digital flood-inundation maps for a 12.5-mile reach of the Big Papillion Creek from 0.6 mile upstream from the State Street Bridge to the 72nd Street Bridge in Omaha, Nebraska, were created by the U.S. Geological Survey (USGS) in cooperation with the Papio-Missouri River Natural Resources District. The flood-inundation maps, which can be accessed through the USGS Flood Inundation Mapping Science Web site at http://water.usgs.gov/osw/flood_inundation/, depict estimates of the areal extent and depth of flooding corresponding to selected water levels (stages) at the USGS streamgage on the Big Papillion Creek at Fort Street at Omaha, Nebraska (station 06610732). Near-real-time stages at this streamgage may be obtained on the Internet from the USGS National Water Information System at http://waterdata.usgs.gov/ or the National Weather Service Advanced Hydrologic Prediction Service at http:/water.weather.gov/ahps/, which also forecasts flood hydrographs at this site.

Structural and electrical properties of La{sub 0.5}Ca{sub 0.5}Mn{sub 0.95}Fe{sub 0.05}O{sub 3+{delta}} perovskite

Energy Technology Data Exchange (ETDEWEB)

Mohamed, E.A., E-mail: emanattamohammed@yahoo.com [Department of Physics, Faculty of Science (Girl' s Branch), Al Azhar University, Nasr City, Cairo (Egypt)

2012-12-05

Highlights: Black-Right-Pointing-Pointer La{sub 0.5}Ca{sub 0.5}Mn{sub 0.95}Fe{sub 0.05}O{sub 3+{delta}} synthesis has been achieved by co-precipitation process. Black-Right-Pointing-Pointer Moessbauer results show an evidence for the local distortion of Mn(Fe)O{sub 6} octahedron. Black-Right-Pointing-Pointer Metal-Semiconductor transition temperature (T{sub p}) is observed. - Abstract: La{sub 0.5}Ca{sub 0.5}Mn{sub 0.95}Fe{sub 0.05}O{sub 3+{delta}} was synthesized by co-precipitation method. The structure refinement by using the Rietveld method indicates that the sample was single phase with the presence of small impurities (Mn{sub 3}O{sub 4}) and crystallizes in an orthorhombic (Pbmn) structure. The room temperature (RT) Moessbauer spectrum shows clear evidence of the local structural distortion of the Mn(Fe)O{sub 6} octahedron on the basis of non-zero nuclear quadrupole interactions for high-spin Fe{sup 3+} ions. The Jahn-Teller coupling strength (E{sub JT}) was estimated from the Moessbauer results. Metal-Semiconductor transition temperature (T{sub p}) is observed at 80 K. At high temperature (T{sub P} < T < {theta}{sub D}/2) conductivity data satisfy the variable range hopping (VRH) model. For T > {theta}{sub D}/2 the small polaron hopping model is more appropriate than the VRH model.

The stored energy in processed Cu-0.4 wt.%Cr-0.12 wt.%Zr-0.02 wt.%Si-0.05 wt.%Mg

International Nuclear Information System (INIS)

Li, X.F.; Dong, A.P.; Wang, L.T.; Yu, Z.; Meng, L.

2011-01-01

Research highlights: → The crystal orientation in processed Cu-0.4 wt.%Cr-0.12 wt.%Zr-0.02 wt.%Si-0.05 wt.%Mg is deviating from the as-cast specimens and microstrain of the alloy is gradually increasing as the draw ratio rising before η ≤ 6.7. → The dynamic recovery has taken place as 6.7 texture is formed with the draw ratio rising. Meanwhile, the stored energy also increases with the draw ratio rising and a peak is reached with draw ratio of 6.7. The release of stored energy is primarily due to the decrease of dislocation density. The flow stress estimated from the stored energy has a similar variation trend with the measured data with a stress difference ∼20 to 120 MPa. The main strengthening effect is attributed to dislocation mechanism.

DNA excision repair in human cells treated with ultraviolet radiation and 7,12-dimethylbenz(a)anthracene 5,6-oxide

Energy Technology Data Exchange (ETDEWEB)

Ahmed, F.E.; Gentil, A.; Renstein, B.S.; Setlow, R.B.

1980-01-01

Excision repair was measured in normal human and xeroderma pigmentosum group C cells treated with 7,12-dimethylbenz(a)anthracene 5,6-oxide and with ultraviolet radiation by the techniques of unscheduled DNA synthesis, repair replication, a modification and bromodeoxyuridine photolysis and endonuclease-sensitive sites assay. Radiautography and repair replication showed that in normal cells the magnitude of repair after a saturation dose of the epoxide to be 0.1 to 0.2, that after a saturating ultraviolet dose, though survival data showed that both doses gave nearly similar killings. Repair was of the long-patch type and repair kinetics after the epoxide treatment were similar to ultraviolet. After a combined treatment with both agents, unscheduled synthesis in normal cells was more than additive. The data indicate that there are different rate-limiting steps in the removal of the ultraviolet and the epoxide damages, and that the residual repair activity in xeroderma pigmentosum cells is accomplished by different, not just fewer, enzymes than in normal cells.

A new insight into high-strength Ti62Nb12.2Fe13.6Co6.4Al5.8 alloys with bimodal microstructure fabricated by semi-solid sintering.

Science.gov (United States)

Liu, L H; Yang, C; Kang, L M; Qu, S G; Li, X Q; Zhang, W W; Chen, W P; Li, Y Y; Li, P J; Zhang, L C

2016-03-31

It is well known that semi-solid forming could only obtain coarse-grained microstructure in a few alloy systems with a low melting point, such as aluminum and magnesium alloys. This work presents that semi-solid forming could also produce novel bimodal microstructure composed of nanostructured matrix and micro-sized (CoFe)Ti2 twins in a titanium alloy, Ti62Nb12.2Fe13.6Co6.4Al5.8. The semi-solid sintering induced by eutectic transformation to form a bimodal microstructure in Ti62Nb12.2Fe13.6Co6.4Al5.8 alloy is a fundamentally different approach from other known methods. The fabricated alloy exhibits high yield strength of 1790 MPa and plastic strain of 15.5%. The novel idea provides a new insight into obtaining nano-grain or bimodal microstructure in alloy systems with high melting point by semi-solid forming and into fabricating high-performance metallic alloys in structural applications.

Novel routes to 1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazines and 5,6,9,10,11,11a-hexahydro-8H-pyrido[1,2-a]pyrrolo[2,1-c]pyrazines.

Science.gov (United States)

Katritzky, Alan R; Jain, Ritu; Xu, Yong-Jiang; Steel, Peter J

2002-11-15

Condensation reactions of benzotriazole and 2-(pyrrol-1-yl)-1-ethylamine (1) with formaldehyde and glutaric dialdehyde, respectively, afforded intermediates 2 and 6. Subsequent nucleophilic substitutions of the benzotriazole group in 2 and 6 with Grignard reagents, sodium cyanide, and sodium borohydride gave 1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazines 3a-e, 4, 5 and 5,6,9,10,11,11a-hexahydro-8H-pyrido[1,2-a]pyrrolo[2,1-c]pyrazines 7a-c, 8, 9, respectively, in good yields.

Effects of MnO{sub 2} doping on structure, dielectric and piezoelectric properties of 0.825NaNbO{sub 3}-0.175Ba{sub 0.6}(Bi{sub 0.5}K{sub 0.5}){sub 0.4}TiO{sub 3} lead-free ceramics

Energy Technology Data Exchange (ETDEWEB)

Fan, Ximing; Lin, Dunmin; Zheng, Qiaoji; Sun, Hailing; Wan, Yang; Wu, Xiaochun [College of Chemistry and Materials Science, and Visual Computing and Virtual Reality Key Laboratory of Sichuan Province, Sichuan Normal University, Chengdu 610066 (China); Wu, Lang [State Key Laboratory Cultivation Base for Nonmetal Composites and Functional Materials, Southwest University of Science and Technology, Mianyang 621010 (China)

2012-12-15

Lead-free ceramics 0.825NaNbO{sub 3}-0.175Ba{sub 0.6}(Bi{sub 0.5}K{sub 0.5}){sub 0.4}TiO{sub 3} + xmol% MnO{sub 2} were prepared by an ordinary sintering technique and the effects of MnO{sub 2} doping on the structure, dielectric, and piezoelectric properties of the ceramics were studied. The ceramics with perovskite structure are transformed from tetragonal to pseudocubic phases by increasing the doping level of MnO{sub 2}. After the addition of MnO{sub 2}, the Curie temperature T{sub C} of the ceramics decreases and the ferroelectric-paraelectric phase transition at T{sub C} becomes more diffusive. Because of the donor and acceptor doping effects of Mn ions simultaneously, the piezoelectric constant d{sub 33}, electromechanical coupling coefficient k{sub p}, relative permittivity {epsilon}{sub r}, and mechanical quality factor Q{sub m} are enhanced considerably after the addition of 1 mol% MnO{sub 2}. The ceramic with 1 mol% MnO{sub 2} doping possesses the optimum piezoelectricity (d{sub 33} = 131 pC/N and k{sub p} = 21.8%) and relatively high Q{sub m} = 627. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Substantial photovoltaic response and morphology tuning in benzo[1,2-b:6,5-b']dithiophene (bBDT) molecular donors.

Science.gov (United States)

Harschneck, Tobias; Zhou, Nanjia; Manley, Eric F; Lou, Sylvia J; Yu, Xinge; Butler, Melanie R; Timalsina, Amod; Turrisi, Riccardo; Ratner, Mark A; Chen, Lin X; Chang, Robert P H; Facchetti, Antonio; Marks, Tobin J

2014-04-21

The influence of solubilizing substituents on the photovoltaic performance and thin-film blend morphology of new benzo[1,2-b:6,5-b']dithiophene (bBDT) based small molecule donor semiconductors is investigated. Solar cells based on bBDT(TDPP)2-PC71BM with two different types of side chains exhibit high power conversion efficiencies, up to 5.53%.

Irreversibility Curve on Y1–xLuxBa2Cu3O7–δ (x=0.4, 0.5 and 0.6) superconducting

International Nuclear Information System (INIS)

Grimaldos, J F Cepeda; Supelano G, I; Santos, A Sarmiento; Chiquillo, M V; Martínez B, D; Vargas, C A Parra

2014-01-01

The irreversibility line in the H–T plane divides the irreversible and reversible behaviour of the magnetization which is of importance for the characterization of high T c superconductors. In this work, we report the production of Y 1–X Lu X Ba 2 Cu 3 O 7–δ (X=0.4, 0.5 and 0.6) superconducting system using the usual solid state reaction method. The irreversibility line H–T plane for the Y 1–X Lu X Ba 2 Cu 3 O 7–δ polycrystalline sample was investigated. The curves of magnetization ZFC (cero field cooled)- FC (field cooled) were measured in magnetic fields between 100 Oe and 4000 Oe, and allowed to obtain the values for irreversibility and critical temperatures

Preparation of La{sub 0.75}Sr{sub 0.25}Cr{sub 0.5}Mn{sub 0.5}O{sub 3-{delta}} fine powders by carbonate coprecipitation for solid oxide fuel cells

Energy Technology Data Exchange (ETDEWEB)

Ha, Sang Bu; Cho, Pyeong-Seok; Cho, Yoon Ho; Lee, Dokyol; Lee, Jong-Heun [Department of Materials Science and Engineering, Korea University, Anam-dong, Sungbuk-ku, Seoul 136-713 (Korea)

2010-01-01

A range of La{sub 0.75}Sr{sub 0.25}Cr{sub 0.5}Mn{sub 0.5}O{sub 3-{delta}} (LSCM) powders is prepared by the carbonate coprecipitation method for use as anodes in solid oxide fuel cells. The supersaturation ratio (R = [(NH{sub 4}){sub 2}CO{sub 3}]/([La{sup 3+}] + [Sr{sup 2+}] + [Cr{sup 3+}] + [Mn{sup 2+}])) during the coprecipitation determines the relative compositions of La, Sr, Cr, and Mn. The composition of the precursor approaches the stoichiometric one at the supersaturation range of 4 {<=} R {<=} 12.5, whereas Sr and Mn components are deficient at R < 4 and excessive at R = 25. The fine and phase-pure LSCM powders are prepared by heat treatment at very low temperature (1000 C) at R = 7.5 and 12.5. By contrast, the solid-state reaction requires a higher heat-treatment temperature (1400 C). The catalytic activity of the LSCM electrodes is enhanced by using carbonate-derived powders to manipulate the electrode microstructures. (author)

Synthesis and characterization of the novel rare earth orthophosphates Y0.5Er0.5PO4 and Y0.5Yb0.5PO4

International Nuclear Information System (INIS)

Schildhammer, Daniel; Petschnig, Lucas L.; Fuhrmann, Gerda; Heymann, Gunter; Schottenberger, Herwig; Huppertz, Hubert; Tribus, Martina

2016-01-01

The new mixed rare earth (RE) orthophosphates Y 0.5 Er 0.5 PO 4 and Y 0.5 Yb 0.5 PO 4 were synthesized by a classical solid state reaction in an electrical furnace at 1200 C. As starting materials, the corresponding rare earth oxides and diammonium hydrogen phosphate were used. The powder diffraction analyses revealed that the new compounds Y 0.5 Er 0.5 PO 4 and Y 0.5 Yb 0.5 PO 4 crystallize in a zircon-type structure being isostructural with the rare earth orthophosphate YPO 4 . Y 0.5 Er 0.5 PO 4 and Y 0.5 Yb 0.5 PO 4 crystallize in the tetragonal space group I4 1 /amd (no. 141) with four formula units in the unit cell. The structural parameters based on Rietveld refinements are a = 687.27(2), c = 601.50(2) pm, V = 0.28412(1) nm 3 , R p = 0.0143, and R wp = 0.0186 (all data) for Y 0.5 Er 0.5 PO 4 and a = 684.61(2), c = 599.31(2) pm, V = 0.28089(2) nm 3 , R p = 0.0242, and R wp = 0.0313 (all data) for Y 0.5 Yb 0.5 PO 4 . Furthermore, the structure of Y 0.5 Er 0.5 PO 4 was refined from single-crystal X-ray diffraction data: a = 687.78(5), c = 601.85(4) pm, V = 0.28470(5) nm 3 , R 1 = 0.0165, and wR 2 = 0.0385 (all data). In both compounds, the rare earth metal ions are eightfold coordinated by oxygen atoms, forming two unique interlocking tetrahedra with two individual RE-O distances. The tetrahedral phosphate groups [PO 4 ] 3- are slightly distorted in both compounds. The individual rare earth ions share a common position (Wyckoff site 4a). The presence of two rare earth ions in the structures of the new orthophosphates Y 0.5 Er 0.5 PO 4 and Y 0.5 Yb 0.5 PO 4 was additionally confirmed by single-crystal EDX spectroscopy revealing a ratio of 1:1.

[Allergic asthma and interleukins 2, 4, 5, 6 and 12 and gamma interferon levels].

Science.gov (United States)

Bastida Segura, Diana Lyzbeth; López Velásquez, Benjamin; Castrejón Vázquez, María Isabel; Galicia Tapía, Jorge; Cano Altamirano, Silvia; Miranda Feria, Alfonso Javier

2004-01-01

Asthma is an inflammatory chronic illness, in which mastocyt cells, basophils, T lymphocytes, eosinophils and cytokines play a role. Its association with the production of TH2 cytokines is not well known, but it is considered an aberrant immune response, yielding the activation and recruitment of a number of effector cells (mastocyts/eosinophils) and the appearance of clinical symptoms. To determine the serum values of the interleukins 2, 4, 5, 6 and 12 and gamma interferon in relation to the severity degree of asthma and the time of immunotherapy in patients with stable chronic allergic bronchial asthma. Clinical records of allergic asthmatic patients from the external consultation at Servicio de Alergia e Immunología Clínica were reviewed in a period of 12 months (1st January 2002 to 1st January 2003) and those of healthy volunteers, forming three groups: Group 1, allergic asthmatics with immunotherapy less than 24 months; Group 2, allergic asthmatics with more than 24 months of immunotherapy, and Group 3, healthy volunteers (control group). Previous informed consent, a serum sample was taken of all subjects. Ninety-two subjects were included: 41 (45%) allergic asthmatics and 51 (55%) healthy volunteers. Significant differences were found in interleukins 2, 4, 5, 6 and 12 levels between healthy volunteers and asthmatics without relating the immunotherapy time. In the total group gamma interferon levels were not found. A relation of interleukins Th2 levels with the severity degree of asthma was not found. Differences of serum interleukins Th1 and Th2 in allergic patients related to immunotherapy time were not significant; even though, irrespective of immunotherapy time, IgG levels were always high. Patients with allergic asthma have a predominance of serum interleukins Th2 and, despite of the immunotherapy, in the maintaining phase, these continue high, which may be due to an immune system dysregulation maybe including other factors. Immunotherapy continues

12 CFR 16.6 - Sales of nonconvertible debt.

Science.gov (United States)

2010-01-01

... 12 Banks and Banking 1 2010-01-01 2010-01-01 false Sales of nonconvertible debt. 16.6 Section 16.6... RULES § 16.6 Sales of nonconvertible debt. (a) The OCC will deem offers or sales of bank issued... grade; (5) Prior to or simultaneously with the sale of the debt, each purchaser receives an offering...

12.5 Gb/s carrier-injection silicon Mach—Zehnder optical modulator

International Nuclear Information System (INIS)

Chen Hongtao; Ding Jianfeng; Yang Lin

2012-01-01

We demonstrate a 12.5 Gb/s carrier-injection silicon Mach—Zehnder optical modulator. Under a nonreturn-zero (NRZ) pre-emphasized electrical drive signal with voltage swing of 6.3 V and forward bias of 0.7 V, the eye is clearly opened with an extinction ratio of 8.4 dB. The device exhibits high modulation efficiency, with a figure of merit V π L of 0.036 V·mm. (semiconductor devices)

Ablation in teeth with the free-electron laser around the absorption peak of hydroxyapatite (9.5 μm) and between 6.0 and 7.5 μm

Science.gov (United States)

Ostertag, Manfred; Walker, Rudolf; Weber, Heiner; van der Meer, Lex; McKinley, Jim T.; Tolk, Norman H.; Jean, Benedikt J.

1996-04-01

Pulsed IR laser ablation on dental hard substances was studied in the wavelength range between 9.5 and 11.5 micrometers with the Free-Electron Laser (FEL) in Nieuwegein/NL and between 6.0 and 7.5 micrometers with the FEL at Vanderbilt University in Nashville/TN. Depth, diameter and volume of the ablation crater were determined with a special silicon replica method and subsequent confocal laser topometry. The irradiated surfaces and the ejected debris were examined with an SEM 9.5 - 11.5 micrometers : depth, diameter and volume of the ablation crater are greater and the ablation threshold is lower for ablation with a wavelength corresponding to the absorption max. of hydroxyapatite (9.5 micrometers ), compared to ablation at wavelengths with lower absorption (10.5 - 11.5 micrometers ). For all wavelengths, no thermal cracking can be observed after ablation in dentine, however a small amount of thermal cracking can be observed after ablation in enamel. After ablation at 9.5 micrometers , a few droplets of solidified melt were seen on the irradiated areas, whereas the debris consisted only of solidified melt. In contrast, the surface and the debris obtained from ablation using the other wavelengths showed the natural structure of dentine 6.0 - 7.5 micrometers : the depth of the ablation crater increases and the ablation threshold decreases for an increasing absorption coefficient of the target material. Different tissue components absorbed the laser radiation of different wavelengths (around 6.0 micrometers water and collagen, 6.5 micrometers collagen and water, 7.0 micrometers carbonated hydroxyapatite). Nevertheless the results have shown no major influence on the primary tissue absorber.

Moessbauer spectroscopy studies of spin reorientations in amorphous and crystalline (Co0.2Fe0.8)72.5Si12.5B15 glass coated micro-wires

International Nuclear Information System (INIS)

Nowik, I.; Felner, I.; Garcia-Miquel, H.

2007-01-01

Thermo-gravimetric, differential scanning calorimetry and comprehensive 57 Fe Moessbauer spectroscopy studies of amorphous and crystalline ferromagnetic glass coated (Co 0.2 Fe 0.8 ) 72.5 Si 12.5 B 15 micro-wires have been recorded. The Curie temperature of the amorphous phase is T C (amorp) ∼730 K. The analysis of the Moessbauer spectra reveals that below 623 K the easy axis of the magnetization is axial-along the wires, and that a tangential or/and radial orientation occurs at higher temperatures. At 770 K, in the first 4 hours the Moessbauer spectrum exhibits a pure paramagnetic doublet. Crystallization and decomposition to predominantly α-Fe(Si) and Fe 2 B occurs either by raising the temperature above 835 K or isothermally in time at lower temperatures. Annealing for a day at 770 K, leads to crystallization. In the crystalline material the magnetic moments have a complete random orientation. After cooling back to ambient temperature, both α-Fe(Si) and Fe 2 B in the glass coated wire show pure axial magnetic orientation like in the original amorphous state. The observed spin reorientations are associated with changes in the stress induced by the glass coating

Mo0.5W0.5S2 for Q-switched pulse generation in ytterbium-doped fiber laser

Science.gov (United States)

Wang, Junli; Chen, Lei; Dou, Chenxi; Yan, Haiting; Meng, Lingjie; Wei, Zhiyi

2018-06-01

In this work, we fabricate the Mo0.5W0.5S2 by microwave-assisted solvothermal method, and report the Q-switched Yb-doped fiber lasers (YDFL) using Mo0.5W0.5S2 polymer film and tapered fiber as the saturable absorbers (SAs). The modulation depth and saturable intensity of the film SA are 5.63% and 6.82 MW cm‑2. The shortest pulse duration and the maximum single pulse energy are 1.22 μs and 148.8 nJ for the film SA, 1.46 μs and 339 nJ for the fiber-taper SA. To the best of our knowledge, this is the first report on the Q-switched YDFL using Mo0.5W0.5S2 SAs.

MERLIN observations of the OH/IR stars OH 53.6-0.2, OH 138.0+7.2 and OH 141.7+3.5

International Nuclear Information System (INIS)

Chapman, J.; Cohen, R.J.; Norris, R.P.; Diamond, P.J.; Booth, R.S.

1984-01-01

OH maser emission from the three OH/IR stars OH 53.6-0.2, OH 138.0+7.2 and OH 141.7+3.5 has been mapped with an angular resolution of 0.28 arcsec and a velocity resolution of 0.7 km s -1 using the Jodrell Bank MERLIN array. Maps are presented of the 1612-MHz OH emission over individual velocity ranges. The maps are consistent with a uniform expanding shell model, and by fitting such models to the data the angular diameters of the shells have been estimated to an accuracy of approx. 25 per cent. (author)

Ocular penetration and pharmacokinetics of topical gatifloxacin 0.3% and moxifloxacin 0.5% ophthalmic solutions after keratoplasty.

Science.gov (United States)

Holland, Edward J; Lane, Stephen S; Kim, Terry; Raizman, Michael; Dunn, Steven

2008-04-01

To compare the corneal and aqueous penetration and pharmacokinetics of gatifloxacin 0.3% and moxifloxacin 0.5% ophthalmic solutions and their effect on corneal reepithelialization after penetrating keratoplasty. In this randomized, open-label, parallel-controlled study, corneal and aqueous penetration and the pharmacokinetic parameters of topically applied gatifloxacin 0.3% and moxifloxacin 0.5% (2 preoperative doses of 1 drop given 5 minutes apart) were estimated by using a sparse sampling method. Corneal and aqueous samples were collected 0.25, 0.5, 1, or 2 hours after the final dose. The concentration was determined by a high-performance liquid chromatography method. Stromal Cmax:MBC50 (maximum drug concentration in serum to 50% minimum bactericidal concentration) ratios for selected ocular pathogens were also assessed. Postoperative corneal reepithelialization at days 1, 3, and 7 was evaluated and compared between groups. The calculated pharmacokinetic parameters were higher with moxifloxacin 0.5% than with gatifloxacin 0.3%. The stromal Cmax was 48.5 versus 15.7 microg/g (P = 0.04), and the stromal AUC0-2 (area under the concentration-time curve from 0 to 2 hours) was 30.9 versus 13.6 mug.h/g (P 0.05), and the endothelial AUC0-2 was 43.9 versus 9.8 microg.h/g (P 0.05), and the aqueous AUC0-2 was 1.2 versus 0.4 microg.h/mL (P < 0.05). Stromal Cmax:MBC50 ratios were higher in the moxifloxacin 0.5% group for each pathogen tested. The corneal reepithelialization rates were comparable between groups. Topical preoperative moxifloxacin 0.5% achieved greater corneal and aqueous penetration than did gatifloxacin 0.3%. The clinical significance of this difference is not known. Postoperative use of these agents had similar effects on corneal reepithelialization.

12 CFR 5.35 - Bank service companies.

Science.gov (United States)

2010-01-01

.... (d) Definitions—(1) Bank service company means a corporation or limited liability company organized... liability company. (2) Limited liability company means any non-corporate company, partnership, trust, or..., obligation, or liability of the company solely by reason of being, or acting as, a member or manager of such...