Supercurrents in HgBa{sub 2}CaCu{sub 2}O{sub 6+{delta}} and TlBa{sub 2}CaCu{sub 2}O{sub 7} epitaxial thin films

Energy Technology Data Exchange (ETDEWEB)

Gapud, A.A.; Wu, J.Z.; Fang, L.; Yan, S.L.; Xie, Y.Y. [Department of Physics and Astronomy, University of Kansas, Lawrence, Kansas 66045-2151 (United States); Siegal, M.P.; Overmyer, D.L. [Sandia National Laboratories, Albuquerque, New Mexico 87185 (United States)

1999-06-01

The availability of high-quality epitaxial thin films of HgBa{sub 2}CaCu{sub 2}O{sub 6+{delta}} (Hg-1212) and TlBa{sub 2}CaCu{sub 2}O{sub 7} (Tl-1212) with high critical current densities (J{sub c}) has made it possible to examine and compare the J{sub c} of these species. Results reveal that the J{sub c} of 1212 species have very similar temperature behavior at low fields, strongly suggesting that the 30 K shift in critical temperature (T{sub c}) induced by the exchange of Hg and Tl in the 1212 structure is due largely to a change in charge carrier density and/or electronic band structure. {copyright} {ital 1999 American Institute of Physics.}

Determination of standard Gibbs free energy of formation for Ca2P2O7 and Ca(PO3)2 from solid-state EMF measurements using yttria stabilised zirconia as solid electrolyte

International Nuclear Information System (INIS)

Sandstroem, Malin Hannah; Bostroem, Dan; Rosen, Erik

2006-01-01

The equilibrium reactions: 3Ca 2 P 2 O 7 (s)+6Ni(s)-bar 2Ca 3 (PO 4 ) 2 (s)+2Ni 3 P(s)+52O 2 (g) and 2Ca(PO 3 ) 2 (s)+6Ni(s)-bar Ca 2 P 2 O 7 (s)+2Ni 3 P(s)+52O 2 (g) were studied in the temperature range 890K to 1140K. The oxygen equilibrium pressures were determined using galvanic cells incorporating yttria stabilized zirconia as solid electrolyte. From the measured data and using the literature values of standard Gibbs free energy of formation for Ca 3 (PO 4 ) 2 and Ni 3 P, the following relationship of the standard Gibbs free energy of formation for Ca 2 P 2 O 7 and Ca(PO 3 ) 2 were calculated:Δ f G o (Ca 2 P 2 O 7 )+/-11/(kJ.mol -1 )=-3475.9+1.5441(T/K)-0.1051(T/K).ln(T/K)andΔ f G o (Ca(PO 3 ) 2 )+/-12/(kJ.mol -1 )=-3334.8+6.1561(T/K)-0.6950(T/K).ln(T/K)

Maximum oxygen uptake and objectively measured physical activity in Danish children 6-7 years of age: the Copenhagen school child intervention study

DEFF Research Database (Denmark)

Eiberg, Stig; Hasselstrøm, Henriette; Grønfeldt, Vivian

2005-01-01

Objectives: To provide normative data on maximum oxygen uptake (V·O2MAX) and physical activity in children 6-7 years of age and analyse the association between these variables. Methods: VO2MAX was measured in 366 boys (mean (SD) 6.8 (0.4) years of age) and 332 girls (6.7 (0.4) years of age) from.......5 (6.0) v 44.8 (5.6) ml/kg/min (+8%); pgirls. The difference in VO2MAX between boys and girls decreased to +2% when expressed relative to lean body mass (LBM). Absolute VO2MAX was related to LBM, body mass, and stature (all pBoys were more physically active than girls (mean counts...... +9.4%, pboys and girls with the same VO2MAX were compared, boys were more active. The difference in physical activity between the sexes was higher when sustained activity of higher intensity was compared. Conclusions: VO2MAX is higher in boys than girls (+11%), even when...

Characterization of Ti6Al7Nb alloy foams surface treated in aqueous NaOH and CaCl2 solutions.

Science.gov (United States)

Bütev, Ezgi; Esen, Ziya; Bor, Şakir

2016-07-01

Ti6Al7Nb alloy foams having 53-73% porosity were manufactured via evaporation of magnesium space holders. A bioactive 1µm thick sodium hydrogel titanate layer, NaxH2-xTiyO2y+1, formed after 5M NaOH treatment, was converted to crystalline sodium titanate, Na2TiyO2y+1, as a result of post-heat treatment. On the other hand, subsequent CaCl2 treatment of NaOH treated specimens induced calcium titanate formation. However, heat treatment of NaOH-CaCl2 treated specimens led to the loss of calcium and disappearance of the titanate phase. All of the aforementioned surface treatments reduced yield strengths due to the oxidation of the cell walls of the foams, while elastic moduli remained mostly unchanged. Accordingly, equiaxed dimples seen on the fracture surfaces of as-manufactured foams turned into relatively flat and featureless fracture surfaces after surface treatments. On the other hand, Ca- and Na-rich coating preserved their mechanical stabilities and did not spall during fracture. The relation between mechanical properties of foams and macro-porosity fraction were found to obey a power law. The foams with 63 and 73% porosity met the desired biocompatibility requirements with fully open pore structures and elastic moduli similar to that of bone. In vitro tests conducted in simulated body fluid (SBF) showed that NaOH-heat treated surfaces exhibit the highest bioactivity and allow the formation of Ca-P rich phases having Ca/P ratio of 1.3 to form within 5 days. Although Ca-P rich phases formed only after 15 days on NaOH-CaCl2 treated specimens, the Ca/P ratio was closer to that of apatite found in bone. Copyright © 2016 Elsevier Ltd. All rights reserved.

Fusion and nonfusion phenomena in the 6Li+40Ca reaction at 156 MeV

International Nuclear Information System (INIS)

Brzychczyk, J.; Freindl, L.; Grotowski, K.

1982-01-01

Reaction products from 6 Li-induced reactions on 40 Ca at 156 MeV have been studied using the dE x E identification as well as the inclusive γ-ray method. The complete fusion cross-section has been found to be σsub(f)=(77 +- 11)mb. The Z distribution of fusion evaporation residues is compared with statistical model predictions. The Z spectrum of reaction products shows a maximum at 15 6 Li break-up. (author)

Fusion and nonfusion phenomena in the 6Li+40Ca reaction at 156 MeV

International Nuclear Information System (INIS)

Brzychczyk, J.; Freindl, L.; Grotowski, K.; Majka, Z.; Micek, S.; Planeta, R.; Uniwersytet Jagiellonski, Krakow; Albinska, M.; Buschmann, J.; Klewe-Nebenius, H.; Gils, H.J.; Rebel, H.; Zagromski, S.

1984-01-01

Reaction products from 6 Li-induced reactions on 40 Ca at 156 MeV have been studied using the dExE idenitification as well as the inclusive γ-ray method. The complete fusion cross section has been found to be sigmasub(F)=67 +- 20 mb. The Z-distribution of fusion evaporation residues is compared with statistical model predictions. The Z-spectrum of reaction products shows a maximum at 15 6 Li-break-up processes. (orig.)

Quantum percolation transition in Eu{sub 1-x}Ca{sub x}B{sub 6}

Energy Technology Data Exchange (ETDEWEB)

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

2010-03-15

The study of transport and magnetic properties performed on Eu{sub 1-x}Ca{sub x}B{sub 6} single crystals with nominal Ca content 0 {<=} x {<=} 0.4 at temperatures 1.8-300 K in magnetic fields up to 80 kOe provides the direct experimental evidence of metal-to-insulator transition (MIT) earlier proposed for the system by V. M. Pereira et al. [Phys. Rev. Lett., 93, 147202 (2004)]. A giant enhancement of magnetoresistance up to the values of ({rho}(0) - {rho}(H))/{rho}(H) {proportional_to} 7 x 10{sup 7}% was detected for x = 0.4 in the wide vicinity of the ferromagnetic insulating state. The field induced crossover from hole-like to electron-like regime of charge transport observed for the first time in the paramagnetic phase of Eu{sub 0.6}Ca{sub 0.4}B{sub 6} is discussed in terms of quantum percolation transition predicted for this low carrier density system within double exchange model. (Abstract Copyright [2010], Wiley Periodicals, Inc.)

Enhanced magnetoresistance in La0.7Ca0.3Mn03/Nd0.7Ca0.3Mn03 epitaxial multilayers

International Nuclear Information System (INIS)

Sharma, Himanshu; Khan, Md. S.; Tomy, C.V.; Jain, Sourabh; Tulapurkar, Ashwin

2014-01-01

Magnanite multilayers of La 0.7 Ca 0.3 MnO 3 /Nd 0.7 Ca 0.5 MnO 3 have been fabricated on SrTiO 3 (100) substrate using Nd 0.7 Ca 0.5 MnO 3 as the spacer layers. An enhanced magnetoresistance (MR) of more than 80% is observed in the multilayers compared with LCMO thin film (∼50%). Result suggests that the interface strains between LCMO and NCMO layers may have influences on the transport properties and a suitable film structure could be used to increase the large low field magnetoresistance. (author)

High-temperature resistivity and thermoelectric properties of coupled substituted Ca3Co2O6

Directory of Open Access Journals (Sweden)

Meenakshisundaram Senthilkumar and Rajagopalan Vijayaraghavan

2009-01-01

Full Text Available Polycrystalline samples of Ca3−xNaxCo2−xMnxO6 (x=0.0–0.5 have been prepared by the sol-gel cum combustion method using sucrose in order to investigate the effects of the coupled substitution of Na and Mn on Ca and Co sites on the transport properties of Ca3Co2O6(Co326. The products were characterized by Fourier transform infrared spectroscopy, powder x-ray diffraction (XRD, thermogravimetry (TGA, differential thermal analysis and scanning electron microscopy. XRD patterns reveal the formation of single-phase products up to x=0.5. Coupled substitution increases the solubility of both Na and Mn on Ca and Co sites, respectively, in contrast to the limited solubility of Na and Mn (x=0.2 when separately substituted. TGA confirms the formation of the Ca3Co2O6 phase at temperatures ~720 °C. The grain size of the parent and substituted products is in the range 150–250 nm. Electrical resistivity and Seebeck coefficient were measured in the temperature range 300–800 K. Resistivity shows semiconducting behavior for all the compositions, particularly in the low-temperature regime. The Seebeck coefficient increases with temperature throughout the measured temperature range for all compositions. The maximum Seebeck coefficient (200 μV K−1 is observed for x=0.5 at 825 K, and this composition may be optimal for high-temperature thermoelectric applications.

Structural chemistry of the cation-ordered perovskites Sr2CaMo1-xTexO6 (0=

International Nuclear Information System (INIS)

Prior, Timothy J.; Couper, Victoria J.; Battle, Peter D.

2005-01-01

The crystal structures of Sr 2 CaMoO 6 and Sr 2 CaTeO 6 have been determined at room temperature by neutron powder diffraction. Both compounds crystallize in the perovskite structure with a rock-salt ordered array of Ca 2+ and M 6+ cations (M=Mo, Te) on the six-coordinate sites (space group P2 1 /n (no. 14); for M=Mo, a=5.76228(7), b=5.84790(7), c=8.18707(9)A, β=90.194(1) o , for M=Te, a=5.79919(9), b=5.83756(8), c=8.2175(1)A, β=90.194(1) o ). Compositions in the solid solution Sr 2 CaMo 1-x Te x O 6 have been synthesized and shown by X-ray diffraction to adopt the same ordered structure. The results are used in a discussion of the cation oxidation states in Ca 2 FeMoO 6 and to establish the similarity between the structural chemistry of hexavalent Mo and Te

Formation reactions and thermal stability of Ca/sub 2/NbCoO/sub 6/ and Ca/sub 2/TaCoO/sub 6/

Energy Technology Data Exchange (ETDEWEB)

Kuleshova, T B; Razumovskaya, O N; Belyaev, I N; Salei, V S [Rostovskij-na-Donu Gosudarstvennyj Univ. (USSR)

1979-11-01

Ca/sub 2/M/sup 5/CoO/sub 6/ compounds and reactions of their formation from oxides were investigated by thermogravimetric and X-ray phase analysis methods. Optimum conditions for synthesizing the above compounds have been found, and the degree of oxidation of Co therein, determined. The thermal stability of the compounds was also studied. It was shown, that the stability of Co (3) in Ca/sub 2/NbCaO/sub 6/ Ca/sub 2/TaCoO/sub 6/ is higher than that in similar compounds containing Pb. The resultant compounds are pure perovskites. Presented are the calculated and the experimental values of perovskite cell parameters.

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

International Nuclear Information System (INIS)

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

2012-01-01

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

Facile solution-precipitation assisted synthesis and luminescence property of greenish-yellow emitting Ca{sub 6}Ba(PO{sub 4}){sub 4}O:Eu{sup 2+} phosphor

Energy Technology Data Exchange (ETDEWEB)

Ji, Haipeng [School of Materials Science and Technology, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, China University of Geosciences, Beijing 100083 (China); Huang, Zhaohui, E-mail: huang118@cugb.edu.cn [School of Materials Science and Technology, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, China University of Geosciences, Beijing 100083 (China); Xia, Zhiguo, E-mail: xiazg@ustb.edu.cn [The Beijing Municipal Key Laboratory of New Energy Materials and Technologies, School of Materials Sciences and Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Xie, Yao [School of Materials Science and Technology, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, China University of Geosciences, Beijing 100083 (China); Molokeev, Maxim S. [Laboratory of Crystal Physics, Kirensky Institute of Physics, SB RAS, Krasnoyarsk 660036 (Russian Federation); Department of Physics, Far Eastern State Transport University, Khabarovsk 680021 (Russian Federation); Atuchin, Victor V. [Laboratory of Optical Materials and Structures, Institute of Semiconductor Physics, SB RAS, Novosibirsk 630090 (Russian Federation); Functional Electronics Laboratory, Tomsk State University, Tomsk 634050 (Russian Federation); Laboratory of Semiconductor and Dielectric Materials, Novosibirsk State University, Novosibirsk 630090 (Russian Federation)

2016-03-15

Highlights: • Ca{sub 6}Ba(PO{sub 4}){sub 4}O:Eu{sup 2+} phosphor was prepared by the solution-precipitation assisted route. • The phosphors have satisfactory smooth grain surface and particle size. • It shows greenish-yellow color emission (maximum at 540 nm) upon blue light excitation. • Eu{sup 2+} is coordinated with isolated oxygen atoms and those from PO{sub 4} polyhedra. - Abstract: Greenish-yellow emitting microcrystalline Ca{sub 6}Ba(PO{sub 4}){sub 4}O:Eu{sup 2+} phosphor was successfully prepared by a solution-precipitation assisted high temperature reaction method. Phase structure, morphology and/or luminescence properties of the precursor and the as-prepared phosphors were characterized. The phase-pure Ca{sub 6}Ba(PO{sub 4}){sub 4}O:Eu{sup 2+} phosphors were obtained with smooth grain surface and particle size of 2–8 μm. Ca{sub 6}Ba(PO{sub 4}){sub 4}O:Eu{sup 2+} exhibits bright greenish-yellow color emission with its maximum at 540 nm upon UV-blue light excitation. The maximum position of the broad emission band is independent on the calcination temperature. The emission intensity increases with increasing calcination temperature due to improved crystallinity. Besides, the presence of two Eu{sup 2+} emission centers in the Ca{sub 6}Ba(PO{sub 4}){sub 4}O crystal lattice was confirmed and the coordination effects are considered concerning the roles of isolated O atoms and those from the PO{sub 4} tetrahedra.

Synthesis and photoluminescence properties of Ba{sub 2}CaZn{sub 2}Si{sub 6}O{sub 17}:Eu{sup 3+} red phosphors for white LED applications

Energy Technology Data Exchange (ETDEWEB)

Annadurai, G.; Kennedy, S. Masilla Moses, E-mail: kennedysmm@ssn.edu.in

2016-01-15

Novel pellyite type Ba{sub 2}CaZn{sub 2}Si{sub 6}O{sub 17}:Eu{sup 3+} red emitting phosphors with different Eu{sup 3+} contents were synthesized by the solid state reaction method. The crystal structure, photoluminescence properties and concentration quenching of Ba{sub 2}CaZn{sub 2}Si{sub 6}O{sub 17}:Eu{sup 3+} phosphors were investigated. Powder X-ray diffraction measurements confirmed the structure of the samples. The photoluminescence emission (PL) and excitation (PLE) spectra were measured. The results showed that the dominant hypersensitive red emission peak of the phosphors Ba{sub 2}CaZn{sub 2}Si{sub 6}O{sub 17}:Eu{sup 3+} was located at 613 nm attributed to the Eu{sup 3+} transition ({sup 5}D{sub 0}→{sup 7}F{sub 2}) which could be effectively excited by 395 nm (near-UV). The latter band matched well with the emission from the near-UV LED chips. The intensity ratio of {sup 5}D{sub 0}→{sup 7}F{sub 2} to {sup 5}D{sub 0}→{sup 7}F{sub 1} transition showed slight variation with Eu{sup 3+} concentrations. The Eu{sup 3+} emission intensity was maximum for 9 mol%. The luminescence quantum efficiency was determined and also the decay profiles were obtained and analyzed. In addition, the Commission International del'Eclairage (CIE) chromaticity coordinates of Ba{sub 2}CaZn{sub 2}Si{sub 6}O{sub 17}:0.09Eu{sup 3+} phosphor were calculated to be 0.637 and 0.362. The experimental results demonstrated that the Ba{sub 2}CaZn{sub 2}Si{sub 6}O{sub 17}:Eu{sup 3+} red emitting phosphor is a potential candidate for white light emitting diodes (WLEDs) pumped by near-UV chip. - Highlights: • A novel Ba{sub 2}CaZn{sub 2}Si{sub 6}O{sub 17}:Eu{sup 3+} red phosphor was synthesized. • The samples yielded a dominant PL emission of Eu{sup 3+} at 613 nm. • Eu{sup 3+} concentration was optimized to be 9 mol% in Ba{sub 2}CaZn{sub 2}Si{sub 6}O{sub 17.} • CIE chromaticity coordinates were estimated from the emission spectrum.

Host sensitized novel red phosphor CaZrSi{sub 2}O{sub 7} : Eu{sup 3+} for near UV and blue LED-based white LEDs

Energy Technology Data Exchange (ETDEWEB)

Bandi, Vengala Rao; Jeong, Junho; Jang, Kiwan; Lee, Ho Sueb [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Jayasimhadri, M [Department of Applied Physics, Delhi Technological University, Delhi (India); Yi, Soung-Soo [Department of Photonics, Silla University, Busan (Korea, Republic of); Jeong, Jung-Hyun, E-mail: kwjang@changwon.ac.k [Department of Physics, Pukyong National University, Busan (Korea, Republic of)

2010-10-06

A series of red phosphors Ca{sub 1-x}ZrSi{sub 2}O{sub 7} : Eu{sub x} (x = 0.5,1,5,10,12 mol%) were prepared by a solid-state reaction technique at various temperatures and their structural and optical properties were investigated. The x-ray diffraction profiles showed that all peaks could be attributed to the monoclinic phase CaZrSi{sub 2}O{sub 7} doped with Eu{sup 3+}. SEM, FTIR, TG and DTA profiles have also been characterized to explore their structural properties. The luminescence properties of these resulting phosphors have been characterized by photoluminescence spectra. The host matrix itself has shown a strong blue emission which has its maximum intensity at 470 nm. The excitation spectra of CaZrSi{sub 2}O{sub 7} : Eu{sup 3+} revealed two excitation bands at 395 and 464 nm which correspond to the sharp {sup 7}F{sub 0}-{sup 5}L{sub 6} and {sup 7}F{sub 0}-{sup 5}D{sub 2} transitions of Eu{sup 3+} and matches well with the two popular emissions from n-UV/blue GaN-based LEDs. The prominent red emission was obtained at 615 nm by the excitation transitions {sup 5}L{sub 6}, {sup 5}D{sub 2} of Eu{sup 3+} through the non-radiative energy transfer process from the host to the Eu{sup 3+} ion. The effects of charge compensation by monovalent ions on the luminescence behaviour of a red emitting phosphor CaZrSi{sub 2}O{sub 7} : Eu{sup 3+} were investigated. The high colour saturation and the low thermal quenching effect of these phosphors make it a potential red component for white light emitting diodes (w-LEDs).

Neutron Powder Diffraction Studies of Ca2-xSrxCoWO6 Double Perovskites

International Nuclear Information System (INIS)

Zhou, Qingdi; Kennedy, Brendan; Elcombe, Margaret

2005-01-01

Full text: A series of double perovskite compounds of A 2-x Sr x CoWO 6 (A = Ca, Ba) were synthesized and the room- and variable-temperature structural phase transitions have been studied by synchrotron and neutron powder diffraction techniques. These studies demonstrated that the symmetry increases as the average size of the A-site cation increases. These transitions are associated with the gradual reduction and ultimately removal of the octahedral tiles of the BO 6 octahedra. Temperature dependent structural studies have been undertaken for selected samples. The transition to cubic is continuous in the three Ca doped samples studied as a function of temperature, Ca 2-x Sr x CoWO 6 x = 1.8, 1.7, 1.6, however in each case analysis of the spontaneous strain shows the transition to be tricritical rather than second order in nature. Where observed the temperature induced P2 1 /n to I4/m transition is first order as required by symmetry. (authors)>>>>

Unusual spin frozen state in a frustrated pyrochlore system NaCaCo{sub 2}F{sub 7} as observed by NMR

Energy Technology Data Exchange (ETDEWEB)

Sarkar, R.; Brueckner, F.; Klauss, H.H. [IFP, TU Dresden (Germany); Krizan, J.W.; Cava, R.J. [Department of Chemistry, Princeton University, Princeton, NJ (United States)

2016-07-01

We present {sup 23}Na -and {sup 19}F NMR results on the magnetically frustrated pyrochlore NaCaCo{sub 2}F{sub 7} with a frustration index of f = θ{sub CW}/T{sub f} ∝ 56. Recent neutron scattering experiments proposed XY like antiferromagnetic spin clusters at low energies in NaCaCo{sub 2}F{sub 7}. {sup 23}Na NMR -spectra reveal the presence of two magnetically non equivalent Na sites in conjunction with the local Co{sup 2+} spin structure. Below 3.6 K both the {sup 23}Na -and {sup 19}F spectra broaden due to the formation of static spin correlations. A huge reduction of the {sup 19}F -and {sup 23}Na NMR signal intensity hints at a quasi-static field distribution in NaCaCo{sub 2}F{sub 7} in this regime. The {sup 19}F spin-lattice relaxation rate {sup 19}(1/T{sub 1}) exhibits a peak at around 2.9 K, at the same temperature range where ac and dc susceptibility data show a broad maximum. The character of the spin fluctuation appears to be isotropic. The overall temperature dependence of {sup 19}(1/T{sub 1}) can be described by the BPP theory considering a fluctuating hyperfine field with an autocorrelation function. The correlation time of the autocorrelation function exhibits an activation behavior further indicating the spin-frozen state. While the present NMR studies suggest the spin frozen state at low temperatures, μSR investigations however reveal the presence of so called persistent spin dynamics down to 20 mK implying an exotic ground state in NaCaCo{sub 2}F{sub 7}.

Formation of CaB6 in the thermal decomposition of the hydrogen storage material Ca(BH4)2.

Science.gov (United States)

Sahle, Christoph J; Sternemann, Christian; Giacobbe, Carlotta; Yan, Yigang; Weis, Christopher; Harder, Manuel; Forov, Yury; Spiekermann, Georg; Tolan, Metin; Krisch, Michael; Remhof, Arndt

2016-07-20

Using a combination of high resolution X-ray powder diffraction and X-ray Raman scattering spectroscopy at the B K- and Ca L2,3-edges, we analyzed the reaction products of Ca(BH4)2 after annealing at 350 °C and 400 °C under vacuum conditions. We observed the formation of nanocrystalline/amorphous CaB6 mainly and found only small contributions from amorphous B for annealing times larger than 2 h. For short annealing times of 0.5 h at 400 °C we observed neither CaB12H12 nor CaB6. The results indicate a reaction pathway in which Ca(BH4)2 decomposes to B and CaH2 and finally reacts to form CaB6. These findings confirm the potential of using Ca(BH4)2 as a hydrogen storage medium and imply the desired cycling capabilities for achieving high-density hydrogen storage materials.

Activation of human IK and SK Ca2+ -activated K+ channels by NS309 (6,7-dichloro-1H-indole-2,3-dione 3-oxime)

DEFF Research Database (Denmark)

Strøbaek, Dorte; Teuber, Lene; Jørgensen, Tino D

2004-01-01

We have identified and characterized the compound NS309 (6,7-dichloro-1H-indole-2,3-dione 3-oxime) as a potent activator of human Ca2+ -activated K+ channels of SK and IK types, whereas it is devoid of effect on BK type channels. IK- and SK-channels have previously been reported to be activated...

Phase diagram of Se-CaIn4Se7 system

International Nuclear Information System (INIS)

Musaeva, R.I.; Aliev, I.I; Ismailova, F.I; Aliev, A.A

2011-01-01

Full text: The Se-CaIn 4 Se 7 system has been studied using methods of differential thermal analysis, X-ray diffraction, micro structural analysis, density measurements and its phase diagram has been constructed. It has been established that the section Se-CaIn 4 Se 7 is a quasibinary section of the ternary system Ca-In-Se. At room temperature, on the basis of CaIn 2 Se 4 and Se no solid solution has been found

Modification of a loop sequence between α-helices 6 and 7 of virus capsid (CA protein in a human immunodeficiency virus type 1 (HIV-1 derivative that has simian immunodeficiency virus (SIVmac239 vif and CA α-helices 4 and 5 loop improves replication in cynomolgus monkey cells

Directory of Open Access Journals (Sweden)

Adachi Akio

2009-08-01

Full Text Available Abstract Background Human immunodeficiency virus type 1 (HIV-1 productively infects only humans and chimpanzees but not cynomolgus or rhesus monkeys while simian immunodeficiency virus isolated from macaque (SIVmac readily establishes infection in those monkeys. Several HIV-1 and SIVmac chimeric viruses have been constructed in order to develop an animal model for HIV-1 infection. Construction of an HIV-1 derivative which contains sequences of a SIVmac239 loop between α-helices 4 and 5 (L4/5 of capsid protein (CA and the entire SIVmac239 vif gene was previously reported. Although this chimeric virus could grow in cynomolgus monkey cells, it did so much more slowly than did SIVmac. It was also reported that intrinsic TRIM5α restricts the post-entry step of HIV-1 replication in rhesus and cynomolgus monkey cells, and we previously demonstrated that a single amino acid in a loop between α-helices 6 and 7 (L6/7 of HIV type 2 (HIV-2 CA determines the susceptibility of HIV-2 to cynomolgus monkey TRIM5α. Results In the study presented here, we replaced L6/7 of HIV-1 CA in addition to L4/5 and vif with the corresponding segments of SIVmac. The resultant HIV-1 derivatives showed enhanced replication capability in established T cell lines as well as in CD8+ cell-depleted primary peripheral blood mononuclear cells from cynomolgus monkey. Compared with the wild type HIV-1 particles, the viral particles produced from a chimeric HIV-1 genome with those two SIVmac loops were less able to saturate the intrinsic restriction in rhesus monkey cells. Conclusion We have succeeded in making the replication of simian-tropic HIV-1 in cynomolgus monkey cells more efficient by introducing into HIV-1 the L6/7 CA loop from SIVmac. It would be of interest to determine whether HIV-1 derivatives with SIVmac CA L4/5 and L6/7 can establish infection of cynomolgus monkeys in vivo.

Investigation of the stability of glass-ceramic composites containing CeTi2O6 and CaZrTi2O7 after ion implantation

Science.gov (United States)

Paknahad, Elham; Grosvenor, Andrew P.

2017-12-01

Glass-ceramic composite materials have been investigated for nuclear waste sequestration applications due to their ability to incorporate large amounts of radioactive waste elements. A key property that needs to be understood when developing nuclear waste sequestration materials is how the structure of the material responds to radioactive decay of nuclear waste elements, which can be simulated by high energy ion implantation. Borosilicate glass-ceramic composites containing brannerite-type (CeTi2O6) or zirconolite-type (CaZrTi2O7) oxides were synthesized at different annealing temperatures and investigated after being implanted with high-energy Au ions to mimic radiation induced structural damage. Backscattered electron (BSE) images were collected to investigate the interaction of the brannerite crystallites with the glass matrix before and after implantation and showed that the morphology of the crystallites in the composite materials were not affected by radiation damage. Surface sensitive Ti K-edge glancing angle XANES spectra collected from the implanted composite materials showed that the structures of the CeTi2O6 and CaZrTi2O7 ceramics were damaged as a result of implantation; however, analysis of Si L2,3-edge XANES spectra indicated that the glass matrix was not affected by ion implantation.

Investigation of the stability of glass-ceramic composites containing CeTi 2 O 6 and CaZrTi 2 O 7 after ion implantation

Energy Technology Data Exchange (ETDEWEB)

Paknahad, Elham; Grosvenor, Andrew P.

2017-12-01

Glass-ceramic composite materials have been investigated for nuclear waste sequestration applications due to their ability to incorporate large amounts of radioactive waste elements. A key property that needs to be understood when developing nuclear waste sequestration materials is how the structure of the material responds to radioactive decay of nuclear waste elements, which can be simulated by high energy ion implantation. Borosilicate glass-ceramic composites containing brannerite-type (CeTi2O6) or zirconolite-type (CaZrTi2O7) oxides were synthesized at different annealing temperatures and investigated after being implanted with high-energy Au ions to mimic radiation induced structural damage. Backscattered electron (BSE) images were collected to investigate the interaction of the brannerite crystallites with the glass matrix before and after implantation and showed that the morphology of the crystallites in the composite materials were not affected by radiation damage. Surface sensitive Ti K-edge glancing angle XANES spectra collected from the implanted composite materials showed that the structures of the CeTi2O6 and CaZrTi2O7 ceramics were damaged as a result of implantation; however, analysis of Si L2,3-edge XANES spectra indicated that the glass matrix was not affected by ion implantation.

Synthesis and photoluminescence properties of Sm3+-doped CaWO4 nanoparticles

International Nuclear Information System (INIS)

Xiao Qi; Zhou Qitao; Li Ming

2010-01-01

The Sm 3+ -doped CaWO 4 nanoparticles were synthesized by hydrothermal method. The room temperature photoluminescence (PL) spectra of Sm 3+ -doped CaWO 4 nanoparticles doped with different Sm 3+ concentrations under 405 nm excitation have been investigated. The PL spectra showed four strong emission peaks at 460, 571, 609, and 653 nm. The first emission peak at 460 nm could be due to a structural defect of the lattice, an oxygen-deficient WO 3 complex. The other three emissions at 571, 609, and 653 nm were due to the f-f forbidden transitions of the 4f electrons of Sm 3+ , corresponding to 4 G 5/2 → 6 H 5/2 (571 nm), 6 H 7/2 (609 nm), and 6 H 9/2 (653 nm), respectively. In addition, the optimum Sm 3+ concentration in CaWO 4 nanoparticles for optical emission was determined to be 1.0%. The Sm 3+4 G 5/2 → 6 H 7/2 (609 nm) emission intensity of Sm 3+ -doped CaWO 4 nanoparticles significantly increased with the increase of Sm 3+ concentration, and showed a maximum when Sm 3+ doping content was 1.0%. If Sm 3+ concentration continued to increase, namely more than 1.0%, the Sm 3+4 G 5/2 → 6 H 7/2 emission intensity would decrease. The present materials might be a promising phosphor for white-light LED applications.

Luminescent properties of complexly substituted oxides Ме2Ln8 (XO46O2 (Me=Sr, Ca; Ln=La, Gd, Eu; X= Si, P

Directory of Open Access Journals (Sweden)

A. A. Vasin

2014-11-01

Full Text Available In the current work it is established that the maximum intensity of a luminescence of crystalline phosphors with structure silicate-apatite of general formulae: Ca2Eu8Si6(1-xP6xO26, Sr2Gd7.2Eu0.8Si6(1-xP6xO26 and Ca2La8(1-xEu8xSi6O26 is reached at concentration of europium equal 0,15. The maximum intensity of a luminescence of these substances, at replacement in an anion sublattice of tetrahedrons [SiO4]4- on tetrahedrons [PO4]3- takes place at concentration of phosphorus 0,05.

Synthesis of Ca(PF6)2, formed via nitrosonium oxidation of calcium.

Science.gov (United States)

Keyzer, Evan N; Matthews, Peter D; Liu, Zigeng; Bond, Andrew D; Grey, Clare P; Wright, Dominic S

2017-04-20

The development of rechargeable Ca-ion batteries as an alternative to Li systems has been limited by the availability of suitable electrolyte salts. We present the synthesis of complexes of Ca(PF 6 ) 2 (a key potential Ca battery electrolyte salt) via the treatment of Ca metal with NOPF 6 , and explore their conversion to species containing PO 2 F 2 - under the reaction conditions.

Fracto- mechanoluminescence and thermoluminescence properties of orange-red emitting Eu3+ doped Ca2Al2SiO7 phosphors

International Nuclear Information System (INIS)

Tiwari, Geetanjali; Brahme, Nameeta; Sharma, Ravi; Bisen, D.P.; Sao, Sanjay K.; Khare, Ayush

2017-01-01

The suitability of nano-structured Ca 2 Al 2 SiO 7 :Eu 3+ phosphors for thermoluminescence and mechanoluminescence dosimeter were investigated. Europium doped di-calcium di-aluminum silicate phosphor was synthesised by the combustion assisted method and annealed at 1100 °C for 4 h in reducing and oxidizing environments. The prepared Ca 2 Al 2 SiO 7 :Eu 3+ phosphor was characterized by X-ray diffractometer (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM) with energy dispersive x-ray spectroscopy (EDX), photoluminescence (PL) and decay characteristics. The phase structure of sintered phosphor has akermanite type which belongs to the tetragonal crystallography; this structure is a member of the melilite group and forms a layered compound. The chemical composition of the sintered Ca 2 Al 2 SiO 7 :Eu 3+ phosphor was confirmed by EDX spectra. Mechanoluminescence (ML) and thermoluminescence (TL) studies revealed that the ML and TL intensity increases with activator concentration. Optimum ML was observed for the sample having 2 mol% of Eu ions. The TL intensity of Ca 2 Al 2 SiO 7 :Eu 3+ was recorded for different exposure times of γ -irradiation and it was observed that TL intensity is maximum for γ dose of 1770 Gy. The PL spectra indicated that Ca 2 Al 2 SiO 7 :Eu 3+ could be excited effectively by near ultraviolet (NUV) light and exhibited bright orange-red emission with excellent colour stability. CIE colour coordinates of the prepared Ca 2 Al 2 SiO 7 :Eu 3+ phosphor was found suitable as orange-red light emitting phosphor with a CIE value of (x=0.6142, y=0.3849) and correlated colour temperature (CCT) is 1250 K. Therefore, it is considered to be a new promising orange-red emitting phosphor for white light emitting diode (LED) application.

Magnetic and magnetocaloric properties of La{sub 1.4-x}Yb{sub x}Ca{sub 1.6}Mn{sub 2}O{sub 7}

Energy Technology Data Exchange (ETDEWEB)

Himcinschi, C. [Babes-Bolyai Univ., Cluj-Napoca (Romania). Faculty of Physics; GSI, Strasbourg (France). Inst. de Physique et Chemie des Materiaux; Burzo, E. [Babes-Bolyai Univ., Cluj-Napoca (Romania). Faculty of Physics; Deville, J.P. [GSI, Strasbourg (France). Inst. de Physique et Chemie des Materiaux

2001-07-01

Magnetic and magnetocaloric properties of La{sub 1.4-x}Yb{sub x}Ca{sub 1.6}Mn{sub 2}O{sub 7} system were studied. Polycrystalline samples with x = 0 and 0.2 were prepared by solid state reaction. Magnetic measurements show that Curie temperatures decrease from 246 K for x = 0 down to 211 K for x = 0.2. The temperature dependences of the magnetic entropy change {delta}S{sub M}, show peaks close to the magnetic transition temperatures. Peak values of {delta}S{sub M} = 2.7 J/kg K and 2.1 J/kg K were obtained for compositions x = 0 and 0.2. The decrease in {delta}S{sub M} when changing composition was correlated with the diminution of exchange interactions. (orig.)

Hydrogen and electricity production in a light-assisted microbial photoelectrochemical cell with CaFe2O4 photocathode

Science.gov (United States)

Chen, Qing-Yun; Zhang, Kai; Liu, Jian-Shan; Wang, Yun-Hai

2017-04-01

A microbial photoelectrochemical cell (MPEC) was designed with a p-type CaFe2O4 semiconductor as the photoelectrode for simultaneous hydrogen and electricity production under light illumination. The CaFe2O4 photoelectrode was synthesized by the sol-gel method and well characterized by x-ray diffraction, field emission scanning electron microscope, and UV-Vis-NIR spectrophotometer. The linear sweep voltammogram of the CaFe2O4 photoelectrode presented the cathodic photocurrent output. For the MPEC, with an external resistance of 2000 Ω, the maximum power density of 143 mW was obtained. Furthermore, with an external resistance of 100 Ω, the maximum hydrogen production rate of 6.7 μL·cm-2 could be achieved. The MPEC with CaFe2O4 photocathode was compared to MPEC with other photocathodes as well as photocatalytic water splitting technology.

Quantifying Ca2+ release and inactivation of Ca2+ release in fast- and slow-twitch muscles.

Science.gov (United States)

Barclay, C J

2012-12-01

The aims of this study were to quantify the Ca(2+) release underlying twitch contractions of mammalian fast- and slow-twitch muscle and to comprehensively describe the transient inactivation of Ca(2+) release following a stimulus. Experiments were performed using bundles of fibres from mouse extensor digitorum longus (EDL) and soleus muscles. Ca(2+) release was quantified from the amount of ATP used to remove Ca(2+) from the myoplasm following stimulation. ATP turnover by crossbridges was blocked pharmacologically (N-benzyl-p-toluenesulphonamide for EDL, blebbistatin for soleus) and muscle heat production was used as an index of Ca(2+) pump ATP turnover. At 20°C, Ca(2+) release in response to a single stimulus was 34 and 84 μmol (kg muscle)(-1) for soleus and EDL, respectively, and increased with temperature (30°C: soleus, 61 μmol kg(-1); EDL, 168 μmol kg(-1)). Delivery of another stimulus within 100 ms of the first produced a smaller Ca(2+) release. The maximum magnitude of the decrease in Ca(2+) release was greater in EDL than soleus. Ca(2+) release recovered with an exponential time course which was faster in EDL (mean time constant at 20°C, 32.1 ms) than soleus (65.6 ms) and faster at 30°C than at 20°C. The amounts of Ca(2+) released and crossbridge cycles performed are consistent with a scheme in which Ca(2+) binding to troponin-C allowed an average of ∼1.7 crossbridge cycles in the two muscles.

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

Indian Academy of Sciences (India)

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

Low-Temperature Sintering Li3Mg1.8Ca0.2NbO6 Microwave Dielectric Ceramics with LMZBS Glass

Science.gov (United States)

Wang, Gang; Zhang, Huaiwu; Liu, Cheng; Su, Hua; Jia, Lijun; Li, Jie; Huang, Xin; Gan, Gongwen

2018-05-01

Li3Mg1.8Ca0.2NbO6 ceramics doped with Li2O-MgO-ZnO-B2O3-SiO2 glass (LMZBS) were prepared via a solid-state route. The LMZBS glass effectively reduced the sintering temperature of Li3Mg1.8Ca0.2NbO6 ceramics to 950°C. The effects of the LMZBS glass on the sintering behavior, microstructures and microwave dielectric properties of Li3Mg1.8Ca0.2NbO6 ceramics are discussed in detail. Among all the LMZBS doped Li3Mg1.8Ca0.2NbO6 ceramics, the sample with 1 wt.% of LMZBS glass sintered at 950°C for 4 h exhibited good dielectric properties: ɛ r = 16.7, Q × f = 31,000 GHz (9.92 GHz), τ f = - 1.3 ppm/°C. The Li3Mg1.8Ca0.2NbO6 ceramics possessed excellent chemical compatibility with Ag electrodes, and could be applied in low temperature co-fired ceramics (LTCC) applications.

Unresolved problems in superconductivity of CaC6

NARCIS (Netherlands)

Mazin, I.I.; Boen, L.; Dolgov, O.V.; Golubov, Alexandre Avraamovitch; Bachelet, G.B.; Giantomassi, M.; Andersen, O.K.

2007-01-01

We discuss the current status of the theory of the “high-temperature” superconductivity in intercalated graphites YbC6 and CaC6. We emphasize that while the general picture of conventional, phonon-driven superconductivity has already emerged and is generally accepted, there are still interesting

Unraveling the Role of Structural Order in the Transformation of Electrical Conductivity in Ca2FeCoO6-δ, CaSrFeCoO6-δ, and Sr2FeCoO6-δ.

Science.gov (United States)

Hona, Ram Krishna; Huq, Ashfia; Ramezanipour, Farshid

2017-12-04

The ability to control the electrical conductivity of solid-state oxides using structural parameters has been demonstrated. A correlation has been established between the electrical conductivity and structural order in a series of oxygen-deficient perovskites using X-ray and neutron diffraction, X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and electrical conductivity studies at a wide temperature range, 25-800 °C. The crystal structure of CaSrFeCoO 6-δ has been determined, and its stark contrast to Ca 2 FeCoO 6-δ and Sr 2 FeCoO 6-δ has been demonstrated. The Fe/Co distribution over tetrahedral and octahedral sites has been determined using neutron diffraction. There is a systematic increase in the structural order in progression from Sr 2 FeCoO 6-δ (δ = 0.5) to CaSrFeCoO 6-δ (δ = 0.8) and Ca 2 FeCoO 6-δ (δ = 0.9) . The oxygen contents of these materials were determined using iodometric titration and TGA. At room temperature, there is an inverse correlation between the electrical conductivity and structural order. The ordered Ca 2 and CaSr compounds are semiconductors, while the disordered Sr 2 compund shows metallic behavior. The metallic nature of the Sr 2 material persists up to 1073 K (800 °C), while the Ca 2 and CaSr compounds undergo a semiconductor-to-metal transition above 500 and 300 °C, respectively, highlighting another important impact of the structural order. At high temperature, the CaSr compound has the highest conductivity compared to the Ca 2 and Sr 2 materials. There appears to be an optimum degree of structural order that leads to the highest conductivity at high temperature. Another consequence of the structural order is the observation of mixed ionic-electronic conductivity in CaSr and Ca 2 compounds, as is evident from the hysteresis in the conductivity data obtained during heating and cooling cycles. The average ionic radius required for each structural transition was

Synaptotagmin-7 is a principal Ca2+ sensor for Ca2+ -induced glucagon exocytosis in pancreas

DEFF Research Database (Denmark)

Gustavsson, Natalia; Wei, Shun-Hui; Hoang, Dong Nhut

2009-01-01

Hormones such as glucagon are secreted by Ca(2+)-induced exocytosis of large dense-core vesicles, but the mechanisms involved have only been partially elucidated. Studies of pancreatic beta-cells secreting insulin revealed that synaptotagmin-7 alone is not sufficient to mediate Ca(2+)-dependent i...

Histone deacetylase 6 inhibition reduces cysts by decreasing cAMP and Ca2+ in knock-out mouse models of polycystic kidney disease.

Science.gov (United States)

Yanda, Murali K; Liu, Qiangni; Cebotaru, Valeriu; Guggino, William B; Cebotaru, Liudmila

2017-10-27

Autosomal dominant polycystic kidney disease (ADPKD) is associated with progressive enlargement of multiple renal cysts, often leading to renal failure that cannot be prevented by a current treatment. Two proteins encoded by two genes are associated with ADPKD: PC1 ( pkd1 ), primarily a signaling molecule, and PC2 ( pkd2 ), a Ca 2+ channel. Dysregulation of cAMP signaling is central to ADPKD, but the molecular mechanism is unresolved. Here, we studied the role of histone deacetylase 6 (HDAC6) in regulating cyst growth to test the possibility that inhibiting HDAC6 might help manage ADPKD. Chemical inhibition of HDAC6 reduced cyst growth in PC1-knock-out mice. In proximal tubule-derived, PC1-knock-out cells, adenylyl cyclase 6 and 3 (AC6 and -3) are both expressed. AC6 protein expression was higher in cells lacking PC1, compared with control cells containing PC1. Intracellular Ca 2+ was higher in PC1-knock-out cells than in control cells. HDAC inhibition caused a drop in intracellular Ca 2+ and increased ATP-simulated Ca 2+ release. HDAC6 inhibition reduced the release of Ca 2+ from the endoplasmic reticulum induced by thapsigargin, an inhibitor of endoplasmic reticulum Ca 2+ -ATPase. HDAC6 inhibition and treatment of cells with the intracellular Ca 2+ chelator 1,2-bis(2-aminophenoxy)ethane- N , N , N ', N '-tetraacetic acid tetrakis(acetoxymethyl ester) reduced cAMP levels in PC1-knock-out cells. Finally, the calmodulin inhibitors W-7 and W-13 reduced cAMP levels, and W-7 reduced cyst growth, suggesting that AC3 is involved in cyst growth regulated by HDAC6. We conclude that HDAC6 inhibition reduces cell growth primarily by reducing intracellular cAMP and Ca 2+ levels. Our results provide potential therapeutic targets that may be useful as treatments for ADPKD. © 2017 by The American Society for Biochemistry and Molecular Biology, Inc.

Effect of Ca doping level on the laser-induced voltages in tilted La{sub 1-x}Ca{sub x}MnO{sub 3} (0.1 ≤ x ≤ 0.7) thin films

Energy Technology Data Exchange (ETDEWEB)

Ma, Ji; Zhang, Hui; Chen, Qingming; Liu, Xiang [Kunming University of Science and Technology, Faculty of Materials Science and Engineering, Kunming (China); Theingi, Mya [Kunming University of Science and Technology, Faculty of Materials Science and Engineering, Kunming (China); University of Yangon, Department of Chemistry, Yangon (Myanmar)

2014-03-15

Tilted La{sub 1-x}Ca{sub x}MnO{sub 3} (0.1 ≤ x ≤ 0.7) thin films have been grown on vicinal cut LaAlO{sub 3} (100) substrate by pulsed laser deposition. The laser-induced voltage effect was studied at room temperature with the KrF excimer laser using as the thermal source. The relationships between Ca doping level and voltage signal, response time and anisotropy Seebeck coefficient were established. The voltage signal and anisotropy Seebeck coefficient increase at first with increasing Ca doping level, reach a maximum at the same Ca content around x = 0.5, and then decrease. The respond time decreases with the Ca concentration increasing, and changes very little after x = 0.5. The figure of merit F{sub m} was also the largest at this doping level, indicating a potential good performance of the photodetector devices. The variation of intrinsic structural and transport anisotropy induced by the change of Ca concentration has been proposed to account for the different LIV effects observed in LCMO thin films. (orig.)

Reconstruction of calmodulin single-molecule FRET states, dye interactions, and CaMKII peptide binding by MultiNest and classic maximum entropy

Science.gov (United States)

DeVore, Matthew S.; Gull, Stephen F.; Johnson, Carey K.

2013-08-01

We analyzed single molecule FRET burst measurements using Bayesian nested sampling. The MultiNest algorithm produces accurate FRET efficiency distributions from single-molecule data. FRET efficiency distributions recovered by MultiNest and classic maximum entropy are compared for simulated data and for calmodulin labeled at residues 44 and 117. MultiNest compares favorably with maximum entropy analysis for simulated data, judged by the Bayesian evidence. FRET efficiency distributions recovered for calmodulin labeled with two different FRET dye pairs depended on the dye pair and changed upon Ca2+ binding. We also looked at the FRET efficiency distributions of calmodulin bound to the calcium/calmodulin dependent protein kinase II (CaMKII) binding domain. For both dye pairs, the FRET efficiency distribution collapsed to a single peak in the case of calmodulin bound to the CaMKII peptide. These measurements strongly suggest that consideration of dye-protein interactions is crucial in forming an accurate picture of protein conformations from FRET data.

Reconstruction of Calmodulin Single-Molecule FRET States, Dye-Interactions, and CaMKII Peptide Binding by MultiNest and Classic Maximum Entropy.

Science.gov (United States)

Devore, Matthew S; Gull, Stephen F; Johnson, Carey K

2013-08-30

We analyze single molecule FRET burst measurements using Bayesian nested sampling. The MultiNest algorithm produces accurate FRET efficiency distributions from single-molecule data. FRET efficiency distributions recovered by MultiNest and classic maximum entropy are compared for simulated data and for calmodulin labeled at residues 44 and 117. MultiNest compares favorably with maximum entropy analysis for simulated data, judged by the Bayesian evidence. FRET efficiency distributions recovered for calmodulin labeled with two different FRET dye pairs depended on the dye pair and changed upon Ca 2+ binding. We also looked at the FRET efficiency distributions of calmodulin bound to the calcium/calmodulin dependent protein kinase II (CaMKII) binding domain. For both dye pairs, the FRET efficiency distribution collapsed to a single peak in the case of calmodulin bound to the CaMKII peptide. These measurements strongly suggest that consideration of dye-protein interactions is crucial in forming an accurate picture of protein conformations from FRET data.

Dosimeter properties of Ce and Eu doped LiCaAlF6

International Nuclear Information System (INIS)

Yanagida, Takayuki; Fujimoto, Yutaka; Watanabe, Kenichi; Fukuda, Kentaro

2014-01-01

Optical, scintillation properties, optical stimulated luminescence, and thermally stimulated luminescence of Ce 1, 3, and 5% doped and Eu 1, 1.5, and 2% doped LiCaAlF 6 crystals fabricated by Tokuyama Corp. were investigated. In transmittance, absorption was proportional to dopant concentrations and typical optical quantum yield of Ce and Eu-doped LiCaAlF 6 were 40 and 100%, respectively. Scintillation wavelength and decay time profiles were investigated under X-ray irradiation. Ce 3+ and Eu 2+ 5d-4f luminescence appeared around 300 nm and 370 nm with typical decay time of 40 ns and 1.5 μs, respectively. Optically stimulated luminescence of Ce-doped ones appeared under 405 nm stimulation with detectable intensity while those of Eu doped ones were quite weak. Thermally stimulated luminescence of Ce- and Eu-doped LiCaAlF 6 were enough strong and they exhibited good response function from 1 to 1000 mGy exposure. - Highlights: • Optical, scintillation, OSL, and TSL properties of Ce or Eu differently doped LiCaAlF6 were studied. • PL quantum yield of Ce and Eu doped LiCaAlF6 showed 40% and 100%, respectively. • OSL was observed in Ce-doped LiCaAlF6. • TSL was observed in both material systems and exhibited a good dose response from 1 to 1000 mGy

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

International Nuclear Information System (INIS)

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

2010-01-01

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

Photoluminescence characteristics of Sm{sup 3+}-doped Ba{sub 2}CaWO{sub 6} as new orange–red emitting phosphors

Energy Technology Data Exchange (ETDEWEB)

Yu, Ruiijn [College of Science, Northwest A and F University, Yangling, Shaanxi 712100 (China); Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of); Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Mi Noh, Hyeon; Kee Moon, Byung; Chun Choi, Byung [Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of); Hyun Jeong, Jung, E-mail: jhjeong@pknu.ac.kr [Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of); Sueb Lee, Ho [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Jang, Kiwan, E-mail: kwjang@changwon.ac.kr [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Soo Yi, Soung [Department of Electronic Material Engineering, Silla University, Busan 617-736 (Korea, Republic of)

2014-08-01

The orange–red emitting Ba{sub 2}CaWO{sub 6}:xSm{sup 3+} (0.01≤x≤0.25) phosphors were synthesized via solid state reaction process. The crystal structure of the phosphor was characterized by XRD. The photoluminescence excitation and emission spectra, concentration effect were investigated. The results show an efficient energy transfer from WO{sub 6}{sup 6−} group to Sm{sup 3+} occurs. The emission spectra of the Ba{sub 2}CaWO{sub 6}:Sm{sup 3+} phosphors consisted of some sharp emission peaks of Sm{sup 3+} ions centre at 579 nm, 618 nm, 625 nm, and 675 nm. The strongest one is located at 610 nm due to {sup 4}G{sub 5/2}→{sup 6}H{sub 7/2} transition of Sm{sup 3+}, generating bright orange–red light. The optimum dopant concentration of Sm{sup 3+} ions in Ba{sub 2}CaWO{sub 6}:xSm{sup 3+} is around 5 mol% and the critical transfer distance of Sm{sup 3+} is calculated as 18 Å. The fluorescence lifetime of Sm{sup 3+} in Ba{sub 2}CaWO{sub 6}:0.05Sm{sup 3+} is 2.36 ms. The Ba{sub 2}CaWO{sub 6}:Sm{sup 3+} phosphors may be potentially used as orange–red phosphors for white light-emitting diodes. - Highlights: • A new host-sensitized Sm{sup 3+}-doped Ba{sub 2}CaWO{sub 6} phosphor was firstly synthesized. • Its structure, luminescent properties are well studied and characterized. • There exists an efficient energy transfer from WO{sub 6}{sup 6−} group to Sm{sup 3+}. • The thermal quenching properties of Ba{sub 2}CaWO{sub 6}:Sm{sup 3+} was firstly evaluated.

Giant T{sub c} shift in HgBa{sub 2}CaCu{sub 2}O{sub 6+{delta}} and TlBa{sub 2}CaCu{sub 2}O{sub 7{minus}{delta}} superconductors due to Hg-Tl exchange

Energy Technology Data Exchange (ETDEWEB)

Gapud, A.A.; Wu, J.Z.; Kang, B.W.; Yan, S.L.; Xie, Y.Y. [Department of Physics and Astronomy, University of Kansas, Lawrence, Kansas 66045-2151 (United States); Siegal, M.P. [Sandia National Laboratories, Albuquerque, New Mexico 87185 (United States)

1999-01-01

The irreversibility lines of epitaxial thin films of HgBa{sub 2}CaCu{sub 2}O{sub 6+{delta}} and TlBa{sub 2}CaCu{sub 2}O{sub 7{minus}{delta}}, whether deduced from field-induced magnetoresistive broadening or onset of nonhysteretic magnetization, were found to coincide when plotted against reduced temperature, showing the same exponential-decay temperature behavior for T/T{sub c}{lt}0.8 and power-law behavior for T/T{sub c}{gt}0.8 (where T{sub c} is zero-field, zero-resistivity critical temperature). These results indicate that replacing Tl with Hg has no noticeable effect on the anisotropy and suggests that T{sub c} is not determined by anisotropy. {copyright} {ital 1999} {ital The American Physical Society}

Crystal growth, optical properties, and continuous-wave laser operation of Nd3+-doped CaNb2O6 crystal

International Nuclear Information System (INIS)

Cheng, Y; Xu, X D; Xiao, X D; Li, D Z; Zhao, C C; Zhou, S M; Xin, Z; Yang, X B; Xu, J

2009-01-01

Laser crystal Nd:CaNb 2 O 6 with excellent quality has been grown by Czochralski technique. The effective segregation coefficient of Nd 3+ was studied by X-ray fluorescence method. The polarized absorption spectra and the fluorescence spectra of Nd:CaNb 2 O 6 were measured at room temperature. The peak absorption cross section was calculated to be 6.202×10 -20 cm 2 with a broad FWHM of 7 nm at 808 nm for E ∥ a light polarization. The emission cross section at 1062 nm is 9.87×10 -20 cm 2 . We report what we believe to be the first demonstration of the continuous-wave Nd:CaNb 2 O 6 laser operation under diode pumping. Output power of 1.86 W at 1062 nm was obtained with a slope efficiency of 19% in the CW regime

Crystal growth, optical properties, and continuous-wave laser operation of Nd3+-doped CaNb2O6 crystal

Science.gov (United States)

Cheng, Y.; Xu, X. D.; Xin, Z.; Yang, X. B.; Xiao, X. D.; Li, D. Z.; Zhao, C. C.; Xu, J.; Zhou, S. M.

2009-10-01

Laser crystal Nd:CaNb2O6 with excellent quality has been grown by Czochralski technique. The effective segregation coefficient of Nd3+ was studied by X-ray fluorescence method. The polarized absorption spectra and the fluorescence spectra of Nd:CaNb2O6 were measured at room temperature. The peak absorption cross section was calculated to be 6.202×10-20 cm2 with a broad FWHM of 7 nm at 808 nm for E ∥ a light polarization. The emission cross section at 1062 nm is 9.87×10-20 cm2. We report what we believe to be the first demonstration of the continuous-wave Nd:CaNb2O6 laser operation under diode pumping. Output power of 1.86 W at 1062 nm was obtained with a slope efficiency of 19% in the CW regime.

Synthesis of Ca(PF$_6$)$_2$, formed $\\textit{via}$ nitrosonium oxidation of calcium

OpenAIRE

Keyzer, Evan; Matthews, PD; Liu, Zigeng; Bond, Andrew David; Grey, Clare Philomena; Wright, Dominic Simon

2017-01-01

The development of rechargeable Ca-ion batteries as an alternative to Li systems has been limited by the availability of suitable electrolyte salts. We present the synthesis of complexes of Ca(PF$_6$)$_2$ (a key potential Ca battery electrolyte salt) $\\textit{via}$ the treatment of Ca metal with NOPF$_6$, and explore their conversion to species containing PO$_2$F$_2$$^{-}$ under the reaction conditions. NSERC of Canada PGSD; Gonville and Caius College; Cambridge Commonwealth, European, and...

Mol 7C/6; Mol 7C/6

Energy Technology Data Exchange (ETDEWEB)

Aberle, J.; Schleisiek, K.; Schmuck, I.; Schmidt, L.; Romer, O.; Weih, G.

1995-08-01

The Mol 7C/6 coolant blockage experiment in the Belgian BR2 reactor yielded results different from Mol 7C experiments with low burnup pins: At 10% burnup local failure is not self-limiting, but requires active systems for detection and scram. The Mol 7C series was finished in 1991. In each of the test bundles Mol 7C/4, /5 and /6, 30 Mk I pins pre-irradiated in KNK II were used. The central blockage consisted of enriched UO{sub 2} covering 30 percent of the bundle cross-section, with a height of 40 mm. The most important system for timely detection of coolant blockages of the type studied in Mol 7C/6 is based on DND. (orig.)

Optimization of pH, temperature and CaCl2 concentrations for Ricotta cheese production from Buffalo cheese whey using Response Surface Methodology.

Science.gov (United States)

Rashid, Abdul Ahid; Huma, Nuzhat; Zahoor, Tahir; Asgher, Muhammad

2017-02-01

The recovery of milk constituents from cheese whey is affected by various processing conditions followed during production of Ricotta cheese. The objective of the present investigation was to optimize the temperature (60-90 °C), pH (3-7) and CaCl2 concentration (2·0-6·0 mm) for maximum yield/recovery of milk constituents. The research work was carried out in two phases. In 1st phase, the influence of these processing conditions was evaluated through 20 experiments formulated by central composite design (CCD) keeping the yield as response factor. The results obtained from these experiments were used to optimize processing conditions for maximum yield using response surface methodology (RSM). The three best combinations of processing conditions (90 °C, pH 7, CaCl2 6 mm), (100 °C, pH 5, CaCl2 4 mm) and (75 °C, pH 8·4, CaCl2 4 mm) were exploited in the next phase for Ricotta cheese production from a mixture of Buffalo cheese whey and skim milk (9 : 1) to determine the influence of optimized conditions on the cheese composition. Ricotta cheeses were analyzed for various physicochemical (moisture, fat, protein, lactose, total solids, pH and acidity indicated) parameters during storage of 60 d at 4 ± 2 °C after every 15 d interval. Ricotta cheese prepared at 90 °C, pH 7 and CaCl2 6 mm exhibited the highest cheese yield, proteins and total solids, while high fat content was recorded for cheese processed at 100 °C, pH 5 and 4 mm CaCl2 concentration. A significant storage-related increase in acidity and NPN was recorded for all cheese samples.

Overexpression of CaDSR6 increases tolerance to drought and salt stresses in transgenic Arabidopsis plants.

Science.gov (United States)

Kim, Eun Yu; Seo, Young Sam; Park, Ki Youl; Kim, Soo Jin; Kim, Woo Taek

2014-11-15

The partial CaDSR6 (Capsicum annuum Drought Stress Responsive 6) cDNA was previously identified as a drought-induced gene in hot pepper root tissues. However, the cellular role of CaDSR6 with regard to drought stress tolerance was unknown. In this report, full-length CaDSR6 cDNA was isolated. The deduced CaDSR6 protein was composed of 234 amino acids and contained an approximately 30 amino acid-long Asp-rich domain in its central region. This Asp-rich domain was highly conserved in all plant DSR6 homologs identified and shared a sequence identity with the N-terminal regions of yeast p23(fyp) and human hTCTP, which contain Rab protein binding sites. Transgenic Arabidopsis plants overexpressing CaDSR6 (35S:CaDSR6-sGFP) were tolerant to high salinity, as identified by more vigorous root growth and higher levels of total chlorophyll than wild type plants. CaDSR6-overexpressors were also more tolerant to drought stress compared to wild type plants. The 35S:CaDSR6-sGFP leaves retained their water content and chlorophyll more efficiently than wild type leaves in response to dehydration stress. The expression of drought-induced marker genes, such as RD20, RD22, RD26, RD29A, RD29B, RAB18, KIN2, ABF3, and ABI5, was markedly increased in CaDSR6-overexpressing plants relative to wild type plants under both normal and drought conditions. These results suggest that overexpression of CaDSR6 is associated with increased levels of stress-induced genes, which, in turn, conferred a drought tolerant phenotype in transgenic Arabidopsis plants. Overall, our data suggest that CaDSR6 plays a positive role in the response to drought and salt stresses. Copyright © 2014 Elsevier B.V. All rights reserved.

Bioactivity and mineralization of hydroxyapatite with bioglass as sintering aid and bioceramics with Na3Ca6(PO4)5 and Ca5(PO4)2SiO4 in a silicate matrix

International Nuclear Information System (INIS)

Demirkiran, Hande; Mohandas, Arunesh; Dohi, Motokazi; Fuentes, Alonso; Nguyen, Kytai; Aswath, Pranesh

2010-01-01

Hydroxyapatite and Bioglass-45S5 were sintered together creating new ceramic compositions that yielded increased apatite deposition and osteoblast differentiation and proliferation in vitro compared to hydroxyapatite. The sintered products characterized by X-ray diffraction, revealed hydroxyapatite as the main phase when small quantities (1, 2.5 and 5 wt.%) of bioglass was added. Bioglass behaved as a sintering aid with β-TCP (Ca 3 (PO 4 ) 2 ) being the minor phase. The amount of β-TCP increased with the amount of bioglass added. In compositions with larger additions of bioglass (10 and 25 wt.%), new phases with compositions of calcium phosphate silicate (Ca 5 (PO 4 ) 2 SiO 4 ) and sodium calcium phosphate (Na 3 Ca 6 (PO 4 ) 5 ) were formed respectively within amorphous silicate matrices. In vitro cell culture studies of the ceramic compositions were examined using bone marrow stromal cell (BMSC). Cell proliferation and differentiation of bone marrow stromal cells into osteoblasts were determined by Pico Green DNA assays and alkaline phosphatase (ALP) activity, respectively. All hydroxyapatite-bioglass co-sintered ceramics exhibited larger cell proliferation compared to pure hydroxyapatite samples. After 6 days in cell culture, the ceramic with Ca 5 (PO 4 ) 3 SiO 4 in a silicate matrix formed by reacting hydroxyapatite with 10 wt.% bioglass exhibited the maximum proliferation of the BMSC's. The ALP activity was found to be largest in the ceramic with Na 3 Ca 6 (PO 4 ) 5 embedded in a silicate matrix synthesized by reacting hydroxyapatite with 25 wt.% bioglass.

Effect of variable doses of ultraviolet radiation (253.7 nm) on thermoluminescence NaCl:Ca(T) material

International Nuclear Information System (INIS)

Nehate, A.K.; Joshi, T.R.; Kathuria, S.P.; Joshi, R.V.

1986-01-01

This paper studies the thermoluminescence (TL) glow curves of NaCl:Ca(T) phosphors to various doses of 253.7-nm ultraviolet (UV) radiation at room temperature. TLD grade NaCl:Ca(T) material was obtained by crystallization from solution and was subsequently annealed at 750 degrees C for 2 h, followed by sudden quenching. We undertook measurement of the effect of variable UV radiation doses (10(2) to 10(6) J m-2) on the TL behaviour of NaCl:Ca(T) phosphors. It was observed that the phosphor exhibits a dominant peak around 167 degrees C along with a weak peak at lower temperature. The high-temperature peak (Peak II) is found to grow linearly with the increase in UV dose in the range of 10(2) to 10(6) J m-2. Since the nature of the glow curves under the influence of different doses remains more or less identical, it is believed that the phosphor does not undergo radiation damage and displays high intrinsic TL around Peak II. Examination of the system for fundamental dosimetry requirements shows that it can be used in dosimetry work at 253.7 nm

[S100A7 promotes the metastasis and epithelial-mesenchymal transition on HeLa and CaSki cells].

Science.gov (United States)

Tian, T; Hua, Z; Wang, L Z; Wang, X Y; Chen, H Y; Liu, Z H; Cui, Z M

2018-02-25

Objective: To elucidate the impact of over-expression of S100A7 on migration, invasion, proliferation, cell cycle, and epithelial-mesenchymal transition (EMT) in human cervical cancer HeLa and CaSki cells. Methods: (1) Immunohistochemistry of SP was used to examine the expression of S100A7 in 40 cases of squamous cervical cancer tissues and 20 cases of normal cervical tissues. (2) The vectors of pLVX-IRES-Neo-S100A7 and pLVX-IRES-Neo were used to transfect human cervical cancer HeLa and CaSki cells, and the positive clones were screened and identified. Next, transwell migration assay, cell counting kit-8 (CCK-8) assay and fluorescence activating cell sorter (FACS) were used to detect the effect of S100A7-overexpression on the migration, invasion, proliferation and cell cycle of cervical cancer cells. Furthermore, western blot was performed to observe the expression of epithelial marker (E-cadherin) and mesenchymal markers (N-cadherin, vimentin, and fibronectin) of EMT. Results: (1) S100A7 expression was significantly higher in cervical squamous cancer tissues (median 91.6) than that in normal cervical tissues (median 52.1; Z=- 2.948, P= 0.003) . (2) Stable S100A7-overexpressed cells were established using lentiviral-mediated gene delivery in HeLa and CaSki cells. S100A7 was detected by real-time quantitative reverse transcription PCR, S100A7 mRNA of S100A7-overexpressed cells were 119±3 and 177±16, increased significantly compared with control groups of median ( Pcells, the number of S100A7-overexpressed HeLa and CaSki cells that passed the transwell membrane assay were increased significanatly (572±51 vs 337±25, PHeLa and CaSki cells that passed the transwell membrane were respectively 441±15 and 110±14, elevated significantly compared with control cells (156±21 and 59±7; Pcell cycle progression of HeLa and CaSki cells ( P> 0.05) . Expression of E-cadherin was dramatically decreased, while N-cadherin, vimentin, and fibronectin increased in S100A7

Oxygen excess in the '114' cobaltite hexagonal structure: The ferrimagnet CaBaCo4O7.50

International Nuclear Information System (INIS)

Pralong, V.; Caignaert, V.; Sarkar, T.; Lebedev, O.I.; Duffort, V.; Raveau, B.

2011-01-01

The study of the oxidation of the '114' orthorhombic cobaltite CaBaCo 4 O 7 , using first electrochemistry and then soft chemistry based on oxidation by NaClO, has allowed a new phase, CaBaCo 4 O 7.50 , to be prepared topotactically. The structural study of this phase shows that its hexagonal structure, closely related to that of orthorhombic CaBaCo 4 O 7 , is curiously similar to that of the members of the LnBaCo 4 O 7 series, in spite of its excess oxygen. Its magnetic study shows that this phase, like CaBaCo 4 O 7 , is ferrimagnetic with the same T C (60 K), but differently exhibits an unusual magnetic hysteresis. This exceptional behavior of CaBaCo 4 O 7 with respect to oxidation as well as the magnetic properties of CaBaCo 4 O 7.50 is interpreted in terms of the presence of defects due to oxidation. - Graphical Abstract: The study of the oxidation of the '114' orthorhombic cobaltite CaBaCo 4 O 7 , using first electrochemistry and then soft chemistry based on oxidation by NaClO, has allowed a new phase, CaBaCo 4 O 7.50 , to be prepared topotactically. The structural study of this phase shows that its hexagonal structure, closely related to that of orthorhombic CaBaCo 4 O 7 , is curiously similar to that of the members of the LnBaCo 4 O 7 series, in spite of its oxygen excess. Its magnetic study shows that this phase, like CaBaCo 4 O 7 , is ferrimagnetic. Highlights: → Topotactic oxidation by means of electrochemistry and soft chemistry of the '114' orthorhombic cobaltite CaBaCo 4 O 7 . → This new phase, CaBaCo 4 O 7.5 shows an hexagonal structure, is closely related to that of orthorhombic mother phase CaBaCo 4 O 7 . → CaBaCo 4 O 7.5 is ferrimagnetic and exhibits an unusual magnetic hysteresis, due to defect pinning centers.

Thermal conductivity of Ca3Co2O6 single crystals

Science.gov (United States)

Che, H. L.; Shi, J.; Wu, J. C.; Rao, X.; Liu, X. G.; Zhao, X.; Sun, X. F.

2018-05-01

Ca3Co2O6 is a rare example of one-dimensional Ising spin-chain material with the moments preferentially aligned along the c axis. In this work, we study the c-axis thermal conductivity (κc) of Ca3Co2O6 single crystal at low temperatures down to 0.3 K and in magnetic fields up to 14 T. The zero-field κc(T) shows a large phonon peak and can be well fitted by using the classical Debye model, which indicates that the heat transport is purely phononic. Moreover, the low-T κc(H) isotherms with H || c display a field-independent behavior. These results indicate that there is no contribution of magnetic excitations to the thermal conductivity in Ca3Co2O6, neither carrying heat nor scattering phonons, which can be attributed to the Ising-like spin anisotropy.

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

Science.gov (United States)

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

2018-04-01

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

Mucins CA 125, CA 19.9, CA 15.3 and TAG-72.3 as tumor markers in patients with lung cancer: comparison with CYFRA 21-1, CEA, SCC and NSE.

Science.gov (United States)

Molina, Rafael; Auge, Jose Maria; Escudero, Jose Miguel; Marrades, Ramon; Viñolas, Nuria; Carcereny, Emilio; Ramirez, Jose; Filella, Xavier

2008-01-01

Tumor marker serum levels were prospectively studied in 289 patients with suspected, but unconfirmed, lung cancer and in 513 patients with lung cancer [417 non-small cell lung cancer (NSCLC) patients and 96 small cell lung cancer (SCLC) patients]. In patients with benign disease, abnormal serum levels were found for the following tumor markers: CEA (in 6.6% of patients); CA 19.9 (6.2%); CA 125 (28.7%); NSE (0.7%); CYFRA (8.7%); TAG-72.3 (4.2%); SCC (3.5%), and CA 15.3 (3.5%). Excluding patients with renal failure or liver diseases, tumor marker specificity improved with abnormal levels in 0.5% for NSE, 0.9% for SCC, 2.8% for CEA, CA 15.3 and TAG-72.3, 3.8% for CA 19.9, 4.2% for CYFRA and 21.4% for CA 125. Excluding CA 125, one of the markers was abnormal in 15% of patients without malignancy. Tumor marker sensitivity was related to cancer histology and tumor extension. NSE had the highest sensitivity in SCLC and CYFRA and CEA in NSCLC. Significantly higher concentrations of CEA, SCC, CA 125, CA 15.3 and TAG-72.3 were found in NSCLC than in SCLC. Likewise, significantly higher CEA (p tumors. Using a combination of 3 tumor markers (CEA, CYFRA 21-1 in all histologies, SCC in squamous tumors and CA 15.3 in adenocarcinomas), a high sensitivity may be achieved in all histological types. Tumor markers may be useful in the histological differentiation of NSCLC and SCLC. Using specific criteria for the differentiation of SCLC and NSCLC, the sensitivity was 84.2 and 68.8%, the specificity was 93.8 and 99.7%, the positive predictive value was 98.3 and 98.5% and the negative predictive value was 57.7 and 93.3%, respectively. Copyright 2008 S. Karger AG, Basel.

High-pressure crystal growth and electromagnetic properties of 5d double-perovskite Ca3OsO6

International Nuclear Information System (INIS)

Feng, Hai Luke; Shi, Youguo; Guo, Yanfeng; Li, Jun; Sato, Akira; Sun, Ying; Wang, Xia; Yu, Shan; Sathish, Clastin I.; Yamaura, Kazunari

2013-01-01

Single crystals of the osmium-containing compound Ca 3 OsO 6 have been successfully grown under high-pressure conditions, for the first time. The crystal structure of Ca 3 OsO 6 were characterized as an ordered double-perovskite structure of space group P2 1 /n with the Ca and Os atoms being fully ordered at the perovskite B-site. The electromagnetic analysis shows that the crystal exhibits a semiconductor-like behavior below 300 K and undergoes an antiferromagnetic transition at 50 K. - Graphical Abstract: Schematic image of crystal structure of Ca 3 OsO 6 as determined by X-ray diffraction, where the gray and black octahedrons are occupied by Ca and Os, respectively. Top inset reveals an optic image of a typical Ca 3 OsO 6 single crystal. Highlights: ► Single crystals of Ca 3 OsO 6 have been successfully grown under high-pressure. ► Ca 3 OsO 6 crystalizes into an ordered double-perovskite structure. ► The Ca 3 OsO 6 undergoes an antiferromagnetic transition at 50 K

The Partial Molar Volume and Compressibility of the FeO Component in Model Basalts (Mixed CaAl2Si2O8-CaMgSi2O6-CaFeSi2O6 Liquids) at 0 GPa: evidence of Fe2+ in 6-fold coordination

Science.gov (United States)

Guo, X.; Lange, R. A.; Ai, Y.

2010-12-01

FeO is an important component in magmatic liquids and yet its partial molar volume at one bar is not as well known as that for Fe2O3 because of the difficulty of performing double-bob density measurements under reducing conditions. Moreover, there is growing evidence from spectroscopic studies that Fe2+ occurs in 4, 5, and 6-fold coordination in silicate melts, and it is expected that the partial molar volume and compressibility of the FeO component will vary accordingly. We have conducted both density and relaxed sound speed measurements on four liquids in the An-Di-Hd (CaAl2Si2O8-CaMgSi2O6-CaFeSi2O6) system: (1) Di-Hd (50:50), (2) An-Hd (50:50), (3) An-Di-Hd (33:33:33) and (4) Hd (100). Densities were measured between 1573 and 1838 K at one bar with the double-bob Archimedean method using molybdenum bobs and crucibles in a reducing gas (1%CO-99%Ar) environment. The sound speeds were measured under similar conditions with a frequency-sweep acoustic interferometer, and used to calculate isothermal compressibility. All the density data for the three multi-component (model basalt) liquids were combined with density data on SiO2-Al2O3-CaO-MgO-K2O-Na2O liquids (Lange, 1997) in a fit to a linear volume equation; the results lead to a partial molar volume (±1σ) for FeO =11.7 ± 0.3(±1σ) cm3/mol at 1723 K. This value is similar to that for crystalline FeO at 298 K (halite structure; 12.06 cm3/mol), which suggests an average Fe2+ coordination of ~6 in these model basalt compositions. In contrast, the fitted partial molar volume of FeO in pure hedenbergite liquid is 14.6 ± 0.3 at 1723 K, which is consistent with an average Fe2+ coordination of 4.3 derived from EXAFS spectroscopy (Rossano, 2000). Similarly, all the compressibility data for the three multi-component liquids were combined with compressibility data on SiO2-Al2O3-CaO-MgO liquids (Ai and Lange, 2008) in a fit to an ideal mixing model for melt compressibility; the results lead to a partial molar

Investigation of the reaction 6Li + 40Ca at 156 MeV in a coincidence experiment

International Nuclear Information System (INIS)

Freindl, L.; Grotowski, K.; Uniwersytet Jagiellonski, Krakow; Planeta, R.; Klewe-Nebenius, H.; Neumann, B.; Buschmann, J.; Gils, H.J.; Rebel, H.; Zagromski, S.

1983-12-01

The cross sections for inelastic break up have been studied for the 6 Li + 40 Ca reaction at Esub(Li) = 156 MeV. For this, gamma ray spectra from the heavy residual nuclei were measured in coincidence with beam velocity projectile fragments. The cross sections were found to be: 34 +- 9 14 mb for protons, 30 +- 7 12 mb for deuterons, and 78 +- 41 142 mb for α-particles, respectively. These values are small when compared to total break up cross sections. A comparison of the cross section sum of all known reaction paths induced by 6 Li + 40 Ca at 156 MeV with total reaction cross section indicates a missing cross section of the order of a few hundred millibarns. It is discussed whether this cross section may be attributed to pick up reactions. (orig.) [de

The superconductor (Tl,Hg,Ca)2(Ba,Sr)2(Ca,Sr,Tl)Cu2O7.6

International Nuclear Information System (INIS)

Valldor, M.; Bryntse, I.; Morawski, A.

2002-01-01

In the title 2212-type superconductor (thallium mercury calcium barium strontium copper oxide), which contains both Tl and Hg in the charge reservoir (CR), Sr is located at both alkali-earth (AE) metal sites. Ca enters the CR at the same time as Tl shares the smaller AE site, which increases the apical Cu-Cu distance significantly. The structure causes the superconducting Cu-O layers to become significantly puckered. (orig.)

Blue and red dual emission nanophosphor CaMgSi2O6:Eun+; crystal structure and electronic configuration

International Nuclear Information System (INIS)

Pawar, A.U.; Jadhav, Abhijit P.; Pal, U.; Kim, Byung Kyu; Kang, Young Soo

2012-01-01

Well dispersed Eu doped CaMgSi 2 O 6 (CMS) nanoparticles of 12–19 nm average sizes were synthesized by the co-precipitation method using different ratios of water and ethanol mixture as a solvent and subsequent air annealing. While ethanol as solvent produced pure CMS in monoclinic phase, pure water produced Ca 2 MgSi 2 O 7 (C2MS) and CMS in the mixed phase. Apart from the composition of CMS and C2MS, concentration and ionization state of the activator depended strongly on the composition (effective dielectric constant) of the solvent. Both the blue and red emission bands could be revealed for the europium activated CMS nanoparticles using single europium precursor. Efficiency of blue and red emissions in the nanophosphors, controlled by the relative abundance of europium in Eu 2+ and Eu 3+ oxidation states, could be controlled by adjusting the water content in the solvent. The relative intensity of the red emission (615 nm) decreased with the increase of water content in the solvent. - Highlights: ► We have synthesized Eu doped CaMgSi 2 O 6 using different volume ratios of water and ethanol solvent. ► We observed Ca 2 MgSi 2 O 7 phase increases with increasing amount of water in solvent. ► Dual emission was observed using single europium precursor. ► As synthesized material can be used for wavelength conversion application.

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

Energy Technology Data Exchange (ETDEWEB)

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

2016-07-25

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

Local microstructure and photoluminescence of Er-doped 12CaO·7Al2O3 powder

Institute of Scientific and Technical Information of China (English)

WANG Dan; LIU Yuxue; XU Changshan; LIU Yichun; WANG Guorui; LI Xinghua

2008-01-01

Er-doped 12CaO·7Al2O3 (C12A7:Er) powders were prepared using the sol-gel method followed by annealing inorganic precursors. X-ray diffraction (XRD), Raman and absorption spectra revealed that Er ions existed and substituted Ca2+ lattice site in C12A7. The photoluminescence of C12A7:Er at room temperature was observed in the visible and infrared region using 488 nm (2.54 eV) Ar+ line as excitation source, respectively. The sharp and intense green emission bands with multi-peaks around 520 nm and 550 nm correspond to the transitions from the excited states 2H11/2 and 4S3/2 to the ground state 4I15/2, respectively. Furthermore, red emission band around 650 nm was also observed. It was attributed to the electronic transition from excited states 4F9/2 to the ground state 4I15/2 inside 4f-shell of Er3+ ions. The intensive infrared emission at 1.54μm was attributed to the transition from the first excited states of 4I13/2 to the ground state (4I15/2). The temperature dependent photoluminescence of infrared emission showed that the integrated intensity reached a maximum value at near room temperature. The forbidden transitions of intra-4f shell electrons in free Er3+ ions were allowed in C12A7 owing to lack of the inversion symmetry in the Er3+ position in C12A7 crystal field. Our results suggested that C12A7:Er was a candidate for applications in Er-doped laser materials, and full color display.

Novel 6- and 7-Substituted Coumarins with Inhibitory Action against Lipoxygenase and Tumor-Associated Carbonic Anhydrase IX

Directory of Open Access Journals (Sweden)

Aikaterini Peperidou

2018-01-01

Full Text Available A series of carboxamide derivatives of 6- and 7-substituted coumarins have been prepared by an original procedure starting from the corresponding 6- or 7-hydroxycoumarins which were alkylated with ethyl iodoacetate, and the obtained ester was converted to the corresponding carboxylic acids which were thereafter reacted with a series of aromatic/aliphatic/heterocyclic amines leading to the desired amides. The new derivatives were investigated as inhibitors of two enzymes, human carbonic anhydrases (hCAs and soy bean lipoxygenase (LOX. Compounds 4a and 4b were potent LOX inhibitors, whereas many effective hCA IX inhibitors (KIs in the range of 30.2–30.5 nM were detected in this study. Two compounds, 4b and 5b, showed the phenomenon of dual inhibition. Furthermore, these coumarins did not significantly inhibit the widespread cytosolic isoforms hCA I and II, whereas they were weak hCA IV inhibitors, making them hCA IX-selective inhibitors. As hCA IX and LOX are validated antitumor targets, these results are promising for the investigation of novel drug targets involved in tumorigenesis.

Effects of 45Ca on murine skeletal muscle. 2

International Nuclear Information System (INIS)

Asotra, K.; Katoch, S.S.; Krishan, K.; Malhotra, R.K.

1983-01-01

Swiss albino mice were injected intraperitoneally with 3.7x10 4 Bq and 7.4x10 4 Bq 45 Ca/g body weight. 45 Ca-treated mice were sacrificed on days 1, 3, 5, 7, 14 and 28 and activities of acid phosphatase, alkaline phosphatase and glucose 6-phosphatase bioassayed in diaphragm and gastrocnemius. Activities of acid and alkaline phosphatases decreased after the 1st day of 45 Ca treatment in both the muscles compared with the normal controls. These two enzymes apparently do not contribute to myofiber necrosis in irradiated skeletal muscle. Glucose 6-phosphatase levels increased in the two irradiated muscles and with 7.4x10 4 Bq 45 Ca dose as much as 20-fold and 7-fold elevations are recorded in diaphragm and gastrocnemius, respectively, indicating a radiation-induced stimulation of inhibition of glucose 6-phosphatase channelization for energy generation. The possible role of elevated glucose 6-phosphatase levels in glycogen accumulation on account of radiations in skeletal muscle has been discussed. (author)

Spin-glass behavior in the S=1/2 fcc ordered perovskite Sr2CaReO6

International Nuclear Information System (INIS)

Wiebe, C.R.; Greedan, J.E.; Luke, G.M.; Gardner, J.S.

2002-01-01

The ordered perovskite Sr 2 CaReO 6 of monoclinic symmetry [space group P2 1 /n,a=5.7556(3) A,b=5.8534(3) A,c=8.1317(4) A,β=90.276(5) deg. at T=4 K] has been synthesized using standard solid-state chemistry techniques. The difference in the size and charge of the cations induces an ordering of the B site Ca 2+ and Re 6+ ions which leads to a distorted fcc lattice of spin-(1/2) Re 6+ (5d 1 ) moments. dc magnetic susceptibility measurements indicate a maximum at T G ∼14 K and an irreversibility in the field-cooled and zero-field-cooled data at ∼22 K that is believed to be caused by the geometric frustration inherent in the fcc structure. Neutron-scattering measurements confirm the absence of magnetic long-range order, and muon spin relaxation experiments indicate the presence of an abrupt spin freezing at T G . Specific heat measurements reveal a broad anomaly typical of spin glasses and no sharp feature. 65% of the spin entropy is released at low temperatures. The low-temperature data do not show the expected linear temperature dependence, but rather a T 3 relationship, as is observed, typically, for antiferromagnetic spin waves. The material is characterized as an unconventional, essentially disorder-free, spin glass

Phase selection in the containerless solidification of undercooled CaO · 6Al2O3 melts

International Nuclear Information System (INIS)

Li Mingjun; Kuribayashi, Kazuhiko

2004-01-01

The CaO · 6Al 2 O 3 melts were solidified on an aero-acoustic levitator under a containerless processing condition at various undercoolings. A high-speed video was operated to monitor the recalescence behavior, from which the growth velocity as a function of melt undercooling was determined. The microstructures were observed and the crystalline phases were identified using the X-ray diffraction technique, indicting that the Al 2 O 3 was solidified when the melt temperature was higher than the peritectic temperature, T p . When the melt was undercooled below T p , the CaO · 6Al 2 O 3 (CA 6 ) peritectic phase was crystallized directly from the undercooled melts. With respect to the direct formation of the peritectic phase, further analysis from the viewpoints of competitive nucleation indicated that the minimum free energy principle may be applied to elucidate the nucleation of CA 6 phase. In terms of the competitive growth behavior, the interface attachment kinetics for Al 2 O 3 and CA 6 phases are calculated by using the classical BCT model indicating that although the Al 2 O 3 phase doped by CaO has about four times larger interface kinetic coefficient than that of the CA 6 peritectic phase, the growth kinetics of Al 2 O 3 in the melt with the CaO · 6Al 2 O 3 chemical composition is not sufficiently high to replace the CA 6 phase as the primary phase. Therefore, once CA 6 is nucleated, it can develop into a macro crystal as the primary phase. The competitive nucleation and growth behavior in the CA 6 system is different from those in other well-studied peritectic alloys and the present investigation on the phase formation will be an essential supplement to the phase selection theory

Calcium Isotope (δ44/40Ca) Composition of Morozovella Velascoensis During the Paleocene Eocene Thermal Maximum Ocean Acidification Event

Science.gov (United States)

Kitch, G. D.; Jacobson, A. D.; Hurtgen, M.; Sageman, B. B.; Harper, D. T.; Zachos, J. C.

2017-12-01

Ocean acidification (OA) events are transient disruptions to the carbonate chemistry of seawater that involve decreases in pH, [CO32-] and carbonate mineral saturation states (Ω). Numerical modeling studies predict that the Ca isotope (δ44/40Ca) composition of primary marine carbonate should be sensitive to OA1, and recent evidence from the rock record may support this hypothesis2. Boron isotope (δ11B) data for the planktonic foraminifera Morozovella velascoensis indicate that the Paleocene-Eocene Thermal Maximum (PETM; 55 Mya) was an interval of pronounced OA3, although the Ca isotope composition of the bulk carbonate record appears to show post-burial diagenetic effects4. To further evaluate the Ca isotope proxy, we used a high-precision (2σSD=±0.04‰), double-spike (43Ca-42Ca) TIMS method5 to measure δ44/40Ca values of well-preserved M. velascoensis tests spanning the PETM. M. velascoensis tests (250-355 µm) were picked from samples recovered during ODP Leg 198, Site 1209 on Shatsky Rise in the equatorial Pacific. Five M. velascoensis tests were combined per sample, dissolved, spiked, and analyzed using a Triton TIMS. Repeat dissolutions of ten samples gave δ44/40Ca values within ±0.04‰ of the original measurements. Method and procedural blanks were negligible. δ44/40Ca values are elevated, even before the negative carbon isotope excursion (CIE) that marks the PETM. When δ11/10B values decrease during the CIE, δ44/40Ca values remain elevated, but then decrease by 0.10‰ as δ11B values return to pre-CIE levels. The apparent inverse correlation between δ44/40Ca and δ11B values suggests that Ca isotope fractionation by M. velascoensis was sensitive to OA. A decrease in pH indicated by lower δ11B values is consistent with higher δ44/40Ca values (decreased fractionation) due to elevated [Ca2+]/[CO32-] ratios and reduced W. The Ca isotope composition of pristine foraminiferal calcite may have potential for reconstructing [CO32-]. The current

LiCaAlF sub 6 :Ce crystal: a new scintillator

CERN Document Server

Gektin, A V; Neicheva, S; Gavrilyuk, V; Bensalah, A; Fukuda, T; Shimamura, K

2002-01-01

Scintillation properties of LiCaAlF sub 6 :Ce crystal, well known as the effective UV laser material, is reported. Ce sup 3 sup + emission at 286-305 nm with a single exponential decay time of 35 ns provides a scintillation pulse. Radiation damage in pure and Ce-doped crystals is studied. In contrast to the majority of fluoride crystals, cerium is responsible for the ultradeep traps formation revealing thermostimulated luminescence. Overlapping of color center absorption and Ce sup 3 sup + ion emission bands limits the scintillation efficiency of LiCaAlF sub 6 :Ce at high radiation doses.

Photoluminescence properties of Eu(3+)/ Sm(3+) activated CaZr4(PO4)6 phosphors.

Science.gov (United States)

Nair, Govind B; Dhoble, S J

2016-09-01

Solid state reaction method was employed for the synthesis of a series of CaZr4(PO4)6: Eu(3+)/Sm(3+) phosphors. The red-emitting CaZr4(PO4)6:Eu(3+) phosphors can be efficiently excited at 396 nm and thereby, exhibit a strong red luminescence predominantly corresponding to the electric dipole transition at 615 nm. Under 405 nm excitation, CaZr4(PO4)6:Sm(3+) phosphors display orange emission with color temperatures approximately around 2200 K. The acquired results reveal that CaZr4(PO4)6: RE(3+) (RE = Eu, Sm) phosphors could be potential candidates for red and orange emitting phosphor, respectively, for UV/blue-pump LEDs.

Ca(AlH4)2, CaAlH5, and CaH2+6LiBH4: Calculated dehydrogenation enthalpy, including zero point energy, and the structure of the phonon spectra.

Science.gov (United States)

Marashdeh, Ali; Frankcombe, Terry J

2008-06-21

The dehydrogenation enthalpies of Ca(AlH(4))(2), CaAlH(5), and CaH(2)+6LiBH(4) have been calculated using density functional theory calculations at the generalized gradient approximation level. Harmonic phonon zero point energy (ZPE) corrections have been included using Parlinski's direct method. The dehydrogenation of Ca(AlH(4))(2) is exothermic, indicating a metastable hydride. Calculations for CaAlH(5) including ZPE effects indicate that it is not stable enough for a hydrogen storage system operating near ambient conditions. The destabilized combination of LiBH(4) with CaH(2) is a promising system after ZPE-corrected enthalpy calculations. The calculations confirm that including ZPE effects in the harmonic approximation for the dehydrogenation of Ca(AlH(4))(2), CaAlH(5), and CaH(2)+6LiBH(4) has a significant effect on the calculated reaction enthalpy. The contribution of ZPE to the dehydrogenation enthalpies of Ca(AlH(4))(2) and CaAlH(5) calculated by the direct method phonon analysis was compared to that calculated by the frozen-phonon method. The crystal structure of CaAlH(5) is presented in the more useful standard setting of P2(1)c symmetry and the phonon density of states of CaAlH(5), significantly different to other common complex metal hydrides, is rationalized.

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

Science.gov (United States)

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

2017-05-01

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

Fracto- mechanoluminescence and thermoluminescence properties of orange-red emitting Eu{sup 3+} doped Ca{sub 2}Al{sub 2}SiO{sub 7} phosphors

Energy Technology Data Exchange (ETDEWEB)

Tiwari, Geetanjali, E-mail: geetanjali.tiwari10@gmail.com [School of Studies in Physics and Astrophysics, Pt. Ravishankar Shukla University, Raipur, C.G., 492010 (India); Brahme, Nameeta, E-mail: namitabrahme@gmail.com [School of Studies in Physics and Astrophysics, Pt. Ravishankar Shukla University, Raipur, C.G., 492010 (India); Sharma, Ravi [Department of Physics, Govt. Arts and Commerce Girls College, Devendra Nagar, Raipur, C.G. (India); Bisen, D.P.; Sao, Sanjay K. [School of Studies in Physics and Astrophysics, Pt. Ravishankar Shukla University, Raipur, C.G., 492010 (India); Khare, Ayush [Department of Physics, National Institute of Technology, Raipur - 492 010 (India)

2017-03-15

The suitability of nano-structured Ca{sub 2}Al{sub 2}SiO{sub 7}:Eu{sup 3+} phosphors for thermoluminescence and mechanoluminescence dosimeter were investigated. Europium doped di-calcium di-aluminum silicate phosphor was synthesised by the combustion assisted method and annealed at 1100 °C for 4 h in reducing and oxidizing environments. The prepared Ca{sub 2}Al{sub 2}SiO{sub 7}:Eu{sup 3+} phosphor was characterized by X-ray diffractometer (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM) with energy dispersive x-ray spectroscopy (EDX), photoluminescence (PL) and decay characteristics. The phase structure of sintered phosphor has akermanite type which belongs to the tetragonal crystallography; this structure is a member of the melilite group and forms a layered compound. The chemical composition of the sintered Ca{sub 2}Al{sub 2}SiO{sub 7}:Eu{sup 3+} phosphor was confirmed by EDX spectra. Mechanoluminescence (ML) and thermoluminescence (TL) studies revealed that the ML and TL intensity increases with activator concentration. Optimum ML was observed for the sample having 2 mol% of Eu ions. The TL intensity of Ca{sub 2}Al{sub 2}SiO{sub 7}:Eu{sup 3+} was recorded for different exposure times of γ -irradiation and it was observed that TL intensity is maximum for γ dose of 1770 Gy. The PL spectra indicated that Ca{sub 2}Al{sub 2}SiO{sub 7}:Eu{sup 3+} could be excited effectively by near ultraviolet (NUV) light and exhibited bright orange-red emission with excellent colour stability. CIE colour coordinates of the prepared Ca{sub 2}Al{sub 2}SiO{sub 7}:Eu{sup 3+} phosphor was found suitable as orange-red light emitting phosphor with a CIE value of (x=0.6142, y=0.3849) and correlated colour temperature (CCT) is 1250 K. Therefore, it is considered to be a new promising orange-red emitting phosphor for white light emitting diode (LED) application.

Measurement of cytoplasmic Ca2+ concentration in Saccharomyces cerevisiae induced by air cold plasma

Science.gov (United States)

Xiaoyu, DONG

2018-03-01

In this study, a novel approach to measure the absolute cytoplasmic Ca2+ concentration ([Ca2+]cyt) using the Ca2+ indicator fluo-3 AM was established. The parameters associated with the probe fluo-3 AM were optimized to accurately determine fluorescence intensity from the Ca2+-bound probe. Using three optimized parameters (final concentration of 6 mM probe, incubation time of 135 min, loading probe before plasma treatment), the maximum fluorescence intensity (F max = 527.8 a.u.) and the minimum fluorescence intensity (F min = 63.8 a.u.) were obtained in a saturated Ca2+ solution or a solution of lacking Ca2+. Correspondingly, the maximum [Ca2+]cyt induced by cold plasma was 1232.5 nM. Therefore, the Ca2+ indicator fluo-3 AM was successfully applied to measure the absolute [Ca2+]cyt in Saccharomyces cerevisiae stimulated by cold plasma at atmospheric air pressure.

Magnetic and magnetocaloric properties of La{sub 0.7}Ca{sub 0.3}Mn{sub 1−x}Zn{sub x}O{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Ho, T.A. [Department of Materials Science and Engineering, Korea University, Seoul 02841 (Korea, Republic of); Lim, S.H., E-mail: sangholim@korea.ac.kr [Department of Materials Science and Engineering, Korea University, Seoul 02841 (Korea, Republic of); Tho, P.T.; Phan, T.L. [Department of Physics and Oxide Research Center, Hankuk University of Foreign Studies, Yongin 17035 (Korea, Republic of); Yu, S.C. [Department of Physics, Chungbuk National University, Cheongju 28644 (Korea, Republic of)

2017-03-15

The magnetic Mn{sup 3+} ions in La{sub 0.7}Ca{sub 0.3}MnO{sub 3} are partially replaced by nonmagnetic Zn{sup 2+} ions to form La{sub 0.7}Ca{sub 0.3}Mn{sub 1−x}Zn{sub x}O{sub 3} compounds (x=0.0, 0.06, 0.08, and 0.1), and their magnetic and magnetocaloric properties are investigated. The Curie temperature decreases drastically from 245 to 70 K as x increases from 0 to 0.1. An analysis using the Banerjee's criterion of the experimental results for magnetization as a function of temperature and magnetic field indicates that the first-to-second order magnetic phase transformation occurs at a threshold composition of x=0.06, which is further supported by the universal curves of the normalized entropy change versus reduced temperature. The maximum magnetic entropy change measured at a magnetic field span of 50 kOe, which occurs near the Curie temperature, decreases from 10.30 to 2.15 J/kg K with the increase of x from 0.0 to 0.1. However, the relative cooling power, an important parameter for practical applications, shows a maximum value of 404 J/kg at x=0.08, which is 1.5 times greater than that observed for the undoped sample. - Highlights: • Magnetic and MCE of La{sub 0.7}Ca{sub 0.3}Mn{sub 1−x}Zn{sub x}O{sub 3} are investigated. • Order of magnetic phase transition is dependent on the Zn doping concentration. • Although the |∆S{sub max}| decreases with increasing x, RCP increase remarkably.

In vivo evaluation of alpha7 nicotinic acetylcholine receptor agonists [11C]A-582941 and [11C]A-844606 in mice and conscious monkeys.

Directory of Open Access Journals (Sweden)

Jun Toyohara

Full Text Available BACKGROUND: The alpha7 nicotinic acetylcholine receptors (nAChRs play an important role in the pathophysiology of neuropsychiatric diseases such as schizophrenia and Alzheimer's disease. The goal of this study was to evaluate the two carbon-11-labeled alpha7 nAChR agonists [(11C]A-582941 and [(11C]A-844606 for their potential as novel positron emission tomography (PET tracers. METHODOLOGY/PRINCIPAL FINDINGS: The two tracers were synthesized by methylation of the corresponding desmethyl precursors using [(11C]methyl triflate. Effects of receptor blockade in mice were determined by coinjection of either tracer along with a carrier or an excess amount of a selective alpha7 nAChR agonist (SSR180711. Metabolic stability was investigated using radio-HPLC. Dynamic PET scans were performed in conscious monkeys with/without SSR180711-treatment. [(11C]A-582941 and [(11C]A-844606 showed high uptake in the mouse brain. Most radioactive compounds in the brain were detected as an unchanged form. However, regional selectivity and selective receptor blockade were not clearly observed for either compound in the mouse brain. On the other hand, the total distribution volume of [(11C]A-582941 and [(11C]A-844606 was high in the hippocampus and thalamus but low in the cerebellum in the conscious monkey brain, and reduced by pretreatment with SSR180711. CONCLUSIONS/SIGNIFICANCE: A nonhuman primate study suggests that [(11C]A-582941 and [(11C]A-844606 would be potential PET ligands for imaging alpha7 nAChRs in the human brain.

Structural phase transition and magnetic properties of double perovskites Ba2CaMO6 (M=W, Re, Os)

International Nuclear Information System (INIS)

Yamamura, Kazuhiro; Wakeshima, Makoto; Hinatsu, Yukio

2006-01-01

Structures and magnetic properties for double perovskites Ba 2 CaMO 6 (M=W, Re, Os) were investigated. Both Ba 2 CaReO 6 and Ba 2 CaWO 6 show structural phase transitions at low temperatures. For Ba 2 CaReO 6 , the second order transition from cubic Fm3-bar m to tetragonal I4/m has been observed near 120K. For Ba 2 CaWO 6 , the space group of the crystal structure is I4/m at 295K and the transition to monoclinic I2/m has been observed between 220K. Magnetic susceptibility measurements show that Ba 2 CaReO 6 (S=1/2) and Ba 2 CaOsO 6 (S=1) transform to an antiferromagnetic state below 15.4 and 51K, respectively. Anomalies corresponding to their structural phase transition and magnetic transition have been also observed through specific heat measurements

First investigations on the quaternary system Na2O-K2O-CaO-SiO2: synthesis and crystal structure of the mixed alkali calcium silicate K1.08Na0.92Ca6Si4O15

Science.gov (United States)

Kahlenberg, Volker; Mayerl, Michael Jean-Philippe; Schmidmair, Daniela; Krüger, Hannes; Tribus, Martina

2018-04-01

In the course of an exploratory study on the quaternary system Na2O-K2O-CaO-SiO2 single crystals of the first anhydrous sodium potassium calcium silicate have been obtained from slow cooling of a melt in the range between 1250 and 1050 °C. Electron probe micro analysis suggested the following idealized molar ratios of the oxides for the novel compound: K2O:Na2O:CaO:SiO2 = 1:1:12:8 (or KNaCa6Si4O15). Single-crystal diffraction measurements on a crystal with chemical composition K1.08Na0.92Ca6Si4O15 resulted in the following basic crystallographic data: monoclinic symmetry, space group P 21/ c, a = 8.9618(9) Å, b = 7.3594(6) Å, c = 11.2453(11) Å, β= 107.54(1)°, V = 707.2(1) Å3, Z = 2. Structure solution was performed using direct methods. The final least-squares refinement converged at a residual of R(|F|) = 0.0346 for 1288 independent reflections and 125 parameters. From a structural point of view, K1.08Na0.92Ca6Si4O15 belongs to the group of mixed-anion silicates containing [Si2O7]- and [SiO4]-units in the ratio 1:2. The mono- and divalent cations occupy a total of four crystallographically independent positions located in voids between the tetrahedra. Three of these sites are exclusively occupied by calcium. The fourth site is occupied by 54(1)% K and 46%(1) Na, respectively. Alternatively, the structure can be described as a heteropolyhedral framework based on corner-sharing silicate tetrahedra and [CaO6]-octahedra. The network can build up from kröhnkite-like [Ca(SiO4)2O2]-chains running along [001]. A detailed comparison with other A2B6Si4O15-compounds including topological and group-theoretical aspects is presented.

Effects of chlorides on the hydration of 12CaO{center_dot}7Al2O3 solid solution

Energy Technology Data Exchange (ETDEWEB)

Sango, H.; Miyakawa, T.; Yasue, T.; Arai, Y. [Nihon Univ., Tokyo (Japan). Faculty of Science and Engineering

1995-01-01

The purpose of this paper was to compare the hydration rate of C12A7ss and to study the effects of chlorides on the hydration products and the hydration rate of C12A7ss. In this paper, `C12A7ss` is a general term for C11A7{center_dot}Ca(OH)2, 11CaO{center_dot}7Al2O3{center_dot}CaF2 and 11CaO{center_dot}7Al2O3{center_dot}CaCl2. The hydration process and the hydration rate of 12CaO{center_dot}7Al2O3 solution (C12A7ss) with and without various chlorides (CaCl2, MgCl2, NaCl, NH4Cl and AlCl3) has been determined at 25{degree}C. Various C12A7ss were prepared in burning method. When C12A7ss with various chlorides are hydrated, 3CaO{center_dot} Al2O3{center_dot}CaCl2{center_dot}10H2O(Friedel`s salt) is formed as the primary hydrate. The hydration rate of C12A7ss is decreased by the coexistence of CaCl2, MgCl2, NaCl or NH4Cl except AlCl3. As a result, the setting time of C12A7ss is extended and the unhydrate exists for a long time comparatively. 14 refs., 7 figs., 1 tab.

Lattice dynamics of CaC.sub.6./sub. by Raman spectroscopy

Czech Academy of Sciences Publication Activity Database

Hlinka, Jiří; Gregora, Ivan; Pokorný, Jan; Hérold, C.; Emery, N.; Mareché, J.F.; Lagrange, P.

2007-01-01

Roč. 76, č. 14 (2007), 144512/1-144512/6 ISSN 1098-0121 Institutional research plan: CEZ:AV0Z10100520 Keywords : Raman scattering * phonon spectra * CaC 6 * superconductivity Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 3.172, year: 2007

Infrared spectroscopic study of CaFe0.7Co0.3O3

Science.gov (United States)

Zhang, C. X.; Xia, H. L.; Dai, Y. M.; Qiu, Z. Y.; Sui, Q. T.; Long, Y. W.; Qiu, X. G.

2017-08-01

Temperature-dependent infrared spectroscopy has been investigated for CaFe0.7Co0.3O3 which undergoes a ferromagnetic transition at TC≈177 K . It is observed that the spectral weight is transferred from ˜4800 -14 000 cm-1 to ˜0 -4800 cm-1 as the temperature is lowered around TC. Such a large-range spectral weight transfer is attributed to the Hund's interaction. The phonons in CaFe0.7Co0.3O3 show minor asymmetric line shapes, implying relatively weak electron-phonon coupling compared with the parent compound CaFeO3. The optical conductivity also reveals a broad peak structure in the range of ˜700 -1500 cm-1. Fit by the model of single-polaron absorption, the broad peak is interpreted by the excitation of polarons. From the fitting parameters of the polaron peak, we estimate the electron-phonon coupling constant α ˜ 0.4 -0.5 , implying that CaFe0.7Co0.3O3 falls into the weak-coupling regime.

Synthesis and structure of ternary lithium, calcium, copper phosphate Ca9CuLi(PO4)7

International Nuclear Information System (INIS)

Yanov, O.V.; Morozov, V.A.; Koznyakov, I.V.; Lazoryak, B.I.; Khasanov, S.S.

1998-01-01

New Ca 9 CuLi(PO 4 ) 7 compound is synthesized and specified through the methods of roentgenographic and thermogravimetric analysis. This compound is crystallized in trigonal syngony (sp.gr. R3c, Z=6) and is related to the structural type of the vitlokite natural mineral. The crystal structure (a=10.3231(2), c=37.111(1)A, V=3425(2)A 3 , R WP =5.99, R p =4/35, R I =2.25, R F =1.11, R E =3.28) is verified through the Ritweld method. The calcium cations are positioned in three nonequivalent octaapexed. The copper cations are located in a distorted octahedron. The lithium cations occupy irregularly and statistically two types of positions Li(A) (75(6)%) and Li(B) (25(6)%)uLi(PO 4 ) 7

Densification and mechanical properties of ZrO2-CaAl4O7 composites obtained by reaction sintering

International Nuclear Information System (INIS)

Bruni, Yesica; Aglietti, Esteban

2016-01-01

Composites of the ZrO 2 -CaO-Al 2 O 3 system exhibit high corrosion resistance and high chemical stability, these being suitable properties for enhanced performance as refractories. In this work composites based on ZrO 2 -CaAl 4 O 7 (CA 2 ) were developed by reaction sintering of two pure ZrO 2 powders with different particle size (d 50 = 0.44 μm and d 50 = 8 μm) mixed with high-alumina cement. The effects of CaO to ZrO 2 molar ratio, particle size of ZrO 2 and sintering temperature on densification, c-ZrO 2 formation, microstructure and mechanical properties (Vickers hardness, dynamic Young's modulus and compressive strength) were determined. Porosity and mean pore size of composites reduced with decreasing both particle size of ZrO 2 and CaO content. The highest compression strength of ∝350 MPa and hardness of 6 GPa corresponded to dense ZrO 2 -based composite with 15 vol.% CA 2 sintered at 1400 C.

Synthesis and electrical characterization of Ca2Nd4Ti6O20 ceramics

Directory of Open Access Journals (Sweden)

Muhammad Raz

2016-03-01

Full Text Available Ca2Nd4Ti6O20, a layered perov skite structured material was synthesized via a chemical (citrate sol-gel route for the first time using nitrates and alkoxide precursors. Phase analysis of a sample sintered at 1625 °C revealed the formation of an orthorhombic (Pbn21 symmetry. The microstructure of the sample after sintering comprised rod-shaped grains of a size of 1.5 to 6.5µm. The room temperature dielectric constant of the sintered sample was 38 at 100 kHz. The remnant polarization (Pr and the coercive field (Ec were about 400 μC/cm2 and 8.4 kV/cm, respectively. Impedance spectroscopy revealed that the capacitance (13.7 pF and activation energy (1.39 eV of the grain boundary was greater than the capacitance (5.7 pF and activation energy (1.13 eV of the grain.

The synthesis and luminescence properties of a novel red-emitting phosphor: Eu3+-doped Ca9La(PO4)7

Science.gov (United States)

Liang, Zehui; Mu, Zhongfei; Wang, Qiang; Zhu, Daoyun; Wu, Fugen

2017-10-01

A series of novel red-emitting phosphors Ca9La1- x (PO4)7: xEu3+ were synthesized by high-temperature solid state reactions. The photoluminescence excitation and photoluminescence spectra of these phosphors were investigated in detail. O2--Eu3+ charge transfer band peaking at about 261 nm is dominant in the PLE spectra of Eu3+-doped Ca9La(PO4)7, indicating that the phosphors are suitable for tricolor fluorescent lamps. The phosphors also show a good absorption in near ultraviolet (around 395 nm) and blue (around 465 nm) spectral region, which indicates that it can be pumped with NUV and blue chips for white light-emitting diodes. The transition of 5D0 → 7F2 of Eu3+ in this lattice can emit bright red light. Ca9La(PO4)7 could accommodate a large amount of Eu3+ with an optimal concentration of 60 mol%. The dipole-dipole interaction between Eu3+ is the dominant mechanism for concentration quenching of Eu3+. The calculated color coordinates lie in red region ( x = 0.64, y = 0.36), which is close to Y2O3: 0.05Eu3+ ( x = 0.65, y = 0.34). The integral emission intensity of Ca9La0.4(PO4)7: 0.6Eu3+ is 1.9 times stronger than that of widely used commercial red phosphor Y2O3: 0.05Eu3+. All these results indicate that Eu3+-doped Ca9La(PO4)7 is a promising red-emitting phosphor which can be used in tricolor fluorescent lamps and white light-emitting diodes.

Ca isotopes in refractory inclusions

International Nuclear Information System (INIS)

Niederer, F.R.; Papanastassiou, D.A.

1984-01-01

We report measurements of the absolute isotope abundance of Ca in Ca-Al-rich inclusions from the Allende and Leoville meteorites. Improved high precision measurements are reported also for 46 Ca. We find that nonlinear isotope effects in Ca are extremely rare in these inclusions. The absence of nonlinear effects in Ca, except for the effects in FUN inclusions, is in sharp contrast to the endemic effects in Ti. One fine-grained inclusion shows an excess of 46 Ca of (7 +- 1) per mille, which is consistent with addition of only 46 Ca or of an exotic (*) component with 46 Ca* approx. 48 Ca*. FUN inclusion EK-1-4-1 shows a small 46 Ca excess of (3.3 +- 1.0) per mille; this confirms that the exotic Ca components in EK-1-4-1 were even more deficient in 46 Ca relative to 48 Ca than is the case for normal Ca. The Ca in the Ca-Al-rich inclusions shows mass dependent isotope fractionation effects which have a range from -3.8 to +6.7 per mille per mass unit difference. This range is a factor of 20 wider than the range previously established for bulk meteorites and for terrestrial and lunar samples. Ca and Mg isotope fractionation effects in the Ca-Al-rich inclusions are common and attributed to kinetic isotope effects. (author)

Reactive spark plasma synthesis of CaZrTi2O7 zirconolite ceramics for plutonium disposition

Science.gov (United States)

Sun, Shi-Kuan; Stennett, Martin C.; Corkhill, Claire L.; Hyatt, Neil C.

2018-03-01

Near single phase zirconolite ceramics, prototypically CaZrTi2O7, were fabricated by reactive spark plasma sintering (RSPS), from commercially available CaTiO3, ZrO2 and TiO2 reagents, after processing at 1200 °C for only 1 h. Ceramics were of theoretical density and formed with a controlled mean grain size of 1.9 ± 0.6 μm. The reducing conditions of RSPS afforded the presence of paramagnetic Ti3+, as demonstrated by EPR spectroscopy. Overall, this study demonstrates the potential for RSPS to be a disruptive technology for disposition of surplus separated plutonium stockpiles in ceramic wasteforms, given its inherent advantage of near net shape products and rapid throughput.

Crystal structures of CCa2CuO5 and CSr1.9Ca1.1Cu2O7 refined from single crystal data

International Nuclear Information System (INIS)

Kopnin, E.M.; Matveev, A.T.; Salamakha, P.S.; Sato, A.; Takayama-Muromachi, E.

2003-01-01

Single crystals were grown for new layered oxycarbonates CCa 2 CuO 5 and CSr 1.9 Ca 1.1 Cu 2 O 7 at 6 GPa using a belt-type apparatus. Their crystal structures were determined using single crystal X-ray diffraction data with R1(wR2)=0.0294(0.0659) and 0.0199(0.0457) for CCa 2 CuO 5 and CSr 1.9 Ca 1.1 Cu 2 O 7 , respectively. These phases crystallize in the space group P4/mmm (No. 123), Z=1 with a=3.8157(1) Angst, c=7.1426(3) Angst for CCa 2 CuO 5 and a=3.8753(1) Angst, c=10.6765(5) Angst for CSr 1.9 Ca 1.1 Cu 2 O 7 . In contrast to CSr 2 CuO 5 , no ordering in the orientation of the triangular CO 3 groups was revealed in CCa 2 CuO 5 and CSr 1.9 Ca 1.1 Cu 2 O 7

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.)

Luminescence in Eu2+ and Ce3+ doped SrCaP2O7 phosphors

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K.N. Shinde

Full Text Available Eu2+ and Ce3+ doped SrCaP2O7 has been achieved by modified solid state diffusion in reducing atmosphere. The prepared phosphor powders have been identified by their characteristic X-ray diffraction patterns. The mixed phases of α-Sr2P2O7 type with orthorhombic and α-Ca2P2O7 type with monoclinic form were investigated. Its excitation wavelength ranging from 250 to 430 nm fits well with the characteristic emission of UV light-emitting diode (LED. The excitation and emission spectra indicate that these phosphors can be effectively excited by the near-UV light, and emits blue (visible range due to 4f7 → 4f65d1 transition of Eu2+ particularly, SrCaP2O7: Eu2+ whereas, photoluminescence excitation spectrum measurements of Ce3+ activated SrCaP2O7 shows that the phosphor can be efficiently excited by UV–Vis light from 280 to 310 nm to realize emission in the near visible range due to the 5d–4f transition of Ce3+ ions which is applicable for scintillation purpose. The impacts of doping of divalent europium and trivalent cerium on photoluminescence properties on SrCaP2O7 pyrophosphate phosphors were investigated and I propose a feasible interpretation. Keywords: Phosphor, Luminescence, XRD, LED, FTIR

CaV 3.1 and CaV 3.3 account for T-type Ca2+ current in GH3 cells

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M.A. Mudado

2004-06-01

Full Text Available T-type Ca2+ channels are important for cell signaling by a variety of cells. We report here the electrophysiological and molecular characteristics of the whole-cell Ca2+ current in GH3 clonal pituitary cells. The current inactivation at 0 mV was described by a single exponential function with a time constant of 18.32 ± 1.87 ms (N = 16. The I-V relationship measured with Ca2+ as a charge carrier was shifted to the left when we applied a conditioning pre-pulse of up to -120 mV, indicating that a low voltage-activated current may be present in GH3 cells. Transient currents were first activated at -50 mV and peaked around -20 mV. The half-maximal voltage activation and the slope factors for the two conditions are -35.02 ± 2.4 and 6.7 ± 0.3 mV (pre-pulse of -120 mV, N = 15, and -27.0 ± 0.97 and 7.5 ± 0.7 mV (pre-pulse of -40 mV, N = 9. The 8-mV shift in the activation mid-point was statistically significant (P < 0.05. The tail currents decayed bi-exponentially suggesting two different T-type Ca2+ channel populations. RT-PCR revealed the presence of a1G (CaV3.1 and a1I (CaV3.3 T-type Ca2+ channel mRNA transcripts.

Investigations towards the use of Gd0.7Ca0.3CoOx as membrane in an exhaust gas sensor for NOx

NARCIS (Netherlands)

Romer, E.W.J.; Nigge, Ulrich; Schulte, Thomas; Wiemhöfer, Hans-Dieter; Bouwmeester, Henricus J.M.

2001-01-01

Application of a material with the nominal composition Gd0.7Ca0.3CoOx is considered for use as membrane material in an exhaust gas sensor for NOx. SEM–EDX and XRD measurements revealed that after sintering at 1200°C in air, three co-existing phases are present: (Gd0.6Ca0.4)2CoOx (60 vol.%), GdCoO3

Electronic, Optical, and Lattice Dynamical Properties of Tetracalcium Trialuminate (Ca4Al6O13

Directory of Open Access Journals (Sweden)

Huayue Mei

2018-03-01

Full Text Available The electronic, optical, and lattice dynamical properties of tetracalcium trialuminate (Ca4Al6O13 with a special sodalite cage structure were calculated based on the density functional theory. Theoretical results show that Ca4Al6O13 is ductile and weakly anisotropic. The calculated Young’s modulus and Poisson ratio are 34.18 GPa and 0.32, respectively. Ca4Al6O13 is an indirect-gap semiconductor with a band gap of 5.41 eV. The top of the valence band derives from O 2p states, and the bottom of conduction band consists of Ca 3d states. Transitions from O 2p, 2s states to empty Ca 4s, 3d and Al 3s, 3p states constitute the major peaks of the imaginary part of the dielectric function. Ca4Al6O13 is a good UV absorber for photoelectric devices due to the high absorption coefficient and low reflectivity. The lattice vibration analysis reveals that O atoms contribute to the high-frequency portions of the phonon spectra, while Ca and Al atoms make important contributions to the middle- and low-frequency portions. At the center of the first Brillouin zone, lattice vibrations include the Raman active modes (E, A1, infrared active mode (T2, and silentmodes (T1, A2. Typical atomic displacement patterns were also investigated to understand the vibration modes more intuitively.

CaCO3-III and CaCO3-VI, high-pressure polymorphs of calcite: Possible host structures for carbon in the Earth's mantle

Science.gov (United States)

Merlini, M.; Hanfland, M.; Crichton, W. A.

2012-06-01

Calcite, CaCO3, undergoes several high pressure phase transitions. We report here the crystal structure determination of the CaCO3-III and CaCO3-VI high-pressure polymorphs obtained by single-crystal synchrotron X-ray diffraction. This new technical development at synchrotron beamlines currently affords the possibility of collecting single-crystal data suitable for structure determination in-situ at non-ambient conditions, even after multiphase transitions. CaCO3-III, observed in the pressure range 2.5-15 GPa, is triclinic, and it presents two closely related structural modifications, one, CaCO3-III, with 50 atoms in the unit cell [a=6.281(1) Å, b=7.507(2) Å, c=12.516(3) Å, α=93.76(2)°, β=98.95(2)°, γ=106.49(2)°, V=555.26(20) Å3 at 2.8 GPa], the second, CaCO3-IIIb, with 20 atoms [a=6.144(3) Å, b=6.3715(14) Å, c=6.3759(15) Å, α= 93.84(2)°, β=107.34(3)°, γ=107.16(3)°, V=224.33(13) Å3 at 3.1 GPa]. Different pressure-time experimental paths can stabilise one or the other polymorph. Both structures are characterised by the presence of non-coplanar CO3 groups. The densities of CaCO3-III (2.99 g/cm3 at 2.8 GPa) and CaCO3-IIIb (2.96 g/cm3 at 3.1 GPa) are lower than aragonite, in agreement with the currently accepted view of aragonite as the thermodynamically stable Ca-carbonate phase at these pressures. The presence of different cation sites, with variable volume and coordination number (7-9), suggests however that these structures have the potential to accommodate cations with different sizes without introducing major structural strain. Indeed, this structure can be adopted by natural Ca-rich carbonates, which often exhibit compositions deviating from pure calcite. Mg-calcites are found both in nature (Frezzotti et al., 2011) and in experimental syntheses at conditions corresponding to deep subduction environments (Poli et al., 2009). At these conditions, the low pressure rhombohedral calcite structure is most unlikely to be stable, and, at the same

Spin glass properties of Y0.7Ca0.3MnO3 and Th0.35Ba0.37Ca0.28MnO3

Science.gov (United States)

Sedmidubský, D.; Hejtmánek, J.; Maryško, M.; Jirák, Z.; Hardy, V.; Martin, C.

2002-05-01

Two perovskite manganites with the same nominal concentration of Mn4+ have been studied by the magnetic susceptibility and specific heat measurements: the Y0.7Ca0.3MnO3 single crystal (YCa) with low tolerance factor and negligible ionic radii variance and the Th0.35Ba0.37Ca0.28MnO3 (ThBaCa) ceramics with favorable tolerance factor but huge substitution induced disorder. Both systems were found to possess an insulating ground state with activated conductivity. The ac susceptibility data exhibit a frequency dependent peak at Tsg=32 K for YCa and Tsg=43 K for ThBaCa. The Cole-Cole analysis revealed a sharper than exponential increase of the relaxation time for the former sample while almost linear slowly growing characteristics below Tsg were observed for the latter one. Using the heat capacity curves, the magnetic contribution was separated and magnetic peaks with typical linear on-set tails were obtained. This observation and the abovementioned characteristics are all indicative of spin or cluster glass character. The necessary magnetic frustration is here induced by a considerable tilting of MnO6 octahedra and deformation of Mn-O bonds which occur in a cooperative manner for YCa and locally for ThBaCa.

Ca(AlH4)2, CaAlH5, and CaH2+6LiBH4 : Calculated dehydrogenation enthalpy, including zero point energy, and the structure of the phonon spectra

NARCIS (Netherlands)

Marashdeh, A.; Frankcombe, T.J.

2008-01-01

The dehydrogenation enthalpies of Ca(AlH4)2, CaAlH5, and CaH2+6LiBH4 have been calculated using density functional theory calculations at the generalized gradient approximation level. Harmonic phonon zero point energy (ZPE) corrections have been included using Parlinski’s direct method. The

Application of C_6_0, C_7_2 and carbon nanotubes as anode for lithium-ion batteries: A DFT study

International Nuclear Information System (INIS)

Najafi, Meysam

2017-01-01

The application of C_6_0, C_7_2, CNT (8, 0) and CNT (10, 0) as anode materials for Lithium-ion batteries were investigated by density functional theory (DFT) calculations. Results show that the average values of voltage cell (V_c_e_l_l) and adsorption energy (E_a_d) of CNT (8, 0) and CNT (10, 0) were higher than C_6_0 and C_7_2 ca 0.327 V and 6.52 kcal/mol, respectively. The NH_2 functionalization of studied nanostructures as a strategy to improve the performance of these systems as anode materials of Lithium-ion batteries were investigated. Results show that, NH_2 functionalization of studied nanostructures increase the average values of voltage cell and adsorption energy ca 0.197 V and 8.20 kcal/mol, respectively. Obtained results propose that NH_2 functionalized C_7_2 and CNT (10, 0) have larger V_c_e_l_l and E_a_d values and therefore these nanostructures have higher potential as anode material for Lithium-ion battery. - Highlights: • C_6_0 and CNT (10, 0) as anode materials for Lithium-ion batteries were investigated. • V_c_e_l_l and E_a_d of CNT (8, 0) and CNT (10, 0) were higher than C_6_0 and C_7_2 ca. • NH_2 functionalization of C_6_0 improve the performance of it as anode materials of Lithium-ion batteries.

Microstructure, Tensile Properties, and Corrosion Behavior of Die-Cast Mg-7Al-1Ca- xSn Alloys

Science.gov (United States)

Wang, Feng; Dong, Haikuo; Sun, Shijie; Wang, Zhi; Mao, Pingli; Liu, Zheng

2018-02-01

The microstructure, tensile properties, and corrosion behavior of die-cast Mg-7Al-1Ca- xSn ( x = 0, 0.5, 1.0, and 2.0 wt.%) alloys were studied using OM, SEM/EDS, tensile test, weight loss test, and electrochemical test. The experimental results showed that Sn addition effectively refined grains and intermetallic phases and increased the amount of intermetallic phases. Meanwhile, Sn addition to the alloys suppressed the formation of the (Mg,Al)2Ca phase and resulted in the formation of the ternary CaMgSn phase and the binary Mg2Sn phase. The Mg-7Al-1Ca-0.5Sn alloy exhibited best tensile properties at room temperature, while Mg-7Al-1Ca-1.0Sn alloy exhibited best tensile properties at elevated temperature. The corrosion resistance of studied alloys was improved by the Sn addition, and the Mg-7Al-1Ca-0.5Sn alloy presented the best corrosion resistance.

[{sup 11}C]A-69024: A potent and selective non-benzazepine radiotracer for in vivo studies of dopamine D1 receptors

Energy Technology Data Exchange (ETDEWEB)

Kassiou, Michael; Scheffel, Ursula; Ravert, Hayden T; Mathews, William B; Musachio, John L; Lambrecht, Richard M; Dannals, Robert F

1995-02-01

[{sup 11}C]A-69024, ({+-})-1-(2-bromo-4,5-dimethoxybenzyl)-7-hydroxy-6-methoxy-2-[{sup 11}C]methyl-1,2= ,3,4-tetrahydroisoquinoline, is a specific and selective dopamine D1 radiotracer. The in vivo biodistribution of this novel radioligand in mice showed a high uptake in the striatum (6.7% ID/g) at 5 min, followed by clearance with a half-life of 16.1 min. As a measure of specificity, the striatal/cerebellar ratio reached a maximum of 7.4 at 30 min post-injection. Radioactivity in the striatum was reduced to the level of the cerebellum by pre-administration of the D1 antagonist SCH 23390 (1 mg/kg). Pretreatment of mice with spiperone (D2), 7-hydroxydipropylaminotetralin (7-OH-DPAT) (D3), clozapine (D4), ketanserin (5-HT2/5-HT2C), mazindol (monoamine reuptake), prazosin ({alpha}{sub 1}), and haloperidol (D2/{sigma}) had no inhibitory effect on [{sup 11}C]A-69024 uptake in the striatum. The dextrotatory enantiomer of the dopamine antagonist butaclamol inhibited striatal uptake, while the less active isomer (-)-butaclamol did not. [{sup 11}C]A-69024 binding was inhibited by unlabeled A-69024 in a dose dependent manner (ED{sub 50} = 0.3 mg/kg) in the striatum while no change occurred in the cerebellum. [{sup 11}C]A-69024 warrants further investigation as a PET ligand for examination of central dopamine D1 receptors in humans.

High-spin states of 39K and 42Ca, ch. 4

International Nuclear Information System (INIS)

Eggenhuisen, H.H.; Elstrom, L.P.; Engelbertink, G.A.P.; Aarts, H.J.M.

1978-01-01

High-spin states of 39 K and 42 Ca have been investigated with the 28 Si( 16 O, αpγ) 39 K and 28 Si( 16 O, 2pγ) 42 Ca reactions at a beam energy of 45 MeV. Gamma-gamma coincidence, γ-ray angular distribution and linear polarization measurements were performed with a Ge(Li)-NaI(Tl) Compton suppression spectrometer and a three-crystal Ge(Li) Compton polarimeter. High-spin states of 39 K at Esub(x)=7.14, 7.78 and 8.03 and of 42 Ca at Esub(x)=7.75 MeV are established. Unambiguous spin-parity assignments of Jsup(π)=11/2 - , 13/2 - , 15/2 + , 15/2 - , 17/2 + and 19/2 - to the 39 K levels at Esub(x)=5.35, 5.72, 6.48, 7.14, 7.78 and 8.03 MeV and of 6 - , 7 - , 8 - , 9 - and (8,10) to the 42 Ca levels at Esub(x)=5.49, 6.15, 6.41, 6.55 and 7.37 MeV, respectively, have been obtained. Further spin-parity restrictions, lifetime limits, excitation energies, branching ratios and multipole mixing ratios are reported. Discrepancies with previous Jsup(π) assignments are discussed in detail. (Auth.)

Luminescence properties of Ca2 Ga2 SiO7 :RE phosphors for UV white-light-emitting diodes.

Science.gov (United States)

Jiao, Mengmeng; Lv, Wenzhen; Lü, Wei; Zhao, Qi; Shao, Baiqi; You, Hongpeng

2015-03-16

A series of Eu(2+) -, Ce(3+) -, and Tb(3+) -doped Ca2 Ga2 SiO7 phosphors is synthesized by using a high-temperature solid-state reaction. The powder X-ray diffraction and structure refinement data indicate that our prepared phosphors are single phased and the phosphor crystalizes in a tetrahedral system with the ${P\\bar 42m}$ (113) space group. The Eu(2+) - and Ce(3+) -doped phosphors both have broad excitation bands, which match well with the UV light-emitting diodes chips. Under irradiation of λ=350 nm, Ca2 Ga2 SiO7 :Eu(2+) and Ca2 Ga2 SiO7 :Ce(3+) , Li(+) have green and blue emissions, respectively. Luminescence of Ca2 Ga2 SiO7 :Tb(3+) , Li(+) phosphor varies with the different Tb(3+) contents. The thermal stability and energy-migration mechanism of Ca2 Ga2 SiO7 :Eu(2+) are also studied. The investigation results indicate that the prepared Ca2 Ga2 SiO7 :Eu(2+) and Ca2 Ga2 SiO7 :Ce(3+) , Li(+) samples show potential as green and blue phosphors, respectively, for UV-excited white-light-emitting diodes. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Electronic structure of TlBa2CaCu2O7-δ

Science.gov (United States)

Vasquez, R. P.; Novikov, D. L.; Freeman, A. J.; Siegal, M. P.

1997-06-01

The core levels of TlBa2CaCu2O7-δ (Tl-1212) epitaxial films have been measured with x-ray photoelectron spectroscopy (XPS). The valence electronic structure has been determined using the full-potential linear muffin-tin-orbital band-structure method and measured with XPS. The calculations show that a van Hove singularity (VHS) lies above the Fermi level (EF) for the stoichiometric compound (δ=0), while for 50% oxygen vacancies in the Tl-O layer (δ=0.5) EF is in close proximity to the VHS. Samples annealed in nitrogen (to reduce the hole overdoping by the removal of oxygen) exhibit higher core-level binding energies and a higher Tc, consistent with a shift of EF closer to the VHS. Comparisons are made to the core levels and valence bands of Tl2Ba2CaCu2O8+δ (Tl-2212) and HgBa2CaCu2O6+δ (Hg-1212). The similarity of the Cu 2p3/2 spectra for Tl-1212 and Tl-2212 indicates that the number of Tl-O layers has little effect on the Cu-O bonding. However, the Tl-1212 and Hg-1212 Cu 2p3/2 signals exhibit differences which suggest that the replacement of Tl3+ with Hg2+ results in a decrease in the O 2p-->Cu 3d charge-transfer energy and differences in the probabilities of planar vs apical oxygen charge transfer and/or Zhang-Rice singlet-state formation. Differences between the Tl-1212 and the Tl-2212 and Hg-1212 measured valence bands are consistent with the calculated Cu 3d and (Tl,Hg) 6s/5d partial densities of states.

Electronic structure of TlBa2CaCu2O7-δ

International Nuclear Information System (INIS)

Vasquez, R.P.; Novikov, D.L.; Freeman, A.J.; Siegal, M.P.

1997-01-01

The core levels of TlBa 2 CaCu 2 O 7-δ (Tl-1212) epitaxial films have been measured with x-ray photoelectron spectroscopy (XPS). The valence electronic structure has been determined using the full-potential linear muffin-tin-orbital band-structure method and measured with XPS. The calculations show that a van Hove singularity (VHS) lies above the Fermi level (E F ) for the stoichiometric compound (δ=0), while for 50% oxygen vacancies in the Tl-O layer (δ=0.5) E F is in close proximity to the VHS. Samples annealed in nitrogen (to reduce the hole overdoping by the removal of oxygen) exhibit higher core-level binding energies and a higher T c , consistent with a shift of E F closer to the VHS. Comparisons are made to the core levels and valence bands of Tl 2 Ba 2 CaCu 2 O 8+δ (Tl-2212) and HgBa 2 CaCu 2 O 6+δ (Hg-1212). The similarity of the Cu 2p 3/2 spectra for Tl-1212 and Tl-2212 indicates that the number of Tl-O layers has little effect on the Cu-O bonding. However, the Tl-1212 and Hg-1212 Cu 2p 3/2 signals exhibit differences which suggest that the replacement of Tl 3+ with Hg 2+ results in a decrease in the O 2p→Cu 3d charge-transfer energy and differences in the probabilities of planar vs apical oxygen charge transfer and/or Zhang-Rice singlet-state formation. Differences between the Tl-1212 and the Tl-2212 and Hg-1212 measured valence bands are consistent with the calculated Cu 3d and (Tl,Hg) 6s/5d partial densities of states. copyright 1997 The American Physical Society

Electronic Structure of TlBa2CaCu2O(7-Delta)

Science.gov (United States)

Vasquez, R. P.; Novikov, D. L.; Freeman, A. J.; Siegal, M. P.

1997-01-01

The core levels of TlBa2CaCu2O(7-delta) (Tl-1212) epitaxial films have been measured with X-ray photoelectron spectroscopy (XPS). The valence electronic structure has been determined using the full-potential linear muffin-tin-orbital band-structure method and measured with XPS. The calculations show that a van Hove singularity (VHS) lies above the Fermi level (E(sub F)) for the stoichiometric compound (delta = 0.5), while for 50% oxygen vacancies in the Tl-O layer (delta = 0.5) E(sub F) is in close proximity to the VHS. Samples annealed in nitrogen (to reduce the hole overdoping by the removal of oxygen) exhibit higher core-level binding energies and a higher T(sub c), consistent with a shift of E(sub F) closer to the VHS. Comparisons are made to the core levels and valence bands of Tl2Ba2CaCu2O(8 + delta)(Tl-2212) and HgBa2CaCu2O)6 + delta) (Hg- 1212). The similarity of the Cu 2p(sub 3/2) spectra for Tl-1212 and Tl-2212 indicates that the number of Tl-O layers has little effect on the Cu-O bonding. However, the Tl-1212 and Hg-1212 Cu 2p(sub 3/2) signals exhibit differences which suggest that the replacement of T(sup 3+) with Hg(sup 2+) results in a decrease in the O 2p right arrow Cu 3d charge-transfer energy and differences in the probabilities of planar vs apical oxygen charge transfer and/or Zhang-Rice singlet-state formation. Differences between the Tl-1212 and the Tl-2212 and Hg-1212 measured valence bands are consistent with the calculated Cu 3d and (Tl,Hg) 6s/5d partial densities of states.

Magnetic and transport properties of La0.3Ca0.7Mn0.9T0.1O3 (T = Cr, Fe, and W)

International Nuclear Information System (INIS)

Sudyoadsuk, T.; Suryanarayanan, R.; Winotai, P.

2005-01-01

We have carried out structural, magnetic and magneto transport measurements of the electron-doped manganite La 0.3 Ca 0.7 MnO 3 substituted with 10% of Cr, Fe and W on the Mn site. The substitution by Cr, Fe and W suppresses the charge order transition present at 260 K in the parent compound. All the samples show a semiconducting behavior. Whereas the parent compound does not show any magneto resistance (MR) even in a field of 14 T, a maximum MR of 6% in 5 T at 25 K is observed for the Cr substituted sample that is attributed to a spin-cluster glass like states induced by Cr. The Fe and W substituted samples showed a MR of 1.5 and 3%, respectively which may be attributed to a smaller number of FM domains/spin-clusters and to an increase in anti-ferromagnetic interaction

RFX6 Regulates Insulin Secretion by Modulating Ca2+ Homeostasis in Human β Cells

Directory of Open Access Journals (Sweden)

Vikash Chandra

2014-12-01

Full Text Available Development and function of pancreatic β cells involve the regulated activity of specific transcription factors. RFX6 is a transcription factor essential for mouse β cell differentiation that is mutated in monogenic forms of neonatal diabetes. However, the expression and functional roles of RFX6 in human β cells, especially in pathophysiological conditions, are poorly explored. We demonstrate the presence of RFX6 in adult human pancreatic endocrine cells. Using the recently developed human β cell line EndoC-βH2, we show that RFX6 regulates insulin gene transcription, insulin content, and secretion. Knockdown of RFX6 causes downregulation of Ca2+-channel genes resulting in the reduction in L-type Ca2+-channel activity that leads to suppression of depolarization-evoked insulin exocytosis. We also describe a previously unreported homozygous missense RFX6 mutation (p.V506G that is associated with neonatal diabetes, which lacks the capacity to activate the insulin promoter and to increase Ca2+-channel expression. Our data therefore provide insights for understanding certain forms of neonatal diabetes.

Preparation, characterization and activity evaluation of CaZrTi2O7 photocatalyst

International Nuclear Information System (INIS)

Chen Shifu; Ji Mingsong; Yuang Yunguang; Liu Wei

2012-01-01

CaZrTi 2 O 7 photocatalyst sample was prepared by a polymerizable complex method. The photocatalyst was characterized by X-ray powder diffraction, scanning electron microscopy, UV–Vis diffuse reflectance spectroscopy, photoluminescence emission spectroscopy, Brunauer–Emmett–Teller analysis, N 2 adsorption measurements, and terephthalic acid probed fluorescence technique. The photocatalytic activity of the sample was evaluated by photocatalytic oxidation of methyl orange and photocatalytic reduction of Cr 2 O 7 2− and nitrobenzene. The results showed that when the reaction solution was illuminated by UV light for 50 min, the photooxidation efficiency of methyl orange and the photoreduction efficiency of Cr 2 O 7 2− were 83.1% and 87.9%, respectively. When methanol was used as the holes scavengers and the illumination time was 10 h in the photocatalytic reduction experiment of nitrobenzene, the production efficiency of aniline was 70.3%. The effect of the heat treatment conditions on the photocatalytic activity was also investigated. The optimum preparation condition for CaZrTi 2 O 7 sample is 800 °C for 12 h. The mechanisms of influence on the photocatalytic activity of the sample were also discussed with the valance band theory. - Highlights: ► CaZrTi 2 O 7 photocatalyst was prepared by a polymerizable complex method. ► The heat treatment has a significant influence on the photocatalytic activity. ► The optimal heat treatment condition is approximately 800 °C for 12 h. ► The CaZrTi 2 O 7 has the band bap of about 2.89 eV with particle size of about 80 nm.

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

Photoluminescence properties of blue light excited Ca{sub 8}La{sub 2}(PO{sub 4}){sub 6}O{sub 2}:Eu{sup 3+} red phosphors

Energy Technology Data Exchange (ETDEWEB)

Fang, Yongzheng; Liu, Fengxin; Hou, Jingshan; Zhang, Yan; Zheng, Xinfeng; Zhang, Na [School of Materials Science and Engineering, Shanghai Institute of Technology, Shanghai 201418 (China); Zhao, Guoying, E-mail: zhaogy135@sit.edu.cn [School of Materials Science and Engineering, Shanghai Institute of Technology, Shanghai 201418 (China); Liao, Meisong [Key Laboratory of Materials for High Powder Laser, Shanghai Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, Shanghai 201800 (China); Dai, Guozhang; Long, Mengqiu [School of Physics and Electronics, Central South University, Changsha, Hunan 410083 (China); Liu, Yufeng, E-mail: yfliu@mail.sitp.ac.cn [School of Materials Science and Engineering, Shanghai Institute of Technology, Shanghai 201418 (China)

2016-09-15

A series of red emitting Ca{sub 8}La{sub 2}(PO{sub 4}){sub 6}O{sub 2}:xEu{sup 3+} (0≤x≤0.4) phosphors were synthesized by the conventional solid state reaction, and their photoluminescence properties were investigated in this work. Upon excitation of blue light, the Ca{sub 8}La{sub 2}(PO{sub 4}){sub 6}O{sub 2}:xEu{sup 3+} phosphors exhibit strong red emission at 616 nm, which corresponds to the dominant transition of Eu{sup 3+} ions in Ca{sub 8}La{sub 2}(PO{sub 4}){sub 6}O{sub 2} host, originating from the electric dipole transition {sup 5}D{sub 0}–{sup 7}F{sub 2}. Moreover, Ca{sub 8}La{sub 2}(PO{sub 4}){sub 6}O{sub 2}:0.3Eu{sup 3+} phosphor shows more intense photoluminescence than that of other phosphors, where the concentration of Eu{sup 3+} ion is not equal to 0.3. The CIE chromaticity coordinate (0.657, 0.343) of Ca{sub 8}La{sub 2}(PO{sub 4}){sub 6}O{sub 2}:0.3Eu{sup 3+} phosphor is close to National Television Standard Committee standard value (0.670, 0.330) of red phosphors, which indicates Ca{sub 8}La{sub 2}(PO{sub 4}){sub 6}O{sub 2}:0.3Eu{sup 3+} is potential to apply in white light-emitting diodes as an excellent red emitting phosphor.

Investigations on the crystal-structure and non-ambient behaviour of K2Ca2Si8O19 - a new potassium calcium silicate

Science.gov (United States)

Schmidmair, Daniela; Kahlenberg, Volker; Praxmarer, Alessandra; Perfler, Lukas; Mair, Philipp

2017-09-01

Within the context of a systematic re-investigation of phase relationships between compounds of the ternary system K2O-CaO-SiO2 a new potassium calcium silicate with the chemical formula K2Ca2Si8O19 was synthesized via solid state reactions as well as the flux method using KCl as a solvent. Its crystal structure was determined from single-crystal X-ray diffraction data by applying direct methods. The new compound crystallizes in the triclinic space group P 1 bar . Unit cell dimensions are a = 7.4231(7) Å, b = 10.7649(10) Å, c = 12.1252(10) Å, α = 70.193(8)°, β = 83.914(7)° and γ = 88.683(7)°. K2Ca2Si8O19 is built up of corner-connected, slightly distorted [SiO4]-tetrahedra forming double-sheets, which are linked by double-chains of edge-sharing [CaO6]-octahedra. Electroneutrality of the material is provided by additional potassium atoms that are located within the voids of the silicate layers and between adjacent [Ca2O6]-double-chains. Further characterization of the compound was performed by Raman spectroscopy and differential thermal analysis. The behaviour of K2Ca2Si8O19 under high-temperature and high-pressure was investigated by in-situ high-temperature powder X-ray diffraction up to a maximum temperature of 1125 °C and a piston cylinder experiment at 1.5 GPa and 1100 °C. Additionally an overview of known double-layer silicates is given as well as a comparison of K2Ca2Si8O19 to closely related structures.

(Patho)physiological implications of the novel epithelial Ca2+ channels TRPV5 and TRPV6.

NARCIS (Netherlands)

Nijenhuis, T.; Hoenderop, J.G.J.; Nilius, B.; Bindels, R.J.M.

2003-01-01

The epithelial Ca(2+) channels TRPV5 and TRPV6 constitute the apical Ca(2+) entry mechanism in active Ca(2+) (re)absorption. These two members of the superfamily of transient receptor potential (TRP) channels were cloned from the vitamin-D-responsive epithelia of kidney and small intestine and

Performance Characteristics of CA 19-9 Radioimmunoassay and Clinical Significance of Serum CA 19-9 Assay in Patients with Malignancy

International Nuclear Information System (INIS)

Kim, Sang Eun; Shong, Young Kee; Cho, Bo Youn; Kim, Noe Kyeong; Koh, Chang Soon; Lee, Mun Ho; Hong, Seong Woon; Hong, Kee Suk

1985-01-01

To evaluate the performance characteristics of CA 19-9 radioimmunoassay and the clinical significance of serum CA 19-9 assay in patients with malignancy, serum. CA 19-9 levels were measured by radioimmunoassay using monoclonal antibody in 135 normal controls, 81 patients with various untreated malignancy, 9 patients of postoperative colon cancer without recurrence and 20 patients with benign gastrointestinal diseases, who visited Seoul National University Hospital from June, 1984 to March, 1985. The results were as follows; 1) The CA 19-9 radioimmunoassay was simple to perform and can be completed in one work day. And the between-assay reproducibility and the assay recovery were both excellent. 2) The mean serum CA 19-9 level in 135 normal controls was 8.4±4.2 U/mL. Normal upper limit of serum CA 19-9 was defined as 21.0 U/mL. 4 out of 135 (3.0%) normal controls showed elevated CA 19-9 levels above the normal upper limit. 3) One out of 20 (5.0%) patients with benign gastrointestinal diseases showed elevated serum CA 19-9 level above the normal upper limit. 4) In 81 patients with various untreated malignancy, 41 patients (50.6%) showed elevated serum CA 19-9 levels. 66.7% of 18 patients with colorectal cancer, 100% of 2 patients with pancreatic cancer, 100% of 3 patients with common bile duct cancer, 47.1% of 17 patients with stomach cancer, 28.6% of 28 patients with hepatoma and 60.0% of 5 gastrointestinal tract cancers showed elevated serum CA 19-9 levels. 5) The sensitivities of serum CA 19-9 related to respectability in colorectal and stomach cancer were 33.3% in resectable colorectal cancer, 83.3% in unresectable colorectal cancer, 41.7% in resectable stomach cancer, 60.0% in unresectable stomach cancer respectively. 6) The sensitivity of serum CA 19-9 in 9 patients of postoperative colorectal cancer without recurrence were 33.3% and significantly decreased compared with that of untreated colorectal cancer, 66.7% (p<0.05). 7) In Patients with colorectal cancer

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

Energy Technology Data Exchange (ETDEWEB)

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

2010-09-15

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

TRPV5 and TRPV6 in transcellular Ca(2+) transport: regulation, gene duplication, and polymorphisms in African populations.

Science.gov (United States)

Peng, Ji-Bin

2011-01-01

TRPV5 and TRPV6 are unique members of the TRP super family. They are highly selective for Ca(2+) ions with multiple layers of Ca(2+)-dependent inactivation mechanisms, expressed at the apical membrane of Ca(2+) transporting epithelia, and robustly responsive to 1,25-dihydroxivitamin D(3). These features are well suited for their roles as Ca(2+) entry channels in the first step of transcellular Ca(2+) transport pathways, which are involved in intestinal absorption, renal reabsorption of Ca(2+), placental transfer of Ca(2+) to fetus, and many other processes. While TRPV6 is more broadly expressed in a variety of tissues such as esophagus, stomach, small intestine, colon, kidney, placenta, pancreas, prostate, uterus, salivary gland, and sweat gland, TRPV5 expression is relatively restricted to the distal convoluted tubule and connecting tubule of the kidney. There is only one TRPV6-like gene in fish and birds in comparison to both TRPV5 and TRPV6 genes in mammals, indicating TRPV5 gene was likely generated from duplication of TRPV6 gene during the evolution of mammals to meet the needs of complex renal function. TRPV5 and TRPV6 are subjected to vigorous regulations under physiological, pathological, and therapeutic conditions. The elevated TRPV6 level in malignant tumors such as prostate and breast cancers makes it a potential therapeutic target. TRPV6, and to a lesser extent TRPV5, exhibit unusually high levels of single nucleotide polymorphisms (SNPs) in African populations as compared to other populations, indicating TRPV6 gene was under selective pressure during or after humans migrated out of Africa. The SNPs of TRPV6 and TRPV5 likely contribute to the Ca(2+) conservation mechanisms in African populations.

Combustion phasing for maximum efficiency for conventional and high efficiency engines

International Nuclear Information System (INIS)

Caton, Jerald A.

2014-01-01

Highlights: • Combustion phasing for max efficiency is a function of engine parameters. • Combustion phasing is most affected by heat transfer, compression ratio, burn duration. • Combustion phasing is less affected by speed, load, equivalence ratio and EGR. • Combustion phasing for a high efficiency engine was more advanced. • Exergy destruction during combustion as functions of combustion phasing is reported. - Abstract: The importance of the phasing of the combustion event for internal-combustion engines is well appreciated, but quantitative details are sparse. The objective of the current work was to examine the optimum combustion phasing (based on maximum bmep) as functions of engine design and operating variables. A thermodynamic, engine cycle simulation was used to complete this assessment. As metrics for the combustion phasing, both the crank angle for 50% fuel mass burned (CA 50 ) and the crank angle for peak pressure (CA pp ) are reported as functions of the engine variables. In contrast to common statements in the literature, the optimum CA 50 and CA pp vary depending on the design and operating variables. Optimum, as used in this paper, refers to the combustion timing that provides the maximum bmep and brake thermal efficiency (MBT timing). For this work, the variables with the greatest influence on the optimum CA 50 and CA pp were the heat transfer level, the burn duration and the compression ratio. Other variables such as equivalence ratio, EGR level, engine speed and engine load had a much smaller impact on the optimum CA 50 and CA pp . For the conventional engine, for the conditions examined, the optimum CA 50 varied between about 5 and 11°aTDC, and the optimum CA pp varied between about 9 and 16°aTDC. For a high efficiency engine (high dilution, high compression ratio), the optimum CA 50 was 2.5°aTDC, and the optimum CA pp was 7.8°aTDC. These more advanced values for the optimum CA 50 and CA pp for the high efficiency engine were

Calcium Sulfoaluminate Sodalite (Ca 4 Al 6 O 12 SO 4 ) Crystal Structure Evaluation and Bulk Modulus Determination

KAUST Repository

Hargis, Craig W.

2013-12-12

The predominant phase of calcium sulfoaluminate cement, Ca 4(Al6O12)SO4, was investigated using high-pressure synchrotron X-ray diffraction from ambient pressure to 4.75 GPa. A critical review of the crystal structure of Ca4(Al 6O12)SO4 is presented. Rietveld refinements showed the orthorhombic crystal structure to best match the observed peak intensities and positions for pure Ca4(Al6O 12)SO4. The compressibility of Ca4(Al 6O12)SO4 was studied using cubic, orthorhombic, and tetragonal crystal structures due to the lack of consensus on the actual space group, and all three models provided similar results of 69(6) GPa. With its divalent cage ions, the bulk modulus of Ca4(Al6O 12)SO4 is higher than other sodalites with monovalent cage ions, such as Na8(AlSiO4)6Cl2 or Na8(AlSiO4)6(OH)2·H 2O. Likewise, comparing this study to previous ones shows the lattice compressibility of aluminate sodalites decreases with increasing size of the caged ions. Ca4(Al6O12)SO4 is more compressible than other cement clinker phases such as tricalcium aluminate and less compressible than hydrated cement phases such as ettringite and hemicarboaluminate. © 2013 The American Ceramic Society.

Phase diagram and EXAFS study of La sub 0 sub . sub 7 Ca sub 0 sub . sub 3 sub - sub x Ba sub x MnO sub 3 manganites

CERN Document Server

Ulyanov, A N; Yang, D S

2003-01-01

The phase diagram and local structure of La sub 0 sub . sub 7 Ca sub 0 sub . sub 3 sub - sub x Ba sub x MnO sub 3 (x=0; 0.03; 0.06; ... 0.3) lanthanum manganites were studies. The Curie temperature, T sub c , of the compositions showed a sharp change near the concentrational structural orthorhombic-rhombohedral phase transition. Maximums of dispersion, sigma sub M sub n sub - sub O sup 2 , and asymmetry, sigma M sub n sub - sub O sup 3 , of pair distribution function for the Mn-O bond distances of MnO sub 6 octahedron on x-dependence were observed by extended X-ray absorption fine structure (EXAFS) analysis. The maximum of sigma sub M sub n sub - sub O sup 2 is caused by increase of dynamic rms displacements of Mn-O bond distances near the T sub c. The observed x dependence of sigma sub M sub n sub - sub O sup 3 reflects the reduction of charge carriers mobility at approaching to T sub c. (author)

Synthesis of Defect Perovskites (He_2–x⟂_x)(CaZr)F₆ by Inserting Helium into the Negative Thermal Expansion Material CaZrF₆

Energy Technology Data Exchange (ETDEWEB)

Hester, Brett R. [Georgia Inst. of Technology, Atlanta, GA (United States); dos Santos, António M. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Molaison, Jamie J. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Hancock, Justin C. [Georgia Inst. of Technology, Atlanta, GA (United States); Wilkinson, Angus P. [Georgia Inst. of Technology, Atlanta, GA (United States)

2017-09-11

Defect perovskites (He_2–x⟂_x)(CaZr)F₆ can be prepared by inserting helium into CaZrF₆ at high pressure. They can be recovered to ambient pressure at low temperature. There are no prior examples of perovskites with noble gases on the A-sites. The insertion of helium gas into CaZrF₆ both elastically stiffens the material and reduces the magnitude of its negative thermal expansion. It also suppresses the onset of structural disorder, which is seen on compression in other media. Measurements of the gas released on warming to room temperature and Rietveld analyses of neutron diffraction data at low temperature indicate that exposure to helium gas at 500 MPa leads to a stoichiometry close to (He₁⟂₁)(CaZr)F₆. Helium has a much higher solubility in CaZrF₆ than silica glass or crystobalite. An analogue with composition (H₂)₂(CaZr)F₆ would have a volumetric hydrogen storage capacity greater than current US DOE targets. We anticipate that other hybrid perovskites with small neutral molecules on the A-site can also be prepared and that they will display a rich structural chemistry.

Evaluation of live attenuated H7N3 and H7N7 vaccine viruses for their receptor binding preferences, immunogenicity in ferrets and cross reactivity to the novel H7N9 virus.

Directory of Open Access Journals (Sweden)

Qi Xu

Full Text Available Live attenuated influenza vaccine (LAIV candidates of the H7 subtype, A/Netherlands/219/03 (H7N7, NL03 ca and A/chicken/British Columbia/CN-6/2004 (H7N3, BC04 ca, were evaluated for their receptor binding specificity and immunogenicity in ferrets. The BC04 ca virus exhibited α2,3-SA and α2,6-SA dual receptor binding preference while the NL03 ca virus preferentially bound to α2,3-SA. Substitution of the Q226 and G228 (Q-G by the L226 and S228 (L-S residues in the HA improved binding to α2,6-SA for NL03 ca. The vaccine viruses with L-S retained the attenuation phenotype. NL03 L-S ca replicated more efficiently than the original NL03 ca virus in the upper respiratory tract of ferrets, and induced higher levels of humoral and cellular immune responses. Prior vaccination with seasonal LAIV reduced H7-specific antibody responses, but did not reduce the H7N7 vaccine mediated protection against a heterologous H7N3 BC04 wt virus infection in ferrets. In addition, the H7N3 and H7N7 vaccine immunized ferret sera cross reacted with the newly emerged H7N9 virus. These data, in combination with the safety data from previously conducted Phase 1 studies, suggest that these vaccines may have a role in responding to the threat posed by the H7N9 virus.

New metal-organic frameworks of [M(C6H5O7)(C6H6O7)(C6H7O7)(H2O)] . H2O (M=La, Ce) and [Ce2(C2O4)(C6H6O7)2] . 4H2O

International Nuclear Information System (INIS)

Weng Shengfeng; Wang, Yun-Hsin; Lee, Chi-Shen

2012-01-01

Two novel materials, [M(C 6 H 5 O 7 )(C 6 H 6 O 7 )(C 6 H 7 O 7 )(H 2 O)] . H 2 O (M=La(1a), Ce(1b)) and [Ce 2 (C 2 O 4 )(C 6 H 6 O 7 ) 2 ] . 4H 2 O (2), with a metal-organic framework (MOF) were prepared with hydrothermal reactions and characterized with photoluminescence, magnetic susceptibility, thermogravimetric analysis and X-ray powder diffraction in situ. The crystal structures were determined by single-crystal X-ray diffraction. Compound 1 crystallized in triclinic space group P1-bar (No. 2); compound 2 crystallized in monoclinic space group P2 1 /c (No. 14). The structure of 1 is built from a 1D MOF, composed of deprotonated citric ligands of three kinds. Compound 2 contains a 2D MOF structure consisting of citrate and oxalate ligands; the oxalate ligand arose from the decomposition in situ of citric acid in the presence of Cu II ions. Photoluminescence spectra of compounds 1b and 2 revealed transitions between the 5d 1 excited state and two levels of the 4f 1 ground state ( 2 F 5/2 and 2 F 7/2 ). Compounds 1b and 2 containing Ce III ion exhibit a paramagnetic property with weak antiferromagnetic interactions between the two adjacent magnetic centers. - Graphical Abstract: [M(C 6 H 5 O 7 )(C 6 H 6 O 7 )(C 6 H 7 O 7 )(H 2 O)] . H 2 O (M=La(1a), Ce(1b)) and [Ce 2 (C 2 O 4 )(C 6 H 6 O 7 ) 2 ] . 4H 2 O (2)—with 1D and 2D structures were synthesized and characterized. Highlights: ► Two MOF – [M(C 6 H 5 O 7 )(C 6 H 6 O 7 )(C 6 H 7 O 7 )(H 2 O)] . H 2 O (M=La(1a), Ce(1b)) and [Ce 2 (C 2 O 4 )(C 6 H 6 O 7 ) 2 ] . 4H 2 O (2) – with 1D and 2D structures. ► The adjacent chains of the 1D framework were correlated with each other through an oxalate ligand to form a 2D layer structure. ► The source of the oxalate ligand was the decomposition in situ of citric acid oxidized in the presence of Cu II ions.

Bioactivity and mineralization of hydroxyapatite with bioglass as sintering aid and bioceramics with Na{sub 3}Ca{sub 6}(PO{sub 4}){sub 5} and Ca{sub 5}(PO{sub 4}){sub 2}SiO{sub 4} in a silicate matrix

Energy Technology Data Exchange (ETDEWEB)

Demirkiran, Hande [Materials Science and Engineering Department, University of Texas at Arlington, Arlington, TX 76019 (United States); Mohandas, Arunesh; Dohi, Motokazi; Fuentes, Alonso; Nguyen, Kytai [Bioengineering Department, University of Texas at Arlington, Arlington, TX 76019 (United States); Aswath, Pranesh, E-mail: aswath@uta.edu [Materials Science and Engineering Department, University of Texas at Arlington, Arlington, TX 76019 (United States)

2010-01-30

Hydroxyapatite and Bioglass-45S5 were sintered together creating new ceramic compositions that yielded increased apatite deposition and osteoblast differentiation and proliferation in vitro compared to hydroxyapatite. The sintered products characterized by X-ray diffraction, revealed hydroxyapatite as the main phase when small quantities (1, 2.5 and 5 wt.%) of bioglass was added. Bioglass behaved as a sintering aid with {beta}-TCP (Ca{sub 3}(PO{sub 4}){sub 2}) being the minor phase. The amount of {beta}-TCP increased with the amount of bioglass added. In compositions with larger additions of bioglass (10 and 25 wt.%), new phases with compositions of calcium phosphate silicate (Ca{sub 5}(PO{sub 4}){sub 2}SiO{sub 4}) and sodium calcium phosphate (Na{sub 3}Ca{sub 6}(PO{sub 4}){sub 5}) were formed respectively within amorphous silicate matrices. In vitro cell culture studies of the ceramic compositions were examined using bone marrow stromal cell (BMSC). Cell proliferation and differentiation of bone marrow stromal cells into osteoblasts were determined by Pico Green DNA assays and alkaline phosphatase (ALP) activity, respectively. All hydroxyapatite-bioglass co-sintered ceramics exhibited larger cell proliferation compared to pure hydroxyapatite samples. After 6 days in cell culture, the ceramic with Ca{sub 5}(PO{sub 4}){sub 3}SiO{sub 4} in a silicate matrix formed by reacting hydroxyapatite with 10 wt.% bioglass exhibited the maximum proliferation of the BMSC's. The ALP activity was found to be largest in the ceramic with Na{sub 3}Ca{sub 6}(PO{sub 4}){sub 5} embedded in a silicate matrix synthesized by reacting hydroxyapatite with 25 wt.% bioglass.

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

Science.gov (United States)

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

2012-09-19

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

2.4 μm diode-pumped Dy2+:CaF2 laser

Science.gov (United States)

Švejkar, Richard; Papashvili, Alexander G.; Šulc, Jan; Němec, Michal; Jelínková, Helena; Doroshenko, Maxim E.; Batygov, Sergei H.; Osiko, Vyacheslav V.

2018-01-01

In this work, a cryogenic cooled, longitudinal diode-pumped Dy2+ :CaF2 laser was investigated for the first time. The temperature dependence of the spectroscopy and the laser properties of Dy2+ :CaF2 are presented. The tested Dy2+ :CaF2 crystal was a longitudinal pump in a near-IR region (926 nm) by laser diode radiation. The maximal mean output power and slope efficiency at 78 K during the pulse regime of the laser were 57.5 mW and 7%, respectively. Furthermore, the CW regime was successfully tested and a maximum output power of 0.37 W was obtained for the absorbed pumping power 5.7 W. The emission laser wavelength was 2367 nm.

Synthesis, crystal structure, and photocatalytic activity of a new two-layer Ruddlesden-Popper phase, Li2CaTa2O7

International Nuclear Information System (INIS)

Liang Zhenhua; Tang Kaibin; Shao Qian; Li Guocan; Zeng Suyuan; Zheng Huagui

2008-01-01

A new two-layer Ruddlesden-Popper phase Li 2 CaTa 2 O 7 has been synthesized for the first time. The detailed structure determination of Li 2 CaTa 2 O 7 performed by powder X-ray diffraction (XRD) and electron microscopy (ED) shows that it crystallizes in the space group Fmmm [a∼5.5153(1), b∼5.4646(1), c∼18.2375(3)A]. UV-visible diffuse reflection spectrum of the prepared Li 2 CaTa 2 O 7 indicates that it had absorption in the UV region. The photocatalytic activity of the Li 2 CaTa 2 O 7 powders was evaluated by degradation of RhB molecules in water under ultra visible light irradiation. The results showed that Li 2 CaTa 2 O 7 has high photocatalytic activity at room temperature. Therefore, the preparation and properties studies of Li 2 CaTa 2 O 7 with a two-layer Ruddlesden-Popper structure suggest potential future applications in photocatalysis. - Graphical abstract: Crystal structure of a two-layer Ruddlesden-Popper phase Li 2 CaTa 2 O 7 A new two-layer Ruddlesden-Popper phase Li 2 CaTa 2 O 7 has been synthesized for the first time. Li 2 CaTa 2 O 7 crystallizes in the space group Fmmm determined by powder X-ray and electron diffraction. UV-visible diffuse reflection spectra and the photocatalytic degradation of RhB molecules in water under ultra visible light irradiation show that Li 2 CaTa 2 O 7 is a potential material in photocatalysis

Superconducting Cd and Ca doped 123 phase in Cdo.8Ba2(Y0.7Ca0.4) Cu3.5Oy

International Nuclear Information System (INIS)

Balchev, N.; Kovachev, V; THOMAS, J.; BIEGER, W.; Konstantinov, K.; Kunev, B.

1999-01-01

A new Cd-containing superconductor with nominal composition of Cd 0.8 Ba 2 (Y 0.7 Ca 0.4 ) Cu 3.5 O y and T c = 80 K was synthesized and investigated. The obtained XRD pattern shows that the dominating phase is an orthorhombic 123. It was shown that the presence of Cd and Ca facilitates the 123 phase formation. The results of the EDX analysis on SEM and TEM have shown that the distribution of the Cd and Ca in the samples is inhomogeneous. The two elements enter the 123 phase in most of the investigated crystals and form a new Cd-Ba-Y-Ca-Cu-O superconducting compound

Effect of exercise training on Ca2+ release units of left ventricular myocytes of spontaneously hypertensive rats.

Science.gov (United States)

Carneiro-Júnior, M A; Quintão-Júnior, J F; Drummond, L R; Lavorato, V N; Drummond, F R; Amadeu, M A; Oliveira, E M; Felix, L B; Cruz, J S; Mill, J G; Natali, A J; Prímola-Gomes, T N

2014-08-29

In cardiomyocytes, calcium (Ca2+) release units comprise clusters of intracellular Ca2+ release channels located on the sarcoplasmic reticulum, and hypertension is well established as a cause of defects in calcium release unit function. Our objective was to determine whether endurance exercise training could attenuate the deleterious effects of hypertension on calcium release unit components and Ca2+ sparks in left ventricular myocytes of spontaneously hypertensive rats. Male Wistar and spontaneously hypertensive rats (4 months of age) were divided into 4 groups: normotensive (NC) and hypertensive control (HC), and normotensive (NT) and hypertensive trained (HT) animals (7 rats per group). NC and HC rats were submitted to a low-intensity treadmill running protocol (5 days/week, 1 h/day, 0% grade, and 50-60% of maximal running speed) for 8 weeks. Gene expression of the ryanodine receptor type 2 (RyR2) and FK506 binding protein (FKBP12.6) increased (270%) and decreased (88%), respectively, in HC compared to NC rats. Endurance exercise training reversed these changes by reducing RyR2 (230%) and normalizing FKBP12.6 gene expression (112%). Hypertension also increased the frequency of Ca2+ sparks (HC=7.61±0.26 vs NC=4.79±0.19 per 100 µm/s) and decreased its amplitude (HC=0.260±0.08 vs NC=0.324±0.10 ΔF/F0), full width at half-maximum amplitude (HC=1.05±0.08 vs NC=1.26±0.01 µm), total duration (HC=11.51±0.12 vs NC=14.97±0.24 ms), time to peak (HC=4.84±0.06 vs NC=6.31±0.14 ms), and time constant of decay (HC=8.68±0.12 vs NC=10.21±0.22 ms). These changes were partially reversed in HT rats (frequency of Ca2+ sparks=6.26±0.19 µm/s, amplitude=0.282±0.10 ΔF/F0, full width at half-maximum amplitude=1.14±0.01 µm, total duration=13.34±0.17 ms, time to peak=5.43±0.08 ms, and time constant of decay=9.43±0.15 ms). Endurance exercise training attenuated the deleterious effects of hypertension on calcium release units of left ventricular myocytes.

Effect of exercise training on Ca2+ release units of left ventricular myocytes of spontaneously hypertensive rats

Directory of Open Access Journals (Sweden)

M.A. Carneiro-Júnior

2014-11-01

Full Text Available In cardiomyocytes, calcium (Ca2+ release units comprise clusters of intracellular Ca2+ release channels located on the sarcoplasmic reticulum, and hypertension is well established as a cause of defects in calcium release unit function. Our objective was to determine whether endurance exercise training could attenuate the deleterious effects of hypertension on calcium release unit components and Ca2+ sparks in left ventricular myocytes of spontaneously hypertensive rats. Male Wistar and spontaneously hypertensive rats (4 months of age were divided into 4 groups: normotensive (NC and hypertensive control (HC, and normotensive (NT and hypertensive trained (HT animals (7 rats per group. NC and HC rats were submitted to a low-intensity treadmill running protocol (5 days/week, 1 h/day, 0% grade, and 50-60% of maximal running speed for 8 weeks. Gene expression of the ryanodine receptor type 2 (RyR2 and FK506 binding protein (FKBP12.6 increased (270% and decreased (88%, respectively, in HC compared to NC rats. Endurance exercise training reversed these changes by reducing RyR2 (230% and normalizing FKBP12.6 gene expression (112%. Hypertension also increased the frequency of Ca2+ sparks (HC=7.61±0.26 vs NC=4.79±0.19 per 100 µm/s and decreased its amplitude (HC=0.260±0.08 vs NC=0.324±0.10 ΔF/F0, full width at half-maximum amplitude (HC=1.05±0.08 vs NC=1.26±0.01 µm, total duration (HC=11.51±0.12 vs NC=14.97±0.24 ms, time to peak (HC=4.84±0.06 vs NC=6.31±0.14 ms, and time constant of decay (HC=8.68±0.12 vs NC=10.21±0.22 ms. These changes were partially reversed in HT rats (frequency of Ca2+ sparks=6.26±0.19 µm/s, amplitude=0.282±0.10 ΔF/F0, full width at half-maximum amplitude=1.14±0.01 µm, total duration=13.34±0.17 ms, time to peak=5.43±0.08 ms, and time constant of decay=9.43±0.15 ms. Endurance exercise training attenuated the deleterious effects of hypertension on calcium release units of left ventricular myocytes.

Effect of exercise training on Ca2+ release units of left ventricular myocytes of spontaneously hypertensive rats

International Nuclear Information System (INIS)

Carneiro-Júnior, M.A.; Quintão-Júnior, J.F.; Drummond, L.R.; Lavorato, V.N.; Drummond, F.R.; Amadeu, M.A.; Oliveira, E.M.; Felix, L.B.; Cruz, J.S.; Mill, J.G.; Natali, A.J.; Prímola-Gomes, T.N.

2014-01-01

In cardiomyocytes, calcium (Ca 2+ ) release units comprise clusters of intracellular Ca 2+ release channels located on the sarcoplasmic reticulum, and hypertension is well established as a cause of defects in calcium release unit function. Our objective was to determine whether endurance exercise training could attenuate the deleterious effects of hypertension on calcium release unit components and Ca 2+ sparks in left ventricular myocytes of spontaneously hypertensive rats. Male Wistar and spontaneously hypertensive rats (4 months of age) were divided into 4 groups: normotensive (NC) and hypertensive control (HC), and normotensive (NT) and hypertensive trained (HT) animals (7 rats per group). NC and HC rats were submitted to a low-intensity treadmill running protocol (5 days/week, 1 h/day, 0% grade, and 50-60% of maximal running speed) for 8 weeks. Gene expression of the ryanodine receptor type 2 (RyR2) and FK506 binding protein (FKBP12.6) increased (270%) and decreased (88%), respectively, in HC compared to NC rats. Endurance exercise training reversed these changes by reducing RyR2 (230%) and normalizing FKBP12.6 gene expression (112%). Hypertension also increased the frequency of Ca 2+ sparks (HC=7.61±0.26 vs NC=4.79±0.19 per 100 µm/s) and decreased its amplitude (HC=0.260±0.08 vs NC=0.324±0.10 ΔF/F 0 ), full width at half-maximum amplitude (HC=1.05±0.08 vs NC=1.26±0.01 µm), total duration (HC=11.51±0.12 vs NC=14.97±0.24 ms), time to peak (HC=4.84±0.06 vs NC=6.31±0.14 ms), and time constant of decay (HC=8.68±0.12 vs NC=10.21±0.22 ms). These changes were partially reversed in HT rats (frequency of Ca 2+ sparks=6.26±0.19 µm/s, amplitude=0.282±0.10 ΔF/F 0 , full width at half-maximum amplitude=1.14±0.01 µm, total duration=13.34±0.17 ms, time to peak=5.43±0.08 ms, and time constant of decay=9.43±0.15 ms). Endurance exercise training attenuated the deleterious effects of hypertension on calcium release units of left ventricular myocytes

Ca2 Al2 SiO7 :Ce3+ phosphors for mechanoluminescence dosimetry.

Science.gov (United States)

Tiwari, Geetanjali; Brahme, Nameeta; Sharma, Ravi; Bisen, D P; Sao, Sanjay Kumar; Sahu, Ishwar Prasad

2016-12-01

A series of Ce 3+ ion single-doped Ca 2 Al 2 SiO 7 phosphors was synthesized by a combustion-assisted method at an initiating temperature of 600 °C. The samples were annealed at 1100 °C for 3 h and their X-ray diffraction patterns confirmed a tetragonal structure. The phase structure, particle size, surface morphology and elemental analysis were analyzed using X-ray diffraction (XRD), transmission electron microscope (TEM), scanning electron microscopy (SEM) and energy dispersive X-ray (EDX) spectroscopy techniques. Thermoluminescence (TL) intensity increased with increase in ultraviolet (UV) light exposure time up to 15 min. With further increase in the UV irradiation time the TL intensity decreases. The increase in TL intensity indicates that trap concentration increased with UV exposure time. A broad peak at 121 °C suggested the existence of a trapping level. The peak of mechanoluminescence (ML) intensity versus time curve increased linearly with increasing impact velocity of the moving piston. Mechanoluminescence intensity increased with increase in UV irradiation time up to 15 min. Under UV-irradiation excitation, the TL and ML emission spectra of Ca 2 Al 2 SiO 7 :Ce 3+ phosphor showed the characteristic emission of Ce 3+ peaking at 400 nm (UV-violet) and originating from the Ce 3+ transitions of 5d-4f ( 2 F 5/2 and 2 F 7/2 ). The photoluminescence (PL) emission spectra for Ca 2 Al 2 SiO 7 :Ce 3+ were similar to the ML/TL emission spectra. The mechanism of ML excitation and the suitability of the Ca 2 Al 2 SiO 7 :Ce 3+ phosphor for radiation dosimetry are discussed. Copyright © 2016 John Wiley & Sons, Ltd. Copyright © 2016 John Wiley & Sons, Ltd.

49 CFR 398.6 - Hours of service of drivers; maximum driving time.

Science.gov (United States)

2010-10-01

... REGULATIONS TRANSPORTATION OF MIGRANT WORKERS § 398.6 Hours of service of drivers; maximum driving time. No person shall drive nor shall any motor carrier permit or require a driver employed or used by it to drive...

Crystal growth and optical properties of Sm:CaNb2O6 single crystal

International Nuclear Information System (INIS)

Di Juqing; Xu Xiaodong; Xia Changtai; Zeng Huidan; Cheng Yan; Li Dongzhen; Zhou Dahua; Wu Feng; Cheng Jimeng; Xu Jun

2012-01-01

Highlights: ► Sm:CaNb 2 O 6 single crystal was grown by the Czochralski method. ► Thermal expansion coefficients and J–O parameters were calculated. ► We found that this crystal had high quantum efficiency of 97%. - Abstract: Sm:CaNb 2 O 6 single crystal has been grown by the Czochralski method. Its high-temperature X-ray powder diffraction, optical absorption, emission spectroscopic as well as lifetime have been studied. Thermal expansion coefficients (α), J–O parameters (Ω i ), radiative lifetime (τ rad ), branching ratios (β) and stimulated emission cross-sections (σ e ) were calculated. The quantum efficiency (η) was calculated to be 97%. The intense peak emission cross section at 610, 658 nm were calculated to be 2.40 × 10 −21 , 2.42 × 10 −21 cm 2 . These results indicate that Sm:CaNb 2 O 6 crystal has potential use in visible laser and photonic devices area.

Effects of Ca-dopant on the pyroelectric, piezoelectric and dielectric properties of (Sr 0.6Ba 0.4) 4Na 2Nb 10O 30 ceramics

KAUST Repository

Yao, Yingbang

2012-12-01

Calcium-doped sodium strontium barium niobate (SBNN, (Sr 0.6Ba 0.4) 4-xCa xNa 2Nb 10O 30, 0 ≤ x ≤ 0.5) ceramics were prepared by a conventional solid-state reaction method. SBNN showed \\'filled\\' tetragonal tungsten-bronze structure with fully occupied A-sites. The tetragonal structure, as revealed by X-ray diffraction (XRD) and Raman spectroscopy, was not affected by the Ca-dopant. Effects of Ca-doping concentration on the phase transitions as well as ferroelectric, piezoelectric and pyroelectric properties of the SBNN ceramics were investigated. From the dielectric studies, two anomalies were observed, namely, a sharp normal ferroelectric transition at 260 °C and a broad maximum at round -110 °C. The later was affected by the Ca-doping concentration and its origin was discussed. At x = 0.3, the sample exhibited the highest pyroelectric coefficient of 168 μC/m 2 K and the largest piezoelectric coefficient (d 33) of 63 pC/N at room temperature. On the basis of our results, the pyroelectric properties of the SBNN were improved by Ca-doping. © 2012 Elsevier B.V. All rights reserved.

Effects of Ca-dopant on the pyroelectric, piezoelectric and dielectric properties of (Sr 0.6Ba 0.4) 4Na 2Nb 10O 30 ceramics

KAUST Repository

Yao, Yingbang; Mak, C. L.

2012-01-01

Calcium-doped sodium strontium barium niobate (SBNN, (Sr 0.6Ba 0.4) 4-xCa xNa 2Nb 10O 30, 0 ≤ x ≤ 0.5) ceramics were prepared by a conventional solid-state reaction method. SBNN showed 'filled' tetragonal tungsten-bronze structure with fully occupied A-sites. The tetragonal structure, as revealed by X-ray diffraction (XRD) and Raman spectroscopy, was not affected by the Ca-dopant. Effects of Ca-doping concentration on the phase transitions as well as ferroelectric, piezoelectric and pyroelectric properties of the SBNN ceramics were investigated. From the dielectric studies, two anomalies were observed, namely, a sharp normal ferroelectric transition at 260 °C and a broad maximum at round -110 °C. The later was affected by the Ca-doping concentration and its origin was discussed. At x = 0.3, the sample exhibited the highest pyroelectric coefficient of 168 μC/m 2 K and the largest piezoelectric coefficient (d 33) of 63 pC/N at room temperature. On the basis of our results, the pyroelectric properties of the SBNN were improved by Ca-doping. © 2012 Elsevier B.V. All rights reserved.

Mol 7C/6

International Nuclear Information System (INIS)

Aberle, J.; Schleisiek, K.; Schmuck, I.; Schmidt, L.; Romer, O.; Weih, G.

1995-01-01

The Mol 7C/6 coolant blockage experiment in the Belgian BR2 reactor yielded results different from Mol 7C experiments with low burnup pins: At 10% burnup local failure is not self-limiting, but requires active systems for detection and scram. The Mol 7C series was finished in 1991. In each of the test bundles Mol 7C/4, /5 and /6, 30 Mk I pins pre-irradiated in KNK II were used. The central blockage consisted of enriched UO 2 covering 30 percent of the bundle cross-section, with a height of 40 mm. The most important system for timely detection of coolant blockages of the type studied in Mol 7C/6 is based on DND. (orig.)

Experimental studies on cycling stable characteristics of inorganic phase change material CaCl2·6H2O-MgCl2·6H2O modified with SrCl2·6H2O and CMC

Science.gov (United States)

He, Meizhi; Yang, Luwei; Zhang, Zhentao

2018-01-01

By means of mass ratio method, binary eutectic hydrated salts inorganic phase change thermal energy storage system CaCl2·6H2O-20wt% MgCl2·6H2O was prepared, and through adding nucleating agent 1wt% SrCl2·6H2O and thickening agent 0.5wt% carboxy methyl cellulose (CMC), inoganic phase change material (PCM) modified was obtained. With recording cooling-melting curves simultaneously, this PCM was frozen and melted for 100 cycles under programmable temperature control. After per 10 cycles, the PCM was charaterized by differential scanning calorimeter (DSC), X-ray diffraction (XRD) and density meter, then analysing variation characteristics of phase change temperature, supercooling degree, superheat degree, latent heat, crystal structure and density with the increase of cycle index. The results showed that the average values of average phase change temperature for cooling and heating process were 25.70°C and 27.39°C respectively with small changes. The average values of average supercooling and superheat degree were 0.59°C and 0.49°C respectively, and the maximum value was 1.10°C. The average value and standard deviation of latent heat of fusion were 120.62 J/g and 1.90 J/g respectively. Non-molten white solid sediments resulted from phase separation were tachyhydrite (CaMg2Cl6·12H2O), which was characterized by XRD. Measuring density of the PCM after per 10 cycles, and the results suggested that the total mass of tachyhydrite was limited. In summary, such modified inoganic PCM CaCl2·6H2O-20wt% MgCl2·6H2O-1wt% SrCl2·6H2O-0.5wt% CMC could stay excellent circulation stability within 100 cycles, and providing reference value in practical use.

The diagnostic value of serum tumor markers CEA, CA19-9, CA125, CA15-3, and TPS in metastatic breast cancer.

Science.gov (United States)

Wang, Weigang; Xu, Xiaoqin; Tian, Baoguo; Wang, Yan; Du, Lili; Sun, Ting; Shi, Yanchun; Zhao, Xianwen; Jing, Jiexian

2017-07-01

This study aims to understand the diagnostic value of serum tumor markers carcinoembryonic antigen (CEA), cancer antigen 19-9 (CA19-9), cancer antigen 125 (CA125), cancer antigen 15-3 (CA15-3), and tissue polypeptide-specific antigen (TPS) in metastatic breast cancer (MBC). A total of 164 metastatic breast cancer patients in Shanxi Cancer Hospital were recruited between February 2016 and July 2016. 200 breast cancer patients without metastasis in the same period were randomly selected as the control group. The general characteristics, immunohistochemical, and pathological results were investigated between the two groups, and tumor markers were determined. There were statistical differences in the concentration and the positive rates of CEA, CA19-9, CA125, CA15-3, and TPS between the MBC and control group (Ptumor marker at 56.7% and 97.0%, respectively. In addition, two tumor markers were used for the diagnosis of MBC and the CEA and TPS combination had the highest diagnostic sensitivity with 78.7%, while the CA15-3 and CA125 combination had the highest specificity of 91.5%. Analysis of tumor markers of 164 MBC found that there were statistical differences in the positive rates of CEA and CA15-3 between bone metastases and other metastases (χ 2 =6.00, P=0.014; χ 2 =7.32, P=0.007, respectively). The sensitivity and specificity values of the CEA and CA15-3 combination in the diagnosis of bone metastases were 77.1% and 45.8%, respectively. The positive rate of TPS in the lung metastases group was lower than in other metastases (χ 2 =8.06, P=0.005).There were significant differences in the positive rates of CA15-3 and TPS between liver metastases and other metastases (χ 2 =15.42, Ptumor markers have varying diagnostic value. Copyright © 2017 Elsevier B.V. All rights reserved.

The effects of temperature, salinity, and the carbonate system on Mg/Ca in Globigerinoides ruber (white): A global sediment trap calibration

Science.gov (United States)

Gray, William R.; Weldeab, Syee; Lea, David W.; Rosenthal, Yair; Gruber, Nicolas; Donner, Barbara; Fischer, Gerhard

2018-01-01

The Mg/Ca of planktic foraminifera Globigerinoides ruber (white) is a widely applied proxy for tropical and sub-tropical sea-surface temperature. The accuracy with which temperature can be reconstructed depends on how accurately relationships between Mg/Ca and temperature and the multiple secondary controls on Mg/Ca are known; however, these relationships remain poorly quantified under oceanic conditions. Here, we present new calibrations based on 440 sediment trap/plankton tow samples from the Atlantic, Pacific and Indian Oceans, including 130 new samples from the Bay of Bengal/Arabian Sea and the tropical Atlantic Ocean. Our results indicate temperature, salinity and the carbonate system all significantly influence Mg/Ca in G. ruber (white). We propose two calibration models: The first model assumes pH is the controlling carbonate system parameter. In this model, Mg/Ca has a temperature sensitivity of 6.0 ± 0.8%/°C (2σ), a salinity sensitivity of 3.3 ± 2.2%/PSU and a pH sensitivity of - 8.3 ± 7.7%/0.1 pH units; The second model assumes carbonate ion concentration ([3 2-CO]) is the controlling carbonate system parameter. In this model, Mg/Ca has a temperature sensitivity of 6.7 ± 0.8%/°C, a salinity sensitivity of 5.0 ± 3.0%/PSU and a [3 2-CO] sensitivity of - 0.24 ± 0.11%/μmol kg-1. In both models, the temperature sensitivity is significantly lower than the widely-applied sensitivity of 9.0 ± 0.6%/°C. Application of our new calibrations to down-core data from the Last Glacial Maximum, considering whole ocean changes in salinity and carbonate chemistry, indicate a cooling of 2.4 ± 1.6°C in the tropical oceans if pH is the controlling parameter and 1.5 ± 1.4°C if [3 2-CO] is the controlling parameter.

46 CFR 7.120 - Mexican/United States border to Point Fermin, CA.

Science.gov (United States)

2010-10-01

... 46 Shipping 1 2010-10-01 2010-10-01 false Mexican/United States border to Point Fermin, CA. 7.120 Section 7.120 Shipping COAST GUARD, DEPARTMENT OF HOMELAND SECURITY PROCEDURES APPLICABLE TO THE PUBLIC... from the southerly tower of the Coronado Hotel in approximate position latitude 32°40.8′ N. longitude...

Crystal structures of the double perovskites Ba2Sr1-x Ca x WO6

International Nuclear Information System (INIS)

Fu, W.T.; Akerboom, S.; IJdo, D.J.W.

2007-01-01

Structures of the double perovskites Ba 2 Sr 1- x Ca x WO 6 have been studied by the profile analysis of X-ray diffraction data. The end members, Ba 2 SrWO 6 and Ba 2 CaWO 6 , have the space group I2/m (tilt system a 0 b - b - ) and Fm3-barm (tilt system a 0 a 0 a 0 ), respectively. By increasing the Ca concentration, the monoclinic structure transforms to the cubic one via the rhombohedral R3-bar phase (tilt system a - a - a - ) instead of the tetragonal I4/m phase (tilt system a 0 a 0 c - ). This observation supports the idea that the rhombohedral structure is favoured by increasing the covalency of the octahedral cations in Ba 2 MM'O 6 -type double perovskites, and disagrees with a recent proposal that the formation of the π-bonding, e.g., d 0 -ion, determines the tetragonal symmetry in preference to the rhombohedral one. - Graphical abstract: Enlarged sections showing the evolution of the basic (222) and (400) reflections in Ba 2 Sr 1- x Ca x WO 6 . Tick marks below are the positions of Bragg's reflections calculated using the space groups I2/m (x=0), R3-bar (x=0.25, 0.5 and 0.75) and Fm3-barm (x=1), respectively

Taurine effects on 45Ca2+ transport in retinal subcellular fractions

International Nuclear Information System (INIS)

Pasantes-Morales, H.; Ademe, R.M.; Lopez-Colome, A.M.

1979-01-01

The effect of taurine on 45 Ca 2+ transport by subcellular fractions from the chick retina was examined. An inhibitory action of taurine on 45 Ca 2+ uptake was observed in retinal fractions incubated for 1-5 min in a Krebs-bicarbonate medium, pH 7.4. In the crude nuclear fraction, 25 mM taurine produced a decrease of 50% in 45 Ca 2+ uptake; in the crude synaptosomal fraction, taurine reduced 45 Ca 2+ accumulation by 70%; the maximum inhibitory effect of taurine on 45 Ca 2+ uptake (80%) was observed in a fraction containing outer segments and pigment epithelium cells. Taurine effect was specific, dose-dependent and related to osmotically sensitive particles. The results suggest a role of taurine in the regulation of calcium fluxes in the retina. (Auth.)

Scintillation and optical properties of Ce{sup 3+}-doped CaGdAl{sub 3}O{sub 7} single crystals

Energy Technology Data Exchange (ETDEWEB)

Mori, Masaki, E-mail: masaki.mori.mz4@ms.naist.jp [Graduate School of Materials Science, Nara Institute of Science and Technology (NAIST), 8916-5 Takayama-cho, Ikoma-shi, Nara 630-0192 (Japan); Nakauchi, Daisuke; Okada, Go [Graduate School of Materials Science, Nara Institute of Science and Technology (NAIST), 8916-5 Takayama-cho, Ikoma-shi, Nara 630-0192 (Japan); Fujimoto, Yutaka [Department of Applied Chemistry, Graduate School of Engineering, Tohoku University, 6-6-07 Aoba, Aramaki, Aoba-ku, Sendai, 980-8579 (Japan); Kawaguchi, Noriaki [Graduate School of Materials Science, Nara Institute of Science and Technology (NAIST), 8916-5 Takayama-cho, Ikoma-shi, Nara 630-0192 (Japan); Koshimizu, Masanori [Department of Applied Chemistry, Graduate School of Engineering, Tohoku University, 6-6-07 Aoba, Aramaki, Aoba-ku, Sendai, 980-8579 (Japan); Yanagida, Takayuki [Graduate School of Materials Science, Nara Institute of Science and Technology (NAIST), 8916-5 Takayama-cho, Ikoma-shi, Nara 630-0192 (Japan)

2017-06-15

The single crystals of 0, 0.6, 1, 1.6 and 2 mol% Ce doped CaGdAl{sub 3}O{sub 7} (Ce:CGAM) were grown by the Floating Zone method, and investigated on photoluminescence (PL) and scintillation properties. In the PL spectra, a broad emission appeared over 380–500 nm under 280 and 360 nm excitations with the quantum yield of 33.8–38.8%. Under a vacuum ultraviolet excitation (90 nm) using a synchrotron source, non-doped CGAM single crystal showed broad emissions over 250–650 nm. The PL decay time profiles followed a monotonic exponential decay with a decay time constant of around 33 ns. The scintillation spectra were similar to those of PL. All of the samples exhibited a clear photoabsorption peak and Compton edge in the pulse height spectra measured under {sup 137}Cs γ-ray irradiation, and the absolute scintillation light yield (LY) was highest for the 2% Ce-doped sample with the value of 3300±300 ph/MeV. The scintillation decay profiles were approximated by a third order exponential decay function, and the extracted decay time of Ce{sup 3+} emission component was around 36–44 ns. Among all the samples, 2%Ce:CGAM single crystal sample showed the best afterglow level as a scintillator under X-ray irradiation. - Highlights: •Ce{sup 3+}-doped CaGdAl{sub 3}O{sub 7} single crystals were synthesized by the FZ method. •Optical and scintillation properties of Ce{sup 3+}-doped CaGdAl{sub 3}O{sub 7} were investigated. •Photoabsorption peak in a pulse height spectrum was clearly observed under γ-rays.

40 CFR 721.10018 - Calcium hydroxide oxide silicate (Ca6(OH)2O2(Si2O5)3).

Science.gov (United States)

2010-07-01

... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Calcium hydroxide oxide silicate (Ca6... New Uses for Specific Chemical Substances § 721.10018 Calcium hydroxide oxide silicate (Ca6(OH)2O2... substance identified as calcium hydroxide oxide silicate (Ca6(OH)2O2(Si2O5)3) (PMN P-01-442; CAS No. 13169...

A single-phase white light emitting Pr3+ doped Ba2CaWO6 phosphor: synthesis, photoluminescence and optical properties

Science.gov (United States)

Sreeja, E.; Vidyadharan, Viji; Jose, Saritha K.; George, Anns; Joseph, Cyriac; Unnikrishnan, N. V.; Biju, P. R.

2018-04-01

Pr3+ doped Ba2CaWO6 phosphor were prepared by traditional high-temperature solid-state reaction technique. The structure evolution was systematically investigated by X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) analysis. The X-ray powder diffraction patterns indicate that the prepared phosphors crystallized in the cubic double-perovskite structure. The functional groups were identified using FTIR spectra and the elements present in the composition were confirmed by the EDS profile. The morphology of the phosphor was identified using SEM and TEM analysis. The PL spectra illustrated that these phosphors could be efficiently excited by charge transfer band of host and the maximum luminescence intensity was observed at 0.06 wt% of Pr3+ ion. Upon the charge transfer band excitation, emission spectra showed peaks at 489, 532, 647, 685 and 737 nm corresponding to 3P0→3H4, 3P1→3H5, 3P0→3F2, 3P0→3F3 and 3P0→3F4 transitions respectively. The concentration quenching of Ba2CaWO6:Pr3+ phosphor can be mainly attributed to dipole-dipole interaction. The CIE coordinates were estimated to be close to the white region. The decay curves are well fitted with double exponential decay models. The standard and modified Judd-Ofelt (JO) theories were used to determine the Judd-Ofelt intensity parameters, radiative transition probabilities and branching ratios. The optical properties indicate that Ba2CaWO6:Pr3+ phosphors can produce white light emission from a single phase host and its potential application for solid-state lighting and display devices.

Study on fast luminescence component induced by gamma-rays in Ce doped LiCaAlF6 scintillators

International Nuclear Information System (INIS)

Watanabe, Kenichi; Kondo, Yoshiyuki; Yamazaki, Atsushi; Uritani, Akira; Iguchi, Tetsuo; Kawaguchi, Noriaki; Fukuda, Kentaro; Ishizu, Sumito; Yanagida, Takayuki; Fujimoto, Yutaka; Yoshikawa, Akira

2014-01-01

We discuss the origin of the fast luminescence component induced by fast electrons generated in gamma-ray interactions in Ce doped LiCaAlF 6 scintillators. Although the slow luminescence component induced by Ce 3+ emissions depends on the Ce concentration in the LiCaAlF 6 scintillator, the fast component is independent. The fast component is suggested to be generated in the host matrix of the LiCaAlF 6 crystal. From quantitative considerations based on Frank–Tamm equation, which shows the light yield of the Cherenkov radiation, the Cherenkov radiation was determined as the origin of the fast component. We, additionally, found that the slow rise time of main Ce 3+ emissions in the Ce:LiCaAlF 6 scintillator plays an important role to perform the pulse shape discrimination. - Highlights: • The fast luminescence in Ce:LiCaAlF 6 scintillator is generated in the host matrix. • The origin of the fast luminescence is determined as the Cherenkov radiation. • The slow rise time also plays an important role to perform PSD

Derived (mutated)-types of TRPV6 channels elicit greater Ca²+ influx into the cells than ancestral-types of TRPV6: evidence from Xenopus oocytes and mammalian cell expression system.

Science.gov (United States)

Sudo, Yuka; Matsuo, Kiyotaka; Tetsuo, Tomoyuki; Tsutsumi, Satoshi; Ohkura, Masamichi; Nakai, Junichi; Uezono, Yasuhito

2010-01-01

The frequency of the allele containing three derived nonsynonymous SNPs (157C, 378M, 681M) of the gene encoding calcium permeable TRPV6 channels expressed in the intestine has been increased by positive selection in non-African populations. To understand the nature of these SNPs, we compared the properties of Ca²+ influx of ancestral (in African populations) and derived-TRPV6 (in non-African populations) channels with electrophysiological, Ca²+-imaging, and morphological methods using both the Xenopus oocyte and mammalian cell expression systems. Functional electrophysiological and Ca²+-imaging analyses indicated that the derived-TRPV6 elicited more Ca²+ influx than the ancestral one in TRPV6-expressing cells where both channels were equally expressed in the cells. Ca²+-inactivation properties in the ancestral- and derived-TRPV6 were almost the same. Furthermore, fluorescence resonance energy transfer (FRET) analysis showed that both channels have similar multimeric formation properties, suggesting that derived-TRPV6 itself could cause higher Ca²+ influx. These findings suggest that populations having derived-TRPV6 in non-African areas may absorb higher Ca²+ from the intestine than ancestral-TRPV6 in the African area.

Group theoretical treatment of the low-temperature phase transition of the Cd6Ca 1/1-cubic approximant

International Nuclear Information System (INIS)

Tamura, R.; Shibata, K.; Nishimoto, K.; Takeuchi, S.; Edagawa, K.; Saitoh, K.; Isobe, M.; Ueda, Y.

2005-01-01

An antiparallel orientational transition is reported for an intermetallic compound, i.e., Cd 6 Ca crystal, which is a 1/1-1/1-1/1 crystalline approximant to the icosahedral quasicrystal Cd 5.7 Ca. A group theoretical analysis based on the Landau theory predicts that the space group of the low-temperature phase is either C2/c or C2/m, in good agreement with the observations. Accordingly, two types of orientational orderings of Cd 4 tetrahedra, which are located in the center of icosahedral clusters, may occur below 100 K: In both cases, the Cd 4 tetrahedra are orientationally ordered in an antiparallel fashion along the [110] direction of the high temperature body-centered-cubic phase. Such a transition in a metal is reminiscent of orientational transitions in molecular solids

Rapid effects of 17beta-estradiol on epithelial TRPV6 Ca2+ channel in human T84 colonic cells.

LENUS (Irish Health Repository)

Irnaten, Mustapha

2008-11-01

The control of calcium homeostasis is essential for cell survival and is of crucial importance for several physiological functions. The discovery of the epithelial calcium channel Transient Receptor Potential Vaniloid (TRPV6) in intestine has uncovered important Ca(2+) absorptive pathways involved in the regulation of whole body Ca(2+) homeostasis. The role of steroid hormone 17beta-estradiol (E(2)), in [Ca(2+)](i) regulation involving TRPV6 has been only limited at the protein expression levels in over-expressing heterologous systems. In the present study, using a combination of calcium-imaging, whole-cell patch-clamp techniques and siRNA technology to specifically knockdown TRPV6 protein expression, we were able to (i) show that TRPV6 is natively, rather than exogenously, expressed at mRNA and protein levels in human T84 colonic cells, (ii) characterize functional TRPV6 channels and (iii) demonstrate, for the first time, the rapid effects of E(2) in [Ca(2+)](i) regulation involving directly TRPV6 channels in T84 cells. Treatment with E(2) rapidly (<5 min) enhanced [Ca(2+)](i) and this increase was partially but significantly prevented when cells were pre-treated with ruthenium red and completely abolished in cells treated with siRNA specifically targeting TRPV6 protein expression. These results indicate that when cells are stimulated by E(2), Ca(2+) enters the cell through TRPV6 channels. TRPV6 channels in T84 cells contribute to the Ca(2+) entry\\/signalling pathway that is sensitive to 17beta-estradiol.

Effect of exercise training on Ca{sup 2+} release units of left ventricular myocytes of spontaneously hypertensive rats

Energy Technology Data Exchange (ETDEWEB)

Carneiro-Júnior, M.A. [Universidade Federal do Espírito Santo, Departamento de Ciências Fisiológicas, Vitória, ES (Brazil); Universidade Federal de Viçosa, Laboratório de Biologia do Exercício, Departamento de Educação Física, Viçosa, MG (Brazil); Quintão-Júnior, J.F.; Drummond, L.R.; Lavorato, V.N.; Drummond, F.R. [Universidade Federal de Viçosa, Laboratório de Biologia do Exercício, Departamento de Educação Física, Viçosa, MG (Brazil); Amadeu, M.A.; Oliveira, E.M. [Universidade de São Paulo, Laboratório de Bioquímica e Biologia Molecular do Exercício, Escola de Educação Física e Esportes, São Paulo, SP (Brazil); Felix, L.B. [Universidade Federal de Viçosa, Departamento de Engenharia Elétrica, Viçosa, MG (Brazil); Cruz, J.S. [Universidade Federal de Minas Gerais, Laboratório de Membranas Excitáveis e Biologia Cardiovascular, Departamento de Bioquímica e Imunologia, Belo Horizonte, MG (Brazil); Mill, J.G. [Universidade Federal do Espírito Santo, Departamento de Ciências Fisiológicas, Vitória, ES (Brazil); Natali, A.J.; Prímola-Gomes, T.N. [Universidade Federal de Viçosa, Laboratório de Biologia do Exercício, Departamento de Educação Física, Viçosa, MG (Brazil)

2014-08-29

In cardiomyocytes, calcium (Ca{sup 2+}) release units comprise clusters of intracellular Ca{sup 2+} release channels located on the sarcoplasmic reticulum, and hypertension is well established as a cause of defects in calcium release unit function. Our objective was to determine whether endurance exercise training could attenuate the deleterious effects of hypertension on calcium release unit components and Ca{sup 2+} sparks in left ventricular myocytes of spontaneously hypertensive rats. Male Wistar and spontaneously hypertensive rats (4 months of age) were divided into 4 groups: normotensive (NC) and hypertensive control (HC), and normotensive (NT) and hypertensive trained (HT) animals (7 rats per group). NC and HC rats were submitted to a low-intensity treadmill running protocol (5 days/week, 1 h/day, 0% grade, and 50-60% of maximal running speed) for 8 weeks. Gene expression of the ryanodine receptor type 2 (RyR2) and FK506 binding protein (FKBP12.6) increased (270%) and decreased (88%), respectively, in HC compared to NC rats. Endurance exercise training reversed these changes by reducing RyR2 (230%) and normalizing FKBP12.6 gene expression (112%). Hypertension also increased the frequency of Ca{sup 2+} sparks (HC=7.61±0.26 vs NC=4.79±0.19 per 100 µm/s) and decreased its amplitude (HC=0.260±0.08 vs NC=0.324±0.10 ΔF/F{sub 0}), full width at half-maximum amplitude (HC=1.05±0.08 vs NC=1.26±0.01 µm), total duration (HC=11.51±0.12 vs NC=14.97±0.24 ms), time to peak (HC=4.84±0.06 vs NC=6.31±0.14 ms), and time constant of decay (HC=8.68±0.12 vs NC=10.21±0.22 ms). These changes were partially reversed in HT rats (frequency of Ca{sup 2+} sparks=6.26±0.19 µm/s, amplitude=0.282±0.10 ΔF/F{sub 0}, full width at half-maximum amplitude=1.14±0.01 µm, total duration=13.34±0.17 ms, time to peak=5.43±0.08 ms, and time constant of decay=9.43±0.15 ms). Endurance exercise training attenuated the deleterious effects of hypertension on calcium release units of

Crystal structure and magnetoresistance of La0.7Ca0.3MnO3 perovskite at room temperature

International Nuclear Information System (INIS)

Engkir Sukirman; Wisnu Ari Adi; Yustinus Purwamargapratala

2012-01-01

A comparative study on crystal structure and magnetoresistance (MR) of La 0.7 Ca 0.3 MnO 3 (LCMO) perovskite toward LaMnO 3 (LMO) and CaMnO 3 (CMO) parent compounds have been carried out to study the change of LCMO due to magnetic fields variations at room temperature. The LCMO, LMO and CMO were synthesized using high energy milling (HEM) method. The precursors obtained were pressed into pellet and sintered at T s = 1350°C for 6 hours. The qualitative analysis were conducted by x-rays diffraction technique using Rietveld method. The MR effect on the samples were measured using four point probe (FPP) method and the surface structure of pellets were observed by scanning electron microscope (SEM). The samples have the same crystal structure, namely orthorhombic, space group: Pnma, No. 62. The lattice parameters of LCMO were successfully confirmed until four decimal precision, namely a = 5.4851(3) Å, b = 7.7601(4) Å, c = 5.5185(2) Å. The lattice parameters for LMO and CMO successively are a = 5.4405(9) Å, b = 7.717(1) Å, c = 5.537(1) Å and a = 5.2973(6) Å, b = 7.477(1) Å, c = 5.281 (1) Å. All samples have grain diameter of around 1,000 nm with a globule like form and every grain consists of 27 crystallites. The MR for LCMO, LMO and CMO samples at room temperature are -10.1; -7.3 dan -12.3%, respectively, and comparable with the one of multilayers based GMR [Cu/NiFeCo] x10 /Ta. The LCMO perovskite bulk can be used to detect the magnetic microbeads and ferrofluid. (author)

Crystal Growth and Scintillation Properties of Eu2+ doped Cs4CaI6 and Cs4SrI6

Science.gov (United States)

Stand, L.; Zhuravleva, M.; Chakoumakos, B.; Johnson, J.; Loyd, M.; Wu, Y.; Koschan, M.; Melcher, C. L.

2018-03-01

In this work we present the crystal growth and scintillation properties of two new ternarymetal halide scintillators activated with divalent europium, Cs4CaI6 and Cs4SrI6. Single crystals of each compound were grown in evacuated quartz ampoules via the vertical Bridgman technique using a two-zone transparent furnace. Single crystal X-ray diffraction experiments showed that both crystals have a trigonal (R-3c) structure, with a density of 3.99 g/cm3 and 4.03 g/cm3. The radioluminescence and photoluminescence measurements showed typical luminescence properties due to the 5d-4f radiative transitions in Eu2+. At this early stage of development Cs4SrI6:Eu and Cs4CaI6:Eu have shown very promising scintillation properties, with light yields and energy resolutions of 62,300 ph/MeV and 3.3%, and 51,800 photons/MeV and 3.6% at 662 keV, respectively.

7 CFR 7.6 - Determination of elective areas.

Science.gov (United States)

2010-01-01

... 7 Agriculture 1 2010-01-01 2010-01-01 false Determination of elective areas. 7.6 Section 7.6 Agriculture Office of the Secretary of Agriculture SELECTION AND FUNCTIONS OF AGRICULTURAL STABILIZATION AND... county committee shall give public notice of the community boundaries in advance of the election. ...

Low field magnetoresistance effects in fine particles of La sub 0 sub . sub 6 sub 7 Ca sub 0 sub . sub 3 sub 3 MnO sub 3 perovskites

CERN Document Server

Rivas, J; Fondado, A; Rivadulla, F; López-Quintela, M A

2000-01-01

In this work magnetic and magnetotransport experimental data in well-characterized small particles of La sub 0 sub . sub 6 sub 7 Ca sub 0 sub . sub 3 sub 3 MnO sub 3 are presented. Grain size reduction leads to a larger resistivity and a decrease in metal-insulator transition temperature. Intrinsic colossal magnetoresistance (CMR) is destroyed while intergranular one is promoted to larger values. This low field MR can be explained taking into account magnetization data through spin-polarized tunneling model, which ensures an acceptable first-order fit between both magnitudes. Finally, low-temperature resistivity upturn present in small particle size samples can be understood in terms of an electrostatic barrier between grains.

Vibrational spectroscopic study of poldervaartite CaCa[SiO3(OH)(OH)

Science.gov (United States)

Frost, Ray L.; López, Andrés; Scholz, Ricardo; Lima, Rosa Malena Fernandes

2015-02-01

We have studied the mineral poldervaartite CaCa[SiO3(OH)(OH)] which forms a series with its manganese analogue olmiite CaMn[SiO3(OH)](OH) using a range of techniques including scanning electron microscopy, thermogravimetric analysis, Raman and infrared spectroscopy. Chemical analysis shows the mineral is reasonably pure and contains only calcium and manganese with low amounts of Al and F. Thermogravimetric analysis proves the mineral decomposes at 485 °C with a mass loss of 7.6% compared with the theoretical mass loss of 7.7%. A strong Raman band at 852 cm-1 is assigned to the SiO stretching vibration of the SiO3(OH) units. Two Raman bands at 914 and 953 cm-1 are attributed to the antisymmetric vibrations. Intense prominent peaks observed at 3487, 3502, 3509, 3521 and 3547 cm-1 are assigned to the OH stretching vibration of the SiO3(OH) units. The observation of multiple OH bands supports the concept of the non-equivalence of the OH units. Vibrational spectroscopy enables a detailed assessment of the molecular structure of poldervaartite.

6/sup +/ isomer state in /sup 46/Ca

Energy Technology Data Exchange (ETDEWEB)

Bizzeti, P G; Maurenzig, P R; Poggi, G [Florence Univ. (Italy). Istituto di Fisica; Lo Bianco, G [Milan Univ. (Italy). Istituto di Fisica

1975-01-11

The decay of the expected isomer, obtained from the reaction /sup 48/Ca(p,p2n)/sup 46/Ca, has been observed as a delayed activity after bombardment of a 97.2% enriched /sup 48/CaC0/sub 3/ target with 35 MeV protons. The experimental apparatus used at AUF cyclotron of Milan is described. Data are reported and discussed.

Clinical value of preoperative serum CA 19-9 and CA 125 levels in predicting the resectability of hilar cholangiocarcinoma.

Science.gov (United States)

Hu, Hai-Jie; Mao, Hui; Tan, Yong-Qiong; Shrestha, Anuj; Ma, Wen-Jie; Yang, Qin; Wang, Jun-Ke; Cheng, Nan-Sheng; Li, Fu-Yu

2016-01-01

To examine the predictive value of tumor markers for evaluating tumor resectability in patients with hilar cholangiocarcinoma and to explore the prognostic effect of various preoperative factors on resectability in patients with potentially resectable tumors. Patients with potentially resectable tumors judged by radiologic examination were included. The receiver operating characteristic (ROC) analysis was conducted to evaluate serum carbohydrate antigenic determinant 19-9 (CA 19-9), carbohydrate antigen 125 (CA 125) and carcino embryonie antigen levels on tumor resectability. Univariate and multivariate logistic regression models were also conducted to analysis the correlation of preoperative factors with resectability. In patients with normal bilirubin levels, ROC curve analysis calculated the ideal CA 19-9 cut-off value of 203.96 U/ml in prediction of resectability, with a sensitivity of 83.7 %, specificity of 80 %, positive predictive value of 91.1 % and negative predictive value of 66.7 %. Meanwhile, the optimal cut-off value for CA 125 to predict resectability was 25.905 U/ml (sensitivity, 78.6 %; specificity, 67.5 %). In a multivariate logistic regression model, tumor size ≤3 cm (OR 4.149, 95 % CI 1.326-12.981, P = 0.015), preoperative CA 19-9 level ≤200 U/ml (OR 20.324, 95 % CI 6.509-63.467, P hilar cholangiocarcinoma. Preoperative CA 19-9 and CA 125 levels predict resectability in patients with radiological resectable hilar cholangiocarcinoma. Increased preoperative CA 19-9 levels and CA 125 levels are associated with poor resectability rate.

Preparation dependent superconductivity in T1CaBa2Cu3O7.5+-d above 100 K

International Nuclear Information System (INIS)

Porjesz, T.; Halasz, I.; Traeger, T.; Kovacs, G.; Kirschner, I.; Zsolt, G.; Karman, T.

1988-08-01

Different heat treatment procedures were applied during the sample preparation process, which result in different superconducting properties in the samples of the same nominal composition of TlCaBa 2 Cu 3 O 7.5+-d . It manifests itself in the different critical temperatures having values of 104 K, 107 K and 93 K. The effect of heat treatments is reflected in the structural and magnetic properties as well. (author). 6 refs, 5 figs

Effect of exercise training on Ca²⁺ release units of left ventricular myocytes of spontaneously hypertensive rats.

Science.gov (United States)

Carneiro-Júnior, M A; Quintão-Júnior, J F; Drummond, L R; Lavorato, V N; Drummond, F R; Amadeu, M A; Oliveira, E M; Felix, L B; Cruz, J S; Mill, J G; Natali, A J; Prímola-Gomes, T N

2014-11-01

In cardiomyocytes, calcium (Ca²⁺) release units comprise clusters of intracellular Ca²⁺ release channels located on the sarcoplasmic reticulum, and hypertension is well established as a cause of defects in calcium release unit function. Our objective was to determine whether endurance exercise training could attenuate the deleterious effects of hypertension on calcium release unit components and Ca²⁺ sparks in left ventricular myocytes of spontaneously hypertensive rats. Male Wistar and spontaneously hypertensive rats (4 months of age) were divided into 4 groups: normotensive (NC) and hypertensive control (HC), and normotensive (NT) and hypertensive trained (HT) animals (7 rats per group). NC and HC rats were submitted to a low-intensity treadmill running protocol (5 days/week, 1 h/day, 0% grade, and 50-60% of maximal running speed) for 8 weeks. Gene expression of the ryanodine receptor type 2 (RyR2) and FK506 binding protein (FKBP12.6) increased (270%) and decreased (88%), respectively, in HC compared to NC rats. Endurance exercise training reversed these changes by reducing RyR2 (230%) and normalizing FKBP12.6 gene expression (112%). Hypertension also increased the frequency of Ca²⁺ sparks (HC=7.61 ± 0.26 vs NC=4.79 ± 0.19 per 100 µm/s) and decreased its amplitude (HC=0.260 ± 0.08 vs NC=0.324 ± 0.10 ΔF/F0), full width at half-maximum amplitude (HC=1.05 ± 0.08 vs NC=1.26 ± 0.01 µm), total duration (HC=11.51 ± 0.12 vs NC=14.97 ± 0.24 ms), time to peak (HC=4.84 ± 0.06 vs NC=6.31 ± 0.14 ms), and time constant of decay (HC=8.68 ± 0.12 vs NC=10.21 ± 0.22 ms). These changes were partially reversed in HT rats (frequency of Ca²⁺ sparks=6.26 ± 0.19 µm/s, amplitude=0.282 ± 0.10 ΔF/F0, full width at half-maximum amplitude=1.14 ± 0.01 µm, total duration=13.34 ± 0.17 ms, time to peak=5.43 ± 0.08 ms, and time constant of decay=9.43 ± 0.15 ms). Endurance exercise training attenuated the deleterious effects of hypertension on calcium release

38 CFR 7.6 - Benefits.

Science.gov (United States)

2010-07-01

... 38 Pensions, Bonuses, and Veterans' Relief 1 2010-07-01 2010-07-01 false Benefits. 7.6 Section 7.6... Soldiers' and Sailors' Civil Relief Act Amendments of 1942 § 7.6 Benefits. Any policy found to be entitled... such monetary benefits arising out of the contract or by reason thereof, will be held subject to...

High-pressure crystal growth and electromagnetic properties of 5d double-perovskite Ca3OsO6

Science.gov (United States)

Feng, Hai Luke; Shi, Youguo; Guo, Yanfeng; Li, Jun; Sato, Akira; Sun, Ying; Wang, Xia; Yu, Shan; Sathish, Clastin I.; Yamaura, Kazunari

2013-05-01

Single crystals of the osmium-containing compound Ca3OsO6 have been successfully grown under high-pressure conditions, for the first time. The crystal structure of Ca3OsO6 were characterized as an ordered double-perovskite structure of space group P21/n with the Ca and Os atoms being fully ordered at the perovskite B-site. The electromagnetic analysis shows that the crystal exhibits a semiconductor-like behavior below 300 K and undergoes an antiferromagnetic transition at 50 K.

Metallicity of Ca{sub 2}Cu{sub 6}P{sub 5} with single and double copper-pnictide layers

Energy Technology Data Exchange (ETDEWEB)

Li, Li, E-mail: lil2@ornl.gov [Materials Science & Technology Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831 (United States); Parker, David [Materials Science & Technology Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831 (United States); Chi, Miaofang [Center for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, TN 37831 (United States); Tsoi, Georgiy M.; Vohra, Yogesh K. [Department of Physics, University of Alabama at Birmingham, Birmingham, AL 35294 (United States); Sefat, Athena S., E-mail: sefata@ornl.gov [Materials Science & Technology Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831 (United States)

2016-06-25

We report thermodynamic and transport properties, and also theoretical calculations, for Cu-based compound Ca{sub 2}Cu{sub 6}P{sub 5} and compare with CaCu{sub 2-δ}P{sub 2}. Both materials have layers of edge-sharing copper pnictide tetrahedral CuP{sub 4}, similar to Fe–As and Fe–Se layers (with FeAs{sub 4}, FeSe{sub 4}) in the iron-based superconductors. Despite the presence of this similar transition-metal pnictide layer, we find that both Ca{sub 2}Cu{sub 6}P{sub 5} and CaCu{sub 2-δ}P{sub 2} have temperature-independent magnetic susceptibility and show metallic behavior with no evidence of either magnetic ordering or superconductivity down to 1.8 K CaCu{sub 2-δ}P{sub 2} is slightly off-stoichiometric, with δ = 0.14. Theoretical calculations suggest that unlike Fe 3d-based magnetic materials with a large density of states (DOS) at the Fermi surface, Cu have comparatively low DOS, with the majority of the 3d spectral weight located well below Fermi level. The room-temperature resistivity value of Ca{sub 2}Cu{sub 6}P{sub 5} is only 9 μΩ-cm, due to a substantial plasma frequency and an inferred electron-phonon coupling λ of 0.073 (significantly smaller than that of metallic Cu). Also, microscopy result shows that Cu–Cu distance along the c-axis within the double layers can be very short (2.5 Å), even shorter than metallic elemental copper bond (2.56 Å). The value of dρ/dT for CaCu{sub 2-δ}P{sub 2} at 300 K is approximately three times larger than in Ca{sub 2}Cu{sub 6}P{sub 5}, which suggests the likelihood of stronger electron-phonon coupling. This study shows that the details of Cu–P layers and bonding are important for their transport characteristics. In addition, it emphasizes the remarkable character of the DOS of ‘122’ iron-based materials, despite much structural similarities. - Highlights: • A comprehensive study on Cu-based compound Ca{sub 2}Cu{sub 6}P{sub 5} and compare with CaCu{sub 2-δ}P{sub 2}. • Both materials have layers of

Deployed Flight Test of the Iraqi Air Force Comp Air 7SLX (CA-7)

Science.gov (United States)

2014-02-28

been built with a castering nose wheel mounted to the engine mount, a simple yet effective design. The team purchased new engine mounts and castering ...nose wheels from Aero Comp Inc. to solve these problems on all the CA-7s they refurbished, which Fred Webster called “a pretty big modification .”22...from a Cessna 310. The UAE had made numerous other modifications .2 The United States Central Command Air Forces (CENTAF) was working with the

Phase transformation of Ca4[Al6O12]SO4 and its disordered crystal structure at 1073 K

International Nuclear Information System (INIS)

Kurokawa, Daisuke; Takeda, Seiya; Colas, Maggy; Asaka, Toru; Thomas, Philippe; Fukuda, Koichiro

2014-01-01

The phase transformation of Ca 4 [Al 6 O 12 ]SO 4 and the crystal structure of its high-temperature phase were investigated by differential thermal analysis, temperature-dependent Raman spectroscopy and high-temperature X-ray powder diffraction (CuKα 1 ). We determined the starting temperature of the orthorhombic-to-cubic transformation during heating (=711 K) and that of the reverse transformation during cooling (=742 K). The thermal hysteresis was negative (=−31 K), suggesting the thermoelasticity of the transformation. The space group of the high temperature phase is I4 ¯ 3m with the unit-cell dimensions of a=0.92426(2) nm and V=0.78955(2) nm 3 (Z=2) at 1073 K. The initial structural model was derived by the direct methods and further refined by the Rietveld method. The final structural model showed the orientational disordering of SO 4 tetrahedra. The maximum-entropy method-based pattern fitting method was used to confirm the validity of the split-atom model, in which conventional structure bias caused by assuming intensity partitioning was minimized. At around the transformation temperature during heating, the vibrational spectra, corresponding to the Raman-active SO 4 internal stretching mode, showed the continuous and gradual change in the slope of full width at half maximum versus temperature curve. This strongly suggests that the orthorhombic-to-cubic phase transformation would be principally accompanied by the statistical disordering in orientation of the SO 4 tetrahedra, without distinct dynamical reorientation. - Graphical abstract: (Left) Three-dimensional electron-density distributions of the SO 4 tetrahedron with the split-atom model, and (right) a bird's eye view of electron densities on the plane parallel to (111). - Highlights: • Crystal structure of Ca 4 [Al 6 O 12 ]SO 4 at 1073 K is determined by powder XRD. • The atom arrangements are represented by the split-atom model. • The MPF method is used to confirm the validity of the model. �

Effects of DK-002, a synthesized (6aS,cis)-9,10-Dimethoxy-7,11b-dihydro-indeno[2,1-c]chromene-3,6a-diol, on platelet activity.

Science.gov (United States)

Lee, Ki-Seon; Khil, Lee-Yong; Chae, Sang-Ho; Kim, Deukjoon; Lee, Byung-Hoon; Hwang, Gwi-Seo; Moon, Chang-Hyun; Chang, Tong-Shin; Moon, Chang-Kiu

2006-02-02

In the present study, the mechanism of antiplatelet activity of DK-002, a synthesized (6aS,cis)-9,10-Dimethoxy-7,11b-dihydro-indeno[2,1-c]chromene-3,6a-diol, was investigated. DK-002 inhibited the thrombin, collagen, and ADP-induced rat platelet aggregation in a concentration-dependent manner, with IC50 values of 120, 27, and 47 microM, respectively. DK-002 also inhibited thrombin-induced dense granule secretion, thromboxane A2 synthesis, and [Ca2+]i elevation in platelets. DK-002 did not show any significant effect on ADP-induced inhibition of cyclic AMP elevation by prostaglandin E1, but DK-002 was confirmed to inhibit ADP-induced [Ca2+]i elevation and shape change. DK-002 inhibited 4-bromo-A23187-induced [Ca2+]i elevation in the presence of creatine phosphate/creatine phosphokinase (CP/CPK, a ADP scavenging system) and indomethacin (a specific inhibitor of cyclooxygenase). DK-002 also inhibited Ca2+ mobilization in thrombin- or 4-bromo-A23187-stimulated platelets through its inhibitory effects on both Ca2+ release from intracellular stores and Ca2+ influx, in the presence of CP/CPK and indomethacin. Taken together, the present study shows that DK-002 has inhibitory effects on stimulation of platelets, and suggests that its antiplatelet activity might be related to the inhibitory mechanism on Ca2+ mobilization in stimulated platelets.

Climate-simulated raceway pond culturing: quantifying the maximum achievable annual biomass productivity of Chlorella sorokiniana in the contiguous USA

Energy Technology Data Exchange (ETDEWEB)

Huesemann, M.; Chavis, A.; Edmundson, S.; Rye, D.; Hobbs, S.; Sun, N.; Wigmosta, M.

2017-09-13

Chlorella sorokiniana (DOE 1412) emerged as one of the most promising microalgae strains from the NAABB consortium project, with a remarkable doubling time under optimal conditions of 2.57 hr-1. However, its maximum achievable annual biomass productivity in outdoor ponds in the contiguous United States remained unknown. In order to address this knowledge gap, this alga was cultured in indoor LED-lighted and temperature-controlled raceways in nutrient replete freshwater (BG-11) medium at pH 7 under conditions simulating the daily sunlight intensity and water temperature fluctuations during three seasons in Southern Florida, an optimal outdoor pond culture location for this organism identified by biomass growth modeling. Prior strain characterization indicated that the average maximum specific growth rate (µmax) at 36 ºC declined continuously with pH, with µmax corresponding to 5.92, 5.83, 4.89, and 4.21 day-1 at pH 6, 7, 8, and 9, respectively. In addition, the maximum specific growth rate declined nearly linearly with increasing salinity until no growth was observed above 35 g/L NaCl. In the climate-simulated culturing studies, the volumetric ash-free dry weight-based biomass productivities during the linear growth phase were 57, 69, and 97 mg/L-day for 30-year average light and temperature simulations for January (winter), March (spring), and July (summer), respectively, which corresponds to average areal productivities of 11.6, 14.1, and 19.9 g/m2-day at a constant pond depth of 20.5 cm. The photosynthetic efficiencies (PAR) in the three climate-simulated pond culturing experiments ranged from 4.1 to 5.1%. The annual biomass productivity was estimated as ca. 15 g/m2-day, nearly double the U.S. Department of Energy (DOE) 2015 State of Technology annual cultivation productivity of 8.5 g/m2-day, but this is still significantly below the projected 2022 target of ca. 25 g/m2-day (U.S. DOE, 2016) for economic microalgal biofuel production, indicating the need for

Synthesis, crystal structure, and magnetism of A{sub 2}Co{sub 12}As{sub 7} (A=Ca, Y, Ce–Yb)

Energy Technology Data Exchange (ETDEWEB)

Tan, Xiaoyan [Department of Chemistry and Biochemistry, Florida State University, Tallahassee, FL 32306 (United States); Ovidiu Garlea, V. [Quantum Condensed Matter Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831 (United States); Chai, Ping [Department of Chemistry and Biochemistry, Florida State University, Tallahassee, FL 32306 (United States); Geondzhian, Andrey Y. [National Research Nuclear University “Moscow Engineering Physics Institute”, 115409 Moscow (Russian Federation); Yaroslavtsev, Alexander A. [National Research Nuclear University “Moscow Engineering Physics Institute”, 115409 Moscow (Russian Federation); European XFEL GmbH, 22761 Hamburg (Germany); Xin, Yan [National High Magnetic Field Laboratory, Tallahassee, FL 32310 (United States); Menushenkov, Alexey P. [National Research Nuclear University “Moscow Engineering Physics Institute”, 115409 Moscow (Russian Federation); Chernikov, Roman V. [DESY Photon Science, 22603 Hamburg (Germany); Shatruk, Michael, E-mail: shatruk@chem.fsu.edu [Department of Chemistry and Biochemistry, Florida State University, Tallahassee, FL 32306 (United States)

2016-04-15

Ternary intermetallics, A{sub 2}Co{sub 12}As{sub 7} (A=Ca, Y, Ce–Yb), have been synthesized by annealing mixtures of elements in molten Bi at 1223 K. The materials obtained crystallize in the P6{sub 3}/m variant of the Zr{sub 2}Fe{sub 12}P{sub 7} structure type. The unit cell volume shows a monotonic decrease with the increasing atomic number of the rare-earth metal, with the exception of Ce-, Eu-, and Yb-containing compounds. An examination of these outliers with X-ray absorption near edge structures (XANES) spectroscopy revealed mixed valence of Ce, Eu, and Yb, with the average oxidation states of +3.20(1), +2.47(5), and +2.91(1), respectively, at room temperature. Magnetic behavior of A{sub 2}Co{sub 12}As{sub 7} is generally characterized by ferromagnetic ordering of Co 3d moments at 100–140 K, followed by low-temperature ordering of rare-earth 4f moments. The 3d-4f magnetic coupling changes from antiferromagnetic for A=Pr–Sm to ferromagnetic for A=Ce and Eu–Yb. Polarized neutron scattering experiments were performed to support the postulated ferro- and ferrimagnetic ground states for Ce{sub 2}Co{sub 12}As{sub 7} and Nd{sub 2}Co{sub 12}As{sub 7}, respectively. - Graphical abstract: Title arsenides were synthesized by Bi‐flux method. They exhibit mixed valence for A = Ce, Eu, Yb, ferrimagnetism for A = Ca, Y, Pr–Sm, and ferromagnetism for A = Eu–Tm. - Highlights: • A2Co12As7 (A=Ca, Y, Ce–Yb) were synthesized in Bi flux. • Ce, Eu, Yb exhibit mixed valence in the corresponding structures. • The character of 3d‐4f magnetic coupling changes at the half‐filled f shell. • Materials behave as ferrimagnets for A=Ca, Y, Pr–Sm and as ferromagnets for A=Eu–Yb.

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

International Nuclear Information System (INIS)

Lee, Hong-Sub; Park, Hyung-Ho

2015-01-01

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

Tumor markers CA19-9, CA242 and CEA in the diagnosis of pancreatic cancer: a meta-analysis.

Science.gov (United States)

Zhang, Yimin; Yang, Jun; Li, Hongjuan; Wu, Yihua; Zhang, Honghe; Chen, Wenhu

2015-01-01

Pancreatic cancer has the worst prognosis and early detection is crucial for improving patient prognosis. Therefore, we performed a meta-analysis to evaluate and compare the sensitivity and specificity of single test of CA19-9, CA242, and CEA, as well as combination test in pancreatic cancer detection. We searched PubMed, Embase, Medline, and Wanfang databases for studies that evaluated the diagnostic validity of CA19-9, CA242, and CEA between January 1990 and September 2014. Data were analyzed by Meta-Disc and STATA software. A total of 21 studies including 3497 participants, which fulfilled the inclusion criteria were considered for analysis. The pooled sensitivities for CA19-9, CA242, and CEA were 75.4 (95% CI: 73.4-77.4), 67.8 (95% CI: 65.5-70), and 39.5 (95% CI: 37.3-41.7), respectively. The pooled specificities of CA19-9, CA242, and CEA were 77.6 (95% CI: 75.4-79.7), 83 (95% CI: 81-85), and 81.3 (95% CI: 79.3-83.2), respectively. Parallel combination of CA19-9+CA242 has a higher sensitivity (89, 95% CI: 80-95) without impairing the specificity (75, 95% CI: 67-82). Our meta-analysis showed that CA242 and CA19-9 have better performance in the diagnosis of pancreatic cancer than CEA. Furthermore, parallel combination test of CA19-9+CA242 could be of better diagnostic value than individual CA242 or CA19-9 test.

Luminescence in undoped CaYAl{sub 3}O{sub 7} produced via the Pechini method

Energy Technology Data Exchange (ETDEWEB)

Bispo, Giordano F.C., E-mail: gfredericoc@gmail.com [Physics Department, Federal University of Sergipe, 49100-000 São Cristovão, SE (Brazil); Andrade, Adriano B.; S Bezerra, Claudiane dos [Physics Department, Federal University of Sergipe, 49100-000 São Cristovão, SE (Brazil); Teixeira, Verônica C.; Galante, Douglas [Brazilian Synchrotron Light Laboratory, Brazilian Center for Research in Energy and Materials, 13083-970 Campinas, SP (Brazil); Valerio, Mário E.G. [Physics Department, Federal University of Sergipe, 49100-000 São Cristovão, SE (Brazil)

2017-02-15

The luminescent properties of CaYAl{sub 3}O{sub 7} (CYAM) were carried out in undoped powder samples produced via Pechini method. The thermal analysis combined with XRD measurements showed that 1000 °C/4 h is the best condition for the CYAM synthesis. Morphological analysis showed submicrometric particles with irregular shape. Photoluminescence (PL) emission and excitation spectra were studied with excitation in the ultraviolet and vacuum ultraviolet spectral region using synchrotron radiation. The CYAM band gap energy was measured and found to be around 6.8 eV. Low intense emission band around 4.4 eV, upon excitation at 6.5 eV, was assigned to the self-trapped excitons (STE) that are generated during the VUV excitation. Three main emission bands peaking at 2.57, 2.94 and 3.23 eV are responsible for most of the PL emission and radioluminescence (RL) emission in CYAM. Time-resolved measurements under pulsed 4.7 eV light showed that the PL decay curve is composed by 3 main processes with very short lifetime, smaller than 30 ns, and a small amount of long time constant process. Time-resolved RL measurements exciting with 4056 eV photons, above the Ca K edge, showed that the decay curve is composed by two processes with time constants around 27 and 130 ns and a small component due to a long decay constant bigger. All this features allowed the identification of the main emissions centres at 2.94 and 3.23 eV to the F{sup +} centres, while the emission centre at 2.57 eV is due to the F type centre.

Crystal structure and magnetic properties of the solid-solution phase Ca3Co2-v Sc v O6

International Nuclear Information System (INIS)

Hervoches, Charles H.; Fredenborg, Vivian Miksch; Kjekshus, Arne; Fjellvag, Helmer; Hauback, Bjorn C.

2007-01-01

The two crystallographically non-equivalent Co atoms of the quasi-one-dimensional crystal structure of Ca 3 Co 2 O 6 form chains with alternating, face-sharing polyhedra of Co2O 6 trigonal prisms and Co1O 6 octahedra. This compound forms a substitutional solid-solution phase with Sc, in which the Sc atoms enter the Co2 sublattice exclusively. The homogeneity range of Ca 3 Co 2- v Sc v O 6 (more specifically Ca 3 Co1Co2 1- v Sc v O 6 ) extends up to v∼0.55. The crystal structure belongs to space group R3-barc with lattice parameters (in hexagonal setting): 9.0846(3)≤a≤9.1300(2) A and 10.3885(4)≤c≤10.4677(4) A. The magnetic moment decreases rapidly with increasing amount of the non-magnetic Sc solute in the lattice. - Graphical abstract: The quasi-one-dimensional Ca 3 Co 2 O 6 phase forms a substitutional solid-solution system with Sc, in which the Sc atoms enter the Co2 sublattice exclusively. The homogeneity range of Ca 3 Co 2- v Sc v O 6 extends up to v∼0.55. The magnetic moment decreases rapidly with increasing amount of the non-magnetic Sc solute in the lattice

Electric field control of the small-polaron hopping conduction in spatial confined Pr0.7(Ca0.6Sr0.40.3MnO3/PMN-PT heterostructure

Directory of Open Access Journals (Sweden)

Hao Kuang

2017-05-01

Full Text Available The electric field dependent high-temperature small-polaron hopping conduction was investigated in patterned Pr0.7(Ca0.6Sr0.40.3MnO3 strips. The small-polaronic activation energy EA and the carrier localization were found to decrease with the reduction of the strip size. Meanwhile, a similar dependence on the strip size was also obtained for the calculated small-polaron coupling constants, which could be related to the strain relaxation in strips. These results indicate that the spatial confinement prefers to delocalize the carrier and reduce the electron-phonon interaction. Furthermore, opposite variation trends of EA under negative and positive electric field were found in the strips with small size, which could be attributed to the enhancement of polarization effect induced by the reduction of strip size.

Controlled Surface Modification of Polyamide 6.6 Fibres Using CaCl2/H2O/EtOH Solutions

Directory of Open Access Journals (Sweden)

Barbara Rietzler

2018-02-01

Full Text Available Polyamide 6.6 is one of the most widely used polymers in the textile industry due to its durability; however, it has rather limited modification potential. In this work, the controlled surface modification of polyamide 6.6 fibres using the solvent system CaCl2/H2O/EtOH was studied. The effects of solvent composition (relative proportions of the three components and treatment time on fibre properties were studied both in situ (with fibres in solvent and ex situ (after the solvent was washed off. The fibres swell and/or dissolve in the solvent depending on its composition and the treatment time. We believe that the fibre–solvent interaction is through complex formation between the fibre carbonyl groups and the CaCl2. On washing, there is decomplexation and precipitation of the polymer. The treated fibres exhibit greater diameters and surface roughness, structural difference between an outer shell and an inner core is observable, and water retention is higher. The solvent system is more benign than current alternatives, and through suitable tailoring of the treatment conditions, e.g., composition and time, it may be used in the design of advanced materials for storage and release of active substances.

Calcium Sulfoaluminate Sodalite (Ca 4 Al 6 O 12 SO 4 ) Crystal Structure Evaluation and Bulk Modulus Determination

KAUST Repository

Hargis, Craig W.; Moon, Juhyuk; Lothenbach, Barbara; Winnefeld, Frank; Wenk, Hans-Rudolf; Monteiro, Paulo J. M.

2013-01-01

The predominant phase of calcium sulfoaluminate cement, Ca 4(Al6O12)SO4, was investigated using high-pressure synchrotron X-ray diffraction from ambient pressure to 4.75 GPa. A critical review of the crystal structure of Ca4(Al 6O12)SO4 is presented

Cold fusion reactions with 48Ca

International Nuclear Information System (INIS)

Gaeggeler, H.W.; Jost, D.T.; Tuerler, A.

1989-04-01

Cold fusion reactions with 48 Ca on the targets 208 Pb, 209 Bi, 197 Au, 184 W, 180 Hf are reported. The experiments were performed at the velocity filter SHIP of GSI. The maximum cross sections show a steep descent by about four orders of magnitude when going from 224 Th to 228 U as compound nuclei. Between uranium and einsteinium the cross sections stay rather low and increase by about two orders of magnitude for nobelium. For lawrencium the cross section decrease again. 7 figs., 1 tab., 38 refs

Secondary electron emission and glow discharge properties of 12CaO·7Al2O3 electride for fluorescent lamp applications

International Nuclear Information System (INIS)

Watanabe, Satoru; Watanabe, Toshinari; Ito, Kazuhiro; Miyakawa, Naomichi; Ito, Setsuro; Hosono, Hideo; Mikoshiba, Shigeo

2011-01-01

12CaO·7Al 2 O 3 electride, a sub-nanoporous compound having a work function of 2.4 eV, was examined as a candidate cathode material in fluorescent lamps. The electron emission yield was higher and the discharge voltage was lower for 12CaO·7Al 2 O 3 than for existing cathode materials such as Ni, Mo or W; therefore, the energy consumption of the fluorescent lamps can be improved using 12CaO·7Al 2 O 3 cathodes. Prototype glow-discharge lamps using 12CaO·7Al 2 O 3 were constructed and exhibited reasonable durability.

Secondary electron emission and glow discharge properties of 12CaO·7Al2O3 electride for fluorescent lamp applications.

Science.gov (United States)

Watanabe, Satoru; Watanabe, Toshinari; Ito, Kazuhiro; Miyakawa, Naomichi; Ito, Setsuro; Hosono, Hideo; Mikoshiba, Shigeo

2011-06-01

12CaO·7Al 2 O 3 electride, a sub-nanoporous compound having a work function of 2.4 eV, was examined as a candidate cathode material in fluorescent lamps. The electron emission yield was higher and the discharge voltage was lower for 12CaO·7Al 2 O 3 than for existing cathode materials such as Ni, Mo or W; therefore, the energy consumption of the fluorescent lamps can be improved using 12CaO·7Al 2 O 3 cathodes. Prototype glow-discharge lamps using 12CaO·7Al 2 O 3 were constructed and exhibited reasonable durability.

Secondary electron emission and glow discharge properties of 12CaOcenterdot7Al2O3 electride for fluorescent lamp applications

Directory of Open Access Journals (Sweden)

Satoru Watanabe, Toshinari Watanabe, Kazuhiro Ito, Naomichi Miyakawa, Setsuro Ito, Hideo Hosono and Shigeo Mikoshiba

2011-01-01

Full Text Available 12CaOcenterdot7Al2O3 electride, a sub-nanoporous compound having a work function of 2.4 eV, was examined as a candidate cathode material in fluorescent lamps. The electron emission yield was higher and the discharge voltage was lower for 12CaOcenterdot7Al2O3 than for existing cathode materials such as Ni, Mo or W; therefore, the energy consumption of the fluorescent lamps can be improved using 12CaOcenterdot7Al2O3 cathodes. Prototype glow-discharge lamps using 12CaOcenterdot7Al2O3 were constructed and exhibited reasonable durability.

Growth of solid solutions with colquiriite structure LiCa0,2Sr0,8AlF6: Ce3+

International Nuclear Information System (INIS)

Shavelev, A A; Nizamutdinov, A S; Semashko, V V; Marisov, M A

2014-01-01

Aim of this work were experiments on growing new materials based on fluoride crystals with the colquiriite structure LiSr 0,8 Ca 0,2 F 6 , as well as the study of their phase composition. It is shown that for a series of crystals LiSr 0,8 Ca 0,2 F 6 distribution of reflections observed corresponds to the colquiriite structure, and the dependence of the lattice constant in the transition from LiCaAlF 6 crystal to LiSrAlF 6 crystal is linear. Also it found that absorption coefficient in mixed samples is much larger than in not mixed

CaMKII effects on inotropic but not lusitropic force frequency responses require phospholamban

Science.gov (United States)

Wu, Yiming; Luczak, Elizabeth D; Lee, Eun-Jeong; Hidalgo, Carlos; Yang, Jinying; Gao, Zhan; Li, Jingdong; Wehrens, Xander; Granzier, Henk; Anderson, Mark E

2014-01-01

Increasing heart rate enhances cardiac contractility (force frequency relationship, FFR) and accelerates cardiac relaxation (frequency-dependent acceleration of relaxation, FDAR). The positive FFR together with FDAR promotes rapid filling and ejection of blood from the left ventricle (LV) at higher heart rates. Recent studies indicate that the multifunctional Ca2+/calmodulin-dependent protein kinase II (CaMKII) is involved in regulating FFR and FDAR. We used isolated perfused mouse hearts to study the mechanisms of FFR and FDAR in different genetic models, including transgenic myocardial CaMKII inhibition (AC3-I) and phosphalamban knockout (PLN−/−). When the rate was increased from 360 beats/min to 630 beats/min in wild type mouse hearts, the LV developed pressure (LVDP) and the maximum rate of increase in pressure (dP/dt max) increased by 37.6 ± 4.7% and 77.0 ± 8.1%, respectively. However, hearts from AC3-I littermates showed no increase of LVDP and a relatively modest (20.4 ± 3.9 %) increase in dP/dt max. PLN−/− hearts had a negative FFR, and myocardial AC3-I expression did not change the FFR in PLN−/− mice. PLN−/− mouse hearts did not exhibit FDAR, while PLN−/−mice with myocardial AC3-I expression showed further frequency dependent reductions in cardiac relaxation, suggesting CaMKII targets in addition to PLN were critical to myocardial relaxation. We incubated a constitutively active form of CaMKII with chemically-skinned myocardium and found that several myofilament proteins were phosphorylated by CaMKII. However, CaMKII did not affect myofilament calcium sensitivity. Our study shows that CaMKII plays an important role in modulating FFR and FDAR in murine hearts and suggest that PLN is a critical target for CaMKII effects on FFR, while CaMKII effects on FDAR partially require PLN-alternative targets. PMID:22796260

Crystallographic and electronic structure of the Ca2TiMnO6 double perovskite

International Nuclear Information System (INIS)

López, J.P. Garzón; Cardona, R.; Santos, A. Sarmiento; Téllez, D.A. Landínez; Roa-Rojas, J.

2014-01-01

In this work, we report synthesis and crystalline structure study of the Ca 2 TiMnO 6 complex perovskite, by X-ray diffraction experiments and through the application of the Rietveld refinement using the GSAS code. Results revealed the crystallization of the system in a tetragonal perovskite with the characteristic structure given by I4/m (#87) space group and lattice parameters a=5.339(4) Å and c=7.736(6) Å. Ab initio calculations of density of states (DOS) and electronic structure were carried out for this perovskite-like system, by the Density Functional Theory (DFT) and using the Full-potential Linearized Augmented Plane Waves (FP-LAPW) method. The exchange-correlation potential was treated using the Generalized Gradient Approximation (GGA). All calculations were carried-out using spin polarization. For the up spin orientation the compound has a semiconducting behavior and for down spin polarization it behaves like a conductor. The calculated effective magnetic moment in cell was 4.02 μ B , which is close to the expected value calculated from Hund's rules

Dynamics of Ca2+i and pHi in Ehrlich ascites tumor cells after Ca2+-mobilizing agonists or exposure to hypertonic solution

DEFF Research Database (Denmark)

Pedersen, Stine F.; Jørgensen, Nanna K.; Hoffmann, Else Kay

1998-01-01

Intracellular free calcium concentration ([Ca2+]i) and intracellular pH (pHi) were monitored in Ehrlich ascites tumor cells using Fura-2 or 2',7',-bis-(2-carboxyethyl)-5,6-carboxyfluorescein (BCECF), or both probes in combination. An increase in [Ca2+]i induced by thrombin or bradykinin, agonists...

Summary of the 10th International Conference on Human Herpesviruses-6 and -7 (HHV-6A, -6B, and HHV-7).

Science.gov (United States)

Komaroff, Anthony L; Boeckh, Michael; Eliason, Eva; Phan, Tuan; Kaufer, Benedikt B

2018-04-01

The 10th International Conference on Human herpesviruses-6 and -7 (HHV-6A, HHV-6B, and HHV-7) was held at the Freie Universität, Berlin, Germany from July 23-26, 2017. It attracted more than 130 basic, translational and clinical scientists from 19 countries. Important new information was presented regarding: the biology of HHV-6A and -6B; the biology and epidemiology of inherited chromosomally integrated HHV-6A and -6B; improved diagnostic tests; animal models for and animal viruses with similarities to HHV-6A, -6B, and -7; established and possible disease associations; and new treatment strategies. Here, we summarize work presented at the meeting that is of particular interest. © 2017 Wiley Periodicals, Inc.

40 CFR 130.7 - Total maximum daily loads (TMDL) and individual water quality-based effluent limitations.

Science.gov (United States)

2010-07-01

... 40 Protection of Environment 21 2010-07-01 2010-07-01 false Total maximum daily loads (TMDL) and individual water quality-based effluent limitations. 130.7 Section 130.7 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) WATER PROGRAMS WATER QUALITY PLANNING AND MANAGEMENT § 130.7 Total...

Molecular detection of ‘Candidatus Phytoplasma australasia’ and ‘Ca. P. cynodontis’ in Iraq

Directory of Open Access Journals (Sweden)

Alkuwaiti Nawres Abdulelah Sadeq

2017-10-01

Full Text Available The association of phytoplasma was investigated in symptomatic tomato (Solanum lycopersicum L., eggplant (Solanum melongen L., mallow (Malva spp. and Bermuda grass (Cynodon dactylon L. plants exhibiting witches’ broom and white leaf diseases, respectively. Total DNA was extracted from tomato (n=3, eggplant (n=2, mallow (n=2 and Bermuda grass (n=8 samples. Direct polymerase chain reaction (PCR was performed using P1/P7 primer set, then PCR products were sequenced. Sequences obtained from tomato, eggplant and mallow shared 99% maximum nucleotide identity with phytoplasma belonging to subgroup 16SrII-D, and resulted therefore ‘Candidatus Phytoplasma australasia’-related. Sequences obtained from Bermuda grass showed 100% maximum nucleotide identity to 16SrXIV-A subgroup and were ‘Ca. P. cynodontis’-related. The study presents the first molecular confirmation and sequence data of presence of ‘Ca. P. australasia’ and ‘Ca. P. cynodontis’ in Iraq.

Microstructure and Mechanical Properties of ASTM A743 CA6NM Steel Welded by FCAW Process

OpenAIRE

Silva, Rafael de Paula; Faria, Maria Ismenia Sodero Toledo; Almeida, Luiz Fernando Cursino Briet de; Nunes, Carlos Angelo; Vieira, Décio; Borges Júnior, Wanderlei

2017-01-01

CA6NM steel is widely used in the manufacture of hydraulic turbines metallic parts, due to its resistance to corrosion and cavitation damage, combined with good weldability and fatigue properties. However, welding of this type of steel is complex and to ensure a minimum residual stress after welding it is necessary perform a post welding heat treatment (PWHT) of the part. This study aims to analyze the effect of a PWHT on the microstructure and mechanical properties of CA6NM steel weld joint ...

correlation between maximum dry density and cohesion

African Journals Online (AJOL)

HOD

represents maximum dry density, signifies plastic limit and is liquid limit. Researchers [6, 7] estimate compaction parameters. Aside from the correlation existing between compaction parameters and other physical quantities there are some other correlations that have been investigated by other researchers. The well-known.

THE LICK/SDSS LIBRARY. II. [Ca/Fe] AND [Mg/Fe] IN F, G, AND K STARS FROM SDSS-DR7

International Nuclear Information System (INIS)

Franchini, M.; Morossi, C.; Di Marcantonio, P.; Malagnini, M. L.; Chavez, M.

2011-01-01

We analyzed the spectra of 17,600 F, G, and K stars extracted from the seventh Sloan Digital Sky Survey Data Release (SDSS-DR7) database in order to derive ([α/Fe]), [Ca/Fe], and [Mg/Fe] ratios. Particular attention has been devoted to estimating homogeneous and self-consistent atmospheric parameter values, T eff , log g, and [Fe/H], by comparing synthetic and observational Lick/SDSS indices. We present results for the sub-sample of more than 4000 spectra whose overall quality allowed us to derive fairly accurate stellar atmospheric parameter values and, therefore, reliable abundance ratios. A Monte Carlo approach was adopted to evaluate both the errors in the observational Lick/SDSS indices and in the derived parameter estimates. The analysis of the trends of [Ca/Fe] and [Mg/Fe] versus [Fe/H] pointed out that (1) the [Ca/Fe] and [Mg/Fe] ratios increase with decreasing [Fe/H] with different slopes reaching maximum average levels of +0.25 and +0.40 dex at [Fe/H] ≅ -1.75, respectively; (2) our sample contains, at a given [Fe/H], stars characterized by significantly different amounts of α-enhancement, thus belonging to different Galactic populations; and (3) the analyzed sample shows a predominance of thick disk stars for [Fe/H] > - 0.5 and the presence of stars belonging to the h igh-αhalo population for -2.0 < [Fe/H] <-0.5.

Thermal neutron imaging with rare-earth-ion-doped LiCaAlF6 scintillators and a sealed 252Cf source

International Nuclear Information System (INIS)

Kawaguchi, Noriaki; Yanagida, Takayuki; Fujimoto, Yutaka; Yokota, Yuui; Kamada, Kei; Fukuda, Kentaro; Suyama, Toshihisa; Watanabe, Kenichi; Yamazaki, Atsushi; Chani, Valery; Yoshikawa, Akira

2011-01-01

Thermal neutron imaging with Ce-doped LiCaAlF 6 crystals has been performed. The prototype of the neutron imager using a Ce-doped LiCaAlF 6 scintillating crystal and a position sensitive photomultiplier tube (PSPMT) which had 64 multi-channel anode was developed. The Ce-doped LiCaAlF 6 single crystal was grown by the Czochralski method. A plate with dimensions of a diameter of 50x2 mm 2 was cut from the grown crystal, polished, and optically coupled to PSPMT by silicone grease. The 252 Cf source ( 6 .

Influence of Calcium Chloride (CaCl/sub 2/) on Fruit Quality of Pear (Pyrus communis) cv. le conte During Storage

International Nuclear Information System (INIS)

Sajid, M.; Mukhtiar, M.; Rab, M.; Shah, S.R.; Jan, I.

2014-01-01

An experiment was conducted at Postharvest laboratory, Department of Horticulture, The University of Agriculture Peshawar, during 2010 to evaluate the 'Influence of calcium chloride (CaCl/sub 2/) on fruit quality of pear (Pyrus communis) cv. Le-conte'. The experiment was laid out in Randomized Complete Block Design (RCBD) with three factors i.e. (CaCl/sub 2/) concentration (0,3,6 and 9%), dipping time (5,10 and 15 minutes) and storage durations (0,10,20,30 and 40 days). The maximum ascorbic acid (7.93 mg/100 g), reducing sugar (5.86%), while the least percent weight loss (4.52%), pH of fruit juice (4.42), total soluble solids (TSS) (19.83%) and percent disease incidence (2.56%) were observed in fruits treated with 9% CaCl/sub 2/ solution. The dipping time also significantly influenced the quality attributes of pear fruits during storage. The more ascorbic acid (6.88 mg/100 g) and reducing sugar (5.44%) were recorded in the pear fruits dipped for 15 minutes. Storage duration significantly affected the fruit quality 40 days storage. The highest reducing sugar recorded in fresh pear fruits while the highest ascorbic acid (7.83 mg/100 g) were observed in pear fruit stored for 10 days storage duration, while more non-reducing sugar (7.03%) recorded in the fruits stored for 30 days. In the interaction of CaCl/sub 2/ concentration x dipping time, the highest total soluble solid (31.88%) noted in the fruits stored for 40 days and dipped for 5 minutes in CaCl/sub 2/ solution. It is concluded that pear fruit perform best in the postharvest life when treated with 9% CaCl/sub 2/ solution and dipped for 15 minutes. It retained most of the quality attributes up to 10 days storage at ambient temperature while a significant decline was recorded in fruit quality when extended the storage duration from 20 to 40 days. (author)

Effect of Gd–Ca combined additions on the microstructure and creep properties of Mg–7Al–1Si alloys

International Nuclear Information System (INIS)

Liu, Jian; Wang, Wuxiao; Zhang, Sha; Zhang, Dongjie; Zhang, Haiyan

2015-01-01

Highlights: • The effect of compound addition of Ca and Gd on the microstructure and creep properties of Mg–7Al–1Si alloys was investigated. • After adding 1 wt.% of (Ca + Gd), the creep strain and steady-state creep rate were reduced by about 80% and 84%, respectively. • After adding 1 wt.% of (Ca + Gd), the creep properties of Mg–7Al–1Si alloys were superior to that containing single Gd additive. • The improvement of creep properties after compound addition of Gd and Ca is a result of multiple factors. - Abstract: The microstructure and creep properties of Mg–7Al–1Si alloys with combined additions of alkaline earth element Ca and rare earth element (RE) Gd were investigated using scanning electron microscope (SEM), optical microscope, energy dispersive spectrometer (EDS), X-ray diffraction (XRD), and compressive creep tests. It was found that the combined additions of Ca and Gd contributed to grain refinement, modification of the morphology of coarse Chinese script Mg 2 Si phase, and reduction of β-Mg 17 Al 12 content. Mg–7Al–1Si alloys containing 1 wt.% compound modifier (0.5 wt.% Gd + 0.5 wt.% Ca) exhibited the minimal steady-state creep rate, and were even superior to Mg–7Al–1Si alloys containing single Gd addition. The great improvement of creep properties is mainly attributed to the reduction in the amount and continuity of eutectic β-Mg 17 Al 12 phase, morphology modification of Mg 2 Si phase, solution strengthening of Gd, as well as the formation of thermally stable intermetallic Al 2 Gd, which acted as an effective barrier against grain boundary sliding and dislocation movement

Selectividad de caña de azúcar en bovinos

Directory of Open Access Journals (Sweden)

E. M. Aranda

2009-01-01

Full Text Available Se condujo este trabajo con el objetivo de conocer la aceptación del forraje de caña de azúcar integral en la dieta con base de pasto para bovinos adultos fistulados en rumen y duodeno estabulados; para ello, se ofreció pasto estrella africana (Cynodon plectostachyus y caña de azúcar (Saccharum officinarum mezclada con 1% de urea a voluntad, por separado. Se midió la composición de los alimentos, consumo de materia seca, pH ruminal y duodenal. Se utilizaron técnicas de la estadística descriptiva, como la media aritmética y error estándar. La proteína, paredes celulares y hemicelulosa fueron mayores para el pasto estrella. El consumo de MS fue de 46.6 y 38.1% para la caña de azúcar y el pasto, respectivamente; el pH ruminal tuvo valores de 7.3, disminuyendo a 6.7 a las 12 h.; y el pH de la digesta duodenal osciló de 3.7 a 4.7. Se concluye que hubo mayor aceptación por la caña de azúcar y el pH ruminal no indica valores que afecten la celulólisis ruminal.

Structural and magnetotransport properties of the Y doped A-site deficient double layered manganites La{sub 1.2−x}□{sub 0.2}Y{sub x}Ca{sub 1.6}Mn{sub 2}O{sub 7}

Energy Technology Data Exchange (ETDEWEB)

Mahamdioua, N., E-mail: mahamdioua.nabil@gmail.com [LEND, Faculty of Science and Technology, Jijel University, Jijel 18000 (Algeria); Amira, A. [LEND, Faculty of Science and Technology, Jijel University, Jijel 18000 (Algeria); Altintas, S.P. [Department of Physics, Faculty of Arts and Sciences, AIB University, Bolu 14280 (Turkey); Koc University, Surface Science and Technology Center (KUYTAM), 34450-Sariyer, Istanbul (Turkey); Varilci, A.; Terzioglu, C. [Department of Physics, Faculty of Arts and Sciences, AIB University, Bolu 14280 (Turkey)

2016-08-15

We present structural, magnetic and electrical properties of the polycrystalline A-site-deficient yttrium doped double layered manganites La{sub 1.2−x}□{sub 0.2}Y{sub x}Ca{sub 1.6}Mn{sub 2}O{sub 7} (x=0.2, 0.3 and 0.4) prepared by a solid state reaction method. The samples crystallize in the tetragonal structure with the space group I4/mmm. Doping with Y decreases the cell parameters and causes a decrease of the metal-insulator transition temperature. The same evolution with doping is also seen for the deduced Curie temperature from susceptibility curves which present a clear paramagnetic-ferromagnetic transition. The significant positive intrinsic magnetoresistance, shown in all samples, reaches 85% at 122 K under 7 T for 0.3 doped sample and can be attributed to the suppression of spin fluctuations via aligning the spins under external magnetic field, while the extrinsic one is attributed to the inter-grain spin-polarized tunneling across the grain boundaries. The simulation of the resistivity curves in the entire temperature range show that the percolation model is suitable to fit our results. The applied magnetic field increases the density of states near the Fermi level, which is in accordance with the observed decrease of resistivity. - Graphical abstract: Resistivity and magnetoresistance of La{sub 1.2−x}□{sub 0.2}Y{sub x}Ca{sub 1.6}Mn{sub 2}O{sub 7} (x=0.2, 0.3, 0.4). Solid lines correspond to the fitting results. Display Omitted.

TAS2R38 and CA6 genetic polymorphisms, frequency of bitter food intake, and blood biomarkers among elderly woman.

Science.gov (United States)

Mikołajczyk-Stecyna, Joanna; Malinowska, Anna M; Chmurzynska, Agata

2017-09-01

Taste sensitivity is one of the most important biological determinants of food choice. Three SNPs of the TAS2R38 gene (rs713598, rs1726866, and rs10246939) give rise to two common haplotypes: PAV and AVI. These haplotypes, as well as an SNP within the CA6 gene (rs2274333) that encodes carbonic anhydrase VI (CA6), correlate with bitterness perception. The extent of consumption of bitter food may influence some health outcomes. The aim of this study is thus to investigate the impact of the TAS2R38 and CA6 genetic polymorphisms on the choice of bitter food, BMI, blood lipoprotein, and glucose concentrations as well as systemic inflammation in elderly women. The associations between the TAS2R38 diplotype, CA6 genotype, and the intake of bitter-tasting foods were studied in a group of 118 Polish women over 60 years of age. The intake of Brassica vegetables, grapefruit, and coffee was assessed using a food frequency questionnaire. Biochemical parameters were measured using the spectrophotometric method. Genotyping was performed using the high resolution melting method. We found a correlation between lipid profile, glucose and CRP levels, and frequency of bitter food intake. The AVI/AVI subjects drank coffee more frequently than did the PAV/PAV homozygotes, as did the A carriers of CA6 in comparison with the GG homozygotes. We also observed that simultaneous carriers of the PAV haplotype and A allele of TAS2R38 and CA6, respectively, choose white cabbage more frequent and had lower plasma levels of CRP and glucose than did AVI/AVI and GG homozygotes. In elderly women, the TAS2R38 and CA6 polymorphisms may affect the frequency of consumption of coffee and white cabbage, but not of other bitter-tasting foods. Copyright © 2017 Elsevier Ltd. All rights reserved.

The synthesis and luminescence properties of a novel red-emitting phosphor. Eu{sup 3+}-doped Ca{sub 9}La(PO{sub 4}){sub 7}

Energy Technology Data Exchange (ETDEWEB)

Liang, Zehui [Guangdong University of Technology, Experimental Teaching Department, Guangzhou (China); Guangdong University of Technology, School of Chemical Engineering and Light Industry, Guangzhou (China); Mu, Zhongfei; Zhu, Daoyun [Guangdong University of Technology, Experimental Teaching Department, Guangzhou (China); Wang, Qiang; Wu, Fugen [Guangdong University of Technology, School of Materials and Energy, Guangzhou (China)

2017-10-15

A series of novel red-emitting phosphors Ca{sub 9}La{sub 1-x}(PO{sub 4}){sub 7}: xEu{sup 3+} were synthesized by high-temperature solid state reactions. The photoluminescence excitation and photoluminescence spectra of these phosphors were investigated in detail. O{sup 2-}-Eu{sup 3+} charge transfer band peaking at about 261 nm is dominant in the PLE spectra of Eu{sup 3+}-doped Ca{sub 9}La(PO{sub 4}){sub 7}, indicating that the phosphors are suitable for tricolor fluorescent lamps. The phosphors also show a good absorption in near ultraviolet (around 395 nm) and blue (around 465 nm) spectral region, which indicates that it can be pumped with NUV and blue chips for white light-emitting diodes. The transition of {sup 5}D{sub 0} → {sup 7}F{sub 2} of Eu{sup 3+} in this lattice can emit bright red light. Ca{sub 9}La(PO{sub 4}){sub 7} could accommodate a large amount of Eu{sup 3+} with an optimal concentration of 60 mol%. The dipole-dipole interaction between Eu{sup 3+} is the dominant mechanism for concentration quenching of Eu{sup 3+}. The calculated color coordinates lie in red region (x = 0.64, y = 0.36), which is close to Y{sub 2}O{sub 3}: 0.05Eu{sup 3+} (x = 0.65, y = 0.34). The integral emission intensity of Ca{sub 9}La{sub 0.4}(PO{sub 4}){sub 7}: 0.6Eu{sup 3+} is 1.9 times stronger than that of widely used commercial red phosphor Y{sub 2}O{sub 3}: 0.05Eu{sup 3+}. All these results indicate that Eu{sup 3+}-doped Ca{sub 9}La(PO{sub 4}){sub 7} is a promising red-emitting phosphor which can be used in tricolor fluorescent lamps and white light-emitting diodes. (orig.)

Effects of calcium binding and of EDTA and CaEDTA on the clotting of bovine fibrinogen by thrombin.

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Perizzolo, K E; Sullivan, S; Waugh, D F

1985-03-01

Studies were carried out at pH 7.0 and gamma/2 0.15 before addition of CaCl2 or EDTA. Clotting time, tau, at 3.03 microM fibrinogen and 0.91 u/ml thrombin was determined for equilibrium systems. With added Ca2+, tau decreases, from tau 0 at 0 added Ca2+ (mean, 29.7 +/- 3 s), by approximately 3 s at 5 mM added Ca2+. With added EDTA, tau increases sigmoidally from tau 0 at 0 EDTA to a maximum (mean tau m = 142 +/- 23 s) at approximately 200 microM EDTA. tau then decreases slightly to a minimum at approximately 1.3 mM and finally increases to infinity at approximately 10 mM EDTA. Between 0 and 1.3 mM EDTA, effects on clotting time are completely reversed by adding Ca2+ and, after equilibration at 400 microM EDTA, tau is independent of EDTA concentration. Thus, up to 400 microM EDTA, effects on clotting time are attributed to decreasing fibrinogen bound Ca2+. Between 5 mM Ca2+ and 200 microM EDTA it is assumed that an equilibrium distribution of fibrinogen species having 3, 2, 1, or 0 bound calcium ions is established and that a clotting time is determined by the sum of products of species fractional abundance and pure species clotting time. Analysis indicates that pure species clotting times increase proportionately with decreasing Ca2+ binding, binding sites are nearly independent, and the microscopic association constant for the first bound Ca2+ is approximately 4.9 X 10(6) M-1. Effects of adding Ca2+ at times t1 after thrombin addition to systems initially equilibrated at 200 microM EDTA were determined. Analysis of the relation between tau and t1 indicates that as Ca2+ binding decreases, rate constants for release of B peptides decrease less than those for release of A peptides. As EDTA concentration is increased above 1.3 mM, inhibitory effects of EDTA and CaEDTA progressively increase.

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

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Shinde, K N; Dhoble, S J

2013-01-01

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

Structural and magnetic investigations of CaBaCo{sub 4−x}Fe{sub x}O{sub 7} solid solutions

Energy Technology Data Exchange (ETDEWEB)

Turkin, D.I., E-mail: turkin@ihim.uran.ru [Institute of Solid State Chemistry, Ural Branch of the Russian Academy of Sciences, Ekaterinburg GSP-145, 620990 (Russian Federation); Bazuev, G.V. [Institute of Solid State Chemistry, Ural Branch of the Russian Academy of Sciences, Ekaterinburg GSP-145, 620990 (Russian Federation); Korolev, A.V. [Institute of Metal Physics, Ural Branch of the Russian Academy of Sciences, 620041 Ekaterinburg GSP-145, 620999 (Russian Federation)

2017-01-15

Solid solutions of CaBaCo{sub 4−x}Fe{sub x}O{sub 7} (x=0, 0.05, 0.2, 1, 2) were synthesized by glycine-nitrate combustion process. Their structural and magnetic properties were characterized by means of x-ray diffraction and magnetization measurements. In the examined range of the solid solutions, their crystal lattice symmetry changes from orthorhombic with space group Pbn2{sub 1} (06{sub 3}mc (x>0.5). The magnetic measurements revealed that even small doping (x=0.05) of the transition metal sublattice noticeably suppresses ferrimagnetism of the parent compound and induces an AF transition at 88 K. An increase in the doping concentration lowers the frustration parameter |θ{sub CW}|/T{sub C} from 17.2 (for x=0.05) to 13.7 (for x=2) and strengthens the antiferromagnetic interactions, which manifests itself in the Curie–Weiss temperature (θ{sub CW}) growth. The samples with x=0.05 and x=0.2 also show an additional magnetic transition at temperatures T{sub g} (55 and 70 K respectively). The temperature irreversibility between the ZFC and FC magnetization curves may suggest the formation of a spin-glass state below that temperature. - Highlights: • CaBaCo{sub 4−x}Fe{sub x}O{sub 7} solid solutions were synthesized by glycine-nitrate process. • At x=1 symmetry became hexagonal instead orthorhombic. • Fe-doping abruptly suppresses ferrimagnetism of CaBaCo{sub 4}O{sub 7}. • Increase of x is followed by enhancing of antiferromagnetic interactions.

Interaction of peridotite with Ca-rich carbonatite melt at 3.1 and 6.5 GPa: Implication for merwinite formation in upper mantle, and for the metasomatic origin of sublithospheric diamonds with Ca-rich suite of inclusions

Science.gov (United States)

Sharygin, Igor S.; Shatskiy, Anton; Litasov, Konstantin D.; Golovin, Alexander V.; Ohtani, Eiji; Pokhilenko, Nikolay P.

2018-03-01

We performed an experimental study, designed to reproduce the formation of an unusual merwinite + olivine-bearing mantle assemblage recently described as a part of a Ca-rich suite of inclusions in sublithospheric diamonds, through the interaction of peridotite with an alkali-rich Ca-carbonatite melt, derived from deeply subducted oceanic crust. In the first set of experiments, we studied the reaction between powdered Mg-silicates, olivine and orthopyroxene, and a model Ca-carbonate melt (molar Na:K:Ca = 1:1:2), in a homogeneous mixture, at 3.1 and 6.5 GPa. In these equilibration experiments, we observed the formation of a merwinite + olivine-bearing assemblage at 3.1 GPa and 1200 °C and at 6.5 GPa and 1300-1400 °C. The melts coexisting with this assemblage have a low Si and high Ca content (Ca# = molar 100 × Ca/(Ca + Mg) > 0.57). In the second set of experiments, we investigated reaction rims produced by interaction of the same Ca-carbonate melt (molar Na:K:Ca = 1:1:2) with Mg-silicate, olivine and orthopyroxene, single crystals at 3.1 GPa and 1300 °C and at 6.5 GPa and 1400 °C. The interaction of the Ca-carbonate melt with olivine leads to merwinite formation through the expected reaction: 2Mg2SiO4 (olivine) + 6CaCO3 (liquid) = Ca3MgSi2O8 (merwinite) + 3CaMg(CO3)2 (liquid). Thus, our experiments confirm the idea that merwinite in the upper mantle may originate via interaction of peridotite with Ca-rich carbonatite melt, and that diamonds hosting merwinite may have a metasomatic origin. It is remarkable that the interaction of the Ca-carbonate melt with orthopyroxene crystals does not produce merwinite both at 3.1 and 6.5 GPa. This indicates that olivine grain boundaries are preferable for merwinite formation in the upper mantle.

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

Science.gov (United States)

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

2018-05-01

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

Synergistic augmentation of ATP-induced interleukin-6 production by arsenite in HaCaT cells.

Science.gov (United States)

Sumi, Daigo; Asao, Masashi; Okada, Hideta; Yogi, Kuniko; Miyataka, Hideki; Himeno, Seiichiro

2016-06-01

Chronic arsenic exposure causes cutaneous diseases such as hyperkeratosis and skin cancer. However, little information has been available regarding the molecular mechanisms underlying these symptoms. Because extracellular ATP and interleukin-6 (IL-6) are involved in pathological aspects of cutaneous diseases, we examined whether sodium arsenite (As(III)) affects ATP-induced IL-6 production in human epidermal keratinocyte HaCaT cells. The results showed that the addition of As(III) into the medium of HaCaT cells dose dependently increased the production of IL-6 induced by extracellular ATP, although As(III) alone had no effect on IL-6 production. To elucidate the mechanism of the synergistic effect of As(III) on IL-6 production by extracellular ATP, we next examined the phosphorylation of p38, ERK and epidermal growth factor receptor (EGFR), since we found that these signaling molecules were stimulated by exposure to extracellular ATP. The results indicated that ATP-induced phosphorylation of p38, ERK and EGFR was synergistically enhanced by co-exposure to As(III). To clarify the mechanisms underlying the enhanced phosphorylation of p38, ERK and EGFR by As(III), we explored two possible mechanisms: the inhibition of extracellular ATP degradation and the inhibition of protein tyrosine phosphatases (PTPs) activity by As(III). The degradation of extracellular ATP was not changed by As(III), whereas the activity of PTPs was significantly inhibited by As(III). Our results suggest that As(III) augments ATP-induced IL-6 production in HaCaT cells through enhanced phosphorylation of the EGFR and p38/ERK pathways, which is associated with the inhibition of PTPs activity.

literacy.ca EXPRESS. April 2010

Science.gov (United States)

Movement for Canadian Literacy, 2010

2010-01-01

This issue of "literacy.ca EXPRESS" focuses on poverty. The articles included in this issue are: (1) Poverty Overview; (2) Tony's Story; (3) LAN (Learner Advisory Network) Member's Story (Dianne Smith); (4) Linking Adult Literacy to Poverty Reduction; (5) MCL (Movement for Canadian Literacy) Update; (6) Highlights from the LAN; (7) Good…

The Pr and Ca substitution in GdBa2Cu3O7-8

International Nuclear Information System (INIS)

Shakeri, H.; Akhavan, M.

2002-01-01

The granular Gd 1 -x-zPr x Ca z Ba 2 Cu 3 O 7 -8 (Gd Pr Ca-123) high-temperature cuprate samples with 0.0≤x≤0.3 and 0.0≤z≤0.35 are prepared by standard solid state reaction and characterized by XRD and SEM techniques. The BaCuO 2 and impurity phases are less than 1% in the samples having high levels of Pr and Ca concentrations. The electrical resistivity measurements show a nonlinear reduction in T c (x,z=etc) versus x. Moreover, the T c (z) curve with x=0 is nonlinear and a plateau appears at z≅0.05-0.015. For Pr-Ca-doped samples with a constant concentration of Pr, T c increases with the increase of Ca up to an optimum value of Ca doping and then in decreases. Based on these observations, we suggest that hole filling and hole localization the main effects of Pr ion substitution. The magnetic measurements indicate that the value of H C 1 is in the order of 10 m T. The magnetoresistance measurements have been measured and analyzed. The superconducting transition region is broadened by the application of magnetic field. The experimental data near the on sen of superconductivity are fitted with the Ambegakor and Halperin (A H) phase-slip model. We observe that the A H parameter, γ(H), depends not only on the temperature and the magnetic field, but also on the Pr and Ca ions concentrations. It is observed that the critical current density increases with Ca substitution and decreases with pr substitution in Gd-123 system. We suggest that the pr ion substitution probably enhances the weak link, but the Ca ion acts as flux pinning center in the Gd Pr Ca-123 system

Ca doping of TSMTG-YBa2Cu3O7-δ/Y2BaCuO5 composites

International Nuclear Information System (INIS)

Delorme, F.; Harnois, C.; Monot-Laffez, I.; Marinel, S.

2002-01-01

Calcium doped YBa 2 Cu 3 O 7-δ /Y 2 BaCuO 5 bulk samples have been synthesised by the top-seeding-melt-texture growth (TSMTG) process up to 1 wt.% of CaCO 3 . Calcium additions up to 0.25 wt.% of CaCO 3 do not change the decomposition temperature whereas additions of 1 wt.% of CaCO 3 lead to an increase of the decomposition temperature of about 10 deg. C. This difference is not important enough to change the thermal cycle used to process YBa 2 Cu 3 O 7-δ undoped bulk samples. Microstructure studies show that no precursor or secondary phases containing calcium are present in the samples. Energy dispersive spectroscopy analyses have shown that Ca is present both in the YBa 2 Cu 3 O 7-δ matrix and the Y 2 BaCuO 5 particles. The position of the calcium atoms in the superconducting matrix is discussed. The calcium doped samples present slightly depressed critical temperatures but drastically depressed critical current densities

Ca2+ toxicity due to reverse Na+/Ca2+ exchange contributes to degeneration of neurites of DRG neurons induced by a neuropathy-associated Nav1.7 mutation

Science.gov (United States)

Estacion, M.; Vohra, B. P. S; Liu, S.; Hoeijmakers, J.; Faber, C. G.; Merkies, I. S. J.; Lauria, G.; Black, J. A.

2015-01-01

Gain-of-function missense mutations in voltage-gated sodium channel Nav1.7 have been linked to small-fiber neuropathy, which is characterized by burning pain, dysautonomia and a loss of intraepidermal nerve fibers. However, the mechanistic cascades linking Nav1.7 mutations to axonal degeneration are incompletely understood. The G856D mutation in Nav1.7 produces robust changes in channel biophysical properties, including hyperpolarized activation, depolarized inactivation, and enhanced ramp and persistent currents, which contribute to the hyperexcitability exhibited by neurons containing Nav1.8. We report here that cell bodies and neurites of dorsal root ganglion (DRG) neurons transfected with G856D display increased levels of intracellular Na+ concentration ([Na+]) and intracellular [Ca2+] following stimulation with high [K+] compared with wild-type (WT) Nav1.7-expressing neurons. Blockade of reverse mode of the sodium/calcium exchanger (NCX) or of sodium channels attenuates [Ca2+] transients evoked by high [K+] in G856D-expressing DRG cell bodies and neurites. We also show that treatment of WT or G856D-expressing neurites with high [K+] or 2-deoxyglucose (2-DG) does not elicit degeneration of these neurites, but that high [K+] and 2-DG in combination evokes degeneration of G856D neurites but not WT neurites. Our results also demonstrate that 0 Ca2+ or blockade of reverse mode of NCX protects G856D-expressing neurites from degeneration when exposed to high [K+] and 2-DG. These results point to [Na+] overload in DRG neurons expressing mutant G856D Nav1.7, which triggers reverse mode of NCX and contributes to Ca2+ toxicity, and suggest subtype-specific blockade of Nav1.7 or inhibition of reverse NCX as strategies that might slow or prevent axon degeneration in small-fiber neuropathy. PMID:26156380

A live attenuated H7N7 candidate vaccine virus induces neutralizing antibody that confers protection from challenge in mice, ferrets and monkeys

Science.gov (United States)

A live attenuated H7N7 candidate vaccine virus was generated by reverse genetics using the modified hemagglutinin (HA) and neuraminidase (NA) genes of HP A/Netherlands/219/03 (NL/03) (H7N7) wild-type (wt) virus and the six internal protein genes of the cold-adapted (ca) A/Ann Arbor/6/60 ca (AA ca) (...

In vitro and in vivo evaluation of zinc-modified ca-si-based ceramic coating for bone implants.

Science.gov (United States)

Yu, Jiangming; Li, Kai; Zheng, Xuebin; He, Dannong; Ye, Xiaojian; Wang, Meiyan

2013-01-01

The host response to calcium silicate ceramic coatings is not always favorable because of their high dissolution rates, leading to high pH within the surrounding physiological environment. Recently, a zinc-incorporated calcium silicate-based ceramic Ca2ZnSi2O7 coating, developed on a Ti-6Al-4V substrate using plasma-spray technology, was found to exhibit improved chemical stability and biocompatibility. This study aimed to investigate and compare the in vitro response of osteoblastic MC3T3-E1 cells cultured on Ca2ZnSi2O7 coating, CaSiO3 coating, and uncoated Ti-6Al-4V titanium control at cellular and molecular level. Our results showed Ca2ZnSi2O7 coating enhanced MC3T3-E1 cell attachment, proliferation, and differentiation compared to CaSiO3 coating and control. In addition, Ca2ZnSi2O7 coating increased mRNA levels of osteoblast-related genes (alkaline phosphatase, procollagen α1(I), osteocalcin), insulin-like growth factor-I (IGF-I), and transforming growth factor-β1 (TGF-β1). The in vivo osteoconductive properties of Ca2ZnSi2O7 coating, compared to CaSiO3 coating and control, was investigated using a rabbit femur defect model. Histological and histomorphometrical analysis demonstrated new bone formation in direct contact with the Ca2ZnSi2O7 coating surface in absence of fibrous tissue and higher bone-implant contact rate (BIC) in the Ca2ZnSi2O7 coating group, indicating better biocompatibility and faster osseointegration than CaSiO3 coated and control implants. These results indicate Ca2ZnSi2O7 coated implants have applications in bone tissue regeneration, since they are biocompatible and able to osseointegrate with host bone.

In vitro and in vivo evaluation of zinc-modified ca-si-based ceramic coating for bone implants.

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Jiangming Yu

Full Text Available The host response to calcium silicate ceramic coatings is not always favorable because of their high dissolution rates, leading to high pH within the surrounding physiological environment. Recently, a zinc-incorporated calcium silicate-based ceramic Ca2ZnSi2O7 coating, developed on a Ti-6Al-4V substrate using plasma-spray technology, was found to exhibit improved chemical stability and biocompatibility. This study aimed to investigate and compare the in vitro response of osteoblastic MC3T3-E1 cells cultured on Ca2ZnSi2O7 coating, CaSiO3 coating, and uncoated Ti-6Al-4V titanium control at cellular and molecular level. Our results showed Ca2ZnSi2O7 coating enhanced MC3T3-E1 cell attachment, proliferation, and differentiation compared to CaSiO3 coating and control. In addition, Ca2ZnSi2O7 coating increased mRNA levels of osteoblast-related genes (alkaline phosphatase, procollagen α1(I, osteocalcin, insulin-like growth factor-I (IGF-I, and transforming growth factor-β1 (TGF-β1. The in vivo osteoconductive properties of Ca2ZnSi2O7 coating, compared to CaSiO3 coating and control, was investigated using a rabbit femur defect model. Histological and histomorphometrical analysis demonstrated new bone formation in direct contact with the Ca2ZnSi2O7 coating surface in absence of fibrous tissue and higher bone-implant contact rate (BIC in the Ca2ZnSi2O7 coating group, indicating better biocompatibility and faster osseointegration than CaSiO3 coated and control implants. These results indicate Ca2ZnSi2O7 coated implants have applications in bone tissue regeneration, since they are biocompatible and able to osseointegrate with host bone.

Synthesis, Structural Characterization, and Antitumor Activity of a Ca(II Coordination Polymer Based on 1,6-Naphthalenedisulfonate and 4,4′-Bipyridyl

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Xishi Tai

2013-08-01

Full Text Available A novel Ca(II coordination polymer, [CaL(4,4′-bipyridyl(H2O4]n (L = 1,6-naphthalenedisulfonate, was synthesized by reaction of calcium perchlorate with 1,6-naphthalenedisulfonic acid disodium salt and 4,4′-bipyridyl in CH3CH2OH/H2O. It was characterized by elemental analysis, IR, molar conductivity and thermogravimetric analysis. X-ray crystallography reveals that the Ca(II coordination polymer belongs to the orthorhombic system, with space group P212121. The geometry of the Ca(II ion is a distorted CaNO6 pengonal bipyramid, arising from its coordination by four water molecules, one nitrogen atom of 4,4′-bipyridyl molecule, and two oxygen atoms from two L ligands. The complex molecules form a helical chain by self-assembly. The antitumor activity of 1,6-naphthalenedisulfonic acid disodium salt and the Ca(II coordination polymer against human hepatoma smmc-7721 cell line and human lung adenocarcinoma A549 cell line reveals that the Ca(II coordination polymer inhibits cell growth of human lung adenocarcinoma A549 cell line with IC50 value of 27 μg/mL, and is more resistive to human lung adenocarcinoma A549 cell line as compared to 1,6-naphthalenedisulfonic acid disodium salt.

Effects of hyperthermia on intracellular CA/sup 2+/ monitored by digitized video image fluorescence microscopy

International Nuclear Information System (INIS)

Asher, C.R.; Mikkelsen, R.B.

1987-01-01

With digitized video image fluorescence microscopy and the fluorescent Ca/sup 2+/ dye, fuca-2, the authors examined heat effects on intracellular free Ca/sup 2+/, [Ca/sup 2/]/sub f/. HT-29 human colon cancer cells grown on coverslip were equilibrated with 2.0 μM fura-2 in RPMI 1540 (20 0 , 15 min), washed three times and incubated at 20 0 for 1 h. Coverslips were mounted in a Dvorok perfusion chamber sitting within a temperature controlled microscope stage. Fluorescence was monitored at 500 nm by epi-illumination at 385 nm, excitation maximum for free dye, and 340 nm, maximum for Ca/sup 2+/ complexed dye, with a computer controlled filter wheel. The emission intensity ratio, I/sub 340//I/sub 385/, which corrects for dye leakage, photo-bleaching and cell thickness was used to calculate [Ca/sup 2+/]/sub f/. Measurements of 200 cells at 37 0 using a bit pad and mouse to select 0.6 x 0.6 μ cytoplasmi areas indicated 3 populations of cells in terms of [Ca/sup 2+/]/sub f/ (70%, 40-60nM; 15% 70-110nM; 15%, 120-200 nM). Heating to 43 0 for 1 h resulted in an overall decrease in [Ca/sup 2+/]/sub f/ with greater than 90% cells within 30-50 nM. Not all cells responded to heat. Post-incubation for 3 h at 37 0 showed the identical cell distribution; at 24 h, cell distribution was that of non-heated cells. The relationship of these results to cell killing and thermotolerance are not understood, but these results indicated the importance of cell heterogeneity in response to heat

AGR-5/6/7 Irradiation Test Predictions using PARFUME

Energy Technology Data Exchange (ETDEWEB)

Skerjanc, William F. [Idaho National Lab. (INL), Idaho Falls, ID (United States)

2017-09-14

PARFUME, (PARticle FUel ModEl) a fuel performance modeling code used for high temperature gas-cooled reactors (HTGRs), was used to model the Advanced Gas Reactor (AGR)-5/6/7 irradiation test using predicted physics and thermal hydraulics data. The AGR-5/6/7 test consists of the combined fifth, sixth, and seventh planned irradiations of the AGR Fuel Development and Qualification Program. The AGR-5/6/7 test train is a multi-capsule, instrumented experiment that is designed for irradiation in the 133.4-mm diameter north east flux trap (NEFT) position of Advanced Test Reactor (ATR). Each capsule contains compacts filled with uranium oxycarbide (UCO) unaltered fuel particles. This report documents the calculations performed to predict the failure probability of tristructural isotropic (TRISO)-coated fuel particles during the AGR-5/6/7 experiment. In addition, this report documents the calculated source term from the driver fuel. The calculations include modeling of the AGR-5/6/7 irradiation that is scheduled to occur from October 2017 to April 2021 over a total of 13 ATR cycles, including nine normal cycles and four Power Axial Locator Mechanism (PALM) cycle for a total between 500 – 550 effective full power days (EFPD). The irradiation conditions and material properties of the AGR-5/6/7 test predicted zero fuel particle failures in Capsules 1, 2, and 4. Fuel particle failures were predicted in Capsule 3 due to internal particle pressure. These failures were predicted in the highest temperature compacts. Capsule 5 fuel particle failures were due to inner pyrolytic carbon (IPyC) cracking causing localized stresses concentrations in the SiC layer. This capsule predicted the highest particle failures due to the lower irradiation temperature. In addition, shrinkage of the buffer and IPyC layer during irradiation resulted in formation of a buffer-IPyC gap. The two capsules at the two ends of the test train, Capsules 1 and 5 experienced the smallest buffer-IPyC gap

Scoparia dulcis (SDF7) endowed with glucose uptake properties on L6 myotubes compared insulin.

Science.gov (United States)

Beh, Joo Ee; Latip, Jalifah; Abdullah, Mohd Puad; Ismail, Amin; Hamid, Muhajir

2010-05-04

Insulin stimulates glucose uptake and promotes the translocation of glucose transporter 4 (Glut 4) to the plasma membrane on L6 myotubes. The aim of this study is to investigate affect of Scoparia dulcis Linn water extracts on glucose uptake activity and the Glut 4 translocation components (i.e., IRS-1, PI 3-kinase, PKB/Akt2, PKC and TC 10) in L6 myotubes compared to insulin. Extract from TLC fraction-7 (SDF7) was used in this study. The L6 myotubes were treated by various concentrations of SDF7 (1 to 50 microg/ml) and insulin (1 to 100 nM). The glucose uptake activities of L6 myotubes were evaluated using 2-Deoxy-D-glucose uptake assay in with or without fatty acid-induced medium. The Glut 4 translocation components in SDF7-treated L6 myotubes were detected using immunoblotting and quantified by densitometry compared to insulin. Plasma membrane lawn assay and glycogen colorimetry assay were carried out in SDF7- and insulin-treated L6 myotubes in this study. Here, our data clearly shows that SDF7 possesses glucose uptake properties on L6 myotubes that are dose-dependent, time-dependent and plasma membrane Glut 4 expression-dependent. SDF7 successfully stimulates glucose uptake activity as potent as insulin at a maximum concentration of 50 microg/ml at 480 min on L6 myotubes. Furthermore, SDF7 stimulates increased Glut 4 expression and translocation to plasma membranes at equivalent times. Even in the insulin resistance stage (free fatty acids-induced), SDF7-treated L6 myotubes were found to be more capable at glucose transport than insulin treatment. Thus, we suggested that Scoparia dulcis has the potential to be categorized as a hypoglycemic medicinal plant based on its good glucose transport properties. (c) 2010 Elsevier Ireland Ltd. All rights reserved.

41Ca standardization by the CIEMAT/NIST LSC method

International Nuclear Information System (INIS)

Rodriguez Barquero, L.; Los Arcos, J.M.

1996-01-01

A procedure for the liquid scintillation counting standardization of the electron-capture nuclide 41 Ca has been successfully developed and applied with 41 CaCl 2 and 41 Ca-(HDEHP) n samples synthesized in the laboratory from 41 CaCO 3 supplied by Oak Ridge National Laboratory. Six scintillators were tested: the organic samples were stable in toluene-alcohol, Ultima-Gold TM and HiSafe III TM for 30 d, whereas the inorganic samples were only stable in toluene-alcohol and HiSafe III TM for the same period of time. Despite of the low counting efficiencies (1%-13%) due to the very low-energy of less than 3.6 keV of the X-rays and Auger electrons of 41 Ca, the stable samples were standardized by the CIEMAT/NIST method to a combined uncertainty of 2.4% over a range of figures of merit of 1.75 to 7.25 ( 3 H equivalent efficiency of 40% to 7%). (orig.)

Optical spectroscopy and band gap analysis of hybrid improper ferroelectric Ca{sub 3}Ti{sub 2}O{sub 7}

Energy Technology Data Exchange (ETDEWEB)

Cherian, Judy G.; Harms, Nathan C. [Department of Chemistry, University of Tennessee, Knoxville, Tennessee 37996 (United States); Birol, Turan; Vanderbilt, David [Department of Physics and Astronomy, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854 (United States); Gao, Bin; Cheong, Sang-Wook [Department of Physics and Astronomy, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854 (United States); Rutgers Center for Emergent Materials, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854 (United States); Musfeldt, Janice L., E-mail: musfeldt@utk.edu [Department of Chemistry, University of Tennessee, Knoxville, Tennessee 37996 (United States); Department of Physics, University of Tennessee, Knoxville, Tennessee 37996 (United States)

2016-06-27

We bring together optical absorption spectroscopy, photoconductivity, and first principles calculations to reveal the electronic structure of the room temperature ferroelectric Ca{sub 3}Ti{sub 2}O{sub 7}. The 3.94 eV direct gap in Ca{sub 3}Ti{sub 2}O{sub 7} is charge transfer in nature and noticeably higher than that in CaTiO{sub 3} (3.4 eV), a finding that we attribute to dimensional confinement in the n = 2 member of the Ruddlesden-Popper series. While Sr substitution introduces disorder and broadens the gap edge slightly, oxygen deficiency reduces the gap to 3.7 eV and gives rise to a broad tail that persists to much lower energies.

Optical property investigations of polystyrene capped Ca2P2O7:Dy3+ persistent phosphor

International Nuclear Information System (INIS)

Jain, Abhilasha; Kumar, Ashwini; Dhoble, S.J; Peshwe, D.R

2015-01-01

Highlights: • Synthesis of polymer capped pyrophosphate phosphors by citrate gel method. • Radiative lifetime is calculated from parameters of Judd-Ofelt theory and ICP-AES. • Reaction mechanism is discussed leading to high photoluminescence efficiency. • PL emission spectrum reveals broad band emission suitable for solid state lighting. - Abstract: By virtue of enhanced photosensivity, good optical response and better thermal stability, organic–inorganic hybrid materials are contemplated as one of the alternatives for designing advanced optoelectronic devices and innovative photonic applications. A novel inorganic organic hybrid Ca 2 P 2 O 7 :Dy 3+ phosphor has been fabricated by Pechini method. The optical property of synthesized phosphor is successfully altered by the in corporation of polystyrene sulfonic acid as capping agent in the colloidal solution. The phase purity and the average particle size of the prepared phosphor were calculated from X-ray diffraction (XRD) employing Debye Scherrer method. The morphological and chemical investigations were carried out through scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS) analysis. The radiative transitions are explained on the basis of Judd-Ofelt theory and on the basis of derived parameters, the radiative lifetime of persistent hybrid Ca 2 P 2 O 7 :Dy 3+ phosphor is calculated as 5.33 ms. This paper explores the mechanism leading to high photoluminescence efficiency using organic capping additives. The photoluminescence (PL) graphs reveal broad band emission at 482 nm (blue) and 573 nm (yellow) corresponding to 4 F 9/2 - 6 H 15/2 and 4 F 9/2 - 6 H 13/2 transitions of Dy 3+ , respectively. The Commission International De I-Eclairage (CIE) chromaticity co-ordinates were calculated from emission spectra and the values (x, y) were approaching to standard value of white emission. The synthesized pyrophosphate phosphors can thereby account in multiple potential applications

Luminescence properties of red-emitting M2Si5N8:Eu2+ (M = Ca, Sr, Ba) LED conversion phosphors

NARCIS (Netherlands)

Li, Y.Q.; Steen, van J.E.J.; Krevel, van J.W.H.; Botty, G.; Delsing, A.C.A.; DiSalvo, F.J.; With, de G.; Hintzen, H.T.J.M.

2006-01-01

The influence of the type of the alkaline-earth ion and the Eu2+ concentration on the luminescence properties of Eu2+-doped M2Si5N8 (M = Ca, Sr, Ba) has been investigated. XRD analysis shows that Eu2+-doped Ca2Si5N8 forms a limited solid solution with a maximum solubility of about 7 mol% having a

Transmission electron microscopic study of reduced Ca2UO5

International Nuclear Information System (INIS)

Krasevec, V.; Prodan, A.; Holc, J.; Kolar, D.

1983-01-01

Structural changes of Ca 2 UO 5 during reduction in hydrogen were studied by transmission electron microscopy. It was shown that monoclinic Ca 2 UO 5 changes into triclinic Ca 4 U 2 O 9 . They are related, respectively, to the fluorite and the bixbyite (C-M 2 O 3 ) structures, so that the product is a superstructure of the latter. Reduction occurs along the (100)/sub t/ planes originating from the (006)/sub m/ planes of the parent structure by diminishing the coordination number of the Ca cation from 7 to 6. 5 figures

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

Directory of Open Access Journals (Sweden)

Fushao Li

2015-10-01

Full Text Available Series compounds Ca3(Co0.9M0.12O6 (M=Co, Fe, Mn, Ni with hexagonal crystal structure were prepared by sol–gel route as the cathode materials for solid oxide fuel cells (SOFCs. Effects of the varied atomic compositions on the structure, electrical conductivity, thermal expansion and electrochemical performance were systematically evaluated. Experimental results showed that the lattice parameters of Ca3(Co0.9Fe0.12O6 and Ca3(Co0.9Mn0.12O6 were both expanded to certain degree. Electron-doping and hole-doping effects were expected in Ca3(Co0.9Mn0.12O6 and Ca3(Co0.9Ni0.12O6 respectively according to the chemical states of constituent elements and thermal-activated behavior of electrical conductivity. Thermal expansion coefficients (TEC of Ca3(Co0.9M0.12O6 were measured to be distributed around 16×10−6 K−1, and compositional elements of Fe, Mn, and Ni were especially beneficial for alleviation of the thermal expansion problem of cathode materials. By using Ca3(Co0.9M0.12O6 as the cathodes operated at 800 °C, the interfacial area-specific resistance varied in the order of M=CoCa3(Co0.9Fe0.12O6 showed the best electrochemical performance and the power density as high as ca. 500 mW cm−2 at 800 °C achieved in the single cell with La0.8Sr0.2Ga0.83Mg0.17O2.815 as electrolyte and Ni–Ce0.8Sm0.2O1.9 as anode. Ca3(Co0.9M0.12O6 (M=Co, Fe, Mn, Ni can be used as the cost-effective cathode materials for SOFCs.

Oxidative metabolism and Ca2+ handling in isolated brain mitochondria and striatal neurons from R6/2 mice, a model of Huntington's disease.

Science.gov (United States)

Hamilton, James; Pellman, Jessica J; Brustovetsky, Tatiana; Harris, Robert A; Brustovetsky, Nickolay

2016-07-01

Alterations in oxidative metabolism and defects in mitochondrial Ca 2+ handling have been implicated in the pathology of Huntington's disease (HD), but existing data are contradictory. We investigated the effect of human mHtt fragments on oxidative metabolism and Ca 2+ handling in isolated brain mitochondria and cultured striatal neurons from the R6/2 mouse model of HD. Non-synaptic and synaptic mitochondria isolated from the brains of R6/2 mice had similar respiratory rates and Ca 2+ uptake capacity compared with mitochondria from wild-type (WT) mice. Respiratory activity of cultured striatal neurons measured with Seahorse XF24 flux analyzer revealed unaltered cellular respiration in neurons derived from R6/2 mice compared with neurons from WT animals. Consistent with the lack of respiratory dysfunction, ATP content of cultured striatal neurons from R6/2 and WT mice was similar. Mitochondrial Ca 2+ accumulation was also evaluated in cultured striatal neurons from R6/2 and WT animals. Our data obtained with striatal neurons derived from R6/2 and WT mice show that both glutamate-induced increases in cytosolic Ca 2+ and subsequent carbonilcyanide p-triflouromethoxyphenylhydrazone-induced increases in cytosolic Ca 2+ were similar between WT and R6/2, suggesting that mitochondria in neurons derived from both types of animals accumulated comparable amounts of Ca 2+ Overall, our data argue against respiratory deficiency and impaired Ca 2+ handling induced by human mHtt fragments in both isolated brain mitochondria and cultured striatal neurons from transgenic R6/2 mice. © The Author 2016. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

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

Science.gov (United States)

Ding, Chong; Tang, Wanjun

2018-02-01

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

7 CFR 1219.6 - Customs.

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2010-01-01

... 7 Agriculture 10 2010-01-01 2010-01-01 false Customs. 1219.6 Section 1219.6 Agriculture..., AND INFORMATION Hass Avocado Promotion, Research, and Information Order Definitions § 1219.6 Customs. Customs means the United States Customs Service. ...

Sr/Ca-Sea surface temperature calibration in the branching Caribbean coral Acropora palmata

Science.gov (United States)

Gallup, Christina D.; Olson, Donna M.; Edwards, R. Lawrence; Gruhn, Leah M.; Winter, Amos; Taylor, Frederick W.

2006-02-01

We measured Sr/Ca ratios by thermal ionization mass spectrometry in radial and axial growth of modern Caribbean Acropora palmata corals. Comparison of our results with sea surface temperature (SST) allows radial and axial Sr/Ca-SST calibrations of Sr/Ca (mmol/mol) = 11.30 - 0.07072 × SST (°C) and Sr/Ca (mmol/mol) = 11.32 - 0.06281 x SST (°C), respectively. Application of the calibrations to fossil Acropora palmata from the last glacial maximum in Barbados (Guilderson et al., 1994) imply ~7°C cooler conditions than the present, much larger than the 1-1.5° cooling suggested by modern analog technique foraminifera-based estimates (Trend-Staid and Prell, 2002). If the foraminifera-based estimates are correct, then the excess cooling suggested by the Barbados corals could be explained by a 5% shift in the marine Sr/Ca ratio or an addition of ~20% abiotic secondary aragonite.

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.

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

International Nuclear Information System (INIS)

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

2000-01-01

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

Phase diagrams of systems of Sr2V2O7-M2V2O7 and of Ba2V2O7-M2V2O7 (M=Ca,Cd)

International Nuclear Information System (INIS)

Fotiev, A.A.; Zhuravlev, V.D.; Zhukov, V.P.

1982-01-01

Using the methods of X-ray phase and differential thermal anlyses phase equilibria in the systems Sr 2 V 2 O 7 -M 2 V 2 O 7 and Ba 2 V 2 O 7 -M 2 V 2 O 7 , where M--Ca, Cd, are studied, their phase diagrams being built. New double pyrovanadates Mosub(0.5)Srsub(1.5)Vsub(2)Osub(7) and MBaV 2 O 7 are found [ru

36 CFR 6.7 - Mining wastes.

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2010-07-01

... 36 Parks, Forests, and Public Property 1 2010-07-01 2010-07-01 false Mining wastes. 6.7 Section 6... DISPOSAL SITES IN UNITS OF THE NATIONAL PARK SYSTEM § 6.7 Mining wastes. (a) Solid waste from mining includes but is not limited to mining overburden, mining byproducts, solid waste from the extraction...

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

Energy Technology Data Exchange (ETDEWEB)

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

2015-05-18

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

7 CFR 500.6 - Gambling.

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2010-01-01

... 7 Agriculture 6 2010-01-01 2010-01-01 false Gambling. 500.6 Section 500.6 Agriculture Regulations... NATIONAL ARBORETUM Conduct on U.S. National Arboreturm Property § 500.6 Gambling. Participating in games for money or other personal property, or the operation of gambling devices, the conduct of a lottery...

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

Energy Technology Data Exchange (ETDEWEB)

Craddock, Sarah; Senn, Mark S.

2017-04-15

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

Effect of small quantity of chromium on the electrical, magnetic and magnetocaloric properties of Pr{sub 0.7}Ca{sub 0.3}Mn{sub 0.98}Cr{sub 0.02}O{sub 3} manganite

Energy Technology Data Exchange (ETDEWEB)

Bettaibi, A.; Rahmouni, H. [Universite de Gabes, Laboratoire de Physique des Materiaux et des Nanomateriaux appliquee a l' Environnement, Faculte des Sciences de Gabes cite Erriadh, Gabes (Tunisia); M' nassri, R. [Kairouan University, Higher Institute of Applied Sciences and Technology of Kasserine, Kasserine (Tunisia); Universite de Monastir, Laboratoire de Physico-Chimie des Materiaux, Departement de Physique, Faculte des Sciences de Monastir, Monastir (Tunisia); Selmi, A.; Cheikhrouhou, A. [Sfax University, Laboratory of Physics of Materials, Faculty of Sciences of Sfax, Sfax (Tunisia); Khirouni, K. [Kairouan University, Higher Institute of Applied Sciences and Technology of Kasserine, Kasserine (Tunisia); Chniba Boudjada, N. [Institut NEEL, Grenoble Cedex 09 (France)

2016-03-15

Structural, electrical and thermomagnetic properties of Pr{sub 0.7}Ca{sub 0.3}Mn{sub 0.98}Cr{sub 0.02}O{sub 3} were investigated. Sample was prepared by solid-state reaction method. X-ray diffraction revealed that the sample crystallizes in the orthorhombic system with Pnma space group. Electrical conductivity and complex impedance studies of Pr{sub 0.7}Ca{sub 0.3}Mn{sub 0.98}Cr{sub 0.02}O{sub 3} system are analyzed. The investigated compound exhibits a semiconductor behavior in the whole explored temperature range. From 100 to 206 K, the increase in DC conductance is more than two decade. At higher temperatures, the conductance varies slowly and a saturation region appears. The conduction mechanism is found to be governed by small polaron hopping process which is explained by the short range thermally activated energy. Conductance spectrum is well described by Jonsher law, and the temperature dependence of the frequency exponent confirms that conduction mechanism is governed by hopping process of the localized carriers. Using complex impedance analysis, the compound is modeled by an electrical equivalent circuit. Also, such analysis confirms the contribution of grain boundary to the transport properties. The substitution of Mn by 2 % Cr destroyed the charge order state observed in the parent compound and induced a ferromagnetic phase at low temperatures. For a magnetic field change of 5 T, the material shows a maximum magnetic entropy change ∇S {sup max} = 2.69 J kg{sup -1} K{sup -1} with a full width at half maximum δ {sub TFWHM} = 145 K, and a relative cooling power RCP = 389 J kg{sup -1}. Pr{sub 0.7}Ca{sub 0.3}Mn{sub 0.98}Cr{sub 0.02}O{sub 3} material demonstrates potential proprieties to be used in electronic and thermal devices and as magnetic refrigerant. (orig.)

High-Field Quench Behavior and Protection of $Bi_2 Sr_2 Ca Cu_2 O_x$ Coils: Minimum and Maximum Quench Detection Voltages

Energy Technology Data Exchange (ETDEWEB)

Shen, Tengming [Fermilab; Ye, Liyang [NCSU, Raleigh; Turrioni, Daniele [Fermilab; Li, Pei [Fermilab

2015-01-01

Small insert coils have been built using a multifilamentary Bi2Sr2CaCu2Ox round wire, and characterized in background fields to explore the quench behaviors and limits of Bi2Sr2CaCu2Ox superconducting magnets, with an emphasis on assessing the impact of slow normal zone propagation on quench detection. Using heaters of various lengths to initiate a small normal zone, a coil was quenched safely more than 70 times without degradation, with the maximum coil temperature reaching 280 K. Coils withstood a resistive voltage of tens of mV for seconds without quenching, showing the high stability of these coils and suggesting that the quench detection voltage shall be greater than 50 mV to not to falsely trigger protection. The hot spot temperature for the resistive voltage of the normal zone to reach 100 mV increases from ~40 K to ~80 K with increasing the operating wire current density Jo from 89 A/mm2 to 354 A/mm2 whereas for the voltage to reach 1 V, it increases from ~60 K to ~140 K, showing the increasing negative impact of slow normal zone propagation on quench detection with increasing Jo and the need to limit the quench detection voltage to < 1 V. These measurements, coupled with an analytical quench model, were used to access the impact of the maximum allowable voltage and temperature upon quench detection on the quench protection, assuming to limit the hot spot temperature to <300 K.

7 CFR 1230.6 - Council.

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2010-01-01

... 7 Agriculture 10 2010-01-01 2010-01-01 false Council. 1230.6 Section 1230.6 Agriculture Regulations of the Department of Agriculture (Continued) AGRICULTURAL MARKETING SERVICE (MARKETING AGREEMENTS... CONSUMER INFORMATION Pork Promotion, Research, and Consumer Information Order Definitions § 1230.6 Council...

7 CFR 1215.6 - Department.

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2010-01-01

... 7 Agriculture 10 2010-01-01 2010-01-01 false Department. 1215.6 Section 1215.6 Agriculture Regulations of the Department of Agriculture (Continued) AGRICULTURAL MARKETING SERVICE (MARKETING AGREEMENTS... CONSUMER INFORMATION Popcorn Promotion, Research, and Consumer Information Order Definitions § 1215.6...

7 CFR 1540.6 - Information.

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2010-01-01

... 7 Agriculture 10 2010-01-01 2010-01-01 false Information. 1540.6 Section 1540.6 Agriculture Regulations of the Department of Agriculture (Continued) FOREIGN AGRICULTURAL SERVICE, DEPARTMENT OF... § 1540.6 Information. Persons desiring information from the Department of Agriculture regarding the...

The value of clinical expression of CA series in malignancy diagnosis

International Nuclear Information System (INIS)

Wei Zhenyuan; Wang Jie

2002-01-01

Objective: To study the diagnosis of liver cancer, coloprocto-carcinoma, ovary cancer, pancreatic carcinoma, breast cancer, lung cancer and stomach cancer by labelling immunoassay of CA50, CA125, CA199 and CA153. Methods: The authors had measured the serum content of these tumor markers in 67 liver cancer, 88 coloprocto-carcinoma, 48 ovary cancer, 36 pancreatic carcinoma, 34 breast cancer, 128 lung cancer, 271 stomach cancer and 68 normal controls with labelling immunoassay (LIA). The mean coefficient of variation for intra and inter batch-assay of CA50, CA125, CA199 and CA153 were 3.7% and 8.1%, 4.8% and 10.1%, 7.6% and 12.3%, 8.1% and 10.4% respectively. The average recovery ratio was between 95% and 107%. Results: The levels of CA50 in stomach cancer and coloprocto-carcinoma were significantly higher than those in normal controls (p < 0.001). The levels of CA125 in ovary cancer and lung cancer were significantly higher than in normal controls (p < 0.001). The levels of CA199 in pancreatic carcinoma cancer was significantly higher than those in normal controls (p < 0.001). The levels of CA153 in breast cancer was significantly higher than those in normal controls (p < 0.001). The mean levels of CA50, CA125, CA199 and CA153 in 68 normal controls were 12.4 +- 3.9 U/ml, 14.3 +- 3.9 U/ml, 14.3 +- 10.5 U/ml, 10.0 +- 8.4 U/ml and 15.2 +- 7.5 U/ml respectively. Conclusion: In present study of 672 cases, CA50 measurement seems to be most useful for diagnosis of gastric and coloprocto-carcinoma, CA125 for ovarian cancer, CA199 for pancreatic cancer and CA153 for breast cancer (p < 0.001)

The Pr and Ca Substitution in GdBa2Cu3O7- & delta

Directory of Open Access Journals (Sweden)

H. S. H.

2001-12-01

Full Text Available   The granular Gd1-x-zPrxCazBa2Cu3O7-δ high-temperature cuprate samples with 0.0 ≤ x ≤ 0.3 and 0.0≤ x ≤ 0.35 are prepared by standard solid state reaction and characterized by XRD and SEM techniques. The BaCuO2 and impurity phases are less than 1% in the samples having high levels of pr and Ca concentrations. The electrical resistivity measurements show a nonlinear reduction in Tc(x,z=etc versus x. Moreover, the Tc(z curve with x=0 is nonlinear and aplateau appears at z≈ 0.05-0.015. For Pr-Ca-doped samples with a constant concentration of Pr, Tc increases with the increase of Ca up to an optimum value of Ca doping and then in decreases. Based on these observations, we suggest that hole filling and hole localization the main effects of Pr ion substiution. The magnetic measurements indicate that the value of Hc1 is in the order of 10 mT. The mangetoresistance measurements have been measured and analyzed. The superconducting transition region is broadened by the application of magnetic field. The experimental data near the onsen of superconductivity are fitted with the Ambegakor and Halperin (AH phase-slip model. We observe that the AH parameter,γ (H, depends not only on the temperature and the magnetic field, but also on the Pr and Ca ions concentrations. It is observed that the critical current density increases with Ca substitution and decreases with Pr substitution in Gd-123 system. We suggest that the Pr ion substitution probably enhances the weak link, but the Ca ion acts as flux pinning center in the GdPrCa-123 system.

7 CFR 501.6 - Gambling.

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2010-01-01

... 7 Agriculture 6 2010-01-01 2010-01-01 false Gambling. 501.6 Section 501.6 Agriculture Regulations... CONDUCT ON U.S. MEAT ANIMAL RESEARCH CENTER, CLAY CENTER, NEBRASKA § 501.6 Gambling. Participating in games for money or other personal property, or the operation of gambling devices, the conduct of a...

PLC-dependent intracellular Ca2+ release was associated with C6-ceramide-induced inhibition of Na+ current in rat granule cells.

Science.gov (United States)

Liu, Zheng; Fei, Xiao-Wei; Fang, Yan-Jia; Shi, Wen-Jie; Zhang, Yu-Qiu; Mei, Yan-Ai

2008-09-01

In this report, the effects of C(6)-ceramide on the voltage-gated inward Na(+) currents (I(Na)), two types of main K(+) current [outward rectifier delayed K(+) current (I(K)) and outward transient K(+) current (I(A))], and cell death in cultured rat cerebellar granule cells were investigated. At concentrations of 0.01-100 microM, ceramide produced a dose-dependent and reversible inhibition of I(Na) without alteration of the steady-state activation and inactivation properties. Treatment with C(2)-ceramide caused a similar inhibitory effect on I(Na). However, dihydro-C(6)-ceramide failed to modulate I(Na). The effect of C(6)-ceramide on I(Na) was abolished by intracellular infusion of the Ca(2+)-chelating agent, 1,2-bis (2-aminophenoxy) ethane-N, N, N9, N9-tetraacetic acid, but was mimicked by application of caffeine. Blocking the release of Ca(2+) from the sarcoplasmic reticulum with ryanodine receptor blocker induced a gradual increase in I(Na) amplitude and eliminated the effect of ceramide on I(Na). In contrast, the blocker of the inositol 1,4,5-trisphosphate-sensitive Ca(2+) receptor did not affect the action of C(6)-ceramide. Intracellular application of GTPgammaS also induced a gradual decrease in I(Na) amplitude, while GDPbetaS eliminated the effect of C(6)-ceramide on I(Na). Furthermore, the C(6)-ceramide effect on I(Na) was abolished after application of the phospholipase C (PLC) blockers and was greatly reduced by the calmodulin inhibitors. Fluorescence staining showed that C(6)-ceramide decreased cell viability and blocking I(Na) by tetrodotoxin did not mimic the effect of C(6)-ceramide, and inhibiting intracellular Ca(2+) release by dantrolene could not decrease the C(6)-ceramide-induced cell death. We therefore suggest that increased PLC-dependent Ca(2+) release through the ryanodine-sensitive Ca(2+) receptor may be responsible for the C(6)-ceramide-induced inhibition of I(Na), which does not seem to be associated with C(6)-ceramide-induced granule

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

Energy Technology Data Exchange (ETDEWEB)

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

2017-09-11

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

6 CFR 7.2 - Scope.

Science.gov (United States)

2010-01-01

..., National Industrial Security Program, and its implementing directives. (c) This part is independent of and... 6 Domestic Security 1 2010-01-01 2010-01-01 false Scope. 7.2 Section 7.2 Domestic Security DEPARTMENT OF HOMELAND SECURITY, OFFICE OF THE SECRETARY CLASSIFIED NATIONAL SECURITY INFORMATION § 7.2 Scope...

Corrosion behaviour of the welded steel 1.4313/CA6-NM

OpenAIRE

Lovíšek, Martin; Liptáková, Tatiana; Pešlová, Františka

2014-01-01

The stainless steel 1.4313/CA6-NM (EN X3CrNiMo13-4) is used for turbine production. The weld joints are therefore very sensitive localities from mechanical and corrosion point of view. The subject of the work is corrosion studying of the steel welded by TIG method with consequent heat treatment. Corrosion resistance of the weld joints and base material are evaluated through potentiodynamic polarization test measured on the surface after heat treatment and on the surface cleaned by grinding an...

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

Directory of Open Access Journals (Sweden)

Díez, J. C.

2008-06-01

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

Structural, vibrational and luminescence properties of the (1−x)CaWO{sub 4}−xCdWO{sub 4} system

Energy Technology Data Exchange (ETDEWEB)

Taoufyq, A. [Institut Matériaux Microélectronique et Nanosciences de Provence, Aix Marseille Université, CNRS, Université de Toulon, IM2NP UMR 7334, 83957, La Garde (France); Laboratoire Matériaux et Environnement LME, Faculté des Sciences, Université Ibn Zohr, BP 8106, Cité Dakhla, Agadir, Maroc (Morocco); CEA/DEN, Département d’Études des Réacteurs, Laboratoire Dosimétrie Capteurs Instrumentation, CEA Cadarache, 13108, Saint-Paul-lez-Durance (France); Société CESIGMA, Signals and Systems, 1576 Chemin de La Planquette, 83130 La Garde (France); Guinneton, F.; Valmalette, J-C.; Arab, M. [Institut Matériaux Microélectronique et Nanosciences de Provence, Aix Marseille Université, CNRS, Université de Toulon, IM2NP UMR 7334, 83957, La Garde (France); Benlhachemi, A.; Bakiz, B. [Laboratoire Matériaux et Environnement LME, Faculté des Sciences, Université Ibn Zohr, BP 8106, Cité Dakhla, Agadir, Maroc (Morocco); Villain, S. [Institut Matériaux Microélectronique et Nanosciences de Provence, Aix Marseille Université, CNRS, Université de Toulon, IM2NP UMR 7334, 83957, La Garde (France); and others

2014-11-15

In the present work, we investigate the structural, microstructural, vibrational and luminescence properties of the system (1−x)CaWO{sub 4}−xCdWO{sub 4} with x ranging between 0 and 1. Polycrystalline samples were elaborated using a coprecipitation technique followed by thermal treatment at 1000 °C. The samples were then characterized using X-ray diffraction, scanning electron microscopy, Raman spectroscopy and luminescence analyses. X-ray diffraction profile analyses using Rietveld method showed that two kinds of solid solutions Ca{sub 1−x}Cd{sub x}WO{sub 4} having scheelite and wolframite structures, with respectively tetragonal and monoclinic crystal cells, were observed, with a biphasic system for compositions x=0.6 and 0.7. The scanning electron microscopy experiments showed a complex evolution of morphologies and crystallite sizes as x increased. The vibration modes of Raman spectra were characteristic of composition-dependent disordered solid solutions with decreasing wavenumbers as x increased. Luminescence experiments were performed under UV-laser light irradiation. The energies of emission bands increased linearly with cadmium composition x. The integrated intensity of luminescence reached a maximum value for the substituted wolframite phase with composition x=0.8. - Graphical abstract: Luminescence on UV excitation (364.5 nm) of (1−x)CaWO{sub 4−x}CdWO{sub 4} system, elaborated from coprecipitation technique at 1000 °C, with 0Ca{sub 1−x}Cd{sub x}WO{sub 4} polycrystalline phases with 0≤x≤0.5. (b) Maximum of luminescence intensity for the composition x=0.8. - Highlights: • Solid solutions Ca{sub 1−x}Cd{sub x}WO{sub 4} are elaborated from coprecipitation technique. • The structures of two types of solid solutions are refined using Rietveld method. • A maximum of luminescence is obtained for an intermediate composition x=0.8.

6 CFR 13.7 - Complaint.

Science.gov (United States)

2010-01-01

... 6 Domestic Security 1 2010-01-01 2010-01-01 false Complaint. 13.7 Section 13.7 Domestic Security DEPARTMENT OF HOMELAND SECURITY, OFFICE OF THE SECRETARY PROGRAM FRAUD CIVIL REMEDIES § 13.7 Complaint. (a) On or after the date the Department of Justice approves the issuance of a Complaint in accordance...

Luminescence properties of Eu{sup 2+} in silver decacalcium heptakis-orthophosphate AgCa{sub 10}(PO{sub 4}){sub 7}

Energy Technology Data Exchange (ETDEWEB)

Zhang, Hongzhi [School of Materials Science and Engineering, Central South University of Forestry and Technology, Changsha 410004 (China); Zhang, Xinmin, E-mail: zhangxm@csuft.edu.cn [School of Materials Science and Engineering, Central South University of Forestry and Technology, Changsha 410004 (China); Wu, Luyi; Zheng, Wei; Jiang, Wei [School of Materials Science and Engineering, Central South University of Forestry and Technology, Changsha 410004 (China); He, Mengdong [Institute of Mathematics and Physics, Central South University of Forestry and Technology, Changsha 410004 (China); Yuan, Guangming [School of Materials Science and Engineering, Central South University of Forestry and Technology, Changsha 410004 (China); Seo, Hyo Jin [Department of Physics and Interdisciplinary Program of Biomedical, Mechanical & Electrical Engineering, Pukyong National University, Busan 608-737 (Korea, Republic of)

2017-05-15

The luminescence properties of Eu{sup 2+} in AgCa{sub 10}(PO{sub 4}){sub 7} has been studied at room and low temperature and the decay times of Eu{sup 2+} in this matrix have been measured and analyzed. According to the crystal structure of AgCa{sub 10}(PO{sub 4}){sub 7}, photoluminescence (PL) spectra and decay curves, the substitution of Eu{sup 2+} ions is possible to four different Ca{sup 2+} sites. The red-shift of emission wavelength and energy transfer process between Eu{sup 2+} activator ions are discussed.

31 CFR 7.6 - Effect of awards.

Science.gov (United States)

2010-07-01

... 31 Money and Finance: Treasury 1 2010-07-01 2010-07-01 false Effect of awards. 7.6 Section 7.6 Money and Finance: Treasury Office of the Secretary of the Treasury EMPLOYEE INVENTIONS § 7.6 Effect of awards. The acceptance by an employee of a cash award for performance which constitutes an invention...

Substitution effect of Sr2+ by Ca2+ on structure and superconducting properties of Bi2Sr1.6La0.4CuO6+δ (Bi-2201) ceramics

Science.gov (United States)

Boudjaoui, S.; Amira, A.; Mahamdioua, N.; Altintas, S.; varilci, A.; Terzioglu, C.

2018-02-01

In this work, the effect of Ca2+ iso-valence substitution for Sr2+ on properties of Bi2Sr1.6La0.4CuO6+δ superconductors is presented. Samples series with nominal composition of Bi2Sr1.6-xCaxLa0.4CuO6+δ (x= 0, 0.2, 0.4, 0.6 and 0.8) are prepared by a solid-state reaction method. When Ca content is increased, the X-ray diffraction technique shows that the cell parameters a and c decrease, while b one is almost constant. The scanning electron microscopy analysis reveals that the substitution has no significant effect on the porosity and the grain size of the samples. The physical properties of the samples are studied by the analysis of the magneto-resistivity curves measured under magnetic fields in the range 0-1 T. As Ca is added, the results show that the high temperature transition appears and is pushed up to 94.87 K for x=0.8. The substitution also improves the bulk onset critical transition temperature, the transition width, the residual resistivity, the activation energy of vortices and the irreversibility field. The best results are seen for x=0.4 of Ca content.

Crystal structures of double vanadates Ca9R(VO4)7. 1. R = La, Pr and Eu

International Nuclear Information System (INIS)

Belik, A.A.; Morozov, V.A.; Lazoryak, B.I.; Khasanov, S.S.

1997-01-01

Crystalline structures of Ca 9 R(VO 4 ) 7 (R = La(1), Pr(2), Eu(3)) were studied by means of the complete profile analysis. The compounds crystallize in trigonal syngony (sp.gr. R3c, Z=6) with the following parameters of the elementary cells: 1 - a=10.8987(5), c = 38.147(1) A, V = 3924.1(3) A; 2 - a 10.8808(7), c = 38.135(1) A, V = 3910.0(3) A; 3 - a = 10.8651(1), c 38.089(1) A, V = 3894.0(3) A 3 . The rare-earth element cations together with calcium population density of the rare-earth element cations in the positions changes regularly depending on their radius. In some compounds starting from La up to Eu the population density of the rare-earth element cations in M(3) position decreases, while that in M(1) and M(2) position - increases

Tinjauan Teologis: Allah Menyesal Berdasarkan Perspektif Kitab Kejadian Pasal 6:6-7

Directory of Open Access Journals (Sweden)

Yetris Elbaar

2013-10-01

Full Text Available Tujuan penelitian ini adalah Pertama, untuk menjelaskan makna Allahmenyesal melalui pemaparan eksposisi nas di dalam kitab Kejadian 6:6-7, supayadapat menghasilkan kerangka pemahaman yang benar tentang Allah sebagaiPencipta. Kedua, untuk mendapatkan pemahaman yang benar mengenai Allahmenyesal berdasarkan penjelasan implikasi teologis. Ketiga, supaya orang percayadapat mengerti makna mengenai Allah menyesal dalam kitab Kejadian 6:6-7 yangdijabarkan dalam implikasi praktis.Penulisan karya ilmiah ini menggunakan metodologi eksposisi, denganmenggunakan prinsip-prinsip hermeneutika, yaitu dengan kajian eksegesis Alkitabmengenai Allah menyesal berdasarkan Kejadian 6:6-7 dan melalui penelitiankualitatif, yaitu dengan penggunaan buku-buku di perpustakaan yang berkaitandengan konsep judul karya ilmiah.Kesimpulan karya ilmiah ini adalah: Pertama, Allah yang menyesal adalahAllah yang konsisten terhadap sifat dan karakter-Nya. Kedua, Allah yang menyesaladalah Allah yang harus dipahami melalui konteks firman Tuhan. Berdasarkankonteks Kejadian 6:6-7 Allah menyesal adalah Allah yang menyatakan pengakuan-Nya sebagai pencipta (6:6. Dan Mengungkapkan keputusan Allah (6:7. Ketiga,Allah menyesal adalah Allah yang tidak dapat menyangkal diri-Nya sebagai Allahyang ingin menyatakan bahwa Ia sangat berduka, tetapi harus menyatakankeadilannya sebagai Allah dan harus menghukum kejahatan manusia. Keempat,Allah menyesal adalah Allah yang menghendaki supaya manusia hidup dalamperaturan dan hukum-hukum yang Allah tetapkan dalam kehidupannya.

7 CFR 12.6 - Administration.

Science.gov (United States)

2010-01-01

... 7 Agriculture 1 2010-01-01 2010-01-01 false Administration. 12.6 Section 12.6 Agriculture Office....6 Administration. (a) General. A determination of ineligibility for benefits in accordance with the... making such determinations, as provided in this section. (b) Administration by FSA. (1) The provisions of...

New vanadium oxides with perovskite type structure: AThV/sub 2/O/sub 6/ (A=Ca,Sr)

Energy Technology Data Exchange (ETDEWEB)

Vidyasagar, K; Gopalakrishnan, J

1982-07-01

New perovskite oxides of the formula AThV/sub 2/O/sub 6/ (A=Ca,Sr) have been prepared by reduction of the corresponding AThV/sub 2/O/sub 8/ under hydrogen atmosphere. CaThV/sub 2/O/sub 6/ crystallizes in an orthorhombic LaVO/sub 3/ type structure, while the strontium compound exhibiting cation-deficient nonstoichiometry. SrThsub(1-x)V/sub 2/O/sub 6/ (x approx. 0.4), is cubic. The magnetic susceptibility behaviour of the calcium compound is similar to that of V/sup 3 +/ perovskites, while the strontium compound exhibits a large increase in susceptibility below 130K, the behaviour being likely to be associated with the mixed-valence character of vanadium.

No-carrier-added (NCA) synthesis of 6-[18F]fluoro-L-DOPA using 3,5,6,7,8,8a-hexahydro-7,7,8a-trimethyl-[6S-(6α, 8α, 8αβ)]-6,8-methano-2H-1,4-benzoxazin-2-one

International Nuclear Information System (INIS)

Horti, A.; Yale Univ., West Haven, CT; Redmond, D.E. Jr.; Soufer, R.

1995-01-01

3,5,6,7,8,8a-Hexahydro-7,7,8a-trimethyl-[6S-(6α,8α , 8αβ)]-6,8-methano-2H-1,4-benzoxazino-2-one (2) was investigated as chiral auxiliary for asymmetric NCA nucleophilic synthesis of 6-[ 18 F]Fluoro-L-DOPA. Direct condensation of 3,4-dimethoxy-2-[ 18 F]fluorobenzaldehyde (1a) or 6-[ 18 F]fluoro-piperonal (1b) in the presence of NaH with 2 gave the corresponding [ 18 F]-3-[(2-fluorophenyl)methylene]-3,5,6,7,8,8a-hexahydro-7,7,8 a-trimethyl-[6S-(3Z,3α,6α,8α,8αβ)]-6, 8-methano-2H-1,4-benzoxazin-2-one derivative 3a or 3b as a single stereoisomer. L-Selectride promoted hydrogenation of the olefinic double bond of these derivatives, in presence of tertbutyl alcohol, afforded the corresponding [ 18 F]-3-[(2-fluorophenyl) methyl]-3,5,6,7,8,8a-hexahydro-7,7,8a-trimethyl-[3S-(3α, 6α, 8α8αβ)]-6,8-methano-2H-1,4-benzoxazin-2-one derivatives (4a,b) without affecting the orientation of diasterofacial discrimination. Deprotection of the derivatives 4a,b yielded 6-[ 18 F]fluoro-L-DOPA (e.e. >90%, 3% radiochemical yield (EOB), total synthesis time 125 min, specific activity >2000 mCi/μmol). Direct deprotection/reduction of the compounds 3a,b provides the enantiomeric mixture of 6-[ 18 F]fluoro-D,L-DOPA (10-12% radiochemical yield) and, after chiral separation, 6-[ 18 F]fluoro-L-DOPA (e.e. 98%, 4-5% radiochemical yield). (author)

Crystallographic and electronic structure of the Ca{sub 2}TiMnO{sub 6} double perovskite

Energy Technology Data Exchange (ETDEWEB)

López, J.P. Garzón [Grupo de Física de Nuevos Materiales, Departamento de Física, Universidad Nacional de Colombia, AA 5997 Bogotá DC (Colombia); Grupo de Estudios de Materiales – GEMA, Departamento de Física, Universidad Nacional de Colombia, AA 5997 Bogotá DC (Colombia); Cardona, R. [Grupo de Estudios de Materiales – GEMA, Departamento de Física, Universidad Nacional de Colombia, AA 5997 Bogotá DC (Colombia); Santos, A. Sarmiento [Grupo de Superficies, Electroquímica y Corrosión, Universidad Pedagógica y Tecnológica de Colombia, Tunja (Colombia); Téllez, D.A. Landínez [Grupo de Física de Nuevos Materiales, Departamento de Física, Universidad Nacional de Colombia, AA 5997 Bogotá DC (Colombia); Roa-Rojas, J., E-mail: jroar@unal.edu.co [Grupo de Física de Nuevos Materiales, Departamento de Física, Universidad Nacional de Colombia, AA 5997 Bogotá DC (Colombia)

2014-12-15

In this work, we report synthesis and crystalline structure study of the Ca{sub 2}TiMnO{sub 6} complex perovskite, by X-ray diffraction experiments and through the application of the Rietveld refinement using the GSAS code. Results revealed the crystallization of the system in a tetragonal perovskite with the characteristic structure given by I4/m (#87) space group and lattice parameters a=5.339(4) Å and c=7.736(6) Å. Ab initio calculations of density of states (DOS) and electronic structure were carried out for this perovskite-like system, by the Density Functional Theory (DFT) and using the Full-potential Linearized Augmented Plane Waves (FP-LAPW) method. The exchange-correlation potential was treated using the Generalized Gradient Approximation (GGA). All calculations were carried-out using spin polarization. For the up spin orientation the compound has a semiconducting behavior and for down spin polarization it behaves like a conductor. The calculated effective magnetic moment in cell was 4.02 μ{sub B}, which is close to the expected value calculated from Hund's rules.

ORIGIN FOR IRRADIATION EFFECT OF 0．56GeV C6＋ ON CaVSn：YIG

Institute of Scientific and Technical Information of China (English)

熊宏齐; 侯明东; 等

1995-01-01

This paper presents numerous physical characteristics of Ca,V.Sn doped yttrium iron garnet(CaVSn:YIG) irradiated with 0.56GeV carbon ions delivered by the Heavy Ion Research Facility of Lanzhou (HIRFL).The reason for change of the magnetic properties of the samples induced by energetic carbon ions bombardment is discussed.By comparison of this results with the irradiation effects of YIG induced by eneregetic argon,krypton and xenon oibtained on the GANIL,Caen,France,it is concluded that the irradiation effect of 0.56GeV C6+ on CaVSn:YIG arises from the electronic energy losses.

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

International Nuclear Information System (INIS)

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

1997-01-01

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

New borohydride anion B6H7-

International Nuclear Information System (INIS)

Kuznetsov, I.Yu.; Vinitskij, D.M.; Solntsev, K.A.

1985-01-01

The [Ni(Bipy) 3 ] (B 6 H 7 ) 2 , (Ph 4 P)B 6 H 7 , [Ni(Phen) 3 ](B 6 H 7 ) 2 crystals (where Bipy = bipyridine, Phen = phenathroline, Ph = phenyl) are obtained via the exchange reaction with a subsequent recrystallization from aqua-acetonic and acetonic solutions. The structure is studied of a new borohydride anion B 6 H 7 - possessing a four-valence bond unique for polyhedral borohydride anions. A triangular face of boride skeleton coordinating a hydrogen atom is considerably larger than other faces, and the electron density on this hydrogen atom is evidently much higher than at the end hydride hydrogen atoms. The trend of B 6 H 7 - anion to form statistically disordered structurs testifies to a rather slight effect of the seventh hydrogen atom position on the structure pattern of the ionic crystal lattice

Hydriding and dehydriding properties of CaSi

International Nuclear Information System (INIS)

Aoki, Masakazu; Ohba, Nobuko; Noritake, Tatsuo; Towata, Shin-ichi

2005-01-01

The hydriding and dehydriding properties of CaSi were investigated both theoretically and experimentally. First-principles calculations suggested that CaSiH n is thermodynamically stable. Experimentally, the p -c isotherms clearly demonstrated plateau pressures in a temperature range of 473-573 K and the maximum hydrogen content was 1.9 weight % (wt.%) under a hydrogen pressure of 9 MPa at 473 K. The structure of CaSiH n is different from those of ZrNi hydrides, although CaSi has the CrB-type structure as well as ZrNi

7 CFR 6.20 - Introduction.

Science.gov (United States)

2010-01-01

... 7 Agriculture 1 2010-01-01 2010-01-01 false Introduction. 6.20 Section 6.20 Agriculture Office of the Secretary of Agriculture IMPORT QUOTAS AND FEES Dairy Tariff-Rate Import Quota Licensing § 6.20 Introduction. (a) Presidential Proclamation 6763 of December 23, 1994, modified the Harmonized Tariff Schedule...

Luminescent properties of phosphor converted LED using an orange-emitting Rb{sub 2}CaP{sub 2}O{sub 7}:Eu{sup 2+} phosphor

Energy Technology Data Exchange (ETDEWEB)

Song, Hee Jo; Yim, Dong Kyun [Department of Materials Science and Engineering, College of Engineering, Seoul National University, Daehak-dong, Gwanak-gu, Seoul 151-744 (Korea, Republic of); Cho, In-Sun [Department of Mechanical Engineering, Stanford University, CA 94305 (United States); Roh, Hee-Suk; Kim, Ju Seong [Department of Materials Science and Engineering, College of Engineering, Seoul National University, Daehak-dong, Gwanak-gu, Seoul 151-744 (Korea, Republic of); Kim, Dong-Wan, E-mail: dwkim@ajou.ac.kr [Department of Materials Science and Engineering, Ajou University, Woncheon-dong, San 5, Yeongtong-gu, Suwon 443-749 (Korea, Republic of); Hong, Kug Sun, E-mail: kshongss@plaza.snu.ac.kr [Department of Materials Science and Engineering, College of Engineering, Seoul National University, Daehak-dong, Gwanak-gu, Seoul 151-744 (Korea, Republic of)

2012-12-15

Graphical abstract: Display Omitted Highlights: ► Phase-pure Rb{sub 2}CaP{sub 2}O{sub 7}:Eu{sup 2+} powders were synthesized by a solid state reaction process. ► The optimum emission intensity was observed at the Eu{sup 2+} ion concentration of 0.006. ► The dipole–dipole interaction was the major concentration quenching mechanism. ► The pc-LED coated with Rb{sub 2}CaP{sub 2}O{sub 7}:Eu{sup 2+} had higher CRI than commercial red phosphor. -- Abstract: A series of orange-emitting Rb{sub 2}CaP{sub 2}O{sub 7}:Eu{sup 2+} phosphors were synthesized by a conventional solid-state reaction method. The as-prepared phosphors were characterized by X-ray powder diffraction (XRD), fluorescence spectroscopy, and spectroradiometry. XRD showed that all prepared samples exhibited a monoclinic Rb{sub 2}CaP{sub 2}O{sub 7} phase. Fluorescence spectroscopy showed that the photoluminescence efficiency of Rb{sub 2}Ca{sub 1−x}P{sub 2}O{sub 7}:Eu{sub x}{sup 2+} phosphors increased with increasing Eu{sup 2+} concentration until x = 0.006, then decreased at higher concentrations, due to a concentration quenching effect. The thermal activation energy was also measured to be 0.40 eV. Furthermore, a phosphor-converted LED (pc-LED) coated with Rb{sub 2}Ca{sub 0.994}P{sub 2}O{sub 7}:Eu{sub 0.006}{sup 2+} was fabricated, which exhibited bright orange emission under a forward bias, from 200 to 300 mA. The color rendering index (CRI) of pc-LED coated with Rb{sub 2}Ca{sub 0.994}P{sub 2}O{sub 7}:Eu{sub 0.006}{sup 2+} was higher than the CRI of pc-LED coated with commercial red phosphor, due to the broad emission band of Rb{sub 2}CaP{sub 2}O{sub 7}:Eu{sup 2+} phosphor. In applying with three-band pc-LEDs, moreover, white pc-LED using Rb{sub 2}CaP{sub 2}O{sub 7}:Eu{sup 2+} phosphor had a higher CRI, than using commercial phosphor. These results indicated that Rb{sub 2}CaP{sub 2}O{sub 7}:Eu{sup 2+} phosphor could be a good candidate for a near-UV based w-LED.

Synthesis of Al₂Ca Dispersoids by Powder Metallurgy Using a Mg-Al Alloy and CaO Particles.

Science.gov (United States)

Fujita, Junji; Umeda, Junko; Kondoh, Katsuyoshi

2017-06-28

The elemental mixture of Mg-6 wt %Al-1 wt %Zn-0.3 wt %Mn (AZ61B) alloy powder and CaO particles was consolidated by an equal-channel angular bulk mechanical alloying (ECABMA) process to form a composite precursor. Subsequently, the precursor was subjected to a heat treatment to synthesize fine Al₂Ca particles via a solid-state reaction between the Mg-Al matrix and CaO additives. Scanning electron microscopy-energy-dispersive spectroscopy (SEM-EDS) and electron probe micro-analysis on the precursor indicated that 4.7-at % Al atoms formed a supersaturated solid solution in the α-Mg matrix. Transmission electron microscopy-EDS and X-ray diffraction analyses on the AZ61B composite precursor with 10-vol % CaO particles obtained by heat treatment confirmed that CaO additives were thermally decomposed in the Mg-Al alloy, and the solid-soluted Ca atoms diffused along the α-Mg grain boundaries. Al atoms also diffused to the grain boundaries because of attraction to the Ca atoms resulting from a strong reactivity between Al and Ca. As a result, needle-like (Mg,Al)₂Ca intermetallics were formed as intermediate precipitates in the initial reaction stage during the heat treatment. Finally, the precipitates were transformed into spherical Al₂Ca particles by the substitution of Al atoms for Mg atoms in (Mg,Al)₂Ca after a long heat treatment.

Magnetic and magnetocaloric properties in Ba-doped La0.7Ca0.3MnO3 nanoparticles

International Nuclear Information System (INIS)

Thanh, Tran Dang; Linh, Dinh Chi; Uyen Tuyen, Ngo Thi; Phan, The-Long; Yu, Seong-Cho

2015-01-01

La 0.7 Ca 0.3−x Ba x MnO 3 nanoparticles with the crystalline size d = 38 and 39 nm for x = 0.025, and 0.05, respectively, were synthesized by utilizing the solid-state reaction and mechanical ball milling methods. We have used the Banerjee's criteria, the mean-field, and the thermodynamic theories, and isothermal magnetization, M(H), data around Curie temperature (T C ) to investigate the magnetic phase transformation and the temperature (T) and magnetic field (H) dependences of magnetic entropy change, ΔS m (T, H), for nanoparticles. These exhibit the samples undergoing a second-order magnetic phase transition with an existence of the short-range ferromagnetic order in the samples. Under an applied magnetic field change ΔH = 30 kOe, the maximum value of ΔS m (denoted as |ΔS max |) are obtained about 4.4 J kg −1 K −1 corresponding to a relative cooling power (RCP) value about 140 J kg −1 . Field dependences of |ΔS max | and RCP can be expressed by the power laws, |ΔS max | = a × H n and RCP = b × H N , where a and b are coefficients, n and N are the field exponents, respectively. Interestingly, all the ΔS m (T, H) curves measured at different applied fields are collapsed onto a universal curve, ΔS m (T, H)/ΔS max versus θ = (T − T C )/(T r − T C ), where T r is the reference temperature. - Highlights: • An existence of the short-range FM order in the La 0.7 Ca 0.3−x Ba x MnO 3 nanoparticles. • High magnetic entropy change, wide operative temperature range, and high RCP value. • Field dependences of |ΔS max | and RCP can be expressed by the power laws. • All the ΔS m (T, H) data are followed a universal master curve

7 CFR 6.9 - Information.

Science.gov (United States)

2010-01-01

... 7 Agriculture 1 2010-01-01 2010-01-01 false Information. 6.9 Section 6.9 Agriculture Office of the Secretary of Agriculture IMPORT QUOTAS AND FEES General Provisions § 6.9 Information. Persons desiring information from the Department of Agriculture regarding section 22 or section 8(a), or any action with...

Processing, structure and magnetic properties correlation in co-precipitated Ca-ferrite

Energy Technology Data Exchange (ETDEWEB)

Abasht, Behzad, E-mail: abasht@gmail.com [Space Thruster Research Institute, Iranian Space Research Center, Tabriz (Iran, Islamic Republic of); Department of Metallurgy and Materials Engineering, Iran University of Science and Technology, Tehran (Iran, Islamic Republic of); Beitollahi, Ali; Mirkazemi, Seyyed Mohammad [Department of Metallurgy and Materials Engineering, Iran University of Science and Technology, Tehran (Iran, Islamic Republic of)

2016-12-15

La-substituted hexagonal calcium ferrite, Ca{sub 1−X}La{sub X}Fe{sub 12}O{sub 19} (x varies from 0 to 0.6 with the step of 0.2), was synthesized by applying co-precipitation method, in which the molar ratio of Fe{sup 3+}/(Ca{sup 2+}+La{sup 2+}) was 11. The ferrite precursors were prepared from aqueous solution of calcium nitrate, ferric nitrate and lanthanum nitrate by co-precipitation of calcium, iron and lanthanum ions by using an aqueous base of sodium hydroxide (1.5 M) at the pH of 14 and at room temperature. These precursors were calcinated with different amount of La at different temperature of 700, 1100 and 1200 °C for constant calcination time of 1 h in a static air atmosphere. Some tests such as simultaneous thermal analysis (STA), X-ray diffraction (XRD), scanning electron microscopy (SEM) and vibrating sample magnetometer (VSM) were carried out to investigate the thermal behavior, crystallographic properties, morphology and magnetic properties of the precursor powders which were calcinated at different temperatures. The powder XRD patterns of samples which consisted of La as dopant and were calcinated at 1200 °C for 1 h, indicates the formation of calcium hexaferrite and also α-Fe{sub 2}O{sub 3} besides Magnetoplumbite-phase (M-phase). However, the results showed that CaFe{sub 4}O{sub 7} and α-Fe{sub 2}O{sub 3} phases were formed in the sample with the same condition but without using any dopant. The results of SEM showed that the calcium hexaferrite particle were regular hexagonal platelets with the size range of 1–2 µm. The magnetic properties such as maximum magnetization (M{sub Max}), remanent magnetization (M{sub r}) and coercivity (H{sub c}) were measured from the hysteresis loops. Low values of coercive field (16.3 kA m{sup −1}) and maximum magnetization (50.6 A m{sup 2} kg{sup −1}) were obtained from calcium hexaferrite particle in optimum amount of La (X=0.4) which calcinated at the temperature of 1200 °C. - Highlights: • In this

Electronic Structure of TIBa(sub 2)CaCu(sub 2)O(sub 7-delta)

Science.gov (United States)

Vasquez, R. P.; Novikov, D. L.; Freeman, A. J.; Siegal, M. P.

1996-01-01

The core levels of TIBa(sub 2)CaCu(sub 2)O(sub 7-delta) epitaxial films have been measured with x-ray photoelectron spectroscopy (XPS). The valence electronic structure has been determined using the full-potential linear muffin tin orbital band structure method and measured with XPS.

NIR to visible upconversion in Er3+/Yb3+ co-doped CaYAl3O7 phosphor obtained by solution combustion process

International Nuclear Information System (INIS)

Singh, Vijay; Rai, Vineet Kumar; Al-Shamery, Katharina; Nordmann, Joerg; Haase, Markus

2011-01-01

Using the combustion synthesis, CaYAl 3 O 7 :Er 3+ phosphor powders co-doped with Yb 3+ have been prepared at low temperatures (550 o C) in a few minutes. Formation of the compound was confirmed by X-ray powder diffraction. Near-infrared to visible upconversion fluorescence emission in the Er 3+ doped CaYAl 3 O 7 phosphor powder has been observed. The effect of co-doping with triply ionized ytterbium in the CaYAl 3 O 7 :Er 3+ phosphor has been studied and the process involved is discussed. - Highlights: → The green emitting up-conversion CaYAl 3 O 7 :Er 3+ phosphor powders co-doped with Yb 3+ have been prepared by easy combustion method. → The combustion method is a simple, energy saving, fast and economical viable process. → The luminescence intensity in the co-doped phosphor is enhanced by several times compared to that of the singly (Er 3+ ) doped phosphor.

Activation of functional α7-containing nAChRs in hippocampal CA1 pyramidal neurons by physiological levels of choline in the presence of PNU-120596.

Directory of Open Access Journals (Sweden)

Bopanna I Kalappa

2010-11-01

Full Text Available The level of expression of functional α7-containing nicotinic acetylcholine receptors (nAChRs in hippocampal CA1 pyramidal neurons is believed to be very low compared to hippocampal CA1 interneurons, and for many years this expression was largely overlooked. However, high densities of expression of functional α7-containing nAChRs in CA1 pyramidal neurons may not be necessary for triggering important cellular and network functions, especially if activation of α7-containing nAChRs occurs in the presence of positive allosteric modulators such as PNU-120596.An approach previously developed for α7-containing nAChRs expressed in tuberomammillary neurons was applied to investigate functional CA1 pyramidal α7-containing nAChRs using rat coronal hippocampal slices and patch-clamp electrophysiology. The majority (∼71% of tested CA1 pyramidal neurons expressed low densities of functional α7-containing nAChRs as evidenced by small whole-cell responses to choline, a selective endogenous agonist of α7 nAChRs. These responses were potentiated by PNU-120596, a novel positive allosteric modulator of α7 nAChRs. The density of functional α7-containing nAChRs expressed in CA1 pyramidal neurons (and thus, the normalized net effect of activation, i.e., response net charge per unit of membrane capacitance per unit of time was estimated to be ∼5% of the density observed in CA1 interneurons. The results of this study demonstrate that despite low levels of expression of functional pyramidal α7-containing nAChRs, physiological levels of choline (∼10 µM are sufficient to activate these receptors and transiently depolarize and even excite CA1 pyramidal neurons in the presence of PNU-120596. The observed effects are possible because in the presence of 10 µM choline and 1-5 µM PNU-120596, a single opening of an individual pyramidal α7-containing nAChR ion channel appears to transiently depolarize (∼4 mV the entire pyramidal neuron and occasionally

Regulation of capacitative and non-capacitative Ca2+ entry in A7r5 vascular smooth muscle cells

Directory of Open Access Journals (Sweden)

COLIN W TAYLOR

2004-01-01

Full Text Available A capacitative Ca2+ entry (CCE pathway, activated by depletion of intracellular Ca2+ stores, is thought to mediate much of the Ca2+ entry evoked by receptors that stimulate phospholipase C (PLC. However, in A7r5 vascular smooth muscle cells, vasopressin, which stimulates PLC, empties intracellular Ca2+ stores but simultaneously inhibits their ability to activate CCE. The diacylglycerol produced with the IP3 that empties the stores is metabolized to arachidonic and this leads to activation of nitric oxide (NO synthase, production of NO and cyclic GMP, and consequent activation of protein kinase G. The latter inhibits CCE. In parallel, NO directly activates a non-capacitative Ca2+ entry (NCCE pathway, which is entirely responsible for the Ca2+ entry that occurs in the presence of vasopressin. This reciprocal regulation of two Ca2+ entry pathways ensures that there is sequential activation of first NCCE in the presence of vasopressin, and then a transient activation of CCE when vasopressin is removed. We suggest that the two routes for Ca2+ entry may selectively direct Ca2+ to processes that mediate activation and then recovery of the cell.

7 CFR 996.6 - Importation.

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2010-01-01

... 7 Agriculture 8 2010-01-01 2010-01-01 false Importation. 996.6 Section 996.6 Agriculture Regulations of the Department of Agriculture (Continued) AGRICULTURAL MARKETING SERVICE (Marketing Agreements... peanuts into channels of commerce of the United States. ...

Deformation processed Al/Ca nano-filamentary composite conductors for HVDC applications

Science.gov (United States)

Czahor, C. F.; Anderson, I. E.; Riedemann, T. M.; Russell, A. M.

2017-07-01

Efficient long-distance power transmission is necessary as the world continues to implement renewable energy sources, often sited in remote areas. Light, strong, high-conductivity materials are desirable for this application to reduce both construction and operational costs. In this study an Al/Ca (11.5% vol.) composite with nano-filamentary reinforcement was produced by powder metallurgy then extruded, swaged, and wire drawn to a maximum true strain of 12.7. The tensile strength increased exponentially as the filament size was reduced to the sub-micron level. In an effort to improve the conductor’s ability to operate at elevated temperatures, the deformation-processed wires were heat-treated at 260°C to transform the Ca-reinforcing filaments to Al2Ca. Such a transformation raised the tensile strength by as much as 28%, and caused little change in ductility, while the electrical conductivity was reduced by only 1% to 3%. Al/Al2Ca composites are compared to existing conductor materials to show how implementation could affect installation and performance.

Self-injection length in La0.7Ca0.3MnO3–YBa2Cu3 O7−δ ...

Indian Academy of Sciences (India)

Critical current, Ic, was measured at 77 K on both the control side as well as the LCMO side for different YBCO film thickness. It was observed that while the control ... devices which are essentially a heterostructure consisting of a layer of YBa2Cu3O7−δ (YBCO), grown over La0.7Ca0.3MnO3 (LCMO). The critical current of.

Tricolor emission Ca3Si2O7:Ln (Ln=Ce, Tb, Eu) phosphors for near-UV white light-emitting-diode

International Nuclear Information System (INIS)

Mao, Zhi-yong; Zhu, Ying-chun; Gan, Lin; Zeng, Yi; Xu, Fang-fang; Wang, Yang; Tian, Hua; Li, Jian; Wang, Da-jian

2013-01-01

Tricolor emission in a same Ca 3 Si 2 O 7 host with independent Ln (Ln=Ce 3+ , Eu 2+ , Tb 3+ ) dopants is demonstrated to construct a near-UV white light emitting diode (LED). The luminescence properties and thermal quenching properties, as well as the applications in near-UV white LED are investigated. These phosphors show typical blue, red, and green, three-basal-color, luminescence in the CIE chromaticity diagram for Ce 3+ , Eu 2+ and Tb 3+ dopants, respectively. Thermal quenching properties show that the luminescence thermal stability strongly depends on the different dopant types; better thermal quenching property of Ce 3+ and Tb 3+ is recorded in comparison with that of Eu 2+ . The white LED prototype fabricated with near-UV chip and as-prepared tricolor phosphors exhibits acceptable CIE chromaticity coordinates (0.32, 0.30) with a CCT of 6000 K and a CRI of 87, indicating the potential application of Ca 3 Si 2 O 7 :Ln phosphors in near-UV white LED. - Highlights: ► Tricolor Ca 3 Si 2 O 7 : Ln phosphors were demonstrated to construct near-UV white LED. ► Eu 2+ doped Ca 3 Si 2 O 7 red-emitting phosphor was confirmed by this work once again. ► Thermal quenching properties for Ca 3 Si 2 O 7 :Ln phosphors were reported for the first time. ► Performances of fabricated white LED indicated the potential application of phosphors.

Binding of 45Ca2+ to particulate fractions of coleoptile tissue

International Nuclear Information System (INIS)

Vesper, M.J.; Saftner, R.A.; Sharma, D.; Evans, M.L.

1976-01-01

Using recently developed techniques, we have investigated the binding of 45 Ca 2+ to membrane preparations from corn (Zea mays L) and oat (Avena sativa L) colcoptile tissue. Scatchard plot analysis reveals at least two Ca 2+ binding sites in each tissue, a high affinity binding site (Ksub(m)=7.7 x 10 -7 M, n=6.9 x 10 -10 mol . 0.5g f.w. -1 in corn, Ksub(m)=4.93 x 10 -6 M, n=2.29 x 10 -9 mol . 0.5g f.w. -1 in Avena) and a low affinity binding site (Ksub(m)=9.01 x 10 -5 M, n=5.4 x 10 -8 mol . 0.5g f.w. -1 in corn; Ksub(m)=1.03 x 10 -4 M, n=3.40 x 10 -8 mol . 0.5g f.w. -1 in Avena). There is also some evidence of a third, lower affinity binding site in each tissue, especially corn. More detailed studies with corn coleoptile homogenates show that they contain a potent dialyzable inhibitor of Ca 2+ binding. Monovalent cations were observed to be ineffective as inhibitors of Ca 2+ binding in corn. However, of six divalent cations tested, all were capable of strong inhibition of Ca 2+ binding and there appeared to be a relationship between size of the atomic radius of the ion and potency as an inhibitor of calcium binding. (orig.) [de

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

Science.gov (United States)

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

1997-01-01

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

Thermal neutron imaging with rare-earth-ion-doped LiCaAlF{sub 6} scintillators and a sealed {sup 252}Cf source

Energy Technology Data Exchange (ETDEWEB)

Kawaguchi, Noriaki, E-mail: famicom@mail.tagen.tohoku.ac.jp [Tokuyama Corporation, Shibuya 3-chome, Shibuya-ku, Tokyo 150-8383 (Japan); IMRAM, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai, Miyagi 980-8577 (Japan); Yanagida, Takayuki; Fujimoto, Yutaka; Yokota, Yuui; Kamada, Kei [IMRAM, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai, Miyagi 980-8577 (Japan); Fukuda, Kentaro; Suyama, Toshihisa [Tokuyama Corporation, Shibuya 3-chome, Shibuya-ku, Tokyo 150-8383 (Japan); Watanabe, Kenichi; Yamazaki, Atsushi [Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8603 (Japan); Chani, Valery [IMRAM, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai, Miyagi 980-8577 (Japan); Yoshikawa, Akira [IMRAM, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai, Miyagi 980-8577 (Japan); New Industry Creation Hatchery Center, Tohoku University, Sendai 980-8579 (Japan)

2011-10-01

Thermal neutron imaging with Ce-doped LiCaAlF{sub 6} crystals has been performed. The prototype of the neutron imager using a Ce-doped LiCaAlF{sub 6} scintillating crystal and a position sensitive photomultiplier tube (PSPMT) which had 64 multi-channel anode was developed. The Ce-doped LiCaAlF{sub 6} single crystal was grown by the Czochralski method. A plate with dimensions of a diameter of 50x2 mm{sup 2} was cut from the grown crystal, polished, and optically coupled to PSPMT by silicone grease. The {sup 252}Cf source (<1 MBq) was sealed with 43 mm of polyethylene for neutron thermalization. Alphabet-shaped Cd pieces with a thickness of 2 mm were used as a mask for the thermal neutrons. After corrections for the pedestals and gain of each pixel, we successfully obtained two-dimensional neutron images using Ce-doped LiCaAlF{sub 6}.

Thermoluminescence properties of Mn-doped CaYAl3O7 phosphor irradiated with ultra-violet, mega-voltage and gamma radiation

International Nuclear Information System (INIS)

Pathak, Pushpraj; Selot, Anupam; Kurchania, Rajnish

2014-01-01

Low temperature combustion synthesis was employed for the preparation of CaYAl 3 O 7 (Mn 2+ ) phosphor. X-Ray diffraction (XRD) patterns were recorded to confirm the phase formation. Estimated particle size was found to be ∼19.9 nm by using the Debye Scherrer's formula. FTIR study confirms the formation of CaYAl 3 O 7 compound, escape of nitrates and other organic products. Thermoluminescence (TL) glow curves of the prepared phosphor were recorded after exposing the sample with Ultra-violet (UV), 6-Mega-voltage (MV), 16-MV and Co-60(Cobalt-60, 1.25-MeV average gamma energy) radiation. Trapping parameters namely activation energy (E), order of kinetics (b) and frequency factor(s) of main peak, centered around 186 °C in the sample irradiated with UV source for 20 min, were determined using glow curve shape (Chen's) method. It has been observed that the TL peak intensity increases with increasing the exposure from UV source. Also with increases the energy of incident radiation a decrease in TL peak intensity were observed. This could be due to higher penetration power and less absorbance of incident beam in the phosphor material. Analysis suggests that possibility of utilizing this phosphor in futuristic low and high energy dosimetric applications as well as in solid state lighting devices. - Highlights: • The average particle size was found to be 19.9 nm of CaYAl 3 O 7 :Mn 2+ phosphor synthesized by the combustion method. • Two glow peaks were recorded in UV exposed sample. However with Gamma and MV irradiated sample a single glow peak was observed. • TL intensity in the sample irradiated with UV is higher as compared to Gamma and MV. • Glow peaks of the phosphor obeys second order kinetic has 0.637 eV activation energy and 9.9×10 7 S −1 frequency factor. • Useful in radiation dosimetry as well as solid state lighting

7 CFR 1006.6 - Supply plant.

Science.gov (United States)

2010-01-01

... 7 Agriculture 9 2010-01-01 2009-01-01 true Supply plant. 1006.6 Section 1006.6 Agriculture Regulations of the Department of Agriculture (Continued) AGRICULTURAL MARKETING SERVICE (Marketing Agreements... Handling Definitions § 1006.6 Supply plant. See § 1000.6. ...

7 CFR 1033.6 - Supply plant.

Science.gov (United States)

2010-01-01

... 7 Agriculture 9 2010-01-01 2009-01-01 true Supply plant. 1033.6 Section 1033.6 Agriculture Regulations of the Department of Agriculture (Continued) AGRICULTURAL MARKETING SERVICE (Marketing Agreements... Handling Definitions § 1033.6 Supply plant. See § 1000.6. ...

7 CFR 1005.6 - Supply plant.

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2010-01-01

... 7 Agriculture 9 2010-01-01 2009-01-01 true Supply plant. 1005.6 Section 1005.6 Agriculture Regulations of the Department of Agriculture (Continued) AGRICULTURAL MARKETING SERVICE (Marketing Agreements... Handling Definitions § 1005.6 Supply plant. See § 1000.6. ...

7 CFR 1030.6 - Supply plant.

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2010-01-01

... 7 Agriculture 9 2010-01-01 2009-01-01 true Supply plant. 1030.6 Section 1030.6 Agriculture Regulations of the Department of Agriculture (Continued) AGRICULTURAL MARKETING SERVICE (Marketing Agreements... Handling Definitions § 1030.6 Supply plant. See § 1000.6. ...

7 CFR 1007.6 - Supply plant.

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2010-01-01

... 7 Agriculture 9 2010-01-01 2009-01-01 true Supply plant. 1007.6 Section 1007.6 Agriculture Regulations of the Department of Agriculture (Continued) AGRICULTURAL MARKETING SERVICE (Marketing Agreements... Handling Definitions § 1007.6 Supply plant. See § 1000.6. ...

7 CFR 1032.6 - Supply plant.

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2010-01-01

... 7 Agriculture 9 2010-01-01 2009-01-01 true Supply plant. 1032.6 Section 1032.6 Agriculture Regulations of the Department of Agriculture (Continued) AGRICULTURAL MARKETING SERVICE (Marketing Agreements... Handling Definitions § 1032.6 Supply plant. See § 1000.6. ...

7 CFR 1126.6 - Supply plant.

Science.gov (United States)

2010-01-01

... 7 Agriculture 9 2010-01-01 2009-01-01 true Supply plant. 1126.6 Section 1126.6 Agriculture Regulations of the Department of Agriculture (Continued) AGRICULTURAL MARKETING SERVICE (Marketing Agreements... Handling Definitions § 1126.6 Supply plant. See § 1000.6. ...

7 CFR 1001.6 - Supply plant.

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2010-01-01

... 7 Agriculture 9 2010-01-01 2009-01-01 true Supply plant. 1001.6 Section 1001.6 Agriculture Regulations of the Department of Agriculture (Continued) AGRICULTURAL MARKETING SERVICE (Marketing Agreements... Handling Definitions § 1001.6 Supply plant. See § 1000.6. ...

7 CFR 1131.6 - Supply plant.

Science.gov (United States)

2010-01-01

... 7 Agriculture 9 2010-01-01 2009-01-01 true Supply plant. 1131.6 Section 1131.6 Agriculture Regulations of the Department of Agriculture (Continued) AGRICULTURAL MARKETING SERVICE (Marketing Agreements... Handling Definitions § 1131.6 Supply plant. See § 1000.6. ...

U-Pb and Lu-Hf zircon geochronology of the Cañadón Asfalto Basin, Chubut, Argentina: Implications for the magmatic evolution in central Patagonia

Science.gov (United States)

Hauser, N.; Cabaleri, N. G.; Gallego, O. F.; Monferran, M. D.; Silva Nieto, D.; Armella, C.; Matteini, M.; Aparicio González, P. A.; Pimentel, M. M.; Volkheimer, W.; Reimold, W. U.

2017-10-01

The Cañadón Asfalto basin, central Chubut, Argentina, comprises a volcano-sedimentary sequence related to the opening of the Atlantic Ocean during Mesozoic times. The Lonco Trapial, Cañadón Asfalto and Cañadón Calcáreo formations are the main units related to the evolution of this basin. The Las Chacritas and Puesto Almada members are distinguished in the Cañadón Asfalto Formation. LA-HR-ICP-MS U-Pb and Lu-Hf data on zircon were obtained on these units. The Lonco Trapial Formation gave a weighted average age of 172.3 ± 1.8 Ma. A pyroclastic level from the Las Chacritas Member gave a weighted average age of 168.2 ± 2.2 Ma. Two U-Pb concordant ages of 160.3 ± 1.7 Ma on a laminated tuffite and 158.3 ± 1.3 Ma on a pyroclastic level were obtained for the Puesto Almada Member. Two maximum depositional ages constrain the sedimentary provenance areas for the basin: 1) A sample from the Sierra de la Manea range, where a controversial unit related either to the Cañadón Asfalto or to the Cañadón Calcáreo formation occurs, gave an age of 176.6 ± 1.0 Ma. Two younger zircon crystals indicate that this unit may be related to the Cañadón Calcáreo Formation. 2) A sandstone with cross-stratification from the Puesto Almada Member gave a maximum depositional age of 173.6 ± 6.4 Ma. In terms of U-Pb and Lu-Hf isotopes, two magmatic events are identified in central Patagonia: the Mamil Choique magmatic event characterized by negative εHf values around -5.0 and representing recycling during Permian times of Mesoproterozoic crust (TDM of ∼1.5 Ga), and the Cañadón Asfalto magmatic event with negative (-8.2) to positive (+4) εHf values and Meso- to Neoproterozoic TDM between 1.5 and 0.8 Ga. The younger event is characterized by three main cycles: C1 related to the Lonco Trapial magmatism, C2 to the Las Chacritas volcanism, and C3 to the Puesto Almada volcanism. These cycles are related with Marifil, Chon Aike and El Quemado formations volcanics events of

Electronic structure study of wide band gap magnetic semiconductor (La0.6Pr0.4)0.65Ca0.35MnO3 nanocrystals in paramagnetic and ferromagnetic phases

Science.gov (United States)

Dwivedi, G. D.; Joshi, Amish G.; Kumar, Shiv; Chou, H.; Yang, K. S.; Jhong, D. J.; Chan, W. L.; Ghosh, A. K.; Chatterjee, Sandip

2016-04-01

X-ray circular magnetic dichroism (XMCD), X-ray photoemission spectroscopy (XPS), and ultraviolet photoemission spectroscopy (UPS) techniques were used to study the electronic structure of nanocrystalline (La0.6Pr0.4)0.65Ca0.35MnO3 near Fermi-level. XMCD results indicate that Mn3+ and Mn4+ spins are aligned parallel to each other at 20 K. The low M-H hysteresis curve measured at 5 K confirms ferromagnetic ordering in the (La0.6Pr0.4)0.65Ca0.35MnO3 system. The low temperature valence band XPS indicates that coupling between Mn3d and O2p is enhanced and the electronic states near Fermi-level have been suppressed below TC. The valence band UPS also confirms the suppression of electronic states near Fermi-level below Curie temperature. UPS near Fermi-edge shows that the electronic states are almost absent below 0.5 eV (at 300 K) and 1 eV (at 115 K). This absence clearly demonstrates the existence of a wide band-gap in the system since, for hole-doped semiconductors, the Fermi-level resides just above the valence band maximum.

No-carrier-added (NCA) synthesis of 6-[{sup 18}F]fluoro-L-DOPA using 3,5,6,7,8,8a-hexahydro-7,7,8a-trimethyl-[6S-(6{alpha}, 8{alpha}, 8{alpha}{beta})]-6,8-methano-2H-1,4-benzoxazin-2-one

Energy Technology Data Exchange (ETDEWEB)

Horti, A. [Yale Univ., New Haven, CT (United States). School of Medicine]|[Yale Univ., West Haven, CT (United States). PET Center; Redmond, D.E. Jr. [Yale Univ., New Haven, CT (United States). School of Medicine; Soufer, R. [Yale Univ., West Haven, CT (United States). PET Center

1995-12-31

3,5,6,7,8,8a-Hexahydro-7,7,8a-trimethyl-[6S-(6{alpha},8{alpha} , 8{alpha}{beta})]-6,8-methano-2H-1,4-benzoxazino-2-one (2) was investigated as chiral auxiliary for asymmetric NCA nucleophilic synthesis of 6-[{sup 18}F]Fluoro-L-DOPA. Direct condensation of 3,4-dimethoxy-2-[{sup 18}F]fluorobenzaldehyde (1a) or 6-[{sup 18}F]fluoro-piperonal (1b) in the presence of NaH with 2 gave the corresponding [{sup 18}F]-3-[(2-fluorophenyl)methylene]-3,5,6,7,8,8a-hexahydro-7,7,8 a-trimethyl-[6S-(3Z,3{alpha},6{alpha},8{alpha},8{alpha}{beta})]-6, 8-methano-2H-1,4-benzoxazin-2-one derivative 3a or 3b as a single stereoisomer. L-Selectride promoted hydrogenation of the olefinic double bond of these derivatives, in presence of tertbutyl alcohol, afforded the corresponding [{sup 18}F]-3-[(2-fluorophenyl) methyl]-3,5,6,7,8,8a-hexahydro-7,7,8a-trimethyl-[3S-(3{alpha}, 6{alpha}, 8{alpha}8{alpha}{beta})]-6,8-methano-2H-1,4-benzoxazin-2-one derivatives (4a,b) without affecting the orientation of diasterofacial discrimination. Deprotection of the derivatives 4a,b yielded 6-[{sup 18}F]fluoro-L-DOPA (e.e. >90%, 3% radiochemical yield (EOB), total synthesis time 125 min, specific activity >2000 mCi/{mu}mol). Direct deprotection/reduction of the compounds 3a,b provides the enantiomeric mixture of 6-[{sup 18}F]fluoro-D,L-DOPA (10-12% radiochemical yield) and, after chiral separation, 6-[{sup 18}F]fluoro-L-DOPA (e.e. 98%, 4-5% radiochemical yield). (author).

Quality, precision and accuracy of the maximum No. 40 anemometer

Energy Technology Data Exchange (ETDEWEB)

Obermeir, J. [Otech Engineering, Davis, CA (United States); Blittersdorf, D. [NRG Systems Inc., Hinesburg, VT (United States)

1996-12-31

This paper synthesizes available calibration data for the Maximum No. 40 anemometer. Despite its long history in the wind industry, controversy surrounds the choice of transfer function for this anemometer. Many users are unaware that recent changes in default transfer functions in data loggers are producing output wind speed differences as large as 7.6%. Comparison of two calibration methods used for large samples of Maximum No. 40 anemometers shows a consistent difference of 4.6% in output speeds. This difference is significantly larger than estimated uncertainty levels. Testing, initially performed to investigate related issues, reveals that Gill and Maximum cup anemometers change their calibration transfer functions significantly when calibrated in the open atmosphere compared with calibration in a laminar wind tunnel. This indicates that atmospheric turbulence changes the calibration transfer function of cup anemometers. These results call into question the suitability of standard wind tunnel calibration testing for cup anemometers. 6 refs., 10 figs., 4 tabs.

Thermally and optically stimulated radiative processes in Eu and Y co-doped LiCaAlF6 crystal

International Nuclear Information System (INIS)

Fukuda, Kentaro; Yanagida, Takayuki; Fujimoto, Yutaka

2015-01-01

Yttrium co-doping was attempted to enhance dosimeter performance of Eu doped LiCaAlF 6 crystal. Eu doped and Eu, Y co-doped LiCaAlF 6 were prepared by the micro-pulling-down technique, and their dosimeter characteristics such as optically stimulated luminescence (OSL) and thermally stimulated luminescence (TSL) were investigated. By yttrium co-doping, emission intensities of OSL and TSL were enhanced by some orders of magnitude. In contrast, scintillation characteristics of yttrium co-doped crystal such as intensity of prompt luminescence induced by X-ray and light yield under neutron irradiation were degraded

7 CFR 1124.6 - Supply plant.

Science.gov (United States)

2010-01-01

... 7 Agriculture 9 2010-01-01 2009-01-01 true Supply plant. 1124.6 Section 1124.6 Agriculture Regulations of the Department of Agriculture (Continued) AGRICULTURAL MARKETING SERVICE (Marketing Agreements... Regulating Handling Definitions § 1124.6 Supply plant. See § 1000.6. ...

Eu and Rb co-doped LiCaAlF6 scintillators for neutron detection

International Nuclear Information System (INIS)

Yamaji, Akihiro; Yanagida, Takayuki; Kawaguchi, Noriaki; Yokota, Yuui; Fujimoto, Yutaka; Kurosawa, Shunsuke; Pejchal, Jan; Watanabe, Kenichi; Yamazaki, Atsushi; Yoshikawa, Akira

2013-01-01

Eu and Rb co-doped LiCaAlF 6 (LiCAF) single crystals with different dopant concentrations were grown by the micro-pulling-down method for neutron detection. Their transmittance spectra showed strong absorption bands at 200–220 and 290–350 nm, and under 241 Am alpha-ray excitation, their radioluminescence spectra exhibited an intense emission peak at 373 nm that was attributed to the Eu 2+ 5d–4f transition. These results were consistent with those for the Rb-free Eu:LiCAF. The highest light yield among the grown crystals was 36,000 ph/n, which was 20% greater than that of the Rb-free crystal. In addition, the neutron-excited scintillation decay times were 650–750 ns slower than that of the Rb-free Eu:LiCAF. -- Highlights: •Eu and Rb co-doped LiCaAlF 6 crystals were grown by the micro-pulling down method. •Transmittance, photoluminescence and radioluminescence spectra were measured. •The light yields and scintillation decays were evaluated under 252 Cf neutron irradiation

Gravity variation before the Akto Ms6.7 earthquake, Xinjiang

Directory of Open Access Journals (Sweden)

Hongtao Hao

2017-03-01

Full Text Available The relationship between gravity variation and the Akto Ms6.7 earthquake on November 11, 2016, was studied by use of mobile gravity observation data from the China continental structural environmental monitoring network. The result revealed that before the Akto earthquake, a high positive gravity variation was observed in the Pamir tectonic knots region (within a maximum magnitude of approximately +80 microgal, which was consistent with the existing knowledge of gravity abnormality and the locations of strong earthquakes. In view of the recent strong seismic activities in the Pamir tectonic knots region, as well as the strong upward crust movement and compressive strain, it is believed that gravity change in the Pamir tectonic knots region reflects the recent strong seismic activities and crust movement.

7 CFR 35.6 - Shipment.

Science.gov (United States)

2010-01-01

... 7 Agriculture 2 2010-01-01 2010-01-01 false Shipment. 35.6 Section 35.6 Agriculture Regulations of the Department of Agriculture AGRICULTURAL MARKETING SERVICE (Standards, Inspections, Marketing... country regardless of the number of consignees, receivers, or ports of destination in that country. [41 FR...

Experimental investigation of highly excited states of the 5,6He and 5,6Li nuclei in the (6Li, 7Be) and (6Li, 7Li) one-nucleon-pick-up reactions

International Nuclear Information System (INIS)

Sakuta, S.B.; Novatskij, B.G.; Stepanov, D.N.; Aleksandrov, D.V.; Glukhov, Yu.A.; Nikol'skij, E.Yu.

2002-01-01

( 6 Li, 7 Be) and ( 6 Li, 7 Li) reactions on the 6 Li, 7 Li nuclei have been investigated in the angular range of 0-20 deg in laboratory system at the 93-MeV 6 Li energy. Besides low-lying states of 5,6 He and 5,6 Li nuclei, broad structures have been observed in the measured spectra close to the t( 3 He) + d and t( 3 He) + t threshold at excitation energies of 16.75 (3/2 + ) and ∼ 20 MeV ( 5 He), 16.66 (3/2 + ) and ∼ 20 MeV ( 5 Li), 14.0 and 25 MeV ( 6 He), and ∼ 20 MeV ( 6 Li). Angular distributions, which have been measured for transitions to the ground (0 + ) and exited states at E x =1.8 MeV (2 + ) and 14.0 MeV of the 6 He nucleus in the 7 Li( 6 Li, 7 Be) 6 He reaction, have been analyzed in the framework of the finite-range distorted-waves method assuming the 1p- and 1s-proton pick-up mechanism. It has been shown that ( 6 Li, 7 Be) and ( 6 Li, 7 Li) reactions predominately proceed by one-step pick-up mechanism and broad structures which are observed at high excitation energies should be considered as quasimolecular states of the t( 3 He) + d and t( 3 He) + t type [ru

Ionic conductivity in new perovskite type oxides: NaAZrMO6 (A = Ca or Sr; M = Nb or Ta)

International Nuclear Information System (INIS)

Rajendran, Deepthi N.; Ravindran Nair, K.; Prabhakar Rao, P.; Sibi, K.S.; Koshy, Peter; Vaidyan, V.K.

2008-01-01

New oxides of the type, NaAZrMO 6 (M = Ca or Sr; M = Nb or Ta), have been prepared by the solid-state reaction technique. Phase identification by powder X-ray diffraction (XRD) shows that NaCaZrMO 6 has orthorhombic perovskite type structure (Pnma) and NaSrZrMO 6 has cubic perovskite type structure (Pm3m). The grain morphology observation by scanning electron microscope (SEM) shows well-sintered grains. ac impedance spectra and electrical conductivity measurements in air, oxygen and nitrogen atmospheres indicate that they are probable oxide ion conductors with ionic conductivities of the order of 10 -3 S cm -1 at 750 deg. C

Photodynamic processes in LiCaAlF6:Ce3+ UV active medium

International Nuclear Information System (INIS)

Galiev, A I; Semashko, V V; Akhtyamov, O R; Shnaidman, S A; Marisov, M A; Shavelev, A A

2014-01-01

The objectives of this paper are experimental studies of pump-induced effects in LiCaAlF 6 : Ce 3+ single crystals and computer model elaboration and appropriated software package engineering. The elaborated experimental technique and software allow either to calculate the nonlinear absorption/gain characteristics of the active medium on the basis of known parameters, or to find its previously unknown parameters from pump-probe experimental dependences

Enhancing Sm{sup 3+} red emission via energy transfer from Bi{sup 3+}→Sm{sup 3+} based on terbium bridge mechanism in Ca{sub 2}Al{sub 2}SiO{sub 7} phosphors

Energy Technology Data Exchange (ETDEWEB)

Li, Minhong; Wang, LiLi; Ran, Weiguang; Ren, Chunyan; Song, Zeling; Shi, Jinsheng, E-mail: jsshiqn@aliyun.com

2017-04-15

Currently, the key change for white-LED is to improve the luminescence efficiency of red phosphor. Sm{sup 3+} activated phosphor was considered due to suitable emission position of red light. However, the luminescence intensity in the red region is weak. For enhancing red-emitting of Sm{sup 3+}, Bi{sup 3+} and Tb{sup 3+} ions were introduced into Ca{sub 2}Al{sub 2}SiO{sub 7}:Sm{sup 3+} phosphors based on the concept of energy transfer. For Ca{sub 2}Al{sub 2}SiO{sub 7}:Bi{sup 3+}, Sm{sup 3+} samples, it can be observed that the energy transfer process was blocked. Hence, Tb{sup 3+} was introduced into Ca{sub 2}Al{sub 2}SiO{sub 7}:Bi{sup 3+}, Sm{sup 3+} samples to increase Sm{sup 3+} luminescence intensity based on Bi{sup 3+}→Tb{sup 3+}→Sm{sup 3+} energy transfer process. Compared with Sm{sup 3+} single-doped Ca{sub 2}Al{sub 2}SiO{sub 7} phosphor, the luminescence intensity of Sm{sup 3+} was enhanced by 2.6 times. It can be found that Tb{sup 3+} ions play a role of storing the energy or transfer bridge from Bi{sup 3+}→ Sm{sup 3+} by investigating the Ca{sub 2}Al{sub 2}SiO{sub 7}:Bi{sup 3+}, Tb{sup 3+} and Ca{sub 2}Al{sub 2}SiO{sub 7}:Tb{sup 3+}, Sm{sup 3+} energy transfer mechanism. All these results suggest that terbium branch mechanism plays an important role on enhancing activators luminescence intensity.

Cell surface topology creates high Ca2+ signalling microdomains

DEFF Research Database (Denmark)

Brasen, Jens Christian; Olsen, Lars Folke; Hallett, Maurice B

2010-01-01

It has long been speculated that cellular microdomains are important for many cellular processes, especially those involving Ca2+ signalling. Measurements of cytosolic Ca2+ report maximum concentrations of less than few micromolar, yet several cytosolic enzymes require concentrations of more than...

CDPKs CPK6 and CPK3 function in ABA regulation of guard cell S-type anion- and Ca(2+-permeable channels and stomatal closure.

Directory of Open Access Journals (Sweden)

Izumi C Mori

2006-10-01

Full Text Available Abscisic acid (ABA signal transduction has been proposed to utilize cytosolic Ca(2+ in guard cell ion channel regulation. However, genetic mutants in Ca(2+ sensors that impair guard cell or plant ion channel signaling responses have not been identified, and whether Ca(2+-independent ABA signaling mechanisms suffice for a full response remains unclear. Calcium-dependent protein kinases (CDPKs have been proposed to contribute to central signal transduction responses in plants. However, no Arabidopsis CDPK gene disruption mutant phenotype has been reported to date, likely due to overlapping redundancies in CDPKs. Two Arabidopsis guard cell-expressed CDPK genes, CPK3 and CPK6, showed gene disruption phenotypes. ABA and Ca(2+ activation of slow-type anion channels and, interestingly, ABA activation of plasma membrane Ca(2+-permeable channels were impaired in independent alleles of single and double cpk3cpk6 mutant guard cells. Furthermore, ABA- and Ca(2+-induced stomatal closing were partially impaired in these cpk3cpk6 mutant alleles. However, rapid-type anion channel current activity was not affected, consistent with the partial stomatal closing response in double mutants via a proposed branched signaling network. Imposed Ca(2+ oscillation experiments revealed that Ca(2+-reactive stomatal closure was reduced in CDPK double mutant plants. However, long-lasting Ca(2+-programmed stomatal closure was not impaired, providing genetic evidence for a functional separation of these two modes of Ca(2+-induced stomatal closing. Our findings show important functions of the CPK6 and CPK3 CDPKs in guard cell ion channel regulation and provide genetic evidence for calcium sensors that transduce stomatal ABA signaling.

Comparison between clinical significance of serum proinflammatory proteins (IL-6 and CRP) and classic tumor markers (CEA and CA 19-9) in gastric cancer.

Science.gov (United States)

Lukaszewicz-Zając, Marta; Mroczko, Barbara; Gryko, Mariusz; Kędra, Bogusław; Szmitkowski, Maciej

2011-06-01

Gastric cancer (GC) is a second most common cause of cancer-related death and represents an inflammation-driven malignancy. It has been suggested that interleukin 6 (IL-6) and C-reactive protein (CRP) play a potential role in the growth and progression of GC. The aim of the present study was to compare clinical significance of IL-6 and CRP with classic tumor markers-carcinoembryonic antigen (CEA) and carbohydrate antigen (CA 19-9) in GC patients. The study included 92 patients with GC and 70 healthy subjects. The serum concentrations of IL-6, CEA and CA 19-9 were determined using immunoenzyme assays, whereas CRP using immunoturbidimetric method. We defined the diagnostic criteria and prognostic value for proteins tested. In GC patients, the serum concentrations of all the proteins tested were significantly higher than in healthy subjects. The IL-6, CEA and CA 19-9 levels correlated with nodal metastases, while CRP with tumor stage, gastric wall invasion, presence of nodal and distant metastases. Diagnostic sensitivity of IL-6 was higher (85%) than those of other markers (CRP 66%, CA 19-9 34%, CEA 22%) and increased in combined use with CRP or CEA (88%). The area under ROC curve for IL-6 was larger than those of CRP and classic tumor markers (CEA and CA 19-9). None of the proteins tested was independent prognostic factor for the survival of GC patients. Our findings indicate better usefulness of serum proinflammatory proteins-IL-6 and CRP than classic tumor markers-CEA and CA 19-9 in the diagnosis of GC.

Dendrochronologically dated pine stumps document phase-wise bog expansion at a northwest German site between ca. 6700 and ca. 3400 BC

Science.gov (United States)

Maike Achterberg, Inke Elisabeth; Eckstein, Jan; Birkholz, Bernhard; Bauerochse, Andreas; Leuschner, Hanns Hubert

2018-01-01

The investigated northwest German mire site at Totes Moor is densely covered with subfossil pine stumps (Pinus sylvestris L.) from the fen-bog transition. This facilitates the spatio-temporal reconstruction of mire development, which is based on 212 in situ tree stumps in the case study presented here. Six dendrochronologically dated site chronologies together cover 2345 years between 6703 and 3403 BC. The gaps in between are 6 to 550 years long. Additionally, a floating chronology of 309 years, containing 30 trees, was radiocarbon-dated to the beginning of the 7th millennium cal BC. Peat-stratigraphical survey was carried out additionally, and elevations a.s.l. were determined at several locations. Tree dying-off phases, which indicate water level rise at the site, mostly in context of the local fen-bog transition, are evident for ca. 6600-6450, ca. 6350-5750, ca. 5300-4900, ca. 4700-4550, ca. 3900-3850, ca. 3700-3600, ca. 3500-3450 and ca. 3400 BC. The spatial distribution of the dated in situ trees illustrates the phase-wise expansion of raised bog over fen peat at the site. The documented bog expansion pulses likely correspond to climatic wet sifts.

Preparation of core-shell structured CaCO3 microspheres as rapid and recyclable adsorbent for anionic dyes

Science.gov (United States)

Zhao, Mengen; Chen, Zhenhua; Lv, Xinyan; Zhou, Kang; Zhang, Jie; Tian, Xiaohan; Ren, Xiuli; Mei, Xifan

2017-09-01

Core-shell structured CaCO3 microspheres (MSs) were prepared by a facile, one-pot method at room temperature. The adsorbent dosage and adsorption time of the obtained CaCO3 MSs were investigated. The results suggest that these CaCO3 MSs can rapidly and efficiently remove 99-100% of anionic dyes within the first 2 min. The obtained CaCO3 MSs have a high Brunauer-Emmett-Teller surface area (211.77 m2 g-1). In addition, the maximum adsorption capacity of the obtained CaCO3 MSs towards Congo red was 99.6 mg g-1. We also found that the core-shell structured CaCO3 MSs have a high recycling capability for removing dyes from water. Our results demonstrate that the prepared core-shell structured CaCO3 MSs can be used as an ideal, rapid, efficient and recyclable adsorbent to remove dyes from aqueous solution.

Complex cubic metallides AM{sub ∝6} (A=Ca, Sr; M=Zn, Cd, Hg). Synthesis, crystal chemistry and chemical bonding

Energy Technology Data Exchange (ETDEWEB)

Schwarz, Michael; Wendorff, Marco; Roehr, Caroline [Freiburg Univ. (Germany). Inst. fuer Anorganische und Analytische Chemie

2017-09-01

In a systematic synthetic, crystallographic and bond theoretical study, the stability ranges as well as the distribution of the isoelectronic late d-block elements Zn, Cd and Hg (M) in the polyanions of the YCd{sub 6}-type phases (Ca/Sr)Cd{sub 6} have been investigated. Starting from Ca(Cd/Hg){sub 6}, 12-30% of the M atoms can be substituted by Zn, which gradually occupies the center of the empty cubes. In all ternary compounds, smaller/less electronegative Zn/Cd atoms occupy the disordered tetrahedra explaining the lack of the YCd{sub 6}-type for pure mercurides. Along the section SrCd{sub 6}-SrHg{sub 6}, the ordered Eu{sub 4}Cd{sub 25}-type is formed (Sr{sub 4}Cd{sub 16.1}Hg{sub 8.9}: cF1392, Fd anti 3, a=3191.93(5) pm, R1=0.0404). Besides, two new complex cubic Ca phases appear at increased Zn proportion: Ca{sub 2}Zn{sub 5.1}Cd{sub 5.8}, which exhibits a nearly complete site preference of Zn and Cd, crystallizes in the rare cubic Mg{sub 2}Zn{sub 11}-type structure (cP39-δ, Pm anti 3, a=918.1(1) pm, R1=0.0349). In the Ca-Hg system, an increased Zn proportion yielded the new compound CaZn{sub 1.31}Hg{sub 3.69} (cF480, F anti 43m, a=2145.43(9) pm, R1=0.0572), with a complex cubic structure closely related to Ba{sub 20}Hg{sub 103}. All structures, which are commonly described using nested polyhedra around high-symmetric sites, are alternatively described in accordance with the calculated electron densities and charge distribution: building blocks are face-sharing [M{sub 4}] tetrahedra (star polyhedra such as TS, IS, OS), each with a cage-critical point in its center, and [M{sub 8}] cubes (deformed TS), which are either empty, distorted or filled. The M element distribution in the anion is determined by size criteria and the difference in electronegativity, which induces a preferred formation of heteroatomic polar bonds.

6 CFR 7.26 - Derivative classification.

Science.gov (United States)

2010-01-01

... 6 Domestic Security 1 2010-01-01 2010-01-01 false Derivative classification. 7.26 Section 7.26 Domestic Security DEPARTMENT OF HOMELAND SECURITY, OFFICE OF THE SECRETARY CLASSIFIED NATIONAL SECURITY INFORMATION Classified Information § 7.26 Derivative classification. (a) Derivative classification is defined...

I. The properties of hot Ca-like fragments from the 40Ca+40Ca reaction at 35 AMeV

International Nuclear Information System (INIS)

Planeta, R.; Gawlikowicz, W.; Wieloch, A.

2001-01-01

The creation of hot Ca-like fragments was investigated in the 40 Ca + 40 Ca reaction at 35 AMeV. Using the AMPHORA 4π detector system, the primary projectile-like fragment was reconstructed and its properties were determined. Both primary and secondary distributions are compared with the predictions of a Monte Carlo code describing a heavy-ion collision as a two-step process. Some of the nucleons which are identified as participants in the first step are transferred in the second step to these final states, which correspond on the average to the maximum value of entropy (thermodynamic probability). The model allows for competition between mean-field effects and nucleon-nucleon interactions in the overlap zone of the interacting nuclei. The analysis presented here suggests a thermalized source picture of the decay of the projectile-like fragment. The validity of the reconstruction procedure for projectile-like fragments is discussed. (orig.)

Solubility of calcium in CaO-CaCl2

International Nuclear Information System (INIS)

Perry, G.S.; Shaw, S.J.

1991-06-01

The Direct Oxide Reduction (DOR) process is well established as a process to produce plutonium metal from plutonium dioxide by reaction with calcium. Calcium chloride is added to dissolve the calcium oxide produced, allowing the metal to coalesce into a button. Since calcium metal melts at 840 0 C and DOR can take place successfully below this temperature, it is likely calcium dissolved in calcium chloride reacts with the plutonium dioxide. The solubility of calcium in calcium chloride is reasonably well established but the effect of the CaO formed during the DOR process on the solubility of calcium has not been previously determined. For this reason the solubility of calcium in CaCl 2 -CaO melts at 800 o C has been studied. The solubility decreases from 2.7 mol % in CaCl 2 to 0.4 mol % in 9 mol % CaO-CaCl 2 . (author)

Charge transfer-type fluorescence of Ti-doped Ca{sub 14}Al{sub 10}Zn{sub 6}O{sub 35}

Energy Technology Data Exchange (ETDEWEB)

Satoh, Yuta; Takemoto, Minoru, E-mail: takemoto@chem.kanagawa-it.ac.jp

2017-05-15

The calcium aluminum zincates Ca{sub 14}(Al{sub 1-2x}Ti{sub x}Zn{sub x}){sub 10}Zn{sub 6}O{sub 35}, in which Al{sup 3+} sites in the host material Ca{sub 14}Al{sub 10}Zn{sub 6}O{sub 35} are simultaneously substituted by Ti{sup 4+} and Zn{sup 2+}, were synthesized by a polymerized complex method. Al{sup 3+} ions could be replaced up to an x value of 0.1. The host material does not exhibit fluorescence, while the cation-substituted samples show an emission band centered at 383 nm under excitation by UV light at 243 nm. The emission intensity increases with x up to 0.1 and then gradually decreases as x is further increased. The emission wavelength also becomes longer with increasing temperature. Based on the properties of other Ti{sup 4+}-containing fluorescent materials, the emission of Ca{sub 14}(Al{sub 1-2x}Ti{sub x}Zn{sub x}){sub 10}Zn{sub 6}O{sub 35} is attributed to charge transfer-type fluorescence resulting from [TiO{sub 6}] octahedra.

Thermoluminescence characteristics of copper activated calcium borate nanocrystals (CaB{sub 4}O{sub 7}:Cu)

Energy Technology Data Exchange (ETDEWEB)

Erfani Haghiri, Maryam, E-mail: maryam.erfani59@gmail.com [Department of Physics, Faculty of Science, University Putra Malaysia, 43400 UPM Serdang, Selangor (Malaysia); Saion, Elias; Soltani, Nayereh [Department of Physics, Faculty of Science, University Putra Malaysia, 43400 UPM Serdang, Selangor (Malaysia); Wan Abdullah, Wan Saffiey [Radiation Protection and Health Division, Malaysian Nuclear Agency (Nuclear Malaysia), Bangi, 43000 Kajang (Malaysia); Navasery, Manizheh; Hashim, Mansor [Department of Physics, Faculty of Science, University Putra Malaysia, 43400 UPM Serdang, Selangor (Malaysia)

2013-09-15

The copper activated calcium tetraborate (CaB{sub 4}O{sub 7}:Cu) nanophosphor was synthesized by a combination of facile co-precipitation and thermal treatment methods for the first time. Thermoluminescence and dosimetric characteristics of the gamma irradiated CaB{sub 4}O{sub 7}:Cu nanophosphor was reported. The glow curves shows two well resolved TL peaks centered at about 120 °C and 260 °C. The copper concentration was varied from 1 to 3 mol% and it was found that the nanocrystalline CaB{sub 4}O{sub 7}:Cu with a dopant concentration of 2 mol% has the highest sensitivity among the other dopant concentrations. The results demonstrated that copper can enhance TL efficiency to 2.26 times more than that of un-doped nanocrystalline samples. Moreover, the dose response of the dosimetric peak at 260 °C follows a good linearity up to 3 kGy whereas the linearity of lower temperature peak at 120 °C extended up to 30 Gy. The linearity characteristic of the present nanophosphor suggests it as a candidate towards dosimetric applications. -- Highlights: • The TL characterization of calcium tetraborate nanoparticles was reported for the first time. • The addition of copper to host lattice can enhance the TL efficiency well. • The interesting feature of this study is a linearity of nanophosphor for wide range of doses. • The nanophosphor showed simple glow curve, good reproducibility and high sensitivity.

49 CFR 7.6 - Deletion of identifying detail.

Science.gov (United States)

2010-10-01

... 49 Transportation 1 2010-10-01 2010-10-01 false Deletion of identifying detail. 7.6 Section 7.6... To Be Made Public by DOT § 7.6 Deletion of identifying detail. Whenever it is determined to be... the deletion will accompany the record published or made available for inspection. ...

E6 and E7 Gene Polymorphisms in Human Papillomavirus Types-58 and 33 Identified in Southwest China.

Directory of Open Access Journals (Sweden)

Zuyi Chen

Full Text Available Cancer of the cervix is associated with infection by certain types of human papillomavirus (HPV. The gene variants differ in immune responses and oncogenic potential. The E6 and E7 proteins encoded by high-risk HPV play a key role in cellular transformation. HPV-33 and HPV-58 types are highly prevalent among Chinese women. To study the gene intratypic variations, polymorphisms and positive selections of HPV-33 and HPV-58 E6/E7 in southwest China, HPV-33 (E6, E7: n = 216 and HPV-58 (E6, E7: n = 405 E6 and E7 genes were sequenced and compared to others submitted to GenBank. Phylogenetic trees were constructed by Maximum-likelihood and the Kimura 2-parameters methods by MEGA 6 (Molecular Evolutionary Genetics Analysis version 6.0. The diversity of secondary structure was analyzed by PSIPred software. The selection pressures acting on the E6/E7 genes were estimated by PAML 4.8 (Phylogenetic Analyses by Maximun Likelihood version4.8 software. The positive sites of HPV-33 and HPV-58 E6/E7 were contrasted by ClustalX 2.1. Among 216 HPV-33 E6 sequences, 8 single nucleotide mutations were observed with 6/8 non-synonymous and 2/8 synonymous mutations. The 216 HPV-33 E7 sequences showed 3 single nucleotide mutations that were non-synonymous. The 405 HPV-58 E6 sequences revealed 8 single nucleotide mutations with 4/8 non-synonymous and 4/8 synonymous mutations. Among 405 HPV-58 E7 sequences, 13 single nucleotide mutations were observed with 10/13 non-synonymous mutations and 3/13 synonymous mutations. The selective pressure analysis showed that all HPV-33 and 4/6 HPV-58 E6/E7 major non-synonymous mutations were sites of positive selection. All variations were observed in sites belonging to major histocompatibility complex and/or B-cell predicted epitopes. K93N and R145 (I/N were observed in both HPV-33 and HPV-58 E6.

Nuclear structure of 41Ca from inelastic proton scattering

International Nuclear Information System (INIS)

Vold, P.B.; Cline, D.; Voigt, M.J.A. de

1977-01-01

Angular distributions have been measured for inelastic and elastic scattering of 19 MeV protons on 40 41 Ca. A total of 89 levels were identified below 6.4 MeV in 41 Ca with an energy resolution of 12 keV. Inelastic transition strengths have been extracted using DWBA theory with a vibrational model form factor. These transition strengths correlate well with inelastic α-scattering and electromagnetic values. The quadrupole strengths are interpreted in terms of the coexistence model and imply that the excited-core admixture in the ground states of both 40 Ca and 41 Ca are approximately 5%. The octupole strengths in 41 Ca exhibits features characteristic of the weak coupling of an fsub(7/2) neutron to the lowest 3 - state in 40 Ca. The l = 5 strength exhibits a similar weak-coupling behavior. In both cases the microscopic structure appreciably reduces the transition strength for the highest spin member of the weak-coupling multiplets. (Auth.)

Magnetic and magnetocaloric properties in La{sub 0.7}Ca{sub 0.3−x}Na{sub x}MnO{sub 3} exhibiting first-order and second-order magnetic phase transitions

Energy Technology Data Exchange (ETDEWEB)

Ho, T.A. [Department of Materials Science and Engineering, Korea University, Seoul 136-713 (Korea, Republic of); Dang, N.T. [Institute of Research and Development, Duy Tan University, Da Nang (Viet Nam); Phan, The-Long [Department of Physics and Oxide Research Center, Hankuk University of Foreign Studies, Yongin 449-791 (Korea, Republic of); Yang, D.S. [Physics Division, School of Science Education, Chungbuk National University, Cheongju 361-763 (Korea, Republic of); Lee, B.W. [Department of Physics and Oxide Research Center, Hankuk University of Foreign Studies, Yongin 449-791 (Korea, Republic of); Yu, S.C., E-mail: scyu@chungbuk.ac.kr [Department of Physics, Chungbuk National University, Cheongju 361-763 (Korea, Republic of)

2016-08-15

Polycrystalline orthorhombic samples La{sub 0.7}Ca{sub 0.3−x}Na{sub x}MnO{sub 3} (x = 0–0.09) were prepared by solid-state reaction. The study of magnetic properties revealed that the ferromagnetic-paramagnetic (FM-PM) transition temperature (T{sub C}) increases from 255 to about 271 K with increasing Na-doping content (x) from 0 to 0.09, respectively. Around the T{sub C}, we have found the samples showing a large magnetocaloric (MC) effect with maximum values of magnetic entropy change (|ΔS{sub max}|) of 7–8 J kg{sup −1} K{sup −1} and relative cooling power RCP = 232–236 J/kg for the samples x = 0.03–0.09 in a magnetic-field interval ΔH = 40 kOe. Detailed analyses of isothermal magnetization data M(T, H) based on Banerjee's criteria indicated a first-to-second-order magnetic-phase transformation taking place at a threshold Na-doping concentration x{sub c} ≈ 0.06. This could also be observed clearly from the feature of entropy universal curves. An assessment of the magnetic-ordering exponent N = dLn|ΔS{sub m}|/dLnH demonstrates an existence of short-range magnetic order in the samples. We believe that the changes of the magnetic properties and MC effect in La{sub 0.7}Ca{sub 0.3−x}Na{sub x}MnO{sub 3} caused by Na doping are related to the changes in the structural parameters and Mn{sup 4+}/Mn{sup 3+} ratio, which are confirmed by the geometrical and electronic analyses based on X-ray diffraction and X-ray absorption fine structure. - Highlights: • Geometrical and electronic structures of La{sub 0.7}Ca{sub 0.3−x}Na{sub x}MnO{sub 3}. • Threshold of first-to-second-order phase transformation in La{sub 0.7}Ca{sub 0.3−x}Na{sub x}MnO{sub 3}. • Large magneto-caloric effect with |ΔS{sub max}| ≈ 7–8 J kg{sup −1} K{sup −1}, and RCP = 232–236 J/kg. • Universal curve of magnetic-entropy change.

6 CFR 25.7 - Litigation management.

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2010-01-01

... 6 Domestic Security 1 2010-01-01 2010-01-01 false Litigation management. 25.7 Section 25.7 Domestic Security DEPARTMENT OF HOMELAND SECURITY, OFFICE OF THE SECRETARY REGULATIONS TO SUPPORT ANTI-TERRORISM BY FOSTERING EFFECTIVE TECHNOLOGIES § 25.7 Litigation management. (a) Liability for all claims...

6 CFR 7.30 - Classification challenges.

Science.gov (United States)

2010-01-01

... 6 Domestic Security 1 2010-01-01 2010-01-01 false Classification challenges. 7.30 Section 7.30... INFORMATION Classified Information § 7.30 Classification challenges. (a) Authorized holders of information... classified are encouraged and expected to challenge the classification status of that information pursuant to...

Synthesis and Photoluminescence Properties of Ca2Ga2SiO7:Eu(3+) Red Phosphors with an Intense (5)D0 → (7)F4 Transition.

Science.gov (United States)

Behrh, Gaganpreet Kaur; Gautier, Romain; Latouche, Camille; Jobic, Stéphane; Serier-Brault, Hélène

2016-09-19

Novel melilite-type Ca2Ga2SiO7:Eu(3+) red-emitting phosphors with different Eu(3+) contents were synthesized via high-temperature solid-state reaction. The crystal structure, optical absorption, and photoluminescence properties were investigated, while density functional theory calculations were performed on the host lattice. The excitation spectra indicate that phosphors can be effectively excited by near-UV light for a potential application in white-light-emitting diodes. Because of the abnormally high intensity emission at about 700 nm arising from the (5)D0 → (7)F4 transition of Eu(3+), the phosphors Ca2Ga2SiO7:Eu(3+) show a deep-red emission with chromaticity coordinates (0.639, 0.358).

Effect of scandium on structure and hardening of Al–Ca eutectic alloys

Energy Technology Data Exchange (ETDEWEB)

Belov, N.A., E-mail: nikolay-belov@yandex.ru [National Research and Technological University “MISIS”, 4, Leninsky pr., Moscow 119049 (Russian Federation); Naumova, E.A. [Bauman Moscow State Technical University, 5, 2 ul. Baumanskaya, Moscow, 105005 (Russian Federation); Alabin, A.N. [National Research and Technological University “MISIS”, 4, Leninsky pr., Moscow 119049 (Russian Federation); UC RUSAL, 13/1, Nikoloyamskaya st., Moscow, 109240 (Russian Federation); Matveeva, I.A. [UC RUSAL, 13/1, Nikoloyamskaya st., Moscow, 109240 (Russian Federation)

2015-10-15

The phase composition, structure and hardening of alloys in the aluminium corner of the Al–Ca–Sc system were studied in the range up to 10% Ca and up to 1% S≿. The experimental study (optical, scanning and transmission electron microscopy with electron-microprobe analysis, differential thermal analysis and hardness measurements) was combined with Thermo-Calc software simulation for the optimization of the alloy composition. It was shown that only phases of the binary systems (Al{sub 4}Ca and Al{sub 3}Sc) might be in equilibrium with the aluminium solid solution. It was shown that the (Al) + Al{sub 4}Ca eutectic had a much finer structure as compared with the Al–Si eutectic, which suggests a possibility of reaching higher mechanical properties as compared to commercial alloys of the A356 type. The influence of the annealing temperature within the range up to 600 °C on the structure and hardness of the Al–Ca–Sc experimental alloys was studied. It was determined that the maximum hardening corresponded to the annealing at 300 °C, which was due to the precipitation of Al{sub 3}Sc nanoparticles with their further coarsening. With an example of an Al-7.6% Ca-0.3% Sc model experimental alloy, a principal possibility of manufacturing aluminium casting alloys based on the (Al) + Al{sub 4}Ca eutectic was demonstrated. Unlike commercial alloys of the A356 type, the model alloy does not require quenching, as hardening particles are formed in the course of annealing of casting. - Highlights: • Al–Ca–Sc phase diagram in aluminum corner. • Formation of Al{sub 3}Sc nanoparticles in eutectic (Al) + Al{sub 4}Ca during heating at 300–450 °C. • Hardening and thermal stability of proposed (Al–Ca–Sc) and commercial (Al–Si–Mg, 356 type) eutectic alloys.

Tris(dibenzoylmethanido-κ2O,O′[(6S,8S-(+-7,7-dimethyl-3-(2-pyridyl-5,6,7,8-tetrahydro-6,8-methanoisoquinoline-κ2N,N′]gadolinium(III

Directory of Open Access Journals (Sweden)

Xi-Li Li

2009-09-01

Full Text Available In the title compound, [Gd(C15H11O23(C17H18N2], the GdIII atom is coordinated by six O atoms from three β-diketonate ligands and two N atoms from a chiral ligand LS,S-(+-7,7-dimethyl-3-(2-pyridyl-5,6,7,8-tetrahydro-6,8-methanoisoquinoline, in a coordination geometry best described as distorted square-antiprismatic.

Highly active and durable Ca-doped Ce-SBA-15 catalyst for biodiesel production

International Nuclear Information System (INIS)

Thitsartarn, Warintorn; Maneerung, Thawatchai; Kawi, Sibudjing

2015-01-01

In this work, Ca-doped Ce-incorporated SBA-15 (Ca/CeS) catalyst was successfully synthesized by using direct synthesis of Ce-incorporated SBA-15 followed by impregnation of CaO (calcium oxide). The maximum Si/Ce molar ratio that Ce atoms can be incorporated successfully into the mesoporous framework was found to be 5 (CeS-5). After the impregnation of 30 wt. % Ca, the obtained 30Ca/CeS-5 catalysts showed the superior catalytic performance for transesterification reaction of palm oil with methanol and also the higher catalytic activity as compared to other supported catalysts, i.e. CaO/CeO 2 and CaO–CeO 2 /SBA-15. This can be attributed to the well-dispersion of CaO on the CeS-5 support surface. Furthermore, it was found that the leaching of Si, Ce and Ca from the catalyst into biodiesel produced was negligible (i.e. <1 ppm after 7 cycles), indicating the strong interaction between CaO and CeS-5 support. As a result, the 30Ca/CeS-5 catalyst can be reused at least 15 cycles with insignificant decrease in catalytic activity, offering the efficient CaO-based catalyst for biodiesel production. - Highlights: • Mesoporous Ca-based catalyst was successfully developed for biodiesel production. • Catalyst exhibited high activity towards transesterification (FAME yield > 98%). • Catalyst can be effectively re-used at least 15 cycles. • Extremely low catalyst contaminant (<1 ppm) was presented

Determination of Ca, Fe, Cu and Zn content in hair by EDXRF method

International Nuclear Information System (INIS)

Yang Mingtai; Chen Jinhua; Qi Honglian; Gao Ge

1994-01-01

The authors introduce an analysing method that can determine simultaneously Ca, Fe, Cu and Zn in hair by using energy-dispersive X ray fluorescence analyzer of tube-excite type made in China. The added element Y is used as internal standard in hair sample. The hair is resolved by chemical reagent to make test sample, then the energy-dispersive X ray fluorescence analyzer is used to determine Ca, fe, Cu and Zn contents in hair sample. The lower limits of detection are 7 x 10 -6 , 1 x 10 -6 , 4 x 10 -6 , 3 x 10 -6 , respectively. Correlative coefficients of variations are 6%, 1%, 2%, 2%

MPK6 controls H2 O2-induced root elongation by mediating Ca2+ influx across the plasma membrane of root cells in Arabidopsis seedlings.

Science.gov (United States)

Han, Shuan; Fang, Lin; Ren, Xuejian; Wang, Wenle; Jiang, Jing

2015-01-01

Mitogen-activated protein kinases (MPKs) play critical roles in signalling and growth, and Ca(2+) and H2 O2 control plant growth processes associated with abscisic acid (ABA). However, it remains unclear how MPKs are involved in H2 O2 - and Ca(2+) -mediated root elongation. Root elongation in seedlings of the loss-of-function mutant Atmpk6 (Arabidopsis thaliana MPK6) was less sensitive to moderate H2 O2 or ABA than that in wild-type (WT) plants. The enhanced elongation was a result of root cell expansion. This effect disappeared when ABA-induced H2 O2 accumulation or the cytosolic Ca(2+) increase were defective. Molecular and biochemical evidence showed that increased expression of the cell wall peroxidase PRX34 in Atmpk6 root cells enhanced apoplastic H2 O2 generation; this promoted a cytosolic Ca(2+) increase and Ca(2+) influx across the plasma membrane. The plasma membrane damage caused by high levels of H2 O2 was ameliorated in a Ca(2+) -dependent manner. These results suggested that there was intensified PRX34-mediated H2 O2 generation in the apoplast and increased Ca(2+) flux into the cytosol of Atmpk6 root cells; that is, the spatial separation of apoplastic H2 O2 from cytosolic Ca(2+) in root cells prevented H2 O2 -induced inhibition of root elongation in Atmpk6 seedlings. © 2014 The Authors. New Phytologist © 2014 New Phytologist Trust.

Study of LiF:Mg,Ti and CaSO4:Dy dosimeters TL response to electron beams of 6 MeV applied to radiotherapy using PMMA and solid water phantoms

International Nuclear Information System (INIS)

Bravim, A.; Sakuraba, R.K.; Cruz, J.C.; Campos, L.L.

2011-01-01

The performance of CaSO 4 :Dy and LiF:Mg,Ti dosimeters to electron beams applied to radiotherapy was investigated. The TL response of these dosimeters was studied for 6 MeV electron beams using PMMA and Solid Water (SW) phantoms. The dosimeters were previously separated in groups according to their TL individual sensitivities to 60 Co gamma-radiation in air under electronic equilibrium conditions. After that, they were irradiated with 6 MeV electron doses of 0.1, 0.5, 1, 5 and 10 Gy using a linear accelerator Clinac 2100C Varian of Hospital Israelita Albert Einstein – HIAE. The electron beam irradiations were performed using a 10 × 10 cm 2 field size, 100 cm source-phantom surface distance and the dosimeters were positioned at the depth of maximum dose (1.2 cm). The TL readings were carried out between 24 and 32 h after irradiation using a Harshaw 3500 TL reader. The TL dose–response of both type of dosimeters and phantoms presented linear behavior on the electron dose range from 0.1 to 5 Gy CaSO 4 :Dy dosimeter is 21 times more sensitive than LiF:Mg,Ti, dosimeter commonly used in clinical dosimetry. The obtained results indicate that the performance of CaSO 4 :Dy dosimeters is similar to LiF:Mg,Ti dosimeters and this material can be an alternative dosimetric material to be used to clinical electron beams dosimetry.

7 CFR 948.6 - Seed potatoes.

Science.gov (United States)

2010-01-01

... 7 Agriculture 8 2010-01-01 2010-01-01 false Seed potatoes. 948.6 Section 948.6 Agriculture... and Orders; Fruits, Vegetables, Nuts), DEPARTMENT OF AGRICULTURE IRISH POTATOES GROWN IN COLORADO Order Regulating Handling Definitions § 948.6 Seed potatoes. Seed potatoes or seed means any potatoes...

7 CFR 371.6 - Wildlife Services.

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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...

7 CFR 981.6 - Shelled almonds.

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2010-01-01

... 7 Agriculture 8 2010-01-01 2010-01-01 false Shelled almonds. 981.6 Section 981.6 Agriculture... and Orders; Fruits, Vegetables, Nuts), DEPARTMENT OF AGRICULTURE ALMONDS GROWN IN CALIFORNIA Order Regulating Handling Definitions § 981.6 Shelled almonds. Shelled almonds mean raw or roasted almonds after...

7 CFR 1773.6 - Auditor communication.

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2010-01-01

... 7 Agriculture 12 2010-01-01 2010-01-01 false Auditor communication. 1773.6 Section 1773.6... AGRICULTURE (CONTINUED) POLICY ON AUDITS OF RUS BORROWERS RUS Audit Requirements § 1773.6 Auditor... the auditor to communicate certain information regarding the nature and extent of testing and...

Altered Ca fluxes and contractile state during pH changes in cultured heart cells

International Nuclear Information System (INIS)

Kim, D.; Smith, T.W.

1987-01-01

The authors studied mechanisms underlying changes in myocardial contractile state produced by intracellular (pH/sub i/) or extracellular (pH 0 ) changes in pH using cultured chick embryo ventricular cells. A change in pH 0 of HEPES-buffered medium from 7.4 to 6.0 or to 8.8 changed the amplitude of cell motion by -85 or +60%, and 45 Ca uptake at 10 s by -29 or +22%, respectively. The pH 0 induced change in Ca uptake was not sensitive to nifedipine but was Na gradient dependent. Changes in pH/sub i/ produced by NH 4 Cl or preincubation in media at pH values ranging from 6.0 to 8.8 failed to alter significantly 45 Ca uptake or efflux. However, larger changes in pH/sub i/ were associated with altered Ca uptake. Changes in pH 0 from 7.5 to 6.0 or to 8.8 were associated with initial changes in 45 Ca efflux by +17 or -18%, respectively, and these effects were not Na dependent. Exposure of cells to 20 mM NH 4 Cl produced intracellular alkalinization and a positive inotropic effect, whereas subsequent removal of NH 4 Cl caused intracellular acidification and a negative inotropic effect. There was, however, a lack of close temporal relationships between pH/sub i/ and contractile state. These results indicated that pH 0 -induced changes in contractile state in cultured heart cells are closely correlated with altered transarcolemmal Ca movements and presumably are due to these Ca flux changes

Electrical Conductivity of Cancrinite-Type Na8 - 2 x Ca x [Al6Si6O24][CO3] · 2H2O ( x ≤ 0.03) Crystals

Science.gov (United States)

Sorokin, N. I.

2018-05-01

The electrical conductivity of crystals of artificial cancrinite Na8 - 2 x Ca x [Al6Si6O24][CO3] · 2H2O ( x ≤ 0.03) has been studied in the temperature range of 498-604 K. These crystals were grown by hydrothermal synthesis on a seed in the Na2O-Al2O3-SiO2-H2O system ( t = 380-420°C, P = 3 × 107-9 × 107 Pa). The ionic conductivity of a single-crystal sample (sp. gr. P63), measured along the crystallographic axis c, is low: σ = 8 × 10-7 S/cm at 300°C. The electric transport activation energy is E a = 0.81 ± 0.05 eV. The relationship between the ionic conductivity and specific features of the atomic structure of cancrinites is discussed.

Thermally and optically stimulated radiative processes in Eu and Y co-doped LiCaAlF{sub 6} crystal

Energy Technology Data Exchange (ETDEWEB)

Fukuda, Kentaro, E-mail: ken-fukuda@tokuyama.co.jp [Tokuyama Corporation, 1-1 Mikage-cho, Shunan-shi, Yamaguchi 745-8648 (Japan); Yanagida, Takayuki; Fujimoto, Yutaka [Kyushu Institute of Technology, 2-4 Hibikino, Wakamatsu, Kitakyushu, Fukuoka 808-0196 (Japan)

2015-06-01

Yttrium co-doping was attempted to enhance dosimeter performance of Eu doped LiCaAlF{sub 6} crystal. Eu doped and Eu, Y co-doped LiCaAlF{sub 6} were prepared by the micro-pulling-down technique, and their dosimeter characteristics such as optically stimulated luminescence (OSL) and thermally stimulated luminescence (TSL) were investigated. By yttrium co-doping, emission intensities of OSL and TSL were enhanced by some orders of magnitude. In contrast, scintillation characteristics of yttrium co-doped crystal such as intensity of prompt luminescence induced by X-ray and light yield under neutron irradiation were degraded.

Age and adaptation to Ca and P deficiencies: 2. Impacts on amino acid digestibility and phytase efficacy in broilers.

Science.gov (United States)

Li, W; Angel, R; Kim, S-W; Jiménez-Moreno, E; Proszkowiec-Weglarz, M; Plumstead, P W

2015-12-01

A total of 1,152 straight-run hatchling Heritage 56M×fast feathering Cobb 500F broiler birds were used to determine Ca, age, and adaptation effects on apparent ileal digestibility of crude protein (AID of CP), amino acids (AID of AA) and phytase efficacy. Twelve treatments with 8 replicates, each were fed from 7 to 9 d (6 birds per replicate), 7 to 21 d (6 birds per replicate) and 19 to 21 d (3 birds per replicate) d of age. Diets were prepared with 3 Ca (0.65, 0.80, and 0.95%) and 2 non-phytate P, (0.20 and 0.40%) concentrations. A 6-phytase was added at 500 or 1,000 FTU/kg to the 0.20% nPP diet at each Ca concentration. The age and adaptation effects were determined by comparing the responses between birds fed from 7 to 9 and 19 to 21 d of age, 19 to 21, and 7 to 21 d of age, respectively. An age effect was observed regardless of Ca, nPP, or phytase concentration, with older birds (19 to 21 d) having greater apparent ileal digestibility (AID) of amino acids (AA) and CP than younger birds (7 to 9 d; Pphytase concentrations. Constant lower AID of CP and AA was seen in adapted birds (7 to 21 d) compared to unadapted bird (19 to 21 d) when 0.20% nPP diets were fed at 0.95% Ca concentrations (PPhytase efficacy was significantly lower in younger (7 to 9 d) compared to older birds (19 to 21 d; PPhytase inclusion increased AID of CP and AA regardless of Ca (P<0.05). In conclusion, the AID of CP and AA can be affected by diet, age, and adaptation. © 2015 Poultry Science Association Inc.

Productivity response of calcareous nannoplankton to Eocene Thermal Maximum 2 (ETM2

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M. Dedert

2012-05-01

Full Text Available The Early Eocene Thermal Maximum 2 (ETM2 at ~53.7 Ma is one of multiple hyperthermal events that followed the Paleocene-Eocene Thermal Maximum (PETM, ~56 Ma. The negative carbon excursion and deep ocean carbonate dissolution which occurred during the event imply that a substantial amount (10³ Gt of carbon (C was added to the ocean-atmosphere system, consequently increasing atmospheric CO₂(pCO₂. This makes the event relevant to the current scenario of anthropogenic CO₂ additions and global change. Resulting changes in ocean stratification and pH, as well as changes in exogenic cycles which supply nutrients to the ocean, may have affected the productivity of marine phytoplankton, especially calcifying phytoplankton. Changes in productivity, in turn, may affect the rate of sequestration of excess CO₂ in the deep ocean and sediments. In order to reconstruct the productivity response by calcareous nannoplankton to ETM2 in the South Atlantic (Site 1265 and North Pacific (Site 1209, we employ the coccolith Sr/Ca productivity proxy with analysis of well-preserved picked monogeneric populations by ion probe supplemented by analysis of various size fractions of nannofossil sediments by ICP-AES. The former technique of measuring Sr/Ca in selected nannofossil populations using the ion probe circumvents possible contamination with secondary calcite. Avoiding such contamination is important for an accurate interpretation of the nannoplankton productivity record, since diagenetic processes can bias the productivity signal, as we demonstrate for Sr/Ca measurements in the fine (<20 μm and other size fractions obtained from bulk sediments from Site 1265. At this site, the paleoproductivity signal as reconstructed from the Sr/Ca appears to be governed by cyclic changes, possibly orbital forcing, resulting in a 20–30% variability in Sr/Ca in dominant genera as obtained by ion probe. The ~13 to 21

7 CFR 2903.6 - Project types.

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2010-01-01

... 7 Agriculture 15 2010-01-01 2010-01-01 false Project types. 2903.6 Section 2903.6 Agriculture... AGRICULTURE BIODIESEL FUEL EDUCATION PROGRAM Program Description § 2903.6 Project types. OEPNU intends to... predetermined project period with a statement of intention to provide additional support at a future date...

7 CFR 1000.6 - Supply plant.

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2010-01-01

... 7 Agriculture 9 2010-01-01 2009-01-01 true Supply plant. 1000.6 Section 1000.6 Agriculture Regulations of the Department of Agriculture (Continued) AGRICULTURAL MARKETING SERVICE (Marketing Agreements... Definitions § 1000.6 Supply plant. Supply plant means a plant approved by a duly constituted regulatory agency...

6-Bromohypaphorine from Marine Nudibranch Mollusk Hermissenda crassicornis is an Agonist of Human α7 Nicotinic Acetylcholine Receptor

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Igor E. Kasheverov

2015-03-01

Full Text Available 6-Bromohypaphorine (6-BHP has been isolated from the marine sponges Pachymatisma johnstoni, Aplysina sp., and the tunicate Aplidium conicum, but data on its biological activity were not available. For the nudibranch mollusk Hermissenda crassicornis no endogenous compounds were known, and here we describe the isolation of 6-BHP from this mollusk and its effects on different nicotinic acetylcholine receptors (nAChR. Two-electrode voltage-clamp experiments on the chimeric α7 nAChR (built of chicken α7 ligand-binding and glycine receptor transmembrane domains or on rat α4β2 nAChR expressed in Xenopus oocytes revealed no action of 6-BHP. However, in radioligand analysis, 6-BHP competed with radioiodinated α-bungarotoxin for binding to human α7 nAChR expressed in GH4C1 cells (IC50 23 ± 1 μM, but showed no competition on muscle-type nAChR from Torpedo californica. In Ca2+-imaging experiments on the human α7 nAChR expressed in the Neuro2a cells, 6-BHP in the presence of PNU120596 behaved as an agonist (EC50 ~80 μM. To the best of our knowledge, 6-BHP is the first low-molecular weight compound from marine source which is an agonist of the nAChR subtype. This may have physiological importance because H. crassicornis, with its simple and tractable nervous system, is a convenient model system for studying the learning and memory processes.

Phase transformation of Ca{sub 4}[Al{sub 6}O{sub 12}]SO{sub 4} and its disordered crystal structure at 1073 K

Energy Technology Data Exchange (ETDEWEB)

Kurokawa, Daisuke [Department of Materials Science and Engineering, Nagoya Institute of Technology, Nagoya 466-8555 (Japan); R and D Center, Taiheiyo Cement Corporation, Chiba 285-8655 (Japan); Takeda, Seiya [Department of Materials Science and Engineering, Nagoya Institute of Technology, Nagoya 466-8555 (Japan); Colas, Maggy [Science des Proce' de' s Ce' ramiques et de Traitements de Surface (SPCTS), UMR 7315 CNRS, Universite' de Limoges, Centre Europe' en de la Ce' ramique, 12 Rue Atlantis, 87068 Limoges Cedex (France); Asaka, Toru [Department of Materials Science and Engineering, Nagoya Institute of Technology, Nagoya 466-8555 (Japan); Thomas, Philippe [Science des Proce' de' s Ce' ramiques et de Traitements de Surface (SPCTS), UMR 7315 CNRS, Universite' de Limoges, Centre Europe' en de la Ce' ramique, 12 Rue Atlantis, 87068 Limoges Cedex (France); Fukuda, Koichiro, E-mail: fukuda.koichiro@nitech.ac.jp [Department of Materials Science and Engineering, Nagoya Institute of Technology, Nagoya 466-8555 (Japan)

2014-07-01

The phase transformation of Ca{sub 4}[Al{sub 6}O{sub 12}]SO{sub 4} and the crystal structure of its high-temperature phase were investigated by differential thermal analysis, temperature-dependent Raman spectroscopy and high-temperature X-ray powder diffraction (CuKα{sub 1}). We determined the starting temperature of the orthorhombic-to-cubic transformation during heating (=711 K) and that of the reverse transformation during cooling (=742 K). The thermal hysteresis was negative (=−31 K), suggesting the thermoelasticity of the transformation. The space group of the high temperature phase is I4{sup ¯}3m with the unit-cell dimensions of a=0.92426(2) nm and V=0.78955(2) nm{sup 3} (Z=2) at 1073 K. The initial structural model was derived by the direct methods and further refined by the Rietveld method. The final structural model showed the orientational disordering of SO{sub 4} tetrahedra. The maximum-entropy method-based pattern fitting method was used to confirm the validity of the split-atom model, in which conventional structure bias caused by assuming intensity partitioning was minimized. At around the transformation temperature during heating, the vibrational spectra, corresponding to the Raman-active SO{sub 4} internal stretching mode, showed the continuous and gradual change in the slope of full width at half maximum versus temperature curve. This strongly suggests that the orthorhombic-to-cubic phase transformation would be principally accompanied by the statistical disordering in orientation of the SO{sub 4} tetrahedra, without distinct dynamical reorientation. - Graphical abstract: (Left) Three-dimensional electron-density distributions of the SO{sub 4} tetrahedron with the split-atom model, and (right) a bird's eye view of electron densities on the plane parallel to (111). - Highlights: • Crystal structure of Ca{sub 4}[Al{sub 6}O{sub 12}]SO{sub 4} at 1073 K is determined by powder XRD. • The atom arrangements are represented by the split

In situ formation of CA6 platelets in Al2O3 and Al2O3/ZrO2 matrices

International Nuclear Information System (INIS)

Belmonte, M.; Sanchez-Herencia, A.J.; Moreno, R.; Miranzo, P.; Moya, J.S.; Tomsia, A.P.

1993-01-01

Al 2 O 3 and Al 2 O 3 /ZrO 2 compacts containing CaO as a dopant have been sintered under different conditions and atmospheres: air, high vacuum (> 10 -6 torr). SEM observations have been made on the polished surfaces of sintered and also of annealed samples. Only after the annealing treatment in air at temperatures ranging from 1400 to 1500 C, a massive formation of CA 6 platelets was detected in samples sintered in low oxygen partial pressure atmospheres. In order to clarify the mechanism of formation of this secondary phase at the grain boundaries, CaO has been introduced in the form of either plaster of Paris (to reproduce a possible contamination provided by the molds in slip casting) or CaCO 3 . The obtained results indicate the important role of the firing atmosphere on the precipitation of secondary phases at grain boundary. (orig.)

A novel high color purity blue-emitting phosphor: CaBi{sub 2}B{sub 2}O{sub 7}:Tm{sup 3+}

Energy Technology Data Exchange (ETDEWEB)

Li, Jiangong, E-mail: lijiangong01@gmail.com [Department of Electronic Science and Engineering, Huanghuai University, Zhumadian 463000 (China); Yan, Huifang [Department of Foreign Languages and Literature, Huanghuai University, Zhumadian 463000 (China); Yan, Fengmei [Department of Chemistry and Chemical Engineering, Huanghuai University, Zhumadian 463000 (China)

2016-07-15

Graphical abstract: - Highlights: • A series of Tm{sup 3+}-doped CaBi{sub 2}B{sub 2}O{sub 7} blue-emitting phosphors were prepared. • The optimum doping content of Tm{sup 3+} ions was found. • The critical distance and concentration quenching mechanism was discussed. • The color purity of as prepared sample was analyzed and compared. - Abstract: A series of Tm{sup 3+}-doped CaBi{sub 2−x}B{sub 2}O{sub 7}:xTm{sup 3+} (0.02 ≤ x ≤ 0.12) blue-emitting phosphors with high color purity were prepared by solid-state reaction method. The crystal structure and luminescence properties of the as-prepared phosphors were studied. This phosphor shows a satisfactory blue performance (peak at 453 nm) due to the {sup 1}D{sub 2} → {sup 3}F{sub 4} transition of Tm{sup 3+} excited by 357 nm light. Investigation of Tm{sup 3+} content dependent emission spectra indicates that x = 0.04 is the optimum doping content of Tm{sup 3+} ions in the CaBi{sub 2}B{sub 2}O{sub 7} host. The critical distance and the concentration quenching mechanism were also investigated. In particular, the color purity of as prepared sample was analyzed and the result shows that the color purity of CaBi{sub 2}B{sub 2}O{sub 7}:Tm{sup 3+} is higher than the commercial blue phosphor BaMgAl{sub 10}O{sub 17}:Eu{sup 2+} (BAM:Eu{sup 2+}) and the latest reported Tm{sup 3+} doped blue phosphors. The present work suggests that the CaBi{sub 2}B{sub 2}O{sub 7}:Tm{sup 3+} phosphor is a potential blue-emitting candidate for the application in the near-UV WLEDs.

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

International Nuclear Information System (INIS)

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

2003-01-01

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

Effect of calcium fluoride on sintering behaviour of SiO2-CaO-Na2O-MgO glass-ceramic system

Directory of Open Access Journals (Sweden)

Bahman Mirhadi

2012-09-01

Full Text Available The crystallization characteristics of glasses based on the SiO2-CaO-Na2O-MgO (SCNM system containing calcium fluoride (CaF2 have been investigated by differential thermal analysis (DTA, X-ray diffraction (XRD and scanning electron microscopy (SEM. The partial replacement of CaO by CaF2 in the studied glass-ceramics led to the development of different crystalline phase assemblages, including wollastonite and diopside using various heat-treatment processes. With the increase of CaF2 content, the crystallization temperature of the glass and the strength of the crystallization peak temperature decreases. Addition of CaF2 up to 6.0 mol%, as expected, improved the sinterability. This sample reached to maximum density by sintering at 950 °C.

Synthesis and Fungicidal Activities of (Z/E-3,7-Dimethyl-2,6-octadienamide and Its 6,7-Epoxy Analogues

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Mingyan Yang

2015-11-01

Full Text Available In order to find new lead compounds with high fungicidal activity, (Z/E-3,7-dimethyl-2,6-octadienoic acids were synthesized via selective two-step oxidation using the commercially available geraniol/nerol as raw materials. Twenty-eight different (Z/E-3,7-dimethyl-2,6-octadienamide derivatives were prepared by reactions of (Z/E-carboxylic acid with various aromatic and aliphatic amines, followed by oxidation of peroxyacetic acid to afford their 6,7-epoxy analogues. All of the compounds were characterized by HR-ESI-MS and 1H-NMR spectral data. The preliminary bioassays showed that some of these compounds exhibited good fungicidal activities against Rhizoctonia solani (R. solani at a concentration of 50 µg/mL. For example, 5C, 5I and 6b had 94.0%, 93.4% and 91.5% inhibition rates against R. solani, respectively. Compound 5f displayed EC50 values of 4.3 and 9.7 µM against Fusahum graminearum and R. Solani, respectively.

Measurement and estimation of maximum skin dose to the patient for different interventional procedures

International Nuclear Information System (INIS)

Cheng Yuxi; Liu Lantao; Wei Kedao; Yu Peng; Yan Shulin; Li Tianchang

2005-01-01

Objective: To determine the dose distribution and maximum skin dose to the patient for four interventional procedures: coronary angiography (CA), hepatic angiography (HA), radiofrequency ablation (RF) and cerebral angiography (CAG), and to estimate the definitive effect of radiation on skin. Methods: Skin dose was measured using LiF: Mg, Cu, P TLD chips. A total of 9 measuring points were chosen on the back of the patient with two TLDs placed at each point, for CA, HA and RF interventional procedures, whereas two TLDs were placed on one point each at the postero-anterior (PA) and lateral side (LAT) respectively, during the CAG procedure. Results: The results revealed that the maximum skin dose to the patient was 1683.91 mGy for the HA procedure with a mean value of 607.29 mGy. The maximum skin dose at the PA point was 959.3 mGy for the CAG with a mean value of 418.79 mGy; While the maximum and the mean doses at the LAT point were 704 mGy and 191.52 mGy, respectively. For the RF procedure the maximum dose was 853.82 mGy and the mean was 219.67 mGy. For the CA procedure the maximum dose was 456.1 mGy and the mean was 227.63 mGy. Conclusion: All the measured dose values in this study are estimated ones which could not provide the accurate maximum value because it is difficult to measure using a great deal of TLDs. On the other hand, the small area of skin exposed to high dose could be missed as the distribution of the dose is successive. (authors)