Formation process of micro arc oxidation coatings obtained in a sodium phytate containing solution with and without CaCO{sub 3} on binary Mg-1.0Ca alloy

Energy Technology Data Exchange (ETDEWEB)

Zhang, R.F. [School of Material and Electromechanics, Jiangxi Science and Technology Normal University, Nanchang 330013 (China); Zhang, Y.Q. [Zhejiang DunAn Light Alloy Technology CO,.LTD, Zhuji 311835 (China); Hunan University of Science and Technology, Xiangtan 411201 (China); Zhang, S.F.; Qu, B. [School of Material and Electromechanics, Jiangxi Science and Technology Normal University, Nanchang 330013 (China); Guo, S.B. [Hunan University of Science and Technology, Xiangtan 411201 (China); Xiang, J.H., E-mail: xiangjunhuai@163.com [School of Material and Electromechanics, Jiangxi Science and Technology Normal University, Nanchang 330013 (China)

2015-01-15

Highlights: • Compared to the Mg phase, the area of Mg{sub 2}Ca phase is much smaller. • The coatings are preferentially developed on the area adjacent to Mg{sub 2}Ca phase. • During MAO process, some sodium phytate molecules are hydrolyzed. • Anodic coatings are developed from uneven to uniform. - Abstract: Micro arc oxidation (MAO) is an effective method to improve the corrosion resistance of magnesium alloys. In order to reveal the influence of alloying element Ca and CaCO{sub 3} electrolyte on the formation process and chemical compositions of MAO coatings on binary Mg-1.0Ca alloy, anodic coatings after different anodizing times were prepared on binary Mg-1.0Ca alloy in a base solution containing 3 g/L sodium hydroxide and 15 g/L sodium phytate with and without addition of CaCO{sub 3}. The coating formation was studied by using scanning electron microscope (SEM), energy dispersive X-ray spectroscopy (EDS) and X-ray diffraction (XRD). The results show that Mg-1.0Ca alloy is composed of two phases, the Mg phase and Mg{sub 2}Ca phase. After treating for 5 s, the coating began to develop and was preferentially formed on the area nearby Mg{sub 2}Ca phase, which may be resulted from the intrinsic electronegative potential of the Mg phase than that of Mg{sub 2}Ca phase. Anodic coatings unevenly covered the total surface after 20 s. After 80 s, the coatings were uniformly developed on Mg-1.0Ca alloy with micro pores. During MAO process, some sodium phytate molecules are hydrolyzed into inorganic phosphate. CaCO{sub 3} has minor influence on the calcium content of the obtained MAO coatings.

High-pressure densified solid solutions of alkaline earth hexaborides (Ca/Sr, Ca/Ba, Sr/Ba) and their high-temperature thermoelectric properties

International Nuclear Information System (INIS)

Gürsoy, M.; Takeda, M.; Albert, B.

2015-01-01

Solid solutions of alkaline earth hexaborides were synthesized and densified by spark plasma sintering at 100 MPa. The high-temperature thermoelectric properties (Seebeck coefficients, electrical and thermal diffusivities, heat capacities) were measured between room temperature and 1073 K. CaB 6 , SrB 6 , BaB 6 and the ternary hexaborides Ca x Sr 1−x B 6 , Ca x Ba 1−x B 6 , Sr x Ba 1−x B 6 (x = 0.25, 0.5, 0.75) are n-type conducting compounds over the whole compositional and thermal ranges. The values of the figure of merit ZT for CaB 6 (ca. 0.3 at 1073 K) were found to be significantly increased compared to earlier investigations which is attributed to the densification process. - Highlights: • Solid solutions of alkaline earth hexaborides were synthesized. • High-temperature thermoelectric properties of mixed calcium borides are excellent. • Spark plasma source densification results in high ZT values. • Borides are rare-earth free and refractory materials

Development of biodegradable Zn-1X binary alloys with nutrient alloying elements Mg, Ca and Sr

Science.gov (United States)

Li, H. F.; Xie, X. H.; Zheng, Y. F.; Cong, Y.; Zhou, F. Y.; Qiu, K. J.; Wang, X.; Chen, S. H.; Huang, L.; Tian, L.; Qin, L.

2015-01-01

Biodegradable metals have attracted considerable attentions in recent years. Besides the early launched biodegradable Mg and Fe metals, Zn, an essential element with osteogenic potential of human body, is regarded and studied as a new kind of potential biodegradable metal quite recently. Unfortunately, pure Zn is soft, brittle and has low mechanical strength in the practice, which needs further improvement in order to meet the clinical requirements. On the other hand, the widely used industrial Zn-based alloys usually contain biotoxic elements (for instance, ZA series contain toxic Al elements up to 40 wt.%), which subsequently bring up biosafety concerns. In the present work, novel Zn-1X binary alloys, with the addition of nutrition elements Mg, Ca and Sr were designed (cast, rolled and extruded Zn-1Mg, Zn-1Ca and Zn-1Sr). Their microstructure and mechanical property, degradation and in vitro and in vivo biocompatibility were studied systematically. The results demonstrated that the Zn-1X (Mg, Ca and Sr) alloys have profoundly modified the mechanical properties and biocompatibility of pure Zn. Zn-1X (Mg, Ca and Sr) alloys showed great potential for use in a new generation of biodegradable implants, opening up a new avenue in the area of biodegradable metals. PMID:26023878

Development of biodegradable Zn-1X binary alloys with nutrient alloying elements Mg, Ca and Sr.

Science.gov (United States)

Li, H F; Xie, X H; Zheng, Y F; Cong, Y; Zhou, F Y; Qiu, K J; Wang, X; Chen, S H; Huang, L; Tian, L; Qin, L

2015-05-29

Biodegradable metals have attracted considerable attentions in recent years. Besides the early launched biodegradable Mg and Fe metals, Zn, an essential element with osteogenic potential of human body, is regarded and studied as a new kind of potential biodegradable metal quite recently. Unfortunately, pure Zn is soft, brittle and has low mechanical strength in the practice, which needs further improvement in order to meet the clinical requirements. On the other hand, the widely used industrial Zn-based alloys usually contain biotoxic elements (for instance, ZA series contain toxic Al elements up to 40 wt.%), which subsequently bring up biosafety concerns. In the present work, novel Zn-1X binary alloys, with the addition of nutrition elements Mg, Ca and Sr were designed (cast, rolled and extruded Zn-1Mg, Zn-1Ca and Zn-1Sr). Their microstructure and mechanical property, degradation and in vitro and in vivo biocompatibility were studied systematically. The results demonstrated that the Zn-1X (Mg, Ca and Sr) alloys have profoundly modified the mechanical properties and biocompatibility of pure Zn. Zn-1X (Mg, Ca and Sr) alloys showed great potential for use in a new generation of biodegradable implants, opening up a new avenue in the area of biodegradable metals.

Chemical solution deposition of CaCu3Ti4O12 thin film

Indian Academy of Sciences (India)

Administrator

CaCu3Ti4O12; thin film; chemical solution deposition; dielectric properties. 1. Introduction. The CaCu3Ti4O12. (CCTO) compound has recently attracted considerable ... and Kelvin probe force microscopy (Chung et al 2004). Intrinsic .... SEM images of CCTO thin films as a function of sintering temperature. silicon based ...

Search for superheavy elements in the bombardment of 248Cm with 48Ca

International Nuclear Information System (INIS)

Hulet, E.K.; Lougheed, R.W.; Wild, J.F.; Landrum, J.H.; Stevenson, P.C.; Ghiorso, A.; Nitschke, J.M.; Otto, R.J.; Morrissey, D.J.; Baisden, P.A.; Gavin, B.F.; Lee, D.; Silva, R.J.; Fowler, M.M.; Seaborg, G.T.

1977-01-01

We have searched for superheavy elements 110 to 116 with half-lives between 10 4 and 10 8 s in fractions chemically separated after each of a series of bombardments of 248 Cm made with 267-MeV 48 Ca ions. After 6 months of α and spontaneous-fission counting, our results provide no persuasive evidence for the presence of super-heavy elements. The most plausible explanation for not finding the superheavy elements is that they have either short half-lives or very small formation cross sections

Solutions of group IV elements in liquid lithium

International Nuclear Information System (INIS)

Dadd, A.T.; Hubberstey, P.; Roberts, P.G.

1982-01-01

The solubilities of tin (0.00 = 22 Sn 5 . A simple thermochemical cycle is used to demonstrate that, whereas carbon dissolves endothermically in both liquid lithium and liquid sodium, the heavier Group IV elements dissolve exothermically. A similar cycle is used to derive solvation enthalpies (for the neutral gaseous species) for all Group IV elements in the two solvents. The trend in solvation enthalpy: C > Si > Ge > Sn > Pb is indicative of a diminishing affinity of solvent for solute and is attributed to the increasing metallic character of the solute as the Group is descended. (author)

Ca{sub 2−x}Li{sub 2x}GeO{sub 4} solid solutions. Chemical composition range and flux crystal growth

Energy Technology Data Exchange (ETDEWEB)

Ivanov, V.A. [N.I. Lobachevsky State University of Nizhni Novgorod, Nizhni Novgorod, 603950 (Russian Federation); Marychev, M.O., E-mail: marychev@yandex.ru [N.I. Lobachevsky State University of Nizhni Novgorod, Nizhni Novgorod, 603950 (Russian Federation); Andreev, P.V.; Lykov, V.A.; Faddeev, M.A. [N.I. Lobachevsky State University of Nizhni Novgorod, Nizhni Novgorod, 603950 (Russian Federation); Koseva, I. [Bulgarian Academy of Science, Institute of General and Inorganic Chemistry, BU-1113 Sofia (Bulgaria); Nikolov, V. [N.I. Lobachevsky State University of Nizhni Novgorod, Nizhni Novgorod, 603950 (Russian Federation)

2015-11-01

A series of Ca{sub 2−x}Li{sub 2x}GeO{sub 4} specimens with 0 < 2x < 2, were synthesized by the classical solid state method. X-ray analysis revealed that for 0 < 2x < 0.6 only Ca{sub 2−x}Li{sub 2x}GeO{sub 4} solid solutions of Ca{sub 2}GeO{sub 4} structure crystallized. The cell parameters of these solid solutions linearly decreased upon increasing the lithium concentration, which means that the solutions are in accordance with the Vegard's law. For 2x > 0.6 the specimens contained two phases: (i) Ca{sub 2−x}Li{sub 2x}GeO{sub 4} solid solutions with maximum lithium concentration approximately equal to that for 2x = 0.6 and minimum values of the cell parameters and (ii) Li{sub 2}CaGeO{sub 4} phase. Li{sub 2}O·MoO{sub 3}–Ca{sub 2}GeO{sub 4} high-temperature solutions were used to grow Ca{sub 2−x}Li{sub 2x}GeO{sub 4} solid solutions and Li{sub 2}CaGeO{sub 4} single crystals by the high temperature solution (flux) method. Li{sub 2}CaGeO{sub 4} crystals were grown in the concentration range 8–26 wt. % Ca{sub 2}GeO{sub 4} in the temperature range 830–980 °C. Crystals with chemical compositions of the Ca{sub 2−x}Li{sub 2x}GeO{sub 4} solid solutions with different Li concentrations were grown in the concentration range 26–40 wt. % Ca{sub 2}GeO{sub 4} in the temperature range 980–1090 °C. - Highlights: • Ca{sub 2−x}Li{sub 2x}GeO{sub 4} solid solutions are established for the first time. • The Li concentration range into the solutions is between 0 and 0.6. • The solid solutions are in accordance to Vegard's law. • Suitable solutions are found out for Ca{sub 2−x}Li{sub 2x}GeO{sub 4} and Li{sub 2}CaGeO{sub 4} crystal growth.

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.

76 FR 59167 - Siemens Medical Solutions USA, Inc., Oncology Care Systems Division, Concord, CA; Siemens Medical...

Science.gov (United States)

2011-09-23

... Medical Solutions USA, Inc., Oncology Care Systems Division, Concord, CA; Siemens Medical Solutions USA... Solutions USA, Inc. (Siemens), Oncology Care Systems Division, Concord, California (subject firm). The...., Oncology Care Systems Division, Concord, California (TA-W-73,158) and Siemens Medical Solutions USA, Inc...

Methodology to obtain exchange properties of the calcite surface-Application to major and trace elements: Ca(II), HCO3-, and Zn(II)

International Nuclear Information System (INIS)

Tertre, E.; Beaucaire, C.; Juery, A.; Ly, J.; Tertre, E.; Beaucaire, C.; Juery, A.; Ly, J.

2010-01-01

Sorption of inorganic elements onto carbonate minerals has been intensively described in the literature by two reaction steps: (1) a first one rapid and completed within a few hours and (2) a second one slower, eventually irreversible, and occurring at a constant rate. The first step is often attributed to an ion-exchange process, but its reversibility is rarely investigated. Consequently, discrimination of the global sorption phenomenon into two different mechanisms is not always justified. In this study, we investigated, by batch experiments, both sorption and desorption of Ca(II), HCO 3 - , and Zn(II), radiolabeled with isotopes 45 Ca(II), H 14 CO 3 - , and 65 Zn(II), respectively, onto synthetic pure calcite. Solutions were pre-equilibrated with atmospheric p(CO 2 ) and saturated with respect to calcite. Therefore, our purpose was to: (1) obtain experimental distribution coefficients of major elements (Ca(II) and HCO 3 - ) and a trace element (Zn(II)) onto calcite from sorption and desorption experiments, (2) test the validity of a first-occurring ion-exchange process generally noted in the literature, by calculating distribution coefficients for the 'sole' exchange process, and (3) quantify the amounts of Ca(II), HCO 3 - , and Zn(II) sorbed on the calcite surface by the sole 'exchange process' and compare them with surface crystallochemical data. Ca(II) or HCO 3 - sorption experimental data suggest that a significant fraction of these two elements was sorbed irreversibly onto or in the calcite. By using a method based on isotopic ratios, the Ca(II) or HCO 3 - concentrations, which are reversibly adsorbed on the calcite, have been quantified. These concentrations are respectively estimated at 4. 0 ± 2. 0 * 10 -4 and 7. 0 ± 1. 5 * 10 -4 mol/kg. The obtained Ca(II) surface concentration value is one order of magnitude lower than the one obtained from isotopic measurement by former authors [Geochim. Cosmochim. Acta 55 (1991) 1549; Geochim. Cosmochim. Acta 51

Redox reactions for group 5 elements, including element 105, in aqueous solutions

International Nuclear Information System (INIS)

Ionova, G.V.; Pershina, V.; Johnson, E.; Fricke, B.; Schaedel, M.

1992-08-01

Standard redox potentials Edeg(M z+x /M z+ ) in acidic solutions for group 5 elements including element 105 (Ha) and the actinide, Pa, have been estimated on the basis of the ionization potentials calculated via the multiconfiguration Dirac-Fock method. Stability of the pentavalent state was shown to increase along the group from V to Ha, while that of the tetra- and trivalent states decreases in this direction. Our estimates have shown no extra stability of the trivalent state of hahnium. Element 105 should form mixed-valence complexes by analogy with Nb due to the similar values of their potentials Edeg(M 3+ /M 2+ ). The stability of the maximum oxidation state of the elements decreases in the direction 103 > 104 > 105. (orig.)

Distribution Pattern of Fe, Sr, Zr and Ca Elements as Particle Size Function in the Code River Sediments from Upstream to Downstream

International Nuclear Information System (INIS)

Sri Murniasih; Muzakky

2007-01-01

The analysis of Fe, Sr, Zr and Ca elements concentration of granular sediment from upstream to downstream of Code river has been done. The aim of this research is to know the influence of particle size on the concentration of Fe, Sr, Zr and Ca elements in the Code river sediments from upstream to downstream and its distribution pattern. The instrument used was x-ray fluorescence with Si(Li) detector. Analysis results show that more Fe and Sr elements are very much found in 150 - 90 μm particle size, while Zr and Ca elements are very much found in < 90 μm particle size. Distribution pattern of Fe, Sr, Zr and Ca elements distribution in Code river sediments tends to increase relatively from upstream to downstream following its conductivity. The concentration of Fe, Sr, Zr and Ca elements are 1.49 ± 0.03 % - 5.93 ± 0.02 % ; 118.20 ± 10.73 ppm - 468.21 ± 20.36 ppm; 19.81 ppm ± 0.86 ppm - 76.36 ± 3.02 ppm and 3.22 ± 0.25 % - 11.40 ± 0.31 % successively. (author)

Novel biocompatible magnesium alloys design with nutrient alloying elements Si, Ca and Sr: Structure and properties characterization

Energy Technology Data Exchange (ETDEWEB)

Wang, Weidan; Han, Junjie [Institute of Metal Research, Chinese Academy of Sciences, 72 Wenhua Road, Shenyang 110016 (China); Yang, Xuan; Li, Mei [Department of Orthopedics, Guangdong Key Lab of Orthopaedic Technology and Implant Materials, Guangzhou General Hospital of Guangzhou Military Command, 111 Liuhua Road, Guangzhou 510010 (China); Wan, Peng, E-mail: pwan@imr.ac.cn [Institute of Metal Research, Chinese Academy of Sciences, 72 Wenhua Road, Shenyang 110016 (China); Tan, Lili [Institute of Metal Research, Chinese Academy of Sciences, 72 Wenhua Road, Shenyang 110016 (China); Zhang, Yu [Department of Orthopedics, Guangdong Key Lab of Orthopaedic Technology and Implant Materials, Guangzhou General Hospital of Guangzhou Military Command, 111 Liuhua Road, Guangzhou 510010 (China); Yang, Ke, E-mail: kyang@imr.ac.cn [Institute of Metal Research, Chinese Academy of Sciences, 72 Wenhua Road, Shenyang 110016 (China)

2016-12-15

Highlights: • A non-toxic Mg-based alloy system with nutrient elements Si, Sr, Ca is proposed. • Properties improved due to morphology of coarse Mg{sub 2}Si change into small polygon. • Fewer, finer and homogenized Mg{sub 2}Si particles are obtained after anneal-treated. • Cytocompatibility results indicate a potential application in orthopedic. - Abstract: Magnesium has been widely studied as a biodegradable material, where its mechanical property and biocompatibility make it preferred candidate for orthopedic implant. Proper alloying can further improve the properties of Mg. First and foremost, to guarantee the biosafety for biomedical application, the alloying element should be toxic free. To address this point, nutrient elements including Si, Sr and Ca were selected due to their biological functions in human body, especially in bone regeneration and repair. In this study, 0.5–1.0 wt% Sr and Ca were used to refine and modify the morphology of coarse Mg{sub 2}Si in Mg-1.38wt% Si to obtain an uniform microstructure. Microstructure, mechanical and degradation properties of as-cast and homogenizing-annealed quaternary Mg-1.38Si-xSr-yCa (x, y = 0.5–1 wt%) alloys were investigated by optical microscopy, scanning electronic microscopy, X-ray diffraction, tensile and electrochemical measurement. Addition of Sr and Ca element cause a morphological change in Mg{sub 2}Si particles from coarse Chinese script shape to small polygonal type. The presences of intermetallic phases, such as Mg{sub 2}Si, CaMgSi and Mg{sub 17}Sr{sub 2}, were confirmed in quaternary alloys, of which content was applied to interpret the results for the quaternary system. Compared with the as-cast state, fewer, finer and homogenized microstructure were observed after an anneal heat treatment under 500 °C. The mechanical properties were improved with increase of Ca and Sr additions, which was related to the evolution of the microstructure and second phases, however, also causing an

On reactions of polymerization of p-element hydroxides in aqueous solutions

International Nuclear Information System (INIS)

Tikavyj, V.F.; Lesnikovich, A.I.

1978-01-01

The tendency of p-element hydroxides towards polymerization in aqueous solutions has been considered with respect to their location in the Periodic Table. Stable hydroxides of d-elements are practically all polymerized; among s-elements only berillium and magnesium hydroxides polymerize as the least dissociated ones. Hydroxides of the elements located to the right of the 4 Group and above the 5-th Period do not polymerize in aqueous solutions. The structure and tendency towards polymerization of In, Te, and I compounds have been studied. The tendency to polymerization of all hydroxides of p-elements located below the 4-th Period is explained from the standpoint of electron structure and the simplest thermodynamic analysis (entropy, enthalpy)

Tribological behaviors of graphite sliding against cemented carbide in CaCl2 solution

International Nuclear Information System (INIS)

Guo, Fei; Tian, Yu; Liu, Ying; Wang, Yuming

2015-01-01

The tribological behaviors of graphite sliding against cemented carbide were investigated using a standard tribological tester Plint TE92 in a ring-on-ring contact configuration in both CaCl 2 solution and deionized water. An interesting phenomenon occurred: as the CaCl 2 solution concentration increased, the friction coefficient firstly decreased and was lower than that in the deionized water, and then gradually increased, exceeding the friction coefficient in the deionized water. The wear rate of the ,graphite also presented the same variation trend. According to the polarization curves of cemented carbide, contact angle measurements, Raman spectrum analysis and scanning electron microscope (SEM) images analysis, the above friction and wear behaviors of graphite sliding against cemented carbide were attributed to the graphite surface wettability and the cemented carbide surface corrosion property. (paper)

Removal of Calcium from Scheelite Leaching Solution by Addition of CaSO4 Inoculating Crystals

Science.gov (United States)

Liu, Wenting; Li, Yongli; Zeng, Dewen; Li, Jiangtao; Zhao, Zhongwei

2018-04-01

In this work, the solubility behaviors of gypsum and anhydrite in the H2SO4-H3PO4-H2O system were investigated over the temperature range T = 30-80°C, and the results showed that the solubility of anhydrite was considerably lower than that of gypsum. On the basis of the differential solubilities of gypsum and anhydrite, a method was developed to remove calcium from the scheelite leaching solution by adding anhydrite as an inoculating crystal. The effects of the reaction time, concentration of the CaSO4 inoculating crystals, and temperature were investigated. With an addition of CaSO4 inoculating crystals at a concentration of 60 g/L, the Ca2+ concentration of the scheelite leaching solution decreased to a low level of approximately 0.76 g/L after 10 h at 70°C.

Molybdenum: the element and aqueous solution chemistry

International Nuclear Information System (INIS)

Sykes, A.G.

1987-01-01

This chapter on the chemistry of the coordination compounds of molybdenum concentrates on the element itself, its recovery from ores and its use in the manufacture of steels. Most of the chapter is devoted to the aqueous solution chemistry of molybdenum in oxidation states II, III and IV. (UK)

A multigrid solution method for mixed hybrid finite elements

Energy Technology Data Exchange (ETDEWEB)

Schmid, W. [Universitaet Augsburg (Germany)

1996-12-31

We consider the multigrid solution of linear equations arising within the discretization of elliptic second order boundary value problems of the form by mixed hybrid finite elements. Using the equivalence of mixed hybrid finite elements and non-conforming nodal finite elements, we construct a multigrid scheme for the corresponding non-conforming finite elements, and, by this equivalence, for the mixed hybrid finite elements, following guidelines from Arbogast/Chen. For a rectangular triangulation of the computational domain, this non-conforming schemes are the so-called nodal finite elements. We explicitly construct prolongation and restriction operators for this type of non-conforming finite elements. We discuss the use of plain multigrid and the multilevel-preconditioned cg-method and compare their efficiency in numerical tests.

Effect of organic substrates on available elemental contents in nutrient solution

Energy Technology Data Exchange (ETDEWEB)

Ao, Y.S.; Sun, M.; Li, Y.Q. [Shanghai Jiao Tong University, Shanghai (China). School for Agriculture & Biology

2008-07-15

In this paper, the changes of available elemental contents in the nutrient solution extracts of organic substrates (peat moss, charred rice husk, chicken manure, sawdust, turfgrass clipping and weathered coal) were studied and compared with that in the water extracts. Results showed that available elemental contents in the nutrient solution extracts are significantly different between organic substrates, whereas ionic concentrations are basically under steady condition after treatment for 36-108 h. Ionic contents in the nutrient solution extracts are not equal to the value of adding ionic concentrations in the supplied nutrient solution to that in the water extract. Thus, a mathematical model was proposed for adjusting the composition of supplied nutrient solution to match plant requirements in the organic soilless culture system.

Synthesis and photoluminescence properties of CaSixOy:Tb3+ phosphors prepared using solution-combustion method

CSIR Research Space (South Africa)

Dejene, FB

2011-07-01

Full Text Available Effect of Tb3+ ion concentrations on the structural and persistence luminescence properties of CaSixOy:Tb3+ crystals were evaluated using powders grown by the solution combustion technique. The XRD study indicates the change of phase from CaSiO3...

A Summary of the Space-Time Conservation Element and Solution Element (CESE) Method

Science.gov (United States)

Wang, Xiao-Yen J.

2015-01-01

The space-time Conservation Element and Solution Element (CESE) method for solving conservation laws is examined for its development motivation and design requirements. The characteristics of the resulting scheme are discussed. The discretization of the Euler equations is presented to show readers how to construct a scheme based on the CESE method. The differences and similarities between the CESE method and other traditional methods are discussed. The strengths and weaknesses of the method are also addressed.

A finite element solution method for quadrics parallel computer

International Nuclear Information System (INIS)

Zucchini, A.

1996-08-01

A distributed preconditioned conjugate gradient method for finite element analysis has been developed and implemented on a parallel SIMD Quadrics computer. The main characteristic of the method is that it does not require any actual assembling of all element equations in a global system. The physical domain of the problem is partitioned in cells of n p finite elements and each cell element is assigned to a different node of an n p -processors machine. Element stiffness matrices are stored in the data memory of the assigned processing node and the solution process is completely executed in parallel at element level. Inter-element and therefore inter-processor communications are required once per iteration to perform local sums of vector quantities between neighbouring elements. A prototype implementation has been tested on an 8-nodes Quadrics machine in a simple 2D benchmark problem

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

Preparation of Ca-alginate coated nZVI core shell beads for uranium (VI) removal from aqueous solution

International Nuclear Information System (INIS)

Shuhong Hu; Xiaoyan Lin; Yahui Zhang; Meiling Shi

2017-01-01

In this study, the core-shell nanoscale zero-valent iron (nZVI)@Alg-Ca beads were synthesized by coaxial electronic injection method for removal of U (VI) from aqueous solution, and characterized by SEM, EDX and XPS. The results showed that the pseudo-second-order models and the Langmuir isotherm model fitted well with the data obtained. The removal mechanism may include both physical adsorption of U (VI) on the surface or inside of core-shell nZVI@Alg-Ca beads and subsequent reduction of U (VI) to U (IV). Therefore, the core-shell nZVI@Alg-Ca beads would have an application prospect in effective removal of U (VI) contamination from aqueous solution. (author)

Solution of problems with material nonlinearities with a coupled finite element/boundary element scheme using an iterative solver. Yucca Mountain Site Characterization Project

International Nuclear Information System (INIS)

Koteras, J.R.

1996-01-01

The prediction of stresses and displacements around tunnels buried deep within the earth is an important class of geomechanics problems. The material behavior immediately surrounding the tunnel is typically nonlinear. The surrounding mass, even if it is nonlinear, can usually be characterized by a simple linear elastic model. The finite element method is best suited for modeling nonlinear materials of limited volume, while the boundary element method is well suited for modeling large volumes of linear elastic material. A computational scheme that couples the finite element and boundary element methods would seem particularly useful for geomechanics problems. A variety of coupling schemes have been proposed, but they rely on direct solution methods. Direct solution techniques have large storage requirements that become cumbersome for large-scale three-dimensional problems. An alternative to direct solution methods is iterative solution techniques. A scheme has been developed for coupling the finite element and boundary element methods that uses an iterative solution method. This report shows that this coupling scheme is valid for problems where nonlinear material behavior occurs in the finite element region

Trace elements and nutrients adsorption onto nano-maghemite in a contaminated-soil solution: A geochemical/statistical approach.

Science.gov (United States)

Martínez-Fernández, Domingo; Bingöl, Deniz; Komárek, Michael

2014-07-15

Two experiments were carried out to study the competition for adsorption between trace elements (TEs) and nutrients following the application of nano-maghemite (NM) (iron nano-oxide; Fe2O3) to a soil solution (the 0.01molL(-1) CaCl2 extract of a TEs-contaminated soil). In the first, the nutrients K, N, and P were added to create a set of combinations: potential availability of TEs during their interaction with NM and nutrients were studied. In the second, response surface methodology was used to develop predictive models by central composite design (CCD) for competition between TEs and the nutrients K and N for adsorption onto NM. The addition of NM to the soil solution reduced specifically the concentrations of available As and Cd, but the TE-adsorption capacity of NM decreased as the P concentration increased. The CCD provided more concise and valuable information, appropriate to estimate the behavior of NM sequestering TEs: according to the suggested models, K(+) and NH4(+) were important factors for Ca, Fe, Mg, Mn, Na, and Zn adsorption (Radj(2)=95%, except for Zn with Radj(2)=87%). The obtained information and models can be used to predict the effectiveness of NM for the stabilization of TEs, crucial during the phytoremediation of contaminated soils. Copyright © 2014 Elsevier B.V. All rights reserved.

Organic radionuclide compounds in soil solutions and their role in elements absorption in plants

International Nuclear Information System (INIS)

Agapkin, G.I.; Tikhomirov, F.A.

1991-01-01

The results of reference experiments with introduction of radioactive labels ( 35 S, 45 Ca, 59 Fe, 85 , 125 I) into 5 types of climatophytic soils by the method of radiogel-chromatography allow to ascertain that in soil solutions 59 Fe and 125 I incorporate completely and 35 S, 45 Ca and 85 Sr incorporate by 60-90 % into the composition of one of three fractions of organic compounds with molecular masses of 4x10 2 -6x10 4 . It is shown that significant variations between soils in the absorption of such radionuclides as 4 5 Ca, 58 Fe, 85 Sr and 125 I are celated to a different degree of their transport into soil solutions as well as to differencies in their distribution by molecular-mass fractions of water-soluble organic compounds

Mg/Ca partitioning between aqueous solution and aragonite mineral: a molecular dynamics study

NARCIS (Netherlands)

Ruiz-Hernandez, S.E.; Grau-Crespo, R.; Almora-Barrios, N.; Wolthers, M.; Ruiz-Salvador, A.R.; Fernandez, N.; Leeuw, N.H. de

2012-01-01

We have calculated the concentrations of Mg in the bulk and surfaces of aragonite CaCO3 in equilibrium with aqueous solution, based on molecular dynamics simulations and grand-canonical statistical mechanics. Mg is incorporated in the surfaces, in particular in the (001) terraces,

Evaluation of element migration from food plastic packagings into simulated solutions using radiometric method

International Nuclear Information System (INIS)

Soares, Eufemia Paez; Saiki, Mitiko; Wiebeck, Helio

2005-01-01

In the present study a radiometric method was established to determine the migration of elements from food plastic packagings to a simulated acetic acid solution. This radiometric method consisted of irradiating plastic samples with neutrons at IEA-R1 nuclear reactor for a period of 16 hours under a neutron flux of 10 12 n cm -2 s -1 and, then to expose them to the element migration into a simulated solution. The radioactivity of the activated elements transferred to the solutions was measured to evaluate the migration. The experimental conditions were: time of exposure of 10 days at 40 deg C and 3% acetic acid solution was used as simulated solution, according to the procedure established by the National Agency of Sanitary Monitoring (ANVISA). The migration study was applied for plastic samples from soft drink and juice packagings. The results obtained indicated the migration of elements Co, Cr and Sb. The advantage of this methodology was no need to analyse the blank of simulantes, as well as the use of high purity simulated solutions. Besides, the method allows to evaluate the migration of the elements into the food content instead of simulated solution. The detention limits indicated high sensitivity of the radiometric method. (author)

An upwind space-time conservation element and solution element scheme for solving dusty gas flow model

Science.gov (United States)

Rehman, Asad; Ali, Ishtiaq; Qamar, Shamsul

An upwind space-time conservation element and solution element (CE/SE) scheme is extended to numerically approximate the dusty gas flow model. Unlike central CE/SE schemes, the current method uses the upwind procedure to derive the numerical fluxes through the inner boundary of conservation elements. These upwind fluxes are utilized to calculate the gradients of flow variables. For comparison and validation, the central upwind scheme is also applied to solve the same dusty gas flow model. The suggested upwind CE/SE scheme resolves the contact discontinuities more effectively and preserves the positivity of flow variables in low density flows. Several case studies are considered and the results of upwind CE/SE are compared with the solutions of central upwind scheme. The numerical results show better performance of the upwind CE/SE method as compared to the central upwind scheme.

The Time Course of the Loss and Recovery of Contracture Ability in Frog Striated Muscle Following Exposure to Ca-Free Solutions

Science.gov (United States)

Milligan, J. V.

1965-01-01

Using area under the contracture curve to quantitate contractures, the diffusion coefficient of calcium ions within the frog toe muscle during washout in a calcium-free solution and subsequent recovery after reintroduction of calcium to the bathing solution was calculated to be about 2 x 10-6 cm2/sec. The diffusion coefficient measured during washout was found to be independent of temperature or initial calcium ion concentration. During recovery it was found to decrease if the temperature was lowered. This was likely due to the repolarization occurring after the depolarizing effect of the calcium-free solution. The relation between contracture area and [Ca]o was found to be useful over a wider range than that between maximum tension and [Ca]o. The normalized contracture areas were larger at lower calcium concentrations if the contractures were produced with cold potassium solutions or if NO3 replaced Cl in the bathing solutions. Decreasing the potassium concentration of the contracture solution to 50 mM from 115 mM did not change the relation between [Ca]o and the normalized area. If the K concentration of the bathing solution was increased, the areas were decreased at lower concentrations of Ca. PMID:14324991

Prediction of thermodynamic properties of solute elements in Si solutions using first-principles calculations

International Nuclear Information System (INIS)

Iwata, K.; Matsumiya, T.; Sawada, H.; Kawakami, K.

2003-01-01

The method is presented to predict the activity coefficients and the interaction parameters of the solute elements in infinite dilute Si solutions by the use of first-principles calculations based on density functional theory. In this method, the regular solution model is assumed. The calculated activity coefficients in solid Si are converted to those in molten Si by the use of the solid-liquid partition coefficients. Furthermore, the interaction parameters in solid Si solutions are calculated and compared with reported experimental values of those in liquid Si solutions. The results show that the calculated activity coefficients and interaction parameters of Al, Fe, Ti and Pb in Si solutions are in good agreement with the tendency of the experiments. However, the calculations have some quantitative discrepancy from the experiments. It is expected that consideration of the excess entropy would reduce this discrepancy

Solution of the conjugated heat transfer problem for the fuel elements assemblies

International Nuclear Information System (INIS)

Golba, V.S.; Ivanenko, I.J.; Zinina, G.A.

1997-01-01

The paper presents the assemblies conjugated heat conductivity problem calculation and experimental method. The method is based on the temperature superposition modified concept and subchannel method and allows to predict the fuel elements surface temperatures with availability of fuel elements inside structure of any complication caused by technological and working defects and with availability of depositions with low heat conductivity on the fuel elements surfaces. According to the method developed the partial solutions of the heat conductivity equation at the heat removal boundaries (solid-liquid) are found separately for the fuel elements and for the liquid. The heat conductivity equation partial solutions for the fuel elements are predicted by calculations. The coolant heat conductivity equation partial solution ('influence functions') data massif is obtained in present work experimentally in the fuel assembly model consists of 7 tube bundle of fuel elements imitators placed in right grating with relative grating step equal to 1.1 and cooled by eutectic alloy Pb-Bi. It is shown that 'subchannel prediction method' decreases the crosswise heat transfer in comparison with crosswise heat transfer, when the fuel element inside structure is taken into account. Also in the paper it is shown that it is possible to realize the assembly temperature prediction method suggested without carrying out the experiments in the assembly's model in order to get the external problem influence functions'. (author)

Synthesis and characterization of CaTiO3 powder by combustion synthesis process

International Nuclear Information System (INIS)

Jung, C. W.; Shin, H. C.; Park, J. Y.; Lee, H. G.; Kim, H. Y.; Hong, K. W.

2000-01-01

Synroc is considered as a one of the most promising candidate for HLW solidification. CaTiO 3 , perovskite, which is a component of Synroc, can immobilize lanthanide and actinides by forming solid solutions. Generally most of the radioactive wastes elements were treated as a nitrate form. Therefore, the combustion process using metal nitrates as reactant materials can be easily applied to immobilize the radioactive waste elements. In this study, the feasibility of preparing fine, single-phase powders of multi-component oxide by a combustion process was investigated. Generally, the powder synthesized by combustion process showed different characteristics depending on the type and amount of fuel. And the spherical CaTiO 3 particles were directly prepared from the aqueous solution by an ultrasonic mist combustion process using an ultrasonic nebulizers as mist generators. The particles prepared with simple spray pyrolysis method using nitrate solution without fuel as precursor solution showed porous and hollow morphology, while the particles prepared with precursor solutions containing fuel showed dense solid morphology. Among various kinds of fuel tested, glycine showed the best result in reaction kinetics and crystalline phase purity

Is The Ca + K + Mg/Al Ratio in the Soil Solution a Predictive Tool for Estimating Forest Damage?

International Nuclear Information System (INIS)

Goeransson, A.; Eldhuset, T. D.

2001-01-01

The ratio between (Ca +K +Mg) and Al in nutrient solution has been suggested as a predictive tool for estimating tree growth disturbance. However, the ratio is unspecific in the sense that it is based on several elements which are all essential for plant growth;each of these may be growth-limiting. Furthermore,aluminium retards growth at higher concentrations. Itis therefore difficult to give causal and objective biological explanations for possible growth disturbances. The importance of the proportion of base-cations to N, at a fixed base-cation/Al ratio, is evaluated with regard to growth of Picea abies.The uptake of elements was found to be selective; nutrients were taken up while most Al remained in solution. Biomass partitioning to the roots increased after aluminium addition with low proportions of basecations to nitrogen. We conclude that the low growthrates depend on nutrient limitation in these treatments. Low growth rates in the high proportion experiments may be explained by high internal Alconcentrations. The results strongly suggest that growth rate is not correlated with the ratio in the rooting medium and question the validity of using ratios as predictive tools for estimating forest damage. We suggest that growth limitation of Picea abies in the field may depend on low proportions of base cations to nitrate. It is therefore important to know the nutritional status of the plant material in relation to the growth potential and environmental limitation to be able to predict and estimate forest damage

Chemical solution deposition of CaCu 3 Ti 4 O 12 thin film

Indian Academy of Sciences (India)

CaCu3Ti4O12 (CCTO) thin film was successfully deposited on boron doped silica substrate by chemical solution deposition and rapid thermal processing. The phase and microstructure of the deposited films were studied as a function of sintering temperature, employing X-ray diffractometry and scanning electron ...

Distribution of major elements (Na, K, Ca, Mg in the various anatomical parts of Fadama crops in Ekiti State, Nigeria

Directory of Open Access Journals (Sweden)

E.I. Adeyeye

2005-12-01

Full Text Available Levels of sodium, potassium, calcium and magnesium were determined in plant organs (bud, flowers, fruit, seed, leaves, stems, roots, cobs, styles, shaft, grains and efflorescences of three Fadama farms located in Ifaki-Ekiti, Ado-Ekiti and Ikere-Ekiti of Ekiti State, Nigeria. The highest levels of Mg, K, Na and Ca were obtained in the bud of Hibiscus esculentus with respective values (ppm dry weight, ppm DW of 4397, 2983, 3928 and 1622; this was closely followed by their levels in Lycopersicon esculentum root: Mg (2734, K (1079, Na (2111 and Ca (678. The levels of all the elements were highly varied in the anatomical parts of each plant and between the various plants. The index of bioaccumulation (ratio in plants/soil was recorded for all the elements with all values falling within 1-101 showing that the degree of accumulation was intensive. The overall levels of the elements were Mg > Na > K > Ca.

An upwind space-time conservation element and solution element scheme for solving dusty gas flow model

Directory of Open Access Journals (Sweden)

Asad Rehman

Full Text Available An upwind space-time conservation element and solution element (CE/SE scheme is extended to numerically approximate the dusty gas flow model. Unlike central CE/SE schemes, the current method uses the upwind procedure to derive the numerical fluxes through the inner boundary of conservation elements. These upwind fluxes are utilized to calculate the gradients of flow variables. For comparison and validation, the central upwind scheme is also applied to solve the same dusty gas flow model. The suggested upwind CE/SE scheme resolves the contact discontinuities more effectively and preserves the positivity of flow variables in low density flows. Several case studies are considered and the results of upwind CE/SE are compared with the solutions of central upwind scheme. The numerical results show better performance of the upwind CE/SE method as compared to the central upwind scheme. Keywords: Dusty gas flow, Solid particles, Upwind schemes, Rarefaction wave, Shock wave, Contact discontinuity

Cadmium and zinc in plants and soil solutions from contaminated soils

DEFF Research Database (Denmark)

Lorenz, S.E.; Hamon, R.E.; Holm, P.E.

1997-01-01

In an experiment using ten heavy metal-contaminated soils from six European countries, soil solution was sampled by water displacement before and after the growth of radish. Concentrations of Cd, Zn and other elements in solution (K, Ca, Mg, Mn) generally decreased during plant growth, probably...

The performance of a surface-applied corrosion inhibitor for the carbon steel in saturated Ca(OH)2 solutions

International Nuclear Information System (INIS)

Zheng, Haibing; Li, Weihua; Ma, Fubin; Kong, Qinglin

2014-01-01

In the present work, the performance of an amino alcohol based surface applied inhibitor was studied by the electrochemical techniques in saturated Ca(OH) 2 solutions. The surface morphology of the carbon steel was observed by scanning electron microscope, and the energy diffraction spectrum was also tested. Results showed that the inhibitor used in this work demonstrated obvious inhibition efficiency on the carbon steel in saturated Ca(OH) 2 solutions. The inhibition mechanism of the inhibitor lies in the quick adsorption of the active component on carbon steel surface

Finite element solution of quasistationary nonlinear magnetic field

International Nuclear Information System (INIS)

Zlamal, Milos

1982-01-01

The computation of quasistationary nonlinear two-dimensional magnetic field leads to the following problem. There is given a bounded domain OMEGA and an open nonempty set R included in OMEGA. We are looking for the magnetic vector potential u(x 1 , x 2 , t) which satisifies: 1) a certain nonlinear parabolic equation and an initial condition in R: 2) a nonlinear elliptic equation in S = OMEGA - R which is the stationary case of the above mentioned parabolic equation; 3) a boundary condition on delta OMEGA; 4) u as well as its conormal derivative are continuous accross the common boundary of R and S. This problem is formulated in two equivalent abstract ways. There is constructed an approximate solution completely discretized in space by a generalized Galerkin method (straight finite elements are a special case) and by backward A-stable differentiation methods in time. Existence and uniqueness of a weak solution is proved as well as a weak and strong convergence of the approximate solution to this solution. There are also derived error bounds for the solution of the two-dimensional nonlinear magnetic field equations under the assumption that the exact solution is sufficiently smooth

On the possibility to measure 0νββ-decay nuclear matrix element for 48Ca

International Nuclear Information System (INIS)

Rodin, Vadim

2011-01-01

As shown in Ref. [2], the Fermi part M F 0ν of the total 0νββ-decay nuclear matrix element M 0ν can be related to the single Fermi transition matrix element between the isobaric analog state (IAS) of the ground state of the initial nucleus and the ground state of the final nucleus. The latter matrix element could be measured in charge-exchange reactions. Here we discuss a possibility of such a measurement for 48 Ca and estimate the cross-section of the reaction 48 Ti(n,p) 48 Sc(IAS).

Synthesis of the isotopes of elements 118 and 116 in the 249Cf and 245Cm+48Ca fusion reactions

International Nuclear Information System (INIS)

Oganessian, Y T; Utyonkov, V K; Lobanov, Y V; Abdullin, F S; Polyakov, A N; Sagaidak, R N; Shirokovsky, I V; Tsyganov, Y S; Voinov, A A; Gulbekian, G G; Bogomolov, S L; Gikal, B N; Mezentsev, A N; Iliev, S; Subbotin, V G; Sukhov, A M; Subotic, K; Zagrebaev, V I; Vostokin, G K; Itkis, M G; Moody, K J; . Patin, J B; Shaughnessy, D A; Stoyer, M A; Stoyer, N J; Wilk, P A; Kenneally, J M; Landrum, J H; Wild, J F; Lougheed, R W

2006-01-01

The decay properties of 290 116 and 291 116, and the dependence of their production cross sections on the excitation energies of the compound nucleus, 293 116, have been measured in the 245 Cm( 48 Ca,xn) 293-x 116 reaction. These isotopes of element 116 are the decay daughters of element 118 isotopes, which are produced via the 249 Cf+ 48 Ca reaction. They performed the element 118 experiment at two projectile energies, corresponding to 297 118 compound nucleus excitation energies of E* = 29.2 ± 2.5 and 34.4 ± 2.3 MeV. During an irradiation with a total beam dose of 4.1 x 10 19 48 Ca projectiles, three similar decay chains consisting of two or three consecutive α decays and terminated by a spontaneous fission (SF) with high total kinetic energy of about 230 MeV were observed. The three decay chains originated from the even-even isotope 294 118 (E α = 11.65 ± 0.06 MeV, T α = 0.89 -0.31 +1.07 ms) produced in the 3n-evaporation channel of the 249 Cf+ 48 Ca reaction with a maximum cross section of 0.5 -0.3 +1.6 pb

Solution of two energy-group neutron diffusion equation by triangular elements

International Nuclear Information System (INIS)

Correia Filho, A.

1981-01-01

The application of the triangular finite elements of first order in the solution of two energy-group neutron diffusion equation in steady-state conditions is aimed at. The EFTDN (triangular finite elements in neutrons diffusion) computer code in FORTRAN IV language is developed. The discrete formulation of the diffusion equation is obtained applying the Galerkin method. The power method is used to solve the eigenvalues' problem and the convergence is accelerated through the use of Chebshev polynomials. For the equation systems solution the Gauss method is applied. The results of the analysis of two test-problems are presented. (Author) [pt

Use of cationites for separation of transplutonium elements from other elements from aqueous and aqua-alcohol solutions of hydrochloric and nitric acids

International Nuclear Information System (INIS)

Guseva, L.I.; Tikhomirova, G.S.

1984-01-01

The behaviour of Am, Cm, Pu and certain fragment elements (Cs, Sr, Y, Zr, Nb, Ru, Eu) on cationite dauex-50 in aqueous and aqueous-alcohol solutions of HCl and HNO 3 has been studied. Dependences of distribution coefficients and separation factors of the elements on the acid concentration and alcohol content in the solutions are presented. The sorption of TPE by cationite from HCl and HNO 3 solutions in the presence of alcohol is shown to increase over the range of concentrations studied (from 0.5 mol/L to 4-5 mol/L), which is explained by the salting-out effect of alcohol. The distribution coefficients of TPE in the solutions, containing >= 50% alcohol, constitute >= 10 2 . The distribution coefficients of the fragment elements in the presence of alcohol also increase, but to a considerably lesser extent, which results in a better separation. The study of the washing-out curves has shown that, to separate TPE from fragment elements on cationites, both HCl and HNO 3 solutions can be used, at that, in the case of aqueous solutions a better separation is attained at acid concentration, equal to 1 mol/L, and in the case of eluating by aqueous-alcohol solutions a good separation is achieved at hig-her concentrations of the acids as well

Elastic-Plastic J-Integral Solutions or Surface Cracks in Tension Using an Interpolation Methodology. Appendix C -- Finite Element Models Solution Database File, Appendix D -- Benchmark Finite Element Models Solution Database File

Science.gov (United States)

Allen, Phillip A.; Wells, Douglas N.

2013-01-01

No closed form solutions exist for the elastic-plastic J-integral for surface cracks due to the nonlinear, three-dimensional nature of the problem. Traditionally, each surface crack must be analyzed with a unique and time-consuming nonlinear finite element analysis. To overcome this shortcoming, the authors have developed and analyzed an array of 600 3D nonlinear finite element models for surface cracks in flat plates under tension loading. The solution space covers a wide range of crack shapes and depths (shape: 0.2 less than or equal to a/c less than or equal to 1, depth: 0.2 less than or equal to a/B less than or equal to 0.8) and material flow properties (elastic modulus-to-yield ratio: 100 less than or equal to E/ys less than or equal to 1,000, and hardening: 3 less than or equal to n less than or equal to 20). The authors have developed a methodology for interpolating between the goemetric and material property variables that allows the user to reliably evaluate the full elastic-plastic J-integral and force versus crack mouth opening displacement solution; thus, a solution can be obtained very rapidly by users without elastic-plastic fracture mechanics modeling experience. Complete solutions for the 600 models and 25 additional benchmark models are provided in tabular format.

The enthalpies of interactions of Ca2+(aq) and C2O{4/2-} (aq) ions in complexon solutions: Competition between complexation and precipitation

Science.gov (United States)

Kustov, A. V.; Smirnova, N. L.; Berezin, B. D.; Trostin, V. N.

2010-04-01

The thermal effects of mixing of aqueous calcium chloride with sodium citrate and ethylenedi-aminetetraacetate in the absence and presence of sodium oxalate have been measured at 25°C. The thermal effects of dilution of aqueous calcium chloride solutions were determined. The thermal effects of calcium oxalate precipitation and formation of calcium complexes with citrate and ethylenediaminetetraacetate ions were calculated. The 1% solution of sodium citrate inhibited the formation of CaC2O4 (s); in a 1% solution of sodium ethylenediaminetetraacetate with [Ca2+][C2O{4/2-}] > 10-5, the endothermal formation of the [CaEdta]2- complex quickly changed to exothermal precipitation. The 3 and 5% solutions of complexons showed a pronounced inhibiting effect on the formation of urinary stones even when the concentration of calcium and oxalate ions in solution exceeded the product of solubility of CaC2O4 by four and more orders of magnitude.

Multisite Ion Model in Concentrated Solutions of Divalent Cations (MgCl2 and CaCl2): Osmotic Pressure Calculations

Science.gov (United States)

2015-01-01

Accurate force field parameters for ions are essential for meaningful simulation studies of proteins and nucleic acids. Currently accepted models of ions, especially for divalent ions, do not necessarily reproduce the right physiological behavior of Ca2+ and Mg2+ ions. Saxena and Sept (J. Chem. Theor. Comput.2013, 9, 3538–3542) described a model, called the multisite-ion model, where instead of treating the ions as an isolated sphere, the charge was split into multiple sites with partial charge. This model provided accurate inner shell coordination of the ion with biomolecules and predicted better free energies for proteins and nucleic acids. Here, we expand and refine the multisite model to describe the behavior of divalent ions in concentrated MgCl2 and CaCl2 electrolyte solutions, eliminating the unusual ion–ion pairing and clustering of ions which occurred in the original model. We calibrate and improve the parameters of the multisite model by matching the osmotic pressure of concentrated solutions of MgCl2 to the experimental values and then use these parameters to test the behavior of CaCl2 solutions. We find that the concentrated solutions of both divalent ions exhibit the experimentally observed behavior with correct osmotic pressure, the presence of solvent separated ion pairs instead of direct ion pairs, and no aggregation of ions. The improved multisite model for (Mg2+ and Ca2+) can be used in classical simulations of biomolecules at physiologically relevant salt concentrations. PMID:25482831

Hybrid Fundamental Solution Based Finite Element Method: Theory and Applications

Directory of Open Access Journals (Sweden)

Changyong Cao

2015-01-01

Full Text Available An overview on the development of hybrid fundamental solution based finite element method (HFS-FEM and its application in engineering problems is presented in this paper. The framework and formulations of HFS-FEM for potential problem, plane elasticity, three-dimensional elasticity, thermoelasticity, anisotropic elasticity, and plane piezoelectricity are presented. In this method, two independent assumed fields (intraelement filed and auxiliary frame field are employed. The formulations for all cases are derived from the modified variational functionals and the fundamental solutions to a given problem. Generation of elemental stiffness equations from the modified variational principle is also described. Typical numerical examples are given to demonstrate the validity and performance of the HFS-FEM. Finally, a brief summary of the approach is provided and future trends in this field are identified.

Application of finite element method in the solution of transport equation

International Nuclear Information System (INIS)

Maiorino, J.R.; Vieira, W.J.

1985-01-01

It is presented the application of finite element method in the solution of second order transport equation (self-adjoint) for the even parity flux. The angular component is treated by expansion in Legendre polinomials uncoupled of the spatial component, which is approached by an expansion in base functions, interpolated in each spatial element. (M.C.K.) [pt

Extraction of transplutonium elements from carbonate solutions by alkylpyrocatechol

International Nuclear Information System (INIS)

Karalova, Z.K.; Myasoedov, B.F.; Rodionova, L.M.; Kuznetsova, V.S.

1983-01-01

Extraction of americium, berkelium as well as Ce, Eu, Th, U, Zr, Cs, Fe with solution of 4(α, α-dioctylethyl)pyrocatechol (DOP) in toluene from carbonate solutions to determine conditions of their separation has been studied. It is established that americium extraction is quite sensitive to the changes of potassium carbonate concentration. The maximum extraction of americium (R >90%) is observed in the case of 0.1-0.5 mol/l of K 2 CO 3 solutions and the minimum one (R=2.5%) - in the case of 8 mol/l K 2 CO 3 . Americium extraction increases sharply when sodium hydroxide is introduced in carbonate solutions. It is shown that varying sodium hydroxide concentration it is possible to achieve qualitative extraction of americium even from saturated solution of potassium carbonate. Reextraction of TPE is easily realized with 3 mol/l HCl solution. The system K 2 CO 3 (KOH)-DOP proved to be perspective for Am separation from Bk, Ce, Cs, actinoid elements as well as from Fe

Kinetics of Roasting Decomposition of the Rare Earth Elements by CaO and Coal

Directory of Open Access Journals (Sweden)

Shuai Yuan

2017-06-01

Full Text Available The roasting method of magnetic tailing mixed with CaO and coal was used to recycle the rare earth elements (REE in magnetic tailing. The phase transformation and decomposition process were researched during the roasting processes. The results showed that the decomposition processes of REE in magnetic tailing were divided into two steps. The first step from 380 to 431 °C mainly entailed the decomposition of bastnaesite (REFCO3. The second step from 605 to 716 °C mainly included the decomposition of monazite (REPO4. The decomposition products were primarily RE2O3, Ce0.75Nd0.25O1.875, CeO2, Ca5F(PO43, and CaF2. Adding CaO could reduce the decomposition temperature of REFCO3 and REPO4. Meanwhile, the decomposition effect of CaO on bastnaesite and monazite was significant. Besides, the effects of the roasting time, roasting temperature, and CaO addition level on the decomposition rate were studied. The optimum technological conditions were a roasting time of 60 min; roasting temperature of 750 °C; and CaO addition level of 20% (w/w. The maximum decomposition rate of REFCO3 and REPO4 was 99.87%. The roasting time and temperature were the major factors influencing the decomposition rate. The kinetics process of the decomposition of REFCO3 and REPO4 accorded with the interfacial reaction kinetics model. The reaction rate controlling steps were divided into two steps. The first step (at low temperature was controlled by a chemical reaction with an activation energy of 52.67 kJ/mol. The second step (at high temperature was controlled by diffusion with an activation energy of 8.5 kJ/mol.

Hanford 100N Area Apatite Emplacement: Laboratory Results of Ca-Citrate-PO4 Solution Injection and Sr-90 Immobilization in 100N Sediments

Energy Technology Data Exchange (ETDEWEB)

Szecsody, James E.; Burns, Carolyn A.; Moore, Robert C.; Fruchter, Jonathan S.; Vermeul, Vincent R.; Williams, Mark D.; Girvin, Donald C.; McKinley, James P.; Truex, Michael J.; Phillips, Jerry L.

2007-10-01

This report summarizes laboratory scale studies investigating the remediation of Sr-90 by Ca-citrate-PO4 solution injection/infiltration to support field injection activities in the Hanford 100N area. This study is focused on experimentally testing whether this remediation technology can be effective under field scale conditions to mitigate Sr-90 migration 100N area sediments into the Columbia River. Sr-90 is found primarily adsorbed to sediments by ion exchange (99% adsorbed, < 1% in groundwater) in the upper portion of the unconfined aquifer and lower vadose zone. Although primarily adsorbed, Sr-90 is still considered a high mobility risk as it is mobilized by seasonal river stage increases and by plumes of higher ionic strength relative to groundwater. This remediation technology relies upon the Ca-citrate-PO4 solution forming apatite precipitate [Ca6(PO4)10(OH)2], which incorporates some Sr-90 during initial precipitation and additionally slowly incorporates Sr-90 by solid phase substitution for Ca. Sr substitution occurs because Sr-apatite is thermodynamically more stable than Ca-apatite. Once the Sr-90 is in the apatite structure, Sr-90 will decay to Y-90 (29.1 y half-life) then Zr-90 (64.1 h half-life) without the potential for migration into the Columbia River. For this technology to be effective, sufficient apatite needs to be emplaced in sediments to incorporate Sr and Sr-90 for 300 years (~10 half-lives of Sr-90), and the rate of incorporation needs to exceed the natural groundwater flux rate of Sr in the 100N area. A primary objective of this study is to supply an injection sequence to deliver sufficient apatite into subsurface sediments that minimizes initial mobility of Sr-90, which occurs because the injection solution has a higher ionic strength compared to groundwater. This can be accomplished by sequential injections of low, then high concentration injection of Ca-citrate-PO4 solutions. Assessment of low concentration Ca-citrate-PO4, citrate-PO4

Eigenvalue solutions in finite element thermal transient problems

International Nuclear Information System (INIS)

Stoker, J.R.

1975-01-01

The eigenvalue economiser concept can be useful in solving large finite element transient heat flow problems in which the boundary heat transfer coefficients are constant. The usual economiser theory is equivalent to applying a unit thermal 'force' to each of a small sub-set of nodes on the finite element mesh, and then calculating sets of resulting steady state temperatures. Subsequently it is assumed that the required transient temperature distributions can be approximated by a linear combination of this comparatively small set of master temperatures. The accuracy of a reduced eigenvalue calculation depends upon a good choice of master nodes, which presupposes at least a little knowledge about what sort of shape is expected in the unknown temperature distributions. There are some instances, however, where a reasonably good idea exists of the required shapes, permitting a modification to the economiser process which leads to greater economy in the number of master temperatures. The suggested new approach is to use manually prescribed temperature distributions as the master distributions, rather than using temperatures resulting from unit thermal forces. Thus, with a little pre-knowledge one may write down a set of master distributions which, as a linear combination, can represent the required solution over the range of interest to a reasonable engineering accuracy, and using the minimum number of variables. The proposed modified eigenvalue economiser technique then uses the master distributions in an automatic way to arrive at the required solution. The technique is illustrated by some simple finite element examples

Formation of ammonia complexes of alkaline earth elements in aqueous solutions

International Nuclear Information System (INIS)

Padar, T.G.; Stupko, T.V.; Isaev, I.D.; Pashkov, G.L.; Mironov, V.E.

1990-01-01

Coefficients of ammonia distribution between aqueous solutions of calcium, strontium, barium and ammonium perchlorate mixtures at ionic strength - 0.50; 1.0 and 1.5 at 298.2 K and ammonia concentrations 0.2-10 mol/dm 3 are measured. Formation of ammonia complexes of M(NH 3 ) n 2+ composition is shown. Logarithms of stepped stability constants for solutions with zero ionic strength for Ca 2+ are: -0.13; -0.25; -0.52 and -0.77, where n=1-4; for Sr 2+ : -0.04; -0.42 and -0.70, where n=1-3 and for Ba 2+ : -0.11; -0.50 and 0.76, where n=1-3

Synthesis, single crystal growth and thermodynamic properties of SrNdAlO4-CaNdAlO4 solid solutions

International Nuclear Information System (INIS)

Novoselov, A.; Ryumin, M.; Pushkina, G.; Spiridonov, F.; Komissarova, L.; Zimina, G.; Pajaczkowska, A.

2005-01-01

Continuous solid solutions in the SrNdAlO 4 -CaNdAlO 4 system are formed. Powder samples of Sr x Ca 1-x NdAlO 4 (0.0≤x≤1.0) were obtained using the carbonate coprecipitation method while single crystals of Sr x Ca 1-x NdAlO 4 (x=0.0,0.162,0.392,0.687,1.0) were grown by the Czochralski method. Structural parameters and thermodynamic properties of the samples were studied by X-ray diffraction and heat flux Calvet calorimetry. Composition dependence of lattice constants was observed to follow Vegard's low. Heat of solution of the Sr x Ca 1-x NdAlO 4 samples in molten 2PbO.B 2 O 3 were measured, and enthalpies of formation and mixing were calculated. (copyright 2005 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

The effect of Ca and RE elements on the precipitation kinetics of Mg17Al12 phase during artificial aging of magnesium alloy AZ91

International Nuclear Information System (INIS)

Amir Esgandari, B.; Mehrjoo, H.; Nami, B.; Miresmaeili, S.M.

2011-01-01

Highlights: → Ca and RE elements decrease the precipitation rate during aging of AZ91 alloy. → Precipitation kinetics and mechanism during aging of the alloys were studied. → Effect of Ca and RE on creep properties of age hardened AZ91 alloy was studied. - Abstract: The effect of simultaneous alloying with Ca and rare earth (RE) elements on the age hardening kinetics of AZ91 was studied through the fitting of the Johnson-Mehl-Avrami (JMA) equation. The results showed that the addition of both Ca and RE elements not only suppress discontinuous precipitation of the Mg 17 Al 12 phase during the age hardening process, but also decrease the alloy hardness. Fitting the JMA equation to the experimental data indicated that the phase transformation during age hardening of an alloy variant containing both Ca and RE (at 170 deg. C and 190 deg. C) and standard AZ91 (at 170 deg. C) takes place by the nucleation of precipitates on dislocations. In contrast, the precipitation during age hardening of AZ91 at 190 deg. C occurs via nucleation at grain boundaries. Although it was observed that the creep strength of age hardened specimens are lower than that of the as cast specimens, but age hardening treatment has lower deleterious influence on the creep resistance of the alloy containing Ca and RE in comparison with conventional AZ91. This may be ascribed to the decreased precipitation rate resulting from the addition of both Ca and RE elements.

Contributions to multiple element speciation in vegetable plants: Studies on the type of bonding of numerous elements, particularly zinc and cadmium

International Nuclear Information System (INIS)

Guenther, K.

1997-03-01

In the first part of the study, the total contents and the solubility characteristics of Zn, Cd, Fe, Mn, Cu, Ca, Sr, K and Rb in 26 different vegetable plants, the majority of them commercially available, are reported, obtained by post-decomposition analyses. The data are given for avocados, bananas, cauliflower, chicory, Chinese cabbage, dill, ice lettuce (two specimens), endive, field salad, cucumbers, kohlrabi, lettuce, chard beet, carrots, peppers, leek, radish, red cabbage, loose leaved lettuce, celery (two specimens), spinach, topinambur, white cabbage, and parsley. Cell decomposition was done by treatment of the plant material with an electric dispersing apparatus (Ultra-Turrax) in buffer solution (liquid shearing). The homogenates were separated into supernatants (cytosoles)and pellets by means of centrifugation. Cell decomposition of the plants by crushing with quartz sand after lyophilization (solid shearing) required much more technical effort and for some elements created problems with the blind values. At least 50% on the average of the elements Zn, Cd, Rb, and K could be transferred to the solutions by the dispersing treatment with Ultra-Turrax. In many cases, the cytosole-borne detectable contents of these 5 elements were above 70%. The solubility of Zn and Cd was more strongly dependent on the plant species than that of Cu, Rb, and K. All five elements thus can be analysed by conventional methods for further enhanced speciation. Mn, Ca, and especially Fe and Sr for the most part were found to be bonded to solid cell constituents. However, the solubility characteristics of Ca and Mn and Sr in particular was very homogeneous. In some plants, the contents of Mn and Sr in the cytosoles was approx. 90%, so that comprehensive speciation of these elements is possible. (orig./AJ) [de

Identifying Military Impacts on Archaeological Deposits Based on Differences in Soil Organic Carbon and Chemical Elements at Soil Horizon Interfaces

Science.gov (United States)

2012-03-01

Robotic pH meter (AS-3000 Dual pH Analyzer, LabFit, Burswood, Australia) using a 1:1 soil / solution ratio (0.01 M CaCl2) (Kissel et al., 2009). Soil lime...displacement of elements in the soil profile, and alterations in mineralization processes which affect the leachable element concentration in soil solution . Leachable

A comparison of phytoremediation capability of selected plant species for given trace elements

International Nuclear Information System (INIS)

Fischerova, Zuzana; Tlustos, Pavel; Jirina Szakova; Kornelie Sichorova

2006-01-01

In our experiment, As, Cd, Pb, and Zn remediation possibilities on medium contaminated soil were investigated. Seven plant species with a different trace element accumulation capacity and remediation potential were compared. We found good accumulation capabilities and remediation effectiveness of Salix dasyclados similar to studied hyperaccumulators (Arabidopsis halleri and Thlaspi caerulescens). We have noticed better remediation capability in willow compared to poplar for most of the elements considered in this experiment. On the contrary, poplar species were able to remove a larger portion of Pb as opposed to other species. Nevertheless, the removed volume was very small. The elements found in plant biomass depend substantially on the availability of these elements in the soil. Different element concentrations were determined in natural soil solution and by inorganic salt solution extraction (0.01 mol L -1 CaCl 2 ). Extracted content almost exceeded the element concentration in the soil solution. Element concentrations in soil solution were not significantly affected by sampling time. - Selected accumulator trees grown on medium contaminated soil may have remediation capacity similar to hyperaccumulator species

The Influence of Mg(II and Ca(II Ions on Rutin Autoxidation in Weakly Alkaline Aqueous Solutions

Directory of Open Access Journals (Sweden)

Živanović Slavoljub C.

2016-09-01

Full Text Available Rutin (quercetin-3-O-rutinoside is one of the most abundant bioflavonoids with various biological and pharmacological activities. Considering the ubiquitous presence of Mg(II and Ca(II ions in biological systems we decided to investigate their influence on the autoxidation of rutin in weakly alkaline aqueous solutions. Changes in UV-Vis spectra recorded during the rutin autoxidation in aqueous solution at pH 8.4 revealed that this process was very slow in the absence of metal ions. The presence of Mg(II and, especially Ca(II ion, increased the transformation rate of rutin. UV-Vis spectra recorded after prolonged autoxidation indicated the formation of humic acidlike products in the presence of Mg(II and Ca(II ions. Four new compounds formed during the initial stage of rutin autoxidation in the presence of Mg(II and Ca(II ions were detected by HPLCDAD. Based on the analysis of their DAD UV-Vis spectra and comparison of their retention times with the retention time value for rutin, we concluded that the initial rutin transformation products were formed by the water addition on double bond in ring C and hydroxylation of ring B. A very small decrease of the initial rutin concentration (4% was observed by HPLC-DAD in the absence of metal ions for the period of 90 minutes. However, rutin concentration decrease was much larger in the presence of Mg(II and Ca(II ions (14% and 24%, respectively. The more pronounced effect of Ca(II ion on the rutin autoxidation may be explained by the stronger binding of Mg(II ion to rutin and thus greater stabilizing effect on reaction intermediates caused by its higher ionic potential (charge/ionic radius ratio in comparison to Ca(II ion. The results of this study may contribute to the better understanding of interactions of Mg(II and Ca(II ions with natural phenolic antioxidants which are important for their various biological activities.

LIBS detection of heavy metal elements in liquid solutions by using wood pellet as sample matrix

International Nuclear Information System (INIS)

Wen Guanhong; Sun Duixiong; Su Maogen; Dong Chenzhong

2013-01-01

Laser-induced breakdown spectroscopy (LIBS) has been applied to the analysis of heavy metals in liquid sample. A new approach was presented to improve the detection limit and minimize the sample matrix effects, in which dried wood pellets absorbed the given amounts of Cr standard solutions and then were baked because they have stronger and rapid absorption properties for liquid samples as well as simple elemental compositions. In this work, we have taken a typical heavy metal Cr element as an example, and investigated the spectral feasibility of Cr solutions and dried wood pellets before and after absorbing Cr solutions at the same experimental conditions, respectively. The results were demonstrated to successfully produce a superior analytical response for heavy metal elements by using wood pellet as sample matrix according to obtained LOD of 0.07 ppm for Cr element in solutions. (author)

LIBS Detection of Heavy Metal Elements in Liquid Solutions by Using Wood Pellet as Sample Matrix

International Nuclear Information System (INIS)

Wen Guanhong; Sun Duixiong; Su Maogen; Dong Chenzhong

2014-01-01

Laser-induced breakdown spectroscopy (LIBS) has been applied to the analysis of heavy metals in liquid samples. A new approach was presented to lower the limit of detection (LOD) and minimize the sample matrix effects, in which dried wood pellets absorbed the given amounts of Cr standard solutions and then were baked because they have stronger and rapid absorption properties for liquid samples as well as simple elemental compositions. In this work, we have taken a typical heavy metal Cr element as an example, and investigated the spectral feasibility of Cr solutions and dried wood pellets before and after absorbing Cr solutions at the same experimental conditions. The results were demonstrated to successfully produce a superior analytical response for heavy metal elements by using wood pellet as sample matrix according to the obtained LOD of 0.07 ppm for Cr element in solutions

La2O3/CaO CATALYSTS AND ITS APPLICATION IN THE OXIDATIVE COUPLING OF METHANE

OpenAIRE

Garrido-Schaeffer, A.; Dedios Yenque, G.; Ponce Alvaréz, S.

2014-01-01

La2O3/CaO catalysts were prepared at different weight percentages of La2O3.Por the coprecipitation method described porRaO, CaCO3 is prepared and then it was impregnated in a solution of La (NO) 3.6H2O thus obtaining the catalyst precursor . precursors dried at 393K and calcined at 973K, obtaining 0-15% La2O3/CaO catalysts. XRF elemental qualitative analysis was performed. By FTIR carbonates adsorbed species was observed. The presence of La2O3 and CaO phases was confirmed by XRD and BET surfa...

Experiments on the Synthesis of Element 115 in the Reaction ^{243}Am (^{48}Ca, xn)^{291-x}115

CERN Document Server

Oganessian, Yu T; Lobanov, Yu V; Abdullin, F S; Polyakov, A N; Shirokovsky, I V; Tsyganov, Yu S; Gulbekyan, G G; Bogomolov, S L; Mezentsev, A N; Iliev, S; Subbotin, V G; Sukhov, A M; Voinov, A A; Buklanov, G V; Subotic, K M; Zagrebaev, V I; Itkis, M G; Patin, J B; Moody, K J; Wild, J F; Stoyer, M A; Stoyer, N J; Shaughnessy, D A; Kenneally, J M; Lougheed, R W

2003-01-01

The results of experiments designed to synthesize element 115 isotopes in the ^{243}Am(^{48}Ca,xn)^{291-x}115 reaction are presented. With a beam dose of 4.3\\cdot 10^{18} 248-Mev ^{48}Ca projectiles, we observed three similar decay chains consisting of five consecutive alpha-decays, all detected in time intervals of about 20 s and terminated at a later time by a spontaneous fission with a high energy release (TKE \\sim 220 MeV). At a higher bombarding energy of 253 MeV, with an equal ^{48}Ca beam dose, we registered a different decay chain of four consecutive alpha-decays detected in a time interval of about 0.5 s, also terminated by spontaneous fission. The alpha-decay energies and half-lives for nine new alpha-decaying nuclei were determined. The decay properties of these synthesized nuclei are consistent with consecutive alpha-decays originating from the parent isotopes of the new element 115, ^{288}115 and ^{287}115, produced in the 3n- and 4n-evaporation channels with cross sections of about 3 and 1 pb, r...

The elements distribution of Fe, Cd, Ca, Co and Cr on the well water and river in area Wonosari Gunung Kidul

International Nuclear Information System (INIS)

Rosidi; Agus Taftazani; Sukirno

2010-01-01

The analysis of Fe, Cd, Ca, Co and Cr on the well water and river were detected by γ spectrometer with HPGe detector using NAA method. The main objective of this research was carried out to characterize the Fe, Cd, Ca, Co and Cr on the well water and river in area Gunung Kidul Yogyakarta, which accommodate of the present of environment data in support the clean water program. The result indicated that concentration of elements in well and river water at the Wonosari were still in standard level by Govenor of Daerah Istimewa Yogyakarta no 214/KPTS/1991, were Cd = 0,005 mg/L; Ca = 200 mg/L; Fe = 0,5 mg/L; Co = 0,2 mg/L and Cr = 0,050 mg/L. The concentration in water of Cd, Fe, Ca, Co, and Cr were (0.0002-0.006), (16-40), (5-20), (0.0002-0.37) and (0.0003-0.005) mg/L respectively. The result of analysis give the information that these elements concentration were still proper to use for domestic activities. (author)

Photoluminescence in solid solutions and thin films of tungstates CaWO{sub 4}-CdWO{sub 4}

Energy Technology Data Exchange (ETDEWEB)

Taoufyq, A.; Mauroy, V.; Guinneton, F.; Valmalette, J-C. [University of Toulon, IM2NP, UMR CNRS 7334, La Garde, (France); Fiorido, T. [Aix Marseille University, IM2NP, UMR CNRS, 7334, Marseille, (France); Benlhachemi, A. [IBN ZOHR University, Faculty of sciences, Environment and Materials Laboratory, Agadir, (Morocco); Lyoussi, A. [CEA of Cadarache, DEN, Departement of reactors studies, experimental physics, Instrumentation Sensors and Dosimetry Laboratory, (France); Nolibe, G. [Cesigma society, signals and systems, La Garde, (France); Gavarri, J-R. [University of Toulon, IM2NP, UMR CNRS 7334, La Garde, (France)

2015-07-01

In this study, we present two types of studies on the luminescence properties under UV and X-ray excitations of solid solutions Ca{sub 1-x}Cd{sub x}WO{sub 4} and of thin layers of CaWO{sub 4} and CdWO{sub 4}. These tungstate based solid solutions are susceptible to be integrated into new radiation sensors, in order to be used in different fields of applications such as reactor measurements, safeguards, homeland security, nuclear nondestructive assays, LINAC emission radiation measurement. However these complex materials were rarely investigated in the literature. One first objective of our studies was to establish correlations between luminescence efficiency, chemical substitution and the degree of crystallization resulting from elaboration conditions. A second objective will be to determine the efficiency of luminescence properties of thin layers of these materials. In the present work, we focus our attention on the role of chemical substitution on photon emissions under UV and X-ray irradiations. The luminescence spectra of Ca{sub 1-x}Cd{sub x}WO{sub 4} polycrystalline materials have been investigated at room temperature as a function of composition (0≤x≤1). In addition, we present a preliminary study of the luminescence of CaWO{sub 4} and CdWO{sub 4} thin layers: oscillations observed in the case of X-ray excitations in the luminescence spectra are discussed. (authors)

The Influence of the Addition of Polyacrylic Hydrogel on the Content of Proteins, Minerals and Trace Elements in Milk Protein Solutions

Directory of Open Access Journals (Sweden)

Aleksandar Ž. Kostić

2014-01-01

Full Text Available Solutions of milk protein concentrate, whey protein concentrate and bovine serum albumin (BSA were treated with polyacrylic hydrogel to establish whether the hydrogel could be used for decontamination of heavy metal ions from milk protein-based products. The obtained results indicated that swelling of hydrogel in these solutions had different effects on their mineral, trace element and total protein content. Total protein and phosphorus content increased in milk protein concentrate and whey protein concentrate solutions after swelling of hydrogel without changes in their protein compositions. On the other hand, the protein content in BSA solution decreased after swelling. The content of Na did not change in milk protein concentrate solution, whereas it significantly increased in whey protein concentrate solution after hydrogel swelling. The content of Ca and Mg was reduced after the swelling in milk protein concentrate and whey protein concentrate solutions for 20.3–63.4 %, depending on the analysed sample and the mineral. The content of Zn did not change during swelling, whereas the content of Fe, Cu, Mn, Ni and Pb significantly decreased after hydrogel swelling in all analysed samples. According to the obtained results, the addition of polyacrylic hydrogel to milk and whey protein concentrate solutions can significantly decrease the content of heavy metal ions without affecting their protein composition. Therefore, this work could be useful in developing a new technological process for heavy metal purification of milk protein-based products.

Nucleation of CaCO3 polymorphs from a colloidal alcoholic solution of Ca(OH)2 nanocrystals exposed to low humidity conditions

OpenAIRE

Gómez Villalba, Luz Stella; López-Arce, Paula; Fort González, Rafael

2011-01-01

A study of the stability of calcium carbonate polymorphs formed as a result of the carbonation process from an alcoholic colloidal solution of nanocrystals of Ca(OH)2 in low relative humidity (RH) conditions (33% and 54% RH) is presented in this research. The crystalline behavior, the time dependence of nucleation and the phases’ transformations as a result of exposure to low humidity conditions are evaluated. The carbonation process is slow, starting with the nucleation of amorphous calcium ...

Effect of organic matrices on the determination of the trace element chemistry (Mg, Sr, Mg/Ca, Sr/Ca) of aragonitic bivalve shells (Arctica islandica). Comparison of ICP-OES and LA-ICP-MS data

International Nuclear Information System (INIS)

Schoene, Bernd R.; Zhang, Zengjie; Jacob, Dorrit; Soldate, Analia; Gillikin, David P.; Tuetken, Thomas; Garbe-Shoenberg, Dieter; McConnaughey, Ted

2010-01-01

The element chemistry of biogenic carbonates can provide important data on past environments. However, the Sr/Ca and Mg/Ca ratios as well as the Mg and Sr concentrations of biological carbonates, especially aragonitic bivalves often depart from apparent thermodynamic equilibrium. When measured in situ by means of LA-ICP-MS, the Mg concentration is often substantially enriched (two- to threefold) near the organic-rich, annual growth lines. To test the hypothesis that some organic components exert a major influence on the skeletal metal content, the element chemistry of different shell components (insoluble organic matrix, IOM; dissolved CaCO 3 and soluble organics, SOM) of Arctica islandica was measured by means of ICP-OES and LA-ICP-MS. The ICP-OES data indicate that the IOM is strongly enriched in Mg (130 ppm) and depleted in Sr and Ca (10 ppm and 0.22 wt%, respectively) when compared to the whole biomineral (Mg: 68 to 99 ppm, Sr: 860 to 1,060 ppm, Ca: ∼35.72 wt%). Although the average relative abundance of the IOM barely exceeds 0.46 wt%, its chemical composition in combination with its heterogeneous distribution across the shell can significantly increase estimates of the Mg concentration if measured in situ by LA-ICP-MS. Depending on the distribution of the IOM, the Ca concentration may be significantly lower locally than the average Ca concentration of the whole shell (35.72 wt%). If this remains undetected, the Mg concentration of shell portions with higher than average IOM content is overestimated by LA-ICP-MS and, conversely, the Mg concentration is underestimated in shell portions with lower than average IOM content. Removal of the IOM prior to the chemical analysis by LA-ICP-MS or mathematical correction for the IOM-derived magnesium concentrations is therefore strongly advised. The different chemistry of the IOM may also exert a major control on the trace element to calcium ratios. Shell portions enriched in IOM will show up to 200 times higher Mg/Ca

Solution of Fokker–Planck equation by finite element and finite ...

Indian Academy of Sciences (India)

The response of a structural system to white noise excitation (delta-correlated) constitutes a Markov vector process whose transitional probability density function (TPDF) is governed by both the forward Fokker–Planck and backward Kolmogorov equations. Numerical solution of these equations by finite element and finite ...

PERSONAL, INDOOR, AND OUTDOOR CONCENTRATIONS OF PM2.5, PARTICULATE NITRATE, AND ELEMENTAL CARBON FOR INDIVIDUALS WITH COPD IN LOS ANGELES, CA

Science.gov (United States)

This study characterizes the personal, indoor, and outdoor concentrations of PM2.5 and the major components of PM2.5, including nitrate (NO3-), elemental carbon (EC), and the elements for individuals with chronic obstructive pulmonary disease (COPD) living in Los Angeles, CA. ...

Coordination and structure of Ca(II)-acetate complexes in aqueous solution studied by a combination of Raman and XAFS spectroscopies

Science.gov (United States)

Muñoz Noval, Álvaro; Nishio, Daisuke; Kuruma, Takuya; Hayakawa, Shinjiro

2018-06-01

The determination of the structure of Ca(II)-acetate in aqueous solution has been addressed by combining Raman and X-ray absorption fine structure spectroscopies. The pH-dependent speciation of the acetate/Ca(II) system has been studied observing modifications in specific Raman bands of the carboxyl group. The current results evidence the Ca(II)-acetate above acetate pKa forms a bidentate complex and presents a coordination 6, in which the Ca-O shell radius decrease of about 0.1 Å with respect the hydrated Ca2+ with coordination 8. The experimental results show the OCO angle of the carboxyl in the complex is close to 124°, being the OCaO angle about 60°.

Numerical solutions of multi-dimensional solidification/melting problems by the dual reciprocity boundary element method

International Nuclear Information System (INIS)

Jo, Jong Chull; Shin, Won Ky

1997-01-01

This paper presents an effective and simple procedure for the simulation of the motion of the solid-liquid interfacial boundary and the transient temperature field during phase change process. To accomplish this purpose, an iterative implicit solution algorithm has been developed by employing the dual reciprocity boundary element method. The dual reciprocity boundary element approach provided in this paper is much simpler than the usual boundary element method applying a reciprocity principle and an available technique for dealing with domain integral of boundary element formulation simultaneously. The effectiveness of the present analysis method have been illustrated through comparisons of the calculation results of an example with its semi-analytical or other numerical solutions where available

Magnetic susceptibilities of Ca/sub y/U/sub 1-y/O/sub 2+x/ solid solutions

International Nuclear Information System (INIS)

Hinatsu, Y.; Fujino, T.

1988-01-01

Magnetic susceptibilities of Ca/sub y/U/sub 1-y/O/sub 2+x/ solid solutions with fluorite structure were measured from 4.2 K to room temperature. An antiferromagnetic transition was observed for all the solid solutions examined in this study (y ≤ 0.33). The Neel temperature of the oxygen-hypostoichiometric solid solutions (x 2 solid solutions, but different from that of (U,Th)O 2 solid solutions. The effective magnetic moment decreased with increasing calcium concentration, which indicates the oxidation of uranium in the solid solutions. From the analysis of the magnetic susceptibility data, it was found that the oxidation state of uranium was either tetravalent or pentavalent. The Neel temperature of the hyperstoichiometric solid solutions (x > 0) did not change appreciably with calcium concentrations. From the comparison of the magnetic susceptibility data of the hypostoichiometric solid solutions with those of the hyperstoichiometric solid solutions, the effect of oxygen vacancies is more significant than that of interstitial oxygens on the decrease of magnetic interactions between uranium ions

Determination of trace elements in seawater by neutron activation analysis and electrochemical separation

International Nuclear Information System (INIS)

Jorstad, K.; Salbu, B.

1980-01-01

The combination of neutron activation analysis and electrolysis at a constant, controlled potential has proved itself to be a useful multielement method for the determination of 28 elements in seawater. After freeze-drying and irradiation, the samples are dissolved and electrolyzed for 1 h. The radioactive species deposited on the mercury cathode allow determination of 14 elements (Ag, As, Au, Cd, Co, Cr, Fe, Ga, Hg, La, Mo, Sb, Se, Zn). Another 14 elements (Ba, Br, Ca, Ce, Cs, Eu, Na, Rb, Sc, Sm, Sr, Th, U, Yb) are quantitatively determined by measuring the activities in the residual solution. To obtain a reproducible electrolysis, radioactive tracers have been used to study the decrease of element concentrations in solution as a function of time of electrolysis, the influence of the initial element concentration on the rate constant k, the effect of cathode material and of the pH in the solution. 4 figures, 4 tables

Feasibility study on using three element TLD badge based on CaSO4:Dy as environmental dosimeter

International Nuclear Information System (INIS)

Choudhary, Sreeletha; BharathiLashmi, G.V.; Yasotha, E.; Devanathan, P.S.; Annalakshmi, O.; Mathiyarasu, R.

2018-01-01

A three element thermoluminescence badge based on CaSO 4 :Dy is used for personnel monitoring in India. The three discs of the badge is heated in sequential manner by hot nitrogen gas and from the amount of light emitted while heating, the doses are estimated. This badge was redesigned as a two element system and is used for environmental monitoring. Though the two element badge has some advantages, the software used for processing of TLDs in the semiautomatic reader has to be modified and separate badges has to be maintained for environmental dose measurements. In this work a feasibility study has been carried out to use the three element personnel monitoring badge itself for environmental monitoring also. This study was also carried out to understand the abnormal pattern of the glow curves observed in some field cards

Methods for removing transuranic elements from waste solutions

International Nuclear Information System (INIS)

Slater, S.A.; Chamberlain, D.B.; Connor, C.; Sedlet, J.; Srinivasan, B.; Vandegrift, G.F.

1994-11-01

This report outlines a treatment scheme for separating and concentrating the transuranic (TRU) elements present in aqueous waste solutions stored at Argonne National Laboratory (ANL). The treatment method selected is carrier precipitation. Potential carriers will be evaluated in future laboratory work, beginning with ferric hydroxide and magnetite. The process will result in a supernatant with alpha activity low enough that it can be treated in the existing evaporator/concentrator at ANL. The separated TRU waste will be packaged for shipment to the Waste Isolation Pilot Plant

Investigations on the use of pneumatic cross-flow nebulizers with dual solution loading including the correction of matrix effects in elemental determinations by inductively coupled plasma optical emission spectrometry

International Nuclear Information System (INIS)

Bauer, Mathieu; Broekaert, Jose A.C.

2007-01-01

The use of a so-called trihedral and a T-shaped cross-flow pneumatic nebulizer with dual solution loading for inductively coupled plasma optical emission spectrometry has been studied. By these devices analyte clouds from two solutions can be mixed during the aerosol generation step. For both nebulizers the correction of matrix effects using internal standardization and standard addition calibration in an on-line way was investigated and compared to elemental determinations using a conventional cross-flow nebulizer and calibration with synthetic standard solutions without matrix matching. A significant improvement of accuracy, both for calibration with internal standardization and standard addition, was obtained in the case of four synthetic solutions containing each 40 mmol L -1 Na, K, Rb and Ba as matrix elements and 300 μg L -1 Cd, Co, Cr, Cu, Fe, Mn, Ni and Pb as analytes. Calibration by standard addition in the case of dual solution loading has been shown to be very useful in the determination of elements at minor and trace levels in steel and alumina reference materials. The results of analysis for minor concentrations of Cr, Cu and Ni in steel as well as for Ca, Fe, Ga, Li, Mg, Mn, Na, Si and Zn in alumina powder certified reference materials subsequent to sample dissolution were found to be in good agreement with the certificates. Limits of detection were found to be only slightly above those for a conventional cross-flow nebulizer and a precision better than 3% was realized with both novel nebulizers

Fundamental solutions and dual boundary element methods for fracture in plane Cosserat elasticity.

Science.gov (United States)

Atroshchenko, Elena; Bordas, Stéphane P A

2015-07-08

In this paper, both singular and hypersingular fundamental solutions of plane Cosserat elasticity are derived and given in a ready-to-use form. The hypersingular fundamental solutions allow to formulate the analogue of Somigliana stress identity, which can be used to obtain the stress and couple-stress fields inside the domain from the boundary values of the displacements, microrotation and stress and couple-stress tractions. Using these newly derived fundamental solutions, the boundary integral equations of both types are formulated and solved by the boundary element method. Simultaneous use of both types of equations (approach known as the dual boundary element method (BEM)) allows problems where parts of the boundary are overlapping, such as crack problems, to be treated and to do this for general geometry and loading conditions. The high accuracy of the boundary element method for both types of equations is demonstrated for a number of benchmark problems, including a Griffith crack problem and a plate with an edge crack. The detailed comparison of the BEM results and the analytical solution for a Griffith crack and an edge crack is given, particularly in terms of stress and couple-stress intensity factors, as well as the crack opening displacements and microrotations on the crack faces and the angular distributions of stresses and couple-stresses around the crack tip.

Distribution of trace elements between clays and zeolites and aqueous solutions similar to sea water

International Nuclear Information System (INIS)

Berger, G.

1992-01-01

The mechanisms of solid-solution partitioning during mineral crystallization in sea water have been investigated for Rb, Cs, Co, Sr, U, Th and lanthanides as trace elements, and Fe, Mg-chlorite/smectites and Na-zeolites as solid phases. These minerals have been synthesized by alteration at 40 o C in saline solutions of silicate glasses of appropriate compositions. The variation of the distribution coefficients (D) with the concentration of the elements as well as competition mechanisms between elements of analogous crystallochemical properties have been studied. The ''trapping'' of trace elements is shown to be governed by two mechanisms, according to D values or to water-rock ratios. At low values of D the incorporation of elements is controlled only by D, whereas at high values it is controlled by the number of available crystallochemical sites. (Author)

Effect of calcium on the microstructure and corrosion behavior of microarc oxidized Mg-xCa alloys.

Science.gov (United States)

Pan, Yaokun; Chen, Chuanzhong; Feng, Rui; Cui, Hongwei; Gong, Benkui; Zheng, Tingting; Ji, Yarou

2018-01-16

Magnesium alloys are potential biodegradable implants for biomedical applications, and calcium (Ca) is one kind of ideal element being examined for magnesium alloys and biodegradable ceramic coatings owing to its biocompatibility and mechanical suitability. In this study, microarc oxidation (MAO) coatings were prepared on Mg-xCa alloys to study the effect of Ca on the microstructure and corrosion resistance of Mg-xCa alloys and their surface MAO coatings. The electrochemical corrosion behavior was investigated using an electrochemical workstation, and the degradability and bioactivity were evaluated by soaking tests in simulated body fluid (SBF) solutions. The corrosion products were characterized by scanning electron microscopy, x-ray diffractometry, and Fourier transform infrared spectrometry. The effects of Ca on the alloy phase composition, microstructure, MAO coating formation mechanism, and corrosion behavior were investigated. Results showed that the Mg-0.82Ca alloy and MAO-coated Mg-0.82Ca exhibited the highest corrosion resistance. The number and distribution of Mg 2 Ca phases can be controlled by adjusting the Ca content in the Mg-xCa alloys. The proper amount of Ca in magnesium alloy was about 0.5-0.8 wt. %. The pore size, surface roughness, and corrosion behavior of microarc oxidized Mg-xCa samples can be controlled by the number and distribution of the Mg 2 Ca phase. The corrosion behaviors of microarc oxidized Mg-Ca in SBF solutions were discussed.

Application of thermodynamics to silicate crystalline solutions

Science.gov (United States)

Saxena, S. K.

1972-01-01

A review of thermodynamic relations is presented, describing Guggenheim's regular solution models, the simple mixture, the zeroth approximation, and the quasi-chemical model. The possibilities of retrieving useful thermodynamic quantities from phase equilibrium studies are discussed. Such quantities include the activity-composition relations and the free energy of mixing in crystalline solutions. Theory and results of the study of partitioning of elements in coexisting minerals are briefly reviewed. A thermodynamic study of the intercrystalline and intracrystalline ion exchange relations gives useful information on the thermodynamic behavior of the crystalline solutions involved. Such information is necessary for the solution of most petrogenic problems and for geothermometry. Thermodynamic quantities for tungstates (CaWO4-SrWO4) are calculated.

Numerical solutions of multi-dimensional solidification/melting problems by the dual reciprocity boundary element method

Energy Technology Data Exchange (ETDEWEB)

Jo, Jong Chull; Shin, Won Ky [Korea Institute of Nuclear Safety, Taejon (Korea, Republic of)

1998-12-31

This paper presents an effective and simple procedure for the simulation of the motion of the solid-liquid interfacial boundary and the transient temperature field during phase change process. To accomplish this purpose, an iterative implicit solution algorithm has been developed by employing the dual reciprocity boundary element method. The dual reciprocity boundary element approach provided in this paper is much simpler than the usual boundary element method applying a reciprocity principle and an available technique for dealing with domain integral of boundary element formulation simultaneously. The effectiveness of the present analysis method have been illustrated through comparisons of the calculation results of an example with its semi-analytical or other numerical solutions where available. 22 refs., 3 figs. (Author)

Numerical solutions of multi-dimensional solidification/melting problems by the dual reciprocity boundary element method

Energy Technology Data Exchange (ETDEWEB)

Jo, Jong Chull; Shin, Won Ky [Korea Institute of Nuclear Safety, Taejon (Korea, Republic of)

1997-12-31

This paper presents an effective and simple procedure for the simulation of the motion of the solid-liquid interfacial boundary and the transient temperature field during phase change process. To accomplish this purpose, an iterative implicit solution algorithm has been developed by employing the dual reciprocity boundary element method. The dual reciprocity boundary element approach provided in this paper is much simpler than the usual boundary element method applying a reciprocity principle and an available technique for dealing with domain integral of boundary element formulation simultaneously. The effectiveness of the present analysis method have been illustrated through comparisons of the calculation results of an example with its semi-analytical or other numerical solutions where available. 22 refs., 3 figs. (Author)

Desirable levels of exchangeable K and Ca and their concentration in the soil solution to reduce uptake of radioactive Cs by rice plants

International Nuclear Information System (INIS)

Sekimoto, Hitoshi; Yamada, Takashi; Hotsuki, Tomoe; Matsuzaki, Akio; Mimura, Tetsuro

2014-01-01

K in the soil solution can control the uptake of radioactive Cs by rice plants, but this control is not accomplished only by K; it is affected by other ionic species. It is therefore important to investigate uptake of radioactive Cs from the perspective of the concentration of major cations such as Ca in the soil solution and the levels of exchangeable cations in the soil. To clarify the effects of K and Ca in the soil solution and of the levels of soil exchangeable cations to prevent uptake of radioactive Cs, we conducted a pot experiment and field experiments in a paddy soil in 2011 and 2012. To reduce the uptake of radioactive Cs, it was necessary to achieve a K concentration in the soil solution of 0.5 mmol L"-"1, and a Ca concentration higher than 2 mmol L"-"1 based on the results of the pot experiment. In addition, we obtained the desirable levels of exchangeable cations and the cation exchange capacity (CEC) in the soil from previous reports and the results of our field experiments. On this basis, we propose the following threshold levels for exchangeable cations and CEC in the soil as a standard: 0.53 K cmol_c kg"-"1, 18.0 Ca cmol_c kg"-"1, 2.0 Mg cmol_c kg"-"1, i.e. 25 mg K_2O 100 g"-"1, 505 mg CaO 100 g"-"1, 40 Mg O mg 100 g"-"1, and a CEC of 30 cmol_c kg"-"1. Converting these values into the corresponding levels in the soil solution, we obtained concentrations of 0.71 mmol K L"-"1, 4.22 mmol Ca L"-"1, and 1.35 mmol Mg L"-"1. These levels are within the improving standard for fertility of paddy soils in Japan. Consequently, it will be necessary to improve the fertility of paddy soils to control the uptake of radioactive Cs by rice plants. (author)

Investigation on a two-stage solar liquid-desiccant (LiBr) dehumidification system assisted by CaCl2 solution

International Nuclear Information System (INIS)

Xiong, Z.Q.; Dai, Y.J.; Wang, R.Z.

2009-01-01

A two-stage solar powered liquid-desiccant dehumidification system, for which two kinds of desiccant solution (lithium chloride and calcium bromide) are fed to the two dehumidification stages separately, has been studied. In the studied system air moisture (latent) load is separately removed by a pre-dehumidifier using cheap calcium chloride (CaCl 2 ) and a main dehumidifier using stable lithium bromide (LiBr). Side-effect of mixing heat rejected during dehumidification process is considerably alleviated by an indirect evaporative cooling unit added between the two dehumidification stages. The feasibility of high-desiccant concentration difference achieved by reusing desiccant solution to dehumidify air and regenerating desiccant repeatedly is analyzed. By increasing desiccant concentration difference, desiccant storage capacity is effectively explored. It is found that the pre-dehumidification effect of CaCl 2 solution is significant in high ambient humidity condition. Also seen is that the desiccant investment can be decreased by 53%, though the cost of equipments is somewhat increased, and the Tcop and COP of the proposed system can reach 0.97 and 2.13, respectively

Maximum-principle-satisfying space-time conservation element and solution element scheme applied to compressible multifluids

KAUST Repository

Shen, Hua; Wen, Chih-Yung; Parsani, Matteo; Shu, Chi-Wang

2016-01-01

A maximum-principle-satisfying space-time conservation element and solution element (CE/SE) scheme is constructed to solve a reduced five-equation model coupled with the stiffened equation of state for compressible multifluids. We first derive a sufficient condition for CE/SE schemes to satisfy maximum-principle when solving a general conservation law. And then we introduce a slope limiter to ensure the sufficient condition which is applicative for both central and upwind CE/SE schemes. Finally, we implement the upwind maximum-principle-satisfying CE/SE scheme to solve the volume-fraction-based five-equation model for compressible multifluids. Several numerical examples are carried out to carefully examine the accuracy, efficiency, conservativeness and maximum-principle-satisfying property of the proposed approach.

Maximum-principle-satisfying space-time conservation element and solution element scheme applied to compressible multifluids

KAUST Repository

Shen, Hua

2016-10-19

A maximum-principle-satisfying space-time conservation element and solution element (CE/SE) scheme is constructed to solve a reduced five-equation model coupled with the stiffened equation of state for compressible multifluids. We first derive a sufficient condition for CE/SE schemes to satisfy maximum-principle when solving a general conservation law. And then we introduce a slope limiter to ensure the sufficient condition which is applicative for both central and upwind CE/SE schemes. Finally, we implement the upwind maximum-principle-satisfying CE/SE scheme to solve the volume-fraction-based five-equation model for compressible multifluids. Several numerical examples are carried out to carefully examine the accuracy, efficiency, conservativeness and maximum-principle-satisfying property of the proposed approach.

Chemical Identification of Dubnium as a Decay Product of Element 115 Produced in the Reaction $\\rm {^{48}Ca}+{^{243}Am}$

CERN Document Server

Dmitriev, S N; Utyonkov, V K; Shishkin, S V; Eremin, A V; Lobanov, Yu V; Chepigin, V I; Sokol, E A; Tsyganov, Yu S; Vostokin, G K; Aksenov, N V; Hussonnois, M; Itkis, M G; Aggeler, H W; Schumann, D; Bruchertseifer, H; Eichler, R; Shaughnessy, D A; Wilk, P A; Kenneally, J M; Stoyer, M A; Wild, J F

2004-01-01

The results of an experiment designed to identify $^{268}$Db as the terminal isotope in the $\\alpha $-decay chain of element 115 produced via the ${\\rm {^{243}Am}}({\\rm {^{48}Ca}},3n){\\rm {^{288}115}}$ reaction are presented. The $^{243}$Am target was bombarded with a beam dose of $3.4\\cdot 10^{18}$ $^{48}$Ca projectiles at an energy of 247 MeV at the center of the target. The reaction products were collected in the surface layer of a copper catcher block, which was removed with a lathe and then dissolved in concentrated HNO$_{3}$. The group-5 elements were separated by sorption onto Dowex $50{\\times} 8$ cation-exchange resin with subsequent desorption using 1 M HF, which forms anionic fluoride complexes of group-5 elements. The eluent was evaporated onto a 0.4 $\\mu$m thick polyethylene foil that was placed between a pair of semiconductor detectors surrounded by $^{3}$He neutron counters for measurement of $\\alpha$ particles, fission fragments, and neutrons. In the course of the experiment, we observed 15 spo...

Electrochemical characteristics of bioresorbable binary MgCa alloys in Ringer's solution: Revealing the impact of local pH distributions during in-vitro dissolution

Energy Technology Data Exchange (ETDEWEB)

Mareci, D., E-mail: danmareci@yahoo.com [Faculty of Chemical Engineering and Environmental Protection, The “Gheorghe Asachi” Technical University of Iasi, 700050, Iasi (Romania); Bolat, G. [Faculty of Chemical Engineering and Environmental Protection, The “Gheorghe Asachi” Technical University of Iasi, 700050, Iasi (Romania); Izquierdo, J. [Department of Chemistry, University of La Laguna, P.O. Box 456, E-38200 La Laguna (Tenerife) (Spain); Crimu, C.; Munteanu, C. [Faculty of Mechanical Engineering, The “Gheorghe Asachi” Technical University of Iasi, 700050, Iasi (Romania); Antoniac, I. [Faculty of Materials Science and Engineering, Politehnica of Bucharest, 060042 Bucharest (Romania); Souto, R.M., E-mail: rsouto@ull.es [Department of Chemistry, University of La Laguna, P.O. Box 456, E-38200 La Laguna (Tenerife) (Spain); Faculty of Materials Science and Engineering, Politehnica of Bucharest, 060042 Bucharest (Romania)

2016-03-01

Biodegradable magnesium–calcium (MgCa) alloy is a very attractive biomaterial. Two MgCa alloys below the solid solubility of Ca were considered, as to solely investigate the effect of Ca content on the behavior of magnesium and the pH changes associated to metal dissolution. X-ray diffraction analysis and optical microscopy showed that both Mg–0.63Ca and Mg–0.89Ca alloys were solely composed of α(Mg) phase. Degradation characteristics and electrochemical characterization of MgCa alloys were investigated during exposure to Ringer's solution at 37 °C by electrochemical impedance spectroscopy and scanning electrochemical microscopy. The impedance behavior showed both capacitive and inductive features that are related to the alloy charge transfer reaction and the relaxation of the absorbed corrosion compounds, and can be described in terms of an equivalent circuit. Scanning electron microscopy (SEM) was employed to view the surface morphology of the MgCa samples after 1 week immersion in Ringer's solution showing extensive precipitation of corrosion products, whereas the substrate shows evidence of a non-uniform corrosion process. Energy dispersive analysis showed that the precipitates contained oxygen, calcium, magnesium and chlorine, and the Mg:Ca ratios were smaller than in the alloys. Scanning electrochemical microscopy (SECM) was used to visualize local pH changes associated to these physicochemical processes with high spatial resolution. The occurrence of pH variations in excess of 3 units between anodic and cathodic half-cell reactions was monitored in situ. - Highlights: • Spontaneous degradation of MgCa alloys in Ringer's solution characterized at 37 °C • Reactivity differences between Mg0.63Ca and Mg0.89Ca are evidenced using multiscale electrochemical characterization. • Electrochemical activation occurs heterogeneously on the alloy surface. • Metal dissolution is accompanied by local pH changes. • Mg0.63Ca degrades faster

Isolation of transplutonium elements on ion exchangers from solutions of high salt concentration

International Nuclear Information System (INIS)

Guseva, L.I.; Tikhomirova, G.S.; Stepushkina, V.V.

1985-01-01

The behaviour of transplutonium elements (TPE) on cation and anion exchangers in aqueous alcoholic solutions of chlorides and nitrates of some alkali and alkaline earth metals depending on different factors: salt concentration, content of alcohol and of acid in the solution as well as the nature of a cation was studied. The data obtained were used to determine the optimal conditions of concentration of TPE on ion exchangers from solutions containing great quantities of salts. The advantages of the use of aqueous alcoholic solutions of nitric acid in the isolation of TPE are shown. (author)

Removal of Ca(II) and Mg(II) from potassium chromate solution on Amberlite IRC 748 synthetic resin by ion exchange

International Nuclear Information System (INIS)

Yu Zhihui; Qi Tao; Qu Jingkui; Wang Lina; Chu Jinglong

2009-01-01

Experimental measurements have been made on the batch ion exchange of Ca(II) and Mg(II) from potassium chromate solution using cation exchanger of Amberlite IRC 748 as K + form. The ion exchange behavior of two alkaline-earth metals on the resin, depending on contact time, pH, temperature and resin dosage was studied. The adsorption isotherms were described by means of the Langmuir and Freundlich isotherms. For Ca(II) ion, the Langmuir model represented the adsorption process better than the Freundlich model. The maximum ion exchange capacity was found to be 47.21 mg g -1 for Ca(II) and 27.70 mg g -1 for Mg(II). The kinetic data were tested using Lagergren-first-order and pseudo-second-order kinetic models. Kinetic data correlated well with the pseudo-second-order kinetic model, indicating that the chemical adsorption was the rate-limiting step. Various thermodynamic parameters such as Gibbs free energy (ΔG o ), enthalpy (ΔH o ) and entropy (ΔS o ) were also calculated. These parameters showed that the ion exchange of Ca(II) and Mg(II) from potassium chromate solution was feasible, spontaneous and endothermic process in nature. The activation energy of ion-exchange (E a ) was determined as 12.34 kJ mol -1 for Ca(II) and 9.865 kJ mol -1 for Mg(II) according to the Arrhenius equation.

A Study on Microstructural Change and Properties of Mg-1.4 wt%Ca-xwt%Zn Alloys by Two-Step Solid Solution and Aging Treatment

International Nuclear Information System (INIS)

Koo, Seong Mo; Kim, Hye Sung; Jeong, Ha-Guk; Kim, Teak-Soo

2015-01-01

Optimum heat treatment conditions to improve the hardness and corrosion resistance of ternary Mg-Ca-Zn alloys have been studied, based on the theoretical models and DSC (Differential scanning calorimetry) experimental data. Two-step heating process at 420 ℃ and 480 ℃ has been applied and we have found that the low melting point phase, Ca_2Mg_6Zn_3 can effectively be dissolved into α-Mg matrix without premature melting. Due to preceding treatment at lower temperature followed by the second stage solid solution heat treatment at 480 ℃, Mg-1.4 wt%Ca-xwt%Zn alloys (x=0, 1.5 and 4.0) exhibit improved corrosion resistance than that from the single step solid solution treated alloy at 480 ℃. However, aging treatment of the alloy at 200 ℃ has led to the homogeneous precipitation of Ca_2Mg_6Zn_3 and Mg_2Ca phases in the matrix as well as at the grain boundary. This microstructural change results in the deterioration of corrosion resistance mainly originated from galvanic corrosion between the matrix and the precipitates. The hardness of Mg-1.4%Cax%Zn alloy, on the other hand, significantly increases with Zn addition by applying two-step solid solution and aging heat treatment.

SNL/CA Environmental Management System Program Manual.

Energy Technology Data Exchange (ETDEWEB)

Larsen, Barbara L.

2007-04-01

The Sandia National Laboratories, California (SNL/CA) Environmental Management System (EMS) Program Manual documents the elements of the site EMS Program. The SNL/CA EMS Program conforms to the International Standard on Environmental Management Systems, ISO 14001:2004. Elements of the ISO standard overlap with those of Department of Energy (DOE) Order 450.1, thus SNL/CA's EMS program also meets the DOE requirements.

Corrosion study of resorbable Ca60Mg15Zn25 bulk metallic glasses in physiological fluids

Directory of Open Access Journals (Sweden)

Rafał Babilas

2017-10-01

Full Text Available The corrosion activity of amorphous plates of Ca60Mg15Zn25 alloy was investigated. The biocompatible elements were selected for the alloy composition. The electrochemical corrosion and immersion tests were carried out in a multi-electrolyte fluid and Ringer's solution. Better corrosion behavior was observed for the samples tested in a multi-electrolyte fluid despite the active dissolution of Ca and Mg in Ringer's solution. The experimental results indicated that reducing concentration of NaCl from 8.6 g/dm3 for Ringer's solution to 5.75 g/dm3 caused the decrease of the corrosion rate. The volume of the hydrogen evolved after 480 min in Ringer's solution (40.1 ml/cm2 was higher in comparison with that obtained in a multi-electrolyte fluid (24.4 ml/cm2. The values of open-circuit potential (EOCP for the Ca60Mg15Zn25 glass after 1 h incubation in Ringer's solution and a multi-electrolyte fluid were determined to be −1553 and −1536 mV vs. a saturated calomel electrode (SCE. The electrochemical measurements indicated a shift of the corrosion current density (jcorr from 1062 μA/cm2 for the sample tested in Ringer's solution to 788 μA/cm2 for the specimen immersed in a multi-electrolyte fluid. The corrosion products analysis was conducted by using the X-ray photoelectron spectroscopy (XPS. The corrosion products were identified to be CaCO3, Mg(OH2, CaO, MgO and ZnO. The mechanism of corrosion process was proposed and described based on the microscopic observations. The X-ray diffraction and Fourier transform infrared spectroscopy (FTIR also indicated that Ca(OH2, CaCO3, Zn(OH2 and Ca(Zn(OH32·2H2O mainly formed on the surface of the studied alloy. Keywords: Ca-based metallic glasses, X-ray photoelectron spectroscopy, FTIR spectroscopy, X-ray diffraction, Corrosion resistance, Hydrogen evaluation

Finite-element solutions of the AER-2 rod ejection benchmark by CRONOS

International Nuclear Information System (INIS)

Kolev, N.P.; Lenain, R.; Fedon-Magnaud, C.

2001-01-01

The finite-element option in CRONOS was used to analyse the AER-2 rod-ejection benchmark for WWER-440. The objective is to obtain spatially converged solutions by means of node subdivision and approximation refinement. This paper presents the first phase of analysis dealing with the initial and just-ejected states used for calculation of the initial reactivity. Fine-mesh and extrapolated to zero mesh size solutions were obtained and verified by comparison to MAG code solutions. These differences provide potential for large deviations in the transient results and deserve further attention in reactor safety analysis (Authors)

Transfer of alkaline earth elements in mothers' milk and doses from 45Ca, 90Sr and 226Ra

International Nuclear Information System (INIS)

Smith, T.J.; Phipps, A.W.; Fell, T.P.; Harrison, J.D.

2003-01-01

An international programme of work is currently under way to develop methods for calculating doses to infants from ingestion of radionuclides present in mothers' milk. This paper considers the special case of the alkaline earth elements. Models have been developed for 45 Ca, 90 Sr and 226 Ra and the sensitivity of results to various changes in parameter values is discussed. A complication when calculating doses from intakes of radium is that the International Commission on Radiological Protection has previously recommended that doses from decay products of radium should be calculated using element-specific biokinetic models (so-called independent biokinetics). An extension of this method to the models for breastfeeding is proposed. Preliminary estimates of the doses received by the infant for a number of maternal intake scenarios show that doses to the infant can exceed the corresponding adult dose, such as for 45 Ca (ratio = 3.1) while, in other cases such as 90 Sr, the infant dose can be a significant fraction of the adult dose. (author)

Development Of PIXE Measurement Of Ca Changes Resulting From Viral Transduction In Cells

Science.gov (United States)

Whitlow, Harry J.; Chienthavorn, Orapin; Eronen, Hannele; Sajavaara, Timo; Laitinen, Mikko; Norarat, Rattanaporn; Gilbert, Leona K.

2011-06-01

Ca is a life-element of particular interest because it is both bound to proteins, and as Ca2+ which functions as a signal molecule in apoptosis. Here we report development of chemical-matrix blind assaying the Ca fluxes from transduced HepG2 cells using particle induced X-ray emission. The cells were transduced with recombinant baculoviruses hosting the DNA for non-structural protein 1 (NS1) of the human pavovirus B19. Different recombinant baculoviruses were used that carried different DNA payloads of this NS1. Two different approaches have been developed to assay Ca in cells. The first is where the cells were directly cultured using a self-supporting pioloform as a substrate. In the second approach the cells are permeabilized, and bound-Ca content in the debris, and unbound-Ca in the wash solutions were measured using an internal V reference standard. The results support a difference in the Ca contents depending on the payload of the infecting virus, however the PIXE signals were too close to the minimum detection limit to draw reliable conclusions.

Transition from Endothermic to Exothermic Dissolution of Hydroxyapatite Ca5(PO43OH–Johnbaumite Ca5(AsO43OH Solid Solution Series at Temperatures Ranging from 5 to 65 °C

Directory of Open Access Journals (Sweden)

Bartosz Puzio

2018-06-01

Full Text Available Five crystalline members of the hydroxyapatite (HAP; Ca5(PO43OH–johnbaumite (JBM; Ca5(AsO43OH series were crystallized at alkaline pH from aqueous solutions and used in dissolution experiments at 5, 25, 45, and 65 °C. Equilibrium was established within three months. Dissolution was slightly incongruent, particularly at the high-P end of the series. For the first time, the Gibbs free energy of formation ΔGf0, enthalpy of formation ΔHf0, entropy of formation Sf0, and specific heat of formation Copf were determined for HAP–JBM solid solution series. Based on the dissolution reaction, Ca5(AsO4m(PO43−mOH = 5Ca2+(aq + mAsO43−(aq + (3 − mPO43−(aq + OH−(aq, their solubility product Ksp,298.15 was determined. Substitution of arsenic (As for phosphorus (P in the structure of apatite resulted in a linear increase in the value of Ksp: from HAP logKsp,298.15 = −57.90 ± 1.57 to JBM logKsp,298.15 = −39.22 ± 0.56. The temperature dependence of dissolution in this solid solution series is very specific; in the temperature range of 5 °C to 65 °C, the enthalpy of dissolution ΔHr varied around 0. For HAP, the dissolution reaction at 5 °C and 25 °C was endothermic, which transitioned at around 40 °C and became exothermic at 45 °C and 65 °C.

Solution of finite element problems using hybrid parallelization with MPI and OpenMP Solution of finite element problems using hybrid parallelization with MPI and OpenMP

Directory of Open Access Journals (Sweden)

José Miguel Vargas-Félix

2012-11-01

Full Text Available The Finite Element Method (FEM is used to solve problems like solid deformation and heat diffusion in domains with complex geometries. This kind of geometries requires discretization with millions of elements; this is equivalent to solve systems of equations with sparse matrices and tens or hundreds of millions of variables. The aim is to use computer clusters to solve these systems. The solution method used is Schur substructuration. Using it is possible to divide a large system of equations into many small ones to solve them more efficiently. This method allows parallelization. MPI (Message Passing Interface is used to distribute the systems of equations to solve each one in a computer of a cluster. Each system of equations is solved using a solver implemented to use OpenMP as a local parallelization method.The Finite Element Method (FEM is used to solve problems like solid deformation and heat diffusion in domains with complex geometries. This kind of geometries requires discretization with millions of elements; this is equivalent to solve systems of equations with sparse matrices and tens or hundreds of millions of variables. The aim is to use computer clusters to solve these systems. The solution method used is Schur substructuration. Using it is possible to divide a large system of equations into many small ones to solve them more efficiently. This method allows parallelization. MPI (Message Passing Interface is used to distribute the systems of equations to solve each one in a computer of a cluster. Each system of equations is solved using a solver implemented to use OpenMP as a local parallelization method.

Up-regulation of Ca2+/CaMKII/CREB signaling in salicylate-induced tinnitus in rats.

Science.gov (United States)

Zhao, Jiuhan; Wang, Biao; Wang, Xiaohong; Shang, Xiuli

2018-02-09

The purpose of the study was to investigate the changes of Ca 2+ /calmodulin-dependent protein kinases II (CaMKII)/cAMP response element-binding protein (CREB) signaling pathway in a rat tinnitus model. Eighteen Wistar rats were randomly divided into three groups: normal control (NC), normal saline (NS), and tinnitus model (TM) groups. Tinnitus model was induced by intraperitoneal injection of salicylate. The concentration of intracellular calcium level in auditory cortex cells was determined using Fura-2 acetoxymethyl ester (Fura-2 AM) method with fluorospectrophotometer. Expressions of calmodulin (CaM), N-methyl-D-aspartate receptor 2B subunit (NR2B), calcium-calmodulin kinase II (CaMKII), and cAMP response element-binding protein (CREB) were detected with Western blot. Tinnitus model was successfully established by the intraperitoneal administration of salicylate in rats. Compared with rats in NC and NS groups, salicylate administration significantly elevated CaM, NR2B, phospho-CaMKII and phospho-CREB expression in auditory cortex from tinnitus model group (p salicylate administration causes tinnitus symptoms and elevates Ca 2+ /CaMKII/CREB signaling pathway in auditory cortex cells. Our study likely provides a new understanding of the development of tinnitus.

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.

SOLUTION OF TRANSIENT HEAT CONDUCTION PROBLEM BY THE FINITE ELEMENT METHOD

Directory of Open Access Journals (Sweden)

Süleyman TAŞGETİREN

1995-01-01

Full Text Available Determination of temperature distribution is generally the first step in the design of machine elements subjected to ubnormal temperatures in their service life and for selection of materials. During this heat transfer analysis, the boundary and enviromental conditions must be modeled realistically and the geometry must be well represented. A variety of materials deviating from simple constant property isotropic material to composit materials having different properties according to direction of reinforcements are to be analysed. Then, the finite element method finds a large application area due to its use of same notation in heat transfer analysis and mechanical analysis of elements. In this study, the general formulation of two dimensional transient heat conduction is developed and a sample solution is given for arectangular bar subjected to convection baundary condition.

Electrochemical characteristics of bioresorbable binary MgCa alloys in Ringer's solution: Revealing the impact of local pH distributions during in-vitro dissolution.

Science.gov (United States)

Mareci, D; Bolat, G; Izquierdo, J; Crimu, C; Munteanu, C; Antoniac, I; Souto, R M

2016-03-01

Biodegradable magnesium-calcium (MgCa) alloy is a very attractive biomaterial. Two MgCa alloys below the solid solubility of Ca were considered, as to solely investigate the effect of Ca content on the behavior of magnesium and the pH changes associated to metal dissolution. X-ray diffraction analysis and optical microscopy showed that both Mg-0.63Ca and Mg-0.89Ca alloys were solely composed of α(Mg) phase. Degradation characteristics and electrochemical characterization of MgCa alloys were investigated during exposure to Ringer's solution at 37 °C by electrochemical impedance spectroscopy and scanning electrochemical microscopy. The impedance behavior showed both capacitive and inductive features that are related to the alloy charge transfer reaction and the relaxation of the absorbed corrosion compounds, and can be described in terms of an equivalent circuit. Scanning electron microscopy (SEM) was employed to view the surface morphology of the MgCa samples after 1 week immersion in Ringer's solution showing extensive precipitation of corrosion products, whereas the substrate shows evidence of a non-uniform corrosion process. Energy dispersive analysis showed that the precipitates contained oxygen, calcium, magnesium and chlorine, and the Mg:Ca ratios were smaller than in the alloys. Scanning electrochemical microscopy (SECM) was used to visualize local pH changes associated to these physicochemical processes with high spatial resolution. The occurrence of pH variations in excess of 3 units between anodic and cathodic half-cell reactions was monitored in situ. Copyright © 2015 Elsevier B.V. All rights reserved.

Excretion of biotrace elements using the multitracer technique in mice

International Nuclear Information System (INIS)

Wang, X.; Wu, M.; Yin, X.M.; Zhang, X.; Li, Z.W.; Tian, J.; Sheng, X.L.

1999-01-01

A radioactive multitracer solution obtained from the nuclear reaction of selenium with 25 MeV/nucleon 40 Ar ions was applied to the investigation of the trace elements behavior in feces and urine of mouse. The excretion rates of 23 elements, Na, K, Rb, Mg, Ca, Sr, Ga, As, Sc, V, Cr, Mn, Co, Fe, Zn, Y, Zr, Mo, Nb, Tc, Ru, Ag and In were simultaneously detected under strictly identical experimental conditions, in order to clarify the excretion behavior of the elements in Mice. Fecal and urinary excretion rates of the elements in mice reached the highest value separately at 48 and 24 hours. The total excretion of Mo, Tc and Co within 96 hours were all larger, more than 60%. Accumulative excretion rates of Ca, Nb, Mg, Sr, V, Sc, Na, Cr, Fe, Ag, Mn and Zr were 60-30%. The total rates of Ru, K, As, Zn, Rb, Y, Ga and In were less than 30%, and low excretion. The main excretion pathway of Mo, Co, Mg, Fe and Ag was through urine, and Na, K, As and Rb were eliminated from the body also in urine. But fecal excretion of Tc, Nb, Sr, Y, Ru, and In were larger than urinary excretion, and Ca, Sc, Mn, Zr, Zn were eliminated from the body in feces. (author)

Measuring calcium, potassium, and nitrate in plant nutrient solutions using ion-selective electrodes in hydroponic greenhouse of some vegetables.

Science.gov (United States)

Vardar, Gökay; Altıkatoğlu, Melda; Ortaç, Deniz; Cemek, Mustafa; Işıldak, İbrahim

2015-01-01

Generally, the life cycle of plants depends on the uptake of essential nutrients in a balanced manner and on toxic elements being under a certain concentration. Lack of control of nutrient levels in nutrient solution can result in reduced plant growth and undesired conditions such as blossom-end rot. In this study, sensitivity and selectivity tests for various polyvinylchloride (PVC)-based ion-selective membranes were conducted to identify those suitable for measuring typical concentration ranges of macronutrients, that is, NO(3-), K(+), and Ca(2+), in hydroponic solutions. The sensitivity and selectivity of PVC-membrane-based ion-selective sensors prepared with tetradodecylammoniumnitrate for NO(3-), valinomycin for K(+), and Ca ionophore IV for Ca(2+) were found to be satisfactory for measuring NO(3-), K(+), and Ca(2+) ions in nutrient solutions over typical ranges of hydroponic concentrations. Potassium, calcium, and nitrate levels that were utilized by cucumber and tomato seedlings in the greenhouse were different. The findings show that tomato plants consumed less amounts of nitrate than cucumber plants over the first 2 months of their growth. We also found that the potassium intake was higher than other nutritional elements tested for all plants. © 2014 International Union of Biochemistry and Molecular Biology, Inc.

Comparison of closed-form and finite-element solutions of thick laminated anisotropic rectangular plates

Energy Technology Data Exchange (ETDEWEB)

Reddy, J N; Chao, W C [Virginia Polytechnic Inst. and State Univ., Blacksburg (USA). Dept. of Engineering Science and Mechanics

1981-04-01

In this study the effects of reduced integration, mesh size, and element type (i.e. linear or quadratic) on the accuracy of a penalty-finite element based on the theory governing thick, laminated, anisotropic composite plates are investigated. In order to assess the accuracy of the present finite element, exact closed-form solutions are developed for cross-ply and antisymmetric angle-ply rectangular plates simply supported and subjected to sinusoidally distributed mechanical and/or thermal loadings, and free vibration.

Value assignment and uncertainty evaluation for single-element reference solutions

Science.gov (United States)

Possolo, Antonio; Bodnar, Olha; Butler, Therese A.; Molloy, John L.; Winchester, Michael R.

2018-06-01

A Bayesian statistical procedure is proposed for value assignment and uncertainty evaluation for the mass fraction of the elemental analytes in single-element solutions distributed as NIST standard reference materials. The principal novelty that we describe is the use of information about relative differences observed historically between the measured values obtained via gravimetry and via high-performance inductively coupled plasma optical emission spectrometry, to quantify the uncertainty component attributable to between-method differences. This information is encapsulated in a prior probability distribution for the between-method uncertainty component, and it is then used, together with the information provided by current measurement data, to produce a probability distribution for the value of the measurand from which an estimate and evaluation of uncertainty are extracted using established statistical procedures.

Semiconductor-metal transition in CaMO3-CaTiO2 (M-Ru,Ir) systems

International Nuclear Information System (INIS)

Lazarev, V.B.; Shaplygin, I.S.

1982-01-01

Properties of CaRusub(x)Tisub(1-x)Osub(3) and CaIsub(2x)Tisub(1-x)Osub(3) solid solutions were studied in the whole range of concentrations by the methods of X-ray diffraction, electric conductivity and magnetic susceptibility. It was ascertained that the transition of semiconductor-metal type proceeded in the both families of solid solutions at x approximately 0.77 and 0.85 respectively and was accompanied by the change of structural type of solid solutions

Molecular dynamics study of structure and vibrational spectra at zwitterionoic lipid/aqueous KCl, NaCl, and CaCl2 solution interfaces

Science.gov (United States)

Ishiyama, Tatsuya; Shirai, Shinnosuke; Okumura, Tomoaki; Morita, Akihiro

2018-06-01

Molecular dynamics (MD) simulations of KCl, NaCl, and CaCl2 solution/dipalmytoylphosphatidylcholine lipid interfaces were performed to analyze heterodyne-detected vibrational sum frequency generation (HD-VSFG) spectra in relation to the interfacial water structure. The present MD simulation well reproduces the experimental spectra and elucidates a specific cation effect on the interfacial structure. The K+, Na+, and Ca2+ cation species penetrate in the lipid layer more than the anions in this order, due to the electrostatic interaction with negative polar groups of lipid, and the electric double layer between the cations and anions cancels the intrinsic orientation of water at the water/lipid interface. These mechanisms explain the HD-VSFG spectrum of the water/lipid interface and its spectral perturbation by adding the ions. The lipid monolayer reverses the order of surface preference of the cations at the solution/lipid interface from that at the solution/air interface.

Numerical solution of multi group-Two dimensional- Adjoint equation with finite element method

International Nuclear Information System (INIS)

Poursalehi, N.; Khalafi, H.; Shahriari, M.; Minoochehr

2008-01-01

Adjoint equation is used for perturbation theory in nuclear reactor design. For numerical solution of adjoint equation, usually two methods are applied. These are Finite Element and Finite Difference procedures. Usually Finite Element Procedure is chosen for solving of adjoint equation, because it is more use able in variety of geometries. In this article, Galerkin Finite Element method is discussed. This method is applied for numerical solving multi group, multi region and two dimensional (X, Y) adjoint equation. Typical reactor geometry is partitioned with triangular meshes and boundary condition for adjoint flux is considered zero. Finally, for a case of defined parameters, Finite Element Code was applied and results were compared with Citation Code

Contributions to multiple element speciation in vegetable plants: Studies on the type of bonding of numerous elements, particularly zinc and cadmium; Beitraege zur Multielement-Speziation in pflanzlichen Lebensmitteln: Studien zur Bindungsform zahlreicher Elemente unter besonderer Beruecksichtigung von Zink und Cadmium

Energy Technology Data Exchange (ETDEWEB)

Guenther, K.

1997-03-01

In the first part of the study, the total contents and the solubility characteristics of Zn, Cd, Fe, Mn, Cu, Ca, Sr, K and Rb in 26 different vegetable plants, the majority of them commercially available, are reported, obtained by post-decomposition analyses. The data are given for avocados, bananas, cauliflower, chicory, Chinese cabbage, dill, ice lettuce (two specimens), endive, field salad, cucumbers, kohlrabi, lettuce, chard beet, carrots, peppers, leek, radish, red cabbage, loose leaved lettuce, celery (two specimens), spinach, topinambur, white cabbage, and parsley. Cell decomposition was done by treatment of the plant material with an electric dispersing apparatus (Ultra-Turrax) in buffer solution (liquid shearing). The homogenates were separated into supernatants (cytosoles)and pellets by means of centrifugation. Cell decomposition of the plants by crushing with quartz sand after lyophilization (solid shearing) required much more technical effort and for some elements created problems with the blind values. At least 50% on the average of the elements Zn, Cd, Rb, and K could be transferred to the solutions by the dispersing treatment with Ultra-Turrax. In many cases, the cytosole-borne detectable contents of these 5 elements were above 70%. The solubility of Zn and Cd was more strongly dependent on the plant species than that of Cu, Rb, and K. All five elements thus can be analysed by conventional methods for further enhanced speciation. Mn, Ca, and especially Fe and Sr for the most part were found to be bonded to solid cell constituents. However, the solubility characteristics of Ca and Mn and Sr in particular was very homogeneous. In some plants, the contents of Mn and Sr in the cytosoles was approx. 90%, so that comprehensive speciation of these elements is possible. (orig./AJ) [Deutsch] Im ersten Teil dieser Studie wurden die Gesamtgehalte und das Loeslichkeitsverhalten von Zn, Cd, Fe, Mn, Cu, Ca, Sr, K und Rb in 26 verschiedenen - ueberwiegend

Cumulative and competitive effects of chemical elements on nuclear glass alteration

International Nuclear Information System (INIS)

Arena, Helene

2016-01-01

This work takes place in the context of the long-term behavior of nuclear glasses under repository conditions. The main objective is to identify, understand and compare the effects of some chemical elements present in the glass composition and/or in the repository media (Zn, Mg, Ni, Co, Fe, Ca, Gd, Ce, K, Cs, Cr and Ag) on the processes involved in glass alteration by water. The cumulative or competitive nature of the effects of these chemical elements was determined. To reach this goal, a 6 oxides simple glass (ISG) has been altered for more than 500 days in a solution containing one or more of the chemical elements of interest. The results indicate that Zn, Mg, Ni, Co and Fe elements increase glass alteration forming secondary phases with the same structure and stoichiometry (tri-octahedral smectites). To form, these silicates consume chemical elements (Si, Al) from the environment and induce a pH decrease until a limiting value of pH. Beyond this pH the precipitation of secondary phases is inhibited and these chemical elements can be integrated into the gel, replacing Ca whose solubility increases at lower pH. As long as they form secondary phases, the effects of these elements are cumulative. Rare earths Gd and Ce also increase glass alteration forming secondary phases but their effects are lower as they contain less silicon. These elements are not integrated in the gel. Chromium increases glass alteration by precipitating with Ca and leading to a less protective gel, depleted in Ca. Silver precipitates as AgCl and has no effect on the alteration of the glass. The chemical elements K, Cs and Ca limit glass alteration by integrating into the gel and slowing down the transport phenomena therein. This integration is competitive: the order of integration (quantity and effectiveness glass alteration limitation) is the following Ca≥≥Cs≥K. Thus, the increase of glass alteration may be proportional to the quantity of elements promoting the precipitation of

Two-dimensional finite element solution for the simultaneous transport of water and solutes through a nonhomogeneous aquifer under transient saturated unsaturated flow conditions

International Nuclear Information System (INIS)

Gureghian, A.B.

1979-01-01

A mathematical model of ground water transport through an aquifer is presented. The solute of interest is a metal tracer or radioactive material which may undergo decay through a sorbing unconfined aquifer. The subject is developed under the following headings: flow equation, solute equation, boundary conditions, finite element formulation, element formulation, solution scheme (flow equation, solute equation), results and discussions, water movement in a ditch drained aquifer under transient state, water and solute movement in a homogeneous and unsaturated soil, transport of 226 Ra in nonhomogeneous aquifer, tailings pond lined, and tailings pond unlined. It is concluded that this mathematical model may have a wide variety of applications. The uranium milling industry may find it useful to evaluate the hydrogeological suitability of their disposal sites. It may prove suited for the design of clay disposal ponds destined to hold hazardous liquids. It may also provide a means of estimating the long-term impact of radionuclides or other pollutants on the quality of ground water. 31 references, 9 figures, 3 tables

Effects of solute interstitial elements on swelling of stainless steel

International Nuclear Information System (INIS)

Stiegler, J.O.; Leitnaker, J.M.; Bloom, E.E.

1975-01-01

High-purity stainless steel (HPS), equivalent to type 316 stainless steel in major alloy elements but with greatly reduced interstitial elements and manganese contents, was irradiated in the temperature range 725 to 875 K to fluences ranging from 1.0 to 3.5 x 10 26 neutrons/m 2 (>0.1 MeV). The HPS swelled 20 to 50 times more than commercial grade 316 stainless steel (316 SS), and about the same as commercial-purity nickel, which has about the same interstitial content as HPS. A fine-grained 316 SS in which interstitial elements but not manganese were precipitated by thermomechanical treatments also showed exaggerated swelling, approaching that of HPS, which suggests that swelling in commercial stainless steels is retarded by small amounts of interstitial elements normally present in them and not by the major alloying elements. Interstitials tend to precipitate from solution during irradiation, and bulk extractions of precipitate particles were made to evaluate the extent of the precipitation reactions. At both 643 and 853 K precipitation was clearly enhanced by irradiation significantly enough to alter the matrix composition, which suggests that swelling may be increased at high fluences over that predicted by extrapolation of lower fluence data. These observations are discussed in terms of potential behaviour of fuel cladding materials and of the validity and interpretation of accelerated schemes for simulating neutron damage. (author)

Finite element simulation of moisture movement and solute transport in a large caisson

International Nuclear Information System (INIS)

Huyakorn, P.S.; Jones, B.G.; Parker, J.C.; Wadsworth, T.D.; White, H.O. Jr.

1987-01-01

The results of the solute transport experiments performed on compacted, crushed Bandelier Tuff in caisson B of the experimental cluster described by DePoorter (1981) are simulated. Both one- and three-dimensional simulations of solute transport have been performed using two selected finite element codes. Results of bromide and iodide tracer experiments conducted during near-steady flow conditions have been analyzed for pulse additions made on December 6, 1984, and followed over a period of up to 60 days. In addition, a pulse addition of nonconservative strontium tracer on September 28, 1984, during questionably steady flow conditions has been analyzed over a period of 240 days. One-dimensional finite element flow and transport simulations were carried out assuming the porous medium to be homogeneous and the injection source uniformly distributed. To evaluate effects of the nonuniform source distribution and also to investigate effects of inhomogeneous porous medium properties, three dimensional finite element analyses of transport were carried out. Implications of the three-dimensional effects for the design and analysis of future tracer studies are discussed

Optimization of the crystal growth of the superconductor CaKFe4As4 from solution in the FeAs -CaFe2As2-KFe2As2 system

Science.gov (United States)

Meier, W. R.; Kong, T.; Bud'ko, S. L.; Canfield, P. C.

2017-06-01

Measurements of the anisotropic properties of single crystals play a crucial role in probing the physics of new materials. Determining a growth protocol that yields suitable high-quality single crystals can be particularly challenging for multicomponent compounds. Here we present a case study of how we refined a procedure to grow single crystals of CaKFe4As4 from a high temperature, quaternary liquid solution rich in iron and arsenic ("FeAs self-flux"). Temperature dependent resistance and magnetization measurements are emphasized, in addition to the x-ray diffraction, to detect intergrown CaKFe4As4 , CaFe2As2 , and KFe2As2 within what appear to be single crystals. Guided by the rules of phase equilibria and these data, we adjusted growth parameters to suppress formation of the impurity phases. The resulting optimized procedure yielded phase-pure single crystals of CaKFe4As4 . This optimization process offers insight into the growth of quaternary compounds and a glimpse of the four-component phase diagram in the pseudoternary FeAs -CaFe2As2-KFe2As2 system.

SNL/CA Environmental Management System Program Manual.

Energy Technology Data Exchange (ETDEWEB)

Larsen, Barbara L.

2005-09-01

The Sandia National Laboratories, California (SNL/CA) Environmental Management System (EMS) Program Manual documents the elements of the site EMS Program. The SNL/CA EMS Program was developed in accordance with Department of Energy (DOE) Order 450.1 and incorporates the elements of the International Standard on Environmental Management Systems, ISO 14001.

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.

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

Science.gov (United States)

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

1996-10-01

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

Analysis of Fe, Ca, Ti, Ba, Ce, Zr and La element in the Sea sediment at Muria peninsula by X RF method

International Nuclear Information System (INIS)

Sukirno and Sri Murniasih

2009-01-01

he analysis of metals (Fe, Ca, Ti, Ba, Ce, Zr and La) in the sea sediment environmental samples at Muria peninsula has been carried out with X-Ray Fluorescence (XRF) method. The aim of this analysis is to know the distribution metals which accommodate the recent environmental data in supporting the license of site and Environmental Impact Assessment (EIA) for the Nuclear Power Plants (NPP). Samples taken preparation and analysis based on the procedures of environmental analysis. The result analysis that contents of mayor elements in 7 sea sediment location of sampling were Ca, Ti and Fe with concentration are (6.74 – 11.69 ) %; (0.74 – 6.89 ) % and (0.45 -1.94 ) % successively; while minor elements were Ba, Ce, Zr and La with concentration are 451.4 – 1331.6 ) mg/kg; (201.8 – 427.3) mg/kg; (192.3 – 338.5) mg/kg dan (171.7 – 298.4) mg/kg. The statistic test result shows that sampling location there is a significant difference all of element with the level significant of 95 %. (author)

Experiments on different materials (polyamide, stainless & galvanized steel) influencing geothermal CaCO3 scaling formation: Polymorphs & elemental incorporation

Science.gov (United States)

Wedenig, Michael; Dietzel, Martin; Boch, Ronny; Hippler, Dorothee

2016-04-01

Thermal water is increasingly used for heat and electric power production providing base-load capable renewable and virtually unlimited geothermal energy. Compared to other energy sources geothermal facilities are less harmful to the environment, i.e. chemically and visually. In order to promote the economic viability of these systems compared to other traditional and renewable energy sources, production hindering processes such as corrosion and scaling of components arising from the typically high salinity thermal waters have to be considered as important economic factors. In this context, using proper materials being in contact with the thermal water is crucial and a playground for further improvements. Aim of the study presented, are basic experiments and observations of scaling and corrosive effects from hydrothermal water interacting with different materials and surfaces (stainless steel, polyamide, galvanized steel) and in particular the nucleation and growth effects of these materials regarding the precipitation of solid carbonate phases. The incorporation of Mg, Sr and Ba cations into the carbonate scalings are investigated as environmental proxy. For this purpose, hydrothermal carbonate precipitating experiments were initialized by mixing NaHCO3 and Ca-Mg-Sr-Ba-chloride solutions at temperatures ranging from 40 to 80 °C in glass reactors hosting artificial substrates of the above mentioned materials. The experiments show a strong dependence of the precipitation behaviour of calcium carbonate polymorphs on the particular material being present. Stainless steel and polyamide seem to restrict aragonite formation, whereas galvanized steel supports aragonite nucleation. Vaterite formation is promoted by polyamide surfaces. Importantly, vaterite is more soluble (less stable) compared to the other anhydrous calcium carbonate polymorphs, i.e. vaterite can be more easily re-dissolved. Thus, the use of polyamide components might reduce the amount and durability of

Effect of wood ash application on soil solution chemistry of tropical acid soils: incubation study.

Science.gov (United States)

Nkana, J C Voundi; Demeyer, A; Verloo, M G

2002-12-01

The objective of this study was to determine the effect of wood ash application on soil solution composition of three tropical acid soils. Calcium carbonate was used as a reference amendment. Amended soils and control were incubated for 60 days. To assess soluble nutrients, saturation extracts were analysed at 15 days intervals. Wood ash application affects the soil solution chemistry in two ways, as a liming agent and as a supplier of nutrients. As a liming agent, wood ash application induced increases in soil solution pH, Ca, Mg, inorganic C, SO4 and DOC. As a supplier of elements, the increase in the soil solution pH was partly due to ligand exchange between wood ash SO4 and OH- ions. Large increases in concentrations of inorganic C, SO4, Ca and Mg with wood ash relative to lime and especially increases in K reflected the supply of these elements by wood ash. Wood ash application could represent increased availability of nutrients for the plant. However, large concentrations of basic cations, SO4 and NO3 obtained with higher application rates could be a concern because of potential solute transport to surface waters and groundwater. Wood ash must be applied at reasonable rates to avoid any risk for the environment.

Control of ciliary motility by Ca2+: Integration of Ca2+-dependent functions and targets for Ca2+ action

International Nuclear Information System (INIS)

Evans, T.C.

1988-01-01

To identify functions that regulate Ca 2+ -induced ciliary reversal in Paramecium, mutants defective in terminating depolarization-induced backward swimming were selected. Six independent recessive mutations (k-shy) comprising two complementation groups, k-shyA and k-shyB, were identified. All mutants exhibited prolonged backward swimming in depolarizing solutions. Voltage clamp studies revealed that mutant Ca 2+ current amplitudes were reduced, but could be restored to wild type levels by EGTA injection. The recovery of the mutant Ca 2+ current from Ca 2+ -dependent inactivation, and the decay of the Ca 2+ -dependent K + and Ca 2+ -dependent Na + currents after depolarization were slow in k-shy compared to wild type. To identify protein targets of Ca 2+ action, ciliary proteins that interact with calmodulin (CaM) were characterized. With a 125 I-CaM blot assay, several CaM-binding proteins were identified including axonemal, soluble, and membrane-bound polypeptides. Competitive displacement studies with unlabeled Paramecium CaM, bovine CaM, and troponinC suggested that both protein types bind CaM with high affinity and specificity. To examine the presence of CaM-binding sites in intact axonemes, a filtration binding assay was developed

The excretion of biotrace elements using the multitracer technique in tumour-bearing mice.

Science.gov (United States)

Wang, X; Tian, J; Yin, X M; Zhang, X; Wang, Q Z

2000-12-01

A radioactive multitracer solution obtained from the nuclear reaction of selenium with 25 MeV/nucleon 40Ar ions was used for investigation of trace element excretion into the faeces and urine of cancerous mice. The excretion rates of 22 elements (Na, K, Rb, Mg, Ca, Sr, Ga, As, Sc, V, Cr, Mn, Co, Fe, Y, Zr, Mo, Nb, Tc, Ru, Ag and In) were simultaneously measured under strictly identical experimental conditions, in order to clarify the excretion behavior of these elements in cancerous mice. The faecal and urinary excretion rates of Mg, Sr, Ga, As, Sc, V, Cr, Mn, Co, Fe, Y, Zr, Nb, Ru and Mo in cancerous mice, showed the in highest value at 0-8 hours. The accumulative excretion of Ca, Mo, Y and Zr was decreased and Na, Fe, Mn and Co increased in tumour-bearing mice, when compared to normal mice.

The excretion of biotrace elements using the multitracer technique in tumour-bearing mice

Energy Technology Data Exchange (ETDEWEB)

Wang, X.; Tian, J. E-mail: tianjun@public.lz.gs.cn; Yin, X.M.; Zhang, X.; Wang, Q.Z

2000-12-15

A radioactive multitracer solution obtained from the nuclear reaction of selenium with 25 MeV/nucleon {sup 40}Ar ions was used for investigation of trace element excretion into the faeces and urine of cancerous mice. The excretion rates of 22 elements (Na, K, Rb, Mg, Ca, Sr, Ga, As, Sc, V, Cr, Mn, Co, Fe, Y, Zr, Mo, Nb, Tc, Ru, Ag and In) were simultaneously measured under strictly identical experimental conditions, in order to clarify the excretion behavior of these elements in cancerous mice. The faecal and urinary excretion rates of Mg, Sr, Ga, As, Sc, V, Cr, Mn, Co, Fe, Y, Zr, Nb, Ru and Mo in cancerous mice, showed the in highest value at 0-8 hours. The accumulative excretion of Ca, Mo, Y and Zr was decreased and Na, Fe, Mn and Co increased in tumour-bearing mice, when compared to normal mice.

The excretion of biotrace elements using the multitracer technique in tumour-bearing mice

International Nuclear Information System (INIS)

Wang, X.; Tian, J.; Yin, X.M.; Zhang, X.; Wang, Q.Z.

2000-01-01

A radioactive multitracer solution obtained from the nuclear reaction of selenium with 25 MeV/nucleon 40 Ar ions was used for investigation of trace element excretion into the faeces and urine of cancerous mice. The excretion rates of 22 elements (Na, K, Rb, Mg, Ca, Sr, Ga, As, Sc, V, Cr, Mn, Co, Fe, Y, Zr, Mo, Nb, Tc, Ru, Ag and In) were simultaneously measured under strictly identical experimental conditions, in order to clarify the excretion behavior of these elements in cancerous mice. The faecal and urinary excretion rates of Mg, Sr, Ga, As, Sc, V, Cr, Mn, Co, Fe, Y, Zr, Nb, Ru and Mo in cancerous mice, showed the in highest value at 0-8 hours. The accumulative excretion of Ca, Mo, Y and Zr was decreased and Na, Fe, Mn and Co increased in tumour-bearing mice, when compared to normal mice

Effects of Al2O3 and/or CaO on properties of yttria stabilized zirconia electrolyte doped with multi-elements

International Nuclear Information System (INIS)

Lv Zhengang; Guo Ruisong; Yao Pei; Dai Fengying

2007-01-01

Yttria stabilized zirconia (YSZ) has a high oxide ion conductivity at high temperatures. Some rare earth elements (e.g., Yb, Sc, Dy) with similar cation radii to Zr 4+ can dissolve into ZrO 2 , increasing its vacancy concentration and crystal lattice distortion, and therefore enhancing its conductivity and lowering the activation energy. It is expected this material could be used as intermediate temperature electrolyte. In the present work, YSZ electrolyte materials doped by multi-elements (Sc 2 O 3 or Dy 2 O 3 and Yb 2 O 3 ) were prepared by high temperature solid-state method. The high temperature conductivity was improved obviously, reaching 0.18 S/cm at 1000 deg. C, but the density and mechanical properties of sintered materials were not sufficiently high. It is found that sinterability and mechanical properties could be improved by inclusion of a small amount of Al 2 O 3 and/or CaO into the multi-elements doped YSZ materials and our results proved it. The results showed density and bending strength of sintered bodies were enhanced by Al 2 O 3 addition by 4.6% and 30%, respectively, while the conductivity did not degrade remarkably. But the degradation in bending strength and conductivity resulting from the CaO addition happened due to the second phase formed at the grain boundary. XRD patterns showed that all samples had cubic fluorite structure and crystalline lattice parameter was increased. SEM photographs obviously revealed the grain growth for the samples with CaO inclusion

Process development for elemental recovery from PGM tailings by thermochemical treatment: Preliminary major element extraction studies using ammonium sulphate as extracting agent.

Science.gov (United States)

Mohamed, Sameera; van der Merwe, Elizabet M; Altermann, Wladyslaw; Doucet, Frédéric J

2016-04-01

Mine tailings can represent untapped secondary resources of non-ferrous, ferrous, precious, rare and trace metals. Continuous research is conducted to identify opportunities for the utilisation of these materials. This preliminary study investigated the possibility of extracting major elements from South African tailings associated with the mining of Platinum Group Metals (PGM) at the Two Rivers mine operations. These PGM tailings typically contain four major elements (11% Al2O3; 12% MgO; 22% Fe2O3; 34% Cr2O3), with lesser amounts of SiO2 (18%) and CaO (2%). Extraction was achieved via thermochemical treatment followed by aqueous dissolution, as an alternative to conventional hydrometallurgical processes. The thermochemical treatment step used ammonium sulphate, a widely available, low-cost, recyclable chemical agent. Quantification of the efficiency of the thermochemical process required the development and optimisation of the dissolution technique. Dissolution in water promoted the formation of secondary iron precipitates, which could be prevented by leaching thermochemically-treated tailings in 0.6M HNO3 solution. The best extraction efficiencies were achieved for aluminium (ca. 60%) and calcium (ca. 80%). 35% iron and 32% silicon were also extracted, alongside chromium (27%) and magnesium (25%). Thermochemical treatment using ammonium sulphate may therefore represent a promising technology for extracting valuable elements from PGM tailings, which could be subsequently converted to value-added products. However, it is not element-selective, and major elements were found to compete with the reagent to form water-soluble sulphate-metal species. Further development of this integrated process, which aims at achieving the full potential of utilisation of PGM tailings, is currently underway. Copyright © 2016 Elsevier Ltd. All rights reserved.

Effect of local environment on crossluminescence kinetics in SrF{sub 2}:Ba and CaF{sub 2}:Ba solid solutions

Energy Technology Data Exchange (ETDEWEB)

Terekhin, M.A. [P.N. Lebedev Physical Institute, Leninskij Prospekt 53, 119991 Moscow (Russian Federation); Makhov, V.N., E-mail: makhov@sci.lebedev.ru [P.N. Lebedev Physical Institute, Leninskij Prospekt 53, 119991 Moscow (Russian Federation); Lebedev, A.I.; Sluchinskaya, I.A. [Lomonosov Moscow State University, Moscow 119991 (Russian Federation)

2015-10-15

Spectral and kinetic properties of extrinsic crossluminescence (CL) in SrF{sub 2}:Ba (1%) and CaF{sub 2}:Ba (1%) are compared with those of intrinsic CL in BaF{sub 2} and are analyzed taking into account EXAFS data obtained at the Ba L{sub III} edge and results of first-principles calculations. The CL decay time was revealed to be longer in SrF{sub 2}:Ba and CaF{sub 2}:Ba compared to BaF{sub 2}. This fact contradicts the expected acceleration of luminescence decay which could result from an increased overlap of wave functions in solid solutions due to shortening of the Ba-F distance obtained in both EXAFS measurements and first-principles calculations. This discrepancy is explained by the effect of migration and subsequent non-radiative decay of the Ba (5p) core holes in BaF{sub 2} and by decreasing of the probability of optical transitions between Ba (5p) states and the valence band in SrF{sub 2}:Ba and CaF{sub 2}:Ba predicted by first-principles calculations. - Highlights: • The crossluminescence kinetics in SrF{sub 2}:Ba and CaF{sub 2}:Ba is slower than in BaF{sub 2}. • Ba{sup 2+} ions substitute for host Ca{sup 2+}(Sr{sup 2+}) ions in the on-center positions. • The nearest Ba-F distances in SrF{sub 2}:Ba and CaF{sub 2}:Ba are shorter than in BaF{sub 2}. • EXAFS data and first-principles calculations of the local structure agree well. • First-principles calculations explain slower luminescence decay in solid solutions.

Solution of three-dimensional energy equation using finite element method

International Nuclear Information System (INIS)

Bhasin, V.; Singh, R.K.; Dutta, B.K.; Kushwaha, H.S.

1993-01-01

In the present work an attempt has been made to formulate an efficient 3-D finite element program for solving coupled momentum-energy equation with unsymmetric frontal solver and a suitable upwinding scheme. Based on the above solution technique of energy equation it can be concluded that upwinding scheme can lead to fairly accurate and smooth results even with coarse mesh. Otherwise the mesh size requirement will be extremely stringent for most of the practical problems. With upwinding the additional computer time required is marginally more. This effort has resulted in getting practical solution for large size real life problems in nuclear industry. The program was used for computation of temperature field in heavy water moderator of Madras Atomic Power Station (MAPS) reactor, in new mode of operation. (author). 9 refs., 7 figs

Ion-microprobe measurements of Mg, Ca, Ti and Fe isotopic ratios and trace element abundance in hibonite-bearing inclusions in primitive meteorites

International Nuclear Information System (INIS)

Fahey, A.J.

1988-01-01

This thesis reports the isotopic abundances of Mg, Ca, and Ti and rare earth element (REE) abundances in 19 hibonite-bearing inclusions from primative meteorites. The isotopic ratios of Fe were measured in one of the samples, Lance HH-1. These measurements were made by means of secondary ion mass spectrometry (CAMECA IMS-3f). The novel hardware and software developments that made this work possible are described in detail. The samples were studied in thin section in order to investigate the relationship between the inclusions and their mineralogical environments. Inclusions from a number of different meteorites, specifically, Mighei, Murray, Murchison, Lance, Efremovka, Vigarano, Qingzhen, Dhajala, and Semarkona, were studied. The isotopes of Ca and Ti show large and correlated abundance anomalies in their most neutron-rich isotopes, 48 Ca and 50 Ti. The largest anomalies among the samples studied here are in the Murray inclusion MY-F6, with a 4.6% deficit in 48 Ca and a 5.2% deficit in 50 Ti, and Lance HH-1, with 3.3% and 6.0% deficits in 48 Ca and 50 Ti respectively. Correlated excesses of 48 Ca and 50 Ti, up to 2.4% and 1.4% respectively, are found in some other samples studied here. The fact that there is a correlation of isotopic anomalies in two different elements is clear evidence for a nucleosynthetic origin of these effects. Various possibilities for the origin of these isotopic anomalies are discussed and it is shown that a Cosmic Chemical Memory-like model of the incomplete mixing of dust grains from one or several supernovae is sufficient to explain the data. Magnesium isotopes show excesses of 26 Mg, attributable to the in-situ decay of 26 Al, in 7 of these inclusions

Sustainable Soil Washing: Shredded Card Filtration of Potentially Toxic Elements after Leaching from Soil Using Organic Acid Solutions.

Directory of Open Access Journals (Sweden)

Christopher Ash

Full Text Available Shredded card (SC was assessed for use as a sorbent of potentially toxic elements (PTE carried from contaminated soil in various leachates (oxalic acid, formic acid, CaCl2, water. We further assessed SC for retention of PTE, using acidified water (pH 3.4. Vertical columns and a peristaltic pump were used to leach PTE from soils (O and A/B horizons before passing through SC. Sorption onto SC was studied by comparing leachates, and by monitoring total PTE contents on SC before and after leaching. SC buffers against acidic soil conditions that promote metals solubility; considerable increases in solution pH (+4.49 were observed. Greatest differences in solution PTE content after leaching with/without SC occurred for Pb. In oxalic acid, As, Cd, Pb showed a high level of sorption (25, 15, and 58x more of the respective PTE in leachates without SC. In formic acid, Pb sorption was highly efficient (219x more Pb in leachate without SC. In water, only Pb showed high sorption (191x more Pb in leachate without SC. In desorption experiments, release of PTE from SC varied according to the source of PTE (organic/mineral soil, and type of solvent used. Arsenic was the PTE most readily leached in desorption experiments. Low As sorption from water was followed by fast release (70% As released from SC. A high rate of Cd sorption from organic acid solutions was followed by strong retention (~12% Cd desorption. SC also retained Pb after sorption from water, with subsequent losses of ≤8.5% of total bound Pb. The proposed use of this material is for the filtration of PTE from extract solution following soil washing. Low-molecular-mass organic acids offer a less destructive, biodegradable alternative to strong inorganic acids for soil washing.

Sustainable Soil Washing: Shredded Card Filtration of Potentially Toxic Elements after Leaching from Soil Using Organic Acid Solutions

Science.gov (United States)

Ash, Christopher; Drábek, Ondřej; Tejnecký, Václav; Jehlička, Jan; Michon, Ninon; Borůvka, Luboš

2016-01-01

Shredded card (SC) was assessed for use as a sorbent of potentially toxic elements (PTE) carried from contaminated soil in various leachates (oxalic acid, formic acid, CaCl2, water). We further assessed SC for retention of PTE, using acidified water (pH 3.4). Vertical columns and a peristaltic pump were used to leach PTE from soils (O and A/B horizons) before passing through SC. Sorption onto SC was studied by comparing leachates, and by monitoring total PTE contents on SC before and after leaching. SC buffers against acidic soil conditions that promote metals solubility; considerable increases in solution pH (+4.49) were observed. Greatest differences in solution PTE content after leaching with/without SC occurred for Pb. In oxalic acid, As, Cd, Pb showed a high level of sorption (25, 15, and 58x more of the respective PTE in leachates without SC). In formic acid, Pb sorption was highly efficient (219x more Pb in leachate without SC). In water, only Pb showed high sorption (191x more Pb in leachate without SC). In desorption experiments, release of PTE from SC varied according to the source of PTE (organic/mineral soil), and type of solvent used. Arsenic was the PTE most readily leached in desorption experiments. Low As sorption from water was followed by fast release (70% As released from SC). A high rate of Cd sorption from organic acid solutions was followed by strong retention (~12% Cd desorption). SC also retained Pb after sorption from water, with subsequent losses of ≤8.5% of total bound Pb. The proposed use of this material is for the filtration of PTE from extract solution following soil washing. Low-molecular-mass organic acids offer a less destructive, biodegradable alternative to strong inorganic acids for soil washing. PMID:26900684

The concentration ratio of alkaline earth elements calcium, barium and strontium in grains of diploid, tetraploid and hexaploid wheat

Directory of Open Access Journals (Sweden)

Maksimović Ivana V.

2017-01-01

Full Text Available Even though calcium (Ca, strontium (Sr and barium (Ba belong to the same group of the periodic table of elements, and thus have similar chemical features, their importance for plants differs greatly. Since plants do not have the ability to completely dis­criminate between essential (e.g. Ca and non-essential elements (e.g. Sr and Ba, they read­ily take all of them up from soil solution, which is reflected in the ratios of concentrations of those elements in plant tissues, and it influences their nutritive characteristics. The ability of plant species and genotypes to take up and accumulate chemical elements in their different tissues is related to their genetic background. However, differences in chemical composition are the least reflected in their reproductive parts. Hence, the aim of this study was to evaluate ratios of concentrations of Ca, Sr and Ba in the whole grain of diploid and tetraploid wheat - ancestors of common wheat, as well as in hexaploid commercial cultivars, grown in the field, at the same location, over a period of three years. The investigated genotypes accumulated Ca, Sr and Ba at different levels, which is reflected in the ratio of their concentrations in the grain. The lowest ratio was established between Ba and Sr, followed by Ca and Ba, while the highest ratio was between Ca and Sr. Moreover, the results have shown that the year of study, genotype and the combination highly significantly affected the ratio of the concentration Ca:Sr, Ca:Ba, and Ba:Sr.

A variational numerical method based on finite elements for the nonlinear solution characteristics of the periodically forced Chen system

Science.gov (United States)

Khan, Sabeel M.; Sunny, D. A.; Aqeel, M.

2017-09-01

Nonlinear dynamical systems and their solutions are very sensitive to initial conditions and therefore need to be approximated carefully. In this article, we present and analyze nonlinear solution characteristics of the periodically forced Chen system with the application of a variational method based on the concept of finite time-elements. Our approach is based on the discretization of physical time space into finite elements where each time-element is mapped to a natural time space. The solution of the system is then determined in natural time space using a set of suitable basis functions. The numerical algorithm is presented and implemented to compute and analyze nonlinear behavior at different time-step sizes. The obtained results show an excellent agreement with the classical RK-4 and RK-5 methods. The accuracy and convergence of the method is shown by comparing numerically computed results with the exact solution for a test problem. The presented method has shown a great potential in dealing with the solutions of nonlinear dynamical systems and thus can be utilized in delineating different features and characteristics of their solutions.

Kinetics of transuranium element oxidation-reduction reactions in solution; Cinetique des reactions d'oxydo-reduction des elements transuraniens en solution

Energy Technology Data Exchange (ETDEWEB)

Gourisse, D [Commissariat a l' Energie Atomique, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

1966-09-01

A review of the kinetics of U, Np, Pu, Am oxidation-reduction reactions is proposed. The relations between the different activation thermodynamic functions (compensatory effect, formal entropy of the activated complex, magnitude of reactions velocities) are considered. The effects of acidity, ionic strength deuterium and mixed solvents polarity on reactions rates are described. The effect of different anions on reactions rates are explained by variations of the reaction standard free energy and variations of the activation free energy (coulombic interactions) resulting from the complexation of dissolved species by these anions. (author) [French] Une revue systematique de la cinetique des reactions d'oxydo-reduction des elements U, Np, Pu, Am, en solution perchlorique est proposee. Des considerations relatives aux grandeurs thermodynamiques d'activation associees aux actes elementaires (effet de compensation, entropie standard des complexes actives, rapidite des reactions) sont developpees. L'influence de l'acidite, de la force ionique, de l'eau lourde et de la polarite des solvants mixtes sur la vitesse des reactions est decrite. Enfin l'influence des differents anions sur la vitesse des reactions est expliquee par les variations de l'enthalpie libre standard de la reaction et de l'enthalpie libre d'activation (travail des forces electrostatiques) resultant de la complexation des especes dissoutes dans la solution. (auteur)

Thick films of Bi-Sr-Ca-Cu-O and Tl-Ba-Ca-Cu-O by solution processes

International Nuclear Information System (INIS)

Barboux, P.; Tarascon, J.M.; Shokoohi, F.; Wilkens, B.J.; Schwartz, C.L.

1988-01-01

We have prepared superconducting thick films of the Bi-based and the Tl-based cuprates via the decomposition of aqueous-glycerol solutions containing the salts of the elements. Preliminary results are presented in this work. The substrates are coated prior to heat treating, either by dipping or by spraying on various substrates heated at 200 0 C. Short firing times are required in order to minimize the loss of the constituent Bi (Tl). We find that nitrates of the constituents dissolved in a water-glycerol solution increase the reaction rate in comparison to pure nitrate aqueous solutions. They also help to produce the correct superconducting phase before some reaction with the substrate occurs or too much of the constituent Bi (Tl) is lost during heating to form the superconducting phase. However, the thallium phases cannot be obtained if the films are not fired in the presence of a high pressure of thallium in a sealed capsule. The films are composed of platelets, a few microns large, that are on average oriented parallel to the substrate with their c axis normal. The Bi films show an onset temperature at 85 K and zero resistance at 75 K while the Tl films show an onset temperature of 105 K and zero resistance at 95 K. The critical currents obtained to date are quite low (∼50 A/cm 2 at 77 K for the thallium phase)

Influence of Ca/Mg ratio on phytoextraction properties of Salix viminalis. II. Secretion of low molecular weight organic acids to the rhizosphere.

Science.gov (United States)

Magdziak, Z; Kozlowska, M; Kaczmarek, Z; Mleczek, M; Chadzinikolau, T; Drzewiecka, K; Golinski, P

2011-01-01

A hydroponic experiment in a phytotron was performed to investigate the effect of two different Ca/Mg ratios (4:1 and 1:10) and trace element ions (Cd, Cu, Pb and Zn) in solution on the efficiency of low molecular weight organic acid (LMWOA) formation in Salix viminalis rhizosphere. Depending on the Ca/Mg ratio and presence of selected trace elements at 0.5mM concentration, the amount and kind of LMWOAs in the rhizosphere were significantly affected. In physiological 4:1 Ca/Mg ratio the following complex of acids was observed: malonic (Pb, Zn), citric, lactic, maleic and succinic (Zn) acids. Under 1:10 Ca/Mg ratio, citric (Cd, Zn), maleic and succinic (Cd, Cu, Pb, Zn) acids were seen. Additionally, high accumulation of zinc and copper in all systems was observed, with the exception of those where one of the metals was at higher concentration. Summing up, the results indicate a significant role of LMWOAs in Salix phytoremediation abilities. Both effects can be modulated depending on the mutual Ca/Mg ratio. Copyright © 2010 Elsevier Inc. All rights reserved.

Mutual influences in solution spectroscopy of Fe, Ni Cr, Ti elements taken two by two

International Nuclear Information System (INIS)

Baudin, Guy; Henon, Genevieve

1960-01-01

The effect of third elements in solution spectroscopy has been studied for Fe, Ni Cr, Ti elements taken two by two. The existence of a linear relation Δc x /c x = f(c y ) between this effect and the third element concentration has been evidenced and opens interesting perspectives for the analysis of stainless steels. Reprint of a paper published in Comptes rendus des seances de l'Academie des Sciences, t. 250, p. 1463-1465, sitting of 22 February 1960 [fr

Physical conditions in CaFe interstellar clouds

OpenAIRE

Gnacinski, P.; Krogulec, M.

2007-01-01

Interstellar clouds that exhibit strong Ca I and Fe I lines were called CaFe clouds. The ionisation equilibrium equations were used to model the column densities of Ca II, Ca I, K I, Na I, Fe I and Ti II in CaFe clouds. The chemical composition of CaFe clouds is that of the Solar System and no depletion of elements onto dust grains is seen. The CaFe clouds have high electron densities n=1 cm^-3 that leads to high column densities of neutral Ca and Fe.

Finite element based composite solution for neutron transport problems

International Nuclear Information System (INIS)

Mirza, A.N.; Mirza, N.M.

1995-01-01

A finite element treatment for solving neutron transport problems is presented. The employs region-wise discontinuous finite elements for the spatial representation of the neutron angular flux, while spherical harmonics are used for directional dependence. Composite solutions has been obtained by using different orders of angular approximations in different parts of a system. The method has been successfully implemented for one dimensional slab and two dimensional rectangular geometry problems. An overall reduction in the number of nodal coefficients (more than 60% in some cases as compared to conventional schemes) has been achieved without loss of accuracy with better utilization of computational resources. The method also provides an efficient way of handling physically difficult situations such as treatment of voids in duct problems and sharply changing angular flux. It is observed that a great wealth of information about the spatial and directional dependence of the angular flux is obtained much more quickly as compared to Monte Carlo method, where most of the information in restricted to the locality of immediate interest. (author)

Synthesis, characterisation, luminescence and defect centres in solution combustion synthesised CaZrO3:Tb3+ phosphor

International Nuclear Information System (INIS)

Singh, Vijay; Watanabe, S.; Gundu Rao, T.K.; Al-Shamery, Katharina; Haase, Markus; Jho, Young-Dahl

2012-01-01

Tb 3+ doped CaZrO 3 has been prepared by an easy solution combustion synthesis method. The combustion derived powder was investigated by X-ray diffraction, Fourier-transform infrared spectrometry and scanning electron microscopy techniques. A room temperature photoluminescence study showed that the phosphors can be efficiently excited by 251 nm light with a weak emission in the blue and orange region and a strong emission in green light region. CaZrO 3 :Tb 3+ exhibits three thermoluminescence (TL) glow peaks at 126 °C, 200 °C and 480 °C. Electron Spin Resonance (ESR) studies were carried out to study the defect centres induced in the phosphor by gamma irradiation and also to identify the centres responsible for the TL peaks. The room temperature ESR spectrum of irradiated phosphor appears to be a superposition of two distinct centres. One of the centres (centre I) with principal g-value 2.0233 is identified as an O − ion. Centre II with an axial symmetric g-tensor with principal values g ⊥ =1.9986 and g ⊥ =2.0023 is assigned to an F + centre (singly ionised oxygen vacancy). An additional defect centre is observed during thermal annealing experiments and this centre (assigned to F + centre) seems to originate from an F centre (oxygen vacancy with two electrons). The F centre and also the F + centre appear to correlate with the observed high temperature TL peak in CaZrO 3 :Tb 3+ phosphor. - Highlights: ► Powder phosphor of CaZrO 3 :Tb 3+ was prepared by an easy solution combustion synthesis method. ► The phosphor exhibits a bright green emission at 545 nm ( 5 D 4 → 7 F 5 ) of the Tb 3+ ion. ► Electron Spin Resonance studies have been carried out to identify the defect centres responsible for the observed thermoluminescence peaks.

Correlation between the extracting solutions, Modified KCl-Olsen and Mehlich 3, used in soil laboratories in Costa Rica

International Nuclear Information System (INIS)

Bertsch, Floria; Bejarano, Jose Antonio; Corrales, Marco

2005-01-01

The correlation found, between the 2 most commonly used extraction solutions in soil laboratories of Costa Rica, is discussed for Ca, Mg, K, Zn and P determinations in soil analyses. Given the coexistence of extraction methodologies, it is of great relevance to provide users with information allowing an adequate interpretation of the analysis results. Using data exchanged among laboratories, at the national level, relationships between modified KCl-Olsen and Mehlich 3 solutions were established. For all elements determined, except for P, the association between both solutions is very clear and well-defined. Both solutions extract the same amounts of Ca and Mg; Mehlich 3 extracts 1.5 times more K than Modified Olsen. In the case of Zn, in Ca-rich soils (>10 cmol(+) 1 -1 ) Mehlich 3 extracts more Zn, so the critical level must be raised to 3.5 mg 1''- 1 ; whereas, in soils low in Ca ( -1 ), Mehlich 3 extracts less Zn than Modified Olsen, so the critical level must be lowered to 2.5 mg 1 -1 . As for P, the association is not clear at all. (author) [es

Multi-element neutron activation analysis and solution of classification problems using multidimensional statistics

International Nuclear Information System (INIS)

Vaganov, P.A.; Kol'tsov, A.A.; Kulikov, V.D.; Mejer, V.A.

1983-01-01

The multi-element instrumental neutron activation analysis of samples of mountain rocks (sandstones, aleurolites and shales of one of gold deposits) is performed. The spectra of irradiated samples are measured by Ge(Li) detector of the volume of 35 mm 3 . The content of 22 chemical elements is determined in each sample. The results of analysis serve as reliable basis for multi-dimensional statistic information processing, they constitute the basis for the generalized characteristics of rocks which brings about the solution of classification problem for rocks of different deposits

Design of photon energy compensation filters for the new four element CaSO4:Dy TLD badge

International Nuclear Information System (INIS)

Mishra, D.R.; Kulkarni, M.S.; Pradeep, Ratna; Kannan, S.

2001-01-01

A new four element TLD badge using CaSO 4 :Dy is being developed for the estimation of personal dose equivalents Hp(10) and Hp(0.07) and to discriminate them in the mix field (low energy x-ray and high energy γ-ray). Design of energy compensation filters for the new TLD badge is discussed. The total metal filter thickness is kept less than 1 mm. The first and second elements of the badge are planned to be open and plastic (≅180 gm/cm 2 ) window. For the third element a combination of 0.2 mm Sn + 0.7mm Cu + 0.1 mm Al with mass thickness ≅ 1100 mg/cm 2 is proposed which gives energy dependent response similar to Hp(10) within ± 20% (above 80 keV). For the fourth dosimeter a filter combination of 0.4 mm Al + 0.07 mm Sn is proposed which gives Hp(10)xR response for diagnostic x-rays within ± 10% in the mix field. (author)

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

Energy Technology Data Exchange (ETDEWEB)

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

2010-05-15

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

First superheavy element experiments at the GSI recoil separator TASCA: The production and decay of element 114 in the 244Pu(48Ca,3-4n) reaction

International Nuclear Information System (INIS)

Gates, J. M.; Duellmann, Ch. E.; Schaedel, M.; Ackermann, D.; Block, M.; Bruechle, W.; Essel, H. G.; Hartmann, W.; Hessberger, F. P.; Huebner, A.; Jaeger, E.; Khuyagbaatar, J.; Kindler, B.; Krier, J.; Kurz, N.; Lommel, B.; Schaffner, H.; Schausten, B.; Schimpf, E.; Steiner, J.

2011-01-01

Experiments with the new recoil separator, Transactinide Separator and Chemistry Apparatus (TASCA), at the GSI were performed by using beams of 48 Ca to irradiate targets of 206-208 Pb, which led to the production of 252-254 No isotopes. These studies allowed for evaluation of the performance of TASCA when coupled to a new detector and electronics system. By following these studies, the isotopes of element 114 ( 288-291 114) were produced in irradiations of 244 Pu targets with 48 Ca beams at compound nucleus excitation energies around 41.7 and 37.5 MeV, demonstrating TASCA's ability to perform experiments with picobarn-level cross sections. A total of 15 decay chains were observed and were assigned to the decay of 288-291 114. A new α-decay branch in 281 Ds was observed, leading to the new nucleus 277 Hs.

Sequestration of Sr-90 Subsurface Contamination in the Hanford 100-N Area by Surface Infiltration of a Ca-Citrate-Phosphate Solution

Energy Technology Data Exchange (ETDEWEB)

Szecsody, James E.; Rockhold, Mark L.; Oostrom, Martinus; Moore, R. C.; Burns, Carolyn A.; Williams, Mark D.; Zhong, Lirong; Fruchter, Jonathan S.; McKinley, James P.; Vermeul, Vincent R.; Covert, Matthew A.; Wietsma, Thomas W.; Breshears, Andrew T.; Garcia, Ben J.

2009-03-01

The objective of this project is to develop a method to emplace apatite precipitate in the 100N vadose zone, which results in sorption and ultimately incorporation of Sr-90 into the apatite structure. The Ca-citrate-PO4 solution can be infiltrated into unsaturated sediments to result in apatite precipitate to provide effective treatment of Sr-90 contamination. Microbial redistribution during solution infiltration and a high rate of citrate biodegradation for river water microbes (water used for solution infiltration) results in a relatively even spatial distribution of the citrate biodegradation rate and ultimately apatite precipitate in the sediment. Manipulation of the Ca-citrate-PO4 solution infiltration strategy can be used to result in apatite precipitate in the lower half of the vadose zone (where most of the Sr-90 is located) and within low-K layers (which are hypothesized to have higher Sr-90 concentrations). The most effective infiltration strategy to precipitate apatite at depth (and with sufficient lateral spread) was to infiltrate a high concentration solution (6 mM Ca, 15 mM citrate, 60 mM PO4) at a rapid rate (near ponded conditions), followed by rapid, then slow water infiltration. Repeated infiltration events, with sufficient time between events to allow water drainage in the sediment profile can be used to buildup the mass of apatite precipitate at greater depth. Low-K heterogeneities were effectively treated, as the higher residual water content maintained in these zones resulted in higher apatite precipitate concentration. High-K zones did not receive sufficient treatment by infiltration, although an alternative strategy of air/surfactant (foam) was demonstrated effective for targeting high-K zones. The flow rate manipulation used in this study to treat specific depths and heterogeneities are not as easy to implement at field scale due to the lack of characterization of heterogeneities and difficulty tracking the wetting front over a large

Mg/Ca of Continental Ostracode Shells

Science.gov (United States)

Ito, E.; Forester, R. M.; Marco-Barba, J.; Mezquita, F.

2007-12-01

Marine ionic chemistry is thought to remain constant. This, together with the belief that marine calcifiers partition Mg/Ca in a systematic manner as functions of temperature (and Mg/Ca) of water forms the basis of the Mg/Ca thermometer. In continental settings both of these assumptions are usually not true. Continental waters contain a wide variety of solutes in absolute and relative ion concentrations. Hence, waters with identical Mg/Ca may have very different concentrations of Mg and Ca and very different anions. Here we use two examples to focus on the effects of ion chemistry on Mg/Ca partitioning in continental ostracode shells and we ignore the complexities of solute evolution, which can change Mg/Ca over timescales of minutes to millennia. Palacios-Fest and Dettman (2001) conducted a monthly study of ,Cypridopsis vidua at El Yeso Lake in Sonora, Mexico. They established a relation between temperature and average shell Mg/Ca using regression analyses on averaged data. When their Mg/Ca-temperature relation is applied to monthly ,C. vidua data from Page Pond near Cleveland, Ohio, water temperatures of -8 to -1°C are obtained. The observed Mg/Ca ranges for El Yeso Lake (0.31 to 0.46) and Page Pond (0.33 to 0.46) are similar, as are their specific conductivities (700 to 850μS for El Yeso Lake; 400 to 600μS for Page Pond). However, [Ca] is 140-260 mg/L for El Yeso, but only 70-90 mg/L for Page Pond. Page Pond data, in fact, shows a good temperature shell Mg/Ca relation for .C. vidua, but the relation is different from that at El Yeso. Hence, shell Mg/Ca is a multi-valued, family of curves function of temperature and Mg/Ca of water that depends on the [Mg] and [Ca] values in water and perhaps other factors. Our second example comes from sites near Valencia, Spain and involves shell data for ,Cyprideis torosa, an estuarine ostracode that is tolerant of a wide range of salinity and can live in continental waters as long as the carbonate alkalinity to Ca ratio is

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} (00.5). 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.

Inorganic elements in sugar samples

International Nuclear Information System (INIS)

Salles, Paulo M.B. de; Campos, Tarcisio P.R. de

2013-01-01

Sugar is considered a safe food ingredient; however, it can be contaminated by organic elements since its planting until its production process. Thus, this study aims at checking the presence of inorganic elements in samples of crystal, refined and brown sugar available for consumption in Brazil. The applied technique was neutron activation analysis, the k 0 method, using the TRIGA MARK - IPR-R1 reactor located at CDTN/CNEN, in Belo Horizonte. It was identified the presence of elements such as, Au, Br, Co, Cr, Hf, K, Na, Sb, Sc and Zn in the samples of crystal/refined sugar and the presence of As, Au, Br, Ca, Co, Cr, Cs, Fe, Hf, K, Na, Sb, Sc, Sm, Sr, Th and Zn in the brown sugar samples. The applied technique was appropriate to this study because it was not necessary to put the samples in solution, essential condition in order to apply other techniques, avoiding contaminations and sample losses, besides allowing a multi elementary detection in different sugar samples. (author)

Inorganic elements in sugar samples

Energy Technology Data Exchange (ETDEWEB)

Salles, Paulo M.B. de; Campos, Tarcisio P.R. de, E-mail: pauladesalles@yahoo.com.br, E-mail: tprcampos@pq.cnpq.br [Universidade Federal de Minas Gerais (DEN/UFMG), Belo Horizonte, MG (Brazil). Departamento de Engenharia Nuclear; Menezes, Maria Angela de B.C., E-mail: menezes@cdtn.br [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil)

2013-07-01

Sugar is considered a safe food ingredient; however, it can be contaminated by organic elements since its planting until its production process. Thus, this study aims at checking the presence of inorganic elements in samples of crystal, refined and brown sugar available for consumption in Brazil. The applied technique was neutron activation analysis, the k{sub 0} method, using the TRIGA MARK - IPR-R1 reactor located at CDTN/CNEN, in Belo Horizonte. It was identified the presence of elements such as, Au, Br, Co, Cr, Hf, K, Na, Sb, Sc and Zn in the samples of crystal/refined sugar and the presence of As, Au, Br, Ca, Co, Cr, Cs, Fe, Hf, K, Na, Sb, Sc, Sm, Sr, Th and Zn in the brown sugar samples. The applied technique was appropriate to this study because it was not necessary to put the samples in solution, essential condition in order to apply other techniques, avoiding contaminations and sample losses, besides allowing a multi elementary detection in different sugar samples. (author)

Segregation of solute elements at grain boundaries in an ultrafine grained Al-Zn-Mg-Cu alloy

International Nuclear Information System (INIS)

Sha, Gang; Yao, Lan; Liao, Xiaozhou; Ringer, Simon P.; Chao Duan, Zhi; Langdon, Terence G.

2011-01-01

The solute segregation at grain boundaries (GBs) of an ultrafine grained (UFG) Al-Zn-Mg-Cu alloy processed by equal-channel angular pressing (ECAP) at 200 o C was characterised using three-dimensional atom probe. Mg and Cu segregate strongly to the grain boundaries. In contrast, Zn does not always show clear segregation and may even show depletion near the grain boundaries. Trace element Si selectively segregates at some GBs. An increase in the number of ECAP passes leads to a decrease in the grain size but an increase in solute segregation at the boundaries. The significant segregation of alloying elements at the boundaries of ultrafine-grained alloys implies that less solutes will be available in the matrix for precipitation with a decrease in the average grain size. -- Research Highlights: → Atom probe tomography has been employed successfully to reveal unique segregation of solutes at ultrafine grained material. → Mg and Cu elements segregated strongly at the grain boundary of an ultrafine grained Al-Zn-Mg-Cu alloy processed by 4-pass and 8-pass ECAP at 200 o C. Zn frequently depleted at GBs with a Zn depletion region of 7-15 nm in width on one or both sides of the GBs. Only a small fraction (3/13) of GBs were observed with a low level of Zn segregation where the combined Mg and Cu excess is over 3.1 atom/nm 2 . Si appeared selectively segregated at some of the GBs. → The increase in number of ECAP passes from 4 to 8 correlated with the increase in mean level segregation of Mg and Cu for both solute excess and peak concentration. → The change of plane normal of a grain boundary within 30 o only leads to a slight change in the solute segregation level.

A unified approach to model uptake kinetics of trace elements in complex aqueous – solid solution systems

International Nuclear Information System (INIS)

Thien, Bruno M.J.; Kulik, Dmitrii A.; Curti, Enzo

2014-01-01

Highlights: • There are several models able to describe trace element partitioning in growing minerals. • To describe complex systems, those models must be embedded in a geochemical code. • We merged two models into a unified one suitable for implementation in a geochemical code. • This unified model was tested against coprecipitation experimental data. • We explored how our model reacts to solution depletion effects. - Abstract: Thermodynamics alone is usually not sufficient to predict growth-rate dependencies of trace element partitioning into host mineral solid solutions. In this contribution, two uptake kinetic models were analyzed that are promising in terms of mechanistic understanding and potential for implementation in geochemical modelling codes. The growth Surface Entrapment Model (Watson, 2004) and the Surface Reaction Kinetic Model (DePaolo, 2011) were shown to be complementary, and under certain assumptions merged into a single analytical expression. This Unified Uptake Kinetics Model was implemented in GEMS3K and GEM-Selektor codes ( (http://gems.web.psi.ch)), a Gibbs energy minimization package for geochemical modelling. This implementation extends the applicability of the unified uptake kinetics model to accounting for non-trivial factors influencing the trace element partitioning into solid solutions, such as the changes in aqueous solution composition and speciation, or the depletion effects in closed geochemical systems

First-principles study of (Ba ,Ca ) TiO3 and Ba (Ti ,Zr ) O3 solid solutions

Science.gov (United States)

Amoroso, Danila; Cano, Andrés; Ghosez, Philippe

2018-05-01

(Ba ,Ca ) TiO3 and Ba (Ti ,Zr ) O3 solid solutions are the building blocks of lead-free piezoelectric materials that attract a renewed interest. We investigate the properties of these systems by means of first-principles calculations, with a focus on the lattice dynamics and the competition between different ferroelectric phases. We first analyze the four parent compounds in order to compare their properties and their different tendency towards ferroelectricity. The core of our study is systematic characterization of the binary systems (Ba ,Ca ) TiO3 and Ba (Ti ,Zr ) O3 within both the virtual crystal approximation and direct supercell calculations. In the case of Ca doping, we find a gradual transformation from B -site to A -site ferroelectricity due to steric effects that largely determines the behavior of the system. In the case of Zr doping, in contrast, the behavior is eventually dominated by cooperative Zr-Ti motions and the local electrostatics. In addition, our comparative study reveals that the specific microscopic physics of these solids sets severe limits to the applicability of the virtual crystal approximation for these systems.

Ca isotope fractionation and Sr/Ca partitioning associated with anhydrite formation at mid-ocean ridge hydrothermal systems: An experimental approach

Science.gov (United States)

Syverson, D. D.; Scheuermann, P.; Pester, N. J.; Higgins, J. A.; Seyfried, W. E., Jr.

2016-12-01

The elemental and isotopic mass balance of Ca and Sr between seawater and basalt at mid-ocean ridge (MOR) hydrothermal systems is an integrated reflection of the various physiochemical processes, which induce chemical exchange, in the subseafloor. Specifically, the processes of anhydrite precipitation and recrystallization are recognized to be important controls on governing the Ca and Sr elemental and isotope compositions of high temperature vent fluids, however, few experimental data exist to constrain these geochemical effects. Thus, to better understand the associated Sr/Ca partitioning and Ca isotope fractionation and rate of exchange between anhydrite and dissolved constituents, anhydrite precipitation and recrystallization experiments were performed at 175, 250, and 350°C and 500 bar at chemical conditions indicative of active MOR hydrothermal systems. The experimental data suggest that upon entrainment of seawater into MOR hydrothermal systems, anhydrite will precipitate rapidly and discriminate against the heavy isotopes of Ca (Δ44/40Ca(Anh-Fluid) = -0.68 - -0.25 ‰), whereas Sr/Ca partitioning depends on the saturation state of the evolving hydrothermal fluid with respect to anhydrite at each PTX (KD(Anh-Fluid) = 1.24 - 0.55). Coupling experimental constraints with the temperature gradient inferred for high temperature MOR hydrothermal systems in the oceanic crust, data suggest that the Ca isotope and Sr elemental composition of anhydrite formed near the seafloor will be influenced by disequilibrium effects, while, at higher temperatures further into the oceanic crust, anhydrite will be representative of equilibrium Sr/Ca partitioning and Ca isotope fractionation conditions. These experimental observations are consistent with analyzed Sr/Ca and Ca isotope compositions of anhydrites and vent fluids sampled from modern MOR hydrothermal systems1,2 and can be used to further constrain the geochemical effects of hydrothermal circulation in the oceanic crust

Effects of Ca on microstructure, mechanical and corrosion properties and biocompatibility of Mg-Zn-Ca alloys.

Science.gov (United States)

Yin, Ping; Li, Nian Feng; Lei, Ting; Liu, Lin; Ouyang, Chun

2013-06-01

Zn and Ca were selected as alloying elements to develop an Mg-Zn-Ca alloy system for biomedical application due to their good biocompatibility. The effects of Ca on the microstructure, mechanical and corrosion properties as well as the biocompatibility of the as-cast Mg-Zn-Ca alloys were studied. Results indicate that the microstructure of Mg-Zn-Ca alloys typically consists of primary α-Mg matrix and Ca₂Mg₆Zn₃/Mg₂Ca intermetallic phase mainly distributed along grain boundary. The yield strength of Mg-Zn-Ca alloy increased slightly with the increase of Ca content, whilst its tensile strength increased at first and then decreased. Corrosion tests in the simulated body fluid revealed that the addition of Ca is detrimental to corrosion resistance due to the micro-galvanic corrosion acceleration. In vitro hemolysis and cytotoxicity assessment disclose that Mg-5Zn-1.0Ca alloy has suitable biocompatibility.

Understanding corrosion behavior of Mg–Zn–Ca alloys from subcutaneous mouse model: Effect of Zn element concentration and plasma electrolytic oxidation

Energy Technology Data Exchange (ETDEWEB)

Jang, Yongseok [Engineering Research Center for Revolutionizing Metallic Biomaterials (ERC-RMB), North Carolina A and T State University, Greensboro, NC 27411 (United States); Tan, Zongqing [Department of Internal Medicine, College of Medicine, University of Cincinnati, Cincinnati, OH 45221 (United States); Jurey, Chris [Luke Engineering, Wadsworth, OH 44282 (United States); Xu, Zhigang [Engineering Research Center for Revolutionizing Metallic Biomaterials (ERC-RMB), North Carolina A and T State University, Greensboro, NC 27411 (United States); Dong, Zhongyun [Department of Internal Medicine, College of Medicine, University of Cincinnati, Cincinnati, OH 45221 (United States); Collins, Boyce [Engineering Research Center for Revolutionizing Metallic Biomaterials (ERC-RMB), North Carolina A and T State University, Greensboro, NC 27411 (United States); Yun, Yeoheung, E-mail: yyun@ncat.edu [Engineering Research Center for Revolutionizing Metallic Biomaterials (ERC-RMB), North Carolina A and T State University, Greensboro, NC 27411 (United States); Sankar, Jagannathan [Engineering Research Center for Revolutionizing Metallic Biomaterials (ERC-RMB), North Carolina A and T State University, Greensboro, NC 27411 (United States)

2015-03-01

Mg–Zn–Ca alloys are considered as suitable biodegradable metallic implants because of their biocompatibility and proper physical properties. In this study, we investigated the effect of Zn concentration of Mg–xZn–0.3Ca (x = 1, 3 and 5 wt.%) alloys and surface modification by plasma electrolytic oxidation (PEO) on corrosion behavior in in vivo environment in terms of microstructure, corrosion rate, types of corrosion, and corrosion product formation. Microstructure analysis of alloys and morphological characterization of corrosion products were conducted using x-ray computed tomography (micro-CT) and scanning electron microscopy (SEM). Elemental composition and crystal structure of corrosion products were determined using x-ray diffraction (XRD) and electron dispersive x-ray spectroscopy (EDX). The results show that 1) as-cast Mg–xZn–0.3Ca alloys are composed of Mg matrix and a secondary phase of Ca{sub 2}Mg{sub 6}Zn{sub 3} formed along grain boundaries, 2) the corrosion rate of Mg–xZn–0.3Ca alloys increases with increasing concentration of Zn in the alloy, 3) corrosion rates of alloys treated by PEO sample are decreased in in vivo environment, and 4) the corrosion products of these alloys after in vivo tests are identified as brucite (Mg(OH){sub 2}), hydroxyapatite (Ca{sub 10}(PO{sub 4}){sub 6}(OH){sub 2}), and magnesite (MgCO{sub 3}·3H{sub 2}O). - Highlights: • Effects of PEO and Zn concentration in Mg–xZn–0.3Ca alloys on biodegradation • Corrosion rate of Mg–xZn–0.3Ca alloys increases with increasing Zn concentration. • Plasma electrolytic oxidation retards the biodegradation of Mg–xZn–0.3Ca alloys.

Role of Ca in Modifying Corrosion Resistance and Bioactivity of Plasma Anodized AM60 Magnesium Alloys

Energy Technology Data Exchange (ETDEWEB)

Anawati, Anawati; Asoh, Hidetaka; Ono, Sachiko [Kogakuin University, Tokyo (Japan)

2016-06-15

The effect of alloying element Ca (0, 1, and 2 wt%) on corrosion resistance and bioactivity of the as-received and anodized surface of rolled plate AM60 alloys was investigated. A plasma electrolytic oxidation (PEO) was carried out to form anodic oxide film in 0.5 mol dm{sup -3} Na{sub 3}PO{sub 4} solution. The corrosion behavior was studied by polarization measurements while the in vitro bioactivity was tested by soaking the specimens in Simulated Body Fluid (1.5xSBF). Optical micrograph and elemental analysis of the substrate surfaces indicated that the number of intermetallic particles increased with Ca content in the alloys owing to the formation of a new phase Al2Ca. The corrosion resistance of AM60 specimens improved only slightly by alloying with 2 wt% Ca which was attributed to the reticular distribution of Al2Ca phase existed in the alloy that might became barrier for corrosion propagation across grain boundaries. Corrosion resistance of the three alloys was significantly improved by coating the substrates with anodic oxide film formed by PEO. The film mainly composed of magnesium phosphate with thickness in the range 30 - 40 μm. The heat resistant phase of Al{sub 2}Ca was believed to retard the plasma discharge during anodization and, hence, decreased the film thickness of Ca-containing alloys. The highest apatite forming ability in 1.5xSBF was observed for AM60-1Ca specimens (both substrate and anodized) that exhibited more degradation than the other two alloys as indicated by surface observation. The increase of surface roughness and the degree of supersaturation of 1.5xSBF due to dissolution of Mg ions from the substrate surface or the release of film compounds from the anodized surface are important factors to enhance deposition of Ca-P compound on the specimen surfaces.

Structural and luminescence properties of Ca{sub x}Ba{sub 1−x}Ga{sub 2}S{sub 4}:Eu{sup 2+} chalcogenide semiconductor solid solutions

Energy Technology Data Exchange (ETDEWEB)

Tagiyev, B.G. [Institute of Physics of Azerbaijan National Academy of Sciences, 131 H.Javid ave., Baku Az-1143 (Azerbaijan); Tagiyev, O.B. [Institute of Physics of Azerbaijan National Academy of Sciences, 131 H.Javid ave., Baku Az-1143 (Azerbaijan); Baku Branch of M.V. Lomonosov Moscow State University, Baku AZ-1143 (Azerbaijan); Mammadov, A.I. [Institute of Physics of Azerbaijan National Academy of Sciences, 131 H.Javid ave., Baku Az-1143 (Azerbaijan); Quang, Vu Xuan [Institute of Research and Development, Duy Tan University, 550000 Da Nang (Viet Nam); Naghiyev, T.G., E-mail: tural@nagiyev.net [Institute of Physics of Azerbaijan National Academy of Sciences, 131 H.Javid ave., Baku Az-1143 (Azerbaijan); Jabarov, S.H. [Institute of Physics of Azerbaijan National Academy of Sciences, 131 H.Javid ave., Baku Az-1143 (Azerbaijan); Bayerisches Geoinstitute, University Bayreuth, d-95440 Bayreuth (Germany); Leonenya, M.S.; Yablonskii, G.P. [Institute of Physics of National Academy Sciences of Belarus, 220072 Minsk (Belarus); Dang, N.T. [Institute of Research and Development, Duy Tan University, 550000 Da Nang (Viet Nam)

2015-12-01

The structural and luminescence properties of chalcogenide semiconductor Ca{sub x}Ba{sub 1−x}Ga{sub 2}S{sub 4} solid solutions (x=0.1–0.9) doped with 7 at% of Eu{sup 2+} ions were studied at room temperature. It was found, that the crystal structure of Ca{sub x}Ba{sub 1−x}Ga{sub 2}S{sub 4} solid solutions varies with the amount of Ca{sup 2+} cations and phase transition from cubic to orthorhombic takes place with increase of x value. Ca{sub x}Ba{sub 1−x}Ga{sub 2}S{sub 4}:Eu{sup 2+} solid solutions exhibit intense photoluminescence in cyan to yellow spectral region depending on x due to 5d→4f electron–dipole transitions in Eu{sup 2+} ions. The peak position of the emission band shifts from 506 nm for x=0.1 to 555 nm for x=0.9 and the full width at half maximum of the emission band varies from 62 nm to 72 nm depending on the symmetry of the crystal lattice. The PL excitation spectrum of Ca{sub x}Ba{sub 1−x}Ga{sub 2}S{sub 4}:Eu{sup 2+} covers the range at half maximum from 310 nm to 480 nm for x=0.1 and to 520 nm for x=0.9. It was shown that long-wavelength shift is caused by influence of the growing crystal field strength on Eu{sup 2+} ions.

Efficiency Evaluation of Food Waste Materials for the Removal of Metals and Metalloids from Complex Multi-Element Solutions.

Science.gov (United States)

Massimi, Lorenzo; Giuliano, Antonella; Astolfi, Maria Luisa; Congedo, Rossana; Masotti, Andrea; Canepari, Silvia

2018-02-26

Recent studies have shown the potential of food waste materials as low cost adsorbents for the removal of heavy metals and toxic elements from wastewater. However, the adsorption experiments have been performed in heterogeneous conditions, consequently it is difficult to compare the efficiency of the individual adsorbents. In this study, the adsorption capacities of 12 food waste materials were evaluated by comparing the adsorbents' efficiency for the removal of 23 elements from complex multi-element solutions, maintaining homogeneous experimental conditions. The examined materials resulted to be extremely efficient for the adsorption of many elements from synthetic multi-element solutions as well as from a heavy metal wastewater. The 12 adsorbent surfaces were analyzed by Fourier transform infrared spectroscopy and showed different types and amounts of functional groups, which demonstrated to act as adsorption active sites for various elements. By multivariate statistical computations of the obtained data, the 12 food waste materials were grouped in five clusters characterized by different elements' removal efficiency which resulted to be in correlation with the specific adsorbents' chemical structures. Banana peel, watermelon peel and grape waste resulted the least selective and the most efficient food waste materials for the removal of most of the elements.

Nuclear spectroscopy of Ca and Sc isotopes from inelastic scattering and one-nucleon transfer reactions on a radioactive 41Ca target

International Nuclear Information System (INIS)

Vold, P.

1978-04-01

The structure of energy levels in 40 , 42 Ca and 42 Sc has been studied using inelastic proton scattering and one-nucleon stripping and pick-up transfer reactions on a 41 Ca target. Data has given the following information on the properties of the 41 Ca ground state wave function; i) the 41 Ca (g.s.) looks very much like an f (sub7/2) neutron coupled to the 40 Ca (g.s.) core. ii) The core-excited component of the 41 Ca (g.s.) is determined to be 10 or less. It was inferred that the main constituents of the spectroscopic strength leading to the (f(sub7/2)) 2 , (f(sub7/2)p(sub3/2))(subt=1) and (f(sub7/2)p(sub1/2))(subT=1) configurations have been identified. This was used to deduce the effective two-particle matrix elements for these configurations. The 42 Sc and 42 Ca data result in excellent agreement for the T=1 members of the (f(sub7/2)) 2 multiplet while the (f(sub7/2)p(sub3/2))(subT=1) matrix elements derived from the 42 Sc data are about 0.2 MeV more repulsive than those obtained from the 42 Ca data. The (f(sub7/2)d(sub3/2) -1 ) matrix elements derived from the present ( 3 He,α) data were compared to the corresponding values obtained from one-nucleon stripping to mass 34 nuclei. The two sets of matrix elements are in very good agreement. The 40 Ca values are also well reproduced by calculations using the modified surface delta interaction. The experimental spectroscopic factors to both the T=0 and T=1 states of the (f(sub7/2)) 2 multiplet are in remarkably good agreement with the predicted values of the coexistence model considering the simplicity of this model. (JIW)

Boundary Element Solution of Geometrical Inverse Heat Conduction Problems for Development of IR CAT Scan

International Nuclear Information System (INIS)

Choi, C. Y.; Park, C. T.; Kim, T. H.; Han, K. N.; Choe, S. H.

1995-01-01

A geometrical inverse heat conduction problem is solved for the development of Infrared Computerized-Axial-Tomography (IR CAT) Scan by using a boundary element method in conjunction with regularization procedure. In this problem, an overspecified temperature condition by infrared scanning is provided on the surface, and is used together with other conditions to solve the position of an unknown boundary (cavity). An auxiliary problem is introduced in the solution of this problem. By defining a hypothetical inner boundary for the auxiliary problem domain, the cavity is located interior to the domain and its position is determined by solving a potential problem. Boundary element method with regularization procedure is used to solve this problem, and the effects of regularization on the inverse solution method are investigated by means of numerical analysis

Neutron diffraction studies on Ca1-xBaxZr4P6O24 solid solutions

International Nuclear Information System (INIS)

Achary, S.N.; Jayakumar, O.D.; Patwe, S.J.; Kulshreshtha, S.K.; Tyagi, A.K.; Shinde, A.B.; Krishna, P.S.R.

2008-01-01

Herein we report the results of detailed crystallographic studies of Ca 1-x Ba x Zr 4 P 6 O 24 compositions from combined Rietveld refinements of powder X-ray and neutron diffraction data. All the studied compositions crystallize in rhombohedral lattice (space group R-3 No. 148). A continuous solid solution is concluded from the systematic variation of unit cell parameters. The variation of unit cell parameters with the composition indicates decreasing trend in α parameter with increasing Ba 2+ concentration contrast to an increasing trend in c parameter. (author)

Understanding corrosion behavior of Mg-Zn-Ca alloys from subcutaneous mouse model: effect of Zn element concentration and plasma electrolytic oxidation.

Science.gov (United States)

Jang, Yongseok; Tan, Zongqing; Jurey, Chris; Xu, Zhigang; Dong, Zhongyun; Collins, Boyce; Yun, Yeoheung; Sankar, Jagannathan

2015-03-01

Mg-Zn-Ca alloys are considered as suitable biodegradable metallic implants because of their biocompatibility and proper physical properties. In this study, we investigated the effect of Zn concentration of Mg-xZn-0.3Ca (x=1, 3 and 5wt.%) alloys and surface modification by plasma electrolytic oxidation (PEO) on corrosion behavior in in vivo environment in terms of microstructure, corrosion rate, types of corrosion, and corrosion product formation. Microstructure analysis of alloys and morphological characterization of corrosion products were conducted using x-ray computed tomography (micro-CT) and scanning electron microscopy (SEM). Elemental composition and crystal structure of corrosion products were determined using x-ray diffraction (XRD) and electron dispersive x-ray spectroscopy (EDX). The results show that 1) as-cast Mg-xZn-0.3Ca alloys are composed of Mg matrix and a secondary phase of Ca2Mg6Zn3 formed along grain boundaries, 2) the corrosion rate of Mg-xZn-0.3Ca alloys increases with increasing concentration of Zn in the alloy, 3) corrosion rates of alloys treated by PEO sample are decreased in in vivo environment, and 4) the corrosion products of these alloys after in vivo tests are identified as brucite (Mg(OH)2), hydroxyapatite (Ca10(PO4)6(OH)2), and magnesite (MgCO3·3H2O). Copyright © 2014 Elsevier B.V. All rights reserved.

Kinetics of transuranium element oxidation-reduction reactions in solution; Cinetique des reactions d'oxydo-reduction des elements transuraniens en solution

Energy Technology Data Exchange (ETDEWEB)

Gourisse, D. [Commissariat a l' Energie Atomique, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

1966-09-01

A review of the kinetics of U, Np, Pu, Am oxidation-reduction reactions is proposed. The relations between the different activation thermodynamic functions (compensatory effect, formal entropy of the activated complex, magnitude of reactions velocities) are considered. The effects of acidity, ionic strength deuterium and mixed solvents polarity on reactions rates are described. The effect of different anions on reactions rates are explained by variations of the reaction standard free energy and variations of the activation free energy (coulombic interactions) resulting from the complexation of dissolved species by these anions. (author) [French] Une revue systematique de la cinetique des reactions d'oxydo-reduction des elements U, Np, Pu, Am, en solution perchlorique est proposee. Des considerations relatives aux grandeurs thermodynamiques d'activation associees aux actes elementaires (effet de compensation, entropie standard des complexes actives, rapidite des reactions) sont developpees. L'influence de l'acidite, de la force ionique, de l'eau lourde et de la polarite des solvants mixtes sur la vitesse des reactions est decrite. Enfin l'influence des differents anions sur la vitesse des reactions est expliquee par les variations de l'enthalpie libre standard de la reaction et de l'enthalpie libre d'activation (travail des forces electrostatiques) resultant de la complexation des especes dissoutes dans la solution. (auteur)

Determination of micro-quantities of several elements in soil solution by isotope dilution and activation analyses

International Nuclear Information System (INIS)

Cho, C.M.; Axmann, H.

1965-01-01

Determination of small quantities of plant nutrients in the soil solution of flooded rice soils is a difficult problem. The concentrations of Mn, Fe and P, for example, in some soil solutions are so small that no chemical method gives any accurate result. Neutron activation analysis was reported to give a much lower limit of detectability for several elements, while for elements with low-induced activity after neutron irradiation, substoichiometric isotopic dilution analysis was applied. One of the advantages of neutron activation analysis lies in the fact that simultaneous activation of every inducible element in a sample takes place. This gives an opportunity to determine many elements by one sample preparation and irradiation. This, however, is not a simple task since identification of the activated products and their quantitative estimation becomes very difficult. Certain operations of separation must be carried out before activity measurements. Ion-exchange resin columns and chemical separation following the addition of carriers were successfully used for the determination of many elements after neutron irradiation. These procedures, however, cannot be directly applied to the determination of the elements of agronomic interest. A procedure was developed to determine several elements of agronomic interest. Times of irradiation and cooling, quick separation by ion-exchange columns, together with chemical precipitation for β-emitters of relatively long half-lives, were all combined to get the maximum benefit from neutron activation analysis. For Fe, for which no satisfactory neutron activation analysis has yet been developed, a modified substoichiometric double isotope dilution procedure is applied

Mg/Ca and Sr/Ca as novel geochemical proxies for understanding sediment transport processes within coral reefs

Science.gov (United States)

Gacutan, J.; Vila-Concejo, A.; Nothdurft, L. D.; Fellowes, T. E.; Cathey, H. E.; Opdyke, B. N.; Harris, D. L.; Hamylton, S.; Carvalho, R. C.; Byrne, M.; Webster, J. M.

2017-10-01

Sediment transport is a key driver of reef zonation and biodiversity, where an understanding of sediment dynamics gives insights into past reef processes and allows the prediction of geomorphic responses to changing environmental conditions. However, modal conditions within the back-reef seldom promote sediment transport, hence direct observation is inherently difficult. Large benthic foraminifera (LBF) have previously been employed as 'tracers' to infer sediment transport pathways on coral reefs, as their habitat is largely restricted to the algal flat and post-mortem, their calcium carbonate test is susceptible to sediment transport forces into the back-reef. Foraminiferal test abundance and post-depositional test alteration have been used as proxies for sediment transport, although the resolution of these measures becomes limited by low test abundance and the lack of variation within test alteration. Here we propose the novel use of elemental ratios as a proxy for sediment transport. Two species, Baculogypsina sphaerulata and Calcarina capricornia, were analysed using a taphonomic index within One Tree and Lady Musgrave reefs, Great Barrier Reef (Australia). Inductively coupled plasma-atomic emission spectrometry (ICP-AES) was used to determine Mg/Ca and Sr/Ca and these ratios were compared with taphonomic data. Decreases in test Mg/Ca accompany increases in Sr/Ca in specimens from algal-flat to lagoonal samples in both species, mirroring trends indicated by taphonomic values, therefore indicating a relationship with test alteration. To delineate mechanisms driving changes in elemental ratios, back-scattered electron (BSE) images, elemental mapping and in situ quantitative spot analyses by electron microprobe microanalysis (EPMA) using wavelength dispersive X-ray spectrometers (WDS) were performed on un-altered algal flat and heavily abraded tests for both species. EPMA analyses reveal heterogeneity in Mg/Ca between spines and the test wall, implying the loss of

Deletion of an Endoplasmic Reticulum Stress Response Element in a ZmPP2C-A Gene Facilitates Drought Tolerance of Maize Seedlings.

Science.gov (United States)

Xiang, Yanli; Sun, Xiaopeng; Gao, Shan; Qin, Feng; Dai, Mingqiu

2017-03-06

Drought is a major abiotic stress that causes the yearly yield loss of maize, a crop cultured worldwide. Breeding drought-tolerant maize cultivars is a priority requirement of world agriculture. Clade A PP2C phosphatases (PP2C-A), which are conserved in most plant species, play important roles in abscisic acid (ABA) signaling and plant drought response. However, natural variations of PP2C-A genes that are directly associated with drought tolerance remain to be elucidated. Here, we conducted a candidate gene association analysis of the ZmPP2C-A gene family in a maize panel consisting of 368 varieties collected worldwide, and identified a drought responsive gene ZmPP2C-A10 that is tightly associated with drought tolerance. We found that the degree of drought tolerance of maize cultivars negatively correlates with the expression levels of ZmPP2C-A10. ZmPP2C-A10, like its Arabidopsis orthologs, interacts with ZmPYL ABA receptors and ZmSnRK2 kinases, suggesting that ZmPP2C-A10 is involved in mediating ABA signaling in maize. Transgenic studies in maize and Arabidopsis confirmed that ZmPP2C-A10 functions as a negative regulator of drought tolerance. Further, a causal natural variation, deletion allele-338, which bears a deletion of ERSE (endoplasmic reticulum stress response element) in the 5'-UTR region of ZmPP2C-A10, was detected. This deletion causes the loss of endoplasmic reticulum (ER) stress-induced expression of ZmPP2C-A10, leading to increased plant drought tolerance. Our study provides direct evidence linking ER stress signaling with drought tolerance and genetic resources that can be used directly in breeding drought-tolerant maize cultivars. Copyright © 2016 Elsevier Ltd. All rights reserved.

Brain trace elements and aging

International Nuclear Information System (INIS)

Hebbrecht, Geert; Maenhaut, Willy; Reuck, Jacques de

1999-01-01

Degenerative mechanisms involved in the aging process of the brain are to a certain extent counteracted by repair mechanisms. In both degenerative and recovery processes, trace elements are involved. The present study focused on the role of two minor (i.e., K and Ca) and six trace elements (i.e., Mn, Fe, Cu, Zn, Se and Rb) in the aging process. The elements were determined by PIXE in cerebral cortex and white matter, basal ganglia, brainstem and cerebellar cortex of 18 postmortem human brains, from persons without a history of neurologic or psychiatric disease who deceased between the age of 7 and 79. This age range allowed us to study the relationship between elemental concentrations and age. The most prominent findings were a concentration decrease for K and Rb and a concentration increase for the elements Ca, Fe, Zn and Se. The study supports recent findings that Ca and Fe are involved in brain degenerative processes initiated by oxygen free radicals, whereas Zn and Se are involved in immunological reactions counteracting the aging process

Comparative Study of Electronic Structure and Magnetic Properties of Osmate Double Perovskites: Ca2FeOsO6 versus Ca2Co(Ni)OsO6

Science.gov (United States)

Samanta, Kartik; Saha-Dasgupta, Tanusri

2018-04-01

Employing density functional theory, we study the trend in the electronic and magnetic properties of 3d-5d double perovskites, upon varying the 3d element for a fixed choice of 5d element, namely Ca2BOsO6 (B = Fe/Co/Ni). While all three compounds are reported to be ferrimagnets, the magnetic transition temperature of Ca2FeOsO6 is reported to be 2-2.4 times larger than that of Ca2CoOsO6 or Ca2NiOsO6. Our first-principles study provides microscopic insight into this trend. This trend is found to be caused by the downward shift in the position of d level energies of the B site element with respect to that of the Os t2g level upon moving across the 3d series from Fe to Co and Ni. This in turn changes the nominal valence of the Os ion from 5+ in Ca2FeOsO6 to 6+ in Ca2CoOsO6 and Ca2NiOsO6, resulting in differing superexchange paths between Ca2FeOsO6 and Ca2Co(Ni)OsO6, and additionally enabling the hybridization-mechanism-driven magnetism in Ca2FeOsO6. These together significantly enhance the magnetic transition temperature in Ca2FeOsO6 compared with that in Ca2Co(Ni)OsO6.

Limitless Analytic Elements

Science.gov (United States)

Strack, O. D. L.

2018-02-01

We present equations for new limitless analytic line elements. These elements possess a virtually unlimited number of degrees of freedom. We apply these new limitless analytic elements to head-specified boundaries and to problems with inhomogeneities in hydraulic conductivity. Applications of these new analytic elements to practical problems involving head-specified boundaries require the solution of a very large number of equations. To make the new elements useful in practice, an efficient iterative scheme is required. We present an improved version of the scheme presented by Bandilla et al. (2007), based on the application of Cauchy integrals. The limitless analytic elements are useful when modeling strings of elements, rivers for example, where local conditions are difficult to model, e.g., when a well is close to a river. The solution of such problems is facilitated by increasing the order of the elements to obtain a good solution. This makes it unnecessary to resort to dividing the element in question into many smaller elements to obtain a satisfactory solution.

TRIP: a finite element computer program for the solution of convection heat transfer problems

International Nuclear Information System (INIS)

Slagter, W.; Roodbergen, H.A.

1976-01-01

The theory and use of the finite element code TRIP are described. The code calculates temperature distributions in three-dimensional continua subjected to convection heat transfer. A variational principle for transport phenomena is applied to solve the convection heat transfer problem with temperature and heat flux boundary conditions. The finite element discretization technique is used to reduce the continuous spatial solution into a finite number of unknowns. The method is developed in detail to determine temperature distributions in coolant passages of fuel rod bundles which are idealized by hexahedral elements. The development of the TRIP code is discussed and the listing of the program is given in FORTRAN IV. An example is given to illustrate the validity and practicality of the method

Transfer of alkaline earth elements in mothers' milk and doses from {sup 45}Ca, {sup 90}Sr and {sup 226}Ra

Energy Technology Data Exchange (ETDEWEB)

Smith, T.J.; Phipps, A.W.; Fell, T.P.; Harrison, J.D

2003-07-01

An international programme of work is currently under way to develop methods for calculating doses to infants from ingestion of radionuclides present in mothers' milk. This paper considers the special case of the alkaline earth elements. Models have been developed for {sup 45}Ca, {sup 90}Sr and {sup 226}Ra and the sensitivity of results to various changes in parameter values is discussed. A complication when calculating doses from intakes of radium is that the International Commission on Radiological Protection has previously recommended that doses from decay products of radium should be calculated using element-specific biokinetic models (so-called independent biokinetics). An extension of this method to the models for breastfeeding is proposed. Preliminary estimates of the doses received by the infant for a number of maternal intake scenarios show that doses to the infant can exceed the corresponding adult dose, such as for {sup 45}Ca (ratio = 3.1) while, in other cases such as {sup 90}Sr, the infant dose can be a significant fraction of the adult dose. (author)

Efficiency Evaluation of Food Waste Materials for the Removal of Metals and Metalloids from Complex Multi-Element Solutions

Science.gov (United States)

Giuliano, Antonella; Astolfi, Maria Luisa; Congedo, Rossana; Masotti, Andrea; Canepari, Silvia

2018-01-01

Recent studies have shown the potential of food waste materials as low cost adsorbents for the removal of heavy metals and toxic elements from wastewater. However, the adsorption experiments have been performed in heterogeneous conditions, consequently it is difficult to compare the efficiency of the individual adsorbents. In this study, the adsorption capacities of 12 food waste materials were evaluated by comparing the adsorbents’ efficiency for the removal of 23 elements from complex multi-element solutions, maintaining homogeneous experimental conditions. The examined materials resulted to be extremely efficient for the adsorption of many elements from synthetic multi-element solutions as well as from a heavy metal wastewater. The 12 adsorbent surfaces were analyzed by Fourier transform infrared spectroscopy and showed different types and amounts of functional groups, which demonstrated to act as adsorption active sites for various elements. By multivariate statistical computations of the obtained data, the 12 food waste materials were grouped in five clusters characterized by different elements’ removal efficiency which resulted to be in correlation with the specific adsorbents’ chemical structures. Banana peel, watermelon peel and grape waste resulted the least selective and the most efficient food waste materials for the removal of most of the elements. PMID:29495363

Efficiency Evaluation of Food Waste Materials for the Removal of Metals and Metalloids from Complex Multi-Element Solutions

Directory of Open Access Journals (Sweden)

Lorenzo Massimi

2018-02-01

Full Text Available Recent studies have shown the potential of food waste materials as low cost adsorbents for the removal of heavy metals and toxic elements from wastewater. However, the adsorption experiments have been performed in heterogeneous conditions, consequently it is difficult to compare the efficiency of the individual adsorbents. In this study, the adsorption capacities of 12 food waste materials were evaluated by comparing the adsorbents’ efficiency for the removal of 23 elements from complex multi-element solutions, maintaining homogeneous experimental conditions. The examined materials resulted to be extremely efficient for the adsorption of many elements from synthetic multi-element solutions as well as from a heavy metal wastewater. The 12 adsorbent surfaces were analyzed by Fourier transform infrared spectroscopy and showed different types and amounts of functional groups, which demonstrated to act as adsorption active sites for various elements. By multivariate statistical computations of the obtained data, the 12 food waste materials were grouped in five clusters characterized by different elements’ removal efficiency which resulted to be in correlation with the specific adsorbents’ chemical structures. Banana peel, watermelon peel and grape waste resulted the least selective and the most efficient food waste materials for the removal of most of the elements.

Selection of the Best Process Stream to Remove Ca2+ Ion Using Electrodialysis from Sugar Solution

Directory of Open Access Journals (Sweden)

Jogi Ganesh Dattatreya Tadimeti

2014-01-01

Full Text Available Electrodialytic removal of calcium chloride (CaCl2, 25–50 mol·m−3 from 5% sugar solution was executed in batch recirculation mode. Calcium ion removal rate was monitored with (i applied potential, (ii feed flow rate, (iii solution viscosity and conductivity, and (iv catholyte streams (NaOH or sodium salt of ethylene diamine tetraacetic acid-acetic acid, Na2EDTA-AA. Unsteady state model for ion concentration change was written for the ED cell used. Linearized Nernst-Planck equation instead of Ohm’s law was applied to closely obtain the current density and concentration change theoretically. The model developed could closely predict the experimental observation. Mass transfer coefficients and specific energy densities were estimated for each combination of catholyte stream used. NaOH showed better performance for a short duration over Na2EDTA-acetic acid combination.

Influence of Heat Treatment on Biocorrosion and Hemocompatibility of Biodegradable Mg-35Zn-3Ca Alloy

Directory of Open Access Journals (Sweden)

Jeong-Hui Ji

2015-01-01

Full Text Available Mg-35Zn-3Ca (wt.% alloy containing nontoxic and biocompatible Zn and Ca as alloying elements was prepared and subjected to heat treatment and artificial aging for different duration of time to reduce its rate of degradation. Solution heat treatment was performed at 310°C while artificial aging was performed at 170°C for 0, 2.5, 5.0, 7.5, and 10.0 h and they were designated as AT0, AT1, AT2, AT3, and AT4, respectively. The finest and most homogenous reticulum was observed on the surface of the AT2 group. The result of immersion test in Hank’s balanced salt solution (HBSS showed that the corrosion rate of the AT2 group was 2.32 mg/(cm2 day, which was significantly lower as compared to other groups P<0.05. The hemolysis value was ≤5% in all groups, indicating no toxicity during short-term blood reaction.

Caed Interactions During A Product Life Cycle Oriented Towards the Decision-Making in the Design of Polymeric Elements

Science.gov (United States)

Suffo, M.

2017-08-01

In this work, we present the real case of an industrial product was placed prematurely on the market without having checked the different stages of its life cycle. This type of products must be validated by numerical methods and by mechanical tests to verify their rheological behavior. In particular, the product consists of two small pieces in contact, one made of HDPE and the other one corresponding to a stainless steel. The polymeric piece supports the metal pressure under a constant static load over time. As a result of normal operation, the polymer experienced a “crazing” breakdown, which caused the failure to occur. In the study, design methods and computer assisted analysis software (CAED) have been used. These methods were complemented by scanning electron microscopy that confirmed the initial failure hypothesis. Using the finite element method (FEM), a series of load scenarios were carried out, where the different load hypothesis the product must go through prior to its placing on the market were simulated. It is shown that the failure was initiated by stress concentration on one of the edges of the polymeric piece. The proposed solution of the problem based on the analysis focuses on a simple redesign of the piece, which should have been round, or to the reduction of the thickness of the metal piece. As a result of the alteration of its natural life cycle, the company assumed both monetary costs and the definitive loss of customer confidence.

Trace elemental analysis of leaching solutions of hijiki seaweeds by a portable total reflection X-ray fluorescence spectrometer

International Nuclear Information System (INIS)

Liu, Ying; Imashuku, Susumu; Kawai, Jun

2014-01-01

A portable total reflection X-ray fluorescence spectrometer (TXRF) was used to analyze leaching solutions of hijiki seaweeds. S, Cl, K, Ca, Ti, Fe, Ni, As and Br were detected in the solutions. Arsenic quantification results were compared to those from ICP-AES. The TXRF quantification results of arsenic were not significantly different from those of ICP-AES, as two-way analysis of variance (ANOVA) method was applied to the significance test. This kind of small and high sensitive TXRF spectrometer can be used in food quality and environmental pollution investigation. (author)

A numerical comparison between the multiple-scales and finite-element solution for sound propagation in lined flow ducts

NARCIS (Netherlands)

Rienstra, S.W.; Eversman, W.

2001-01-01

An explicit, analytical, multiple-scales solution for modal sound transmission through slowly varying ducts with mean flow and acoustic lining is tested against a numerical finite-element solution solving the same potential flow equations. The test geometry taken is representative of a high-bypass

Trace Elements and Minerals in Fumarolic Sulfur: The Case of Ebeko Volcano, Kuriles

Directory of Open Access Journals (Sweden)

E. P. Shevko

2018-01-01

Full Text Available Native sulfur deposits on fumarolic fields at Ebeko volcano (Northern Kuriles, Russia are enriched in chalcophile elements (As-Sb-Se-Te-Hg-Cu and contain rare heavy metal sulfides (Ag2S, HgS, and CuS, native metal alloys (Au2Pd, and some other low-solubility minerals (CaWO4, BaSO4. Sulfur incrustations are impregnated with numerous particles of fresh and altered andesite groundmass and phenocrysts (pyroxene, magnetite as well as secondary minerals, such as opal, alunite, and abundant octahedral pyrite crystals. The comparison of elemental abundances in sulfur and unaltered rocks (andesite demonstrated that rock-forming elements (Ca, K, Fe, Mn, and Ti and other lithophile and chalcophile elements are mainly transported by fumarolic gas as aerosol particles, whereas semimetals (As, Sb, Se, and Te, halogens (Br and I, and Hg are likely transported as volatile species, even at temperatures slightly above 100°C. The presence of rare sulfides (Ag2S, CuS, and HgS together with abundant FeS2 in low-temperature fumarolic environments can be explained by the hydrochloric leaching of rock particles followed by the precipitation of low-solubility sulfides induced by the reaction of acid solutions with H2S at ambient temperatures. The elemental composition of native sulfur can be used to qualitatively estimate elemental abundances in low-temperature fumarolic gases.

Study of Ca-ATMP precipitation in the presence of magnesium ion.

Science.gov (United States)

Tantayakom, V; Fogler, H Scott; de Moraes, F F; Bualuang, M; Chavadej, S; Malakul, P

2004-03-16

ATMP (aminotri(methylenephosphonic acid)), a phosphonate scale inhibitor used in the petroleum industry, was used as a model scale inhibitor in this study. One of the goals of this work was to determine the range of conditions under which Mg ions, which are formed in reservoir formations containing dolomite, modulate the formation of Ca-ATMP precipitate as a scale inhibitor. The results revealed that the amount of ATMP precipitated decreased with addition of Mg ions in solution at all values of the solution pH. Furthermore, an increase in both the solution pH and the concentration of the divalent cations in solution resulted in a change of the molar ratio of (Ca + Mg) to ATMP in the precipitates. At a low solution pH (pH 1.5), Mg ions had little effect on the composition of the Ca-ATMP precipitate. However, at higher values of the solution pH (pH 4 and 7), the Ca to ATMP molar ratio in the precipitates decreased with increasing concentration of the Mg. Here it was found that Mg ions replaced Ca ions on available reactive sites of ATMP molecules. These results determined the limits of the Mg ion concentration, which affects the precipitation of Ca-ATMP, Mg-ATMP, and (Ca + Mg)-ATMP. The dissolution of the scale inhibitors was studied using a rotating disk reactor. These experiments showed that the total divalent cation molar ratio (Ca + Mg) to ATMP in the precipitates is the primary factor that controls the rate of dissolution (release) of the phosphonate precipitates. The phosphonate precipitate dissolution rates decreased as the molar ratio of divalent cations to ATMP in the precipitates increased.

45Ca2+movements induced by Ca2+chloride in isolated rat aorta under K+-free conditions

NARCIS (Netherlands)

Wermelskirchen, D.; Nebel, U.; Wirth, A.; Wilffert, B.

1991-01-01

Increasing the extracellular Ca2+concentration induced a dihydropyridine-insensitive contraction in the isolated rat aorta bathed in K+-free solution. To obtained further insight into the mechanisms of this contraction45Ca2+uptake measurements were carried out with isolated rat aorta. Increasing the

CA-45(2+) MOVEMENTS INDUCED BY CA2+ CHLORIDE IN ISOLATED RAT AORTA UNDER K+-FREE CONDITIONS

NARCIS (Netherlands)

WERMELSKIRCHEN, D; NEBEL, U; WIRTH, A; WILFFERT, B

1991-01-01

Increasing the extracellular Ca2+ concentration induced a dihydropyridine-insensitive contraction in the isolated rat aorta bathed in K+-free solution. To obtain further insight into the mechanism of this contraction Ca-45(2+) uptake measurements were carried out with isolated rat aorta. Increasing

Adjustment of the ratio of Ca/P in the ceramic coating on Mg alloy by plasma electrolytic oxidation

International Nuclear Information System (INIS)

Yao Zhongping; Li Liangliang; Jiang Zhaohua

2009-01-01

The ceramic coatings containing Ca and P were prepared on AZ91D Mg alloy by plasma electrolytic oxidation technique in NaOH system and Na 2 SiO 3 system, respectively. The phase composition, morphology and the element distribution of the coatings was studied by X-ray diffraction, scanning electron microscopy and energy dispersive spectroscopy. The corrosion resistance of the coatings was examined by polarizing curve methods in a 0.9% NaCl solution. In NaOH system, there were a large number of micro-holes distributing evenly on the surface of the coating, and the coating was mainly composed of Mg, Al, P and Ca. In Na 2 SiO 3 system, the micro-holes in the coatings were reduced greatly in number and the distribution of the micro-holes was uneven, and the coating was mainly composed of Mg, Al, Si, P and Ca. The ratio of Ca/P in the coating can be controlled by the adjustment of the technique parameters to a certain extent. The adjustment of the concentration of Ca 2+ in the electrolyte was an effective method to change the ratio of Ca/P in the coating in both systems; the reaction time and the working voltage for the adjustment of the ratio of Ca/P in the coating was more suitable for the NaSi 2 O 3 system than the NaOH system. The polarizing curve tests showed the coatings improved the corrosion resistance of the AZ91D Mg alloy in 0.9% NaCl solution by nearly two orders of magnitude.

Element/Ca, C and O isotope ratios in modern brachiopods

DEFF Research Database (Denmark)

Ullmann, C. V.; Frei, Robert; Korte, Christoph

2017-01-01

Fossil brachiopods are of major importance for the reconstruction of palaeoenvironmental conditions, particularly of the Paleozoic. In order to better understand signals of ancient shell materials, modern analogue studies have to be conducted. Here we present C and O isotope data in conjunction...... with ambient seawater. Some species – especially in the suborder Terebratellidina – show partly distinct disequilibrium signals, suggesting some degree of phylogenetic control on the expression of vital effects. Mn/Ca and Fe/Ca ratios measured in the modern species form a baseline to assess fossil preservation...

Effects of CaCl2 solutions to alleviate drought stress effects in potted ornamentals Salvia splendens and Ageratum houstonianum

Directory of Open Access Journals (Sweden)

Agata Jędrzejuk

2016-09-01

Full Text Available Bedding plants are often subjected to soil water deficit – either after planting and/or during the market chain. Methods to alleviate the negative water stress effects are sought for to preserve ornamental values of plants. The aim of this study was to evaluate the response of two bedding plants, Ageratum houstonianum Mill. and Salvia splendens Sellow ex Scult., to water stress and treatments with calcium chloride aimed to alleviate drought effects. Plants were subjected either to 45 days of periodical stress (five cycles when watering was off for 5 consecutive days, followed by four cycles on for 5 consecutive days or 10 days of radical drought (complete water withdrawal. On the first day, before the onset of drought, plants were watered with 0.5% Ca or 1% Ca w/v as a solution of calcium chloride (5 g or 10 g Ca per 1 dm3 of the growing substrate. The similarly Ca-treated but routinely watered plants provided controls to evaluate the water shortage effects. Plant height, inflorescence length/number, leaf number, leaf area (in Salvia splendens only, aboveground plant part weight, and root weight (in Salvia splendens only as well as leaf relative water content (RWC were measured at the beginning and at the end of the experiments. Water withdrawal during 10 days of growth (radical drought reduced by half RWC in leaves of withering Salvia splendens and Ageratum houstonianum plants. Its effects on the growth parameters were less pronounced and mitigated by Ca applications. Also in the periodically stressed plants of both species, RWC and most growth parameters were reduced by water shortage but Ca applications alleviated the negative stress effects.

Towards a unified solution of localization failure with mixed finite elements

Science.gov (United States)

Benedetti, Lorenzo; Cervera, Miguel; Chiumenti, Michele; Zeidler, Antonia; Fischer, Jan-Thomas

2015-04-01

Notwithstanding computational scientists made significant steps in the numerical simulation of failure in last three decades, the strain localization problem is still an open question. Especially in a geotechnical setting, when dealing with stability analysis of slopes, it is necessary to provide correct distribution of displacements, to evaluate the stresses in the ground and, therefore, to be able to identify the slip lines that brings to progressive collapse of the slope. Finite elements are an attractive method of solution thanks to profound mathematical foundations and the possibility of describing generic geometries. In order to account for the onset of localization band, the smeared crack approach [1] is introduced, that is the strain localization is assumed to occur in a band of finite width where the displacements are continuous and the strains are discontinuous but bounded. It is well known that this kind of approach poses some challenges. The standard irreducible formulation of FEM is known to be heavily affected by spurious mesh dependence when softening behavior occurs and, consequently, slip lines evolution is biased by the orientation of the mesh. Moreover, in the case of isochoric behavior, unbounded pressure oscillations arise and the consequent locking of the stresses pollutes the numerical solution. Both problems can be shown not to be related to the mathematical statement of the continuous problem but instead to its discrete (FEM) counterpart. Mixed finite element formulations represent a suitable alternative to mitigate these drawbacks. As it has been shown in previous works by Cervera [2], a mixed formulation in terms of displacements and pressure not only provides a propitious solution to the problem of incompressibility, but also it was found to possess the needed robustness in case of strain concentration. This presentation introduces a (stabilized) mixed finite element formulation with continuous linear strain and displacement

Solid-soluted content of cerium in solid solution of sphene

International Nuclear Information System (INIS)

Zhao Wei; Teng Yuancheng; Li Yuxiang; Ren Xuetan; Huang Junjun

2010-01-01

The sphene solid solution was synthesized by solid-state method,with calcium carbonate, silica, titanium dioxide, cerium oxalate and alumina as raw materials. The solid-soluted content of cerium in sphene was researched by means of X-ray diffraction (XRD), backscattering scanning electron microscopy (BSE), energy dispersive spectroscopy (EDS) and so on. The influence of A l3+ ion introduction to sphene on the solid-soluted content of cerium in sphene solid solution was studied. The results indicate that when introducing Al 3+ to sphene as electrovalence compensation, Ce 4+ could be well solidified to Ca 1-x Ce x Ti 1-2x A l2x SiO 5 , and the solid-soluted content is approximately 12.61%. With no electrovalence compensation, Ce 4+ could be solidified to Ca 1-2x Ce x TiSiO 5 , and the solid-soluted content is approximately 10.98%. The appropriate synthesis temperature of sphene solid solution is 1 260 degree C.(authors)

Synthesis, characterisation, luminescence and defect centres in solution combustion synthesised CaZrO{sub 3}:Tb{sup 3+} phosphor

Energy Technology Data Exchange (ETDEWEB)

Singh, Vijay, E-mail: vijayjiin2006@yahoo.com [School of Information and Communications, Gwangju Institute of Science and Technology, Gwangju 500-712 (Korea, Republic of); Watanabe, S.; Gundu Rao, T.K. [Institute of Physics, University of Sao Paulo, 05508-090 Sao Paulo/SP (Brazil); Al-Shamery, Katharina [Physical Chemistry, Institute for Pure and Applied Chemistry and Center of Interface Science University of Oldenburg, 26129 Oldenburg (Germany); Haase, Markus [Department of Inorganic Chemistry I-Materials Research, Institute of Chemistry, University of Osnabrueck, Barbarastrabe 7, 49069 Osnabrueck (Germany); Jho, Young-Dahl, E-mail: jho@gist.ac.kr [School of Information and Communications, Gwangju Institute of Science and Technology, Gwangju 500-712 (Korea, Republic of)

2012-08-15

Tb{sup 3+} doped CaZrO{sub 3} has been prepared by an easy solution combustion synthesis method. The combustion derived powder was investigated by X-ray diffraction, Fourier-transform infrared spectrometry and scanning electron microscopy techniques. A room temperature photoluminescence study showed that the phosphors can be efficiently excited by 251 nm light with a weak emission in the blue and orange region and a strong emission in green light region. CaZrO{sub 3}:Tb{sup 3+} exhibits three thermoluminescence (TL) glow peaks at 126 Degree-Sign C, 200 Degree-Sign C and 480 Degree-Sign C. Electron Spin Resonance (ESR) studies were carried out to study the defect centres induced in the phosphor by gamma irradiation and also to identify the centres responsible for the TL peaks. The room temperature ESR spectrum of irradiated phosphor appears to be a superposition of two distinct centres. One of the centres (centre I) with principal g-value 2.0233 is identified as an O{sup -} ion. Centre II with an axial symmetric g-tensor with principal values g{sub Up-Tack }=1.9986 and g{sub Up-Tack }=2.0023 is assigned to an F{sup +} centre (singly ionised oxygen vacancy). An additional defect centre is observed during thermal annealing experiments and this centre (assigned to F{sup +} centre) seems to originate from an F centre (oxygen vacancy with two electrons). The F centre and also the F{sup +} centre appear to correlate with the observed high temperature TL peak in CaZrO{sub 3}:Tb{sup 3+} phosphor. - Highlights: Black-Right-Pointing-Pointer Powder phosphor of CaZrO{sub 3}:Tb{sup 3+} was prepared by an easy solution combustion synthesis method. Black-Right-Pointing-Pointer The phosphor exhibits a bright green emission at 545 nm ({sup 5}D{sub 4}{yields}{sup 7}F{sub 5}) of the Tb{sup 3+} ion. Black-Right-Pointing-Pointer Electron Spin Resonance studies have been carried out to identify the defect centres responsible for the observed thermoluminescence peaks.

Behaviour of trivalent actinides and lanthanide elements in chloride solution; Comportement des lanthanides et transuraniens trivalents en milieu chlorhydrique

Energy Technology Data Exchange (ETDEWEB)

Marin, B [Commissariat a l' Energie Atomique, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

1969-07-01

The aim of this work is to compare the complexation in chloride solutions of trivalent lanthanides and actinides. We have first studied the solvatation of these cations without complexation. We found a difference between Am, Cm and Rare Earths (we can separate lanthanides into Light and Heavy Rare Earths). For studying the complexation we choose the technic of electrophoresis on paper after establishing a simple theory of mobilities in complex solutions. The hydrolysis of these cations was studied and compared in chloride solutions. We have then studied the complexation with the Cl{sup -} ligand in some solutions: HCl, NH{sub 4}Cl, CaCl{sub 2}, CeCl{sub 3}, LiCl. We have established that the complexation is the same in dilute HCl solutions but in concentrated solutions the trivalent actinides are more complexed. This difference is sharper in LiCl solutions. We also proposed the different models of complex in these solutions. (author) [French] Le but de ce travail est de comparer les transuraniens et lanthanides trivalents au point de vue de leur complexation en solution chlorhydrique. Nous avons ete amenes tout d'abord a etudier la solvatation de ces cations non complexes. C'est ainsi que nous pouvons constater une difference entre Am, Cm et les lanthanides. Ces derniers pouvant se separer en lanthanides legers et lanthanides lourds. Pour etudier la complexation nous avons utilise l'electrophorese sur papier apres avoir donne une theorie simple des mobilites en milieu complexant. Apres avoir etudie et compare l'hydrolyse de ces divers cations en solution chlorhydrique, nous avons etudie leur complexation avec l'ion Cl{sup -} dans dans divers milieux: HCl, NH{sub 4}Cl, CaCl{sub 2}, CeCl{sub 3}, LiCl. ous avons note qu'en solution HCl les deux series se comportent de la meme facon pour des concentrations faibles en Cl{sup -} mais que les transuraniens se complexent plus fortement dans les solutions concentrees. Cette difference s'accroit encore dans les milieux

Computer modelling of defect structure and rare earth doping in LiCaAlF sub 6 and LiSrAlF sub 6

CERN Document Server

Amaral, J B; Valerio, M E G; Jackson, R A

2003-01-01

This paper describes a computational study of the mixed metal fluorides LiCaAlF sub 6 and LiSrAlF sub 6 , which have potential technological applications when doped with a range of elements, especially those from the rare earth series. Potentials are derived to represent the structure and properties of the undoped materials, then defect properties are calculated, and finally solution energies for rare earth elements are calculated, enabling preferred dopant sites and charge compensation mechanisms to be predicted.

A study of elemental migration from poly(ethylene terephthalate) of food packagings to simulated solutions by radiometric method

International Nuclear Information System (INIS)

Soares, Eufemia Paez; Saki, Mitiko; Silva, Leonardo G.A.

2007-01-01

Brazilian plastic production for food packagings, in recent years, has grown in the same proportion as food consumption. Considering that the plastic manufacturing involves catalytic processes and the use of additives, when the foods are in direct contact with these materials, the components present in plastics may migrate to the food. The Brazilian Health Surveillance Agency (ANVISA) has established boundary-values of migrants as well as procedures to evaluate migration of elements and substances from plastic packaging to food. In this study elemental composition of poly (ethylene terephthalate) - PET - packaging and results of elemental migration were obtained. Instrumental Neutron Activation Analysis (INAA) was used to determine elemental concentrations in PET packagings and the radiometric method was applied for elemental migration determination. This radiometric method consisted of irradiating the PET samples with neutrons, followed by migration exposition and radioactivity measurement in food-simulated solution. Experimental conditions used for migration were 10 days exposure period at 40 deg C. Migration was evaluated for soft drink, juice and water PET packaging. The analytical results indicated that PET packagings contain Co and Sb and those elements are transferred to the simulated solutions. However, these migration results were lower than the maximum tolerance values established by ANVISA. The migration detection limits also indicated high sensitivity of the radiometric method. (author)

Parallel iterative procedures for approximate solutions of wave propagation by finite element and finite difference methods

Energy Technology Data Exchange (ETDEWEB)

Kim, S. [Purdue Univ., West Lafayette, IN (United States)

1994-12-31

Parallel iterative procedures based on domain decomposition techniques are defined and analyzed for the numerical solution of wave propagation by finite element and finite difference methods. For finite element methods, in a Lagrangian framework, an efficient way for choosing the algorithm parameter as well as the algorithm convergence are indicated. Some heuristic arguments for finding the algorithm parameter for finite difference schemes are addressed. Numerical results are presented to indicate the effectiveness of the methods.

Preparation and characterization of Bi2Sr2CaCu2O8+δ thin films on MgO single crystal substrates by chemical solution deposition

DEFF Research Database (Denmark)

Grivel, Jean-Claude; Kepa, Katarzyna; Hlásek, T.

2013-01-01

Bi2Sr2CaCu2O8 thin films have been deposited on MgO single crystal substrates by spin-coating a solution based on 2-ethylhexanoate precursors. Pyrolysis takes place between 200°C and 450°C and is accompanied by the release of 2-ethylhexanoic acid, CO2 and H2O vapour. Highly c-axis oriented Bi2Sr2Ca...

Solution of the neutron diffusion equation at two groups of energy by method of triangular finite elements

International Nuclear Information System (INIS)

Correia Filho, A.

1981-04-01

The Neutron Diffusion Equation at two groups of energy is solved with the use of the Finite - Element Method with first order triangular elements. The program EFTDN (Triangular Finite Elements on Neutron Diffusion) was developed using the language FORTRAN IV. The discrete formulation of the Diffusion Equation is obtained with the application of the Galerkin's Method. In order to solve the eigenvalue - problem, the Method of the Power is applied and, with the purpose of the convergence of the results, Chebshev's polynomial expressions are applied. On the solution of the systems of equations Gauss' Method is applied, divided in two different parts: triangularization of the matrix of coeficients and retrosubstitution taking in account the sparsity of the system. Several test - problems are solved, among then two P.W.R. type reactors, the ZION-1 with 1300 MWe and the 2D-IAEA - Benchmark. Comparision of results with standard solutions show the validity of application of the EFM and precision of the results. (Author) [pt

CO2 solubility in aqueous solutions containing Na+, Ca2+, Cl−, SO42− and HCO3-: The effects of electrostricted water and ion hydration thermodynamics

International Nuclear Information System (INIS)

Gilbert, Kimberly; Bennett, Philip C.; Wolfe, Will; Zhang, Tongwei; Romanak, Katherine D.

2016-01-01

Dissolution of CO 2 into deep subsurface brines for carbon sequestration is regarded as one of the few viable means of reducing the amount of CO 2 entering the atmosphere. Ions in solution partially control the amount of CO 2 that dissolves, but the mechanisms of the ion's influence are not clearly understood and thus CO 2 solubility is difficult to predict. In this study, CO 2 solubility was experimentally determined in water, NaCl, CaCl 2 , Na 2 SO 4, and NaHCO 3 solutions and a mixed brine similar to the Bravo Dome natural CO 2 reservoir; ionic strengths ranged up to 3.4 molal, temperatures to 140 °C, and CO 2 pressures to 35.5 MPa. Increasing ionic strength decreased CO 2 solubility for all solutions when the salt type remained unchanged, but ionic strength was a poor predictor of CO 2 solubility in solutions with different salts. A new equation was developed to use ion hydration number to calculate the concentration of electrostricted water molecules in solution. Dissolved CO 2 was strongly correlated (R 2  = 0.96) to electrostricted water concentration. Strong correlations were also identified between CO 2 solubility and hydration enthalpy and hydration entropy. These linear correlation equations predicted CO 2 solubility within 1% of the Bravo Dome brine and within 10% of two mixed brines from literature (a 10 wt % NaCl + KCl + CaCl 2 brine and a natural Na + , Ca 2+ , Cl − type brine with minor amounts of Mg 2+ , K + , Sr 2+ and Br − ). - Highlights: • Measured CO 2 solubility in Na + , Cl − , HCO 3 - , Ca 2+ and SO 4 2− solutions at high PCO 2 . • A new equation calculates electrostricted water (mol/kgw) from hydration number. • CO 2 solubility strongly correlates (R 2  = 0.96) to electrostricted water. • Ion electrostriction of water limits its availability for CO 2 caging and solvation. • Correlations predict CO 2 solubility of several mixed brines to within 1–9%.

Preliminary Formulation of Finite Element Solution for the 1-D, 1-G Time Dependent Neutron Diffusion Equation without Consideration about Delay Neutron

Energy Technology Data Exchange (ETDEWEB)

Ryu, Eun Hyun; Song, Yong Mann; Park, Joo Hwan [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2013-05-15

If time-dependent equation is solved with the FEM, the limitation of the input geometry will disappear. It has often been pointed out that the numerical methods implemented in the RFSP code are not state-of-the-art. Although an acceleration method such as the Coarse Mesh Finite Difference (CMFD) for Finite Difference Method (FDM) does not exist for the FEM, one should keep in mind that the number of time steps for the transient simulation is not large. The rigorous formulation in this study will richen the theoretical basis of the FEM and lead to an extension of the dynamics code to deal with a more complicated problem. In this study, the formulation for the 1-D, 1-G Time Dependent Neutron Diffusion Equation (TDNDE) without consideration of the delay neutron will first be done. A problem including one multiplying medium will be solved. Also several conclusions from a comparison between the numerical and analytic solutions, a comparison between solutions with various element orders, and a comparison between solutions with different time differencing will be made to be certain about the formulation and FEM solution. By investigating various cases with different values of albedo, theta, and the order of elements, it can be concluded that the finite element solution is agree well with the analytic solution. The higher the element order used, the higher the accuracy improvements are obtained.

Diffusion coefficients of alloying elements in dilute Mg alloys: A comprehensive first-principles study

International Nuclear Information System (INIS)

Zhou, Bi-Cheng; Shang, Shun-Li; Wang, Yi; Liu, Zi-Kui

2016-01-01

First-principles calculations based on density functional theory have been used to calculate the temperature-dependent dilute tracer diffusion coefficients for 47 substitutional alloying elements in hexagonal closed packed (hcp) Mg by combining transition state theory and an 8-frequency model. The minimum energy pathways and the saddle point configurations during solute migration are calculated with the climbing image nudged elastic band method. Vibrational properties are obtained using the quasi-harmonic Debye model with inputs from first-principles calculations. An improved generalized gradient approximation of PBEsol is used in the present first-principles calculations, which is able to well describe both vacancy formation energies and vibrational properties. It is found that the solute diffusion coefficients in hcp Mg are roughly inversely proportional to the bulk modulus of the dilute alloys, which reflects the solutes' bonding to Mg. Transition metal elements with d electrons show strong interactions with Mg and have large diffusion activation energies. Correlation effects are not negligible for solutes Ca, Na, Sr, Se, Te, and Y, in which the direct solute migration barriers are much smaller than the solvent (Mg) migration barriers. Calculated diffusion coefficients are in remarkable agreement with available experimental data in the literature.

Formulation of natural convection around repository for dual reciprocity boundary element solution

International Nuclear Information System (INIS)

Vrankar, L.; Sarler, B.

1998-01-01

The disposal of high-level radioactive wastes in deep geological formations is of pronounced technological importance for nuclear safety. The understanding of related fluid flow, heat and mass transport in geological systems is of great interest. This article prepares necessary physical, mathematical and numerical fundamentals for computational modeling of related phenomena. The porous media is described by the simple Darcy law and momentum-energy coupling is due to Boussinesq approximation. The Dual Reciprocity of Boundary Element Method (DRBEM) is used for solving coupled mass, momentum and energy equations in two-dimensions for the steady buoyancy induced convection problem in an semi-infinite porous media. It is structured by weighting with the fundamental solution of the Laplace equation. The inverse multi quadrics are used in the DRBEM transformation. The solution is obtained in an iterative way.(author)

Luminescence Properties of CaF2 Nanostructure Activated by Different Elements

Directory of Open Access Journals (Sweden)

Numan Salah

2015-01-01

Full Text Available Nanostructures of calcium fluoride (CaF2 doped with Eu, Tb, Dy, Cu, and Ag were synthesized by the coprecipitation method and studied for their thermoluminescence (TL and photoluminescence (PL properties. The PL emission spectrum of pure CaF2 nanostructure has a broad band in the 370–550 nm range. Similar spectra were observed in case of doped samples, beside extra bands related to these impurities. The maximum PL intensity was observed in Eu doped sample. The TL results of Eu, Cu, Ag, and Tb doped samples show weak glow peaks below 125°C, whereas Dy doped one is found to be highly sensitive with a prominent peak at 165°C. This sample was further exposed to a wide range of gamma rays exposures from 137Cs source. The response curve is linear in the 100 Gy-10 kGy range. It is also observed that the particle size of CaF2 nanostructure was significantly reduced by increasing Dy concentration. These results showed that Dy is a proper activator in the host of CaF2 nanostructure, providing a highly sensitive dosimeter in a wide range of exposures and also plays a role as a controlling agent for particle size growth.

The analytical solution to the problem on the temperature field in a structural element of rectangular profile for third kind boundary conditions

International Nuclear Information System (INIS)

Kulich, N.V.; Nemtsev, V.A.

1986-01-01

The analytical solution to the problem on the stationary temperature field in an infinite structural element of rectangular profile characteristic of the conjugation points of a vessel and a tube sheet of a heat exchanger (or of a finned surface) at the third-kind boundary conditions has been obtained by the methods of the complex variable function theory. With the help of the obtained analytical dependences the calculations of the given element of the design and the comparison with the known data have been conducted. The proposed analytical solution can be effectively used in calculations of temperature fields in finned surfaces and structural elements of the power equipment of the considered profile and the method is applied for solution of the like problems

Metallic elements (Ca, Hg, Fe, K, Mg, Mn, Na, Zn) in the fruiting bodies of Boletus badius.

Science.gov (United States)

Kojta, Anna K; Falandysz, Jerzy

2016-06-01

The aim of this study was to investigate and compare the levels of eight metallic elements in the fruiting bodies of Bay Bolete (Boletus badius; current name Imleria badia) collected from ten sites in Poland to understand better the value of this popular mushroom as an organic food. Bay Bolete fruiting bodies were collected from the forest area near the towns and villages of Kętrzyn, Poniatowa, Bydgoszcz, Pelplin, Włocławek, Żuromin, Chełmno, Ełk and Wilków communities, as well as in the Augustów Primeval Forest. Elements such as Ca, Fe, K, Mg, Mn, Na and Zn were analyzed by inductively coupled plasma atomic emission spectroscopy (ICP-OES), and mercury by cold vapor atomic absorption spectrometry (CV-AAS). This made it possible to assess the nutritional value of the mushroom, as well as possible toxicological risks associated with its consumption. The results were subjected to statistical analysis (Kruskal-Wallis test, cluster analysis, principal component analysis). Copyright © 2016 Elsevier Ltd. All rights reserved.

Solution of free-boundary problems using finite-element/Newton methods and locally refined grids - Application to analysis of solidification microstructure

Science.gov (United States)

Tsiveriotis, K.; Brown, R. A.

1993-01-01

A new method is presented for the solution of free-boundary problems using Lagrangian finite element approximations defined on locally refined grids. The formulation allows for direct transition from coarse to fine grids without introducing non-conforming basis functions. The calculation of elemental stiffness matrices and residual vectors are unaffected by changes in the refinement level, which are accounted for in the loading of elemental data to the global stiffness matrix and residual vector. This technique for local mesh refinement is combined with recently developed mapping methods and Newton's method to form an efficient algorithm for the solution of free-boundary problems, as demonstrated here by sample calculations of cellular interfacial microstructure during directional solidification of a binary alloy.

Smartphone-based immunosensor for CA125 detection.

Science.gov (United States)

Hosu, Oana; Ravalli, Andrea; Lo Piccolo, Giuseppe Mattia; Cristea, Cecilia; Sandulescu, Robert; Marrazza, Giovanna

2017-05-01

In this work, we report the design, the development and the characterization of the analytical performances of a colorimetric smartphone-based immunosensor for the detection of cancer antigen 125 (CA125). The immunosensor was based on a sandwich strategy in which the primary antibody was immobilized by spotting onto the 3D nitrocellulose membrane. The immunospots were subsequently incubated with CA125 solutions, followed by the affinity reaction with a secondary antibody labeled with gold nanoparticles (AuNPs). The antibody-AuNPs captured onto immunospots induced the silver deposition from a silver enhancer solution leading to the formation of gold-silver nanoparticles of different grey color spots depending on CA125 concentration. The 8 megapixels smartphone camera was integrated in a home-made dark box and used as transducer of color image acquisition and data handling. The pixel intensity of the captured images was determined by an image processing algorithm. The experimental parameters involved in each step of the immunosensor design were studied and optimized, obtaining a limit of detection of 30U/mL CA125. The selectivity of the immunoassay was proven against different concentration solutions of Vascular Endothelial Growth Factor (VEGF) antigen as an unspecific protein when a blank signal was obtained for all tested solutions. Finally, preliminary experiments in human serum samples spiked with CA125 protein were also performed. Therefore, the proposed system could represent a powerful point-of-care tool for the next generation technology for detecting and monitoring cancer biomarkers at early stages by taking advantage of nowadays gadgets with enhanced features such as smartphones. Copyright © 2017 Elsevier B.V. All rights reserved.

In vitro evaluation of bioactivity of SiO2-CaO-P2O5-Na2O-CaF2-ZnO glass-ceramics

Science.gov (United States)

Riaz, Madeeha; Zia, Rehana; Saleemi, Farhat; Bashir, Farooq; Hossain, Tousif; Kayani, Zohra

2014-09-01

Zinc is an essential trace element that stimulates bone formation but it is also known as an inhibitor of apatite crystal growth. In this work addition of ZnO to SiO2-CaO-P2O5-Na2O-CaF2 glass-ceramic system was made by conventional melt-quenching technique. DSC curves showed that the addition of ZnO moved the endothermic and exothermic peaks to lower temperatures. X-ray diffraction analysis did not reveal any additional phase caused by ZnO addition and showed the presence of wollastonite and hydroxyapatite crystalline phases only in all the glass-ceramic samples. As bio-implant apatite forming ability is an essential condition, the surface reactivity of the prepared glass-ceramic specimens was studied in vitro in Kokubo's simulated body fluid (SBF) [1] with ion concentration nearly equal to human blood plasma for 30 days at 37 °C under static condition. Atomic absorption spectroscopy (AAS) was used to study the changes in element concentrations in soaking solutions and XRD, FT-IR and SEM were used to elucidate surface properties of prepared glass-ceramics, which confirmed the formation of HCAp on the surface of all glass-ceramics. It was found that the addition of ZnO had a positive effect on bioactivity of glass-ceramics and made it a potential candidate for restoration of damaged bones.

Influence of liquid structure on diffusive isotope separation in molten silicates and aqueous solutions

Energy Technology Data Exchange (ETDEWEB)

Watkins, J.M.; DePaolo, D.J.; Ryerson, F.J.; Peterson, B.

2011-03-01

Molecular diffusion in natural volcanic liquids discriminates between isotopes of major ions (e.g., Fe, Mg, Ca, and Li). Although isotope separation by diffusion is expected on theoretical grounds, the dependence on mass is highly variable for different elements and in different media. Silicate liquid diffusion experiments using simple liquid compositions were carried out to further probe the compositional dependence of diffusive isotopic discrimination and its relationship to liquid structure. Two diffusion couples consisting of the mineral constituents anorthite (CaAl{sub 2}Si{sub 2}O{sub 8}; denoted AN), albite (NaAlSi{sub 3}O{sub 8}; denoted AB), and diopside (CaMgSi{sub 2}O{sub 6}; denoted DI) were held at 1450°C for 2 h and then quenched to ambient pressure and temperature. Major-element as well as Ca and Mg isotope profiles were measured on the recovered quenched glasses. In both experiments, Ca diffuses rapidly with respect to Si. In the AB–AN experiment, D{sub Ca}/D{sub Si} ~ 20 and the efficiency of isotope separation for Ca is much greater than in natural liquid experiments where D{sub Ca}/D{sub Si} ~ 1. In the AB–DI experiment, D{sub Ca}/D{sub Si} ~ 6 and the efficiency of isotope separation is between that of the natural liquid experiments and the AB–AN experiment. In the AB–DI experiment, D{sub Mg}/D{sub Si} ~ 1 and the efficiency of isotope separation for Mg is smaller than it is for Ca yet similar to that observed for Mg in natural liquids. The results from the experiments reported here, in combination with results from natural volcanic liquids, show clearly that the efficiency of diffusive separation of Ca isotopes is systematically related to the solvent-normalized diffusivity—the ratio of the diffusivity of the cation (D{sub Ca}) to the diffusivity of silicon (D{sub Si}). The results on Ca isotopes are consistent with available data on Fe, Li, and Mg isotopes in silicate liquids, when considered in terms of the parameter D{sub cation

Influence of liquid structure on diffusive isotope separation in molten silicates and aqueous solutions

Science.gov (United States)

Watkins, James M.; DePaolo, Donald J.; Ryerson, Frederick J.; Peterson, Brook T.

2011-06-01

Molecular diffusion in natural volcanic liquids discriminates between isotopes of major ions (e.g., Fe, Mg, Ca, and Li). Although isotope separation by diffusion is expected on theoretical grounds, the dependence on mass is highly variable for different elements and in different media. Silicate liquid diffusion experiments using simple liquid compositions were carried out to further probe the compositional dependence of diffusive isotopic discrimination and its relationship to liquid structure. Two diffusion couples consisting of the mineral constituents anorthite (CaAl 2Si 2O 8; denoted AN), albite (NaAlSi 3O 8; denoted AB), and diopside (CaMgSi 2O 6; denoted DI) were held at 1450 °C for 2 h and then quenched to ambient pressure and temperature. Major-element as well as Ca and Mg isotope profiles were measured on the recovered quenched glasses. In both experiments, Ca diffuses rapidly with respect to Si. In the AB-AN experiment, D Ca/ D Si ≈ 20 and the efficiency of isotope separation for Ca is much greater than in natural liquid experiments where D Ca/ D Si ≈ 1. In the AB-DI experiment, D Ca/ D Si ≈ 6 and the efficiency of isotope separation is between that of the natural liquid experiments and the AB-AN experiment. In the AB-DI experiment, D Mg/ D Si ≈ 1 and the efficiency of isotope separation for Mg is smaller than it is for Ca yet similar to that observed for Mg in natural liquids. The results from the experiments reported here, in combination with results from natural volcanic liquids, show clearly that the efficiency of diffusive separation of Ca isotopes is systematically related to the solvent-normalized diffusivity - the ratio of the diffusivity of the cation ( D Ca) to the diffusivity of silicon ( D Si). The results on Ca isotopes are consistent with available data on Fe, Li, and Mg isotopes in silicate liquids, when considered in terms of the parameter D cation/ D Si. Cations diffusing in aqueous solutions display a similar relationship

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

Energy Technology Data Exchange (ETDEWEB)

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

2015-03-15

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

ICP-MS with hexapole collision cell for isotope ratio measurements of Ca, Fe, and Se.

Science.gov (United States)

Boulyga, S F; Becker, J S

2001-07-01

To avoid mass interferences on analyte ions caused by argon ions and argon molecular ions via reactions with collision gases, an rf hexapole filled with helium and hydrogen has been used in inductively coupled plasma mass spectrometry (ICP-MS), and its performance has been studied. Up to tenfold improvement in sensitivity was observed for heavy elements (m > 100 u), because of better ion transmission through the hexapole ion guide. A reduction of argon ions Ar+ and the molecular ions of argon ArX+ (X = O, Ar) by up to three orders of magnitude was achieved in a hexapole collision cell of an ICP-MS ("Platform ICP", Micromass, Manchester, UK) as a result of gas-phase reactions with hydrogen when the hexapole bias (HB) was set to 0 V; at an HB of 1.6 V argon, and argon-based ions of masses 40 u, 56 u, and 80 u, were reduced by approximately four, two, and five orders of magnitude, respectively. The signal-to-noise ratio 80Se/ 40Ar2+ was improved by more than five orders of magnitude under optimized experimental conditions. Dependence of mass discrimination on collision-cell properties was studied in the mass range 10 u (boron) to 238 u (uranium). Isotopic analysis of the elements affected by mass-spectrometric interference, Ca, Fe, and Se, was performed using a Meinhard nebulizer and an ultrasonic nebulizer (USN). The measured isotope ratios were comparable with tabulated values from IUPAC. Precision of 0.26%, 0.19%, and 0.12%, respectively, and accuracy of 0.13% 0.25%, and 0.92%, respectively, was achieved for isotope ratios 44Ca/ 40Ca and 56Fe/57Fe in 10 microg L(-1) solution nebulized by means of a USN and for 78Se/80Se in 100 microg L(-1) solution nebulized by means of a Meinhard nebulizer.

Finite element method solution of simplified P3 equation for flexible geometry handling

International Nuclear Information System (INIS)

Ryu, Eun Hyun; Joo, Han Gyu

2011-01-01

In order to obtain efficiently core flux solutions which would be much closer to the transport solution than the diffusion solution is, not being limited by the geometry of the core, the simplified P 3 (SP 3 ) equation is solved with the finite element method (FEM). A generic mesh generator, GMSH, is used to generate linear and quadratic mesh data. The linear system resulting from the SP 3 FEM discretization is solved by Krylov subspace methods (KSM). A symmetric form of the SP 3 equation is derived to apply the conjugate gradient method rather than the KSMs for nonsymmetric linear systems. An optional iso-parametric quadratic mapping scheme, which is to selectively model nonlinear shapes with a quadratic mapping to prevent significant mismatch in local domain volume, is also implemented for efficient application of arbitrary geometry handling. The gain in the accuracy attainable by the SP 3 solution over the diffusion solution is assessed by solving numerous benchmark problems having various core geometries including the IAEA PWR problems involving rectangular fuels and the Takeda fast reactor problems involving hexagonal fuels. The reference transport solution is produced by the McCARD Monte Carlo code and the multiplication factor and power distribution errors are assessed. In addition, the effect of quadratic mapping is examined for circular cell problems. It is shown that significant accuracy gain is possible with the SP 3 solution for the fast reactor problems whereas only marginal improvement is noted for thermal reactor problems. The quadratic mapping is also quite effective handling geometries with curvature. (author)

A deflation based parallel algorithm for spectral element solution of the incompressible Navier-Stokes equations

Energy Technology Data Exchange (ETDEWEB)

Fischer, P.F. [Brown Univ., Providence, RI (United States)

1996-12-31

Efficient solution of the Navier-Stokes equations in complex domains is dependent upon the availability of fast solvers for sparse linear systems. For unsteady incompressible flows, the pressure operator is the leading contributor to stiffness, as the characteristic propagation speed is infinite. In the context of operator splitting formulations, it is the pressure solve which is the most computationally challenging, despite its elliptic origins. We seek to improve existing spectral element iterative methods for the pressure solve in order to overcome the slow convergence frequently observed in the presence of highly refined grids or high-aspect ratio elements.

Solution of the diffusion equations for several groups by the finite elements method

International Nuclear Information System (INIS)

Arredondo S, C.

1975-01-01

The code DELFIN has been implemented for the solution of the neutrons diffusion equations in two dimensions obtained by applying the approximation of several groups of energy. The code works with any number of groups and regions, and can be applied to thermal reactors as well as fast reactor. Providing it with the diffusion coefficients, the effective sections and the fission spectrum we obtain the results for the systems multiplying constant and the flows of each groups. The code was established using the method of finite elements, which is a form of resolution of the variational formulation of the equations applying the Ritz-Galerkin method with continuous polynomial functions by parts, in one case of the Lagrange type with rectangular geometry and up to the third grade. The obtained results and the comparison with the results in the literature, permit to reach the conclusion that it is convenient, to use the rectangular elements in all the cases where the geometry permits it, and demonstrate also that the finite elements method is better than the finite differences method. (author)

Preparation of 45Ca(HDEHP)n and (CaH1502)2 samples for liquid scintillation counting, compared to 45caCl2 results

International Nuclear Information System (INIS)

Rodriguez, L.; Arcos, J. M. los; Grau Malonda, A.

1994-01-01

A procedure for preparation of liquid scintillation counting organic samples of the Di-2-ethylhexyl phosphate calcium complex and the 2-ethylhexanoate calcium salt, labelled with 45Ca, is described. The chemical quench, the counting stability and spectral evolution of both compounds is studied in six scintillators,Toluene-alcohol, Dioxane-naphtalene, Hi safe II, Ultimate-Gold and Instagel, and compared to results obtained from a commercial solution of 4 5CaCl2. (Author) 7 refs

[Effects of LED spectrum combinations on the absorption of mineral elements of hydroponic lettuce].

Science.gov (United States)

Chen, Xiao-Li; Guo, Wen-Zhong; Xue, Xu-Zhang; Mmanake Beauty, Morewane

2014-05-01

Lettuce (Lactuca sativa) was hydroponically cultured in a completely enclosed plant factory, in which spectrum proportion-adjustable LED panels were used as sole light source for plant growth. Absorption and content of eleven mineral elements such as K, P, Ca, Mg, Na, Fe, Mn, Zn, Cu, B and Mo in Lactuca sativa under different spectral component conditions were studied by ICP -AES technology. The results showed that: (1) Single or combined spectrums corresponding to the absorbing peaks of chlorophyll a and b (450, 660 nm) could enhance the absorbing ability of roots especially for mineral elements Na, Fe, Mn, Cu and Mo, the single red spectrum had the most significant promoting effect under which contents of those four elements were respectively 7. 8, 4. 2, 4. 0 and 3. 7 times more than that under FL; (2) Absorption of K and B was the highest under FL which was 10. 309 mg g-1 and 32. 6 microg g-1 while the values decreased significantly under single or combined spectrum of red and blue; (3) Plants grown under single blue spectrum had the lowest absorption of Ca and Mg which respectively decreased by 35% and 33% than FL; (4) Lettuce grown under the spectrum combination of 30% blue and 70% red had the highest accumulations of biomass while those grown under 20% blue and 80% red had the highest accumulations of the following seven elements Ca, Mg, Na, Fe, Mn, Zn and B. The results provided theoretical basis for adjusting nutrient solution formula and selecting light spectrum of hydroponic lettuce.

An approximative solution for limit load of piping branch junctions with circumferential crack and finite element validation

International Nuclear Information System (INIS)

Xuan Fuzhen; Liu Changjun; Li Peining

2005-01-01

This paper is concerned with the prediction of limit load of the piping branch junctions with circumferential crack under internal pressure. Recently, we have developed a new approach for predicting the limit load of two-cylinder intersection structures with diameter ratio larger than 0.5, which has been successfully applied to defect free cases under various loading conditions. In the present work, we consider the extension of the approach to cover cracked piping branch junctions. On the basis of stress analysis in the vicinity of intersection line, a closed form of limit load solution for piping branch junctions with circumferential crack was developed. Then, 36 finite element (FE) models of piping branch junction with various dimensions of structure and crack were analyzed by using nonlinear finite element software. The limit loads from FE analysis and the proposed solution are compared with each other. Overall good agreement between the estimated solutions and the FE results provides confidence in the use of the proposed formulae for defect assessment of piping branch junctions in practice

Indirect boundary element method for three dimensional problems. Analytical solution for contribution to wave field by triangular element; Sanjigen kansetsu kyokai yosoho. Sankakukei yoso no kiyo no kaisekikai

Energy Technology Data Exchange (ETDEWEB)

Yokoi, T [Building Research Institute, Tokyo (Japan); Sanchez-Sesma, F [Universidad National Autonoma de Mexico, (Mexico). Institute de Ingenieria

1997-05-27

Formulation is introduced for discretizing a boundary integral equation into an indirect boundary element method for the solution of 3-dimensional topographic problems. Yokoi and Takenaka propose an analytical solution-capable reference solution (solution for the half space elastic body with flat free surface) to problems of topographic response to seismic motion in a 2-dimensional in-plane field. That is to say, they propose a boundary integral equation capable of effectively suppressing the non-physical waves that emerge in the result of computation in the wake of the truncation of the discretized ground surface making use of the wave field in a semi-infinite elastic body with flat free surface. They apply the proposed boundary integral equation discretized into the indirect boundary element method to solve some examples, and succeed in proving its validity. In this report, the equation is expanded to deal with 3-dimensional topographic problems. A problem of a P-wave vertically landing on a flat and free surface is solved by the conventional boundary integral equation and the proposed boundary integral equation, and the solutions are compared with each other. It is found that the new method, different from the conventional one, can delete non-physical waves from the analytical result. 4 figs.

Preparation and properties of superconducting Bi-Sr-Ca-Cu-O materials by the alkoxide process

International Nuclear Information System (INIS)

Uchikawa, Fusaoki; Kobayashi, Toshio; Usami, Ryo; Yoshizaki, Kiyoshi

1989-01-01

Homogeneous starting solutions were synthesized using Bi, Sr, Ca and Cu alkoxides. Powders, thick films and gel fibers were prepared respectively by controlling hydrolysis using the same solutions. The synthesized powder had a homogeneous particle size. The fired powder showed a good crystallization property. The thick film coated on MgO substrate using the synthesized sol solution had a smooth surface and a uniformity of each metal elements. The film showed the c-axis orientation and was shown to have the zero resistance temperature of 90 K and the critical current density of 180 A/cm 2 at 77 K. The fiber drawn from the viscous gel solution showed a comparatively large shrinkage with hear treatment. The fired fiber was brittle and had a low strength. It was also found for the fired fiber that zero resistance temperature was 70 K and the critical current density was 90 A/cm 2 at 77 K

Effect of the addition CNTs on performance of CaP/chitosan/coating deposited on magnesium alloy by electrophoretic deposition.

Science.gov (United States)

Zhang, Jie; Wen, Zhaohui; Zhao, Meng; Li, Guozhong; Dai, Changsong

2016-01-01

CaP/chitosan/carbon nanotubes (CNTs) coating on AZ91D magnesium alloy was prepared via electrophoretic deposition (EPD) followed by conversion in a phosphate buffer solution (PBS). The bonding between the layer and the substrate was studied by an automatic scratch instrument. The phase compositions and microstructures of the composite coatings were determined by using X-ray diffraction (XRD), Fourier-transformed infrared spectroscopy (FTIR), Raman spectroscopy and scanning electron microscope (SEM). The element concentration and gentamicin concentration were respectively determined by inductively coupled plasma optical emission spectrometer (ICP-OES) test and ultraviolet spectrophotometer (UV). The cell counting kit (CCK) assay was used to evaluate the cytotoxicity of samples to SaOS-2 cells. The results showed that a few CNTs with their original tubular morphology could be found in the CaP/chitosan coating and they were beneficial for the crystal growth of phosphate and improvement of the coating bonding when the addition amount of CNTs in 500 ml of electrophoretic solution was from 0.05 g to 0.125 g. The loading amount of gentamicin increased and the releasing speed of gentamicin decreased after CNTs was added into the CaP/chitosan coating for immersion loading and EPD loading. The cell viability of Mg based CaP/chitosan/CNTs was higher than that of Mg based CaP/chitosan from 16 days to 90 days. Copyright © 2015 Elsevier B.V. All rights reserved.

Effect of the addition CNTs on performance of CaP/chitosan/coating deposited on magnesium alloy by electrophoretic deposition

Energy Technology Data Exchange (ETDEWEB)

Zhang, Jie [Department of Neuro Intern, First Affiliated Hospital of Harbin Medical University, Harbin 150001 (China); Pharmaceutical Research Institute in Heilongjiang Province, Jiamusi University, Jiamusi 154007 (China); Wen, Zhaohui, E-mail: wenzhaohui1968@163.com [Department of Neuro Intern, First Affiliated Hospital of Harbin Medical University, Harbin 150001 (China); Zhao, Meng [Department of Neuro Intern, First Affiliated Hospital of Harbin Medical University, Harbin 150001 (China); Li, Guozhong, E-mail: hydlgz1962@163.com [Department of Neuro Intern, First Affiliated Hospital of Harbin Medical University, Harbin 150001 (China); Dai, Changsong, E-mail: changsd@hit.edu.cn [School of Chemistry Engineering and Technology, Harbin Institute of Technology, Harbin 150001 (China)

2016-01-01

CaP/chitosan/carbon nanotubes (CNTs) coating on AZ91D magnesium alloy was prepared via electrophoretic deposition (EPD) followed by conversion in a phosphate buffer solution (PBS). The bonding between the layer and the substrate was studied by an automatic scratch instrument. The phase compositions and microstructures of the composite coatings were determined by using X-ray diffraction (XRD), Fourier-transformed infrared spectroscopy (FTIR), Raman spectroscopy and scanning electron microscope (SEM). The element concentration and gentamicin concentration were respectively determined by inductively coupled plasma optical emission spectrometer (ICP-OES) test and ultraviolet spectrophotometer (UV). The cell counting kit (CCK) assay was used to evaluate the cytotoxicity of samples to SaOS-2 cells. The results showed that a few CNTs with their original tubular morphology could be found in the CaP/chitosan coating and they were beneficial for the crystal growth of phosphate and improvement of the coating bonding when the addition amount of CNTs in 500 ml of electrophoretic solution was from 0.05 g to 0.125 g. The loading amount of gentamicin increased and the releasing speed of gentamicin decreased after CNTs was added into the CaP/chitosan coating for immersion loading and EPD loading. The cell viability of Mg based CaP/chitosan/CNTs was higher than that of Mg based CaP/chitosan from 16 days to 90 days. - Highlights: • CaP/chitosan/CNTs coating on AZ91D was prepared. • The addition of CNTs could improve the performance of CaP/chitosan coating. • A new method of loading gentamicin by EPD was proposed.

Fusion dynamics in 40Ca induced reactions

International Nuclear Information System (INIS)

Prasad, E.; Hinde, D.J.; Williams, E.

2017-01-01

Synthesis of superheavy elements (SHEs) and investigation of their properties are among the most challenging research topics in modern science. A non-compound nuclear process called quasi fission is partly responsible for the very low production cross sections of SHEs. The formation and survival probabilities of the compound nucleus (CN) strongly depend on the competition between fusion and quasi fission. A clear understanding of these processes and their dynamics is required to make reliable predictions of the best reactions to synthesise new SHEs. All elements beyond Nh are produced using hot fusion reactions and beams of 48 Ca were used in most of these experiments. In this context a series of fission measurements have been carried out at the Australian National University (ANU) using 40;48 Ca beams on various targets ranging from 142 Nd to 249 Cf. Some of the 40 Ca reactions will be discussed in this symposium

Preliminary analysis of construction of the test drift in boom clay at Mol using plasticity solutions and finite elements

International Nuclear Information System (INIS)

Mair, R.J.; Taylor, R.N.; Higgins, K.G.; Potts, D.M.

1989-01-01

Analyses have been undertaken on an advancing tunnel heading at great depth in a clay formation corresponding to the test drift construction at Mol. Belgium. Simplifying assumptions enable plasticity solutions to be used to model the behaviour of a tunnel heading in a linear elastic-perfectly plastic soil. Finite element analysis with the same soil model has been undertaken of the test drift construction, assuming axisymmetric conditions. The results are compared with the plasticity solutions and with the measurements of lining stresses, soil movements and pore pressures by SCK/CEN. Good agreement is obtained between the plasticity solutions and finite element analysis. The measured immediate build-up of stress on the linings is well-predicted and reasonable agreement is obtained between predicted and measured soil movements. The measured pore-pressure changes are poorly predicted by the analyses

Mineralogy and Trace Element Chemistry of Ferberite/Reinite from Tungsten Deposits in Central Rwanda

Directory of Open Access Journals (Sweden)

Philippe Muchez

2013-04-01

Full Text Available Tungsten mineralization in hydrothermal quartz veins from the Nyakabingo,Gifurwe and Bugarama deposits in central Rwanda occurs as the iron-rich endmember ofthe wolframite solid solution series (ferberite and in the particular form of reinite, whichrepresents a pseudomorph of ferberite after scheelite. Primary ferberite, reinite and latesecondary ferberite are characterized by their trace element chemistry and rare earthelement patterns. The replacement of scheelite by ferberite is also documented in the traceelement composition. Primary ferberite shows high Mg, Zn, Sc, V, Nb, In and Snconcentrations, but very low Ca, Pb, Sr and Ba contents. Reinite and late secondaryferberite display an uncommon trace element composition containing high concentrationsof Ca, Pb, Sr, Ba, As and Ga, but very low levels in Sn, Zr, Hf, In, Ti, Sc, Nb, Ta, Mg andZn. Late secondary ferberite replacing primary ferberite is characterized by additionalenrichments in Bi, Pb, As and Sb. The rare earth element patterns of reinite and secondaryferberite are also similar to hydrothermal scheelite. The formation of the tungsten depositsin central Rwanda is interpreted to be epigenetic in origin, and the hydrothermalmineralizing fluids are related to the intrusion of the G4-granites.

45Ca distribution and transport in saponin skinned vascular smooth muscle

International Nuclear Information System (INIS)

Stout, M.A.; Diecke, F.P.

1983-01-01

45 Ca distribution and transport were studied in chemically skinned strips of caudal artery from Kyoto Wistar rats. Sarcolemmal membranes were made hyperpermeable by exposure for 60 min to solutions containing 0.1 mg/ml of saponin. Skinned helical strips responded with graded contractions to changes in ethylene glycol bis-(beta-aminoethyl ether)-N,N'-tetraacetic acid buffered free Ca solutions (10(-7) to 10(-5) M) and were sensitive to the Mg-ATP concentration. Tissues loaded in the presence of 10(-7) M Ca contracted in response to 10 mM caffeine. These experiments indicate the strips are skinned and possess a functional regulatory and contractile system and an intact Ca sequestering system. 45 Ca distributes in three compartments in skinned caudal artery strips. The Ca contents of two components are linear functions of the Ca-ethylene glycol bis-(beta-aminoethyl ether)-N,N'-tetraacetic acid concentration and desaturate at rapid rates. They correspond to the extracellular and cytoplasmic spaces. A significantly smaller component releases Ca at comparatively slower rates. 45 Ca uptake by the slow component consists of an ATP-dependent and an ATP-independent fraction. The 45 Ca content of the ATP-dependent fraction is a function of the free Ca concentration and is independent of the Ca-ethylene glycol bis-(beta-aminoethyl ether)-N,N'-tetraacetic acid concentration. Its content was enhanced by oxalate and was abolished by Triton X-100 skinning solutions. The ATP-independent component was not affected by Triton X-100 skinning and may represent Ca binding to cytoplasmic molecules and structures. The sequestered Ca was released with caffeine or Ca but not by epinephrine. The observations indicate that the sarcoplasmic reticulum and mitochondria of vascular smooth muscle strips skinned with saponin retain their functional integrity after saponin skinning

Distributions of 14 elements on 60 selected absorbers from two simulant solutions (acid-dissolved sludge and alkaline supernate) for Hanford HLW Tank 102-SY

International Nuclear Information System (INIS)

Marsh, S.F.; Svitra, Z.V.; Bowen, S.M.

1993-10-01

Sixty commercially available or experimental absorber materials were evaluated for partitioning high-level radioactive waste. These absorbers included cation and anion exchange resins, inorganic exchangers, composite absorbers, and a series of liquid extractants sorbed on porous support-beads. The distributions of 14 elements onto each absorber were measured from simulated solutions that represent acid-dissolved sludge and alkaline supernate solutions from Hanford high-level waste (HLW) Tank 102-SY. The selected elements, which represent fission products (Ce, Cs, Sr, Tc, and Y); actinides (U, Pu, and Am); and matrix elements (Cr, Co, Fe, Mn, Zn, and Zr), were traced by radionuclides and assayed by gamma spectrometry. Distribution coefficients for each of the 1680 element/absorber/solution combinations were measured for dynamic contact periods of 30 min, 2 h, and 6 h to provide sorption kinetics information for the specified elements from these complex media. More than 5000 measured distribution coefficients are tabulated

Structural and magnetic properties of the (Ca1-xNax)(Fe2-xTix)O4 solid solution (0 ≤ x ≤ 1)

International Nuclear Information System (INIS)

Zouari, S.; Ranno, L.; Cheikh-Rouhou, A.; Isnard, O.; Wolfers, P.; Bordet, P.; Strobel, P.

2008-01-01

New compounds corresponding to the (Ca 1-x Na x )(Fe 2-x Ti x )O 4 formula with 0 ≤ x ≤ 1 were prepared by solid state reactions at 1100 deg. C in air. A continuous solid solution was found between end members CaFe 2 O 4 and NaFeTiO 4 . The evolution of structural parameters and bonding geometry with composition is discussed in detail. Magnetic measurements show that the antiferromagnetic ordering known in CaFe 2 O 4 is suppressed for all x values investigated (x ≥ 0.2). The absence of crystallographic transition at low temperature was checked by X-ray diffraction down to 10 K. The magnetic structure of CaFe 2 O 4 was redetermined from powder neutron diffraction. Spins on the two iron sites order antiparallel (F z F z spin arrangement), as described previously. The difference in magnetic moments on Fe 1 and Fe 2 sites result in a ferrimagnetic configuration with net moment 2.72μ B at 2 K

Approximate solutions of pulse transport in turbulent flow in narrow fuel element bundle geometries, using the FE method

International Nuclear Information System (INIS)

Kaiser, H.G.

1985-01-01

The author is concerned with the flow conditions in case of narrow fuel element grids of pressurised-water reactors. Starting from the mathematical formulation of the flow processes for incompressible, isothermal flows, models of the turbulence characteristics are being developed. Besides turbulence models, and network structure the finite element method is treated as numeric solution process. Finally the results are summarized and discussed. (HAG) [de

Thorium-d-metals compounds and solid solutions

International Nuclear Information System (INIS)

Chachkhiani, Z.B.; Chechernikov, V.I.; Chachkhiani, L.G.

1986-01-01

Thorium compounds with Fe, Co, Ni dependence of their magnetic properties on temperature, pressure and concentration of the second element are considered. Anomalous magnetic behaviour of alloys in the Th-Fe system is noted. Special attention is paid to compounds with CaCu 5 type hexagonal structure and their solid solutions. Th-Co-Ni specimens containing up to 25% Ni are ferromagnetics and the rest are paramagnetics. Specimens with 60% cobalt content do not display ferromagnetic properties up to 4.2 K. Hydrides of Th 7 M 3 H 30 type (M - Fe, Co, Ni) are also considered. Highly hydrogenized specimens (under high pressure) appear to be stronger ferromagnetics

Effect of solute elements in Ni alloys on blistering under He + and D + ion irradiation

Science.gov (United States)

Wakai, E.; Ezawa, T.; Takenaka, T.; Imamura, J.; Tanabe, T.; Oshima, R.

2007-08-01

Effects of solute atoms on microstructural evolution and blister formation have been investigated using Ni alloys under 25 keV He + and 20 keV D + irradiation at 500 °C to a dose of about 4 × 10 21 ions/m 2. The specimens used were pure Ni, Ni-Si, Ni-Co, Ni-Cu, Ni-Mn and Ni-Pd alloys. The volume size factors of solute elements for the Ni alloys range from -5.8% to +63.6%. The formations of blisters were observed in the helium-irradiated specimens, but not in the deuteron-irradiated specimens. The areal number densities of blisters increased with volume size difference of solute atoms. The dependence of volume size on the areal number densities of blisters was very similar to that of the number densities of bubbles on solute atoms. The size of the blisters inversely decreased with increasing size of solute atoms. The formation of blisters was intimately related to the bubble growth, and the gas pressure model for the formation of blisters was supported by this study.

Elemental markers in elasmobranchs: effects of environmental history and growth on vertebral chemistry.

Science.gov (United States)

Smith, Wade D; Miller, Jessica A; Heppell, Selina S

2013-01-01

Differences in the chemical composition of calcified skeletal structures (e.g. shells, otoliths) have proven useful for reconstructing the environmental history of many marine species. However, the extent to which ambient environmental conditions can be inferred from the elemental signatures within the vertebrae of elasmobranchs (sharks, skates, rays) has not been evaluated. To assess the relationship between water and vertebral elemental composition, we conducted two laboratory studies using round stingrays, Urobatis halleri, as a model species. First, we examined the effects of temperature (16°, 18°, 24°C) on vertebral elemental incorporation (Li/Ca, Mg/Ca, Mn/Ca, Zn/Ca, Sr/Ca, Ba/Ca). Second, we tested the relationship between water and subsequent vertebral elemental composition by manipulating dissolved barium concentrations (1x, 3x, 6x). We also evaluated the influence of natural variation in growth rate on elemental incorporation for both experiments. Finally, we examined the accuracy of classifying individuals to known environmental histories (temperature and barium treatments) using vertebral elemental composition. Temperature had strong, negative effects on the uptake of magnesium (DMg) and barium (DBa) and positively influenced manganese (DMn) incorporation. Temperature-dependent responses were not observed for lithium and strontium. Vertebral Ba/Ca was positively correlated with ambient Ba/Ca. Partition coefficients (DBa) revealed increased discrimination of barium in response to increased dissolved barium concentrations. There were no significant relationships between elemental incorporation and somatic growth or vertebral precipitation rates for any elements except Zn. Relationships between somatic growth rate and DZn were, however, inconsistent and inconclusive. Variation in the vertebral elemental signatures of U. halleri reliably distinguished individual rays from each treatment based on temperature (85%) and Ba exposure (96%) history. These

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.

Rare Earth Element Phases in Bauxite Residue

Directory of Open Access Journals (Sweden)

Johannes Vind

2018-02-01

Full Text Available The purpose of present work was to provide mineralogical insight into the rare earth element (REE phases in bauxite residue to improve REE recovering technologies. Experimental work was performed by electron probe microanalysis with energy dispersive as well as wavelength dispersive spectroscopy and transmission electron microscopy. REEs are found as discrete mineral particles in bauxite residue. Their sizes range from <1 μm to about 40 μm. In bauxite residue, the most abundant REE bearing phases are light REE (LREE ferrotitanates that form a solid solution between the phases with major compositions (REE,Ca,Na(Ti,FeO3 and (Ca,Na(Ti,FeO3. These are secondary phases formed during the Bayer process by an in-situ transformation of the precursor bauxite LREE phases. Compared to natural systems, the indicated solid solution resembles loparite-perovskite series. LREE particles often have a calcium ferrotitanate shell surrounding them that probably hinders their solubility. Minor amount of LREE carbonate and phosphate minerals as well as manganese-associated LREE phases are also present in bauxite residue. Heavy REEs occur in the same form as in bauxites, namely as yttrium phosphates. These results show that the Bayer process has an impact on the initial REE mineralogy contained in bauxite. Bauxite residue as well as selected bauxites are potentially good sources of REEs.

Structural basis for the differential effects of CaBP1 and calmodulin on CaV1.2 calcium-dependent inactivation

Science.gov (United States)

Findeisen, Felix; Minor, Daniel L.

2010-01-01

Calcium-binding protein 1 (CaBP1), a calmodulin (CaM) homolog, endows certain voltage-gated calcium channels (CaVs) with unusual properties. CaBP1 inhibits CaV1.2 calcium-dependent inactivation (CDI) and introduces calcium-dependent facilitation (CDF). Here, we show that the ability of CaBP1 to inhibit CaV1.2 CDI and induce CDF arises from interaction between the CaBP1 N-lobe and interlobe linker residue Glu94. Unlike CaM, where functional EF hands are essential for channel modulation, CDI inhibition does not require functional CaBP1 EF-hands. Furthermore, CaBP1-mediated CDF has different molecular requirements than CaM-mediated CDF. Overall, the data show that CaBP1 comprises two structural modules having separate functions: similar to CaM, the CaBP1 C-lobe serves as a high-affinity anchor that binds the CaV1.2 IQ domain at a site that overlaps with the Ca2+/CaM C-lobe site, whereas the N-lobe/linker module houses the elements required for channel modulation. Discovery of this division provides the framework for understanding how CaBP1 regulates CaVs. PMID:21134641

Structural basis for the differential effects of CaBP1 and calmodulin on Ca(V)1.2 calcium-dependent inactivation.

Science.gov (United States)

Findeisen, Felix; Minor, Daniel L

2010-12-08

Calcium-binding protein 1 (CaBP1), a calmodulin (CaM) homolog, endows certain voltage-gated calcium channels (Ca(V)s) with unusual properties. CaBP1 inhibits Ca(V)1.2 calcium-dependent inactivation (CDI) and introduces calcium-dependent facilitation (CDF). Here, we show that the ability of CaBP1 to inhibit Ca(V)1.2 CDI and induce CDF arises from interaction between the CaBP1 N-lobe and interlobe linker residue Glu94. Unlike CaM, where functional EF hands are essential for channel modulation, CDI inhibition does not require functional CaBP1 EF hands. Furthermore, CaBP1-mediated CDF has different molecular requirements than CaM-mediated CDF. Overall, the data show that CaBP1 comprises two structural modules having separate functions: similar to CaM, the CaBP1 C-lobe serves as a high-affinity anchor that binds the Ca(V)1.2 IQ domain at a site that overlaps with the Ca²+/CaM C-lobe site, whereas the N-lobe/linker module houses the elements required for channel modulation. Discovery of this division provides the framework for understanding how CaBP1 regulates Ca(V)s. Copyright © 2010 Elsevier Ltd. All rights reserved.

Multi-element RIMS Analysis of Genesis Solar Wind Collectors

Science.gov (United States)

Veryovkin, I. V.; Tripa, C. E.; Zinovev, A. V.; King, B. V.; Pellin, M. J.; Burnett, D. S.

2009-12-01

and 3.6±2.5×1013 at/cm2 in #60476 were measured. Thus, only one element in each sample showed reasonable agreement with the expected values, Ca in #60179 and Cr in #60476. However the cleaning procedures applied to these samples were different: #60179 was only Megasonicated in ultra-pure water, while #60476 was subjected to longer Megasonication and an RCA cleaning procedure involving multiple rinsing steps with acid solutions. It is apparent that the surface contamination and cleaning procedures influenced the results of our measurements. We will present these experimental results and discuss procedures - including improved sample cleaning, dual-beam high resolution sputter depth profiling from front and back sides of the sample, and modeling of near-surface impurity transport - aimed at improving the accuracy of determination of elemental abundances by ion sputtering based analytical methods. This work is supported by NASA through a grant NNH08AH761 and by UChicago Argonne, LLC, under contract No. DE-AC02-06CH11357.

Superconductivity under high pressure in the binary compound CaLi2

Science.gov (United States)

Debessai, M.; Matsuoka, T.; Hamlin, J. J.; Gangopadhyay, A. K.; Schilling, J. S.; Shimizu, K.; Ohishi, Y.

2008-12-01

Feng predicted for CaLi2 highly anomalous properties with possible superconductivity under very high pressures, including for the hcp polymorph a significant lattice bifurcation at pressures above 47 GPa. More recently, however, Feng suggested that for pressures exceeding 20 GPa CaLi2 may dissociate into elemental Ca and Li. Here we present for hcp CaLi2 measurements of the electrical resistivity and ac susceptibility to low temperatures under pressures as high as 81 GPa. Pressure-induced superconductivity is observed in the pressure range of 11-81 GPa, with Tc reaching values as high as 13 K. X-ray diffraction studies to 54 GPa at 150 K reveal that hcp CaLi2 undergoes a structural phase transition above 23 GPa to orthorhombic but does not dissociate into elemental Ca and Li. In the hcp phase a fit of the equation of state with the Murnaghan equation yields the bulk modulus Bo=15(2)GPa and dBo/dP=3.2(6) .

Relationships Between Element Contents in Polish Children's and Adolescents' Hair.

Science.gov (United States)

Długaszek, Maria; Skrzeczanowski, Wojciech

2017-11-01

Environment, sex, and age are the main factors which determine the elemental composition of hair. The objective of the study is to determine the contents of calcium (Ca), magnesium (Mg), zinc (Zn), copper (Cu), iron (Fe), lead (Pb), and cadmium (Cd) in girls' and boys' hair in five age groups (within 1-19-year range) corresponding to successive human ontogenesis phases as well as to evaluate the relationships between these elements. Quantitative analysis has been carried out using atomic absorption spectrometry (AAS). Experimental results were analyzed using classic and principal component (PCA) statistical analyses. In particular, differences between contents of particularly Ca, Mg, and Zn in girls' and boys' hair were found, and substantial differences between age groups were stated. In general, larger amounts of Ca, Mg, and Zn as compared to boys' hair have been observed for girls' hair and higher toxic element (Pb, Cd) contents for boys were measured in some age groups. An increasing trend was found for bioelements (Ca, Mg, Zn) both for girls and boys in all age groups, while for Cu and Fe content, changes are insignificant and even decreasing for teenagers. The most frequently correlating element pairs are Ca-Mg, Ca-Zn, Mg-Zn, and Pb-Cd. Classic and PCA statistics show, in general, a satisfactory consistence. The elemental composition of hair varies depending on the gender and age of children and young people.

Optimization and application of ICPMS with dynamic reaction cell for precise determination of 44Ca/40Ca isotope ratios.

Science.gov (United States)

Boulyga, Sergei F; Klötzli, Urs; Stingeder, Gerhard; Prohaska, Thomas

2007-10-15

An inductively coupled plasma mass spectrometer with dynamic reaction cell (ICP-DRC-MS) was optimized for determining (44)Ca/(40)Ca isotope ratios in aqueous solutions with respect to (i) repeatability, (ii) robustness, and (iii) stability. Ammonia as reaction gas allowed both the removal of (40)Ar+ interference on (40)Ca+ and collisional damping of ion density fluctuations of an ion beam extracted from an ICP. The effect of laboratory conditions as well as ICP-DRC-MS parameters such a nebulizer gas flow rate, rf power, lens potential, dwell time, or DRC parameters on precision and mass bias was studied. Precision (calculated using the "unbiased" or "n - 1" method) of a single isotope ratio measurement of a 60 ng g(-1) calcium solution (analysis time of 6 min) is routinely achievable in the range of 0.03-0.05%, which corresponded to the standard error of the mean value (n = 6) of 0.012-0.020%. These experimentally observed RSDs were close to theoretical precision values given by counting statistics. Accuracy of measured isotope ratios was assessed by comparative measurements of the same samples by ICP-DRC-MS and thermal ionization mass spectrometry (TIMS) by using isotope dilution with a (43)Ca-(48)Ca double spike. The analysis time in both cases was 1 h per analysis (10 blocks, each 6 min). The delta(44)Ca values measured by TIMS and ICP-DRC-MS with double-spike calibration in two samples (Ca ICP standard solution and digested NIST 1486 bone meal) coincided within the obtained precision. Although the applied isotope dilution with (43)Ca-(48)Ca double-spike compensates for time-dependent deviations of mass bias and allows achieving accurate results, this approach makes it necessary to measure an additional isotope pair, reducing the overall analysis time per isotope or increasing the total analysis time. Further development of external calibration by using a bracketing method would allow a wider use of ICP-DRC-MS for routine calcium isotopic measurements, but it

Bioaccumulation of uranium and thorium from the solution containing both elements using various microorganisms

International Nuclear Information System (INIS)

Tsuruta, T.

2006-01-01

The effects of proton, thorium and uranium on the bioaccumulation of thorium and uranium from the solution (pH 3.5) containing uranium and thorium using Streptomyces levoris cells were examined. The amount of thorium accumulated using the cells decreased by the pre-contact between the cells and the solution (pH 3.5) containing no metals, whereas that of uranium was almost unaffected by the treatment. The amount of thorium was almost unaffected by the existence of uranium. On the other hand, the amount of uranium accumulated was strongly affected by the thorium, especially thorium addition after uranium accumulation. The decrease of uranium accumulated by the addition of thorium after the accumulation of uranium was higher than that from the solution containing both elements. Therefore, the contribution of uranium-thorium exchange reaction was higher than that of competition reaction. Accordingly, proton-uranium-thorium exchange reaction was occurred in the accumulation of thorium from the solution containing thorium and uranium. The gram-positive bacteria, such as Micrococcus luteus, Arthrobacter nicotianae, Bacillus subtilis and B. megaterium, has a much higher separation factor as thorium/uranium than that of actinomycetes. These gram-positive bacterial strains can be used for the accumulation of thorium from the solution containing uranium and thorium

The other side of cardiac Ca2+ signaling: transcriptional control

Directory of Open Access Journals (Sweden)

Alejandro eDomínguez-Rodríquez

2012-11-01

Full Text Available Ca2+ is probably the most versatile signal transduction element used by all cell types. In the heart, it is essential to activate cellular contraction in each heartbeat. Nevertheless Ca2+ is not only a key element in excitation-contraction coupling (EC coupling, but it is also a pivotal second messenger in cardiac signal transduction, being able to control processes such as excitability, metabolism, and transcriptional regulation. Regarding the latter, Ca2+ activates Ca2+-dependent transcription factors by a process called excitation-transcription coupling (ET coupling. ET coupling is an integrated process by which the common signaling pathways that regulate EC coupling activate transcription factors. Although ET coupling has been extensively studied in neurons and other cell types, less is known in cardiac muscle. Some hints have been found in studies on the development of cardiac hypertrophy, where two Ca2+-dependent enzymes are key actors: Ca2+/Calmodulin kinase II (CaMKII and phosphatase calcineurin, both of which are activated by the complex Ca2+/ /Calmodulin. The question now is how ET coupling occurs in cardiomyocytes, where intracellular Ca2+ is continuously oscillating. In this focused review, we will draw attention to location of Ca2+ signaling: intranuclear ([Ca2+]n or cytoplasmic ([Ca2+]c, and the specific ionic channels involved in the activation of cardiac ET coupling. Specifically, we will highlight the role of the 1,4,5 inositol triphosphate receptors (IP3Rs in the elevation of [Ca2+]n levels, which are important to locally activate CaMKII, and the role of transient receptor potential channels canonical (TRPCs in [Ca2+]c, needed to activate calcineurin.

Surface interactions of a W-DLC-coated biomedical AISI 316L stainless steel in physiological solution.

Science.gov (United States)

Antunes, Renato A; de Lima, Nelson Batista; Rizzutto, Márcia de Almeida; Higa, Olga Zazuco; Saiki, Mitiko; Costa, Isolda

2013-04-01

The corrosion stability of a W-DLC coated surgical AISI 316L stainless steel in Hanks' solution has been evaluated. Particle induced X-ray emission (PIXE) measurements were performed to evaluate the incorporation of potentially bioactive elements from the physiological solution. The film structure was analyzed by X-ray diffractometry and micro-Raman spectroscopy. The wear behavior was assessed using the sphere-on-disc geometry. The in vitro biocompatibility of the W-DLC film was evaluated by cytotoxicity tests. The corrosion resistance of the stainless steel substrate decreased in the presence of the PVD layer. EIS measurements suggest that this behavior was closely related to the corrosion attack through the coating pores. PIXE measurements revealed the presence of Ca and P in the W-DLC film after immersion in Hanks' solution. This result shows that the PIXE technique can be applied to identify and evaluate the incorporation of bioactive elements by W-DLC films. The film showed good wear resistance and biocompatibility.

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

Ca{sup 2+}/calmodulin-dependent protein kinase phosphatase (CaMKP/PPM1F) interacts with neurofilament L and inhibits its filament association

Energy Technology Data Exchange (ETDEWEB)

Ozaki, Hana [Laboratory of Molecular Brain Science, Graduate School of Integrated Arts and Sciences, Hiroshima University, Higashi-Hiroshima, 739-8521 (Japan); Katoh, Tsuyoshi [Department of Biochemistry, Asahikawa Medical University, Asahikawa, 078-8510 (Japan); Nakagawa, Ryoko; Ishihara, Yasuhiro [Laboratory of Molecular Brain Science, Graduate School of Integrated Arts and Sciences, Hiroshima University, Higashi-Hiroshima, 739-8521 (Japan); Sueyoshi, Noriyuki; Kameshita, Isamu [Department of Life Sciences, Faculty of Agriculture, Kagawa University, Kagawa, 761-0795 (Japan); Taniguchi, Takanobu [Department of Biochemistry, Asahikawa Medical University, Asahikawa, 078-8510 (Japan); Hirano, Tetsuo; Yamazaki, Takeshi [Laboratory of Molecular Brain Science, Graduate School of Integrated Arts and Sciences, Hiroshima University, Higashi-Hiroshima, 739-8521 (Japan); Ishida, Atsuhiko, E-mail: aishida@hiroshima-u.ac.jp [Laboratory of Molecular Brain Science, Graduate School of Integrated Arts and Sciences, Hiroshima University, Higashi-Hiroshima, 739-8521 (Japan)

2016-09-02

Ca{sup 2+}/calmodulin-dependent protein kinase phosphatase (CaMKP/PPM1F) is a Ser/Thr phosphatase that belongs to the PPM family. Growing evidence suggests that PPM phosphatases including CaMKP act as a complex with other proteins to regulate cellular functions. In this study, using the two-dimensional far-western blotting technique with digoxigenin-labeled CaMKP as a probe, in conjunction with peptide mass fingerprinting analysis, we identified neurofilament L (NFL) as a CaMKP-binding protein in a Triton-insoluble fraction of rat brain. We confirmed binding of fluorescein-labeled CaMKP (F-CaMKP) to NFL in solution by fluorescence polarization. The analysis showed that the dissociation constant of F-CaMKP for NFL is 73 ± 17 nM (n = 3). Co-immunoprecipitation assay using a cytosolic fraction of NGF-differentiated PC12 cells showed that endogenous CaMKP and NFL form a complex in cells. Furthermore, the effect of CaMKP on self-assembly of NFL was examined. Electron microscopy revealed that CaMKP markedly prevented NFL from forming large filamentous aggregates, suggesting that CaMKP-binding to NFL inhibits its filament association. These findings may provide new insights into a novel mechanism for regulating network formation of neurofilaments during neuronal differentiation. - Highlights: • NFL was identified as a CaMKP-binding protein in an insoluble fraction of rat brain. • CaMKP bound to NFL in solution with a K{sub d} value of 73 ± 17 nM. • A CaMKP-NFL complex was found in NGF-differentiated PC12 cells. • CaMKP-binding to NFL inhibited its filament association. • CaMKP may regulate network formation of neurofilaments in neurons.

Multielement determination of major-to-ultratrace elements in plant reference materials by ICP-AES/ICP-MS and evaluation of their enrichment factors

International Nuclear Information System (INIS)

Hokura, Akiko; Matsuura, Hirotaka; Katsuki, Fumie; Haraguchi, Hiroki

2000-01-01

The multielement determination of major-to-ultratrace elements in plant reference materials (SRM Pine Needles, SRM Tomato Leaves, and NIES Tea Leaves) was carried out by ICP-AES (inductively coupled plasma atomic emission spectrometry) and ICP-MS (inductively coupled plasma mass spectrometry). The plant sample was decomposed with nitric acid and hydrofluoric acid in a Teflon beaker on a hot plate. The digest was dissolved in 1 M HNO 3 solution, and then subjected to elemental analyses. As a consequence, the analytical data for about 40 elements including rare earth elements (REEs) were obtained over a wide concentration range, for example, from 49600 μg g -1 of Ca to 6.2 ng g -1 of Lu in Tomato Leaves. The enrichment factors, which were estimated by normalizing the observed concentrations of analyte elements in plant reference materials to their soil abundances, were evaluated in order to discuss the relative abundances of various elements between plants and soil. It was found that most of the elements, except for REEs in Pine Needles and Tea Leaves, were significantly accumulated in the plant reference materials. In particular, the essential elements (K, Mg, Ca, Mn, Cu, Zn, B and P) for plant growth provided large enrichment factors. (author)

XRF and TXRF techniques for multi-element determination of trace elements in whole blood and human hair samples

International Nuclear Information System (INIS)

Khuder, A.; Karjou, J.; Sawan, M.Kh.; Bakir, M.A.

2007-01-01

XRF and TXRF were established as useful techniques for multi-element analysis of whole blood and human head hair samples. Direct-XRF with different collimation units and different X-ray excitation modes was successfully used for the determination of S, P, K, Ca, Fe, and Br elements in blood samples and K, Ca, Mn, Fe elements in human hair samples. Direct analysis by TXRF was used for the determination of Rb and Sr in digested blood and human hair samples, respectively, while, the co-precipitation method using APDC for TXRF analysis was used for the determination of Ni, Cu, Zn, and Pb elements in both matrices. As a result, the improved XRF and TXRF methods were applied for multi-element determination of elements in whole blood and human hair samples in non-occupational exposed population living in Damascus city. The mean concentrations of analyzed elements in both matrices were on the reported range values for non-occupational population in other countries. (author)

XRF and TXRF techniques for multi-element determination of trace elements in whole blood and human hair samples

International Nuclear Information System (INIS)

Khuder, A.; Karjou, J.; Sawan, M.Kh.; Bakir, M.A.

2008-01-01

XRF and TXRF were established as useful techniques for multi-element analysis of whole blood and human head hair samples. Direct-XRF with different collimation units and different X-ray excitation modes was successfully used for the determination of S, P, K, Ca, Fe, and Br elements in blood samples and K, Ca, Mn, Fe elements in human hair samples. Direct analysis by TXRF was used for the determination of Rb and Sr in digested blood and human hair samples, respectively, while, the co-precipitation method using APDC for TXRF analysis was used for the determination of Ni, Cu, Zn, and Pb elements in both matrices. As a result, the improved XRF and TXRF methods were applied for multi-element determination of elements in whole blood and human hair samples in non-occupational exposed population living in Damascus city. The mean concentrations of analyzed elements in both matrices were on the reported range values for non-occupational population in other countries. (author)

Solidification and Immobilization of Heavy metals in Soil using with nano-metallic Ca/CaO Dispersion Mixture

Directory of Open Access Journals (Sweden)

Mallampati S. R.

2013-04-01

Full Text Available In the present work, the use of nano-metallic calcium (Ca and calcium oxide (CaO dispersion mixture for the immobilization of heavy metals (As, Cd, Cr and Pb in soil was investigated. With simple grinding, 85-90% of heavy metals immobilization could be achieved, while it could be enhanced to 98-100% by grinding with the addition of nano-metallic Ca/CaO dispersion mixture. By SEM-EDS elemental maps as well as semi-quantitative analysis observed that the amount of As, Cd, Cr and Pb measurable on soil particle surface decreases after nano-metallic Ca/CaO treatment. The leachable heavy metals concentrations were reduced, to the concentration lower than the Japan soil elution standard regulatory threshold, i. e., < 0.01 mg/l for As, Cd and Pb and 0.05mg/l for Cr. Whereas, the effect of soil moisture and pH on heavy metals immobilization was not much influenced. The results suggest that nano-metallic Ca/CaO mixture is suitable to be used for the gentle immobilization of heavy metals contaminated soil at normal moisture conditions.

Study of trace element metabolism in normal and cancerous mice using multitracer technique

International Nuclear Information System (INIS)

Wang Xiao; Kong Fuquan; Zhao Kui; Zhang Xiang; Qin Zhi

2008-01-01

A radioactive multitracer solution of the 24 elements, e.g. Be, Na, K, Rb, Mg, Ca, Sr, Ga, As, Sc, V, Cr, Mn, Co, Fe, Zn, Y, Zr, Mo, Nb, To, Ru, Ag and In, was obtained from the nuclear reaction of 25 MeV/u 40 Ar + Se with a series of chemical process. The multitracer solution was orally administered to normal and muscular turnout-bearing mice of male Balb/c mice. Urine and faeces samples of mice were collected. The two group mice were saerificed after 96 h. The uptake of 17 elements, Na, Rb, Ga, As, Sc, V, Cr, Mn, Co, Fe, Zn, Y, Zr, Tc, Ru, Ag and In, were simultaneously detected in normal mice while 15 elements, Na, Rb, Ga, Sc, V, Cr, Mn, Co, Fe, Y, Zr, Tc, Ru, Ag and In, were simultaneously detected in tumour-bearing mice. Our results indicate that the majority of the detected elements were distributed in liver, kidney, pelt, turnout while a small fraction of the biotrace elements were distributed in heart and spleen. (tumour-bearing mice) in the two groups of mice. The higher concentrations of Fe, Na, Mn were detected in heart or kidney of normal mice. Na, Mn, Fe and Co showed better absorption in most tissues in the normal mice, except for Na and Mn in heart. (authors)

Measurement of Ca, Zn and Sr in enamel of human teeth by XRF

Energy Technology Data Exchange (ETDEWEB)

Wielopolski, L.; Featherstone, J.D.B.; Cohn, S.H.

1984-01-01

Energy dispersive x-ray fluorescence (EDXRF) has been employed to measure Ca, Zn, and Sr in enamel of human teeth. The calibration of the EDXRF system was performed by comparing Sr/Ca ratios with values obtained by atomic absorption analysis of acid etched biopsies of the enamel surface. Two calibration lines were obtained, one line for untreated teeth and the second line for teeth immersed (treated) in solutions containing Sr. A simple analytical model demonstrated that the two calibration lines were the result of the difference in the depth of the enamel sampled by EDXRF and by the acid-etched biopsy. The multi-elemental, non-destructive and quantitative aspects of EDXRF permit the sequential monitoring of the effects of Sr and Zn ions on the mineralization and demineralization processes in human enamel. The portability of the system and adaptability to non-invasive measurements makes it suitable for field studies. 26 references, 4 figures.

Measurement of Ca, Zn and Sr in enamel of human teeth by XRF

International Nuclear Information System (INIS)

Wielopolski, L.; Featherstone, J.D.B.; Cohn, S.H.

1984-01-01

Energy dispersive x-ray fluorescence (EDXRF) has been employed to measure Ca, Zn, and Sr in enamel of human teeth. The calibration of the EDXRF system was performed by comparing Sr/Ca ratios with values obtained by atomic absorption analysis of acid etched biopsies of the enamel surface. Two calibration lines were obtained, one line for untreated teeth and the second line for teeth immersed (treated) in solutions containing Sr. A simple analytical model demonstrated that the two calibration lines were the result of the difference in the depth of the enamel sampled by EDXRF and by the acid-etched biopsy. The multi-elemental, non-destructive and quantitative aspects of EDXRF permit the sequential monitoring of the effects of Sr and Zn ions on the mineralization and demineralization processes in human enamel. The portability of the system and adaptability to non-invasive measurements makes it suitable for field studies. 26 references, 4 figures

Measurement of Ca, Zn, and Sr in enamel of human teeth by XRF

International Nuclear Information System (INIS)

Wielopolski, L.; Featherstone, J.D.b.; Cohn, S.H.

1984-01-01

Energy dispersive x-ray fluorescence (EDXRF) has been employed to measure Ca, Zn, and Sr in enamel of human teeth. The calibration of the EDXRF system was performed by comparing Sr/Ca ratios with values obtained by atomic absorption analysis of acid etched biopsies of the enamel surface. Two calibration lines were obtained, one line for untreated teeth and the second line for teeth immersed (treated) in solutions containing Sr. A simple analytical model demonstrated that the two calibration lines were the result of the difference in the depth of the enamel sampled by EDXRF and by the acid-etched biopsy. The multi-elemental, non-destructive and quantitative aspects of EDXRF permit the sequential monitoring of the effects of Sr and Zn ions on the mineralization and demineralization processes in human enamel. The portability of the system and adaptability to non-invasive measurements makes it suitable for field studies. 26 references, 4 figures

A mathematical model for chemical reactions with actinide elements in the aqueous nitric acid solution: REACT

International Nuclear Information System (INIS)

Tachimori, Shoichi

1990-02-01

A mathematical model of chemical reactions with actinide elements: REACT code, was developed to simulate change of valency states of U, Pu and Np in the aqueous nitric acid solution. Twenty seven rate equations for the redox reactions involving some reductants, disproportionation reactions, and radiolytic growth and decay reaction of nitrous acid were programmed in the code . Eight numerical solution methods such as Porsing method to solve the rate equations were incorporated parallel as options depending on the characteristics of the reaction systems. The present report gives a description of the REACT code, e.g., chemical reactions and their rate equations, numerical solution methods, and some examples of the calculation results. A manual and a source file of the program was attached to the appendix. (author)

A study on removal of elemental mercury in flue gas using fenton solution

International Nuclear Information System (INIS)

Liu, Yangxian; Wang, Yan; Wang, Qian; Pan, Jianfeng; Zhang, Yongchun; Zhou, Jianfei; Zhang, Jun

2015-01-01

Highlights: • A novel technique on oxidation of Hg 0 using Fenton was proposed. • The effects of several process parameters on Hg 0 removal were studied. • Products and ·OH in solution were detected. • Reaction mechanism of Hg 0 removal was studied. • Simultaneous removal of Hg 0 , NO and SO 2 was also studied. - Abstract: A novel technique on oxidation-separation of elemental mercury (Hg 0 ) in flue gas using Fenton solution in a bubbling reactor was proposed. The effects of several process parameters (H 2 O 2 concentration, Hg 0 inlet concentration, Fe 2+ concentration, solution temperature, solution pH, gas flow) and several flue gas components (NO, SO 2 , O 2 , CO 2 , inorganic ions and particulate matters on Hg 0 removal were studied. The results indicate that H 2 O 2 concentration, Fe 2+ concentration, solution pH and gas flow have great effects on Hg 0 removal. Solution temperature, Hg 0 , NO, SO 2 , CO 3 2− and HCO 3 − concentrations also have significant effects on Hg 0 removal. However, Cl − , SO 4 2− , NO 3 − , O 2 and CO 2 concentrations only have slight effects on Hg 0 removal. Furthermore, reaction mechanism of Hg 0 removal and simultaneous removal process of Hg 0 , NO and SO 2 were also studied. Hg 0 is removed by oxidation of ·OH and oxidation of H 2 O 2 . The simultaneous removal efficiencies of 100% for SO 2 , 100% for Hg 0 and 88.3% for NO were obtained under optimal test conditions. The results demonstrated the feasibility of Hg 0 removal and simultaneous removal of Hg 0 , SO 2 and NO using Fenton solution in a bubbling reactor

Soil solution chemistry and element fluxes in three European heathlands and their responses to warming and drought

DEFF Research Database (Denmark)

Schmidt, I.K.; Tietema, A.; Williams, D.

2004-01-01

Soil water chemistry and element budgets were studied at three northwestern European Calluna vulgaris heathland sites in Denmark (DK), The Netherlands (NL), and Wales (UK). Responses to experimental nighttime warming and early summer drought were followed during a two-year period. Soil solution...

Natural rain - induced element leaching from coal ASH; La pluie naturelle - lixiviation d'element de la cendre de charbon

Energy Technology Data Exchange (ETDEWEB)

Popovic, A.; Djordjevic, D.; Polic, P. [Belgrade Univ., Dept. of Chemistry, IChTM, Chemistry Center, Belgrade (Yugoslavia)

2000-07-01

Six composite samples of coal ash from power plants 'Nikola Tesla' A and B, located in the vicinity of Obrenovac, near Belgrade (Yugoslavia), were subjected to extraction with 1 M acetate solution, pH 5.5, in order to imitate possible leaching of the ash by natural acidic rain. Seven trace and five major elements have been examined, and the obtained amounts were in the range from 0.003 {+-} 0.001 ppm (Cd), to 117 {+-} 27 ppm (Ca), dry ash basis. Though some of the concentrations were higher than allowed by domestic and international regulations it can be concluded that neither of the examined elements represents a serious threat for the environment (at least for the conditions applied in this experiment). Also, both magnesium and iron are carriers of copper, chromium and arsenic, while cadmium is associated with magnesium and manganese. Calcium and manganese are beside magnesium and iron, scavengers of arsenic. (authors)

Studies on the numerical solution of three-dimensional stationary diffusion equations using the finite element method

International Nuclear Information System (INIS)

Franke, H.P.

1976-05-01

The finite element method is applied to the solution of the stationary 3D group diffusion equations. For this, a programme system with the name of FEM3D is established which also includes a module for semi-automatic mesh generation. Tetrahedral finite elements are used. The neutron fluxes are described by complete first- or second-order Lagrangian polynomials. General homogeneous boundary conditions are allowed. The studies show that realistic three-dimensional problems can be solved at less expense by iterative methods, in particular so when especially adapted matrix handling and storage schemes are used efficiently. (orig./RW) [de

Atoms, molecules & elements

CERN Document Server

Graybill, George

2007-01-01

Young scientists will be thrilled to explore the invisible world of atoms, molecules and elements. Our resource provides ready-to-use information and activities for remedial students using simplified language and vocabulary. Students will label each part of the atom, learn what compounds are, and explore the patterns in the periodic table of elements to find calcium (Ca), chlorine (Cl), and helium (He) through hands-on activities.

Quantitative analysis of sodium di-uranate for Al, Ca, Fe, Mg, Mn, Na by flame-atomic absorption spectrometric method

International Nuclear Information System (INIS)

Jat, J.R.; Balaji Rao, Y.; Subba Rao, Y.

2015-01-01

Nuclear Fuel Complex (NFC) receives Sodium Di-Uranate (SDU) from Uranium Corporation of India Limited (UCIL) for producing sinterable UO 2 pellets for manufacturing fuel sub assemblies. Several impurities present in ore find their way into SDU during its conversion. Stringent specification have been laid down by the reactor designs for achieving the optimum performance of the fuel and several impurity element like Al, Ca, Fe, Mg, Mn, Na among others affects severely performance of UO 2 fuel. Most of the impurity including the above mentioned elements are generally analysed by ICP-OES method. However, determination of Al, Ca, Fe, Mg, Mn and Na by ICP-OES requires lot of dilution as they are present at high levels in SDU. Apart from introducing dilution error, dilution process is very tedious and time consuming work and not a preferred choice in an industrial lab like control lab where large analytical load exists and time bound analysis is a requirement. To avoid these difficulties a simple and reliable Flame Atomic absorption spectrometric technique has been developed for regular analysis. Present method involves dissolution of SDU sample in Conc. HNO 3 and after the complete dissolution the sample solution has been evaporated to near dryness on a hot plate. Subsequently sample solution has been brought into 4N HNO 3 medium

Accumulation of elements by edible mushroom species II. A comparison of aluminium, barium and nutritional element contents.

Science.gov (United States)

Mleczek, Mirosław; Siwulski, Marek; Stuper-Szablewska, Kinga; Sobieralski, Krzysztof; Magdziak, Zuzanna; Goliński, Piotr

2013-01-01

The aim of the study was to compare accumulation efficiency of Al, Ba and nutritional elements (Ca, Fe, K, Mg, Mn, Na) exhibited by six edible mushrooms collected in particular regions of Poland during the last 20 years. The studied mushroom species were Boletus edulis, Cantharellus cibarius, Lactarius deliciosus, Leccinum aurantiacum, Suillus luteus and Xerocomus badius. The highest and the lowest concentrations of the elements in tested mushroom species were 11 - 410, 34 - 337, 16785 - 34600, 140 - 607, 12 - 75 and 16 - 143 mg kg(-1)d.m., respectively. The highest average concentrations of Al, Mg and Mn were observed in Suillus luteus fruiting bodies, while for Ba, Ca, K and Na it was in Lactarius deliciosus. BCF >1 was found for K and Mg in all tested mushroom species and additionally for the highest Ca and Na concentrations of all tested mushroom species except for C. cibarius and S. luteus, respectively. For the other tested elements (Al, Ba, Fe and Mn) BCF values < 1 were recorded.

An Experimental and Finite Element Protocol to Investigate the Transport of Neutral and Charged Solutes across Articular Cartilage.

Science.gov (United States)

Arbabi, Vahid; Pouran, Behdad; Zadpoor, Amir A; Weinans, Harrie

2017-04-23

Osteoarthritis (OA) is a debilitating disease that is associated with degeneration of articular cartilage and subchondral bone. Degeneration of articular cartilage impairs its load-bearing function substantially as it experiences tremendous chemical degradation, i.e. proteoglycan loss and collagen fibril disruption. One promising way to investigate chemical damage mechanisms during OA is to expose the cartilage specimens to an external solute and monitor the diffusion of the molecules. The degree of cartilage damage (i.e. concentration and configuration of essential macromolecules) is associated with collisional energy loss of external solutes while moving across articular cartilage creates different diffusion characteristics compared to healthy cartilage. In this study, we introduce a protocol, which consists of several steps and is based on previously developed experimental micro-Computed Tomography (micro-CT) and finite element modeling. The transport of charged and uncharged iodinated molecules is first recorded using micro-CT, which is followed by applying biphasic-solute and multiphasic finite element models to obtain diffusion coefficients and fixed charge densities across cartilage zones.

High-pressure synthesis and structural, physical properties of CaIr1-xPtxO3 and CaIr1-xRhxO3

Science.gov (United States)

Hirai, S.; Bromiley, G. D.; Klemme, S.; Irifune, T.; Ohfuji, H.; Attfield, P.; Nishiyama, N.

2010-12-01

Since the discovery of the perovskite to post-perovskite transition in MgSiO3 in a laser-heated DAC, wide attention has been focussed on the post-perovskite phase of MgSiO3. This is because the post-perovskite phase is likely to play a key role in Earth’s lowermost mantle, and because the perovskite to post-perovskite transition can explain many features of the D” seismic discontinuity. While it is meaningful to conduct further studies of MgSiO3, the post-perovskite phase of MgSiO3 cannot be quenched to ambient pressure/temperature conditions. Thus, further studies must be conducted using analogue compounds of MgSiO3 post-perovskite, which are quenchable to ambient pressure/temperature conditions. The post-perovskite phase of MgSiO3 crystallizes in a layered structure with CaIrO3-structure. Therefore, it is useful to investigate compounds with CaIrO3-structure. There are only four quenchable oxides with CaIrO3-structure reported to date: CaIrO3, CaPtO3, CaRhO3 and CaRuO3. CaIrO3 can be synthesized at ambient pressure, whilst the other three oxides can only be obtained at high pressure/temperature conditions using a multi-anvil apparatus. Further studies on these materials have revealed structural phase transitions at high P-T and a metal-insulator transition by hole doping. In the case of CaIrO3, The post-perovskite phase of CaIrO3 synthesized at 2GPa, 1373K transforms into a perovskite phase at 2GPa, 1673K. In other words, the perovskite phase can be synthesized at temperatures higher than those needed for synthesizing the post-perovskite phase. This is also the case for CaRhO3 (6GPa, 1873K) and CaRuO3 (23GPa, 1343K), while CaPtO3 remained post-perovskite at higher temperatures. We have succeeded in synthesizing solid solutions between CaIrO3, CaPtO3 and CaRhO3. We have found the systematic change in structural and physical properties of post-perovskite oxides, with composition and P-T, which broadens the future opportunity for studying post-perovskite systems

Corrosion studies of thermally sensitised AGR fuel element brace in pH7 and pH9.2 borate solutions

International Nuclear Information System (INIS)

Tyfield, S.P.; Smith, C.A.

1987-04-01

Brace and cladding of AGR fuel elements sensitised in reactor are susceptible to intergranular and crevice corrosion, which may initiate in the pH7 borate pond storage environment of CEGB/SSEB stations. This report considers the benefit in corrosion control that is provided by raising the pond solution pH to 9.2, whilst maintaining the boron level at 1250 gm -3 . The greater corrosion protection provided by pH9.2 solution compared to the pH7 borate solution is demonstrated by a series of tests with non-active laboratory sensitised brace samples exposed to solutions dosed with chloride or sulphate in order to promote localised corrosion. The corrosion tests undertaken consisted of 5000 hour immersions at 32 0 C and shorter term electrochemically monitored experiments (rest potential, impedance, anodic current) generally conducted at 22 0 C. The pH9.2 solution effectively inhibited the initiation of crevice and intergranular corrosion in the presence of low levels of chloride and sulphate, whereas the pH7 solution did not always do so. However, the pH9.2 solution, dosed with 40 gm -3 chloride, failed to suppress fully crevice corrosion initiated in unborated 40 gm -3 chloride solution at 22 0 C. Fluoride is not deleterious at low levels ∼ 10 gm -3 in the borate solutions. The significant improvement in corrosion control demonstrated for the change from pH7 to pH9.2 borate solution on laboratory sensitised brace samples should ideally be confirmed using complete irradiated AGR fuel elements. (U.K.)

Distribution of copper and other elements in ryegrass roots, determined with a scanning proton microprobe

International Nuclear Information System (INIS)

Mazzolini, A.P.; Legge, G.J.F.

1982-01-01

A scanning proton microprobe has been used to determine the distribution of Cu and other elements in Wimmera ryegrass roots grown in solution cultures. Cu was found to be localized on or near the surface of the roots in randomly distributed discrete zones. The distribution of Cu was partially correlated with those of Fe, P and Ca and possibly indicates some form of association; co-precipitation in a precipitate of ferric phosphate or hydroxy-oxide is favoured

On the application of finite element method in the solution of steady state diffusion equation

International Nuclear Information System (INIS)

Ono, S.

1982-01-01

The solution of the steady state neutron diffusion equation is obtained by using the finite element method. Specifically the variational approach is used for one dimensional problems and the weighted residual method (Galerkin) for one and two dimensional problems. The spatial domain is divided into retangular elements and the neutron flux is approximated by linear (one dimensional case), and bilinear (two-dimensional case) functions. Numerical results are obtained with a FORTRAN IV computer program and compared with those obtained by the finite difference CITATION code. The results show that linear or bilinear functions, do not satisfactorily describe the differential parameters in highly heterogeneous reactor cases, but provide good results for integral parameters such as multiplication factor. (Author) [pt

Spectrographic determination of impurities in enriched uranium solutions

International Nuclear Information System (INIS)

Capdevila, C.; Roca, M.

1980-01-01

A spectrographic procedure for the determination of trace amounts of Al, B, Ba, Be, Bi, Ca, Cd, Co, Cr, Cu, Fe, K, L i , Hg, Mn, Mo, Na, Nb, Ni, P, Pb, Ru, Sb, Sn, Sr, Ti, V, Zn, and Zr in enriched uranyl nitrate solutions from the reprocessing of spent nuclear fuels is described. After removal of uranium by either TBP or TNOA solvent extraction, the aqueous phase Is analysed by the graphite spark technique. TBP is adequate for all impurities, excepting boron and phosphorus; both of these elements can sat is factory be determined by using TNOA after the addition of mannitol to avoid boron losses. (Author) 4 refs

Extraction of Eu, Am, Ca a Sr by the nitrobenzene solution of dicarbollylcobaltate in nitrobenzene in the presence of diphosphine oxides

International Nuclear Information System (INIS)

Vanura, P.; Makrlik, E.; Selucky, P.

2015-01-01

Extraction of microamounts of Eu 3+ , Am 3+ , Ca 2+ and Sr 2+ with a nitrobenzene solution of hydrogen dicarbollylcobaltate (H+B) in the presence of substituted bis-diphenylphosphine dioxides was investigated and discussed. It was find that diphenylphosphine dioxides can be used for the extraction of the above metal. The most efficient extraction reagent is bis(diphenylphosphino)methane dioxide. The stability constants of some species formed in the organic phase were calculated. (author)

Kinetics of element profile pattern during life cycle stage of morning-glory

International Nuclear Information System (INIS)

Nakanishi, T.M.; Tamada, M.

1999-01-01

The kinetics of seven element profiles, macroscopic elements, Na, Mg, Cl, K and Ca, as well as Al and Br, in every tissue of morning-glory (Ipomoea nil L. c.v. Murasaki), from seedling to flowering stage are presented. Barriers for the elements were formed even in the same tissue during different growing phases. Most of Na and Al remained in root tissue, showing the first barrier to the upper part of the plant. During the juvenile phase, the tissues lower than cotyledon stored the elements, especially Ca and Mg. The barrier at cotyledon did not disappear completely until seed ripening stage, except for K. Generally, late developing stem showed lower accumulation of the elements, which seemed to regulate the inflow of Mg, Ca, Cl and Br into flowering tissue. The concentrations of K, Ca, Cl and Br in leaf were kept constant in spite of twice or three times higher concentration of these elements in leaf petiole. After flowering, selective element accumulation was observed during seed development, where most of the elements were accumulated into seed wall, not in seed. Higher concentration of the elements in elder leaf, which falls into ground and will be reused as plant nutrient, might reflect the recycling system of the elements in plants. (author)

Application of neutron activation analysis to the determination of minor-and trace elements in magnesite ore

International Nuclear Information System (INIS)

Sepulveda Munita, C.J.A.; Atalla, L.T.

1979-01-01

A method employing analysis with thermal neutrons was developed for analyzing magnesite samples coming from the States do Ceara and Bahia (Brazil). Ten samples were analyzed. Qualitative analysis of the samples indicated the presence of Mn, Fe, Sc, Ca, Cu, Co and some of the lanthanides. Mn was analyzed by non-destructive activation analysis and the other elements were analyzed, individually or in group, after sample dissolution with 8 N HCl solution. A detailed study of the possible interferences in neutron activation analysis of the elements considered was also undertaken. The precision and accuracy of the results obtained and the sensitivity of the method are discussed. (Author) [pt

Improved creep strength of nickel-base superalloys by optimized γ/γ′ partitioning behavior of solid solution strengthening elements

International Nuclear Information System (INIS)

Pröbstle, M.; Neumeier, S.; Feldner, P.; Rettig, R.; Helmer, H.E.; Singer, R.F.; Göken, M.

2016-01-01

Solid solution strengthening of the γ matrix is one key factor for improving the creep strength of single crystal nickel-base superalloys at high temperatures. Therefore a strong partitioning of solid solution hardening elements to the matrix is beneficial for high temperature creep strength. Different Rhenium-free alloys which are derived from CMSX-4 are investigated. The alloys have been characterized regarding microstructure, phase compositions as well as creep strength. It is found that increasing the Titanium (Ti) as well as the Tungsten (W) content causes a stronger partitioning of the solid solution strengtheners, in particular W, to the γ phase. As a result the creep resistance is significantly improved. Based on these ideas, a Rhenium-free alloy with an optimized chemistry regarding the partitioning behavior of W is developed and validated in the present study. It shows comparable creep strength to the Rhenium containing second generation alloy CMSX-4 in the high temperature / low stress creep regime and is less prone to the formation of deleterious topologically close packed (TCP) phases. This more effective usage of solid solution strengtheners can enhance the creep properties of nickel-base superalloys while reducing the content of strategic elements like Rhenium.

Modeling in architectural-planning solutions of agrarian technoparks as elements of the infrastructure

Science.gov (United States)

Abdrassilova, Gulnara S.

2017-09-01

In the context of development of the agriculture as the driver of the economy of Kazakhstan it is imperative to study new types of agrarian constructions (agroparks, agrotourists complexes, "vertical" farms, conservatories, greenhouses) that can be combined into complexes - agrarian technoparks. Creation of agrarian technoparks as elements of the infrastructure of the agglomeration shall ensure the breakthrough in the field of agrarian goods production, storing and recycling. Modeling of architectural-planning solutions of agrarian technoparks supports development of the theory and practice of designing objects based on innovative approaches.

Fixation and separation of the elements thorium and uranium using anion exchange resins in nitrate solution

International Nuclear Information System (INIS)

Korgaonkar, V.

1967-10-01

The exchange of thorium and uranium between a strong base anion resin and a mixed water + ethanol solvent containing nitrate ions is studied. It is assumed that in the resin the thorium and uranium are fixed in the form of the complexes Th(NO 3 ) 6 2- and UO 2 (NO 3 ) 4 2- in solution these elements are present in the form of complexes having the general formula: Th(NO 3 ) 6-n n-2 and UO 2 (NO 3 ) 4-n n-2 It has been possible to deduce a law for the changes in the partition functions of thorium and uranium as a function of the concentrations of the various species in solution and of the complexing ion NO 3 . From this has been deduced the optimum operational conditions for separating a mixture of these two elements. Finally, in these conditions, the influence of a few interfering ions has been studied: Ba, Bi, Ce, La, Mo, Pb, Zr. The method proposed can be used either as a preparation, or for the dosage of thorium by a quantitative separation. (author) [fr

Mineral elements and essential trace elements in blood of seals of the North Sea measured by total-reflection X-ray fluorescence analysis

International Nuclear Information System (INIS)

Griesel, S.; Mundry, R.; Kakuschke, A.; Fonfara, S.; Siebert, U.; Prange, A.

2006-01-01

Mineral and essential trace elements are involved in numerous physiological processes in mammals. Often, diseases are associated with an imbalance of the electrolyte homeostasis. In this study, the concentrations of mineral elements (P, S, K, Ca) and essential trace elements (Fe, Cu, Zn, Se, Rb, Sr) in whole blood of harbor seals (Phoca vitulina) were determined using total-reflection X-ray fluorescence spectrometry (TXRF). Samples from 81 free-ranging harbor seals from the North Sea and two captive seals were collected during 2003-2005. Reference ranges and element correlations for health status determination were derived for P, S, K, Ca, Fe, Cu, and Zn level in whole blood. Grouping the seals by age, gender and sample location the concentration levels of the elements were compared. The blood from two captive seals with signs of diseases and four free-ranging seals showed reduced element levels of P, S, and Ca and differences in element correlation of electrolytes were ascertained. Thus, simultaneous measurements of several elements in only 500 μL volumes of whole blood provide the possibility to obtain information on both, the electrolyte balance and the hydration status of the seals. The method could therefore serve as an additional biomonitoring tool for the health assessment

Separation and Recycling for Rare Earth Elements by Homogeneous Liquid-Liquid Extraction (HoLLE Using a pH-Responsive Fluorine-Based Surfactant

Directory of Open Access Journals (Sweden)

Shotaro Saito

2015-08-01

Full Text Available A selective separation and recycling system for metal ions was developed by homogeneous liquid-liquid extraction (HoLLE using a fluorosurfactant. Sixty-two different elemental ions (e.g., Ag, Al, As, Au, B, Ba, Be, Bi, Ca, Cd, Ce, Co, Cr, Cu, Dy, Er, Eu, Fe, Ga, Gd, Ge, Hf, Hg, Ho, In, Ir, La, Lu, Mg, Mn, Mo, Nb, Nd, Ni, Os, P, Pb, Pd, Pr, Pt, Re, Rh, Ru, Sb, Sc, Se, Si, Sm, Sn, Sr, Ta, Tb, Te, Ti, Tl, Tm, V, W, Y, Yb, Zn, and Zr were examined. By changing pH from a neutral or alkaline solution (pH ≥ 6.5 to that of an acidic solution (pH < 4.0, gallium, zirconium, palladium, silver, platinum, and rare earth elements were extracted at >90% efficiency into a sedimented Zonyl FSA® (CF3(CF2n(CH22S(CH22COOH, n = 6–8 liquid phase. Moreover, all rare earth elements were obtained with superior extraction and stripping percentages. In the recycling of rare earth elements, the sedimented phase was maintained using a filter along with a mixed solution of THF and 1 M sodium hydroxide aqueous solution. The Zonyl FSA® was filtrated and the rare earth elements were recovered on the filter as a hydroxide. Furthermore, the filtrated Zonyl FSA was reusable by conditioning the subject pH.

Elements and inorganic ions as source tracers in recent Greenland snow

Science.gov (United States)

Lai, Alexandra M.; Shafer, Martin M.; Dibb, Jack E.; Polashenski, Chris M.; Schauer, James J.

2017-09-01

Atmospheric transport of aerosols leads to deposition of impurities in snow, even in areas of the Arctic as remote as Greenland. Major ions (e.g. Na+, Ca2+, NH4+, K+, SO42-) are frequently used as tracers for common aerosol sources (e.g. sea spray, dust, biomass burning, anthropogenic emissions). Trace element data can supplement tracer ion data by providing additional information about sources. Although many studies have considered either trace elements or major ions, few have reported both. This study determined total and water-soluble concentrations of 31 elements (Al, As, Ca, Cd, Ce, Co, Cr, Dy, Eu, Fe, Gd, K, La, Mg, Mn, Na, Nb, Nd, Pb, Pr, S, Sb, Si, Sm, Sn, Sr, Ti, V, U, Y, Zn) in shallow snow pits at 22 sampling sites in Greenland, along a transect from Summit Station to sites in the northwest. Black carbon (BC) and inorganic ions were measured in colocated samples. Sodium, which is typically used as a tracer of sea spray, did not appear to have any non-marine sources. The rare earth elements, alkaline earth elements (Mg, Ca, Sr), and other crustal elements (Fe, Si, Ti, V) were not enriched above crustal abundances relative to Al, indicating that these elements are primarily dust sourced. Calculated ratios of non-sea salt Ca (nssCa) to estimated dust mass affirm the use of nssCa as a dust tracer, but suggest up to 50% uncertainty in that estimate in the absence of other crustal element data. Crustal enrichment factors indicated that As, Cd, Pb, non-sea-salt S, Sb, Sn, and Zn were enriched in these samples, likely by anthropogenic sources. Principal component analysis indicated more than one crustal factor, and a variety of factors related to anthropogenically enriched elements. Analysis of trace elements alongside major tracer ions does not change interpretation of ion-based source attribution for sources that are well-characterized by ions, but is valuable for assessing uncertainty in source attribution and identifying sources not represented by major ions.

[Study on the determination of 14 inorganic elements in coffee by inductively coupled plasma mass spectrometry].

Science.gov (United States)

Nie, Xi-Du; Fu, Liang

2013-07-01

Samples of coffee were digested by microwave digestion, and inorganic elements amounts of Na, Mg, P, Ca, Cr, Mn, Fe, Co, Cu, Zn, As, Se, Mo and Pb in sample solutions were determined by inductively coupled plasma mass spectrometry (ICP-MS). HNO3 + H2O2 was used to achieve the complete decomposition of the organic matrix in a closed-vessel microwave oven. The working parameters of the instrument were optimized. The results showed that the relative standard deviation (RSD) was less than 3.84% for all the elements, and the recovery was found to be 92.00% -106.52% by adding standard recovery experiment. This method was simple, sensitive and precise and can perform simultaneous multi-elements determination of coffee, which could satisfy the sample examination request and provide scientific rationale for determining inorganic elements of coffee.

A spatially adaptive grid-refinement approach for the finite element solution of the even-parity Boltzmann transport equation

International Nuclear Information System (INIS)

Mirza, Anwar M.; Iqbal, Shaukat; Rahman, Faizur

2007-01-01

A spatially adaptive grid-refinement approach has been investigated to solve the even-parity Boltzmann transport equation. A residual based a posteriori error estimation scheme has been utilized for checking the approximate solutions for various finite element grids. The local particle balance has been considered as an error assessment criterion. To implement the adaptive approach, a computer program ADAFENT (adaptive finite elements for neutron transport) has been developed to solve the second order even-parity Boltzmann transport equation using K + variational principle for slab geometry. The program has a core K + module which employs Lagrange polynomials as spatial basis functions for the finite element formulation and Legendre polynomials for the directional dependence of the solution. The core module is called in by the adaptive grid generator to determine local gradients and residuals to explore the possibility of grid refinements in appropriate regions of the problem. The a posteriori error estimation scheme has been implemented in the outer grid refining iteration module. Numerical experiments indicate that local errors are large in regions where the flux gradients are large. A comparison of the spatially adaptive grid-refinement approach with that of uniform meshing approach for various benchmark cases confirms its superiority in greatly enhancing the accuracy of the solution without increasing the number of unknown coefficients. A reduction in the local errors of the order of 10 2 has been achieved using the new approach in some cases

A spatially adaptive grid-refinement approach for the finite element solution of the even-parity Boltzmann transport equation

Energy Technology Data Exchange (ETDEWEB)

Mirza, Anwar M. [Department of Computer Science, National University of Computer and Emerging Sciences, NUCES-FAST, A.K. Brohi Road, H-11, Islamabad (Pakistan)], E-mail: anwar.m.mirza@gmail.com; Iqbal, Shaukat [Faculty of Computer Science and Engineering, Ghulam Ishaq Khan (GIK) Institute of Engineering Science and Technology, Topi-23460, Swabi (Pakistan)], E-mail: shaukat@giki.edu.pk; Rahman, Faizur [Department of Physics, Allama Iqbal Open University, H-8 Islamabad (Pakistan)

2007-07-15

A spatially adaptive grid-refinement approach has been investigated to solve the even-parity Boltzmann transport equation. A residual based a posteriori error estimation scheme has been utilized for checking the approximate solutions for various finite element grids. The local particle balance has been considered as an error assessment criterion. To implement the adaptive approach, a computer program ADAFENT (adaptive finite elements for neutron transport) has been developed to solve the second order even-parity Boltzmann transport equation using K{sup +} variational principle for slab geometry. The program has a core K{sup +} module which employs Lagrange polynomials as spatial basis functions for the finite element formulation and Legendre polynomials for the directional dependence of the solution. The core module is called in by the adaptive grid generator to determine local gradients and residuals to explore the possibility of grid refinements in appropriate regions of the problem. The a posteriori error estimation scheme has been implemented in the outer grid refining iteration module. Numerical experiments indicate that local errors are large in regions where the flux gradients are large. A comparison of the spatially adaptive grid-refinement approach with that of uniform meshing approach for various benchmark cases confirms its superiority in greatly enhancing the accuracy of the solution without increasing the number of unknown coefficients. A reduction in the local errors of the order of 10{sup 2} has been achieved using the new approach in some cases.

Phase diagrams of Ca(Fe,Ru){sub 2}As{sub 2} system

Energy Technology Data Exchange (ETDEWEB)

Zhao, Kan; Gegenwart, Philipp [Experimentalphysik VI, Elektronische Korrelationen und Magnetismus, Institut fuer Physik, Universitaet Augsburg, D-86135 Augsburg (Germany)

2015-07-01

Single crystalline Ca(Fe,Ru){sub 2}As{sub 2} series have been grown and characterized by structural, magnetic, and transport measurements. These measurement shows Ca(Fe,Ru){sub 2}As{sub 2} undergoes successive phase transitions with increasing Ru element doping. The antiferromagnetic phase with orthorhombic structure at x<0.023 (x means the doping concentration of Ru element) is directly driven to a Fermi-liquid type collapsed tetragonal (cT) phase at 0.023CaFe{sub 2}As{sub 2} under hydrostatic pressure.

Labile rhizosphere soil solution fraction for prediction of bioavailability of heavy metals and rare earth elements to plants.

Science.gov (United States)

Shan, Xiao-Quan; Wang, Zhongwen; Wang, Weisheng; Zhang, Shuzhen; Wen, Bei

2003-02-01

A labile rhizosphere soil solution fraction has been recommended to predict the bioavailability of heavy metals and rare earth elements to plants. This method used moist rhizosphere soil in combination with a mixture of 0.01 mol L(-1) of low-molecular-weight organic acids (LMWOAs) as extractant. The extracted soil solutions were fractionated into two colloidal fractions of soil solution fraction, F(lrss). For the soil solutions extracted with a mixture of LMWOAs the concentrations of heavy metals and rare earth elements in F(2) and F(3) were quite similar. However, the mean concentrations of Cr, Ni, Zn, Cu, Pb, Cd, La, Ce, Pr, and Nd in F(lrss) accounted for 79.9%, 91.3%, 90.8%, 60.1%, 77.5%, 75.3%, 81.2%, 77.2%, 80.3%, and 79.5%, respectively, of their concentrations in F(2). In contrast, there were no differences in the extractable metal concentrations between the three fractions while the first step of the method recommended by the European Community of Reference (BCR), where 0.1 mol L(-1) acetic acid was used as an extractant. The single correlation analysis was made between metal concentrations in the different fractions of soil solutions and their concentrations in wheat. If the first step of BCR method was used there was no good correlation between heavy metals in soil pools and that in wheat shoots and roots. When LMWAOs were used a good correlation was obtained between the concentrations of heavy metals in soil pools and that in wheat roots, which followed a general order of r(1 kD, LMWOAs) >r(0.2 microm, LMWOAs) approximately r(0.45 microm, LMWOAs). In the case of rare earth elements the good correlation was obtained for both the wheat roots and shoots. Generally, the correlation coefficients obtained by LMWAOs were better than that obtained by the first step of BCR method. Therefore, LMWAOs and F(lrss) were strongly recommended to predict the bioavailability of metals in soil pools to plants.

Use of heterogeneous finite elements generated by collision probability solutions to calculate a pool reactor core

International Nuclear Information System (INIS)

Calabrese, C.R.; Grant, C.R.

1990-01-01

This work presents comparisons between measured fluxes obtained by activation of Manganese foils in the light water, enriched uranium research pool reactor RA-2 MTR (Materials Testing Reactors) fuel element) and fluxes calculated by the finite element method FEM using DELFIN code, and describes the heterogeneus finite elements by a set of solutions of the transport equations for several different configurations obtained using the collision probability code HUEMUL. The agreement between calculated and measured fluxes is good, and the advantage of using FEM is showed because to obtain the flux distribution with same detail using an usual diffusion calculation it would be necessary 12000 mesh points against the 2000 points that FEM uses, hence the processing time is reduced in a factor ten. An interesting alternative to use in MTR fuel management is presented. (Author) [es

Elemental analysis of the suspended particulate matter in the air of Tehran using INAA and AAS techniques. Appendix 11

International Nuclear Information System (INIS)

Sohrabpour, M.; Rostami, S.; Athari, M.

1995-01-01

A network of ten sampling stations for monitoring the elemental concentration of the suspended particulate matter (SPM) in the air of Tehran has been established. Instrumental neutron activation analysis (INAA) and atomic absorption spectrometry (AAS) techniques have been used for analysis of the Whatman-41 filters collected during the year 1994. Assessment of the preliminary results using the two techniques has produced the following twenty-one elements: Al, Br, Ca, Cd, Ce, Cl, Co, Cr, Cs, Fe, K, Mg, Mn, Na, Ni, Pb, Sb, Sc, Ti, V, Zn. Various standard solutions with known concentrations of elements, together with standard reference materials, have been used for quality assurance of the measured concentrations. (author)

New procedure of quantitative mapping of Ti and Al released from dental implant and Mg, Ca, Fe, Zn, Cu, Mn as physiological elements in oral mucosa by LA-ICP-MS.

Science.gov (United States)

Sajnóg, Adam; Hanć, Anetta; Koczorowski, Ryszard; Barałkiewicz, Danuta

2017-12-01

A new procedure for determination of elements derived from titanium implants and physiological elements in soft tissues by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) is presented. The analytical procedure was developed which involved preparation of in-house matrix matched solid standards with analyte addition based on certified reference material (CRM) MODAS-4 Cormorant Tissue. Addition of gelatin, serving as a binding agent, essentially improved physical properties of standards. Performance of the analytical method was assayed and validated by calculating parameters like precision, detection limits, trueness and recovery of analyte addition using additional CRM - ERM-BB184 Bovine Muscle. Analyte addition was additionally confirmed by microwave digestion of solid standards and analysis by solution nebulization ICP-MS. The detection limits are in range 1.8μgg -1 to 450μgg -1 for Mn and Ca respectively. The precision values range from 7.3% to 42% for Al and Zn respectively. The estimated recoveries of analyte addition line within scope of 83%-153% for Mn and Cu respectively. Oral mucosa samples taken from patients treated with titanium dental implants were examined using developed analytical method. Standards and tissue samples were cryocut into 30µm thin sections. LA-ICP-MS allowed to obtain two-dimensional maps of distribution of elements in tested samples which revealed high content of Ti and Al derived from implants. Photographs from optical microscope displayed numerous particles with µm size in oral mucosa samples which suggests that they are residues from implantation procedure. Copyright © 2017 Elsevier B.V. All rights reserved.

Poisson-Nernst-Planck Equations for Simulating Biomolecular Diffusion-Reaction Processes I: Finite Element Solutions.

Science.gov (United States)

Lu, Benzhuo; Holst, Michael J; McCammon, J Andrew; Zhou, Y C

2010-09-20

In this paper we developed accurate finite element methods for solving 3-D Poisson-Nernst-Planck (PNP) equations with singular permanent charges for electrodiffusion in solvated biomolecular systems. The electrostatic Poisson equation was defined in the biomolecules and in the solvent, while the Nernst-Planck equation was defined only in the solvent. We applied a stable regularization scheme to remove the singular component of the electrostatic potential induced by the permanent charges inside biomolecules, and formulated regular, well-posed PNP equations. An inexact-Newton method was used to solve the coupled nonlinear elliptic equations for the steady problems; while an Adams-Bashforth-Crank-Nicolson method was devised for time integration for the unsteady electrodiffusion. We numerically investigated the conditioning of the stiffness matrices for the finite element approximations of the two formulations of the Nernst-Planck equation, and theoretically proved that the transformed formulation is always associated with an ill-conditioned stiffness matrix. We also studied the electroneutrality of the solution and its relation with the boundary conditions on the molecular surface, and concluded that a large net charge concentration is always present near the molecular surface due to the presence of multiple species of charged particles in the solution. The numerical methods are shown to be accurate and stable by various test problems, and are applicable to real large-scale biophysical electrodiffusion problems.

PMR spectroscopy of Ca(II) complexes of ethylenediamine-N,N,N',N' - tetraacetic acid

International Nuclear Information System (INIS)

Novomesky, P.; Balgavy, P.; Majer, J.

1977-01-01

Proton magnetic resonance spectra for the EDTA complexes of Ca(II) were measured in aqueous solutions as a function of solution pH. It follows from the analysis of chemical shift changes that the nitrogen atoms rather than the carboxylate groups are protonated (as the pH is lowered) in the tetraanion of EDTA. The same conclusion follows for the protonization of the [CaEDTA] 2- complex in the acid pH range where the hydrogen complex [CaH(EDTA)] - is formed. The formation of [Ca(OH)EDTA] 3- was not observed at pH less than 12.6, at [CaEDTA] 2- concentration of 0.5 mol/l. In solutions with a metal-to-ligand molar ratio 1:1.5 two sets of resonance signals appear in the pH range from 12.8 to 6.0, the former for the free ligand and the latter for the stable [CaEDTA] 2- complex. However, from pH 6.0 to 4.35 only one set of broadened signals was observed, which indicates that an exchange process between free ligand, normal [CaEDTA] 2- complex and [CaH(EDTA)] - takes place. (author)

The CaV2.3 R-type voltage-gated Ca2+ channel in mouse sleep architecture.

Science.gov (United States)

Siwek, Magdalena Elisabeth; Müller, Ralf; Henseler, Christina; Broich, Karl; Papazoglou, Anna; Weiergräber, Marco

2014-05-01

Voltage-gated Ca(2+) channels (VGCCs) are key elements in mediating thalamocortical rhythmicity. Low-voltage activated (LVA) CaV 3 T-type Ca(2+) channels have been related to thalamic rebound burst firing and to generation of non-rapid eye movement (NREM) sleep. High-voltage activated (HVA) CaV 1 L-type Ca(2+) channels, on the opposite, favor the tonic mode of action associated with higher levels of vigilance. However, the role of the HVA Non-L-type CaV2.3 Ca(2+) channels, which are predominantly expressed in the reticular thalamic nucleus (RTN), still remains unclear. Recently, CaV2.3(-/-) mice were reported to exhibit altered spike-wave discharge (SWD)/absence seizure susceptibility supported by the observation that CaV2.3 mediated Ca(2+) influx into RTN neurons can trigger small-conductance Ca(2+)-activated K(+)-channel type 2 (SK2) currents capable of maintaining thalamic burst activity. Based on these studies we investigated the role of CaV2.3 R-type Ca(2+) channels in rodent sleep. The role of CaV2.3 Ca(2+) channels was analyzed in CaV2.3(-/-) mice and controls in both spontaneous and artificial urethane-induced sleep, using implantable video-EEG radiotelemetry. Data were analyzed for alterations in sleep architecture using sleep staging software and time-frequency analysis. CaV2.3 deficient mice exhibited reduced wake duration and increased slow-wave sleep (SWS). Whereas mean sleep stage durations remained unchanged, the total number of SWS epochs was increased in CaV2.3(-/-) mice. Additional changes were observed for sleep stage transitions and EEG amplitudes. Furthermore, urethane-induced SWS mimicked spontaneous sleep results obtained from CaV2.3 deficient mice. Quantitative Real-time PCR did not reveal changes in thalamic CaV3 T-type Ca(2+) channel expression. The detailed mechanisms of SWS increase in CaV2.3(-/-) mice remain to be determined. Low-voltage activated CaV2.3 R-type Ca(2+) channels in the thalamocortical loop and extra

Uranium dissolution in hyper-alkaline TMA-OH solutions: Preliminary results

Energy Technology Data Exchange (ETDEWEB)

Cachoir, C.; Salah, S.; Mennecart, T.; Lemmens, K. [Belgian Research Nuclear Centre - SCK-CEN, Boeretang 200, 2400 Mol (Belgium)

2016-07-01

Leaching experiments were performed with depleted UO{sub 2} powders in tetramethylammonium solutions (TMA-OH) at pH 13.5 and 12.5, and at different UO{sub 2} surface area to volume of solution (SA/V) ratio's to determine the solubility and the dissolution kinetics of UO{sub 2} at high pH in absence of cations dominating cementitious waters (Ca, Na, K). The solubility of UO{sub 2} increased from pH 12.5 to 13.5 and by increasing the SA/V ratio up to 100 m{sup -1}. However, no known U secondary-phases were predicted by geochemical calculations to control the measured U-concentrations. We interpreted the UO{sub 2} dissolution process as a 2-step process. For all experiments, we observe a fast initial rate, hydroxo promoted and likely surface controlled. Afterwards the rate is apparently negative at low SA/V over time while it is positive at higher SA/V ratio's. The former is interpreted to be related to a sorption process, while the latter reveals a continuous residual dissolution process. No solubility enhancing effect of U-colloids was observed in the TMA-OH media. However, there is much less uranium colloid formation in TMA-OH tests with low Ca (Na, K) concentration than in previous tests with higher Ca (Na, K) concentrations. This suggests that the colloid formation is promoted by alkali and/or alkali-earth elements.

Hydraulic modeling of riverbank filtration systems with curved boundaries using analytic elements and series solutions

Science.gov (United States)

Bakker, Mark

2010-08-01

A new analytic solution approach is presented for the modeling of steady flow to pumping wells near rivers in strip aquifers; all boundaries of the river and strip aquifer may be curved. The river penetrates the aquifer only partially and has a leaky stream bed. The water level in the river may vary spatially. Flow in the aquifer below the river is semi-confined while flow in the aquifer adjacent to the river is confined or unconfined and may be subject to areal recharge. Analytic solutions are obtained through superposition of analytic elements and Fourier series. Boundary conditions are specified at collocation points along the boundaries. The number of collocation points is larger than the number of coefficients in the Fourier series and a solution is obtained in the least squares sense. The solution is analytic while boundary conditions are met approximately. Very accurate solutions are obtained when enough terms are used in the series. Several examples are presented for domains with straight and curved boundaries, including a well pumping near a meandering river with a varying water level. The area of the river bottom where water infiltrates into the aquifer is delineated and the fraction of river water in the well water is computed for several cases.

Determination of 17 impurity elements in nuclear quality uranium compounds by atomic absorption spectroscopy

International Nuclear Information System (INIS)

Andonie, O.; Smith, L.A.; Cornejo, S.

1985-01-01

A method is described for the determination of 17 elements (Al, Ca, Cd, Co, Cr, Cu, Fe, K, Li, Mg, Mn, Mo, Na, Ni, Pb, V and Zn) in the ppm level, in nuclearly pure uranium compounds by flame atomic absorption spectroscopy. The analysis is performed by first dissolving the uranium sample in nitric acid and then extracting the uranium with tributyl phosphate solution. The aqueous phase, free of uranium, which contains the elements to analyze is inspirated into the flame of an atomic absorption spectrophotometer using air-acetylene or nitrous oxide-acetylene flame according to the element in study. This method allows to extract the uranium selectively in more than 99.0% and the recovery of the elements sudied was larger 90% (for K) to 100% (for Cr). The sensitivity of the method vary from 0.096 μg/g U (for Cd) to 5.5 μg/g U (for Na). (Author)

ICP-MS with hexapole collision cell for isotope ratio measurements of Ca, Fe, and Se

Energy Technology Data Exchange (ETDEWEB)

Boulyga, S.F. [Radiation Physics and Chemistry Problems Inst., Minsk (Belarus); Becker, J.S. [Central Department for Analytical Chemistry, Research Centre Juelich (Germany)

2001-07-01

To avoid mass interferences on analyte ions caused by argon ions and argon molecular ions via reactions with collision gases, an rf hexapole filled with helium and hydrogen has been used in inductively coupled plasma mass spectrometry (ICP-MS), and its performance has been studied. Up to tenfold improvement in sensitivity was observed for heavy elements (m > 100 u), because of better ion transmission through the hexapole ion guide. A reduction of argon ions Ar{sup +} and the molecular ions of argon ArX{sup +} (X = O, Ar) by up to three orders of magnitude was achieved in a hexapole collision cell of an ICP-MS (''Platform ICP'', Micromass, Manchester, UK) as a result of gas-phase reactions with hydrogen when the hexapole bias (HB) was set to 0 V; at an HB of 1.6 V argon, and argon-based ions of masses 40 u, 56 u, and 80 u, were reduced by approximately four, two, and five orders of magnitude, respectively. The signal-to-noise ratio {sup 80}Se/ {sup 40}Ar{sub 2}{sup +} was improved by more than five orders of magnitude under optimized experimental conditions. Dependence of mass discrimination on collision-cell properties was studied in the mass range 10 u (boron) to 238 u (uranium). Isotopic analysis of the elements affected by mass-spectrometric interference, Ca, Fe, and Se, was performed using a Meinhard nebulizer and an ultrasonic nebulizer (USN). The measured isotope ratios were comparable with tabulated values from IUPAC. Precision of 0.26%, 0.19%, and 0.12%, respectively, and accuracy of 0.13% 0.25%, and 0.92%, respectively, was achieved for isotope ratios {sup 44}Ca/ {sup 40}Ca and {sup 56}Fe/{sup 57}Fe in 10 {mu}g L{sup -1} solution nebulized by means of a USN and for {sup 78}Se/{sup 80}Se in 100 {mu}g L{sup -1} solution nebulized by means of a Meinhard nebulizer. (orig.)

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.

DISTRIBUTION OF MAJOR ELEMENTS (NA, K, CA, MG) IN THE ...

African Journals Online (AJOL)

Levels of sodium, potassium, calcium and magnesium were determined in plant organs (bud, flowers, fruit, seed, leaves, stems, roots, cobs, styles, shaft, grains and efflorescences) of three Fadama farms located in Ifaki-Ekiti, Ado-Ekiti and Ikere-Ekiti of Ekiti State, Nigeria. The highest levels of Mg, K, Na and Ca were ...

Adaptive solution of the multigroup diffusion equation on irregular structured grids using a conforming finite element method formulation

International Nuclear Information System (INIS)

Ragusa, J. C.

2004-01-01

In this paper, a method for performing spatially adaptive computations in the framework of multigroup diffusion on 2-D and 3-D Cartesian grids is investigated. The numerical error, intrinsic to any computer simulation of physical phenomena, is monitored through an a posteriori error estimator. In a posteriori analysis, the computed solution itself is used to assess the accuracy. By efficiently estimating the spatial error, the entire computational process is controlled through successively adapted grids. Our analysis is based on a finite element solution of the diffusion equation. Bilinear test functions are used. The derived a posteriori error estimator is therefore based on the Hessian of the numerical solution. (authors)

Molecular dynamics simulations of the electrical double layer on smectite surfaces contacting concentrated mixed electrolyte (NaCl-CaCl2) solutions.

Science.gov (United States)

Bourg, Ian C; Sposito, Garrison

2011-08-15

We report new molecular dynamics results elucidating the structure of the electrical double layer (EDL) on smectite surfaces contacting mixed NaCl-CaCl(2) electrolyte solutions in the range of concentrations relevant to pore waters in geologic repositories for CO(2) or high-level radioactive waste (0.34-1.83 mol(c) dm(-3)). Our results confirm the existence of three distinct ion adsorption planes (0-, β-, and d-planes), often assumed in EDL models, but with two important qualifications: (1) the location of the β- and d-planes are independent of ionic strength or ion type and (2) "indifferent electrolyte" ions can occupy all three planes. Charge inversion occurred in the diffuse ion swarm because of the affinity of the clay surface for CaCl(+) ion pairs. Therefore, at concentrations ≥0.34 mol(c) dm(-3), properties arising from long-range electrostatics at interfaces (electrophoresis, electro-osmosis, co-ion exclusion, colloidal aggregation) will not be correctly predicted by most EDL models. Co-ion exclusion, typically neglected by surface speciation models, balanced a large part of the clay mineral structural charge in the more concentrated solutions. Water molecules and ions diffused relatively rapidly even in the first statistical water monolayer, contradicting reports of rigid "ice-like" structures for water on clay mineral surfaces. Published by Elsevier Inc.

A study on removal of elemental mercury in flue gas using fenton solution

Energy Technology Data Exchange (ETDEWEB)

Liu, Yangxian; Wang, Yan; Wang, Qian; Pan, Jianfeng [School of Energy and Power Engineering, Jiangsu University, Zhenjiang, Jiangsu 212013 (China); Zhang, Yongchun [Jiangsu Province Special Equipment Safety Supervision Inspection Institute (Branch of Wuxi), Wuxi 214000 (China); Zhou, Jianfei [School of Energy and Power Engineering, Jiangsu University, Zhenjiang, Jiangsu 212013 (China); Zhang, Jun [Key Laboratory of Energy Thermal Conversion and Control of Ministry of Education, Southeast University, Nanjing 210096 (China)

2015-07-15

Highlights: • A novel technique on oxidation of Hg{sup 0} using Fenton was proposed. • The effects of several process parameters on Hg{sup 0} removal were studied. • Products and ·OH in solution were detected. • Reaction mechanism of Hg{sup 0} removal was studied. • Simultaneous removal of Hg{sup 0}, NO and SO{sub 2} was also studied. - Abstract: A novel technique on oxidation-separation of elemental mercury (Hg{sup 0}) in flue gas using Fenton solution in a bubbling reactor was proposed. The effects of several process parameters (H{sub 2}O{sub 2} concentration, Hg{sup 0} inlet concentration, Fe{sup 2+} concentration, solution temperature, solution pH, gas flow) and several flue gas components (NO, SO{sub 2}, O{sub 2}, CO{sub 2}, inorganic ions and particulate matters on Hg{sup 0} removal were studied. The results indicate that H{sub 2}O{sub 2} concentration, Fe{sup 2+} concentration, solution pH and gas flow have great effects on Hg{sup 0} removal. Solution temperature, Hg{sup 0}, NO, SO{sub 2}, CO{sub 3}{sup 2−} and HCO{sub 3}{sup −} concentrations also have significant effects on Hg{sup 0} removal. However, Cl{sup −}, SO{sub 4}{sup 2−}, NO{sub 3}{sup −}, O{sub 2} and CO{sub 2} concentrations only have slight effects on Hg{sup 0} removal. Furthermore, reaction mechanism of Hg{sup 0} removal and simultaneous removal process of Hg{sup 0}, NO and SO{sub 2} were also studied. Hg{sup 0} is removed by oxidation of ·OH and oxidation of H{sub 2}O{sub 2}. The simultaneous removal efficiencies of 100% for SO{sub 2}, 100% for Hg{sup 0} and 88.3% for NO were obtained under optimal test conditions. The results demonstrated the feasibility of Hg{sup 0} removal and simultaneous removal of Hg{sup 0}, SO{sub 2} and NO using Fenton solution in a bubbling reactor.

Measurements of natural 41Ca concentrations

International Nuclear Information System (INIS)

Steinhof, A.

1989-05-01

Atomic mass spectroscopic examinations on 41 Ca were carried out in the UNILAC accelerator. A sensitivity of about 10 -15 was achieved. This would allow the measurement of present natural 41 Ca concentrations as soon as the problem of the transmission determination is solved. In this respect suggestions were worked out and their feasibility discussed. The detection of 41 Ca-ions is especially free of background when high UNILAC-energies are applied. An estimation showed a background level corresponding with a 41 Ca concentration of less then 10 -17 referred to 40 Ca. Besides an independent concept for the electromagnetic concentration of 41 Ca with variable concentration factors was developed. After being concentrated up to 50 respectively 25 times the initial concentration in the GSI mass separator, the 41 Ca concentration of three recent deer bones found in the Odenwald was measured by atomic mass spectroscopy in the 14UD-Pelletron Tandem in Rehovot (Israel). The measured 41 Ca concentrations ranged between 10 -14 to 10 -13 with consideration of the concentration factor. A theoretical study of the 41 Ca production in the earth's surface based on cosmic radiation illustrates the influence of trace elements on the neutron flux and thus on the 41 Ca production. This influence might be a possible explanation for the observed amplitude of variation of the 41 Ca concentration in recent bones which are of decisive importance for the feasibility of 41 Ca-related dating. In this work a method is suggested that does not depend on the amplitude of variation mentioned above and which would allow the determination of the erosion rate of rocks by its 41 Ca concentrations. (orig./HP) [de

Preparation of 45Ca(HDEHP)n and (CaH{sub 1}50{sub 2})2 samples for liquid scintillation counting, compared to 45caCl{sub 2} results; Preparacion de Ca (HDEHP)n y (C{sub 8}H{sub 1}50{sub 2})2 marcados con 45Ca y estudio comparativo con 4 5ca Cl2 en medidas por centelleo liquido

Energy Technology Data Exchange (ETDEWEB)

Rodriguez, L.; Arcos, J. M. los; Grau Malonda, A.

1994-07-01

A procedure for preparation of liquid scintillation counting organic samples of the Di-2-ethylhexyl phosphate calcium complex and the 2-ethylhexanoate calcium salt, labelled with 45Ca, is described. The chemical quench, the counting stability and spectral evolution of both compounds is studied in six scintillators,Toluene-alcohol, Dioxane-naphtalene, Hi safe II, Ultimate-Gold and Instagel, and compared to results obtained from a commercial solution of 4 5CaCl2. (Author) 7 refs.

Physiological studies in heterozygous calcium sensing receptor (CaSR gene-ablated mice confirm that the CaSR regulates calcitonin release in vivo

Directory of Open Access Journals (Sweden)

Kovacs Christopher S

2004-04-01

Full Text Available Abstract Background The calcium sensing receptor (CaSR regulates serum calcium by suppressing secretion of parathyroid hormone; it also regulates renal tubular calcium excretion. Inactivating mutations of CaSR raise serum calcium and reduce urine calcium excretion. Thyroid C-cells (which make calcitonin express CaSR and may, therefore, be regulated by it. Since calcium stimulates release of calcitonin, the higher blood calcium caused by inactivation of CaSR should increase serum calcitonin, unless CaSR mutations alter the responsiveness of calcitonin to calcium. To demonstrate regulatory effects of CaSR on calcitonin release, we studied calcitonin responsiveness to calcium in normal and CaSR heterozygous-ablated (Casr+/- mice. Casr+/- mice have hypercalcemia and hypocalciuria, and live normal life spans. Each mouse received either 500 μl of normal saline or one of two doses of elemental calcium (500 μmol/kg or 5 mmol/kg by intraperitoneal injection. Ionized calcium was measured at baseline and 10 minutes, and serum calcitonin was measured on the 10 minute sample. Results At baseline, Casr+/- mice had a higher blood calcium, and in response to the two doses of elemental calcium, had greater increments and peak levels of ionized calcium than their wild type littermates. Despite significantly higher ionized calcium levels, the calcitonin levels of Casr+/- mice were consistently lower than wild type at any ionized calcium level, indicating that the dose-response curve of calcitonin to increases in ionized calcium had been significantly blunted or shifted to the right in Casr+/- mice. Conclusions These results confirm that the CaSR is a physiological regulator of calcitonin; therefore, in response to increases in ionized calcium, the CaSR inhibits parathyroid hormone secretion and stimulates calcitonin secretion.

Theoretical predictions of hydrolysis and complex formation of group-4 elements Zr, Hf and Rf in HF and HCl solutions

International Nuclear Information System (INIS)

Pershina, V.; Trubert, D.; Le Naour, C.; Kratz, J.V.

2002-01-01

Fully relativistic molecular density-functional calculations of the electronic structures of hydrated, hydrolyzed and fluoride/chloride complexes have been performed for group-4 elements Zr, Hf, and element 104, Rf. Using the electronic density distribution data, relative values of the free energy change for hydrolysis and complex formation reactions were defined. The results show the following trend for the first hydrolysis step of the cationic species: Zr>Hf>Rf in agreement with experiments. For the complex formation in HF solutions, the trend to a decrease from Zr to Hf is continued with Rf, provided no hydrolysis takes place. At pH>0, further fluorination of hydrolyzed species or fluoro-complexes has an inversed trend in the group Rf≥Zr>Hf, with the difference between the elements being very small. For the complex formation in HCl solutions, the trend is continued with Rf, so that Zr>Hf>Rf independently of pH. A decisive energetic factor in hydrolysis or complex formation processes proved to be a predominant electrostatic metal-ligand interaction. Trends in the K d (distribution coefficient) values for the group-4 elements are expected to follow those of the complex formation

Separation of uranium and rare earth elements from Rirang ore leach solution by two-step precipitation

International Nuclear Information System (INIS)

Sradjono; Erni Rifandriyah, A.; Zahardi

1995-01-01

Separation of uranium and rare-earth elements from Rirang ore leach solution was carried out through a two-step precipitation. Several condition affecting the separation processes were examined including solution pH, reagent concentration, and reaction prepitation time. Optimum conditions for the first and second precipitation steps include adjustment of precipitation pH to 1.3 and 2.3, respectively by the addition of 7.3% of NH 4 OH solution and allowing 60 minutes precipitation/reaction time. Based on the conditions, about 6% of Th, 3% of U, 0.9% of PO 4 3- , and none of RE were recovered in the first precipitation step meanwhile, about 99% of RE, 55% of U, 76% of PO 4 3- , and of the Th were recovered in the second step. (author). 3 refs. 4 tabs. 4 figs

Seasonal variation of major elements (Ca, Mg) and trace metals (Fe, Cu, Zn, Mn) and cultured mussel Perna viridis L. and seawater in the Dona Paula Bay, Goa

Digital Repository Service at National Institute of Oceanography (India)

Rivonker, C.U.; Parulekar, A.H.

The major elements and trace metals were analysed from nussel tissue and the seawater taken from three depths (0, 5 and 9 meters) from the culture site. Range of variation in Ca, Mg, Fe, Cu, Zn and Mn were 226-399; 708-1329; 0.005-0.084; BDL-0...

Current extraction and separation of uranium, thorium and rare earths elements from monazite leach solution using organophosphorous extractants

International Nuclear Information System (INIS)

Biswas, Sujoy; Rupawate, V.H.; Hareendran, K.N.; Roy, S.B.

2014-01-01

A new process based on solvent extraction has been developed for separation of uranium, thorium and rare earths from monazite leach solution using organophosphorous extractants. The Thorium cake coming from monazite source was dissolved in HNO 3 medium in presence of trace amount of HF for feed preparation. The separation of U(VI) was carried out by liquid-liquid extraction using tris-2-ethyl hexyl phosphoric acid (TEHP) in dodecane leaving thorium and rare earths elements in the raffinate. The thorium from raffinate was selectively extracted using 1M tri iso amyl phosphate (TiAP) in dodecane in organic phase leaving all rare earths elements in aqueous solution. The uranium and thorium from organic medium was quantitatively stripped using 0.05 M HNO 3 counter current mode. Results indicate the quantitative separation of uranium, thorium and rare earths from thorium cake (monazite source) using organophosphorous extractant in counter current mode

Magnetic Field Effects on CaCO3 Precipitation Process in Hard Water

Directory of Open Access Journals (Sweden)

Nelson Saksono

2010-10-01

Full Text Available Magnetic treatment is applied as physical water treatment for scale prevention especially CaCO3, from hard water in piping equipment by reducing its hardness.Na2CO3 and CaCl2 solution sample was used in to investigate the magnetic fields influence on the formation of particle of CaCO3. By changing the strength of magnetic fields, exposure time and concentration of samples solution, this study presents quantitative results of total scale deposit, total precipitated CaCO3 and morphology of the deposit. This research was run by comparing magnetically and non-magnetically treated  samples. The results showed an increase of deposits formation rate and total number of precipitated CaCO3 of magnetically treated samples. The increase of concentration solution sample will also raised the deposit under magnetic  field. Microscope images showed a greater number but smaller size of CaCO3 deposits form in magnetically treated samples, and aggregation during the processes. X-ray diffraction (XRD analysis showed that magnetically samples were dominated by calcite. But, there was a significant decrease of calcite’s peak intensities from magnetized  samples that indicated the decrease of the amount of calcite and an increase of total amorphous of deposits. This result  showed that magnetization of hard water leaded to the decreasing of ion Ca2+ due to the increasing of total CaCO3 precipitation process.

Confirmation Of Super Heavy Element Production In 48Ca Induced Fusion Reactions A Handshake Of Physics And Chemistry For Element 112

International Nuclear Information System (INIS)

Hofmann, S.; Ackermann, D.; Burkhard, H. G.; Heinz, S.; Hessberger, F. P.; Khuyagbaatar, J.; Kindler, B.; Kojouharov, I.; Lommel, B.; Mann, R.; Muenzenberg, G.; Schoett, H. J.; Sulignano, B.; Antalic, S.; Saro, S.; Streicher, B.; Venhart, M.; Yeremin, A. V.; Comas, V. F.; Heredia, J. A.

2008-01-01

The production of 283 112 in 48 Ca induced nuclear reactions was investigated using physical and chemical separation techniques. In the reaction 48 Ca on 238 U, four events were registered at the SHIP velocity filter. The mean atomic mass of the evaporation residues (EVR)

Structure of the CaMKIIdelta/calmodulin complex reveals the molecular mechanism of CaMKII kinase activation.

Directory of Open Access Journals (Sweden)

Peter Rellos

2010-07-01

Full Text Available Long-term potentiation (LTP, a long-lasting enhancement in communication between neurons, is considered to be the major cellular mechanism underlying learning and memory. LTP triggers high-frequency calcium pulses that result in the activation of Calcium/Calmodulin (CaM-dependent kinase II (CaMKII. CaMKII acts as a molecular switch because it remains active for a long time after the return to basal calcium levels, which is a unique property required for CaMKII function. Here we describe the crystal structure of the human CaMKIIdelta/Ca2+/CaM complex, structures of all four human CaMKII catalytic domains in their autoinhibited states, as well as structures of human CaMKII oligomerization domains in their tetradecameric and physiological dodecameric states. All four autoinhibited human CaMKIIs were monomeric in the determined crystal structures but associated weakly in solution. In the CaMKIIdelta/Ca2+/CaM complex, the inhibitory region adopted an extended conformation and interacted with an adjacent catalytic domain positioning T287 into the active site of the interacting protomer. Comparisons with autoinhibited CaMKII structures showed that binding of calmodulin leads to the rearrangement of residues in the active site to a conformation suitable for ATP binding and to the closure of the binding groove for the autoinhibitory helix by helix alphaD. The structural data, together with biophysical interaction studies, reveals the mechanism of CaMKII activation by calmodulin and explains many of the unique regulatory properties of these two essential signaling molecules.This article can also be viewed as an enhanced version in which the text of the article is integrated with interactive 3-D representations and animated transitions. Please note that a web plugin is required to access this enhanced functionality. Instructions for the installation and use of the Web plugin are available in Text S1.

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

Nanosilica supported CaO: A regenerable and mechanically hard CO2 sorbent at Ca-looping conditions

International Nuclear Information System (INIS)

Sanchez-Jimenez, P.E.; Perez-Maqueda, L.A.; Valverde, J.M.

2014-01-01

Highlights: • A synthetic CO 2 sorbent is prepared by impregnation of calcium nitrate on a nanosilica matrix. • Sintering of the nascent CaO in the calcination stage of carbonation/calcination cycles is hindered. • CaO conversion reaches a stable value well above the residual conversion of natural limestone. • Particle fragmentation as caused by ultrasonic irradiation in a liquid dispersion is hindered. - Abstract: This work presents a CO 2 sorbent that may be synthesized from low-cost and widely available materials following a simple method basically consisting of impregnation of a nanostructured silica support with a saturated solution of calcium nitrate. In a first impregnation stage, the use of a stoichiometric CaO/SiO 2 ratio serves to produce a calcium silicate matrix after calcination. This calcium silicate matrix acts as a thermally stable and mechanically hard support for CaO deposited on it by further impregnation. The CaO-impregnated sorbent exhibits a stable CaO conversion at Ca-looping conditions whose value depends on the CaO wt% deposited on the calcium silicate matrix, which can be increased by successive reimpregnations. A 10 wt% CaO impregnated sorbent reaches a stable conversion above 0.6 whereas the stable conversion of a 30 wt% CaO impregnated sorbent is around 0.3, which is much larger than the residual conversion of CaO derived from natural limestone (between 0.07 and 0.08). Moreover, particle size distribution measurements of samples predispersed in a liquid and subjected to high energy ultrasonic waves indicate that the CaO-impregnated sorbent has a relatively high mechanical strength as compared to limestone derived CaO

Leaching of Major and Minor Elements during the Transport and Storage of Coal Ash Obtained in Power Plant

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Rada Krgović

2014-01-01

Full Text Available In power plant, coal ash obtained by combustion is mixed with river water and transported to the dump. Sequential extraction was used in order to assess pollution caused by leaching of elements during ash transport through the pipeline and in the storage (cassettes. A total of 80 samples of filter ash as well as the ash from active (currently filled and passive (previously filled cassettes were studied. Samples were extracted with distilled water, ammonium acetate, ammonium oxalate/oxalic acid, acidic solution of hydrogen-peroxide, and a hydrochloric acid. Concentrations of the several elements (Al, As, Cd, Co, Cu, Cr, Fe, Ba, Ca, Mg, Ni, Pb, and Zn in all extracts were determined by inductively coupled plasma atomic emission spectrometry. Pattern recognition method was carried out in order to provide better understanding of the nature of distribution of elements according to their origins. Results indicate possible leaching of As, Ca, Cd, Cu, Zn, and Pb. Among these elements As, Cd, and Pb are toxicologically the most important but they were not present in the first two phases with the exception of As. The leaching could be destructive and cause negative effects on plants, water pollution, and damage to some life forms.

Precipitation-filtering technology for uranium waste solution generated on washing-electrokinetic decontamination

Energy Technology Data Exchange (ETDEWEB)

Kim, Gye-Nam, E-mail: kimsum@kaeri.re.kr; Park, Uk-Ryang; Kim, Seung-Soo; Moon, Jei-Kwon

2015-05-15

Graphical abstract: A recycling process diagram for the volume reduction of waste solution generated from washing-electrokinetic decontamination. - Highlights: • A process for recycling a waste solution generated was developed. • The total metal precipitation rate by NaOH in a supernatant after precipitation was the highest at pH 9. • The uranium radioactivity in the treated solution upon injection of 0.2 g of alum was lower. • After drying, the volume of sludge was reduced to 35% of the initial sludge volume. - Abstract: Large volumes of uranium waste solution are generated during the operation of washing-electrokinetic decontamination equipment used to remove uranium from radioactive soil. A treatment technology for uranium waste solution generated upon washing-electrokinetic decontamination for soil contaminated with uranium has been developed. The results of laboratory-size precipitation experiments were as follows. The total amount of metal precipitation by NaOH for waste solution was highest at pH 11. Ca(II), K(I), and Al(III) ions in the supernatant partially remained after precipitation, whereas the concentration of uranium in the supernatant was below 0.2 ppm. Also, when NaOH was used as a precipitant, the majority of the K(I) ions in the treated solution remained. The problem of CaO is to need a long dissolution time in the precipitation tank, while Ca(OH){sub 2} can save a dissolution time. However, the volume of the waste solution generated when using Ca(OH){sub 2} increased by 8 mL/100 mL (waste solution) compared to that generated when using CaO. NaOH precipitant required lower an injection volume lower than that required for Ca(OH){sub 2} or CaO. When CaO was used as a precipitant, the uranium radioactivity in the treated solution at pH 11 reached its lowest value, compared to values of uranium radioactivity at pH 9 and pH 5. Also, the uranium radioactivity in the treated solution upon injection of 0.2 g of alum with CaO or Ca(OH){sub 2} was

Performance Issues Along the Six Elements of Holcim Solusi Rumah's Marketing Mix and Solution Recommedations

OpenAIRE

Susana, Apriliani Dewi; Titus, Amol

2013-01-01

This study aims at identifying key issues in SR franchise business along the six elements of marketing mix: people, partner, place, product, promotion, and price, and then propose solution recommendations for the identified issues. Data is collected through a method of in-depth interviews with key SR stakeholders, internally and externally, namely end customers, SR personnels, and SR franchisees. Issues identified are mapped into a Problem Tree Analysis diagram to determine causal relations...

Atomic absorption spectrometric determination of mineral elements in mammalian bones

International Nuclear Information System (INIS)

Udoh, Anthony P.

2000-01-01

The phosphorus content of the major bones of male and female selected mammals was determined using the yellow vanadomolybdate colorimetric method. For each animal, the bone with the highest phosphorus content was used as pilot sample. Varying concentrations of strontium were added to solutions of the ashed pilot samples to minimize phosphorus interference in the determination of calcium and magnesium using flame atomic absorption spectrophotometry operated on the air-acetylene mode. At least 6,000 ppm (0.6%) of strontium was required to give optimum results for calcium. The amount of magnesium obtained from the analysis was not affected by the addition of strontium. With the incorporation of strontium in the sample solution, all elements of interest can be determined in the same sample solution. Based on this, a procedure is proposed for the determination of calcium and other elements in bones. Average recoveries of spiked calcium and magnesium were 97.85% and 98.16%, respectively at the 95% confidence level. The coefficients of variation obtained for replicate determinations using one of the samples were 0.00% for calcium, lead and sodium, 2.93% for magnesium, 3.27% for iron and 3.92% for zinc at the concentration levels found in that sample. Results from the proposed procedure compared well with those from classical chemical methods at the 95% confidence level. It is evident that calcium phosphorus, magnesium and sodium which are the most abundant elements in the bones are distributed in varying amounts both in the different types of bones and different animal species, although the general trend is Ca > P > Na > Mg for each bone considered. The calcium - phosphorus ratio is generally 3:1. The work set out to propose an atomic absorption spectrometric method for the multi-element analysis of mammalian bones with a single sample preparation and to study the distribution pattern of these elements in the bones. (Author)

A three-dimensional spectral element model for the solution of the hydrostatic primitive equations

CERN Document Server

Iskandarani, M; Levin, J C

2003-01-01

We present a spectral element model to solve the hydrostatic primitive equations governing large-scale geophysical flows. The highlights of this new model include unstructured grids, dual h-p paths to convergence, and good scalability characteristics on present day parallel computers including Beowulf-class systems. The behavior of the model is assessed on three process-oriented test problems involving wave propagation, gravitational adjustment, and nonlinear flow rectification, respectively. The first of these test problems is a study of the convergence properties of the model when simulating the linear propagation of baroclinic Kelvin waves. The second is an intercomparison of spectral element and finite-difference model solutions to the adjustment of a density front in a straight channel. Finally, the third problem considers the comparison of model results to measurements obtained from a laboratory simulation of flow around a submarine canyon. The aforementioned tests demonstrate the good performance of th...

Element-topology-independent preconditioners for parallel finite element computations

Science.gov (United States)

Park, K. C.; Alexander, Scott

1992-01-01

A family of preconditioners for the solution of finite element equations are presented, which are element-topology independent and thus can be applicable to element order-free parallel computations. A key feature of the present preconditioners is the repeated use of element connectivity matrices and their left and right inverses. The properties and performance of the present preconditioners are demonstrated via beam and two-dimensional finite element matrices for implicit time integration computations.

High-temperature electrical properties of the Bi2.1Sr1.9(Ca1-xYx)Cu2Oy solid solution

International Nuclear Information System (INIS)

Hong, Byungsun; Mason, T.O.

1993-01-01

By a combination of conventional physical property measurements and high temperature electrical property studies, the solid solution limit, transport parameters, and potential defect regimes of the Bi 2.1 Sr 1.9 (Ca 1 - x Y x )Cu 2 O y solid solution were established. A continuous solid solution extends to x = 0.7 or 0.8. The electrical properties indicate that the product of the hole density-of-states and mobility for semiconducting compositions is approximately an order of magnitude smaller than for the other p-type superconducting cuprates. A pronounced drop in hole concentration accompanies the tetragonal-to-orthorhombic transition at x = 0.5, where after superconductivity disappears. The electrical properties also indicate that a composition x ≥ 0.7 is the appropriate ''reference'' compound for the solid solution series. Upon doping this yttrium-rich insulating composition with calcium, holes are introduced. With increased calcium content (decreased yttrium content) the system exhibits several defect regimes reminiscent of the behavior in the La 2 - x AE x CuO 4 (AE = Sr or Ba) system. Oxygen defects (interstitial and vacancies) are believed to play an important role in the defect structure

Differences of the essential mineral element levels in the milk of Croatian Coldblood horse and Littoral-Dinaric donkey

Directory of Open Access Journals (Sweden)

Nina Bilandžić

2014-03-01

Full Text Available The concentrations of essential elements in the milk of Croatian Coldblood mares and Littoral- Dinaric donkey were measured. The mean element contents in horse milk were (mg/kg: Ca 687.1, Mg 72.1, K 637.7, Na 143.5, Cu 0.126, Fe 0.235, Se 0.01, Zn 2.06, Mn<0.01. In donkey milk, the mean element contents were (mg/kg: Ca 815.4, Mg 80.8, K 887.7, Na 217.6, Cu 0.027, Fe 0.196, Zn 2.36, Mn 0.016. In horse milk, moderate correlations were found between the elements: Ca-K, Mg-Se, Mg-K, Mg-Cu, Se-Cu, Se-Fe, Mn-K. Strong correlations were found among elements in donkey milk: Ca-Na, Ca-K, Ca-Cu, K-Na, K-Cu, Cu-Mn. Significant differences between Na, K and Cu concentrations were obtained between the two species. Other elements concentrations were similar in both species.

PIXE analysis for bioaccumulation studies of trace elements

International Nuclear Information System (INIS)

Iwata, Y.; Satoh, A.; Sasaki, Y.; Ito, R.; Kuramachi, K.

2005-01-01

Bioaccumulation by micro-alga in the ocean was simulated in nutritive seawater containing known amounts of trace metals, and the concentration factors for Fe, Zn and Cd were measured by PIXE. Trace transition metals in nearshore seawater were removed by Chelex-100. Then a culture solution was prepared by adding known amounts of trace metals and nutritive salts to the purified seawater. Marine micro-algae (Nannochloropsis sp., and Phaeodactylum sp.,) were purely cultured in the culture solution. An interested metal ion was added to the culture solution (0.01-5.0 mg/l). Alga in 10 ml of the culture solution was collected on a polycarbonate filter (pore size: 1.0 ) by suction filtration and subjected to 2.9 MeV proton bombardment. Na, Mg, Al, Si, P, S, Cl, K, Ca, Cr, Mn, Fe, Zn and Cd were simultaneously determined. PIXE multi-element analysis was possible using less than 1 mg of analytical sample. The quantity of the metal in the alga was increased in proportion to the concentration in the culture solution. The concentration factors for Zn, Fe and Cd were measured, e.g., 10200 ± 300 ml/g to Zn for Phaeodactylum. The trend of the affinity for the trace metals in the case of Nannochloropsis was Fe 3+ > Zn 2+ > Pb 2+ > Cd 2+ . (author)

Obtention of agricultural gypsum traced on 34 S (Ca34 SO4.2H2O), by chemical reaction between H234 SO4 and Ca(OH)2

International Nuclear Information System (INIS)

Rossete, Alessandra L.R.M.; Bendassolli, Jose A.; Ignoto, Raquel de Fatima; Batagello, Hugo Henrique

2002-01-01

The gypsum (CaSO 4 .2H 2 O) has double function in the soil: as source of calcium and sulfur and reducing agent of aluminum saturation. The sulfur for the plants has acting in the vital functions and it is proven fact increase of the S deficiency in Brazilian soils. The isotope tracer 34 S can elucidate important aspects in the sulfur cycle. The Ca 34 SO 4 .2H 2 O was obtained by chemical reaction between Ca(OH) 2 and H 2 34 SO 4 solution. The acid was obtained by chromatography ionic change, using cationic resin Dowex 50WX8 and Na 2 34 SO 4 solution. The reaction was realized under slow agitation. After the reaction, the precipitate was separated and dried in ventilated stove at 60 deg C temperature. The Mass of the Ca 34 SO 4 .2H 2 O produced was determined by method gravimetric. This way, a system contends resin 426 cm 3 , considering volume of 2.2 liters can be obtained a solution contends 44.2 g of H 2 34 SO 4 , theoretically could be produced 78.0 g of Ca 34 SO 4 .2H 2 O approximately. With results of the tests were verified that there was not total precipitation of the Ca 34 SO 4 .2H 2 O. Were produced 73.7± 0.6 g of Ca 34 SO 4 .2H 2 O representing average income 94.6±0.8 %. The purity of the produced CaSO 4 .2H 2 O was 98%. (author)

Bi--Sr--Ca--Cu--O superconducting films fabricated using metal alkoxides

International Nuclear Information System (INIS)

Katayama, S.; Sekine, M.

1991-01-01

Superconducting films in the Bi--Sr--Ca--Cu--O systems were made using metal alkoxides. To prepare a dip-coating solution using a mixed alkoxide solution, insoluble Cu and Bi alkoxides were dissolved by modification with 2-dimethylaminoethanol and formation of a double alkoxide, respectively. Formation of the double alkoxides of Bi with Ca or Sr was confirmed using FT-IR and 1 H-NMR. Bi--Sr--Ca--Cu--O films on yttria-stabilized ZrO 2 and single crystal MgO(100) substrates were made using this solution. The films were closely oriented along the c-axis perpendicular to the substrate. The film on MgO(100) fired at 850 degree C for 48 h showed two resistance drops around 115 and 85 K, corresponding to the high-T c and low-T c phases, respectively, and zero resistance at 72 K

The use of physiological solutions or media in calcium phosphate synthesis and processing.

Science.gov (United States)

Tas, A Cuneyt

2014-05-01

This review examined the literature to spot uses, if any, of physiological solutions/media for the in situ synthesis of calcium phosphates (CaP) under processing conditions (i.e. temperature, pH, concentration of inorganic ions present in media) mimicking those prevalent in the human hard tissue environments. There happens to be a variety of aqueous solutions or media developed for different purposes; sometimes they have been named as physiological saline, isotonic solution, cell culture solution, metastable CaP solution, supersaturated calcification solution, simulated body fluid or even dialysate solution (for dialysis patients). Most of the time such solutions were not used as the aqueous medium to perform the biomimetic synthesis of calcium phosphates, and their use was usually limited to the in vitro testing of synthetic biomaterials. This review illustrates that only a limited number of research studies used physiological solutions or media such as Earle's balanced salt solution, Bachra et al. solutions or Tris-buffered simulated body fluid solution containing 27mM HCO3(-) for synthesizing CaP, and these studies have consistently reported the formation of X-ray-amorphous CaP nanopowders instead of Ap-CaP or stoichiometric hydroxyapatite (HA, Ca10(PO4)6(OH)2) at 37°C and pH 7.4. By relying on the published articles, this review highlights the significance of the use of aqueous solutions containing 0.8-1.5 mMMg(2+), 22-27mM HCO3(-), 142-145mM Na(+), 5-5.8mM K(+), 103-133mM Cl(-), 1.8-3.75mM Ca(2+), and 0.8-1.67mM HPO4(2-), which essentially mimic the composition and the overall ionic strength of the human extracellular fluid (ECF), in forming the nanospheres of X-ray-amorphous CaP. Copyright © 2013 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

Surface morphology and molecular bonding of CaCO3 nanocrystallites by gas diffusion method

Science.gov (United States)

Sulimai, N. H.; Rani, Rozina Abdul; Khusaimi, Z.; Abdullah, S.; Salifairus, M. J.; Alrokayan, Salman; Khan, Haseeb; Rusop, M.

2018-05-01

Calcium carbonate with the chemical formula of (CaCO3) is the most abundant element in the world. Its usage on certain applications is largely affected by its properties. The best means to control its properties is through controlled preparation of CaCO3. This study uses diffusion method between the precursors Calcium Chloride and Ammonium Carbonate. Instead of using water, ethanol was used to prepare the salt. Reaction was done in room temperature (RT) for 6h-24h. Smallest average crystallite size measured by FESEM micrograph is 500nm produced by synthesis of CaCO3 reacted for 168 hours. From energy-dispersive X-ray spectrum also indicated the smallest particle size is by CaCO3 reacted for 168 hours. Changes was seen for element Ca at 3.7keV.

Determination of trace elements in chicken feeds in Khartoum state

International Nuclear Information System (INIS)

Hassan, Salma Yahya Mohammed

2017-03-01

Trace elements are very important for chicken because thy contribute in biochemical processes required for normal growth, development and formation of the eggshell. The deficiency or the elevation of these trace elements may affect the normal physiological activity and biochemical process of their bodies. In this study the concentrations of trace elements in chicken feed samples were determined by X RF spectrometry. The results showed that there were 9 trace elements in sample ( K, Ca Mn, Fe Cu Zn, Pb, Rb, Sr) the mean concentration were K ( 2.12 x 10 4 ), Ca (2.22x10 4 ), Mn (48.1). Fe (191), Cu(9.81), Zn (24.6), Pb (1.63), Rb (7.79), Sr(4.09) ppm. Comparing the trace elements concentrations obtained in this study with the recommended values showed that some of them e.g Mn, Cu, Zn, Fe were found higher concentration than the recommended values, which stipulated by national research council NRC European Union. While lead concentration was in the permissible limit (5mg/kg). However, the statistical Alan's revealed than there were no significant difference between all concentrations of trace elements in the two types of chicken feeds i.e layer and broiler. The pearson correlation test displayed a strong correlation between K-Rb (0.885), Mn-Zn (0.874). The negative correlation between Mn-Rb (0.680), K-Mn (0.6000), K-Ca (0.565), Zn-Rb (-0.541). Ca-Rb (0.458) were found . Further investigations were performed using the principal component analysis (PCA) which involved the extraction of principal factor to study the total variance in the feed samples in terms of the trace elements concentrations in each. The obtained results revealed that the first principal component have a positive correlation with the elements Ca, Mn, Pb, and Zn, while K and Rb showed negative correlation with it. Similarly, the second principal compound showed positive correlation with the elements Mn, PB and Zn, while Ca and Sr showed negative, on the perth hand the third component was found to

Sr/Ca and Mg/Ca in Glycymeris glycymeris (Bivalvia) shells from the Iberian upwelling system: Ontogeny and environmental control

Science.gov (United States)

Freitas, Pedro; Richardson, Christopher; Chenery, Simon; Monteiro, Carlos; Butler, Paul; Reynolds, David; Scourse, James; Gaspar, Miguel

2017-04-01

Bivalve shells have a great potential as high-resolution geochemical proxy archives of marine environmental conditions. In addition, sclerochronology of long-lived bivalve species (e.g. Arctica islandica) provides a timeline of absolutely dated shell material for geochemical analysis that can extend into the past beyond the lifetime of single individuals through the use of replicated crossmatched centennial to millennial chronologies. However, the interpretation of such records remains extremely challenging and complex, with multiple environmental and biological processes affecting element incorporation in the shell (e.g. crystal fabrics, organic matrix, biomineralization mechanisms and physiological processes). As a result, the effective use of bivalve shell elemental/Ca ratios as palaeoenvironmental proxies has been limited, often to species-specific applications or applications restricted to particular environmental settings. The dog-cockle, Glycymeris glycymeris, is a relatively long-lived bivalve (up to 200 years) that occurs in coarse-grained subtidal sediments of coastal shelf seas of Europe and North West Africa. Glycymeris glycymeris shells provide a valuable, albeit not fully explored, archive to reconstruct past environmental variability in an area lacking sclerochronological studies due to the rarity of long-lived bivalves and lack of coral reefs. In this study, we evaluate the potential of Sr/Ca and Mg/Ca ratios in G. glycymeris shells as geochemical proxies of upwelling conditions in the Iberian Upwelling System, the northern section of the Canary Current Eastern Boundary Upwelling System. Sr/Ca and Mg/Ca generally co-varied significantly and a clear ontogenetic, non-environmental related change in Sr/Ca and Ba/Ca variability was observed. High Sr/Ca and Mg/Ca ratios in older shells (> 10 years old) were found to be associated with the occurrence of growth lines deposited during the winter reduction in shell growth. Nevertheless, Sr/Ca and Mg/Ca

23 Elemental Composition of Suspended Particulate Matter ...

African Journals Online (AJOL)

`123456789jkl''''#

The samples were analysed by energy dispersive x-ray fluorescence. (EDXRF) and atomic absorption spectroscopy (AAS) for up to 10 elements. It was found that 66% of the ..... coefficients between the various crustal elements Ca, Ti, Mn, ...

Synthesis and photoluminescence of Ca-(Sn,Ti)-Si-O compounds

International Nuclear Information System (INIS)

Abe, Shunsuke; Yamane, Hisanori; Yoshida, Hisashi

2010-01-01

The phase relation of the compounds prepared in the CaO-SnO 2 -SiO 2 system at 1673 K and in the CaO-TiO 2 -SiO 2 system at 1573 K was investigated in order to explore new Ti 4+ -activated stannate phosphors. Solid solutions of Ca(Sn 1-x Ti x )SiO 5 and Ca 3 (Sn 1-y Ti y )Si 2 O 9 were synthesized at x = 0-1.0 and y = 0-0.10, respectively, and their crystal structures were analyzed by powder X-ray diffraction. Photoluminescence of these solid solutions was observed in a broad range of a visible light wavelength region under ultraviolet (UV) light excitation. The peaks of the emission band of Ca(Sn 0.97 Ti 0.03 )SiO 5 and Ca 3 (Sn 0.925 Ti 0.075 )Si 2 O 9 were at 510 nm under excitation of 252 nm and at 534 nm under excitation of 258 nm, respectively. The absorption edges estimated by the diffuse reflectance spectra were at 300 nm (4.1 eV) for CaSnSiO 5 and at 270 nm (4.6 eV) for Ca 3 SnSi 2 O 9 , suggesting that the excitation levels in Ca(Sn 1-x Ti x )SiO 5 were above the band gap of the host, although the levels in Ca 3 (Sn 1-y Ti y )Si 2 O 9 were within the band gap and near the conduction band edge.

Determination of the micro-nutrient elements and the toxic in food of peruvian children of the city of Lima. Part I: determination through instrumental neutron activation of Ca, Cl, K, Mg and Na in samples of milk and milk with cereal consumed by peruvian children in the age of weaning

International Nuclear Information System (INIS)

Montoya R, E.; Bedregal, P.; Diaz, A.; Zavaleta, N.; Berlanga, R.

1993-01-01

The contents of Ca, Cl, K, Mg and Na in milk and milk with cereal, consumed by the peruvian children were determined by short irradiation INAA using RP-10 reactor, with a thermal flux of 10 13 n/cm -2 s -1 and a pneumatic system. The comparative method with solutions of primary standards of each element determined was used. The IAEA-A11-milk powder, IAEA-H4-animal muscle and IAEA-V10-hay powder, reference materials were periodically analyzed, together with the samples, in order to check the quality of analytical results. (authors) 3 refs., 3 tabs, 2 figs

The calcium oxide influence on formation of manganese, calcium pyrovanadate solid solutions

International Nuclear Information System (INIS)

Vatolin, N.A.; Volkova, P.I.; Sapozhnikova, T.V.; Ovchinnikova, L.A.

1988-01-01

The X-ray graphic, derivatographic, microscopic and chemical methods are used to study solid solutions of manganese, calcium pyrovanadates containing 1-10 mass% CaO and the products of interaction of reprocessing charges of vanadium-containing converter slags intended for he formation of manganese and calcium pyrovanadates with additions of calcium oxide within 10-90 mass%. It is established that in the case of 1-6 mass% CaO content in manganese pyrovanadate solid interstitial solutions appear, while at 6-20 mass% CaO - solid substitution solutions form. The results of calculating elementary cell parameters as well as melting temperatures and pyrovanadate solid solution solubility depending on CaO content are presented. The best solubility of introduction solid solutions during vanadium extraction according to the lime technology is found

Distributions of 14 elements on 63 absorbers from three simulant solutions (acid-dissolved sludge, acidified supernate, and alkaline supernate) for Hanford HLW Tank 102-SY

International Nuclear Information System (INIS)

Marsh, S.F.; Svitra, Z.V.; Bowen, S.M.

1994-08-01

As part of the Hanford Tank Waste Remediation System program at Los Alamos, we evaluated 63 commercially available or experimental absorber materials for their ability to remove hazardous components from high-level waste (HLW). These absorbers included cation and anion exchange resins, inorganic exchangers, composite absorbers, and a series of liquid extractants sorbed on porous support-beads. We tested these absorbers with three solutions prepared to simulate acid-dissolved sludge (pH 0.6), acidified supernate (pH 3.5), and alkaline supernate (pH 13.9) from underground storage tank 102-SY at the Hanford Reservation near Richland, Washington. To these simulants we added the appropriate radionuclides and used gamma spectrometry to measure fission products (Ce, Cs, Sr, Tc, and Y), actinides (U, Pu, and Am), and matrix elements (Cr, Co, Fe, Mn, Zn, and Zr). For each of more than 2500 element/absorber/solution combinations, we measured distribution coefficients for dynamic contact periods of 30 min, 2 h, and 6 h to obtain information about sorption kinetics. Because we measured the sorption of many different elements, the tabulated results indicate those elements most likely to interfere with the sorption of elements of greater interest. On the basis of nearly 7500 measured distribution coefficients, we determined that many of these absorbers appear suitable for processing HLW. This study supersedes the previous version of LA-12654, in which results attributed to a solution identified as an alkaline supernate simulant were misleading because that solution contained insufficient hydroxide

Improvement of the mechanical properties and corrosion resistance of biodegradable β-Ca3(PO4)2/Mg-Zn composites prepared by powder metallurgy: the adding β-Ca3(PO4)2, hot extrusion and aging treatment.

Science.gov (United States)

Yan, Yang; Kang, Yijun; Li, Ding; Yu, Kun; Xiao, Tao; Deng, Youwen; Dai, Han; Dai, Yilong; Xiong, Hanqing; Fang, Hongjie

2017-05-01

In this study, 10%β-Ca 3 (PO 4 ) 2 /Mg-6%Zn (wt.%) composites with Mg-6%Zn alloy as control were prepared by powder metallurgy. After hot extrusion, the as-extruded composites were aged for 72h at 150°C. The effects of the adding β-Ca 3 (PO 4 ) 2 , hot extrusion and aging treatment on their microstructure, mechanical properties and corrosion resistance were investigated. The XRD results identified α-Mg, MgZn phase and β-Ca 3 (PO 4 ) 2 phase in these composites. After hot extrusion, grains were significantly refined, and the larger-sized β-Ca 3 (PO 4 ) 2 particles and coarse MgZn phases were broken into linear-distributed β-Ca 3 (PO 4 ) 2 and MgZn phases along the extrusion direction. After aging treatment, the elements of Zn, Ca, P and O presented a more homogeneous distribution. The compressive strengths of the β-Ca 3 (PO 4 ) 2 /Mg-Zn composites were approximately double those of natural bone, and their densities and elastic moduli matched those of natural bone. The immersion tests and electrochemical tests revealed that the adding β-Ca 3 (PO 4 ) 2 , hot extrusion and aging treatment could promote the formation of protective corrosion product layer on the sample surface in Ringer's solution, which improved corrosion resistance of the β-Ca 3 (PO 4 ) 2 /Mg-Zn composites. The XRD results indicated that the corrosion product layer contained Mg(OH) 2 , β-Ca 3 (PO 4 ) 2 and hydroxyapatite (HA). The cytotoxicity assessments showed the as-extruded β-Ca 3 (PO 4 ) 2 /Mg-Zn composite aged for 72h was harmless to L-929 cells. These results suggested that the β-Ca 3 (PO 4 ) 2 /Mg-Zn composites prepared by powder metallurgy were promising to be used for bone tissue engineering. Copyright © 2017 Elsevier B.V. All rights reserved.

Adsorption effect in non-reaction wetting: In-Ti on CaF2

International Nuclear Information System (INIS)

Glickman, E.; Fuks, D.; Frage, N.; Barzilai, S.; Froumin, N.

2012-01-01

The experiments show that the alloying liquid In with only (0.1-0.5) at% Ti dramatically reduces the equilibrium contact angle Θ ∞ formed by In on the surface of CaF 2 . The aim of this paper is to clarify whether this practically important and conceptually challenging effect can be explained solely by Ti adsorption at the F-terminated solid-liquid interface without resorting to any other Ti-induced effect. The combination of ab initio calculations and regular solution approximation was proposed for finding the binding energy, ΔE Ti of Ti adatom with the interface ''CaF 2 /liquid solutions In-Ti.'' With thus obtained ΔE Ti =1.16 eV, we calculated from the Shishkovsky isotherm the reduction in the solid-liquid interface energy, Δγ SL induced by Ti adsorption from liquid In with various Ti concentration, C. It was found that Δγ SL (C) dependence demonstrated close inverse correspondence with Θ ∞ (C) and that the theory fitted very well all available experimental data on the concentration and temperature dependence of Δγ SL . It was concluded that the Ti adsorption effect is large enough to account for the observed wetting improvement. The proposed multiscale modeling approach to the role of adsorption in wetting can be applied also to other nonreactive systems ''liquid metal-ceramics'' where the substrate determines the surface density of the adsorption sites for the active element. (orig.)

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

Separation of thorium and uranium by liquid-liquid extraction from mixed aqueous nitric acidic-methanolic solutions

International Nuclear Information System (INIS)

Schmid, E.R.; Kenndler, E.

1976-01-01

A method is described for the separation of Th and U from each other and from other elements, usually occuring in minerals, by liquid-liquid extraction with Aliquat Nitrate (tricaprylmethyl ammoniumnitrate, 6 vol%) in benzene from a mixed solution of 2.5 M HNO 3 and methanol (1:1 volume ratio). Permissible upper concentration ratios of interfering elements, such as Li, Na, K, Mg, Ca, Al, Cu, Co(II), Fe(III), Mn(II), Ti(IV), La(III), U(VI), Cl - , ClO 4 - , SO 4 2- , PO 4 3- , have been determined. Following the separation, Th has been determined by spectrophotometry using Thorin, and U by fluorometry. Results for yield under varying conditions, together with elemental concentrations in the ppm range for U and Th in minerals, are given. (B.T.)

Ca-48 handling for a cyclotron ECR ion source to produce highly intense ion beams

International Nuclear Information System (INIS)

Lebedev, V.Ya.; Bogomolov, S.L.; Dmitriev, S.N.; Kutner, V.B.; Shamanin, A.N.; Yakushev, A.B.

2002-01-01

Ca ion beam intensities in the U-400 cyclotron. To control the 48 Ca movement during the preparation of metallic calcium, recuperation of the calcium and to obtain a picture of the distribution of the 48 Ca deposits inside the ECR ion source, we used 47 Ca as a radiotracer. This was obtained from the 48 Ca(γ,n) 47 Ca reaction by irradiating a mixture of 48 CaO + Al, prepared for the reduction of the calcium, with the bremsstrahlung (E e = 22 MeV) of the microtron MT-25 of JINR FLNR. The radiotracer technique provided us with 48 Ca control in all processes of calcium of the ECR ion source after stopping and calcium separation from acidic solutions, that allowed us to minimize our losses of 48 Ca. The whole technique was very effective in dealing with such expensive isotope as 48 Ca. During the last years at FLNR JINR (Dubna) several isotopes of element 114 and 116 have been obtained by irradiation of Pu and Cm targets with highly intense 48 Ca ion beams

CaO insulator coatings on a vanadium-base alloy in liquid 2 at.% calcium-lithium

International Nuclear Information System (INIS)

Park, J.H.; Kassner, T.F.

1996-01-01

The electrical resistance of CaO coatings produced on V-4%Cr-4%Ti and V-15%Cr-5%Ti by exposure of the alloy (round bottom samples 6-in. long by 0.25-in. dia.) to liquid lithium that contained 2 at.% dissolved calcium was measured as a function of time at temperatures between 300-464 degrees C. The solute element, calcium in liquid lithium, reacted with the alloy substrate at these temperatures for 17 h to produce a calcium coating ∼7-8 μm thick. The calcium-coated vanadium alloy was oxidized to form a CaO coating. Resistance of the coating layer on V-15Cr-5Ti, measured in-situ in liquid lithium that contained 2 at.% calcium, was 1.0 x 10 10 Ω-cm 2 at 300 degrees C and 400 h, and 0.9 x 10 10 Ω-cm 2 at 464 degrees C and 300 h. Thermal cycling between 300 and 464 degrees C changed the resistance of the coating layer, which followed insulator behavior. Examination of the specimen after cooling to room temperature revealed no cracks in the CaO coating. The coatings were evaluated by optical microscopy, scanning electron microscopy (SEM), electron dispersive spectroscopy (EDS), and X-ray analysis. Adhesion between CaO and vanadium alloys was enhanced as exposure time increased

Macro-Elements and Trace Elements in Cereal Grains Cultivated in Latvia

Directory of Open Access Journals (Sweden)

Jākobsone Ida

2015-09-01

Full Text Available Cereal-based foods have great importance in the compensation of micro- and trace element deficiency, because 50% of the foods produced worldwide are made up of cereal grains. The aim of the research was to determine the concentration of macro-elements and trace elements in different cereals cultivated in Latvia. Various cereals were used in the research: rye (n = 45, barley (n = 54, spring wheat (n = 27, winter wheat (n = 53, triticale (n = 45 and oats (n = 42. Thirteen macro- and trace elements (Cd, Pb, Ni, Cr, Al, Cu, K, Na, Mn, Fe, Zn, Mg, Ca were determined in cereal grain samples (n = 266. Macro-elements and trace elements varied significantly (p < 0.01 or p < 0.001. The highest concentrations of macro- and trace elements were found in oats and the lowest in rye. The obtained data will expand the opportunity for food and nutrition scientists to evaluate content of the examined elements in grain products, and dietary consumption (bioavailability of the examined macro-elements and trace elements.

Finite Volume Element (FVE) discretization and multilevel solution of the axisymmetric heat equation

Science.gov (United States)

Litaker, Eric T.

1994-12-01

The axisymmetric heat equation, resulting from a point-source of heat applied to a metal block, is solved numerically; both iterative and multilevel solutions are computed in order to compare the two processes. The continuum problem is discretized in two stages: finite differences are used to discretize the time derivatives, resulting is a fully implicit backward time-stepping scheme, and the Finite Volume Element (FVE) method is used to discretize the spatial derivatives. The application of the FVE method to a problem in cylindrical coordinates is new, and results in stencils which are analyzed extensively. Several iteration schemes are considered, including both Jacobi and Gauss-Seidel; a thorough analysis of these schemes is done, using both the spectral radii of the iteration matrices and local mode analysis. Using this discretization, a Gauss-Seidel relaxation scheme is used to solve the heat equation iteratively. A multilevel solution process is then constructed, including the development of intergrid transfer and coarse grid operators. Local mode analysis is performed on the components of the amplification matrix, resulting in the two-level convergence factors for various combinations of the operators. A multilevel solution process is implemented by using multigrid V-cycles; the iterative and multilevel results are compared and discussed in detail. The computational savings resulting from the multilevel process are then discussed.

Cellular Response to Doping of High Porosity Foamed Alumina with Ca, P, Mg, and Si

Directory of Open Access Journals (Sweden)

Edwin Soh

2015-03-01

Full Text Available Foamed alumina was previously synthesised by direct foaming of sulphate salt blends varying ammonium mole fraction (AMF, foaming heating rate and sintering temperature. The optimal product was produced with 0.33AMF, foaming at 100 °C/h and sintering at 1600 °C. This product attained high porosity of 94.39%, large average pore size of 300 µm and the highest compressive strength of 384 kPa. To improve bioactivity, doping of porous alumina by soaking in dilute or saturated solutions of Ca, P, Mg, CaP or CaP + Mg was done. Saturated solutions of Ca, P, Mg, CaP and CaP + Mg were made with excess salt in distilled water and decanted. Dilute solutions were made by diluting the 100% solution to 10% concentration. Doping with Si was done using the sol gel method at 100% concentration only. Cell culture was carried out with MG63 osteosarcoma cells. Cellular response to the Si and P doped samples was positive with high cell populations and cell layer formation. The impact of doping with phosphate produced a result not previously reported. The cellular response showed that both Si and P doping improved the biocompatibility of the foamed alumina.

The Rengen Grassland experiment: bryophytes biomass and element concentrations after 65 years of fertilizer application.

Science.gov (United States)

Hejcman, Michal; Száková, Jirina; Schellberg, Jürgen; Srek, Petr; Tlustos, Pavel; Balík, Jirí

2010-07-01

The Rengen Grassland Experiment in Germany, established in 1941, consists of the following fertilizer treatments applied under a two cut management: control, Ca, CaN, CaNP, CaNP-KCl, and CaNP-K(2)SO(4). The aim of this study was (1) to identify effects of fertilizer application on biomass and species composition of bryophytes and (2) to investigate the impact of fertilizer application on macro- (N, P, K, Ca, Mg), micro- (Cu, Fe, Mn, Zn), and toxic (As, Cd, Cr, Pb, Ni) element concentrations in bryophyte biomass. In June 2006, Rhytidiadelphus squarrosus was the only bryophyte species recorded in the control. In treatment Ca, R. squarrosus was the dominant bryophyte species whereas Brachythecium rutabulum occurred sporadically only in a single plot of that treatment. The latter was the only bryophyte species collected in CaN, CaNP, CaNP-KCl, and CaNP-K(2)SO(4) treatments. Dry matter accumulation of bryophytes was highest in the control (180 g m(-2)) followed by Ca (46 g m(-2)), CaNP (25 g m(-2)), CaNP-KCl (15 g m(-2)), CaNP-K(2)SO(4) (9 g m(-2)), and CaN (2 g m(-2)) treatments. A negative correlation between biomass production of bryophytes and dry matter production of vascular plants was revealed up to a threshold value of 400 g m(-2). Above this limit, biomass production of bryophytes remained obviously unaffected by further increase in biomass production of vascular plants. A significant effect of treatment on As, Cd, Cr, Fe, Mn, Ni, Pb, P, Ca, Mg, K, and N concentrations was revealed. Concentrations of these elements were a function of amount of elements supplied with fertilizers. Bryophytes seem to be promising bio-indicators not only for airborne deposition of toxic element but also for fertilizer introduced as well.

The effect of theophylline on the labelling of nitracellular myocardial calcium with 45Ca

International Nuclear Information System (INIS)

Sausen, F.H.

1973-01-01

The effect of theophylline of varying concentration on the labelling of intracellular myocardial calcium was investigated by isotope tests with radioactively labelled Ca ( 45 Ca) in isolated, electrically stimulated left auricles of guinea pigs. The preparates were incubated in a 45 Ca solution for 60 minutes, and activity uptake and intracellular Ca concentration were determined. In contrast to earlier investigations, the extracellular Ca was removed after charge by rinsing the resting auricles with inactive, Ca ++ - and Na + -free choline chloride solution. Under controlled conditions, the intercellular Ca was found to be 45 Ca-labelled by about 36% theophylline in 'therapeutical' concentration (5 x 10 -4 g/ml) induced a significant increase of the labelled Ca fraction of 16.9% as compared to the controls. 'Toxic' theophylline concentrations, too, lead to a significantly higher absorption of 45 Ca. The interchangeable intracellular Ca fraction increased by 11.7% and 10.3% as compared to the untreated preparates. The findings are discussed with regard to earlier investigations on the influence of methylxanthines on the Ca metabolism of the heart. The author assumes that the positively inotropic effect of theophylline and the theophylline-induced contracture may be ascribed to a shift in the intracellular Ca distribution towards ionized Ca. This shift could be explained by a suppression of Ca rebinding in intracellular Ca storage places or by Ca release from these structures. (orig./AK) [de

Matrix equation decomposition and parallel solution of systems resulting from unstructured finite element problems in electromagnetics

Energy Technology Data Exchange (ETDEWEB)

Cwik, T. [California Institute of Technology, Pasadena, CA (United States); Katz, D.S. [Cray Research, El Segundo, CA (United States)

1996-12-31

Finite element modeling has proven useful for accurately simulating scattered or radiated electromagnetic fields from complex three-dimensional objects whose geometry varies on the scale of a fraction of an electrical wavelength. An unstructured finite element model of realistic objects leads to a large, sparse, system of equations that needs to be solved efficiently with regard to machine memory and execution time. Both factorization and iterative solvers can be used to produce solutions to these systems of equations. Factorization leads to high memory requirements that limit the electrical problem size of three-dimensional objects that can be modeled. An iterative solver can be used to efficiently solve the system without excessive memory use and in a minimal amount of time if the convergence rate is controlled.

Composition-structure-property (Zn2+ and Ca2+ ion release) evaluation of Si-Na-Ca-Zn-Ce glasses: Potential components for nerve guidance conduits

International Nuclear Information System (INIS)

Zhang, X.F.; Kehoe, S.; Adhi, S.K.; Ajithkumar, T.G.; Moane, S.; O'Shea, H.; Boyd, D.

2011-01-01

Bioactive glasses have demonstrated tailored therapeutic ion release, primarily with respect to the augmentation of hard tissues. However, controlled degradation and release of therapeutic ions from biomaterials may also play an important role in soft tissue regeneration such as repair of peripheral nerve discontinuities. In this study, three silica based glasses (0.5SiO 2 -0.2CaO-0.13ZnO-XNa 2 O-(0.17-X) CeO 2 ) where, (0.04 29 Si isotope was probed for each glass using 29 Si MAS-NMR, whilst the thermal characteristics of each glass were examined using DTA. Following these analyses, ion release profiles for Ca 2+ and Zn 2+ were evaluated; an equivalent specific surface area of 1 m 2 of each glass powder was incubated (37 deg. C) in 10 ml of citric acid buffer and TRIS-HCI buffer solution (pH 3.0 and pH 7.4 respectively) for incubation periods of up to 30 days. The Zn 2+ concentration of each filtrate was analysed using flame Atomic Absorption Spectroscopy (Varian AA240FS Fast Sequential AAS) and the Ca 2+ concentration of each filtrate was determined using Inductively Coupled Plasma-Mass Spectrometer (Varian 820 ICP-MS). Results obtained from the 29 Si MAS-NMR spectra indicated Q 2 structures pervading the network. An analytical model was proposed to analyse the ion release profiles for each glass, and indicated heterogeneous dissolution of glass networks. The ion release data demonstrates that ion release in the range (19.26-3130 ppm) for Ca 2+ and in the range (5.97-4904 ppm) for Zn 2+ occurred. Release of such elements, at appropriate levels, from peripheral nerve guidance conduits may be advantageous with respect to the repair of peripheral nerve discontinuities.

Fast solution of neutron diffusion problem by reduced basis finite element method

International Nuclear Information System (INIS)

Chunyu, Zhang; Gong, Chen

2018-01-01

Highlights: •An extremely efficient method is proposed to solve the neutron diffusion equation with varying the cross sections. •Three orders of speedup is achieved for IAEA benchmark problems. •The method may open a new possibility of efficient high-fidelity modeling of large scale problems in nuclear engineering. -- Abstract: For the important applications which need carry out many times of neutron diffusion calculations such as the fuel depletion analysis and the neutronics-thermohydraulics coupling analysis, fast and accurate solutions of the neutron diffusion equation are demanding but necessary. In the present work, the certified reduced basis finite element method is proposed and implemented to solve the generalized eigenvalue problems of neutron diffusion with variable cross sections. The order reduced model is built upon high-fidelity finite element approximations during the offline stage. During the online stage, both the k eff and the spatical distribution of neutron flux can be obtained very efficiently for any given set of cross sections. Numerical tests show that a speedup of around 1100 is achieved for the IAEA two-dimensional PWR benchmark problem and a speedup of around 3400 is achieved for the three-dimensional counterpart with the fission cross-sections, the absorption cross-sections and the scattering cross-sections treated as parameters.

Stress Analysis of a TRISO Coated Particle Fuel by Using ABAQUS Finite Element Visco-Elastoplastic Solutions

International Nuclear Information System (INIS)

Cho, Moon Sung; Kim, Y. M.; Lee, Y. W.

2006-01-01

The fundamental design for a gas-cooled reactor relies on an understanding of the behavior of a coated particle fuel. KAERI, which has been carrying out the Korean VHTR (Very High Temperature modular gas cooled Reactor) Project since 2004, is developing a fuel performance analysis code for a VHTR named COPA (COated Particle fuel Analysis). A validation of COPA was attempted by comparing its benchmark results with the visco-elastic solutions obtained from the ABAQUS code calculations for the IAEA-CRP-6 TRISO coated particle benchmark problems involving a creep, swelling, and pressure. However, the ABAQUS finite element model used for the above-mentioned analysis did not consider the material nonlinearity of the SiC coating layer that showed stress levels higher than the assumed yield point of the material. In this study, a consideration of the material nonlinearity is included in the ABAQUS model to obtain the visco-elastoplastic solutions and the results are compared with the visco-elastic solutions obtained from the previous ABAQUS model

Synthesis of leucite, sanidine and a melt of sanidine at 930-10300C and 2 Kb: partition coefficients of Rb, Ca, Sr and Ba between these phases and hydrothermal solution of KCl. Geological utilizations

International Nuclear Information System (INIS)

Moreira, A.H.P.

1988-01-01

This work shows the results of hydrothermal experiments to determine the distribution coefficients of alcali and alcaline earth elements in trace concentrations between sanidine and liquids of same composition and between leucite and liquid. At 2 Kb pressure and 930 0 C for sanidine, 930 0 and 1030 0 C for leucite and 1030 0 C for a melt of sanidine composition the concentration of trace elements (TE) in the coexisting potassium bearing aqueous fluid phase was varied between 10 -1 to 10 -6 mole to one mol of K + . By use of radioactive tracers (Rb 86 , Ca 45 , Sr 85 , Ba 133 ) the concentrations in TE of the aqueous phase, the solids and melts has been determined. This indirect method will give a good aproximation of the behaviour of TE between a melt and crystallising solids. These aprotimations lead to following conclusions: a) during the crystallisation of leucite, this phase incorporates large quantities of Ba and Rb, depleting the residual melt in those elements. Sr and Ca, on the other hand are enriched in the residual melt. b) the crystallisation of sanidine depletes even more the residual melt in Ba, Sr shows similias behaviour, Rb and Ca, however, are enriched in the residual melt phase. (author) [pt

A new potentiometric method for the estimation of the rare earth elements

International Nuclear Information System (INIS)

Selig, W.S.

1988-01-01

Chinese workers recently described a new potentiometric method for lead using sodium tetraphenylborate (NaTPB) as a titrant. Based on a previous Chinese publication, the authors have recently developed a method for the estimation of the alkaline earth metals by sequential titration with NaTPB. In the present work, the authors report a similar method for the estimation of the rare earth elements, including Sc and Y. The sensing electrode is a spectrographic graphite rod, coated with a solution of poly(vinyl chloride) and dioctylphthalate in tetrahydrofuran as previously described. The reference electrode was a double-junction Ag/AgCl electrode. The titration system is controlled by a Tektronix 4051 graphics computer system. Single cations or mixtures up to 0.5 mequiv are determined by potentiometric titration with 0.05 N NaTPB, after formation of the oxonium cations by reaction with an aqueous solution of poly(ethylene glycol) (PEG). Best results are obtained with PEGs of molecular weights from 8,000 to 20,000. Sequential estimation of Pb + Ba, Sr, and Ca, and the sum of the rare earth elements is also reported, plus possible applications to Al, Ga, and anions precipitated by lead

Extraction and separation of Am and rare earth elements in HNO3 solution with P507-sulphonating kerosene

International Nuclear Information System (INIS)

Li Zhenhu; Jiao Rongzhou; Zhu Yongjun

1994-01-01

A study has been made of the extraction equilibrium of Am(III) and rare earth elements (III) in HNO 3 solution with P507-sulphonating kerosene. It has been found that this equilibrium depends on saponification ratio of P507, feed acidity, metal concentration as well as phase ratio. The extraction ability in order is La< Ce< Am< Pr< Nd< Sm. The model of distribution ratio has been founded. The agreement for calculated and experimental values of distribution ratio is fairly good. These values can be used to design the extraction and separation process of Am and rare earth elements

Determination of the potential and coherent scattering cross-sections of the elements Si, Ca, Cr, Mn, Co, Zn, Zr, Sb and Ta

International Nuclear Information System (INIS)

Adib, M.; Abdel-Kawy, A.; Hamouda, I.

1976-01-01

The potential scattering cross-sections for slow neutrons have been measured for Si, Ca, Cr, Mn, Co, Zn, Zr, Sb and Ta in order to determine the nuclear potential radius and to investigate the prediction of nuclear optical model. The coherent scattering cross-sections for these elements have been measured from the obtained values of the Bragg cut-offs observed in the behaviour of the total cross-sections at cold neutron energies. The measurements were based on the total neutron cross-sections resulting from transmission experiments performed with the neutron chopper at ET-RR-1 reactor

In-situ thermal analysis and macroscopical characterization of Mg-xCa and Mg-0.5Ca-xZn alloy systems

Energy Technology Data Exchange (ETDEWEB)

Farahany, Saeed [Department of Materials Engineering, Faculty of Mechanical Engineering, Universiti Teknologi Malaysia, 81310 Johor Bahru, Johor (Malaysia); Bakhsheshi-Rad, Hamid Reza, E-mail: Rezabakhsheshi@gmail.com [Department of Materials Engineering, Faculty of Mechanical Engineering, Universiti Teknologi Malaysia, 81310 Johor Bahru, Johor (Malaysia); Idris, Mohd Hasbullah [Department of Materials Engineering, Faculty of Mechanical Engineering, Universiti Teknologi Malaysia, 81310 Johor Bahru, Johor (Malaysia); Abdul Kadir, Mohammed Rafiq [Medical Implants Technology Group, Universiti Teknologi Malaysia, 81310 Johor Bahru, Johor (Malaysia); Department of Biomechanics and Biomedical Materials, Faculty of Biomedical Engineering and Health Sciences, Universiti Teknologi Malaysia, 81310 Johor Bahru, Johor (Malaysia); Lotfabadi, Amir Fereidouni [Department of Manufacturing and Industrial Engineering, Faculty of Mechanical Engineering, Universiti Teknologi Malaysia, 81310 Johor Bahru, Johor (Malaysia); Ourdjini, Ali [Department of Materials Engineering, Faculty of Mechanical Engineering, Universiti Teknologi Malaysia, 81310 Johor Bahru, Johor (Malaysia)

2012-01-10

Highlights: Black-Right-Pointing-Pointer The effect of Ca and Zn addition on Mg-Ca and Mg-Ca-Zn were investigated. Black-Right-Pointing-Pointer Ca and Zn addition decreased solid fraction at coherency point. Black-Right-Pointing-Pointer T{sub N}-T{sub DCP} increased by adding Ca and Zn in Mg-Ca and Mg-Ca-Zn, respectively. Black-Right-Pointing-Pointer Three reactions were detected when Zn/Ca atomic ratio less than 1.25 in Mg-Ca-Zn. Black-Right-Pointing-Pointer A new peak Mg{sub 51}Zn{sub 20} was identified in Mg-0.5Ca-9Zn in addition of other peaks. - Abstract: This research described the identification phases by thermal analysis and microscopy inspection of Mg-xCa and Mg-0.5%Ca-xZn alloys that were solidified at slow cooling rate. Analysis of cooling curve after Ca addition shows the evolution of the Mg{sub 2}Ca intermetallic phase at around 520 Degree-Sign C in addition to {alpha}-Mg phase. First derivative curves of alloys after the addition of Zn to Mg-0.5Ca alloy reveals three peaks related to {alpha}-Mg, Mg{sub 2}Ca and Ca{sub 2}Mg{sub 6}Zn{sub 3} for alloys that have Zn/Ca atomic ratio less than 1.23. The peak of Mg{sub 2}Ca reaction on the first derivative curves disappeared for alloys containing Zn/Ca ratio more than 1.23. A new peak was also observed at 330 Degree-Sign C for Mg-0.5Ca-9Zn which was identified as Mg{sub 51}Zn{sub 20}. Solid fraction at coherency point decreased with increasing Ca and Zn elements. However, coherency time and difference between the nucleation and coherency temperatures (T{sub N}-T{sub DCP}) increased by adding Ca and Zn in Mg-Ca and Mg-Ca-Zn systems.

Effects of solute elements on hardening of thermally-aged RPV model alloys

International Nuclear Information System (INIS)

Dohi, Kenji; Nishida, Kenji; Nomoto, Akiyoshi; Soneda, Naoki; Liu, Li; Sekimura, Naoto; Li Zhengcao

2012-01-01

The investigation of effects of solute elements on the copper-enriched cluster, which is a cause of radiation embrittlement of reactor pressure vessel steels, is needed in order to understand the mechanism of the hardening and the cluster formation. The dependence of the hardness change and the formation of thermally-aged Fe-Cu model alloys doped Ni, Si and Mn on aging time are investigated using Vickers harness tester and three dimensional atom probe. Ni addition suppresses hardening, and Si addition accelerates hardening slightly at the initial stage of the aging. Mn addition accelerates hardening much more but does not almost affect the peak hardness. Ni and Si addition increase the number density and the size of the cluster, while Mn addition remarkably increases the number density and the size of the cluster at the initial stage of the aging. In addition, there is no clear correlation between the square root of the volume fraction of the clusters and the hardness change for all of the alloys. The reasons are considered to be the decrease in the solute hardening caused by the cluster formation and the difference in the shear modulus of the cluster due to the difference in the chemical composition of the cluster. (author)

Study of calcium-dependent lead-tolerance on plants differing in their level of Ca-deficiency tolerance

International Nuclear Information System (INIS)

Antosiewicz, Danuta Maria

2005-01-01

The main aim of the study was to determine the role of calcium in the amelioration of lead toxic effects in plants with accordingly high/low level of Pb-tolerance and high/low Ca-deficiency tolerance. The study was performed on maize, rye, tomato and mustard. Plants were cultivated in modified Knop's solution. They were subjected to Ca-deficiency, and to lead nitrate administered in the presence of four calcium nitrate concentrations 3.0, 2.4, 1.2, 0.3 mM. Lead-tolerance and tolerance to Ca-deficiency were determined, as were concentration of the studied elements in plant tissues, and the Pb deposition pattern at the ultrastructural level (electron microscopy study, X-ray microanalysis). In all studied plants, lead toxicity increased as medium calcium content decreased, however, only in the Ca-deficiency sensitive mustard with low Pb-tolerance was it accompanied by a rise in tissue lead concentration. In contrast, lead root and shoot levels did not increase in the highly Ca-deficiency tolerant tomato, mustard and rye with high Pb-tolerance irrespective of the Ca 2+ regimens applied. Thus, in these plants, lead's unfavourable effects resulted only from the higher toxicity of the same amount of lead in tissues at low calcium in the medium. Of particular relevance is the finding by electron microscopy and X-ray microanalysis, that under low calcium in both highly Ca-deficiency tolerant and Ca-deficiency sensitive plants, less efficient Pb 2+ detoxification was accompanied by the restriction of the formation of large lead deposits in cell walls. Obtained results are novel in demonstrating calcium involvement in the lead deposition in the cell wall, thus in the regulation of the internal lead detoxification. - Calcium regulated lead deposition in cell walls of plants

Solution microcalorimeter for measuring heats of solution of radioactive elements and compounds

International Nuclear Information System (INIS)

Raschella, D.L.

1978-12-01

The microcalorimeter vessel is constructed of tantalum metal, with a nominal volume of 5 cm 3 . Its energy equivalent is 24 J K -1 when containing 5 cm 3 H 2 O. The thermal leakage modulus is 0.010 min -1 . A thermistor is employed as the temperature sensor. The operating sensitivity is about 1 x 10 -5 K (300 μJ). The performance of the calorimetry system was tested using tris(hydroxymethyl)aminomethane (TRIS) and magnesium metal. The results of the TRIS experiments, at a concentration of 1 g dm -3 in 0.1 N HCl at 298 K, yielded a heat of solution of -29.606 +- 0.063 kJ mol -1 . The magnesium experiments, in 1 N HCl at 298 K, gave a heat of solution of -465.965 +- 1.136 kJ mol -1 . The heat of solution of curium-248 metal in 1 N HCl at 298 K was measured. The experiments, which should not be considered definitive, yielded a heat of solution of -606.4 +- 1.8 kJ mol -1 . A single measurement in 6 N HCl gave a heat of solution of -602.3 kJ mol -1 . From these results the heat of formation of Cm 3+ /sub (aq)/ is calculated to be -607.2 +- 2.5 kJ mol -1

Effects of intercropping of oat (Avena sativa L.) with white lupin (Lupinus albus L.) on the mobility of target elements for phytoremediation and phytomining in soil solution.

Science.gov (United States)

Wiche, Oliver; Székely, Balazs; Kummer, Nicolai-Alexeji; Moschner, Christin; Heilmeier, Hermann

2016-09-01

This study aims to investigate how intercropping of oat (Avena sativa L.) with white lupin (Lupinus albus L.) affects the mobile fractions of trace metals (Fe, Mn, Pb, Cd, Th, U, Sc, La, Nd, Ge) in soil solution. Oat and white lupin were cultivated in monocultures and mixed cultures with differing oat/white lupin ratios (11% and 33% lupin, respectively). Temporal variation of soil solution chemistry was compared with the mobilization of elements in the rhizosphere of white lupin and concentrations in plant tissues. Relative to the monocrops, intercropping of oat with 11% white lupin significantly increased the concentrations of Fe, Pb, Th, La and Nd in soil solution as well as the concentrations of Fe, Pb, Th, Sc, La and Nd in tissues of oat. Enhanced mobility of the mentioned elements corresponded to a depletion of elements in the rhizosphere soil of white lupin. In mixed cultures with 33% lupin, concentrations in soil solution only slightly increased. We conclude that intercropping with 11% white lupin might be a promising tool for phytoremediation and phytomining research enhancing mobility of essential trace metals as well as elements with relevance for phytoremediation (Pb, Th) and phytomining (La, Nd, Sc) in soil.

On the distribution of trace element concentrations in multiple bone elements in 10 Danish medieval and post-medieval individuals.

Science.gov (United States)

Lund Rasmussen, Kaare; Skytte, Lilian; D'imporzano, Paolo; Orla Thomsen, Per; Søvsø, Morten; Lier Boldsen, Jesper

2017-01-01

The differences in trace element concentrations among 19 different bone elements procured from 10 archaeologically derived human skeletons have been investigated. The 10 individuals are dated archaeologically and some by radiocarbon dating to the medieval and post-medieval period, an interval from ca. AD 1150 to ca. AD 1810. This study is relevant for two reasons. First, most archaeometric studies analyze only one bone sample from each individual; so to what degree are the bones in the human body equal in trace element chemistry? Second, differences in turnover time of the bone elements makes the cortical tissues record the trace element concentrations in equilibrium with the blood stream over a longer time earlier in life than the trabecular. Therefore, any differences in trace element concentrations between the bone elements can yield what can be termed a chemical life history of the individual, revealing changes in diet, provenance, or medication throughout life. Thorough decontamination and strict exclusion of non-viable data has secured a dataset of high quality. The measurements were carried out using Inductively Coupled Plasma Mass Spectrometry (for Fe, Mn, Al, Ca, Mg, Na, Ba, Sr, Zn, Pb and As) and Cold Vapor Atomic Absorption Spectroscopy (for Hg) on ca. 20 mg samples. Twelve major and trace elements have been measured on 19 bone elements from 10 different individuals interred at five cemeteries widely distributed in medieval and renaissance Denmark. The ranges of the concentrations of elements were: Na (2240-5660 µg g -1 ), Mg (440-2490 µg g -1 ), Al (9-2030 µg g -1 ), Ca (22-36 wt. %), Mn (5-11450 µg g -1 ), Fe (32-41850 µg g -1 ), Zn (69-2610 µg g -1 ), As (0.4-120 µg g -1 ), Sr (101-815 µg g -1 ), Ba (8-880 µg g -1 ), Hg (7-78730 ng g -1 ), and Pb (0.8-426 µg g -1 ). It is found that excess As is mainly of diagenetic origin. The results support that Ba and Sr concentrations are effective provenance or dietary indicators. Migrating

48Ca+249Bk fusion reaction leading to element Z = 117: long-lived α-decaying 270Db and discovery of 266Lr.

Science.gov (United States)

Khuyagbaatar, J; Yakushev, A; Düllmann, Ch E; Ackermann, D; Andersson, L-L; Asai, M; Block, M; Boll, R A; Brand, H; Cox, D M; Dasgupta, M; Derkx, X; Di Nitto, A; Eberhardt, K; Even, J; Evers, M; Fahlander, C; Forsberg, U; Gates, J M; Gharibyan, N; Golubev, P; Gregorich, K E; Hamilton, J H; Hartmann, W; Herzberg, R-D; Heßberger, F P; Hinde, D J; Hoffmann, J; Hollinger, R; Hübner, A; Jäger, E; Kindler, B; Kratz, J V; Krier, J; Kurz, N; Laatiaoui, M; Lahiri, S; Lang, R; Lommel, B; Maiti, M; Miernik, K; Minami, S; Mistry, A; Mokry, C; Nitsche, H; Omtvedt, J P; Pang, G K; Papadakis, P; Renisch, D; Roberto, J; Rudolph, D; Runke, J; Rykaczewski, K P; Sarmiento, L G; Schädel, M; Schausten, B; Semchenkov, A; Shaughnessy, D A; Steinegger, P; Steiner, J; Tereshatov, E E; Thörle-Pospiech, P; Tinschert, K; Torres De Heidenreich, T; Trautmann, N; Türler, A; Uusitalo, J; Ward, D E; Wegrzecki, M; Wiehl, N; Van Cleve, S M; Yakusheva, V

2014-05-02

The superheavy element with atomic number Z=117 was produced as an evaporation residue in the (48)Ca+(249)Bk fusion reaction at the gas-filled recoil separator TASCA at GSI Darmstadt, Germany. The radioactive decay of evaporation residues and their α-decay products was studied using a detection setup that allowed measuring decays of single atomic nuclei with half-lives between sub-μs and a few days. Two decay chains comprising seven α decays and a spontaneous fission each were identified and are assigned to the isotope (294)117 and its decay products. A hitherto unknown α-decay branch in (270)Db (Z = 105) was observed, which populated the new isotope (266)Lr (Z = 103). The identification of the long-lived (T(1/2) = 1.0(-0.4)(+1.9) h) α-emitter (270)Db marks an important step towards the observation of even more long-lived nuclei of superheavy elements located on an "island of stability."

Preferential removal and immobilization of stable and radioactive cesium in contaminated fly ash with nanometallic Ca/CaO methanol suspension

Energy Technology Data Exchange (ETDEWEB)

Mallampati, Srinivasa Reddy, E-mail: srireddys@ulsan.ac.kr [Department of Civil and Environmental Engineering, University of Ulsan, Ulsan 680-749 (Korea, Republic of); Mitoma, Yoshiharu, E-mail: mitomay@pu-hiroshima.ac.jp [Department of Environmental Sciences, Faculty of Life and Environmental Sciences, Prefectural University of Hiroshima, 562 Nanatsuka-Cho, Shobara City, Hiroshima 727-0023 (Japan); Okuda, Tetsuji [Environmental Research and Management Center, Hiroshima University, 1-5-3 Kagamiyama, Higashi-Hiroshima, Hiroshima 739-8513 (Japan); Sakita, Shogo [Department of Environmental Sciences, Faculty of Life and Environmental Sciences, Prefectural University of Hiroshima, 562 Nanatsuka-Cho, Shobara City, Hiroshima 727-0023 (Japan); Simion, Cristian [Politehnica University of Bucharest, Department of Organic Chemistry, Bucharest 060042 (Romania)

2014-08-30

Graphical abstract: Schematic representation of possible mechanisms determining the Cs extraction and immobilization in fly ash during water, methanol or n-MCaS extraction. - Highlights: • nMCaS suspension for cesium extraction and immobilization in fly ash was developed. • Enhanced cesium immobilization was done by nanometallic Ca/CaO methanol suspension. • By SEM analysis the amount of cesium detectable on soil particle surface decreases. • Leachable cesium concentrations reduced, lower than the standard regulatory limit. • nMCaS unique and a highly potential amendment for the remediation of Cs. - Abstract: In this work, the capability of nanometallic Ca/CaO methanol suspension in removing and/or immobilizing stable ({sup 133}Cs) and radioactive cesium species ({sup 134}Cs and {sup 137}Cs) in contaminated fly ash was investigated. After a first methanol and second water washing yielded only 45% of {sup 133}Cs removal. While, after a first methanol washing, the second solvent with nanometallic Ca/CaO methanol suspension yielded simultaneous enhanced removal and immobilization about 99% of {sup 133}Cs. SEM-EDS analysis revealed that the mass percent of detectable {sup 133}Cs on the fly ash surface recorded a 100% decrease. When real radioactive cesium contaminated fly ash (containing an initial 14,040 Bq kg{sup −1134}Cs and {sup 137}Cs cumulated concentration) obtained from burning wastes from Fukushima were reduced to 3583 Bq kg{sup −1} after treatment with nanometallic Ca/CaO methanol suspension. Elution test conducted on the treated fly ash gave 100 Bq L{sup −1} total {sup 134}Cs and {sup 137}Cs concentrations in eluted solution. Furthermore, both ash content and eluted solution concentrations of {sup 134}Cs and {sup 137}Cs were much lower than the Japanese Ministry of the Environment regulatory limit of 8000 Bq kg{sup −1} and 150 Bq L{sup −1} respectively. The results of this study suggest that the nanometallic Ca/CaO methanol suspension is

Determination of trace elements by neutron activation analysis using dinonylnaphtalene sulfonic acid as a preconcentrating agent

International Nuclear Information System (INIS)

Yang, M.H.; Chen, P.Y.; Tseng, C.L.; Yeh, S.J.; Weng, P.S.

1977-01-01

Dinonylnaphthalene sulfonic acid (HD) has been used as a preconcentrating agent to enrich trace metal ions and to separate the interfering elements such as Na, K, Cl and Br, which normally exist in the natural aqueous systems. Experiments were performed by extracting the ions in the aqueous medium with HD in n-hexane and subsequently backextracted into a minimal volume of acid solution. Factors influencing the extraction efficiency of the ions of interest were investigated. The preconcentration technique has been successfully applied to the determination by neutron activation analysis of trace elements in natural water and biological materials. Both short-lived nuclides (Mg, Al, Ca, Mn) and long-lived nuclides (Sm, Eu, Zn, La, Cr, Sc, Fe, Co) in the ppb-level concentrations were determined. (T.G.)

Synthesis and characterization of Ag-containing calcium phosphates with various Ca/P ratios

International Nuclear Information System (INIS)

Gokcekaya, Ozkan; Ueda, Kyosuke; Narushima, Takayuki; Ergun, Celaletdin

2015-01-01

Ag-containing calcium phosphate (CaP) powders were synthesized by a precipitation method using aqueous solutions of calcium nitrate, silver nitrate, and ammonium phosphate. The powders were sintered at temperatures ranging from 1173 to 1473 K. The charged atomic ratios of (Ca + Ag)/P and Ag/(Ca + Ag) in solution were varied from 1.33 to 1.67 and from 0 to 0.30, respectively. The Ag content in the as-precipitated CaP powders increased with the charged Ag/(Ca + Ag) atomic ratio in solution and was lower than the charged Ag/(Ca + Ag) value. The as-precipitated CaP powders consisted of hydroxyapatite (HA) as the main phase. Ag nanoparticles were observed on the as-precipitated HA particles under all conditions of Ag addition. After the sintering, HA, β-TCP (tricalcium phosphate), α-TCP, and β-CPP (calcium pyrophosphate) were mainly detected as CaPs on the basis of the Ca/P atomic ratio of the as-precipitated powders. The addition of Ag stabilized the β-TCP phase, and the distribution of Ag in β-TCP was homogeneous. A metallic Ag phase coexisted with HA. The solubility of Ag in HA was estimated to be 0.0019–0.0061 (Ag/(Ca + Ag)) atomic ratio, which was lower than that in β-TCP (higher than 0.0536) and higher than that of β-CPP (below the detection limit of analyses). - Highlights: • The HA powders with Ag nanoparticles were synthesized by a precipitation method. • Metallic Ag particles were detected with the HA phase after sintering. • The distribution of Ag in β-TCP was homogeneous after sintering. • The addition of Ag stabilized the β-ΤCP phase. • β-TCP exhibited higher solubility of Ag than HA and β-CPP

Synthesis and characterization of Ag-containing calcium phosphates with various Ca/P ratios

Energy Technology Data Exchange (ETDEWEB)

Gokcekaya, Ozkan, E-mail: gokcekaya@dc.tohoku.ac.jp [Department of Materials Processing, Tohoku University, 6-6-02 Aza Aoba, Aramaki, Aoba-ku, Sendai, Miyagi 980-8579 (Japan); Ueda, Kyosuke; Narushima, Takayuki [Department of Materials Processing, Tohoku University, 6-6-02 Aza Aoba, Aramaki, Aoba-ku, Sendai, Miyagi 980-8579 (Japan); Ergun, Celaletdin [Faculty of Mechanical Engineering, Istanbul Technical University, 65 Inonu Street, Gumussuyu, Istanbul 34437 (Turkey)

2015-08-01

Ag-containing calcium phosphate (CaP) powders were synthesized by a precipitation method using aqueous solutions of calcium nitrate, silver nitrate, and ammonium phosphate. The powders were sintered at temperatures ranging from 1173 to 1473 K. The charged atomic ratios of (Ca + Ag)/P and Ag/(Ca + Ag) in solution were varied from 1.33 to 1.67 and from 0 to 0.30, respectively. The Ag content in the as-precipitated CaP powders increased with the charged Ag/(Ca + Ag) atomic ratio in solution and was lower than the charged Ag/(Ca + Ag) value. The as-precipitated CaP powders consisted of hydroxyapatite (HA) as the main phase. Ag nanoparticles were observed on the as-precipitated HA particles under all conditions of Ag addition. After the sintering, HA, β-TCP (tricalcium phosphate), α-TCP, and β-CPP (calcium pyrophosphate) were mainly detected as CaPs on the basis of the Ca/P atomic ratio of the as-precipitated powders. The addition of Ag stabilized the β-TCP phase, and the distribution of Ag in β-TCP was homogeneous. A metallic Ag phase coexisted with HA. The solubility of Ag in HA was estimated to be 0.0019–0.0061 (Ag/(Ca + Ag)) atomic ratio, which was lower than that in β-TCP (higher than 0.0536) and higher than that of β-CPP (below the detection limit of analyses). - Highlights: • The HA powders with Ag nanoparticles were synthesized by a precipitation method. • Metallic Ag particles were detected with the HA phase after sintering. • The distribution of Ag in β-TCP was homogeneous after sintering. • The addition of Ag stabilized the β-ΤCP phase. • β-TCP exhibited higher solubility of Ag than HA and β-CPP.

Elemental variations in the germinating fungus Phytophthora palmivora

International Nuclear Information System (INIS)

Mazzolini, A.P.; Sealock, R.M.; Legge, G.J.F.; Grant, B.R.

1991-01-01

We have measured the elemental variations between zoospores and germinating cystospores of the fungus Phytophthora palmivora, using a scanning proton microprobe. Averaged over a number of individual cells, our results indicate that the level of Ca is much lower in germinating cystospores than in zoospores. The levels of S, Cl, and Zn also appear to be lower, and the level of K appears to be higher. The spatial distribution of elements within the germinating cystospore is very similar for P, S, Cl, K, Mn, Fe, and Cu, but significantly different for Ca and Zn. (orig.)

Elemental variations in the germinating fungus Phytophthora palmivora

Science.gov (United States)

Mazzolini, A. P.; Grant, B. R.; Sealock, R. M.; Legge, G. J. F.

1991-03-01

We have measured the elemental variations between zoospores and germinating cystospores of the fungus Phytophthora palmivora, using a scanning proton microprobe. Averaged over a number of individual cells, our results indicate that the level of Ca is much lower in germinating cystospores than in zoospores. The levels of S, Cl, and Zn also appear to be lower, and the level of K appears to be higher. The spatial distribution of elements within the germinating cystospore is very similar for P, S, Cl, K, Mn, Fe, and Cu, but significantly different for Ca and Zn.

Vapor pressures and isopiestic molalities of concentrated CaCl2(aq), CaBr2(aq), and NaCl(aq) to T = 523 K

International Nuclear Information System (INIS)

Gruszkiewicz, Miroslaw S.; Simonson, John M.

2005-01-01

The Oak Ridge National Laboratory high-temperature isopiestic apparatus was outfitted with precise pressure gauges to allow for direct vapor pressure measurements. Vapor pressures over concentrated solutions of CaCl 2 (aq), and CaBr 2 (aq) were measured at temperatures between (380.15 and 523.15) K in the range of water activities between 0.2 and 0.85. Isopiestic molalities were used to determine osmotic coefficients at the conditions where NaCl reference standard solutions remained undersaturated. The main goal of this work was to improve the accuracy of isopiestic comparisons based on the calcium chloride reference standard. Osmotic coefficients for CaCl 2 (aq) and CaBr 2 (aq) calculated from both isopiestic and direct vapor pressure results were combined with the literature data and used to build general thermodynamic models based on a variant of extended Pitzer ion-interaction equations and valid at the saturation pressure of water. While these empirical models approach the accuracy of the experimental data in a wider range of concentrations and temperatures than any previously published equations, considerable amounts of accurate data and a substantial effort are required in order to obtain a satisfactory representation using power series-based virial equations. The effect of experimental uncertainties on the accuracy of the direct vapor pressure results is discussed, including in particular the error caused by the presence in the apparatus of a small amount of CO 2 . The substantial decrease of the solubility product of CaCO 3 in concentrated chloride solutions at temperatures above 423 K is a serious defect of calcium chloride as a water activity reference standard

Development of a Certified Reference Material (NMIJ CRM 7203-a) for Elemental Analysis of Tap Water.

Science.gov (United States)

Zhu, Yanbei; Narukawa, Tomohiro; Inagaki, Kazumi; Miyashita, Shin-Ichi; Kuroiwa, Takayoshi; Ariga, Tomoko; Kudo, Izumi; Koguchi, Masae; Heo, Sung Woo; Suh, Jung Ki; Lee, Kyoung-Seok; Yim, Yong-Hyeon; Lim, Youngran

2017-01-01

A certified reference material (CRM), NMIJ CRM 7203-a, was developed for the elemental analysis of tap water. At least two independent analytical methods were applied to characterize the certified value of each element. The elements certified in the present CRM were as follows: Al, As, B, Ca, Cd, Cr, Cu, Fe, K, Mg, Mn, Mo, Na, Ni, Pb, Rb, Sb, Se, Sr, and Zn. The certified value for each element was given as the (property value ± expanded uncertainty), with a coverage factor of 2 for the expanded uncertainty. The expanded uncertainties were estimated while considering the contribution of the analytical methods, the method-to-method variance, the sample homogeneity, the long-term stability, and the concentrations of the standard solutions for calibration. The concentration of Hg (0.39 μg kg -1 ) was given as the information value, since loss of Hg was observed when the sample was stored at room temperature and exposed to light. The certified values of selected elements were confirmed by a co-analysis carried out independently by the NMIJ (Japan) and the KRISS (Korea).

Conforming discretizations of boundary element solutions to the electroencephalography forward problem

Science.gov (United States)

Rahmouni, Lyes; Adrian, Simon B.; Cools, Kristof; Andriulli, Francesco P.

2018-01-01

In this paper, we present a new discretization strategy for the boundary element formulation of the Electroencephalography (EEG) forward problem. Boundary integral formulations, classically solved with the Boundary Element Method (BEM), are widely used in high resolution EEG imaging because of their recognized advantages, in several real case scenarios, in terms of numerical stability and effectiveness when compared with other differential equation based techniques. Unfortunately, however, it is widely reported in literature that the accuracy of standard BEM schemes for the forward EEG problem is often limited, especially when the current source density is dipolar and its location approaches one of the brain boundary surfaces. This is a particularly limiting problem given that during an high-resolution EEG imaging procedure, several EEG forward problem solutions are required, for which the source currents are near or on top of a boundary surface. This work will first present an analysis of standardly and classically discretized EEG forward problem operators, reporting on a theoretical issue of some of the formulations that have been used so far in the community. We report on the fact that several standardly used discretizations of these formulations are consistent only with an L2-framework, requiring the expansion term to be a square integrable function (i.e., in a Petrov-Galerkin scheme with expansion and testing functions). Instead, those techniques are not consistent when a more appropriate mapping in terms of fractional-order Sobolev spaces is considered. Such a mapping allows the expansion function term to be a less regular function, thus sensibly reducing the need for mesh refinements and low-precisions handling strategies that are currently required. These more favorable mappings, however, require a different and conforming discretization, which must be suitably adapted to them. In order to appropriately fulfill this requirement, we adopt a mixed

Efficacy of chlorine dioxide against Listeria monocytogenes in brine chilling solutions.

Science.gov (United States)

Valderrama, W B; Mills, E W; Cutter, C N

2009-11-01

Chilled brine solutions are used by the food industry to rapidly cool ready-to-eat meat products after cooking and before packaging. Chlorine dioxide (ClO(2)) was investigated as an antimicrobial additive to eliminate Listeria monocytogenes. Several experiments were performed using brine solutions made of sodium chloride (NaCl) and calcium chloride (CaCl(2)) inoculated with L. monocytogenes and/or treated with 3 ppm of ClO(2). First, 10 and 20% CaCl(2) and NaCl solutions (pH 7.0) were inoculated with a five-strain cocktail of L. monocytogenes to obtain approximately 7 log CFU/ml and incubated 8 h at 0 degrees C. The results demonstrated that L. monocytogenes survived in 10% CaCl(2), 10 and 20% NaCl, and pure water. L. monocytogenes levels were reduced approximately 1.2 log CFU/ml in 20% CaCl(2). Second, inoculated ( approximately 7 log CFU/ml) brine solutions (10 and 20% NaCl and 10% CaCl(2)) treated with 3 ppm of ClO(2) resulted in a approximately 4-log reduction of the pathogen within 90 s. The same was not observed in a solution of 20% CaCl(2); further investigation demonstrated that high levels of divalent cations interfere with the disinfectant. Spent brine solutions from hot dog and ham chilling were treated with ClO(2) at concentrations of 3 or 30 ppm. At these concentrations, ClO(2) did not reduce L. monocytogenes. Removal of divalent cations and organic material in brine solutions prior to disinfection with ClO(2) should be investigated to improve the efficacy of the compound against L. monocytogenes. The information from this study may be useful to processing establishments and researchers who are investigating antimicrobials in chilling brine solutions.

Physico-Chemical Study of the Separation of Calcium Isotopes by Chemical Exchange Between Amalgam and Salt Solutions; Etude physico-chimique de la separation des isotopes du calcium par echange chimique entre amalgame et solution saline

Energy Technology Data Exchange (ETDEWEB)

Duie, P; Dirian, G [Commissariat a l' Energie Atomique. Centre d' Etudes Nucleaires de Saclay, 91 - Gif-sur-Yvette (France)

1962-07-01

In a preliminary study of the isotopic exchange between Ca amalgam and aqueous or organic solutions of Ca salts, the main parameters governing the feasibility of a separation process based on these systems such as separation factor, exchange kinetics, rate of decomposition of the amalgam were investigated. The separation factor between {sup 40}Ca and {sup 46}Ca was found to be of the order of 1.02. The rate of the exchange reaction is rather low for aqueous solutions, extremely low for organic solutions. The amalgam seems not to be attacked by dimethyl-formamide solutions; but it is rapidly decomposed by aqueous solutions of Ca halides. This decomposition is slow in the case of aqueous solutions of calcium formate and still slower for Ca(OH){sub 2}; however, except in particular conditions, the observed rate is often much higher, owing to interfering reactions between amalgam and water vapor contained in H{sub 2} bubbles. (authors) [French] On a fait une etude preliminaire, pour des systemes amalgame de calcium - solution aqueuse ou organique de sels de calcium, des principaux parametres pouvant intervenir dans l'application d'un procede d'echange a l'enrichissement isotopique du calcium: facteur de separation, cinetique de l'echange, cinetique de la decomposition de l'amalgame. Les facteurs de separation {sup 40}Ca-{sup 46}Ca sont de l'ordre de 1,02. L'echange est assez lent pour les solutions aqueuses, extremement lent pour les solutions organiques. La decomposition de l'amalgame est pratiquement inexistante avec les solutions dans le dimethyl- formamide, appreciable pour les solutions alcooliques, rapide pour les solutions aqueuses d'halogenures; elle est normalement lente pour les solutions aqueuses de formiate et surtout de chaux, mais la decomposition est en general acceleree par une reaction parasite entre l'amalgame et l'eau a l'etat vapeur, reaction que l'on n'evite dans des conditions tres particulieres. (auteurs)

Investigation of microwave assisted drying of samples and evaporation of aqueous solutions in trace element analysis

Energy Technology Data Exchange (ETDEWEB)

Maichin, B.; Knapp, G. [Technische Univ., Graz (Austria). Inst. fuer Analytische Chemie, Mikro- und Radiochemie; Kettisch, P. [Anton Paar GmbH, Graz (Austria)

2000-01-01

Investigations of microwave assisted drying of sample materials and microwave assisted evaporation of aqueous sample solutions and acidic digestion residues were accomplished by means of special rotors for the microwave digestion system MULTIWAVE. To check the results obtained by microwave assisted drying, the samples were also conventionally dried at 105 C in an oven. The following samples have been dried: 10 g each of meat, fish, apple, cucumber, potato, mustard, yogurt, clay and marl; 1 g each of certified reference material TORT 2 (lobster hepatopancreas), BCR 278 (mussel tissue) and BCR 422 (cod muscle); 500 g garden mould. Microwave assisted drying takes 40 min for organic samples and 30 min for inorganic material. Important is a slow increase of microwave power during the first 20 min. The results agree well with conventional drying at 105 C. Losses of As, Se and Hg have been investigated for 3 CRMs. Only Se shows losses in the range of 20%. Losses of As, Be, Cd, Co, Cr, Cu, Fe, Hg, Li, Mg, Mn, Mo, Ni, Pb, Sb, Se, Sr, Ti, Tl, V and Zn after evaporation of aqueous samples and acidic solutions after wet digestion, respectively, have been investigated. 50 mL aqueous solution was evaporated almost to dryness within 25 min. The recovery of Hg is 40-50%, of Se 90-95% and of the other elements 97-102%. 0.2 g each of TORT 2, BCR 278 and BCR 422 have been digested with 4 mL nitric acid and 1 mL hydrochloric acid by means of the microwave digestion system MULTIWAVE. The digestion residue was evaporated almost to dryness and dissolved again in 10 mL diluted nitric acid. In this case no element losses have been observed. The measured concentration of As, Cd, Cu, Fe, Mn, Hg, Pb, Mo, Ni, Se, Sr, V and Zn agree very well with the certified values. An important prerequisite for good recoveries is not to evaporate the solutions to complete dryness. (orig.)

A solution of the dispersion-convection equation of radial tracer transportation by the finite element variational method

International Nuclear Information System (INIS)

Hubert, J.

1979-01-01

The variational finite element method (of the Rayleigh-Ritz type) has been applied to solve the standard diffusion-convection equation of radial flow in a dispersive medium. It was shown that the imposing of the boundary condition ΔC/Δx = 0 (=null concentration gradient) introduced great errors in computation results. To remedy it this condition was imposed at the free end of the artifical domain. Its other end joined to the downstream boundary of the investigated domain. The results of calculations compared with the known analytical solutions of the parallel flow show their good accuracy. The method was used to discuss the applicability of the approximate analytical solutions of the radial flow. (author)

Biosorption of rare earth elements, thorium and uranium using Buccinum tenuissimum shell biomass

International Nuclear Information System (INIS)

Wang, Yudan; Koto, Yusuke; Sakamoto, Nobuo; Kano, Naoki; Imaizumi, Hiroshi

2010-01-01

In order to evaluate the efficiency of shell biomass as sorbent for rare earth elements (REEs), thorium (Th) and uranium (U), sorption experiment from multi-element solutions containing known amount of REEs, Th and U using Buccinum tenuissimum shell was explored. Furthermore, to confirm the characteristics of the shell biomass, the surface morphology, the crystal structure, and the specific surface area of the shell (both original sample and the heat-treatment (480degC, 6h) sample) was determined. Consequently, the following matters have been mainly clarified. (1) By heat-treatment (480degC, 6h), the crystal structure of the shell biomass was transformed from aragonite (CaCO 3 ) into calcite (CaCO 3 ) phase, and the specific surface area of the biomass have decreased remarkably (i.e., by a factor of less than one eighth). (2) The shell biomass (both original sample and the heat-treated sample) showed excellent sorption capacity for REEs, although the sorption capacity decreases slightly after heat-treatment. (3) Adsorption isotherms using the shell biomass can be described by Langmuir and Freundlich isotherms satisfactorily for REEs, but not for Th and U in this work. (4) Shell biomass (usually treated as waste material) could be an efficient sorbent for REEs in future. (author)

Estimation of ultraviolet radiation dose using CaF2:Tb phosphor

International Nuclear Information System (INIS)

Fukuda, Y.; Ohtaki, H.; Owaki, S.

1996-01-01

To observe and estimate the dose of ultraviolet (UV) radiation in sunlight, the available thermoluminescence (TL) materials were studied. Several kinds of lanthanide elements were doped in pure CaF 2 powdered crystal and the properties of the Tl for UV were observed. The TL intensity from CaF 2 :Tb was the highest among the samples doped with various lanthanide elements, and form the TL emission spectra (380-540 nm) the TL is estimated to be due to inner transition of Tb 3+ . The peak wavelength of the TL excitation light was located approximately at 235 nm and light of a longer wavelength than 320 nm was unable to excite the TL. The ultraviolet response of CaF 2 :Tb depended on its sintering temperature. Even without γ ray pre-irradiation the CaF 2 :Tb sample with 1 h exposure to sunlight has enough sensitivity to estimate the change of UV. Seasonal change of UV intensity in sunlight was measured with this TLD during four months in 1993. The results agreed with that of other institutes in Japan. (author)

Effect of sodium carbonate solution on self-setting properties of tricalcium silicate bone cement.

Science.gov (United States)

Zhiguang Huan; Jiang Chang

2008-11-01

In this study, the effects of sodium carbonate (Na(2)CO(3) ) solution with different concentrations (10, 15, 20, and 25 wt%) as liquid phase on the setting time and compressive strength of tricalcium silicate bone cements are investigated. The in vitro bioactivity and degradability of the resultant Ca(3)SiO(5)-Na(2)CO(3) solution paste was also studied. The results indicate that as the concentration of Na(2)CO(3) solution varies from 0 to 25 wt%, the initial and final setting time of the cement decrease significantly from 90 to 20 min and from 180 to 45 min, respectively. After setting for 24 h, the compressive strength of Ca(3)SiO(5)-Na(2)CO(3) solution paste reaches 5.1 MPa, which is significantly higher than that of Ca( 3)SiO(5)-water cement system. The in vitro bioactivity of the cements is investigated by soaking in simulated body fluid (SBF) for 7 days. The results show that the Ca(3)SiO(5)-Na(2)CO( 3) solution bone cement has a good bioactivity and can degrade in Ringer's solution. The results indicate that Na(2)CO(3) solution as a liquid phase significantly improves the self-setting properties of Ca( 3)SiO(5) cement as compared to water. The Ca(3)SiO( 5) cement paste prepared using Na(2)CO(3) solution shows good bioactivity and moderate degradability, and the Ca(3)SiO( 5)-Na(2)CO(3) solution system may be used as degradable and bioactive bone defect filling materials.

preliminary phytochemical screening, proximate and elemental

African Journals Online (AJOL)

DR. AMINU

1*Kawo, A.H., 1Abdullahi, B.A., 2Gaiya, Z.A. 3Halilu, A., 4Dabai, M. and 5Dakare, M.A. ... mineral elements in the seed powder were: Al (144 ± 4 ppm), Ca (602 ± 122 ppm), K (732 ± 164 .... elements as Sr (69 ± 3.0), Rb (122 ± 0.0) and Zr (11.

The finite element solution of two-dimensional transverse magnetic scattering problems on the connection machine

International Nuclear Information System (INIS)

Hutchinson, S.; Costillo, S.; Dalton, K.; Hensel, E.

1990-01-01

A study is conducted of the finite element solution of the partial differential equations governing two-dimensional electromagnetic field scattering problems on a SIMD computer. A nodal assembly technique is introduced which maps a single node to a single processor. The physical domain is first discretized in parallel to yield the node locations of an O-grid mesh. Next, the system of equations is assembled and then solved in parallel using a conjugate gradient algorithm for complex-valued, non-symmetric, non-positive definite systems. Using this technique and Thinking Machines Corporation's Connection Machine-2 (CM-2), problems with more than 250k nodes are solved. Results of electromagnetic scattering, governed by the 2-d scalar Hemoholtz wave equations are presented in this paper. Solutions are demonstrated for a wide range of objects. A summary of performance data is given for the set of test problems