K-Ca and Rb-Sr Dating of Lunar Granite 14321 Revisited

Science.gov (United States)

Simon, Justin I.; Shih, C.-Y.; Nyquist, L. E.

2011-01-01

K-Ca and Rb-Sr age determinations were made for a bulk feldspar-rich portion of an Apollo rock fragment of the pristine lunar granite clast (14321,1062), an acid-leached split of the sample, and the leachate. K-Ca and Rb-Sr data were also obtained for a whole rock sample of Apollo ferroan anorthosite (FAN, 15415). The recent detection [1] of widespread intermediate composition plagioclase indicates that the generation of a diversity of evolved lunar magmas maybe more common and therefore more important to our understanding of crust formation than previously believed. Our new data strengthen the K-Ca and Rb-Sr internal isochrons of the well-studied Apollo sample 14321 [2], which along with a renewed effort to study evolved lunar magmas will provide an improved understanding of the petrogenetic history of evolved rocks on the Moon.

Electronic structure of Ca, Sr, and Ba under pressure.

Science.gov (United States)

Animalu, A. O. E.; Heine, V.; Vasvari, B.

1967-01-01

Electronic band structure calculations phase of Ca, Sr and Ba over wide range of atomic volumes under pressure electronic band structure calculations for fcc phase of Ca, Sr and Ba over wide range of atomic volumes under pressure electronic band structure calculations for fcc phase of Ca, Sr and Ba over wide range of atomic volumes under pressure

Rb/Sr dating of rock samples from Antarctica

International Nuclear Information System (INIS)

Ahmed, A.; Awan, M.A.; Mehjabeen, A.; Jabeen, N.; Majid, C.A.

1996-01-01

Soon after the discovery of radioactivity in 1896 by Becquerel, the phenomenon was applied to geochronology. From 1902 onwards, rapid advances were made in this field of science. Using radiometric techniques of Rb/Sr the whole rock granitic pegmatite samples from two localities in the North Eastern Antarctica have been dated. The rock samples have yielded Rb/Sr ages around 200 nd 173 million year. The ages around 200 million year have been correlated to the orogenic/epeirogenic activities associated with the breaking up of the Pangaea which led to the dispersion of the continents to form Gondwanaland and Laurasia which subsequently gave rise to the present day configuration of the globe. The younger age of 173 million year corresponds to Jurassic dole rites from Western queens Maud Land and other areas of Antarctica. (author)

The Rb-Sr geochronology of the Colossus kimberlite pipe, Zimbabwe

International Nuclear Information System (INIS)

Allsopp, H.L.

1985-01-01

The Colossus kimberlite is one of several such occurrences situated in central Zimbabwe. A relationship with alluvial diamond deposits in the same area has been suggested, and on this basis a pre-Permian age has been inferred. The general geology and petrography of the Colossus kimberlite pipe are described. Rb-Sr age measurements on somewhat weathered kimberlite micas are reported, and the best estimate for the age of the kimberlite is reported as 502+-47 Ma. A model Rb-Sr age of 2 630 Ma for the Formona granite, which forms the country rock to the kimberlite, is also reported

Evidence of three-body correlation functions in Rb+ and Sr2+ acetonitrile solutions

Science.gov (United States)

D'Angelo, P.; Pavel, N. V.

1999-09-01

The local structure of Sr2+ and Rb+ ions in acetonitrile has been investigated by x-ray absorption spectroscopy (XAS) and molecular dynamics simulations. The extended x-ray absorption fine structure above the Sr and Rb K edges has been interpreted in the framework of multiple scattering (MS) formalism and, for the first time, clear evidence of MS contributions has been found in noncomplexing ion solutions. Molecular dynamics has been used to generate the partial pair and triangular distribution functions from which model χ(k) signals have been constructed. The Sr2+ and Rb+ acetonitrile pair distribution functions show very sharp and well-defined first peaks indicating the presence of a well organized first solvation shell. Most of the linear acetonitrile molecules have been found to be distributed like hedgehog spines around the Sr2+ and Rb+ ions. The presence of three-body correlations has been singled out by the existence of well-defined peaks in the triangular configurations. Excellent agreement has been found between the theoretical and experimental data enforcing the reliability of the interatomic potentials used in the simulations. These results demonstrate the ability of the XAS technique in probing the higher-order correlation functions in solution.

Musa's granite and Rio Maria's granodiorite Rb/Sr isotopic ages and geochemistry

International Nuclear Information System (INIS)

Gastal, M.C.P.; Macambira, M.J.B.; Medeiros, H.; Dall'Agnol, R.

1987-01-01

The Musa Granite and the Rio Maria Granodiorite are located at the eastern margin of the Amazonian craton, in the Rio Maria region, where a typical granite-greenstone terrain is characterized. Rb-Sr dating of six samples from different facies of Rio Maria Granodiorite furnished an age of 2564 ± 68 Ma with initial 87 Sr/ 86 Sr radio (IR) of 0.70288 ± 0.00092 (whole rock isochron; 1 ο error; MSWD = 2.26). Thirteen samples from the three facies of Musa Granite (monzogranites, syenogranites and intermediate to felsic hypabyssal rocks) gave Rb-Sr whole rock isochron with an age of 1692 ± 11 Ma and IR of 0.70777 ± 0.00023 (1 ο error, MSWD = 1.89). A preliminary attempt to individualize geochronologically the three facies was done resulting different ages and IRs. There is a coincidence between these ages and the emplacement sequence of these facies of the pluton. The actual meaning of the Rio Maria Granodiorite Rb-Sr age is still uncertain. It could be related to the end of the magmatic crystallization of the batholith as well as to the metamorphic-mylonitic event that affect it. Considering that the Jamon and Musa Granites are petrologically similar that they occur in the same area, it is interesting to note that latter is apparently a little older than the former. The IRs obtained for the two plutons are also not coincident. The isotopic Rb-Sr available data show that the exposed rocks of the Rio Maria Granodiorite have not been able to generate magmas with the compositions of the monzongranitic and the hypabyssal facies of the Musa pluton. On the other hand, rocks isotopically similar to the Rio Maria Granodiorite would theorically be able to generate the Jamon and a magma with the characteristics of the syenogranitic facies of the Musa pluton. (author) [pt

Rb-Sr geochronology of some Miocene West Australian lamproites

International Nuclear Information System (INIS)

Allsopp, H.L.; Scott Smith, B.H.; Danchin, R.V.

1985-01-01

Rb-Sr ages are presented for four lamproite intrusions (Mount North, Old Leopold Hill, Mount Rose and Seltrust Pipe 2) located in the west Kimberley region of West Australia. The data are in agreement with the early Miocene ages previously obtained for the lamproites of this area. The lamproites are characterized by high initial-Sr ratios, indicative of derivation from an enriched source. Localized and regional mantle heterogeneity is indicated by new and existing data

Refinement of crystal structures of CaHCl, SrHCl, BaHCl, BaHBr, and BaHI

International Nuclear Information System (INIS)

Beck, H.P.; Limmer, A.

1983-01-01

The structures of CaHCl, SrHCl, BaHBr, BaHCl, and BaHI have been refined using single crystal data. The comparison of the parameters with the corresponding data of isotypic fluorohalide compounds gives a valuable insight into the bonding interactions in this structure type. (author)

Refinement of crystal structures of CaHCl, SrHCl, BaHCl, BaHBr, and BaHI

Energy Technology Data Exchange (ETDEWEB)

Beck, H.P.; Limmer, A. (Erlangen-Nuernberg Univ., Erlangen (Germany, F.R.). Inst. fuer Anorganische Chemie)

1983-07-01

The structures of CaHCl, SrHCl, BaHBr, BaHCl, and BaHI have been refined using single crystal data. The comparison of the parameters with the corresponding data of isotypic fluorohalide compounds gives a valuable insight into the bonding interactions in this structure type.

Evaluation and application of alumina-based Rb-82 generators charged with high levels of Sr-82/85

International Nuclear Information System (INIS)

Yano, Y.; Budinger, T.F.; Chiang, G.; O'Brien, H.A.; Grant, P.M.

1979-01-01

Generator-produced Rb-82, a 75-sec positron emitter with potential for myocardial blood-flow imaging, was studied with various ion-exchange columns to evaluate the characteristics of alumina as an adsorber for the 25-day Sr-82 parent. Test columns of alumina, Bio Rex 70, and Chelex 100 were loaded with multimillicurie amounts of no-carrier-added Sr-82/Sr-85 (Sr-85 is a production contaminant). The breakthrough of Sr-82/Sr-85, and the yield of Rb-82, were determined for long-term elutions from each column with up to 4 liter of 2% NaCl solution at pH 8 to 9. The breakthrough of Sr-82/85 was 10 -6 to 10 -5 from alumina and 10 -6 to 10 -4 from Chelex 100 and Bio Rex 70. The effects of eluent flow rate and concentration, and of alumina volume, on the breakthrough and yield were also studied. An improved and automated Rb-82 generator was used for myocardial and brain blood-flow studies in experimental animals and in man; it was equipped with solenoid flow-control valves and five in. of lead shielding for the alumina columns, which were charged with 25 to 50 mCi Sr-82 (100 to 150 mCi Sr-85). The Rb-82 generator with alumina column provided up to 20 to 40 mCi of Rb-82 as often as every 5 to 10 min with -5 breakthrough of Sr-82/85 over the 2- to 3-mo, useful life of the generator

Rb-Sr isochronous age of Vepor pluton granitoids

International Nuclear Information System (INIS)

Bagdasaryan, G.P.; Gykasyan, R.Kh.; Cambel, B.

1986-01-01

The result are presented of geochronological investigations of the Vepor pluton granitoids by the Rb-Sr isochronous method. The results prove the Variscan age of granodiorite magmatism of the Sihla type (387±27 m.y.) and the Early Variscan age of leucocratic granitoids of the Vepor and the Ipel types (284±22 m.y.). Since the initial ratio of 87 Sr/ 86 Sr in granitoids of the Sihla type is 0.7054 and of the Vepor type 0.7060, it can be assumed that during the formation of the granitoids of veporides there was an increased supply of matter from the main source affecting genesis of granitoids. The results prove a polyphase character of the Variscan granitoids of Veporicum. (author)

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.

Apollo 17 'melt sheet': chemistry, age and Rb/Sr systematics

Energy Technology Data Exchange (ETDEWEB)

Winzer, S R [Martin Marietta Labs., Baltimore, Md. (USA); Nava, D F; Schuhmann, S; Philpotts, J A [National Aeronautics and Space Administration, Greenbelt, Md. (USA). Goddard Space Flight Center; Schuhmann, P J; Lum, R K.L.; Lindstrom, M M; Lindstrom, D J [Maryland Univ., College Park (USA)

1977-01-01

Major, minor and trace element compositions, age data and Rb/Sr systematics of Apollo 17 boulders have been compiled, and additional analyses performed on a norite breccia clast (77215) included in the Apollo 17, Station 7 boulder. The Apollo 17 boulders are found to be identical or nearly so in major, minor and trace element composition, suggesting that they all originated as an impact melt analogous to melt sheets found in larger terrestrial craters. The matrix dates (/sup 40/Ar//sup 39/Ar) and Rb/Sr systematics available suggest that this impact melt formed by a single impact about 4 b.y. ago. This impact excavated, shocked, brecciated and melted norites, norite cumulates and possibly anorthositic gabbros and dunites about 4.4 b.y. old. The impact was likely a major one, possibly the Serenitatis basin-forming event.

Geochronological studies by Rb/Sr method in rocks of the Jundiai block and surroundings. [Ampario group

Energy Technology Data Exchange (ETDEWEB)

Wernick, E [Faculdade de Filosofia Ciencias e Letras de Rio Claro; Oliveira, M A.F. de; Kawashita, K; Cordani, U G [Sao Paulo Univ. (Brazil). Inst. de Geociencias; Delhal, J [Musee Royal de l' Afrique Centrale, Belgica

1976-01-01

Field and petrological data, as well as radiometric results performed in granulitic, gneissic, migmatitic, and granitic rocks from the 'Jundiai tectonic block' (States of Sao Paulo and Minas Gerais), show for that region the existence of two superposed orogeneses. To the older, of transamazonian age whole rock Rb-Sr isochron 2,010 m.y. Rb/sup 87//Sr/sup 86/ initial = 0.702), belongs the Amparo Group, composed of gneisses, migmatites, and granulites, with intercalation of quartzites, schists and calc-silicate rocks. To the younger, of brazilian age whole rock Rb-Sr isochron 690 m.y. (Sr/sup 87//Sr/sup 86/ initial = 0.702), are related the feldspathization and migmatization of the Amparo Group, as well as the intrusion of granitic bodies. Possibly, also the metasediments around Jacarei belong to the brazilian cycle. This pattern of geologic evolution is similar to that observed for the Serra dos Orgaos region (States of Rio de Janeiro and Minas Gerais).

Results of Rb-Sr dating of metamorphic rocks of crystalline complexes of Male Karpaty Mts

International Nuclear Information System (INIS)

Bagdasaryan, G.P.; Gukasyan, P.Kh.; Cambel, B.; Veselsky, J.

1983-01-01

The paper follows up on a recently published paper on Rb-Sr isochrone dating of granitoid rocks of the Male Karpaty Mts. Data are given on comparative statistical analysis of isochrones obtained for the Bratislava and Modra massifs (isochrone of the latter is complemented with the analyses of two new samples) and the results of age determination of metasedimentary rocks of the Pezinok-Pernek zone and the Bratislava area by the Rb-Sr isochrone. Regression analysis shows that there is no statistically significant difference between the age of the Bratislava massif (347+-4 m.y.) and the Modra massif (326+-22 m.y.) and between their initial ratios 87 Sr/ 86 Sr (i.e., they are synchronous, having the same magma source) which makes it possible to calculate uniform value for age. Whole-rock samples of metamorphic and crystalline schists (gneisses) of the Male Karpaty Mts. also determine the isochrone corresponding to the age 387+-38 m.y. (2σ) and initial ratio ( 87 Sr/ 86 Sr)=0.7100+-0.00O8 (2σ). Rb-Sr isotope analyses of several pairs of biotite-crystalline schist (from which biotite was separated) point out that redistribution of Sr isotopes among the mineral phases of rocks takes place during the periplutonic metamorphism, while the whole-rock samples remain chemically closed systems. (author)

Sr and Nd isotopic and trace element compositions of Quaternary volcanic centers of the Southern Andes

Science.gov (United States)

Futa, K.; Stern, C.R.

1988-01-01

Isotopic compositions of samples from six Quaternary volcanoes located in the northern and southern extremities of the Southern Volcanic Zone (SVZ, 33-46??S) of the Andes and from four centers in the Austral Volcanic Zone (AVZ, 49-54??S) range for 87Sr 86Sr from 0.70280 to 0.70591 and for 143Nd 144Nd from 0.51314 to 0.51255. The ranges are significantly greater than previously reported from the southern Andes but are different from the isotopic compositions of volcanoes in the central and northern Andes. Basalts and basaltic andesites from three centers just north of the Chile Rise-Trench triple junction have 87Sr 86Sr, 143Nd 144Nd, La Yb, Ba La, and Hf Lu that lie within the relatively restricted ranges of the basic magmas erupted from the volcanic centers as far north as 35??S in the SVZ of the Andes. The trace element and Sr and Nd isotopic characteristics of these magmas may be explained by source region contamination of subarc asthenosphere, with contaminants derived from subducted pelagic sediments and seawater-altered basalts by dehydration of subducted oceanic lithosphere. In the northern extremity of the SVZ between 33?? and 34??S, basaltic andesites and andesites have higher 87Sr 86Sr, Rb Cs, and Hf Lu, and lower 143Nd 144Nd than basalts and basaltic andesites erupted farther south in the SVZ, which suggests involvement of components derived from the continental crust. In the AVZ, the most primitive sample, high-Mg andesite from the southernmost volcanic center in the Andes (54??S) has Sr and Nd isotopic compositions and K Rb and Ba La similar to MORB. The high La Yb of this sample suggests formation by small degrees of partial melting of subducted MORB with garnet as a residue. Samples from centers farther north in the AVZ show a regionally regular northward increase in SiO2, K2O, Rb, Ba, Ba La, and 87Sr 86Sr and decrease in MgO, Sr, K Rb, Rb Cs, and 143Nd 144Nd, suggesting increasingly greater degrees of fractional crystallization and associated intra

Isothermal cross-sections of Sr-Al-Ge and Ba-Al-Ge systems at 673 K

International Nuclear Information System (INIS)

Kutsenok, N.L.; Yanson, T.I.

1987-01-01

X-ray and microstructural analyses are used to study phase equilibria in Sr-Al-Ge and Ba-Al-Ge systems. Existence of SrAl 2 Ge 2 , Sr(Al, Ge) 2 Ba(Al, Ge) 2 , Sr 3 Al 2 Ge 2 , Ba 3 Al 2 Ge 2 ternary compounds is confirmed, a new BaGe 4 binary compound and also new ternary compounds of approximate composition Sr 57 Al 30 Ge 13 and Ba 20 Al 40 Ge 40 , which crystal structure is unknown, are detected. Aluminium solubility in SrAl 4 and BaAl 4 binary compounds (0.05 atomic fraction) is determined. Ba(Al, Ge) 2 compound homogeneity region is defined more exactly (aluminium content varies from 0.27 to 0.51 at. fractions)

Rb-Sr isochronous dating of granitoids of Dumbier zone of Low Tatras (Western Carpathians)

International Nuclear Information System (INIS)

Bagdasaryan, G.P.; Gukasyan, R.Kh.; Cambel, B.; Vesel'skij, J.

1985-01-01

The results are discussed of isotopic-geochronological research and age determination of characteristic samples of granitoid rocks, obtained by the Rb/Sr isochronous method. The samples were biotite granodiorites and granites taken from various parts of the Dumbier massif and small granite bodies of the Kralicka type. Rb/Sr isochrones of the rock samples show identical age values: 362+-21 m.y. for the Dumbier massif and 365+-17 m.y. correspnding to the Middle - Upper Devonian. Initial 87 Sr/ 86 Sr ratios equal to 0.7079 and 0.7157, respectively, allow to make a presumption that the rocks of the Dumbier massif may have been derived both from crustal and from mantle sources while granites of the Kralicka type are close to the rocks of the crustal origin

Adsorption removal of Sr by Barium impregnated 4A Zeolite(BaA) from high radioactive seawater waste

Energy Technology Data Exchange (ETDEWEB)

Lee, Eil Hee; Lee, Keun Young; Kim, Kwang Wook; Kim, Ik Soo; Chung, Dong Yong; Moon, Jei Kwon; Choi, Jong Won [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2016-06-15

This study investigated the removal of Sr, which was one of the high radioactive nuclides, by adsorption with Barium (Ba) impregnated 4A zeolite (BaA) from high-radioactive seawater waste (HSW). Adsorption of Sr by BaA (BaA-Sr), in the impregnated Ba concentration of above 20.2wt%, was decreased by increasing the impregnated Ba concentration, and the impregnated Ba concentration was suitable at 20.2wt%. The BaA-Sr adsorption was added to the co-precipitation of Sr with BaSO4 precipitation in the adsorption of Sr by 4A (4A-Sr) within BaA. Thus, it was possible to remove Sr more than 99% at m/V (adsorbent weight/solution volume)=5 g/L for BaA and m/V >20 g/L for 4A, respectively, in the Sr concentration of less than 0.2 mg/L (actual concentration level of Sr in HSW). It shows that BaA-Sr adsorption is better than 4A-Sr adsorption in for the removal capacity of Sr per unit gram of adsorbent, and the reduction of the secondary solid waste generation (spent adsorbent etc.). Also, BaA-Sr adsorption was more excellent removal capacity of Sr in the seawater waste than distilled water. Therefore, it seems to be effective for the direct removal of Sr from HSW. On the other hand, the adsorption of Cs by BaA (BaA-Cs) was mainly performed by 4A within BaA. Accordingly, it seems to be little effect of impregnated Ba into BaA. Meanwhile, BaA-Sr adsorption kinetics could be expressed the pseudosecond order rate equation. By increasing the initial Sr concentrations and the ratios of V/m, the adsorption rate constants (k2) were decreased, but the equilibrium adsorption capacities (qe) were increasing. However, with increasing the temperature of solution, k2 was conversely increased, and qe was decreased. The activation energy of BaA-Sr adsorption was 38 kJ/mol. Thus, the chemical adsorption seems to be dominant rather than physical adsorption, although it is not a chemisorption with strong bonding form.

High field-effect mobility at the (Sr,Ba)SnO{sub 3}/BaSnO{sub 3} interface

Energy Technology Data Exchange (ETDEWEB)

Fujiwara, Kohei, E-mail: kfujiwara@imr.tohoku.ac.jp; Nishihara, Kazuki; Shiogai, Junichi; Tsukazaki, Atsushi [Institute for Materials Research, Tohoku University, Sendai 980-8577 (Japan)

2016-08-15

A perovskite oxide, BaSnO{sub 3}, has been classified as one of transparent conducting materials with high electron mobility, and its application for field-effect transistors has been the focus of recent research. Here we report transistor operation in BaSnO{sub 3}-based heterostructures with atomically smooth surfaces, fabricated on SrTiO{sub 3} substrates by the (Sr,Ba)SnO{sub 3} buffer technique. Indeed, modulation of band profiles at the channel interfaces with the insertion of wide bandgap (Sr,Ba)SnO{sub 3} as a barrier layer results in a significant improvement of field-effect mobility, implying effective carrier doping at the regulated heterointerface. These results provide an important step towards realization of high-performance BaSnO{sub 3}-based field-effect transistors.

The Apollo 17 'melt sheet': chemistry, age and Rb/Sr systematics

International Nuclear Information System (INIS)

Winzer, S.R.; Nava, D.F.; Schuhmann, S.; Philpotts, J.A.

1977-01-01

Major, minor and trace element compositions, age data and Rb/Sr systematics of Apollo 17 boulders have been compiled, and additional analyses performed on a norite breccia clast (77215) included in the Apollo 17, Station 7 boulder. The Apollo 17 boulders are found to be identical or nearly so in major, minor and trace element composition, suggesting that they all originated as an impact melt analogous to melt sheets found in larger terrestrial craters. The matrix dates ( 40 Ar/ 39 Ar) and Rb/Sr systematics available suggest that this impact melt formed by a single impact about 4 b.y. ago. This impact excavated, shocked, brecciated and melted norites, norite cumulates and possibly anorthositic gabbros and dunites about 4.4 b.y. old. The impact was likely a major one, possibly the Serenitatis basin-forming event. (Auth.)

Rb-Sr age of a basic dyke, Schirmacher oasis, east Antarctica

International Nuclear Information System (INIS)

Dayal, A.M.; Hussain, S.M.

1996-01-01

In order to understand the crustal evolution in east Antartica, detailed geological, geochemical and isotopic studies of the various rocks in the area are necessary. This paper reports the Rb-Sr isotopic data on a gabbroic dyke in the Schirmacher oasis

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

Dielectric enhancement of BaTiO3/SrTiO3 superlattices with embedded Ni nanocrystals

International Nuclear Information System (INIS)

Xiong Zhengwei; Sun Weiguo; Wang Xuemin; Jiang Fan; Wu Weidong

2012-01-01

Highlights: ► The BaTiO 3 /SrTiO 3 superlattices with embedded Ni NCs were successfully fabricated by L-MBE. ► The influence with the various concentrations of Ni nanocrystals embedded in BaTiO 3 /SrTiO 3 superlattices was also discussed. ► The BaTiO 3 /SrTiO 3 superlattices with lower concentration of embedded Ni NCs had higher permittivity and dielectric loss compared with the pure BaTiO 3 /SrTiO 3 superlattices. ► The dielectric enhancement of BaTiO 3 /SrTiO 3 superlattices with embedded Ni NCs was proposed to explained by Drude quasi-free-electron theory. - Abstract: The self-organized Ni nanocrystals (NCs) were embedded in BaTiO 3 /SrTiO 3 superlattices using laser molecular beam epitaxy (L-MBE). The stress of the composite films was increased with the increasing concentration of embedded Ni NCs, as investigation in stress calculation. The influence with the various concentrations of Ni NCs embedded in BaTiO 3 /SrTiO 3 superlattices was also discussed. The internal stress of the films was too strong to epitaxial growth of BaTiO 3 /SrTiO 3 superlattices. Compared with the pure BaTiO 3 /SrTiO 3 superlattices, the BaTiO 3 /SrTiO 3 superlattices with lower concentration of embedded Ni NCs had higher permittivity and dielectric loss. Furthermore, the dielectric enhancement of BaTiO 3 /SrTiO 3 superlattices with embedded Ni NCs was proposed to explained by Drude quasi-free-electron theory.

Ab initio study of the RbSr electronic structure: Potential energy curves, transition dipole moments, and permanent electric dipole moments

Energy Technology Data Exchange (ETDEWEB)

Pototschnig, Johann V., E-mail: johann.pototschnig@tugraz.at; Krois, Günter; Lackner, Florian; Ernst, Wolfgang E., E-mail: wolfgang.ernst@tugraz.at [Institute of Experimental Physics, Graz University of Technology, Petersgasse 16, A-8010 Graz (Austria)

2014-12-21

Excited states and the ground state of the diatomic molecule RbSr were calculated by post Hartree-Fock molecular orbital theory up to 22 000 cm{sup −1}. We applied a multireference configuration interaction calculation based on multiconfigurational self-consistent field wave functions. Both methods made use of effective core potentials and core polarization potentials. Potential energy curves, transition dipole moments, and permanent electric dipole moments were determined for RbSr and could be compared with other recent calculations. We found a good agreement with experimental spectra, which have been obtained recently by helium nanodroplet isolation spectroscopy. For the lowest two asymptotes (Rb (5s {sup 2}S) + Sr (5s4d {sup 3}P°) and Rb (5p {sup 2}P°) + Sr (5s{sup 2} {sup 1}S)), which exhibit a significant spin-orbit coupling, we included relativistic effects by two approaches, one applying the Breit-Pauli Hamiltonian to the multireference configuration interaction wave functions, the other combining a spin-orbit Hamiltonian and multireference configuration interaction potential energy curves. Using the results for the relativistic potential energy curves that correspond to the Rb (5s {sup 2}S) + Sr (5s4d {sup 3}P°) asymptote, we have simulated dispersed fluorescence spectra as they were recently measured in our lab. The comparison with experimental data allows to benchmark both methods and demonstrate that spin-orbit coupling has to be included for the lowest states of RbSr.

Ab initio study of the RbSr electronic structure: potential energy curves, transition dipole moments, and permanent electric dipole moments.

Science.gov (United States)

Pototschnig, Johann V; Krois, Günter; Lackner, Florian; Ernst, Wolfgang E

2014-12-21

Excited states and the ground state of the diatomic molecule RbSr were calculated by post Hartree-Fock molecular orbital theory up to 22 000 cm(-1). We applied a multireference configuration interaction calculation based on multiconfigurational self-consistent field wave functions. Both methods made use of effective core potentials and core polarization potentials. Potential energy curves, transition dipole moments, and permanent electric dipole moments were determined for RbSr and could be compared with other recent calculations. We found a good agreement with experimental spectra, which have been obtained recently by helium nanodroplet isolation spectroscopy. For the lowest two asymptotes (Rb (5s (2)S) + Sr (5s4d (3)P°) and Rb (5p (2)P°) + Sr (5s(2) (1)S)), which exhibit a significant spin-orbit coupling, we included relativistic effects by two approaches, one applying the Breit-Pauli Hamiltonian to the multireference configuration interaction wave functions, the other combining a spin-orbit Hamiltonian and multireference configuration interaction potential energy curves. Using the results for the relativistic potential energy curves that correspond to the Rb (5s (2)S) + Sr (5s4d (3)P°) asymptote, we have simulated dispersed fluorescence spectra as they were recently measured in our lab. The comparison with experimental data allows to benchmark both methods and demonstrate that spin-orbit coupling has to be included for the lowest states of RbSr.

Rb-Sr ages and palaeomagnetic data for some Angolan alkaline intrusives

International Nuclear Information System (INIS)

Allsopp, H.L.; Hargraves, R.B.

1985-01-01

New Rb-Sr age measurements are reported for a number of intrusives from Angola. Data for the Njoio and Tchivira nepheline syenite bodies yield mineral isochrons indicating ages of 104,3+-0,8 Ma and 130,8+-1,4 Ma respectively. Palaeomagnetic studies on the same occurrences gave marginal and scattered results respectively. Micas from the Camafuca crater-facies kimberlite yielded and apparent age of 1 822+-151 Ma, a result that is far in excess of the Tertiary (or younger) age inferred for this pipe. Similarly conflicting data were obtained for the Nova Lisboa kimberlite. It is likely that older crustal micas incorporated in the kimberlite breccias are responsible for the anomalous ages reported on the kimberlites. Satisfactory palaeomagnetic data are reported for the Zenza and Bailundu occurrences, not dated by the Rb-Sr method. A convenient K-Ar age of 80+-0,8 Ma was obtainable for Zenza

Phase equilibrium in Al-Li-Ca(Sr, Ba) systems at 423 K

International Nuclear Information System (INIS)

Ganieva, N.I.; Nazarov, Kh.M.; Ganiev, I.N.

1999-01-01

The isothermic cross section of the Al-Li-Ca(Sr, Ba) systems at 423 K is obtained. It is shown that the Al-Li-Sr ternary system as well as the Li-Sr binary system differ by nature of components in interaction from the Al-Li-Ca(Ba) systems. This is obvious by formation of the SrAl 2 Li 2 ternary intermetallide, which is not observed in the systems with participation of barium and calcium [ru

Separation of Sr from Ca, Ba and Ra by means of Ca(OH)2 and Ba(Ra)Cl2 or Ba(Ra)SO4 for the determination of radiostrontium

DEFF Research Database (Denmark)

Chen, Q.J.; Hou, Xiaolin; Yu, Y.X.

2002-01-01

be completed. The new separation procedure has been successfully used for the determination of Sr-90 in samples with high Ca content, such as 451 of seawater and 2001 of drinking water. The analytical quality of the results is comparable to that of the traditional method using fuming nitric acid and BaCrO4......A simple procedure is developed to separate Sr from a large amount of Ca, which relies on the insolubility of Ca(OH)(2) in alkaline solution. Calcium is quantitatively separated from Sr and more than 95% of Sr is recovered from a sample with as much as 50 g of Ca and a Ca/Sr mole ratio of 250....... A new procedure for the separation of Sr from Ba and Ra is also investigated, which is based on the difference in solubility of the chlorides of Sr, Ba and Ra in HCl media. In 9.5 mol 1(-1) HCl or 7.5 mol 1(-1) HCl-10% acetone media, >97% of Ba and Ra can be removed by Ba(Ra)Cl-2 precipitation, and >94...

K, Rb and Sr abundances and Sr isotopic composition of the Tanzawa granitic and associated gabbroic rocks, Japan: low-potash island arc plutonic complex

International Nuclear Information System (INIS)

Ishizaka, K.; Yanagi, T.

1977-01-01

The granitic and associated gabbroic rocks of the Tanzawa plutonic complex of Miocene age occurring in the northern part of the Izu-Bonin arc are characterized by low abundances of K (229-6790 ppm) and Rb (0.414-12.1 ppm), low K 2 O/Na 2 O ratios (0.037-0.21), moderately high K/Rb ratios (541-630), low Rb/Sr ratios (0.00137-0.0579) and low initial 87 Sr/ 86 Sr ratios (0.70332-0.70372). This indicates that acid to intermediate plutonic rocks with these geochemical characteristics also occur in island arc environments besides mid-oceanic ridge environments. They represent, together with associated gabbroic rocks, a low-potash island arc plutonic complex and are expected to occur beneath young island arcs, although now unexposed. The Tanzawa plutonic complex may have been formed by differentiation of low-K calc-alkaline magma. (Auth.)

Phase diagrams for systems Cu2S-AIIS (AII=Mg, Ca, Sr, Ba)

International Nuclear Information System (INIS)

Andreev, O.V.; Sikerina, N.V.; Solov'eva, A.V.

2005-01-01

By the methods of physicochemical analysis phase diagrams of Cu 2 S-A II S (A II =Mg, Ca, Sr, Ba) systems are studied. The system Cu 2 S-SrS is of eutectic type with eutectic coordinates 1095 K and 21.5 mol.% of SrS. Solubility of SrS in Cu 2 S is 2 mol.% at 1095 K. Regularities of phase diagram changes of Cu 2 S-A II S (A II =Mg, Ca, Sr, Ba) system are determined. Thermodynamic analysis is done [ru

Fluid inclusion, geochemical, Rb-Sr and Sm-Nd isotope studies on ...

Indian Academy of Sciences (India)

10

Degana granites is quiet high and ranges from 958 to 1907 ppm except B-24, Zr .... According to Pearson's hard soft acid base (HSAB) principle, tungsten which occurs ... could explain lower Sr abundances in the Balda and Degana granites, Rb ...... Oceanic ridge granites (ORG), within-plate granite (WPG), volcanic arc ...

Rb-Sr And Sm-Nd Ages, and Petrogenesis of Depleted Shergottite Northwest Africa 5990

Science.gov (United States)

Shih, C. Y.; Nyquist, L. E.; Reese, Y.; Irving, A. J.

2011-01-01

Northwest Africa (NWA) 5990 is a very fresh Martian meteorite recently found on Hamada du Draa, Morocco and was classified as an olivine-bearing diabasic igneous rock related to depleted shergottites [1]. The study of [1] also showed that NWA 5990 resembles QUE 94201 in chemical, textural and isotopic aspects, except QUE 94201 contains no olivine. The depleted shergottites are characterized by REE patterns that are highly depleted in LREE, older Sm-Nd ages of 327-575 Ma and highly LREE-depleted sources with Nd= +35+48 [2-7]. Age-dating these samples by Sm-Nd and Rb-Sr methods is very challenging because they have been strongly shocked and contain very low abundances of light rare earth elements (Sm and Nd), Rb and Sr. In addition, terrestrial contaminants which are commonly present in desert meteorites will compromise the equilibrium of isotopic systems. Since NWA 5990 is a very fresh meteorite, it probably has not been subject to significant desert weathering and thus is a good sample for isotopic studies. In this report, we present Rb-Sr and Sm-Nd isotopic results for NWA 5990, discuss the correlation of the determined ages with those of other depleted shergottites, especially QUE 94201, and discuss the petrogenesis of depleted shergottites.

Heat capacity measurement of Ba3SrNb2O9

International Nuclear Information System (INIS)

Singh, B.M.; Samui, Pradeep; Agarwal, Renu; Mukerjee, S.K.

2016-01-01

Barium, Strontium and Niobium are important fission products in nuclear reactor with reasonable fission yields. During irradiation of oxide fuels, they can combine to form compounds of Ba-Sr-Nb-O system. Therefore, thermodynamic properties of Ba 3 SrNb 2 O 9 are required for modelling fuel behaviour however thermodynamic data of this compound is not available in literature. Ba 3 SrNb 2 O 9 was prepared by solid state route, by mixing stoichiometric amounts of finely grounded SrCO 3 , BaCO 3 and Nb 2 O 5 . Finally mixed powder was pressed into a pellet at 5 ton pressure for 2 minutes in a hydraulic press and the pellet was heated at 1123 K for 60 h in air. The pellet was cooled, finely grounded, re-pelletised and heated at 1473 K for 120 h. The formation of compound was confirmed by X-ray diffraction pattern, collected at room temperature using Cu-K α radiation (λ = 1.54 nm), scanned over the angular range 20-80° (2θ) with steps of 0.02°. Heat capacity of the compound was measured by the classical three-step method, in continuous mode, using LABSYS EVO, in temperature range of 370 and 950 K. No transition was observed in the investigated temperature range

Physical and magnetic properties of (Ba/Sr) substituted magnesium nano ferrites

Science.gov (United States)

Ateia, Ebtesam E.; Takla, E.; Mohamed, Amira T.

2017-10-01

In the presented paper, strontium (Sr) and barium (Ba) nano ferrites were synthesized by citrate auto combustion method. The investigated samples are characterized by X-ray diffraction technique (XRD), field emission scanning electron microscopy, high resolution transmission electron microscopy and energy dispersive X-ray spectroscopy. The structural properties of the obtained samples were examined by XRD analysis showing that the synthesized nanoparticles are in cubic spinel structure. The average crystallite sizes are in the range of 22.66 and 21.95 nm for Mg0.7Ba0.3Fe2O4 and Mg0.7 Sr0.3Fe2O4 respectively. The VSM analysis confirms the existence of ferromagnetic nature of Sr2+/Ba2+ substituted magnesium nano particles. Exchange interaction between hard (Sr/Ba) and soft (Mg) magnetic phases improves the structural and magnetic properties of nano ferrite particles. Rigidity modulus, longitudinal and shear wave velocities are predicted theoretically from Raman spectroscopy and structural data of the investigated spinel ferrite. The magnetic and structural properties of magnesium are enhanced by doping with barium and strontium nano particles. The saturation magnetization, remanent magnetization and coercivity reported on vibrating sample magnetometer curve illustrate the promising industrial and magnetic recording applications of the prepared samples.

Computational study of Ca, Sr and Ba under pressure

International Nuclear Information System (INIS)

Jona, F; Marcus, P M

2006-01-01

A first-principles procedure for the calculation of equilibrium properties of crystals under hydrostatic pressure is applied to Ca, Sr and Ba. The procedure is based on minimizing the Gibbs free energy G (at zero temperature) with respect to the structure at a given pressure p, and hence does not require the equation of state to fix the pressure. The calculated lattice constants of Ca, Sr and Ba are shown to be generally closer to measured values than previous calculations using other procedures. In particular for Ba, where careful and extensive pressure data are available, the calculated lattice parameters fit measurements to about 1% in three different phases, both cubic and hexagonal. Rigid-lattice transition pressures between phases which come directly from the crossing of G(p) curves are not close to measured transition pressures. One reason is the need to include zero-point energy (ZPE) of vibration in G. The ZPE of cubic phases is calculated with a generalized Debye approximation and applied to Ca and Sr, where it produces significant shifts in transition pressures. An extensive tabulation is given of structural parameters and elastic constants from the literature, including both theoretical and experimental results

Computational study of Ca, Sr and Ba under pressure

Energy Technology Data Exchange (ETDEWEB)

Jona, F; Marcus, P M [Department of Materials Science and Engineering, State University of New York, Stony Brook, NY 11794-2275 (United States)

2006-05-17

A first-principles procedure for the calculation of equilibrium properties of crystals under hydrostatic pressure is applied to Ca, Sr and Ba. The procedure is based on minimizing the Gibbs free energy G (at zero temperature) with respect to the structure at a given pressure p, and hence does not require the equation of state to fix the pressure. The calculated lattice constants of Ca, Sr and Ba are shown to be generally closer to measured values than previous calculations using other procedures. In particular for Ba, where careful and extensive pressure data are available, the calculated lattice parameters fit measurements to about 1% in three different phases, both cubic and hexagonal. Rigid-lattice transition pressures between phases which come directly from the crossing of G(p) curves are not close to measured transition pressures. One reason is the need to include zero-point energy (ZPE) of vibration in G. The ZPE of cubic phases is calculated with a generalized Debye approximation and applied to Ca and Sr, where it produces significant shifts in transition pressures. An extensive tabulation is given of structural parameters and elastic constants from the literature, including both theoretical and experimental results.

Rb-Sr geochronological study on Tatehira granodiorite, Oshima Peninsula, Southwest Hokkaido, Japan

Energy Technology Data Exchange (ETDEWEB)

Iizumi, Shigeru; Kobayashi, Hideo; Toyoda, Minoru

1984-10-01

It has been known that Tatehira granodiorite, a pluton which occurs sporadically in the southwest region of Hokkaido, is related with Kanoite formation. The radiometric age of this granodiorite still remains unknown. The Tatehira granodiorite intrudes into late Paleozoic or early Mesozoic Matsumae group, and is overlain by Miocene Usubetsu formation unconformably. It occurs as several separated small plutons. The samples for Rb-Sr analysis were collected from one of the plutons in southern part. The determination of the isochron age of rock-minerals and the initial Sr isotopic ratio of Tatehira granodiorite were carried out. This granodiorite is able to be classified into two phases, namely melanocratic (WRM) and leucocratic (WRL) phases. The samples of WRM and WRL were powdered and subjected to X-ray analysis. It was found that the chemical compositions were similar except slight differences in FeO + Fe2O3, CaO and K2O. The Sr isotopic ratio was determined with a MAT 261 mass spectrometer, and the results were analyzed statistically. The Rb and Sr concentrations and the Sr isotopic ratio of WRM, WRL, and PRF (plagio-clase rich fraction) and BRF (biotite rich fraction) separated from the WRL were determined, and the age of 102.5 +- 0.3 Ma and the initial ratio of 0.70538 +- 0.00001 were obtained. The ratio of Tatehira granodiorite is comparable to that of Okushiri Island. Comparing with the data obtained from other region, the granodiorites of Tatehira and Okushiri Island should be related with the granitoids of Abukuma granite province.

Impedance spectroscopy of Li2CO3 doped (Ba,Sr)TiO3 ceramic

Science.gov (United States)

Ham, Yong-Su; Koh, Jung-Hyuk

2013-02-01

(BaxSr1-x)TiO3-based ceramic has been considered as one of the most important electronic materials widely employed in microwave passive device applications. Many researches have been performed to lower the high sintering temperature, by adding various dopants such as B2O3, La2O3, etc. In our previous study, by adding Li2CO3 to (Ba0.5,Sr0.5)TiO3 ceramics, the sintering temperature of Li2CO3 doped (Ba0.5,Sr0.5)TiO3 ceramics decreased from 1350 to 900 °C. This study observed the crystalline structure and electrical properties of Li2CO3 doped (Ba0.5,Sr0.5)TiO3 ceramics. In scanning the crystalline structure of Li2CO3 doped (Ba0.5,Sr0.5)TiO3 ceramics, no pyro phase was observed by X-ray diffraction analysis. To investigate the electrical properties of Li2CO3 doped (Ba0.5,Sr0.5)TiO3 ceramics, real and imaginary parts of the impedances were analyzed. Complex impedance data were measured from 100 Hz to 1 MHz at various temperature ranges.

Sequential separation of cs, ca and ba for 90sr assessment

International Nuclear Information System (INIS)

Dianu, M.; Bucur, C.

2015-01-01

A two-steps chemical treatment technique for strontium assessment from aqueous samples is described in this paper. The method was applied to simulated samples containing stable elements of Ni, Cs, Ca, Ba, Mn, Fe, Co and Eu. The transition elements (Ni, Mn, Fe, Co, Eu) were precipitated as hydroxides, followed by alkaline-earth metals separation (Ca, Ba) as carbonates. Finally, the Sr was purified by extraction chromatography using Triskem International Sr resin. The strength of Sr sorption in nitric acid increases with increasing acid concentration, and the optimal bonding strength is achieved in 8 M HNO3. The combination of successive precipitations with extraction chromatography for complete removal of other interferences from Sr matrix leads to good recovery and decontamination factor values. (authors)

Potentiality if Rb-Sr method for dating the argillous sedimentary rocks

International Nuclear Information System (INIS)

Thomaz Filho, A.

1976-01-01

The potentiality of application Rb-Sr method in argillous sediments, using samples from paleozoic and mesozoic formation in brazilian sedimentaries basin was tested. Physical, chemistry and isotopic analysis of thirty eight samples were made in the laboratories of geochronology Research Center from the University of Sao Paulo. Four isochronic diagrams for the argillous sedimentary rocks were also proposed. (author)

K-Ar and Rb-Sr dating results of the Malyshevsky leucogranite massif (eastern slope of the Middle Urals)

International Nuclear Information System (INIS)

Smirnov, V.N.; Ivanov, K.S.; Ronkin, Yu.L.; Levin, V.Ya.; Bushlyakov, I.N.; Lepikhina, O.P.; Popova, O.Yu.

2005-01-01

The age of leucogranites and minerals forming the Malyshevsky massif was identified by the methods of K-Ar- and Rb-Sr dating for refining the sequence of magmatic complexes formation on the eastern slope of the Middle Urals. The obtained isotope age values, i.e. 229-277 mln. years (K-Ar) and 277.1±1.1 mln. years (Rb-Sr), permit considering the age of 277 mln. years as the period of the leucogranites formation and of the associated molybdenum mineralization [ru

The age of Male Karpaty Mts. granitoid rocks determined by Rb-Sr isochrone method

International Nuclear Information System (INIS)

Badgasaryan, G.P.; Gukasyan, R.Kh.; Veselsky, J.

1982-01-01

The results are presented of nuclear geochronological datings of Male Karpaty Mts. granitoids by Rb-Sr isochrone method. Using the method the age of Bratislava massif granitoids was established to be 347+-4 mil. y. at ( 87 Sr/ 86 Sr)=0.7076+-0.0013 and the age of Modra massif granitoids to be 324+-18 mil. y. at ( 87 Sr/ 86 Sr)=0.7075+-0.00032 (2σ). The relative agreement of age of both massifs as well as the agreement of the primary ratio ( 87 Sr/ 86 Sr) 0 not only testifies to their continuity in age but also in genesis. The same relations also confirm the genetic dependence of pegmatites and leucocratic granitoids on fundamental types of granitoids building up the Bratislava and Modra massifs. (author)

Mechanistic model for Sr and Ba release from severely damaged fuel

International Nuclear Information System (INIS)

Rest, J.; Cronenberg, A.W.

1985-11-01

Among radionuclides associated with fission product release during severe accidents, the primary ones with health consequences are the volatile species of I, Te, and Cs, and the next most important are Sr, Ba, and Ru. Considerable progress has been made in the mechanistic understanding of I, Cs, Te, and noble gas release; however, no capability presently exists for estimating the release of Sr, Ba, and Ru. This paper presents a description of the primary physical/chemical models recently incorporated into the FASTGRASS-VFP (volatile fission product) code for the estimation of Sr and Ba release. FASTGRASS-VFP release predictions are compared with two data sets: (1) data from out-of-reactor induction-heating experiments on declad low-burnup (1000 and 4000 MWd/t) pellets, and (2) data from the more recent in-reactor PBF Severe Fuel Damage Tests, in which one-meter-long, trace-irradiated (89 MWd/t) and normally irradiated (approx.35,000 MWd/t) fuel rods were tested under accident conditions. 10 refs

Rb-Sr and Sm-Nd chronology and genealogy of mare basalts from the Sea of Tranquility

Science.gov (United States)

Papanastassiou, D. A.; Depaolo, D. J.; Wasserburg, G. J.

1977-01-01

Rb-Sr and Sm-Nd ages of two Apollo 11 mare basalts, high-K basalt 10072 and low-K basalt 10062, are reported. Rb-Sr, Sm-Nd, and Ar-40-Ar-39 ages are in good agreement and indicate an extensive time interval for filling of the Sea of Tranquility, presumably by thin lava flows, in agreement with similar observations for the Ocean of Storms. Initial Sr and Nd isotopic compositions on Apollo 11 basalts reveal at least two parent sources producing basalts. The Sm-Nd isotopic data demonstrate that low-K and high-Ti basalts from Apollo 11 and 17 derived from distinct reservoirs, while low-Ti Apollo 15 mare basalt sources have Sm/Nd similar to the sources of Apollo 11 basalts. Groupings of mare basalt based on Ti content and on isotopic data do not coincide.

The effect of diameter ratio between transducers and reactor in sonication-assisted synthesis of Ba{sub 0.7}Sr{sub 0.3}TiO{sub 3} and Ba{sub 0.3}Sr{sub 0.7}TiO{sub 3} nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Manaf, A., E-mail: azwar@ui.ac.id; Fahmi, Agam Aidil [Department of Physics, FMIPA, Universitas Indonesia, Kampus UI Depok (Indonesia); Yustanti, Erlina [Department of Physics, FMIPA, Universitas Indonesia, Kampus UI Depok (Indonesia); Department of Metallurgy, Faculty of Engineering, University of Sultan AgengTirtayasa Jl. Jenderal Sudirman KM 03 Cilegon-Banten 65134 (Indonesia)

2016-04-19

This paper describes the particle size characterization of mechanically alloyed Ba{sub 0.7}Sr{sub 0.3}TiO{sub 3} and Ba{sub 0.3}Sr{sub 0.7}TiO{sub 3} prepared with the aid of a high-power ultrasonic destruction. Analytical-grade BaCO{sub 3}, TiO{sub 2} and SrCO{sub 3} with a purity greater than 99 wt.% were used as precursors for Ba{sub 0.7}Sr{sub 0.3}TiO{sub 3} and Ba{sub 0.3}Sr{sub 0.7}TiO{sub 3}. The mechanically powders were respectively sintered at 1200 °C for 3 hours to form crystalline powders. This work is aimed at studying the effect of diameter ratio between reactor and transducer of a high power sonicator on the Ba{sub 0.7}Sr{sub 0.3}TiO{sub 3} and Ba{sub 0.3}Sr{sub 0.7}TiO{sub 3} nanoparticles formation. The presence of a single phase of the two materials was confirmed by X-Ray Diffraction (XRD). The concentration of the particles in demineralized water was 3.0 g / 100 mL which become the object of 3 hours ultrasonic destruction subjected to the application of transducer in which the ratio between the diameter of the reactor and the transducer (D/d) was fixed at 1.4, 1.6 and 1.8 respectively. It was found that the mean particle size before the ultrasonic destruction was 538 nm for Ba{sub 0.7}Sr{sub 0.3}TiO{sub 3} and 480 nm for Ba{sub 0.3}Sr{sub 0.7}TiO{sub 3}. With D/d of 1.8, the mean particle size of the two materials was found to decrease drastically to 38 nm and 24 nm, respectively. These mean particle sizes were respectively comparable with that of the crystallite size of the particles derived using the Whole Powder Pattern Modelling (WPPM) from which the mean crystallite size of 22 nm for Ba{sub 0.7}Sr{sub 0.3}TiO{sub 3} and 14 nm for Ba{sub 0.3}Sr{sub 0.7}TiO{sub 3} were obtained. It is then confirmed single nanocrystallite Ba{sub 0.7}Sr{sub 0.3}TiO{sub 3} and Ba{sub 0.3}Sr{sub 0.7}TiO{sub 3} particles were already achieved. We can conclude that the ultrasonic destruction to mechanically milled crystalline particles would be one

Application of boat method in emissive flame photometry for determination of Li, Rb, Cs, Na, K, Ca, Sr, Ba

International Nuclear Information System (INIS)

Orlov, N.A.; Pobedonostsev, V.A.; Savel'ev, Yu.A.

1976-01-01

Study of the flame temperature and dependence of adsorbance on the C/O ratio over the boat for the carbide forming elements and the effect of material, thickness, and the height of the boat on the vaporization of alkaline and alkaline earth metals is described. For a boat (70x8, and 0.3 mm thickness), made from Cu, brass, and Ni, the fall in temperature over the boat was 70, 130, 250, and 340 0 , respectively, for air-C 2 H 2 and 50, 100, 210, and 280 0 for N 2 O-C 2 H 2 flame. Introduction of the boat increases the C/O ratio in the analytical zone of the flame, probably caused by a creation of a shaded space, immediately above the boat. Smaller amounts of atmospheric O enter into the space, when compared with the flame in the absence of the boat. The increase in the C/O ratio decreases the absorbance, which in turn, is caused by the fall in temperature and formation of carbides. Time lag between heating of the boat and the initiation of vaporization of the sample and the duration of evaporation impulse were measured. Solutions of CsCl, containing 1 μg Cs/ml were used at 852.1 nm. The boats, previously treated with 0.1% polystyrene in C 6 H 6 , to give a hydrophobic surface and an uniform salt layer distribution, containing the sample were dried under an ir lamp and introduced into the flame. The dependence of Cs emission on the thickness of the different materials (Ni, Cu, Ta) and heights of boats in the air-C 2 H 2 flame is illustrated. The duration of the emission impulse decreases linearly with the decrease of thickness of the boat for all materials tested. Limits of detection of Na, K, Li, Rb, Cs, Ca, Sr, and Ba were determined by using the equilibrium and the boat methods, the latter being some 1-2 orders lower than the former

Tracing subduction zone fluid-rock interactions using trace element and Mg-Sr-Nd isotopes

Science.gov (United States)

Wang, Shui-Jiong; Teng, Fang-Zhen; Li, Shu-Guang; Zhang, Li-Fei; Du, Jin-Xue; He, Yong-Sheng; Niu, Yaoling

2017-10-01

Slab-derived fluids play a key role in mass transfer and elemental/isotopic exchanges in subduction zones. The exhumation of deeply subducted crust is achieved via a subduction channel where fluids from various sources are abundant, and thus the chemical/isotopic compositions of these rocks could have been modified by subduction-zone fluid-rock interactions. Here, we investigate the Mg isotopic systematics of eclogites from southwestern Tianshan, in conjunction with major/trace element and Sr-Nd isotopes, to characterize the source and nature of fluids and to decipher how fluid-rock interactions in subduction channel might influence the Mg isotopic systematics of exhumed eclogites. The eclogites have high LILEs (especially Ba) and Pb, high initial 87Sr/86Sr (up to 0.7117; higher than that of coeval seawater), and varying Ni and Co (mostly lower than those of oceanic basalts), suggesting that these eclogites have interacted with metamorphic fluids mainly released from subducted sediments, with minor contributions from altered oceanic crust or altered abyssal peridotites. The positive correlation between 87Sr/86Sr and Pb* (an index of Pb enrichment; Pb* = 2*PbN/[CeN + PrN]), and the decoupling relationships and bidirectional patterns in 87Sr/86Sr-Rb/Sr, Pb*-Rb/Sr and Pb*-Ba/Pb spaces imply the presence of two compositionally different components for the fluids: one enriched in LILEs, and the other enriched in Pb and 87Sr/86Sr. The systematically heavier Mg isotopic compositions (δ26Mg = - 0.37 to + 0.26) relative to oceanic basalts (- 0.25 ± 0.07) and the roughly negative correlation of δ26Mg with MgO for the southwestern Tianshan eclogites, cannot be explained by inheritance of Mg isotopic signatures from ancient seafloor alteration or prograde metamorphism. Instead, the signatures are most likely produced by fluid-rock interactions during the exhumation of eclogites. The high Rb/Sr and Ba/Pb but low Pb* eclogites generally have high bulk-rock δ26Mg values

Consideration of the band-gap tunability of BaSi2 by alloying with Ca or Sr based on the electronic structure calculations

International Nuclear Information System (INIS)

Imai, Yoji; Watanabe, Akio

2007-01-01

The electronic structures and total energies of BaSi 2 -SrSi 2 and BaSi 2 -CaSi 2 systems have been calculated using the first-principle pseudopotential method to clarify the band gap tunability of BaSi 2 by alloying with Sr or Ca. From an energetic consideration of the compounds where all the Ba I sites or all the Ba II sites of the BaSi 2 lattice are preferentially replaced by Sr or Ca, it is expected that the Ba I site will be preferentially replaced by Sr rather than the Ba II sites. Compounds where all the Ba II sites are replaced by Sr or all the Ba II or all the Ba I sites are replaced by Ca are energetically unfavorable compared to the undissolved system of BaSi 2 and SrSi 2 or CaSi 2 . The effect of the addition of Sr or Ca into the BaSi 2 lattice on the gap value is different depending on the replaced sites of Ba. The replacement of Ba I site by Sr will broaden the band gap of BaSi 2 , which is consistent with the observed results

First-principles study of the (001) surface of cubic Ba0.5Sr0.5TiO3

International Nuclear Information System (INIS)

Wang, Yuan Xu

2008-01-01

We have theoretically investigated basic properties of the (001) surface of cubic Ba 0.5 Sr 0.5 TiO 3 (BST) by the plane-wave pseudopotential method within the local-density approximation. For the BaSrO 2 -terminated surface, the surface-layer Sr atoms move inward and the surface-layer Ba atoms move outward. Moreover, the displacement of the surface-layer Sr atoms is much larger than the surface-layer Ba atoms. The rumpling of the BaSrO 2 -terminated surface is much larger than that of the Ti 2 O 4 -terminated one. The surface state appears in the band structure of the Ti 2 O 4 -terminated surface of BST. Based on the results of the calculated grand thermodynamic potential, only the BaSrO 2 -terminated surface can exist in the (001) surface of cubic BST. (copyright 2008 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

Rb-Sr, Pb-Pb, U-Pb dating in the Bandja plutonic series of Western Cameroon. Donnees geochronologiques (Rb-Sr, Pb-Pb, U-Pb) sur le complexe plutonique de Bandja (Centre-Ouest Cameroun)

Energy Technology Data Exchange (ETDEWEB)

Tchankam, C N [Nancy-1 Univ., 54 (France); Vialette, Y [Clermont-Ferrand-2 Univ., 63 - Aubiere (France)

1994-08-01

The results of U-Pb zircon and Pb-Pb on minerals and whole rocks are reported on a charnockite syn-D1 from the Bandja series in the western Cameroon. Data are interpreted as representing a plutonic emplacement at 640 Ma. A syn- to post-tectonic pluton is dated at 557 [+-] 8 Ma (Rb-Sr whole rocks isochron). These results confirm the Pan-African age of the charnockitic intrusive body. Initial isotopic [sup 87]Sr/[sup 86]Sr ratios of charnockite (0.709) and granite (0.7089) show the importance of crustal imprint in the magma genesis. (authors).

A Rb-Sr geochronological study on Tatehira granodiorite, Oshima Peninsula, Southwest Hokkaido, Japan

International Nuclear Information System (INIS)

Iizumi, Shigeru; Kobayashi, Hideo; Toyoda, Minoru.

1984-01-01

It has been known that Tatehira granodiorite, a pluton which occurs sporadically in the southwest region of Hokkaido, is related with Kanoite formation. The radiometric age of this granodiorite still remains unknown. The Tatehira granodiorite intrudes into late Paleozoic or early Mesozoic Matsumae group, and is overlain by Miocene Usubetsu formation unconformably. It occurs as several separated small plutons. The samples for Rb-Sr analysis were collected from one of the plutons in southern part. The determination of the isochron age of rock-minerals and the initial Sr isotopic ratio of Tatehira granodiorite were carried out. This granodiorite is able to be classified into two phases, namely melanocratic (WRM) and leucocratic (WRL) phases. The samples of WRM and WRL were powdered and subjected to X-ray analysis. It was found that the chemical compositions were similar except slight differences in FeO + Fe 2 O 3 , CaO and K 2 O. The Sr isotopic ratio was determined with a MAT 261 mass spectrometer, and the results were analyzed statistically. The Rb and Sr concentrations and the Sr isotopic ratio of WRM, WRL, and PRF (plagio-clase rich fraction) and BRF (biotite rich fraction) separated from the WRL were determined, and the age of 102.5 +- 0.3 Ma and the initial ratio of 0.70538 +- 0.00001 were obtained. The ratio of Tatehira granodiorite is comparable to that of Okushiri Island. Comparing with the data obtained from other region, the granodiorites of Tatehira and Okushiri Island should be related with the granitoids of Abukuma granite province. (Ishimitsu, A.)

87Rb-87Sr chronology of H chondrites: constraint and speculations on the early evolution of their parent body

International Nuclear Information System (INIS)

Minster, J.-F.; Allegre, C.J.

1979-01-01

A precise 87 Rb- 87 Sr whole-rock isochron for H chrondrites and an internal isochron for Tieschitz (H3) have been determined. The age and 87 Sr/ 86 Sr initial ratio of the whole rocks are 4.25 +- 0.05 b.y. and 0.69876 +- 0.00040 (lambda( 87 Rb) = 1.42 X 10 -11 yr -1 ). For Tieschitz, whereas handipicked separates plot on a well-defined line, heavy liquid separates scatter in the 87 Rb/ 86 Sr vs. 87 Sr/ 86 Sr diagram. Leaching experiments by heavy liquids indicate that they might have a sizeable effect on Tieschitz minerals. The age and 87 Sr/ 86 Sr initial ratio as determined by handpicked separates are 4.53 +- 0.06 b.y. and 0.69880 +- 0.00020, indistinguishable from the whole-rock isochron. These results are interpreted as 'primitive isochrons' dating the condensation of chondrites from the solar nebula. The best value of this event is given by joining both isochrons together at 4.518 +- 0.026 b.y. and 87 Sr/ 86 Sr = 0.69881 +- 0.00016. The near identity of this initial ratio with the one of Allende white inclusions argues in favor of a sharp isochronism of condensation from a 87 Sr/ 86 Sr homogeneous nebula. Data from Guarena and Richardton are interpreted as secondary internal isochrons, 100 m.y. after the condensation of the whole rocks. The data are then used to constrain a thermal evolution model of the H chondrite parent body. This body might have a 150-175 km radius, and might have been heated by 26 Al. An 26 Al/ 27 Al ratio of 4-6 X 10 -6 is enough for heating such a body. Further tests for this model are proposed. (Auth.)

Derivation of Apollo 14 High-Al Basalts at Discrete Times: Rb-Sr Isotopic Constraints

Science.gov (United States)

Hui, H.; Neal, C. R.; Shih, C.-Y.; Nyquist, L. E.

2012-03-01

Four eruption episodes were identified for A-14 high-Al basalts. Rb-Sr isotopic data and ITE ratios show that their parental melt compositions of are correlated through mixing of evolved components with a relatively primitive magma ocean cumulate.

Orthorhombic strontium titanate in BaTiO sub 3 -SrTiO sub 3 superlattices

CERN Document Server

Rios, S; Jiang, A Q; Scott, J F; Lü, H; Chen, Z

2003-01-01

It has been suggested by several authors that SrTiO sub 3 layers in SrTiO sub 3 -BaTiO sub 3 superlattices should be tetragonal and ferroelectric at ambient temperatures, like the BaTiO sub 3 layers, rather than cubic, as in bulk SrTiO sub 3 , and that free-energy minimization requires continuity of the polarization direction. A recent ab initio calculation constrained solutions to this structure. Surprisingly, our x-ray study shows that the SrTiO sub 3 layers are orthorhombic with 0.03% in-plane strain, with the BaTiO sub 3 c-axis matching the SrTiO sub 3 a- and b-axis better than the c-axis; strain energy overcomes the cost in electrostatic energy. (letter to the editor)

Microstructure and dielectric parameters of epitaxial SrRuO3/BaTiO3/SrRuO3 heterostructures

Science.gov (United States)

Boikov, Yu. A.; Claeson, T.

2001-05-01

Epitaxial films of ferroelectric barium titanate are desirable in a number of applications but their properties are inferior to those of bulk material. Relations between microstructure and dielectric properties may give better understanding of limitations. Trilayer heterostructures SrRuO3/BaTiO3/SrRuO3 were grown by laser ablation on (100)LaAlO3 and (100)MgO substrates. The BaTiO3 layer was granular in structure. When grown on (100)SrRuO3/(100)LaAlO3, it was preferentially a-axis oriented due to tensile mechanical stress. Using (100)MgO as a substrate, on the other hand, produced a mixture of about equal value of a-axis and c-axis oriented grains of BaTiO3. The dielectric permittivity, ɛ, of the BaTiO3 layer was almost twice as large, at T>200 K and f=100 kHz, for the LaAlO3 substrate as compared to the MgO one. Its maximum value (ɛ/ɛ0≈6200) depended on temperature of growth, grain size, and electric field and compares well with optimal values commonly used for ceramic material. The maximum in the ɛ(T) shifted from about 370 to 320 K when the grain size in the BaTiO3 film decreased from 100 to 40 nm. At T300 K, hysteresis loops in polarization versus electric field were roughly symmetric. The BaTiO3 films grown on (100)SrRuO3/(100)MgO exhibit the largest remnant polarizations and coercive fields in the temperature range 100-380 K.

Geochemistry of the Serra das Melancias Pluton in the Serra da Aldeia Suite: a classic post-collisional high Ba-Sr granite in The Riacho do Pontal Fold Belt, NE Brazil

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Marcela Paschoal Perpétuo

Full Text Available ABSTRACT: The Serra da Aldeia Suite is composed by circular or oval-shaped plutons, intrusive in meta-sedimentary and meta-volcanosedimentary rocks in the Riacho do Pontal Fold Belt, NE Brazil. The Serra das Melancias Pluton, belonging to Serra da Aldeia Suite, is located southeastern of Piaui state, near Paulistana city. These plutons represent a major magmatic expression in this area and contain important information about the late magmatic/collisional geologic evolution of the Brasiliano Orogeny. Based on petrographic and geochemical data, three facies were defined in the Serra das Melancias Pluton: granites, syenites and quartz monzonites. The rocks display high-K and alkaline to shoshonitic affinities, are metaluminous and show ferrous character. They are enriched in Light Rare Earth Elements and Large Ion Lithophile Elements, with negative anomalies in Nb, Ta and Ti. Their high Ba, Sr, K/Rb, low Rb, relatively low U, Th, Nb to very low Heavy Rare Earth Elements and Y resemble those of typical high Ba-Sr granitoids. The geochemical data suggest the emplacement of Serra das Melancias Pluton in a transitional, late to post-orogenic setting in the Riacho do Pontal Fold Belt during the late Brasiliano-Pan African Orogeny.

Rb-Sr ages of Precambrian sediments from the Ovruch mountain range, northwestern Ukraine (U.S.S.R.)

International Nuclear Information System (INIS)

Gorokhov, I.M.; Varshavskaya, E.S.; Kutyavin, E.P.; Clauer, N.; Drannik, A.S.

1981-01-01

A mineralogical and Rb-Sr geochronological study of Precambrian sediments and metasediments from the Ovruch mountain range (northwestern Ukraine) shows two distinct events: a slight metamorphism of the Belokorovichi Formation 1575 +- 30 Ma ago which precedes the deposition of the Zbranki Formation at 1389 +- 71 Ma (lambda 87 Rb = 1.42 x 10 -11 y -1 ). (Auth.)

Thermal properties of perovskite RCeO{sub 3} (R = Ba, Sr)

Energy Technology Data Exchange (ETDEWEB)

Shukla, Aarti, E-mail: aarti.phy@gmail.com [Department of Physics, Barkatullah University, Bhopal 462026 (India); Parey, Vanshree; Thakur, Rasna [Department of Physics, Barkatullah University, Bhopal 462026 (India); Srivastava, Archana [Department of Physics, Sri Sathya Sai College for women, Bhopal 462024 (India); Gaur, N.K. [Department of Physics, Barkatullah University, Bhopal 462026 (India)

2015-08-20

Highlights: • (Ba,Sr)CeO{sub 3} are high temperature protonic conductor materials. • This makes their thermal properties very interesting. • MRIM has successfully predicted the thermodynamic properties. • The computed results are in good agreement with the available experimental data. • Present results will serve as guide to experimental workers in future. - Abstract: We have investigated the bulk modulus and thermal properties of proton conducting perovskite RCeO{sub 3} (R = Ba, Sr) for the first time by incorporating the effect of lattice distortion in modified rigid ion models (MRIM). The computed bulk modulus, specific heat, thermal expansion coefficient and other thermal properties of BaCeO{sub 3} and SrCeO{sub 3} reproduce well with the available experimental data. In addition the cohesive energy (ϕ), molecular force constant (f), reststrahlen frequency (ν), Debye temperature (θ{sub D}) and Gruneisen parameter (γ) are also reported and discussed. The specific heat results can further be improved by taking into account the spin and the orbital ordering contribution in the specific heat formulae.

Defect analysis of BaSrFBr:Eu irradiated by X-ray

International Nuclear Information System (INIS)

Lee, C. Y.; Jeong, J. M.; Kim, J. H.

2010-01-01

The mechanical property of the BaSrFBr:Eu phosphor layer of X-ray image plates was investigated by using image quality (IQ), resolution (LP/mm), and coincidence Doppler broadening (CDB) positron annihilation. The screen samples of BaSrFBr:Eu phosphors were irradiated with hospital X-rays in the course of diagnostic radiography at an average rate of 20,000 times per year and were used for various periods of time. The LP/mm values of the irradiated BaSrFBr:Eu image plates varied between 2.4 and 2.0 for three years while the IQ values varied between 35 and 11 over the same period. CDB positron annihilation spectroscopy was used to analyze the defect structures in the phosphor layer. The S parameter values increased in correlation with increased exposure time, which indicated that more defects were generated. There was a positive relationship between the IQ and S parameters. Measurements of the defects indicate that most of the defects were likely to have been generated by the X-ray radiation.

High-pressure modifications of CaZn2, SrZn2, SrAl2, and BaAl2: Implications for Laves phase structural trends

International Nuclear Information System (INIS)

Kal, Subhadeep; Stoyanov, Emil; Belieres, Jean-Philippe; Groy, Thomas L.; Norrestam, Rolf; Haeussermann, Ulrich

2008-01-01

High-pressure forms of intermetallic compounds with the composition CaZn 2 , SrZn 2 , SrAl 2 , and BaAl 2 were synthesized from CeCu 2 -type precursors (CaZn 2 , SrZn 2 , SrAl 2 ) and Ba 21 Al 40 by multi-anvil techniques and investigated by X-ray powder diffraction (SrAl 2 and BaAl 2 ), X-ray single-crystal diffraction (CaZn 2 ), and electron microscopy (SrZn 2 ). Their structures correspond to that of Laves phases. Whereas the dialuminides crystallize in the cubic MgCu 2 (C15) structure, the dizincides adopt the hexagonal MgZn 2 (C14) structure. This trend is in agreement with the structural relationship displayed by sp bonded Laves phase systems at ambient conditions. - Graphical abstract: CeCu 2 -type polar intermetallics can be transformed to Laves phases upon simultaneous application of pressure and temperature. The observed structures are controlled by the valence electron concentration

Unusual Rb-Sr data on the age of two typical peralkaline granitoid plutons in West Transbeikalia

International Nuclear Information System (INIS)

Litvinovskij, B.A.; Posokhov, V.F.; Zanvilevich, A.N.

1995-01-01

Rb-Sr isotope study of two typical plutons in West Transbaikalia (Bryansk and Kharitonov) has been carried out. For alkaline and peralkaline suits of the Bryansk pluton the obtained data are 287 ± m.y., I Sx =0.7054 ± 3 and 285 ± 1 m.y., I Sr =0.7037 ± 3 respectively. Rb-Sr age of peralkaline syenites and granites from the Kharitonov pluton are in more or less consistency with those on the Malokunal pluton (233 ± 5 m.y.) and much less than the age of the Khorinsk pluton (253 ± 3 m.y.). Taking into account the K-Ar data on amphibole from the peralkaline granitoids it is concluded that probable age of these rocks span the interval 250-220 m.y. However results obtained from the Bryansk pluton suggest that within the Mongolia-Transbaikalia belt one more stage of peralkaline granitoid generation i.e. the Early Permian stage could be manifested as well. 20 refs.; 5 figs.; 3 tabs

Compounds of the type Ba/sub 3/Bsup(II)M/sub 2/sup(V)O/sub 9/ with Bsup(II) = Mg, Ca, Sr, Ba, and Msup(V) = Nb, Ta

Energy Technology Data Exchange (ETDEWEB)

Kemmler-Sack, S; Thumm, I; Herrmann, M [Tuebingen Univ. (Germany, F.R.). Lehrstuhl fuer Anorganische Chemie 2

1981-08-01

The hexagonal perovskites Ba/sub 3/Bsup(II)M/sub 2/sup(V)O/sub 9/ (Msup(V) = Nb, Ta) crystallize with Bsup(II) = Mg, Ca in a 3 L structure (sequence (c)/sub 3/) and Bsup(II) = Sr in the hexagonal BaTiO/sub 3/ type (6 L; sequence (hcc)/sub 2/) with an 1:2 order for the B and M ions. Intensity calculations for Ba/sub 3/SrNb/sub 2/O/sub 9/ and Ba/sub 3/SrTa/sub 2/O/sub 9/ gave in the space group P6/sub 3//mmc a refined, intensity related R' value of 8.4% (Nb) and 9.0% (Ta) respectively. For Bsup(II) = Ba the perovskite Ba/sub 3/BaTa/sub 2/O/sub 9/ has an orthorhombic distorted 6 L structure and forms with Ba/sub 3/SrTa/sub 2/O/sub 9/ a continuous series of mixed crystals (Ba/sub 3/Srsub(1-x)Basub(x)Ta/sub 2/O/sub 9/). In the system Ba/sub 3/Srsub(1-x)Basub(x)Nb/sub 2/O/sub 9/ the range of existence of the hexagonal BaTiO/sub 3/ type is confined to the Sr richer end. The pure Ba compound posesses a proper structure type (5 L: Ba/sub 5/BaNb/sub 3/vacantOsub(13.5)vacantsub(1.5)).

The Transhimalaya (Gangdese) plutonism in the Ladakh region: A U-Pb and Rb-Sr study

International Nuclear Information System (INIS)

Schaerer, U.; Hamet, J.; Allegre, C.J.

1984-01-01

The age and origin of the Transhimalaya (Gangdese) plutonic belt in the Ladakh area has been studied by high-resolution U-Pb analyses of accessory minerals (zircon and monazite/allanite) and Rb-Sr measurements on whole rock samples. The ages determined of 101+-2 m.y. for a granodiorite and of 60.7+-0.4 m.y. for a granite substantiate that the Transhimalaya plutonism was active at least in mid-Cretaceous (Albian) and earliest Tertiary (Palaeocene) times. A Rb-Sr isochron of 73.4+-2.4 m.y. might be fortuitous because the Rb-Sr systematics shows important heterogeneities on the whole rock scale. The inherited radiogenic lead in zircon demonstrates that anatexis of continental crust was involved in magma genesis. The thus recycled continental material was heterogeneous with respect to its primary ages and/or metamorphic history; the approximate minimum ages of the continental sources range from 350 to 590 m.y. The 101+-2 m.y. old Transhimalaya granodiorite, which intrudes a series of mainly basaltic island arc rocks (Dras Series) shows that this island arc was attached to the continental margin at that times. This is consistent with the hypothesis that the ''Ladakh Tethys'' closed through two subduction regimes: (1) an early Cretaceous subduction, which formed the Dras island arc, and (2) a late Cretaceous to Palaeocene subduction at the continental margin, which caused the emplacement of the Transhimalaya plutonic belt. (orig.)

Thermochemical properties of oxides in Y-Ba-Cu-O, Sr-Bi-O, Cu-Nb-O, Sr-Cu-O, Ca-Cu-O, Cu-O and Hg-Ba-Ca-Cu-O systems

International Nuclear Information System (INIS)

Moiseev, G.K.; Vatolin, N.A.; Il'inykh, N.I.

2000-01-01

Thermochemical properties (ΔH 0 298 , S 0 298 , H 0 298 -H 0 0 , C p (T), C p at T>T melt ) of complex oxides in Y-Ba-Cu-O, Sr-Bi-O, Cu-Nb-O, Sr-Cu-O, Ca-Cu-O, Cu-O and Hg-Ba-Ca-Cu-O systems obtained with application of calculation methods are presented. Nonexperimental methods of estimation, revision and correction of standard formation enthalpies of inorganic compounds are described [ru

The use of Rb-Sr and K-Ar dating methods as a stratigraphic tool applied to sedimentary rocks and minerals

International Nuclear Information System (INIS)

Bonhomme, M.G.

1982-01-01

Rb-Sr and K-Ar methods can be used for direct numerical chronostratigraphy of sediments using the clay silicates they contain. The interpretation of the ages calculated depends on the satisfaction of the following requirements: (1) The series studied must include diagenetic clay sediments. Coarsely-detrital or slightly-metamorphic formations must be excluded. Studies in progress concerning decarbonatation may lead to the application of direct dating of sediments being extended to carbonate sediments. (2) Careful mineralogical study of the clay minerals must prove early diagenetic recrystallization or new formation. This part of the study must precede any isotopic work. (3) The isotopic study must involve the use of both Rb-Sr and K-Ar methods. The extreme sensibility of the K-Ar isotopic system to late diagenesis helps to choose between early or late diagenesis: a younger K-Ar age may generally be regarded as that of the late diagenesis, whereas the Rb-Sr age may be that of the early diagenesis. (4) The initial 87 Sr/ 86 Sr isotopic ratio is not always a reliable criterion, owing to the effects of the dilution of the radiogenic 87 Sr by the great amounts of primary Sr contained in carbonates. (5) The regularly-decreasing succession of isotopic ages must follow the stratigraphic succession. When this condition is satisfied, there is a high probability that the calculated ages are indeed those of the deposition dates. (Auth.)

Rb-Sr geochronology of leucocratic granitoid rocks from the Spissko-Gemerske Rudohorie Mts. and Veporicum

International Nuclear Information System (INIS)

Cambel, B.; Veselsky, J.

1989-01-01

Information is given on new Rb-Sr data from leucocratic types of rocks occurring in the Gemericum and Veporicum. Basses on isochron geochronological data, mutual geochronological and geochemical relations are discussed. (author). 3 figs., 47 tabs., 14 refs

Electrical properties of resistive switches based on Ba1-χSrχTiO3 thin films prepared by RF co-sputtering

International Nuclear Information System (INIS)

Marquez H, A.; Hernandez R, E.; Zapata T, M.; Guillen R, J.; Cruz, M. P.; Calzadilla A, O.; Melendez L, M.

2010-01-01

In this work, was proposed the use of Ba 1-χ Sr χ TiO 3 (0≤x≤1) thin films for the construction of metal-insulator-metal heterostructures; and their great potential for the development of non-volatile resistance memories (ReRAM) is shown. The deposition of Ba 1-χ Sr χ TiO 3 thin films was done by the RF co-sputtering technique using two magnetron sputtering cathodes with BaTiO 3 and SrTiO 3 targets. The chemical composition (x parameter) in the deposited Ba 1-χ Sr χ TiO 3 thin films was varied through the RF powder applied to the targets. The constructed metal-insulator-metal heterostructures were Al/Ba 1-χ Sr χ TiO 3 /nichrome. The I-V measurements of the heterostructures showed that their hysteretic characteristics change depending on the Ba/Sr ratio of the Ba 1-χ Sr χ TiO 3 thin films; the Ba/Sr ratio was determined by employing the energy dispersive spectroscopy; Sem micrographs showed that Ba 1-χ Sr χ TiO 3 thin films were uniform without cracks or pinholes. Additionally, the analysis of the X-ray diffraction results indicated the substitutional incorporation of Sr into the BaTiO 3 lattice and the obtainment of crystalline films for the entire range of the x values. (Author)

Rb-Sr geochronology of the rocks of the Himalayas, Eastern Nepal, (1)

International Nuclear Information System (INIS)

Kai, Kunio

1981-01-01

Rb-Sr isotopic measurements were carried out for whole rock and small sliced rock from the Himalayan gneiss which constitutes the metamorphosed basement of the Tethyan sediments. The results of the measurements on whole rock from the Barun migmatite, the Barun gneiss and the Irkhua gneiss indicate that complete Sr isotopic redistribution occurred about 520 m.y. ago. This age is interpreted as the time of the regional metamorphism. The analytical results of the small sliced slabs of the Himalayan gneiss indicate that Sr isotopic redistribution occurred among the sliced slabs 33.3 +- 13.2 m.y. ago. This age is interpreted as the time of the metamorphism in the sillimanite-amphibolite facies. The high initial 87 Sr/ 86 Sr ratio of 0.7372 +- 0.0031 from the Barun migmatite of the Himalayan gneiss suggests the Precambrian Origin of the source rocks. The analytical results on the sliced slab of the Barun migmatite indicate that the original age of the rocks is about 800 m.y. The rock is interpreted as the remobilized Precambrian crustal rock. The high initial 87 Sr/ 86 Sr ratio of the Barun gneiss and the Irkhua gneiss of the Himalayan gneiss (0.7234 +- 0.0013) indicates also the Precambrian origin of the source rocks. (author)

Crystallization and properties of Sr-Ba aluminosilicate glass-ceramic matrices

Science.gov (United States)

Bansal, Narottam P.; Hyatt, Mark J.; Drummond, Charles H., III

1991-01-01

Powders of roller quenched (Sr,Ba)O-Al2O3-2SiO2 glasses of various compositions were uniaxially pressed into bars and hot isostatically pressed at 1350 C for 4 hours or cold isostatically pressed and sintered at different temperatures between 800 to 1500 C for 10 or 20 hours. Densities, flexural strengths, and linear thermal expansion were measured for three compositions. The glass transition and crystallization temperatures were determined by Differential Scanning Calorimetry (DSC). The liquidus and crystallization temperature from the melt were measured using high temperature Differential Thermal Analysis (DTA). Crystalline phases formed on heat treatment of the glasses were identified by powder X ray diffraction. In Sr containing glasses, the monoclinic celsian phase always crystallized at temperatures above 1000 C. At lower temperatures, the hexagonal analog formed. The temperature for orthorhombic to hexagonal structural transformation increased monotonically with SrO content, from 327 C for BaO-Al2O3-2SiO2 to 758 C for SrO-Al2O3-2SiO2. These glass powders can be sintered to almost full densities and monoclinic celsian phase at a relatively low temperature of 1100 C.

Screening of plant species for comparative uptake abilities of radioactive Co, Rb, Sr and Cs from soil

International Nuclear Information System (INIS)

Gouthu, S.; Arie, T.; Ambe, S.; Yamaguchi, I.

1997-01-01

In case of radioactive fallout, persistence of long lived nuclides in soil and subsequent transfer into the food chain through plants over a long period is the key factor. The possibility of 'phytoremediation'is suggested to reduce the radionuclides in soil. To exploit the natural potential of some plants in absorbing or accumulating certain radionuclides and depleting the soil radioactivity, thirty-two plant species were tested under laboratory conditions for their comparative ability in taking up radioactive Rb, Co, Sr and Cs. Broccoli and tomato for Co; tomato, chard, sunflower and cucumber for Rb; cucumber, sunflower and turnip (Kyona) for Sr; and tomato, chard and cucumber for Cs were found to be effective compared to other species tested. (author)

Reconnaissance Rb-Sr dates for the Himalayan Central Gneiss, Northwest India

International Nuclear Information System (INIS)

Powell, C. McA.; Crawford, A.R.; Armstrong, R.L.; Wynne-Edwards, H.R.; Prakash, R.

1979-01-01

Rb-Sr analysis of whole-rock samples and biotite and biotite - or muscovite - whole rock pairs suggests that the Himalayan Central Gneiss in the crystalline nappes of the Lesser Himalaya and the root zone in the High Himalaya was formed during Oligocene to mid-Miocene times by deformation and metamorphism of older rocks, including Precambrian. Four whole-rock samples from the Almora-Askot thrust sheets define an isochron of 1620 +- 90 Ma with a high initial 87 Sr/ 86 Sr ratio of 0.749 +- 0.007; other single whole-rock samples give dates in the range 268 to 1065 Ma, assuming an initial 87 Sr/ 86 Sr ratio of 0.704. These dates are considered to represent either depositional or early instructive/deformational events. Three biotite-whole rock pairs from the root zone of the Himalayan Central Gneiss in Lahaul give aqes of 16 to 19 Ma and two muscovite-whole rock pairs give similar mid-Cenozoic ages (12 and 26 Ma); two muscovite-whole rock pairs give Paleozoic ages, which suggests incomplete resetting of the muscovite by the Cenozoic metamorphism. The pattern of ages is similar to recent results from adjacent areas, and consistent with models of Himalayan tectonics involving formation of the Central Gneiss from older Indian crust during the mid-Cenozoic. (auth.)

Ferromagnetic Instability in AFe4Sb12 (A = Ca, Sr, and Ba)

OpenAIRE

Matsuoka, E.; Hayashi, K.; Ikeda, A.; Tanaka, K.; Takabatake, T.; Higemoto, W.; Matsumura, M.

2004-01-01

Magnetic, transport and thermal properties of AFe4Sb12 (A = Ca, Sr, Ba) are reported. All three compounds show a maximum in both the magnetic susceptibility and thermopower at 50 K, and a large electronic specific heat coefficient of 100 mJ/mol K2. These properties are the characteristics of a nearly ferromagnetic metal. Furthermore, a remanent moment of the order of 10-3muB/Fe was observed below 54, 48, and 40 K for A = Ca, Sr, and Ba, respectively. The volume fraction of the ferromagnetic c...

Geochronology (Rb-Sr, Sm-Nd and Pb-Pb) of the proterozoic granulitic and granitic rocks around Usilampatti, Madurai district, Tamil Nadu: implication on age of various lithounits

International Nuclear Information System (INIS)

Pandey, U.K.; Pandey, B.K.; Krishnamurthy, P.

2005-01-01

Rb-Sr, Sm-Nd and Pb-Pb systematics on mafic granulites, intermediate- charnockites, charnockites, calc-granulites, orthogneisses, leptynites, granites and two (2) mineral samples (microcline and muscovite) from pegmatite have been studied. Sm-Nd model ages (T DM ) for most of the rocks cluster around 2.1 Ga. Calc-granulites gave Rb-Sr whole rock isochron age of 1339 ± 110 Ma with initial 87 Sr/ 86 Sr ratio (I.R.) = 0.709. Mesoproterozoic age for the Metasedimentary Group of rocks (calc-granulites) has been inferred based on their 87 Sr/ 86 Sr ratio also. Granites and leptynites have yielded Rb-Sr whole rock isochron ages of 823± 38 Ma, with I.R. = 0.713 and 894± 82 Ma, with I.R. = 0.708 respectively which are younger than the calc-granulites. Microcline and muscovite from pegmatite gave Rb-Sr model ages as 532 and 491 Ma respectively. Granites, leptynites and calc-granulites are derived from the crustal source as indicated by their high initial 87 Sr/ 86 Sr ratios. Most probably the protolith of the granitic and granulitic rocks is of Palaeoproterozoic age in this part of the Madurai Block. The minimum age of granulite grade of metamorphism has been inferred at c. 850 Ma, indirectly on the basis of Rb-Sr ages of leptynites, which normally form during the evolution of granulite facies assemblages. Both granulite facies metamorphism and granitic magmatism probably took place during Neoproterozoic period correlatable to the early phase of Pan-African orogeny. Later decompression, causing mineral scale resetting of the Rb-Sr and Sm-Nd systematics, around 450-550 Ma, may correspond to the final exhumation, which brought the middle to lower crustal granulites to upper crustal levels, during the last phase of Pan-African activity. As per ages obtained on various lithounits in the present study the Metasedimentary Group of rocks (Mesoproterozoic) are younger than the Charnockite Group of rocks (Palaeoproterozoic) followed by the rocks belonging to the Migmatite Complex

Geochronology (Rb-Sr, Sm-Nd and Pb-Pb) of the proterozoic granulitic and granitic rocks around Usilampatti, Madurai District, Tamil Nadu: implication on age of various lithounits

International Nuclear Information System (INIS)

Pandey, U.K.; Pandey, B.K.; Krishnamurthy, P.

2005-01-01

Rb-Sr, Sm-Nd and Pb-Pb systematics on mafic granulites, intermediate-charnockites, charnockites, calc- granulites, orthogneisses, leptynites, granites and two (2) mineral samples (microcline and muscovite) from pegmatite have been studied. Sm-Nd model ages (T DM ) for most of the rocks cluster around 2.1 Ga. Calc-granulites gave Rb-Sr whole rock isochron age of 1339± 110 Ma with initial 87 Sr/ 86 Sr ratio (IR)= 0.709. Mesoproterozoic age for the metasedimentary group of rocks (calc-granulites) has been inferred based on their 86 Sr/ 86 Sr ratio also. Granites and leptynites have yielded Rb-Sr whole rock isochron ages of 823 ± 38 Ma, with I.R. = 0.713 and 894± 82 Ma, with I.R.= 0.708 respectively which are younger than the calc-granulites. Microcline and muscovite from pegmatite gave Rb-Sr model ages as 532 and 491 Ma respectively. Granites, leptynites and calc-granulites are derived from the crustal source as indicated by their high initial 87 Sr/ 86 Sr ratios. Most probably the protolith of the granitic and granulitic rocks is of Palaeoproterozoic age in this part of the Madurai Block. The minimum age of granulite grade of metamorphism has been inferred at c. 850 Ma, indirectly on the basis of Rb-Sr ages of leptynites, which normally form during the evolution of granulite facies assemblages. Both granulite facies metamorphism and granitic magmatism probably took place during Neoproterozoic period correlatable to the early phase of Pan-African orogeny. Later decompression, causing mineral scale resetting of the Rb-Sr and Sm-Nd systematics, around 450-550 Ma, may correspond to the final exhumation, which brought the middle to lower crustal granulites to upper crustal levels, during the last phase of Pan-African activity. As per ages obtained on various lithounits in the present study the Metasedimentary Group of rocks (Mesoproterozoic) are younger than the Charnockite Group of rocks (Palaeoproterozoic) followed by the rocks belonging to the Migmatite Complex

AEMnSb2 (AE=Sr, Ba): a new class of Dirac materials

International Nuclear Information System (INIS)

Farhan, M Arshad; Lee, Geunsik; Shim, Ji Hoon

2014-01-01

The Dirac fermions of Sb square net in AEMnSb 2 (AE=Sr, Ba) are investigated by using first-principles calculation. BaMnSb 2 contains Sb square net layers with a coincident stacking of Ba atoms, exhibiting Dirac fermion behavior. On the other hand, SrMnSb 2 has a staggered stacking of Sr atoms with distorted zig-zag chains of Sb atoms. Application of hydrostatic pressure on the latter induces a structural change from a staggered to a coincident arrangement of AE ions accompanying a transition from insulator to a metal containing Dirac fermions. The structural investigations show that the stacking type of cation and orthorhombic distortion of Sb layers are the main factors to decide the crystal symmetry of the material. We propose that the Dirac fermions can be obtained by controlling the size of cation and the volume of AEMnSb 2 compounds. (fast track communication)

Tuning the electrocaloric effect by varying Sr concentration in ferroelectric Ba1 -xSrxTiO3

Science.gov (United States)

Lisenkov, S.; Ponomareva, I.

2018-05-01

The electrocaloric effect is investigated systematically in Ba1 -xSrxTiO3 ferroelectrics using a semiclassical direct computational approach. The data are reported for the technologically important range of Sr concentrations of 0.0-0.6, electric fields up to 1000 kV/cm, and temperatures ranging from 5 to 600 K. A detailed comparison of computational data with experimental data from the literature reveals semiquantitative agreement and suggests the origin of discrepancies. The electrocaloric change in temperature Δ T shows strong dependence on Sr concentration which offers a way to tune electrocaloric response. In particular, the maximum electrocaloric Δ T is found to decrease with the increase in Sr concentration, whereas the location of the maximum shifts towards lower temperatures following the Curie point of the ferroelectric. Surprisingly, the width of the peak in the dependence of Δ T on the initial temperature is independent of the Sr concentration but shows a strong dependence on the applied electric field. Computational data are used to propose a compositionally graded ferroelectric Ba0.70Sr0.30TiO3/Ba0.55Sr0.45TiO3/Ba0.50Sr0.50TiO3/Ba0.45Sr0.55TiO3 whose Δ T shows almost no temperature dependence in the technologically important range of temperatures and electric fields. Such a desirable feature could potentially lead to the enhancement of relative cooling power.

Rb-Sr age of the Sivamalai alkaline complex, Tamil Nadu

International Nuclear Information System (INIS)

Subba Rao, T.V.; Narayana, B.L.; Gopalan, K.

1994-01-01

The Sivamalai alkaline complex comprises ferro-, pyroxene- hornblende-and nepheline-syenites. Field relations show that the nepheline syenites followed the emplacement of non-feldspathoidal syenites. Mineralogical data on the syenite suite have been reviewed. The Sivamalai alkaline rocks are not strongly enriched in rare-earth elements like most miaskites. Rb-Sr isotopic analyses of a suite of six samples from the various members of the complex define an isochron corresponding to an age of 623 ± 21 Ma (2σ) and initial Sr ratio of 0.70376 ± 14 (2σ). This is consistent with a model of fractional crystallization of a parent magma derived from an upper mantle source with apparently no isotopic evidence for more than one magma source for the complex. The Sivamalai alkaline complex represents a Pan-African alkaline magmatic event in the southern granulite terrane of peninsular India. (author). 26 refs., 4 figs., 4 tabs

Is otolith microchemistry (Sr: Ca and Ba:Ca ratios useful to identify Mugil curema populations in the southeastern Caribbean Sea?

Directory of Open Access Journals (Sweden)

E. Avigliano

Full Text Available Abstract The aim of the present study was to evaluate the potential use of otolith microchemistry (Sr:Ca and Ba:Ca ratios to identify silver mullet, Mugil curema, populations in Southeastern Caribbean Sea. Fish samples were collected in 7 areas of Nueva Esparta State (Venezuela. The otolith Sr:Ca and Ba:Ca ratios and water Sr:Ca were determined (by ICP-OES and EDTA volumetric method. Otoliths Sr:Ca and Ba:Ca ratios and Sr:Ca partition coefficient of mullets in Cubagua island (south of the State were significantly different from ratios in La Guardia (north of the State. A discriminant analysis of otolith Sr:Ca and Ba:Ca ratios separated Cubagua Island from La Guardia values. These results suggest the existence of different mullet groups in the Southeastern Caribbean Sea. For this, the simultaneous use of Sr:Ca and Ba:Ca ratios could be a potential tool to identify populations in the study area.

Is otolith microchemistry (Sr: Ca and Ba:Ca ratios) useful to identify Mugil curema populations in the southeastern Caribbean Sea?

Science.gov (United States)

Avigliano, E; Callicó-Fortunato, R; Buitrago, J; Volpedo, A V

2015-11-01

The aim of the present study was to evaluate the potential use of otolith microchemistry (Sr:Ca and Ba:Ca ratios) to identify silver mullet, Mugil curema, populations in Southeastern Caribbean Sea. Fish samples were collected in 7 areas of Nueva Esparta State (Venezuela). The otolith Sr:Ca and Ba:Ca ratios and water Sr:Ca were determined (by ICP-OES and EDTA volumetric method). Otoliths Sr:Ca and Ba:Ca ratios and Sr:Ca partition coefficient of mullets in Cubagua island (south of the State) were significantly different from ratios in La Guardia (north of the State). A discriminant analysis of otolith Sr:Ca and Ba:Ca ratios separated Cubagua Island from La Guardia values. These results suggest the existence of different mullet groups in the Southeastern Caribbean Sea. For this, the simultaneous use of Sr:Ca and Ba:Ca ratios could be a potential tool to identify populations in the study area.

Rb-Sr systematics of granitoids of the central gneissic complex, Arunachal Himalaya: implications on tectonism, stratigraphy and source

International Nuclear Information System (INIS)

Dikshitulu, G.R.; Dhana Raju, R.; Pandey, B.K.; Krishna, Veena

1995-01-01

Precambrian central gneissic complex (CGC) in the Kameng district of Arunachal Pradesh comprises the oldest Sela group thrusting over the Bomdila group, with the Salari group being the youngest. Augen gneiss of the Bomdila group, granite of the Salari group and hornblende granite gneiss of the Sela group define Rb-Sr isochron ages of 1914±23, 1536±60 and 481± 23 Ma, respectively. The 481 Ma age on the hornblende gneiss from the oldest Sela group is attributed to the resetting of Rb-Sr clock due to tectonic imprint of the main central thrust (MCT). The 1914 Ma age of the augen gneiss, the oldest reported so far from the Arunachal Himalaya, is either the emplacement age or latest metamorphic event. The 1536 Ma old emplacement age of the granite intruding the black shale of the Salari group disproves the hitherto considered Gondwana age for the black shale, and, thus, necessitates revision in its chronostratigraphy ( 87 Sr/ 86 Sr), of the hornblende granite gneiss and Salari granite is high (0.719 and 0.709) indicating a crustal source for these, whereas it is low for the augen gneiss (0.703) suggesting an inherited signature of the upper mantle source together with some crustal contamination. Rb-Sr whole-rock isochron ages from the Arunachal Himalaya are correlatable with those reported from other parts of the Indian Himalaya. These cumulatively point to at least three major periods of activity in the Himalaya at ca. 2060±250, 1530±90 and 530± 75 Ma. (author). 22 refs., 2 figs., 3 tabs

Rb-Sr systematics of granitoids of the central gneissic complex, Arunachal Himalaya: implications on tectonism, stratigraphy and source

Energy Technology Data Exchange (ETDEWEB)

Dikshitulu, G R; Dhana Raju, R [Dept. of Atomic Energy, Bangalore (India). Atomic Minerals Division; Pandey, B K; Krishna, Veena [Department of Atomic Energy, Hyderabad (India). Atomic Minerals Div.

1995-01-01

Precambrian central gneissic complex (CGC) in the Kameng district of Arunachal Pradesh comprises the oldest Sela group thrusting over the Bomdila group, with the Salari group being the youngest. Augen gneiss of the Bomdila group, granite of the Salari group and hornblende granite gneiss of the Sela group define Rb-Sr isochron ages of 1914{+-}23, 1536{+-}60 and 481{+-} 23 Ma, respectively. The 481 Ma age on the hornblende gneiss from the oldest Sela group is attributed to the resetting of Rb-Sr clock due to tectonic imprint of the main central thrust (MCT). The 1914 Ma age of the augen gneiss, the oldest reported so far from the Arunachal Himalaya, is either the emplacement age or latest metamorphic event. The 1536 Ma old emplacement age of the granite intruding the black shale of the Salari group disproves the hitherto considered Gondwana age for the black shale, and, thus, necessitates revision in its chronostratigraphy ({sup 87}Sr/{sup 86}Sr), of the hornblende granite gneiss and Salari granite is high (0.719 and 0.709) indicating a crustal source for these, whereas it is low for the augen gneiss (0.703) suggesting an inherited signature of the upper mantle source together with some crustal contamination. Rb-Sr whole-rock isochron ages from the Arunachal Himalaya are correlatable with those reported from other parts of the Indian Himalaya. These cumulatively point to at least three major periods of activity in the Himalaya at ca. 2060{+-}250, 1530{+-}90 and 530{+-} 75 Ma. (author). 22 refs., 2 figs., 3 tabs.

Absolute branching intensities in the decay of 92Rb to 92Sr

CERN Document Server

Lhersonneau, G; Rizzi, V; Alyakrinskiy, O; Lanchais, A; Volkov, Yu.M; Barzakh, A.E; Fedorov, D.V; Ionan, A.M; Ivanov, V.S; Mezilev, K.A; Moroz, F.V; Orlov, S.Yu; Panteleev, V.N; Lau, C; Bajeat, O; Essabaa, S; Leroy, R; Jardin, P; Stroe, L; 10.1103/PhysRevC.74.017308

2006-01-01

The branching of the 2+ to 0+ transition in 92Sr has been measured to 0.032(4) per 92Rb decay. It confirms an earlier measurement however discarded in nuclear data evaluations since in contradiction with accepted lower logft limits. The conflict could be solved assuming that close to half of the decay intensity, mostly as high-energy ground-state transitions, is missing in th edecay scheme.

Rb-Sr ages and initial 87Sr/86Sr ratios of late paleozoic granitic rocks from northern Chile

International Nuclear Information System (INIS)

Shibata, Ken; Ishihara, Shunso; Ulriksen, C.E.

1984-01-01

Rb-Sr whole-rock isochron ages were determined on three suites of so-called Paleozoic granitic rocks from northern coastal Chile. The granitic rocks from the Valparaiso and Ci Funcho areas are dated as 296.3 +- 5.4 Ma and 262.2 +- 4.6 Ma, respectively, which are in accord with geologically estimated age. The rocks from the Chanaral area is dated as 212.8 +- 8.6 Ma, which is correlated close to the Triassic-Jurassic boundary age. A K-Ar age of 196 +- 6 Ma was obtained on biotite in granite from Esmeralda between Ci Funcho and Chanaral. These age results demonstrate that no Precambrian plutonism occurred in the studied area, and that so-called Paleozoic granitic rocks in the Ci Funcho-Chanaral area are divided into Permian and early Mesozoic in age. Initial 87 Sr/ 86 Sr ratios of the ilmenite-series granitic rocks from the coastal region are 0.70641 (Valparaiso), 0.70635 (Ci Funcho) and 0.70455 (Chanaral). These relatively low ratios deny substantial crustal contribution to the granitoids. The initial ratios of magnetite-series granitoids from porphyry- and manto-type mineralized areas (Chiquicamata, El Salvador and Tocopilla) are as low as 0.70344 to 0.70464. (author)

Rb-Sr Isotopic Systematics of Alkali-Rich Fragments in the Yamato-74442 LL-Chondritic Breccia

Science.gov (United States)

Yokoyama, T.; Misawa, K.; Okano, O.; Shih, C.-Y.; Nyquist, L. E.; Simo, J. I.; Tappa, M. J.; Yoneda, S.

2012-01-01

Alkali-rich igneous fragments were identified in the brecciated LL-chondrites, Kr henberg (LL5)], Bhola (LL3-6) and Yamato (Y)-74442 (LL4), and show characteristic fractionation patterns of alkaline elements. The K-Rb-Cs-rich fragments in Kr henberg, Bhola, and Y-74442 are very similar in mineralogy and petrography (olivine + pyroxene + glass), suggesting that they could have come from related precursor materials. We have undertaken Rb-Sr isotopic studies on alkali-rich fragments in Y-74442 to precisely determine their crystallization ages and the isotopic signatures of their precursor material(s).

Screening of plant species for comparative uptake abilities of radioactive Co, Rb, Sr and Cs from soil

Energy Technology Data Exchange (ETDEWEB)

Gouthu, S; Arie, T; Ambe, S; Yamaguchi, I [Institute of Physical and Chemical Research, Wako, Saitama (Japan)

1997-08-01

In case of radioactive fallout, persistence of long lived nuclides in soil and subsequent transfer into the food chain through plants over a long period is the key factor. The possibility of `phytoremediation`is suggested to reduce the radionuclides in soil. To exploit the natural potential of some plants in absorbing or accumulating certain radionuclides and depleting the soil radioactivity, thirty-two plant species were tested under laboratory conditions for their comparative ability in taking up radioactive Rb, Co, Sr and Cs. Broccoli and tomato for Co; tomato, chard, sunflower and cucumber for Rb; cucumber, sunflower and turnip (Kyona) for Sr; and tomato, chard and cucumber for Cs were found to be effective compared to other species tested. (author). 13 refs.

Correlation of Structure, Tunable Colors, and Lifetimes of (Sr, Ca, Ba)Al₂O₄:Eu2+, Dy3+ Phosphors.

Science.gov (United States)

Xie, Qidi; Li, Bowen; He, Xin; Zhang, Mei; Chen, Yan; Zeng, Qingguang

2017-10-18

(Sr, Ca, Ba)Al₂O₄:Eu 2+ , Dy 3+ phosphors were prepared via a high temperature solid-state reaction method. The correlation of phase structure, optical properties and lifetimes of the phosphors are investigated in this work. For the (Sr, Ca)Al₂O₄:Eu 2+ ,Dy 3+ phosphors, the different phase formation from monoclinic SrAl₂O₄ phase to hexagonal SrAl₂O₄ phase to monoclinic CaAl₂O₄ phase was observed when the Ca content increased. The emission color of SrAl₂O₄:Eu 2+ , Dy 3+ phosphors varied from green to blue. For the (Sr, Ba)Al₂O₄:Eu 2+ , Dy 3+ phosphors, different phase formation from the monoclinic SrAl₂O₄ phase to the hexagonal BaAl₂O₄ phase was observed, along with a shift of emission wavelength from 520 nm to 500 nm. More interestingly, the decay time of SrAl₂O₄:Eu 2+ , Dy 3+ changed due to the different phase formations. Lifetime can be dramatically shortened by the substitution of Sr 2+ with Ba 2+ cations, resulting in improving the performance of the alternating current light emitting diode (AC-LED). Finally, intense LEDs are successfully obtained by combining these phosphors with Ga(In)N near UV chips.

Magnetothermopower in A2−xLaxFeMoO6 (A = Sr, Ba

Directory of Open Access Journals (Sweden)

G. V. M. Williams

2017-01-01

Full Text Available A magnetothermopower has been observed in electronically spin-polarized polycrystalline Sr2-xLaxFeMoO6 and Ba2FeMoO6. The magnetothermopower is linear up to ~50 K for Sr2-xLaxFeMoO6 and linear up to ~270 K for Ba2FeMoO6. We suggest that the magnetothermopower may arise from a spin-tunneling magnetothermopower between the grains.

First-principles study of the (001) surface of cubic Ba{sub 0.5}Sr{sub 0.5}TiO{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Wang, Yuan Xu [Computational Materials Science Center, National Institute for Materials Science, Tsukuba 305-0044 (Japan); Institute for Computational Materials Science, School of Physics and Electronics, Henan University, Kaifeng 475004 (China)

2008-06-15

We have theoretically investigated basic properties of the (001) surface of cubic Ba{sub 0.5}Sr{sub 0.5}TiO{sub 3} (BST) by the plane-wave pseudopotential method within the local-density approximation. For the BaSrO{sub 2}-terminated surface, the surface-layer Sr atoms move inward and the surface-layer Ba atoms move outward. Moreover, the displacement of the surface-layer Sr atoms is much larger than the surface-layer Ba atoms. The rumpling of the BaSrO{sub 2}-terminated surface is much larger than that of the Ti{sub 2}O{sub 4}-terminated one. The surface state appears in the band structure of the Ti{sub 2}O{sub 4}-terminated surface of BST. Based on the results of the calculated grand thermodynamic potential, only the BaSrO{sub 2}-terminated surface can exist in the (001) surface of cubic BST. (copyright 2008 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

Prospects for transferring 87Rb84Sr dimers to the rovibrational ground state based on calculated molecular structures

Science.gov (United States)

Chen, Tao; Zhu, Shaobing; Li, Xiaolin; Qian, Jun; Wang, Yuzhu

2014-06-01

Using fitted model potential curves of the ground and lowest three excited states yielded by the relativistic Kramers-restricted multireference configuration interaction method with 19 electrons correlated, we theoretically investigate the rovibrational properties including the number of vibrational state and diagonally distributed Franck-Condon factors for a 87Rb84Sr molecule. Benefiting from a turning point at about v'=20 for the Franck-Condon factors between the ground state and spin-orbit 2(Ω=1/2) excited state, we choose |2(Ω=1/2),v'=21,J'=1> as the intermediate state in the three-level model to theoretically analyze the possibility of performing stimulated Raman adiabatic passage to transfer weakly bound RbSr molecules to the rovibrational ground state. With 1550 nm pump laser (2 W/cm2) and 1342 nm dump laser (10 mW/cm2) employed and appropriate settings of pulse time length (about 300 μs), we have formalistically achieved a round-trip transfer efficiency of 60%, namely 77% for one-way transfer. The results demonstrate the possibility of producing polar 87Rb84Sr molecules efficiently in a submicrokelvin regime, and further provide promising directions for future theoretical and experimental studies on alkali-alkaline(rare)-earth dimers.

Ca, Sr and Ba stable isotopes reveal the fate of soil nutrients along a tropical climosequence

Science.gov (United States)

Bullen, Thomas D.; Chadwick, Oliver A.

2016-01-01

Nutrient biolifting is an important pedogenic process in which plant roots obtain inorganic nutrients such as phosphorus (P) and calcium (Ca) from minerals at depth and concentrate those nutrients at the surface. Here we use soil chemistry and stable isotopes of the alkaline earth elements Ca, strontium (Sr) and barium (Ba) to test the hypothesis that biolifting of P has been an important pedogenic process across a soil climosequence developed on volcanic deposits at Kohala Mountain, Hawaii. The geochemical linkage between these elements is revealed as generally positive site-specific relationships in soil mass gains and losses, particularly for P, Ba and Ca, using the ratio of immobile elements titanium and niobium (Ti/Nb) to link individual soil samples to a restricted compositional range of the chemically and isotopically diverse volcanic parent materials. At sites where P is enriched in surface soils relative to abundances in deeper soils, the isotope compositions of exchangeable Ca, Sr and Ba in the shallowest soil horizons ( 10 cm depth) at those sites is consistently heavier than the volcanic parent materials. The isotope compositions of exchangeable Ca and Sr trend toward heavier compositions with depth more gradually, reflecting increasing leakiness from these soils in the order Ba < Sr < Ca and downward transfer of light biocycled Ca and Sr to deeper exchange sites. Given the long-term stability of ecosystem properties at the sites where P is enriched in surface soils, a simple box model demonstrates that persistence of isotopically light exchangeable Ca, Sr and Ba in the shallowest soil horizons requires that the uptake flux to plants from those near-surface layers is less than the recycling flux returned to the surface as litterfall. This observation implicates an uptake flux from an additional source which we attribute to biolifting. We view the heavy exchangeable Ba relative to soil parent values in deeper soils at sites where P is enriched in

Rb-Sr dating of low-grade metamorphics in the U.S.S.R

International Nuclear Information System (INIS)

Gorokhov, I.M.; Varshavskaya, E.S.; Kutyavin, E.P.; Melnikov, N.N.

1982-01-01

Geologically well-dated low-grade metasedimentary and metavolcanic rocks from five localities have been studied using the whole-rock Rb-Sr age method. All age values obtained are younger than those suggested by stratigraphy. When whole-rock points fit either an isochron or an errorchron with low value of the mean square of weighted deviates, the slope of this line gives the age of metamorphism. (Auth.)

Reverse micellar synthesis, structural characterization and dielectric properties of Sr-doped BaZrO_3 nanoparticles

International Nuclear Information System (INIS)

Ahmad, Tokeer; Ubaidullah, Mohd; Shahazad, Mohd; Kumar, Dinesh; Al-Hartomy, Omar A.

2017-01-01

Sr-doped BaZrO_3 nanoparticles with strontium content varying from 5 to 20 mol % were successfully synthesized by reverse micellar method at 900 °C for the first time. Systematic studies have been carried out to establish the structural and electrical properties of the as prepared nanoparticles. These nanoparticles were characterized using powder X-ray diffraction, transmission electron microscopy, BET surface area and dielectric measurements. X-ray diffraction analysis showed the formation of monophasic and highly crystalline nanoparticles which could be indexed in cubic BaZrO_3 with contraction of lattice on strontium substitution. A monotonic shift of diffraction pattern towards higher angel confirms the formation of solid solutions of Ba_1_−_xSr_xZrO_3 (0.05 ≤ x ≤ 0.20) which was corroborating well with lattice parameter studies. Transmission electron microscopic studies showed the formation of cubic, spherical and hexagonal nanoparticles with an average grain size of 40–65 nm. Energy dispersive X-ray spectroscopic studies confirmed the presence of dopant (Sr"2"+) in the BaZrO_3 matrix and estimated chemical species corroborate well with the loaded composition. Specific surface area of the solid solution comes out to be in the range of 104–244 m"2 g"-"1. Smallest particle of size 40 nm shows highest surface area 244 m"2 g"-"1 for 20 mol% Sr-doped BaZrO_3. Dielectric and impedance studies were also carried out as a function of frequency and temperature to explore the electrical properties of Sr-doped BaZrO_3. The dielectric constant of Ba_1_−_xSr_xZrO_3 (0.05 ≤ x ≤ 0.20) was found to be in the range of 13–25 for x = 0.05 to x = 0.20 with nearly similar dielectric loss of the order of 0.02. The conductance increases linearly with increase in frequency at room temperature, however the impedance has an inverse effect. - Highlights: • Monophasic nanocrystalline Ba_1_−_xSr_xZrO_3 at low dopant concentration using reverse micelles for the first

Study of chromites YbMIICr2O5,5 (MII - Mg, Ca, Sr, Ba by X-ray diffraction

Directory of Open Access Journals (Sweden)

B. Kasenov

2012-03-01

Full Text Available Compounds of composition YbMeMnFeO5,5 (Me – Mg, Ca, Sr, Ba are synthesized from Yb2O3, , Cr2O3 and MgCO3, CaCO3, SrCO3, BaCO3 by solid phase method. X-ray powder diffraction showed that the compound YbMgCr2O5,5, YbCaCr2O5,5, YbSrCr2O5,5, YbBaCr2O5,5 crystallizes in the tetragonal crystal system.

Structures and self-activating photoluminescent properties of Sr3−xAxGaO4F (A=Ba, Ca) materials

International Nuclear Information System (INIS)

Green, Robert; Vogt, Thomas

2012-01-01

The synthesis, structures and photoluminescent properties of mixed oxyfluorides of the type Sr 3−x A x GaO 4 F are compared to Sr 3−x A x AlO 4 F (A=Ca, Ba) materials. In these compounds the F − and O 2− ions are ordered and located on two distinct crystallographic sites. When substituting Sr 2+ by Ba 2+ and Ca 2+ , we find in Sr 3−x A x GaO 4 F materials an ordering of the alkaline earth cations over the two crystallographic sites. The amount of Ba 2+ ions that can be substituted into Sr 3−x A x GaO 4 F is x≤1.2, which is slightly more than can be incorporated into the previously reported Al-analog Sr 3−x A x AlO 4 F (x=1.0). Conversely, the amount of Ca 2+ ions that can be substituted into Sr 3−x Ca x GaO 4 F (x=0.3) is significantly less than in Sr 3−x Ca x AlO 4 F (x=1.0). A post-synthesis reduction step causes these materials to exhibit self-activating broad band photoluminescence where the emitted colors vary with the amount of ions substituted into the host lattice. - Graphical abstract: TOC Statement The structures of the self-activating phosphors Sr 3−x A x MO 4 F (A=Ba, Ca and M=Al, Ga) can be rationalized as alternating layers of bond compression and elongation, which impact the photoluminescence. Highlights: ► Comparison of the structural changes in Sr 3−x A x AlO 4 F and Sr 3−x A x GaO 4 F (A=Ba, Ca) and its influence on the photoluminescence of these self-activating phosphors. ► Analysis of the Global Instability Index of the Sr 3−x A x AlO 4 F and Sr 3−x A x GaO 4 F (A=Ba, Ca). ► Comparison of the photoluminescence between the self-activating phosphors Sr 3−x A x AlO 4 F and Sr 3−x A x GaO 4 F (A=Ba, Ca).

Rb-Sr geochronology of neoproterozoic syenites in parts of northern Tamil Nadu: implication on Pan-African magmatism

International Nuclear Information System (INIS)

Pandey, U.K.; Prasad, R.N.; Krishna, Veena; Paneer Selvam, A.; Chabria, Tikam

1996-01-01

This paper presents Rb-Sr whole rock isochron age data on two syenite plutons viz. Elagiri and Rasimalai, and results of this study may constrain the timing of magmatic event and crystal evolution in northern granulite segment

Ground-state hyperfine splitting for Rb, Cs, Fr, Ba+, and Ra+

Science.gov (United States)

Ginges, J. S. M.; Volotka, A. V.; Fritzsche, S.

2017-12-01

We have systematically investigated the ground-state hyperfine structure for alkali-metal atoms 87Rb,133Cs, and 211Fr and alkali-metal-like ions +135Ba and +225Ra, which are of particular interest for parity violation studies. The quantum electrodynamic one-loop radiative corrections have been rigorously evaluated within an extended Furry picture employing core-Hartree and Kohn-Sham atomic potentials. Moreover, the effect of the nuclear magnetization distribution on the hyperfine structure intervals has been studied in detail and its uncertainty has been estimated. Finally, the theoretical description of the hyperfine structure has been completed with full many-body calculations performed in the all-orders correlation potential method.

Rb-Sr Autunian age of cordierite-bearing migmatites from northern Cevennes (French Massif Central)

International Nuclear Information System (INIS)

Chenevoy, M.; Gay, M.; Duthou, J.L.

1995-01-01

On the basis of whole rock Rb-Sr data, an Autunian age (287 ± 6 Ma) is ascribed to the cordierite-bearing migmatites occurring south of Mt Pilat. The related anatexis is therefore linked with the low pressure metamorphism, and is distinct from the Devonian anatexis with gave rise to the Barrovian cordierite migmatites in the Lyonnais area. (authors). 34 refs., 2 figs

Rb-Sr and K-Ar isotopic evidence for neoproterozoic (Pan-African) granulite metamorphism from the basement of Mumbai offshore basin, India

International Nuclear Information System (INIS)

Rathore, S.S.; Vijan, A.R.; Singh, M.P.; Misra, K.N.; Prabhu, B.N.

2000-01-01

Precambrian basement from well HBM-1 in the Heera oil field of Mumbai offshore basin has been dated by Rb-Sr and K-Ar methods. Five granulitic basement samples from three conventional drill cores have yielded Rb-Sr isochron age of 502±25 Ma with an initial Sr ratio of 0.70855±0.00013. This age has been interpreted as the time of granulite facies metamorphism of the basement rocks in the region. Two whole rock samples from the basement of this well have yielded mutually concordant K-Ar ages of 505±16 Ma and 507±17 Ma. The K-Ar ages are significantly similar to Rb-Sr age obtained from this well, suggesting complete isotopic reequilibration around 500 Ma ago. The time of secondary thermal heating around 500 Ma ago in the basement of Heera field coincides with the widespread neoproterozoic (Pan-African) thermo-tectonic event extending from the Arabian Peninsula and eastern Africa covering Madagascar, southern India. Sri Lanka and East Antarctica. This study widens the limit of the Pan-African zone, which hitherto was thought to be confined to the western part (presently southern part) of the Indian subcontinent, towards further east. (author)

Trace-element and Sr, Nd, Pb, and O isotopic composition of Pliocene and Quaternary alkali basalts of the Patagonian Plateau lavas of southernmost South America

Science.gov (United States)

Stern, C.R.; Frey, F.A.; Futa, K.; Zartman, R.E.; Peng, Z.; Kurtis, Kyser T.

1990-01-01

The Pliocene and Quaternary Patagonian alkali basalts of southernmost South America can be divided into two groups. The "cratonic" basalts erupted in areas of Cenozoic plateau volcanism and continental sedimentation and show considerable variation in 87Sr/86Sr (0.70316 to 0.70512), 143Nd/144Nd (e{open}Nd) and 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratios (18.26 to 19.38, 15.53 to 15.68, and 38.30 to 39.23, respectively). These isotopic values are within the range of oceanic island basalts, as are the Ba/La, Ba/Nb, La/Nb, K/Rb, and Cs/Rb ratios of the "cratonic" basalts. In contrast, the "transitional" basalts, erupted along the western edge of the outcrop belt of the Pliocene and Quaternary plateau lavas in areas that were the locus of earlier Cenozoic Andean orogenic arc colcanism, have a much more restricted range of isotopic composition which can be approximated by 87Sr/86Sr=0.7039??0.0004, e{open}Nd, 206Pb/204Pb=18.60??0.08, 207Pb/204Pb=15.60??0.01, and 208Pb/204Pb=38.50??0.10. These isotopic values are similar to those of Andean orogenic are basalts and, compared to the "cratonic" basalts, are displaced to higher 87Sr/86Sr at a given 143Nd/144Nd and to higher 207Pb/204Pb at a given 208Pb/204Pb. The "transitional" basalts also have Ba/La, Ba/Nb, La/Nb, and Cs/Rb ratios higher than the "cratonic" and oceanic island basalts, although not as high as Andean orogenic are basalts. In contrast to the radiogenic isotopes, ??18O values for both groups of the Patagonian alkali basalts are indistinguishable and are more restricted than the range reported for Andean orogenic are basalts. Whole rock ??18O values calculated from mineral separates for both groups range from 5.3 to 6.5, while measured whole rock ??18O values range from 5.1 to 7.8. The trace element and isotopic data suggest that decreasing degrees of partial melting in association with lessened significance of subducted slabderived components are fundamental factors in the west to east transition from arc

Reaction of Rb and oxygen overlayers with single-crystalline Bi2Sr2CaCu2O/sub 8+//sub δ/ superconductors

International Nuclear Information System (INIS)

Lindberg, P.A.P.; Shen, Z.; Wells, B.O.; Dessau, D.S.; Mitzi, D.B.; Lindau, I.; Spicer, W.E.; Kapitulnik, A.

1989-01-01

Single crystals of Bi 2 Sr 2 CaCu 2 O/sub 8+//sub δ/ superconductors, in situ cleaved and modified by Rb and oxygen overlayers, have been studied using ultraviolet and x-ray photoemission spectroscopy. The core-level results show that Rb strongly reacts with the Bi and O states, while the Cu and Sr states are left unchanged. This observation strongly indicates that the Bi-O plane forms the surface layer. Subsequent exposure to oxygen results in new oxygen states at the surface as monitored by the O 1s core-level data. For both Rb and oxygen overlayers the valence-band spectra are severely altered. In particular, new valence-band states, presumably of oxygen character, are formed

Granitoids of the Mala Fatra and Velka Fatra Mts.: Rb/Sr isochron geochronology (Western Carpathians)

International Nuclear Information System (INIS)

Bagdasaryan, G.P.; Gukasyan, R.C.; Cambel, B.; Kamenicky, L.; Macek, J.

1992-01-01

New data formerly lacking (with exceptions - Dubna Skala, 1990) were gained from the Western Carpathian core mountain - Mala Fatra and Velka Fatra - by the Rb/Sr method. The isochron based on 13 samples gave the age of 361±10 Ma for Mala Fatra and Velka Fatra intrusions. (author) 4 tabs., 4 figs., 8 refs

Influence of Ba2+ and Sr2+ ions on the hydration process of portland cement and blended cements

Directory of Open Access Journals (Sweden)

Živanović, B. M.

1987-12-01

Full Text Available This study concerns the influence of the concentration of Sr2+ and Ba2+ ions in mortar batch waters upon the hydration process of various Portland and additive cements. An increase in the mechanical resistence of said cements is observed, after 28 days, when the concentration of Ba2+ and Sr2+ ions in the mortar batch waters increases. This suggests a possible microstructural explanation of said phenomenon.En el presente trabajo se estudia la influencia de la concentración de los iones Sr2+ y Ba2+ en las aguas de amasado sobre el proceso de hidratación de varios cementos portland y de adición. Se comprueba un incremento de las resistencias mecánicas de dichos cementos, a los 28 días, cuando aumenta la concentración de los iones Ba2+ y Sr2+ en las aguas de amasado, lo cual sugiere una posible explicación microestructural a dicho fenómeno.

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

International Nuclear Information System (INIS)

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

2014-01-01

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

Effect of Wood Aging on Wine Mineral Composition and 87Sr/86Sr Isotopic Ratio.

Science.gov (United States)

Kaya, Ayse D; Bruno de Sousa, Raúl; Curvelo-Garcia, António S; Ricardo-da-Silva, Jorge M; Catarino, Sofia

2017-06-14

The evolution of mineral composition and wine strontium isotopic ratio 87 Sr/ 86 Sr (Sr IR) during wood aging were investigated. A red wine was aged in stainless steel tanks with French oak staves (Quercus sessiliflora Salisb.), with three industrial scale replicates. Sampling was carried out after 30, 60, and 90 days of aging, and the wines were evaluated in terms of general analysis, phenolic composition, total polysaccharides, multielement composition, and Sr IR. Li, Be, Mg, Al, Sc, Ti, V, Mn, Co, Ni, Cu, Zn, Ga, Ge, As, Rb, Sr, Y, Zr, Mo, Sb, Cs, Ba, Pr, Nd, Sm, Eu, Dy, Ho, Er, Yb, Lu, Tl, and Pb elements and 87 Sr/ 86 Sr were determined by quadrupole inductively coupled plasma mass spectrometry (Q-ICP-MS) and Na, K, Ca, and Fe by flame atomic absorption spectrometry (FAAS). Two-way ANOVA was applied to assess wood aging and time effect on Sr IR and mineral composition. Wood aging resulted in significantly higher concentrations of Mg, V, Co, Ni, and Sr. At the end of the aging period, wine exhibited statistically identical Sr IR compared to control. Study suggests that wood aging does not affect 87 Sr/ 86 Sr, not precluding the use of this parameter for wine traceability purposes.

Absolute transition intensities in decay of 92Rb

International Nuclear Information System (INIS)

Lhersonneau, G.; Rizzi, V.; Barzakh, A.

2005-01-01

In a first step studied the evolution of the ion current of 92 Rb and 94 Sr produced by surface ionisation versus temperature. Ratios of peak areas of γ lines emitted in Sr (1428 keV) and Rb (837 keV) decays are shown. The temperature is decreased from working conditions until the ion currents become very weak. The plateau at low temperature can be understood by the fact that Sr is not ionised anymore and there is no more decease possible. Then, the only contribution to the Sr decay peak is from the decay of Rb collected before transport of the activity to the counting station

Rb/Sr ages of metamorphites of the Herbert Mountains, Shackleton Range, Antarctica

International Nuclear Information System (INIS)

Hofmann, J.; Pilot, J.; Schlichting, M.

1981-01-01

Results of Rb/Sr-age determinations from six mica schists, sampled in the upper part of the Shackleton metamorphic complex (Herbert Mountains, Shackleton Range, Antarctica) are reported. A three point isochrone gives an age of 470 +- 36 mio. yrs., a two point isochrone an age of 1414 +- 185 mio yrs. The first age marks a thermo-magmatic activation of early paleozoic age, the second one is interpretated as the age of regional metamorphism from the upper parts of the Shackleton metamorphic complex. The results are discussed under consideration of former age determinations. (author)

Formation of layered microstructure in the Y-Ba-Cu-O and Bi-Sr-Ca-Cu-O superconductors

International Nuclear Information System (INIS)

Jin, S.; Kammlott, G.W.; Tiefel, T.H.; Chen, S.K.

1992-01-01

The layered grain microstructure is essential for overcoming the weak link problem and ensuring high transport critical currents in the cuprate superconductors. In this paper we discuss the processing and the mechanisms for layer information in Y-Ba-Cu-O and Bi-Sr-Ca-Cu-O. In melt-processed Y-Ba-Cu-O, sympathetic nucleation on previously nucleated YBa 2 Cu 3 O 7-δ plates during solidification appears to be dominant mechanism for the formation of parallel plate-shaped grains. In the Y-Ba-Cu-O and Bi-Sr-Ca-Cu-O ribbons, the interface reaction between the superconductor layer and the silvers substrate seems to be the main mechanism for the c-axis texturing of the layered grains. The drastically different critical current behavior in the c-axis textured Y-Ba-Cu-O and Bi-Sr-Ca-Cu-O ribbons is discussed in terms of possible differences in the nature of the twist and tilt grain boundaries. (orig.)

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

International Nuclear Information System (INIS)

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

2007-01-01

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

Correlation of Structure, Tunable Colors, and Lifetimes of (Sr, Ca, Ba)Al2O4:Eu2+, Dy3+ Phosphors

Science.gov (United States)

Xie, Qidi; Li, Bowen; He, Xin; Zhang, Mei; Chen, Yan; Zeng, Qingguang

2017-01-01

(Sr, Ca, Ba)Al2O4:Eu2+, Dy3+ phosphors were prepared via a high temperature solid-state reaction method. The correlation of phase structure, optical properties and lifetimes of the phosphors are investigated in this work. For the (Sr, Ca)Al2O4:Eu2+, Dy3+ phosphors, the different phase formation from monoclinic SrAl2O4 phase to hexagonal SrAl2O4 phase to monoclinic CaAl2O4 phase was observed when the Ca content increased. The emission color of SrAl2O4:Eu2+, Dy3+ phosphors varied from green to blue. For the (Sr, Ba)Al2O4:Eu2+, Dy3+ phosphors, different phase formation from the monoclinic SrAl2O4 phase to the hexagonal BaAl2O4 phase was observed, along with a shift of emission wavelength from 520 nm to 500 nm. More interestingly, the decay time of SrAl2O4:Eu2+, Dy3+ changed due to the different phase formations. Lifetime can be dramatically shortened by the substitution of Sr2+ with Ba2+ cations, resulting in improving the performance of the alternating current light emitting diode (AC-LED). Finally, intense LEDs are successfully obtained by combining these phosphors with Ga(In)N near UV chips. PMID:29057839

Correlation of Structure, Tunable Colors, and Lifetimes of (Sr, Ca, BaAl2O4:Eu2+, Dy3+ Phosphors

Directory of Open Access Journals (Sweden)

Qidi Xie

2017-10-01

Full Text Available (Sr, Ca, BaAl2O4:Eu2+, Dy3+ phosphors were prepared via a high temperature solid-state reaction method. The correlation of phase structure, optical properties and lifetimes of the phosphors are investigated in this work. For the (Sr, CaAl2O4:Eu2+,Dy3+ phosphors, the different phase formation from monoclinic SrAl2O4 phase to hexagonal SrAl2O4 phase to monoclinic CaAl2O4 phase was observed when the Ca content increased. The emission color of SrAl2O4:Eu2+, Dy3+ phosphors varied from green to blue. For the (Sr, BaAl2O4:Eu2+, Dy3+ phosphors, different phase formation from the monoclinic SrAl2O4 phase to the hexagonal BaAl2O4 phase was observed, along with a shift of emission wavelength from 520 nm to 500 nm. More interestingly, the decay time of SrAl2O4:Eu2+, Dy3+changed due to the different phase formations. Lifetime can be dramatically shortened by the substitution of Sr2+ with Ba2+ cations, resulting in improving the performance of the alternating current light emitting diode (AC-LED. Finally, intense LEDs are successfully obtained by combining these phosphors with Ga(InN near UV chips.

Structural, electronic and optical characteristics of SrGe{sub 2} and BaGe{sub 2}: A combined experimental and computational study

Energy Technology Data Exchange (ETDEWEB)

Kumar, Mukesh, E-mail: mkgarg79@gmail.com [Environmental Remediation Materials Unit, National Institute for Materials Science, Ibaraki 305-0044 (Japan); Umezawa, Naoto [Environmental Remediation Materials Unit, National Institute for Materials Science, Ibaraki 305-0044 (Japan); Imai, Motoharu [Superconducting Properties Unit, National Institute for Materials Science, Ibaraki 305-0047 (Japan)

2015-05-05

Highlights: • Charge transfer between cation and anion atoms observed first time in digermandies. • Study yields a band gap of ∼1 eV and ∼0.85 eV for SrGe{sub 2} and BaGe{sub 2}, respectively. • Band gap decrease with the application of hydrostatic pressure. • Localized cation d states lead to a large absorption coefficient (>7.5 × 10{sup 4} cm{sup −1}). - Abstract: SrGe{sub 2} and BaGe{sub 2} were characterized for structural, electronic and optical properties by means of diffuse reflectance and first-principles density functional theory. These two germanides crystallize in the BaSi{sub 2}-type structure, in which Ge atoms are arranged in tetrahedral configuration. The calculation indicates a charge transfer from Sr (or Ba) atoms to Ge atoms along with the formation of covalent bonds among Ge atoms in Ge tetrahedral. The computational results confirm that these two germanies are Zintl phase described as Sr{sub 2}Ge{sub 4} (or Ba{sub 2}Ge{sub 4}), which are characterized by positively charged [Sr{sub 2} (or Ba{sub 2})]{sup 2.59+} and negatively charged [Ge{sub 4}]{sup 2.59−} units acting as cation and anion, respectively. These compounds are indirect gap semiconductors with band gap estimated to be E{sub g} = 1.02 eV for BaGe{sub 2} and E{sub g} = 0.89 eV for SrGe{sub 2} which are in good agreement with our experimental measured values (E{sub g} = 0.97 eV for BaGe{sub 2} and E{sub g} = 0.82 eV for SrGe{sub 2}). Our calculations demonstrate that the band gaps are narrowed by application of hydrostatic pressure; the pressure coefficients are estimated to be −10.54 for SrGe{sub 2} and −10.06 meV/GPa for BaGe{sub 2}. Optical properties reveal that these compounds have large absorption coefficient (∼7.5 × 10{sup 4} cm{sup −1} at 1.5 eV) and the estimated high frequency (static) dielectric constant are, ε{sub ∞}(ε{sub 0}) ≈ 12.8(20.97) for BaGe{sub 2} and ε{sub ∞}(ε{sub 0}) ≈ 14.27(22.87) for SrGe{sub 2}.

Reverse micellar synthesis, structural characterization and dielectric properties of Sr-doped BaZrO{sub 3} nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Ahmad, Tokeer, E-mail: tahmad3@jmi.ac.in [Nanochemistry Laboratory, Department of Chemistry, Jamia Millia Islamia, New Delhi, 110025 (India); Ubaidullah, Mohd [Nanochemistry Laboratory, Department of Chemistry, Jamia Millia Islamia, New Delhi, 110025 (India); Department of Chemistry, Banasthali University, Tonk, Rajasthan, 304022 (India); School of Science and Technology, Glocal University, Mirzapur, Saharanpur, 247121, Uttar Pradesh (India); Shahazad, Mohd [Nanochemistry Laboratory, Department of Chemistry, Jamia Millia Islamia, New Delhi, 110025 (India); Kumar, Dinesh [Department of Chemistry, Banasthali University, Tonk, Rajasthan, 304022 (India); Al-Hartomy, Omar A. [Department of Physics, Faculty of Science, King Abdulaziz University, Jeddah, 21589 (Saudi Arabia)

2017-01-01

Sr-doped BaZrO{sub 3} nanoparticles with strontium content varying from 5 to 20 mol % were successfully synthesized by reverse micellar method at 900 °C for the first time. Systematic studies have been carried out to establish the structural and electrical properties of the as prepared nanoparticles. These nanoparticles were characterized using powder X-ray diffraction, transmission electron microscopy, BET surface area and dielectric measurements. X-ray diffraction analysis showed the formation of monophasic and highly crystalline nanoparticles which could be indexed in cubic BaZrO{sub 3} with contraction of lattice on strontium substitution. A monotonic shift of diffraction pattern towards higher angel confirms the formation of solid solutions of Ba{sub 1−x}Sr{sub x}ZrO{sub 3} (0.05 ≤ x ≤ 0.20) which was corroborating well with lattice parameter studies. Transmission electron microscopic studies showed the formation of cubic, spherical and hexagonal nanoparticles with an average grain size of 40–65 nm. Energy dispersive X-ray spectroscopic studies confirmed the presence of dopant (Sr{sup 2+}) in the BaZrO{sub 3} matrix and estimated chemical species corroborate well with the loaded composition. Specific surface area of the solid solution comes out to be in the range of 104–244 m{sup 2} g{sup -1}. Smallest particle of size 40 nm shows highest surface area 244 m{sup 2} g{sup -1} for 20 mol% Sr-doped BaZrO{sub 3}. Dielectric and impedance studies were also carried out as a function of frequency and temperature to explore the electrical properties of Sr-doped BaZrO{sub 3}. The dielectric constant of Ba{sub 1−x}Sr{sub x}ZrO{sub 3} (0.05 ≤ x ≤ 0.20) was found to be in the range of 13–25 for x = 0.05 to x = 0.20 with nearly similar dielectric loss of the order of 0.02. The conductance increases linearly with increase in frequency at room temperature, however the impedance has an inverse effect. - Highlights: • Monophasic nanocrystalline Ba{sub 1−x}Sr

Thermal expansion behaviour in the oxygen deficient perovskites Sr2BSbO5.5 (B=Ca, Sr, Ba). Competing effects of water and oxygen ordering

International Nuclear Information System (INIS)

Zhou Qingdi; Kennedy, Brendan J.; Avdeev, Maxim

2011-01-01

Neutron diffractions studies reveal the presence of oxygen disorder in the oxygen deficient perovskites Sr 2 BSbO 5.5 (B=Ca, Sr, Ba). Synchrotron X-ray studies demonstrate that these oxides have a double perovskite-type structure with the cell size increasing as the size of the B cation increases from 8.2114(2) A for B=Ca to 8.4408(1) A for B=Ba. It is postulated that a combination of local clustering of the anions and vacancies together with water-water and water-host hydrogen bonds plays a role in defining the volume of the encapsulated water clusters and that changes in the local structure upon heating result in anomalous thermal expansion observed in variable temperature diffraction measurements. - Graphical abstract: The oxides Sr 2 BSbO 5.5 (B=Ca, Sr, Ba) have unusual anion disorder. There is a lag in the contraction in the cell size of Sr 2 CaSbO 5.5 nH 2 O established from X-ray diffraction measurements following the loss of water suggesting changes on the local structure are important. Highlights: → The average structures of the defect perovskites Sr 2 MSbO 5.5 established. → Anion and cation disorder quantified by neutron and synchrotron X-ray diffraction. → Anomalous thermal expansion due to local clustering of anions and vacancies observed.

Rb-Sr and Sm-Nd Isotopic Studies of Lunar Green and Orange Glasses

Science.gov (United States)

Shih, C.-Y.; Nyquist, L. E.; Reese, Y.

2012-01-01

Lunar volcanic glassy beads have been considered as quenched basaltic magmas derived directly from deep lunar mantle during fire-fountaining eruptions [1]. Since these sub-mm size glassy melt droplets were cooled in a hot gaseous medium during free flight [2], they have not been subject to mineral fractionations. Thus, they represent primary magmas and are the best samples for the investigation of the lunar mantle. Previously, we presented preliminary Rb- Sr and Sm-Nd isotopic results for green and orange glassy samples from green glass clod 15426,63 and orange soil 74220,44, respectively [3]. Using these isotopic data, initial Sr-87/Sr-86 and Nd ratios for these pristine mare glass sources can be calculated from their respective crystallization ages previously determined by other age-dating techniques. These isotopic data were used to evaluate the mineralogy of the mantle sources. In this report, we analyzed additional glassy samples in order to further characterize isotopic signatures of their source regions. Also, we'll postulate a relationship between these two major mare basalt source mineralogies in the context of lunar magma ocean dynamics.

Impedance spectroscopy and structural properties of the perovskite-like Sn(Ba,Sr)O3 stagnate

International Nuclear Information System (INIS)

Cuervo Farfán, J.; Olaya, J.J.; Vera López, E.; Landínez Téllez, D.A.; Roa-Rojas, J.

2012-01-01

An exhaustive study of structural, electrical and transport properties on the perovskite stagnate Sn(Ba,Sr)O 3 was performed. Samples of SnBa 1-x Sr x O 3 with 0≤x≤1.00 were prepared by the solid state reaction method. The crystallographic structure was studied by X-ray diffraction experiments and Rietveld refinement using the GSAS code. Results reveal the material synthesized in a cubic structure (space group Pm3-bar m, no. 221) for 0≤x≤0.50 and in an orthorhombic (space group Pnma, no. 62) for x>0.50. The approximate grain size was found from experiments' Scanning Electron Microscopy. The electric response was studied by the Impedance Spectroscopy technique from 10.0 mHz up to 0,10 MHz. Electric polarization measurements for SnSrO 3 and SnBaO 3 were determined through curves of polarization as a function of applied electric field, which reveal the ferroelectric character of the material. From the saturation polarization the dielectric constants of materials were calculated.

Dielectric behaviour of (Ba,Sr)TiO3 perovskite borosilicate glass ceramics

International Nuclear Information System (INIS)

Yadav, Avadhesh Kumar; Gautam, C.R.

2013-01-01

Various perovskite (Ba,Sr)TiO 3 borosilicate glasses were prepared by rapid melt-quench technique in the glass system ((Ba 1-x Sr x ).TiO 3 )-(2SiO 2 .B 2 O 3 )-(K 2 O)-(La 2 O 3 ). On the basis of differential thermal analysis results, glasses were converted into glass ceramic samples by regulated heat treatment schedules. The dielectric behaviour of crystallized barium strontium titanate borosilicate glass ceramic samples shows diffuse phase transition. The study depicts the dielectric behaviour of glass ceramic sample BST5K1L0.2S814. The double relaxation was observed in glass ceramic samples corresponding 80/20% Ba/Sr due to change in crystal structure from orthorhombic to tetragonal and tetragonal to cubic with variation of temperature. The highest value of dielectric constant was found to be 48289 for the glass ceramic sample BST5K1L0.2S814. The high value of dielectric constant attributed to space charge polarization between the glassy phase and perovskite phase. Due to very high value of dielectric constant, such glass ceramics are used for high energy storage devices. La 2 O 3 acts as nucleating agent for crystallization of glass to glass ceramics and enhances the dielectric constant and retarded dielectric loss. Such glass ceramics can be used in high energy storage devices such as barrier layer capacitors, multilayer capacitors etc. (author)

Elastic properties of nano structured AZrO3 (A=Ba, Sr) single perovskites

International Nuclear Information System (INIS)

Pazhani, R.; Thomas, J.K.; Moses Ezhil Raj, A.; Solomon, S.; Bena Jothy, V.; Mathai, K.C.

2011-01-01

Nanocrystals of barium zirconate and strontium zirconate AZrO 3 (A=Ba and Sr) were synthesized by a unique self-sustained single-step combustion of an aqueous solution, containing Ba, Sr and Zr ions by using citric acid as complexing agent and liquor ammonia as fuel, thus giving rise to phase pure AZrO 3 nanopowder. In this process, a single phase pure nanopowder of AZrO 3 has been obtained without the need of calcination steps. The formation and stability of the compound was confirmed through the tolerance factor on the basis of the ionic radii of all the atoms of the compound. Phase-purity of the as-prepared powders was examined using X-ray diffraction. As-prepared powder was single phase, crystalline, and composed of uniform particles with sizes 20-30 nm. The crystal structure of AZrO 3 are respective cubic (Pm3-bar m, a=4.1839A) and orthorhombic (Pnma, a=5.7937A, b=8.17648A and c=5.7694A). Annealed samples of SrZrO 3 has improved crystal structure with a=5.764A, b=8.2292A and c=5.7989A, comparable to the standards. Microstrain acting on all the planes of the material is positive which indicates presence of tensile stress on the material. The calculated compressive stress on the surface of' the nanopowder is of the order 0.213 GPa to -0.274 GPa for BaZrO 3 and 4.443 GPa to -0.220 GPa for SrZrO 3 along various planes of the particles. (author)

Dependence of transfer number of fluorine on cation type in glasses of Ba(PO3)2-MeF2 systems (Me=Ba,Sr,Ca,Mg)

International Nuclear Information System (INIS)

Pronkin, A.A.

1978-01-01

The influence of Ba, Sr, Ca, Mg cations on transfer numbers of fluorine in glasses of Ba(PO 3 ) 2 - MeF 2 pseudobinary systems is studied. Transfer numbers are essentially different in one and the same fluorine ion concentration in glasses, containing various alkali-earth cations: increase of the cation field force brings about decrease of the transfer numbers of fluorine, and the glass-formation region in the Ba-Sr-Ca-Mg series rises. The dependence of transfer numbers of fluorine on the fluorine concentration logarithm is presented. It is established, that alkali-earth metals influence the transfer numbers of fluorine on account of selective interaction with the phosphate constituent of glass structure

Investigations of the solid solution in the system SrI2-BaI2 at ambient pressures and at 2.0 GPa

International Nuclear Information System (INIS)

Beck, H.P.; Holley, C.; Limmer, A.

1984-01-01

The P,T,x-diagram of the system SrI 2 -BaI 2 has been investigated at ambient pressures and at 2.0 GPa. The amount of solid solution in the four structure types occuring in this system (SrI 2 - or PbCl 2 -ZrAs 2 -type with SrI 2 and PbCl 2 - or anti-Fe 2 P-type with BaI 2 ) differs considerably. Structural geometries belonging to the same PbCl 2 structure family show marked differences in their toleration to cation substitution. Solid solution is especially pronounced in the BaI 2 -rich phases which incorporate up to 60 mol-% Sr 2+ in the high pressure phase of BaI 2 . (author)

Numerical solutions of anharmonic vibration of BaO and SrO molecules

Energy Technology Data Exchange (ETDEWEB)

Pramudito, Sidikrubadi; Sanjaya, Nugraha Wanda [Theoretical Physics Division, Department of Physics, Bogor Agricultural University, Jalan Meranti Kampus IPB Dramaga Bogor 16680 (Indonesia); Sumaryada, Tony, E-mail: tsumaryada@ipb.ac.id [Theoretical Physics Division, Department of Physics, Bogor Agricultural University, Jalan Meranti Kampus IPB Dramaga Bogor 16680 (Indonesia); Computational Biophysics and Molecular Modeling Research Group (CBMoRG), Department of Physics, Bogor Agricultural University, Jalan Meranti Kampus IPB Dramaga Bogor 16680 (Indonesia)

2016-03-11

The Morse potential is a potential model that is used to describe the anharmonic behavior of molecular vibration between atoms. The BaO and SrO molecules, which are two almost similar diatomic molecules, were investigated in this research. Some of their properties like the value of the dissociation energy, the energy eigenvalues of each energy level, and the profile of the wavefunctions in their correspondence vibrational states were presented in this paper. Calculation of the energy eigenvalues and plotting the wave function’s profiles were performed using Numerov method combined with the shooting method. In general we concluded that the Morse potential solved with numerical methods could accurately produce the vibrational properties and the wavefunction behavior of BaO and SrO molecules from the ground state to the higher states close to the dissociation level.

Synthesis and luminescent properties of novel red-emitting M7Sn(PO46:Eu3+ (M = Sr, Ba phosphors

Directory of Open Access Journals (Sweden)

Guo Feng

2018-03-01

Full Text Available Novel Eu3+-activated M7Sn(PO46 (where M = Sr, Ba red-emitting phosphors were synthesized via conventional solid-state reaction method at 1200 °C for 2 h. The luminescence properties of the prepared samples and quenching concentration of Sr7-xSn(PO46:xEu3+ and Ba7-xSn(PO46:xEu3+ were investigated. These phosphors can be efficiently excited by UV (395 nm and visible blue (465 nm light nicely matching the output wavelengths of the near-UV LEDs and InGaN blue LED chips and emit the red light. The critical concentrations of the Eu3+ activator were found to be 0.175 mol and 0.21 mol per formula unit for Sr7-xSn(PO46:xEu3+ and Ba7-xSn(PO46:xEu3+, respectively. The M7-xSn(PO46:xEu3+ (M = Sr, Ba phosphor may be a good candidate for light-emitting diodes application.

Mechanical properties of hexaferite based magnet composite of SrFe12019 and BaFe12O19 with natural rubber bonding agent

International Nuclear Information System (INIS)

Waluyo, T.; Herman, Y.A.; Sudirman; Ridwan

2000-01-01

Research on mechanical properties at magnet composite of SrFe 12 0 19 (SrM) and BaFe 12 O 19 (BaM)magnet powder with natural rubber bonding agent have been done. The natural rubber used was rubber made of latex without vulcanization, The SrM powder having average particle size of 1.6 μm and flat shaped. and the BaM powder having particle size of 1.2 μm and nodular shaped. The production of composite carried out in Labo Plastomill at 100 o C and mixer speed of 30 rpm for 7 minutes. The result obtained from Labo Plastomill then made into sheets. Mechanical properties of the composite tested were strain, elongation break and hardness, The results showed that the highest strain of the SrM composite obtained at composition of 70% vol of powder that is 2,22 MPa, and 3,84 MPa for BaM composite at 50% vol. of powder The elongation break of SrM composite decreased by increasing of powder volume fraction, that is 90% at the composition or 70% vol. of powder, and 370% for BaM composite at 50% vol. fraction of powder. The highest hardness for SrM composite obtained at composition of of 70% vol. of powder, that is 95 SHA. and for the BaM composite at 50% vol. of powder. that is 52 SHA

Structural studies of the rhombohedral and orthorhombic monouranates: CaUO{sub 4}, α-SrUO{sub 4}, β-SrUO{sub 4} and BaUO{sub 4}

Energy Technology Data Exchange (ETDEWEB)

Murphy, Gabriel [School of Chemistry, The University of Sydney, Sydney, NSW 2006 (Australia); Kennedy, Brendan J., E-mail: kennedyb@chem.usyd.edu.au [School of Chemistry, The University of Sydney, Sydney, NSW 2006 (Australia); Johannessen, Bernt; Kimpton, Justin A. [Australian Synchrotron, 800 Blackburn Road, Clayton, Victoria 3168 (Australia); Avdeev, Maxim; Griffith, Christopher S.; Thorogood, Gordon J.; Zhang, Zhaoming [Australian Nuclear Science and Technology Organisation, Lucas Heights, NSW 2234 (Australia)

2016-05-15

The structures of some AUO{sub 4} (A=Ca, Sr, or Ba) oxides have been determined using a combination of neutron and synchrotron X-ray diffraction, supported by X-ray absorption spectroscopic measurements at the U L{sub 3}-edge. The smaller Ca cation favours a rhombohedral AUO{sub 4} structure with 8-coordinate UO{sub 8} moieties whilst an orthorhombic structure based on UO{sub 6} groups is found for BaUO{sub 4}. Both the rhombohedral and orthorhombic structures can be stabilised for SrUO{sub 4}. The structural studies suggest that the bonding requirements of the A site cation play a significant role in determining which structure is favoured. In the rhombohedral structure, Bond Valence Sums demonstrate the A site is invariably overbonded, which, in the case of rhombohedral α-SrUO{sub 4}, is compensated for by the formation of vacancies in the oxygen sub-lattice. The uranium cation, with its flexible oxidation state, is able to accommodate this by inducing vacancies along its equatorial coordination site as demonstrated by neutron powder diffraction. - Graphical abstract: Diffraction studies of AUO{sub 4} (A = Ca, Sr, or Ba) oxides reveal the importance of the bonding requirements of the A site cation in determining whether the structure is rhombohedral or orthorhombic. - Highlights: • Structures of AUO{sub 4} ( A = Ca Sr, Ba) refined against X-ray and Neutron diffraction. • The alkali cations size has a dramatic effect on the crystal structure. • Smaller cations favouring a rhombohedral structure. • Oxygen vacancies to stabilise the rhombohedral structure in SrUO{sub 4}.

Rb/Sr and K/Ar dating of Slovakia's rocks, its possibilities and interpretation

International Nuclear Information System (INIS)

Cambel, B.; Bagdasaryan, G.P.; Gukasyan, P.Kh.; Veselskij, I.

1979-01-01

Nuclear geochronological data are evaluated and summarized into histograms. On the basis of an evaluation, the results are compared obtained using various methods (K/Ar, Rb/Sr and U-Th-Pb) and the age of rocks in West Carpathians determined. It is pointed out that the age determination is dependent on the geochemical state of the studied minerals and rocks. The obtained results confirm the palaeozoic age of the majority of rocks of West Carpathians. Direct nuclear geochronological evidence of precambrium rocks has not yet been obtained. (author)

Effect of divalent (Sr, Ba) doping on the structural and magnetic properties of BiFeO{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Rangi, Manisha, E-mail: mrangi100@gmail.com; Sanghi, Sujata; Agarwal, Ashish; Jangra, Sandhaya; Singh, Ompal [Department of Applied Physics, Guru Jambheshwar University of Science and Technology, Hisar, Haryana- 125001 (India)

2015-06-24

The effect of divalent substitution on the crystal structure and magnetic properties of BiFeO{sub 3} has been investigated using X-ray diffraction and magnetic measurements technique. Single phase Bi{sub 0.8}A{sub 0.2}FeO{sub 3} (A= Sr, Ba) multiferroics have been synthesized by solid state reaction method. Rietveld analysis of the XRD patterns revealed that the prepared ceramics exhibit rhombohedral structure with space group R3c. M–H hysteresis loops were recorded at 5K revealed that Sr and Ba substitution transformed antiferromagnetic BiFeO3 into weak ferromagnetic. The enhanced magnetization with Sr and Ba addition is confirmed by the MT curve recorded at 1T. It is closely related to intrinsic structural distortion and modification of the antiparallel spin structure.

Trigermanides AEGe{sub 3} (AE = Ca, Sr, Ba). Chemical bonding and superconductivity

Energy Technology Data Exchange (ETDEWEB)

Castillo, Rodrigo; Schnelle, Walter; Baranov, Alexey I.; Burkhardt, Ulrich; Bobnar, Matej; Cardoso-Gil, Raul; Schwarz, Ulrich; Grin, Yuri [Max-Planck-Institut fuer Chemische Physik Fester Stoffe, Dresden (Germany)

2016-08-01

The crystal structures of the trigermanides AEGe{sub 3}(tI32) (AE = Ca, Sr, Ba; space group I4/mmm, for SrGe{sub 3}: a = 7.7873(1), c = 12.0622(3) Aa) comprise Ge{sub 2} dumbbells forming layered Ge substructures which enclose embedded AE atoms. The chemical bonding analysis by application of the electron localizability approach reveals a substantial charge transfer from the AE atoms to the germanium substructure. The bonding within the dumbbells is of the covalent two-center type. A detailed analysis of SrGe{sub 3} reveals that the interaction on the bond-opposite side of the Ge{sub 2} groups is not lone pair-like - as it would be expected from the Zintl-like interpretation of the crystal structure with anionic Ge layers separated by alkaline-earth cations - but multi-center strongly polar between the Ge{sub 2} dumbbells and the adjacent metal atoms. Similar atomic interactions are present in CaGe{sub 3} and BaGe{sub 3}. The variation of the alkaline-earth metal has a merely insignificant influence on the superconducting transition temperatures in the s,p-electron compounds AEGe{sub 3}.

Glass formation and physicochemical properties of glasses of Ba(PO3)2-LiRAlF6 (R=Mg, Ca, Sr, Ba) system

International Nuclear Information System (INIS)

Khalilev, V.D.; Chkhenkeli, G.D.; Vakhrameev, V.I.

1987-01-01

Glass formation regions, crystallizability, optical constants, thermal linear expansion coefficient and IR absorption spectra of glass are studied in Ba(PO) 3 ) 2 - LiRAlF 6 system where R=Mg, Ca, Sr, Ba. The carried out investigation confirms participation of introduced fluorides (as modified cryolites) in structural transformations manifested in increase of glass formation regions and nonlinear variations of properties

Low temperature rf sputtering deposition of (Ba, Sr) TiO3 thin film with crystallization enhancement by rf power supplied to the substrate

International Nuclear Information System (INIS)

Yoshimaru, Masaki; Takehiro, Shinobu; Abe, Kazuhide; Onoda, Hiroshi

2005-01-01

The (Ba, Sr) TiO 3 thin film deposited by radio frequency (rf) sputtering requires a high deposition temperature near 500 deg. C to realize a high relative dielectric constant over of 300. For example, the film deposited at 330 deg. C contains an amorphous phase and shows a low relative dielectric constant of less than 100. We found that rf power supplied not only to the (Ba, Sr) TiO 3 sputtering target, but also to the substrate during the initial step of film deposition, enhanced the crystallization of the (Ba, Sr) TiO 3 film drastically and realized a high dielectric constant of the film even at low deposition temperatures near 300 deg. C. The 50-nm-thick film with only a 10 nm initial layer deposited with the substrate rf biasing is crystallized completely and shows a high relative dielectric constant of 380 at the deposition temperature of 330 deg. C. The (Ba, Sr) TiO 3 film deposited at higher temperatures (upwards of 400 deg. C) shows preferred orientation, while the film deposited at 330 deg. C with the 10 nm initial layer shows a preferred orientation on a -oriented ruthenium electrode. The unit cell of (Ba, Sr) TiO 3 (111) plane is similar to that of ruthenium (001) plane. We conclude that the rf power supplied to the substrate causes ion bombardments on the (Ba, Sr) TiO 3 film surface, which assists the quasiepitaxial growth of (Ba, Sr) TiO 3 film on the ruthenium electrode at low temperatures of less than 400 deg. C

Low temperature rf sputtering deposition of (Ba, Sr) TiO3 thin film with crystallization enhancement by rf power supplied to the substrate

Science.gov (United States)

Yoshimaru, Masaki; Takehiro, Shinobu; Abe, Kazuhide; Onoda, Hiroshi

2005-05-01

The (Ba, Sr) TiO3 thin film deposited by radio frequency (rf) sputtering requires a high deposition temperature near 500 °C to realize a high relative dielectric constant over of 300. For example, the film deposited at 330 °C contains an amorphous phase and shows a low relative dielectric constant of less than 100. We found that rf power supplied not only to the (Ba, Sr) TiO3 sputtering target, but also to the substrate during the initial step of film deposition, enhanced the crystallization of the (Ba, Sr) TiO3 film drastically and realized a high dielectric constant of the film even at low deposition temperatures near 300 °C. The 50-nm-thick film with only a 10 nm initial layer deposited with the substrate rf biasing is crystallized completely and shows a high relative dielectric constant of 380 at the deposition temperature of 330 °C. The (Ba, Sr) TiO3 film deposited at higher temperatures (upwards of 400 °C) shows preferred orientation, while the film deposited at 330 °C with the 10 nm initial layer shows a preferred orientation on a -oriented ruthenium electrode. The unit cell of (Ba, Sr) TiO3 (111) plane is similar to that of ruthenium (001) plane. We conclude that the rf power supplied to the substrate causes ion bombardments on the (Ba, Sr) TiO3 film surface, which assists the quasiepitaxial growth of (Ba, Sr) TiO3 film on the ruthenium electrode at low temperatures of less than 400 °C.

Electrical behavior of Ca, Sr, Ba, and Eu at very high pressures and low temperatures

International Nuclear Information System (INIS)

Bundy, F.P.; Dunn, K.J.

1981-01-01

Compression of Ca and Sr initially causes an increase in resistivity, probably because of uncrossing of conduction and valence bands. Then at about 180 kbar for Ca and about 35 kbar for Sr the resistivity drops quite abruptly, following which the resistivity again increases with additional pressure, similar to the behavior of Ba starting at room pressure. The high pressure forms of Ba have already been reported to be superconducting, and the experiments confirm this. Superconductivity appears in Sr at about 350 kbar and develops strongly at higher pressures. In the 440 kbar experiment on Ca a resistance drop started at the lower threshold of the temperature capability, 2.1K, suggesting that Ca, too, becomes superconducting at sufficiently high pressures. The high pressure form of Eu above 125 kbar was tested for superconductivity down to 2.2K with negative results. (Auth.)

High Q ceramics in the ACe2(MoO4)4 (A = Ba, Sr and Ca) system for LTCC applications

International Nuclear Information System (INIS)

Surjith, A.; Ratheesh, R.

2013-01-01

Highlights: ► Solid state synthesis of phase pure ACe 2 (MoO 4 ) 4 (A = Ba, Sr and Ca) ceramics. ► Structural and microstructural evaluation of the synthesized ceramic materials. ► Microwave dielectric property studies of ACe 2 (MoO 4 ) 4 (A = Ba, Sr and Ca) ceramics. ► Structure-property correlation through Laser Raman studies. - Abstract: Novel low temperature sinterable high Q ceramic systems ACe 2 (MoO 4 ) 4 (A = Ba, Sr and Ca) have been prepared through solid state ceramic method. The effect of ionic radii of alkaline earth cations on the structure, microstructure and microwave dielectric properties of these ceramics were studied using powder X-ray diffraction, Laser Raman spectroscopy, scanning electron microscopy and Vector Network Analyzer. A structural change from monoclinic to tetragonal structure was observed while substituting Sr 2+ and Ca 2+ cations in place of Ba 2+ . The Sr and Ca analogues possess better microwave dielectric properties compared to BaCe 2 (MoO 4 ) 4 . All the ceramics were well sintered below 840 °C with dielectric constant in the range 10.2–12.3 together with good quality factor. The SrCe 2 (MoO 4 ) 4 ceramic exhibits an unloaded quality factor of 6762 at 8.080662 GHz with a temperature coefficient of resonant frequency of −46 ppm/°C while the CaCe 2 (MoO 4 ) 4 ceramic shows an unloaded quality factor of 7549 at 6.928868 GHz and a temperature coefficient of resonant frequency of −44 ppm/°C.

Ferromagnetism and half metallicity induced by oxygen vacancies in the double perovskite BaSrNiWO{sub 6}: DFT study

Energy Technology Data Exchange (ETDEWEB)

Aharbil, Y. [Laboratoire de Chimie Physique des Matériaux LCPM, Faculté des Sciences Ben M' Sik, Casablanca (Morocco); Labrim, H. [Unité Science de la Matière/DERS/Centre National de l’Energie, des Sciences et des Techniques Nucléaires (CNESTEN), Rabat (Morocco); Benmokhtar, S.; Haddouch, M. Ait [Laboratoire de Chimie Physique des Matériaux LCPM, Faculté des Sciences Ben M' Sik, Casablanca (Morocco); Bahmad, L., E-mail: bahmad@fsr.ac.ma [Mohammed V University in Rabat, Laboratoire de Magnétisme et Physique des Hautes Energies L.M.P.H.E. URAC-12, B.P. 1014, Rabat (Morocco); Belhaj, A. [LIRST, Département de Physique, Faculté Poly-disciplinaire, Université Sultan Moulay Slimane, Béni Mellal (Morocco); Ez-Zahraouy, H.; Benyoussef, A. [Mohammed V University in Rabat, Laboratoire de Magnétisme et Physique des Hautes Energies L.M.P.H.E. URAC-12, B.P. 1014, Rabat (Morocco)

2016-11-01

Using the spin polarized density functional theory (DFT) and exploring the Plane-Wave Self-Consistent Field (PWscf) code implemented in Quantum-ESPRESSO package, we investigate the effect of the Oxygen vacancies (V{sub O}) and the Oxygen interstitial (O{sub i}) on the double perovskite BaSrNiWO{sub 6}. This deals with the magnetic ordering and the electronic structure in such a pure sample exhibiting the insulating anti-ferromagnetic (AFM) state. This study shows that the presence of oxygen deficient defects converts the insulating to half metal with ferromagnetic or anti-ferromagnetic states. The magnetic ordering in BaSrNiWO{sub 6−δ} depends on the position of the Oxygen vacancy in the unit cell. However, it has been shown that the Oxygen interstitial preserves the anti-ferromagnetic propriety. We have computed the formation energies of different positions of the Oxygen vacancy (V{sub O}) and the Oxygen interstitial (O{sub i}) in the BaSrNiWO{sub 6} compound. We showed that the formation of V{sub O} is easier and vice versa for the O{sub i} formation. The obtained results reveal(V{sub O}) and the Oxygen interstitial (O{sub i}) that the anti-ferromagnetic can be converted to ferromagnetic in the double perovskite BaSrNiWO{sub 6} induced by Oxygen vacancies V{sub O}. - Highlights: • We have studied the ferromagnetism and Half Metallicity in Double Perovskite BaSrNiWO{sub 6}. • We have applied the Ab-inito calculations using the DFT approach. • We showed the effects induced by Oxygen Vacancies and Oxygen interstitial. • We found that the magnetic ordering in BaSrNiWO{sub 6−δ} depends on the position of the Oxygen vacancy in the unit cell.

Impedance spectroscopy and structural properties of the perovskite-like Sn(Ba,Sr)O{sub 3} stagnate

Energy Technology Data Exchange (ETDEWEB)

Cuervo Farfan, J. [Grupo de Fisica de Nuevos Materiales, Departamento de Fisica, Universidad Nacional de Colombia, AA 5997, Bogota DC (Colombia); Ciencias Basicas, Universidad Manuela Beltran, Bogota DC (Colombia); Olaya, J.J. [Departamento de Ingenieria Mecanica y Mecatronica, Universidad Nacional de Colombia, Bogota DC (Colombia); Vera Lopez, E. [Grupo de Superficies, Electroquimica y Corrosion, Universidad Pedagogica y Tecnologica de Colombia, Tunja (Colombia); Landinez Tellez, D.A. [Grupo de Fisica de Nuevos Materiales, Departamento de Fisica, Universidad Nacional de Colombia, AA 5997, Bogota DC (Colombia); Roa-Rojas, J., E-mail: jroar@unal.edu.co [Grupo de Fisica de Nuevos Materiales, Departamento de Fisica, Universidad Nacional de Colombia, AA 5997, Bogota DC (Colombia)

2012-08-15

An exhaustive study of structural, electrical and transport properties on the perovskite stagnate Sn(Ba,Sr)O{sub 3} was performed. Samples of SnBa{sub 1-x}Sr{sub x}O{sub 3} with 0{<=}x{<=}1.00 were prepared by the solid state reaction method. The crystallographic structure was studied by X-ray diffraction experiments and Rietveld refinement using the GSAS code. Results reveal the material synthesized in a cubic structure (space group Pm3-bar m, no. 221) for 0{<=}x{<=}0.50 and in an orthorhombic (space group Pnma, no. 62) for x>0.50. The approximate grain size was found from experiments' Scanning Electron Microscopy. The electric response was studied by the Impedance Spectroscopy technique from 10.0 mHz up to 0,10 MHz. Electric polarization measurements for SnSrO{sub 3} and SnBaO{sub 3} were determined through curves of polarization as a function of applied electric field, which reveal the ferroelectric character of the material. From the saturation polarization the dielectric constants of materials were calculated.

The transfer of 45Ca, 85Sr and 140Ba from mother to newborn in rats

International Nuclear Information System (INIS)

Taylor, D.M.; Bligh, P.H.

1992-01-01

Comparative studies of the transfer of 45 Ca, 85 Sr and 140 Ba from mother to offspring were made in August rats following intravenous injection of the radionuclides either during gestation or 40 to 90 days prior to mating. Immediately following parturition, and before suckling could begin, the newborn rats were removed from the dam and killed. For each radionuclide the percentage of the initial maternal activity transferred to individual offspring decreased exponentially with time between injection and parturition with a mean half-time of 3.1 ± 0.7 (SD) days. Transfer ratios measured in rats injected either during or prior to gestation were similar and could be described by the rounded values Ca: Sr: Ba = 1.00: 0.4:0.2. Placental transfer ratios were not significantly different from those for gastrointestinal absorption of the three radionuclides, plus 226 Ra, in adult rats of the same strain. For humans transfer ratios from mother to baby of Ca: Sr: Ba: Ra = 1.0: 0.6: 0.4: 0.4 are suggested. (author)

Structures, phase transitions and microwave dielectric properties of the 6H perovskites Ba3BSb2O9, B=Mg, Ca, Sr, Ba

International Nuclear Information System (INIS)

Ling, Chris D.; Rowda, Budwy; Avdeev, Maxim; Pullar, Robert

2009-01-01

We present a complete temperature-composition phase diagram for Ba 3 BSb 2 O 9 , B=Mg, Ca, Sr, Ba, along with their electrical behavior as a function of B. These compounds have long been recognized as 6H-type perovskites, but (with the exception of B=Mg) their exact structures and properties were unknown due to their low symmetries, temperature-dependent phase transitions, and difficulties in synthesizing pure samples. The full range of possible space group symmetries is observed, from ideal hexagonal P6 3 /mmc to monoclinic C2/c to triclinic P1-bar. Direct second-order transitions between these phases are plausible according to group theory, and no evidence was seen for any further intermediate phases. The phase diagram with respect to temperature and the effective ionic radius of B is remarkably symmetrical for B=Mg, Ca, and Sr. For B=Ba, a first-order phase transition to a locally distorted phase allows a metastable hexagonal phase to persist to lower temperatures than expected before decomposing around 600 K. Electrical measurements revealed that dielectric permittivity corrected for porosity does not change significantly as a function of B and is in a good agreement with the values predicted by the Clausius-Mossotti equation. - Graphical abstract: Thermodynamic phase diagram for Ba 3 BSb 2 O 9 , B=Mg, Ca, and Sr, as a function of temperature T and effective ionic radius (IR) of the B 2+ cation

On the chemical resolution of the {sup 87}Rb{sup +} (s{sup 0})/{sup 87}Sr{sup +} (s{sup 1}) isobaric interference: A kinetic search for an optimum reagent

Energy Technology Data Exchange (ETDEWEB)

Cheng Ping; Koyanagi, Gregory K. [Department of Chemistry, Centre for Research in Mass Spectrometry and Centre for Research in Earth and Space Science, York University, Toronto, Ontario, M3J 1P3 (Canada); Bohme, Diethard K. [Department of Chemistry, Centre for Research in Mass Spectrometry and Centre for Research in Earth and Space Science, York University, Toronto, Ontario, M3J 1P3 (Canada)], E-mail: dkbohme@yorku.ca

2008-10-03

Room-temperature reactions of the atomic cations Sr{sup +} and Rb{sup +} have been surveyed systematically with a variety of gases using an Inductively-Coupled Plasma/Selected-Ion Flow Tube (ICP/SIFT) tandem mass spectrometer. Rate coefficients and product distributions have been measured in He buffer gas at 0.35 Torr and 295 K for reactions of Sr{sup +} and Rb{sup +} with CH{sub 3}F, CH{sub 3}Cl, N{sub 2}O, CO{sub 2}, CS{sub 2}, SF{sub 6}, D{sub 2}O and NH{sub 3}. Rb{sup +} (s{sup 0}) is seen to be quite inert with these molecules and reacts either slowly by molecule addition or not at all, while Sr{sup +} (s{sup 1}) is much more reactive with all these 8 molecules, especially with CH{sub 3}F, CH{sub 3}Cl, N{sub 2}O and SF{sub 6}. Sr{sup +} reacts with CH{sub 3}F and SF{sub 6} by F-atom transfer, with CH{sub 3}Cl by Cl-atom transfer and with N{sub 2}O by O-atom transfer, and the reaction rate coefficients are all quite high, k {>=} 1.4 x 10{sup -11} cm{sup 3} molecules{sup -1} s{sup -1}. The extreme differences in reactivity with CH{sub 3}F, SF{sub 6}, CH{sub 3}Cl and N{sub 2}O provide a chemical basis for the separation of isobaric interferences of {sup 87}Rb{sup +} and {sup 87}Sr{sup +} often encountered in ICP-MS. Among these four molecules, SF{sub 6} exhibits the largest difference in reactivity, almost a factor of 10{sup 4}, and so is identified as the kinetically recommended reagent for the chemical resolution of the isobaric interference of {sup 87}Rb{sup +} and {sup 87}Sr{sup +}.

Les Néandertaliens étaient-ils essentiellement carnivores ? Résultats préliminaires sur les teneurs en Sr et en Ba de la paléobiocénose mammalienne de Saint-CésaireWere Neandertalians essentially carnivores? Sr and Ba preliminary results of the mammalian palaeobiocoenosis of Saint-Césaire

Science.gov (United States)

Balter, Vincent; Person, Alain; Labourdette, Nathalie; Drucker, Dorothée; Renard, Maurice; Vandermeersch, Bernard

2001-01-01

Strontium-calcium (Sr/Ca) and barium-calcium (Ba/Ca) ratios are reduced constantly between diet and bioapatite in mammal organisms. This phenomenon leads to a reduction in the Sr/Ca and Ba/Ca ratios at higher trophic level in predator-prey mammalian communities, and is applied here to the reconstruction of a castelperronian food web, which includes a Neanderthal specimen. Adapted chemical pretreatment allows to isolate bioapatite from diagenetic compounds for analysis of Ca, Sr and Ba. Sr/Ca and Ba/Ca results of the fauna are consistent with trophic predictions. Initial results for the Neandertal suggest that he was mostly carnivorous. Distribution of Ba/Ca values of bones of herbivorous taxa reveals that ruminant animals can be distinguished from non-ruminants. The biosegregation model predicts that the diet of the Neandertal was composed by about 97 % in weight of meat with a weak contribution of vegetable or fish, and that the association of fish and plant is excluded in any proportion.

Luminescent properties of Sr{sub 2.5-3x/2}Ba{sub 0.5}Sm{sub x}AlO{sub 4}F oxyfluorides

Energy Technology Data Exchange (ETDEWEB)

Park, Sangmoon, E-mail: spark@silla.ac.kr [Department of Engineering in Energy and Applied Chemistry, Silla University, Busan 617-736 (Korea, Republic of)

2012-04-15

Effective orange Sm{sup 3+}-doped Sr{sub 2.5}Ba{sub 0.5}AlO{sub 4}F phosphors excited at 254 and 408 nm excitation were prepared by the solid-state method. The excitation and emission spectra of Sr{sub 2.5-3x/2}Ba{sub 0.5}Sm{sub x}AlO{sub 4}F and Sr{sub 2.5-3x/2}Ba{sub 0.5}Sm{sub x}AlO{sub 4-{alpha}}F{sub 1-{delta}} (x=0.001{approx}0.1) based on photoluminescence spectroscopy are investigated. The defects in anion-deficient Sr{sub 2.5-3x/2}Ba{sub 0.5}Sm{sub x}AlO{sub 4-{alpha}}F{sub 1-{delta}} (x=0.001, 0.01) are monitored by broad-band photoluminescence emission centered near 480 nm along with the orange emission transitions of Sm{sup 3+}. CIE values and relative luminescent intensities of Sr{sub 2.5-3x/2}Ba{sub 0.5}Sm{sub x}AlO{sub 4}F and Sr{sub 2.5-3x/2}Ba{sub 0.5}Sm{sub x}AlO{sub 4-{alpha}}F{sub 1-{delta}} by changing the Sm{sup 3+} content (x=0.001{approx}0.1) are discussed. - Highlights: Black-Right-Pointing-Pointer Under the excitation of 408 nm competent orange emitting Sr{sub 2.5-3x/2}Ba{sub 0.5}Sm{sub x}AlO{sub 4}F phosphor is initiated. Black-Right-Pointing-Pointer Sm{sup 3+}-activated oxyfluoride phosphor is quite effective to prepare white-emitting light for near-UV LED applications. Black-Right-Pointing-Pointer Defects could be visibly created in the Sr{sub 2.5-3x/2}Ba{sub 0.5}Sm{sub x}Al O{sub 4}F host lattices when Sm{sup 3+} ions are doped less than 5 mol %. Black-Right-Pointing-Pointer The gradual substitution of Sm{sup 3+} contents in oxyfluoride hosts is amenable to change CIE values and desired emitting intensity.

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

International Nuclear Information System (INIS)

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

2007-01-01

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

Rb-Sr measurements on metamorphic rocks from the Barro Alto Complex, Goias, Brazil

International Nuclear Information System (INIS)

Fuck, R.A.; Neves, B.B.B.; Cordani, U.G.; Kawashita, K.

1988-01-01

The Barro Alto Complex comprises a highly deformed and metamorphosed association of plutonic, volcanic, and sedimentary rocks exposed in a 150 x 25 Km boomerang-like strip in Central Goias, Brazil. It is the southernmost tip of an extensive yet discontinuous belt of granulite and amphibolite facies metamorphic rocks which include the Niquelandia and Cana Brava complexes to the north. Two rock associations are distinguished within the granulite belt. The first one comprises a sequence of fine-grained mafic granulite, hypersthene-quartz-feldspar granulite, garnet quartzite, sillimanite-garnet-cordierite gneiss, calc-silicate rock, and magnetite-rich iron formation. The second association comprises medium-to coarse-grained mafic rocks. The medium-grade rocks of the western/northern portion (Barro Alto Complex) comprise both layered mafic rocks and a volcanic-sedimentary sequence, deformed and metamorphosed under amphibolite facies conditions. The fine-grained amphibolite form the basal part of the Juscelandia meta volcanic-sedimentary sequence. A geochronologic investigation by the Rb-Sr method has been carried out mainly on felsic rocks from the granulite belt and gneisses of the Juscelandia sequence. The analytical results for the Juscelandia sequence are presented. Isotope results for rocks from different outcrops along the gneiss layer near Juscelandia are also presented. In conclusion, Rb-Sr isotope measurements suggest that the Barro Alto rocks have undergone at least one important metamorphic event during Middle Proterozoic times, around 1300 Ma ago. During that event volcanic and sedimentary rocks of the Juscelandia sequence, as well as the underlying gabbro-anorthosite layered complex, underwent deformation and recrystallization under amphibolite facies conditions. (author)

Proterozoic biotite Rb-Sr dates in the northwestern part of the Yilgarn Craton, Western Australia

International Nuclear Information System (INIS)

Libby, W.G.; De Laeter, J.R.; Armstrong, R.A.

1999-01-01

Rb-Sr dating of biotite in the northwestern corner of the Yilgarn Craton identified four areas with distinctive age ranges. Biotite in the northwestern area, which includes the Narryer Terrane and part of the Murchison Terrane, yields reset Rb-Sr dates of ca 1650 Ma. In the western area, along the margin of the craton, biotite has been reset to 629 Ma. Eastward of these areas, mainly in the Murchison Terrane, the modal biotite date is near 2450 Ma, though because of a skewed distribution the mean date is closer to 2300 Ma. Dates in a transition zone between the western and eastern areas range broadly between 2000 and 1000 Ma, averaging about 1775 Ma. The western area and the transition zone are continuous with analogous areas south of the limits of the present study. The 1650 Ma dates in the northwestern area are probably related to plutonic and tectonic activity of similar age in the Gascoyne Province to the north. They may represent cooling after thermal resetting during tectonic loading by southward thrust-stacking of slices of Narryer Terrane and allochthonous Palaeoproterozoic volcanic arc and back arc rocks during the Capricorn Orogeny. This episode of crustal shortening resulted from the collision of the Yilgarn and Pilbara Cratons to form the West Australian Craton. The dates reflect cooling associated with subsequent erosion-induced rebound. The 2450 Ma biotite dates of the eastern area are similar to biotite dates found over most of the Yilgarn Craton and represent a background upon which the later dates have been superimposed. The origin of dates in the western area is unknown but may be related to an associated dolerite dyke swarm or to possible thrusting from the west. There is some evidence of minor later intrusion of felsic hypabyssal rock between 2000 and 2200 Ma and localised shearing in the Narryer area at about 1350 to 1400 Ma. One small area near Yalgoo with biotite Rb-Sr dates near 2200 Ma may be co genetic with the Muggamurra Swarm of dolerite

Ba{sub y}Sr{sub 1−y}TiO{sub 3} buffer layers for strain tuning of infinite-layer Sr{sub 1−x}La{sub x}CuO{sub 2} thin films

Energy Technology Data Exchange (ETDEWEB)

Sakuma, Keita, E-mail: sakuma.keita@d.mbox.nagoya-u.ac.jp; Ito, Masataka; He, Yilun; Hajiri, Tetsuya; Ueda, Kenji; Asano, Hidefumi

2016-08-01

We report on the precise tuning of lattice strain in an infinite-layer electron-doped high temperature superconductor Sr{sub 1−x}La{sub x}CuO{sub 2} (SLCO; a{sub SLCO} = 0.3949 nm for x = 0.1), which is a perovskite-related oxide, using perovskite BaTiO{sub 3}–SrTiO{sub 3} (BSTO; Ba{sub y}Sr{sub 1−y}TiO{sub 3}) buffer layers. The BSTO buffer layers formed on (001) (La{sub 0.18}Sr{sub 0.82})(Al{sub 0.59}Ta{sub 0.41})O{sub 3} substrates by magnetron sputtering were fully relaxed with high crystalline quality due to high oxygen partial pressure deposition and post annealing at 950 °C. The lattice constants of the BSTO buffer layers could be controlled in the range of 0.3926–0.3973 nm by changing the Ba content (y = 0.2–0.7). These BSTO buffer layers allow coherent growth of SLCO thin films, and a clear dependence of the superconducting transition temperature on the lattice strain was observed. The fabrication of these BSTO/superconductor heterostructures may provide novel devices composed of functional perovskite thin films, in addition to a general approach for the precise control of lattice strain in functional perovskite thin films. - Highlights: • Ba{sub y}Sr{sub 1−y}TiO{sub 3} buffer layers were developed for the strain tuning of perovskite-related oxides. • Strain effect in Sr{sub 1−x}La{sub x}CuO{sub 2} was investigated by using Ba{sub y}Sr{sub 1−y}TiO{sub 3} buffer layers. • Ba{sub y}Sr{sub 1−y}TiO{sub 3} buffer layers can be used to tune the strain in other perovskite oxides.

Precambrain Rb-Sr isochron ages from the crystalline complexes of inner Forsblads Fjord, East Greenland fold belt

International Nuclear Information System (INIS)

Rex, D.C.; Gledhill, A.R.; Higgins, A.K.

1977-01-01

Several collections of samples were made from crystalline units in inner Forsblads Fjord in 1974. Results of whole rock Rb-Sr analyses on two of these collections are presented, and give an Archaean age for banded gneisses and a middle Proterozoic age for quartzitic metasediments. These ages confirm the occurence of major Precambrian complexes within the East Greenland Caledonian fold belt. (author)

Lanthanide doped BaTiO{sub 3}−SrTiO{sub 3} solid-solution phosphors: Structure, optical spectroscopy and upconverted temperature sensing behavior

Energy Technology Data Exchange (ETDEWEB)

Chen, Daqin, E-mail: dqchen@hdu.edu.cn; Xu, Wei; Zhou, Yang; Chen, Yan, E-mail: chenyan@hdu.edu.cn

2016-08-15

Lanthanide doped Ba{sub 1-x}Sr{sub x}TiO{sub 3} (x = 0–1) solid-solution phosphors were successfully prepared by a conventional solid-state reaction. Using Eu{sup 3+} dopants as the structural probe, the variation of {sup 5}D{sub 0} → {sup 7}F{sub 2}/{sup 5}D{sub 0} → {sup 7}F{sub 1} emission intensity ratio with increase of Eu{sup 3+} content and the excitation-wavelength-dependent luminescence in the Ba{sub 1-x}Sr{sub x}TiO{sub 3} sample were demonstrated to be originated from the different emission behaviors of Eu{sup 3+} in Ba{sup 2+}/Sr{sup 2+} site and Ti{sup 4+} site. Furthermore, upconversion luminescence for the Yb{sup 3+}/Er{sup 3+} co-doped Ba{sub 1-x}Sr{sub x}TiO{sub 3} samples were investigated, and it was found that the emission intensity of Yb{sup 3+}/Er{sup 3+}: Ba{sub 0.5}Sr{sub 0.5}TiO{sub 3} phosphor was about 5 and 2 times as high as those of Yb{sup 3+}/Er{sup 3+}: BaTiO{sub 3} and Yb{sup 3+}/Er{sup 3+}: SrTiO{sub 3} ones. Using the investigated Yb{sup 3+}/Er{sup 3+}: Ba{sub 0.5}Sr{sub 0.5}TiO{sub 3} solid-solution as the optical thermometric medium, the temperature sensitivity was determined to be 0.76% K{sup −1} at the temperature of 610 K based on the temperature-dependent fluorescence intensity ratio of the thermally coupled {sup 2}H{sub 11/2} and {sup 4}S{sub 3/2} emitting-states of Er{sup 3+}. - Highlights: • Lanthanide doped Ba{sub 1-x}Sr{sub x}TiO{sub 3} (x = 0–1) solid-solutions were fabricated. • Excitation-wavelength-dependent Eu{sup 3+} emissions were recorded. • Enhanced Er{sup 3+} luminescence was realized by partial substitution of Ba{sup 2+} by Sr{sup 2+}. • T-sensitive emissions of two Er{sup 3+} thermally coupled states were observed. • The upconversion phosphor exhibited a high sensitivity of 0.76% K{sup −1}.

Chemical, structural and magnetic studies of new mono- and diphosphates appearing in ternary diagrams AO-CuO-(P2O5); A= Mg, Ca, Sr, Ba

International Nuclear Information System (INIS)

Moqine, A.

1990-01-01

A systematic study of mixed mono- and diphosphates of AO-CuO-(P 2 O 5 ) systems (A= Mg, Ca, Sr, Ba) has been carried out. This study showed up, on one hand, continuous and wide ranges in magnesium system and on the other hand, eight new phases in the other systems: Sr sub 18 Cu sub 3 (PO 4 ) 14 , A 2 Cu (PO 4 ) 2 , (A= Sr, Ba), Sr 3 Cu 3 (PO 4 ) 4 , BaCu 2 (PO 4 ) 2 and ACu(P 2 O 7 ) (A= Ca, Sr, Ba). The crystalline structures of SrCu(P 2 O 7 ), BaCu(P 2 O 7 ),Sr 3 Cu 3 (PO 4 ) 4 and BaCu 2 (PO 4 ) 2 phosphates have been described and discussed. The first compound presents a Tunnel structure and the three others have Foliation structures. The magnetic behaviours of some Cu sup 2+ ions phos-phates have been correlated to their crystalline structures. The experimental data have been parametered using the Ising model and/or the Heisenberg model. In this work, three Ising theoretical models have been developed. This magnetic study showed up new chains of antiferro- or ferrimagnetic Cu sup 2+ ions. 59 figs., 32 tabs., 113 refs. (author)

Microstructure investigations of Ba-Sr mixed ferrites, using SEM technique

International Nuclear Information System (INIS)

Amighian, J.; Mozaffari, M.

1996-01-01

A series of isotropic Ba-Sr mixed ferrites were prepared, using a conventional dry technique. The starting materials were hematite by product of Isfahan steel factory, strontium carbonate from Merck company and barium carbonate obtained from local source. The principle phase of the samples was chosen to have a composition in the form of (BaO) sub 1-x (SrO) sub x nFe sub 2 O sub 3, in which x varied between 0 to l and n was varied between 5 to 6. The raw materials were thoroughly mixed and fired in an electrical furnace for 2 hours. They were then milled in an vibrating ball mill, in which the optimum milling time for each sample was obtained. After annealing at 750 degree C, the powders were compacted in a cylindrical die under 5 tons/cm sup 2. The compacts were then mixed with a binder and sintered in air for 10 minutes at their optimum temperatures. Using SEM technique, the microstructure of the samples were investigated. Using a permeameter, the coercive force Hc and remanent induction Br were measured. The microstructures obtained from SEM technique can be used to control the sintering stage in ferrite fabrication

Influences of Indium Tin Oxide Layer on the Properties of RF Magnetron-Sputtered (BaSr)TiO3 Thin Films on Indium Tin Oxide-Coated Glass Substrate

Science.gov (United States)

Kim, Tae Song; Oh, Myung Hwan; Kim, Chong Hee

1993-06-01

Nearly stoichiometric ((Ba+Sr)/Ti=1.08-1.09) and optically transparent (BaSr)TiO3 thin films were deposited on an indium tin oxide (ITO)-coated glass substrate by means of rf magnetron sputtering for their application to the insulating layer of an electroluminescent flat panel display. The influence of the ITO layer on the properties of (BaSr)TiO3 thin films deposited on the ITO-coated substrate was investigated. The ITO layer did not affect the crystallographic orientation of (BaSr)TiO3 thin film, but enhanced the grain growth. Another effect of the ITO layer on (BaSr)TiO3 thin films was the interdiffusion phenomenon, which was studied by means of secondary ion mass spectrometry (SIMS). As the substrate temperature increased, interdiffusion intensified at the interface not only between the grown film and ITO layer but also between the ITO layer and base glass substrate. The refractive index (nf) of (BaSr)TiO3 thin film deposited on a bare glass substrate was 2.138-2.286, as a function of substrate temperature.

Dielectric and Energy Storage Properties of Ba0.65Sr0.35TiO3 Ceramics Modified by BiNbO4

Science.gov (United States)

Zheng, Yi; Zhang, Jihua; Wei, Meng; Dong, Xiangxiang; Huang, Jiapeng; Wu, Kaituo; Chen, Hongwei

2018-02-01

(1 - x) (Ba0.65Sr0.35TiO3)-xBiNbO4 (x = 0.0-0.15) ceramic were prepared by solid-state reaction method. The phase composition, microstructure, dielectric properties, polarization-electric field, breakdown strength and energy storage behaviors for the BiNbO4-modified Ba0.65Sr0.35TiO3 ceramics were investigated. With the addition of BiNbO4, the remnant polarization and saturation polarization decreased and the nonlinearity was suppressed. When x = 0.07, the maximum recoverable energy storage achieved was 0.5 J/cm3, 1.5 times that of un-doped Ba0.65Sr0.35TiO3 ceramics, with an efficiency of 96.89% and a breakdown electric field reaching 15.3 kV/mm. Therefore, BiNbO4 doping could improve the energy storage properties of Ba0.65Sr0.35TiO3 for high-energy pulse capacitor application.

Synthesis and luminescence properties of glass ceramics containing MSiO3:Eu2+ (M=Ca, Sr, Ba) phosphors for white LED

International Nuclear Information System (INIS)

Cui Zhiguang; Jia Guohua; Deng Degang; Hua Youjie; Zhao Shilong; Huang Lihui; Wang Huanping; Ma Hongping; Xu Shiqing

2012-01-01

Eu 2+ doped silicate glasses were prepared of the system 52SiO 2 -48MO: xEu 2+ (in molar ratio, M=Ca, Sr, Ba; x=1, 3, 5, 7, 9) by a high temperature melt-quenching method in a reducing atmosphere. Glass ceramics containing MSiO 3 :Eu 2+ (M=Ca, Sr, Ba) nano-phosphors were obtained after the heat treatment of the glass samples. The excitation, emission spectra and lifetime decay curves of 4f 6 5d 1 →4f 7 of Eu 2+ were measured and interpreted with respect to their crystal structures and multi-site occupations of divalent europium in the hosts. Their excitation bands mainly extend from 450 to 250 nm, which is adaptable to the main emission region of the UV LED chip. With UV light excitation, the Eu 2+ emission in CaSiO 3 , SrSiO 3 and BaSiO 3 shows blue, green and yellow colors centered at 440, 505 and 555 nm, respectively. The critical Eu 2+ concentration was studied and determined to be x=5 for both CaSiO 3 and SrSiO 3 and x=7 for BaSiO 3 phosphors. The results show that the Eu 2+ doped glass ceramic phosphors containing MSiO 3 (M=Ca, Sr, Ba) nano-crystals can be used as potential matrix materials for a high power white LED pumped by the UV LED chip. - Highlights: → Glass ceramic containing MSiO 3 :Eu 2+ (M=Ca, Sr, Ba) phosphors prepared. → Derived phosphors emit intensively blue, green and yellow colors. → Their luminescence properties and crystal structures have been investigated. → Concentration quenching effects observed and analyzed. → Potential application for UV chip exciting white LED evaluated.

The influences of mole composition of strontium (x) on properties of barium strontium titanate (Ba{sub 1−x}Sr{sub x}TiO{sub 3}) prepared by solid state reaction method

Energy Technology Data Exchange (ETDEWEB)

Sandi, Dianisa Khoirum; Supriyanto, Agus; Iriani, Yofentina, E-mail: yopen-2005@yahoo.com [Physics Department, Faculty of Mathematics and Natural Science, Sebelas Maret University (Indonesia); Jamaluddin, Anif [Physics Department, Faculty of Teacher Training and Education, Sebelas Maret University (Indonesia)

2016-02-08

Barium Strontium Titanate (Ba{sub 1-x}Sr{sub x}TiO{sub 3}) or BST was prepared by solid state reaction method. Raw materials are BaCO{sub 3}, SrCO{sub 3}, and TiO{sub 2}. Those materials are mixed for 8 h, pressed, and sintered at temperature 1200°C for 2 h. Mole composition of Sr (x) was varied to study its influences on structural, morphological, and electrical properties of BST. Variation of (x) are x = 0; x = 0.1; and x = 0.5. XRD patterns showed a single phase of BST, which mean that mixture of raw materials was homogenous. Crystal structure was influenced by x. BaTiO{sub 3} and Ba{sub 0.9}Ti{sub 0.1}TiO{sub 3} have tetragonal crystal structure, while Ba{sub 0.5}Sr{sub 0.5}TiO{sub 3} is cubic. The diffraction angle shifted to right side (angle larger) as the increases of x. Crystalline size of BaTiO{sub 3}, Ba{sub 0.9}Sr{sub 0.1}TiO{sub 3}, and Ba{sub 0.5}Sr{sub 0.5}TiO{sub 3} are 38.13 nm; 38.62 nm; and 37.13 nm, respectively. SEM images showed that there are still of pores which were influenced by x. Ba{sub 0.9}Sr{sub 0.1}TiO{sub 3} has densest surface (pores are few and small in size). Sawyer Tower circuit showed that BaTiO{sub 3} and Ba{sub 0.9}Sr{sub 0.1} TiO{sub 3} is ferroelectric, while Ba{sub 0.5}Sr{sub 0.5}TiO{sub 3} is paraelectric. The dielectric constants of BaTiO{sub 3}, Ba{sub 0.9}Sr{sub 0.1}TiO{sub 3} and Ba{sub 0.5}Sr{sub 0.5}TiO{sub 3} at frequency of 1 KHz are 156; 196; and 83, respectively. Ba{sub 0.9}Sr{sub 0.1}TiO{sub 3} has relatively highest dielectric constant. It is considered that Ba{sub 0.9}Sr{sub 0.1}TiO{sub 3} has densest surface.

Observation of forbidden (E2) lines in the ultraviolet spectra of Ca II, Sr II, and Ba II by inductively coupled plasma emission spectroscopy

International Nuclear Information System (INIS)

Doidge, Peter S.

2013-01-01

Forbidden (electric quadrupole, E2) transitions of the type ns 2 S 1/2 –nd 2 D 3/2 and ns 2 S 1/2 –nd 2 D 5/2 in the ultraviolet spectra of singly ionized Ca, Sr, and Ba (with n = 4, 5 or 6 for Ca, Sr, and Ba, respectively) have been observed in the emission spectrum of an inductively coupled argon plasma. Wavelengths and wavenumbers of the six lines are reported and the values are in good agreement with those expected from literature data for the energy levels involved. - Highlights: • Wavelengths measured using commercially available ICP emission spectrometer • First wavelength and wavenumber measurements of some E2 lines of Ba +, Ca +, Sr + • Evidence for small plasma shifts in the wavenumbers of Ba + and Sr +

Investigations of the solid solution in the system SrI/sub 2/-BaI/sub 2/ at ambient pressures and at 2. 0 GPa

Energy Technology Data Exchange (ETDEWEB)

Beck, H.P.; Holley, C.; Limmer, A. (Erlangen-Nuernberg Univ., Erlangen (Germany, F.R.). Inst. fuer Anorganische Chemie)

1984-09-01

The P,T,x-diagram of the system SrI/sub 2/-BaI/sub 2/ has been investigated at ambient pressures and at 2.0 GPa. The amount of solid solution in the four structure types occuring in this system (SrI/sub 2/- or PbCl/sub 2/-ZrAs/sub 2/-type with SrI/sub 2/ and PbCl/sub 2/- or anti-Fe/sub 2/P-type with BaI/sub 2/) differs considerably. Structural geometries belonging to the same PbCl/sub 2/ structure family show marked differences in their toleration to cation substitution. Solid solution is especially pronounced in the BaI/sub 2/-rich phases which incorporate up to 60 mol-% Sr/sup 2 +/ in the high pressure phase of BaI/sub 2/.

Interface Control of Ferroelectricity in an SrRuO3 /BaTiO3 /SrRuO3 Capacitor and its Critical Thickness.

Science.gov (United States)

Shin, Yeong Jae; Kim, Yoonkoo; Kang, Sung-Jin; Nahm, Ho-Hyun; Murugavel, Pattukkannu; Kim, Jeong Rae; Cho, Myung Rae; Wang, Lingfei; Yang, Sang Mo; Yoon, Jong-Gul; Chung, Jin-Seok; Kim, Miyoung; Zhou, Hua; Chang, Seo Hyoung; Noh, Tae Won

2017-05-01

The atomic-scale synthesis of artificial oxide heterostructures offers new opportunities to create novel states that do not occur in nature. The main challenge related to synthesizing these structures is obtaining atomically sharp interfaces with designed termination sequences. In this study, it is demonstrated that the oxygen pressure (PO2) during growth plays an important role in controlling the interfacial terminations of SrRuO 3 /BaTiO 3 /SrRuO 3 (SRO/BTO/SRO) ferroelectric (FE) capacitors. The SRO/BTO/SRO heterostructures are grown by a pulsed laser deposition method. The top SRO/BTO interface, grown at high PO2 (around 150 mTorr), usually exhibits a mixture of RuO 2 -BaO and SrO-TiO 2 terminations. By reducing PO2, the authors obtain atomically sharp SRO/BTO top interfaces with uniform SrO-TiO 2 termination. Using capacitor devices with symmetric and uniform interfacial termination, it is demonstrated for the first time that the FE critical thickness can reach the theoretical limit of 3.5 unit cells. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Age of meta-rhyolite of Marata sequence, Araxa Group, Goias: geochronology study by U-Pb in zircon, Rb-Sr and Sm-Nd methods

International Nuclear Information System (INIS)

Pimentel, M.M.; Heaman, L.; Fuck, R.A.

1992-01-01

U-Pb isotopic analyses in eight zircon fractions separated from a meta-rhyolite sample of the Marata sequence (Araxa Group, Goias) are presented. Two morphologically distinct zircon populations were identified: stubby prismatic crystals (width:length of 1:2 to 1:3) in which core-overgrowth relationships are observed; long prismatic crystals (needles) with width:length ratios of ca. 1:10. Analyses performed on group zircons indicated the presence of a ca. 2.0 Ga. old inherited component. Analyses of group zircons plot very close to the concordia and yield an upper intercepts age of 794 ± 10 Ma for the crystallization of the volcanic protolith. The study was complemented with whole-rock isotopic analyses by the Rb-Sr and Sm-Nd methods. Rb-Sr isochron obtained with samples from two different outcrops gave data of 829 ± 82 Ma (initial 87 Sr/ 86 Sr of 0.7057 ± 0.0157) and 691 ± 30 Ma (initial 87 Sr/ 86 Sr of 0.7337 ± 0.0034). The latter reflects a later Sr-isotopic re-homogenization episode, possibly associated with the intense deformation and metamorphism suffered by these rocks. Sm-Nd isotopic analyses on three samples reveal EN d (T) (T =794 Ma) values in the range of -6.1 to -9.5 which indicate the presence of older (early Proterozoic) crustal Nd. This is consistent with the inheritance pattern shown in the U-Pb isotopic results. (author)

Rb-Sr geochronology from Barro Alto Complex, Goias: metamorphism evidence of high degree and continental collision around 1300 Ma ago in Central Brazil

International Nuclear Information System (INIS)

Fuck, R.A.; Neves, B.B.B.; Cordani, U.G.; Kawashita, K.

1989-01-01

Rb-Sr geochronologic investigation carried out on rocks from the Barro Alto Complex, Goias, yielded iso chronic ages of 1266 +- 17 Ma, for felsic rocks from the granulite belt and 1330 +- 67 Ma, for gneisses belonging to the Juscelandia Sequence. Rb-Sr isotope measurements suggest that Barro Alto rocks have undergone an important metamorphic event during middle Proterozoic times, around 1300 Ma ago. During that event, volcanic and sedimentary rocks of Juscelandia Sequence, as well as the underlying gabbros-anorthosite layered complex, underwent deformation and recrystallization under amphibolite facies conditions. Deformation and metamorphism took place during the collision of two continental blocks, which resulted in a southeastward directed thrust complex, allowing the exposure of granulite slices from the middle-lower crust of the overthrusted block. (author)

Relativistic calculations of the fine-structure intervals of the ns2np2P terms and the ionization energies of the Ca-, Sr-and Ba- ions

International Nuclear Information System (INIS)

Wijesundera, W.P.; Vosko, S.H.; Parpia, F.A.

1996-01-01

We report new calculations of the energy differences between the ns 1/2 2 np 1/2 and ns 1/2 2 np 3/2 levels of the Ca - , Sr - and Ba - ions; here n 4, 5 and 6 for Ca - , Sr - and Ba - , respectively. The electron affinities of Ca, Ba and Sr have also been calculated. All estimates were obtained by performing a series of multiconfiguration Dirac-Fock calculations for the neutral atoms and their anions. Correlations among valence electrons in both the ground and excited states were included in these calculations. Our estimate of the fine structure of the ground state of Sr - is in good agreement with recent measurements. Our estimates of the electron affinities of Ca, Sr and Ba are in reasonable agreement with experiment. (author)

Rb-Sr ages of the biotite and muscovite of the Himalayas, eastern Nepal

International Nuclear Information System (INIS)

Kai, Kunio

1981-01-01

Rb-Sr ages of biotite from the southern flank of Mt. Everest, eastern Nepal, range from 14.1 to 1.3 m.y., the youngest biotite coexists with muscovite of 7.3 m.y. These different ages for different samples reflect the difference in cooling history related to the uplift of the Himalayas. The biotite ages decrease with increasing distance from the high mountain range, suggesting that the high range, i.e., the northern area, was uplifted earlier than the southern area. The relationship between the ages and altitutes of sampling sites indicates that the uplift rate of the northern area was 0.60 mm/yr. (author)

Surface morphology analysis of nanostructured (Ba sub x , Sr sub 1 sub - sub x)TiO sub 3 thin films using fractal method

CERN Document Server

Hong, K J; Choi, W K; Cho, J C

2003-01-01

Based on the fractal theory, this paper uses scanning electron microscopy images to investigate the roughness characteristics of nanostructured (Ba Sr)TiO sub 3 thin films by sol-gel methods. The percentage grain area, surface fractal dimensions and 3D image are evaluated using image analysis methods. The thickness of the (Ba Sr)TiO sub 3 thin films was 260-280 nm. The surface fractal dimensions were increased with strontium doping, and grain area, were decreased with it. The fractal dimension and the grain areas of the (Ba sub 0 sub . sub 7 Sr sub 0 sub . sub 3)TiO sub 3 thin films were 1.81 and 81%. Based on the image analysis, the roughness height of 3D images as 256 levels was about 3 nm and its distribution was about 35-40% for the (Ba sub 0 sub . sub 8 Sr sub 0 sub . sub 2)TiO sub 3 and (Ba sub 0 sub . sub 7 Sr sub 0 sub . sub 3)TiO sub 3 thin films. The roughness height of the BST thin films was distributed from 35% to 40% ranging from 3 nm to 4 nm. By increasing the strontium doping, the roughness hei...

Band-gap tuning and magnetic properties of heterovalent ions (Ba, Sr and Ca) substituted BiFeO_3 nanoparticles

International Nuclear Information System (INIS)

Chauhan, Sunil; Kumar, Manoj; Katyal, S. C.

2016-01-01

A Comparative study of heterovalent Ba, Sr and Ca ions substitution on the structural, vibrational, optical and magnetic properties of BiFeO_3 nanoparticles was carried out. The distorted rhombohedral structure was confirmed from both X-ray diffraction and Raman spectroscopy techniques in pure BiFeO_3 and Bi_0_._8_5A_0_._1_5FeO_3 (A= Ba, Sr and Ca) samples. UV-Visible spectroscopy results show that the band-gap of BiFeO_3 nanoparticles can be tuned by heterovalent ions substitution from 2.12 eV for BiFeO_3 to 2.10, 2.06 and 2.03 eV for Ca, Sr and Ba substituted BiFeO_3 nanoparticles respectively. The magnetic measurements indicate enhancement in magnetization for heterovalent A"2"+ substituted BiFeO_3 samples and the magnetization increases with increase of ionic radius of the substituted ions.

Study of photo-stimulated luminescence in Ba0.95M0.05FBr:Eu2+ (M = Sr, Ca) powder

International Nuclear Information System (INIS)

Zhou Yingxue; Wang Dongsheng; Zhang Xinyi

2001-01-01

The luminescence centered at about 390 nm due to 4f 6 5d→4f 7 transition of Eu 2+ can be observed without X-ray or UV-light pre-irradiation for BaFBr:Eu 2+ , Ba 0.95 Sr 0.05 FBr:Eu 2+ and Ba 0.95 Ca 0.05 FBr:Eu 2+ powder samples which can be excited by light with wave length longer than 400 nm. It could be attributed to F centers which are formed in the preparation of samples. There are two broad bands in the photo-stimulated spectra. One peaked at 535 nm results from the excitation of electrons at F(F - ) center, and the other at 708 nm might be originated from the electron excitation of F(Br - ) center or F(Br - ) accumulators. If the Ba 2+ (ion's radius equals to 0.135 nm) in the samples were replaced by about 50% mol. of Sr 2+ (ion's radius equals to 0.113 nm) or Ca 2+ (ion's radius equals to 0.099 nm), the intensities of 535 nm and 708 nm bands decrease with the decreasing of ion radius. On the other hand, the shoulders at 580 nm and 650 nm or 575 nm and 645 nm can appear. In absorption spectra of 50-400 nm range, one can observe the red-shift of 79 nm, 83 nm peaks and new absorption peaks. It means that the new color centers: F(F - , Sr 2+ ), F(br - , Sr 2+ ) or F(F - , Ca 2+ ), F(br - , Ca 2+ ) are formed, when Ba 2+ were replaced with Sr 2+ or Ca 2+ in samples. It corresponds to the shoulders in photo-stimulated spectra

Perovskite phases in the systems AO-SE/sub 2/O/sub 3/-UO/sub 2,x/ with A=alkaline earth metal and SE=rare earths, La, and Y. IX. The systems Ba/sub 2/SrUO/sub 6/-Ba/sub 2/Gd/sub 0. 67/UO/sub 6/ and Ba/sub 2/SrUO/sub 6/-Ba/sub 2/Y/sub 0. 67/UO/sub 6/

Energy Technology Data Exchange (ETDEWEB)

Kemmler-Sack, S; Seemann, I [Tuebingen Univ. (F.R. Germany). Inst. fuer Anorganische Chemie I

1976-07-01

The ordered perovskite Ba/sub 2/SrUO/sub 6/ forms a solid solution series with Ba/sub 2/Gdsub(0.67)UO/sub 6/ and Ba/sub 2/Ysub(0.67)UO/sub 6/ respectively. The deviations from the ideal behaviour are studied by X-ray, diffuse reflectance and vibrational methods.

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

International Nuclear Information System (INIS)

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

2003-01-01

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

Analysis of (Ba,Ca,Sr){sub 3}MgSi{sub 2}O{sub 8}:Eu{sup 2+}, Mn{sup 2+} phosphors for application in solid state lighting

Energy Technology Data Exchange (ETDEWEB)

Han, J.K. [University of California, San Diego, Materials Science and Engineering Program, La Jolla, CA 92093 (United States); Piqutte, A.; Hannah, M.E. [OSRAM SYLVANIA Central Research, 71 Cherry Hill Drive Beverly, MA 01915 (United States); Hirata, G.A. [Centro de Nanociencias y Nanotecnolgía, Universidad Nacional Autónoma de México, Km. 107 Carretera Tijuana-Ensenada Apdo, Ensenada MX CP 22860 (Mexico); Talbot, J.B. [University of California, San Diego, Materials Science and Engineering Program, La Jolla, CA 92093 (United States); University of California, San Diego, Department of Nanoengineering, La Jolla, CA 92093 (United States); Mishra, K.C. [OSRAM SYLVANIA Central Research, 71 Cherry Hill Drive Beverly, MA 01915 (United States); McKittrick, J., E-mail: jmckittrick@ucsd.edu [University of California, San Diego, Materials Science and Engineering Program, La Jolla, CA 92093 (United States); University of California, San Diego, Department of Mechanical and Aerospace Engineering, La Jolla, CA 92093 (United States)

2014-04-15

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

Structure, luminescence and thermal quenching properties of Eu doped Sr{sub 2−x}Ba{sub x}Si{sub 5}N{sub 8} red phosphors

Energy Technology Data Exchange (ETDEWEB)

Liu, Y.H.; Chen, L.; Zhou, X.F.; Liu, R.H., E-mail: griremlrh@126.com; Zhuang, W.D.

2017-02-15

Eu{sup 2+} doped Sr{sub 2-x}Ba{sub x}Si{sub 5}N{sub 8} phosphors were synthesized at 1610 ℃ for 4 h via the solid-state reaction method. The XRD results confirm that the complete solid solutions are formed. With the increase of x, the emission spectra show an obvious blue-shift from 610 nm to 585 nm under the excitation of 460 nm. The color tone can be tuned from yellow to red. The corresponding mechanism for the blue-shift of peak-wavelength is studied in detail. The results of decomposed Gaussian spectra and fluorescence lifetime show that the local coordination structure surrounding activator ions changes with increasing x value. It is found that the probability of Eu occupying Sr1 and Sr2 site is dependent on Ba/Sr ratio. The variation of thermal quenching properties and the corresponding mechanism is discussed in detail. The results indicate that Eu{sup 2+} doped Sr{sub 2-x}Ba{sub x}Si{sub 5}N{sub 8} is a promising orange red-emitting phosphor for near UV or blue light-pumped white light-emitting-diodes (wLEDs). - Graphical abstract: Eu{sup 2+} doped Sr{sub 2-x}Ba{sub x}Si{sub 5}N{sub 8} solid solutions were prepared by the solid-state reaction method. The structure, luminescence and thermal quenching properties with varying Ba/Sr ratio were investigated in detail. - Highlights: • The stucture and luminescence properties of Eu doped Sr{sub 2-x}Ba{sub x}Si{sub 5}N{sub 8} phosphors were investigated. • The samples with the intermediate compositions(x=1.0,1.5) show better stability than the end members of both Sr{sub 2}Si{sub 5}N{sub 8}:Eu{sup 2+} and Ba{sub 2}Si{sub 5}N{sub 8}:Eu{sup 2+}. • The possible mechanism for the improvement of thermal quenching properties was proposed.

Structural and thermodynamic characterization of the perovskite-related BA{sub 1+y}UO{sub 3+x} and (BA,SR){sub 1+y}UO{sub 3+x} phases

Energy Technology Data Exchange (ETDEWEB)

Cordfunke, E.H.P. [Netherlands Energy Research Foundation (ECN), Petten (Netherlands); Booij, A.S. [Netherlands Energy Research Foundation (ECN), Petten (Netherlands); Smit-Groen, V. [Netherlands Energy Research Foundation (ECN), Petten (Netherlands); Vlaanderen, P. van [Netherlands Energy Research Foundation (ECN), Petten (Netherlands); IJdo, D.J.W. [Rijksuniversiteit Leiden (Netherlands). Gorlaeus Labs.

1996-11-01

The perovskite-type BaUO{sub 3} structure has been investigated by X-ray and neutron diffraction. The Ba/U ratio, the (Ba, Sr)/U ratio, and the oxygen stoichiometry in Ba{sub 1+y}UO{sub 3+x} were varied, and the integral enthalpies of formation determined by solution calorimetry. In addition, equilibrium oxygen partial pressures were measured using a reversible EMF cell. The chemical defect mechanism is discussed, and it is shown that a continuous series BaUO{sub 3}-Ba{sub 1+y}UO{sub 3+x}-Ba{sub 3}UO{sub 6} exist in which uranium vacancies are gradually filled up with barium ions, whereas uranium is oxidized via the pentavalent to the hexavalent state in Ba{sub 3}UO{sub 6}(=Ba{sub 2}(Ba, U)O{sub 6}). (orig.).

Rock Rb-Sr ages from Bananal region - Sao Paulo State, Brazil

International Nuclear Information System (INIS)

Dias Neto, C.M.; Tassinari, C.G.C.; Silva, M.E.

1996-01-01

New Rb-Sr whole rock isochron ages have been determined for the main lithological units that occur in Sao Paulo and Rio de Janeiro States. These rocks belong to Serra do Mar domain. The purpose of this work is to characterize the sequence of the geological events as well as the possible relationship between the different rocks. The geochronological data suggest that the paragneisses and the basement rocks, represented by ortho gneisses nuclei, were generated under amphibolite conditions around 700 Ma. At the same time the leucogranites were generated by partial melting processes and injected into both gneiss types. Tarditectonic granitic magmatic activities took place within ductile shear zones. One of the granites, the Getulandia granite, yielded an age of 514 Ma, falling in the range of the late Brasiliano Cycle which extended into the Middle Cambrian. (author). 9 figs., 1 tab

Electrical properties and structure of glasses in the Ba(PO3)2-MF2 systems, where M = Mg, Ca, Sr, Ba

International Nuclear Information System (INIS)

Sokolov, I.A.; Tarlakov, Yu.P.; Murin, I.V.; Pronkin, A.A.

2000-01-01

Using the methods of conductometry and IR spectroscopy the concentrational dependences of electric conductivity are studied, the nature of current carriers is determined, the concentrational dependence of transfer numbers is ascertained and structural changes in glasses of the system Ba(PO 3 ) 2 -MF 2 (M = Mg, Ca, Sr, Ba), depending on MF 2 content, are considered. It is shown that F - ions take part in electric current transfer. Influence of crystallochemical nature of alkaline-earth cations on physicochemical properties and structure of the glasses studied is analyzed [ru

New Rb-Sr isotopic ages and geochemistry of granitic gneisses from southern Bastar: implications for crustal evolution

International Nuclear Information System (INIS)

Sarkar, G.; Gupta, S.N.; Bishui, P.K.

1994-01-01

Deformed gneisses from the southern Bastar craton yield Rb-Sr whole-rock ages of 2560 Ma and 2659 Ma with initial Sr ratios ranging between 0.70899 and 0.70726 respectively. The isotopic data are found to be scattered even at the outcrop scale which possibly indicate large-scale reworking of the gneisses during the period. The high initial Sr ratios that associate with scattering of the isotopic data reflect reworking of older gneisses. Geochemically, these gneisses are considered to be derived from an amphibolitic or basaltic protolith. The 2095 Ma (initial Sr ratio of 0.74312) old leucocratic granite intrusive into these gneisses represent early Proterozoic magmatic activity. Based on the available isotopic and geochemical data, it is suggested that the Bastar craton represents a polyphase, multicomponent terrain developed by repeated magmatism at a much earlier, probably during mid-Archaean, time and was extensively reworked during the time span between end-Archaean and early Proterozoic period. This reworking may be synchronous with coalescing of smaller crustal components possibly during the end-Archaean time. (author). 21 refs., 5 figs., 2 tabs

Primordial crustal growth in northern Nigeria: preliminary Rb-Sr and Sm-Nd constraints from Kaduna migmatite-gneiss complex

International Nuclear Information System (INIS)

Dada, S. S.; Briqueu, L.; Birck, J. L.

1998-01-01

The Kaduna Migmatite-Gneiss Complex in the central area of the Northern shield includes variably migmatised granitotrondhjemitic gneisses and amphibolite of hitherto unknown age. The amphibolite enclaves and dykes are metatholeiites with comparatively unfractionated rare-earth patterns. The two main rock units (TTG and amphibolite) exhibit complementary geochemical signatures in the normalised abundance patterns of relatively incompatible elements and suggest possible derivation of the gneisses from subduction related mafic material. Sm-Nd and Rb-Sr isotopic data document early Archaean crustal formation of new crust and its subsequent late Archaean differentiation. These preliminary results form an evidence for a more extended crustal history in the heart of the Pan-African domain (ca. 600 Ma.). They suggest the differentiation of juvenile crustal protolith from a chondritic reservoir about 3.5 Ga. for the gneiss-amphibolite bimodal suite. A tectonothermal event about 3.1-3.0 Ga led to the emplacement of an early gneiss as indicated from Rb-Sr and U-Ph zircon analyses. Subsequent differentiation and/or reworking around 2.8-2.7 Ga is coherent with the Liberian orogeny within the West African- Latino American subregion

Nano-SIMS analysis of Mg, Sr, Ba and U in natural calcium carbonate

International Nuclear Information System (INIS)

Sano, Yuji; Shirai, Kotaro; Takahata, Naoto; Hirata, Takafumi; Sturchio, Neil C.

2005-01-01

Concentrations of minor (Mg and Sr) and trace (Ba and U) elements in four natural calcium carbonate samples were first analyzed by inductively coupled plasma mass spectrometry (ICP-MS) after chemical dissolution and calibrated against a standard dolomite. Their homogeneities were checked by in situ laser ablation (LA) ICP-MS with 10-20 spots. The carbonate samples were measured by using a high lateral resolution secondary ion mass spectrometer (Nano-SIMS NS50). A ∼4 nA O - primary beam was used to sputter a 5 - 6-μm diameter crater on the sample surface, and secondary positive ions were extracted for mass analysis using an accelerating voltage of 8 kV and a Mattauch-Herzog geometry. A multi-collector system was adjusted to detect 26 Mg + , 43 Ca + , 88 Sr + , 138 Ba + , 238 U 16 O 2 + ions at the same time. A resolving power of 2500 - 5000 at 10% peak height was attained by an entrance slit set at 40 μm, and each exit slit at 50 μm with adequate flat-topped peaks. The observed 26 Mg/ 43 Ca, 88 Sr/ 43 Ca, 138 Ba/ 43 Ca and 238 U 16 O 2 / 43 Ca ratios agreed well with those measured by LA-ICP-MS. Foraminifera shells were analyzed at 5 - 6 μm scale by Nano-SIMS. There was a large variation of the Mg/Ca ratios, up to ±38%, even in a single fragment of the shell, suggesting that although the ratios provide a useful paleoceanographic proxy at bulk scale, they may reflect a more complex pattern at <10 μm scale. (author)

A Rb-Sr isotope study of a young granite sheet at Marble Delta, southern Natal

International Nuclear Information System (INIS)

Naidoo, D.D.; Eglington, B.M.; Harmer, R.E.

1989-01-01

Rb-Sr isotope data are presented for two apophyses of a granite sheet intrusive into marble at Marble Delta, southern Natal. Granite samples collected near the margins of these apophyses contain calcite and are thought to have been contaminated by the marble during intrusion of the granite magma. In contrast, those further away from contacts lack calcite. The 'uncontaminated' granite samples define an isochron date of 899 ± 11 Ma. This data is thought to represent the intrusive age of the granite sheet. 11 refs., 5 figs., 2 tabs

A high 87Sr 86Sr mantle source for low alkali tholeiite, northern Great Basin

Science.gov (United States)

Mark, R.K.; Lee, Hu C.; Bowman, H.R.; Asaro, F.; McKee, E.H.; Coats, R.R.

1975-01-01

Olivine tholeiites, the youngest Tertiary units (about 8-11 m.y. old) at five widely spaced localities in northeastern Nevada, are geologically related to the basalts of the Snake River Plain, Idaho, to the north and are similar in major element and alkali chemistry to mid-ocean ridge basalts (MORB) and island arc tholeiites. The measured K (1250-3350 ppm), Rb (1??9-6??2 ppm) and Sr (140-240 ppm) concentrations overlap the range reported for MORB. Three of the five samples have low, unfractionated rare earth element (REE) patterns, the other two show moderate light-REE enrichment. Barium concentration is high and variable (100-780 ppm) and does not correlate with the other LIL elements. The rocks have 87Sr/86Sr = 0??7052-0??7076, considerably higher than MORB (~0??702-0??703). These samples are chemically distinct (i.e. less alkalic) from the olivine tholeiites from the adjacent Snake River Plain, but their Sr isotopic compositions are similar. They contain Sr that is distinctly more radiogenic than the basalts from the adjacent Great Basin. About 10 b.y. would be required for the mean measured Rb/Sr (~ 0??02) of these samples to generate, in a closed system, the radiogenic Sr they contain. The low alkali content of these basalts makes crustal contamination an unlikely mechanism. If the magma is uncontaminated, the time-averaged Rb/Sr of the source material must have been ~0??04. A significant decrease in Rb/Sr of the source material (a factor 2??) thus most probably occurred in the relatively recent (1??09 yr) past. Such a decrease of Rb/Sr in the mantle could accompany alkali depletion produced by an episode of partial melting and magma extraction. In contrast, low 87Sr 86Sr ratios indicate that the source material of the mid-ocean ridge basalts may have been depleted early in the Earth's history. ?? 1975.

Electronic structure of (La,Sr)2CuO4 and Ba0.6K0.4BiO3

International Nuclear Information System (INIS)

Howell, R.H.; Sterne, P.A.; Fluss, M.J.; Kaiser, J.H.; Kitazawa, K.; Kojima, H.; Mosley, W.D.; Dykes, J.W.; Shelton, R.N.

1995-01-01

We have measured and calculated the electron-positron momentum distribution of La 2-x Sr x CuO 4 samples for Sr concentrations of 0, 0.1,0.13, and 0.2 and Ba 0.6 K 0.4 BiO 3 . The momentum distribution of all samples contained features derived from the overlap of the positron distribution with the valence electrons. In addition, discontinuities typical of a Fermi surface are seen in the superconducting samples. The form and position of these features are in general agreement with band theory for both La 2-x Sr x CuO 4 and Ba 0.6 K 0.4 BiO 3 . However the evolution of the Fermi surface with doping in La 2-x Sr x CuO 4 differed significantly from expectations based on single electron band theories. (orig.)

Investigation into the metamorphic Nappes of the Central Scandinavian Caledonides on the basis of Rb-Sr and K-Ar age determination

International Nuclear Information System (INIS)

Reymer, A.P.S.

1979-01-01

This study concerns age determinations on several rock units of metamorphic nappes in the central Scandinavian Caledonides. Rb-Sr analyses on whole-rocks and minerals (biotite, muscovite/phengite, feldspars, garnet) were made as well as K-Ar determinations on biotite, muscovite/phengite, amphibole and feldspar. (Auth.)

Electrical transport across nanometric SrTiO3 and BaTiO3 barriers in conducting/insulator/conducting junctions

Science.gov (United States)

Navarro, H.; Sirena, M.; González Sutter, J.; Troiani, H. E.; del Corro, P. G.; Granell, P.; Golmar, F.; Haberkorn, N.

2018-01-01

We report the electrical transport properties of conducting/insulator/conducting heterostructures by studying current-voltage IV curves at room temperature. The measurements were obtained on tunnel junctions with different areas (900, 400 and 100 μm2) using a conducting atomic force microscope. Trilayers with GdBa2Cu3O7 (GBCO) as the bottom electrode, SrTiO3 or BaTiO3 (thicknesses between 1.6 and 4 nm) as the insulator barrier, and GBCO or Nb as the top electrode were grown by DC sputtering on (100) SrTiO3 substrates For SrTiO3 and BaTiO3 barriers, asymmetric IV curves at positive and negative polarization can be obtained using electrodes with different work function. In addition, hysteretic IV curves are obtained for BaTiO3 barriers, which can be ascribed to a combined effect of the FE reversal switching polarization and an oxygen vacancy migration. For GBCO/BaTiO3/GBCO heterostructures, the IV curves correspond to that expected for asymmetric interfaces, which indicates that the disorder affects differently the properties at the bottom and top interfaces. Our results show the role of the interface disorder on the electrical transport of conducting/insulator/conduction heterostructures, which is relevant for different applications, going from resistive switching memories (at room temperature) to Josephson junctions (at low temperatures).

Influence of Ba²⁺ and Sr²⁺ ions on the hydration process of portland cement and blended cements

OpenAIRE

Živanović, B. M.; Petrašinović, Lj.; Milovanović, T.; Karanović, Lj.; Krstanović, I.

1987-01-01

This study concerns the influence of the concentration of Sr2+ and Ba2+ ions in mortar batch waters upon the hydration process of various Portland and additive cements. An increase in the mechanical resistence of said cements is observed, after 28 days, when the concentration of Ba2+ and Sr2+ ions in the mortar batch waters increases. This suggests a possible microstructural explanation of said phenomenon.En el presente trabajo se estudia la influencia de la concentración de los iones Sr2+ y...

Study of non-stoichiometric BaSrTiFeO3 oxide dedicated to semiconductor gas sensors

International Nuclear Information System (INIS)

Fasquelle, D.; Verbrugghe, N.; Deputier, S.

2016-01-01

Developing instrumentation systems compatible with the European RoHS directive (restriction of hazardous substances) to monitor our environment is of great interest for our society. Our research therefore aims at developing innovating integrated systems of detection dedicated to the characterization of various environmental exposures. These systems, which integrate new gas sensors containing lead-free oxides, are dedicated to the detection of flammable and toxic gases. We have firstly chosen to study semiconductor gas sensors implemented with lead-free oxides in view to develop RoHS devices. Therefore thick films deposited by spin-coating and screen-printing have been chosen for their robustness, ease to realize and ease to finally obtain cost-effective sensors. As crystalline defects and ionic vacancies are of great interest for gas detection, we have decided to study a non-stoichiometric composition of the BaSrTiFeO 3 sensible oxide. Nonstoichiometric BaSrTiFeO 3 lead-free oxide thick films were deposited by screen-printing on polycrystalline AFO 3 substrates covered by a layer of Ag-Pd acting as bottom electrode. The physical characterizations have revealed a crystalline structure mainly composed of BaTiO 3 pseudo-cubic phase and Ba 4 Ti 12 O 27 monoclinic phase for the powder, and a porous microstructure for the thick films. When compared to a BSTF thick film with a stoichiometric composition, a notable increase in the BSTF dielectric constant value was observed when taking into account of a similar microstructure and grain size. The loss tangent mean value varies more softly for the non-stoichiometric BaSrTiFeO 3 films than for the perovskite BSTF film as tanδ decreases from 0.45 to 0.04 when the frequency increases from 100 Hz to 1 MHz. (paper)

Systems of Ba(PO3)2-Sr(Pu3)2, Cd(PO3)2-Ca(PO3)2

International Nuclear Information System (INIS)

Tokman, I.A.; Bukhalova, G.A.

1977-01-01

Phase diagrams of the Ba(PO 3 ) 2 -Sr(PO 3 ) 2 and Cd(PO 3 ) 2 -Ca(PO 3 ) 2 systems have been studied and plotted by the methods of differential-thermal analysis (DTA), visual-polythermal, X-ray phase and infrared spectroscopy. The Ba(PO 3 ) 2 -Sr(PO 3 ) 2 system is of the eutectic type. In the binary system Cd(PO 3 ) 2 -Ca(PO 3 ) 2 the existence of a continuous series of solid solutions with a minimum at 858 deg C and 27.5 mol.% Ca(PO 3 ) 2 has been established

Structural distortions in Sr3-xAxMO4F (A=Ca, Ba; M=Al, Ga, In) anti-Perovskites and corresponding changes in photoluminescence

International Nuclear Information System (INIS)

Sullivan, Eirin; Avdeev, Maxim; Vogt, Thomas

2012-01-01

The ordered oxyfluoride family Sr 3 − x A x MO 4 F (A=Ca, Ba and M=Al, Ga) has formed the basis of several new inorganic phosphors, and shows great potential for use in phosphor-conversion LED lamp devices. This study examines the correlation between subtle structural changes and photoluminescent behaviour in some of these materials. In order to ascertain whether cation charge compensation has any influence on structure and subsequent photoluminescent behaviour, a comparison was carried out between phases with the nominal compositions Sr 2.975 Ce 0.025 AlO 4 F and Sr 2.95 Ce 0.025 Na 0.025 AlO 4 F using structural characterisation based upon high-resolution neutron powder diffraction (NPD) data. Additionally, NPD data has been used to elucidate the role of different M cations in these materials, using Sr 2.25 Ba 0.6 Eu 0.1 M 0.95 In 0.05 O 4−α F 1−δ (M=Al, Ga) to determine the effect M cation size has on structure and photoluminescent properties. - Graphical abstract: The structure of Sr3-xAxMO4F (A=Ca, Ba and M=Al, Ga) and excitation and emission spectra for Sr 2.25 Ba 0.6 Eu 0.1 Ga 0.95 In 0.05 O 4−α F 1−δ . Highlights: ► Correlation between structural changes and photoluminescence in Sr 3−x A x MO 4 F (A=Ca, Ba, M=Al, Ga). ► Comparison of Sr 2.975 Ce 0.025 AlO 4 F and Sr 2.95 Ce 0.025 Na 0.025 AlO 4 F using high-resolution NPD. ► Study of the effect of cation charge-compensation on structure and photoluminescent behaviour. ► Examination of high-resolution NPD data for Sr 2.25 Ba 0.6 Eu 0.1 M 0.95 In 0.05 O 4−α F 1−δ (M=Al, Ga). ► Determination of the effect M cation size has on structure and photoluminescent properties.

Structural study of Sr0.3Ba0.7Nb2O6 and La0.030Sr0.255Ba0.700Nb2O6 ceramic systems

International Nuclear Information System (INIS)

Luna-Lopez, J.A.; Portelles, J.; Raymond, O.; Siqueiros, J.M.

2009-01-01

Sr 0.3 Ba 0.7 Nb 2 O 6 (SBN) and La 0.030 Sr 0.255 Ba 0.700 Nb 2 O 6 (LSBN) ceramic compounds have been prepared using the traditional ceramic method at two different calcination temperatures (900 and 1000 deg. C) and later sintered both at 1400 deg. C. A study of the effects of the calcination temperatures and La substitution on the morphological, compositional, and structural properties of SBN and LSBN is presented using scanning electronic microscopy (SEM), energy dispersive spectroscopy (EDS), and X-ray diffraction (XRD) analysis. From Rietveld refinement processes, the XRD patterns were interpreted to evaluate such effects in the structural parameters and the site occupation factors of the heavy metals and oxygen atoms. The effect of the incorporation of La resulted in a 0.25% cell contraction and turned out to be higher than the 0.08% dilation effect produced by the increase of calcination temperature. The La ion with similar effective ionic radius and higher electronegativity is incorporated into the structure occupying the A 1 site just like the Sr ions in the SBN compound. Differences in the site occupation factors between the SBN and LSBN samples lead to substantial changes in the physical properties such as temperature of relative dielectric constant maximum, relative dielectric constant, and dielectric loss, correlated with the distortion and the relative orientation of the oxygen octahedra.

Rapid and efficient visible light photocatalytic dye degradation using AFe2O4 (A = Ba, Ca and Sr) complex oxides

International Nuclear Information System (INIS)

Vijayaraghavan, T.; Suriyaraj, S.P.; Selvakumar, R.; Venkateswaran, R.; Ashok, Anuradha

2016-01-01

Highlights: • Alkaline earth ferrites AFe 2 O 4 (A = Ba, Ca and Sr) were synthesized by sol–gel method. • Visible light photocatalytic activity of these ferrites were studied using congo red dye degradation. • BaFe 2 O 4 exhibited the best photocatalytic activity under visible light (xenon lamp) irradiation; CaFe 2 O 4 was the best photocatalyst under natural sun light irradiation. - Abstract: Photocatalytic activity of spinel type complex oxides has been investigated in this study. Alkaline earth ferrites AFe 2 O 4 (A = Ba, Ca, Sr) were synthesized by sol–gel method. Structural characterizations reveal that the synthesized ferrites have orthorhombic crystal structures with different space groups and cell dimensions when they have different alkaline earth metals in their A site. All the synthesized ferrites exhibited their bandgap in the range 2.14–2.19 eV. Their photocatalytic activities were studied using congo red dye under sunlight and xenon lamp radiation. The substitution of Ba, Ca and Sr at A site of these ferrites had varying impact on dye degradation process. Under xenon lamp irradiation, BaFe 2 O 4 exhibited the highest percentage of dye degradation (92% after 75 min). However, CaFe 2 O 4 showed the fastest degradation of the dye (70% within 15 min). In the absence of irradiation, SrFe 2 O 4 showed the highest dye adsorption (44% after 75 min).

Properties of half metallic (Ba0.8Sr0.2)2-x La2x/3x/3FeMoO6 double perovskites

International Nuclear Information System (INIS)

Serrate, D.; De Teresa, J.M.; Blasco, J.; Morellon, L.; Ibarra, M.R.

2005-01-01

Previous work in (Ba 0.8 Sr 0.2 ) 2- x La x FeMoO 6 and Ba 1+ x Sr 1-3 x La 2 x FeMoO 6 have stated electron doping as the most important parameter in terms of T c enhancement. Here we report complementary structural, magnetic and transport properties, say a series where there is no doping and only structural parameters are changed: (Ba 0.8 Sr 0.2 ) 2- x La 2 x /3 x /3 FeMoO 6 . We propose a complete phase diagram where structural and bandfilling impact on the Curie temperature is clearly evidenced

Study on the equilibrium in the MBr2-CH3OH-H2O system (M = Sr2+, Ba2+) at 25 0C

International Nuclear Information System (INIS)

Zlateva, I.; Stoev, M.

1985-01-01

The dehydration processes in the three-component system MBr 2 -CH 3 OH-H 2 O (M = Sr 2+ , Ba 2+ ) have been studied at 25 0 C by physio-chemical analyses. Crystallization fields for the lower crystal hydrates SrBr 2 x H 2 O and BaBr 2 x H 2 O have been found. The solubility curves exhibit complex-formation processes. The dehydration and solvation processes in three-component system such as MBr 2 -CH 3 OH-H 2 O at 25 0 C with M = Mg 2+ , Ca 2+ , Sr 2+ , Ba 2+ have been discussed in general terms. (author)

The Effect Of Coupling Agent On Composite Magnet Characteristic Based On Hexa ferrite (Sr M/Ba M) With Polyester And Epoxy Binder

International Nuclear Information System (INIS)

Sudirman; Ridwan; Mujamilah; Karo Karo, Aloma; Handayani, Ari; Rukihati

2004-01-01

Magnetic composites are mixtures of hexa ferrite powder and non magnetic materials such as polymers as binders. These composites have been investigated because they are light, elastic, and cheap. In this study thermoset polymer (epoxy and polyester) were used as binders. Inside study of coupling agent added effect on mechanical properties, hardness and microstructure. The composites were prepared by mixture thermoset polymer epoxy or polyester with hexa ferrite powder Sr M (SrFe 12 O 19 ) or Ba M (BaFe 12 O 19 ) with volume fraction of 40,50 and 60 % v/v, coupling agent of the Tetra Isopropyl Titanate in the amount of 5 ml or 10 ml are added before mix turing of the thermoset polymer epoxy or polyester with hexa ferrite powder. The resulting composite were characterized mechanically (tensile strength), hardness and microstructure test. The results showed that the tensile strength and hardness of the composite magnet were increased by increasing the composition of magnetic powder, either Sr M or Ba M, it caused by microstructure of particle Sr M magnetic powder 1.6 μm in the form splinter, where as the Ba M magnetic powder 1,2 μm in nodular form. Thermoset polymer epoxy as binder have tensile strength and hardness is bigger than composite magnet based on polyester, either Sr M or Ba M. The addition of coupling agent is very influenced on the tensile strength and hardness composite magnet, the more coupling magnet addition causes the more tensile strength and hardness of the composite magnet

Diamagnetism to ferromagnetism in Sr-substituted epitaxial BaTiO{sub 3} thin films

Energy Technology Data Exchange (ETDEWEB)

Singamaneni, Srinivasa Rao, E-mail: ssingam@ncsu.edu; Prater, John T. [Materials Science Division, Army Research Office, Research Triangle Park, North Carolina 27709 (United States); Department of Materials Science and Engineering, North Carolina State University, Raleigh, North Carolina 27695 (United States); Punugupati, Sandhyarani; Narayan, Jagdish [Department of Materials Science and Engineering, North Carolina State University, Raleigh, North Carolina 27695 (United States)

2016-04-04

We report on the ferromagnetic-like behavior in otherwise diamagnetic BaTiO{sub 3} (BTO) thin films upon doping with non-magnetic element Sr having the composition Ba{sub 0.4}Sr{sub 0.6}TiO{sub 3} (BST). The epitaxial integration of BST (∼800 nm) thick films on Si (100) substrate was achieved using MgO (40 nm) and TiN (20 nm) as buffer layers to prepare BST/MgO/TiN/Si (100) heterostructure by pulsed laser deposition. The c-axis oriented and cube-on-cube epitaxial BST is formed on Si (100) as evidenced by the in-plane and out-of-plane X-ray diffraction. All the deposited films are relaxed through domain matching epitaxy paradigm as observed from X-ray diffraction pattern and A{sub 1}TO{sub 3} mode (at 521.27 cm{sup −1}) of Raman spectra. As-deposited BST thin films reveal ferromagnetic-like properties, which persist up to 400 K. The magnetization decreases two-fold upon oxygen annealing. In contrast, as-deposited un-doped BTO films show diamagnetism. Electron spin resonance measurements reveal no evidence of external magnetic impurities. XRD and X-ray photoelectron spectroscopy spectra show significant changes influenced by Sr doping in BTO. The ferromagnetic-like behavior in BST could be due to the trapped electron donors from oxygen vacancies resulting from Sr-doping.

Theoretical investigation on thermoelectric properties of (Ca,Sr,Ba)Fe2(As/Bi)2 compounds under temperature

Science.gov (United States)

Jayalakshmi, D. S.; Sundareswari, M.; Viswanathan, E.; Das, Abhijeet

2018-04-01

The electrical conductivity, resistivity and Seebeck coefficient, Pauli magnetic susceptibility and power factor are computed under temperature (100 K - 800 K) in steps of 100 K for the theoretically designed compounds namely (Ca,Sr,Ba)Fe2Bi2 and their parent compounds namely (Ca,Sr,Ba)Fe2As2 by using Boltzmann transport theory interfaced to the Wien2k program. The Bulk modulus, electron phonon coupling constant, thermoelectric figure of merit (ZT) and transition temperature are calculated for the optimized anti ferromagnetic phase of the proposed compounds. The results are discussed for the novel compounds in view of their superconductivity existence and compared with their parent unconventional superconducting compounds.

Lattice mismatch and energy transfer of Eu- and Dy-codoped MO–Al2O3–SrO (M=Mg, Ca, Ba) ternary compounds affecting luminescence behavior

International Nuclear Information System (INIS)

Liang, Chen-Jui; Huang, Kuan-Yu

2017-01-01

A systematic investigation of energy transfers and luminescence behaviors for M x Sr 0.94−x Al 2 O 4 :Eu 0.02 , Dy 0.04 (M=Mg, Ca, Ba; x=0, 0.235, 0.47, 0.705, 0.94) ternary compounds was accomplished. The results demonstrated that six phenomena must be fitted into the energy-transfer mechanisms of the ternary compounds: (1) the optical band-gap energy of Mg 0.94 Al 2 O 4 :Eu 0.02 Dy 0.04 is extremely low and does not allow photoemission; (2) Ca 2+ and Ba 2+ ions are the main hosts when x≥0.47 in Ca x Sr 1−x Al 2 O 4 :Eu 0.02 Dy 0.04 and Ba x Sr 1−x Al 2 O 4 :Eu 0.02 Dy 0.04 , respectively; (3) Eu 3+ ions are the main activator ions in Ca x Sr 1−x Al 2 O 4 :Eu 0.02 Dy 0.04 with x=0.47 and in Ba x Sr 1−x Al 2 O 4 :Eu 0.02 Dy 0.04 with x=0.353−0.705; (4) Sr 2+ and Eu 2+ ions are the main host and activator ions, respectively, when x<0.353 in each ternary compound; (5) energy transfers from the MO phases to the SrO phase because the conduction band energy of SrO is the lowest; and (6) mutual substitution between alkaline-earth ions does not alter the resultant structures’ crystal field and nephelauxetic effects, as determined by measuring their luminescence. Two energy transfer paths were discovered to be possible in CaO–Al 2 O 3 –SrO and BaO–Al 2 O 3 –SrO ternary compounds, and the boundaries determining which path was chosen were the atomic ratios Ca:Sr and Ba:Sr, both approximately 1.6:1 (x=0.353). Because second path increased the energy transferred from the MO band gap to the SrO band gap, the corresponding structure's spectrum emission intensity was approximately 4.3 times higher than that of the SrO−Al 2 O 3 binary compound, and their photoluminescence was thus substantially higher.

Fractal formation of a Y-Ba-Cu-O thin film on SrTiO3

International Nuclear Information System (INIS)

Chow, L.; Chen, J.; Desai, V.; Sundaram, K.; Arora, S.

1989-01-01

Fractal formation has been observed after thermal annealing of the rf-sputtered Y-Ba-Cu-O thin film on SrTiO 3 substrate. Through energy-dispersive x-ray analysis, it was found that the composition of the fractal was YBa 2 Cu 3 O x and the surrounding film composition wasY 2 Ba 2 Cu 3 O x . The fractal dimensions D ranging from 1.26 to 1.65 were obtained using the standard sandbox method with different thresholds

Structure of the new Tl(Ba sub 1.0 Sr sub 1.0) PrCu sub 2 O sub 7-x by Rietveld analysis

International Nuclear Information System (INIS)

Yang, P.; Fun, H. K.; Lee, T.J.; Ku, H.C.; Lai, C.C.

1994-01-01

The crystalline structure of Tl(Ba sub 1.0 Sr sub 1.0)PrCu sub 2 O sub 7-x was obtained at room temperature from x-ray powder diffraction with CuK sub α radiation using Rietveld analysis. Tl(Ba sub 1.0 Sr sub 1.0)PrCu sub 2 O sub 7-x isomorphous at both room temperature (300 K) and low temperature (100 K) with TlBa sub 2 ca Cu sub 2 O sub 7-x type (1212) structure, crystallized with space group P4/mmm and one formula in the unit cell. At 300 K, cell parameters a=3.8892(2) A, c=12.3099(6) A, the structure was refined with 25 parameters to R sub WP = 6.30%, R sub P = 4.38% for 3551 step intensities and R sub b = 5.01%, R sub f = 4.20% for 156 reflections. The goodness of fitting S=3.18. At 100K, cell parameters a=3.8866(4) A, c= 12.289(1) A, the structure was refined with 26 parameters to R sub WP = 8.42%, R sub P = 6.21% for 2676 step intensities and R sub b = 6.72%, R sub f = 5.28% for 120 reflections. The goodness of fitting S=2.32. Reasonable anisotropic thermal parameters were obtained. The compositions of Ba and Sr atoms were refined to about Ba sub 1.1 Sr sub 0.9 compared with the stoichiometric Ba sub 1.0 Sr sub 1.0

Rb-Sr systematics in drill core samples of the Eye-Dashwa Lakes pluton at the whole rock and mineral scale

International Nuclear Information System (INIS)

Peterman, Z.E.; Futa, K.; Kamineni, D.C.

1990-01-01

Twenty-one whole-rock samples from boreholes ATK-1 and ATK-6 define a precise Rb-Sr isochron with an age of 2637 ± 33 Ma and initial 87 Sr/ 86 Sr intercept, IR(Sr), of 0.70144 ± 0.00006. An internal mineral isochron for ATC-1 (991-997) and biotites from ATK-1 (35.63) and ATK-1 (3.84) give younger ages of 2541 ± 14 Ma 2574 ± 25 Ma, and 2534 ± 25 Ma, respectively. Data for samples from fracture zones scatter but correlate around an isochron of 2281 ± 153 Ma. The internal isochron and biotite ages record cooling below about 300 C due to uplift and erosion. The younger age, 2281 ± 153 Ma, records an episode or episodes of brittle failure at relatively high crustal levels. These fractures provided pathways for infiltration of water, which facilitated the mineralogical alteration

(Sr,Ba)(Si,Ge)2 for thin-film solar-cell applications: First-principles study

International Nuclear Information System (INIS)

Kumar, Mukesh; Umezawa, Naoto; Imai, Motoharu

2014-01-01

In order to meet the increasing demand for electric power generation from solar energy conversion, the development of efficient light absorber materials has been awaited. To this end, the electronic and optical properties of advanced alkaline-earth-metals disilicides and digermanides (SrSi 2 , BaSi 2 , SrGe 2 , and BaGe 2 ) are studied by means of the density functional theory using HSE06 exchange-correlation energy functional. Our calculations show that all these orthorhombic structured compounds have fundamental indirect band gaps in the range E g ≈ 0.89–1.25 eV, which is suitable for solar cell applications. The estimated lattice parameters and band gaps are in good agreement with experiments. Our calculations show that the electronic band structures of all four compounds are very similar except in the vicinity of the Γ-point. The valence band of these compounds is made up by Si(Ge)-p states, whereas the conduction band is composed of Sr(Ba)-d states. Their band alignments are carefully determined by estimating the work function of each compound using slab model. The optical properties are discussed in terms of the complex dielectric function ε(ω) = ε 1 (ω) + iε 2 (ω). The static and high-frequency dielectric constants are calculated, taking into account the ionic contribution. The absorption coefficient α(ω) demonstrates that a low energy dispersion of the conduction band, which results in a flat conduction band minimum, leads to large optical activity in these compounds. Therefore, alkaline-earth-metals disilicides and digermanides possess great potential as light absorbers for applications in thin-film solar cell technologies.

Possible two-stage 87Sr evolution in the Stockdale Rhyolite

International Nuclear Information System (INIS)

Compston, W.; McDougall, I.; Wyborn, D.

1982-01-01

The Rb-Sr total-rock data for the Stockdale Rhyolite, of significance for the Palaeozoic time scale, are more scattered about a single-stage isochron than expected from experimental error. Two-stage 87 Sr evolution for several of the samples is explored to explain this, as an alternative to variation in the initial 87 Sr/ 86 Sr which is customarily used in single-stage dating models. The deletion of certain samples having very high Rb/Sr removes most of the excess scatter and leads to an estimate of 430 +- 7 m.y. for the age of extrusion. There is a younger alignment of Rb-Sr data within each sampling site at 412 +- 7 m.y. We suggest that the Stockdale Rhyolite is at least 430 m.y. old, that its original range in Rb/Sr was smaller than now observed, and that it experienced a net loss in Sr during later hydrothermal alteration at ca. 412 m.y. (orig.)

Rb-Sr geochronology from Sao Felix to Xingu: preliminary results

International Nuclear Information System (INIS)

Lafon, J.M.; Pereira, E.D.; Silva Barradas, J.A. da

1991-01-01

Rb-Sr systematics have been applied on rocks from the Sao Felix do Xingu region, in the southeastern part of the State of Para. An age of 2716 ± 34 Ma with IR of 0.70292 ± 0.00030 (MSWD = 1.54) and an age of 2677 ± 50 Ma with IR of 0.70161 ± 0.00022 (MSWD = 5.21) had been obtained for a granitic body and a tonalitic body respectively, both of them associated to the green stones belts that occur in this area. Gneisses from the Xingu complex gave an age of 2574 ± 57 Ma with an IR of 0.70416 ± 0.00054 (MSWD = 5.06). An age of 1653 ± 14 Ma with IR of 0.70823 ± 0.02361 (MSWD = 1.71) had been obtained for the Velho Guilherme granite that crosscut the granite-green stones terrains. Such geochronological data show the existence of a magmatic event between 2.72 Ga and 2.68 Ga and permit us to conclude on the archaean age of the green stones terrains. (author)

Influence of bismuth on properties and microstructures of Sr0⋅ 5Ba0 ...

Indian Academy of Sciences (India)

Home; Journals; Bulletin of Materials Science; Volume 29; Issue 5. Influence of bismuth on properties and microstructures of Sr0.5Ba0.5–Bi TiO3 thin films. Tao Wenhong Wang Yin Fu Xinghua Wei Qihong. Thin Films Volume 29 Issue 5 October 2006 pp 523-527 ...

The effect of secondary apatite on the initial 87Sr/86Sr ratio determination in granitic rocks: a case study of the Tadamigawa pluton, northeastern Japan

Science.gov (United States)

Wakasugi, Y.; Ichino, K.; Tanioka, Y.; Wakaki, S.; Tsuboi, M.; Ishikawa, T.

2017-12-01

Apatite is a major accessory mineral in igneous rocks. Because Rb contents in apatite are very low, 87Sr/86Sr ratios of magmatic apatite are useful to estimate the initial 87Sr/86Sr ratio (SrI) of igneous rocks. Secondary post-magmatic event such as hydrothermal alteration may also crystallize secondary apatite, which may inhibit the estimation of SrI of igneous rocks. In this study, we examine the effects of secondary apatite on the initial 87Sr/86Sr ratio determination of granitic rocks by using acid leaching technique. Leached apatite samples were first separated from the whole rock powder as a heavy mineral fraction by heavy liquid technique, and the heavy mineral fraction was then leached by 3 M HNO3. The isotopic ratios of Sr and the concentrations of Rb and Sr were analyzed by TIMS and ICP-MS at Kochi Core Center, respectively. The Tadamigawa Older-stage granites, which locate in the Taishaku Mountains at the northeastern part of Japan, intrude into the Ashio Jurassic complex, and the ages of these rocks are late Cretaceous to Paleogene. The U-Pb ages of zircon and the K-Ar ages of biotite for these rocks are c. 100 Ma [1, 2]. Rb-Sr whole-rock isochron age of the pluton is 96.5 ± 1.3 Ma (SrI = 0.70534 ± 0.00003) and it is concordant with other radiometric ages. Rb-Sr mineral isochron ages range from 84.4 to 97.3 Ma and these ages are relatively younger than the Rb-Sr whole-rock isochron age. The difference among radiometric ages may reflect the difference of the closure temperature in each isotopic system. The Tadamigawa Older-stage granites have SrI for Rb-Sr mineral isochron range from 0.7053 to 0.7061 and are very similar to that (0.70534) for Rb-Sr whole-rock isochron. These may suggest that the Tadamigawa Older-stage granites are generated from same parental magma. However, 87Sr/86Sr ratios of the leached apatite samples were 0.70544-0.70856 and are relatively higher than SrI obtained from the Rb-Sr mineral isochrons (0.7053-0.7061). This result

Precambrian-Cambrian boundary in the Tal formation of Garhwal Lesser Himalaya : Rb-Sr age evidence from black shales underlying phosphorites

International Nuclear Information System (INIS)

Sharma, K.K.; Rameshwar Rao, D.; Azmi, R.J.; Gopalan, K.; Pantulu, G.V.C.

1991-01-01

The recently reported faunal evidence for placing the Precambrian-Cambrian boundary within the main phosphorite unit of the Chert-Phosphorite Member of the Tal Formation, Garhwal Lesser Himalaya, is supported by the present report of 626 ± 13 myr for the whole-rock Rb-Sr isochron age of the black shales directly underlying the phosphorite band. (author). 15 refs., 2 figs., 1 tab

Emergence of the sub-THz central peak at phase transitions in artificial BaTiO3/(Ba,Sr)TiO3 superlattices

International Nuclear Information System (INIS)

Tikhonov, Yu.A.; Razumnaya, A.G.; Torgashev, V.I.; Zakharchenko, I.N.; Yuzyuk, Yu.I.; El Marssi, M.; Ortega, N.; Kumar, A.; Katiyar, R.S.

2015-01-01

A prominent central peak in the sub-THz frequency range was observed in the Raman spectra of BaTiO 3 /(Ba,Sr)TiO 3 (BT/BST) superlattice grown on (001)MgO substrate. Both soft and central mode show an anomaly around 200 K and 280 K, which can be correlated with orthorhombic to monoclinic phase transition of BST and BT, respectively. The observed temperature dependence of the central mode enabled us to explain rather broad temperature dependence of the dielectric permittivity previously observed in BT/BST superlattices. (copyright 2015 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

Application of specific extraction chromatographic methods to the Rb-Sr, Sm-Nd isotope study of geological samples: The Hombreiro-Santa Eulalia Granite (Lugo, NW Spain)

OpenAIRE

Santos Zalduegui, J. F.; Pin, C.; Aranguren, A.; Gil Ibarguchi, José Ignacio

1996-01-01

The analytical application to geological samples of three new chromatographic resins, TRU-Spec ®, Sr-Spec ® and LN-Spec ®) has been investigated. Seven samples of the Hombreiro massif (Lugo, NW Spain) have been studied, that yield a Rb-Sr age of 298 ±5 Ma (SrQ = 0.7086, MSWD = 7.64) for the magma crystallization. Sm-Nd data results for the same massif give eNd values dose to -2 at 300 Ma. This suggests that the origin of the magma might be related to the partial melting of immature sediments,...

Fabrication and characterization of Ba sub x Sr sub 1 sub - sub x TiO sub 3 /YBa sub 2 Cu sub 3 O sub x /SrTiO sub 3 structure

CERN Document Server

Choi, J; Park, S Y; Lee Jae Sik; No, K; Sung, T H; Park, Y

2002-01-01

Ba sub x Sr sub 1 sub - sub x TiO sub 3 (BST)/YBa sub 2 Cu sub 3 O sub x (YBCO)/SrTiO sub 3 (STO) structures were deposited, and the microstructure, orientation and electrical characteristics were investigated. (00l) oriented YBCO thin films were deposited on STO substrates using pulsed laser deposition, and (h00) oriented BST thin films were deposited on YBCO/STO substrates using electron cyclotron resonance (ECR) plasma assisted metal organic chemical vapor deposition (MOCVD). A new phase was formed at the interface between YBCO and BST films and was speculated to be (Ba sub x Y sub 1 sub - sub x)(Ti sub y Y sub 1 sub - sub y)O sub 3. Ba-rich BST films showed a higher dielectric loss than Sr-rich BST films did, which indicates that Sr-rich BST films are more suited for application to microwave devices. The dielectric loss of the films was reduced as temperature decreased, which may be due to the conductivity change of YBCO film and the formation of a conduction path rather than a dielectric property change ...

Possible two-stage /sup 87/Sr evolution in the Stockdale Rhyolite

Energy Technology Data Exchange (ETDEWEB)

Compston, W.; McDougall, I. (Australian National Univ., Canberra. Research School of Earth Sciences); Wyborn, D. (Department of Minerals and Energy, Canberra (Australia). Bureau of Mineral Resources)

1982-12-01

The Rb-Sr total-rock data for the Stockdale Rhyolite, of significance for the Palaeozoic time scale, are more scattered about a single-stage isochron than expected from experimental error. Two-stage /sup 87/Sr evolution for several of the samples is explored to explain this, as an alternative to variation in the initial /sup 87/Sr//sup 86/Sr which is customarily used in single-stage dating models. The deletion of certain samples having very high Rb/Sr removes most of the excess scatter and leads to an estimate of 430 +- 7 m.y. for the age of extrusion. There is a younger alignment of Rb-Sr data within each sampling site at 412 +- 7 m.y. We suggest that the Stockdale Rhyolite is at least 430 m.y. old, that its original range in Rb/Sr was smaller than now observed, and that it experienced a net loss in Sr during later hydrothermal alteration at ca. 412 m.y.

History of the Pasamonte achondrite: relative susceptibility of the Sm-Nd, Rb-Sr, and U-Pb systems to metamorphic events

International Nuclear Information System (INIS)

Unruh, D.M.; Tatsumoto, M.; Nakamura, N.

1977-01-01

The Rb-Sr, Sm-Nd, and U-Pb systematics of the eucrite Pasamonte have been studied in order to investigate the relative susceptibility of the different systems to post-crystallization events and to determine the age and history of the meteorite. The Rb-Sr and 238 U- 206 Pb data of mineral separates do not define an isochron but the Sm-Nd data define an internal isochron which corresponds to the formation age of 4.58+-0.12 b.y. (10 9 years). The 207 Pb- 206 Pb data of mineral separates define an apparent age of 4.53+-0.03 b.y., however it is concluded that this age, while in agreement with the Sm-Nd age, is not strictly valid since the U-Pb data indicate at least three stages of evolution. The U-Pb data indicate that the parent body of the meteorite experienced brecciation shortly after the formation of the parent body surface (approximately 4.2-4.45 b.y. ago) and a recent disturbance (collision) 6+-30 m.y. ago. The latter age is within the range of cosmic ray exposure ages for achondrites. (Auth.)

Comparative study of the ionic exchange of Ca++, Sr++, and Ba++ cations on resins and inorganic exchangers

International Nuclear Information System (INIS)

Sanchez Batanero, P.

1969-03-01

With a view to applying the results to certain problems related to chemical separations in activation analysis, a study has been made, of the possibilities of separating the alkaline-earth elements Ca, Sr and Ba on organic resins and inorganic exchangers using the radioactive indicator method. The partition coefficients of the cations Ca 2+ , Sr 2+ and Ba 2+ have been measured on Dowex 50 W (NH 4 + ) x 8 resin in the presence of EDTA - NTA - EGTA and DCTA as complexing agents, and on zirconium phosphate, tungstate and molybdate in the presence of HCl and NH 4 Cl. Methods have been developed for separating mixtures of alkaline-earth elements using DCTA-NH 4 + followed by elution on Dowex 50 W (NH 4 + ) x 8 resin columns and on zirconium phosphate. Amongst the complexing agents used on the ion-exchange resins the most promising appears to be DCTA which leads to partition coefficients Ca, Sr and Ba which are very different. The results of measurements of partition coefficients on zirconium phosphate (NH 4 + form) using DCTA-NH 4 + show the interesting possibilities of separations on columns. The separation of the alkaline-earth elements on zirconium phosphate seems to be less quantitative than on Dowex 50 resin; it is however much faster in the former case and this can be useful for treating short half-life radioisotopes in activation analysis. (author) [fr

Rb-Sr and Nd-Sr isotope geochemistry and petrogenesis of the Misho Mountains mafic dikes (NW Iran

Directory of Open Access Journals (Sweden)

Maryam Ahankoub

2017-02-01

Full Text Available Introduction There are some theories about the Paleotethys event during the Paleozoic that have been proposed by geologists (Metcalfe, 2006. Some scientist offered some pieces of evidence about the northern margin of Gondwana (Zhu et al., 2010. The Paleotethys Ocean and Hercynian orogenic report first in Iran, have been Offered from the Morrow and Misho Mountain (Eftekharnejad, 1981. Misho Mountains is located between the north and south Misho faults and cause the formation of a positive flower structure (Moayyed and Hossainzade, 2011. There is theory about Misho southern fault as the best candidate of the Paleotethys suture zone (Moayyed and Hossainzade, 2011. Geochemistry and Sr –Nd isotopic data of the A2 granitic and Synite rocks of the East Misho, indicate that the magmatism post collision has occurred in the active continental margin by extensional zones of the following the closure of the Paleotethys (Ahankoub, 2012. Granite and syenite rocks have been cut by mafic dikes. Mafic dikes are often formed in extensional tectonic settings related to mantle plume or continental break –up (Zhu et al., 2009. In this paper, we use the geochemistry and Nd-Sr isotope data to determined petrogenesis, tectono-magmatic setting and age of Misho mafic dikes. Materials and methods After petrography study of 30 thin sections of mafic dike rocks, 8 samples were selected for whole-rock chemical analyses using ICP-MS and ICP-AES instruments by ACME Company in Vancouver, Canada. We prepared 6 sample For Sm-Nd and Rb-Sr analysis. Sr and Nd isotope ratios were measured with a thermal ionization mass spectrometer, VG Sector 54–30 at the Nagoya University. The isotope abundances of Rb, Sr, Nd, and Sm were measured by the ID method with a Finnigan MAT Thermoquad THQ thermal ionization quadrupole mass spectrometer at the Nagoya University. NBS987 and JNdi-1 were measured as natural Sr and Nd isotope ratio standards (Tanaka et al., 2000. Averages and 2σ errors

Luminescence investigations of rare earth doped lead-free borate glasses modified by MO (M = Ca, Sr, Ba)

Energy Technology Data Exchange (ETDEWEB)

Janek, Joanna, E-mail: janek.joanna@gmail.com; Sołtys, Marta; Żur, Lidia; Pietrasik, Ewa; Pisarska, Joanna; Pisarski, Wojciech A.

2016-09-01

Series of lead-free borate glasses with different oxide modifiers and lanthanide ions were prepared. The effect of oxide modifiers MO (M = Ca, Sr, Ba) on spectroscopic properties of trivalent Ln{sup 3+} (Ln = Eu, Er, Pr) were systematically investigated. Especially, the luminescence spectra of Ln{sup 3+}-doped lead-free borate glasses are presented and discussed in relation to the impact of selective components (CaO, SrO and BaO). Several spectroscopic parameters, such as the fluorescence intensity ratio R/O (Eu{sup 3+}) and measured luminescence lifetimes for the {sup 5}D{sub 0} (Eu{sup 3+}), {sup 4}I{sub 13/2} (Er{sup 3+}) and {sup 1}D{sub 2} (Pr{sup 3+}) excited states of lanthanide ions were analyzed in details. The research proved that spectroscopic properties of trivalent Ln{sup 3+} depend significantly on kind of presence oxide modifiers MO (M = Ca, Sr, Ba) in glass host matrices. - Highlights: • Luminescence of Ln{sup 3+}-doped borate glasses was presented and discussed. • Effect of glass modifiers on spectroscopic properties of rare earths was studied. • Measured luminescence lifetimes of Ln{sup 3+} (Ln = Eu, Er, Pr) were analyzed. • Luminescence intensity ratios R/O (Eu{sup 3+}) were determined.

Comparative study of the ionic exchange of Ca{sup ++}, Sr{sup ++}, and Ba{sup ++} cations on resins and inorganic exchangers; Etude comparative de l'echange ionique des cations Ca{sup ++}, Sr{sup ++} et Ba{sup ++} sur resine et sur echangeurs mineraux

Energy Technology Data Exchange (ETDEWEB)

Sanchez Batanero, P [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1969-03-01

With a view to applying the results to certain problems related to chemical separations in activation analysis, a study has been made, of the possibilities of separating the alkaline-earth elements Ca, Sr and Ba on organic resins and inorganic exchangers using the radioactive indicator method. The partition coefficients of the cations Ca{sup 2+}, Sr{sup 2+} and Ba{sup 2+} have been measured on Dowex 50 W (NH{sub 4}{sup +}) x 8 resin in the presence of EDTA - NTA - EGTA and DCTA as complexing agents, and on zirconium phosphate, tungstate and molybdate in the presence of HCl and NH{sub 4}Cl. Methods have been developed for separating mixtures of alkaline-earth elements using DCTA-NH{sub 4}{sup +} followed by elution on Dowex 50 W (NH{sub 4}{sup +}) x 8 resin columns and on zirconium phosphate. Amongst the complexing agents used on the ion-exchange resins the most promising appears to be DCTA which leads to partition coefficients Ca, Sr and Ba which are very different. The results of measurements of partition coefficients on zirconium phosphate (NH{sub 4}{sup +} form) using DCTA-NH{sub 4}{sup +} show the interesting possibilities of separations on columns. The separation of the alkaline-earth elements on zirconium phosphate seems to be less quantitative than on Dowex 50 resin; it is however much faster in the former case and this can be useful for treating short half-life radioisotopes in activation analysis. (author) [French] En vue de l'application a certains problemes de separations chimiques en analyse par activation, on a etudie les possibilites de separation des elements alcalino-terreux Ca-Sr et Ba sur resine organique et sur echangeurs mineraux par la methode des indicateurs radioactifs. Les coefficients de partage des cations Ca{sup +2}, Sr{sup +2} et Ba{sup +2} sur resine Dowex 50 W (NH{sub 4}{sup +}) x 8 en milieux complexants EDTA - NTA - EGTA et DCTA et sur phosphate, tungstate et molybdate de zirconium en milieu HCl et NH{sub 4}Cl ont ete mesures. Des

Effect of Sr substitution on superconductivity in Hg2(Ba1-ySry)2YCu2O8-d (part 1): a neutron powder diffraction study

OpenAIRE

Toulemonde, P.; Odier, P.; Bordet, P.; Floch, S. Le; Suard, E.

2002-01-01

The effect of Sr chemical pressure on superconductivity was investigated in Hg2(Ba1-ySry)2YCu2O8-d. The samples were synthesized at high pressure-high temperature from y = 0.0 to full substitution, y = 1.0. These Sr-substituted compounds are superconducting, without Ca doping on the Y site, and show an increasing Tc with Sr, reaching 42 K for y = 1.0. A detailed neutron powder diffraction study compares the structural changes induced by this chemical Sr/Ba substitution and the mechanical pres...

Effects of Sr2+ substitution on photoluminescence characteristics of Ba1−x−ySryZrSi3O9:xEu2+ phosphors

International Nuclear Information System (INIS)

Chiang, Chung-Hao; Gong, Syuan-Jhih; Lin, Han-Yu; Zhan, Ting-Shi; Chu, Sheng-Yuan

2014-01-01

In this work, single-phase Ba 1−x−y Sr y ZrSi 3 O 9 :xEu 2+ phosphors were synthesized via the solid-state reaction method. The crystal structure and luminescence properties were investigated using X-ray diffraction and photoluminescence measurements, respectively. An increase of the dopant Sr 2+ increased the emission intensity of the phosphors. The peak intensity of the samples was at y = 0.4 under near-ultraviolet light excitation (397 nm). The wavelength of the emission peaks red-shifts slightly from 477 to 483 nm due to the splitting of the 5d energy level. Sr 2+ ions have a smaller ionic radius than that of Ba 2+ ions, and thus the dopant changes the crystal structure, improving the energy transfer efficiency between luminescence centers. More Eu 2+ solid solubility was found in Ba 0.6−x Sr 0.4 ZrSi 3 O 9 :xEu 2+ phosphors (10 mol. %) than in the host BaZrSi 3 O 9 (6 mol. %), which enhanced the emission intensity. In addition, the thermal reliability of the phosphors was studied

A reconnaissance Rb-Sr, Sm-Nd, U-Pb, and K-Ar study of some host rocks and ore minerals in the West Shasta Cu- Zn district, California ( USA).

Science.gov (United States)

Kistler, R.W.; McKee, E.H.; Futa, K.; Peterman, Z.E.; Zartman, R.E.

1985-01-01

The Copley Greenstone, Balaklala Rhyolite, and Mule Mountain stock in the West Shasta Cu-Zn district, California, have Rb-Sr, Sm-Nd, U-Pb, and K-Ar systematics that indicate they are a cogenetic suite of ensimatic island-arc rocks about 400 Ma. Pervasive alteration and mineralization of these rocks, for the most part, was syngenetic and the major component of the mineralizing fluid was Devonian seawater. K-Ar ages of quarz-sericite concentrates from ore horizons and Rb-Sr systematics of a few rock and ore specimens record a later thermal and mineralizing event in the district of about 260 Ma. Contamination of some rocks with pelagic sediments is indicated by the Sm-Nd data. -Authors

Ab initio hybrid DFT calculations of BaTiO{sub 3}, PbTiO{sub 3}, SrZrO{sub 3} and PbZrO{sub 3} (111) surfaces

Energy Technology Data Exchange (ETDEWEB)

Eglitis, Roberts I., E-mail: rieglitis@gmail.com

2015-12-15

Highlights: • Surface energies for AO{sub 3}-term (111) surfaces are larger than for Ti (Zr)-term surfaces. • A increase of Ti−O (Zr−O) bond covalency near the ABO{sub 3} (111) surface relative to the bulk is observed. • The ABO{sub 3} (111) surface energy is larger than the earlier calculated (001) surface energy. • Band gap for PbTiO{sub 3}, SrZrO{sub 3} and PbZrO{sub 3} (111) surfaces becomes smaller, but for BaTiO{sub 3} (111) larger with respect to the bulk . - Abstract: The results of ab initio calculations for polar BaTiO{sub 3}, PbTiO{sub 3}, SrZrO{sub 3} and PbZrO{sub 3} (111) surfaces using the CRYSTAL code are presented. By means of the hybrid B3LYP approach, the surface relaxation has been calculated for two possible B (B = Ti or Zr) or AO{sub 3} (A = Ba, Pb or Sr) BaTiO{sub 3}, PbTiO{sub 3}, SrZrO{sub 3} and PbZrO{sub 3} (111) surface terminations. According to performed B3LYP calculations, all atoms of the first surface layer, for both terminations, relax inwards. The only exception is a small outward relaxation of the PbO{sub 3}-terminated PbTiO{sub 3} (111) surface upper layer Pb atom. B3LYP calculated surface energies for BaO{sub 3}, PbO{sub 3}, SrO{sub 3} and PbO{sub 3}-terminated BaTiO{sub 3}, PbTiO{sub 3}, SrZrO{sub 3} and PbZrO{sub 3} (111) surfaces are considerably larger than the surface energies for Ti (Zr)-terminated (111) surfaces. Performed B3LYP calculations indicate a considerable increase of Ti−O (Zr−O) chemical bond covalency near the BaTiO{sub 3}, PbTiO{sub 3}, SrZrO{sub 3} and PbZrO{sub 3} (111) surface relative to the BaTiO{sub 3}, PbTiO{sub 3}, SrZrO{sub 3} and PbZrO{sub 3} bulk. Calculated band gaps at the Γ-point near the PbTiO{sub 3}, SrZrO{sub 3} and PbZrO{sub 3} (111) surfaces are reduced, but near BaTiO{sub 3} (111) surfaces increased, with respect to the BaTiO{sub 3}, PbTiO{sub 3}, SrZrO{sub 3} and PbZrO{sub 3} bulk band gap at the Γ-point values.

Luminescence Properties of Self-Activated Mm(VO4)2 (M = Mg, Ca, Sr, and Ba) Phosphors Synthesized by Solid-State Reaction Method.

Science.gov (United States)

Min, Xin; Huang, Zhaohui; Fang, Minghao; Liu, Yan'gai; Tang, Chao; Wu, Xiaowen

2016-04-01

In this paper, M3(VO4)2 (M = Mg, Ca, Sr, and Ba) self-activated phosphors were prepared by a solid-state reaction method at 1,000 °C for 5 h. The phase formation and micrographs were analyzed by X-ray diffraction and scanning electron microscopy. The Ca3(VO4)2 phosphor does not show any emission peaks under excitation with ultraviolet (UV) light. However, the M3(VO4)2 (M = Mg, Sr, and Ba) samples are effectively excited by UV light chips ranging from 200 nm to 400 nm and exhibit broad emission bands due to the charge transfer from the oxygen 2p orbital to the vacant 3d orbital of the vanadium in the VO4. The color of these phosphors changes from yellow to light blue via blue-green with increasing ionic radius from Mg to Sr to Ba. The luminescence lifetimes and quantum yield decrease with the increasing unit cell volume and V-V distance, in the order of Mg3(VO4)2 to Sr3(VO4)2 to Ba3(VO4)2. The emission intensity decreases with the increase of temperatures, but presents no color shift. This confirms that these self-activated M3(VO4)2 phosphors can be suggested as candidates of the single-phase phosphors for light using UV light emitting diodes (LEDs).

Luminescence characteristics of Sr{sub 1-x}Ba{sub x}Si{sub 2}O{sub 2}N{sub 2}:Eu{sup 2+} phosphors for white light emitting diodes

Energy Technology Data Exchange (ETDEWEB)

Anoop, G.; Cho, I.H.; Suh, D.W.; Yoo, J.S. [Display Materials Laboratory, School of Chemical Engineering and Materials Science, Chung-Ang University, Heukseok-Dong 221, Dongjak-gu, Seoul 156-756 (Korea, Republic of)

2012-12-15

Sr{sub 1-x}Ba{sub x}Si{sub 2}O{sub 2}N{sub 2}:Eu{sup 2+} phosphors were synthesized using high temperature solid state reaction. The effect of Ba incorporation on the structural and luminescence characteristics of SrSi{sub 2}O{sub 2}N{sub 2}:Eu{sup 2+} phosphors were studied. The phosphors were crystallized in triclinic crystal structure and the cell volume increases monotonically with Ba addition. The PL emission peak wavelength red shifts with Ba up to x = 0.50 beyond which no red shift is observed. The XPS analysis shows that nitrogen is being incorporated into the host lattice along with Ba addition up to x = 0.50. The as synthesized phosphors show high thermal stability. Phosphor converted light emitting diodes were realized using Sr{sub 1-x}Ba{sub x}Si{sub 2}O{sub 2}N{sub 2}:Eu{sup 2+} phosphors (x = 0 and x = 0.40) showing luminance efficacies of 108 and 101 lm W{sup -1}. The CIE chromaticity coordinates of Sr{sub 1-x}Ba{sub x}Si{sub 2}O{sub 2}N{sub 2}:Eu (x = 0 and x = 0.40) phosphors. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Effects of La{sub 2}O{sub 3}-doping and sintering temperature on the dielectric properties of BaSrTiO{sub 3} ceramics

Energy Technology Data Exchange (ETDEWEB)

Zhao, Hong Wei; Chang, Chun Rui [College of Science, North China University of Science and Technology, Hebei Province (China); Li, Yuan Liang [Hebei Provincial Key Laboratory of Inorganic Nonmetallic Materials, North China University of Science and Technology, Hebei Province (China); Yan, Chun Liang [Analysis and Testing Center, North China University of Science and Technology, Hebei Province (China)

2016-03-15

Using BaCO{sub 3}, SrCO{sub 3} and TiO{sub 2}, et al as crude materials, La{sub 2}O{sub 3} as dopant, Ba{sub 0.8}Sr{sub 0.2}TiO{sub 3} (BST) Ceramics of perovskite structure were prepared by solid state reaction method. We investigated the effects of La{sub 2}O{sub 3} -doping and sintering temperature on the dielectric properties of BaSrTiO{sub 3} ceramics. The experiment results show that: The amount of La{sub 2}O{sub 3} can increase the dielectric constant of the sample, with the doping amount increasing, the dielectric constant increases. The sintering temperature has also significant impact on the dielectric properties. The dielectric constant of the sample reaches its highest point at 1280 °C. (author)

Effect of oxygen gas and annealing treatment for magnetically enhanced reactive ion etched (Ba0.65,Sr0.35)TiO3 thin films

International Nuclear Information System (INIS)

Zhang Baishun; Quan Zuci; Zhang Tianjin; Guo Tao; Mo Shaobo

2007-01-01

Sol-gel-derived (Ba 0.65 ,Sr 0.35 )TiO 3 (BST) thin films were etched in CF 4 /Ar and CF 4 /Ar/O 2 plasmas using magnetically enhanced reactive ion etching technology. Experimental results show that adding appropriate O 2 to CF 4 /Ar can better the etching effects of BST films for the increase of etching rate and decrease of etched residues. The maximum etching rate is 8.47 nm/min when CF 4 /Ar/O 2 gas-mixing ratio is equal to 9/36/5. X-ray photoelectron spectroscopy (XPS) data confirm accumulation of reaction products on the etched surface due to low volatility of reaction products such as Ba and Sr fluorides, and these residues could be removed by annealing treatment. The exact peak positions and chemical shifts of the interested elements were deduced by fitting XPS narrow-scan spectra with symmetrical Gaussian-Lorentzian product function for Ba 3d, Sr 3d, and O 1s peaks, meanwhile asymmetrical Gaussian-Lorentzian sum function was used to fit Ti 2p doublet to adjust the multiple splitting and/or shake-up process of transition-metal Ti cations. Compared to the unetched counterparts, the etched Ba 3d 5/2 , Ba 3d 3/2 , Sr 3d 5/2 , Sr 3d 3/2 , Ti 2p 3/2 , Ti 2p 1/2 , and O 1s peaks shift towards higher binding energy regions by amounts of 1.31, 1.30, 0.60, 0.79, 0.09, 0.46, and 0.50 eV, respectively. While the etched Ti 2p 3/2 and Ti 2p 1/2 peaks have small chemical shifts for two reasons. One is that Ti fluoride (TiF z ) is mostly removed from the etched surface because of its higher volatility in the process of thermal desorption. The other is that there is a shift compensation between TiF z and the etched BST matrix in which Ti 4+ cations are partially reduced to form Ti x+ (0 0.65 ,Sr 0.35 )Ti 0.97 O 2.86 , (Ba 0.70 ,Sr 0.30 )Ti 0.24 O 1.39 , and (Ba 0.68 ,Sr 0.32 )Ti 0.95 O 2.74 , and then the average valence of Ti cations is estimated to be +3.84, +3.25, and +3.66 with respect to the electroneutrality principle, respectively. It is inferred that electrical

Multi-proxy Reconstructions of the Eastern Equatorial Pacific: Measuring Sr/Ca, Ba/Ca, and Li/Mg in Modern Corals Using ICP-OES

Science.gov (United States)

Cheung, A. H.; Cole, J. E.; Vetter, L.; Jimenez, G.; Thompson, D. M.; Tudhope, A. W.

2017-12-01

Sea surface temperature (SST) in the Eastern Equatorial Pacific (EEP) exhibits large variability on multiple timescales. These variations are often related to modes of climate variability that exert significant influence on global climate, such as the El Niño Southern Oscillation. However, the short length and sparsity of instrumental data in the EEP limits our ability to discern changes in this region. Geochemical signals in corals can help extend instrumental data further back in time. While δ18O and Sr/Ca are the most commonly analyzed geochemical tracers of SST in corals, they often have site-specific complications. Several alternatives (e.g., Li/Mg) have been proposed to overcome these challenges, but have yet to be applied to long climate records, in part due to the cost and time required to measure these elements. Here, we develop a new method that uses Inductively Coupled Plasma-Optical Emission Spectrometry (ICP-OES) to analyze Li/Mg, Sr/Ca, and Ba/Ca ratios in coral aragonite. We apply this method to two Porites spp. corals collected from the northern Galapagos archipelago (Wolf and Darwin Islands). We specifically assess the fidelity of Li/Mg and Sr/Ca to reconstruct SST, and Ba/Ca to reconstruct upwelling conditions. Our results confirm that both Li/Mg and Sr/Ca track SST. We show that despite analytical noise, downcore reconstructions of Li/Mg have the potential to provide additional information about SST that is not present in reconstructions generated from Sr/Ca alone. Skeletal Ba/Ca shows little relationship with upwelling, perhaps because of the distance of our sites from the center of upwelling in the southern Galapagos. These results demonstrate the potential for analyzing Sr, Li, Ba, Mg simultaneously in corals with a cost- and time- efficient method, which may be applied to coral paleoclimate sites worldwide.

Age of granitoids from the Kohut Veporic zone according to Rb-Sr isochrone analysis

International Nuclear Information System (INIS)

Cambel, B.; Bagdasaryan, G.P.; Gukasyan, R.K.; Dupej, J.

1988-01-01

Rb-Sr isochrone analyses of granitoid rocks from the southern part of the Veporic zone - the so-called Kohut zone - are presented. In this region, the Sinec (Rimavica) type of granitoids formerly considered to be Late Palaeozoic to Neoide, is found. The present isochrone research determines them as equivalents of granitoids of the Sihla type (387±27 m.y.). The Sinec (Rimavica) granite reaches an age of 392±5 m.y. This extended age must partly be attributed to additional processes which took place in the stage of retrograde alterations. The conclusions are of considerable importance in clarifying the metamorphic age and stratigraphy of the crystalline complex in the region of the southern Veporic zone. (author). 9 figs., 4 tabs., 38 refs

Structure evolution upon chemical and physical pressure in (Sr{sub 1−x}Ba{sub x}){sub 2}FeSbO{sub 6}

Energy Technology Data Exchange (ETDEWEB)

Tiittanen, T.; Karppinen, M., E-mail: maarit.karppinen@aalto.fi

2017-02-15

Here we demonstrate the gradual structural transformation from the monoclinic I2/m to tetragonal I4/m, cubic Fm-3m and hexagonal P6{sub 3}/mmc structure upon the isovalent larger-for-smaller A-site cation substitution in the B-site ordered double-perovskite system (Sr{sub 1−x}Ba{sub x}){sub 2}FeSbO{sub 6}. This is the same transformation sequence previously observed up to Fm-3m upon heating the parent Sr{sub 2}FeSbO{sub 6} phase to high temperatures. High-pressure treatment, on the other hand, transforms the hexagonal P6{sub 3}/mmc structure of the other end member Ba{sub 2}FeSbO{sub 6} back to the cubic Fm-3m structure. Hence we may conclude that chemical pressure, physical pressure and decreasing temperature all work towards the same direction in the (Sr{sub 1−x}Ba{sub x}){sub 2}FeSbO{sub 6} system. Also shown is that with increasing Ba-for-Sr substitution level, i.e. with decreasing chemical pressure effect, the degree-of-order among the B-site cations, Fe and Sb, decreases. - Graphical abstract: In the (Sr{sub 1−x}Ba{sub x}){sub 2}FeSbO{sub 6} double-perovskite system the gradual structural transformation from the monoclinic I2/m to tetragonal I4/m, cubic Fm-3m and hexagonal P6{sub 3}/mmc structure is seen upon the isovalent larger-for-smaller A-site cation substitution. High-pressure treatment under 4 GPa extends stability of the cubic Fm-3m structure within a wider substitution range of x. - Highlights: • Gradual structural transitions upon A-cation substitution in (Sr{sub 1−x}Ba{sub x}){sub 2}FeSbO{sub 6.} • With increasing x structure changes from I2/m to I4/m, Fm-3m and P6{sub 3}/mmc. • Degree of B-site order decreases with increasing x and A-site cation radius. • High-pressure treatment extends cubic Fm-3m phase stability for wider x range. • High-pressure treatment affects bond lengths mostly around the A-cation.

Effects of Sr-substitution on the structural and magnetic behavior of Ba-based Y-type hexagonal ferrites

International Nuclear Information System (INIS)

Ahmad, Mukhtar; Ali, Qasim; Ali, Ihsan; Ahmad, Ishtiaq; Azhar Khan, M.; Akhtar, Majid Niaz; Murtaza, G.; Rana, M.U.

2013-01-01

Highlights: •Sr-substituted Y-type hexaferrites synthesized by sol–gel method have been investigated. •Platelet grains with well defined hexagonal shape are suitable for microwave absorbers. •Saturation magnetization values were calculated by the law of approach to saturation. •Coercivity of a few hundred oersteds found for all samples is suitable for EM materials. -- Abstract: Sr-substituted samples of Y-type hexagonal ferrites with chemical formula Ba 2−x Sr x Ni 2 Fe 12 O 22 (x = 0.0, 0.2, 0.4, 0.6, 0.8, 1.0) were synthesized using the sol–gel autocombustion method and were sintered at 1150 °C for 3 h. The samples were investigated by differential thermal and thermogravimetry analysis, X-ray diffraction, scanning electron microscopy, energy dispersive X-ray spectroscopy and vibrating sample magnetometry. X-ray diffraction analysis reveals that single phase samples can be achieved by substituting Sr 2+ ions at Ba 2+ sites in Y-type hexagonal ferrites. X-ray density and bulk density were observed to decrease whereas porosity increased with increasing Sr-concentration. All the samples show well defined hexagonal shape which is favorable for microwave absorbing purposes. The saturation magnetization values were calculated from M–H loops by the law of approach to saturation. The loops show low values of coercivity of a few hundred oersteds which is one of the necessary conditions for electromagnetic (EM) materials and is suitable for security, switching, sensing and high frequency applications

Magnetic and magneto-transport properties of double perovskite Ba{sub 2-x}Sr{sub x}FeMoO{sub 6} system

Energy Technology Data Exchange (ETDEWEB)

Pandey, Vibhav; Verma, Vivek; Aloysius, R.P. [National Physical Laboratory, Dr. K.S. Krishnan Marg, New Delhi-110012 (India); Bhalla, G.L. [Department of Physics and Astrophysics, Delhi University, Delhi (India); Awana, V.P.S.; Kishan, H. [National Physical Laboratory, Dr. K.S. Krishnan Marg, New Delhi-110012 (India); Kotnala, R.K. [National Physical Laboratory, Dr. K.S. Krishnan Marg, New Delhi-110012 (India)], E-mail: rkkotnala@gmail.com

2009-07-15

The structural magnetic and magneto-transport properties of double perovskite system Ba{sub 2-x}Sr{sub x}FeMoO{sub 6} (0{<=}x{<=}1.0) prepared in bulk polycrystalline form are reported in this paper. X-ray diffraction analysis showed that samples are single phase and the lattice constants decreases with increase in the Sr content. The degree of Fe-Mo ordering has been found decreasing in the series with an increase in the Sr content. Parent compound Ba{sub 2}FeMoO{sub 6} exhibits saturation magnetic moment value of 3.54 {mu}{sub B}/f.u. at 85 K in a magnetic field of 6000 Oe. Temperature dependence of resistivity shows metallic behavior for all the samples. The magneto-resistance (MR) of the compound with x=0.4 is higher than that of the other samples. At room temperature this system shows a saturation magnetization value of 1.73 {mu}{sub B}/f.u. and MR value of 7.08% (1 T). The observed variations in the structural and magnetic properties are attributed to the change of chemical pressure due to the substitution of Sr in place of Ba. The effect of antisite disorder (ASD) defects on magneto-transport properties is studied in more detail.

Preparation of cauliflower-like shaped Ba0.6Sr0.4TiO3 powders by modified oxalate co-precipitation method

International Nuclear Information System (INIS)

Li Mingli; Xu Mingxia

2009-01-01

The quantitative barium-strontium titanyl oxalate (Ba 0.6 Sr 0.4 TiO(C 2 O 4 ) 2 .4H 2 O, BSTO) precursor powders were prepared by the modified oxalate co-preparation method. It was based on the cation-exchange reaction between the stoichiometric solutions of oxalotitanic acid (H 2 TiO(C 2 O 4 ) 2 , HTO) and barium + strontium nitrate solution containing stoichiometric quantities of Ba and Sr ions. The pyrolysis of BSTO at 800 deg. C/4 h in air produced the homogeneous cauliflower-like shaped barium-strontium titanate (Ba 0.6 Sr 0.4 TiO 3 , BST) powders. The effect of polyethylene glycol (PEG) on morphology of BSTO and BST powders was also investigated. The characterization studies were carried on the as-dried BSTO and calcined BST powders by various physicochemical techniques, IR, X-ray diffraction (XRD), scanning electron microscopy (SEM), etc. The BSTO and BST powders obtained by aforementioned technique without PEG were homogeneous with spherical shape. The particles grew into spindle shape with the effect of PEG

Accurate calculations of the ground state and low-lying excited states of the (RbBa)⁺ molecular ion: a proposed system for ultracold reactive collisions

DEFF Research Database (Denmark)

Knecht, Stefan; Sørensen, Lasse Kragh; Jensen, Hans Jørgen Aagaard

2010-01-01

Collisions of ultracold Ba+ ions on a Rb Bose–Einstein condensate have been suggested as a possible benchmark system for ultracold ion-neutral collision experiments. However, a priori knowledge of the possible processes is desirable. For this purpose, we here present high-level four-component cou...

Preparation of MAl 2 O 4 : Eu 2+ , Sm 3+ (M = Ca, Sr, Ba) Phosphors ...

African Journals Online (AJOL)

A series of MAl2O4: Eu2+, Sm3+ (M = Ca, Sr, Ba) phosphors was prepared by the combustion method, and the influence of these alkaline earth metals on the structure and luminescent performances for these phosphors was investigated. A relationship was established between their composition, crystallization capacity and ...

Theoretical characterization of quaternary iridium based hydrides NaAeIrH{sub 6} (Ae = Ca, Ba and Sr)

Energy Technology Data Exchange (ETDEWEB)

Bouras, S. [Laboratory of Studies Surfaces and Interfaces of Solids Materials, Department of Physics, Faculty of Science, University of Setif 1, 19000 (Algeria); Ghebouli, B., E-mail: bghebouli@yahoo.fr [Laboratory of Studies Surfaces and Interfaces of Solids Materials, Department of Physics, Faculty of Science, University of Setif 1, 19000 (Algeria); Benkerri, M. [Laboratory of Studies Surfaces and Interfaces of Solids Materials, Department of Physics, Faculty of Science, University of Setif 1, 19000 (Algeria); Ghebouli, M.A., E-mail: med.amineghebouli@yahoo.fr [Microelectronic Laboratory (LMSE), University of Bachir Ibrahimi, Bordj-Bou-Arreridj 34000 (Algeria); Research Unit on Emerging Materials (RUEM), University of Setif 1, 19000 (Algeria); Choutri, H. [Microelectronic Laboratory (LMSE), University of Bachir Ibrahimi, Bordj-Bou-Arreridj 34000 (Algeria); Louail, L.; Chihi, T.; Fatmi, M. [Research Unit on Emerging Materials (RUEM), University of Setif 1, 19000 (Algeria); Bouhemadou, A. [Laboratory for Developing New Materials and Their Characterization, Department of Physics, Faculty of Science, University of Setif 1, 19000 (Algeria); Department of Physics and Astronomy, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451 (Saudi Arabia); Khenata, R.; Khachai, H. [Laboratoire de Physique Quantique et de Modélisation Mathématique, Université de Mascara, 29000 (Algeria)

2015-01-15

The quaternary iridium based hydrides NaAeIrH{sub 6} (Ae = Ca, Ba and Sr) are promising candidates as hydrogen storage materials. We have studied the structural, elastic, electronic, optical and thermodynamic properties of NaAeIrH{sub 6} (Ae = Ca, Ba and Sr) within the generalized gradient approximation, the local density approximation (LDA) and mBj in the frame of density functional perturbation theory. These alloys have a large indirect Γ–X band gap. The thermodynamic functions were computed using the phonon density of states. The origin of the possible transitions from valence band to conduction band was illustrated. By using the complex dielectric function, the optical properties such as absorption, reflectivity, loss function, refractive index and optical conductivity have been obtained. - Graphical abstract: Real and imaginary parts of the dielectric function, the absorption spectrum α(ω), reflectivity R(ω) and energy-loss spectrum L(ω). - Highlights: • NaAeIrH{sub 6} (Ae = Ca, Ba and Sr) alloys have been investigated. • The elastic moduli, energy gaps are predicted. • The optical and thermal properties were studied.

Application of the Rb-Sr, Pb-Pb and Sm-Nd systems on the Salobe 3A polymetallic deposit, Carajas Mineral Province, Para, Brazil; Aplicacao dos sistemas Rb-Sr, Pb-Pb e Sm-Nd do deposito polimetalico do Salobo 3A, Provincia Mineral de Carajas, Para

Energy Technology Data Exchange (ETDEWEB)

Mellito, Katia Maria

1998-07-01

The Salobo 3A polymetallic Cu (Au-Mo-Ag) deposit, located in the northern part of the Carajas Mineral Province, Para, consists of a metavolcano-sedimentary sequence represented by iron formation, amphibolite, schist and quartzite of the Igarape Salobo Group. This rock sequence rest uncomformably on the gneissic basement of the Xingu Complex. The copper mineralization hosted by iron formation consists of bornite-chalcocite and bornite-chalcopyrite disseminations associated with magnetite. The geochronological data determined through the application of the Rb-Sr, Sm-Nd and Pb-Pb methods, contribute to characterize the complex evolution of both the geological setting and the cupriferous mineralization of the Salobo deposit. The 3.11-2.92 Ga interval (T{sub DM}, Sm-Nd, whole rock) represents the age of the igneous protholith of the gneiss. The {epsilon}{sub Nd} values calculated for the time of the gneiss formation (2859 Ma) vary between +1.02 and -1.08, and indicate a short period between the mantle-crust differentiation epoch and the gneiss formation. Moreover, the {epsilon}{sub Nd} parameter suggest a mantle source with late crustal contamination. The application of the leaching technique allows a gradual extraction of Pb at each leaching step and it was applied to chalcocite and magnetite. The 2762 {+-} 180 Ma and 2776 {+-} 240 Ma ages determined on those minerals are interpreted to be close to the epoch of the formation of the copper mineralization with Uu and Th enrichment and of the iron formation deposition, respectively, in a conventional setting. The leaching technique was also applied to tourmaline from gneiss and quartzite, and the age near to 2400 Ma was attributed to its formation. The random variability of the Pb isotope compositions of the tourmaline together with its petrographic characteristics suggest the boron source is not associated with the metassedimentary rocks of the Igarape Salobo Group. The Sm-Nd mineral isochron attributed to schists

Magnetic and electrical transport properties of La0.5A0.5CoO3 nanoparticles (A = Sr, Ca, and Ba)

International Nuclear Information System (INIS)

Roy, B.; Das, S.

2011-01-01

Research highlights: → La 0.5 A 0.5 CoO 3 (A = Sr, Ca, and Ba) nanoparticles prepared by sol-gel technique. → Size-induced metal-insulator transition in Sr- and Ba-doped samples. → Broad paramagnetic to ferromagnetic transition with large magnetic irreversibility. → Co 3+ ions in intermediate and Co 4+ in a mixture of intermediate and high spin states. → ac magnetization suggests magnetic cluster glass nature of the samples. - Abstract: We have investigated the effect of particle size on the electrical transport and magnetic properties of La 0.5 A 0.5 CoO 3 (A = Sr, Ca, and Ba) nanoparticles synthesized by sol-gel technique. A size-induced metal to insulator transition is observed in the resistivity behaviour of Sr- and Ba-doped samples as the dimension changes from higher to lower ones. The magnetoresistance exhibits almost linear behaviour throughout the studied field range. The zero-field-cooled (ZFC) and field-cooled (FC) magnetizations display a broad paramagnetic to ferromagnetic transition at T C with a large magnetic irreversibility. The magnetization results indicate that Co 3+ ions are in the intermediate spin state but Co 4+ ions stay in a mixture of intermediate and high spin states. The observed frequency dependent shoulder in the in-phase and the peak in the out of phase component of the ac susceptibility indicate the glassy nature of the samples. The analysis of the ac magnetization results suggests that the magnetic behaviour is consistent with the cluster glass model.

[Distribution of rubidium, cesium, beryllium, strontium, and barium in blood and urine in general Chinese population].

Science.gov (United States)

Ding, Chunguang; Pan, Yajuan; Zhang, Aihua; Zhu, Chun; Liu, Deye; Xu, Guang; Zheng, Yuxin; Yan, Huifang

2015-12-01

To investigate the distribution of rubidium (Rb), cesium (Cs), beryllium (Be), strontium (Sr), and barium (Ba) in blood and urine in general Chinese population. A total of 18 120 subjects aged 6~60 years were enrolled from 24 regions in 8 provinces in Eastern, Central, and Western China from 2009 to 2010 based on the method of cluster random sampling. Questionnaire survey was conducted to collect the data on living environment and health status. Blood and urine samples were collected from these subjects, and the levels of Rb, Cs, Be, Sr, and Ba in these samples were determined by inductively coupled plasma mass spectrometry. The distribution of these elements in blood and urine in male or female subjects living in different regions was analyzed statistically. In the general Chinese population, the concentration of Be in the whole blood was below the detection limit (0.06 μg/L); the geometric mean (GM) of Ba in the whole blood was below the detection limit (0.45 μg/L), with the 95th percentile (P95)of 1.37 μg/L; the GMs (95% CI)of Rb, Cs, and Sr in the whole blood were 2 374(2 357~2 392) μg/L, 2.01 (1.98~2.05) μg/L, and 23.5 (23.3~23.7) μg/L, respectively; in males and females, the GMs (95%CI)of blood Rb, Cs, and Sr were 2 506 (2 478~2 533) μg/L and 2 248 (2 227~2 270) μg/L, 1.88 (1.83~1.94) μg/L and 2.16 (2.11~2.20) μg/L, and 23.4 (23.1~23.7) μg/L and 23.6 (23.3~23.9) μg/L, respectively(P0.05, and P>0.05). In the general Chinese population, the GM of urine Be was below the detection limit (0.06 μg/L), while the GMs (95%CI)of urine Rb, Cs, Sr, and Ba were 854 (836~873) μg/L, 3.65 (3.56~3.74) μg/L, 39.5 (38.4~40.6) μg/L, and 1.10 (1.07~1.12) μg/L, respectively; in males and females, the GMs (95%CI)of urine Rb, Cs, Sr, and Ba were 876 (849~904) μg/L and 832 (807~858) μg/L, 3.83 (3.70~3.96) μg/L and 3.47 (3.35~3.60) μg/L, 42.5 (40.9~44.2) μg/L and 36.6 (35.1~38.0) μg/L, and 1.15 (1.12~1.19) μg/L and 1.04 (1.01~1.07) μg/L, respectively (all P< 0

Rapid and efficient visible light photocatalytic dye degradation using AFe{sub 2}O{sub 4} (A = Ba, Ca and Sr) complex oxides

Energy Technology Data Exchange (ETDEWEB)

Vijayaraghavan, T. [PSG Institute of Advanced Studies, Coimbatore 641004 (India); Suriyaraj, S.P.; Selvakumar, R. [Nanobiotechnology Laboratory, PSG Institute of Advanced Studies, Coimbatore 641004 (India); Venkateswaran, R. [PSG Institute of Advanced Studies, Coimbatore 641004 (India); Ashok, Anuradha, E-mail: anu@psgias.ac.in [PSG Institute of Advanced Studies, Coimbatore 641004 (India)

2016-08-15

Highlights: • Alkaline earth ferrites AFe{sub 2}O{sub 4} (A = Ba, Ca and Sr) were synthesized by sol–gel method. • Visible light photocatalytic activity of these ferrites were studied using congo red dye degradation. • BaFe{sub 2}O{sub 4} exhibited the best photocatalytic activity under visible light (xenon lamp) irradiation; CaFe{sub 2}O{sub 4} was the best photocatalyst under natural sun light irradiation. - Abstract: Photocatalytic activity of spinel type complex oxides has been investigated in this study. Alkaline earth ferrites AFe{sub 2}O{sub 4} (A = Ba, Ca, Sr) were synthesized by sol–gel method. Structural characterizations reveal that the synthesized ferrites have orthorhombic crystal structures with different space groups and cell dimensions when they have different alkaline earth metals in their A site. All the synthesized ferrites exhibited their bandgap in the range 2.14–2.19 eV. Their photocatalytic activities were studied using congo red dye under sunlight and xenon lamp radiation. The substitution of Ba, Ca and Sr at A site of these ferrites had varying impact on dye degradation process. Under xenon lamp irradiation, BaFe{sub 2}O{sub 4} exhibited the highest percentage of dye degradation (92% after 75 min). However, CaFe{sub 2}O{sub 4} showed the fastest degradation of the dye (70% within 15 min). In the absence of irradiation, SrFe{sub 2}O{sub 4} showed the highest dye adsorption (44% after 75 min).

Iron valence in double-perovskite (Ba,Sr,Ca)2FeMoO6: isovalent substitution effect

International Nuclear Information System (INIS)

Yasukawa, Y.; Linden, J.; Chan, T.S.; Liu, R.S.; Yamauchi, H.; Karppinen, M.

2004-01-01

In the Fe-Mo based B-site ordered double-perovskite, A 2 FeMoO 6.0 , with iron in the mixed-valence II/III state, the valence value of Fe is not precisely fixed at 2.5 but may be fine-tuned by means of applying chemical pressure at the A-cation site. This is shown through a systematic 57 Fe Moessbauer spectroscopy study using a series of A 2 FeMoO 6.0 [A=(Ba,Sr) or (Sr,Ca)] samples with high degree of Fe/Mo order, the same stoichiometric oxygen content and also almost the same grain size. The isomer shift values and other hyperfine parameters obtained from the Moessbauer spectra confirm that Fe remains in the mixed-valence state within the whole range of A constituents. However, upon increasing the average cation size at the A site the precise valence of Fe is found to decrease such that within the A=(Ba,Sr) regime the valence of Fe is closer to II, while within the A=(Sr,Ca) regime it is closer to the actual mixed-valence II/III state. As the valence of Fe approaches II, the difference in charges between Fe and Mo increases, and parallel with this the degree of Fe/Mo order increases. Additionally, for the less-ordered samples an increased tendency of clustering of the antisite Fe atoms is deduced from the Moessbauer data

The transfer factors of I, Ba, Sr, Y and Zr from soil to leafy vegetables

International Nuclear Information System (INIS)

Luo Daling; Li Mianfeng; Weng Senhan; Wen Guanghao; Liu Xiaowei; Zhang Cunxiang; Zhang Zeng; Yu Junyue

1996-01-01

The transfer factors of I, Ba, Sr, Y and Zr from soil to leafy vegetables have been determined using method of radioisotope tracers and element content analysis. The effects of growth period, size of the vegetables, contents of the isotopes in the soil and other climatic factors on the transfer factors have also been studied

Structure and properties of (Sr, Ca)CuO2-BaCuO2 superlattices grown by pulsed laser interval deposition

NARCIS (Netherlands)

Koster, Gertjan; Verbist, Karen; Rijnders, Augustinus J.H.M.; Rogalla, Horst; van Tendeloo, Gustaav; Blank, David H.A.

2001-01-01

We report on the preparation of CuBa2(SrxCa1¿x)nCun¿1Oy compounds by fabrication of (Ba,Sr,Ca)CuO2 superlattices with pulsed laser deposition (PLD). A technique called interval deposition is used to suppress multi-level or island growth resulting in high-quality superlattice structures. Both, the

Study of the effects of additives on structural properties of the Ba{sub x}Sr{sub 1-x}Fe{sub 12}O{sub 19} hexaferrite; Estudo do efeito de aditivos nas propriedades estruturais da hexaferrita Ba{sub x}Sr{sub 1-x}Fe{sub 12}O{sub 19}

Energy Technology Data Exchange (ETDEWEB)

Alves, Y.S.; Pereira, C.A.; Farias, F.C.; Mello, P.S.; Alves, A.G.; Pereira, F.M.; Barroso, M.B., E-mail: yuri.link2@gmail.com [Universidade Federal do Cariri (UFCA), Juazeiro do Norte, CE (Brazil); Saraiva, I.R.; Conde, W.S. [DeVry Fanor, Fortaleza, CE (Brazil); Sombra, A.B. [Laboratorio de Telecomunicacoes e Ciencia e Engenharia de Materiais (LOCEM/UFC), Fortaleza, CE (Brazil)

2016-07-01

The Hexaferrites are magnetic ceramic materials chemically and thermally stable, low-cost and easy processing. The objective of this work was to study the effects of SiO2 and CaO additives on structural properties of hexaferrite Ba{sub x}Sr{sub 1-x}Fe{sub 12}O{sub 19}. The samples were characterized by scanning electron microscopy (SEM), X-Ray Diffraction (XRD) and quantified by the Rietveld method. The doped samples showed no structural change. With the concentration of dopant employed, there was a decrease in the sintering temperature of all samples Ba{sub x}Sr{sub 1-x}Fe{sub 12}O{sub 19} 1100 °C/5h to 1000 °C/2h. After addition of dopants, it was observed that the growth of the grains in the samples did not occur uniformly. This uneven growth can is being influenced by the concentrations of Ba and Sr atoms present in the samples, as well as some sort of reaction with the dopant elements. (author)

Large recoverable electrostrain in Mn-doped (Ba,Sr) TiO3 ceramics

International Nuclear Information System (INIS)

Zhang, L.X.; Chen, W.; Ren, X.

2004-01-01

In this letter we demonstrate that with a different principle, BaTiO 3 ceramics, so far considered as inferior piezoelectrics compared with Pb(Zr,Ti)O 3 (PZT), can show a large recoverable electrostrain. This principle utilizes a point-defect-mediated reversible domain switching mechanism, which can in theory generate 0.368% strain for BaTiO 3 ceramics at the best condition. Experimental results showed that, after aging at room temperature, 1.0 mol % Mn-doped (Ba 0.95 Sr 0.05 )TiO 3 ceramics generate a large recoverable nonlinear strain of about 0.12%-0.15% at a field of 3 kV/mm. This value exceeds that of conventional hard PZT piezoelectric ceramics. A microscopic model for the domain-related electrostrain effect in ceramics is proposed. It is also found that the large electrostrain effect is quite stable with respect to both changing frequency and fatigue cycles. Large electrostrain remains recoverable down to 0.05 Hz and after 10 000 cycles. These results demonstrate the potential of our approach in achieving large recoverable electrostrain in environmental-friendly (Pb-free) ceramics

The Solid Solution Sr(1-x)Ba(x)Ga2: Substitutional Disorder and Chemical Bonding Visited by NMR Spectroscopy and Quantum Mechanical Calculations.

Science.gov (United States)

Pecher, Oliver; Mausolf, Bernhard; Lamberts, Kevin; Oligschläger, Dirk; Niewieszol, Carina; Englert, Ulli; Haarmann, Frank

2015-09-28

Complete miscibility of the intermetallic phases (IPs) SrGa2 and BaGa2 forming the solid solution Sr(1-x)Ba(x)Ga2 is shown by means of X-ray diffraction, thermoanalytical and metallographic studies. Regarding the distances of Sr/Ba sites versus substitution degree, a model of isolated substitution centres (ISC) for up to 10% cation substitution is explored to study the influence on the Ga bonding situation. A combined application of NMR spectroscopy and quantum mechanical (QM) calculations proves the electric field gradient (EFG) to be a sensitive measure of different bonding situations. The experimental resolution is boosted by orientation-dependent NMR on magnetically aligned powder samples, revealing in first approximation two different Ga species in the ISC regimes. EFG calculations using superlattice structures within periodic boundary conditions are in fair agreement with the NMR spectroscopy data and are discussed in detail regarding their application on disordered IPs. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Quasi-2D silicon structures based on ultrathin Me2Si (Me = Mg, Ca, Sr, Ba) films

Science.gov (United States)

Migas, D. B.; Bogorodz, V. O.; Filonov, A. B.; Borisenko, V. E.; Skorodumova, N. V.

2018-04-01

By means of ab initio calculations with hybrid functionals we show a possibility for quasi-2D silicon structures originated from semiconducting Mg2Si, Ca2Si, Sr2Si and Ba2Si silicides to exist. Such a 2D structure is similar to the one of transition metal chalcogenides where silicon atoms form a layer in between of metal atoms aligned in surface layers. These metal surface atoms act as pseudo passivation species stabilizing crystal structure and providing semiconducting properties. Considered 2D Mg2Si, Ca2Si, Sr2Si and Ba2Si have band gaps of 1.14 eV, 0.69 eV, 0.33 eV and 0.19 eV, respectively, while the former one is also characterized by a direct transition with appreciable oscillator strength. Electronic states of the surface atoms are found to suppress an influence of the quantum confinement on the band gaps. Additionally, we report Sr2Si bulk in the cubic structure to have a direct band gap of 0.85 eV as well as sizable oscillator strength of the first direct transition.

Transport and magnetic properties of R sub 1 sub - sub x A sub x CoO sub 3. (R = La, Pr and Nd; A = Ba, Sr and Ca)

CERN Document Server

Masuda, H; Miyashita, T; Soda, M; Yasui, Y; Kobayashi, Y; Sato, M

2003-01-01

Transport and magnetic measurements have been carried out on perovskite Co-oxides R sub 1 sub - sub x A sub x CoO sub 3 (R = La, Pr, and Nd; A = Ba, Sr and Ca; 0 <= x <= 0.5: All sets of the R and A species except Nd sub 1 sub - sub x Ba sub x CoO sub 3 have been studied.). With increasing the Sr- or Ba-concentration x, the system becomes metallic ferromagnet with rather large magnetic moments. For R = Pr and Nd and A = Ca, the system approaches the metal-insulator phase boundary but does not become metallic. The magnetic moments of the Ca-doped systems measured with the magnetic field H = 0.1 T are much smaller than those of the Ba- and Sr-doped systems. The thermoelectric powers of the Ba- and Sr-doped systems decrease from large positive values of lightly doped samples to negative ones with increasing doping level, while those of Ca-doped systems remain positive. These results can be understood by considering the relationship between the average ionic radius of R sub 1 sub - sub x A sub x and the ene...

RB research nuclear reactor - Annual report for 1986, I - III

International Nuclear Information System (INIS)

Markovic, H.; Pesic, M.; Vranic, S.; Petronijevic, M.; Jevremovic, M.; Ilic, I.

1987-01-01

This report includes data concerning the RB reactor operation in 1986, state of the reactor components, data about the employed personnel and the database of experimental and other reactor related devices. It is made of 3 parts: Engineering description and operation of the RB reactor including dosimetry, reactor staff data and financial report; Reactor facility components and maintenance; RB reactor operation and utilization in 1986 [sr

Synthesis and structural characterization of the ternary Zintl phases AE3Al2Pn4 and AE3Ga2Pn4 (AE=Ca, Sr, Ba, Eu; Pn=P, As)

International Nuclear Information System (INIS)

He, Hua; Tyson, Chauntae; Saito, Maia; Bobev, Svilen

2012-01-01

Ten new ternary phosphides and arsenides with empirical formulae AE 3 Al 2 Pn 4 and AE 3 Ga 2 Pn 4 (AE=Ca, Sr, Ba, Eu; Pn=P, As) have been synthesized using molten Ga, Al, and Pb fluxes. They have been structurally characterized by single-crystal and powder X-ray diffraction to form with two different structures—Ca 3 Al 2 P 4 , Sr 3 Al 2 As 4 , Eu 3 Al 2 P 4 , Eu 3 Al 2 As 4 , Ca 3 Ga 2 P 4 , Sr 3 Ga 2 P 4 , Sr 3 Ga 2 As 4 , and Eu 3 Ga 2 As 4 crystallize with the Ca 3 Al 2 As 4 structure type (space group C2/c, Z=4); Ba 3 Al 2 P 4 and Ba 3 Al 2 As 4 adopt the Na 3 Fe 2 S 4 structure type (space group Pnma, Z=4). The polyanions in both structures are made up of TrPn 4 tetrahedra, which share common corners and edges to form 2 ∞ [TrPn 2 ] 3– layers in the phases with the Ca 3 Al 2 As 4 structure, and 1 ∞ [TrPn 2 ] 3– chains in Ba 3 Al 2 P 4 and Ba 3 Al 2 As 4 with the Na 3 Fe 2 S 4 structure type. The valence electron count for all of these compounds follows the Zintl–Klemm rules. Electronic band structure calculations confirm them to be semiconductors. - Graphical abstract: AE 3 Al 2 Pn 4 and AE 3 Ga 2 Pn 4 (AE=Ca, Sr, Ba, Eu; Pn=P, As) crystallize in two different structures—Ca 3 Al 2 P 4 , Sr 3 Al 2 As 4 , Eu 3 Al 2 P 4 , Eu 3 Al 2 As 4 , Ca 3 Ga 2 P 4 , Sr 3 Ga 2 P 4 , Sr 3 Ga 2 As 4 , and Eu 3 Ga 2 As 4 , are isotypic with the previously reported Ca 3 Al 2 As 4 (space group C2/c (No. 15)), while Ba 3 Al 2 P 4 and Ba 3 Al 2 As 4 adopt a different structure known for Na 3 Fe 2 S 4 (space group Pnma (No. 62). The polyanions in both structures are made up of TrPn 4 tetrahedra, which by sharing common corners and edges, form 2 ∞ [TrPn 2 ] 3– layers in the former and 1 ∞ [TrPn 2 ] 3– chains in Ba 3 Al 2 P 4 and Ba 3 Al 2 As 4 . Highlights: ► AE 3 Ga 2 Pn 4 (AE=Ca, Sr, Ba, Eu; Pn=P, As) are new ternary pnictides. ► Ba 3 Al 2 P 4 and Ba 3 Al 2 As 4 adopt the Na 3 Fe 2 S 4 structure type. ► The Sr- and Ca-compounds crystallize with the Ca 3

Recognition of the Kaweka Terrane in northern South Island, New Zealand : preliminary evidence from Rb-Sr metamorphic and U-Pb detrital zircon ages

International Nuclear Information System (INIS)

Adams, C.J.; Mortimer, N.; Campbell, H.J.; Griffin, W.L.

2011-01-01

Detrital zircon U-Pb ages and Rb-Sr metamorphic ages from low-grade Torlesse Supergroup metasedimentary rocks from North Canterbury and Marlborough provide preliminary evidence for a continuation of the Kaweka Terrane of the central North Island into the Torlesse Composite Terrane of the South Island. This would extend from the south side of the Wairau Fault in the upper Wairau River valley southwards to the Lake Tennyson and Lake Sumner areas, and as far as Hawarden. Rb-Sr ages indicate Jurassic metamorphism, 170±24 Ma, with initial 87 Sr/ 86 Sr ratios at that time 0.7073 ± 0.0007 i.e. similar to their North Island counterparts. These Kaweka Terrane rocks have detrital zircon ages that follow the distinctive pattern of the Torlesse rocks in general, i.e. substantial (>30%) Permian-Triassic and Precambrian-Early Palaeozoic groupings, but they also have minor youngest age components c. 175-165 Ma which constrain a maximum Early-Middle Jurassic depositional age. In detail, significant, older zircon components are Late Permian-Early Triassic (260-240 Ma) and Late Triassic (220-210 Ma), but the Precambrian-Early Palaeozoic detrital zircon ages are more scattered. The Kaweka Terrane thus forms a linear belt (c. 500 km) along the length of the Torlesse Composite Terrane in both North and South Islands. In the South Island it coincides with the Esk Head Belt, i.e. east of the Rakaia Terrane (Triassic-Late Permian) and west of the Pahau Terrane (Early Cretaceous-Late Jurassic). (author). 61 refs., 4 figs., 2 tabs.

Rb-Sr and K-Ar age of globular phyllosilicates and biostratigraphy of the Riphean deposits of the Olenek Uplift (North Siberia)

Science.gov (United States)

Zaitseva, T. S.; Gorokhov, I. M.; Semikhatov, M. A.; Ivanovskaya, T. A.; Kuznetsov, A. B.; Dorzhieva, O. V.

2017-11-01

This work presents results of the complex mineralogical, geochemical, and isotope-geochronological investigation of globular dioctahedral 2: 1 phyllosilicates (GPS) of the illite-glauconite series from the Riphean sequences of the Olenek Uplift. It is established that GPS (glauconite, Al-glauconite, Fe-illite) in deposits of the Arymass, Debengda, and Khaipakh formations are represented by mixed-layer varieties of two types: (1) with relatively low (cell of minerals varies from 9.18 to 9.72 Å. The Rb-Sr age dating of GPS was first carried out in combination with the calculation of theoretical pattern of the cation distribution in the mineral structure and comparison of the calculation results obtained with the Mössbauer and IR spectroscopy data. This approach is based on the assumption that development and evolution of isotope systems in GPS are synchronous with the evolution of the crystalline structure of the mineral at various stages of the geological and geochemical history of the development of sedimentary units. Analysis of the obtained data allows us to state that the structural features of the Riphean GPS from the Olenek section reflect the early diagenetic stages of the formation of the minerals studied. The 87Sr/86Sr initial ratios in the studied sediments are consistent with the range of variations in this ratio in the Middle Riphean Ocean (0.7049-0.7061). The Rb-Sr and K-Ar ages of the GPS of the Arymass (1305 ± 8 and 1302 Ma, respectively), Debengda (1265 ± 12 and 1284 ± 22 Ma), and Khaipakh (1172 ± 18 and 1112 ± 24 Ma) formations in the Olenek Uplift section are close to the accumulation time of corresponding deposits and, correspondingly, have significance for stratigraphic correlations.

Effects of Sr-substitution on the structural and magnetic behavior of Ba-based Y-type hexagonal ferrites

Energy Technology Data Exchange (ETDEWEB)

Ahmad, Mukhtar, E-mail: mukhtarahmad25@gmail.com [Department of Physics, Bahauddin Zakariya University, Multan 60800 (Pakistan); Ali, Qasim; Ali, Ihsan; Ahmad, Ishtiaq [Department of Physics, Bahauddin Zakariya University, Multan 60800 (Pakistan); Azhar Khan, M. [Department of Physics, The Islamia University of Bahawalpur 63100 (Pakistan); Akhtar, Majid Niaz [Department of Physics, COMSATS Institute of Information Technology, Lahore (Pakistan); Murtaza, G. [Centre for Advanced Studies in Physics, G.C. University, Lahore (Pakistan); Rana, M.U., E-mail: mazharrana@bzu.edu.pk [Department of Physics, Bahauddin Zakariya University, Multan 60800 (Pakistan)

2013-12-15

Highlights: •Sr-substituted Y-type hexaferrites synthesized by sol–gel method have been investigated. •Platelet grains with well defined hexagonal shape are suitable for microwave absorbers. •Saturation magnetization values were calculated by the law of approach to saturation. •Coercivity of a few hundred oersteds found for all samples is suitable for EM materials. -- Abstract: Sr-substituted samples of Y-type hexagonal ferrites with chemical formula Ba{sub 2−x}Sr{sub x}Ni{sub 2}Fe{sub 12}O{sub 22} (x = 0.0, 0.2, 0.4, 0.6, 0.8, 1.0) were synthesized using the sol–gel autocombustion method and were sintered at 1150 °C for 3 h. The samples were investigated by differential thermal and thermogravimetry analysis, X-ray diffraction, scanning electron microscopy, energy dispersive X-ray spectroscopy and vibrating sample magnetometry. X-ray diffraction analysis reveals that single phase samples can be achieved by substituting Sr{sup 2+} ions at Ba{sup 2+} sites in Y-type hexagonal ferrites. X-ray density and bulk density were observed to decrease whereas porosity increased with increasing Sr-concentration. All the samples show well defined hexagonal shape which is favorable for microwave absorbing purposes. The saturation magnetization values were calculated from M–H loops by the law of approach to saturation. The loops show low values of coercivity of a few hundred oersteds which is one of the necessary conditions for electromagnetic (EM) materials and is suitable for security, switching, sensing and high frequency applications.

Correlation of Structure, Tunable Colors, and Lifetimes of (Sr, Ca, Ba)Al2O4:Eu2+, Dy3+ Phosphors

OpenAIRE

Qidi Xie; Bowen Li; Xin He; Mei Zhang; Yan Chen; Qingguang Zeng

2017-01-01

(Sr, Ca, Ba)Al2O4:Eu2+, Dy3+ phosphors were prepared via a high temperature solid-state reaction method. The correlation of phase structure, optical properties and lifetimes of the phosphors are investigated in this work. For the (Sr, Ca)Al2O4:Eu2+, Dy3+ phosphors, the different phase formation from monoclinic SrAl2O4 phase to hexagonal SrAl2O4 phase to monoclinic CaAl2O4 phase was observed when the Ca content increased. The emission color of SrAl2O4:Eu2+, Dy3+ phosphors varied from green to ...

On the photo-luminescence properties of sol–gel derived undoped and Dy3+ ion doped nanocrystalline Scheelite type AMoO4 (A = Ca, Sr and Ba)

International Nuclear Information System (INIS)

Jena, Paramananda; Gupta, Santosh K.; Natarajan, V.; Padmaraj, O.; Satyanarayana, N.; Venkateswarlu, M.

2015-01-01

Nanocrystalline Scheelite type Dy doped AMoO 4 [where A = Ba, Sr and Ca] samples were prepared by acrylamide assisted sol–gel process and characterized by XRD, FT-Raman, FTIR, SEM and photoluminescence (PL). PL of undoped sample shows blue/green emission in CaMoO 4 and SrMoO 4 but multicolour visible emission leading to near white light in BaMoO 4 nanoparticles; the origin of which is explained. It was observed that on doping 0.5 mol% of Dy 3+ in molybdate samples complete energy transfer takes place in case of SrMoO 4 and BaMoO 4 , but host contributed substantially in Dy doped BaMoO 4 sample, resulting in biexponential decay. It was also observed that symmetry around Dy 3+ decreases as the size of alkaline earth ion increases. Due to combined blue, yellow and red colour emission in dysprosium doped sample; all samples showed near white light emission under UV and near UV excitation

Sm-Nd, Rb-Sr and K-Ar age constraints of the El Molle and Barroso plutons, western Sierra de San Luis, Argentina

International Nuclear Information System (INIS)

Sato, A.M.; Gonzalez, P.D; Petronilho, L.A; Llambias, E.J.; Varela, R; Basei, M.A.S

2001-01-01

Within the Early Paleozoic Famatinian orogeny of Southern Sierras Pampeanas (Sierra de San Luis and Sierra de Cordoba), the post-orogenic granitoids are characterized by circular intrusions. The published Rb-Sr and K-Ar ages from plutons in the Sierra de San Luis range between 408 and 320 Ma (see synthesis in Llambias et al., 1998). The El Molle and Barroso plutons (Sims et al., 1997; Gonzalez and Sato, 2000) are the two main exposures of a post-orogenic intrusive complex located in the western area of the Sierra de San Luis basement. They also exhibit an overall circular map view of almost 8 km in diameter, and are emplaced in a metamorphic complex developed through pre-Famatinian (Proterozoic? to Early Paleozoic) to Famatinian (Early Paleozoic) orogenies (Gonzalez and Llambias, 1998; von Gosen and Prozzi, 1998). We are carrying out isotopic datings of the El Molle and Barroso plutons in order to contribute to the understanding of the magmatic and metamorphic evolution of the final stages of the Famatinian orogenic cycle in the Sierra de San Luis. The first results of the Sm-Nd, Rb-Sr and K-Ar dates are here presented (au)

Incorporation of Mg, Sr, Ba, U, and B in High-Mg Calcite Benthic Foraminifers Cultured Under Controlled pCO2

Science.gov (United States)

Not, C.; Thibodeau, B.; Yokoyama, Y.

2018-01-01

Measurement of elemental ratios (E/Ca) has been performed in two symbiont-bearing species of high-Mg calcite benthic foraminifers (hyaline, Baculogypsina sphaerulata and porcelaneous, Amphisorus hemprichii), cultured under five pCO2 levels, representing preindustrial, modern, and three predicted future values. E/Ca ratios were analyzed by Laser Ablation coupled with Inductively Coupled Plasma Mass Spectrometer (LA-ICP-MS). We measured several E/Ca, such as Mg/Ca, Sr/Ca, Ba/Ca, U/Ca, and B/Ca simultaneously. We observed that high-Mg calcite benthic foraminifers possess higher E/Ca than low-Mg calcite foraminifers, irrespective of their calcification mode (hyaline or porcelaneous). In both modes of calcification, Mg, Sr, Ba, U, and B incorporation could be controlled by Rayleigh fractionation. However, more data are needed to validate and quantify the relative importance of this process and closely investigate the presence/absence of other mechanism. Therefore, it highlights the need for a multielemental approach when looking at trace element incorporation. Finally, no significant relationship was observed between the different ratios and the pCO2 of the water, suggesting that none of the Mg/Ca, Sr/Ca, Ba/Ca, U/Ca, and B/Ca is sensitive to bottom water pCO2 or pH for these species.

Cathode characterization system: preliminary results with (Ba,Sr,Ca) O coated cathodes

International Nuclear Information System (INIS)

Nono, M.C.A.; Goncalves, J.A.N.; Barroso, J.J.; Dallaqua, R.S.; Spassovsky, I.

1993-01-01

The performance of a cathode characterization system for studying the emission parameters of thermal electron emitters is reported. The system consists of vacuum chamber, power supplies and equipment for measuring and control. Measurements have been taken of the emission current as function of cathode temperature and anode voltage. Several (Ba, Sr) O coated cathodes were tested and the results have shown good agreement with Child's and Richardson's laws. The experimental work function is between 1.0 and 2.0 e V. All emission parameters measured are consistent with international literature data. (author)

Magnetization and critical currents of Bi-Sr-Ca-Cu-O and Ba2YCu3O7 superconductors

International Nuclear Information System (INIS)

Gyorgy, E.M.; van Dover, R.B.; Jin, S.; Sherwood, R.C.; Schneemeyer, L.F.; Tiefel, T.H.; Waszczak, J.V.

1988-01-01

We have measured the critical currrent density J/sub c/ as a function of temperature for a Bi-Sr-Ca-Cu-O sample containing a substantial fraction of a phase with T/sub c/≅110 K and for a Ba 2 YCu 3 O 7 sample (TT/sub c/≅92 K). The behavior of J/sub c/ was deduced from magnetization measurements. For both samples the magnetization at fixed temperature and field decayed logarithmically with time. The values of J/sub c/ so derived, allowing for the decay to occur, went to zero for temperatures above 35 K for the Bi-Sr-Ca-Cu-O ceramic and to zero above 70 K for the Ba 2 YCu 3 O 7 sample. These values are substantially lower than those deduced from dynamic M-H loops

Structure and optical band gaps of (Ba,Sr)SnO{sub 3} films grown by molecular beam epitaxy

Energy Technology Data Exchange (ETDEWEB)

Schumann, Timo; Raghavan, Santosh; Ahadi, Kaveh; Kim, Honggyu; Stemmer, Susanne, E-mail: stemmer@mrl.ucsb.edu [Materials Department, University of California, Santa Barbara, California 93106-5050 (United States)

2016-09-15

Epitaxial growth of (Ba{sub x}Sr{sub 1−x})SnO{sub 3} films with 0 ≤ x ≤ 1 using molecular beam epitaxy is reported. It is shown that SrSnO{sub 3} films can be grown coherently strained on closely lattice and symmetry matched PrScO{sub 3} substrates. The evolution of the optical band gap as a function of composition is determined by spectroscopic ellipsometry. The direct band gap monotonously decreases with x from to 4.46 eV (x = 0) to 3.36 eV (x = 1). A large Burnstein-Moss shift is observed with La-doping of BaSnO{sub 3} films. The shift corresponds approximately to the increase in Fermi level and is consistent with the low conduction band mass.

Lattice mismatch and energy transfer of Eu- and Dy-codoped MO–Al{sub 2}O{sub 3}–SrO (M=Mg, Ca, Ba) ternary compounds affecting luminescence behavior

Energy Technology Data Exchange (ETDEWEB)

Liang, Chen-Jui, E-mail: cjliang@fcu.edu.tw; Huang, Kuan-Yu

2017-05-15

A systematic investigation of energy transfers and luminescence behaviors for M{sub x}Sr{sub 0.94−x}Al{sub 2}O{sub 4}:Eu{sub 0.02}, Dy{sub 0.04} (M=Mg, Ca, Ba; x=0, 0.235, 0.47, 0.705, 0.94) ternary compounds was accomplished. The results demonstrated that six phenomena must be fitted into the energy-transfer mechanisms of the ternary compounds: (1) the optical band-gap energy of Mg{sub 0.94}Al{sub 2}O{sub 4}:Eu{sub 0.02}Dy{sub 0.04} is extremely low and does not allow photoemission; (2) Ca{sup 2+} and Ba{sup 2+} ions are the main hosts when x≥0.47 in Ca{sub x}Sr{sub 1−x}Al{sub 2}O{sub 4}:Eu{sub 0.02}Dy{sub 0.04} and Ba{sub x}Sr{sub 1−x}Al{sub 2}O{sub 4}:Eu{sub 0.02}Dy{sub 0.04}, respectively; (3) Eu{sup 3+} ions are the main activator ions in Ca{sub x}Sr{sub 1−x}Al{sub 2}O{sub 4}:Eu{sub 0.02}Dy{sub 0.04} with x=0.47 and in Ba{sub x}Sr{sub 1−x}Al{sub 2}O{sub 4}:Eu{sub 0.02}Dy{sub 0.04} with x=0.353−0.705; (4) Sr{sup 2+} and Eu{sup 2+} ions are the main host and activator ions, respectively, when x<0.353 in each ternary compound; (5) energy transfers from the MO phases to the SrO phase because the conduction band energy of SrO is the lowest; and (6) mutual substitution between alkaline-earth ions does not alter the resultant structures’ crystal field and nephelauxetic effects, as determined by measuring their luminescence. Two energy transfer paths were discovered to be possible in CaO–Al{sub 2}O{sub 3}–SrO and BaO–Al{sub 2}O{sub 3}–SrO ternary compounds, and the boundaries determining which path was chosen were the atomic ratios Ca:Sr and Ba:Sr, both approximately 1.6:1 (x=0.353). Because second path increased the energy transferred from the MO band gap to the SrO band gap, the corresponding structure's spectrum emission intensity was approximately 4.3 times higher than that of the SrO−Al{sub 2}O{sub 3} binary compound, and their photoluminescence was thus substantially higher.

Synthesis and characterisation of the n = 2 Ruddlesden–Popper phases Ln2Sr(Ba)Fe2O7 (Ln = La, Nd, Eu)

International Nuclear Information System (INIS)

Gurusinghe, Nicola N.M.; Figuera, Juand de la; Marco, José F.; Thomas, Michael F.; Berry, Frank J.; Greaves, Colin

2013-01-01

Graphical abstract: - Highlights: • Some Ruddlesden–Popper phases have been characterised. • Substitution on the A site influences cationic order. • The magnetic moment redirects with temperature - Abstract: A series of n = 2 Ruddlesden–Popper phases A 2 B 2 O 7 of composition Ln 2 Sr(Ba)Fe 2 O 7 (Ln = La, Nd, Eu) have been prepared. La 2 SrFe 2 O 7 and La 2 BaFe 2 O 7 crystallise in the tetragonal space group I4/mmm. The structures of Eu 2 SrFe 2 O 7 and Nd 2 SrFe 2 O 7 are best described in space group P4 2 /mnm. Substitution on the A site with smaller lanthanide- and larger alkaline metal- ions leads to enhanced cationic order in these phases and reflects increasing differences in cationic radii. All the compounds are antiferromagnetically ordered between 298 and 2 K. In La 2 SrFe 2 O 7 the magnetic moment lies along [1 1 0] at all temperatures between 298 and 2 K whereas in La 2 BaFe 2 O 7 the magnetic moment at 298 K lies along the crystallographic x-axis but redirects from the [1 0 0] to the [1 1 0] direction between 210 and 190 K and is retained in this direction until 2 K. In Nd 2 SrFe 2 O 7 the magnetic moment at 298 K lies along [1 1 0] but rotates from [1 1 0] to [0 0 1] between 17 and 9 K. A series of 57 Fe Mössbauer spectra recorded from La 2 SrFe 2 O 7 between 290 and 600 K indicate a magnetic ordering temperature of T N ≥ 535 K

Trace elements (Rb, Cs, Sr, Pb, Th, U) bioavailability potential and speciation in the Piracicaba river bottom sediments, Sao Paulo, Brazil

International Nuclear Information System (INIS)

Fernandes, Alexandre Martins; Mortatti, Jefferson; Oliveira, Helder de; Bibian, Joao Paulo Rambelli; Moraes, Graziela Meneghel de; Probst, Jean-Luc

2007-01-01

It was studied the bioavailability potential of Rb, Cs, Sr, Pb, Th and U and their chemical speciation in Piracicaba river bottom sediments. This river system crosses important agricultural and urban areas of Sao Paulo state, which groups about 3 million people and receives a large load of agricultural, industrial and domestic wastes. The procedure used to estimate trace elements bioavailability potential was related to a 7-step sequential chemical extraction. This scheme was designed to dissolved and separate sample chemical phases, which can be affected by changes in physical-chemical conditions; in the following order: water soluble, exchangeable, bound to carbonates or acid fraction, bound to Mn-oxides, bound to Fe-oxides and bound to organic matter. Trace element concentrations were determined by Inductively Coupled Plasma-Atomic Emission Spectrometry (ICP-AES) after each extraction step. With the used extraction procedure, it was possible to identify the fraction where some trace elements could be found in order to evaluate their bioavailability potential. Rb and Cs were particularly involved with the organic fraction, while Sr revealed to be associated mainly to the exchangeable fraction (clay minerals). Pb, Th and U were mainly bound to the residual and Fe-oxide fractions. (author)

Effect of Sr doping on structural and magnetic behavior of SmBa1-xSrxCo2O5+δ (x = 0 and 1)

Science.gov (United States)

Kumari, Archana; Dhanasekhar, C.; Das, A. K.

2018-05-01

Layered double perovskite, SmBa1-xSrxCo2O5+δ (x = 0, δ = 0.5 and x = 1, δ = 1) samples were prepared by solid state reaction method. X-ray diffraction studies show that the SmBaCo2O5.5 sample crystallizes in the orthorhombic crystal structure with Pmmm space group, whereas SmSrCo2O6 sample crystallizes in the orthorhombic crystal structure with Pnma space group. The temperature dependent magnetization of the SmBaCo2O5.5 sample shows a paramagnetic (PM)-ferromagnetic (FM) and a FM-antiferromagnetic (AFM) transitions at TC = 267 K and TN = 221 K, respectively. In contrast, the SmSrCo2O6 sample shows a PM-FM transition at TC = 175 K. According to Goodenough-Kanamori-Anderson rules, the ferromagnetic behavior in SmSrCo2O6 can be understood from the super exchange interaction between the intermediate spin Co3+ and low spin Co4+ via O2- (IS Co3+ -O2- - LS Co4+). The change in magnetic entropy (ΔSMmax) is found to be maximum for the SmSrCo2O6 sample.

Spectroscopic and thermal degradation behavior of Mg(II, Ca(II, Ba(II and Sr(II complexes with paracetamol drug

Directory of Open Access Journals (Sweden)

Moamen S. Refat

2017-05-01

Full Text Available Complexes of Mg(II, Ca(II, Ba(II and Sr(II with paracetamol drug were synthesized and characterized by elemental analysis, conductivity, UV–Vis, IR, and 1H NMR spectroscopy and thermal analysis, as well as screened for antimicrobial activity. The IR spectral data suggested that the ligand behaves as paracetamol behaves as a neutral bidentate ligand coordinated to the metal ions via the lone pair of electrons of nitrogen and carbonyl-O atoms of the amide group. From the microanalytical data, the stoichiometry of the complexes reacts with Mg(II, Ca(II, Ba(II and Sr(II by molar ratios (2:1 (paracetamol:metal ion. The thermal behavior (TG/DTG of the complexes was studied. The ligand and their metal complexes were screened against both of antibacterial and fungicidal activities.

A novel procedure for Rubidium separation and its isotope measurements on geological samples by MC-ICP-MS

Science.gov (United States)

Ma, J.; Zhang, Z.; Wei, G.; Zhang, L.

2017-12-01

A method including a novel column Rb separation procedure and high-precision Rb isotope measurement in geological materials by using multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) in standard-sample-bracketing (SSB) mode has been developed. Sr-Spec resin was employed, in which the distribution coefficients for Rb, K, Ba and Sr are different in nitric acid, to sequentially separate them from the matrix. The dissolved samples were loaded on the column in 3 M HNO3, the main matrix such as Al, Ca, Fe, Mg, Mn and Na were removed by rinsing with 4.5 mL HNO3, Rb and K were then sequentially eluted by 3 M HNO3 in different volumes. After that, Ba was eluted by 8 M HNO3, and Sr was finally eluted by Milli-Q water. This enable us to collect the pure Rb, K, Ba and Sr one by one with recovery close to 100% for their isotopic compositions measurement on MC-ICP-MS. We here focus on Rb isotope measurement. The measurement using MC-ICP-MS yielded an internal precision for δ87Rb of external precision was generally better than ± 0.06‰ (2SD) based on the long-term results of the Rb standard solutions NIST SRM 984. A series of geological rock standards, were analyzed using this method, and the results indicate significant Rb isotope differences in different geologic materials. This will provide a powerful tool to investigate Rb isotope fractionation during geological processes.Based on this method, Rb isotope compositions from a basaltic weathering profile were carried out. The data show the lighter Rb (85Rb) isotope is preferentially leached from the weathering profile and remains heavy Rb isotope (87Rb) in the weathered residues during the incipient weathering stage. From the moderate to advanced weathering stage, the significant variations of Rb isotope were observed and multiple factors, such as leaching, adsorption, desorption, and precipitation, should play important role in fractionating Rb isotope.

The study of the effect of Ba coverage through the accelerations lifetime of activated BaO/SrO cathodes

International Nuclear Information System (INIS)

Hashim, A.A.; Ray, A.K.; Hassan, A.K.; Barratt, D.S.

2005-01-01

A novel type of BaO/SrO oxide cathode with 5% addition of Ni powder by weight on a Ni cap containing an activating impurity was studied. The conductivity and the electron activation energy were studied as a function of temperature in the range of 300-1200 K after conversion and activation of the cathode at 1200 K for 1 h. The experimental results yield three values for the activation energy of 1.49, 2.23 and 3.3 eV, which are close to BaO band structure parameters with a small shift due to the effect of other oxide components and metallic fraction additions. The experiments furthermore confirm that the current density of the cathode was enhanced at high temperature range with the long operation. The conduction mechanisms observed a metallic conduction at low temperature after operation for several 100 h due to improvements in the Ba coverage layer on the grains of oxide layer. Additionally, there appears a qualified conduction stability of the current density J = 10-45 mA cm -2 at the acceleration temperature range of 1100-1150 K under the duty of low voltage. The low voltage duty V = 30 mV is focused on the conduction electrons faraway from the emission electrons

Microwave loss mechanisms in Ba0.25Sr0.75TiO3 films

International Nuclear Information System (INIS)

Vorobiev, A.; Rundqvist, P.; Gevorgian, S.

2005-01-01

Trilayer Au(Pt)/Ba 0.25 Sr 0.75 TiO 3 /(Pt)Au thin film varactors are fabricated on high resistive Si substrate and characterized at dc, rf and microwave frequencies. In the frequency range of 10-45 GHz the varactors reveal relatively low losses, the loss tangent is less than 0.025 at 45 GHz. Due to the thick and highly conductive Pt/Au electrodes the metal losses are less than 10%. However, the loss tangent of the ferroelectric film is still 3-5 times higher than that in Ba 0.27 Sr 0.73 TiO 3 single crystal. The analysis of the dc field dependent loss tangent and permittivity in a wide frequency range show that these additional losses are mainly due to the charged defects. Extrapolation of measured low frequency (1 MHz) loss tangents to the microwave region using the power law ω 1/3 is in good agreement with the experiment. We assume that the oxygen vacancies within the grain boundaries of ferroelectric film act as charged defects and cause extrinsic microwave losses. The knowledge of the extrinsic loss mechanism and corresponding microstructure defects is useful in optimization of the varactor design, deposition, and/or annealing process and further improvement of the varactor performance

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

Energy Technology Data Exchange (ETDEWEB)

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

2016-03-11

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

PIXE analysis of ancient Jordanian pottery

International Nuclear Information System (INIS)

Saleh, N.; Carlsson, L.E.

1981-01-01

Proton-induced X-ray emission (PIXE) has been applied for the determination of 18 elements (Si, K, Ca, Ti, Cr, Mn, Fe, Ni, Cu, Zn, Ga, Rb, Sr, Y, Zr, Nb, Ba and Pb) in two groups of pottery from two different sites in Jordan, Biblical Bozrah (BB) and Amman Citadel (AC). The analysis showed that the elements Zn, Rb, Sr, Zr and Ba were the most useful elements to study to be able to differentiate between the two groups of pottery. (orig.)

Solid electrolytes Sr(Ba)6Nb(Ta)2O11 with structural disordering of oxygen sublattice

International Nuclear Information System (INIS)

Nejman, A.Ya.; Podkorytov, A.L.; Yurkovskaya, N.Yu.; Zhukovskij, V.M.

1986-01-01

Electric conductivity at alternating and direct current and ratio of ionic component of conductivity in M 2 O-M 2 5 O 5 systems (M 2 -Sr, Ba; M 5 -Nb, Ta) are measured. High ionic conductivity of M 6 2 M 2 5 O 11 compounds is shown to be conducted by structural disordering of oxygen sublattice

Impedance spectroscopy of Ba3Sr2DyTi3V7O30 ceramic

Indian Academy of Sciences (India)

Administrator

Polycrystalline sample of Ba3Sr2DyTi3V7O30 was prepared at 950°C using a high-temperature solid-state ... Introduction. Though a large number of ferroelectric oxides of different .... change in its shape with rise in temperature suggesting a change in the .... Singh K S, Sati R and Choudhary R N P 1992 J. Mater. Sci. Lett.

Oxygen perovskites with pentavalent ruthenium A/sub 2/sup(II)Bsup(III)Rusup(V)O/sub 6/ with Asup(II) = Ba, Sr

Energy Technology Data Exchange (ETDEWEB)

Bader, H; Kemmler-Sack, S [Tuebingen Univ. (Germany, F.R.). Lehrstuhl fuer Anorganische Chemie 2

1980-07-01

The perovskites Ba/sub 2/Bsup(III)Rusup(V)O/sub 6/ with Bsup(III) = La, Nd, Sm, Eu, Gd, Dy, Y are cubic (Bsup(III) = La: a = 8.54 A; Y: a = 8.33 A) with a partial order for Bsup(III) and Rusup(V). The Sc compound, Ba/sub 2/ScRuO/sub 6/, has a hexagonal 6L structure (a = 5.79 A; c = 14.22 A; sequence (hcc)/sub 2/). The lattice of the Sr perovskites, Sr/sub 2/Bsup(III)Rusup(V)O/sub 6/, with Bsup(III) = Eu, Gd, Dy, Y is rhombic distorted. The IR and FIR spectra are discussed.

Syntheses, and crystal and electronic structures of the new Zintl phases Na2ACdSb2 and K2ACdSb2 (A=Ca, Sr, Ba, Eu, Yb): Structural relationship with Yb2CdSb2 and the solid solutions Sr2-xAxCdSb2, Ba2-xAxCdSb2 and Eu2-xYbxCdSb2

International Nuclear Information System (INIS)

Saparov, Bayrammurad; Saito, Maia; Bobev, Svilen

2011-01-01

Presented are the details of the syntheses, crystal and electronic structures of a new family of Zintl phases Na 2 ACdSb 2 and K 2 ACdSb 2 (A=Ca, Sr, Ba, Eu, Yb), as well as the solid solutions Sr 2-x A x CdSb 2 , Ba 2-x A x CdSb 2 and Eu 2-x Yb x CdSb 2 . The structures of Na 2 ACdSb 2 and K 2 ACdSb 2 (A=Ca, Sr, Ba, Eu, Yb) were determined to be of a new type with the non-centrosymmetric space group Pmc2 1 (no. 26), Pearson symbol oP12, with lattice parameters a=4.684(1)-4.788(1) A; b=9.099(3)-9.117(2) A; c=7.837(1)-8.057(2) A for the Na 2 ACdSb 2 series, and a=4.6637(9)-5.0368(8) A; b=9.100(2)-9.8183(15) A; and c=7.7954(15)-8.4924(13) A for K 2 ACdSb 2 , respectively. The solid solutions Sr 2-x A x CdSb 2 , Ba 2-x A x CdSb 2 and Eu 2-x Yb x CdSb 2 (x∼1) are isostructural and isoelectronic to the recently reported Yb 2 CdSb 2 (space group Cmc2 1 (no. 36), Pearson symbol cP20). All discussed structures are based upon CdSb 2 4- polyanionic layers, similar to the ones observed in Yb 2 CdSb 2 , with various alkali- and/or alkaline-earth cations coordinated to them. Magnetic susceptibility and Seebeck coefficient measurements on selected Eu 2-x Yb x CdSb 2 samples, taken at low temperatures up to 300 K, are also reported. -- Graphical abstract: The quaternary Zintl phases Na 2 ACdSb 2 and K 2 ACdSb 2 (A=Ca, Sr, Ba, Eu, Yb) with novel layered structures have been synthesized for the first time and structurally characterized by single-crystal X-ray diffraction. Reported as well are the results from crystallographic and property studies of the closely related solid solutions Sr 2-x A x CdSb 2 , Ba 2-x A x CdSb 2 (x∼1), and Eu 2-x Yb x CdSb 2 (1 2 ACdSb 2 and K 2 ACdSb 2 (A=Ca, Sr, Ba, Eu, Yb) are new quaternary Zintl phases. → Sr 2-x A x CdSb 2 , Ba 2-x A x CdSb 2 (x∼1), and Eu 2-x Yb x CdSb 2 (1 4 tetrahedra. → Eu 2-x Yb x CdSb 2 (1< x<2) exhibit high Seebeck coefficient (217 μV/K at RT).

Development of an on-line flow injection Sr/matrix separation method for accurate, high-throughput determination of Sr isotope ratios by multiple collector-inductively coupled plasma-mass spectrometry.

Science.gov (United States)

Galler, Patrick; Limbeck, Andreas; Boulyga, Sergei F; Stingeder, Gerhard; Hirata, Takafumi; Prohaska, Thomas

2007-07-01

This work introduces a newly developed on-line flow injection (FI) Sr/Rb separation method as an alternative to the common, manual Sr/matrix batch separation procedure, since total analysis time is often limited by sample preparation despite the fast rate of data acquisition possible by inductively coupled plasma-mass spectrometers (ICPMS). Separation columns containing approximately 100 muL of Sr-specific resin were used for on-line FI Sr/matrix separation with subsequent determination of (87)Sr/(86)Sr isotope ratios by multiple collector ICPMS. The occurrence of memory effects exhibited by the Sr-specific resin, a major restriction to the repetitive use of this costly material, could successfully be overcome. The method was fully validated by means of certified reference materials. A set of two biological and six geological Sr- and Rb-bearing samples was successfully characterized for its (87)Sr/(86)Sr isotope ratios with precisions of 0.01-0.04% 2 RSD (n = 5-10). Based on our measurements we suggest (87)Sr/(86)Sr isotope ratios of 0.713 15 +/- 0.000 16 (2 SD) and 0.709 31 +/- 0.000 06 (2 SD) for the NIST SRM 1400 bone ash and the NIST SRM 1486 bone meal, respectively. Measured (87)Sr/(86)Sr isotope ratios for five basalt samples are in excellent agreement with published data with deviations from the published value ranging from 0 to 0.03%. A mica sample with a Rb/Sr ratio of approximately 1 was successfully characterized for its (87)Sr/(86)Sr isotope signature to be 0.718 24 +/- 0.000 29 (2 SD) by the proposed method. Synthetic samples with Rb/Sr ratios of up to 10/1 could successfully be measured without significant interferences on mass 87, which would otherwise bias the accuracy and uncertainty of the obtained data.

Synthesis of MSnO{sub 3} (M = Ba, Sr) nanoparticles by reverse micelle method and particle size distribution analysis by whole powder pattern modeling

Energy Technology Data Exchange (ETDEWEB)

Ahmed, Jahangeer; Blakely, Colin K.; Bruno, Shaun R. [Department of Chemistry, Michigan State University, East Lansing, MI 48824 (United States); Poltavets, Viktor V., E-mail: poltavets@chemistry.msu.edu [Department of Chemistry, Michigan State University, East Lansing, MI 48824 (United States)

2012-09-15

Highlights: ► BaSnO{sub 3} and SrSnO{sub 3} nanoparticles synthesized using the reverse micelle method. ► Particle size and size distribution studied by whole powder pattern modeling. ► Nanoparticles are of optimal size for investigation in dye-sensitized solar cells. -- Abstract: Light-to-electricity conversion efficiency in dye-sensitized solar cells critically depends not only on the dye molecule, semiconducting material and redox shuttle selection but also on the particle size and particle size distribution of the semiconducting photoanode. In this study, nanocrystalline BaSnO{sub 3} and SrSnO{sub 3} particles have been synthesized using the microemulsion method. Particle size distribution was studied by whole powder pattern modeling which confirmed narrow particle size distribution with an average size of 18.4 ± 8.3 nm for SrSnO{sub 3} and 15.8 ± 4.2 nm for BaSnO{sub 3}. These values are in close agreement with results of transmission electron microscopy. The prepared materials have optimal microstructure for successive investigation in dye-sensitized solar cells.

Microfabrication of SrRuO3 thin films on various oxide substrates using LaAlO3/BaOx sacrificial bilayers

Science.gov (United States)

Harada, Takayuki; Tsukazaki, Atsushi

2018-02-01

Oxides provide various fascinating physical properties that could find use in future device applications. However, the physical properties of oxides are often affected by formation of oxygen vacancies during device fabrication processes. In this study, to develop a damage-free patterning process for oxides, we focus on a lift-off process using a sacrificial template layer, by which we can pattern oxide thin films without severe chemical treatment or plasma bombardment. As oxides need high thin-film growth temperature, a sacrificial template needs to be made of thermally stable and easily etchable materials. To meet these requirements, we develop a sacrificial template with a carefully designed bilayer structure. Combining a thermally and chemically stable LaAlO3 and a water-soluble BaOx, we fabricated a LaAlO3/BaOx sacrificial bilayer. The patterned LaAlO3/BaOx sacrificial bilayers were prepared on oxide substrates by room-temperature pulsed laser deposition and standard photolithography process. The structure of the sacrificial bilayer can be maintained even in rather tough conditions needed for oxide thin film growth: several hundred degrees Celsius under high oxygen pressure. Indeed, the LaAlO3/BaOx bilayer is easily removable by sonication in water. We applied the lift-off method using the LaAlO3/BaOx sacrificial bilayer to a representative oxide conductor SrRuO3 and fabricated micron-scale Hall-bar devices. The SrRuO3 channels with the narrowest line width of 5 μm exhibit an almost identical transport property to that of the pristine film, evidencing that the developed process is beneficial for patterning oxides. We show that the LaAlO3/BaOx lift-off process is applicable to various oxide substrates: SrTiO3, MgO, and Al2O3. The new versatile patterning process will expand the range of application of oxide thin films in electronic and photonic devices.

Investigation on gamma and neutron radiation shielding parameters for BaO/SrO‒Bi2O3‒B2O3 glasses

Science.gov (United States)

Sayyed, M. I.; Lakshminarayana, G.; Dong, M. G.; Ersundu, M. Çelikbilek; Ersundu, A. E.; Kityk, I. V.

2018-04-01

In this work, mass attenuation coefficients (μ/ρ), effective atomic number (Zeff), electron density (Ne), mean free path (MFP), and half-value layer (HVL) of 20 BaO/SrO‒(x) Bi2O3‒(80‒x) B2O3 glasses (where x=10, 20, 30, 40, 50 and 60 mol%) were calculated using WinXCom program and MCNP5 code. The obtained (μ/ρ) results using both MCNP5 code and WinXCom program were in good agreement. It is found that the addition of Bi2O3 leads to increase the Zeff values in both BaO/SrO‒Bi2O3‒B2O3 glass systems. However, the Zeff values of the BaO‒Bi2O3‒B2O3 glass system are higher than those of the SrO‒Bi2O3‒B2O3 glasses. The fast neutrons effective removal cross sections (ΣR) for 20 SrO‒40 Bi2O3‒40 B2O3 glass is the highest among all studied glasses. The calculated half-value layer values were compared with different glass systems and it was found that the shielding properties of the selected glasses are comparable or even better than other glass systems such as phosphate glasses.

Study of Ne and Kr production in Mg, Al, Rb, Sr and Y targets by 0-180 MeV neutrons. Cosmochemical application

International Nuclear Information System (INIS)

Bertin, P.

1989-07-01

High sensitivity mass spectrometry technique has been used to measure production of noble gases Ne and Kr induced by 0-180 MeV neutrons in Mg, Al, Rb, Sr and Y targets. This experiment allowed us an evaluation of the implied excitation functions, in an energy range where no experimental data were available. These results have exhibited the importance of secondary neutrons induced in the interaction of cosmic rays with meteorites and moon surface [fr

Erosion of the Alps: use of Rb-Sr isotopic data from molassic sediments to identify the ages of the metamorphism recorded by the eroded rocks; Erosion des Alpes: histoire metamorphique des roches erodees par l`analyse du couple Rb-Sr des sediments molassiques

Energy Technology Data Exchange (ETDEWEB)

Henry, P; Deloule, E [Centre National de la Recherche Scientifique (CNRS), 54 - Nancy (France). Centre de Recherches Petrographiques et Geochimiques; Michard, A [Aix-Marseille-3 Univ., 13 - Marseille (France)

1994-06-01

Rb-Sr isotopic data from Oligocene and Miocene peri-alpine molassic sediments allow us to identify the different periods for which the eroded rocks have or have not recorded an alpine metamorphism. The Chattian and the Burdigalian sediments result from the erosion of rocks for which the latest metamorphic event was variscan, while the Stampian, Aquitanian and ``Helvetian`` sediments show evidence for the erosion of rocks which have recorded alpine metamorphic events. The application of this method to old detrital sediments could permit determination of the ages of the tectonic events which occurred in the sediment source regions. (authors). 18 refs., 6 figs.

Electric-field-induced monoclinic phase in (Ba,Sr)TiO3 thin film

International Nuclear Information System (INIS)

Anokhin, A. S.; Yuzyuk, Yu. I.; Golovko, Yu. I.; Mukhortov, V. M.; El Marssi, M.

2011-01-01

We have studied electric-field-induced symmetry lowering in the tetragonal (001)-oriented heteroepitaxial (Ba 0.8 Sr 0.2 )TiO 3 thin film deposited on (001)MgO substrate. Polarized micro-Raman spectra were recorded from the film area in between two planar electrodes deposited on the film surface. Presence of c domains with polarization normal to the substrate was confirmed from polarized Raman study under zero field, while splitting and hardening of the E(TO) soft mode and polarization changes in the Raman spectra suggest monoclinic symmetry under external electric field.

Photophysical electronic structure of double-perovskites A{sub 2}GdTaO{sub 6} (A = Ba and Sr)

Energy Technology Data Exchange (ETDEWEB)

Ghosh, Binita, E-mail: ghosh.binita@gmail.com [Department of Physics, Bose Institute, 93/1 Acharya Prafulla Chandra Road, Kolkata 700009 (India); Dutta, Alo [Department of Physics, Bose Institute, 93/1 Acharya Prafulla Chandra Road, Kolkata 700009 (India); Shannigrahi, Santiranjan [Institute of Materials Research and Engineering, Agency for Science Technology and Research, 3 Research Link, Singapore 117602 (Singapore); Sinha, T.P. [Department of Physics, Bose Institute, 93/1 Acharya Prafulla Chandra Road, Kolkata 700009 (India)

2015-11-05

X-ray photoemission spectroscopy (XPS) measurements of double perovskite oxides, Ba{sub 2}GdTaO{sub 6} and Sr{sub 2}GdTaO{sub 6} are performed in the energy window of 0–1300 eV. Density functional theory calculations are initiated with the Vienna ab initio Simulation Package to understand the electronic structure of the systems. The calculated DOS has been compared with the experimental valence band XPS spectra. It has been observed that the Ta-5d and O-2p states are hybridized in the valence band. The chemical shifts of these compounds suggest a mixed ionic and covalent character of the bonds, which has been used to explain the electrical conduction mechanism of the systems. The calculated ratio of the spin-orbit interaction energy for Ba 3d and 4d states matches well with the observed experimental results. - Highlights: • DFT calculations of Ba{sub 2}GdTaO{sub 6} and Sr{sub 2}GdTaO{sub 6} have been performed with VASP. • XPS measurements are performed in the energy window of 0–1300 eV. • The calculated DOS has been compared with the valence band XPS spectra. • Chemical shifts from XPS spectra have been used to explain the conduction mechanism.

Rb/Sr geochronology in whole rocks and minerals of the Cumaru granodiorite, Serra dos Gradaus, Para state, Brazil

International Nuclear Information System (INIS)

Lafon, J.M.; Scheller, T.; Pereira, E.D.; Macambira, J.B.

1990-01-01

The Cumaru granodiorite occurs in the Serra dos Gradaus region, southeastern part of the Metallogenic Province of Carajas, Para. Rb-Sr systematics have been provided in whole rocks and minerals for samples of the Cumaru granodiorite thus an age of 2543 ± 53 Ma, with an initial isotopic ratio of 0.70311 ± 34 (MSWD+1.87) was obtained for whole rocks samples. Taking in account that these rocks are not affected by metamorphism and/or deformation, we consider the age of 2543 ± 53 Ma as an emplacement age corresponding to the crystallization of the body. Such an age confirms the existence of a late Archaean plutonic event in the Serra dos Gradaus area and the interpretation of the Cumaru granodiorite as a contemporaneous and cogenetic body of the Juruena type granites (Ca. 2000 Ma old), as proposed previously, must be definitively abandoned. Therefore, Archaean ages for the greenstone belt sequence (Gradaus group) as well as for the Xingu complex in this area are also confirmed, although by indirect evidence. The age obtained implies that the latter represents an Archaean metamorphic basement in the Serra dos Gradaus region rather than the reworking of the late archaean granitics rocks during the Transmazonian orogenic event. The initial isotopic ratio of 0.70311 ± 34 is close to a mantellic or low time of crustal residence source material ratios at the end of Archaean times. Therefore, comparison with isotopic initial ratios of other granitic rocks which occur in the Rio Maria region identifies an evolution line with a Rb-Sr ratio of 0.25 for a crustal source material that would have separated from mantle about 2.8 Ga ago. (author)

The initial 87Sr/86Sr ratios of the Kirwan Volcanics of Dronning Maud Land: Comparison with the Kirkpatrick Basalt, Transantarctic Mountains

International Nuclear Information System (INIS)

Faure, G.; Bowman, J.R.; Elliot, D.H.

1979-01-01

A series of lava flows from Mountain B (6 0 13.9'W, 74 0 06.9'S) of the Kirwan Escarpment in Dronning Maud Land, Antarctica, is composed of tholeiite basalts of Jurassic age. Their chemical compositions are similar to those of Jurassic basalts elsewhere in Dronning Maud Land but differ from those of the Kirkpatrick Basalt of the Transantarctic Mountains. The basalts on Mountain B contain 50.39% SiO 2 , 9.7 ppm Rb, 174.4 ppm Sr, have a Rb/Sr ratio of 0.057, and a K/Rb ratio of 417. Their average initial 87 Sr/ 86 Sr ratio is 0.7044 +- 0.0010 (1sigma) which suggests that the magma from which they formed could have been derived from the upper mantle without extensive contamination with 87 Sr and other elements. These results confirm earlier suggestions that the Jurassic basalts of Dronning Maud Land differ significantly from the Kirkpatrick Basalt and the Ferrar Dolerite of the Transantarctic Mountains. These differences in chemical and Sr-isotopic composition may be related to tectonic activity and magma formation during the break-up of Gondwanaland. (Auth.)

Structural and optical properties of (Sr,Ba)2SiO4:Eu2+ thin films grown by magnetron sputtering

International Nuclear Information System (INIS)

Li, Leliang; Zheng, Jun; Zuo, Yuhua; Cheng, Buwen; Wang, Qiming

2014-01-01

(Sr,Ba) 2 SiO 4 :Eu 2+ thin films were deposited on Si at different substrate temperatures by magnetron sputtering. The morphology and crystalline phases of the films were studied by scanning electron microscopy (SEM) and X-ray diffraction (XRD) measurements, respectively. The silicate crystal phase was presented when films were annealed above 900 °C and the annealing temperature had great impact on the film morphology. The samples annealed at 1000 °C in a non-reducing atmosphere for 30 s show intense room temperature Eu 2+ emission. These findings may open a promising way to prepare efficient phosphor thin films for on-chip light emitting diodes application. - Highlights: • The (Sr, Ba) 2 SiO 4 :Eu 2+ films are fabricated by magnetron sputtering. • A very strong RT PL emission at 540 nm is achieved. • The morphology and optical properties dependent on temperature are studied

The Rb/Sr ages for granitoids of the Middle Chukotka: a new approach to the geological history of the region

International Nuclear Information System (INIS)

Efremov, S.V.; Kozlov, V.D.; Sandimirova, G.P.

2000-01-01

For studying the history of geological evolution of the Middle Chukotka in the Mesozoic by the method of Rb-Sr dating the age of granitoids in the region was determined. It was ascertained that the granitoids have different genetic nature, their formation involving the most intensive tectonic restructuring. Magmatism was manifested in two stages. Formation of the first stage granitoids (126-144 mln. years) relates to orogenesis, while that of the second stage granitoids (∼ 80 mln. years) - to the process of the Chukotka folded region activation [ru

Interdiffusion effect on strained La0.8Ba0.2MnO3 thin films by off-axis sputtering on SrTiO3 (100) substrates

International Nuclear Information System (INIS)

Chou, Hsiung; Hsu, S. G.; Lin, C. B.; Wu, C. B.

2007-01-01

Strained La 0.8 Ba 0.2 MnO 3 thin films on SrTiO 3 (100) substrate are grown by an off-axis sputtering technique. It is found that the ferromagnetic temperature T C increases for thinner films. Secondary ion mass spectroscopy indicates that Sr diffuses partially into the film, making it structurally nonuniform. The region close to the film/substrate interface acts as La 1-x (Sr y Ba 1-y ) x MnO 3 with a near negligible y for the as grown film and a non-negligible amount of y for the high-temperature postannealed film. The enhancement of T C is attributed to the combination of the strain and interdiffusion effects

A summary of Rb-Sr isotope studies in the Archean Hopedale Block and the adjacent proterozoic Makkovik subprovince, Labrador

International Nuclear Information System (INIS)

Grant, N.K.; Hickman, M.H.; Marzano, M.S.; Ermanovics, I.F.

1983-01-01

Rb-Sr isotope study of thirteen whole-rock suites of Archean and Proterozoic rocks from Hopedale block and Makkovik Subprovince shows that the crustal history began about 3115 Ma ago. We tentatively recognize younger crustal segments that formed 2920 Ma ago, from which Kanairktok intrusives were derived at 2832 +- 178 Ma. In Makkovik Subprovince the Island Harbour granites range in age from 1843 +- 90 to 1794 +- 71 Ma. These ages overlap with the 1847 +-87 Ma age for Kanairktok shear zone mylonites. The Island Harbour granodiorites from inland localities to the southwest are contaminated with Archean rocks in Makkovik Subprovince and their initial 87 Sr/ 86 ratios imply a crustal contribution to their source. In contrast, the Island Harbour granites of Striped Island were derived from a mantle source. The sills of Striped Island are 1635 +- 47 Ma old. An undeformed northeast trending Kikkertavak dolerite dyke from Hopedale block is 1206 +- 120 Ma

Dating the Martian meteorite Zagami by the ⁸⁷Rb-⁸⁷Sr isochron method with a prototype in situ resonance ionization mass spectrometer.

Science.gov (United States)

Anderson, F Scott; Levine, Jonathan; Whitaker, Tom J

2015-01-30

The geologic history of the Solar System builds on an extensive record of impact flux models, crater counts, and ~270 kg of lunar samples analyzed in terrestrial laboratories. However, estimates of impactor flux may be biased by the fact that most of the dated Apollo samples were only tenuously connected to an assumed geologic context. Moreover, uncertainties in the modeled cratering rates are significant enough to lead to estimated errors for dates on Mars and the Moon of ~1 Ga. Given the great cost of sample return missions, combined with the need to sample multiple terrains on multiple planets, we have developed a prototype instrument that can be used for in situ dating to better constrain the age of planetary samples. We demonstrate the first use of laser ablation resonance ionization mass spectrometry for (87)Rb-(87)Sr isochron dating of geological specimens. The demands of accuracy and precision have required us to meet challenges including regulation of the ambient temperature, measurement of appropriate backgrounds, sufficient ablation laser intensity, avoidance of the defocusing effect of the plasma created by ablation pulses, and shielding of our detector from atoms and ions of other elements. To test whether we could meaningfully date planetary materials, we have analyzed a piece of the Martian meteorite Zagami. In each of four separate measurements we obtained (87)Rb-(87)Sr isochron ages for Zagami consistent with its published age, and, in both of two measurements that reached completion, we obtained better than 200 Ma precision. Combining all our data into a single isochron with 581 spot analyses gives an (87)Rb-(87)Sr age for this specimen of 360 ±90 Ma. Our analyses of the Zagami meteorite represent the first successful application of resonance ionization mass spectrometry to isochron geochronology. Furthermore, the technique is miniaturizable for spaceflight and in situ dating on other planetary bodies. © 2014 The Authors. Rapid Communications in

Defect chemistry and oxygen transport of (La0.6Sr0.4-xMx)(0.99)Co0.2Fe0.8O3-delta, M = Ca (x=0.05, 0.1), Ba (x=0.1, 0.2), Sr Part I: Defect chemistry

DEFF Research Database (Denmark)

Dalslet, Bjarke Thomas; Søgaard, Martin; Bouwmeester, Henry J.M.

2009-01-01

This paper is the first part of a two part series, where the effects of varying the A-site dopant on the defect chemistry, the diffusion coefficient and the surface catalytic properties of the materials (La0.6Sr0.4 − xMx)0.99Co0.2Fe0.8O3 − δ, M = Sr, Ca (x = 0.05, 0.1), Ba (x = 0.1, 0.2) (LSMFC......) have been investigated. In part I, the findings on the defect chemistry are reported, while the transport properties are reported in part II. Substitution of Sr2+ ions with Ca2+ ions (smaller ionic radius) and Ba2+ ions (larger ionic radius) strains the crystal structure differently for each...... composition while keeping the average valence of the cations constant. The Ba2+ containing materials show the largest oxygen loss at elevated temperatures, while the purely Sr2+ doped material showed the smallest oxygen loss. This was reflected in the partial oxidation entropy of the materials. The measured...

The system Ba(H2PO4)2-Sr(H2PO4)2-H3PO4(30%)-H2O at 25, 40 and 60 deg C

International Nuclear Information System (INIS)

Taranenko, N.P.; Serebrennikova, G.M.; Stepin, B.D.; Oboznenko, Yu.V.

1982-01-01

The system Ba(H 2 PO 4 ) 2 -Sr(H 2 PO 4 ) 2 -H 3 PO 4 (30%)-H 2 O (25 deg C) belongs to eutonic type systems. Solubility isotherms of salt components at 40 and 60 deg C are calculated. Polytherms (25-60 deg C) of solubility of monosubstituted barium and strontium phosphates in 30-60% H 3 PO 4 are obtained. The value of cocrystallization coefficient of Sr 2 + and Ba(H 2 PO 4 ) 2 Dsub(Sr)=0.042+-0.005 remains stable in the temperature range of 25-60 deg C and concentrations 30-60% phosphoric acid at initial content [Sr 2 + ]=1x10 - 2 mass%

The isotypic family of the diarsenates MM'As{sub 2}O{sub 7} (M = Sr, Ba; M' = Cd, Hg)

Energy Technology Data Exchange (ETDEWEB)

Weil, Matthias [Technische Univ. Wien (Austria). Inst. for Chemical Technologies and Analytics

2016-08-01

The diarsenates MM'As{sub 2}O{sub 7} (M = Sr, Ba; M' = Cd, Hg) were prepared under hydrothermal conditions (∝200 C, autogenous pressure), starting from As{sub 2}O{sub 5} and the corresponding metal oxides or precursor compounds thereof in aqueous solutions. Structure analyses on the basis of single crystal X-ray data revealed the four structures to be isotypic. They are the first diarsenates to crystallize in the triclinic BaZnP{sub 2}O{sub 7} structure type (space group P anti 1, Z = 2, a ∼ 5.8 Aa, b ∼ 7.3 Aa, c ∼ 7.6 Aa, α ∼ 101 , β ∼ 91 , γ ∼ 98 ). All related MM'As{sub 2}O{sub 7} diarsenates reported so far (M = Sr, Ba, Pb; M' = Mg, Co, Cu, Zn) crystallize in the monoclinic α-Ca{sub 2}P{sub 2}O{sub 7} structure type (P2{sub 1}/n, Z = 4). Hence, the size of the divalent M' cation determines which of the two structure types is adopted.

Oxygen reduction kinetics and transport properties of (Ba,Sr)(Co,Fe)O3-δ solid oxide fuel cell cathode materials

International Nuclear Information System (INIS)

Wang, Lei; Merkle, Rotraut; Baumann, Frank S.; Maier, Joachim; Fleig, Juergen

2007-01-01

Full text: The oxygen reduction at the surface of cathode materials is crucial for the performance of solid oxide fuel cells (SOFC), but a detailed understanding of the mechanism is not available yet. (Ba x Sr 1-x )(Co 1-y Fe y )O 3-δ shows strongly improved oxygen reduction rates compared to previously applied perovskite cathode materials. In this work, surface rate constants as well as bulk transport properties are studied. (Ba x Sr 1-x )(Co 1-y Fe y )O 3-δ with 0≤x≤0.5, 0.2≤y≤1 was synthesized by the Pechini method. Oxygen stoichoimetry was obtained from thermo-gravimetric analysis, confirming that Ba 0.5 Sr 0.5 Co 0.8 Fe 0.2 O 3-δ has an exceptionally low oxygen content which is generally smaller than 2.5. Dense thin films were grown by pulsed laser deposition (PLD) and patterned into circular microelectrodes by photolithography. The surface resistance R s , which dominate the overall electrode resistance, were measured by impedance spectroscopy on individual microelectrodes at different T, pO 2 and applied electrical bias. PLD technique greatly helps to study the oxygen reduction kinetics since only measurements on dense thin films allow to record absolute R s values without interference from morphology effects. These R s values were found to be much lower than those for (La,Sr)(Co,Fe)O 3-δ . The variation of the surface reaction rates with A-site and B-site composition was studied and correlations with bulk materials properties such as oxygen nonstoichiometry, ionic mobility or oxidation enthalpy were examined. Plausible reaction mechanisms as well as possible reasons for the high absolute surface reaction rates will be discussed

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

International Nuclear Information System (INIS)

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

2017-01-01

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

Zintl-phases with layer anions: preparation and crystal structures of the isotypic compounds SrSn sub 2 As sub 2 and Sr sub 0. 87 Ba sub 0. 13 Sn sub 2 As sub 2 and a single crystal structure determination of KSnSb. Zintl-Phasen mit Schichtanionen: Darstellung und Kristallstrukturen der isotypen Verbindungen SrSn sub 2 As sub 2 und Sr sub 0,87 Ba sub 0,13 Sn sub 2 As sub 2 sowie eine Einkristallstrukturbestimmung von KSnSb

Energy Technology Data Exchange (ETDEWEB)

Eisenmann, B; Klein, J [Abt. 2 fuer Anorganische Chemie, Technische Hochschule Darmstadt (Germany)

1991-06-01

The metallic reflecting compounds SrSn{sub 2}As{sub 2} and Sr{sub 0.87}Ba{sub 0.13}Sn{sub 2}As{sub 2} were prepared from the melt, they crystallize in the trigonal rhombohedral system (space group R3m, Z = 3) with lattice constants see ''Inhaltsuebersicht''. In the crystal structure of the isotypic compounds threebonded Sn atoms and threebonded As atoms together form puckered layers which are isostructural to grey As. The mean values of the bond lengths Sn -- As are 277.6 pm (SrSn{sub 2}As{sub 2}) and 279.1 pm (Sr{sub 0.87}Ba{sub 0.13}Sn{sub 2}As{sub 2}) resp. Along (001) the alkaline earth atoms occupy the octahedral interstices of As atoms between each second SnAs layer. The single crystal structure determination of KSnSb confirms the results of the X-ray powder analysis, but leads to slightly different values for the bond lengths.

Dependence of optical properties on the composition of (Ba{sub 1−x−y}Sr{sub x}Eu{sub y})Si{sub 2}O{sub 2}N{sub 2} phosphors for white light emitting diodes

Energy Technology Data Exchange (ETDEWEB)

Zhang, Mei, E-mail: zmjenny@163.com; He, Xin; Luo, Jianyi; Zeng, Qingguang

2014-10-15

BaSi{sub 2}O{sub 2}N{sub 2}: Eu{sup 2+} is an efficient phosphor because of its high quantum yield and quenching temperature. Partial substitution of Ba{sup 2+} by Sr{sup 2+} is the most promising approach to tune the color of phosphors. In this study, a series of (Ba{sub 1−x−y}Sr{sub x}Eu{sub y})Si{sub 2}O{sub 2}N{sub 2} (x = 0.0–0.97, y = 0.00–0.10) phosphors are synthesized via high-temperature solid-state reactions. Intense green to yellow phosphors can be obtained by the partial substitution of the host lattice cation Ba{sup 2+} by either Sr{sup 2+} or Eu{sup 2+}. The luminescent properties and the relationships among the lowest 5d absorption bands, Stokes shifts, centroid shifts, and the splitting of Eu{sup 2+} are studied systematically. Then, based on (Ba{sub 1−x−y}Sr{sub x}Eu{sub y})Si{sub 2}O{sub 2}N{sub 2} phosphors and near-ultraviolet (∼395 nm)/blue (460 nm) InGaN chips, intense green–yellow light emitting diodes (LEDs) and white LEDs are fabricated. (Ba{sub 0.37}Sr{sub 0.60})Si{sub 2}O{sub 2}N{sub 2}: 0.03Eu{sup 2+} phosphors present the highest efficiency, and the luminous efficiency of white LEDs can reach 17 lm/w. These results indicate that (Ba{sub 1−x−y}Sr{sub x}Eu{sub y})Si{sub 2}O{sub 2}N{sub 2} phosphors are promising candidates for solid-state lighting. - Highlights: • The optical properties of Eu{sup 2+} in the (Ba, Sr)Si{sub 2}O{sub 2}N{sub 2} solid-solutions are studied systematically. • The relationship among the lowest 5d absorption bands, Stocks shifts etc.of Eu{sup 2+} are also studied. • The electroluminescent properties of pc-LEDs are studied in details.

Influencia de los iones Ba2+ y Sr2+ en el proceso de hidratación del cemento portland y de los cementos con adiciones activas

OpenAIRE

Živanović, B. M.; Petrašinović, Lj.; Milovanović, T.; Karanović, Lj.; Krstanović, I.

1987-01-01

En el presente trabajo se estudia la influencia de la concentración de los iones Sr2+ y Ba2+ en las aguas de amasado sobre el proceso de hidratación de varios cementos portland y de adición. Se comprueba un incremento de las resistencias mecánicas de dichos cementos, a los 28 días, cuando aumenta la concentración de los iones Ba2+ y Sr2+ en las aguas de amasado, lo cual sugiere una posible explicación microestructural a dicho fenómeno.

Preparation of cauliflower-like shaped Ba{sub 0.6}Sr{sub 0.4}TiO{sub 3} powders by modified oxalate co-precipitation method

Energy Technology Data Exchange (ETDEWEB)

Li Mingli [School of Materials Science and Engineering, Key Laboratory for Advanced Ceramics and Machining Technology of Ministry of Education, Tianjin University, Tianjin 300072 (China)], E-mail: lml@tju.edu.cn; Xu Mingxia [School of Materials Science and Engineering, Key Laboratory for Advanced Ceramics and Machining Technology of Ministry of Education, Tianjin University, Tianjin 300072 (China)

2009-04-17

The quantitative barium-strontium titanyl oxalate (Ba{sub 0.6}Sr{sub 0.4}TiO(C{sub 2}O{sub 4}){sub 2}.4H{sub 2}O, BSTO) precursor powders were prepared by the modified oxalate co-preparation method. It was based on the cation-exchange reaction between the stoichiometric solutions of oxalotitanic acid (H{sub 2}TiO(C{sub 2}O{sub 4}){sub 2}, HTO) and barium + strontium nitrate solution containing stoichiometric quantities of Ba and Sr ions. The pyrolysis of BSTO at 800 deg. C/4 h in air produced the homogeneous cauliflower-like shaped barium-strontium titanate (Ba{sub 0.6}Sr{sub 0.4}TiO{sub 3}, BST) powders. The effect of polyethylene glycol (PEG) on morphology of BSTO and BST powders was also investigated. The characterization studies were carried on the as-dried BSTO and calcined BST powders by various physicochemical techniques, IR, X-ray diffraction (XRD), scanning electron microscopy (SEM), etc. The BSTO and BST powders obtained by aforementioned technique without PEG were homogeneous with spherical shape. The particles grew into spindle shape with the effect of PEG.

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

Science.gov (United States)

Parker, David; Singh, David J

2013-01-01

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

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

Directory of Open Access Journals (Sweden)

David Parker and David J Singh

2013-01-01

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

Suppression of the stellar enhancement factor and the reaction 85Rb(p,n)85Sr

International Nuclear Information System (INIS)

Rauscher, T.; Kiss, G. G.; Gyuerky, Gy.; Simon, A.; Fueloep, Zs.; Somorjai, E.

2009-01-01

It is shown that a Coulomb suppression of the stellar enhancement factor occurs in many endothermic reactions at and far from stability. Contrary to common assumptions, reaction measurements for astrophysics with minimal impact of stellar enhancement should be preferably performed for those reactions instead of their reverses, despite of their negative Q value. As a demonstration, the cross section of the astrophysically relevant 85 Rb(p,n) 85 Sr reaction has been measured by activation between 2.16≤E c.m. ≤3.96 MeV and the astrophysical reaction rates at p process temperatures for (p,n) as well as (n,p) are directly inferred from the data. Additionally, our results confirm a previously derived modification of a global optical proton potential. The presented arguments are also relevant for other α- and proton-induced reactions in the p, rp, and νp processes.

Role of BaO/SrO layers in deciding the electronic structure of Cu0.3Co0.7Ba2-xSrxYCu2O7+δ (CoCu-1212) x = 0, 1 and 2

International Nuclear Information System (INIS)

Singh, Shiva Kumar; Husain, M.; Kishan, H.; Awana, V.P.S.

2011-01-01

Highlights: → Decrease in lattice parameters confirms replacement by Sr ion at Ba ion site. → XPS measurement shows that mixed Cu 1+/2+ and Co 3+/4+ valence state. → With increasing x, Cu valence is non-monotonous whereas Co valence is increasing. → Resistivity reveals that holes in Cu/CoO x planes are taking part in charge transport. → Paramagnetic nature is due to the presence Cu ions in Cu/CoO x chains/planes. - Abstract: In this paper we report the change in electronic structure of Cu 0.3 Co 0.7 Ba 2-x Sr x YCu 2 O 7+δ with change in structural pressure. Rietveld refined X-ray diffraction (XRD) pattern shows that the samples are phase pure. Decrease in lattice parameters with increasing x, confirms replacement by Sr ion at Ba ion site. The calculated tolerance factor of the systems is in accord with lattice parameter changes. The X-ray photoelectron spectroscopy (XPS) is made to find out the variation in ionic state of Co and Cu with ionic size variation in BaO/SrO layers. Effect of the same on the electronic structure and transport properties is explored. The XPS measurement reveals that Cu is in mixed 1+/2+ state and variation in valence state is non-monotonous with increasing x. Whereas Co is in mixed 3+/4+ state and with increasing x its valence state is increasing. The observed changes in electronic structure are subject of structural changes. The resistivity measurement shows that normal state conductivity decreases with increasing x. Resistivity behaviour indicates about holes in Cu/CoO x planes taking part in charge transport. The magnetic measurement (M-T and M-H) shows that paramagnetic nature for all the compositions. The presence of Cu ions in Cu/CoO x chains/planes results in paramagnetic behaviour.

Structural, electronic, optical and thermoelectric investigations of antiperovskites A3SnO (A = Ca, Sr, Ba) using density functional theory

Science.gov (United States)

Hassan, M.; Shahid, A.; Mahmood, Q.

2018-02-01

Density functional theory study of the structural, electrical, optical and thermoelectric behaviors of very less investigated anti-perovskites A3SnO (A = Ca, Sr, Ba) is performed with FP-LAPW technique. The A3SnO exhibit narrow direct band gap, in contrast to the wide indirect band gap of the respective perovskites. Hence, indirect to direct band gap transformation can be realized by the structural transition from perovskite to anti-perovskite. The p-p hybridization between A and O states result in the covalent bonding. The transparency and maximum reflectivity to the certain energies, and the verification of the Penn's model indicate potential optical device applications. Thermoelectric behaviors computed within 200-800 K depict that Ca3SnO exhibits good thermoelectric performance than Ba3SnO and Sr3SnO, and all three operate at their best at 800 K suggesting high temperature thermoelectric device applications.

Theoretical survey on M@C_8_0 (M = Ca, Sr, and Ba): Behavior of different alkaline earth metal impacting the chemical stability and electronic properties

International Nuclear Information System (INIS)

Cui, Jin-Bo; Guo, Yi-Jun; Li, Qiao-Zhi; Zhao, Pei; Zhao, Xiang

2016-01-01

Structures of mono-metallofullerenes M@C_8_0 (M = Ca, Sr, and Ba) that separated in early experiment are determined owning the C_2_v(31920)-C_8_0 cage. The change rule of properties for M@C_8_0 (M = Ca, Sr, and Ba) influenced by different inner metal are discussed. As the trapped metal changes from calcium to barium, performance of thermodynamic stabilities for M@C_2_v(31920)-C_8_0, M@C_2_v(31922)-C_8_0, and M@D_5_h(31923)-C_8_0 are significantly different. Orbital analysis suggests that the lowest unoccupied molecular orbitals (LUMOs) of Ca@C_2_v(31920)-C_8_0 and Ca@D_5_h(31923)-C_8_0 are mostly located on the trapped metal, whereas reduction reactions of Ca@C_2_v(31920)-C_8_0 and Ca@D_5_h(31923)-C_8_0 occur on the fullerene cage. Natural electron configuration analyses demonstrates that the decentralized electron back-donation of Ba@C_2_v(31920)-C_8_0 would take responsible for the instability of itself. Electronic properties such as electron affinities and ionization potentials are significantly affected by encapsulated metal are also found. Computational UV–visible–NIR spectra for M@C_2_v(31920)-C_8_0 (M = Ca, Sr, Ba) are in perfect accord with the spectra obtained experimentally.

Structure refinement of Ba{sub 0.5}Sr{sub 0.5}Co{sub 0.8}Fe{sub 0.2}O{sub 3-d} as cathode materials for intermediate temperature solid oxide fuel cells (IT-SOFC)

Energy Technology Data Exchange (ETDEWEB)

Zakaria, Nurhamidah, E-mail: nurhamidahzakaria@yahoo.com; Idris, Mohd Sobri, E-mail: sobri@unimap.edu.my [Centre of Excellence for Frontier Materials Research, School of Materials Engineering, Universiti Malaysia Perlis (UniMAP), Taman Muhibbah, Jejawi 02600, Arau, Perlis (Malaysia); Osman, Rozana A. M., E-mail: rozana@unimap.edu.my [School of Microelectronics Engineering, Universiti Malaysia Perlis (UniMAP), Pauh Putra, 02600, Arau, Perlis (Malaysia)

2016-07-19

Ba{sub 0.5}Sr{sub 0.5}Co{sub 0.8}Fe{sub 0.2}O{sub 3-δ} was successfully prepared using modified solid-state synthesis routes. The lowest temperature to obtained single phase of Ba{sub 0.5}Sr{sub 0.5}Co{sub 0.8}Fe{sub 0.2}O{sub 3-δ} is about 900°C for 15 hours. Longer period of time are required compared to only 5 hours at 950°C as established in literatures. The X-ray Diffraction (XRD) data confirmed that Ba{sub 0.5}Sr{sub 0.5}Co{sub 0.8}Fe{sub 0.2}O{sub 3-δ} is formed a cubic perovskite with the space group of Pm-3m. The lattice parameters of Ba{sub 0.5}Sr{sub 0.5}Co{sub 0.8}Fe{sub 0.2}O{sub 3-δ} are a = 3.990 (1) Å and unit cell volume is V = 63.5 (1) Å{sup 3}. The Rietveld refinement of XRD data revealed that the crystal structure of Ba{sub 0.5}Sr{sub 0.5}Co{sub 0.8}Fe{sub 0.2}O{sub 3-δ} slightly changes as a function of temperature.

Effect of Sr substitution on superconductivity in Hg2(Ba1-ySry)2YCu2O8-d (part2): bond valence sum approach of the hole distribution

OpenAIRE

Toulemonde, P.; Odier, P.; Bordet, P.; Floch, S. Le; Suard, E.

2004-01-01

The effects of Sr substitution on superconductivity, and more particulary the changes induced in the hole doping mechanism, were investigated in Hg2(Ba1-ySry)2YCu2O8-d by a "bond valence sum" analysis with Sr content from y = 0.0 to y = 1.0. A comparison with CuBa2YCu2O7-d and Cu2Ba2YCu2O8 systems suggests a possible explanation of the Tc enhancement from 0 K for y = 0.0 to 42 K for y = 1.0. The charge distribution among atoms of the unit cell was determined from the refined structure, for y ...

Isotopic and Chemical Evidence for Primitive Aqueous Alteration in the Tagish Lake Meteorite

Science.gov (United States)

Sakuma, Keisuke; Hidaka, Hiroshi; Yoneda, Shigekazu

2018-01-01

Aqueous alteration is one of the primitive activities that occurred on meteorite parent bodies in the early solar system. The Tagish Lake meteorite is known to show an intense parent body aqueous alteration signature. In this study, quantitative analyses of the alkaline elements and isotopic analyses of Sr and Ba from acid leachates of TL (C2-ungrouped) were performed to investigate effects of aqueous alteration. The main purpose of this study is to search for isotopic evidence of extinct 135Cs from the Ba isotopic analyses in the chemical separates from the Tagish Lake meteorite. Barium isotopic data from the leachates show variable 135Ba isotopic anomalies (ε = ‑2.6 ∼ +3.6) which correlatewith 137Ba and 138Ba suggesting a heterogeneous distribution of s- and r-rich nucleosynthetic components in the early solar system. The 87Rb–87Sr and 135Cs–135Ba decay systems on TL in this study do not provide any chronological information. The disturbance of the TL chronometers is likely a reflection of the selective dissolution of Cs and Rb given the relatively higher mobility of Cs and Rb compared to Ba and Sr, respectively, during fluid mineral interactions.

Topotactic reduction as a synthetic route for the preparation of low-dimensional Mn(II) oxide phases: the structure and magnetism of LaAMnO(4-x) (A = Sr, Ba).

Science.gov (United States)

Kitchen, Helen J; Saratovsky, Ian; Hayward, Michael A

2010-07-14

Reaction of LaSrMnO(4) with CaH(2) at 420 degrees C yields LaSrMnO(3.67(3)). Raising the temperature to 480 degrees C yields the Mn(II) phase LaSrMnO(3.50(2)). Neutron powder diffraction data show both phases adopt body-centred orthorhombic crystal structures (LaSrMnO(3.67(3)), Immm: a = 3.7256(1) A, b = 3.8227(1) A, c = 13.3617(4) A; LaSrMnO(3.50(2)), Immm: a = 3.7810(1) A, b = 3.7936(1) A, c = 13.3974(3) A) with anion vacancies located within the equatorial MnO(2-x) planes of the materials. Analogous reactivity is observed between LaBaMnO(4) and CaH(2) to yield body-centred tetragonal reduced phases (LaBaMnO(3.53(3)), I4/mmm: a = 3.8872(1)A, c = 13.6438(2) A). Low-temperature neutron diffraction and magnetisation data show that LaSrMnO(3.5) and LaBaMnO(3.5) exhibit three-dimensional antiferromagnetic order below 155 K and 135 K respectively. Above these temperatures, they exhibit two-dimensional antiferromagnetic order with paramagnetic behaviour observed above 480 K in both phases. The origin of the low dimensional magnetic order and ordering of the anion vacancies in the reduced phases is discussed.

Dating and source determination of volcanic rocks from Khunik area (South of Birjand, South Khorasan using Rb-Sr and Sm-Nd isotopes

Directory of Open Access Journals (Sweden)

Somayeh Samiee

2016-12-01

Full Text Available The Khunik area is located in the south of Birjand, Khorasan province, in the eastern margin of Lut block. Tertiary volcanic rocks have andesite to trachy-andesite composition. Dating analyzing by Rb-Sr method on plagioclase and hornblende as well as whole-rock isochron method was performed on pyroxene-hornblende andesite rock unit. On this basis the emplacement age is Upper Paleocene (58±11 Ma. These rocks have initial 87Sr/86Sr and εNd 0.7046-0.7049 and 2.16-3.12, respectively. According to isotopic data, volcanic rocks originated from depleted mantle and have the least crust contamination while it was fractionated. Geochemically, Khunik volcanic rocks have features typical of calk-alkaline to shoshonite and are metaluminous. Enrichment in LILEs and typical negative anomalies of Nb and Ti are evidences that the volcanic rocks formed in a subduction zone and active continental margin. Modeling suggests that these rocks were derived dominantly from 1–5% partial melting of a mainly spinel garnet lherzolite mantle source that is metasomatized by slab-derived fluid.

Strain induced enhancement of magnetization in Ba{sub 2}FeMoO{sub 6} based heterostructure with (Ba{sub x}Sr{sub 1-x})TiO{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Kim, Kyeong-Won; Norton, David P. [Department of Materials Science and Engineering, University of Florida, Gainesville, Florida 32611 (United States); Ghosh, Siddhartha, E-mail: ghoshsid@gmail.com; Buvaev, Sanal; Hebard, Arthur F. [Department of Physics, University of Florida, Gainesville, Florida 32611 (United States)

2016-05-14

High quality epitaxial Ba{sub 2}FeMoO{sub 6} thin films and Ba{sub 2}FeMoO{sub 6}–(Ba{sub x}Sr{sub 1−x})TiO{sub 3} bi-layer (BL) and superlattice (SL) structures were grown via pulsed laser deposition under low oxygen pressure, and their structural, magnetic, and magneto-transport properties were examined. Superlattice and bi-layer structures were confirmed by X-ray diffraction patterns. Low temperature magnetic measurement shows that the saturation magnetization (M{sub S}) is significantly higher for SLs and almost similar or lower for BLs, when compared to phase pure Ba{sub 2}FeMoO{sub 6} thin films. The variation of the coercive field (H{sub C}) follows exact opposite trend, where BL samples have higher H{sub C} and SL samples have lower H{sub C} than pure Ba{sub 2}FeMoO{sub 6} thin films. Also, a significant decrease of the Curie temperature is found in both BL and SL structures compared to pure Ba{sub 2}FeMoO{sub 6} thin films. Negative magneto-resistance is seen in all the BL and SL structures as well as in pure Ba{sub 2}FeMoO{sub 6} thin films. In contrast to the magnetic properties, the magneto-transport properties do not show much variation with induced strain.

Thermal conductivity of M-Si-N (M = Mg, Ca, Sr, Ba) compounds with varying M/Si ratio

NARCIS (Netherlands)

Hintzen, H.T.J.M.; Bruls, R.J.; Delsing, A.C.A.; Itatani, K.; Tanaka, S.; With, de G.; Metselaar, R.

2002-01-01

The thermal cond. of M-Si-N (M = Mg, Ca, Sr, Ba) compds. was examd. The emphasis is on MgSiN2 (a material which can be derived from AlN by replacing systematically 2Al3+ by Mg2+/Si4+), and Si3N4 (the well known b-modification as well as the recently discovered cubic modification with the spinel

Synthesis and characterization of Sr{sub 1-x}Ba{sub x}Bi{sub 4}Ti{sub 4}O{sub 15} ferroelectric materials

Energy Technology Data Exchange (ETDEWEB)

Xie Dan; Pan Wei; Shi Hui

2003-05-25

Sr{sub 1-x}Ba{sub x}Bi{sub 4}Ti{sub 4}O{sub 15} (SBBT, x=0, 0.2, 0.5, 0.8, 1.0) was prepared by sol-gel method using the salts of strontium (Sr), barium (Ba), bismuth (Bi) and titanium butoxide as sources. The mechanism of hydrolysis and polymetric reaction of precursor solution and the influence of annealing condition on crystal structure and microstructure of SBBT ferroelectric materials were studied by infrared (IR) spectroscopy, X-ray diffraction (XRD), and scanning electron microscopy (SEM). The results of the analysis indicated the formation of stable sol-gel system for SBBT when pH value of the solution was about 3.5. The crystallization temperature of SBBT powder was about 700 deg. C and the particle size was about 100 nm.

Stoichiometry and phase purity control of radio frequency magnetron sputter deposited Ba0.45Sr0.55TiO3 thin films for tunable devices

Science.gov (United States)

Alema, Fikadu; Reinholz, Aaron; Pokhodnya, Konstantin

2013-11-01

The systematic study of the oxygen partial pressure (OPP) and total chamber gas pressure (TGP) effects on the stoichiometry and crystal structure of rf sputtered Ba0.45Sr0.55TiO3 (BST) films and their phase purity allowed identifying close to optimal sputtering parameters for BST single phase polycrystalline film. The film with a Ba/Sr ratio equal to that of the source target and (Ba + Sr)/Ti ratio close to unity demonstrated the enhanced permittivity value of 553 and tunability of 69%. It was confirmed that the increase of TGP enables better match of the film and target stoichiometry. However, using O2/Ar ratio as a parameter should be utilized cautiously since exceeding a threshold OPP (2 mTorr in our case) may facilitate secondary phase formation. Relatively large dielectric losses were observed in both films sputtered at high (30 mTorr) and low (5 mTor) TGPs. The presence of oxygen vacancies was identified as a probable cause of losses, which is indirectly confirmed by the deviation of the film lattice constant from that of the bulk target.

Experimental techniques applied at the RB reactor

International Nuclear Information System (INIS)

Markovic, H.; Takac, S.; Sotic, O.; Dimitrijevic, Z.

1979-12-01

This paper contains a brief description of research and operations at the RB reactor which are concerned with experiments and results of measuring typical reactor parameters, neutron characteristics as well as parameters related to reactor operation and utilization. Annex contains a list of relevant original papers and publications [sr

Trace diffusion of different nuclear reactions products in polycrystalline tantalum

International Nuclear Information System (INIS)

Beyer, G.J.; Fromm, W.D.; Novgorodov, A.F.

1976-07-01

Measurements of the lattice diffusion coefficients for carrier free isotopes of Hf, Lu, Yb, Tm, Tb, Gd, Eu, Ba, Cs, Y, Sr, Rb and As in polycrystalline tantalum were made over the temperature range 1700 Fsub(As)>Fsub(lanthanides)>Fsub(Sr)>Fsub(Ba)>Fsub(Hf)>Fsub(Rb)>Fsub(Cs). The data indicate, that the Arrhenius relation was obeyed over the entire temperature range. Within the lanthanide-group no differences in the diffusion velocities could be detected, this fact points to a diffusion mechanism of Me 3+ -ions of lanthanides, Me 2+ -ions of earth alkaline elements and Me + -ions of alkaline elements. (author)

Phonon dispersion curves of BCC Ba

International Nuclear Information System (INIS)

Mizuki, J.; Stassis, C.; Zarestky, J.

1985-01-01

Ba, as well as Sr and Ca, is a divalent alkaline earth metal. At room temperature and ambient pressure, the structure of Ba is bcc, whereas that of Sr and Ca is fcc. Under pressure, the bcc phase of Ba transforms to an hcp structure at 55 kbar. Also, at 37 kbar Ba becomes a superconductor with T/sub c/ = 0.06 K. These properties are highly dependent on the position of the d bands relative to the Fermi level. Experimental investigation of the elastic and lattice dynamical properties of these metals has been hindered by difficulties in growing single crystals. However, recently the authors were able to grow several single crystals of bcc Ba of sufficient volume for inelastic neutron scattering experiments. Some of the results are summarized here

Kimberlite emplacement time and duration of kimberlite magmatism in the Zimnii Bereg diamond-diferrous district, Arkhangelsk Region: Rb-Sr age of kimberlite sills, Mela River

International Nuclear Information System (INIS)

Pervov, V.A.; Larchenko, V.A.; Minchenko, G.V.; Stepanov, V.P.; Bogomolov, E.S.; Levskij, L.K.; Sergeev, S.A.

2006-01-01

The Rb-Sr isotope data for kimberlites and carbonate-rich sills of the Mela River were obtained for identifying the age and duration of magmatism in the Zimnii Bereg district of the Archangelsk region. It is shown that estimated age of the kimberlite (366.4 mln. years) falls in the age range corresponding to the main phase of alkaline magmatism in the Kola Peninsula (410-362 mln. years) [ru

Luminescent Afterglow Behavior in the M2Si5N8: Eu Family (M = Ca, Sr, Ba

Directory of Open Access Journals (Sweden)

Koen Van den Eeckhout

2011-05-01

Full Text Available Persistent luminescent materials are able to emit light for hours after being excited. The majority of persistent phosphors emit in the blue or green region of the visible spectrum. Orange- or red-emitting phosphors, strongly desired for emergency signage and medical imaging, are scarce. We prepared the nitrido-silicates Ca2Si5N8:Eu (orange, Sr2Si5N8:Eu (reddish, Ba2Si5N8:Eu (yellowish orange, and their rare-earth codoped variants (R = Nd, Dy, Sm, Tm through a solid state reaction, and investigated their luminescence and afterglow properties. In this paper, we describe how the persistent luminescence is affected by the type of codopant and the choice and ratio of the starting products. All the materials exhibit some form of persistent luminescence, but for Sr2Si5N8:Eu,R this is very weak. In Ba2Si5N8:Eu the afterglow remains visible for about 400 s, and Ca2Si5N8:Eu,Tm shows the brightest and longest afterglow, lasting about 2,500 s. For optimal persistent luminescence, the dopant and codopant should be added in their fluoride form, in concentrations below 1 mol%. A Ca3N2 deficiency of about 5% triples the afterglow intensity. Our results show that Ba2Si5N8:Eu(,R and Ca2Si5N8:Eu(,R are promising persistent phosphors for applications requiring orange or red light.

Rb-Sr geochronolgy of the Jervois Range area in the eastern part of the Arunta Block, NT

International Nuclear Information System (INIS)

Black, L.P.

1980-01-01

New Rb-Sr isotopic data are presented for the Jervois Range area in the eastern part of the Arunta Block. The post-metamorphic Jinka and Jervois Granites yield an age of about 1750 m.y. An alaskitic granite is dated at about 1460 m.y. Pegmatite formation occurred about 1660 m.y. ago. Mineral ages are generally younger than total-rock ages, but no values significantly less than that of the alaskitic granite were found. This means that the Alice Springs Orogeny, which extensively reset large areas of the Arunta Block to the west, did not effect the Jervois area. In this and other geochronological comparisons, the Jervois area seems more akin to the rocks of the Tennant Creek Block, 400 km to the northwest, than to those of the Arunta Block

Growth of epitaxial (Sr, Ba){sub n+1}Ru{sub n}O{sub 3n}P+{sub 1}films

Energy Technology Data Exchange (ETDEWEB)

Schlom, D.G.; Knapp, S.B.; Wozniak, S. [Department of Materials Science and Engineering, Penn State University, University Park, PA (United States); Zou, L.N.; Park, J.; Liu, Y. [Department of Physics, Penn State University, University Park, PA (United States); Hawley, M.E.; Brown, G.W. [Center for Materials Science, Los Alamos National Laboratory, Los Alamos, NM (United States); Dabkowski, A.; Dabkowska, H.A. [Institute of Materials Research, McMaster University, Hamilton, Ontario (Canada); Uecker, R.; Reiche, P. [Institute of Crystal Growth, Berlin (Germany)

1997-12-01

We have grown epitaxial (Sr,Ba){sub n+1}Ru{sub n}O{sub 3n+1} films, n = 1, 2 and {infinity}, by pulsed laser deposition (PLD) and controlled their orientation by choosing appropriate substrates. The growth conditions yielding phase-pure films have been mapped out. Resistivity versus temperature measurements show that both a-axis and c-axis films of Sr{sub 2}RuO{sub 4} are metallic, but not superconducting. The latter is probably due to the presence of low-level impurities that are difficult to avoid given the target preparation process involved in growing these films by PLD. (author)

Investigation of the s-process branch-point nucleus {sup 86}Rb at HIγS

Energy Technology Data Exchange (ETDEWEB)

Erbacher, Philipp; Glorius, Jan; Reifarth, Rene; Sonnabend, Kerstin [Goethe Universitaet Frankfurt am Main (Germany); Isaak, Johann; Loeher, Bastian; Savran, Deniz [GSI Helmholzzentrum fuer Schwerionenforschung (Germany); Tornow, Werner [Duke University (United States)

2016-07-01

The branch-point nucleus {sup 86}Rb determines the isotopic abundance ratio {sup 86}Sr/{sup 87}Sr in s-process nucleosynthesis. Thus, stellar parameters such as temperature and neutron density and their evolution in time as simulated by modern s-process network calculations can be constrained by a comparison of the calculated isotopic ratio with the one observed in SiC meteoritic grains. To this end, the radiative neutron-capture cross section of the unstable isotope {sup 86}Rb has to be known with sufficient accuracy. Since the short half-life of {sup 86}Rb prohibits the direct measurement, the nuclear-physics input to a calculation of the cross section has to be measured. For this reason, the γ-ray strength function of {sup 87}Rb was measured using the γ{sup 3} setup at the High Intensity γ-ray Source facility at TUNL in Durham, USA. First experimental results are presented.

Structural, elastic and electronic properties of C14-type Al{sub 2}M (M=Mg, Ca, Sr and Ba) Laves phases

Energy Technology Data Exchange (ETDEWEB)

Lishi, Ma; Yonghua, Duan, E-mail: duanyh@kmust.edu.cn; Runyue, Li

2017-02-15

The structural and mechanical properties, Debye temperatures and anisotropic sound velocities of the Laves phases Al{sub 2}M (M=Mg, Ca, Sr and Ba) with C14-type structure were investigated using the first-principles corresponding calculations. The corresponding calculated structural parameters and formation enthalpies are in good agreement with the available theoretical values, and Al{sub 2}Ca has the best phase stability. The mechanical properties, including elastic constants, bulk modulus B, shear modulus G, Young’s modulus E, and Poisson ratio ν, were deduced within the Voigt-Reuss-Hill approximation. The brittleness and ductility were estimated by the values of Poisson ratio, B/G and Cauchy pressure. Moreover, the elastic anisotropy was investigated by calculating and discussing several anisotropy indexes. Finally, the electronic structures were used to illustrate the bonding characteristics of C14-Al{sub 2}M (M=Mg, Ca, Sr and Ba) phases.

Impedance/modulus analysis of sol-gel Ba{sub x}Sr{sub 1-x}TiO{sub 3} thin films

Energy Technology Data Exchange (ETDEWEB)

Saif, Alaeddin A.; Poopalan, P. [University Malaysia Perlis, Perlis (Malaysia)

2010-12-15

Perovskite-structure-type sol-gel barium-strontium-titanate (BST) thin films with molar formula Ba{sub x}Sr{sub 1-x}TiO{sub 3} (x = 0.5, 0.6, 0.7, and 0.8) have been successfully fabricated as Al/BST/Pt capacitors. In order to study the role of the grain size in the conduction mechanisms, we present atomic force microscopy (AFM) results. The impedance and the electric modulus of Ba{sub x}Sr{sub 1-x}TiO{sub 3} thin films have been analyzed in order to correlate the effect of the film regional processes on the conduction mechanism. The impedance and the electric modulus complex planes show three overlapping regions as response for the bulk, the grain boundary and the film/electrode interface mechanisms, and an equivalent circuit has been proposed for each mechanism. The conduction mechanism resulting from the bulk and the grain boundaries is discussed; the results show that the grain boundaries have less effect on the conduction mechanism than the bulk.

Theoretical survey on M@C{sub 80} (M = Ca, Sr, and Ba): Behavior of different alkaline earth metal impacting the chemical stability and electronic properties

Energy Technology Data Exchange (ETDEWEB)

Cui, Jin-Bo; Guo, Yi-Jun; Li, Qiao-Zhi; Zhao, Pei; Zhao, Xiang, E-mail: xzhao@mail.xjtu.edu.cn

2016-08-02

Structures of mono-metallofullerenes M@C{sub 80} (M = Ca, Sr, and Ba) that separated in early experiment are determined owning the C{sub 2v}(31920)-C{sub 80} cage. The change rule of properties for M@C{sub 80} (M = Ca, Sr, and Ba) influenced by different inner metal are discussed. As the trapped metal changes from calcium to barium, performance of thermodynamic stabilities for M@C{sub 2v}(31920)-C{sub 80}, M@C{sub 2v}(31922)-C{sub 80}, and M@D{sub 5h}(31923)-C{sub 80} are significantly different. Orbital analysis suggests that the lowest unoccupied molecular orbitals (LUMOs) of Ca@C{sub 2v}(31920)-C{sub 80} and Ca@D{sub 5h}(31923)-C{sub 80} are mostly located on the trapped metal, whereas reduction reactions of Ca@C{sub 2v}(31920)-C{sub 80} and Ca@D{sub 5h}(31923)-C{sub 80} occur on the fullerene cage. Natural electron configuration analyses demonstrates that the decentralized electron back-donation of Ba@C{sub 2v}(31920)-C{sub 80} would take responsible for the instability of itself. Electronic properties such as electron affinities and ionization potentials are significantly affected by encapsulated metal are also found. Computational UV–visible–NIR spectra for M@C{sub 2v}(31920)-C{sub 80} (M = Ca, Sr, Ba) are in perfect accord with the spectra obtained experimentally.

Highly efficient red-emitting BaMgBO3F:Eu3+,R+ (R: Li, Na, K, Rb) phosphor for near-UV excitation synthesized via glass precursor solid-state reaction

Science.gov (United States)

Shinozaki, Kenji; Akai, Tomoko

2017-09-01

Eu3+-doped fluoroborate crystals of BaMgBO3F were synthesized by a solid-state reaction using a glassy precursor material, and their photoluminescence (PL) was investigated. To compensate for the incorporation of Eu3+ into Ba2+ sites, samples codoped with alkali ions (Li+, Na+, K+, Rb+) were also prepared. The Eu3+-doped sample showed red PL with a quantum yield (QY) of 65% caused by near-UV excitation (λ = 393 nm), and PL intensity and QY increased with the codoping of Eu3+ and alkali ions. It was found that the Eu3+,Li+-codoped sample showed the highest PL intensity and a QY of 83%.

Synthesis and characterisation of the n = 2 Ruddlesden–Popper phases Ln{sub 2}Sr(Ba)Fe{sub 2}O{sub 7} (Ln = La, Nd, Eu)

Energy Technology Data Exchange (ETDEWEB)

Gurusinghe, Nicola N.M. [School of Chemistry, The University of Birmingham, Edgbaston, Birmingham B15 2TT (United Kingdom); Figuera, Juand de la; Marco, José F. [Instituto de Quimica-Fisica “Rocasolano”, CSIC, Serrano 119, 28006 Madrid (Spain); Thomas, Michael F. [Department of Physics, University of Liverpool, Liverpool. L69 3BX (United Kingdom); Berry, Frank J., E-mail: f.j.berry.1@bham.ac.uk [School of Chemistry, The University of Birmingham, Edgbaston, Birmingham B15 2TT (United Kingdom); Greaves, Colin [School of Chemistry, The University of Birmingham, Edgbaston, Birmingham B15 2TT (United Kingdom)

2013-09-01

Graphical abstract: - Highlights: • Some Ruddlesden–Popper phases have been characterised. • Substitution on the A site influences cationic order. • The magnetic moment redirects with temperature - Abstract: A series of n = 2 Ruddlesden–Popper phases A{sub 2}B{sub 2}O{sub 7} of composition Ln{sub 2}Sr(Ba)Fe{sub 2}O{sub 7} (Ln = La, Nd, Eu) have been prepared. La{sub 2}SrFe{sub 2}O{sub 7} and La{sub 2}BaFe{sub 2}O{sub 7} crystallise in the tetragonal space group I4/mmm. The structures of Eu{sub 2}SrFe{sub 2}O{sub 7} and Nd{sub 2}SrFe{sub 2}O{sub 7} are best described in space group P4{sub 2}/mnm. Substitution on the A site with smaller lanthanide- and larger alkaline metal- ions leads to enhanced cationic order in these phases and reflects increasing differences in cationic radii. All the compounds are antiferromagnetically ordered between 298 and 2 K. In La{sub 2}SrFe{sub 2}O{sub 7} the magnetic moment lies along [1 1 0] at all temperatures between 298 and 2 K whereas in La{sub 2}BaFe{sub 2}O{sub 7} the magnetic moment at 298 K lies along the crystallographic x-axis but redirects from the [1 0 0] to the [1 1 0] direction between 210 and 190 K and is retained in this direction until 2 K. In Nd{sub 2}SrFe{sub 2}O{sub 7} the magnetic moment at 298 K lies along [1 1 0] but rotates from [1 1 0] to [0 0 1] between 17 and 9 K. A series of {sup 57}Fe Mössbauer spectra recorded from La{sub 2}SrFe{sub 2}O{sub 7} between 290 and 600 K indicate a magnetic ordering temperature of T{sub N} ≥ 535 K.

Effect of structural packing on the luminescence properties in tungsten bronze compounds M{sub 2}KNb{sub 5}O{sub 15} (M=Ca, Sr, Ba)

Energy Technology Data Exchange (ETDEWEB)

Yin Xin; Shi Liu [State Key Laboratory of High Performance Ceramics and Superfine Microstructures and CAS Key Laboratory of Materials for Energy Conversion, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050 (China); Wei Ang, E-mail: iamawei@njupt.edu.cn [Key Laboratory for Organic Electronics and Information Displays, 9 Wenyuan Road, Nanjing 210046 (China); Wan Dongyun; Wang Yaoming [State Key Laboratory of High Performance Ceramics and Superfine Microstructures and CAS Key Laboratory of Materials for Energy Conversion, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050 (China); Huang Fuqiang, E-mail: huangfq@mail.sic.ac.cn [State Key Laboratory of High Performance Ceramics and Superfine Microstructures and CAS Key Laboratory of Materials for Energy Conversion, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050 (China); College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China)

2012-08-15

Tungsten bronze compounds M{sub 2}KNb{sub 5}O{sub 15} (M=Ca, Sr, Ba) were successfully synthesized, and the luminescence properties were investigated. Among the three compounds, Ca{sub 2}KNb{sub 5}O{sub 15} showed an obviously broad band of host luminescence at 460 nm with exciting at 269 nm. By doping Eu{sup 3+} into the M sites, Ca{sub 2}KNb{sub 5}O{sub 15}:Eu{sup 3+} displayed strong red emission from Eu{sup 3+} ions characteristic transitions, nearly four times higher than Sr{sub 2}KNb{sub 5}O{sub 15}:Eu{sup 3+} and seven times higher than Ba{sub 2}KNb{sub 5}O{sub 15}:Eu{sup 3+}. Crystal packing factor (PF) was introduced to account for this luminescence difference, lower PF being correlated to higher luminescence intensity for perovskite-related structure. Both the as-prepared compounds and the literature examples were proved to fit this correlation. This can be explained through the influence of the structural packing on the environment distortion and crystal field splitting of the doping site. - Graphical abstract: Tungsten bronze compounds M{sub 2}KNb{sub 5}O{sub 15} (M=Ca, Sr, Ba) show the dependence of luminescence properties on structural packing, among which Ca{sub 2}KNb{sub 5}O{sub 15} has the superior luminescence. Highlights: Black-Right-Pointing-Pointer Tungsten bronze compounds were synthesized by solid state reaction. Black-Right-Pointing-Pointer Ca{sub 2}KNb{sub 5}O{sub 15} displayed remarkably blue host luminescence. Black-Right-Pointing-Pointer Ca{sub 2}KNb{sub 5}O{sub 15}:Eu{sup 3+} showed more intense red emission than M{sub 2}KNb{sub 5}O{sub 15}:Eu{sup 3+} (M=Sr, Ba). Black-Right-Pointing-Pointer The relationship between crystal packing factor and luminescence was obtained.

Synthesis and crystal structure of nanocrystalline phase: Ca1-xMxZr4P6O24 (M = Sr, Ba and x = 0.0-1.0)

International Nuclear Information System (INIS)

Rashmi, Ch.; Shrivastava, O.P.

2011-01-01

The structure of strontium and barium substituted nano crystalline calcium zirconium phosphate (CZP) was determined on the basis of crystal data of solid solutions. It was found that up to 2.42 mol % of strontium and 1.62 mol % of barium could be loaded into CZP formulations without significant changes of the three-dimensional framework structure. The crystal chemistry of Ca 1-x M x Zr 4 P 6 O 24 (M = Sr, Ba and x = 0.0-1.0) phases has been investigated using General Structure Analysis System (GSAS) programming. The Sr and Ba substituted CZP phases crystallize in the space group R-3 and Z = 6. Powder diffraction data have been subjected to Rietveld refinement to arrive at a satisfactory structural convergence of R-factors. The unit cell volume and polyhedral (ZrO 6 and PO 4 ) distortion increases with rise in the size and mole % of loaded cation in the CZP matrix. The PO 4 stretching and bending vibrations in the Infra red (IR) region have been assigned. SEM, TEM and EDAX analysis provide evidence of Sr and Ba in the matrix. (authors)

A comparative study on the magnetic and electrical properties of MFe12O19 (M=Ba and Sr)/BiFeO3 nanocomposites

Science.gov (United States)

Ahmed, M. A.; Mansour, S. F.; Ismael, H.

2015-03-01

M-type hexaferrite (MFe12O19), M=Ba or Sr nanoparticles with hexagonal crystal structure have been successfully synthesized by a citrate auto-combustion method. BiFeO3 (BFO) was prepared by the flash auto-combustion technique. Different nanocomposites were prepared according to the formula [(1-X) MFe12O19+XBiFeO3; M=Ba or Sr, X=0.3, 0.4, 0.5 and 0.6]. The structure and morphology of the obtained nanocomposites have been determined by X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM). From the results, it is observed that the value of saturation magnetization decreases with increasing BFO content, which was mainly due to the contribution of the volume of the weak-magnetic BFO to the total sample volume.

Synthesis and photoluminescence of Sm3+ doped alkali alkaline earth borate hosts NaBa4 (BO3)3 and LiSr4(BO3)3

International Nuclear Information System (INIS)

Chauhan, A.V.; Nagpure, P.A.; Omanwar, S.K.

2012-01-01

In this paper we report the photoluminescence of Sm 3+ doped alkali alkaline borate hosts NaBa 4 (BO 3 ) 3 and LiSr 4 (BO 3 ) 3 . For the synthesis of alkali alkaline borate hosts NaBa 4 (BO 3 ) 3 and LiSr 4 (BO 3 ) 3 doped with different concentrations of Sm 3+ ions, we used the novel combustion technique. The phase purity of the hosts was confirmed by the powder XRD technique. The photoluminescence of the phosphors were carried out within 300 to 700 nm wavelength range. The phosphor shows intense orange red (602 nm) emission for near UV excitation. The FTIR spectra of the phase pure hosts have also been reported. (author)

Precision flow-controlled Rb-82 generator for bolus or constant-infusion studies of the heart and brain

International Nuclear Information System (INIS)

Yano, Y.; Cahoon, J.L.; Budinger, T.F.

1981-01-01

A precision flow-controlled rubidium-82 generator has been constructed to deliver 76-sec Rb-82 at either fast or slow flow rates for bolus or constant-infusion studies. A stepping motor drive is interfaced to a microprocessor for pulsed control of flow rate to deliver the saline eluant solution from a large-volume (150 ml) machined pumping syringe through an alumina column that retains the 25-day Sr-82 parent. The generator system delivers 70-90% of the maximum Rb-82 activity in a 20-25 ml bolus elution of 2% NaCl. The Sr-82/Sr-85 breakthrough is 10 -7 - 10 -6 . Both yield and breakthrough are functions of column length and flow rate. Six separate Sr-82 loadings of the generator were evaluated over a period of nearly 2 yr in studies of myocardial blood perfusion and permeability changes in the blood-brain barrier. Sterility and apyrogenicity of the Rb-82 eluate were maintained during multiple elutions and long-term use of 3-4 mo for each generator loading

Hexagonal perovskites with cationic vacancies. 33. Compounds of type Ba/sub 6-x/Sr/sub x/B/sub 2-y//sup 3 +/SE/sub y//sup 3 +/W/sub 3/vacantO/sub 18/

Energy Technology Data Exchange (ETDEWEB)

Lindner, I; Kemmler-Sack, S [Tuebingen Univ. (Germany, F.R.). Lehrstuhl fuer Anorganische Chemie 2

1982-12-01

In the series Ba/sub 6-x/Sr/sub x/Lu/sub 2-y/SE/sub y//sup 3 +/W/sub 3/vacantO/sub 18/ a substitution of Sr/sup 2 +/ for Ba/sup 2 +/ is possible. According to intensity calculations on powder data of BaSr/sub 5/Lu/sub 1.6/Ho/sub 0.4/W/sub 3/vacantO/sub 18/ the compounds crystallize in a rhombohedral 18 L type with the sequence (hhccc)/sub 3/; space group R-3m. The refined, intensity related R' value is 11.5%. The differences in properties (diffuse reflectance spectra, photoluminescence) between the hexagonal modifications Ba/sub 6/B/sub 2-y//sup 3 +/SE/sub y//sup 3 +/W/sub 3/vacantO/sub 18/ (B/sup 3 +/ = Gd, Y, Lu; SE/sup 3 +/ = Sm, Eu, Tb, Dy, Ho, Er, Tm) and the corresponding cubic HT modifications are discussed.

Positron annihilation study of La2-xMxCuO4 (M=Sr, Ba) system

International Nuclear Information System (INIS)

Lu Qingfeng; Du Baoli; Li Xigui

2004-01-01

The positron lifetime spectra of La 2-x M x CuO 4 (LMCO, M=Sr, Ba, x=0.05, 0.10, 0.125, 0.15, 0.2) were measured at room temperature for studying the long-standing mystery of '1/8 abnormal' in doped lanthanum cuprate. Electron density n e and void concentration (number density) C V were calculated as a function of substitution content x. The appearance of peak (n e ) and valley (C V ) at x=0.125 and the correlation with superconductivity were discussed. (authors)

Energetic prediction on the stability of A2Mg12Si7, A2Mg4Si3, and AMgSi in the A2Si–Mg2Si system (A = Ca, Sr and Ba) and their calculated electronic structures

International Nuclear Information System (INIS)

Imai, Yoji; Mori, Yoshihisa; Nakamura, Shigeyuki; Takarabe, Ken-ichi

2014-01-01

Highlights: • Formation energies of A 2 Mg 4 Si 3 , A 2 Mg 12 Si 7 , and AMgSi (A = Ca,Sr,Ba) were calculated. • All AMgSi are quite stable compared to mixture of A 2 Si and Mg 2 Si. • Ba 2 Mg 4 Si 3 and Sr 2 Mg 4 Si 3 are predicted to be stable, but Ca 2 Mg 4 Si 3 is not. • Ca 2 Mg 12 Si 7 and Sr 2 Mg 12 Si 7 are energetically unstable. • Stability of Ba 2 Mg 12 Si 7 is a tender subject. -- Abstract: In order to evaluate the relative stability of A 2 Mg 4 Si 3 , A 2 Mg 12 Si 7 , and AMgSi (A = Ca, Sr, and Ba) in the A 2 Si–Mg 2 Si system, electronic energy changes in the formation of these compounds were calculated using a density-functional theory with the Perdew–Wang generalized gradient approximations. It was found that (1) AMgSi’s are quite stable compared to equi-molar mixture of A 2 Si and Mg 2 Si, (2) Ba 2 Mg 4 Si 3 and Sr 2 Mg 4 Si 3 are also stable, (3) Ca 2 Mg 4 Si 3 and Ca 2 Mg 12 Si 7 are less stable than the mixture of CaMgSi and Mg 2 Si, and (4) Stability of Ba 2 Mg 12 Si 7 is a tender subject and Sr 2 Mg 12 Si 7 is energetically unstable compared to the mixture of Sr 2 Mg 4 Si 3 (or, SrMgSi) and Mg 2 Si. The presence of Sr 2 Mg 12 Si 7 may be due to the vibrational and/or configurational entropy, which are not treated in the present study. From the calculated electronic densities of state, complex compounds of SrMgSi and Mg 2 Si have both p-type and n-type character, depending on the ratio of SrMgSi and Mg 2 Si in that compound

The geochemistry of marine sediments, island arc magma genesis, and crust-mantle recycling

International Nuclear Information System (INIS)

Ben Othman, D.; Paris-6 Univ., 75; White, W.M.; Cornell Univ., Ithaca, NY; Patchett, J.; Arizona Univ., Tucson

1989-01-01

To assess the role of sediment subduction and recycling in island arc magma genesis and mantle evolution, we have determined Sr, Nd, and Pb isotope ratios and the concentrations of K, Rb, Cs, Ba, Sr, U, Th, Pb and rare earth elements in 36 modern marine sediments, including Mn nodules, biogenic oozes, and pelagic and hemipelagic clays from the Pacific, Antlantic and Indian Oceans. Sr and Nd isotope ratios and the Sr/Nd concentration ratios in sediments are such that mixing between subducted sediment on the one hand and depleted mantle or subducted oceanic crust on the other can produce mixing arrays which may pass either through or outside of the oceanic basalt Sr-Nd isotope 'mantle array'. Thus whether isotope compositions of island arc volcanics (IAV) plot inside our outside of the mantle array is not a good indication of whether or not their sources contain a subducted sediment component. The presence of subducted sediment in the sources of IAV should lead to Cs/Rb and Pb/Ce ratios which are higher than those in oceanic basalts, and Ba/Rb ratios which may be either higher or lower than oceanic basalts. Simple mixing calculations suggest that as little as a percent or so sediment in island arc magma sources can account for the observed Cs/Rb, Pb/Ce, and Ba/Rb ratios in IAV. However, it does not appear that high Ba/La ratios and negative Ce anomalies in IAV are inherited from sediment in IAV magma sources. It is more likely these features reflect fractionation of alkalis and alkaline earths from rare earths during slab dehydration and metasomatism. Pb isotope ratios in sediments from the Warton Basin south of the Sunda Arc are collinear in 208 Pb/ 204 Pb- 207 Pb/ 204 Pb- 206 Bp/ 204 Pb space with volcanics from West Sunda, but not with volcanics from the East Sunda. This collinearity is consistent with the hypothesis that sediments similar to these are being subducted to the magma genesis zone of the West Sunda Arc. (orig./WB)

Synthesis and thermophysical properties of AMoO4 (A = Ca, Sr, Ba)

International Nuclear Information System (INIS)

Maji, Binoy Kumar; Jena, Hrudananda; Asuvathraman, R.; Govindan Kutty, K.V.

2013-01-01

The alkaline earth molybdates AMoO 4 (A=Ca, Sr, Ba) belong to Scheelite type crystal structure with space group 14 1 /a, and are naturally occurring minerals. They are often found as secondary phases in irradiated oxide nuclear fuels as a product of fission product interaction. These compounds can also form as microcrystallites when the high-level nuclear waste is vitrified. As high temperature ceramics, they find applications as sensor materials, oxide ion conductors, etc. The thermophysical properties of these molybdates are essential for understanding their impact on the high temperature properties of the systems and devices containing them. In the present study, these compounds were synthesized by solid state reaction route in air at 823 K, and characterized by powder XRD and TG/DTA. The thermal expansion behavior was investigated by dilatometry in the temperature range of 300-800 K in air. The % thermal expansion of BaMoO 4 was found to be the lowest among the three compounds. The electrical conductivity of the compounds was measured by AC-impedance spectroscopy, and the conductivity was found to be in the range of 10 -4 S.cm -1 at 1073 K in air. The activation energy of electrical conduction was measured to be about 1.3 eV. (author)

Potential of Sr isotopic analysis in ceramic provenance studies: Characterisation of Chinese stonewares

Science.gov (United States)

Li, Bao-Ping; Zhao, Jian-Xin; Greig, Alan; Collerson, Kenneth D.; Zhuo, Zhen-Xi; Feng, Yue-Xin

2005-11-01

We compare the trace element and Sr isotopic compositions of stoneware bodies made in Yaozhou and Jizhou to characterise these Chinese archaeological ceramics and examine the potential of Sr isotopes in provenance studies. Element concentrations determined by ICP-MS achieve distinct characterisation for Jizhou samples due to their restricted variation, yet had limited success with Yaozhou wares because of their large variability. In contrast, 87Sr/86Sr ratios in Yaozhou samples have a very small variation and are all significantly lower than those of Jizhou samples, which show a large variation and cannot be well characterised with Sr isotopes. Geochemical interpretation reveals that 87Sr/86Sr ratios will have greater potential to characterise ceramics made of low Rb/Sr materials such as kaolin clay, yet will show larger variations in ceramics made of high Rb/Sr materials such as porcelain stone.

Potential of Sr isotopic analysis in ceramic provenance studies: Characterisation of Chinese stonewares

International Nuclear Information System (INIS)

Li Baoping; Zhao Jianxin; Greig, Alan; Collerson, Kenneth D.; Zhuo Zhenxi; Feng Yuexin

2005-01-01

We compare the trace element and Sr isotopic compositions of stoneware bodies made in Yaozhou and Jizhou to characterise these Chinese archaeological ceramics and examine the potential of Sr isotopes in provenance studies. Element concentrations determined by ICP-MS achieve distinct characterisation for Jizhou samples due to their restricted variation, yet had limited success with Yaozhou wares because of their large variability. In contrast, 87 Sr/ 86 Sr ratios in Yaozhou samples have a very small variation and are all significantly lower than those of Jizhou samples, which show a large variation and cannot be well characterised with Sr isotopes. Geochemical interpretation reveals that 87 Sr/ 86 Sr ratios will have greater potential to characterise ceramics made of low Rb/Sr materials such as kaolin clay, yet will show larger variations in ceramics made of high Rb/Sr materials such as porcelain stone

Decay studies of Sr isotpes with high resolution and total absorption techniques

CERN Document Server

Perez-Cerdan, Ana-Belen

2012-04-03

High Resolution measurements The beta/EC decay of 77,78Sr and 76,78Rb have been studied in this work. Measurements were carried out of the energies and intensities of the emitted gamma-rays and conversion electrons as well as gamma-gamma and gamma-X-ray coincidences in the decays of 77,78Sr, which have extended our knowledge of their decay schemes including spin and parity assignments to the levels populated in the daughter nucleus, 77Rb and 78Rb respectively. For the decay of 78Sr, 16 new levels and 44 new gamma-ray transitions have been identified. The very much improved experimental knowledge of the 78Rb levels populated in the decay and the strong link between the parent and the daughter states has allowed us to infer some possible level configurations by comparison with HF+BCS calculations using the SG2 Skyrme force. For the decay of 77Sr, 9 new levels and 15 new gamma-ray transitions have been identified. The levels in the low energy part of the level scheme have been discussed in terms of HF+BCS+QRPA c...

High conductive and long-term phase stable anode materials for SOFCs: A2FeMoO6 (A = Ca, Sr, Ba)

Science.gov (United States)

Huan, Yu; Li, Yining; Yin, Baoyi; Ding, Dong; Wei, Tao

2017-08-01

In this work, the mixed oxide-ion/electron conductor (MIEC) double-perovskite compounds A2FeMoO6 (AFMO, A = Ca, Sr, Ba) are investigated as anode materials for O2--ion conducting solid-oxide fuel cells (SOFCs). Several advantages are outlined here; 1) under H2 atmosphere, the conductivities of Ba2FeMoO6 (BFMO), Sr2FeMoO6 (SFMO) and Ca2FeMoO6 (CFMO) reach as high as 243, 302 and 561 S cm-1, respectively, which can be comparable with the commercial NiO-electrolyte anode; 2) excellent structure and phase stability at high temperature and in H2 atmosphere; 3) matched thermodynamic compatibility (such as TECs) with electrolyte materials; 4) fast oxidization for fuel with O2- ions accepted by oxygen vacancies from the electrolyte. Moreover, with H2 as fuel gas, the cell power output, cell's long-term stabilities and the structural parameter are also been examined to evaluate the AFMO anode.

Measurement of strontium isotope ratio in nitric acid extract of peanut testa by ICP-Q-MS after removal of Rb by extraction with pure water.

Science.gov (United States)

Zhu, Yanbei; Hioki, Akiharu; Chiba, Koichi

2014-02-01

The difference in the distributions of Sr and Rb in peanut seeds was utilized to develop a precise method for Sr isotope ratio measurement by inductively coupled plasma quadruple mass spectrometry (ICP-Q-MS). The testa instead of the whole peanut seed was selected as the sample because apparent enrichment of Sr in comparison to Rb was found in the testa. Furthermore, Rb in the testa was removed by pure water extraction with the aid of sonication to remove the isobaric interference in Sr isotope ratio measurement. The testa taken from one peanut seed was treated as one sample for the analysis. After optimization of the operating conditions, pure water (10 mL for each sample) extraction in 30 min with sonication was able to remove over 95% of Rb in the testa, while after the Rb removal Sr could be completely extracted using 10 mL of 0.3 mol L(-1) HNO3 for each sample. The integration time in ICP-Q-MS measurement was optimized to achieve a lower measurement uncertainty in a shorter time; the results showed that 1s was required and enough for the precise measurement of Sr isotope ratios giving a relative standard uncertainty (n=10) of ca. 0.1%. The present method was applied to peanut seeds grown in Japan, China, USA, India, and South Africa. © 2013 Published by Elsevier B.V.

Dual ferroic properties of hexagonal ferrite ceramics BaFe_1_2O_1_9 and SrFe_1_2O_1_9

International Nuclear Information System (INIS)

Kostishyn, V.G.; Panina, L.V.; Timofeev, A.V.; Kozhitov, L.V.; Kovalev, A.N.; Zyuzin, A.K.

2016-01-01

Dual ferroic properties of a strong magnetism and large ferroelectricity have been observed in barium BaFe_1_2O_1_9 and strontium SrFe_1_2O_1_9 hexaferrite ceramics. The samples were fabricated by a modified ceramic technique from highly purified raw materials with addition of boron oxide allowing the control of grain size and enhancement of bulk resistivity. Whereas the samples of PbFe_1_2O_1_9 fabricated by the same technological method did not have sufficient electric resistivity to support an electric field and did not exhibit the ferroelectric properties. The structure of the samples examined by X-ray diffraction is consistent with a single hexagonal phase. The grains are randomly oriented with the average grain size of 300–400 nm coated with boron oxide. The magnetic properties are characterised by standard ferrimagnetic behavior with the Neel temperature of about 450 °C. Large spontaneous polarization was observed with the maximal values of 45–50 μC/cm"2 under an applied electric field of 100–300 kV/m. A strong coupling between magnetic and electric ordering was confirmed by measuring the magnetoelectric (ME) parameter and magnetodielectric ratio. These ME characteristics are more advanced than those for well-known room temperature multiferroic BiFeO_3. Furthermore, by applying an electric field, the manipulation of magnetization in the range of up to 9% was observed, which is even greater than in some substituted hexaferrites with a non-collinear magnetic structure. The obtained results on electrical polarization are similar to the values reported for the corresponding hexaferrites sintered by polymer precursor technique. This suggests a promising potential of M-type hexaferrite ceramics in devices utilizing magnetoelectric coupling. - Highlights: • Ba(Sr)Fe_1_2O_1_9-hexaferrites show large room-temperature multiferroic properties. • Small addition of B_2O_3 increases the hexaferrite resistivity by 4 orders of magnitude. • Large spontaneous

Effects of Nb and Sr doping on crystal structure of epitaxial BaTiO3 thin films on MgO substrates

International Nuclear Information System (INIS)

Kim, Yongsam; Chen, Chunhua; Saiki, Atsushi; Wakiya, Naoki; Shinozaki, Kazuo; Mizutani, Nobuyasu

2002-01-01

Niobium (Nb) and strontium (Sr) doped barium titanate (BT) films were deposited by radio frequency (RF) magnetron sputtering with Nb and Sr doped BT ceramic targets, respectively. The effect of Nb and Sr doping on the crystal structure of epitaxial BaTiO 3 thin films on MgO substrates was investigated. The crystal structure of the films was examined using the reciprocal space mapping measurement. All the films exhibit a cube-on-cube relation with respect to the substrates. As the amount of doped Sr increased, both of the in-plane and out-of-plane lattice constants of Sr doped BT films slowly approached the BT bulk values. On the other hand, the lattice constants of Nb doped BT films were rapidly coming close to the bulk values. These indicated that the lattices of doped BT films were relaxed as the amount of doped elements increased. In addition, Nb doping had greater influence on the relaxation of the films than Sr doping for the same content of dopant. (author)

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

NARCIS (Netherlands)

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

2008-01-01

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

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

Energy Technology Data Exchange (ETDEWEB)

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

2012-12-05

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

Phytoremediation modelling - phytoextraction of 137Cs, 133Ba, and 90Sr from liquid media and artificially contaminated soil

International Nuclear Information System (INIS)

Smrcek, S.; Masnerova, G.

2002-01-01

The phytoremediation model based on experiments with plants cultivated in vitro in media supplemented with radionuclide salts was investigated. The plant species Brassica napus, Sinapis alba, Helianthus annuus, Zea mays and Pisum sativum were cultivated on the Murashige-Skoog basal salt mixture enriched with salts of 137 Cs, 133 Ba, and 90 Sr in aseptic conditions. The time-dependent radioactivity decrease in the medium was determined using LSC, and the phytoextraction curves were plotted. Radioactivity in the plant roots and shoots was measured and the efficiency of phytoextraction and the distribution between the roots and shoots as a measure of radionuclide transport in the plant tissues were calculated for each of the plants used. Cultivation experiments were also performed on artificially contaminated soil. Seeds of the plants were placed into contaminated soil and cultivated for 2 months in conditions similar to those of the in vitro experiments. The extracted radioactivity and distribution between roots and shoots were determined. The in vitro experiments simulated extraction of the radionuclide salt from solution analogously to real extraction from the soil solution, while the processes occurring in the rhizosphere were eliminated. The phytoextraction efficiency in terms of the percentage of the starting radioactivity ranged from 12 to 31 % for 90 Sr, 8 to 24% for 137 Cs, and 12 to 17 % for 133 Ba in a cultivation cycle. The root/shoot radioactivity ratios demonstrate that the plant species used may be suitable for real phytoremediation. The experiments in which the plants were cultivated from seeds in artificial contaminated substrate showed that the ability of roots to extract radionuclide salts from their environment remains unchanged. The relative efficiency values were lower than for the extraction from solutions (3 to 11.5 % for 90 Sr, 1.5 to 4 % for 137 Cs, and 1 to 6.2 %, for 133 Ba), but in this process, the equilibrium between the soil particles

Kr-Ar and Rb-Sr dating and the genesis of tungsten at the Clea tungsten skarn property, Selwyn Mountains, Yukon Territory

International Nuclear Information System (INIS)

Godwin, C.I.; Armstrong, R.L.; Tompson, K.M.

1980-01-01

Tungsten skarn deposits on the Clea property in the Selwyn Mountains, Y.T., are related genetically to a quartz monzonite stock, about 500 metres in diameter at the surface. Lower Paleozoic sedimentary rocks are metamorphosed for a distance of 3 km from the stock. Tugnsten-bearing skarn mineralization within the altered sedimentary rocks is of two types: sulphide-rich pods and calc-silicate beds. The most significant sheelite concentration is in calc-silicate beds near or adjacent to the quartz monzonite stock. Discordant K-Ar and Rb-Sr isotopic dates indicate that the stock is probably of early Late Cretaceous age, 94 Ma or slightly older, and that it cooled slowly. High initial 87 Sr/ 86 Sr ratios and disequilibrium relationships between K-feldspar phenocrysts and groundmass minerals in the porphyritic phase of the granite rock, and between different granite rock specimens, indicate contamination of crystallizing magma by old sialic continental crust which extends westward under the Selwyn Basin. This study is significant to regional tungsten exploration. Granite rocks associated with tungsten deposits, in this part of the Canadian Cordillera at least, appear to have specific isotope characteristics that indicate they were generated at a specific time and in a particular way. (auth)

Potential of Sr isotopic analysis in ceramic provenance studies: Characterisation of Chinese stonewares

Energy Technology Data Exchange (ETDEWEB)

Li Baoping [Advanced Centre for Queensland University Isotope Research Excellence (ACQUIRE), University of Queensland, Brisbane, Qld 4072 (Australia)]. E-mail: b.li@uq.edu.au; Zhao Jianxin [Advanced Centre for Queensland University Isotope Research Excellence (ACQUIRE), University of Queensland, Brisbane, Qld 4072 (Australia); Greig, Alan [Advanced Centre for Queensland University Isotope Research Excellence (ACQUIRE), University of Queensland, Brisbane, Qld 4072 (Australia); Collerson, Kenneth D. [Advanced Centre for Queensland University Isotope Research Excellence (ACQUIRE), University of Queensland, Brisbane, Qld 4072 (Australia); Zhuo Zhenxi [Shaanxi Provincial Institute of Archaeology, Xi' an 710054 (China); Feng Yuexin [Advanced Centre for Queensland University Isotope Research Excellence (ACQUIRE), University of Queensland, Brisbane, Qld 4072 (Australia)

2005-11-15

We compare the trace element and Sr isotopic compositions of stoneware bodies made in Yaozhou and Jizhou to characterise these Chinese archaeological ceramics and examine the potential of Sr isotopes in provenance studies. Element concentrations determined by ICP-MS achieve distinct characterisation for Jizhou samples due to their restricted variation, yet had limited success with Yaozhou wares because of their large variability. In contrast, {sup 87}Sr/{sup 86}Sr ratios in Yaozhou samples have a very small variation and are all significantly lower than those of Jizhou samples, which show a large variation and cannot be well characterised with Sr isotopes. Geochemical interpretation reveals that {sup 87}Sr/{sup 86}Sr ratios will have greater potential to characterise ceramics made of low Rb/Sr materials such as kaolin clay, yet will show larger variations in ceramics made of high Rb/Sr materials such as porcelain stone.

Interdiffusion effect on strained La0.8Ba0.2MnO3 thin films by off-axis sputtering on SrTiO3 (100) substrates

Science.gov (United States)

Chou, Hsiung; Hsu, S. G.; Lin, C. B.; Wu, C. B.

2007-02-01

Strained La0.8Ba0.2MnO3 thin films on SrTiO3 (100) substrate are grown by an off-axis sputtering technique. It is found that the ferromagnetic temperature TC increases for thinner films. Secondary ion mass spectroscopy indicates that Sr diffuses partially into the film, making it structurally nonuniform. The region close to the film/substrate interface acts as La1-x(SryBa1-y)xMnO3 with a near negligible y for the as grown film and a non-negligible amount of y for the high-temperature postannealed film. The enhancement of TC is attributed to the combination of the strain and interdiffusion effects.

4f and 5d energy levels of the divalent and trivalent lanthanide ions in M2Si5N8 (M=Ca, Sr, Ba)

NARCIS (Netherlands)

Kate, ten O.M.; Zhang, Z.; Dorenbos, P.; Hintzen, H.T.J.M.; Kolk, van der E.

2013-01-01

Optical data of Sm, Tb and Yb doped Ca2Si5N8 and Sr2Si5N8 phosphors that have been prepared by solid-state synthesis, are presented. Together with luminescence data from literature on Ce3+ and Eu2+ doping in the M2Si5N8 (M=Ca, Sr, Ba) hosts, energy level schemes were constructed showing the energy

Rb-Sr and Sm-Nd isotopic compositions and Petrogenesis of ore-related intrusive rocks of gold-rich porphyry copper Maherabad prospect area (North of Hanich), east of Iran

International Nuclear Information System (INIS)

Malekzadeh Shafaroudi, A.; Karimpour, M. H.; Mazaheri, S. A.

2010-01-01

The Maherabad gold-rich porphyry copper prospect area is located in the eastern part of Lut block, east of Iran. This is the first porphyry Cu-Au prospecting area which is discovered in eastern Iran. Fifteen mineralization-related intrusive rocks range (Middle Eocene 39 Ma) in composition from diorite to monzonite have been distinguished. Monzonitic porphyries had major role in Cu-Au mineralization. The ore bearing porphyries are I-type, meta luminous, high-Kcalc-alkaline to shoshonite intrusive rocks which were formed in island arc setting. These rocks are characterized by average of SiO 2 > 59 wt %, Al 2 O 3 > 15 wt %, MgO 2 O> 3 wt %, Sr> 870 ppm, Y 55, moderate Light rare earth elements, relatively low heavy rare earth elements and enrichment LILE (Sr, Cs, Rb, K and Ba) relative to HFSE (Nb, Ta, Ti, Hf and Zr). They are chemically similar to some adakites, but their chemical signatures differ in some ways from normal adakites, including higher K 2 O contents and K 2 O/Na 2 O ratios and lower Mg, (La/Yb) N , (Ce/Yb) N and εNd in Maherabad rocks. Maherabad intrusive rocks are the first K-rich adakites that can be related with subduction zone. Partial melting of mantle hybridized by hydrous, silica-rich slab-derived melts or/and input of enriched mantle-derived ultra-potassic magmas during or prior to the formation and migration of adakitic melts could be explain their high K 2 O contents and K 2 O/Na 2r atios. Low Mg values and relatively low MgO, Cr and Ni contents imply limited interaction between adakite-like magma and mantle wedge peridotite. The initial 87 Sr/ 86 Sr and ( 143 Nd/ 144 Nd)i was recalculated to an age of 39 Ma (unpublished data). Initial 87 Sr/ 86 Sr ratios for hornblende monzonite porphyry are 0.7047-0.7048. The ( 143 Nd/ 144 Nd)i isotope composition are 0.512694-0.512713. Initial εNd isotope values 1.45-1.81. These values could be considered as representative of oceanic slab-derived magmas. Source modeling indicates that high-degree of

Infrared emissions in MgSrAl10O17:Er3+ phosphor co-doped with Yb3+/Ba2+/Ca2+ obtained by solution combustion route

International Nuclear Information System (INIS)

Singh, Vijay; Kumar Rai, Vineet; Venkatramu, V.; Chakradhar, R.P.S.; Hwan Kim, Sang

2013-01-01

An intense infrared emitting MgSrAl 10 O 17 :Er 3+ phosphor co-doped with Yb 3+ , Ba 2+ and Ca 2+ ions have been prepared by a solution combustion method. Phase purity of the derived compounds was confirmed by X-ray diffraction technique. The vibrational properties of MgSrAl 10 O 17 phosphor was studied by Fourier transform infrared spectroscopy. The broad and strong infrared emission of Er 3+ ions at around 1.53 μm was observed upon excitation at 980 nm. Effect of co-doping with the Yb 3+ , Ba 2+ and Ca 2+ ions on the infrared luminescence intensity of Er 3+ ions and the mechanism responsible for the variation in the infrared intensity have been discussed. The results indicate that these materials may be suitable for the optical telecommunication window and wavelength division multiplexing applications. - Highlights: ► The hexagonal phase of MgSrAl 10 O 17 could be obtained by the low temperature combustion method. ► The broad and strong infrared emission of Er 3+ ions at around 1.53 μm was observed. ► Effect of co-doping with the Yb 3+ , Ba 2+ and Ca 2+ ions on the infrared luminescence intensity of Er 3+ were reported.

Photoluminescence of trivalent rare earths in perovskite stacking polytypes Ba/sub 2/Lasub(2-x)REsub(x)/sup 3 +/MgW/sub 2/vacantO/sub 12/, Ba/sub 6/Ysub(2-x)REsub(x)/sup 3 +/W/sub 3/vacantO/sub 18/, and Sr/sub 8/SrGdsub(2-x)REsub(x)/sup 3 +/W/sub 4/vacantO/sub 24/

Energy Technology Data Exchange (ETDEWEB)

Kemmler-Sack, S [Tuebingen Univ. (Germany, F.R.). Lehrstuhl fuer Anorganische Chemie 2

1981-12-01

Rhombohedral 12 L staking polytypes Ba/sub 2/Lasub(2-x)REsub(x)/sup 3 +/MgW/sub 2/vacantO/sub 12/ show with RE/sup 3 +/ = Pr, Sm, Eu, Tb, Dy, Ho, Er, Tm; the 18 L stacking polytypes Ba/sub 6/Ysub(2-x)REsub(x)/sup 3 +/W/sub 3/vacantO/sub 18/ and the polymorphic perovskites Sr/sub 8/SrGdsub(2-x)REsub(x)/sup 3 +/W/sub 4/vacantO/sub 24/ with RE/sup 3 +/ = Sm, Eu, Dy, Ho, Er visible photoluminescence. The concentration dependence and the influence of the coordination number of the rare earth are reported.

An X-ray fluorescence method for the determination of Ba, Sr, Mo and Bi in thorium oxide

International Nuclear Information System (INIS)

Dixit, R.M.; Deshpande, S.S.

1988-01-01

A simple and rapid X-ray fluorescence method for the determination of Ba, Sr, Mo and Bi in thoria is described. Thorium oxide samples are dry-mixed thoroughly with pure boric acid in the ratio of 9:1. One gram of mixture is pressed as a double layer over a primary boric acid pellet. The precision and accuracy of the method have been determined. The power limits of detection are found to be around 20 ppm for most analytes. (author). 5 tables

Contribution to the geologic evolution from the Eastern part of Central Amazonia Province by Rb-Sr geochronology from the Carajas Mineral Province and the Sao Felix do Xingu region, Para State

International Nuclear Information System (INIS)

Pereira, Edilea Dutra.

1992-01-01

This work deals with a Rb/Sr geochronological study carried on granitoids and granulites of the Carajas Mineral Province (Rio Maria, Serra dos Gradaus and Serra do Pium regions) and Sao Felix do Xingu regions. The Manelao and Ourilandia granitoids of the Sao Felix do Xingu region are associated with the greenstone terrains of the Tucuma Group, and yield an age of 2749 ± 24 Ma with an initial ratio of 0.07028 ± 19, and 2677 ± 50 Ma with an initial ratio of 0.07016 ± 22, respectively. In the Rio Maria region, an age of 2541 ± 74 Ma with an initial ratio of 0.7104 ± 343 was obtained on the Mata Surrao Granite located near the Marajoara Village. This age confirms an archaean monzogranitic magmatism in this region. In the Gradaus area, the Cumaru Granodiorite give an mineral age of 2577 ± 27 Ma similar to the age obtained by whole rock method. Finally, Rb/Sr ages were obtained from granulitic rocks of the Pium Complex located at the Serra do Pium and near the Catete River. Samples of the Serra do Pium yielded ages of 2325 ± 71 Ma (whole rock) and 1857 ± 48 (minerals). Samples from the Catete River area give a whole rock age of 2018 ± 25 Ma with an initial ratio of 0.7039 ± 25. These data show that the Rb/Sr system in these granulitic rocks suffered changes during the Early Proterozoic times. The geochronological data here obtained confirm promptly an Archaean evolution in the studied regions, besides give rise the discussion about the problem related to the Transamazonian Event inside them. (author). 92 refs., 32 figs., 10 tabs

First observation of isomeric state in {sup 97}Rb

Energy Technology Data Exchange (ETDEWEB)

Rudigier, Matthias; Blazhev, Andrey; Regis, Jean-Marc; Warr, Nigel; Jolie, Jan; Fransen, Christoph; Hackstein, Matthias; Pfeiffer, Michael; Rother, Wolfram; Thomas, Tim [IKP, Univ. Koeln (Germany); Simpson, Gary; Ramdhane, Mourad [LPSC, Grenoble (France); Koester, Ulli; Materna, Thomas; Urban, Waldemar [ILL, Grenoble (France); Daugas, Jean-Michel [CEA, DAM, DIF, Arpajon (France)

2012-07-01

Data on a new microsecond isomer in {sup 97}Rb are presented. The measurement was conducted at the LOHENGRIN mass separator at the ILL, Grenoble. We were able to deduce the level energy and lifetime of the state. The multipolarity of the transition to the ground state was determined using conversion electron spectroscopy. This information enabled us to assign a spin and parity to the state, based on quasi-particle-rotor model calculations. The nucleus {sup 97}Rb has neutron number 60, and is thus situated in the shape-phase transition line of the mass 100 nuclei. It is discussed how the new state fits into the region and the Rb-isotopic chain. Furthermore some new results on the decay of the 9/2{sup +} microsecond isomer of {sup 97}Sr are presented and discussed.

Modification of energy band alignment and electric properties of Pt/Ba{sub 0.6}Sr{sub 0.4}TiO{sub 3}/Pt thin-film ferroelectric varactors by Ag impurities at interfaces

Energy Technology Data Exchange (ETDEWEB)

Hirsch, S.; Komissinskiy, P., E-mail: komissinskiy@oxide.tu-darmstadt.de; Flege, S.; Li, S.; Rachut, K.; Klein, A.; Alff, L. [Institute of Materials Science, Technische Universität Darmstadt, 64287 Darmstadt (Germany)

2014-06-28

We report on the effects of Ag impurities at interfaces of parallel-plate Pt/Ba{sub 0.6}Sr{sub 0.4}TiO{sub 3}/Pt thin film ferroelectric varactors. Ag impurities occur at the interfaces due to diffusion of Ag from colloidal silver paint used to attach the varactor samples with their back side to the plate heated at 600–750 °C during deposition of Ba{sub 0.6}Sr{sub 0.4}TiO{sub 3}. X-ray photoelectron spectroscopy and secondary ion mass spectrometry suggest that amount and distribution of Ag adsorbed at the interfaces depend strongly on the adsorbent surface layer. In particular, Ag preferentially accumulates on top of the Pt bottom electrode. The presence of Ag significantly reduces the barrier height between Pt and Ba{sub 0.6}Sr{sub 0.4}TiO{sub 3} leading to an increased leakage current density and, thus, to a severe degradation of the varactor performance.

Crystallization studies and dielectric properties of (Ba0.7Sr0.3)TiO3 in bariumaluminosilicate glass

Science.gov (United States)

Divya, P. V.; Vignesh, G.; Kumar, V.

2007-12-01

Ferroelectric glass-ceramics with a basic composition (1 - y)(Ba0.70Sr0.30)TiO3 : y(BaO : Al2O3 : 2SiO2) have been synthesized by the sol-gel method. The major crystalline phase is the perovskite. The crystallization of the ferroelectric phase in the glass matrix have been studied using differential thermal analysis and x-ray diffraction and the kinetic parameters characterizing the crystallization have been determined using an Arrhenius model. Glass contents <= 5 mol% promoted liquid phase sintering, which reduced the sintering temperature to 1250 °C. The dielectric permittivity of the glass-ceramic samples decreased and the ferroelectric-paraelectric phase transition became more diffuse with increasing glass content. The dielectric connectivity of the ferroelectric phase in the composite have also been investigated and are reported.

Physical characteristics and magnetic properties of BaFe12O19/SrTiO3 based composites derived from mechanical alloying

International Nuclear Information System (INIS)

Widodo, Rahmat Doni; Manaf, Azwar

2016-01-01

A composite system BaFe 12 O 19 /SrTiO 3 with ferrimagnetic BaFe 12 O 19 phase (BHF) and ferroelectric SrTiO 3 phase (STO) have been prepared by mechanical alloying and subsequent heat treatment. The composite powders were studied by Particle Size Analyze, X-ray diffraction and magnetic measurement. It was found that the particle size of composite powders initially increased due to laminated layers formation of a composite and then decreased to an asymptotic value of ∼8 µm as the milling time extended even to a relatively longer time. However, based on results of line broadening analysis the mean grain size of the particles was found in the nanometer scale. We thus believed that mechanical blending and milling of mixture components for the composite materials has promoted heterogeneous nucleation and only after successive sintering at 1100°C the milled powder transformed into particles of nanograin. In this report, microstructure as well as magnetic properties for the composite is also briefly discussed.

The isotopic and chemical evolution of Mount St. Helens

International Nuclear Information System (INIS)

Halliday, A.N.; Fallick, A.E.; Dickin, A.P.; Mackenzie, A.B.; Stephens, W.E.

1983-01-01

Isotopic and major and trace element analysis of nine samples of eruptive products spanning the history of the Mt. St. Helens volcano suggest three different episodes; (1) 40,000-2500 years ago: eruptions of dacite with epsilonsub(Nd) = +5, epsilonsub(Sr) = -10, variable delta 18 O, 206 Pb/ 204 Pb approx.= 18.76, Ca/Sr approx.= 60, Rb/Ba- approx.= 0.1, La/Yb approx.= 18, (2) 2500-1000 years ago: eruptions of basalt, andesite and dacite with epsilonsub(Nd) = +4 to + 8, epsilonsub(Sr) = -7 to -22, variable delta 18 O (thought to represent melting of differing mantle-crust reservoirs), 206 Pb/ 204 Pb = 18.81-18.87, variable Ca/Sr, Rb/Ba, La/Yb and high Zr, (3) 1000 years ago to present day: eruptions of andesite and dacite with epsilonsub(Nd) = + 6, epsilonsub(Sr) = -13, delta 18 O approx.= 6per mille, variable 206 Pb/ 204 Pb, Ca/Sr approx.= 77, Rb/Ba = 0.1, La/Yb approx.= 11. None of the products exhibit Eu anomalies and all are LREE enriched. There is a strong correlation between 87 Sr/ 86 Sr and differentiation indices. These data are interpreted in terms of a mantle heat source melting young crust bearing zircon and garnet, but not feldspar, followed by intrusion of this crustal reservoir by mantle-derived magma which caused further crustal melting and contaminated the crustal magma system with mafic components. Since 1000 years ago all the eruptions have been from the same reservoir which has displayed a much more gradual re-equilibration of Pb isotopic compositions than other components suggesting that Pb is being transported via a fluid phase. The Nd and Sr isotopic compositions lie along the mantle array and suggest that the mantle underneath Mt. St. Helens is not as depleted as MORB sources. There is no indication of seawater involvement in the source region. (orig.)

The isotopic and chemical evolution of Mount St. Helens

Science.gov (United States)

Halliday, A.N.; Fallick, A.E.; Dickin, A.P.; Mackenzie, A.B.; Stephens, W.E.; Hildreth, W.

1983-01-01

Isotopic and major and trace element analysis of nine samples of eruptive products spanning the history of the Mt. St. Helens volcano suggest three different episodes; (1) 40,000-2500 years ago: eruptions of dacite with ??{lunate}Nd = +5, ??{lunate}Sr = -10, variable ??18O, 206Pb/204Pb ??? 18.76, Ca/Sr ??? 60, Rb/Ba ??? 0.1, La/Yb ??? 18, (2) 2500-1000 years ago: eruptions of basalt, andesite and dacite with ??{lunate}Nd = +4 to +8, ??{lunate}Sr = -7 to -22, variable ??18O (thought to represent melting of differing mantle-crust reservoirs), 206Pb/204Pb = 18.81-18.87, variable Ca/Sr, Rb/Ba, La/Yb and high Zr, (3) 1000 years ago to present day: eruptions of andesite and dacite with ??{lunate}Nd = +6, ??{lunate}Sr = -13, ??18O ???6???, variable 206Pb/204Pb, Ca/Sr ??? 77, Rb/Ba = 0.1, La/Yb ??? 11. None of the products exhibit Eu anomalies and all are LREE enriched. There is a strong correlation between 87Sr/86Sr and differentiation indices. These data are interpreted in terms of a mantle heat source melting young crust bearing zircon and garnet, but not feldspar, followed by intrusion of this crustal reservoir by mantle-derived magma which caused further crustal melting and contaminated the crustal magma system with mafic components. Since 1000 years ago all the eruptions have been from the same reservoir which has displayed a much more gradual re-equilibration of Pb isotopic compositions than other components suggesting that Pb is being transported via a fluid phase. The Nd and Sr isotopic compositions lie along the mantle array and suggest that the mantle underneath Mt. St. Helens is not as depleted as MORB sources. There is no indication of seawater involvement in the source region. ?? 1983.

Preparation of Ba1-xSrxWO4 and Ba1-xCaxWO4 films on tungsten plate by mechanically assisted solution reaction at room temperature

International Nuclear Information System (INIS)

Rangappa, Dinesh; Fujiwara, Takeshi; Watanabe, Tomoaki; Yoshimura, Masahiro

2008-01-01

Preparation of the alkaline earth tungstate films such as Ba 1-x Sr x WO 4 and Ba 1-x Ca x WO 4 on the tungsten substrate was studied with a simple solution process assisted with the ball rotation at room temperature. The solid solution formation and limitations, the effect of oxidizing agent H 2 O 2 and alkaline earth ions concentration on the dissolution of W substrate and the growth of Ba 1-x Sr x WO 4 and Ba 1-x Ca x WO 4 films were studied in detail. The ball rotation assistance plays a very important role to enhance the dissolution of the W substrate and mass transport of the reactant species such as alkaline earth ions and WO 4 2- ions onto the solid/solution interface region, where precipitation occurs. Therefore, the rate of film formation was accelerated by the ball rotation assistance to the reaction system. Ba-rich Ba 1-x Sr x WO 4 and Ba 1-x Ca x WO 4 films were formed without high energy or high temperature treatment

Structural, electrical and multiferroic characteristics of thermo-mechanically fabricated BiFeO3-(BaSr)TiO3 solid solutions

Science.gov (United States)

Behera, C.; Choudhary, R. N. P.; Das, Piyush R.

2018-05-01

A solid solution consisting of two perovskite compounds (BiFeO3 and (BaSr)TiO3) of chemical composition (Bi1/2Ba1/4Sr1/4)(Fe1/2Ti1/2)O3 has been fabricated in the low dimensional regime by thermo-mechanical (ball milling and heating) approach. The effect of particle size on the structural, micro-structural, relative permittivity, switching (ferroelectric and magnetic) and conduction phenomena of the material has been studied using various experimental techniques such as x-rays diffraction, transmission and scanning electron microscopy, ferroelectric and magnetic hysteresis, dynamic magneto-electric coupling measurement and impedance spectroscopy techniques. All the above extracted properties are found to be particle size dependent. The first order magneto-electric coupling constant is found to be 2.56, 6.6 and 8.7 mV cm‑1.Oe for 30, 60 and 90 h milled calcined (hmc) sample respectively. As the above micro/nano-material with different particle size, has a high relative dielectric constant and low tangent loss, it can be used for some multifunctional devices including capacity energy storage device in nano-electronics.

A comparative study on the magnetic and electrical properties of MFe{sub 12}O{sub 19} (M=Ba and Sr)/BiFeO{sub 3} nanocomposites

Energy Technology Data Exchange (ETDEWEB)

Ahmed, M.A., E-mail: moala47@hotmail.com [Materials Science Lab (1), Physics Department, Faculty of Science, Cairo University, Giza (Egypt); Mansour, S.F. [Physics Department, Faculty of Science, Zagazig University (Egypt); Ismael, H. [Materials Science Lab (1), Physics Department, Faculty of Science, Cairo University, Giza (Egypt)

2015-03-15

M-type hexaferrite (MFe{sub 12}O{sub 19}), M=Ba or Sr nanoparticles with hexagonal crystal structure have been successfully synthesized by a citrate auto-combustion method. BiFeO{sub 3} (BFO) was prepared by the flash auto-combustion technique. Different nanocomposites were prepared according to the formula [(1−X) MFe{sub 12}O{sub 19}+XBiFeO{sub 3}; M=Ba or Sr, X=0.3, 0.4, 0.5 and 0.6]. The structure and morphology of the obtained nanocomposites have been determined by X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM). From the results, it is observed that the value of saturation magnetization decreases with increasing BFO content, which was mainly due to the contribution of the volume of the weak-magnetic BFO to the total sample volume. - Highlights: • M-type nanohexaferrite (MFe{sub 12}O{sub 19}) as M=Ba and Sr powders were synthesized by the citrate autocombustion method. • The lattice parameters of composite were negligibly smaller than those of M-type. • FESEM showed that the samples were hexagonal plate-like shape. • M{sub s}, M{sub r}, μ{sub eff.} and H{sub C} were improved to be suitable for perpendicular high density recording media. • ε′ increased with BFO ratio which is useful in microwave devices.

Characterization of quasi-one-dimensional S=1/2 Heisenberg antiferromagnets Sr2Cu(PO4)2 and Ba2Cu(PO4)2 with magnetic susceptibility, specific heat, and thermal analysis

International Nuclear Information System (INIS)

Belik, A.A.; Azuma, M.; Takano, M.

2004-01-01

Properties of Sr 2 Cu(PO 4 ) 2 and Ba 2 Cu(PO 4 ) 2 having [Cu(PO 4 ) 2 ] ∞ linear chains in their structures with Cu-O-P-O-Cu linkages were studied by magnetic susceptibility (T=2-400 K, H=100 Oe) and specific heat measurements (T=0.45-21 K). Magnetic susceptibility versus temperature curves, χ(T), showed broad maxima at T M =92 K for Sr 2 Cu(PO 4 ) 2 and T M =82 K for Ba 2 Cu(PO 4 ) 2 characteristic of quasi-one-dimensional systems. The χ(T) data were excellently fitted by the spin susceptibility curve for the uniform S=1/2 chain (plus temperature-independent and Curie-Weiss terms) with g=2.153(4) and J/k B =143.6(2) K for Sr 2 Cu(PO 4 ) 2 and g=2.073(4) and J/k B =132.16(9) K for Ba 2 Cu(PO 4 ) 2 (Hamiltonian H=JΣS i S i+1 ). The similar J/k B values were obtained from the specific heat data. No anomaly was observed on the specific heat from 0.45 to 21 K for both compounds indicating that the temperatures of long-range magnetic ordering, T N , were below 0.45 K. Sr 2 Cu(PO 4 ) 2 and Ba 2 Cu(PO 4 ) 2 are an excellent physical realization of the S=1/2 linear chain Heisenberg antiferromagnet with k B T N /J 2 CuO 3 (k B T N /J∼0.25%) and γ-LiV 2 O 5 (k B T N /J 2 Cu(PO 4 ) 2 and Ba 2 Cu(PO 4 ) 2 were stable in air up to 1280 and 1150 K, respectively

Crystal structure and surface characteristics of Sr-doped GdBaCo2O6−δ double perovskites: oxygen evolution reaction and conductivity

KAUST Repository

Pramana, Stevin S.

2017-12-04

A cheap and direct solution towards engineering better catalysts through identification of novel materials is required for a sustainable energy system. Perovskite oxides have emerged as potential candidates to replace the less economically attractive Pt and IrO2 water splitting catalysts. In this work, excellent electrical conductivity (980 S cm−1) was found for the double perovskite of composition GdBa0.6Sr0.4Co2O6−δ which is consistent with a better oxygen evolution reaction activity with the onset polarisation of 1.51 V with respect to a reversible hydrogen electrode (RHE). GdBa1−xSrxCo2O6−δ with increasing Sr content was found to crystallise in the higher symmetry tetragonal P4/mmm space group in comparison with the undoped GdBaCo2O6−δ which is orthorhombic (Pmmm), and yields higher oxygen uptake, accompanied by higher Co oxidation states. This outstanding electrochemical performance is explained by the wider carrier bandwidth, which is a function of Co–O–Co buckling angles and Co–O bond lengths. Furthermore the higher oxygen evolution activity was observed despite the formation of non-lattice oxides (mainly hydroxide species) and enrichment of alkaline earth ions on the surface.

Crystal structure and surface characteristics of Sr-doped GdBaCo2O6−δ double perovskites: oxygen evolution reaction and conductivity

KAUST Repository

Pramana, Stevin S.; Cavallaro, Andrea; Li, Cheng; Handoko, Albertus D.; Chan, Kuang Wen; Walker, Robert J.; Regoutz, Anna; Herrin, Jason S.; Yeo, Boon Siang; Payne, David J.; Kilner, John A.; Ryan, Mary P.; Skinner, Stephen J.

2017-01-01

A cheap and direct solution towards engineering better catalysts through identification of novel materials is required for a sustainable energy system. Perovskite oxides have emerged as potential candidates to replace the less economically attractive Pt and IrO2 water splitting catalysts. In this work, excellent electrical conductivity (980 S cm−1) was found for the double perovskite of composition GdBa0.6Sr0.4Co2O6−δ which is consistent with a better oxygen evolution reaction activity with the onset polarisation of 1.51 V with respect to a reversible hydrogen electrode (RHE). GdBa1−xSrxCo2O6−δ with increasing Sr content was found to crystallise in the higher symmetry tetragonal P4/mmm space group in comparison with the undoped GdBaCo2O6−δ which is orthorhombic (Pmmm), and yields higher oxygen uptake, accompanied by higher Co oxidation states. This outstanding electrochemical performance is explained by the wider carrier bandwidth, which is a function of Co–O–Co buckling angles and Co–O bond lengths. Furthermore the higher oxygen evolution activity was observed despite the formation of non-lattice oxides (mainly hydroxide species) and enrichment of alkaline earth ions on the surface.

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

NARCIS (Netherlands)

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

2006-01-01

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

Acoustoelastic effect of textured (Ba,Sr)TiO{sub 3} thin films under an initial mechanical stress

Energy Technology Data Exchange (ETDEWEB)

Kamel, Marwa; Mseddi, Souhir; Njeh, Anouar; Ben Ghozlen, Mohamed Hédi [Laboratoire de Physique des Matériaux, Faculté des Sciences de Sfax, Université de Sfax, Sfax (Tunisia); Donner, Wolfgang [Institute of Materials Science, University of Technology, Alarich-Weiss-Strasse.2, 64287 Darmstadt (Germany)

2015-12-14

Acoustoelastic (AE) analysis of initial stresses plays an important role as a nondestructive tool in current engineering. Two textured BST (Ba{sub 0.65}Sr{sub 0.35}TiO{sub 3}) thin films, with different substrate to target distance, were grown on Pt(111)/TiO{sub 2}/SiO{sub 2}/Si(001) substrate by rf-magnetron sputtering deposition techniques. A conventional “sin{sup 2} ψ” method to determine residual stress and strain in BST films by X-ray diffraction is applied. A laser acoustic waves (LA-waves) technique is used to generate surface acoustic waves (SAW) propagating in both samples. Young's modulus E and Poisson ratio ν of BST films in different propagation directions are derived from the measured dispersion curves. Estimation of effective second-order elastic constants of BST thin films in stressed states is served in SAW study. This paper presents an original investigation of AE effect in prestressed Ba{sub 0.65}Sr{sub 0.35}TiO{sub 3} films, where the effective elastic constants and the effect of texture on second and third order elastic tensor are considered and used. The propagation behavior of Rayleigh and Love waves in BST thin films under residual stress is explored and discussed. The guiding velocities affected by residual stresses, reveal some shifts which do not exceed four percent mainly in the low frequency range.

Crystal structures and thermal decomposition of permanganates AE[MnO{sub 4}]{sub 2} . n H{sub 2}O with the heavy alkaline earth elements (AE=Ca, Sr and Ba)

Energy Technology Data Exchange (ETDEWEB)

Henning, Harald; Bauchert, Joerg M.; Conrad, Maurice; Schleid, Thomas [Stuttgart Univ. (Germany). Inst. fuer Anorganische Chemie

2017-10-01

Reexamination of the syntheses and crystal structures as well as studies of the thermal decomposition of the heavy alkaline earth metal permanganates Ca[MnO{sub 4}]{sub 2} . 4 H{sub 2}O, Sr[MnO{sub 4}]{sub 2} . 3 H{sub 2}O and Ba[MnO{sub 4}]{sub 2} are the focus of this work. As an alternative to the very inelegant Muthmann method, established for the synthesis of Ba[MnO{sub 4}]{sub 2} a long time ago, we employed a cation-exchange column loaded with Ba{sup 2+} cations and passed through an aqueous potassium-permanganate solution. We later used this alternative also with strontium- and calcium-loaded columns and all the compounds synthesized this way were indistinguishable from the products of the established methods. Ca[MnO{sub 4}]{sub 2} . 4 H{sub 2}O exhibiting [CaO{sub 8}] polyhedra crystallizes in the orthorhombic space group Pccn with the lattice parameters a=1397.15(9), b=554.06(4) and c=1338.97(9) pm with Z=4, whereas Sr[MnO{sub 4}]{sub 2} . 3 H{sub 2}O with [SrO{sub 10}] polyhedra adopts the cubic space group P2{sub 1}3 with a=964.19(7) pm and Z=4. So the harder the AE{sup 2+} cation, the higher its demand for hydration in aqueous solution. Consequently, the crystal structure of Ba[MnO{sub 4}]{sub 2} in the orthorhombic space group Fddd with a=742.36(5), b=1191.23(7) and c=1477.14(9) pm with Z=8 lacks any crystal water, but contains [BaO{sub 12}] polyhedra. During the thermal decomposition of Ca[MnO{sub 4}]{sub 2} . 4 H{sub 2}O, the compound expels up to two water molecules of hydration, before the crystal structure collapses after the loss of the third H{sub 2}O molecule at 157 C. The crystal structure of Sr[MnO{sub 4}]{sub 2} . 3 H{sub 2}O breaks down after the expulsion of the third water molecule as well, but this already occurs at 148 C. For both the calcium and the strontium permanganate samples, orthobixbyite-type α-Mn{sub 2}O{sub 3} and the oxomanganates(III,IV) AEMn{sub 3}O{sub 6} (AE=Ca and Sr) remain as final decomposition products at 800 C

Rb-Sr geochronology of coarse-grained greywackes and argillites from the Coffs Harbour Block, eastern Australia

International Nuclear Information System (INIS)

Graham, I.J.; Korsch, R.J.

1985-01-01

The Coffs Harbour Block, eastern Australia, includes a sequence of turbidity-current-deposited greywackes and argillites dominated by quartz-poor to quartz-intermediate, volcanic-lithic and feldspathic types. The rocks have a common provenance consisting of dacite with minor andesite and rhyolite, derived from a continental margin volcanic arc. Rb-Sr whole-rock dating of coarse-grained greywackes and argillites suggests that low-grade regional metamorphism (prehnite-pumpellyite to lowest greenschist facies) has completely equilibrated sediments of all grain sizes, giving an age of 318 +- 8 Ma. A subsequent metamorphism which produced thermal biotite on a regional scale over the southern part of the area, re-equilibrated only the fine-grained sediments 238 +- 5 Ma ago; the coarse-grained sediments were unaffected isotopically and still lie on the older isochron. The wide variations in sandstone petrographic modes imply that the older isochron represents neither the age of volcanism in the magmatic arc nor the age of sedimentation at the deposition site, but rather dates the time of earlier metamorphism. (orig.)

Layered perovskite PrBa0.5Sr0.5CoCuO5+δ as a cathode for intermediate-temperature solid oxide fuel cells

International Nuclear Information System (INIS)

Wang, Biao; Long, Guohui; Ji, Yuan; Pang, Mingjun; Meng, Xiangwei

2014-01-01

Highlights: • A single-phase layered-perovskite PrBa 0.5 Sr 0.5 CoCuO 5+δ (PBSCCu) is prepared by the EDTA–citrate complexing method. • PBSCCu cathode has a good chemical compatible with GDC electrolyte. • Partial substitution of Cu for Co can efficiently lower the thermal expansion coefficient. • Performances of PrBa 0.5 Sr 0.5 CoCuO 5+δ cathode based on Gd 0.1 Ce 0.9 O 1.95 electrolyte is reported firstly. - Abstract: Layered perovskite PrBa 0.5 Sr 0.5 CoCuO 5+δ (PBSCCo) oxide is synthesized by EDTA–citrate complexing method and investigated as a novel cathode material for intermediate-temperature solid oxide fuel cells (IT-SOFCs). X-ray diffraction results show that PBSCCo is chemical compatible with Gd 0.1 Ce 0.9 O 1.95 (GDC) electrolyte below 950 °C. The thermal expansion coefficient of PBSCCo is 17.58 × 10 −6 K −1 between 30 °C and 900 °C. The maximum electrical conductivity of PBSCCo is 483 S cm −1 at 325 °C. The polarization resistance of PBSCCo cathode on GDC electrolyte is as low as 0.06 Ω cm 2 at 800 °C. The maximum power density of the electrolyte-supported single cell with PBSCCo cathode achieves 521 mW cm −2 at 800 °C. Preliminary results indicate that PBSCCo is a potential cathode material for application in IT-SOFCs

Permian alkali granitoids of the transbaikal region (new Rb-Sr dates)

Energy Technology Data Exchange (ETDEWEB)

Sukhanov, M K; Ryakhovskij, V M; Abramov, A V

1984-01-01

Rubidium-strontium isotopic investigations of granitoids from Khorinsk and Middle Oninsk massifs were conducted. Isochrones for two chief-modifications of rocks - subalkaline syenites and alkaline granites-were constructed. The age of syenites is determined to be (293 + 20) x 10/sup 6/ at (/sup 87/Sr//sup 86/Sr)/sub 0/=0.7044 +- 0.0106 that of alkaline granites - (253 +- 3) x 10/sup 6/ at (/sup 87/Sr//sup 86/Sr)/sub 0/=0.7077 +- 0.0033. Analytical data for determination of rubidium-strontium age of rocks of the mentioned massits are presented as well.

Decoupling of magnetism and electric transport in single-crystal (Sr1‑x A x )2IrO4 (A  =  Ca or Ba)

Science.gov (United States)

Zhao, H. D.; Terzic, J.; Zheng, H.; Ni, Y. F.; Zhang, Y.; Ye, Feng; Schlottmann, P.; Cao, G.

2018-06-01

We report a systematical structural, transport and magnetic study of Ca or Ba doped Sr2IrO4 single crystals. Isoelectronically substituting Ca2+ (up to 15%) or Ba2+ (up to 4%) ion for the Sr2+ ion provides no additional charge carriers but effectively changes the lattice parameters in Sr2IrO4. In particular, 15% Ca doping considerably reduces the c-axis and the unit cell by nearly 0.45% and 1.00%, respectively. These significant, anisotropic compressions in the lattice parameters conspicuously cause no change in the Néel temperature which remains at 240 K, but drastically reduces the electrical resistivity by up to five orders of magnitude or even precipitates a sharp insulator-to-metal transition at lower temperatures, i.e. the vanishing insulating state accompanies an unchanged Néel temperature in (Sr1‑x A x )2IrO4. This observation brings to light an intriguing difference between chemical pressure and applied pressure, the latter of which does suppress the long-range magnetic order in Sr2IrO4. This difference reveals the importance of the Ir1–O2–Ir1 bond angle and homogenous volume compression in determining the magnetic ground state. All results, along with a comparison drawn with results of Tb and La doped Sr2IrO4, underscore that the magnetic transition plays a nonessential role in the formation of the charge gap in the spin–orbit-tuned iridate.

Structures and Heats of Formation of Simple Alkaline Earth Metal Compounds II: Fluorides, Chlorides, Oxides, and Hydroxides for Ba, Sr, and Ra.

Science.gov (United States)

Vasiliu, Monica; Hill, J Grant; Peterson, Kirk A; Dixon, David A

2018-01-11

Geometry parameters, vibrational frequencies, heats of formation, bond dissociation energies, cohesive energies, and selected fluoride affinities (difluorides) are predicted for the late alkaline earth (Sr, Ba, and Ra) oxides, fluorides, chlorides, and hydroxides at the coupled cluster theory CCSD(T) level. Additional corrections (scalar relativistic and pseudopotential corrections, vibrational zero-point energies, and atomic spin-orbit effects) were included to accurately calculate the total atomization energies and heats of formation following the Feller-Peterson-Dixon methodology. The calculated values are compared to the experimental data where available. In some cases, especially for Ra compounds, there are no experimental results, or the experimental energetics and geometries are not reliable or have very large error bars. All of the Sr, Ba, and Ra difluorides, dichlorides, and dihydroxides are bent structures with the OMO bond angles decreasing going down the group. The cohesive energies of bulk Be dihalides are predicted to be quite low, while those of Ra are relatively large. The fluoride affinities show that the difluorides are moderately strong Lewis acids and that such trifluorides may form under the appropriate experimental conditions.

Effects of crystallization on structural and dielectric properties of thin amorphous films of (1 - x)BaTiO3-xSrTiO3 (x=0-0.5, 1.0)

Science.gov (United States)

Kawano, H.; Morii, K.; Nakayama, Y.

1993-05-01

The possibilities for fabricating solid solutions of (Ba1-x,Srx)TiO3 (x≤0.5,1.0) by crystallization of amorphous films and for improving their dielectric properties by adjusting the Sr content were investigated. Thin amorphous films were prepared from powder targets consisting of mixtures of BaTiO3 and SrTiO3 by sputtering with a neutralized Ar-ion beam. The amorphous films crystallized into (Ba1-x, Srx)TiO3 solid solutions with a cubic perovskite-type structure after annealing in air at 923 K for more than 1 h. The Debye-type dielectric relaxation was observed for the amorphous films, whereas the crystallized films showed paraelectric behavior. The relative dielectric constants were of the order of 20 for the amorphous samples, but increased greatly after crystallization to about 60-200, depending on the composition; a larger increase in the dielectric constant was observed in the higher Sr content films, in the range x≤0.5, which could be correlated with an increase in the grain size of the crystallites. The crystallization processes responsible for the difference in the grain size are discussed based on the microstructural observations.

Structural and optical properties of electro-optic material. Sputtered (Ba,Sr)TiO3

International Nuclear Information System (INIS)

Suzuki, Masato; Xu, Zhimou; Tanushi, Yuichiro; Yokoyama, Shin

2006-01-01

In order to develop a novel ring resonator optical switch, we have studied the structural and optical properties of the electro-optic material (Ba,Sr)TiO 3 (BST) deposited by RF sputtering on a SiO 2 cladding layer (1.0 μm). The crystallinity of the BST films is evaluated by X-ray diffraction and the optical propagation loss of the waveguides is measured using a He-Ne laser. As a result, it is found that there is a strong relationship between the optical propagation loss and crystallinity of the sputtered film. It is suggested that the propagating light is influenced by the crystal property, for example, the grain size and density of the polycrystalline BST film. (author)

Effects of applied electric field during postannealing on the tunable properties of (Ba,Sr)TiO3 thin films

International Nuclear Information System (INIS)

Xia Yidong; Cheng Jinbo; Pan Bai; Wu Di; Meng Xiangkang; Liu Zhiguo

2005-01-01

The impact of postannealing in electric field on the structure, tunability, and dielectric behavior of rf magnetron sputtering derived (Ba,Sr)TiO 3 films has been studied. It has been demonstrated that postannealing in the proper electric field can increase the dielectric constant and the tunability remarkably and destroy the symmetry of capacitance-voltage characteristics of the films. The increased out-of-plane lattice constant and the appearance of the hysteresis loops in the electric-annealed films indicated the formation of small polar regions with tetragonal structure, which are responsible for the increased dielectric constant and tunability. It was proposed that the segregation of Ti 3+ ions caused by electric annealing could induce the formation of BaTiO 3 -like regions, which are ferroelectric at room temperature

Effects of applied electric field during postannealing on the tunable properties of (Ba,Sr)TiO3 thin films

Science.gov (United States)

Xia, Yidong; Cheng, Jinbo; Pan, Bai; Wu, Di; Meng, Xiangkang; Liu, Zhiguo

2005-08-01

The impact of postannealing in electric field on the structure, tunability, and dielectric behavior of rf magnetron sputtering derived (Ba,Sr)TiO3 films has been studied. It has been demonstrated that postannealing in the proper electric field can increase the dielectric constant and the tunability remarkably and destroy the symmetry of capacitance-voltage characteristics of the films. The increased out-of-plane lattice constant and the appearance of the hysteresis loops in the electric-annealed films indicated the formation of small polar regions with tetragonal structure, which are responsible for the increased dielectric constant and tunability. It was proposed that the segregation of Ti3+ ions caused by electric annealing could induce the formation of BaTiO3-like regions, which are ferroelectric at room temperature.

Structural and optical analysis on europium doped AZrO{sub 3} (A=Ba, Ca, Sr) phosphor for display devices application

Energy Technology Data Exchange (ETDEWEB)

Dubey, Vikas, E-mail: jsvikasdubey@gmail.com [Department of Physics, Bhilai Institute of Technology Raipur, 493661 (India); Tiwari, Neha [Department of Physics, Govt. Model Science College, Jabalpur (India)

2016-05-06

Behavior displayed by europium doped AZrO{sub 3} phosphor which was synthesized by solid state reaction method. For synthesis of BaZrO{sub 3}, SrZrO{sub 3} and CaZrO{sub 3} phosphor with fixed concentration of europium ion was calcination at 1000°C and sintered at 1300°C following intermediate grinding. Synthesized sample was characterized by X-ray diffraction analysis and crystallite sized was calculated by Scherer’s formula. From PL spectra of prepared phosphors shows intense emission centred at 612nm (red emission) with high intensity for SrZrO{sub 3}:Eu{sup 3+}. For europium doped BaZrO{sub 3} and CaZrO{sub 3} (613nm) phosphor shows less intense PL spectra as compared to SrZrO{sub 3}:Eu{sup 3+}. The strong emission peak of AZrO{sub 3}:Eu{sup 3+} phosphor is due to forced electric dipole transition of {sup 5}D{sub 0} to {sup 7}F{sub 2} centered at 612 and 613nm. It is characteristic red emission for europium ion. The excitation spectra of AZrO{sub 3}:Eu{sup 3+} phosphor mainly consists of the charge transfer and (CTB) of Eu{sup 3+} located in 200–350 nm centred at 254nm. The present phosphors can act as single host for red light emission in display devices. The CIE coordinates were calculated by Spectrophotometric method using the spectral energy distribution of the AZrO{sub 3}:Eu{sup 3+} sample.

Thermoelectric properties of doped BaHfO_3

International Nuclear Information System (INIS)

Dixit, Chandra Kr.; Bhamu, K. C.; Sharma, Ramesh

2016-01-01

We have studied the structural stability, electronic structure, optical properties and thermoelectric properties of doped BaHfO_3 by full potential linearized augmented plane wave (FP-LAPW) method. The electronic structure of BaHfO_3 doped with Sr shows enhances the indirect band gaps of 3.53 eV, 3.58 eV. The charge density plots show strong ionic bonding in Ba-Hf, and ionic and covalent bonding between Hf and O. Calculations of the optical spectra, viz., the dielectric function, refractive index and extinction coefficient are performed for the energy range are calculated and analyzed. Thermoelectric properties of semi conducting are also reported first time. The doped BaHfO_3 is approximately wide band gap semiconductor with the large p-type Seebeck coefficient. The power factor of BaHfO_3 is increased with Sr doping, decreases because of low electrical resistivity and thermal conductivity.

44/40Ca and 87Sr/86Sr isotopes as tracers of silicate weathering in small catchments of the Massif Central, France

Science.gov (United States)

Négrel, Philippe; Guerrot, Catherine; Millot, Romain; Petelet-Giraud, Emmanuelle; Bullen, Thomas

2013-04-01

We present calcium stable isotope and strontium radiogenic isotope data for soils and sediments developed on volcanic and igneous rocks forming small catchments in the Massif Central (France). Measurements of 44/40Ca isotope ratios (44/40Ca measured by the double spike method on TIMS and normalized to the value for seawater Ca in delta units) in rocks, sediments and soils from silicate catchments (e.g. granite and basalts) together with 87Sr/86Sr isotope ratios permit an examination of the relationships of these isotope systematics during weathering of silicate rocks. We have analysed the granite, weathered granite (arene) and saprolite, sediment and soil overlying the granite on one hand and the basanite, sediment and soil overlying the basanite on the other. The main bedrock in the volcanic zone (e.g. Allanche catchment) is 11 to 2.5 Ma basanite (nephelinitic to leucitic basalts) having SiO2 between 41-45 wt. %, Na2O + K2O bank have 87Sr/86Sr ratios greater than that of the arene with values increasing in the sediment from the surface down to soil. The 87Sr/86Sr vs. Rb/Sr variation observed in the volcanic area likewise confirms the weathering of low 87Sr/86Sr, low Rb/Sr phases in the bedrock, and there is a linear increase in 87Sr/86Sr and Rb/Sr ratios from those in the sediment up to the values observed in the soils. In the volcanic area, the basanite bedrock has 44/40Ca = -0.94 ± 0.05‰ (n = 7), while the soils and sediments have 44/40Ca of -0.75 to -1.13‰ and -0.79 to -1.01‰, respectively. These results suggest that Ca isotopes are not strongly fractionated during weathering of the basalt. The granite whole-rock has 44/40Ca of -1.29‰, while the soil and sediments have 44/40Ca of -1.93 to -2.07‰ and -1.98 to -2.81‰, respectively, with values decreasing as the Ca content decreases. The 44/40Ca ratios of arene, soil and sediment are similar to or less than that of K- feldspar, reflecting complete loss of the relatively heavy Ca from plagioclase and

On the substitution of Sr ions at Y sites in YBa2Cu3O7-d

International Nuclear Information System (INIS)

Siddiqi, S.A.; Sreedhar, K.; Drobac, D.; Infante, C.; Matacotta, F.C.; Ganguly, P.

1989-10-01

The effect of Sr substitution at the Ba sites in YBa 2 Cu 3 O 7-d has been studied, attempts to substitute Sr exclusively at Y sites have not been successful. We have been able to substitute Sr at Y sites only when the Ba ions are simultaneously substituted by Sr to give solid solutions of the type Y 1-x Sr x Ba 2-2x Sr 2x Cu 3 O 7- x /2-d . These examples show superconducting transitions higher than 78K without significant deterioration in the magnitude of the ac susceptibility. The substitutions are best understood in terms of site constraints on the ions occupying the Y and Ba sites. 4 refs, 2 figs, 2 tabs

Role of diacylglycerol in adrenergic-stimulated sup 86 Rb uptake by proximal tubules

Energy Technology Data Exchange (ETDEWEB)

Baines, A.D.; Drangova, R.; Ho, P. (Univ. of Toronto, Ontario (Canada))

1990-05-01

We used rat proximal tubule fragments purified by Percoll centrifugation to examine the role of diacylglycerol (DAG) in noradrenergic-stimulated Na+ reabsorption. Tubular DAG concentration and ouabain-inhibitable 86Rb uptake increased within 30 s after adding norepinephrine (NE) and remained elevated for at least 5 min. NE (1 microM) increased DAG content 17% and ouabain-inhibitable 86Rb uptake 23%. Cirazoline-stimulated 86Rb uptake was not inhibited by BaCl, quinidine, or bumetanide (1-10 microM) or by the omission of HCO3- or Cl- from the medium, but it was completely inhibited by ouabain and furosemide. Oleoyl-acetyl glycerol, L-alpha-1,2-dioctanoylglycerol, and L-alpha-1,2-dioleoylglycerol (DOG) increased total 86Rb uptake 8-11%. 12-O-tetradecanoylphorbol-13-acetate (TPA) (5 nM) increased uptake by only 4%. Staurosporine at 5 nM inhibited DOG stimulation completely, whereas 50 nM staurosporine was required to inhibit NE stimulation completely. Sphingosine inhibited DOG stimulation by 66% but did not inhibit NE stimulation. Amiloride (1 mM) completely blocked DOG stimulation. Monensin increased 86Rb uptake 31% and completely blocked the DOG effect but reduced the NE effect by only 26% (P = 0.08). In tubules from salt-loaded rats, NE did not increase DAG concentration, but NE-stimulated 86Rb uptake was reduced by only 23% (P = 0.15). Thus DAG released by NE may stimulate Na+ entry through Na(+)-H+ exchange. NE predominantly stimulates Na(+)-K(+)-adenosinetriphosphatase (ATPase) by activating a protein kinase that is insensitive to DAG and TPA and is inhibited by staurosporine but not by sphingosine. NE may also stimulate K+ efflux through a BaCl-insensitive K+ channel that is inhibited by millimolar furosemide.

Microstructure and optical properties of Ba0.65Sr0.35TiO3 thin films prepared by RF magnetron sputtering

International Nuclear Information System (INIS)

Zhang Tianjin; Li Songzhan; Zhang Baishun; Pan Ruikun; Jiang Juan; Huang Weihua

2005-01-01

Ba 0.65 Sr 0.35 TiO 3 thin films have been prepared by RF magnetron sputtering. The crystallization and microstructure of the films were characterized by X-ray diffraction (XRD), scan electronic microstructure (SEM) and atom force microstructure (AFM). As-deposited thin films were found to be amorphous. The more intense characteristic diffraction peaks and improved crystallization can be observed in (Ba,Sr)TiO 3 (BST) thin films deposited at high temperatures and annealed at higher than 650degC. Optical constants were determined from transmittance spectra by using the envelope method. The refractive index increased from 1.778 to 1.961 as the substrate temperature increased from 560 to 650degC. Both the refractive index and extinction coefficient increased with annealing temperature. The refractive index and extinction coefficient increased when the oxygen-to-argon ratio increased from 1:4 to 1:1. The dispersion of relation of the extinction coefficient vs wavelength was also investigated. The optical band gap of BST thin films was found to be about 3.56 eV, which decreased apparently with increasing annealing temperature. (author)

Photoluminescent properties of LiSrxBa1-xPO4:RE3+ (RE = Sm3+, Eu3+) f-f transition phosphors

International Nuclear Information System (INIS)

Tu Dong; Liang Yujun; Liu Rong; Cheng Zheng; Yang Fan; Yang Wenlong

2011-01-01

Highlights: → Novel phosphors LiSr x Ba 1-x PO 4 : Sm 3+ and LiSr x Ba 1-x PO 4 : Eu 3+ have been synthesized by solid-state reaction method. → The LiSr x Ba 1-x PO 4 : Sm 3+ and LiSr x Ba 1-x PO 4 : Eu 3+ phosphors may be potential f-f transition phosphors used in LED. → The emission intensity of the LiSr x Ba 1-x PO 4 : Sm 3+ and LiSr x Ba 1-x PO 4 : Eu 3+ phosphors can be enhanced by increasing the value of x. - Abstract: Rare-earth ions (Sm 3+ or Eu 3+ ) doped LiSr x Ba 1-x PO 4 (x = 0, 0.2, 0.4, 0.6, 0.8, 1.0) f-f transition phosphor powders were prepared by a high temperature solid-state reaction. The resulted phosphors were characterized by X-ray diffraction (XRD) and photoluminescence (PL) spectroscopy. The results of XRD indicate that the phase structure of the sample changes from LiBaPO 4 to LiSrPO 4 when x changes from 0 to 1.0. The excitation spectra indicate that only direct excitation of rare earth ions (Sm 3+ or Eu 3+ ) can be observed. The doped rare earth ions show their characteristic emission in LiSr x Ba 1-x PO 4 , i.e., Eu 3+5 D 0 - 7 F J (J = 0, 1, 2, 3, 4), Sm 3+4 G 5/2 → 6 H J (J = 5/2, 7/2, 9/2, 11/2), respectively. The dependence of the emission intensities of the LiSr x Ba 1-x PO 4 :Sm 3+ and LiSr x Ba 1-x PO 4 :Eu 3+ phosphors on the x value and Ln 3+ (Ln 3+ = Sm 3+ , Eu 3+ ) concentration is also investigated.

Conduction and transport numbers in metacomposites MeWO4 · WO3 (Me = Ca, Sr, Ba)

International Nuclear Information System (INIS)

Nejman, A.Ya.; Pestereva, N.N.; Sharafutdinov, A.R.; Kostikov, Yu.P.

2005-01-01

The conductivity and transfer numbers of charge carriers for composites in the MeWO 4 -WO 3 (Me = Ca, Sr, Ba) systems are studied as a function of the temperature and the activity of oxygen in a gas phase. The transfer numbers are determined by the emf method and are estimated from dependences of conductivity on the activity of oxygen in a gas phase. The deficiencies of the given procedure as applied to investigation of properties of composite phases are analyzed. The materials under study are classified as metacomposites. The concentration intervals of the ionic, mixed, and electronic conductivities are determined. The conductivity of (100-x)MeWO 4 · xWO 3 composites is predominantly ionic at x ≤ 10 (Me = Ca), x ≤ 60 (Me = Sr), and x ≤ 45 (Me = Ba). The obtained data are explained in the framework of a model that represents a composite as a distributed matrix system where a film of surface phase MeW-s with a high mobility of oxygen ions plays the role of a connected matrix. It is presumed that the surface phase MeW-s possesses double-sided surface activity (α MeW-s ≤ α WO 3 , α MeWO 4 ) and a higher mobility with respect to MeWO 4 and WO 3 . The discovered anomalies of dependences σ O 2- (T) and partial conductivities σ O 2- , σ el (T) are explained by a change in the stoichiometry, morphology, and the degree of tie-up of surface phase MeW-s caused by a change in the temperature and composition of composites [ru

Luminescence properties of Ce3+-activated alkaline earth silicon nitride M2Si5N8 (M = Ca, Sr, Ba) materials

NARCIS (Netherlands)

Li, Y.Q.; With, de G.; Hintzen, H.T.J.M.

2006-01-01

The luminescence properties of Ce3+, Li+ or Na+ co-doped alkaline-earth silicon nitride M2Si5N8 (M=Ca, Sr, Ba) are reported. The solubility of Ce3+ and optical properties of M2-2xCexLixSi5N8 (x0.1) materials have been investigated as function of the cerium concentration by X-ray powder diffraction

Synthesis of alkaline-earth metal tungstates in melts of [NaNO3-M(NO3)2]eut-Na2WO4 (M=Ca, Sr, Ba) system

International Nuclear Information System (INIS)

Shurdumov, G.K.; Shurdumova, Z.V.; Cherkesov, Z.A.; Karmokov, A.M.

2006-01-01

Synthesis of alkaline earth metal tungstates in melts of eutectics of NaNO 3 -M(NO 3 ) 2 ] (M=Ca, Sr, Ba) is done. Synthesis is based in exchange reaction of calcium, strontium, and barium nitrates with sodium tungstate [ru

Microstructural and dielectric properties of Ba0.6Sr0.4Ti1-xZrxO3 based combinatorial thin film capacitors library

International Nuclear Information System (INIS)

Liu Guozhen; Wolfman, Jerome; Autret-Lambert, Cecile; Sakai, Joe; Roger, Sylvain; Gervais, Monique; Gervais, Francois

2010-01-01

Epitaxial growth of Ba 0.6 Sr 0.4 Ti 1-x Zr x O 3 (0≤x≤0.3) composition spread thin film library on SrRuO 3 /SrTiO 3 layer by combinatorial pulsed laser deposition (PLD) is reported. X-ray diffraction and energy dispersive x-ray spectroscopy studies showed an accurate control of the film phase and composition by combinatorial PLD. A complex evolution of the microstructure and morphology with composition of the library is described, resulting from the interplay between epitaxial stress, increased chemical pressure, and reduced elastic energy upon Zr doping. Statistical and temperature-related capacitive measurements across the library showed unexpected variations in the dielectric properties. Doping windows with enhanced permittivity and tunability are identified, and correlated to microstructural properties.

Pressure-driven phase transitions in TiOCl and the family (Ca, Sr, Ba)Fe2As2

International Nuclear Information System (INIS)

Zhang YuZhong; Opahle, Ingo; Jeschke, Harald O; ValentI, Roser

2010-01-01

Motivated by recent experimental measurements on pressure-driven phase transitions in Mott insulators as well as the new iron pnictide superconductors, we show that first principles Car-Parrinello molecular dynamics calculations are a powerful method to describe the microscopic origin of such transitions. We present results for (i) the pressure-induced insulator to metal phase transition in the prototypical Mott insulator TiOCl as well as (ii) the pressure-induced structural and magnetic phase transitions in the family of correlated metals AFe 2 As 2 (A = Ca, Sr, Ba). Comparison of our predictions with existing experimental results yields very good agreement.

Electronic structure of the gold/Bi2Sr2CaCu2O8 and gold/EuBa2Cu3O7-δ interfaces as studied by photoemission spectroscopy

International Nuclear Information System (INIS)

Dessau, D.S.; Shen, Z.; Wells, B.O.; Spicer, W.E.; List, R.S.; Arko, A.J.; Bartlett, R.J.; Fisk, Z.; Cheong, S.; Mitzi, D.B.; Kapitulnik, A.; Schirber, J.E.

1990-01-01

High-resolution photoemission has been used to probe the electronic structure of the gold/Bi 2 Sr 2 CaCu 2 O 8 and gold/EuBa 2 Cu 3 O 7-δ interface formed by a low-temperature (20 K) gold evaporation on cleaved high quality single crystals. We find that the metallicity of the EuBa 2 Cu 3 O 7-δ substrate in the near surface region (∼5 A) is essentially destroyed by the gold deposition, while the near surface region of Bi 2 Sr 2 CaCu 2 O 8 remains metallic. This has potentially wide ranging consequences for the applicability of the different types of superconductors in real devices

Perovskite phases in the systems AO-SE/sub 2/O/sub 3/-UOsub(2,x) with A = alkaline earth metal and SE = rare earths, La and Y. 10. The systems Ba/sub 2/CaUO/sub 6/-Ba/sub 2/Lusub(0. 67)UO/sub 6/ and Ba/sub 2/SrUO/sub 6/-Ba/sub 2/Lusub(0. 67)UO/sub 6/

Energy Technology Data Exchange (ETDEWEB)

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

1977-06-01

In the systems Ba/sub 2/Bsub(1-x)Lusub(0.67x)UO/sub 6/ with Bsup(II) = Ca, Sr at the B-rich side rhombic and at the Lu-rich side monoclinic perovskites are formed. The transition is discontinuous and accompanied by order-disorder phenomena.

Spectroscopic and thermal degradation behavior of Mg(II), Ca(II), Ba(II) and Sr(II) complexes with paracetamol drug

OpenAIRE

Moamen S. Refat; Gehad G. Mohamed; Mohamed Y. El-Sayed; Hamada M.A. Killa; Hammad Fetooh

2017-01-01

Complexes of Mg(II), Ca(II), Ba(II) and Sr(II) with paracetamol drug were synthesized and characterized by elemental analysis, conductivity, UV–Vis, IR, and 1H NMR spectroscopy and thermal analysis, as well as screened for antimicrobial activity. The IR spectral data suggested that the ligand behaves as paracetamol behaves as a neutral bidentate ligand coordinated to the metal ions via the lone pair of electrons of nitrogen and carbonyl-O atoms of the amide group. From the microanalytical dat...

The microstructure and composition analysis of (Ba,Sr)O.6Fe_2_1_-_X)(Mn,Ti)_xO_3 (X = 0, 0,25; and 0,5)

International Nuclear Information System (INIS)

Wisnu Ari Adi; Azwar Manaf

2010-01-01

The raw materials were BaCO_3_' srCO_3_' Fe_2O_3_' MnCO_3 and TiO_2. The compound was synthesized by a solid state reaction method. The finely mixed powder was compacted at 5000 psi into pellets. These pellets were sintered in the electric chamber furnace THERMOLYNE at 1050 °C for 15 h with a heating cycle of 5°C/min ramp rate and cooled in the furnace to room temperature. The result showed that the X-ray diffraction pattern obtained can be identified as the SrO.6Fe_2O3 single phase (ICDD PDF 33-1340) for all samples according to the Hanawalt table. The microstructure analyses showed that the particle shapes are polygonal with the varied particle sizes of 2-5 μm distributed homogeneously on the surface of the samples. The element analysis showed that the compound compositions have already suitable to expectation. It is concluded that a single phase Mn-Ti substituted (Ba,Sr)O.6Fe_2O_3 have been made successfully suitable of compound composition was expected. (author)

Strain-mediated magnetic response in La0.67Sr0.33MnO3/SrTiO3/La0.67Sr0.33MnO3/BaTiO3 structure

Science.gov (United States)

Swain, Anupama; Komatsu, Katsuyoshi; Itoh, Mitsuru; Taniyama, Tomoyasu; Gorige, Venkataiah

2018-05-01

Electric field controlled magnetism is an exciting area of condensed matter physics to explore the device applications at ultra-low power consumption compared to the conventional current controlled or magnetic field controlled devices. In this study, an attempt was made to demonstrate electric field controlled magnetoresistance (MR) in a tri-layer structure consisting of La0.67Sr0.33MnO3 (LSMO) (40 nm)/SrTiO3 (10 nm)/LSMO (10 nm) grown on a 500-μm-thick BaTiO3 (001) (BTO) single crystal substrate by pulsed laser deposition technique. Epitaxial growth of the trilayer structure was confirmed by x-ray diffraction measurements. Jumps observed in the temperature-dependent magnetization curve at around the structural phase transitions of BTO ensure the strain-mediated magnetoelectric coupling between LSMO and BTO layers. A significant change in MR of this structure in applied electric fields does not show any polarity dependence. The findings are related to the lattice strain-mediated magnetoelectric coupling in ferromagnetic LSMO/ferroelectric BTO heterostructures.

Erosion of the Alps: use of Rb-Sr isotopic data from molassic sediments to identify the ages of the metamorphism recorded by the eroded rocks

International Nuclear Information System (INIS)

Henry, P.; Deloule, E.

1994-01-01

Rb-Sr isotopic data from Oligocene and Miocene peri-alpine molassic sediments allow us to identify the different periods for which the eroded rocks have or have not recorded an alpine metamorphism. The Chattian and the Burdigalian sediments result from the erosion of rocks for which the latest metamorphic event was variscan, while the Stampian, Aquitanian and ''Helvetian'' sediments show evidence for the erosion of rocks which have recorded alpine metamorphic events. The application of this method to old detrital sediments could permit determination of the ages of the tectonic events which occurred in the sediment source regions. (authors). 18 refs., 6 figs

Defect chemistry and oxygen transport of (La0.6Sr0.4 − xMx)0.99Co0.2Fe0.8O3 − δ, M = Ca (x = 0.05, 0.1), Ba (x = 0.1, 0.2), Sr: Part II: Oxygen transport

DEFF Research Database (Denmark)

Dalslet, Bjarke Thomas; Søgaard, Martin; Hendriksen, Peter Vang

2009-01-01

This paper is the second part of a two part series, where the effects of varying the A-site dopant on the defect chemistry and transport properties of the materials (La0.6Sr0.4 − xMx)0.99Co0.2Fe0.8O3 − δ, M = Sr, Ca (x = 0.05, 0.1), Ba (x = 0.1, 0.2) (LSMFC) have been investigated. In part I......, the findings on the defect chemistry were reported, while the oxygen transport properties are reported here in part II. In the investigated material series, the amount of divalent dopant has been kept constant, while Sr ions have been substituted with Ca ions (smaller ionic radius) or Ba ions (larger ionic...... electrolyte probe were used to extract the permeability and surface resistance, rs. The highest permeability was found for (La0.6Sr0.3Ca0.1)0.99Co0.2Fe0.8O3 − δ. The apparent activation energy of the permeability was 78 kJ/mol. The inverse surface resistance, rs− 1, also had an activated behavior...

Luminescence of a new class of UV-blue-emitting phosphors MSi2O2-deltaN2+2/3delta:Ce3+ (M = Ca, Sr, Ba)

NARCIS (Netherlands)

Li, Y.Q.; With, de G.; Hintzen, H.T.J.M.

2005-01-01

The luminescence properties of Ce3+,Na+-codoped MSi2O22dN2+2/3d (M 5 Ca, Sr, Ba) are reported. The undoped and Ce3+,Na+-codoped MSi2O22dN2+2/3d powders were prepared by a solid-state reaction at temperatures between 1300–1400 uC under N2–H2 (10%) atmosphere in the system MO–SiO2–Si3N4 (M 5 Ca, Sr,

Photoemission study of absorption mechanisms in Bi2.0Sr1.8Ca0.8La0.3Cu2.1O8+δ, BaBiO3, and Nd1.85Ce0.15CuO4

International Nuclear Information System (INIS)

Lindberg, P.A.P.; Shen, Z.; Wells, B.O.; Dessau, D.S.; Ellis, W.P.; Borg, A.; Kang, J.; Mitzi, D.B.; Lindau, I.

1989-01-01

Photoemission measurements in the constant-final-state (absorption) mode were performed on three different classes of high-temperature superconductors Bi 2.0 Sr 1.8 Ca 0.8 La 0.3 Cu 2.1 O 8+δ , BaBiO 3 , and Nd 1.85 Ce 0.15 CuO 4 using synchrotron radiation from 20 to 200 eV. Absorption signals from all elements but Ce are identified. The results firmly show that the Bi 6s electrons are more delocalized in BaBiO 3 than in Bi 2.0 Sr 1.8 Ca 0.8 La 0.3 Cu 2.1 O 8+δ , in agreement with the results of band-structure calculations. Differences in the absorption signals due to O and Bi excitations between BaBiO 3 and Bi 2.0 Sr 1.8 Ca 0.8 La 0.3 Cu 2.1 O 8+δ are discussed. Delayed absorption onsets attributed to giant resonances (Ba 4d→4f, La 4d→4f, and Nd 4d→4f transitions) are also reported

Rb-Sr, K-Ar, and stable isotope evidence for the ages and sources of fluid components of gold-bearing quartz veins in the northern Sierra Nevada foothills metamorphic belt, California

Science.gov (United States)

Böhlke, John Karl; Kistler, R. W.

1986-01-01

Gold-bearing quartz veins occur in and near major fault zones in deformed oceanic and island-arc rocks west of the main outcrop of the Sierra Nevada composite batholith. Veins typically occupy minor reverse faults that crosscut blueschist to amphibolite-grade metamorphic rocks whose metamorphic ages range from early Paleozoic to Jurassic. Vein micas and carbonate-quartz-mica assemblages that formed by hydrothermal metasomatism of ultramafic wall rocks in the Alleghany, Grass Valley, Washington, and Mother Lode districts yield concordant K-Ar and Rb-Sr ages. The dated veins are significantly younger than prograde metamorphism, penetrative deformation, and accretion of their host rocks to the continental margin. New and previously published mineralization ages from 13 localities in the Sierra foothills range from about 140 to 110 m.y. ago, with mean and median between 120 and 115 m.y. The age relations suggest that mineralizing fluids were set in motion by deep magmatic activity related to the resumption of east-dipping subduction along the western margin of North America following the Late Jurassic Nevadan collision event.CO 2 -bearing fluids responsible for metasomatism and much of the vein mica, carbonate, albite, and quartz deposition in several northern mines were isotopically heavy (delta 18 O [asymp] 8-14ppm; delta D between about -10 and -50ppm) and do not resemble seawater, magmatic, or meteoric waters. Metasomatic and vein-filling mica, dolomite, magnesite, and quartz in altered ultramafic rocks generally formed from fluids with similar Sr and O isotope ratios at a given locality. Consistent quartz-mica delta 18 O fractionations (delta 18 O (sub Q-M) = 4.5-4.9ppm) from various localities imply uniform equilibration temperatures, probably between 300 degrees and 350 degrees C. On a local (mine) scale, fluids responsible for both carbonate alteration of mafic and ultramafic wall rocks and albitic alteration of felsic and pelitic rocks had similar Sr isotope

La temperatura de transición en SrxBa1-xHfO3

Directory of Open Access Journals (Sweden)

López-García, A.

2002-02-01

Full Text Available In this contribution the transition temperature TC to the cubic phase in SrxBa1-xHfO3 compounds with x = 0.12, 0.25, 0.50, 0.75 and 0.88 is presented. These temperatures were deduced from the measurements of the perturbed angular correlation on tantalum probes. The purpose of this work is to study how the Sr substitution by Ba affect this temperature. The oxides BaHfO3 and SrHfO3 have at RT cubic and orthorhombic structures, respectively. The Sr-compound transform from tetragonal to cubic at TC1 ≈ 1400. From TC2 ≈ 1000K and up to TC1 the oxygen octahedra are tilted and the tilt angle decreases steadily as T approaches TC1. This rotation is originated by the interaction of strontium with oxygen because the Sr ionic radius (rSr ≈ 1.13 Å allows to be closer than Ba (rBa ≈ 1.35 Å. Then in SrxBa1-xHfO3 compounds a competition between the Ba-O interaction, 2.9502 Å apart and Sr-O interaction at a distance of 2.9098 Å in their respective pure compounds, is established.En este trabajo se presenta las temperaturas de transición TC a la estructura cúbica, en la familia de compuestos SrXBa1-XHfO3 donde x es igual a 0.12, 0.25, 0.50, 0.75 y 0.88, determinadas por medidas de la Correlación Angular Perturbada y usando al tantalio como sonda. El interés es estudiar como la sustitución de estroncio por bario modifica dicha temperatura. El BaHfO3 es cúbico a temperatura ambiente. En cambio, el SrHfO3 presenta una transición estructural de tetragonal a cúbica cuando TC1 ≈ 1400 K. Por debajo de esta temperatura y hasta TC2 ≈ 1000 K los octaedros de oxígeno están rotados uno con respecto al consecutivo, en un ángulo φ alrededor del eje z de la red tetragonal que disminuye a cero a medida que T→TC. Esta rotación está relacionada con la interacción del estroncio con el oxígeno, ya que el radio iónico del catión rSr (≈ 1.13 Å permite un mayor acercamiento entre ambos que el bario al oxígeno, pues rBa (≈ 1.35 Å. Entonces, en