410 research outputs found

    Crystal structure and oxygen content of the double perovskites GdBaCo 2-xFexO6-δ

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    The iron solubility limit, x, in GdBaCo2-xFexO 6-δ determined by means of X-ray diffraction was found to be close to 0.65 in air. The crystal structure changes of the double perovskites GdBaCo2-xFexO6-δ (x=0-0.6) were studied by means of in situ X-ray diffraction in temperature range from 25 to 900 °C in air. The oxygen content, 6-δ, was determined for these double perovskites in air as a function of temperature by means of thermogravimetric technique in range 25≤T, °C≤ 1100. The Pmmm-P4/mmm structure transition was found to occur in GdBaCo2-xFexO 6-δ (0≤x≤0.4) with increasing temperature. This transition is observed at the same temperature for the compositions with 0≤x≤0.1 while the transition temperature reaches maximum for x=0.2 and that decreases linearly with further iron increase. The double perovskite GdBaCo1.4Fe0.6O6-δ was shown to have the tetragonal P4/mmm structure at room temperature. The P4/mmm-Pmmm structure transition occurs at temperature as low as 170 °C for this double perovskite while reverse one is already observed at 290 °C in air. The Pmmm-P4/mmm structure transition was found to be strongly related to the oxygen content for the undoped and slightly doped (x≤0.2) double perovskites while there is no such relation for the double perovskites enriched by iron (x≥0.2). © 2012 Elsevier Inc. All rights reserved

    Oxygen content and thermodynamic stability of YBaCo2O6-δdouble perovskite

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    The thermodynamic stability of the double perovskite YBaCo2O6-δ was studied using the coulometric titration technique and verified by measurements of the overall conductivity depending on oxygen partial pressure at a given temperature. As a result, the stability diagram of YBaCo2O6-δ was plotted. YBaCo2O6-δ was found to be thermodynamically stable in air at 850°C and higher temperatures, whereas its thermodynamic stability at 900°C is limited by the range of oxygen partial pressures -3.56 ≤ log(pO2/atm) ≤ -0.14. Oxygen content in YBaCo2O6-δ slightly decreases at 900°C from 5.035 at log(pO2/atm) = -0.14 to 4.989 in the atmosphere with log(pO2/atm) = -3.565 indicating a crucial role which variation of Co+3/Co+2 ratio plays in its stability. YBaCo2O6-δ decomposes into the mixture of YCoO3 and BaCoO3-z at the high pO2 stability limit, whereas YBaCo4O7, BaCo1-xYxO3-γ, and Y2O3 were identified as the products of its decomposition at the low pO2 one. Copyright © 2018 Anton L. Sednev et al

    30-year lidar observations of the stratospheric aerosol layer state over Tomsk (Western Siberia, Russia)

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    There are only four lidar stations in the world which have almost continuously performed observations of the stratospheric aerosol layer (SAL) state over the last 30 years. The longest time series of the SAL lidar measurements have been accumulated at the Mauna Loa Observatory (Hawaii) since 1973, the NASA Langley Research Center (Hampton, Virginia) since 1974, and Garmisch-Partenkirchen (Germany) since 1976. The fourth lidar station we present started to perform routine observations of the SAL parameters in Tomsk (56.48° N, 85.05° E, Western Siberia, Russia) in 1986. In this paper, we mainly focus on and discuss the stratospheric background period from 2000 to 2005 and the causes of the SAL perturbations over Tomsk in the 2006–2015 period. During the last decade, volcanic aerosol plumes from tropical Mt. Manam, Soufrière Hills, Rabaul, Merapi, Nabro, and Kelut and extratropical (northern) Mt. Okmok, Kasatochi, Redoubt, Sarychev Peak, Eyjafjallajökull, and Grímsvötn were detected in the stratosphere over Tomsk. When it was possible, we used the NOAA HYSPLIT trajectory model to assign aerosol layers observed over Tomsk to the corresponding volcanic eruptions. The trajectory analysis highlighted some surprising results. For example, in the cases of the Okmok, Kasatochi, and Eyjafjallajökull eruptions, the HYSPLIT air mass backward trajectories, started from altitudes of aerosol layers detected over Tomsk with a lidar, passed over these volcanoes on their eruption days at altitudes higher than the maximum plume altitudes given by the Smithsonian Institution Global Volcanism Program. An explanation of these facts is suggested. The role of both tropical and northern volcanic eruptions in volcanogenic aerosol loading of the midlatitude stratosphere is also discussed. In addition to volcanoes, we considered other possible causes of the SAL perturbations over Tomsk, i.e., the polar stratospheric cloud (PSC) events and smoke plumes from strong forest fires. At least two PSC events were detected in 1995 and 2007. We also make an assumption that the Kelut volcanic eruption (Indonesia, February 2014) could be the cause of the SAL perturbations over Tomsk during the first quarter of 2015

    Synthesis of p-tert-butylthiacalix[4]arenes functionalized with tris(2-aminoethyl)amine fragments at the lower rim and their interaction with model lipid membranes

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    © ISUCT Publishing. New tetrasubstituted derivatives of thiacalix[4]arene functionalized with tris(2-aminoethyl)amine fragments at the lower rim in the cone, partial cone and 1,3-alternate conformations have been synthesized. It has been shown that during the interaction of tris(2-aminoethyl)amine with thiacalix[4]arenes in cone and partial cone conformation, еру cyclic fragments are formed. The structure with acyclic fragments is obtained in the case of thiacalix[4]arenes in 1,3- alternate conformation. The interaction of these compounds with a biomembrane model system was studied. It has been shown that the interaction of these compounds with model lipid membranes depends not only on the presence of hydrophilic-hydrophobic groups but also on the spatial orientation of these groups

    Thermodynamics of Formation of Solid Solutions between BaZrO3 and BaPrO3

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    Received: 30.03.2020. Accepted: 11.05.2020. Published: 30.06.2020.A linear relationship between the standard enthalpy of formation from binary oxides, ΔfH°ox, and the Goldschmidt tolerance factor, t, for some AIIBIVO3 (A = Ca, Sr, Ba; B = Ti, Zr, Hf, Ce, Pr, Tb, U, Pu, Am) perovskite oxides was used for estimation of ΔfH°ox of Pr-substituted barium zirconates BaZr1–xPrxO3. A dependence of the relative change of the standard entropies, S°298, on the relative change of the molar volumes in the reactions of formation of AIIBIVO3 (A = Ca, Sr, Ba; B = Ti, Zr, Hf, Ce) from binary oxides was also found to be linear. Using this dependence, a relatively precise method of estimating S°298 was proposed, and S°298 of BaPrO3 was calculated as (162.8 ± 2.8) J·mol–1·K–1. Knowing S°298 of BaPrO3 and using the literature data for S°298 of BaZrO3, the values of S°298 of BaZr1–xPrxO3 were predicted on the assumption that BaZr1–xPrxO3 is a regular or ideal solution of BaPrO3 in BaZrO3 as evidenced by the very small enthalpy of mixing calculated based on the estimated ΔfH°ox. The values of standard entropy changes, ΔfS°ox, and Gibbs energy changes, ΔfG°ox, for the reactions of formation of BaZr1–xPrxO3 from BaO, ZrO2 and PrO2 were also estimated. Substituting Pr for Zr in BaZr1–xPrxO3 results in ΔfH°ox and ΔfG°ox becoming more positive, indicating the decrease of the relative stability with respect to the corresponding binary oxides. Expanded uncertainties of the estimated values of ΔfH°ox and ΔfG°ox are equal to 14 kJ · mol–1, and those of S°298 and ΔfS°ox — less than 2.8 J · mol–1·K–1 and 3.5 J · mol–1·K–1, respectively, for BaZr1–xPrxO3 (x = 0.0–1.0).This work was supported by the Russian Science Foundation (project No. 18‑73‑00022)

    Lipoplexes of dicationic gemini surfactants with DNA: Structural features of DNA compaction and transfection efficiency

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    © 2015, Pleiades Publishing, Ltd. The internal structure of DNA lipoplexes with hydroxyethylated alkylammonium gemini surfactants (GS) with high transfection activity was studied by circular dichroism. It was shown that the efficiency of transfection of HEK293T cells with the pEGFP-N1 circular plasmid was different from zero only in the region of existence of chiral supramolecular DNA-GS complexes and reaches a maximum at concentrations at which the spontaneous aggregation of components is observed

    Hysteresis phenomena during melting of an ultrathin lubricant film

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    The influence of a deformational defect of the shear modulus on the melting of an ultrathin lubricant film was investigated in the framework of the Lorenz model used for describing a viscoelastic medium. It was established that the film can undergo both stepwise and continuous melting. Analysis of the lubricant behavior revealed that there are three modes corresponding to a zero shear stress, a Hookean portion in the loading diagram, and a plastic-flow portion. The hysteresis in the dependences of the stationary shear stress on the strain and the friction surface temperature is examined. When you are citing the document, use the following link http://essuir.sumdu.edu.ua/handle/123456789/1621

    Aligned crystallite powder of NdFeAsO0.86_{0.86}F0.14_{0.14}: magnetic hysteresis and penetration depth

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    We report the basal-plane critical current and superfluid density of magnetically aligned NdFeAsO0.86_{0.86}F0.14_{0.14} powder. This sample has individual crystallite grains permanently oriented with their c axis along the external field. Magnetic irreversibilities at high field suggest strong flux pinning of basal-plane critical currents, with monotonic field dependence and no evidence of the "fishtail" effect. The small particles provide a sensitive indicator of \textit{dc} flux penetration, and allow analysis of the temperature dependence of abab-plane London penetration depth λab,L\lambda_{ab,\mathrm{L}}, which is quadratic at low TT. This feature may not necessarily be due to the nodes in the gap, but may be rather a sign of a strong pair-breaking. A quantitative determination of the absolute magnitude of λab,L\lambda_{ab,\mathrm{L}} is hindered by the need for accurate knowledge of the particle size distribution.Comment: 6 pages, 6 figure

    Production of XeO * in a CW microwave discharge

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    A low-power CW microwave discharge at 2.45 GHz was used to produce XeO * excimer molecules. It was found that a total gas pressure between 5 and 20 Torr, absorbed power of about 20–100 W, and an oxygen-to-xenon ratio of 1∶100 maximized the XeO( 1 S− 1 D) green emission at 5200 to 5600 Å. The XeO * emission appeared in the cooler parts of the discharge near the containment tube walls and in the electric field nodes of the TM 012 resonant mode.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/45480/1/11090_2005_Article_BF01023916.pd
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