Publications by authors named "Ramanujachary K"

Article Synopsis
  • The substitution of Ru by Ta in SrYbRuO leads to changes in its magnetic properties, showing stronger antiferromagnetic interactions in pure SrYbRuO compared to its Ta-substituted variants.
  • As the concentration of Ta increases, the band gap of the material increases nearly linearly, indicating shifts in electronic structure and orbital ordering.
  • The photoelectrocatalytic studies reveal that SrYbRuO has the highest photocurrent density and optimal performance for oxygen evolution reactions, with structural insights gained from techniques like XPS and EPR confirming the oxidation states and the presence of oxygen vacancies.
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The single crystals of a quaternary sulfide, BaFeAgS, have been synthesized by reacting elements at 873 K inside a sealed fused silica tube. The title phase is the first ordered quaternary compound of the Ba-Ag-Fe-S system. The crystal structure of BaFeAgS is characterized by a single-crystal X-ray diffraction study at 298(2) K.

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Article Synopsis
  • GdFeO nanoparticles were created using a straightforward method involving citric acid, resulting in a highly crystalline orthorhombic structure as confirmed by X-ray diffraction and FTIR analysis.!* -
  • Electron microscopy revealed worm-shaped nanoparticles with an average size of 95 nm and a distinct interplanar spacing of 0.12 nm on the (112) crystalline plane.!* -
  • Notably, these nanoparticles exhibited room-temperature ferroelectricity and high dielectric properties, making them promising candidates for use in multistate memory devices.!*
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Three new isostructural quaternary tellurides, BaLnMnTe (Ln = Pr, Gd, and Yb), have been synthesized by the molten-flux method at 1273 K. The single-crystal X-ray diffraction studies at 298(2) K showed that BaLnMnTe crystallize in the space group -C2/m of the monoclinic crystal system. There are six unique crystallographic sites in this structure's asymmetric unit: one Ba site, one Ln site, one Mn site, and three Te sites.

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Human telomeric DNA G-quadruplex has been identified as a good therapeutic target in cancer treatment. G-quadruplex-specific ligands that stabilize the G-quadruplex have great potential to be developed as anticancer agents. Two crystal structures (an apo form of parallel stranded human telomeric G-quadruplex and its holo form in complex with BRACO19, a potent G-quadruplex ligand) have been solved, yet the binding mechanism and pathway remain elusive.

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Green graphene materials prepared by photoreduction of graphite oxide were first time blended with aqueous-based silk fibroin proteins to improve the mechanical and thermal properties of silk biomaterials, and their nanocomposite interaction mechanism was illustrated. Powder X-ray diffraction (XRD) analysis confirmed the complete exfoliation of graphite oxide to graphene in presence of focused pulses of solar radiation. By varying the concentration of graphene (0.

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In this article we present data on the concentration of calcium as determined by Inductively Coupled Plasma (ICP) measurements. Calcium was estimated in the reagents used for native gel electrophoresis of Neuronal Calcium Sensor (NCS) proteins. NCS proteins exhibit calcium-dependent mobility shift in native gels.

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Between 1950 and 1980, lead and chromium along with other metals have been used in paint coatings to protect bridges from corrosion. In New York State with 4500 bridges in 11 Regions 2385 of the bridges have been rehabilitated and subsequently repainted after 1989 when commercial use of lead based paint was prohibited. The purpose of this research was to address the concentration and distribution of trace metals in the paint waste generated during bridge rehabilitation.

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For Department of Transportation (DOT) agencies, bridge rehabilitation involving paint removal results in waste that is often managed as hazardous. Hence, an approach that provides field characterization of the waste classification would be beneficial. In this study, an analysis of variables critical to the leaching process was conducted to develop a predictive tool for waste classification.

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The disposal of paint waste from bridge rehabilitation is a significant issue because of the potential release of contaminants and the consequent impact to human health and the environment. In this study, leaching behavior of paint waste was evaluated for 24 bridges in New York State. Although elevated Pb (5-168,090 mg kg(-1)) and other metal concentrations were observed in the paint samples, leaching experiments that included the toxicity characteristic leaching procedure (TCLP) and the multiple extraction procedure (MEP) revealed toxicity characteristic (TC) limits were not exceeded.

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We have expanded the double perovskite family of materials with the unusual combination of layered order in the A sublattice and rock salt order over the B sublattice to compounds NaLaFeWO6 and NaNdFeWO6. The materials have been synthesized and studied by powder X-ray diffraction, neutron diffraction, electron diffraction, magnetic measurements, X-ray absorption spectroscopy, dielectric measurements, and second harmonic generation. At room temperature, the crystal structures of both compounds can be defined in the noncentrosymmetric monoclinic P2(1) space group resulting from the combination of ordering both in the A and B sublattices, the distortion of the cell due to tilting of the octahedra, and the displacement of certain cations.

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Recently, metals and metalloids have been observed at elevated concentrations in glass beads imported to the US. Average total concentrations in imported batches ranged from 103 to 683 mg kg(-1) for As, 62 to 187 mg kg(-1) for Sb, and 23 to 179 mg kg(-1) for Pb. The labile fraction associated with the glass beads resulted in leached concentrations as great as 538 μg L(-1) for As, 1092 μg L(-1) for Pb, and 160 μg L(-1) for Sb.

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SrFe0.75Mo0.25O3-δ has been recently discovered as an extremely efficient electrode for intermediate temperature solid oxide fuel cells (IT-SOFCs).

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Synthesis of uniform silica shell over Co3O4 nanoparticles was carried out using the colloidal solutions of Tergitol and cyclohexane. The shell could be controlled to a thickness of up to 20 nm by varying different parameters such as the amount of tetraethylorthosilicate, concentration of Co3O4 nanoparticles, reaction time and the presence of water and 1-octanol. Control of the amount of water (required for hydrolysis) appears to be the key factor for controlling the shell thickness.

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Article Synopsis
  • * The synthesis process involves adjusting the niobium precursor to boron ratio and reaction conditions to produce various nanostructures, including core-shell structures, and was characterized using techniques like XRD, HRTEM, and EDX.
  • * Niobium diboride nanorods exhibit superconductivity with a critical transition temperature of 6.4 K, but this superconductivity is hidden in the core-shell structure
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Article Synopsis
  • Researchers created nickel borate nanostructures with specific sizes and shapes using a method involving a precursor made in microemulsions with Tergitol as a surfactant.
  • By experimenting with different co-surfactants like 1-butanol, 1-hexanol, and 1-octanol, they produced uniform nanorods and nanospindles of varying dimensions.
  • The resulting nanorods exhibited antiferromagnetic properties, with a Néel temperature between 44 to 47 K, and showed an increase in magnetic moment as the rods became thinner.
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Anisotropic nanostructures of magnesium oxalate dihydrate were synthesized using cationic surfactant based microemulsion method. The cationic surfactant plays an important role in forming the anisotropic structures. The oxalate nanostructures acts as an excellent precursor for the synthesis of fine magnesium oxide nanoparticles (~10 nm).

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Four new 5-aminoisophthalates of cobalt and nickel have been prepared employing hydro/solvothermal methods: [Co(2)(C(8)H(5)NO(4))(2)(C(4)H(4)N(2))(H(2)O)(2)].3H(2)O (I), [Ni(2)(C(8)H(5)NO(4))(2)(C(4)H(4)N(2))(H(2)O)(2)].3H(2)O (II), [Co(2)(H(2)O)(mu(3)-OH)(2)(C(8)H(5)NO(4))] (III), and [Ni(2)(H(2)O)(mu(3)-OH)(2)(C(8)H(5)NO(4))] (IV).

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Article Synopsis
  • Appropriate microemulsion systems were used to produce hexagonal cobalt and cobalt-nickel alloy nanoparticles with cetyltrimethylammonium bromide as a surfactant at high temperatures, achieving stabilization of hexagonal cobalt at very small sizes.
  • Annealing hcp cobalt nanoparticles in hydrogen at 700 degrees Celsius transformed them into fcc cobalt nanoparticles, with microscopy revealing spherical nanoparticles in different sizes and structures.
  • Electrochemical tests indicated that cobalt nanoparticles outperform cobalt-nickel alloy nanoparticles at voltages below 0.65 V, whereas the alloy shows better efficiency at higher voltages, and all nanoparticles display ferromagnetism, though saturation magnetization is reduced due to potential surface oxidation.
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Rod-shaped nanostructures of cobalt oxalate dihydrate were synthesized at room temperature by the microemulsion (reverse micellar) route. These rods are highly uniform in length and can be modified with temperature (from approximately 6.5 microm at 50 degrees C to approximately 2.

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Article Synopsis
  • * The synthesized nickel and copper nanorods have diameters of 250 nm and 130 nm, respectively, with lengths of about 2.5 microm for nickel and 480 nm for copper, and their shape can be altered by changing the solvent used.
  • * Nickel oxalate nanorods exhibit an antiferromagnetic transition at 34 K, while copper oxalate nanorods show temperature-independent paramagnetism.
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The recent discovery of ferromagnetism above room temperature in low-temperature-processed MnO(2)-ZnO has generated significant interest. Using suitably designed bulk and thin-film studies, we demonstrate that the ferromagnetism in this system originates in a metastable phase rather than by carrier-induced interaction between separated Mn atoms in ZnO. The ferromagnetism persists up to approximately 980 K, and further heating transforms the metastable phase and kills the ferromagnetism.

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We describe the synthesis of two new quadruple perovskites, Sr(2)La(2)CuTi(3)O(12) (I) and Ca(2)La(2)CuTi(3)O(12) (II), by solid-state metathesis reaction between K(2)La(2)Ti(3)O(10) and A(2)CuO(2)Cl(2) (A = Sr, Ca). I is formed at 920 degrees C/12 h, and II, at 750 degrees C/24 h. Both the oxides crystallize in a tetragonal (P4/mmm) quadruple perovskite structure (a = 3.

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Three pleiotropic, quorum sensing-defective Vibrio harveyi mutants were observed to precipitate soluble Pb2+ as an insoluble compound. The compound was purified and subjected to X-ray diffraction and elemental analyses. These assays identified the precipitated compound as Pb9(PO4)6, an unusual and complex lead phosphate salt that is produced synthetically at temperatures of ca.

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