Search results for "pero"

showing 10 items of 3365 documents

Sensitive determination of aliphatic amines in water by high-performance liquid chromatography with chemiluminescence detection.

2004

A sensitive method has been developed for liquid chromatographic determination of short aliphatic amines in water samples. Analytes are preconcentrated and dansylated on solid sorbents (C18 solid-phase extraction cartridges). The dansyl derivatives are chromatographed and post-column mixed with peroxyoxalate (TCPO) and H2O2 in order to perform chemiluminescence detection. Optimal results have been obtained using a sample volume of 5 ml. The method has been applied to the quantification or screening of several aliphatic amines: methylamine, ethylamine, butylamine, diethylamine, pentylamine and hexylamine. The screening procedure has been developed including also polyamines (putrescine, cadav…

DiethylamineDetection limitChromatographyOrganic ChemistryGeneral MedicineBiochemistryHigh-performance liquid chromatographyPeroxyoxalateSensitivity and SpecificityAnalytical Chemistrylaw.inventionchemistry.chemical_compoundSpectrometry FluorescencechemistrylawHexylamineLuminescent MeasurementsSpectrophotometry UltravioletEthylaminePentylamineAminesChromatography High Pressure LiquidChemiluminescenceJournal of chromatography. A
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Defect interaction and local structural distortions in Mg-doped LaGaO3: A combined experimental and theoretical study

2017

A combined experimental and theoretical study of Mg-doped LaGaO3 electrolyte was carried out, with the aim to unveil the interaction between oxygen vacancy (Vo) and perovskite B site cations. LaGaO3 (LG) and LaGa0.875Mg0.125O2.938 (LGM0125) samples were comprehensively characterized by X-ray absorption spectroscopy (XAS) and X-ray diffraction, in order to investigate short- and long-range structures of both undoped and Mg-doped materials. XAS analysis evidenced a preferential Ga-Vo interaction in LGM0125, confirmed by periodic hybrid density functional theory calculations, which were combined with a symmetry-independent classes (SICs) approach in order to (a) obtain a detailed picture of th…

DiffractionAbsorption spectroscopyGeneral Physics and Astronomy02 engineering and technologyCrystal structure010402 general chemistry01 natural sciencesCHEMISTRY1ST PRINCIPLESRAY-ABSORPTION SPECTROSCOPYBODY DISTRIBUTION-FUNCTIONSPhysical and Theoretical ChemistryOXIDE FUEL-CELLSION CONDUCTIVITYPerovskite (structure)CONDENSED MATTERX-ray absorption spectroscopyELECTROLYTESChemistryDoping021001 nanoscience & nanotechnologyTRANSPORT0104 chemical sciencesCrystallographyX-ray crystallographyDensity functional theory0210 nano-technologyLANTHANUM GALLATE PEROVSKITEThe Journal of Chemical Physics
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Physical Properties of Ba0.95Pb0.05TiO3+0.1%Co2O3

2012

The single-phase perovskite structure of the Ba0.95Pb0.05TiO3+0.1%Co2O3 ceramics was confirmed by the X-ray diffraction method. Microstructural studies revealed that the samples were of good quality and chemically homogeneous. The thermal behaviour of ceramics was studied using the in situ high-temperature X-ray synchrotron powder diffraction investigation. The energy gap of about 3.2 eV was estimated using a reflectance spectroscopy. Measurements showed the influence of Pb and Co on the character of phase transition in the BaTiO3 structure. The results were compared to the ones obtained for pure BaTiO3.

DiffractionIn situPhase transitionMaterials scienceBand gapDopingAnalytical chemistryCondensed Matter PhysicsElectronic Optical and Magnetic Materialsvisual_artThermalvisual_art.visual_art_mediumCeramicPerovskite (structure)Ferroelectrics
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X-ray Studies of Debye Temperature of Some ABO 3 Perovskites

2002

Debye temperatures T D of some perovskite compounds are determined by X-ray diffraction. Correlation between T D determined at T=180 °C, mean square displacements of atoms, quasi-elastic coupling, and melting temperature of the perovskite compounds is analysed.

DiffractionPhase transitionMaterials scienceX-rayAnalytical chemistryCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsCondensed Matter::Materials Sciencesymbols.namesakechemistry.chemical_compoundchemistryCondensed Matter::SuperconductivitysymbolsMelting pointStrontium titanateCondensed Matter::Strongly Correlated ElectronsDebye modelDebyePerovskite (structure)Ferroelectrics
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Influence of hydrogen intercalation on the local structure around Re ions in perovskite‐type ReO 3

2005

octahedra with the Re-O-Re angle equal to 169° and the Re-O distance of about 1.90 A [9]. More accurate information on the local atomic and electronic structure of the bronzes can be ob-tained using XAS, which is a structural method complimentary to diffraction. To our knowledge, no such works have been performed until now. In this work, we present the first results of the in-situ XAS study of hydrogen intercalation into ReO

DiffractionX-ray absorption spectroscopyCrystallographyOctahedronHydrogenChemistryIntercalation (chemistry)chemistry.chemical_elementElectronic structureIonPerovskite (structure)physica status solidi (c)
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Ferroelastic Fingerprints in Methylammonium Lead Iodide Perovskite

2016

Methylammonium lead iodide (MAPbI3) perovskite shows an outstanding performance in photovoltaic devices. However, certain material properties, especially the possible ferroic behavior, remain unclear. We observed distinct nanoscale periodic domains in the piezoresponse of MAPbI3(Cl) grains. The structure and the orientation of these striped domains indicate ferroelasticity as their origin. By correlating vertical and lateral piezoresponse force microscopy experiments performed at different sample orientations with X-ray diffraction, the preferred domain orientation is suggested to be the a1–a2-phase. The observation of these ferroelastic fingerprints appears to strongly depend on the film t…

Diffractionchemistry.chemical_classificationPhase transitionMaterials scienceFerroelasticityIodide02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyGeneral EnergyPiezoresponse force microscopychemistryChemical physicsTexture (crystalline)Physical and Theoretical Chemistry0210 nano-technologyNanoscopic scalePerovskite (structure)The Journal of Physical Chemistry C
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Metal ions modify DNA-protecting and mutagen-scavenging capacities of the AV-153 1,4-dihydropyridine.

2019

Abstract 1,4-Dihydropyridines (1,4-DHP) possess important biochemical and pharmacological properties, including antioxidant and antimutagenic activities. AV-153-Na, an antimutagenic and DNA-repair enhancing compound was shown to interact with DNA by intercalation. Here we studied DNA binding of several AV-153 salts to evaluate the impact of AV-153 modifications on its DNA binding capacity, the ability to scavenge the peroxynitrite, to protect HeLa and B-cells cells against DNA damage. Affinity of the AV-153 salts to DNA measured by a fluorescence assay was dependent on the metal ion forming a salt in position 4 of the 1,4-DHP, and it decreased as follows: Mg > Na > Ca > Li > Rb > K. AV-153-…

DihydropyridinesAntioxidantDNA RepairDNA damageHealth Toxicology and Mutagenesismedicine.medical_treatmentMetal ions in aqueous solutionIntercalation (chemistry)[SDV.CAN]Life Sciences [q-bio]/CancerMutagen02 engineering and technologymedicine.disease_causeNiacinAntioxidantsHeLa03 medical and health scienceschemistry.chemical_compoundPeroxynitrous AcidGeneticsmedicineHumansDrug InteractionsDNA Breaks Single-StrandedComputingMilieux_MISCELLANEOUS030304 developmental biology0303 health sciencesB-Lymphocytesbiology021001 nanoscience & nanotechnologybiology.organism_classificationIntercalating AgentsRecombinant ProteinsOxidative StresschemistryMetalsBiophysicstat Gene Products Human Immunodeficiency VirusComet AssaySingle-Cell Analysis0210 nano-technologyDNAPeroxynitriteDNA DamageHeLa CellsMutation research. Genetic toxicology and environmental mutagenesis
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A kinetic model for the oxidation of benzenethiol catalyzed by the [MoVIO2(O2CC(S)(C6H5)2)2]2− complex intercalated in a Zn(II)–Al(III) layered doubl…

2009

Abstract The heterogeneous oxidation of benzenethiol catalyzed by the dianionic bis(2-sulfanyl-2,2-diphenylethanoxycarbonyl) dioxomolybdate (VI) complex intercalated into a Zn(II)–Al(III) layered double hydroxide (LDH) host have been investigated under aerobic conditions. The kinetics of the system has been analysed in detail. In ethanol, the benzenethiol is cleanly oxidized to diphenyl disulfide in the acidic media provided by the protonic resin Amberlite IR-120(H). The reaction is second-order in benzenethiol, and the apparent rate coefficient has been found to be proportional to the catalyst weight and inversely proportional to the initial concentration of the substrate. A catalytic cycl…

Diphenyl disulfideProcess Chemistry and TechnologyInorganic chemistryComproportionationRate-determining stepMedicinal chemistryCatalysisCatalysischemistry.chemical_compoundchemistryCatalytic cycleHydroperoxylOxidation stateHydroxidePhysical and Theoretical ChemistryJournal of Molecular Catalysis A: Chemical
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A small HSP, Lo18, interacts with the cell membrane and modulates lipid physical state under heat shock conditions in a lactic acid bacterium

2005

International audience; The small heat shock proteins (sHSP) are characterized by a chaperone activity to prevent irreversible protein denaturation. This study deals with the sHSP Lo18 induced by multiple stresses in Oenococcus oeni, a lactic acid bacterium. Using in situ immunocytochemistry and cellular fractionation experiments, we demonstrated the association of Lo18 with the membrane in O. oeni cells submitted to heat shock. The same result was obtained after exposure of cells to ethanol or benzyl alcohol, agents known to have an influence on membranes. For the different stresses, the protein was located on the periphery of the cell at membrane level and was also found within the cytopl…

DiphenylhexatrieneHot TemperatureBiophysicsFluorescence PolarizationBiologyBiochemistryImmunolocalizationSmall HSPCell membraneMembrane Lipids03 medical and health scienceschemistry.chemical_compoundHeat shock proteinMembrane fluiditymedicineMembrane fluidityLipid bilayer030304 developmental biologyOenococcus oeni0303 health sciences030306 microbiologyCell MembraneLipid–protein interactionCell Biologybiology.organism_classificationHeat-Shock Proteins SmallGram-Positive CocciMembranemedicine.anatomical_structure[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologychemistryBiochemistryBiophysicsLipochaperoneLaurdanOenococcus oeni
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On the ∗-cocharacter sequence of 3×3 matrices

2000

Abstract Let M 3 (F) be the algebra of 3×3 matrices with involution * over a field F of characteristic zero. We study the ∗ -polynomial identities of M 3 (F) , where ∗=t is the transpose involution, through the representation theory of the hyperoctahedral group B n . After decomposing the space of multilinear ∗ -polynomial identities of degree n under the B n -action, we determine which irreducible B n -modules appear with non-zero multiplicity. In symbols, we write the nth ∗ -cocharacter χ n (M 3 (F),*)=∑ r=0 n ∑ λ⊢r,h(λ)⩽6 μ⊢n−r,h(μ)⩽3 m λ,μ χ λ,μ , where λ and μ are partitions of r and n−r , respectively, χ λ,μ is the irreducible B n -character associated to the pair (λ,μ) and m λ,μ ⩾0 i…

Discrete mathematicsNumerical AnalysisMultilinear mapAlgebra and Number TheoryMultiplicity (mathematics)Hyperoctahedral groupRepresentation theoryPolynomial identitiesCombinatoricsMatrices with involutionCocharacter sequenceDiscrete Mathematics and CombinatoricsGeometry and TopologyMathematicsLinear Algebra and its Applications
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