Search results for "Ionic radius"

showing 10 items of 29 documents

Onset of cohesion in cement paste

2004

It is generally agreed that the cohesion of cement paste occurs through the formation of a network of nanoparticles of a calcium-silicate-hydrate ("C-S-H"). However, the mechanism by which these particles develop this cohesion has not been established. Here we propose a dielectric continuum model which includes all ionic interactions within a dispersion of C-S-H particles. It takes into account all co-ions and counterions explicitly (with pure Coulomb interactions between ions and between ions and the surfaces) and makes no further assumptions concerning their hydration or their interactions with the surface sites. At high surface charge densities, the model shows that the surface charge of…

0211 other engineering and technologiesCementNanoparticleIonic bonding02 engineering and technologyDielectricCSHIonchemistry.chemical_compound021105 building & constructionElectrochemistryGeneral Materials ScienceSurface chargecalcium silicate hydrateCalcium silicate hydrateionic correlationsSpectroscopyMonte Carlo simulation[CHIM.MATE] Chemical Sciences/Material chemistryIonic radiusatomic force microscopySurfaces and Interfaces[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsC-S-HcohesionchemistryChemical physics[ CHIM.MATE ] Chemical Sciences/Material chemistryCohesion (chemistry)nanoparticlesAFM0210 nano-technology
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Optical absorption of divalent metal tungstates: Correlation between the band-gap energy and the cation ionic radius

2008

We have carried out optical-absorption and reflectance measurements at room temperature in single crystals of AWO4 tungstates (A = Ba, Ca, Cd, Cu, Pb, Sr, and Zn). From the experimental results their band-gap energy has been determined to be 5.26 eV (BaWO4), 5.08 eV (SrWO4), 4.94 eV (CaWO4), 4.15 eV (CdWO4), 3.9-4.4 eV (ZnWO4), 3.8-4.2 eV (PbWO4), and 2.3 eV (CuWO4). The results are discussed in terms of the electronic structure of the studied tungstates. It has been found that those compounds where only the s electron states of the A2+ cation hybridize with the O 2p and W 5d states (e.g BaWO4) have larger band-gap energies than those where also p, d, and f states of the A2+ cation contribu…

Accelerator Physics (physics.acc-ph)Condensed Matter - Materials ScienceMaterials scienceIonic radiusBand gapAnalytical chemistryMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesGeneral Physics and AstronomyElectronic structureElectronReflectivityDivalent metalValence bandPhysics - Accelerator PhysicsAbsorption (electromagnetic radiation)EPL (Europhysics Letters)
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High-Pressure Phase Diagram and Superionicity of Alkaline Earth Metal Difluorides

2018

We study the high-pressure–high-temperature phase diagram and superionicity of alkaline earth metal (AEM) difluorides (AF2, A = Ca, Sr, Ba) with first-principles simulation methods. We find that the superionic behavior of SrF2 and BaF2 at high pressures differ appreciably from that previously reported for CaF2 [Phys. Rev. Lett. 2014, 113, 235902]. Specifically, the critical superionic temperature of SrF2 and BaF2 in the low-pressure cubic fluorite phase is not reduced by effect of compression, and the corresponding high-pressure orthorhombic contunnite phases become superionic at elevated temperatures. We get valuable microscopic insights into the superionic features of AEM difluorides in b…

Alkaline earth metalMaterials scienceIonic radiusDifluorideThermodynamics02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesFluorite0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergyPhase (matter)High pressureOrthorhombic crystal systemPhysical and Theoretical Chemistry0210 nano-technologyPhase diagramThe Journal of Physical Chemistry C
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Structural effects of Co and Cr substitution in LaMnO3 + δ

2000

Series of perovskite oxides with the composition LaMn1 − xMxO3 + δ (M = Cr, Co; 0 ≤ x ≤ 1) have been synthesized by thermal treatment of precursors obtained by freeze-drying of acetic acid solutions. The oxides have been characterized by X-ray diffraction, and the Mn4+ content and, thus, the oxygen excess, δ, has been determined by redox back-titration. LaMnO3.14 and LaCrO3 phases have the rhombohedral-LaAlO3 and the orthorhombic-GdFeO3 structures, respectively. The LaMn1 − xCrxO3 + δ phases have the rhombohedral structure for x ≤ 0.3, and the orthorhombic structure for x ≥ 0.5. LaCoO3 has, as LaMnO3.14, the rhombohedral structure. However, the LaMn1 − xCoxO3 + δ phases have orthorhombic st…

CrystallographyIonic radiusChemistryInorganic chemistryMaterials ChemistryOrthorhombic crystal systemGeneral ChemistryCrystal structureThermal treatmentChemical compositionRedoxPerovskite (structure)Solid solutionJournal of Materials Chemistry
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Time-resolved X-ray powder diffraction on a three-way catalyst at the GILDA beamline

2003

Time-resolved X-ray diffraction experiments carried out at the beamline BM08-GILDA of ESRF allowed a study of the structural modifications taking place in a Pt/ceria-zirconia catalyst while the CO oxidation reaction was in progress. The capillary tube in which the sample is stored acts effectively as a chemical microreactor that ensures homogeneity of the sample treatments and minimization of diffusion effects. During the flowing of the reactant CO/He mixture, the investigated catalyst undergoes a fast Ce(IV)-Ce(III) partial reduction that involves the release of one O atom for every two reduced Ce cations. Because Ce(III) has a larger ionic radius than Ce(IV), the structural modification p…

DiffractionNuclear and High Energy PhysicsRadiationMaterials scienceIonic radiusAnalytical chemistryCatalysisCrystallographyLattice constantMixed oxideMicroreactorInstrumentationQuadrupole mass analyzerPowder diffraction
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The hydration enthalpies of Md3+ and Lr3+

1988

Lawrencium (3-min 260Lr) and lighter actinides were produced in the bombardment of a 249Bk target with 18O ions and loaded onto a cation exchange column in 0.05 M α-hydroxyisobutyrate solution at pH=4.85, together with the radioactive lanthanide tracers 166Ho, 171Er and 171Tm. In elutions with 0.12 M α=hydroxyisobutyrate solution (pH=4.85), trivalent Lr was eluted exactly together with the Er tracer and Md was eluted close to Ho. Lr elutes much later than expected based on the known elution positions of the lighter actinides and the expected analogy to the elution positions of the homologous lanthanides. From the measured elution positions, ionic radii were calculated for Lr3+ and Md3+. Sem…

Inorganic ChemistryLanthanideIonic radiusChemistryElutionInorganic chemistryEnthalpyMaterials Chemistrychemistry.chemical_elementActinidePhysical and Theoretical ChemistryIonLawrenciumInorganica Chimica Acta
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Zr- Hf Fractionation During Water-Rock Interaction

2017

International audience; Zr and Hf are two elements having same ionic charge and similar ionic size at a given coordination number. Despite the Zr/Hf ratio is considered to be quite constant in meteorites and lithospheric rocks, seawaters collected from the surface down to varying depths of several Pacific Ocean stations reveal that the Zr/Hf ratio increases by one order of magnitude. Very recent studies have shown that, in both ground waters and lake waters, the Zr/Hf ratio is either higher or lower compared to the interacting minerals displaying a large variability in the distribution of these twin elements. In this communication the possible processes responsible for such a large fraction…

Ionic radius010504 meteorology & atmospheric sciencesCoordination numberEarth and Planetary Sciences(all)Mineralogy[SDU.STU]Sciences of the Universe [physics]/Earth SciencesWeatheringGeneral MedicineFractionation010502 geochemistry & geophysics01 natural sciencesIonZr/Hf weatheringMeteoritenatural watersLithosphereZr/Hf ratioGeologyOrder of magnitude0105 earth and related environmental sciences
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Structural disorder and electronic hybridization in NicMg1−cO solid solutions probed by XANES at the oxygen K edge

2007

A series of NicMg1−cO solid solutions has been studied for the first time looking at the structural disorder by means of x-ray absorption near-edge-structure (XANES) spectroscopy at the oxygen K edge. The experimental XANES signals were analysed within the full multiple scattering formalism and were interpreted taking into account clusters of up to 15 coordination shells around an absorbing oxygen atom. The substitution of nickel atoms by magnesium atoms results in a dramatic decrease of the empty density of states in the conduction band close to the Fermi level due to an exchange of the 3d(Ni)–2p(O) interaction with 3p(Mg)–2p(O). Besides, a simultaneous small decrease of the 3d(Ni)–2p(O) h…

Ionic radiusChemistryFermi levelInorganic chemistryAnalytical chemistrychemistry.chemical_elementCondensed Matter PhysicsXANESsymbols.namesakeNickelK-edgesymbolsDensity of statesGeneral Materials ScienceSpectroscopyMagnesium ionJournal of Physics: Condensed Matter
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Dopant-Host oxide interactions and proton mobility in Gd:BaCeO3

2009

The local structure of Gd:BaCeO3 at different dopant concentrations (2-20%) was studied by X-ray absorption spectroscopy. The EXAFS analysis shows that the environment of the regular Ba2+ and Ce4+ cations is to a limited extent affected by doping. The local structure of gadolinium shows an expansion of the first coordination shell of oxygens, consistent with the ionic radius of Gd3+, but a contraction of the next neighboring shells of cations. In particular, the Ba2+ second neighbors get closer to the dopant, which can be originated by the effective negative charge sharply localized on the dopant. Comparison between EXAFS data of dry and hydrated compounds confirms this interpretation, show…

Ionic radiusDopantAbsorption spectroscopyProtonExtended X-ray absorption fine structureGeneral Chemical EngineeringGadoliniumDopingAnalytical chemistrychemistry.chemical_elementEXAFS proton conductor perovskite barium cerateGeneral ChemistryYttriumCrystallographychemistryMaterials Chemistry
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Classical ionic fluids in the mean spherical approximation

1980

The recently obtained analytical solution of the mean spherical approximation has been used to calculate thermodynamic and structural properties of aqueous solutions of asymmetric electrolytes. The same approximation has also been used to calculate structure functions of pure and mixed molten salts. The agreement between experimental or “quasi-experimental” structure functions and those obtained within the framework of the MSA is quite good especially when the ionic radii are obtained by fitting the long wavelength limit of the structure functions to the isothermal compressibility of the system, under the condition that the diameter ratio is the same as in the crystal.

Ionic radiusLong wavelength limitChemistryIonic bondingThermodynamicsElectrolyteRadial distribution functionInorganic ChemistryCrystalMaterials ChemistryCompressibilityPhysical chemistryPhysical and Theoretical ChemistryMolten saltInorganica Chimica Acta
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