Search results for "Stoichiometry"

showing 10 items of 270 documents

Monitoring the chemical changes in Pd induced by hydrogen absorption using microcantilevers.

2003

Abstract The reactivity of the palladium shaped as a microcantilever is investigated as a function of the hydrogen stoichiometry. A small cell holding the microcantilever is designed to monitor the deflection and the flexural resonance response from high vacuum to a hydrogen gas pressure of several bars. The measurements show that the Young's modulus is accurate if the cantilever is thick enough to be described by a continuum mechanics approach. The orientation distribution function of the palladium grains determined by X-ray diffraction enables to correlate Young's modulus measured using microcantilevers with the elastic constant tensor issued from the literature. The surface stress induce…

CantileverHydrogenHydrideSurface stressUltra-high vacuumAnalytical chemistrychemistry.chemical_elementYoung's modulusAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic Materialssymbols.namesakechemistrysymbolsInstrumentationStoichiometryPalladiumUltramicroscopy
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Detection of gas trace of hydrofluoric acid using microcantilever

2004

Abstract Microcantilevers have been used as a gas sensor in order to detect Hydrofluoric acid (HF) in the concentration range of 0.26–13 ppm. Silicon derived elements (Si 3 N 4 , SiO x ) were chosen to serve as chemical sensitive layer. Cantilever deflection and frequency shift were analyzed and compared as a function of the flow rate and the concentration of the HF molecules. The stoichiometry and roughness of the sensitive layer were found to be of major importance. Results show that the most appropriate signal at the lowest concentration ( x surface by HF. The frequency shift that is mainly governed by the loss in cantilever mass can be used at higher concentration.

CantileverSiliconMetals and AlloysAnalytical chemistrychemistry.chemical_elementSurface finishCondensed Matter PhysicsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsVolumetric flow ratechemistry.chemical_compoundHydrofluoric acidchemistryMaterials ChemistryElectrical and Electronic EngineeringSilicon oxideInstrumentationLayer (electronics)StoichiometrySensors and Actuators B: Chemical
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Evaluating the need for acid treatment prior to d13C and d15N analysis of freshwater fish scales: effects of varying scale mineral content, lake prod…

2010

Carbon isotope Nitrogen isotope Fish scales Acidification De-calcification Stoichiometry
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Distinctive features of diffusion-controlled radiation defect recombination in stoichiometric magnesium aluminate spinel single crystals and transpar…

2020

This work has been performed within the framework of the EUROfusion Enabling Research project: ENR-MFE19.ISSP-UL-02 “Advanced experimental and theoretical analysis of defect evolution and structural disordering in optical and dielectric materials for fusion application”. The views and opinions expressed herein do not necessarily reflect those of the European Commission. Research of A.L, E.F.,, V.S and E.S has been partly supported by the Estonian Research Council grant (PUT PRG619); has been also carried out within the framework of the EUROfusion Consortium and has received funding from the Euratom research and training programme 2014–2018 and 2019–2020 under grant agreement No 633053. The …

CeramicsMaterials scienceKineticsAnalytical chemistrylcsh:Medicine02 engineering and technologyengineering.material01 natural sciencesArticle0103 physical sciencesStructure of solids and liquidsCeramicIrradiationlcsh:Science010302 applied physicsMultidisciplinaryTransparent ceramicsSpinellcsh:R:NATURAL SCIENCES::Physics [Research Subject Categories]021001 nanoscience & nanotechnologyvisual_artSapphirevisual_art.visual_art_mediumengineeringlcsh:QCrystallite0210 nano-technologyStoichiometryScientific Reports
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Effects of overabundant nitrate and warmer temperatures on charophytes: The roles of plasticity and local adaptation

2018

Global change effects, such as warming and increases in nitrogen loading, alter vulnerable Mediterranean aquatic systems, and charophytes can be one of the most affected groups. We addressed the possible interaction between these factors on two populations of the cosmopolitan charophytes Chara hispida and Chara vulgaris. Populations were taken from two different environments, a nitrate-poor mountain lake and a nitrate-rich Mediterranean coastal spring. The laboratory experiment had a 2 × 2 factorial design based on two nitrate levels (similar to and double the local conditions) and two temperatures. Increased temperatures favoured the growth of the four populations, but an increase in nitra…

Charophyte stoichiometry0106 biological sciencesMediterranean climatePhenotypic plasticityPlant ScienceNitrate reactive normsAquatic Science010603 evolutionary biology01 natural scienceschemistry.chemical_compoundNitrate pollutionMacroalgaeNitrateSemi-arid regionEcosystemLocal adaptationPioneer speciesbiologyEcotypeEcology010604 marine biology & hydrobiologyAquatic ecosystembiology.organism_classificationChara vulgarisThermal adaptationchemistryAquatic Botany
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MoO (x≤2) ultrathin film growth from reactions between metallic molybdenum and TiO2 surfaces

2001

Abstract Exposures to oxygen at room temperature and annealings under vacuum were carried out on deposits obtained from molybdenum interacting with (1 1 0) TiO 2 surfaces in order to obtain molybdenum oxide ultra thin films. Exposures to oxygen at room temperature show that the interfacial molybdenum oxide layers resulting from the TiO 2 /Mo interactions are inactive towards oxygen whereas the metallic molybdenum clusters, which grew on top of the interfacial layers, oxidise into MoO 3 . Besides, during annealings under vacuum, substrate oxygen anions can diffuse into the deposit. Thus, between 400 and 500°C, molybdenum oxide layers are progressively oxidised into MoO 2 . Moreover, from the…

ChemistryAnnealing (metallurgy)Inorganic chemistryGeneral Physics and Astronomychemistry.chemical_elementSurfaces and InterfacesGeneral ChemistryCondensed Matter PhysicsSurfaces Coatings and FilmsMetalVacuum depositionX-ray photoelectron spectroscopyMolybdenumPhysical vapor depositionvisual_artvisual_art.visual_art_mediumThin filmStoichiometryApplied Surface Science
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2021

We report on the thermodynamic, structural, and dynamic properties of a recently proposed deep eutectic solvent, formed by choline acetate (ChAc) and urea (U) at the stoichiometric ratio 1:2, hereinafter indicated as ChAc:U. Although the crystalline phase melts at 36–38 °C depending on the heating rate, ChAc:U can be easily supercooled at sub-ambient conditions, thus maintaining at the liquid state, with a glass–liquid transition at about −50 °C. Synchrotron high energy x-ray scattering experiments provide the experimental data for supporting a reverse Monte Carlo analysis to extract structural information at the atomistic level. This exploration of the liquid structure of ChAc:U reveals th…

ChemistryHydrogen bondGeneral Physics and AstronomyDeep eutectic solventCrystallographysymbols.namesakechemistry.chemical_compoundMolecular dynamicsPhase (matter)symbolsUreaPhysical and Theoretical Chemistryvan der Waals forceSupercoolingStoichiometryThe Journal of Chemical Physics
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Adsorption of 3d Transition Elements on a TiO2(110) Surface.

2008

International audience; A first-principles study on the adsorption of 3d transition metal atoms on a stoichiometric TiO2(110) surface is reported. For all 3d elements except Cu, the most stable on-surface adsorption site is a site where the adatom binds to two twofold and one threefold surface oxygen atoms. For Ti, V, and Cr, however, a subsurface site, where the adatom substitutes a sixfold Ti atom, is more stable. The adatoms are oxidized in all cases. The charge transfer to the substrate is larger for the substitutional site than for the on-surface adsorption sites and decreases with atomic number along the 3d series. The relative stabilities of the adsorption sites are discussed in term…

ChemistryInorganic chemistry02 engineering and technologySubstrate (electronics)021001 nanoscience & nanotechnology01 natural sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsElectronegativityA-siteCrystallographyGeneral EnergyAdsorptionTransition metal0103 physical sciencesAtomAtomic numberPhysical and Theoretical Chemistry010306 general physics0210 nano-technologyStoichiometry
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Experimental set up for determining the temperature-oxygen partial pressure conditions during synthesis of spinel oxide nanoparticles

1997

Abstract Nanometric spinel oxide powders, Fe 3− x M x O 4 , where M is a transition element, have been synthetized by soft chemistry. This method generally leads to a non-stoichiometric phase, Fe 3− x M x O 4+δ where δ is the deviation from stoichiometry so that further annealing at low temperatures around 450°C and low oxygen partial pressure around 10 −25 Pa given by N 2 /H 2 /H 2 O gas mixtures is required: this enables a stoichiometric compound to be obtained and a nanometric size to be maintained. The complete set up consisting of a gas mixer, a thermogravimetric apparatus and a preparative furnace is described. Some results concerning the conditions of temperature and oxygen partial p…

ChemistryInorganic chemistrySpinelOxideAnalytical chemistryVanadiumchemistry.chemical_elementGeneral ChemistryPartial pressureengineering.materialCondensed Matter PhysicsOxygenSoft chemistrychemistry.chemical_compoundTransition metalengineeringGeneral Materials ScienceStoichiometry
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A 4-tert-butylcalix[4]arene tetrahydroxamate podand based on the 1-oxypiperidine-2-one (1,2-PIPO−) chelate. Self-assembly into a supramolecular ionop…

2014

An octadentate tetrahydroxamic calix[4]arene podand incorporating 1-hydroxypiperidine-2-one (1,2-PIPOH) binding units has been designed as a specific chelator for tetravalent metal cations like Zr4+ or Hf4+. This receptor, which can be considered as the first ever abiotic ligand possessing only cyclic six-membered hydroxamate groups, has been synthesized and characterized in its tetraprotonated form (1H4). Contrary to expectation, however, this new chelator did not form a 1 : 1 complex upon reaction with M(acac)4 (M = Zr and Hf; acac = acetylacetonate), but rather self-assembled into a dimeric species of 2 : 2 stoichiometry. The latter could be characterized in solution by mass spectrometry…

ChemistryLigandStereochemistryGeneral Chemical EngineeringSupramolecular chemistryIonophoreGeneral ChemistryNuclear magnetic resonance spectroscopyAdductMetalvisual_artPolymer chemistryvisual_art.visual_art_mediumChelationStoichiometryRSC Adv.
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