Search results for "Medium"

showing 10 items of 3746 documents

Structural Characterization of Surfactant-Coated Bimetallic Cobalt/Nickel Nanoclusters by XPS, EXAFS, WAXS, and SAXS

2011

Cobalt nickel bimetallic nanoparticles were synthesized by changing the sequence of the chemical reduction of Co(II) and Ni(II) ions confined in the core of bis(2-ethylhexyl)phosphate (2)., and Ni(DEHP)(2). The reduction was carried out by mixing, sequentially or contemporaneously, fixed amounts of n-heptane solution of Co(DEHP)2 and Ni(DEHP)2 micelles with a solution of sodium borohydride in ethanol at a fixed (reductant)/(total metal) molar ratio. This procedure involves the rapid formation of surfactant-coated nanoparticles, indicated as Co/Ni (Co after Ni), Ni/Co (Ni after Co), and Co + Ni (simultaneous), followed by their slow separation as nanostructures embedded in a sodium bis(2-eth…

inorganic chemicalsendocrine systemMaterials sciencechemistry.chemical_elementNanoparticleNanoclustersMetalSodium borohydridechemistry.chemical_compoundX-ray photoelectron spectroscopyNANOPARTICLESPARTICLESBimetallic Cobalt/Nickel Nanoclusters. XPS. EXAFS. WAXS. SAXS.GOLDPhysical and Theoretical ChemistryBimetallic stripMICELLESSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyNickelGeneral Energychemistryvisual_artNANOPARTICLES; PARTICLES; GOLD; MICELLESvisual_art.visual_art_mediumCobaltNuclear chemistry
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Removal of hexavalent chromium from wastewaters by bone charcoal

1999

The adsorption of hexavalent chromium onto bone charcoal was studied as a function of time, amount of charcoal, pH, concentration of chromium and sample volume. The cross interference with other elements was also investigated. Tests were carried out with solutions of chromium(VI) at concentrations between 5 and 25 mg · L–1. Chromium removal efficiencies higher than 90% were achieved at pH = 1 using 2 g of bone charcoal and a stirring time in the order of 30 min. Acid and alkaline pretreatments of bone charcoal did not improve the sorption capacity of bone charcoal against Cr(VI). The presence of other ions had practically no influence on the chromium removal. The presence of a matrix of tan…

inorganic chemicalsfood and beverageschemistry.chemical_elementMineralogySorptionrespiratory systemequipment and suppliesBiochemistryTannery effluentscarbohydrates (lipids)Matrix (chemical analysis)ChromiumSample volumechemistry.chemical_compoundAdsorptionchemistryvisual_artvisual_art.visual_art_mediumHexavalent chromiumCharcoalNuclear chemistryFresenius' Journal of Analytical Chemistry
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Novel method for determination of tritium depth profiles in metallic samples

2019

Tritium accumulation in fusion reactor materials is considered a serious radiological issue, therefore a lot of effort has been concentrated on the development of radiometric techniques. A novel method, based on gradual dissolution, for the determination of the total tritium content and its depth profiles in metallic samples is demonstrated. This method allows for the measurement of tritium in metallic samples after their exposure to a hydrogen and tritium mixture, tritium containing plasma or after irradiation with neutrons resulting in tritium formation. In this method, successive layers of metal are removed using an appropriate etching agent in the controlled regime and the amount of evo…

inorganic chemicalsfusionNuclear and High Energy PhysicsMaterials scienceNuclear engineeringchemistry.chemical_elementheliumBlanket114 Physical sciences01 natural sciences010305 fluids & plasmasblanketMetalirradiated berylliumjet0103 physical sciencespolycyclic compounds010306 general physicsHeliumbreeding blanketJet (fluid)Fusiontritiumbehaviororganic chemicalshydrogen diffusiontemperatureiter-like-wallFusion powerfirst wallberylliumCondensed Matter Physicschemistryvisual_arttransportcardiovascular systemvisual_art.visual_art_mediumdepth profileTritiumBerylliumNuclear Fusion
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From Single Molecules to Nanoscopically Structured Materials: Self-Assembly of Metal Chalcogenide/Metal Oxide Nanostructures Based on the Degree of P…

2011

A chemically specific and facile method for the immobilization of metal oxide nanoparticles onto the surface of IF-MoS2 nested fullerenes is reported. The modification strategy is based on the chalcophilic affinity of transition metals such as Fe2+/Fe3+, Fe3+, or Zn2+ as described by the Pearson HSAB concept. The binding capabilities of the 3d metals are dictated by their Pearson hardness. Pearson hard cations such as Fe3+ (Fe2O3) do not bind to the chalcogenide surfaces; borderline metals such as Fe2+ (Fe3O4) or Zn2+ (ZnO) bind reversibly. Pearson-soft metals like Au bind irreversibly. The immobilization of metal oxide nanoparticle colloids was monitored by transmission electron microscopy…

inorganic chemicalslayered compound; metal chalcogenide; metal oxide; nanoparticle; reversible surface functionalizationMaterials scienceChalcogenidenanoparticleGeneral Chemical EngineeringInorganic chemistrylayered compoundOxideNanoparticleGeneral Chemistrymetal oxideMetalchemistry.chemical_compoundTransition metalchemistryTransmission electron microscopyvisual_artreversible surface functionalizationMaterials Chemistryvisual_art.visual_art_mediumHSAB theoryHigh-resolution transmission electron microscopymetal chalcogenideChemistry of Materials
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Formation of nanosized strontium substituted hydroxyapatites

2012

Incorporation of specific elements into calcium phosphates offers the combination of a bioactive material and a therapeutic effect. This is important for improving the integration of implants as well as treating medical conditions. Strontium is a suitable candidate and displays the ability to stimulate bone growth and reducing bone resorption. This study investigated the formation of strontium carbonated hydroxyapatite nanoparticles from an amorphous phase. Crystallization of carbonated hydroxyapatite occurred at 585 o C, but samples with an intended 25% and 75% replacement of calcium with strontium crystallized at 624 o C. Heat treatment at the crystallization temperature revealed that str…

inorganic chemicalsmusculoskeletal diseasesBone growthAlkaline earth metalStrontiumMaterials scienceMatériauxMineralogychemistry.chemical_elementCalciumHeat treatmentApatiteHydroxyapatiteNanocrystalslaw.inventionchemistryChemical engineeringStrontiumlawvisual_artCalcium Compoundsvisual_art.visual_art_mediumHydroxyapatitesCrystallizationIOP Conference Series: Materials Science and Engineering
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Hydrothermally Synthesized Strontium Peroxyapatite

2015

The current research focuses on peroxide ion incorporation in the structure of strontium hydroxyapatite (SrHAp) by exposure to H2O2 ina closed hydrothermal vessel under mild conditions at 130 to 170 °C. Peroxide enriched strontium apatite (SrPerAp) was characterized for structure by X-Ray diffraction, for peroxide content- by permanganometric titration and then viewed by SEM. This study continued from previous work that used 30%H2O2 and showed a higher included peroxide content after processing with 50% H2O2 at 130 °C 70% of the theoretical peroxide content in apatitic channels of strontium apatite. This is the highest peroxide content incorporated to date and employs a lower temperature th…

inorganic chemicalspermanganatometric titrationStrontiumInorganic chemistrystrontium peroxyapatiteGeneral Engineeringchemistry.chemical_elementhydrogen peroxideStrontium hydroxyapatitePeroxideLower temperatureApatiteHydrothermal circulationchemistry.chemical_compoundchemistryvisual_artvisual_art.visual_art_mediumTitrationHydrogen peroxideNuclear chemistryAdvanced Materials Research
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Protected but Accessible: Oxygen Activation by a Calixarene-Stabilized Undecagold Cluster

2013

DFT computations show that calixarenes stabilize subnanometer Au11 clusters allowing access of small molecules like O2 to reactive metal sites in the core. Maximum of three dioxygen molecules can bind to the cluster, and they are activated to a superoxo O2(-) state. This study predicts that gold clusters could act as viable oxidation catalysts at ambient conditions based on similar principles as the metal centers in enzymes.

inorganic chemicalsta214ta114ChemistryInorganic chemistrychemistry.chemical_elementGeneral ChemistryPhotochemistryBiochemistrySmall moleculeOxygenCatalysisCatalysisMetalColloid and Surface Chemistryvisual_artUndecagoldCalixarenevisual_art.visual_art_mediumCluster (physics)MoleculeJournal of the American Chemical Society
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Diastereomeric control of enantioselectivity: evidence for metal cluster catalysis

2014

Enantioselective hydrogenation of tiglic acid effected by diastereomers of the general formula [(μ-H)2Ru3(μ3-S)(CO)7(μ-P–P*)] (P–P* = chiral Walphos diphosphine ligand) strongly supports catalysis by intact Ru3 clusters. A catalytic mechanism involving Ru3 clusters has been established by DFT calculations. peerReviewed

intactLigandStereochemistryMetals and AlloysEnantioselective synthesisDiastereomerTiglic acidGeneral Chemistryhydrogenation catalysisCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysisMetalchemistry.chemical_compoundchemistryvisual_artMaterials ChemistryCeramics and Compositesvisual_art.visual_art_mediumCluster (physics)triruthenium clustersta116Chemical Communications
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Intellectual Capital – The Key for Sustainable Competitive Advantage for the SME's Sector

2015

Abstract With the adoption of the Lisbon Agenda and its major objective, namely that the EU would become the most dynamic and competitive knowledge based economy in the world, it became clear the Small and Medium Enterprises (SME's) are the especially affected by these plans, because they represent the driving force for the European economy. In this context of creating and maintaining a competitive advantage for the SME's, it is crucial for them to make good use of the intellectual capital of their employees, in an efficient and proficient manner, in order to increase their potential for innovation. The aim of this article is to show, through an original argumentation, based on the analysis…

intangible assetsbusiness.industryKnowledge economyGeneral EngineeringEnergy Engineering and Power TechnologyContext (language use)International tradeCompetitive advantageArgumentation theoryIntellectual capitalintellectual capitalOrder (exchange)SME's ;Key (cryptography)competitive advantageSmall and medium-sized enterprisesBusinessIndustrial organizationProcedia Economics and Finance
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UV variability and accretion in NGC 2264

2015

Photometric variability is a distinctive feature of young stellar objects; exploring variability signatures at different wavelengths provides insight into the physical processes at work in these sources. We explore the variability signatures at ultraviolet (UV) and optical wavelengths for several hundred accreting and non-accreting members of the star-forming region NGC 2264 (~3Myr). Cone search capability for table J/A+A/581/A66/table2 (Median photometry, variability amplitudes, light curve rms, J index, and color slopes for members monitored at CFHT)

interstellar mediumAccretionUltraviolet astronomyAstrophysics and AstronomyAstrophysics::High Energy Astrophysical PhenomenaPhysicsAstrophysics::Cosmology and Extragalactic Astrophysicsstellar astronomyYoung stellar objectsOptical astronomyPhotometryobservational astronomyAstrophysics::Solar and Stellar AstrophysicsAstrophysics::Earth and Planetary AstrophysicsCCD photometryAstrophysical ProcessesNatural SciencesSloan photometryAstrophysics::Galaxy Astrophysics
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