Search results for "MATTER"

showing 10 items of 16762 documents

X-ray Photoelectron-spectroscopy Investigation of Pumice-supported Nickel-catalysts

1995

Pumice-supported nickel catalysts, prepared by the method of slow homogeneous precipitation with urea, were analysed by x-ray photoelectron spectroscopy (XPS). By comparison with similarly prepared silica- and alumina-supported nickel catalysts, a preferential interaction of Ni2+ with Al3+ of the support has been determined. A quantitative XPS analysis indicated large segregation of nickel to the surface. The treatment with H2 at 673 K and 1073 K produced a partial reduction of Ni+2 to Ni0. The extent of the reduction was largest at 1073 K and in this case the reduced Ni in the metallic phase was detectable by x-ray diffraction. A decrease of the Ni 2p/Si 2p intensity ratio occurring in the…

inorganic chemicalsPrecipitation (chemistry)ChemistryAnalytical chemistrySinteringchemistry.chemical_elementSurfaces and InterfacesGeneral ChemistryCondensed Matter PhysicsSurfaces Coatings and FilmsCatalysisMetalNickelTransition metalX-ray photoelectron spectroscopyvisual_artX-ray crystallographyMaterials Chemistryvisual_art.visual_art_medium
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Study by static SIMS, XPS and UPS of the adsorption of cyanogen on (100) Ni surfaces

2000

Abstract The interaction of cyanogen with (100) Ni surfaces at room temperature was studied using secondary ion mass spectrometry in a static mode, and photoemission spectroscopies (XPS and UPS). It has been shown that cyanogen is adsorbed on this nickel surface in a dissociative mode: atomic carbon and nitrogen are present on the surface as well as CN fragments. These adsorbed species have been characterized by XPS and UPS. Increasing the temperature in the 400 K range increases the rate of the dissociation reaction of CN into atomic carbon and nitrogen. Moreover carbon is found to dissolved into the bulk for temperatures as low as 475 K. No evidence has been found of a polymerized form of…

inorganic chemicalsStatic secondary-ion mass spectrometryChemistryCyanogenAnalytical chemistrychemistry.chemical_elementSurfaces and InterfacesCondensed Matter PhysicsSurfaces Coatings and FilmsSecondary ion mass spectrometrychemistry.chemical_compoundNickelAdsorptionX-ray photoelectron spectroscopyChemisorptionMaterials ChemistryCarbonSurface Science
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Adsorption and desorption surface dynamics of gaseous adsorbate on silicate-1 by molecular dynamics simulation

2013

The dynamics of adsorption and desorption of gaseous molecules on the external surface of a crystal and a membrane of zeolite silicate-1 is investigated by molecular dynamics simulation. The gases ...

inorganic chemicalsSticking coefficientChemistryGeneral Chemical EngineeringAnalytical chemistryGeneral ChemistryCondensed Matter PhysicsSilicaterespiratory tract diseasesQuantitative Biology::Subcellular ProcessesCrystalCondensed Matter::Materials Sciencechemistry.chemical_compoundMolecular dynamicsAdsorptionMembraneChemical physicsModeling and SimulationDesorptionGeneral Materials ScienceAstrophysics::Earth and Planetary AstrophysicsPhysics::Chemical PhysicsZeoliteAstrophysics::Galaxy AstrophysicsInformation SystemsMolecular Simulation
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Structure-based evaluation of the resonance interactions and effectiveness of the charge transfer in nitroamines

2011

Structural data for five nitroamines of general formula Me2N–G–NO2 show effectiveness of the ground-state charge transfer to be most and least efficient in N,N-dimethylnitramine and in 4-N,N-dimethylamino-β-nitrostyrene, respectively. Electron-donor power of the amino nitrogen atom in the latter compound is less than that in 4-nitro-β-N,N-dimethylaminostyrene (these two compounds are isomers). Natural population analysis shows that the charge transfer from the amino to the nitro oxygen atoms is most effective in N,N-dimethylnitramine, Me2N–NO2. The nitro oxygen atoms are not the only acceptors of the negative charge lost by the amino nitrogen atom. The nitro group in two substituted nitrobe…

inorganic chemicalsSubstituentCharge (physics)Resonance (chemistry)Ring (chemistry)Condensed Matter PhysicsMedicinal chemistryNitrobenzenechemistry.chemical_compoundchemistryComputational chemistryNitroMoleculePhysical and Theoretical ChemistryBenzeneStructural Chemistry
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The phase coexistence method to obtain surface free energies and nucleation barriers: a brief review

2018

A recently developed method where one analyses the finite size effects associated with liquid–solid phase equilibria including vapour–crystal coexistence is briefly reviewed. It is shown that the e...

inorganic chemicalsSurface (mathematics)Materials scienceBiophysicsNucleation010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical scienceslaw.inventionColloidChemical physicslawPhase (matter)biological sciences0103 physical sciencesFree energiesPhysical and Theoretical ChemistryCrystallization010306 general physicsMolecular BiologyMolecular Physics
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Novel organo-modifier for thermally-stable polymer-layered silicate nanocomposites

2015

A new novel approach for the stabilisation of polymer-clay nanocomposites has been investigated based on reacting chemically an antioxidant function, a hindered phenol moiety, with an organic modifier based on a quaternary ammonium salt. The chemically linked antioxidant-containing organic modifier (AO-OM) was then introduced into natural montmorillonite (MMt) through a cation-exchange reaction resulting in antioxidant-containing organo-modified clay (AO-OM-MMt). The new antioxidant-containing modified clay, along with other organo-modified clays having a similar organo-modifier but without the reacted antioxidant, were characterised by spectroscopic, thermogravimetric and x-ray diffraction…

inorganic chemicalsThermogravimetric analysisMaterials sciencePolymers and PlasticsPolymer-clay nanocompositeSalt (chemistry)complex mixtureschemistry.chemical_compoundPolymer chemistryMaterials ChemistryMoietyMechanics of MaterialAntioxidant-containing organomodifierchemistry.chemical_classificationMaterials Chemistry2506 Metals and AlloyNanocompositePolymers and PlasticModified montmorillonitePolymerCondensed Matter PhysicsExfoliation jointPA11MontmorilloniteSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryChemical engineeringMechanics of MaterialsDispersion (chemistry)
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Determination of the Absolute Density of Fe3+ and Ni2+ Ions in Langmuir-Blodgett Films

1996

By means of the Langmuir–Blodgett (LB) technique, mono- and multilayers of Ni2+ and Fe3+ containing fatty acid salts are transferred onto silicon wafers. After thermal treatment, oxidic layers can be produced. The absolute amounts of Fe3+ and Ni2+ ions per monolayer of LB film were measured and calculated by three different methods. In the case of nickel, the amount expected from theory and preparation conditions was obtained experimentally. In contrast, about twice the number of Fe3+ ions as expected is transferred. An explanation can be given by the presence of hydroxide groups bound to iron. The mean film thickness of the oxidic layers after thermal treatment was estimated where the thic…

inorganic chemicalsX-rayAnalytical chemistrychemistry.chemical_elementSurfaces and InterfacesGeneral ChemistryThermal treatmentCondensed Matter PhysicsLangmuir–Blodgett filmSurfaces Coatings and FilmsIonchemistry.chemical_compoundNickelchemistryMonolayerMaterials ChemistryHydroxideStearic acidSurface and Interface Analysis
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Gelation of semiflexible polyelectrolytes by multivalent counterions

2012

Filamentous polyelectrolytes in aqueous solution aggregate into bundles by interactions with multivalent counterions. These effects are well documented by experiment and theory. Theories also predict a gel phase in isotropic rodlike polyelectrolyte solutions caused by multivalent counterion concentrations much lower than those required for filament bundling. We report here the gelation of Pf1 virus, a model semiflexible polyelectrolyte, by the counterions Mg(2+), Mn(2+) and spermine(4+). Gelation can occur at 0.04% Pf1 volume fraction, which is far below the isotropic-nematic transition of 0.7% for Pf1 in monovalent salt. Unlike strongly crosslinked gels of semiflexible polymers, which stif…

inorganic chemicalschemistry.chemical_classificationAqueous solutionChemistrymacromolecular substancesGeneral ChemistryPolymerCondensed Matter PhysicsArticlePolyelectrolyteProtein filamentChemical physicsPolymer chemistryVolume fractionElasticity (economics)CounterionSofteningSoft Matter
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On the effect of the nature of counterions on the self-assembly of polyoxyethylene alkyl ether carboxylic acids

2020

In this contribution, we investigate the effect of the type of counterion on the properties of dilute solutions of polyoxyethylene alkyl ether carboxylic acids. Two different surfactants, presenting an oleic acid alkyl chain and on-average five and nine ethylene oxide units, and terminated by a weakly anionic carboxymethyl group were studied. The surfactants were gradually ionized with sodium hydroxide, arginine, and choline hydroxide. The solutions properties were probed by light scattering, electrophoretic mobility, density and sound velocity measurements, as well as by small-angle neutron scattering. To our initial surprise, no specific effect arising from the nature of the counterion co…

inorganic chemicalschemistry.chemical_classificationEthylene oxideCharge density02 engineering and technologyGeneral ChemistryNeutron scattering010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical scienceschemistry.chemical_compoundPulmonary surfactantchemistrySodium hydroxideCounterion condensationSurfactantPolymer chemistryCounterion0210 nano-technologyAlkylSettore CHIM/02 - Chimica FisicaSoft Matter
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Organic matter and wettability characteristics of wildfire ash from Mediterranean conifer forests

2015

Abstract Thermogravimetric analysis (TGA) and water repellency (wettability) determination of ash samples collected following wildfires at four different Mediterranean conifer forest sites in eastern Spain were conducted to provide insights into variations in key chemical and physical characteristics of ash. TGA allowed the evaluation of organic matter (OM) and inorganic carbonate (IC) characteristics and their role in ash wettability. Thermogravimetric profiles were recorded for 40 ash samples (ten from each site). The persistence of water repellency of all ash samples was assessed by the Water Drop Penetration Time (WDPT) test. OM contents decreased, whilst OM stability indices and IC con…

inorganic chemicalschemistry.chemical_classificationMediterranean climateHydrologyThermogravimetric analysisPhysicsCarbon sinkCombustionchemistry.chemical_compoundchemistryWater repellentEnvironmental chemistryEnvironmental scienceCarbonateOrganic matterWettingBiologyEarth-Surface Processes
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