Search results for "Metals"

showing 10 items of 2013 documents

Improvement of the photo-stability of polystyrene-block-polybutadiene-block-polystyrene through carbon nanotubes

2015

Abstract The photo-stability of Polystyrene-Polybutadiene-Polystyrene (SBS) based nanocomposites containing bare multi-walled carbon nanotubes (CNTs) and carbon nanotubes bearing carboxylic functional groups (CNTs-COOH) in comparison to that of pristine SBS has been studied. The photo-oxidation of pristine SBS occurs through crosslinking reactions and oxidized species formation and both these processes begin at early stage of exposure. The formation of crosslinking, formerly in polybutadiene phase, assessed by spectroscopical (FTIR), mechanical, dynamic mechanical and rheological analysis, leads to occurrence of internal mechanical stresses in the solid state and the SBS samples become prem…

Solid-state chemistryPolystyrene-polybutadiene-polystyrene copolymerMaterials sciencePolymers and PlasticsCarbon nanotubesCarbon nanotubes; Photo-stability; Polystyrene-polybutadiene-polystyrene copolymer; Structural changes; Condensed Matter Physics; Mechanics of Materials; Polymers and Plastics; Materials Chemistry; 2506; Metals and AlloysCarbon nanotubeCarbon nanotubelaw.inventionchemistry.chemical_compoundPolybutadieneRheologylawPhase (matter)Structural changeMaterials ChemistryMechanics of MaterialFourier transform infrared spectroscopyComposite materialStructural changesNanocompositePolymers and PlasticMetals and AlloysCondensed Matter PhysicsPhoto-stabilitychemistryChemical engineeringMechanics of MaterialsPolystyrene2506
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Halogen bonding drives the self-assembly of piperazine cyclophanes into tubular structures.

2009

Halogen bonding with 1,4-diiodotetrafluorobenzene leads to the self-assembly of piperazine cyclophanes into well-defined tubular structures with solvent inclusion.

SolventPiperazinechemistry.chemical_compoundHalogen bondchemistryMaterials ChemistryMetals and AlloysCeramics and CompositesOrganic chemistryGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChemical communications (Cambridge, England)
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Design, characterization and evaluation of hydroxyethylcellulose based novel regenerable supersorbent for heavy metal ions uptake and competitive ads…

2017

Abstract Hydroxyethylcellulose succinate-Na (HEC-Suc-Na) was designed and evaluated for removal of some heavy metal ions from aqueous solution. Pristine sorbent HEC-Suc-Na was thoroughly characterized by FTIR and solid-state CP/MAS 13C NMR spectroscopy, SEM-EDS and zero point charge analyses. Langmuir isotherm, pseudo second order kinetic and ion exchange models provided best fit to the experimental data of sorption of metal ions. Maximum sorption capacities of supersorbent HEC-Suc-Na for sorption of heavy metal ions from aqueous solution as calculated by Langmuir isotherm model were found to be 1000, 909.09, 666.6, 588 and 500 mg g−1 for Pb(II), Cr(VI), Co(II), Cu(II) and Ni(II), respectiv…

SorbentMetal ions in aqueous solutionInorganic chemistry02 engineering and technology010501 environmental sciences01 natural sciencesBiochemistryWater Purificationsymbols.namesakeStructural BiologyMetals HeavyGalvanic cellFourier transform infrared spectroscopyCelluloseMolecular Biology0105 earth and related environmental sciencesAqueous solutionIon exchangeChemistryTemperatureLangmuir adsorption modelSorptionGeneral MedicineHydrogen-Ion Concentration021001 nanoscience & nanotechnologyKineticsDrug DesignsymbolsAdsorption0210 nano-technologyWater Pollutants ChemicalInternational Journal of Biological Macromolecules
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Biochar from byproduct to high value added material – A new adsorbent for toxic metal ions removal from aqueous solutions

2018

Abstract An activated biochar coming from pyrolysis of dead Posidonia oceanica residues has been tested as adsorbent material for Cd2+, Pb2+ and Cu2+ ions. The biomass, the activated and the non activated biochars were previously characterized by using several instrumental techniques. The pH of metal ion solution in kinetic and thermodynamic adsorption experiments was fixed at 5 whilst, the dependence on ionic medium, ionic strength and temperature have been evaluated carrying out batch experiments at different experimental conditions. Differential Pulse Anodic Stripping Voltammetry and Inductively Coupled Plasma Optical Emission Spectroscopy have been used to measure the metal ion concentr…

Speciation020209 energyMetal ions in aqueous solutionInorganic chemistryIonic bondingToxic metal02 engineering and technology010501 environmental sciences01 natural sciencesAdsorptionBiochar0202 electrical engineering electronic engineering information engineeringMaterials ChemistryToxic metalsSettore CHIM/01 - Chimica AnaliticaPhysical and Theoretical ChemistryMaterialsSpectroscopy0105 earth and related environmental sciencesAqueous solutionChemistryPosidonia oceanicaCondensed Matter PhysicsAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsBiocharAnodic stripping voltammetryIonic strengthAdsorptionPyrolysisJournal of Molecular Liquids
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Interaction of UO2(2+) with ATP in aqueous ionic media.

2005

Interaction of dioxouranium(VI) (uranyl) ion with ATP was studied by ligand/proton and metal/hydroxide displacement technique, at very low ionic strength and at I=0.15 mol L(-1), in aqueous Me4NCl and NaCl solutions, at t=25 degrees C. Measurements were carried out in the pH range 3-8.5, before the formation of precipitate. Computer analysis allowed us to find the quite stable species UO2(ATP)H2(0), UO2(ATP)H-, UO2(ATP)2-, UO2(ATP)2(6-), UO2(ATP)2H2(4-) and UO2(ATP)(OH)3- whose formation constants are (at I=0 mol L(-1)) logbeta(112)=18.21, logbeta(111)=14.70, logbeta(110)=9.14, logbeta(120)=12.84, logbeta(122)=24.82, and logbeta(11-1)=2.09, respectively. Different values were obtained in th…

SpeciationInorganic chemistryIonic mediaBiophysicsIonic bondingLigandsBiochemistryComplexeIonMetalchemistry.chemical_compoundAdenosine TriphosphateMetals HeavySettore CHIM/01 - Chimica AnaliticaAqueous solutionLigandHydrolysisOrganic ChemistryWaterHydrogen-Ion ConcentrationUranylUranium CompoundsDioxouranium(VI)ATPchemistryStability constants of complexesvisual_artDependence on medium of stability constantvisual_art.visual_art_mediumHydroxideBiophysical chemistry
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Structural reorganisation in polytopic receptors revealed by kinetic studies.

2010

One of the first kinetic studies of metal ion reorganisation between the different sites of a tritopic polyaza ligand reveals well defined pathways for the movement of the metal ion.

Spectrometry Mass Electrospray IonizationBinding SitesMacrocyclic CompoundsMagnetic Resonance SpectroscopyMolecular StructureStereochemistryChemistryLigandMetals and AlloysGeneral ChemistryKinetic energyLigandsCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMetalCrystallographyKineticsvisual_artMaterials ChemistryCeramics and Compositesvisual_art.visual_art_mediumReceptorCopperChemical communications (Cambridge, England)
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Series of Near-IR-Absorbing Transition Metal Complexes with Redox Active Ligands

2020

New soluble and intensely near-IR-absorbing transition metal (Ti, Zr, V, Ni) complexes were synthesized using a redox non-innocent N,N&rsquo

Spectrometry Mass Electrospray IonizationMagnetic Resonance SpectroscopyElectronsChemistry Techniques SyntheticCrystallography X-RayLigandsArticlelcsh:QD241-441Magneticslcsh:Organic chemistryX-Ray DiffractionCoordination ComplexesNickelTransition Elementsorgaaniset yhdisteetSpectroscopy Near-InfraredMolecular Structureredox-active ligandnon-innocent ligandsElectrochemical Techniquesliganditkompleksiyhdisteetmetal organic complexMetalsElectronicsOxidation-Reduction
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Surfactant self-assembly in the gas phase: Bis(2-ethylhexyl)sulfosuccinate- alkaline metal ion aggregates

2008

Molecular dynamics (MD) simulations were conducted for systems in vacuo consisting of n AOT anions (bis(2-ethylhexyl)sulfosuccinate ions) and n 1 or n Na+ ions up to n = 20. For n = 15, positively charged systems with Li+, K+, and Cs+ cations were also considered. All systems were observed to form reverse micelle-like aggregates whose centre is occupied by cations and polar heads in a very compact solid-like way, while globally the aggregate has the form of an elongated and rather flat ellipsoid. Various types of statistical analyses were carried out on the systems to enlighten structural and dynamical properties including gyration radius, atomic pair correlation functions, atomic B-factor …

Spectrometry Mass Electrospray IonizationREVERSE MICELLESElectrospray ionizationInorganic chemistrySupramolecular chemistrySalt (chemistry)LithiumMass SpectrometryIonSurface-Active AgentsPulmonary surfactantMaterials ChemistryWATERPhysical and Theoretical ChemistryAlkylchemistry.chemical_classificationChemistrySodiumSuccinatesAlkali metalSurfaces Coatings and FilmsSolutionsNANOCRYSTALSMetalsMESOSTRUCTURED FLUIDSGasesSelf-assembly
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Testing of the region of Murcia soils by near infrared diffuse reflectance spectroscopy and chemometrics.

2008

A partial least squares near infrared (PLS-NIR) method has been developed for the determination of several physicochemical parameters in soils from different locations of the Region of Murcia. The method was based on the proper chemometric treatment of diffuse reflectance spectra of soil samples. Reflectance spectra were scanned from samples stored in glass vials in the NIR region between 800 and 2600 nm, averaging 36 scans per spectrum at a resolution of 8 cm(-1). Models were built using reference data of 39 samples selected from a dendrogram obtained after hierarchical cluster analysis of NIR spectra of soils and prediction parameters were established from a validation set of 109 addition…

Spectroscopy Near-InfraredSoil testDiffuse reflectance infrared fourier transformChemistryNear-infrared spectroscopyAnalytical chemistryMineralogyInfrared spectroscopyAnalytical ChemistryChemometricsSoilMetalsPartial least squares regressionDiffuse reflectionOrganic ChemicalsSpectroscopyTalanta
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Chemical characterization of ancient liturgical vestment (chasuble) by Inductively Coupled Plasma–Optical Emission Spectrometry (ICP–OES)

2016

Abstract This paper presents the chemical characterization of the yarns of an ancient liturgical vestment (chasuble). The samples have been analyzed for Al, Ag, Au, Cd, Co, Cr, Cu, Ni, Pb and Zn using amounts always less than 1 mg by Inductively Coupled Plasma–Optical Emission Spectrometry (ICP-OES). Except a sample, silver is the most abundant element in all the yarns. In the samples containing silver, it ranged from 68 to 97%. Only two samples contain aluminum. Although the investigated chasuble is recorded in the inventory as an artifact of the XV century, a part of the yarns is composed of materials attributed to later period. In fact, the voluntary use of aluminum in metal alloys is du…

Spectroscopy.Period (periodic table)Analytical chemistrychemistry.chemical_element02 engineering and technology01 natural sciencesSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturaliTextile yarnAnalytical ChemistryMetalAluminiumSettore CHIM/01 - Chimica AnaliticaOptical emission spectrometryICP–OESSpectroscopyChemistryMetal010401 analytical chemistry021001 nanoscience & nanotechnology0104 chemical sciencesCharacterization (materials science)MetalsInductively coupled plasma atomic emission spectroscopyvisual_artvisual_art.visual_art_mediumLiturgical vestmentInductively coupled plasma0210 nano-technologyTextile yarnsChasuble
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