Search results for " solution"

showing 10 items of 3084 documents

Zur polymerisation und copolymerisation des natriumvinylsulfonats

1959

Natriumvinylsulfonat (VS-Na) zeigt in konzentrierten wasrigen Losungen eine ausgepragte Polymerisationsneigung. Die Polymerisationsgeschwindigkeit und der erreichte Umsatz hangen stark von der Aciditat der Losungen ab. Es wurde gefunden, das mit der Polymerisationsdauer und mit wachsendem Umsatz auch die Molekulargewichte der Polymerisate ansteigen. Wasserunlosliche oder nur begrenzt losliche ungesattigte Verbindungen wie Styrol, Vinylacetat und andere konnen in Dimethylsulfoxyd in homogener Losung mit VS-Na copolymerisiert werden. Sodiumvinylsulphonate (VS-Na) shows a strong tendency for polymerization in concentrated aqueous solutions. The rate of polymerization and the conversion depend …

Solventchemistry.chemical_compoundMonomerAqueous solutionPolymerizationChemistryHomogeneousPolymer chemistryStyreneDie Makromolekulare Chemie
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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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Determination of thallium in water samples

2007

Abstract This article illustrates the developments of effective preconcentration techniques and highly sensitive detection methods for accurate measurements of Tl species at extremely low concentration in aqueous solutions. The literature on this topic was taken from the Analytical Abstracts in the period 1990–2005.

SpeciationChromatographyAqueous solutionchemistryEnvironmental chemistrymedia_common.quotation_subjectThalliumchemistry.chemical_elementSpectroscopyVolume concentrationAnalytical ChemistryHighly sensitivemedia_commonMicrochemical Journal
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Advances in the investigation of dioxouranium(VI) complexes of interest for natural fluids

2012

Abstract The interactions of dioxouranium(VI) cation with different organic and inorganic ligands of environmental and biological interest were carefully examined with the aim to draw a chemical speciation picture of this ion in natural aquatic ecosystems and in biological fluids. Since UO22+ ion shows a significant tendency to hydrolyze, particular attention was paid in considering the hydrolysis species formation both in the presence and in absence of ligands. The results reported in the literature show that formation of the hydrolytic species assumes a great importance in the complexation models for all the UO22+-ligand systems considered. In particular, the following ligands have been t…

SpeciationDioxouranium(VI) complexes; Aqueous solutions; Inorganic ligands; Organic ligands; Speciation; SequestrationOrganic ligandsInorganic Chemistrychemistry.chemical_compoundComputational chemistryMaterials ChemistryAqueous solutionDioxouranium(VI) complexesOrganic chemistryMoleculeSettore CHIM/01 - Chimica AnaliticaCarboxylatePhysical and Theoretical ChemistryBinding siteAqueous solutionsDioxouranium(VI) complexechemistry.chemical_classificationInorganic ligandsAqueous solutionLigandSequestrationInorganic ligandUranylAmino acidchemistryOrganic ligandChemical stabilityCoordination Chemistry Reviews
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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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FUNCTIONALIZED HALLOYSITE NANOTUBES FOR ENHANCED REMOVAL OF Hg2+ IONS FROM AQUEOUS SOLUTIONS

2021

AbstractWater is essential for humans, animals, and plants; pollutants, usually derived from anthropogenic activities, can have a serious effect on its quality. Heavy metals are significant pollutants and are often highly toxic to living organisms, even at very low concentrations. Among the numerous removal techniques proposed, adsorption onto suitable adsorbent materials is considered to be one of the most promising. The objective of the current study was to determine the effectiveness of halloysite nanotubes (HNT) functionalized with organic amino or thiol groups as adsorbent materials to decontaminate polluted waters, using the removal of Hg2+ ions, one of the most dangerous heavy metals…

SpeciationInorganic chemistrySoil ScienceIonic bondingRemediation02 engineering and technologyengineering.material010402 general chemistry01 natural sciencesHalloysiteIonMetalAdsorptionGeochemistry and PetrologyEarth and Planetary Sciences (miscellaneous)Settore CHIM/01 - Chimica AnaliticaWater Science and TechnologyAqueous solutionAdsorption; Halloysite; Mercury; Remediation; SpeciationIon exchangeChemistryHalloysiteMercurySettore CHIM/06 - Chimica Organica021001 nanoscience & nanotechnology0104 chemical sciencesIonic strengthvisual_artvisual_art.visual_art_mediumengineeringAdsorption0210 nano-technology
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Studies of CoxMg1-xO Solid Solutions Using Laboratory EXAFS-Spectrometer

1993

Studies of the local electronic structure and the short-range order in solid solutions Co x Mg1-x O with x equal from 0.02 to 1.00 have been carried out on the Co K-edge X-ray absorption spectra measured using the laboratory EXAFS-spectrometer. A non-monotonous change of the Co-O distance in the first coordination shell with the bent at x=0.5 has been established. The second coordination shell of cobalt has been formed by cobalt and magnesium atoms with a distribution close to statistical.

SpectrometerExtended X-ray absorption fine structureAbsorption spectroscopyMagnesiumGeneral EngineeringAnalytical chemistryShell (structure)General Physics and Astronomychemistry.chemical_elementElectronic structureCondensed Matter::Materials ScienceCrystallographychemistryPhysics::Atomic and Molecular ClustersCobaltSolid solutionJapanese Journal of Applied Physics
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Synthesis, Characterization, and Saccharide Binding Studies of Bile Acid − Porphyrin Conjugates

2007

Synthesis and characterization of bile acid-porphyrin conjugates (BAPs) are reported. Binding of saccharides with BAPs in aqueous methanol was studied by monitoring changes in the visible absorption spectral of the porphyrin-moieties. Although these studies clearly showed absorbance changes, suggesting quite high if non-selective binding, the mass spectral studies do not unambiguously support these results.

Spectrometry Mass Electrospray IonizationMagnetic Resonance SpectroscopyPorphyrinsmedicine.drug_classElectrospray ionizationCarbohydratesPharmaceutical ScienceESI MS.ArticleAnalytical ChemistryAbsorbanceBile Acids and Saltslcsh:QD241-441chemistry.chemical_compoundUltraviolet visible spectroscopylcsh:Organic chemistryHeterocyclic Compoundsvisible spectroscopyDrug Discoverymedicinepolycyclic compoundsOrganic chemistryPhysical and Theoretical ChemistrysaccharideAqueous solutionBile acidMolecular StructureOrganic Chemistry1H-NMRPorphyrinCombinatorial chemistryBile acidschemistryChemistry (miscellaneous)Proton NMRMolecular Medicinesense organsporphyrinConjugateMolecules
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Magnetic Ordering and Spin Dynamics of Ba1-xEuxSi Phases

2011

We have investigated the magnetic ordering and spin dynamics of the solid solution series Ba1–xEuxSi with 0 < x ≤ 1 applying X-ray diffraction, electric conductivity measurements, Mossbauer spectroscopy, muon spin depolarization, and neutron diffraction. Our results suggest a spin glass-like behavior of Ba1–xEuxSi for concentrations close to x = 0.3 exist. Different spin ordering phenomena are found, which are dependent on the relative europium concentrations.

Spin glassCondensed matter physicsSpin polarizationChemistryNeutron diffractionchemistry.chemical_elementMuon spin spectroscopy010402 general chemistry01 natural sciences0104 chemical sciencesInorganic ChemistrySpin wave0103 physical sciences010306 general physicsEuropiumSpin-½Solid solutionZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE
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