Search results for "Divalent"

showing 10 items of 102 documents

Gas phase charged aggregates of bis(2-ethylhexyl)sulfosuccinate (AOT) and divalent metal ions: first evidence of AOT solvated aggregates

2011

Assembling and chelating properties of sodium bis(2-ethylhexyl)sulfosuccinate (AOTNa) towards divalent metal ions have been investigated in the gas phase by electrospray ionization mass spectrometry. A variety of positively charged monometallated and mixed metal aggregates are formed. Interestingly, several ions contain solvent (MeOH, H2O) molecules and constitute the most abundant AOT cationic aggregates not containing sodium. These species are the first example of solvated AOT-metal ion aggregates in the gas phase. By increasing the surfactant aggregation number, the abundance of solvated species becomes lower than that of unsolvated ones. Decompositions of ionic species have been studied…

chemistry.chemical_classificationAggregation numberChemistryElectrospray ionizationInorganic chemistryIonic bondingMoleculePhotochemistryMass spectrometrySpectroscopyAlkylDivalentIonJournal of Mass Spectrometry
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Behavior of Actinium, Alkaline, and Rare Earth Elements in Sr-Resin/Mineral Acid Systems

2015

In this work, the interactions between the divalent alkaline earth elements (AEE) (Sr, Ba, Ra), the trivalent rare earth elements (REE) (Ce-Lu, Y), and Ac(III) with Sr-resin were investigated in the presence of HNO3, HCl, HBr, HClO4, and HPF6. Distribution coefficients of these ions on the Sr-resin were determined under batch-loading conditions. Lastly, online column separations were performed to demonstrate the utility of these systems. Substantial differences in the behavior of the ions in solutions comprised of the five different acids were observed. These differences can partly be explained by a combination of ion exchange (primary) and extraction (solvation) mechanisms. From a practica…

chemistry.chemical_classificationAlkaline earth metalIon exchangeGeneral Chemical EngineeringExtraction (chemistry)Inorganic chemistrySolvationchemistry.chemical_elementMineral acidGeneral ChemistryDivalentIonActiniumchemistrySolvent Extraction and Ion Exchange
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Pseudopeptidic ligands: exploring the self-assembly of isophthaloylbisglycine (H2IBG) and divalent metal ions.

2012

We present a systematic study of the complexation of the new pseudopeptidic ligand isophthaloylbisglycine (H(2)IBG) with divalent metal ions of varying ionic radius. This work represents the initial employment of H(2)IBG in the coordination chemistry of alkaline earth, 3d transition, Zn(II) and Cd(II) metal elements. Infrared, NMR, thermal, magnetic, adsorption and theoretical studies of these compounds are also discussed.

chemistry.chemical_classificationAlkaline earth metalIonic radiusMagnetic Resonance SpectroscopySpectrophotometry InfraredInfraredLigandChemistryInorganic chemistryGlycineMolecular ConformationLigandsCoordination complexInorganic ChemistryMetalAdsorptionX-Ray DiffractionCoordination ComplexesMetalsDivalent metal ionsvisual_artvisual_art.visual_art_mediumQD0146ta116OligopeptidesDalton transactions (Cambridge, England : 2003)
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Palladium(II) sequestration by phytate in aqueous solution. Speciation analysis and ionic medium effects.

2010

Environmental context.In the last 20 years, the demand for palladium and other platinum-group elements has intensified, causing a significant increase in their concentration in the environment, with particular accumulation in urban areas. Knowledge about Pd2+ speciation in aqueous media is fundamental for the understanding of its biological and environmental activity in contaminated areas. Phytic acid appears to be a good sequestering agent towards Pd2+ under various conditions, indicating its potential use in the remediation of contaminated sites. Abstract. Palladium(II) speciation in the presence of phytate (Phy12–) was studied by H+ ion selective electrode (ISE) potentiometry at 25°C in…

chemistry.chemical_classificationAqueous solutionMetal ions in aqueous solutionInorganic chemistryFluorescence spectrometrychemistry.chemical_elementcomplexes stability constantsPhytateIon selective electrodeDivalentMetalchemistryComplexesGeochemistry and PetrologyChemistry (miscellaneous)Ionic strengthvisual_artvisual_art.visual_art_mediumEnvironmental ChemistrySettore CHIM/01 - Chimica AnaliticaStability constantsComplexes; Stability constants; Phytate; PalladiumPalladiumPalladium
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Supramolecular assemblies of phenyl-pyridyl-triazolopyridine and β-cyclodextrin as sensor of divalent cations in aqueous solution

2014

The chemosensor 3-phenyl-7-(pyrid-2-yl)-[1,2,3]triazolo[1,5-a]pyridine (PhPTP) used in combination with two different cyclodextrins, enable its solubilization and stabilization in aqueous solution. The behavior of the inclusion complex, and its binding ability in both cyclodextrins were investigated by means of absorption and fluorescence spectroscopy. The best results were obtained for PhPTP-DMβCD assembly, and its orientation in the DMβCD nano cavity was obtained by 2D-NMR. This inclusion geometry was confirmed by docking studies. The binary complex was proved as chemosensor upon the presence of different divalent cations in aqueous solutions. The PhPTP-DMβCD system, displays a high sensi…

chemistry.chemical_classificationAqueous solutionPolymers and PlasticsCyclodextrinCations DivalentPyridinesIronbeta-CyclodextrinsOrganic ChemistryInorganic chemistrySupramolecular chemistryWaterTriazolesFluorescenceFluorescenceFluorescence spectroscopyNanostructuresDivalentchemistry.chemical_compoundchemistryPyridinePolymer chemistryMaterials ChemistryTriazolopyridineCarbohydrate Polymers
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DUAL APPLICATION OF DIVALENT ION-ANCHORED CATALYST: BIODIESEL SYNTHESIS AND PHOTOCATALYTIC DEGRADATION OF CARBAMAZEPINE

2019

chemistry.chemical_classificationBiodieselfood.ingredientfoodchemistryLinseed oilChemical engineeringGeneral MedicineTransesterificationPhotocatalytic degradationDivalentCatalysisIonCatalysis in Green Chemistry and Engineering
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Ionic transport characteristics of negatively and positively charged conical nanopores in 1:1, 2:1, 3:1, 2:2, 1:2, and 1:3 electrolytes

2019

We study experimentally the current (I)-voltage (V) curves of 1:1, 2:1, 3:1, 2:2, 1:2, and 1:3 electrolytes in positively and negatively charged conically-shaped pores of nanoscale dimensions. The positive charges are poly(allylamine hydrochloride) chains functionalized on the pore surface by electrostatic interactions while the negative charges are carboxylic acid groups. Under physiological conditions, these fixed-charge groups are ionized and strongly interact with the different monovalent, divalent, and trivalent ions in the pore solution. The current rectification of the I-V curves and the membrane potentials provide fundamental information on the interaction of the pore charge groups …

chemistry.chemical_classificationCarboxylic acidIonic bonding02 engineering and technologyElectrolyte010402 general chemistry021001 nanoscience & nanotechnologyElectrostatics01 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsDivalentIonBiomaterialsNanoporeColloid and Surface ChemistrychemistryChemical physics0210 nano-technologyTransport phenomenaJournal of Colloid and Interface Science
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A chalcone-based highly selective and sensitive chromofluorogenic probe for trivalent metal cations

2015

[EN] Anew chalcone-based probe for the chromofluorogenic sens-ing of trivalent (Al3 +,Fe3+,Cr3+,Ga3+,In3+and As3 +)overmono-and divalent cationsand anionsisreported. In the presence of trivalent metal cations,the probe was able to displayaremarkable color change from yellow to colorless that wasclearly visible to the naked eye. Also, the initial strongyellowemission was gradually quenched and substituted by aweaklyshifted band.

chemistry.chemical_classificationChalconeQUIMICA INORGANICAGeneral ChemistryHighly selectivePhotochemistrysensorstrivalent cationsDivalentchalcone-based probeMetalchemistry.chemical_compoundchromofluorogenic sensingQUIMICA ORGANICAchemistryvisual_artQUIMICA ANALITICAvisual_art.visual_art_mediumNaked eyeanions
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Liquid Dichlorides and Dichloride-Monochloride Mixtures

1987

We give a short review of the progress done recently in the interpretation of the structure of molten divalent cation chlorides and of the stability of chloro complexes in molten salt mixtures.

chemistry.chemical_classificationChemistryInorganic chemistryMolten saltDivalentInterpretation (model theory)ECS Proceedings Volumes
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Keyhole Limpet Hemocyanin (KLH): Slow In Vitro Reassociation of KLH1 and KLH2 from Immucothel®

1998

Abstract Following our in vitro reassociation of keyhole limpet hemocyanin subunits in the presence of high concentrations (100 mM each) of calcium and magnesium chloride (Harris et al., 1997a, Micron 28, 31–41; 1997b, Micron 28, 43–56), we have now extended our investigations by using a buffer system containing a lower concentration of the two divalent cations (10 mM each). Reassociation of mixed KLH subunits present in the commercially available product Immucothel® was performed using a standardized buffer solution containing 50 mM Tris–HCl, 150 mM NaCl, 10 mM CaCl2 and 10 mM MgCl2 (pH 7.4) over a minimum period of one week, at 4°C. This solution was selected as being close to our KLH sta…

chemistry.chemical_classificationChromatographyMolecular massSize-exclusion chromatographyGeneral Physics and AstronomyCell BiologyBuffer solutionBiologyOligomerDivalentRespiratory proteinchemistry.chemical_compoundchemistryStructural BiologyPEG ratiobiology.proteinGeneral Materials ScienceKeyhole limpet hemocyaninMicron
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