Search results for "aqueous solution"

showing 10 items of 1610 documents

Zirconium and hafnium fractionation and distribution of Rare Earth Elements in neutral–alkaline waters: Case study of Lake Van hydrothermal system, T…

2021

International audience; We investigated the distribution of Zr, Hf, and rare earth elements (REE) as the sum of lanthanides plus Y in the hydrothermal system in the Lake Van area of south-eastern Turkey. This system is characterised by water with variable pH in alkaline conditions resulting from hydrothermal CO2 upraise and neoformation of calcite minerals in near equilibrium with the interacting waters. Zr, Hf, and REE determinations were carried out for aqueous phases and suspended solids in lake water and surrounding thermal springs. We found that dissolved Hf is partitioned relative to Zr during calcite formation and that such fractionation is a function of the Ca2+ activity in warm wat…

CalciteZirconiumAqueous solutionTurkeyChemistryInorganic chemistryCarbonate mineralschemistry.chemical_elementAlkaline lakes REE Turkey Zr/Hf ratioAuthigenicFractionation010501 environmental sciences010502 geochemistry & geophysicsREEAlkaline lakes01 natural sciences6. Clean waterHydrothermal circulationchemistry.chemical_compoundAdsorption[SDU.STU.GC]Sciences of the Universe [physics]/Earth Sciences/GeochemistryGeochemistry and PetrologyZr/Hf ratioEconomic Geology0105 earth and related environmental sciencesJournal of Geochemical Exploration
researchProduct

In-situ suspended aggregate microextraction: A sample preparation approach for the enrichment of organic compounds in aqueous solutions.

2015

Abstract This work presents in-situ suspended aggregate microextraction (iSAME) as a new and expedient sample preparation method. This new concept capitalizes on the general principles of in-situ solvent formation microextraction, in the sense that extraction is carried out in a supramolecular aggregate phase, which is formed in-situ in the sample through one-step process involving ion-association between a cationic surfactant and a benzene sulfonic acid derivative. The suspended aggregate containing the analytes is then collected in the form of a thin-film on the surface of a common filter paper by suction filtration. The entrapped analytes are released by completely dissolving the thin-fi…

Calibration curveLiquid Phase MicroextractionAnalytical chemistryBiochemistryAnalytical Chemistrylaw.inventionMatrix (chemical analysis)ElectrolyteslawSample preparationSolid phase extractionOrganic ChemicalsDissolutionFiltrationAqueous solutionChromatographyChemistryOrganic ChemistryExtraction (chemistry)Osmolar ConcentrationWaterGeneral MedicineHydrogen-Ion ConcentrationSolventsFiltrationWater Pollutants ChemicalJournal of chromatography. A
researchProduct

Desferrioxamine as an appropriate chelator for 90Nb: Comparison of its complexation properties for M-Df-Octreotide (M=Nb, Fe, Ga, Zr)

2014

The niobium-90 radioisotope ((90)Nb) holds considerable promise for use in immuno-PET, due to its decay parameters (t½ = 14.6h, positron yield=53%, Eß(+)(mean) = 0.35 MeV and Eß(+)(max) = 1.5 MeV). In particular, (90)Nb appears well suited to detect in vivo the pharmacokinetics of large targeting vectors (50-150 kDa). In order to be useful for immuno-PET chelators are required to both stabilize the radionuclide in terms of coordination chemistry and to facilitate the covalent attachment to the targeting vector. Different chelators were evaluated for this purpose in terms of radiolabelling efficiency and stability of the radiolabelled Nb(V) complex and in order to determine the most suitable…

Cancer ResearchStereochemistryNiobiumMetal ions in aqueous solutionKineticsOctreotideRadiation DosageCoordination complexTransmetalationDrug StabilityMaterials TestingMoleculeRadiology Nuclear Medicine and imagingChelationChelating AgentsIonsRadioisotopeschemistry.chemical_classificationChemistryMetalsCovalent bondIsotope LabelingMolecular MedicineRadiopharmaceuticalsNuclear chemistryConjugateNuclear Medicine and Biology
researchProduct

Preparation and characterization of hexyl methacrylate monolithic columns for CEC

2008

The preparation of hexyl methacrylate (HMA) monolithic columns for CEC separations has been investigated with two initiation systems: (i) ammonium peroxodisulphate and TEMED to activate the polymerization reaction, and (ii) by thermal initiation with AIBN. For both initiators, the influence of composition of porogenic solvent on morphological and chromatographic properties of monoliths was investigated. Two porogenic solvent systems, aqueous and non-aqueous media, were also studied for monolithic beds polymerized with AIBN. Under optimal conditions, low minimum plate heights (9.6 mum for peroxodisulphate, 8.4 and 10.0 mum for AIBN in aqueous and non-aqueous porogenic solvents, respectively)…

Capillary electrochromatographyChromatographyAqueous solutionChemistryClinical BiochemistryAcrylic ResinsReproducibility of ResultsRepeatabilityEthylenediaminesMethacrylateBiochemistryAnalytical ChemistrySolventPolymerizationCapillary Electrochromatographyvisual_artMicroscopy Electron Scanningvisual_art.visual_art_mediumMethacrylatesAcrylic resinHexyl methacrylateELECTROPHORESIS
researchProduct

QM/MM Determination of Kinetic Isotope Effects for COMT-Catalyzed Methyl Transfer Does Not Support Compression Hypothesis

2004

Secondary alpha-D3 kinetic isotope effects calculated by the hybrid AM1/TIP3P/CHARMM method for the reaction of S-adenosylmethionine with catecholate anion in aqueous solution and catalyzed by rat liver catechol O-methyltransferase at 298 K are 0.94 and 0.85, respectively, in good accord with experiment. The large inverse effect for the enzymatic reaction is not due to compression but arises from significant increases in the stretching and bending force constants involving the isotopically substituted atoms of the transferring methyl group as between the reactant complex and the transition structure, larger than for the reaction in water.

Carbon IsotopesCatecholAqueous solutionMolecular StructureStereochemistryGeneral ChemistryCatechol O-MethyltransferaseMethylationBiochemistryCatalysisCatalysisIonEnzyme catalysisQM/MMKineticschemistry.chemical_compoundColloid and Surface ChemistryModels ChemicalchemistryKinetic isotope effectQuantum TheoryPhysical chemistryComputer SimulationOxidation-ReductionMethyl groupJournal of the American Chemical Society
researchProduct

Reversible coordination of dioxygen by tripodal tetraamine copper complexes incorporated in a porous silica framework.

2010

The present study reports the synthesis and rational design of porous structured materials by using a templating method. A tetraethoxysilylated tripodal tetraamine (TREN) was covalently incorporated in a silica framework with a double imprint: A surfactant template and a metal ion imprint. The presence of a cationic surfactant (CTAB) endowed the material with a high porosity, and the tripodal or square-pyramidal topology of the ligand was preserved thanks to the use of the silylated Cu(II) complex. After removal of the surfactant and de-metalation, the incorporated tetraamine was quantitatively complexed by CuCl(2) and the material has shown after thermal activation that a reversible bindin…

Carbon MonoxideSilicon dioxideLigandNitrogenMetal ions in aqueous solutionOrganic ChemistryInorganic chemistryCationic polymerizationElectron Spin Resonance Spectroscopychemistry.chemical_elementGeneral ChemistrySilicon DioxideCopperCatalysisAdductOxygenchemistry.chemical_compoundchemistryCoordination ComplexesTripodal ligandPolymer chemistryReactivity (chemistry)AminesPorosityCopperChemistry (Weinheim an der Bergstrasse, Germany)
researchProduct

8-Hydroxyquinoline-2-Carboxylic Acid as Possible Molybdophore: A Multi-Technique Approach to Define Its Chemical Speciation, Coordination and Sequest…

2020

8-hydroxyquinoline-2-carboxylic acid (8-HQA) has been found in high concentrations (0.5&ndash

Carboxylic acidInorganic chemistryPotentiometric titrationlcsh:QR1-502metal complexesMolybdate010402 general chemistry01 natural sciencesBiochemistryFerric Compoundschemical speciation; metal complexes; metallophores; molybdate; natural chelants; sequestration; stability constantslcsh:MicrobiologyArticlemetal complexechemistry.chemical_compoundSettore CHIM/01 - Chimica AnaliticaMolecular BiologyVoltammetryDensity Functional TheorySettore CHIM/02 - Chimica Fisicachemistry.chemical_classificationMolybdenumAqueous solutionmetallophore010405 organic chemistryLigandWatersequestrationchemical speciationhumanities0104 chemical sciencesSolutionsmolybdatestability constantsnatural chelantschemistryHydroxyquinolinesnatural chelantTitrationCyclic voltammetrymetallophoresBiomolecules
researchProduct

Electrochemical treatment of aqueous solutions of catechol by various electrochemical advanced oxidation processes: Effect of the process and of oper…

2017

Abstract Catechol, one of the most abundant compounds in olive mills wastewaters, which is generated in the Fenton degradation of various aromatic compounds, is a toxic, possible carcinogen, persistent pollutant and it is not readily biodegradable. Hence, its degradation requires the utilization of advanced oxidation processes (AOPs). Here, the electrochemical treatment of aqueous solutions of catechol was investigated. The utilization of various electrochemical processes, such as electro-Fenton (EF), direct anodic oxidation (AO), indirect oxidation by electro-generated active chlorine and coupled processes was investigated. Furthermore, the effect of various operating conditions (including…

CatecholAqueous solutionChemistryGeneral Chemical EngineeringAdvanced oxidation processInorganic chemistrychemistry.chemical_element02 engineering and technology010501 environmental sciences021001 nanoscience & nanotechnologyElectrochemistry01 natural sciencesCatechol; Advanced oxidation process electro-Fenton anodic oxidation; BDDAnalytical ChemistryAnodeCatalysischemistry.chemical_compoundCatecholElectrochemistryChlorineDegradation (geology)Advanced oxidation process electro-Fenton anodic oxidation0210 nano-technologyBDD0105 earth and related environmental sciences
researchProduct

Au/CeO2 Photocatalyst for the Selective Oxidation of Aromatic Alcohols in Water under UV, Visible and Solar Irradiation

2021

Au nanoparticles supported on CeO2 have been prepared and investigated as photocatalysts for the photocatalytic selective oxidation of benzyl alcohol and 4-methoxybenzyl alcohol to the correspondent benzaldehydes, in aqueous suspensions and room conditions under UV, visible and natural solar light irradiation. Au nanoparticles have been supported by impregnation (1 and 3 wt.%) on two types of CeO2 (i.e., a commercial one and a home prepared oxide obtained in the presence of NaOH as precipitation agent). The Au impregnated samples showed strong visible radiation absorption at 565–570 nm associated to localized surface plasmon resonance (LSPR). The bare CeO2 samples are activated by UV light …

CeOMaterials sciencevisible light photocatalysisAu-CeO; 2; CeO; 2; Plasmonic effect; Visible light photocatalysis2OxideNanoparticleTP1-1185PhotochemistryAldehydeCatalysisplasmonic effectplasmonic effect; CeO<sub>2</sub>; Au-CeO<sub>2</sub>; visible light photocatalysischemistry.chemical_compoundCeO<sub>2</sub>Au-CeOIrradiationVisible light photocatalysisPhysical and Theoretical ChemistrySurface plasmon resonanceQD1-999chemistry.chemical_classificationAqueous solutionChemical technologyChemistryPlasmonic effectchemistryBenzyl alcoholPhotocatalysisAu-CeO2Au-CeO<sub>2</sub>CeO2
researchProduct

Ditopic Aza-Scorpiand Ligands Interact Selectively with ds-RNA and Modulate the Interaction upon Formation of Zn2+ Complexes

2021

Nucleic acids are essential biomolecules in living systems and represent one of the main targets of chemists, biophysics, biologists, and nanotechnologists. New small molecules are continuously developed to target the duplex (ds) structure of DNA and, most recently, RNA to be used as therapeutics and/or biological tools. Stimuli-triggered systems can promote and hamper the interaction to biomolecules through external stimuli such as light and metal coordination. In this work, we report on the interaction with ds-DNA and ds-RNA of two aza-macrocycles able to coordinate Zn2+ metal ions and form binuclear complexes. The interaction of the aza-macrocycles and the Zn2+ metal complexes with duple…

Cell SurvivalMetal ions in aqueous solutionÀcids nucleicsPharmaceutical Science010402 general chemistryLigands01 natural sciencesArticleAnalytical ChemistryMetalchemistry.chemical_compoundQD241-441Coordination ComplexesCell Line TumorDrug DiscoveryChlorocebus aethiopsAnimalsHumansPhysical and Theoretical ChemistryVero CellsRNA Double-Strandedchemistry.chemical_classification010405 organic chemistryCytotoxinsBiomoleculeOrganic Chemistryzinc complexRNADNASmall moleculeFluorescenceCombinatorial chemistry0104 chemical sciencesZincchemistryChemistry (miscellaneous)visual_artDNA and RNA duplexesvisual_art.visual_art_mediumNucleic acidMolecular MedicineRNAaza-macrocycleDNAMolecules
researchProduct