Search results for "uranyl"

showing 10 items of 47 documents

Interactions of Dioxouranium(VI) with Amines in Aqueous Solution

2010

The interaction of the dioxouranium(VI) ion with five low molecular weight polyamines (ethylenediamine, putrescine, cadaverine, spermidine, and spermine) and with poly(allyl)amine (15 kDa) was studied potentiometrically (ISE-H + glass electrode) at T ) 298.15 K. Investigations were carried out in NaNO3 ionic medium, at I ) 0.1 mol · L -1 (and 0.5 mol · L -1 for poly(allyl)amine only), in the pH range 3.5 to 5.5, before the formation of uranyl insoluble species. The results gave evidence for the formation of two species, namely, UO2L 2+ and UO2L(OH) + for the diamine systems (ethylenediamine, putrescine, cadaverine), UO2L 2+ and UO2LH 3+ for spermidine, and UO2LH 3+ and UO2LH2 4+ for spermin…

CadaverineGeneral Chemical EngineeringInorganic chemistryEthylenediamineGeneral Chemistrydioxouranium; sequestrationMedicinal chemistrySpermidinestability constantschemistry.chemical_compoundchemistryaminespeciationStability constants of complexesuranylDiaminePutrescineQualitative inorganic analysisSettore CHIM/01 - Chimica AnaliticaPolyamine
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Extraction of uranyl ions from aqueous solutions using silica-gel-bound macrocycles for alpha contaminated waste water treatment

2004

Abstract The efficiency for the extraction of U(VI) of new modified silica gels, namely N-tripropionate (or N-triacetate)-substituted tetraazamacrocycles-bound silica gels, has been studied. The effect of the nature of the ligand, the pH and the temperature was studied both in batch experiments as well as in continuous extraction. These silica gels are good candidates for the extraction of U(VI) when compared to a commercially available acid-type chelating resin. The breakthrough and regeneration tests showed that the total removal of U(VI) from a contaminated solution can be achieved by using a column packed with such tetraazamacrocycles-bound silica gels. Finally, the use of a modified si…

Chelating resinAqueous solutionSilica gelExtraction (chemistry)chemistry.chemical_elementAmericiumUraniumUranylBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryEnvironmental ChemistrySolid phase extractionSpectroscopyNuclear chemistryAnalytica Chimica Acta
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Specific recognition of fluoride anion using a metallamacrocycle incorporating a uranyl-salen unit

2008

The design and synthesis of a novel fluoride receptor that uses a salen-complexed Lewis acidic uranyl center as the sole binding site is reported here. This receptor binds fluoride anions in DMSO with a high affinity constant (K > 106 M-1) and exhibits a negligible affinity (K < 10 M-1) towards otherwise effective competitors, such as acetate, phosphate and cyanide anions.

CyanideInorganic chemistryAffinity constantGeneral ChemistryPhosphateUranylMedicinal chemistrysupramolecular chemistryCatalysisIonfluoride recognitionchemistry.chemical_compoundchemistryMaterials Chemistrysalen-complexesBinding siteReceptorFluoride
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Effects of preorganization in the chelation of UO22+ by hydroxamate ligands: cyclic PIPO– vs linear NMA–

2018

International audience; Many siderophores incorporate as bidentate chelating subunits linear and more seldomly cyclic hydroxamate groups. In this work, a comparative study of the uranyl binding properties in aqueous solution of two monohydroxamic acids, the prototypical linear N-methylacetohydroxamic acid (NMAH) and the cyclic analog 1-hydroxypiperidine-2-one (PIPOH), has been carried out. The complex [UO2(PIPO)(2)(H2O)] crystallized from slightly acidic water solutions (pH < 5), and its molecular structure was determined by X-ray diffraction. The uranyl speciation in the presence of both ligands has been thoroughly investigated in a 0.1 M KNO3 medium at 298.2 K by the combined use of four …

DenticitySpeciation010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesCatalysisMetalchemistry.chemical_compounduranylMaterials Chemistry[CHIM.CRIS]Chemical Sciences/CristallographyMoleculeChelation[CHIM.COOR]Chemical Sciences/Coordination chemistry[PHYS]Physics [physics]Aqueous solutionLigandChemistryN-methylacetohydroxamic acidGeneral ChemistryUranyl0104 chemical sciencesCrystallographyStability constants of complexesvisual_artSolution thermodynamicscyclic hydroxamic acidvisual_art.visual_art_medium[CHIM.RADIO]Chemical Sciences/Radiochemistry
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Alkaline hydrolysis/methylation-acetylation: a new technique for ultrastructural DNA cytochemistry.

1991

SUMMARY A new technique for the visualization of DNA-containing structures in electron microscopy is described. Samples of glutaraldehyde-fixed bone marrow from rats were subjected to alkaline hydrolysis to remove RNA and the phosphate of phospho-proteins, followed by a combined blockage of protein carboxyl and amino groups through methylation-acetylation. After uranyl acetate staining of epoxy-embedded ultrathin sections, chromatin from all cell types showed a highly selective and intense electron opacity. Staining methods for DNA were also positive in semithin sections. This simple procedure could be very useful in ultrastructural cytochemistry of DNA and chromatin.

HistologyHydrolysisUranyl acetateAcetylationRats Inbred StrainsDNABiologyAlkaline hydrolysis (body disposal)Molecular biologyMethylationChromatinPathology and Forensic MedicineChromatinStainingRatschemistry.chemical_compoundMicroscopy ElectronchemistryBiochemistryBone MarrowUltrastructureNucleic acidCytochemistryAnimalsDNAJournal of microscopy
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Predicting the Breakthrough of Ternary Ca–Uranyl–Carbonate Species in Mineral Water Treated by a Fixed-Bed Granular Ferric Hydroxide Adsorbent

2020

A CD-MUSIC surface complexation model was set up on the basis of batch equilibrium experiments with uranyl ions and akaganeite-based granular ferric hydroxide (GFH), which is often used in water pu...

Inorganic chemistrychemistry.chemical_elementUraniumUranylUranyl carbonateIonMineral waterchemistry.chemical_compoundAdsorptionchemistryChemistry (miscellaneous)Ferric hydroxideEnvironmental ChemistryChemical Engineering (miscellaneous)Ternary operationWater Science and TechnologyACS ES&amp;T Water
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Complex Formation of the Uranyl (UO22+) Ion with the Diethylene Triaminopentaacetate (DTPA) Ligand at 25 °C in 3 M Sodium Perchlorate

2011

The complex formation between the uranyl (UO22+) ion and the diethylene triaminopentaacetate ligand (DTPA) has been investigated at 25 °C, in a 3 M sodium perchlorate medium. The overall protonation constants βjH of the free ligand have been previously determined in this ionic medium: six protonated species (HjA), with j ranging from 1 to 6, together with the free anion A5− have been identified in the concentration range from (3·10−3 to 13·10−3) mol·kg−1. Four complex species, H2UO2A−, HUO2A2−, UO2A3−, and UO2AOH4−, have been identified in the total uranyl concentration range from (1.1·10−3 to 5.7·10−3) mol·kg−1, and their overall stability constants determined, keeping the metal to ligand …

LigandGeneral Chemical EngineeringInorganic chemistrycomplexes formation • solution equilibria • coulometric titration • emf measurements • organic ligand stability constants.Ionic bondingProtonationGeneral ChemistrySodium perchlorateUranylIonMetalchemistry.chemical_compoundchemistryvisual_artvisual_art.visual_art_mediumSettore CHIM/01 - Chimica AnaliticaChelationJournal of Chemical &amp; Engineering Data
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Mixed complexes of alkaline earth uranyl cabonates: A laser-induced time-resolved fluorescence spectroscopic study

2008

The interaction of the alkaline earth ions Mg2+, Sr2+ and Ba2+ with the uranyl tricarbonate complex has been studied by time resolved laser-induced fluorescence spectroscopy. In contrast to the non-luminescent uranyl tricarbonate complex the formed products show slight luminescence properties. These have been used to determine the stoichiometry and complex stabilities of the formed compounds. As the alkaline earth elements are located in an outer shell of the complex the influence of the type of the alkaline earth element on the stability constant is not very drastic. Therefore all obtained data were averaged in order to derive an common stability constant for the described complexes. These…

LuminescenceLightAnalytical chemistryCarbonateschemistry.chemical_elementFluorescence spectroscopyAnalytical ChemistryPhosphatesuraniumchemistry.chemical_compoundAlkaline earth elementscarbonatecomplex formationluminescenceMagnesiumInstrumentationSpectroscopyIonsAlkaline earth metalModels StatisticalTemperatureBariumHydrogen-Ion ConcentrationUranylAtomic and Molecular Physics and OpticsCarbonSpectrometry FluorescencechemistryStability constants of complexesBariumStrontiumUraniumTime-resolved spectroscopyLuminescenceStoichiometry
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Influence of saline and pH on collagen type I fibrillogenesis in vitro: Fibril polymorphism and colloidal gold labelling

2007

We have produced different collagen type I fibrils by in vitro fibrillogenesis of acetic acid-soluble collagen within the pH range 2.5-9.0, in the presence and absence of 150 mM NaCl. The varying relatively stable molecular assemblies and polymorphic fibrillar end-products produced after 24 h incubation have been assessed and compared by the TEM study of specimens negatively stained with uranyl acetate. In the presence of 150 mM NaCl, the assembly of collagen at low pH (2.5) leads to the formation of initial molecular aggregates that progressively link together at slightly higher pH (5.0) to form sub-fibrils and spindle-shaped D-banded bundles of sub-fibrils. At pH 6.0 these D-banded bundle…

Materials scienceGeneral Physics and AstronomyUranyl acetateFibrillogenesisGold ColloidCell BiologyHydrogen-Ion ConcentrationIn Vitro TechniquesSodium ChlorideFibrilNegative stainCollagen Type IRatsGold ColloidMicroscopy ElectronCrystallographychemistry.chemical_compoundchemistryStructural BiologyColloidal goldSide chainAnimalsGeneral Materials ScienceTromethamineBiomineralizationMicron
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Kinetic and equilibrium studies for uranyl removal from aqueous solution by adsorption onto alginate gel beads. DPV and ICP measurements

2014

Settore CHIM/01 - Chimica AnaliticaUranyl Voltammetry DPV ICP-OES Alginate gel beads.
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