Search results for "uranyl"

showing 10 items of 47 documents

Chronospeciation of uranium released in soil during a long-term DU shell weathering experiment.

2021

Corrosion process was investigated of depleted uranium (DU) ammunition fragments buried for three years in aerobic soils continuously irrigated with water. The continuing corrosion process was triggered through formation of soluble uranyl oxyhydrate phases such as metaschoepite and becquerelite, which were identified by micro-Raman and X-ray diffraction spectroscopy. The soil was not amended by phosphates and, therefore, no uranyl phosphates were found as corrosion products on the DU surfaces by X-ray photoelectron spectroscopy. A speciation modelling at high temporal sequence (chronospeciation approach) indicated that the abundant Fe oxyhydroxides in the soil immobilized the U(IV) released…

010504 meteorology & atmospheric sciencesHealth Toxicology and Mutagenesischemistry.chemical_elementWeathering010501 environmental sciences01 natural sciencesCorrosionFerrihydritechemistry.chemical_compoundPore water pressureSoilRadiation MonitoringEnvironmental ChemistrySoil Pollutants RadioactiveWaste Management and Disposal0105 earth and related environmental sciencesTotal organic carbonGeneral MedicineUraniumUranylPollutionCorrosionchemistryEnvironmental chemistrySoil waterUraniumJournal of environmental radioactivity
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The Coordination of Uranyl in Water: A Combined Quantum Chemical and Molecular Simulation Study

2005

The coordination environment of uranyl in water has been studied using a combined quantum mechanical and molecular dynamics approach. Multiconfigurational wave function calculations have been performed to generate pair potentials between uranyl and water. The quantum chemically determined energies have been used to fit parameters in a polarizable force field with an added charge transfer term. Molecular dynamics simulations have been performed for the uranyl ion and up to 400 water molecules. The results show a uranyl ion with five water molecules coordinated in the equatorial plane. The U-O(H(2)O) distance is 2.40 A, which is close to the experimental estimates. A second coordination shell…

Ab initioMolecular simulationBiochemistryCatalysisIonMolecular dynamicschemistry.chemical_compoundColloid and Surface ChemistryAb initio quantum chemistry methodsComputational chemistryComputer SimulationPhysics::Chemical PhysicsQuantum chemicalHydrogen bondSolvationWaterGeneral ChemistryGeneral MedicineUranylSolvation shellchemistryModels ChemicalChemical physicsddc:540Quantum TheoryUranium
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Hydrolysis and chemical speciation of dioxouranium(VI) ion in aqueous media simulating the major ion composition of seawater

2004

Abstract The hydrolysis and chemical speciation of the dioxouranium(VI) ion at 25 °C was studied in a number of binary electrolytes (LiCl, NaCl, MgCl2, CaCl2, Na2SO4) and some mixtures (NaCl–Na2SO4, NaNO3–Na2SO4, CaCl2–MgCl2) as well as artificial seawater (SSWE) as a function of ionic strength. The results in LiCl, CaCl2 and MgCl2 solutions confirmed the formation of (UO2)2(OH)22+, (UO2)3(OH)42+, (UO2)3(OH)5+ and (UO2)3(OH)7− species (at I=0 mol l−1: log Tβ22=−5.76, log Tβ34=−11.82, log Tβ35=−15.89 and log Tβ37=−29.26). For NaNO3, NaCl and artificial seawater the hydrolysis constant for the formation of the UO2(OH)+ species was also determined (at I=0 mol l−1: log Tβ11=−5.19). The results …

Activity coefficientHydrolysis constantUranium speciationAqueous solutionChemistryHydrolysisInorganic chemistryPitzer parametersIonic bondingArtificial seawaterGeneral ChemistryDependence on ionic strengthOceanographyUranylIon pair formationIonDioxouranium(VI)chemistry.chemical_compoundIonic strengthEnvironmental ChemistryChemical speciationHydrolysis; Dioxouranium(VI); Chemical speciation; Seawater; Dependence on ionic strength; Dependence on ionic medium; Pitzer parameters; Ion pair formationSeawaterDependence on ionic mediumWater Science and Technology
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Keyhole limpet haemocyanin: negative staining in the presence of trehalose

1995

Abstract Samples of unpurified and purified haemocyanin from the giant keyhole limpet Megathura crenulata have been studied by transmission electron microscopy (TEM) using mixtures of trehalose with the negative stains, uranyl acetate and ammonium molybdate. Trehalose is a known protein preservative during air and freeze drying, UV irradiation and high temperatures, and therefore offers the possibility of protecting proteins during the drying of negatively-stained specimens and their subsequent electron microscopical study. Evidence is presented that trehalose possesses satisfactory stability within the electron beam during conventional room temperature, negative-staining studies. The combi…

Ammonium molybdatebiologyAnalytical chemistryGeneral Physics and AstronomyUranyl acetateCell BiologyMegathura crenulatabiology.organism_classificationTrehaloseNegative stainchemistry.chemical_compoundFreeze-dryingchemistryStructural BiologyTransmission electron microscopybiology.proteinGeneral Materials ScienceKeyhole limpet hemocyaninNuclear chemistryMicron
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Negative Staining and Cryo-negative Staining: Applications in Biology and Medicine

2013

Negative staining is widely applicable to isolated viruses, protein molecules, macromolecular assemblies and fibrils, subcellular membrane fractions, liposomes and artificial membranes, synthetic DNA arrays, and also to polymer solutions and a variety of nanotechnology samples. Techniques are provided for the preparation of the necessary support films (continuous carbon and holey/perforated carbon). The range of suitable negative stains is presented, with some emphasis on the benefit of using ammonium molybdate and of negative stain-trehalose combinations. Protocols are provided for the single droplet negative staining technique (on continuous and holey carbon support films), the floating a…

Ammonium molybdatechemistry.chemical_compoundMembraneCarbon filmchemistryBiophysicsUranyl formateUranyl acetateNegative stainStainingMacromolecule
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Cholesterol binding to amyloid-β fibrils: A TEM study

2008

There is increasing interest in the role of brain cholesterol in Alzheimer's disease and the contribution of cholesterol to the formation of amyloid plaques. This paper presents a TEM study showing the binding of soluble approximately 10 nm diameter cholesterol-PEG 600 micelles to amyloid-beta(1-42) (Abeta(1-42)) fibrils formed either in the presence of this cholesterol derivative or to preformed fibrils generated under four different fibrillogenesis conditions. Specimens negatively stained with uranyl acetate revealed that during 24 h fibrillogenesis at 37 degrees C the cholesterol-PEG micelles bound periodically to Abeta(1-42) protofibrils and apparently also formed a thin smooth unbroken…

AmyloidAmyloid beta-PeptidesCholesterolCholesterol bindingGeneral Physics and AstronomyUranyl acetateFibrillogenesismacromolecular substancesCell BiologyFibrilNegative stainMicellePolyethylene GlycolsCrystallographychemistry.chemical_compoundCholesterolMicroscopy Electron TransmissionchemistryStructural BiologyHumanslipids (amino acids peptides and proteins)General Materials ScienceHydrogen peroxideMicellesMicron
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Hydrolysis of dioxouranium(VI): a calorimetric study in NaClaq and NaClO4aq, at 25°C

2004

Abstract We report the results of a calorimetric study on the hydrolysis of UO 2 2+ in different ionic media (NaClO 4 aq , NaCl aq ) at 25 °C. Experiments in NaCl were performed at different ionic strength, at I ≤1 mol l −1 . The species considered in both ionic media were UO 2 (OH) + , (UO 2 ) 2 (OH) 2 2+ and (UO 2 ) 3 (OH) 5 + , and in addition (UO 2 ) 3 (OH) 4 2+ and (UO 2 ) 3 (OH) 7 − in NaCl aq . The dependence on ionic strength of enthalpy changes in NaCl aq was expressed by the simple linear equation Δ H pq =Δ H ° pq + aI 1/2 ( a , empirical parameter). Comparison with literature findings is given and some recommended values are reported.

Aqueous solutionChemistryIonic strength dependenceEnthalpyInorganic chemistryIonic bondingCalorimetryCalorimetryCondensed Matter PhysicsSodium perchlorateUranylchemistry.chemical_compoundHydrolysisReaction enthalpyIonic strengthPhysical chemistrySettore CHIM/01 - Chimica AnaliticaPhysical and Theoretical ChemistryHydrolysis of UO22+InstrumentationThermochimica Acta
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Double-Shell Vesicles, Strings of Vesicles and Filaments Found in Crosslinked Micellar Solutions of Poly(1,2-butadiene)-block-poly(ethylene oxide) Di…

2001

Micellar structures of amphiphilic poly(1,2-butadiene)-block-poly(ethylene oxide) diblock copolymers have been crosslinked in aqueous solution by γ-irradiation. By transmission electron microscopy (TEM) of neganively stained specimen it is shown that the precominant structures present are sopolymer sesicles (which appear to be double latered. These fived vesules are stable with respect to their share and can be transferred from water into a good solvent for blue filbeks, such as tetrahydrofuran, this demonstrating the effectiveness of the crosslinking. In addition to the resicles a small number of flexible cylindrichl/filimented structures sequentially fused vesicles/strings of vesicles and…

Aqueous solutionMaterials sciencePolymers and PlasticsEthylene oxideVesicleOrganic ChemistryUranyl acetatechemistry.chemical_compoundCrystallographychemistryTransmission electron microscopyMicellar solutionsAmphiphilePolymer chemistryMaterials ChemistryCopolymerMacromolecular Rapid Communications
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Uranium(VI) sequestration by polyacrylic and fulvic acids in aqueous solution

2011

Stability data on the formation of dioxouranium(VI) species with polyacrylic (PAA) and fulvic acids (FA) are reported with the aim to define quantitatively the sequestering capacity of these high molecular weight synthetic and naturally occurring ligands toward uranium(VI), in aqueous solution. Investigations were carried out at t = 25 °C in NaCl medium at different ionic strengths and in absence of supporting electrolyte for uranyl–fulvate (\( {{\text{UO}}_{2}}^{2+} \)–FA) and uranyl–polyacrylate (\( {{\text{UO}}_{ 2}}^{ 2+ } \)–PAA, PAA MW 2 kDa) systems, respectively. The experimental data are consistent with the following speciation models for the two systems investigated: (i) UO2(FA1),…

Aqueous solutionSupporting electrolyteLigandHealth Toxicology and MutagenesisDioxouranium(VI) cation Uranium sequestration Uranyl–polycarboxylate interactions Fulvic acid Polyacrylic acid Metal complexes in aqueous solutionPolyacrylic acidPublic Health Environmental and Occupational Healthchemistry.chemical_elementIonic bondingUraniumUranylPollutionAnalytical ChemistryIonchemistry.chemical_compoundNuclear Energy and EngineeringchemistryPhysical chemistryRadiology Nuclear Medicine and imagingSettore CHIM/01 - Chimica AnaliticaSpectroscopyNuclear chemistry
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X-Ray crystallographic and computational study on uranyl-salophen complexes bearing nitro groups.

2017

In the solid state, salophen–UO2 complexes bearing one, two, or three NO2 groups lack the pronounced ligand curvature that represents a structural hallmark for this class of compounds. A detailed structural study based on single-crystal X-ray crystallography and computational methods, comprising molecular dynamics, gas-phase Hartree Fock, and DFT calculations, was carried out to investigate the coordination properties of the uranyl cation.

Bearing (mechanical)010405 organic chemistryLigandnitrogen dioxide groupsX-rayHartree–Fock methodMolecular Dynamics; X-ray diffraction; Uranyl complexesMolecular Dynamics010402 general chemistryUranyl01 natural sciencesX-ray diffraction0104 chemical scienceslaw.inventionInorganic ChemistryMolecular dynamicschemistry.chemical_compoundCrystallographyUranyl salophenchemistrylawUranyl complexesNitrouranyl-salophen complexesta116Dalton transactions (Cambridge, England : 2003)
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