Search results for "Actinide"

showing 10 items of 111 documents

Extraction of lanthanides and actinides by a magnetically assisted chemical separation technique based on CMPO-calix[4]arenes

2001

A novel particulate system carrying CMPO ligands pre-organised on a calixarene scaffold has been synthesised and demonstrated to extract Eu3+, Am3+ and Ce3+ at high efficiency from simulated nuclear waste streams.

ChemistryExtraction (chemistry)Metals and AlloysRadioactive wasteGeneral ChemistryActinideCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSolventChemical separationCalixareneMaterials ChemistryCeramics and CompositesParticulate systemNuclear chemistry
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Uptake of actinides by calcium silicate hydrate (C-S-H) phases

2018

Abstract The sorption of actinides (Th, U – Am) was studied in dependence of the solid-to-liquid (S/L) ratio (0.5–20.0 g/L) and the calcium-to-silicon (C:S) ratio. The C:S ratio was varied between 1.80 and 0.70 to simulate the changing composition of the C-S-H phases during cement degradation from high to low C:S ratios. The decrease of the calcium content in the C-S-H phases by time is accompanied by a decrease in pH in the corresponding suspensions from 12.6 to 10.2. X-ray photoelectron spectroscopy (XPS) of the C-S-H phases showed an increasing depletion of Ca on the surface with increasing C:S ratio in comparison to the composition of the solid phase as a whole. The sorption experiments…

cementTechnology02 engineering and technology010501 environmental sciences01 natural sciencesRedoxAmchemistry.chemical_compoundX-ray photoelectron spectroscopyGeochemistry and PetrologyOxidation statePhase (matter)Environmental ChemistryThCalcium silicate hydrateSpectroscopy0105 earth and related environmental sciencesUactinideshigh-energy resolution X-ray absorption near-edge structure (HR-XANES)SorptionX-ray photoelectron spectroscopy (XPS)Pu021001 nanoscience & nanotechnologyPollutionNpC-S-Hchemistryradioactive wasteSorptionAbsorption (chemistry)0210 nano-technologyddc:600Nuclear chemistry
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Exploring the High-Temperature Frontier in Molecular Nanomagnets: From Lanthanides to Actinides.

2019

Molecular nanomagnets based on mononuclear metal complexes, also known as single-ion magnets (SIMs), are crossing challenging boundaries in molecular magnetism. From an experimental point of view, this class of magnetic molecules has expanded from lanthanoid complexes to both d-transition metal and actinoid complexes. From a theoretical point of view, more and more improved models have been developed, and we are now able not only to calculate the electronic structure of these systems on the basis of their molecular structures but also to unveil the role of vibrations in the magnetic relaxation processes, at least for lanthanoid and d-transition metal SIMs. This knowledge has allowed us to o…

LanthanideField (physics)010405 organic chemistryChemistryMagnetismMolecular nanomagnetsUNESCO::QUÍMICAActinideElectronic structure010402 general chemistryMagnetic hysteresis:QUÍMICA [UNESCO]01 natural sciences0104 chemical sciencesInorganic ChemistryChemical physicsMagnetPhysical and Theoretical ChemistryInorganic chemistry
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Efficiency of dihydroxamic and trihydroxamic siderochelates to extract uranium and plutonium from contaminated soils

2021

International audience; Actinide-based mineral phases occurring in contaminated soils can be solubilized by organic chelators excreted by plants, such as citrate. Herein, the efficiency of citrate towards U and Pu extraction is compared to that of siderophores, whose primary function is the acquisition of iron(III) as an essential nutrient and growth factor for many soil microorganisms. To that end, we selected desferrioxamine B (DFB) as an emblematic bacterial trishydroxamic siderophore and a synthetic analog, abbreviated (LCy,Pr)H2, of the tetradentate rhodotorulic acid (RA) produced by yeasts. Firstly, the uranyl speciation with both ligands was assessed in the pH range 2–11 by potentiom…

Siderophore010504 meteorology & atmospheric scienceshydroxamic acidHealth Toxicology and Mutagenesis010501 environmental sciencesFerric Compounds01 natural sciencesActinidesSoilchemistry.chemical_compoundRadiation MonitoringEnvironmental Chemistry[CHIM]Chemical Sciencescitratesolid-liquid distributionWaste Management and DisposalEquilibrium constantChemical decomposition0105 earth and related environmental sciences[PHYS]Physics [physics]Hydroxamic acidExtraction (chemistry)General MedicineUranylPollutionPlutoniumRhodotorulic acidchemistryspeciation[SDE]Environmental SciencesUraniumSelectivityNuclear chemistry
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Actinide and lanthanide thin-layer developments using a drop-on-demand printing system

2023

Actinide and lanthanide thin layers with specific requirements regarding thickness, homogeneity, chemical purity, mechanical stability, and backing properties are applied in a multitude of physics and chemistry experiments. A novel target preparation method, the so-called “Drop-on-Demand” (DoD) technique, based on a commercial nanoliter (nL) dispenser is applied since a few years in the Nuclear Chemistry unit at Johannes Gutenberg University Mainz. The wetting behaviour of the nL droplets on the substrate’s surface is a key parameter determining the spatial distribution of the deposited material after evaporation. By switching from aqueous to organic solvents as well as by substrate surface…

aktinoidit lantanoiditactinideslanthanidesdrop-on-demand printing systemharvinaiset maametallit
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Lawrencium chemistry: no evidence for oxidation states lower than 3+ in aqueous solution

1988

Lawrencium (3-min 260Lr) together with other actinides, was produced in the bombardment of a 249Bk target with 18O ions. There was no sign of a reduction of Lr3+ in dilute hydrochloric acid by V2+ or Cr2+, although in the same experiments, Md3+ was reduced to Md2+ (E°=−0.2 V). The resulting limit for the reduction potential of the Lr3+/Lr1(2)+ couple is E° < −0.44 V.

Inorganic Chemistrychemistry.chemical_compoundAqueous solutionchemistryInorganic chemistryMaterials Chemistrychemistry.chemical_elementHydrochloric acidQualitative inorganic analysisActinidePhysical and Theoretical ChemistryLawrenciumIonInorganica Chimica Acta
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X-ray absorption spectroscopic study of trivalent and tetravalent actinides in solution at varying pH values

2009

Abstract We perform X-ray absorption spectroscopy (XAS) investigations to monitor the stabilization of redox sensitive trivalent and tetravalent actinide ions in solution at acidic conditions in a pH range from 0 to 3 after treatment with holding reductants, hydroxylamine hydrochloride (NH2OHHCl) and Rongalite (sodium hydroxymethanesulfinate, CH3NaO3S). X-ray absorption near edge structure (XANES) measurements clearly demonstrate the stability of the actinide species for several hours under the given experimental conditions. Hence, structural parameters can be accurately derived by extended X-ray absorption fine structure (EXAFS) investigations. The coordination structure of oxygen atoms be…

RongaliteX-ray absorption spectroscopychemistry.chemical_compoundAbsorption spectroscopyExtended X-ray absorption fine structureChemistryMetal ions in aqueous solutionInorganic chemistryActinidePhysical and Theoretical ChemistryAbsorption (chemistry)XANESRadiochimica Acta
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Sensitive laser spectroscopy on trapped barium ions by quenching with hydrogen

1983

The sensitivity of laser spectroscopy on barium ions stored in a radio frequency quadrupole trap was drastically increased by using hydrogen for quenching the optically pumped metastable states. The attained fluorescence intensity per ion permits the detection of single ions. The method will be applied to environmental studies on actinides.

Quenching (fluorescence)Materials sciencePhysics and Astronomy (miscellaneous)HydrogenGeneral EngineeringAnalytical chemistryPhysics::OpticsGeneral Physics and Astronomychemistry.chemical_elementBariumActinideIonchemistryRadio-frequency quadrupolePhysics::Plasma PhysicsMetastabilityPhysics::Atomic PhysicsAtomic physicsSpectroscopyApplied Physics B Photophysics and Laser Chemistry
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Neck fragmentation in fission and quasifission of heavy and superheavy nuclei

2009

The generalized approach is proposed for the ternary fission and the neck fragmentation of the dinuclear system formed in the heavy ion quasifission reactions. The light-charged-particles accompanied the fission and quasifission are the valuable probes for studies of the dynamics of the hyperdeformed nuclear configurations with neck. The developed model describes well the light-charged-particle emission probabilities and their mass distributions in the ternary fission of actinide nuclei. The model is also applied to analyze the double differential distributions of the protons and α-particles accompanied fragmentation in the reaction 86 Kr + 206 Pb at E Kr = 500 and 600 MeV. It was found th…

PhysicsNuclear physicsternary fissionNuclear and High Energy Physicsneck fragmentaionCluster decayFragmentation (mass spectrometry)FissionGeneral Physics and AstronomyHeavy ionActinideTernary fission
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The recoil transfer chamber—An interface to connect the physical preseparator TASCA with chemistry and counting setups

2011

Performing experiments with transactinide elements demands highly sensitive detection methods due to the extremely low production rates (one-atom-at-a-time conditions). Preseparation with a physical recoil separator is a powerful method to significantly reduce the background in experiments with sufficiently long-lived isotopes (t1/2≥0.5 s). In the last years, the new gas-filled TransActinide Separator and Chemistry Apparatus (TASCA) was installed and successfully commissioned at GSI. Here, we report on the design and performance of a Recoil Transfer Chamber (RTC) for TASCA—an interface to connect various chemistry and counting setups with the separator. Nuclear reaction products recoiling o…

PhysicsNuclear reactionNuclear and High Energy Physicschemistry.chemical_elementTransactinide elementRecoil separatorIonNuclear physicsRecoilCardinal pointRigidity (electromagnetism)chemistryRutherfordiumInstrumentationNuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment
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