Search results for "actinide"

showing 10 items of 111 documents

Decomposition studies of group 6 hexacarbonyl complexes. Part 1: Production and decomposition of Mo(CO)6 and W(CO)6

2015

Abstract Chemical studies of superheavy elements require fast and efficient techniques, due to short half-lives and low production rates of the investigated nuclides. Here, we advocate for using a tubular flow reactor for assessing the thermal stability of the Sg carbonyl complex – Sg(CO)6. The experimental setup was tested with Mo and W carbonyl complexes, as their properties are established and supported by theoretical predictions. The suggested approach proved to be effective in discriminating between the thermal stabilities of Mo(CO)6 and W(CO)6. Therefore, an experimental verification of the predicted Sg–CO bond dissociation energy seems to be feasible by applying this technique. By in…

Inorganic chemistryMetal carbonyl02 engineering and technology010402 general chemistry01 natural sciences7. Clean energythermal stability540 ChemistryseaborgiumThermal stabilityNuclideGas compositionPhysical and Theoretical Chemistrycarbonyl complexegroup 6ChemistrytransactinideTransition metals021001 nanoscience & nanotechnologyDecompositionBond-dissociation energy0104 chemical sciencesVolumetric flow rateYield (chemistry)570 Life sciences; biologyPhysical chemistry0210 nano-technology
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Modeling plutonium sorption to kaolinite: Accounting for redox equilibria and the stability of surface species

2015

Abstract Plutonium with its particularly complex redox chemistry may be thermodynamically stable in the states + III to + VI depending on the redox conditions in the environment. Mineral surfaces can also affect Pu redox speciation. Therefore, the interpretation of Pu sorption data becomes particularly challenging, even for simplified laboratory experiments. The present study focuses on Pu sorption to kaolinite. Am(III), Th(IV), Np(V) and U(VI) literature sorption data are used as analogues for the corresponding Pu redox states to calibrate a simple surface complexation model, and the Nernst formalism is applied. Two independent pH–pe diagrams, one for the kaolinite surface and another for …

Inorganic chemistrychemistry.chemical_elementGeologySorptionContext (language use)ActinideRedoxPlutoniumsymbols.namesakechemistryGeochemistry and PetrologyOxidizing agentsymbolsKaoliniteNernst equationNuclear chemistryChemical Geology
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Resonance ionization spectroscopy for trace analysis and fundamental research

1994

Resonance ionization spectroscopy (RIS) and its combination with mass spectrometry (RIMS) have grown to become powerful techniques, which offer high sensitivity as well as elemental and isotopic selectivity. The principles of RIS and RIMS are introduced; they primarily concern the analysis of the optical spectra for the choice of efficient excitation schemes and the suitable design of the experimental apparatus. Recent applications span from studies of short-lived isotopes at on-line mass separators to a wide variety of trace analysis applications for radioactive isotopes, which can range from measurements of solar neutrino flux to environmental assessment.

IsotopeChemistrySolar neutrinoAnalytical chemistryResonanceFluxActinideMass spectrometrySpectroscopyBiochemistryExcitationAnalytical ChemistryComputational physicsFresenius' Journal of Analytical Chemistry
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Uranium from German Nuclear Power Projects of the 1940s— A Nuclear Forensic Investigation

2015

Here we present a nuclear forensic study of uranium from German nuclear projects which used different geometries of metallic uranium fuel. Through measurement of the (230)Th/(234)U ratio, we could determine that the material had been produced in the period from 1940 to 1943. To determine the geographical origin of the uranium, the rare-earth-element content and the (87)Sr/(86)Sr ratio were measured. The results provide evidence that the uranium was mined in the Czech Republic. Trace amounts of (236)U and (239)Pu were detected at the level of their natural abundance, which indicates that the uranium fuel was not exposed to any major neutron fluence.

Isotopes of uraniumbusiness.industryWirtz KarlNuclear forensicsnuclear forensicsRadiochemistrychemistry.chemical_elementGeneral ChemistryActinideNuclear powerUraniumCommunicationsCatalysisuraniumUranium-236chemistryUranium-234Environmental scienceHeisenberg WernerbusinessPlutonium-239mass spectrometryAngewandte Chemie International Edition
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Mobility of the Singly-Charged Lanthanide and Actinide Cations: Trends and Perspectives

2020

The current status of gaseous transport studies of the singly-charged lanthanide and actinide ions is reviewed in light of potential applications to superheavy ions. The measurements and calculations for the mobility of lanthanide ions in He and Ar agree well, and they are remarkably sensitive to the electronic configuration of the ion, namely, whether the outer electronic shells are 6s, 5d6s or 6s$^2$. The previous theoretical work is extended here to ions of the actinide family with zero electron orbital momentum: Ac$^+$ (7s$^2$, $^1$S), Am$^+$ (5f$^7$7s $^9$S$^\circ$), Cm$^+$ (5f$^7$7s$^2$ $^8$S$^\circ$), No$^+$ (5f$^{14}$7s $^2$S) and Lr$^+$ (5f$^{14}$7s$^2$ $^1$S). The calculations rev…

LanthanideAtomic Physics (physics.atom-ph)Ab initioFOS: Physical sciences02 engineering and technologyElectroninteraction potential010402 general chemistry7. Clean energy01 natural sciencesPhysics - Atomic PhysicsIonlcsh:Chemistryion mobilityAtomlanthanideselectronic configurationOriginal ResearchPhysicsIonic radiussuperheavy ionsactinidesGeneral ChemistryActinide021001 nanoscience & nanotechnology3. Good health0104 chemical sciencesChemistrylcsh:QD1-999ddc:540Electron configurationAtomic physics0210 nano-technology
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Fast preparation and gas-chromatographic separation of lanthanide and actinide hexafluoroacetylacetonates

1986

A fast method for the separation of lanthanide elements by gas chromatography of their hexafluoroacetylacetonates is described. Individual lanthanides can be isolated within a few minutes, and the whole group can be separated in less than 10 min. The hexafluoroacetylacetonates are applied in form of mixed complexes with tri-n-butyl phosphate or trioctylphosphine oxide prepared by fast extraction into quasi-solid solvents. The applicability of this method for the separation of trivalent actinide elements is shown, including the fast preparation of thin counting samples.

LanthanideClinical BiochemistryExtraction (chemistry)TrioctylphosphineAnalytical chemistryGeneral MedicineActinideAnalytical Chemistrychemistry.chemical_compoundChromatographic separationchemistryGeneral Materials ScienceGas chromatographyTrioctylphosphine oxideFresenius' Zeitschrift für analytische Chemie
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Fast volatilization of some lanthanide and actinide elements from titanium surfaces

1989

The ad- and desorption of trace quantities of the lanthanide elements lanthanum, praseodymium, neodymium, samarium, europium, gadolinium, dysprosium, and ytterbium and of the actinide elements americium and curium were investigated by thermochromatographic and isothermal measurements with hot titanium columns. The adsorption enthalpies deduced from the experimental data are in reasonable agreement with calculated values which indicate considerable variations in volatility under such conditions. More volatile elements can quickly be separated from less volatile elements by heating the mixture on titanium in high vacuum.

LanthanideCuriumChemistryPraseodymiumClinical BiochemistryInorganic chemistrychemistry.chemical_elementAmericiumGeneral MedicineActinideBiochemistryAnalytical ChemistrySamariumLanthanumGeneral Materials ScienceEuropiumFresenius' Zeitschrift f�r Analytische Chemie
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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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Dendrimer-coated magnetic particles for radionuclide separation

2005

Magnetic particles were synthesised for radionuclide removal from nuclear wastes by magnetic separation. Dendrimers with terminal amino groups attached to the particle surface were used to bind chelating groups for lanthanides and actinides. This led to a 50–400-fold increase of the distribution coefficients for europium and americium in comparison to the reference particles without the dendrimers. Back-extraction studies have demonstrated the possibility of multiple particle recycling.

LanthanideIR-53099RadiochemistryMagnetic separationchemistry.chemical_elementAmericiumMETIS-225399ActinideCondensed Matter Physicsequipment and suppliesElectronic Optical and Magnetic MaterialschemistryDendrimerParticleMagnetic nanoparticlesEuropiumhuman activities
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Narrow rim CMPO/adamantylcalix[4]arenes for the extraction of lanthanides and actinides

2011

Abstract Six p-(1-adamantyl)calix[4]arenes 7, 8 with four differently attached diphenyl-carbamoylmethylphosphine oxide (CMPO) functions at the narrow rim were synthesized. This series was extended by adamantylcalix[4]arenes with two CMPO and two ester, acid or (diethylphosphono)acetylamino groups. Structures of new compounds were proved by NMR, mass-spectrometry and a single-crystal X-ray analysis for the intermediate di-phthalimide 103. The extraction studies towards selected lanthanides and thorium showed that the ligands 7 surpassed the corresponding p-H, p-tert-butyl and p-tert-octyl analogues 3–5 in lanthanide extraction while thorium was extracted with the same or lesser extent. For t…

LanthanideLigandOrganic ChemistryExtraction (chemistry)OxideThoriumchemistry.chemical_elementActinideBiochemistrychemistry.chemical_compoundchemistryDrug DiscoveryCalixareneNuclear chemistryTetrahedron
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