0000000000048348

AUTHOR

Jens Volker Kratz

showing 52 related works from this author

Die experimentelle Bestimmung der Ionisationsenergien von Berkelium und Californium

1996

Materials scienceGeneral MedicineAngewandte Chemie
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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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Extraction behavior of rutherfordium into tributylphosphate from hydrochloric acid

2007

The extraction behavior of rutherfordium (Rf) into tributylphosphate (TBP) from hydrochloric acid (HCl) has been studied together with those of the lighter group-4 elements Zr and Hf. The extractability of261Rf,169Hf, and85Zr into TBP was investigated under identical conditions in 7.2–8.0 M HCl by on-line reversed-phase extraction chromatography. The percent extractions of Rf, Hf, and Zr into the TBP resin increase steeply with increasing HCl concentration, and the order of extraction is Zr &gt; Hf ≈ Rf. By considering the order of chloride complexation among these elements, it is suggested that the stability of the TBP complex of Rf tetrachloride is lower than those of Zr and Hf.

chemistry.chemical_compoundchemistryRutherfordiumTetrachlorideInorganic chemistryExtraction (chemistry)medicinechemistry.chemical_elementHydrochloric acidPhysical and Theoretical ChemistryChloridemedicine.drugNuclear chemistryRadiochimica Acta
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Dosimetric feasibility study for an extracorporeal BNCT application on liver metastases at the TRIGA Mainz

2010

This study investigates the dosimetric feasibility of Boron Neutron Capture Therapy (BNCT) of explanted livers in the thermal column of the research reactor in Mainz. The Monte Carlo code MCNP5 is used to calculate the biologically weighted dose for different ratios of the (10)B-concentration in tumour to normal liver tissue. The simulation results show that dosimetric goals are only partially met. To guarantee effective BNCT treatment the organ has to be better shielded from all gamma radiation.

Radiationbusiness.industryLiver NeoplasmsBoron Neutron Capture TherapyRadiotherapy DosageModels BiologicalExtracorporealTRIGANeutron captureMonte carlo codeLiver tissueHumansMedicineComputer SimulationRadiometryNuclear medicinebusinessApplied Radiation and Isotopes
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Forensic investigation of brick stones using instrumental neutron activation analysis (INAA), laser ablation-inductively coupled plasma-mass spectrom…

2009

Abstract Brick stones collected from different production facilities were studied for their elemental compositions under forensic aspects using laser ablation–inductively coupled plasma–mass spectrometry (LA–ICP–MS), instrumental neutron activation analysis (INAA) and X-ray fluorescence analysis (XRF). The aim of these examinations was to assess the potential of these methods in forensic comparison analyses of brick stones. The accuracy of the analysis methods was evaluated using NIST standard reference materials (679, 98b and 97b). In order to compare the stones to each other, multivariate data analysis was used. The evaluation of the INAA results (based on the concentrations of V, Na, K, …

BrickRadiationLa icp msChemistryElemental analysisLaser ablation inductively coupled plasma mass spectrometryAnalytical chemistryX-ray fluorescenceNeutron activation analysisMass spectrometryAnalysis methodApplied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine
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Chemical studies of elements with Z≥ 104 in liquid phase

2015

Abstract Recent studies of the chemical separation and characterization experiments of the first three transactinide elements, rutherfordium (Rf), dubnium (Db), and seaborgium (Sg), conducted atom-at-a-time in liquid phases, are reviewed. A short description on experimental techniques based on partition methods, specifically automated rapid chemical separation systems, is also given. A newly developed experimental approach to investigate single atoms of the heaviest elements with an electrochemical method is introduced. Perspectives for liquid-phase chemistry experiments on heavier elements are briefly discussed.

PhysicsDubniumNuclear and High Energy PhysicsCountercurrent chromatographyChemical substancechemistrySeaborgiumRutherfordiumAnalytical chemistryLiquid phaseTransactinide elementchemistry.chemical_elementScience technology and societyNuclear Physics A
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Fluoride Complexation of Element 104, Rutherfordium (Rf), Investigated by Cation-exchange Chromatography

2008

We report on new and much more precise cation-exchange data of element 104, rutherfordium (Rf), in the fluoride ion concentration [F−] range of 5.29×10−5−1.04×10−3 M. The result based on one-atom-a...

chemistry.chemical_compoundchemistryRutherfordiumInorganic chemistryIon chromatographyAnalytical chemistrychemistry.chemical_elementGeneral ChemistryFluorideIonChemistry Letters
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First ionization potential of the heaviest actinide lawrencium, element 103

2016

The first ionization potential (IP1 ) of element 103, lawrencium (Lr), has been successfully determined for the first time by using a newly developed method based on a surface ionization process. The measured IP 1 value is 4.9630.08 0.07 eV. This value is the smallest among those of actinide elements and is in excellent agreement with the value of 4.963(15) eV predicted by state-of-the-art relativistic calculations also performed in this work. Our results strongly support that the Lr atom has an electronic configuration of [Rn]7s 2 5f 14 7p 1 1/2 , which is influenced by strong relativistic effects. The present work provides a reliable benchmark for theoretical calculations and also opens t…

PhysicsPhysicsQC1-99905 social sciences050301 educationThermal ionizationchemistry.chemical_elementActinide010403 inorganic & nuclear chemistry01 natural sciences0104 chemical scienceschemistryNuclear Physics - TheoryAtomNuclear Physics - Experimentddc:530Atomic numberElectron configurationAtomic physicsIonization energyRelativistic quantum chemistry0503 educationLawrencium
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Complex chemistry with complex compounds

2016

In recent years gas-phase chemical studies assisted by physical pre-separation allowed for the investigation of fragile single molecular species by gas-phase chromatography. The latest success with the heaviest group 6 transactinide seaborgium is highlighted. The formation of a very volatile hexacarbonyl compound Sg(CO)6 was observed similarly to its lighter homologues molybdenum and tungsten. The interactions of these gaseous carbonyl complex compounds with quartz surfaces were investigated by thermochromatography. Second-generation experiments are under way to investigate the intramolecular bond between the central metal atom of the complexes and the ligands addressing the influence of re…

PhysicsQC1-999Transactinide elementchemistry.chemical_elementTungsten010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciences0104 chemical sciencesMetalchemistryGroup (periodic table)Computational chemistryMolybdenumChemical physicsvisual_artIntramolecular forceSeaborgium540 ChemistryAtomvisual_art.visual_art_medium570 Life sciences; biologyEPJ Web of Conferences
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Few-neutron removal from238U at relativistic energies

1995

As part of a comprehensive study of uranium fragmentation at relativistic energies at the GSI projectile fragment separator, FRS, inclusive neutron-removal cross sections have been measured for severalxn channels at projectile energies of 600 and 950A MeV using targets of Al, Cu and Pb. The variation of the experimental cross sections with target nuclear charge is used to disentangle nuclear and electromagnetic contributions. The electromagnetic cross sections agree surprisingly well with a simple harmonic oscillator calculation of giant dipole resonances based on measured photonuclear cross sections and do not require an extra enhancement of the two-phonon giant dipole excitation as conclu…

PhysicsNuclear and High Energy PhysicsProjectileNuclear Theorychemistry.chemical_elementSimple harmonic motionUraniumEffective nuclear chargeNuclear physicsDipoleFragmentation (mass spectrometry)chemistryNuclear fusionNeutronAtomic physicsNuclear ExperimentNuclear PhysicsZeitschrift für Physik A Hadrons and Nuclei
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Critical Evaluation of the Chemical Properties of the Transactinoid Elements (IUPAC Technical Report)

2003

Polymer scienceChemistryChemical nomenclatureTechnical reportGeneral MedicineChemInform
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First Ionization Potentials of Fm, Md, No, and Lr

2018

We report the first ionization potentials (IP1) of the heavy actinides, fermium (Fm, atomic number Z = 100), mendelevium (Md, Z = 101), nobelium (No, Z = 102), and lawrencium (Lr, Z = 103), determined using a method based on a surface ionization process coupled to an online mass separation technique in an atom-at-a-time regime. The measured IP1 values agree well with those predicted by state-of-the-art relativistic calculations performed alongside the present measurements. Similar to the well-established behavior for the lanthanides, the IP1 values of the heavy actinides up to No increase with filling up the 5f orbital, while that of Lr is the lowest among the actinides. These results clear…

ENERGIESThermal ionizationchemistry.chemical_element01 natural sciencesBiochemistryCatalysisColloid and Surface ChemistrySURFACE-IONIZATIONPhysics in GeneralCHEMISTRYIonization0103 physical sciencesELEMENTS010306 general physicsSPECTROSCOPY010304 chemical physicsChemistryFermiumGeneral ChemistryActinideATOMMendeleviumNobeliumAtomic numberAtomic physicsLawrenciumJournal of the American Chemical Society
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Chronological development of element concentrations in grapes during growth and ripeness and during fermentation of must determined by instrumental n…

2014

Abstract The chronological development of element concentrations during growth and ripeness of grapes described in the literature has only been concerned with the macro elements Mg, K, and Ca. Concentrations of trace elements in must are only described as a snapshot at the end of the ripeness. Therefore, the motivation for the present work was to accompany the growth and the ripening process of grapes successively by systematically determining element concentrations in grapes of Riesling and Cabernet Sauvignon by neutron-activation analyses. While for a number of elements, the concentrations in the grapes increased as a function of grape development (e.g., Na, K, Rb, Al), other concentratio…

ChemistryNondestructive analysisFermentationFood scienceRadiochemical analysisPhysical and Theoretical ChemistryNeutron activation analysisRipenessNeutron temperatureNeutron activationRadiochimica Acta
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Stabilization of polynuclear plutonium(IV) species by humic acid

2014

Abstract Although the formation of tetravalent plutonium (Pu(IV)) polymers with natural organic matter was previously observed by spectroscopy, there is no quantitative evidence of such reaction in batch experiments. In the present study, Pu(IV) interaction with humic acid (HA) was investigated at pH 1.8, 2.5 and 3, as a function of HA concentration and for Pu total concentration equal to 6 × 10−8 M. The finally measured Pu(IV) concentrations ([Pu(IV)]eq) are below Pu(IV) solubility limit. Pu(IV)–HA interaction can be explained by the complexation of Pu(IV) monomers by HA up to [Pu(IV)]eq ∼ 10−8 M. However, the slope of the log–log Pu(IV)–HA binding isotherm changes from ∼0.7 to ∼3.5 for hi…

chemistry.chemical_classificationChemistrychemistry.chemical_elementPlutoniumchemistry.chemical_compoundHydrolysisMonomerTetramerGeochemistry and PetrologyHumic acidSolubilitySpectroscopyStoichiometryNuclear chemistryGeochimica et Cosmochimica Acta
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Anionic Fluoro Complex of Element 105, Db

2009

We report on the characteristic anion-exchange behavior of the superheavy element dubnium (Db) with atomic number Z=105 in HF/HNO3 solution at the fluoride ion concentration [F−]=0.003 M. The resul...

Dubniumchemistry.chemical_compoundChemistryStereochemistryPhysical chemistrychemistry.chemical_elementGeneral ChemistryAtomic numberFluorideIonChemistry Letters
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Chemical properties of rutherfordium (Rf) and dubnium (Db) in the aqueous phase

2016

Recent experimental studies of the chemical characterization of the first two transactinide elements, rutherfordium (Rf) and dubnium (Db), conducted atom-at-a-time in aqueous phases are reviewed. A short description on experimental techniques based on partition methods, specifically automated rapid chemical separation systems, is also given. Perspectives for aqueous-phase chemistry experiments on heavier elements are briefly discussed.

DubniumAqueous solutionPhysicsQC1-999Aqueous two-phase systemAnalytical chemistrychemistry.chemical_elementTransactinide element010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciences0104 chemical sciencesChemical separationchemistryChemical engineeringRutherfordiumEPJ Web of Conferences
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Determination of the partial electron capture- and spontaneous-fission half-lives of254No

1988

The isotope254No was produced in the fusion reaction48Ca +208Pb. Using the velocity filter SHIP and radiochemical techniques it was found that the nuclide254No with a half-life of 55 s decays byα, EC, and spontaneous-fission. Deduced partial half-lives are (61±2) s forα-decay, (550−160+370) s for EC and [2.2−1.0+2.0]×104 s for spontaneous fission.

PhysicsNuclear and High Energy PhysicsFusionFilter (video)Electron captureNuclear fusionAtomic physicsSpontaneous fissionZeitschrift f�r Physik A Atomic Nuclei
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First Experimental Determination of the Ionization Potentials of Berkelium and Californium

1996

BerkeliumChemistryIonizationRadiochemistrychemistry.chemical_elementCaliforniumGeneral MedicineGeneral ChemistryActinideSpectroscopyCatalysisAngewandte Chemie International Edition in English
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First Determination of the Ionization Potential of Actinium and First Observation of Optical Transitions in Ferminm

2002

For the determination of the first ionization potential of actinium, 227Ac was electrodeposited on a Ta backing and covered with ~1 μm Zr. From this filament, Ac atoms were evaporated at ≥ 1250 °C. By resonant excitation with UV light of 388.67 nm and subsequent excitation with light of ca. 568 nm, Ac was ionized in an external electrical field. By determining the ionization thresholds as a function of the electrical field strength and by extrapolation to zero field strength, the first ionization potential of 43398(3) cm−1 = 5.3807(3) eV was measured.About 1 ng of 255Fm, half life 20.1 h, was prepared at ORNL by milking from 255Es produced in the High Flux Isotope Reactor and shipped to Mai…

Nuclear and High Energy PhysicsChemistryBuffer gasAnalytical chemistryThermal ionizationchemistry.chemical_elementIonActiniumNuclear Energy and EngineeringExcited stateIonizationAtomic physicsIonization energyExcitationJournal of Nuclear Science and Technology
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Boron determination in liver tissue by combining quantitative neutron capture radiography (QNCR) and histological analysis for BNCT treatment plannin…

2011

The typical primary malignancies of the liver are hepatocellular carcinoma and cholangiocarcinoma, whereas colorectal liver metastases are the most frequently occurring secondary tumors. In many cases, only palliative treatment is possible. Boron neutron capture therapy (BNCT) represents a technique that potentially destroys tumor tissue selectively by use of externally induced, locally confined secondary particle irradiation. In 2001 and 2003, BNCT was applied to two patients with colorectal liver metastases in Pavia, Italy. To scrutinize the rationale of BNCT, a clinical pilot study on patients with colorectal liver metastases was carried out at the University of Mainz. The distribution o…

NeutronsPathologymedicine.medical_specialtyRadiationPalliative treatmentbusiness.industryRadiographyBiophysicsParticle irradiationmedicine.diseaseRadiographyNeutron captureLiverHepatocellular carcinomaLiver tissueCell Line TumormedicineHumansRadiology Nuclear Medicine and imagingSecondary tumorsbusinessRadiation treatment planningNuclear medicineBoronRadiation research
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Actinides and Transactinides

2020

RadiochemistryKirk‐Othmer Encyclopedia of Chemical Technology
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Backings and targets for chemical and nuclear studies of transactinides with TASCA

2008

Abstract At GSI the gas-filled separator TASCA (TransActinide Separator and Chemistry Apparatus) was set up to investigate the chemical and physical properties of the heaviest elements making use of the highest beam intensities available [ www.gsi.de/tasca ; M. Schadel, D. Ackermann, A. Semchenkov, A. Turler, GSI Scientific Report 2005, GSI Report 2006-1, p. 262]. Appropriate backings and targets have to be developed. Conceivable backing materials are aluminium, titanium, and carbon. Aluminium backings and titanium backings in different thickness and from different companies are produced by cold rolling. Deposition by resistance heating is applied for carbon backings. For experiments in a c…

PhysicsNuclear and High Energy PhysicsMetallurgychemistry.chemical_elementTransactinide elementActinideUranium tetrafluorideUraniumNuclear physicschemistry.chemical_compoundVacuum depositionchemistryAluminiumBerylliumInstrumentationTitaniumNuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment
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Neues von den Transactiniden-Elementen

2000

Das Forschungsgebiet „Chemie der schwersten Elemente” hat eine Fulle neuer Ergebnisse erbracht, unter anderem die erste chemische Untersuchung des Elements 107, Bohrium.

General Chemical EngineeringGeneral ChemistryNachrichten aus der Chemie
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Digital liquid-scintillation counting and effective pulse-shape discrimination with artificial neural networks

2014

Abstract A typical problem in low-level liquid scintillation (LS) counting is the identification of α particles in the presence of a high background of β and γ particles. Especially the occurrence of β-β and β-γ pile-ups may prevent the unambiguous identification of an α signal by commonly used analog electronics. In this case, pulse-shape discrimination (PSD) and pile-up rejection (PUR) units show an insufficient performance. This problem was also observed in own earlier experiments on the chemical behaviour of transactinide elements using the liquid-liquid extraction system SISAK in combination with LS counting. α-particle signals from the decay of the transactinides could not be unambigu…

Artificial neural networkAnalogue electronicsChemistrybusiness.industryLiquid scintillation countingPattern recognitionSignalPulse (physics)Artificial intelligenceTransient (oscillation)Physical and Theoretical ChemistryOscilloscopebusinessDigital recordingRadiochimica Acta
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Dose calculation in biological samples in a mixed neutron-gamma field at the TRIGA reactor of the University of Mainz

2010

To establish Boron Neutron Capture Therapy (BNCT) for non-resectable liver metastases and for in vitro experiments at the TRIGA Mark II reactor at the University of Mainz, Germany, it is necessary to have a reliable dose monitoring system. The in vitro experiments are used to determine the relative biological effectiveness (RBE) of liver and cancer cells in our mixed neutron and gamma fi eld. We work with alanine detectors in combination with Monte Carlo simulations, where we can measure and characterize the dose. To verify our calculations we perform neutron fl ux measurements using gold foil activation and pin-diodes . Material and methods . When L- α -alanine is irradiated with ionizing …

inorganic chemicalsPhysics::Instrumentation and DetectorsQuantitative Biology::Tissues and OrgansPhysics::Medical PhysicsBoron Neutron Capture TherapyValidation Studies as TopicModels BiologicalIonizing radiationTRIGAHospitals UniversityNuclear ReactorsCell Line TumorGermanyRelative biological effectivenessMedicineDosimetryHumansRadiology Nuclear Medicine and imagingNeutronNeutronsbusiness.industryRadiotherapy Planning Computer-AssistedRadiochemistryLiver NeoplasmsRadiotherapy DosageHematologyGeneral MedicineHep G2 CellsNeutron temperatureNeutron captureOncologyGamma RaysAbsorbed dosebusinessNuclear medicineColorectal Neoplasms
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Coulomb excitation of exotic nuclei at the R3B-LAND setup

2012

Exotic Ni isotopes have been measured at the R3B-LAND setup at GSI in Darmstadt, using Coulomb excitation in inverse kinematics at beam energies around 500 MeV/u. As the experimental setup allows kinematically complete measurements, the excitation energy was reconstructed using the invariant mass method. The GDR and additional low-lying strength have been observed in 68Ni, the latter exhausting 4.1(1.9)% of the E1 energy-weighted sum rule. Also, the branching ratio for the non-statistical decay of the excited 68Ni nuclei was measured and amounts to 24(4)%.

PhysicsHistoryInverse kinematicsBranching fractionFOS: Physical sciencesExotic isotopes R3B LAND GSI Coulomb excitation inverse kinematics GDR PDRCoulomb excitationComputer Science ApplicationsEducationNuclear physicsExcited stateInvariant massSum rule in quantum mechanicsNuclear Experiment (nucl-ex)Nuclear ExperimentNuclear ExperimentBeam (structure)Excitation
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Dose determination using alanine detectors in a mixed neutron and gamma field for boron neutron capture therapy of liver malignancies

2011

IntroductionBoron Neutron Capture Therapy for liver malignancies is being investigated at the University of Mainz. One important aim is the set-up of a reliable dosimetry system. Alanine dosimeters have previously been applied for dosimetry of mixed radiation fields in antiproton therapy, and may be suitable for measurements in mixed neutron and gamma fields.Materials and MethodsTwo experiments have been carried out in the thermal column of the TRIGA Mark II reactor at the University of Mainz. Alanine dosimeters have been irradiated in a phantom and in liver tissue.ResultsFor the interpretation and prediction of the dose for each pellet, beside the results of the measurements, calculations …

Monte Carlo methodBoron Neutron Capture TherapyImaging phantomTRIGAIonizing radiationRadiation MonitoringHumansMedicineDosimetryRadiology Nuclear Medicine and imagingNeutronRadiometryNeutronsAlanineDosimeterPhantoms Imagingbusiness.industryLiver NeoplasmsRadiochemistryDose-Response Relationship RadiationHematologyGeneral MedicineNeutron captureLiverOncologyGamma RaysbusinessNuclear medicineMonte Carlo MethodActa Oncologica
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Studies of the ternary systems humic substances – kaolinite – Pu(III) and Pu(IV)

2008

AbstractThe behaviour of plutonium with respect to its migration in the aquifer has been studied under conditions close to nature. Most relevant under these conditions are Pu(III) and Pu(IV) in contact with humic substances (HS) and minerals. As a model for the host rock, kaolinite (KGa-1b) was chosen. The complexation of Pu(III) and Pu(IV) with Aldrich humic acid (AHA) in aqueous solution at ionic strength 0.1 M was investigated by the ultrafiltration method. The sorption of Pu(III) and Am(III) onto kaolinite (K) as a function of pH and metal-ion concentration was studied under aerobic and anaerobic conditions. The pH edge was found at pH∼5.5 independent of the metal-ion concentration and …

chemistry.chemical_classificationAqueous solutionTernary numeral systemchemistryIonic strengthInorganic chemistryUltrafiltrationHumic acidKaoliniteSorptionPhysical and Theoretical ChemistryTernary operationNuclear chemistryRadiochimica Acta
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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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First successful ionization of Lr (Z = 103) by a surface-ionization technique.

2013

We have developed a surface ionization ion-source as part of the JAEA-ISOL (Isotope Separator On-Line) setup, which is coupled to a He/CdI2 gas-jet transport system to determine the first ionization potential of the heaviest actinide lawrencium (Lr, Z = 103). The new ion-source is an improved version of the previous source that provided good ionization efficiencies for lanthanides. An additional filament was newly installed to give better control over its operation. We report, here, on the development of the new gas-jet coupled surface ion-source and on the first successful ionization and mass separation of 27-s (256)Lr produced in the (249)Cf + (11)B reaction.

Materials sciencechemistryIonizationThermal ionizationchemistry.chemical_elementActinideIonization energyAtomic physicsMolar ionization energies of the elementsInstrumentationIon sourceLawrenciumAtmospheric-pressure laser ionizationThe Review of scientific instruments
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Influence of Collective Surface Motion on the Threshold Behavior of Nuclear Fusion

1982

Fusion excitation functions for the systems $^{40}\mathrm{Ar}$+$^{112,116,122}\mathrm{Sn}$ and $^{40}\mathrm{Ar}$+$^{144,148,154}\mathrm{Sm}$ have been determined, covering cross sections ranging from several hundred millibarns down to the microbarn level. The data are interpreted with a fusion model that includes fluctuations of the barrier with an amplitude that is shown to be correlated with the collective surface properties of the nuclei. There is no need to assume an additional enhanced tunneling process.

Nuclear reactionPhysicsSurface (mathematics)FusionAmplitudeGeneral Physics and AstronomyMotion (geometry)Nuclear fusionAtomic physicsQuantum tunnellingExcitationPhysical Review Letters
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Separation of plutonium and neptunium species by capillary electrophoresis-inductively coupled plasma-mass spectrometry and application to natural gr…

2003

Capillary electrophoresis (CE) was coupled to ICPMS in order to combine the good performance of this separation technique with the high sensitivity of the ICPMS for the analysis of plutonium and neptunium oxidation states. The combination of a fused-silica capillary with a MicroMist AR 30-I-FM02 nebulizer and a Cinnabar small-volume cyclonic spray chamber yielded the best separation results. With this setup, it was possible to separate a model element mixture containing neptunium (NpO2(+)), uranium (UO2(2+)), lanthanum (La3+), and thorium (Th4+) in 1 M acetic acid. The same conditions were also suitable for the separation of various oxidation states of plutonium and neptunium in different a…

Detection limitCapillary electrophoresischemistryNeptuniumAnalytical chemistryThoriumchemistry.chemical_elementUraniumMass spectrometryInductively coupled plasma mass spectrometryAnalytical ChemistryPlutoniumAnalytical chemistry
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Isotope selective ultratrace analysis of plutonium by resonance ionisation mass spectrometry

2006

Abstract Resonance ionisation mass spectrometry (RIMS) is a sensitive and selective method for isotopically resolved ultratrace analysis of long-lived radionuclides. For the routine analysis of plutonium three titanium–sapphire lasers pumped by a pulsed Nd:YAG laser in combination with a time-of-flight mass spectrometer are used. The detection limit of this system is as low as 106–107 atoms for the plutonium isotopes 238Pu to 244Pu. The RIMS technique was applied to investigate the isotopic composition and the content of plutonium in a depleted uranium penetrator as used during the Balkan conflict delivering important information on the origin of the depleted uranium in this type of ammunit…

Detection limitRadionuclideIsotopeRadiochemistryAnalytical chemistryResonancechemistry.chemical_elementMass spectrometryPlutoniumIsotope separationlaw.inventionchemistrylawDepleted uranium
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Rapid Synthesis of Radioactive Transition-Metal Carbonyl Complexes at Ambient Conditions

2012

Carbonyl complexes of radioactive transition metals can be easily synthesized with high yields by stopping nuclear fission or fusion products in a gas volume containing CO. Here, we focus on Mo, W, and Os complexes. The reaction takes place at pressures of around 1 bar at room temperature, i.e., at conditions that are easy to accommodate. The formed complexes are highly volatile. They can thus be transported within a gas stream without major losses to setups for their further investigation or direct use. The rapid synthesis holds promise for radiochemical purposes and will be useful for studying, e.g., chemical properties of superheavy elements.

FusionChemistryInorganic chemistrySuperheavy Elements010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciences7. Clean energy0104 chemical sciencesInorganic ChemistryTransition metalNuclear fissionOrganic chemistryPhysical and Theoretical ChemistryInorganic Chemistry
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Liquid-Phase Chemistry of Superheavy Elements

2013

An overview over the chemical separation and characterization experiments of the four transactinide elements so far studied in liquid phases, rutherfordium (Rf), dubnium (Db), seaborgium (Sg), and hassium (Hs), is presented. Results are discussed in view of the position of these elements in the Periodic Table and of their relation to theoretical predictions. Short introductions on experimental techniques in liquid-phase chemistry, specifically automated rapid chemical separation systems, are also given. Studies of nuclear properties of transactinide nuclei by chemical isolation will be mentioned. Some perspectives for further liquid-phase chemistry on heavier elements are briefly discussed.

DubniumNuclear physicschemistrySeaborgiumRutherfordiumchemistry.chemical_elementTransactinide elementSuperheavy ElementsHassiumSpontaneous fissionCharacterization (materials science)
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Fluoride Complexation of Element 104, Rutherfordium

2004

Fluoride complexation of element 104, rutherfordium (Rf), produced in the 248Cm(18O,5n)261Rf reaction has been studied by anion-exchange chromatography on an atom-at-a-time scale. The anion-exchange chromatographic behavior of Rf was investigated in 1.9-13.9 M hydrofluoric acid together with those of the group-4 elements Zr and Hf produced in the 18O-induced reactions on Ge and Gd targets, respectively. It was found that the adsorption behavior of Rf on anion-exchange resin is quite different from those of Zr and Hf, suggesting the influence of relativistic effects on the fluoride complexation of Rf.

DubniumIon chromatographyInorganic chemistryAnalytical chemistrychemistry.chemical_elementGeneral ChemistryBiochemistryCatalysisPartition coefficientchemistry.chemical_compoundColloid and Surface ChemistryAdsorptionHydrofluoric acidchemistryRutherfordiumFluorideJournal of the American Chemical Society
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ChemInform Abstract: Solution Chemistry of Element 106: Theoretical Predictions of Hydrolysis of Group 6 Cations Mo, W, and Sg.

2001

HydrolysisGroup (periodic table)ChemistryPhysical chemistryGeneral MedicineSolution chemistryChemInform
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Gas phase chromatography of halides of elements 104 and 105

1992

On-line isothermal gas phase chromatography was used to study halides of261104 (T1/2=65 s) and262,263105 (T1/2=34 s and 27 s) produced an atom-at-a time via the reactions248Cm(18O, 5n) and249Bk(18O, 5n, 4n), respectively. Using HBr and HCl gas as halogenating agents, we were able to produce volatile bromides and chlorides of the above mentioned elements and study their behavior compared to their lighter homologs in Groups 4 or 5 of the periodic table. Element 104 formed more volatile bromide than its homolog Hf. In contrast, element 105 bromides were found to be less volatile than the bromides of the group 5 elements Nb and Ta. Both 104 and Hf chlorides were observed to be more volatile tha…

ChromatographyChemistryHealth Toxicology and MutagenesisPublic Health Environmental and Occupational HealthHalideHydrochloric acidPollutionChemical reactionChlorideIsothermal processAnalytical Chemistrychemistry.chemical_compoundNuclear Energy and EngineeringBromidemedicineHydrobromic acidRadiology Nuclear Medicine and imagingGas chromatographySpectroscopymedicine.drugJournal of Radioanalytical and Nuclear Chemistry Articles
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Electrodeposition methods in superheavy element chemistry

2008

To prepare electrodeposition experiments with superheavy elements (SHE), their homologs were investigated. In the experiments, various electrode materials and electrolytes were used. Critical potentials (E crit ) where the electrodeposition starts and potentials for the deposition of 50% of the atoms in solution (E 50% ) were determined. Underpotential deposition was observed in most cases. An electrolytic cell for a fast electrochemical deposition was developed and the time for the deposition of 50% of the atoms in solution (t 50% ) was determined. Short lived α-emitting isotopes were produced at Gesellschaft fur Schwerionenforschung (GSI), Darmstadt, transferred to the aqueous phase with …

ChemistryElectrolytic cellInorganic chemistryKineticsAqueous two-phase systemCoupling (piping)ElectrolytePhysical and Theoretical ChemistryElectrochemistryUnderpotential depositionDeposition (chemistry)Radiochimica Acta
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Fluorido Complex Formation of Element 104, Rutherfordium (Rf)

2011

We have investigated the cation-exchange behavior of element 104, rutherfordium (Rf), together with its lighter group-4 homologs Zr and Hf, and the tetravalent pseudo-homolog Th in HF/HNO3 mixed so...

CrystallographychemistryComplex formationRutherfordiumchemistry.chemical_elementGeneral ChemistryBulletin of the Chemical Society of Japan
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HCl gas gettering of low-cost silicon

2013

HCl gas gettering is a cheap and simple technique to reduce transition metal concentrations in silicon. It is attractive especially for low-cost silicon materials like upgraded metallurgical grade (UMG) silicon, which usually contain 3d transition metals in high concentrations. Etching of silicon by HCl gas occurs during HCl gas gettering above a certain onset temperature. The etching rate as well as the gettering efficiency was experimentally determined as a function of the gettering temperature, using UMG silicon wafers. The activation energy of the etching reaction by HCl gas was calculated from the obtained data. The gettering efficiency was determined by analyzing Ni as a representativ…

010302 applied physicsMaterials scienceSiliconEtching rateInorganic chemistrychemistry.chemical_element02 engineering and technologySurfaces and InterfacesActivation energy021001 nanoscience & nanotechnologyCondensed Matter Physics7. Clean energy01 natural sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryTransition metalGetterEtching (microfabrication)0103 physical sciencesMaterials ChemistryWaferElectrical and Electronic Engineering0210 nano-technologyInductively coupled plasma mass spectrometryphysica status solidi (a)
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Liquid-phase Chemistry

2003

Computational chemistryChemistryBioorganic chemistryLiquid phaseTransactinide elementSpontaneous fission
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Evidence for the formation of sodium hassate(VIII)

2004

SummaryHassium, element 108, was produced in the fusion reaction between26Mg and248Cm. The hassium recoils were oxidizedin-situto a highly volatile oxide, presumably HsO4, and were transported in a mixture of He and O2to a deposition and detection system. The latter consisted of 16 silicon PIN-photodiodes facing a layer of NaOH, which served, in the presence of a certain partial pressure of water in the transport gas, as reactive surface for the deposition of the volatile tetroxides. Six correlated α-decay chains of Hs were detected in the first 5 detectors centred around detection position 3. In analogy to OsO4, which forms Na2[OsO4(OH)2], an osmate(VIII), with aqueous NaOH, HsO4presumably…

chemistry.chemical_compoundAqueous solutionchemistrySiliconSodiumInorganic chemistryOxidechemistry.chemical_elementPartial pressurePhysical and Theoretical ChemistryLayer (electronics)Deposition (chemistry)HassiumRadiochimica Acta
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Irradiation facility at the TRIGA Mainz for treatment of liver metastases

2009

Abstract The TRIGA Mark II reactor at the University of Mainz provides ideal conditions for duplicating BNCT treatment as performed in Pavia, Italy, in 2001 and 2003 [Pinelli, T., Zonta, A., Altieri, S., Barni, S., Braghieri, A., Pedroni, P., Bruschi, P., Chiari, P., Ferrari, C., Fossati, F., Nano, R., Ngnitejeu Tata, S., Prati, U., Ricevuti, G., Roveda, L., Zonta, C., 2002. TAOrMINA: from the first idea to the application to the human liver. In: Sauerwein et al. (Eds.), Research and Development in Neutron Capture Therapy. Proceedings of the 10th International Congress on Neutron Capture Therapy, Monduzzi editore, Bologna, pp. 1065–1072]. In order to determine the optimal parameters for the…

PhysicsModels StatisticalRadiationHuman liverbusiness.industryRadiotherapy Planning Computer-AssistedLiver NeoplasmsBoron Neutron Capture TherapyIn Vitro TechniquesTRIGAFast NeutronsNuclear ReactorsGermanyInternational congressHumansNuclear medicinebusinessMonte Carlo MethodApplied Radiation and Isotopes
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The hydration enthalpies of Md3+ and Lr3+

1988

Lawrencium (3-min 260Lr) and lighter actinides were produced in the bombardment of a 249Bk target with 18O ions and loaded onto a cation exchange column in 0.05 M α-hydroxyisobutyrate solution at pH=4.85, together with the radioactive lanthanide tracers 166Ho, 171Er and 171Tm. In elutions with 0.12 M α=hydroxyisobutyrate solution (pH=4.85), trivalent Lr was eluted exactly together with the Er tracer and Md was eluted close to Ho. Lr elutes much later than expected based on the known elution positions of the lighter actinides and the expected analogy to the elution positions of the homologous lanthanides. From the measured elution positions, ionic radii were calculated for Lr3+ and Md3+. Sem…

Inorganic ChemistryLanthanideIonic radiusChemistryElutionInorganic chemistryEnthalpyMaterials Chemistrychemistry.chemical_elementActinidePhysical and Theoretical ChemistryIonLawrenciumInorganica Chimica Acta
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Solution Chemistry of Element 106:  Theoretical Predictions of Hydrolysis of Group 6 Cations Mo, W, and Sg

2001

Fully relativistic molecular density-functional calculations of the electronic structure of hydrated and hydrolyzed complexes have been performed for the group 6 elements Mo, W, and element 106, Sg. By use of the electronic density distribution data, relative values of the free energy changes and constants of hydrolysis reactions were defined. The results show hydrolysis of the cationic species with the formation of neutral molecules to decrease in the order Mo > W > Sg, which is in agreement with experiments for Mo, W, and Sg. For the further hydrolysis process with the formation of anionic species, the trend is reversed:  Mo > Sg > W. A decisive energetic factor in the hydrolysis process …

Inorganic ChemistryHydrolysisChemistryGroup (periodic table)Inorganic chemistryCationic polymerizationPhysical chemistryMoleculeSolution chemistryElectronic structurePhysical and Theoretical ChemistryElectronic densityInorganic Chemistry
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Attempts to Produce Superheavy Elements by Fusion ofCa48withCm248in the Bombarding Energy Range of 4.5-5.2 MeV/u

1985

A search for superheavy elements was made in bombardments of $^{248}\mathrm{Cm}$ with $^{48}\mathrm{Ca}$ ions performed at projectile energies close to the interaction barrier in order to keep the excitation energy of the compound nucleus $Z=116$, $A=296$ as low as possible. No evidence for superheavy nuclei was obtained in a half-life region from 1 \ensuremath{\mu}s to 10 yr with a production cross section greater than ${10}^{\ensuremath{-}34}$ to ${10}^{\ensuremath{-}35}$ ${\mathrm{cm}}^{2}$.

PhysicsNuclear reactionRange (particle radiation)010308 nuclear & particles physicsNuclear TheoryGeneral Physics and AstronomyOrder (ring theory)7. Clean energy01 natural sciencesIonNuclear physics0103 physical sciencesNuclear fusionProduction (computer science)Atomic physicsNuclear Experiment010306 general physicsExcitationEnergy (signal processing)Physical Review Letters
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TASCAを用いたCn, Nh, Fl化学実験のためのHg, Tl, PbのSiO2及びAu表面に対するオンライン化学吸着研究

2018

Online gas-solid adsorption studies with single atom quantities of Hg, Tl, and Pb on SiO$_{2}$ and Au surfaces were carried out using short-lived radioisotopes with half-lives in the range of 4-49 s. This is a model study to measure adsorption enthalpies of superheavy elements Cn, Nh, and Fl. The short-lived isotopes were produced and separated by the gas-filled recoil separator TASCA at GSI. The products were stopped in He gas, and flushed into gas chromatography columns made of Si detectors whose surfaces were covered by SiO$_{2}$ or Au. The short-lived Tl and Pb were successfully measured by the Si detectors with the SiO$_{2}$ surface at room temperature. On the other hand, the Hg did no…

Analytical chemistrychemistry.chemical_elementElectronic structure010402 general chemistry01 natural sciencesadsorption studiethermochromatographyHomologs of superheavy elementRELATIVISTIC PERIODIC DFTMetalGSIAdsorptionCHEMISTRY0103 physical sciencesisothermal chromatographyPhysical and Theoretical ChemistrySUPERHEAVY ELEMENTS010306 general physicsCoperniciumChemistryQUARTZ SURFACE0104 chemical sciencesgas phase chromatography of single atomHEAVIEST ELEMENTSFleroviumELECTRONIC-STRUCTUREvisual_artYield (chemistry)METALvisual_art.visual_art_mediumGas chromatographyRelativistic quantum chemistryphysical preseparationSYSTEMRadiochimica acta
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In-situ formation, thermal decomposition, and adsorption studies of transition metal carbonyl complexes with short-lived radioisotopes

2014

Abstract We report on the in-situ synthesis of metal carbonyl complexes with short-lived isotopes of transition metals. Complexes of molybdenum, technetium, ruthenium and rhodium were synthesized by thermalisation of products of neutron-induced fission of 249Cf in a carbon monoxide-nitrogen mixture. Complexes of tungsten, rhenium, osmium, and iridium were synthesized by thermalizing short-lived isotopes produced in 24Mg-induced fusion evaporation reactions in a carbon monoxide containing atmosphere. The chemical reactions took place at ambient temperature and pressure conditions. The complexes were rapidly transported in a gas stream to collection setups or gas phase chromatography devices.…

In situThermal decomposition02 engineering and technologyCrystal structure010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesBond-dissociation energy0104 chemical scienceschemistry.chemical_compoundAdsorptionTransition metalchemistry540 Chemistry570 Life sciences; biologyThermal stabilityPhysical and Theoretical Chemistry0210 nano-technologyChromium hexacarbonylNuclear chemistryRadiochimica Acta
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Investigation of the Dipole Response in Exotic Nuclei – Experiments at the LAND-R$^3$B Setup

2012

We present experimental results on the electromagnetic excitation of neutron-rich nickel isotopes, making use of the (RB)-B-3-LAND setup at GSI. Exotic beams were produced at approximately 500 MeV/u and their reactions were studied in inverse kinematics. Integral cross sections for Ni-58 are discussed and compared to previous data, providing a validation of our experimental method. The El excitation-energy distribution of the unstable Ni-68 is presented as well, showing an excess in cross section in the 1n decay channel when compared only with a typical Giant Dipole Resonance.

Nuclear physicsPhysicsCross section (physics)DipolePhysics and Astronomy (miscellaneous)IsotopeInverse kinematicsDetectorAtomic physicsNuclear ExperimentResonance (particle physics)ExcitationProgress of Theoretical Physics Supplement
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Speciation of the oxidation states of plutonium in aqueous solutions by UV/Vis spectroscopy, CE-ICP-MS and CE-RIMS

2007

For the speciation of the plutonium oxidation states in aqueous solutions, the online coupling of capillary electrophoresis (CE) with inductively coupled plasma mass spectrometry (ICP-MS) has been developed. Depending on the radius/electrical charge ratio, the oxidation states III, IV, V, and VI of plutonium are separated by CE, based on the different migration times through the capillary and are detected by ICP-MS. The detection limit is 20 ppb,i.e.109–1010atoms (10-12–10-13g) for one oxidation state with an uncertainty of the reproducibility of the migration times of ≤1% and ≤5% for the peak area. The redox kinetics of the different plutonium oxidation states in the presence of humic subs…

chemistry.chemical_classificationAqueous solutionInorganic chemistryAnalytical chemistrychemistry.chemical_elementMass spectrometryRedoxPlutoniumCapillary electrophoresischemistryOxidation stateHumic acidPhysical and Theoretical ChemistryInductively coupled plasma mass spectrometryRadiochimica Acta
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Chemical studies of Fl (element 114): Heaviest chemically studied element

2017

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