Search results for "reactions"

showing 10 items of 631 documents

Investigation of fusion probabilities in the reactions with 52,54Cr, 64Ni, and 68Zn ions leading to the formation of Z = 120 superheavy composite sys…

2020

Background: The formation of superheavy nuclei in fusion reactions is suppressed by a competing quasifission process. The competition between the formation of the compound nucleus and the quasifission depends strongly on the reaction entrance channel. Purpose: The investigation of fission and quasifission processes in the formation of Z=120 superheavy composite systems in the 52,54Cr+248Cm and 68Zn+232Th reactions, and their comparison with the 64Ni+238U reaction at energies in the vicinity of the Coulomb barrier. Methods: Mass-energy distributions of fissionlike fragments formed in the reactions 52,54Cr+248Cm and 68Zn+232Th at energies near the Coulomb barrier were measured using the doubl…

fissiofuusioreaktiolow and intermediate energy heavy-ion reactionsydinfysiikkanuclear fusion
researchProduct

Search for Electron-Capture Delayed Fission in the New Isotope 244Md

2020

The electron-capture decay followed by a prompt fission process was searched for in the hitherto unknown most neutron-deficient Md isotope with mass number 244. Alpha decay with α-particle energies of 8.73-8.86 MeV and with a half-life of 0.30_{-0.09}^{+0.19}  s was assigned to ^{244}Md. No fission event with a similar half-life potentially originating from spontaneous fissioning of the short-lived electron-capture decay daughter ^{244}Fm was observed, which results in an upper limit of 0.14 for the electron-capture branching of ^{244}Md. Two groups of fission events with half-lives of 0.9_{-0.3}^{+0.6}  ms and 5_{-2}^{+3}  ms were observed. The 0.9_{-0.3}^{+0.6}  ms activity was assigned t…

fissioisotoopitydinfysiikkanuclear structure and decaysnuclear reactions
researchProduct

Towards saturation of the electron-capture delayed fission probability : The new isotopes 240Es and 236Bk

2017

The new neutron-deficient nuclei 240Es and 236Bk were synthesised at the gas-filled recoil separator RITU. They were identified by their radioactive decay chains starting from 240Es produced in the fusion–evaporation reaction 209Bi(34S,3n)240Es. Half-lives of 6(2) sand 22+13−6swere obtained for 240Es and 236Bk, respectively. Two groups of αparticles with energies Eα=8.19(3) MeVand 8.09(3) MeVwere unambiguously assigned to 240Es. Electron-capture delayed fission branches with probabilities of 0.16(6)and 0.04(2)were measured for 240Es and 236Bk, respectively. These new data show a continuation of the exponential increase of ECDF probabilities in more neutron-deficient isotopes. peerReviewed

fusion-evaporation reactionsisotoopitmasselectron-capture delayed fissionα decay
researchProduct

117番元素Ts合成のための48Ca+249Bk融合反応

2019

We have performed an experiment to synthesize the element 117 (Ts) with the $^{48}$Ca+$^{249}$Bk fusion reaction. Four $\alpha$-decay chains attributed to the element 117 were observed. Two of them were long decay chains which can be assigned to the one originating from the $\alpha$ decay of $^{294}$Ts. The other two were short decay chains which are consistent with the one originating from the $\alpha$ decay of $^{293}$Ts. We have compared the present results with the literature data, and found that our present results mostly confirmed the literature data, leading to the firm confirmation of the synthesis of the element 117.

gas-filled separatorsuperheavy elementselement 117 (Ts)alpha decaySubatomic PhysicsNuclear Theorylow and intermediate energy heavy-ion reactionsydinfysiikkaNuclear Experimentnuclear structure and decays
researchProduct

Experimental and Theoretical Investigations of the Redox Behavior of the Heterodichalcogenido Ligands [(EPiPr2)(TePiPr2)N]− (E = S, Se): Cyclic Catio…

2008

The two-electron oxidation of the lithium salts of the heterodichalcogenidoimidodiphosphinate anions [(EPiPr2)(TePiPr2)N]− (1a, E = S; 1b, E = Se) with iodine yields cyclic cations [(EPiPr2)(TePiPr2)N]+ as their iodide salts [(SPiPr2)(TePiPr2)N]I (2a) and [(SePiPr2)(TePiPr2)N]I (2b). The five-membered rings in 2a and 2b both display an elongated E−Te bond as a consequence of an interaction between tellurium and the iodide anion. One-electron reduction of 2a and 2b with cobaltocene produces the neutral dimers (EPiPr2NPiPr2Te−)2 (3a, E = S; 3b, E = Se), which are connected exclusively through a Te−Te bond. Two-electron reduction of 2a and 2b with 2 equiv of cobaltocene regenerates the corresp…

hapetus-pelkistys-reaktiotdichalcogenido ligandsredox reactionsdikalkogenidoligandit
researchProduct

The formation, properties and impact of secondary organic aerosol: Current and emerging issues

2009

Hallquist, M. Wenger, J. C. Baltensperger, U. Rudich, Y. Simpson, D. Claeys, M. Dommen, J. Donahue, N. M. George, C. Goldstein, A. H. Hamilton, J. F. Herrmann, H. Hoffmann, T. Iinuma, Y. Jang, M. Jenkin, M. E. Jimenez, J. L. Kiendler-Scharr, A. Maenhaut, W. McFiggans, G. Mentel, Th. F. Monod, A. Prevot, A. S. H. Seinfeld, J. H. Surratt, J. D. Szmigielski, R. Wildt, J.; Secondary organic aerosol (SOA) accounts for a significant fraction of ambient tropospheric aerosol and a detailed knowledge of the formation, properties and transformation of SOA is therefore required to evaluate its impact on atmospheric processes, climate and human health. The chemical and physical processes associated wit…

humic-like substancesAtmospheric Scienceenvironmental chamber data010504 meteorology & atmospheric sciences010501 environmental sciences01 natural sciencessupercritical-fluid extractionlcsh:Chemistrychemistry.chemical_compoundHuman healthddc:550catalyzed heterogeneous reactionsProcess engineeringairborne particulate matter0105 earth and related environmental sciencesTropospheric aerosolpolycyclic aromatic-hydrocarbonsinitiated atmospheric oxidationAtmospheric modelsbusiness.industryPharmacology. Therapy[CHIM.CATA] Chemical Sciences/Catalysis[CHIM.CATA]Chemical Sciences/Catalysischromatography-mass spectrometrylcsh:QC1-999JAerosolChemistrylcsh:QD1-999chemistry13. Climate actionEnvironmental chemistryEarth and Environmental Scienceslow-molecular-weightAerosol mass spectrometrytropospheric chemistry mechanismOrganic componentCurrent (fluid)/dk/atira/pure/subjectarea/asjc/1900/1902businesslcsh:PhysicsOrganosulfate
researchProduct

Theoretical study of neutrino scattering off the stable even Mo isotopes at low and intermediate energies

2011

A systematic study of the cross sections of neutral-current neutrino scattering off the stable even Mo isotopes (mass number A = 92, 94, 96, 98, 100), at low and intermediate neutrino energies (E(nu) <= 130 MeV), is presented and discussed. The required wave functions for the initial (ground state) and all accessible final nuclear states are constructed in the context of the quasi-particle random-phase approximation (QRPA) and tested against data on the low-lying energy spectra of the isotopes in question. The individual contributions coming from the polar-vector and axial-vector components of the hadronic current for the coherent and incoherent channels of each isotope are investigated. Th…

inelastic cross sectionsNuclear and High Energy PhysicsParticle physicsHadronsemi-leptonic electro-weak interactionsneutrino-nucleus reactionsnuclear-data sheetsNuclear physicsdedicated supernova detectionDouble beta decayelastic-scatteringNeutrino Ettore Majorana ObservatoryconversionNuclear ExperimentdetectorsPhysicsMass numberweak-interactionNeutral currentIsotopequasi-particle random-phase approximationspallationSupernovareaction cross-sectionsnetworkHigh Energy Physics::ExperimentNeutrinoburstNuclear Physics A
researchProduct

A solvent-free regioselective iodination route of ortho-carboranes.

2006

Tetraiodo-ortho-carborane based X-ray contrast agents can be readily prepared in a high yield, fast, clean, regioselective fashion by a solvent-free reaction of ortho-carboranes with iodine in sealed tubes.

inorganic chemicalsBoron Compoundschemistry.chemical_elementContrast MediaOrganic-reactions010402 general chemistryIodine01 natural sciencesChemical synthesisInorganic ChemistryQUIMICA ANALITICAOrganic chemistryheterocyclic compoundsSolvent freeintegumentary system010405 organic chemistryChemistryorganic chemicalsRegioselectivityHalogenationCombinatorial chemistry0104 chemical sciencesRadiographyChemical-synthesisOrganic reactionYield (chemistry)SolventsbacteriaDerivativesIodineDalton transactions (Cambridge, England : 2003)
researchProduct

A new simple chromo-fluorogenic probe for NO2 detection in air.

2015

[EN] A new chromo-fluorogenic probe, consisting of a biphenyl derivative containing both a silylbenzyl ether and a N,N-dimethylamino group, for NO2 detection in the gas phase has been developed. A clear colour change from colourless to yellow together with an emission quenching was observed when the probe reacted with NO2. A limit of detection to the naked eye of about 0.1 ppm was determined and the system was successfully applied to the detection of NO2 in realistic atmospheric conditions.

inorganic chemicalsGas phase reactionsAnalytical chemistryEtherPhotochemistryNO2Nitric Oxidecomplex mixturesCatalysisGas phasechemistry.chemical_compoundQUIMICA ORGANICAChromogenic detectionFluorescent DyesDetection limitBiphenylEmission quenchingSIMPLE (dark matter experiment)Molecular StructureSensorsAirOrganic ChemistryQUIMICA INORGANICAGeneral Chemistryrespiratory systemchemistryChromogenic CompoundsNaked eyeDerivative (chemistry)Chemistry (Weinheim an der Bergstrasse, Germany)
researchProduct

Synergistic Anticancer Therapy by Ovalbumin Encapsulation-Enabled Tandem Reactive Oxygen Species Generation

2020

Abstract The anticancer efficacy of photodynamic therapy (PDT) is limited due to the hypoxic features of solid tumors. We report synergistic PDT/chemotherapy with integrated tandem Fenton reactions mediated by ovalbumin encapsulation for improved in vivo anticancer therapy via an enhanced reactive oxygen species (ROS) generation mechanism. O2 .− produced by the PDT is converted to H2O2 by superoxide dismutase, followed by the transformation of H2O2 to the highly toxic .OH via Fenton reactions by Fe2+ originating from the dissolution of co‐loaded Fe3O4 nanoparticles. The PDT process further facilitates the endosomal/lysosomal escape of the active agents and enhances their intracellular deliv…

inorganic chemicalsNanomedicines | Hot PaperOvalbuminmedicine.medical_treatmentRadicalsynergisticcisplatinPhotodynamic therapyAntineoplastic Agents010402 general chemistry01 natural sciencesCatalysisSuperoxide dismutasechemistry.chemical_compoundMicemedicineAnimalsHumansResearch Articleschemistry.chemical_classificationCisplatinReactive oxygen speciesOxidase testPhotosensitizing Agentsbiology010405 organic chemistryFenton reactionsDrug SynergismGeneral MedicineGeneral ChemistryhypoxicEndocytosis0104 chemical sciencesOvalbuminchemistryphotodynamic therapybiology.proteinBiophysicsMCF-7 CellsReactive Oxygen SpeciesNicotinamide adenine dinucleotide phosphatemedicine.drugResearch Article
researchProduct