Search results for "Instrumentation"

showing 10 items of 4914 documents

Precision experiments on exotic nuclei at IGISOL

2006

Abstract Cooling and trapping techniques of low-energy radioactive ion beams of refractory elements employed at the IGISOL facility are presented with emphasis on high-precision measurements of the ground state properties of exotic nuclei. The impact of the new generation Paul and Penning traps on mass measurements of short-lived nuclei is discussed with examples on precision measurements of masses of super-allowed beta emitters and neutron-rich nuclei. As a new concept the trap-assisted spectroscopy of radioactive ions is presented with applications in collinear laser spectroscopy, decay spectroscopy of isobarically purified sources and in nuclear cross-section measurements by ion counting.

ChemistryNuclear TheoryRefractory metalsTrappingCondensed Matter PhysicsPenning trapAtomic massIonBeta (plasma physics)Physics::Atomic PhysicsPhysical and Theoretical ChemistryAtomic physicsNuclear ExperimentGround stateSpectroscopyInstrumentationSpectroscopyInternational Journal of Mass Spectrometry
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Dissociative charge transfer from highly excited Na Rydberg atoms to vibrationally excited Na2 molecules

2001

Abstract We report the observation of the vibrational dependence of dissociative charge transfer (DCT), Na2(X1Σg+, v″) + Na∗∗(nl) → Na− + Na + Na+, in a single Na/Na2 supersonic beam at low intrabeam collision energies (1.6 meV) using the STIRAP technique for selective vibrational excitation of Na2 in the electronic ground state and time-of-flight mass analysis of the ions. The efficiency of this process increases by about an order of magnitude in the range 13 ≤ v″ ≤ 22. Some perspectives are discussed regarding the implementation of a field-free ion-imaging technique for the detection of ions that will allow the direct determination of the kinetic energy distributions of product negative i…

ChemistryPhotodissociationCondensed Matter PhysicsKinetic energyIonExcited stateRydberg atomMoleculePhysical and Theoretical ChemistryAtomic physicsGround stateInstrumentationSpectroscopyExcitationInternational Journal of Mass Spectrometry
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Electron impact mass spectra of chlorinated methyl propanoates

1982

The mass spectral fragmentations of all eleven chlorinated methyl propanoates have been studied. Deuterium labelling and metastable ion analysis were used to elucidate the fragmentation mechanism. The molecular ion peaks of all compounds are small, except methyl 3,3-dichloropanoate (38%). In most cases α-cleavage gives the base peak [COOCH3]+, and the loss of a chlorine atom from the molecular ion is characteristic of the 3-chloro, 3,3-dichloro and 3,3,3-trichloro compounds. Metastable ions showed the losses of small neutral molecules such as CH3OH, CH2CO, CO2 and CO from the [MCl]+ ion. α-Cleavage and the loss of Cl˙ gives an intense [MCOOCH3Cl]+˙ peak, which is the base peak in the spectr…

ChemistryPolyatomic ionAnalytical chemistryBiochemistrySpectral lineIonFragmentation (mass spectrometry)DeuteriumMass spectrumMolecular MedicineMoleculePhysical chemistryInstrumentationSpectroscopyElectron ionizationOrganic Mass Spectrometry
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Gaseous sensors based on solid proton conductors

1992

Abstract he chemical sensors for different gaseous (alcohol, acetone, ammonia, water vapour) detection at room temperature are developed by using polycrystalline β-alumina and xerogel of antimonic acid hydrate (AAH). The sensitivity and selectivity of sensors depend on the ion-exchange and preparative methods. The possibility of producing different types of potentiometric, amperometric, voltammetric and resistance sensors on the basis of these ion-conducting materials is shown. More success is achieved by producing ammonia-sensitive devices on β-alumina as well as on AAH xerogel.

ChemistryPotentiometric titrationInorganic chemistryMetals and AlloysCondensed Matter PhysicsAmperometrySurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundAmmoniaAcetoneCrystalliteElectrical and Electronic EngineeringHydrateSelectivityInstrumentationWater vapor
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Structural and spectroscopic study of the Br2...3-Br-pyridine complex by DFT calculations.

2007

Abstract The structure and the Raman vibrational spectrum of the complex Br 2 ⋯3-Br-pyridine are determined by DFT calculations using different parametrizations. The calculations are performed taking into account the effects of the dichloromethane as solvent by the CPCM method. A value of 39 kJ mol −1 for the formation enthalpy and of 1 kJ mol −1 for the formation free energy at room temperature in presence of the solvent is found. The predicted Raman spectrum is compared with the experimental one and the essential features of the spectrum are well reproduced by the B3LYP parametrization. The intensity changes of the bands when going from the free moieties to the complex are also generally …

ChemistryPyridinesEntropyEnthalpyMolecular ConformationVibrational spectrumBromineSpectrum Analysis RamanAtomic and Molecular Physics and OpticsAnalytical ChemistrySolventchemistry.chemical_compoundsymbols.namesakeModels ChemicalComputational chemistryPyridinesymbolsPhysical chemistrySolvent effectsRaman spectroscopyInstrumentationParametrizationSpectroscopyDichloromethaneSpectrochimica acta. Part A, Molecular and biomolecular spectroscopy
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Studies in organic mass spectrometry. Part 9—mass spectra of 9,10-disubstituted 2,3,6,7-tetraalkoxy-9,10-dihydroanthracenes: A remarkable loss of rad…

1991

The electron impact-induced fragmentations of 23 9,10-disubstituted 2,3,6,7-tetraalkoxy-9,10-dihydroanthracenes, including six stereoisomeric pairs, were studied. The loss of the 9-(or 10-)substituent constitutes the main fragmentation route. The resulting ions give rise to a remarkable violation of the so-called even-electron rule as they eject the second substituent at the 10-(or 9-)position as a radical. The latter aspect was particularly investigated with the aid of low-energy (nominal value 15 eV) and mass-analysed ion kinetic energy spectra

ChemistryRadicalSubstituentAnalytical chemistryMass spectrometryPhotochemistryKinetic energyBiochemistryIonchemistry.chemical_compoundFragmentation (mass spectrometry)Mass spectrumMolecular MedicineInstrumentationSpectroscopyElectron ionizationOrganic Mass Spectrometry
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Triple-resonance autoionization of uranium optimized for diode laser excitation

2007

Abstract The photoionization of uranium via three-step excitation has been optimized for isotope selective trace analysis. A search found 13 new J = 6, 7, and 8 odd-parity states in the 36,850–37,200 cm− 1 region that allow blue–red–red three-photon excitation at wavelengths favorable for commercial diode laser systems. From each of these 13 states, near-threshold autoionization spectra were recorded at a resolution of 3 × 10− 4 cm− 1. Some 30 even-parity autoionizing levels with J = 5 to 9 have also been observed and characterized. Comparison of the spectra allows J assignment for the new intermediate levels as well as selection of an optimized path for trace analysis. We show that, for a …

ChemistryResonancePhotoionizationLaserAtomic and Molecular Physics and OpticsSpectral lineAnalytical ChemistrySemiconductor laser theorylaw.inventionAutoionizationlawAtomic physicsSpectroscopyInstrumentationSpectroscopyExcitationSpectrochimica Acta Part B: Atomic Spectroscopy
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On the phase dependence of the interconversion of the motional modes in a Penning trap by quadrupolar excitation

2012

Abstract The interconversion of the radial motional modes in a Penning trap (magnetron and cyclotron modes) by an external quadrupolar rf-field with a frequency near the true cyclotron frequency ω c plays an important role in the measurement cycle of Penning trap mass spectrometry. Ions to be measured are prepared in a state of magnetron motion which is then resonantly converted into cyclotron motion. The data analysis is usually carried out under the assumption that the initial motional state of the ions has been a pure magnetron state. In reality, however, a small component of cyclotron motion is always present in the ion's initial motional state. This component introduces a dependence on…

ChemistryScatteringCyclotronCyclotron resonanceRadiusCondensed Matter PhysicsPenning trapFourier transform ion cyclotron resonancelaw.inventionlawPhysical and Theoretical ChemistryAtomic physicsInstrumentationSpectroscopyExcitationIon cyclotron resonanceInternational Journal of Mass Spectrometry
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Properties and performance of a quadrupole mass filter used for resonance ionization mass spectrometry

1998

Abstract The performance of commercial quadrupole mass spectrometers (QMS) with a number of imperfections, as compared to the ideal hyperbolic geometry, has been characterized using the computer simulation program simion 3d version 6.0. The analysis of simulated QMS geometries focuses primarily on modeling of the internal potential, the study of field deviations, and the influence of finite length on performance of the QMS. The computer simulation of ion trajectories in the QMS field yields predictions for optimum working conditions and provides estimates for the resolving power and the maximum isotopic abundance sensitivity. Experimental measurements that confirm these expectations are pre…

ChemistrySelected reaction monitoringAnalytical chemistryThermal ionization mass spectrometryCondensed Matter PhysicsMass spectrometryTriple quadrupole mass spectrometerComputational physicsSelected ion monitoringPhysical and Theoretical ChemistryTime-of-flight mass spectrometryInstrumentationQuadrupole mass analyzerSpectroscopyHybrid mass spectrometerInternational Journal of Mass Spectrometry
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Solvatochromy and symmetry breaking in two quadrupolar oligophenylenevinylenes

2020

Electrooptical absorption measurements (EOAM), solvatochromic dependences and quantum chemical simulations testify to large dipole moments change of two quadrupolar oligophenylenevinylenes upon transition to Franck-Condon excited state μeFC. The values of the dipole moments μg and μeFC are in the range [(4.2 - 4.9)1030] C m and (30.8 - 47.0)1030C m, respectively. The relations of dipole moments in the ground and excited states determined by EOAM correlate well with results obtained via the solvatochromic method. Calculations carried out by density functional theory (DFT) show that optimized configuration of the ground state of these molecules is not planar. The results from all methods appl…

ChemistrySolvatochromism02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesMolecular physicsAtomic and Molecular Physics and Optics0104 chemical sciencesAnalytical ChemistryDipoleExcited stateMoleculeDensity functional theorySymmetry breakingAbsorption (chemistry)0210 nano-technologyGround stateInstrumentationSpectroscopySpectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy
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