Search results for "ion source"

showing 10 items of 337 documents

Measurement of low-ppm mixing ratios of water vapor in the upper troposphere and lower stratosphere using chemical ionization mass spectrometry

2018

A chemical ionization mass spectrometer (CIMS) instrument has been developed for the fast, precise, and accurate measurement of water vapor (H2O) at low mixing ratios in the upper troposphere and lower stratosphere (UT/LS). A low-pressure flow of sample air passes through an ionization volume containing an α-particle radiation source, resulting in a cascade of ion-molecule reactions that produce hydronium ions (H3O+) from ambient H2O. The production of H3O+ ions from ambient H2O depends on pressure and flow through the ion source, which were tightly controlled in order to maintain the measurement sensitivity independent of changes in the airborne sampling environment. The instrument w…

Atmospheric ScienceChemical ionizationlcsh:TA715-787Chemistrylcsh:Earthwork. FoundationsAnalytical chemistryAtmosphärische SpurenstoffeWater vapourAtmospheric sciencesMass spectrometryIon sourcelcsh:Environmental engineeringTroposphereIonizationlcsh:TA170-171TropopauseStratosphereWater vapormass spectrometryAtmospheric Measurement Techniques
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Internal ion impact ionization for Fourier-transform ion cyclotron resonance

1994

A general scheme for ionization and fragmentation of ions in Fourier-transform ion cyclotron resonance mass spectrometry (FT-ICRMS) is introduced. The technique is based upon excitation of high-frequency (i.e. lowmass) primary ions (e.g. N, Al+, H2O+·) which may be generated by standard ionization methods (e.g. electron ionization or laser desorption) inside the trap. Generation of the primary ions is followed by excitation of their cyclotron motion to high translational energy to serve as projectile ions. The projectiles serve two functions: to ionize neutral gas atoms and/or molecules (secondary ions) within the trap internal ion impact ionization (IIII), and to collisionally activate the…

Chemical ionizationChemistryOrganic ChemistryAnalytical chemistryThermal ionizationFourier transform ion cyclotron resonanceIon sourceAnalytical ChemistryAtmospheric-pressure laser ionizationPhysics::Plasma PhysicsIonizationAtomic physicsSpectroscopyElectron ionizationIon cyclotron resonanceRapid Communications in Mass Spectrometry
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Studies of electron heating on a 6.4 GHz ECR ion source through measurement of diamagnetic current and plasma bremsstrahlung

2011

Diamagnetic current and low energy (2–70 keV) x-ray bremsstrahlung measurements taken on a 6.4 GHz electron cyclotron resonance ion source (ECRIS) are presented as a function of microwave power, neutral gas pressure and magnetic field configuration. X-ray flux from confined electrons and plasma energy density depend logarithmically on microwave power. This result differs from previous studies performed on ECRISs that operate at higher microwave frequencies, in which the x-ray power increases in an essentially linear fashion with the microwave power. X-ray power and plasma energy density both saturate as the neutral pressure is increased beyond a certain value. The gradient of the magnetic f…

ChemistryAstrophysics::High Energy Astrophysical PhenomenaBremsstrahlungFaraday cupIon currentElectronPlasmaCondensed Matter PhysicsElectron cyclotron resonanceIon sourcesymbols.namesakesymbolsAtomic physicsMicrowavePlasma Sources Science and Technology
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Determination of the first ionization potential of nine actinide elements by resonance ionization mass spectroscopy (RIMS)

1998

The high sensitivity of RIMS enables the precise determination of the first ionization potential of actinide elements with a sample size of ≤1012 atoms. By multiple resonant laser excitation, the actinide atoms under investigation are ionized in the presence of an electric field, and the ions are mass-selectively detected in a time-of-flight spectrometer. The first ionization potential is obtained by scanning the wavelength of the laser used for the last excitation step across the ionization threshold Wth—indicated by a sudden increase of the ion count rate—at various electric field strengths. Extrapolation of Wth to electric field strength zero leads directly to the first ionization potent…

ChemistryMechanical EngineeringMetals and AlloysThermal ionizationPhotoionizationMolar ionization energies of the elementsIon sourceAtmospheric-pressure laser ionizationMechanics of MaterialsIonizationMaterials ChemistryAtomic physicsElectron ionizationAmbient ionizationJournal of Alloys and Compounds
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Negative ions and their importance for the analysis of residual gas

1963

Abstract In the case of heavy molecules, mass spectre obtained with the help of positive ions generally lead to the recording of fragments only, and thus do not indicate the true original mass. In order to overcome this drawback, an attempt was made to attach slow electrons to heavy molecules, since less dissociation products are expected with spectre produced by negative ions. As a preliminary experiment, a simple and cheap form of ion source was constructed which produces mainly atomic negative ions.

ChemistryMoleculeElectronAtomic physicsCondensed Matter PhysicsResidualInstrumentationIon sourceDissociation (chemistry)Surfaces Coatings and FilmsIonVacuum
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Resonant Ionization Laser Ion Source for Radioactive Ion Beams

2009

A resonant ionization laser ion source based on all‐solid‐state, tunable Ti:Sapphire lasers is being developed for the production of pure radioactive ion beams. It consists of a hot‐cavity ion source and three pulsed Ti:Sapphire lasers operating at a 10 kHz pulse repetition rate. Spectroscopic studies are being conducted to develop ionization schemes that lead to ionizing an excited atom through an auto‐ionization or a Rydberg state for numerous elements of interest. Three‐photon resonant ionization of 12 elements has been recently demonstrated. The overall efficiency of the laser ion source measured for some of these elements ranges from 1 to 40%. The results indicate that Ti:Sapphire lase…

ChemistryTi:sapphire laserPhysics::OpticsLaserIon sourcelaw.inventionAtmospheric-pressure laser ionizationIon beam depositionlawIonizationPhysics::Atomic PhysicsAtomic physicsElectron ionizationTunable laserAIP Conference Proceedings
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Microwave emission related to cyclotron instabilities in a minimum-Belectron cyclotron resonance ion source plasma

2015

Electron cyclotron resonance ion sources (ECRIS) have been essential in the research and applications of nuclear physics over the past 40 years. They are extensively used in a wide range of large-scale accelerator facilities for the production of highly charged heavy ion beams of stable and radioactive elements. ECRISs are susceptible to kinetic instabilities due to resonance heating mechanism leading to anisotropic electron velocity distribution function. Instabilities of cyclotron type are a proven cause of frequently observed periodic bursts of 'hot' electrons and bremsstrahlung, accompanied with emission of microwave radiation and followed by considerable drop of multiply charged ions c…

ChemistrylawWaves in plasmasCyclotronCyclotron resonanceBremsstrahlungAtomic physicsCondensed Matter PhysicsIon cyclotron resonanceIon sourceElectron cyclotron resonanceFourier transform ion cyclotron resonancelaw.inventionPlasma Sources Science and Technology
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Evaluation of selected buffers for simultaneous determination of ionic and acidic pesticides including glyphosate using anion exchange chromatography…

2019

Ion chromatography coupled with mass spectrometry is an established technique for determination of ionic analytes, however, sophisticated buffer removal equipment is required to eliminate inorganic compounds from the eluate before introduction into the ion source of mass spectrometer. A standard high-performance liquid chromatography coupled with tandem mass spectrometry setup using an ion exchange column (Metrosep® A Supp 5) is proposed as an alternative approach. For that reason, some buffers including non-volatile carboxylic acid based solutions have been evaluated for simultaneous trace determination of ionic and acidic pesticides including glyphosate in the same extract without a need …

ChromatographyIon exchangeElution010401 analytical chemistryChlorateIon chromatographyFiltration and Separation010501 environmental sciencesBromateTandem mass spectrometryMass spectrometry01 natural sciencesIon source0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundchemistry0105 earth and related environmental sciencesJournal of Separation Science
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An atmospheric pressure chemical ionization-ion-trap mass spectrometer for the on-line analysis of volatile compounds in foods: a tool for linking ar…

2014

An atmospheric pressure chemical ionization ion-trap mass spectrometer was set up for the on-line analysis of aroma compounds. This instrument, which has been successfully employed for some years in several in vitro and in vivo flavour release studies, is described for the first time in detail. The ion source was fashioned from polyether ether ketone and operated at ambient pressure and temperature making use of a discharge corona pin facing coaxially the capillary ion entrance of the ion-trap mass spectrometer. Linear dynamic ranges (LDR), limits of detection (LOD) and other analytical characteristics have been re-evaluated. LDRs and LODs have been found fully compatible with the concentra…

ChromatographybiologyFlavourAnalytical chemistryEthyl hexanoateAtmospheric-pressure chemical ionizationbiology.organism_classificationMass spectrometryIon sourcechemistry.chemical_compoundchemistryIon trapSpectroscopyAromaAmbient pressureJournal of Mass Spectrometry
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Studies in organic mass spectrometry. Part 17—Formation of phenol radical ions by rearrangement of the molecular ions of someN-arylthiophenecarboxami…

1995

It has been shown by exact mass measurements and collision-induced dissociation mass-analysed ion kinetic energy spectra that the structure of the m/z 124 ion observed in the mass spectra of N-(4-methoxyphenyl)thiophene-2-carboxamide, N-(4-methoxyphenyl)thiophene-3-carboxamide, N-(4-methoxyphenyl)-5-nitrothiophene-3-carboxamide and N-(4-methoxyphenyl)benzamide is identical with that of the molecular ion of 4-methoxyphenol. This ion becomes abundant in metastable energy window reactions. A probable mechanism for its formation is discussed.

Collision-induced dissociationChemistryPolyatomic ionMass spectrumAnalytical chemistryFast atom bombardmentMass spectrometryTandem mass spectrometryPhotochemistrySpectroscopyIon sourceIonJournal of Mass Spectrometry
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