Search results for "ionization"

showing 10 items of 1255 documents

Resonance ionization mass spectroscopy for trace analysis of neptunium

1993

Resonance ionization mass spectroscopic (RIMS) measurements for trace analysis and spectroscopy of 237Np, the ecologically most important isotope of neptunium, are described. The chemical procedure for the separation of neptunium from aqueous samples as well as the preparation of filaments for RIMS are outlined. Several two- and three-step excitation schemes have been investigated in order to find suitable conditions for the sensitive detection of 237Np. Using a three-step, three-color excitation and ionization scheme an overall detection efficiency of 3×10−8 was obtained, resulting in a detection limit of 4×108 atoms (160 fg) of 237Np. The hyperfine structure splittings of the levels under…

Detection limitMaterials sciencePhysics and Astronomy (miscellaneous)NeptuniumGeneral EngineeringAnalytical chemistryGeneral Physics and Astronomychemistry.chemical_elementPhotoionizationMass spectrometryNuclear magnetic resonancechemistryIonizationIonization energySpectroscopyHyperfine structureApplied Physics B Photophysics and Laser Chemistry
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Determination of abamectin in citrus fruits by liquid chromatography-electrospray ionization mass spectrometry.

2000

Liquid chromatography coupled to electrospray mass spectrometry (LC-ES-MS) with positive ion detection was used to determine abamectin in oranges. MS conditions were optimized to achieve maximum sensitivity. The main ion for abamectin was [M+Na]+ at a fragmentor voltage of 180 V. Abundant structural information can be obtained at different fragmentor voltages. The detection limit for the standard solution was 12 pg injected, and good linearity and reproducibility were observed. Abamectin residues were extracted using matrix solid-phase dispersion. Orange samples were homogenized with C18 bonded silica placed onto a glass column and eluted with dichloromethane. Recoveries of the abamectin fr…

Detection limitQuality ControlElectrosprayCitrusInsecticidesChromatographyIvermectinElutionElectrospray ionizationOrganic ChemistryReproducibility of ResultsGeneral MedicineMass spectrometryBiochemistryHigh-performance liquid chromatographySensitivity and SpecificityMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundchemistryAbamectinSolid phase extractionChromatography High Pressure LiquidJournal of chromatography. A
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Recent developments in and applications of resonance ionization mass spectrometry

1999

Resonance Ionization Mass Spectrometry (RIMS) has nowadays reached the status of a routine method for sensitive and selective ultratrace determination of long-lived radioactive isotopes in environmental, biomedical and technical samples. It provides high isobaric suppression, high to ultra-high isotopic selectivity and good overall efficiency. Experimental detection limits are as low as 106 atoms per sample and permit the fast and sensitive determination of ultratrace amounts of radiotoxic contaminations. Experimental arrangements for the detection of different radiotoxic isotopes, e.g. 236–244Pu, 89,90Sr and 99Tc in environmental samples are described, and the application of RIMS to the ul…

Detection limitRadionuclideIsotopeChemistryResonance ionizationAnalytical chemistryMass spectrometryBiochemistryOverall efficiencyFresenius' Journal of Analytical Chemistry
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Resonance ionization mass spectrometry for trace analysis of long-lived radionuclides

2008

Resonance ionization mass spectrometry (RIMS) is a sensitive and selective method for the determination of extremely low abundances of long-lived radionuclides. The detection limits are about 106 atoms per sample and an isotopic selectivity up to 1013 has been achieved. The potential of RIMS using different experimental arrangements is outlined for the determination of isotope ratios and lowest abundances of long-lived radioisotopes of interest like 238–244Pu, 90Sr, and 41Ca. Recent developments in improving detection limits and the spatial resolution of this technique are briefly discussed.

Detection limitRadionuclideIsotopeChemistryResonance ionizationAnalytical chemistryTrace analysisThermal ionization mass spectrometryMass spectrometry
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Use of thermal ionization isotope dilution mass spectrometry (TI-IDMS) as an oligo-element method for the determination of photographically relevant …

1998

Thermal ionization isotope dilution mass spectrometry (TI-IDMS) was used as an oligo-element method for the determination of Cr, Cd and Pb in photographic AgCl emulsions. After addition of an appropriate amount of isotopically enriched spikes (53Cr, 116Cd and 206Pb) to the solid samples, the latter were completely dissolved in NH3 solution, permitting isotopic exchange to take place. Thereafter, AgCl was selectively removed by precipitation, whereby ultrasonic treatment was used to enhance the recovery of the elements of interest. Despite the use of concentrated HNO3 and H2O2 during further sample processing, preliminary experiments indicated the presence of a substantial remainder of the o…

Detection limitSilver chloridechemistry.chemical_compoundchemistryIonizationAnalytical chemistryThermal ionizationIsotope dilutionThermal ionization mass spectrometryMass spectrometryBiochemistryIonFresenius' Journal of Analytical Chemistry
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Development of a method for the analysis of seven banned azo-dyes in chilli and hot chilli food samples by pressurised liquid extraction and liquid c…

2008

An automated, confirmatory and sensitive procedure has been developed and validated for the determination of Sudan (I-IV), Sudan Orange G, Sudan Red 7B and Para Red in hot chilli food samples. The proposed method includes pressurised liquid extraction (PLE) with acetone, gel permeation chromatography (GPC) clean-up and detection by liquid chromatography (LC) coupled to electrospray ionization in positive mode tandem mass spectrometry (ESI-MS-MS). The main parameters affecting the performance of the different ionization sources and PLE parameters were previously optimised using statistical design of experiments (DOE). The method was in-house validated on chilli powder and chilli meat. Linear…

Detection limitSpectrometry Mass Electrospray IonizationChemical ionizationElectrosprayChromatographyChemistryElectrospray ionizationFood Coloring AgentsFood ContaminationSudan Red 7BMass spectrometryAnalytical ChemistryGel permeation chromatographychemistry.chemical_compoundMethodsPara RedCapsicumAzo CompoundsFood AnalysisChromatography LiquidTalanta
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Evaluation of solid-phase extraction and stir-bar sorptive extraction for the determination of fungicide residues at low-microg kg(-1) levels in grap…

2004

Abstract A liquid chromatography–mass spectrometry method has been developed for determining bitertanol, carboxin, flutriafol, pyrimethanil, tebuconazole and triadimefon. The evaluation of both atmospheric pressure interfaces (API), atmospheric pressure chemical ionization (APCI) and electrospray (ESI) using positive and negative ionization modes, clearly shows that the studied pesticides are more sensitive using APCI in positive mode. Two procedures based on solid-phase extraction (SPE) and stir-bar sorptive extraction (SBSE) have been assessed for extracting these compounds in grape. The recoveries obtained by SPE in samples spiked at the limit of quantification (LOQ) level ranged from 60…

Detection limitSpectrometry Mass Electrospray IonizationChromatographyChemistryOrganic ChemistryExtraction (chemistry)Pesticide ResiduesReproducibility of ResultsAtmospheric-pressure chemical ionizationGeneral MedicineHydrogen-Ion ConcentrationMass spectrometryBiochemistryHigh-performance liquid chromatographyGas Chromatography-Mass SpectrometryAnalytical ChemistryFungicides Industrialchemistry.chemical_compoundLiquid chromatography–mass spectrometryPyrimethanilVitisSolid phase extractionAdsorptionMicrowavesChromatography High Pressure LiquidJournal of chromatography. A
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Analysis of currently used pesticides in fine airborne particulate matter (PM 2.5) by pressurized liquid extraction and liquid chromatography-tandem …

2008

During and after the application of currently used pesticides (CUPs) a significant fraction of applied pesticides can be lost to the air. A confirmatory and rapid procedure has been developed for the determination of four fungicides (carbendazim, thiabendazol, imazalil and bitertanol), three insecticides (imidacloprid, methidathion and pyriproxyfen), one helicide (methiocarb) and one acaricide (hexythiazox) in fine airborne particulate matter (PM 2.5) at trace level. The proposed method includes extraction of PM 2.5-bound pesticides by pressurized liquid extraction (PLE) followed by a direct injection into LC-MS/MS. The main parameters affecting the performance of the electrospray ionizatio…

Detection limitSpectrometry Mass Electrospray IonizationChromatographyMethiocarbChemistryOrganic ChemistryExtraction (chemistry)Reproducibility of ResultsGeneral MedicineMethidathionPesticideChemical FractionationMass spectrometryBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundLiquid chromatography–mass spectrometryTandem Mass SpectrometryEnvironmental chemistryParticulate MatterPesticidesChromatography LiquidJournal of chromatography. A
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Quantitative analysis of six pesticides in fruits by capillary electrophoresis-electrospray-mass spectrometry.

2005

A method to identify and quantify six pesticide residues - dinoseb, pirimicarb, procymidone, pyrifenox, pyrimethanil, and thiabendazole - in peaches and nectarines using capillary electrophoresis-electrospray ionization-quadrupole ion trap-tandem mass spectrometry (CE-ESI-MS/MS) is described. Separation was carried out using a buffer of 0.3 M ammonium acetate at pH 4 with 10% methanol. Pesticide residues present in peach and nectarine samples were preconcentrated by solid-phase extraction using C(18), eluted with CH(2)Cl(2), concentrated to dryness, and redissolved in buffer to obtain lower detection limits. The recoveries of the analytes ranged from 58 to 99% and the relative standard devi…

Detection limitSpectrometry Mass Electrospray IonizationChromatographyPesticide residueClinical BiochemistryElectrophoresis CapillaryPesticidePirimicarbMass spectrometryBiochemistrySensitivity and SpecificityAnalytical Chemistrychemistry.chemical_compoundCapillary electrophoresischemistryFruitPyrimethanilProcymidonePesticidesElectrophoresis
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Analysis of thiabendazole and procymidone in fruits and vegetables by capillary electrophoresis–electrospray mass spectrometry

2002

Abstract A capillary electrophoresis–mass spectrometry method for determining procymidone and thiabendazole in apples, grapes, oranges, pears, strawberries and tomatoes is described. Separation is achieved using a buffer of formic acid–ammonium formate at pH 3.5 with 2% of methanol. Fungicide residues present in the sample are preconcentrated by both solid-phase extraction and injection of large sample volumes into the capillary by a stacking technique, to obtain lower detection limits. Ionization is performed at atmospheric pressure in an electrospray type source and detection is carried out using positive ionization and selected ion monitoring modes. The quantitation limits are 0.005 and …

Detection limitSpectrometry Mass Electrospray IonizationElectrosprayChromatographyOrganic ChemistryPesticide ResiduesElectrophoresis CapillaryGeneral MedicineMass spectrometrySensitivity and SpecificityBiochemistryFungicides IndustrialAnalytical ChemistryBridged Bicyclo Compoundschemistry.chemical_compoundCapillary electrophoresischemistryFruitThiabendazoleVegetablesSample preparationSelected ion monitoringSolid phase extractionProcymidoneJournal of Chromatography A
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