Search results for " ionization"

showing 10 items of 621 documents

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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Identification of ground water contaminations by landfills using precise boron isotope ratio measurements with negative thermal ionization mass spect…

1997

Precise boron isotope ratio measurements with negative thermal ionization mass spectrometry were used for the identification of ground water contaminations by leakages of landfills. BO 2 - thermal ions were produced to determine the 11 B/ 10 B isotope ratio, which was expressed as δ 11 B value in ‰ normalized to the standard reference material NIST SRM 951. For example, household waste influences the boron isotope ratio by specific components such as washing powder. In the case of one investigated landfill low δ 11 B values correlate well with high boron concentrations in contaminated seepage water samples and vice versa for uncontaminated ground water samples. Possible boron contributions …

Detection limitchemistryIsotopeAnalytical chemistrychemistry.chemical_elementThermal ionizationIsotopes of boronIsotope dilutionThermal ionization mass spectrometryBoronMass spectrometryBiochemistryFresenius' Journal of Analytical Chemistry
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Online atmospheric pressure chemical ionization ion trap mass spectrometry (APCI-IT-MS<sup>n</sup>) for measuring organic…

2012

Abstract. The field application of an aerosol concentrator in conjunction with an atmospheric pressure chemical ionization ion trap mass spectrometer (APCI-IT-MS) at the boreal forest station SMEAR II at Hyytiälä, Finland, is demonstrated in this study. APCI is a soft-ionization technique allowing online measurements of organic acids in the gas and particle phase. The detection limit for the acid species in the particle phase was improved by a factor of 7.5 to 11 (e.g. ∼40 ng m3 for pinonic acid) by using the miniature versatile aerosol concentration enrichment system (mVACES) upstream of the mass spectrometer. The APCI-IT-MS was calibrated in the negative ion mode with two biogenic organic…

Detection limitchemistry.chemical_classificationAtmospheric Science010504 meteorology & atmospheric sciencesChemistryAnalytical chemistryAtmospheric-pressure chemical ionization010501 environmental sciencesMass spectrometry01 natural sciencesAerosolIon13. Climate actionIon trapElectron ionization0105 earth and related environmental sciencesOrganic acidAtmospheric Measurement Techniques
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Direct injection analysis of fatty and resin acids in papermaking process waters by HPLC/MS

2011

A novel HPLC-atmospheric pressure chemical ionization/MS (HPLC-APCI/MS) method was developed for the rapid analysis of selected fatty and resin acids typically present in papermaking process waters. A mixture of palmitic, stearic, oleic, linolenic, and dehydroabietic acids was separated by a commercial HPLC column (a modified stationary C(18) phase) using gradient elution with methanol/0.15% formic acid (pH 2.5) as a mobile phase. The internal standard (myristic acid) method was used to calculate the correlation coefficients and in the quantitation of the results. In the thorough quality parameters measurement, a mixture of these model acids in aqueous media as well as in six different pape…

Detection limitchemistry.chemical_compoundChemical ionizationChromatographychemistryFormic acidPhase (matter)Myristic acidFiltration and SeparationMethanolSelectivityHigh-performance liquid chromatographyAnalytical ChemistryJournal of Separation Science
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An efficient excitation scheme for resonance ionization of tin in a laser ion source

1992

An efficient three-colour, three-step resonant excitation/ionization scheme has been found for tin that leads from the 5p23P2 level of the ground-state multiplet via two excited atomic levels (λ1 = 317.51 nm and λ2 = 811.40 nm) to an autoionizing state 9s3P2(λ3 = 823.49 nm) at 59375.9 cm−1. This excitation path permits the saturation of all transitions with the limited power available from a copper vapour laser pumped dye laser system (Esat ≈ 1.5 mJcm2 for λ3). The high repetition rate of such a laser system is essential for a highly efficient laser ion source.

Dye laserChemistrychemistry.chemical_elementLaserAtomic and Molecular Physics and OpticsIon sourceAnalytical Chemistrylaw.inventionAtmospheric-pressure laser ionizationlawIonizationExcited stateAtomic physicsTinInstrumentationSpectroscopyExcitationSpectrochimica Acta Part B: Atomic Spectroscopy
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Determination of trace elements by resonant ionization mass spectrometry (RIMS)

1988

A resonant ionization mass spectrometer has been developed as an analytical tool for the detection of trace elements, especially of plutonium and other radionuclides. The sample, deposited on a rhenium filament, is evaporated by electrical heating and the atoms of the element under investigation are selectively ionized by laser light delivered from three dye lasers pumped by a copper vapour laser. The resulting photoions are detected in a time-of-flight spectrometer with a channelplate detector. For plutonium a mass resolution of M/δM=1500 was obtained and an overall detection efficiency of 4×10−6 was determined for stepwise excitation and ionization via autoionizing states. With a laser li…

Dye laserSpectrometerPhysics::Instrumentation and DetectorsChemistryClinical BiochemistryAnalytical chemistryGeneral MedicineThermal ionization mass spectrometryMass spectrometryBiochemistryAnalytical ChemistryIonizationGeneral Materials SciencePhysics::Atomic PhysicsAtomic vapor laser isotope separationHyperfine structureHybrid mass spectrometerFresenius Zeitschrift f�r Analytische Chemie
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