Search results for "LIMIT"

showing 10 items of 2826 documents

Bromide/bromate speciation by NTI-IDMS and ICP-MS coupled with ion exchange chromatography

1997

Two different mass spectrometric methods, negative thermal ionization isotope dilution mass spectrometry (NTI-IDMS) and inductively coupled plasma mass spectrometry (ICP-MS), off-line and on-line coupled with anion exchange chromatography, have been developed for simultaneous bromide and bromate determinations in water samples. The detection limits of these methods are in the range of 0.03–0.09 μg/L using a 50 mL sample.The results are independent of the content of other anions, which could be demonstrated by the analyses of six mineral waters containing chloride and sulfate of up to 160 mg/L and 1500 mg/L, respectively. Bromide has been analyzed by the NTI-IDMS method in the range of 10–50…

Detection limitChromatographyIon chromatographyIsotope dilutionBromateBiochemistrychemistry.chemical_compoundchemistryBromideStandard additionmedia_common.cataloged_instanceEuropean unionInductively coupled plasma mass spectrometrymedia_commonFresenius' Journal of Analytical Chemistry
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Development of a molecularly imprinted monolithic polymer disk for agitation-extraction of ecgonine methyl ester from environmental water

2019

Abstract In this study, a new extraction approach based on rotating molecularly imprinted polymer (MIP) disks was developed. The preparation procedure of MIP-disk is simple. Firstly, in order to immobilize MIP onto the surface of polytetrafluoroethylene (PTFE) disk, previous modification and vinylization steps of this fluoropolymer were conducted. Then, MIP synthesis was done by in situ polymerization. The resulting MIP was characterized by Fourier-transform infrared spectroscopy and scanning electron microscopy. Afterwards, two ring magnets were placed in the sides of the MIP-disk to integrate the stirring and preconcentration of sample in just one step. To demonstrate the feasibility of t…

Detection limitChromatographyIon-mobility spectrometry010401 analytical chemistryExtraction (chemistry)Molecularly imprinted polymer02 engineering and technology021001 nanoscience & nanotechnologyMass spectrometry01 natural sciences0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundchemistryFluoropolymerIn situ polymerization0210 nano-technologyMolecular imprintingTalanta
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Uptake and translocation monitoring of imidacloprid to chili and tomato plants by molecularly imprinting extraction - ion mobility spectrometry

2019

Abstract The degradation of imidacloprid in soil and its uptake and translocation to chili and tomato plants was evaluated, as a proof of concept, of the possibilities of the combination of molecularly imprinted polymers (MIPs) and ion mobility spectrometry (IMS) for a fast and sensitive bioprocesses monitoring tool. To do it, a method based on the selective extraction of imidacloprid from soil and plant materials was developed. In the selected conditions, the MIP-IMS procedure provided a recovery of imidacloprid in soil and plant samples from 102 to 114%, for spiked concentration levels from 0.2 to 2.0 μg g−1. Precision of the methodology, expressed as the relative standard deviation (RSD)…

Detection limitChromatographyIon-mobility spectrometryChemistry010401 analytical chemistryRelative standard deviationMolecularly imprinted polymerChromosomal translocation02 engineering and technologyPesticideStandard solution021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundImidacloprid0210 nano-technologySpectroscopyMicrochemical Journal
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Development of an ICP−IDMS Method for Dissolved Organic Carbon Determinations and Its Application to Chromatographic Fractions of Heavy Metal Complex…

1998

A sensitive and fast method for direct determinations of dissolved organic carbon (DOC) in bulk samples and in chromatographically separated fractions by inductively coupled plasma isotope dilution mass spectrometry (ICP−IDMS) is developed. A 13C-enriched spike solution of benzoic acid is used for the isotope dilution step. Equal ionization efficiencies are obtained for carbon, independent of the type and molecular weight of the dissolved organic substance, which is the most important precondition for DOC determinations by ICP−IDMS. The detection limits achieved are 0.3 mg L-1 for bulk analyses and 7 × 10-4 μg s-1 for transient signals of chromatographic peaks. The results for different wat…

Detection limitChromatographyIsotopeChemistryAnalytical chemistrychemistry.chemical_elementIsotope dilutionMass spectrometryAnalytical Chemistrychemistry.chemical_compoundDissolved organic carbonInductively coupled plasmaCarbonBenzoic acidAnalytical Chemistry
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High-performance liquid chromatography of lactose with evaporative light scattering detection, applied to determine fine particle dose of carrier in …

2005

A method for quantification of the fine particle dose of lactose is described, using a hydrophilic interaction chromatography (HILIC) method and evaporative light scattering detection. The HILIC method used an aminopropyl column and a mobile phase consisting of acetonitril/water (80/20, v/v) for isocratic elution. Sensitive chromatography was obtained using a low concentration of water in the extraction solvent. The detection limit (RSD10%) at an injection volume of 10 microL is 10 microg/mL. Linearity was obtained in the range of 10-80 microg/mL (R(2)0.99). A relative standard deviation (RSD) of 0.5% (N=6) demonstrated good precision of the optimized method.

Detection limitChromatographyLightChemistryHydrophilic interaction chromatographyOrganic ChemistryExtraction (chemistry)Analytical chemistryReproducibility of ResultsLactoseGeneral MedicineBiochemistryHigh-performance liquid chromatographyLight scatteringAnalytical ChemistrySolventChromatography detectorAdministration InhalationScattering RadiationParticlePowdersChromatography High Pressure LiquidJournal of Chromatography A
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Solid glucose biosensor integrated in a multi-well microplate coupled to a camera-based detector: Application to the multiple analysis of human serum…

2018

Abstract In the present work, a biosensor adapted in a 96-well microplate has been coupled with a smartphone-based photometer in order to develop a low-cost colorimetric multi-sample dispositive. The strength of this biosensing system is based on the integration of the biosensor into the 96-well microplate and the use of a smartphone and free image analysis software as a microplate reader. The performance of the proposed biosensor has been demonstrated to determine glucose in several human serum samples. This method is simple, cost-effective, sensitive and selective for the determination of glucose in serum, with detection limits of 1.8 mg/dL and a good linearity over the range 6–88 mg/dL. …

Detection limitChromatographyMaterials scienceDetectorRelative standard deviationMetals and Alloys02 engineering and technologyPhotometer010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsSerum samples01 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionMicroplate ReaderlawMaterials ChemistryElectrical and Electronic Engineering0210 nano-technologyInstrumentationBiosensorSensors and Actuators B: Chemical
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Fourier transform infrared determination of imidacloprid in pesticide formulations

2004

A simple method has been developed for Fourier Transform Infrared (FTIR) determination of Imidacloprid in pesticide formulations. Samples were diluted with CHCl3 and the FTIR spectra of samples and standards were obtained at a nominal resolution of 4 cm-1 from 4000 to 900 cm-1 accumulating 25 scans. Imidacloprid determination was based on the measure of either peak area from 1577 to 1567 cm-1 or peak height at 1572 cm-1, both corrected using a horizontal baseline defined at 1900 cm-1. The limits of detection achieved, of the order of 9 µg g-1, were appropriate for the determination of Imidacloprid in commercially available formulations. FTIR results were statistically comparable to those fo…

Detection limitChromatographyMaterials scienceHPLC-UVResolution (mass spectrometry)InfraredImidaclopridGeneral ChemistryHigh-performance liquid chromatographylcsh:Chemistrysymbols.namesakechemistry.chemical_compoundFourier transformchemistrylcsh:QD1-999FTIRImidaclopridsymbolsSample preparationFourier transform infrared spectroscopypesticide formulations
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Determination of amitraz and its transformation products in pears by ethyl acetate extraction and liquid chromatography-tandem mass spectrometry.

2008

A method has been developed for identification and quantification of the acaricide amitraz and its transformation products, 2,4-dimethylaniline (DMA), 2,4-dimethylformamidine (DMF) and N-2,4-dimethylphenyl-N-methylformamidine (DMPF) in pears. The analytes were extracted using ethyl acetate and anhydrous sodium sulphate. Analysis was performed by liquid chromatography-electrospray tandem mass spectrometry (LC-ESI-MS/MS) in the positive ion mode using a triple quadrupole (QqQ) instrument. Two precursor-product ion transitions were monitored for each compound in the selected reaction monitoring (SRM) mode. The method was validated with pears taken from the orchard before the amitraz treatment …

Detection limitChromatographyMaximum Residue LimitAniline CompoundsToluidinesSulfatesOrganic ChemistrySelected reaction monitoringEthyl acetatePesticide ResiduesReproducibility of ResultsGeneral MedicineAcetatesBiochemistryHigh-performance liquid chromatographySensitivity and SpecificityAnalytical ChemistryTriple quadrupole mass spectrometerPyruschemistry.chemical_compoundchemistryLiquid chromatography–mass spectrometryTandem Mass SpectrometryAmitrazChromatography LiquidJournal of chromatography. A
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On-line speciation of mercury in fish by cold vapour atomic fluorescence through ultrasound-assisted extraction

2004

A fully mechanized procedure has been developed for the speciation of mercury in fish samples by using cold vapour atomic fluorescence spectrometry (CV-AFS). Sample slurries in an acid mixture in the presence of a surfactant and with traces of K2Cr2O7, were injected into a flow system, sonicated and merged with 1 ml of an oxidant mixture of KBr/KBrO3 heated at 50 °C in a water bath and total Hg determined by CV-AFS. Sonicated sample slurries were also measured, in the absence of KBr/KBrO3, in order to obtain a second series of data which could be employed to establish the concentrations of free Hg(II). Different compositions of the acidic extractant solutions were evaluated by mixing HCl, H…

Detection limitChromatographyMercury in fishSonicationExtraction (chemistry)Analytical chemistryAnalytical Chemistrychemistry.chemical_compoundCertified reference materialschemistryPulmonary surfactantSlurryMethylmercurySpectroscopyJ. Anal. At. Spectrom.
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Optimization of LC–MS/MS using triple quadrupole mass analyzer for the simultaneous analysis of carbosulfan and its main metabolites in oranges

2006

This paper describes an analytical method involving a simple solvent extraction for the simultaneous liquid chromatography coupled to quadrupole tandem mass spectrometry (LC-MS/MS) determination of carbosulfan, its most toxic metabolite--carbofuran--, and its other main metabolites--3-hydroxycarbofuran, 3-ketocarbofuran, 3-hydroxy-7-phenolcarbofuran, 3-keto-7-phenolcarbofuran, 7-phenolcarbofuran and dibutylamine--in oranges. Chromatography was performed on a Zorbax Bonus-RP (150 mm x 2.1 mm, 5 microm). The mobile phase was a ternary gradient water-methanol-acetonitrile with 1.0 mM ammonium acetate at flow rate of 0.2 ml min(-1). The LC separation and MS/MS optimization were studied to selec…

Detection limitChromatographyMetaboliteAnalytical chemistryTandem mass spectrometryBiochemistryAnalytical ChemistryTriple quadrupole mass spectrometerStandard curvechemistry.chemical_compoundchemistryLiquid chromatography–mass spectrometryEnvironmental ChemistrySample preparationCarbosulfanSpectroscopyAnalytica Chimica Acta
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