Search results for "LIMIT"

showing 10 items of 2826 documents

Some observations on the sensitivity of flow-injection techniques for atomic absorption spectrophotometry

1989

Abstract Different strategies for coupling flow-injection manifolds to atomic absorption spectrometers in order to obtain better sensitivity are compared. Using a T-connector interface, different carriers and flow compensation solvents have been assayed in an attempt to improve the sensitivity of flow-injection analysis. Manganese and copper determinations in sewage sludge have been used as a test system and the analytical parameters of both batch and flow-injection methods are compared.

Detection limitSpectrometerAnalytical chemistrychemistry.chemical_elementManganeseCopperAnalytical ChemistryVolumetric flow ratelaw.inventionchemistrylawSensitivity (control systems)Atomic absorption spectroscopySpectroscopySludgeMicrochemical Journal
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Multi-pumping mechanised determination of selenium in natural waters by light emitting diode (LED) spectrometry

2009

It has been developed a fully mechanised procedure for the determination of selenium in waters employing a LED based spectrometer and solenoid multi-pumps as solution propelling devices. The proposed method is based on the reaction of selenium with potassium iodide in an acidic medium to liberate iodine, which oxidizes Variamine Blue to form a violet-colour species which absorb at 530 nm. The system was mechanised using the multicommutation process and a stopped flow strategy in the final step reaction. The analytical curve was linear between 0.010 and 0.500 mg L-1, with an equation ΔA = 0.501 (± 0.004) C and r = 0.999. The limit of detection (3σ/S) obtained for the proposed method was 0.00…

Detection limitSpectrometerNatural waterwaterRelative standard deviationLED-photometryAnalytical chemistrychemistry.chemical_elementmulti-pumpingGeneral ChemistryMass spectrometryIodinemechanised flow systemlaw.inventionchemistrylawmulticommuted flow systemseleniumSeleniumLight-emitting diodeJournal of the Brazilian Chemical Society
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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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Application of stable isotopes and AF4/ICP-SFMS for simultaneous tracing and quantification of iron oxide nanoparticles in a sediment–slurry matrix

2016

One major challenge in nanomaterial analysis, especially in complex environmental matrices, is the unambiguous differentiation between natural and engineered nanomaterials (ENMs). Particularly with regard to the investigation of ENM's/engineered nanoparticle's (ENPs) fate, analytical methods are needed allowing for tracing and sensitive quantification. Several ENPs are metal-based and contain elements being omnipresent in environmental matrices (e.g., Al, Ti, Zn, Fe and non-metal Si) – hence, high background levels of these elements are expected, compromising sensitive detection. In this work we developed successfully a combined approach of stable isotope labeling (tracing) and reverse post…

Detection limitStable isotope ratioElution010401 analytical chemistryRadiochemistryAnalytical chemistry010501 environmental sciencesIsotope dilution01 natural sciencesSilver nanoparticle0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundColloidchemistryInductively coupled plasma mass spectrometrySpectroscopyIron oxide nanoparticles0105 earth and related environmental sciencesJournal of Analytical Atomic Spectrometry
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Micropumping multicommutation turbidimetric analysis of waters

2007

Abstract A micropumping multicommutation manifold to perform turbidity determinations in waters is described. The procedure is based on the use of a combination of hydrazine sulfate and hexamethylenetetramine, to obtain an external standard of nephelometric turbidity units (NTU), which could compare the absorbance measurements at high wavelengths for samples with a calibration line obtained from a concentrated formazine standard diluted on-line. To minimize sample and reagent consumption and waste generation, the flow system was designed with two solenoid micro-pumps, one of them for the alternative introduction of the formazine standard and samples and the other one for the water carrier. …

Detection limitStandard curveAbsorbancechemistry.chemical_compoundChromatographyChemistryReagentCoefficient of variationAnalytical chemistryTurbidityFormazineAnalytical ChemistryDilutionTalanta
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Fast, low-level detection of strontium-90 and strontium-89 in environmental samples by collinear resonance ionization spectroscopy

1993

Environmental assessment in the wake of a nuclear accident requires the rapid determination of the radiotoxic isotopes 89Sr and 90Sr. Useful measurements must be able to detect 108 atoms in the presence of about 1018 atoms of the stable, naturally occurring isotopes. This paper describes a new approach to this problem using resonance ionization spectroscopy in collinear geometry, combined with classical mass separation. After collection and chemical separation, the strontium from a sample is surface-ionized and the ions are accelerated to an energy of about 30 keV. Initially, a magnetic mass separator provides an isotopic selectivity of about 106. The ions are then neutralized by charge exc…

Detection limitStrontiumIsotopeAnalytical chemistrychemistry.chemical_elementAtomic and Molecular Physics and OpticsAnalytical ChemistryIonsymbols.namesakechemistryExcited stateRydberg atomPhysics::Atomic and Molecular ClustersRydberg formulasymbolsPhysics::Atomic PhysicsAtomic physicsSpectroscopyInstrumentationSpectroscopySpectrochimica Acta Part B: Atomic Spectroscopy
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