Search results for "LIMIT"

showing 10 items of 2826 documents

Selective chlorine determination by gas diffusion in a tandem flow assembly and spectrophotometric detection with o-dianisidine

2001

Abstract A fast, selective, sensitive and automated method for determination of free chlorine in industrial formulations and water samples is proposed. The automation of the flow assembly is based on the “tandem flow” approach, which uses a set of solenoid valves acting as independent switches. The operating cycle for obtaining a typical analytical transient signal can easily be programmed by means of friendly software running in the Windows environment. The manifold is provided with a gas diffusion unit which permits the removal of interfering species as well as concentrating the chlorine. The determination of chlorine is performed on the basis of the oxidation of o-dianisidine as the colo…

Detection limitReproducibilityTandemChemistryAnalytical chemistrychemistry.chemical_elementSolenoidBiochemistryAnalytical ChemistryReagentpolycyclic compoundsChlorineEnvironmental ChemistryGaseous diffusionQuantitative analysis (chemistry)SpectroscopyAnalytica Chimica Acta
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Determination of benzoylurea insecticides in food by pressurized liquid extraction and LC-MS

2010

A method based on pressurized liquid extraction and LC-MS/MS has been developed for determining nine benzoylureas (BUs) in fruit, vegetable, cereals, and animal products. Samples (5 g) were homogenized with diatomaceous earth and extracted in a 22 mL cell with 22 mL of ethyl acetate at 80 degrees C and 1500 psi. After solvent concentration and exchange to methanol, BUs were analyzed by LC-MS/MS using an IT mass analyzer, which achieved several transitions of precursor ions that increase selectivity providing identification. LOQs were between 0.002 and 0.01 mg/kg, which are equal or lower than maximum residue limits established by the Codex Alimentarius. Excellent linearity was achieved over…

Detection limitResidue (complex analysis)ChromatographyBenzoylureaExtraction (chemistry)Ethyl acetateFiltration and SeparationHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistryLiquid chromatography–mass spectrometrymedicineSample preparationmedicine.drugJournal of Separation Science
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Capillary zone electrophoresis for the determination of thiabendazole, prochloraz and procymidone in grapes

2001

Capillary zone electrophoresis with UV detection was applied to the simultaneous determination of thiabendazole, prochloraz and procymidone in grapes. Electrolyte conditions such as pH, composition and concentration of the buffer, addition of organic solvent and working voltage were checked to obtain a high-performance separation of the three fungicides (by measurement of separation efficiency and resolution). The most critical parameter was the pH of the running buffer. The best separation was achieved in 4 mM phosphate solution at pH 3.5. The repeatability of the migration times, expressed as RSD, was <0.44%. The three peaks were completely resolved with a separation efficiency up to 100 …

Detection limitResidue (complex analysis)ChromatographyChemistryExtraction (chemistry)ImidazolesAnalytical chemistryElectrophoresis CapillaryRepeatabilityBiochemistryAnalytical ChemistryBridged Bicyclo Compoundschemistry.chemical_compoundCapillary electrophoresisThiabendazoleElectrochemistryEnvironmental ChemistryVitisProcymidoneTheoretical plateSolid phase extractionSpectroscopyThe Analyst
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Determination of type A and type B trichothecenes in paprika and chili pepper using LC-triple quadrupole-MS and GC-ECD.

2011

There is a need to develop sensitive and accurate analytical methods for determining deoxynivalenol (DON), HT-2 toxin and T-2 toxin in paprika to properly assess the relevant risk of human exposure. An optimized analytical method for determination of HT-2 toxin and T-2 toxin using capillary gas chromatography with electron capture detection and another method for determination of DON by liquid chromatography-mass spectrometry in paprika was developed. The method for determination of HT-2 toxin and T-2 toxin that gave the best recoveries involved extraction of the sample with acetonitrile-water (84:16, v/v), clean-up by solid-phase extraction on a cartridge made of different sorbent material…

Detection limitResidue (complex analysis)ChromatographyChromatography GasElutionChemistryExtraction (chemistry)Mass SpectrometryAnalytical ChemistryTriple quadrupole mass spectrometerT-2 ToxinHumansSample preparationGas chromatographySolid phase extractionCapsicumTrichothecenesChromatography LiquidTalanta
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Non-chromatographic speciation of inorganic arsenic in mushrooms by hydride generation atomic fluorescence spectrometry

2009

Abstract A non-chromatographic speciation method has been developed for the determination of inorganic arsenic in cultivated and wild mushroom samples from different origins. The ultrasound-assisted extraction of the toxic arsenic species As (III) and As (V) was performed for 10 min with 1 mol l −1 H 3 PO 4 and 0.1% (m/v) Triton X-100. After phase separation the residue was washed with 0.1% (w/v) EDTA and centrifuged. As (III) and As (V) were determined by hydride generation atomic fluorescence spectrometry. Speciation was made using proportional equations corresponding to two different measurement conditions, (i) directly feeding sample extracts diluted with HCl and (ii) after reduction wi…

Detection limitResidue (complex analysis)ChromatographyHydrideExtraction (chemistry)Fluorescence spectrometrychemistry.chemical_elementGeneral MedicineAscorbic acidMass spectrometryAnalytical ChemistrychemistryArsenicFood ScienceFood Chemistry
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Multi-class determination of antimicrobials in meat by pressurized liquid extraction and liquid chromatography–tandem mass spectrometry

2008

A multi-residue method using pressurized liquid extraction (PLE) and liquid chromatography-tandem mass spectrometry (LC-MS/MS) has been developed for determining trace levels of 31 antimicrobials, including beta-lactams, lincosamides, macrolides, quinolones, sulfonamides, tetracyclines, nitroimidazoles and trimethoprim. The extraction method required pre-homogeneization of the meat with EDTA-washed sand and subsequent one-static-cycle extraction for 10 min with 40 ml of water at 1500 psi and 70 degrees C. The effect of operation temperature, pressure, flush volume, and static cycles on PLE performance was studied. Average recoveries ranged from 75 to 99% with relative standard deviations <1…

Detection limitResidue (complex analysis)MeatChromatographyMolecular StructureSwineChemistryOrganic ChemistryReproducibility of ResultsGeneral MedicineBiochemistryHigh-performance liquid chromatographyAnti-Bacterial AgentsAnalytical ChemistryHot water extractionTandem Mass SpectrometryLiquid chromatography–mass spectrometryAnimalsmedia_common.cataloged_instanceCattleSample preparationEuropean unionChromatography LiquidAntibacterial agentmedia_commonJournal of Chromatography A
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Optimization of transmission near infrared spectrometry procedures for quality control of pesticide formulations

2006

The use of different response functions to be optimized in the frame of the use of near infrared spectrometry for quality control of active principles in agrochemical formulations has been evaluated. Both, simple functions, based on parameters like sensitivity, repeatability, accuracy, signal to noise ratio, limit of detection or sample throughput, and a complex function, considering all the aforementioned aspects, were employed in the development of a new method for Iprodione determination in agrochemicals. Optimization strategies were based on the previous screening of the most important instrumental factors like number of cumulated scans, nominal resolution, mirror velocity and zero fill…

Detection limitResolution (mass spectrometry)ChemistryRepeatabilityFactorial experimentBiochemistryAnalytical ChemistrySignal-to-noise ratioStatisticsCalibrationEnvironmental ChemistrySensitivity (control systems)Biological systemThroughput (business)SpectroscopyAnalytica Chimica Acta
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Resorcinol Functionalized Gold Nanoparticles for Formaldehyde Colorimetric Detection

2019

[EN] Gold nanoparticles functionalized with resorcinol moieties have been prepared and used for detecting formaldehyde both in solution and gas phases. The detection mechanism is based on the color change of the probe upon the aggregation of the nanoparticles induced by the polymerization of the resorcinol moieties in the presence of formaldehyde. A limit of detection of 0.5 ppm in solution has been determined. The probe can be deployed for the detection of formaldehyde emissions from composite wood boards.

Detection limitResorcinolGeneral Chemical EngineeringFormaldehydeNanoparticleResorcinolArticlelcsh:Chemistrychemistry.chemical_compoundchemistryPolymerizationlcsh:QD1-999Colloidal goldFormaldehydegold nanoparticlescolorimetric detectionGold nanoparticlesformaldehydeGeneral Materials ScienceresorcinolColorimetric detectionNuclear chemistryNanomaterials
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Determination of the new psychoactive substance dichloropane in saliva by microextraction by packed sorbent – Ion mobility spectrometry

2018

Abstract A simple procedure based on microextraction by packed sorbent (MEPS) has been proposed for the extraction of dichloropane in oral fluids and its determination by ion mobility spectrometry (IMS). Extraction conditions such as type of sorbent (octyl and octadecyl silica), sample pH, number of sample loadings, and elution volume were evaluated to obtain the most appropriate values. Dichloropane was extracted from saliva samples using C8 MEPS, loading with 100 μL sample (adjusted to pH 7) in 4 cycles, washing with 100 μL deionized water, and eluting with 50 μL 2-propanol in 10 cycles. The proposed MEPS procedure has been validated in terms of linearity, accuracy, and precision. A limit…

Detection limitSalivaSorbentChromatographyChemistryIon-mobility spectrometryElution010401 analytical chemistryOrganic ChemistryExtraction (chemistry)General Medicine010402 general chemistryMass spectrometry01 natural sciencesBiochemistryGas Chromatography-Mass Spectrometry0104 chemical sciencesAnalytical ChemistryCocaineLimit of DetectionIon Mobility SpectrometryHumansGas chromatography–mass spectrometrySalivaSolid Phase MicroextractionJournal of Chromatography A
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Environmentally friendly analytical chemistry through automation: comparative study of strategies for carbaryl determination with p-aminophenol

1999

Abstract A flow system, based on multicommutation and binary sampling, has been developed for improving the automated spectrophotometric determination of carbaryl with p -aminophenol (PAP) in order to reduce the waste volume and to preserve the maximum analytical performance. The procedure, which was implemented employing a flow network obtained by nesting five, three-way solenoid valves controlled by means of a 386 microcomputer equipped with an electronic interface running software written in quick basic 4.5, provides a limit of detection of 26 μg l −1 , comparable to that obtained using a conventional flow injection (FIA) manifold and lower than that found by sequential injection analysi…

Detection limitSequential injection analysisChromatographyChemistrybusiness.industryAnalytical chemistryFlow networkBiochemistryAutomationEnvironmentally friendlyAnalytical Chemistrychemistry.chemical_compoundVolume (thermodynamics)MicrocomputerCarbarylEnvironmental ChemistrybusinessSpectroscopyAnalytica Chimica Acta
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