Search results for "Standard deviation"

showing 10 items of 282 documents

Improvement of the atomic fluorescence determination of mercury by using multicommutation

2002

Atomic fluorescence spectrometry (AFS) determination of Hg has been improved by exploiting the possibilities of the multicommutation approach in order to outline a fully mechanised system which supplies the same sensitivity as the use of continuous measurements, reducing drastically the reagents consumed and waste generation. The use of multicommutation with a simultaneous reduction of the liquid–gas separator volume and the insertion point modification of argon transport gas provides a sensitivity of the AFS measurements of 300 mV ng−1 ml (using a full scale of 1000 mV), a limit of detection (3 s) of 1.3 ng l−1 and relative standard deviation values below 0.1% for 10 independent measuremen…

Detection limitAtomic fluorescenceChromatographyArgonChemistryRelative standard deviationAnalytical chemistrychemistry.chemical_elementSeparator (oil production)Analytical ChemistryMercury (element)Waste generationReagentSpectroscopyJ. Anal. At. Spectrom.
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Preliminary Results on the Use of Leather Chrome Shavings for Air Passive Sampling

2012

A new passive sampler based on low-density polyethylene (LDPE) layflat tube filled with chrome shavings from tannery waste residues was evaluated to determine volatile organic compounds (VOCs) in indoor and outdoor areas. VOCs were directly determined by head space-gas chromatography-mass spectrometry (HS-GC-MS) without any pretreatment of the sampler and avoiding the use of solvents. Limit of detection values ranging from 20 to 75 ng sampler−1and good repeatability values were obtained for VOCs under study with relative standard deviation values from 2.8 to 9.6% except for carbon disulfide for which it was 22.5%. The effect of the amount of chrome shavings per sampler was studied and resul…

Detection limitCarbon disulfideMaterials sciencelcsh:QD71-142Article SubjectGeneral Chemical EngineeringRelative standard deviationlcsh:Analytical chemistryRepeatabilityPolyethylenePulp and paper industrycomplex mixturesComputer Science ApplicationsAnalytical ChemistryLow-density polyethylenechemistry.chemical_compoundAdsorptionchemistryInstrumentationPassive samplingResearch ArticleJournal of Analytical Methods in Chemistry
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Selective determination of clenbuterol residues in urine by molecular imprinted polymer—Ion mobility spectrometry

2017

Abstract Clenbuterol is banned for sports use and strictly regulated in livestock industry. In this study, a procedure for the determination of clenbuterol residues in water and urine has been developed using selective supports combined with ion mobility spectrometry (IMS) determination. A molecular imprinted polymer (MIP) was used for efficient clean-up and preconcentration of clenbuterol followed to a dispersive liquid-liquid microextraction (DLLME) in order to improve selectivity and sensitivity of IMS determinations. Quantitative recoveries from 81 to 99% were obtained for water and spiked urine samples using MIP-DLLME-IMS method. A precision of 4.5%, established as the relative standar…

Detection limitChromatographyChemistryIon-mobility spectrometry010401 analytical chemistryRelative standard deviationMolecularly imprinted polymer02 engineering and technologyUrine021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAnalytical ChemistryLiquid chromatography–mass spectrometryClenbuterolmedicine0210 nano-technologySpectroscopymedicine.drugMicrochemical Journal
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Die direkte quantitative auswertung von dünnschichtchromatogrammen durch remissions- und fluoreszenzmessungen

1971

Abstract Direct quantitative evaluation of thin-layer chromatograms by remission- and fluorescence measurements. Part 6. Determination of adrenaline, noradrenaline and dopamine from urine Adrenaline, noradrenalineand dopamine were separated from urine on aluminium oxide columns; after elution they were converted into ther O 3 ,O 4 ,N-triacetyl derivatives and separated using thin-layer chromatography. The triacetyl derivatives were in situ converted to fluorescing compounds using ethylene diamine and quantitatively estimated using the Chromatogram-Spectrophotometer (Carl Zeiss, Oberkochen). The advantage of this method over the conventional fluorometric determination of catecholamines in so…

Detection limitChromatographyEthylene diamineChemistryElutionOrganic ChemistryRelative standard deviationThin layerGeneral MedicineBiochemistryAnalytical ChemistryJournal of Chromatography A
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Fast extraction methodologies for the determination of toxic arsenic in meat

2017

Summary A nonchromatographic analytical procedure has been developed for the determination of arsenic in meat samples including the major toxic arsenic species arsenite, arsenate, monomethylarsonic acid (MMA) and dimetylarsinic acid (DMA). The method is based on the extraction of arsenic species in mild conditions, selective trivalent hydride formation and final determination by hydride generation atomic fluorescence spectroscopy (HG-AFS). Different extractant agents and two different procedures, microwave-assisted extraction (MAE) and ultrasound assisted extraction at room temperature, were evaluated for As species extraction. The method provided a limit of detection of 0.013 ng mL−1 and a…

Detection limitChromatographyHydride010401 analytical chemistryExtraction (chemistry)Relative standard deviationArsenatechemistry.chemical_elementMonomethylarsonic acid010501 environmental sciences01 natural sciencesIndustrial and Manufacturing Engineering0104 chemical scienceschemistry.chemical_compoundchemistryEnvironmental chemistryArsenic0105 earth and related environmental sciencesFood ScienceArseniteInternational Journal of Food Science & Technology
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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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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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Flow analysis-spectrophotometric determination of ?-dopa in pharmaceutical formulations by reaction with p-Aminophenol

1994

Abstract A new method has been developed for the spectrophotometric determination of l -dopa in pharmaceutical formulations. The method is based on the reaction between the open-chain quinone of l -dopa, obtained in NaOH, and the benzoqinoneimine form of p-aminophenol, in the presence of KIO4. The reaction product is determined at 574 nm by using both alternately procedures, one based on the stopped-flow and another on a flow injection approach. Under the best experimental conditions L-dopa can be determined with a limit of detection of 52 ng/ml and a relative standard deviation of 0.2% for three replicate measurements of a solution containing 4 μg/ml.

Detection limitChromatographymedicine.diagnostic_testChemistryP-AminophenolRelative standard deviationDosage formAnalytical ChemistryQuinonechemistry.chemical_compoundSpectrophotometrymedicineDerivatizationQuantitative analysis (chemistry)Talanta
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Rapid microwave assisted hydrolysis of formetanate

1993

Abstract A fast microwave-assisted hydrolysis procedure has been developed for the derivatization of formetanate previously to the flow-injection spectrophotometric determination of m -aminophenol by reaction with p -aminophenol. Formetanate is quantitatively hydrolyzed with 0.1 M NaOH in 150 s using a closed polyetrafluoroethylene reactor with 115 ml internal volume and a radiation power of 390 W. The above procedure has been applied, as a previous step, for the flow-injection spectrophotometric determination of formetanate in spiked water samples and accurate and precise results have been found. The method permits to obtain a limit of detection of 0.025 mg 1 −1 of formetanate. The relativ…

Detection limitChromatographymedicine.diagnostic_testRelative standard deviationBiochemistryMicrowave assistedAnalytical Chemistrychemistry.chemical_compoundHydrolysischemistryFormetanateSpectrophotometrymedicineEnvironmental ChemistryTrace analysisDerivatizationSpectroscopyAnalytica Chimica Acta
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HPLC determination of oxadiazon in commercial pesticide formulations

2008

A simple, fast and precise high performance liquid chromatographic (HPLC) procedure has been developed for the determination of oxadiazon in emulsifiable concentrated pesticide formulations. 20 µL of diluted sample in acetonitrile were injected in a Kromasil C18 (250 ×am injetados em uma coluna Kromasil C18 4.6 mm, 5 µm) column, using acetonitrile:water (80:20) as mobile phase at 1 mL min-1 flow rate and oxadiazon determined by absorbance measurement at 292 nm. A theoretical limit of detection of 0.02 µg mL-1, a limit of quantification of 0.047 µg mL-1, corresponding to a 0.02 and 0.07% m/v in the original sample, and a relative standard deviation of 0.08% for three replicate analysis of sa…

Detection limitChromatographymedicine.diagnostic_testhigh performance liquid chromatographyChemistryRelative standard deviationUV-Vis detectionGeneral ChemistryPesticideHigh-performance liquid chromatographyoxadiazonAbsorbancechemistry.chemical_compoundSpectrophotometrymedicineFourier transform infrared spectroscopyAcetonitrilepesticide formulations
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