Search results for "Relative"

showing 10 items of 1094 documents

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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Simultaneous determination of hydride and non-hydride forming elements by inductively coupled plasma optical emission spectrometry

2011

e percentagens de recuperacao entre 97 e 103%. A aplicabilidade do sistema foi demonstrada na determinacao simultânea de Ca, Cd, Co, Cr, Cu, Fe, Mg, Mn, Mo, Ni, Zn, As, Bi, Sb, Se e Te em amostras certificadas para elementos tracos, NIST 1549 (leite em po desnatado), NIST 1570a (folhas de espinafre), DORM-2 (musculo de cacao) e TORT-2 (hepatopâncreas de lagosta). Os resultados obtidos foram concordantes com os teores certificados. The operating characteristics of a dual nebulization system were studied including instrumental and chemical conditions for the hydride generation and analytical figures of merit for both, hydride and non hydride forming elements. Analytical performance of the neb…

Detection limitHydrideChemistryInductively coupled plasma atomic emission spectroscopyRelative standard deviationAnalytical chemistryGeneral ChemistryInductively coupled plasmaOptical emission spectrometryJournal of the Brazilian Chemical Society
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Non-chromatographic speciation of mercury in mushrooms

2016

A fast, sensitive and cheap procedure has been developed for the determination of inorganic mercury (i-Hg) and organic mercury (o-Hg) in mushroom samples. The procedure is based on the use of cold vapour atomic fluorescence spectrometry (CV-AFS). The method involves the extraction of total mercury (t-Hg) with diluted HCl, followed by measurements of the corresponding Hg vapour under two different conditions: (i) directly to determine i-Hg, and (ii) after oxidation with a mixture KBr/KBrO3 to determine t-Hg. o-Hg was estimated from the difference between t-Hg and i-Hg. Previous studies were focused on the assessment of different reagents for mercury extraction and breakdown of organomercury …

Detection limitMushroomChromatographyGeneral Chemical Engineering010401 analytical chemistryAnalyserRelative standard deviationGeneral EngineeringAnalytical chemistryOrganomercury Compoundschemistry.chemical_element04 agricultural and veterinary sciences040401 food science01 natural sciences0104 chemical sciencesAnalytical ChemistryMercury (element)0404 agricultural biotechnologychemistryDry weightReagentAnalytical Methods
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Vanadium and molybdenum concentrations in particulate from Palermo (Italy): analytical methods using voltammetry

2014

The main purpose of this work was to develop a reliable method for the determination of vanadium (V) and molybdenum (Mo) in atmosphere particles or aerosols because they can not be readily measured using conventional techniques. For this research, 30 particulate samples were collected from five different stations located at Palermo, Italy. We used the catalytic adsorptive stripping voltammetry and differential pulsed voltammetry to measure Vand Mo in atmospheric particulate, respectively. The represented method includes advantages of high sensitivity, high selectivity, simplicity, reproducibility, speed and low costs. The quantification limits for V and Mo are, respectively, 0.57 and 0.80 n…

Detection limitReproducibilityRelative standard deviationAnalytical chemistrychemistry.chemical_elementVanadiumParticulatesSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturalichemistryMolybdenumEnvironmental chemistryvanadium molybdenum particulate voltammetry PalermoAdsorptive stripping voltammetrySettore CHIM/01 - Chimica AnaliticaVoltammetryGeneral Environmental Science
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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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Analysis of insoluble silicate: Decomposition with molten sodium hydroxide and determination of Zr(IV) with chloranilic acid in medium-strong acid

1983

A rapid, accurate and precise method for the determination of zirconium in silicates is proposed. Insoluble or sparingly soluble samples are decomposed by means of molten sodium hydroxide. Chloranilic acid is employed as reagent for the spectrophotometric determination of Zr(IV). The limit of detection is 1.2×10−7 M and the relative standard deviation is 0.24%.

Detection limitZirconiumClinical BiochemistryRelative standard deviationInorganic chemistrychemistry.chemical_elementGeneral MedicineDecompositionSilicateAnalytical Chemistrychemistry.chemical_compoundchemistryChloranilic acidSodium hydroxideReagentGeneral Materials ScienceFresenius' Zeitschrift für analytische Chemie
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