Search results for "Relative standard deviation"

showing 10 items of 39 documents

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
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct

Determination of As, Sb, Se, Te and Bi in milk by slurry sampling hydride generation atomic fluorescence spectrometry

2003

A simple and fast analytical procedure has been developed for the determination of As, Sb, Se, Te and Bi in milk samples by hydride generation atomic fluorescence spectrometry (HG-AFS). Samples were treated with aqua regia for 10min in an ultrasound water bath and pre-reduced with KBr for total Se and Te determination or with KI and ascorbic acid for total As and Sb, the determination of Bi being possible in all with or without pre-reduction. Slurries of samples, in the presence of antifoam A, were treated with NaBH(4) in HCl medium to obtain the corresponding hydrides, and AFS measurements were processed in front of external calibrations prepared and measured in the same way as samples. Re…

Detection limitchemistry.chemical_compoundchemistryHydrideRelative standard deviationSlurryAnalytical chemistryAqua regiaChemical elementAscorbic acidAtomic fluorescence spectrometryAnalytical ChemistryTalanta
researchProduct

Speciation of chromium in natural waters by micropumping multicommutated light emitting diode photometry.

2007

Abstract A simple and sensitive multicommutated flow procedure, implemented by employing a homemade light emitting diode (LED) based photometer, has been developed for the determination of chromium (VI) and total chromium in water. The flow system comprised a set of four solenoid micro-pumps, which were assembled to work as fluid propelling and as commutating devices. The core of the detection unit comprised a green LED source, a photodiode and a homemade flow cell of 100 mm length and 2 mm inner diameter. The photometric procedure for the speciation of chromium in natural waters was based on the reaction of Cr (VI) with 1,5-diphenylcarbazide. Cr (III) was previously oxidized to Cr (VI) and…

Detection limitmedicine.diagnostic_testChemistryNatural waterRelative standard deviationAnalytical chemistrychemistry.chemical_elementAnalytical Chemistrylaw.inventionPhotometry (optics)ChromiumlawSpectrophotometrymedicineInner diameterLight-emitting diodeTalanta
researchProduct

Variations in Substitution Rate in Human and Mouse Genomes

2003

We present a method to quantify spatial fluctuations of the substitution rate on different length scales throughout genomes of eukaryotes. The fluctuations on large length scales are found to be predominantly a consequence of a coarse-graining effect of fluctuations on shorter length scales. This is verified for both the mouse and the human genome. We also found that both species show similar standard deviation of fluctuations even though their mean substitution rate differs by a factor of two. Our method furthermore allows to determine time-resolved substitution rate maps from which we can compute auto-correlation functions in order to quantify how fast the spatial fluctuations in substitu…

Genomics (q-bio.GN)GenomeModels GeneticGenome HumanRelative standard deviationSubstitution (logic)AutocorrelationPopulations and Evolution (q-bio.PE)Genetic VariationGeneral Physics and AstronomyGenomicsTime resolutionBiologyQuantitative Biology::GenomicsGenomeMiceEvolutionary biologyFOS: Biological sciencesAnimalsHumansQuantitative Biology - GenomicsHuman genomeQuantitative Biology - Populations and EvolutionRepetitive Sequences Nucleic Acid
researchProduct

Occurrence of fumonisins in organic and conventional cereal-based products commercialized in France, Germany and Spain

2013

A fast and effective method for quantitative determination of fumonisins B1 and B2 (FB1 and FB2) in different cereal-based products was developed. Fumonisins were extracted combining a solid liquid extraction (SLE) pre-treatment and immunoaffinity columns (IACs), which were applied for an effective clean-up. Consecutively, high pressure liquid chromatography (HPLC) coupled to hybrid triple quadrupole-linear ion trap mass spectrometer (QTrap®) was used for the separation, detection and quantification of targeted mycotoxins. The analytical method showed acceptable recoveries ranged from 89.7% to 99.1%, as well as a relative standard deviation (%, RSD) lower than 12%. A total of 1250 samples f…

IAC columnsRelative standard deviationFood ContaminationToxicologyHigh-performance liquid chromatographyFumonisinschemistry.chemical_compoundTandem Mass SpectrometryGermanyMycotoxinSolid liquidChromatography High Pressure LiquidFumonisin B1ChromatographyChemistryExtraction (chemistry)Reproducibility of ResultsGeneral MedicineMycotoxinsQuantitative determinationSpainFood MicrobiologyCereal-based productsIon trapFranceEdible GrainQTrapFood ScienceFood and Chemical Toxicology
researchProduct

Analysis of insecticides in honey by liquid chromatography–ion trap-mass spectrometry: Comparison of different extraction procedures

2010

The feasibility of different extraction procedures was tested and compared for the determination of 12 organophosphorus and carbamates insecticides in honey samples. In this sense, once the samples were pre-treated - essentially dissolved in hot water by stirring - and before they could be analyzed by liquid chromatography-ion trap-second stage mass spectrometry (LC-MS(2)), four different approaches were studied for the extraction step: QuEChERS, solid-phase extraction (SPE), pressurized liquid extraction (PLE) and solid-phase microextraction (SPME). The main aim of this work was to maximise the sensitivity of pesticides and to minimise the presence of interfering compounds in the extract. …

InsecticidesChromatographyChemistrySolid Phase ExtractionOrganic ChemistryExtraction (chemistry)Relative standard deviationPesticide ResiduesReproducibility of ResultsOrganothiophosphorus CompoundsHoneyGeneral MedicineRepeatabilityPesticideQuechersMass spectrometrySensitivity and SpecificityBiochemistryMass SpectrometryAnalytical ChemistryLinear ModelsSolid phase extractionChromatography LiquidIon trap mass spectrometryJournal of Chromatography A
researchProduct