Search results for " Reference"

showing 10 items of 380 documents

Development of a non-chromatographic method for the speciation analysis of inorganic antimony in mushroom samples by hydride generation atomic fluore…

2009

Abstract A simple and sensitive method has been developed for the direct determination of toxic species of antimony in mushroom samples by hydride generation atomic fluorescence spectrometry (HG AFS). The determination of Sb(III) and Sb(V) was based on the efficiency of hydride generation employing NaBH 4 , with and without a previous KI reduction, using proportional equations corresponding to the two different measurement conditions. The extraction efficiency of total antimony and the stability of Sb(III) and Sb(V) in different extraction media (nitric, sulfuric, hydrochloric, acetic acid, methanol and ethanol) were evaluated. Results demonstrated that, based on the extraction yield and th…

Detection limitHydrideExtraction (chemistry)Analytical chemistrychemistry.chemical_elementMass spectrometryAtomic and Molecular Physics and OpticsAnalytical Chemistrychemistry.chemical_compoundCertified reference materialschemistryAntimonyYield (chemistry)MethanolInstrumentationSpectroscopySpectrochimica Acta Part B: Atomic Spectroscopy
researchProduct

Determination of mercury in rice by cold vapor atomic fluorescence spectrometry after microwave-assisted digestion.

2010

Abstract A cold vapor atomic fluorescence spectrometry method (CV-AFS) has been developed for the determination of Hg in rice samples at a few ng g−1 concentration level. The method is based on the previous digestion of samples in a microwave oven with HNO3 and H2O2 followed by dilution with water containing KBr/KBrO3 and hydroxylamine and reduction with SnCl2 in HCl using external calibration. The matrix interferences and the effect of nitrogen oxide vapors have been evaluated and the method validated using a certified reference material. The limit of detection of the method was 0.9 ng g−1 with a recovery percentage of 95 ± 4% at an added concentration of 5 ng g−1. The concentration level …

Detection limitMicrowave ovenAnalytical chemistrychemistry.chemical_elementTin CompoundsOryzaHydrogen PeroxideMercuryBiochemistryNitric AcidAnalytical ChemistryDilutionMercury (element)Cold Temperaturechemistry.chemical_compoundHydroxylamineCertified reference materialsSpectrometry FluorescencechemistryEnvironmental ChemistryNitrogen oxideGasesMicrowave digestionMicrowavesSpectroscopyAnalytica chimica acta
researchProduct

Determination of total mercury in nuts at ultratrace level

2014

Abstract Total mercury, at μg kg−1 level, was determined in different types of nuts (cashew nut, Brazil nuts, almond, pistachio, peanut, walnut) using a direct mercury analyser after previous sample defatting and by cold vapour atomic fluorescence spectrometry. There is not enough sensitivity in the second approach to determine Hg in previously digested samples due to the strong matrix effect. Mercury levels in 25 edible nut samples from Brazil and Spain were found in the range from 0.6 to 2.7 μg kg−1 by using the pyrolysis of sample after the extraction of the nut fat. The accuracy of the proposed method was confirmed by analysing certified reference materials of Coal Fly Ash-NIST SRM 1633…

Detection limitNutfood and beverageschemistry.chemical_elementMercuryRice flourBiochemistryDefattingfood.foodAnalytical ChemistryMercury (element)Spectrometry FluorescenceCertified reference materialsfoodchemistryLimit of DetectionCalibrationNutsEnvironmental ChemistryFood scienceSpectroscopyFood contaminantBrazil nutAnalytica Chimica Acta
researchProduct

Simultaneous determinations of zirconium, hafnium, yttrium and lanthanides in seawater according to a co-precipitation technique onto iron-hydroxide.

2013

Very low concentrations (pg mL(-1) or sub-pg mL(-1) level) along with the high salinity are the main problems in determining trace metal contents in seawater. This problem is mainly considered for investigations of naturally occurring YLOID (Y and Lanthanides) and Zr and Hf in order to provide precise and accurate results. The inductively coupled plasma mass spectrometry (ICP-MS), both in high and low resolution, offers many advantages including simultaneous analyses of all elements and their quantitative determination with detection limits of the order of pg mL(-1). However in the analysis of YLOID in seawater, a better determination needs an efficient combination of ICP-MS measurement wit…

Detection limitQuality ControlZirconiumSpectrophotometry AtomicAnalytical chemistrychemistry.chemical_elementFlocculationYttriumFerric CompoundsLanthanoid Series ElementsAnalytical ChemistryWorking rangeHafniumTrace ElementsCertified reference materialschemistryLimit of DetectionSeawaterSeawaterYttriumZirconiumInductively coupled plasma mass spectrometryHafniumTalanta
researchProduct

Species-Specific GC/ICP-IDMS for Trimethyllead Determinations in Biological and Environmental Samples

2005

An accurate and sensitive species-specific isotope dilution GC/ICPMS method was developed for the determination of trimethyllead (Me3Pb+) in biological and environmental samples. A trimethyllead spike was synthesized from 206Pb-enriched metallic lead by reaction of lead halide with methyllithium and subsequent formation of trimethyllead iodide. The isotopic composition of the spike solution was determined by GC/ICPMS after derivatization with tetraethylborate, and its concentration was determined by reverse isotope dilution analysis. The species-specific GC/ICP-IDMS method was validated by reference material CRM 605 (urban dust) certified for Me3Pb+. The method was also applied to determine…

Detection limitchemistry.chemical_classificationChromatography GasChromatographyIodideIndicator Dilution TechniquesHalideDustFood ContaminationIsotope dilutionMass spectrometryAnalytical Chemistrychemistry.chemical_compoundCertified reference materialsIsotopesLeadSeafoodchemistryTetraethyl LeadEnvironmental PollutantsGas chromatographyDerivatizationAnalytical Chemistry
researchProduct

Non-chromatographic speciation of toxic arsenic in fish

2004

Abstract A rapid, sensitive and economic method has been developed for the direct determination of toxic species of arsenic present in fish and mussel samples. As(III), As(V), dimethylarsinic acid (DMA), and monomethylarsonic acid (MMA) were determined by hydride generation–atomic fluorescence spectrometry using a series of proportional equations without the need of a chromatographic previous separation. The method is based on the extraction of arsenic species from fish through sonication with HNO3 3 mol l−1 and 0.1% (m/v) Triton and washing of the solid phase with 0.1% (m/v) EDTA, followed by direct measurement of the corresponding hydrides in four different experimental conditions. The li…

Detection limitchemistry.chemical_compoundCertified reference materialsChromatographyChemistryNitric acidSonicationExtraction (chemistry)Fluorescence spectrometrychemistry.chemical_elementSample preparationArsenicAnalytical ChemistryTalanta
researchProduct

Determination of arsenic compounds in beverages by high-performance liquid chromatography-inductively coupled plasma mass spectrometry.

2005

Arsenic compounds including arsenous acid (As(III)), arsenic acid (As(V)), dimethylarsinic acid (DMA) and monomethylarsonic acid (MMA) were separated by high-performance liquid chromatography (HPLC) and detected by inductively coupled plasma mass spectrometry (ICP-MS). A Hamilton PRX-100 anionic-exchange column and a pH 8.5 K(2)HPO(4)/KH(2)PO(4) 5.0x10(-3)molL(-1) mobile phase were used to achieve arsenic speciation. The separation of arsenic species provided peaks of As(III) at 2.75min, DMA at 3.33min, MMA at 5.17min and As(V) at 12.5min. The detection limits, defined as three times the standard deviation of the lowest standard measurements, were found to be 0.2, 0.2, 0.3 and 0.5ngmL(-1) f…

Detection limitchemistry.chemical_compoundChromatographyCertified reference materialsChemistryArsenous acidchemistry.chemical_elementArsenic CompoundHigh-performance liquid chromatographyArsenic acidInductively coupled plasma mass spectrometryArsenicAnalytical ChemistryTalanta
researchProduct

Synthetic Aperture Lensless Digital Holographic Microscopy (SALDHM) for Superresolved Biological Imaging

2013

Lensless digital holographic microscopy (LDHM) relates with the capability to achieve microscopic imaging working without lenses in the regime of holography. LDHM uses an extremely simplified setup and provides micron-range lateral and depth resolutions in three-dimensional (3D) imaging. Typically, LDHM uses a pinhole to provide spherical divergent illumination over the sample. Then, two different basic schemes are usually adopted for providing holographic recording. The first one assumes the interference between two in-line waves since diffraction by the sample can be considered as a perturbation of the reference wave. The second scheme uses an external reference beam in an off-line config…

DiffractionSynthetic aperture radarbusiness.industryHolographylaw.inventionOpticsExternal referencelawMicroscopic imagingDigital holographic microscopyBiological imagingbusinessHolographic recordingMathematics
researchProduct

Assessing the particle size of a broadly dispersed powder by complementary techniques

1998

The experimental determination of reliable particle size distribution curves and statistical parameters of broad distributions is known to be a difficult task. This problem is addressed here in an attempt to characterize the granularity of three distinct batches of a pharmaceutical powder (fenofibrate from Fournier Laboratories). The methodology consists in comparing the results, expressed in terms of surface based mean diameter, as obtained by three complementary techniques, namely optical microscopy image analysis, laser light low angle diffraction and surface area measurement by krypton physisorption. These techniques are applied in parallel to the material of interest and to a certified…

Diffractionbusiness.industryKryptonStatistical parameterPharmaceutical Sciencechemistry.chemical_elementlaw.inventionCertified reference materialsOpticschemistryOptical microscopelawParticle-size distributionParticle sizeGranularityBiological systembusinessInternational Journal of Pharmaceutics
researchProduct

Polar motion prediction using the combination of SSA and Copula-based analysis

2018

The real-time estimation of polar motion (PM) is needed for the navigation of Earth satellite and interplanetary spacecraft. However, it is impossible to have real-time information due to the complexity of the measurement model and data processing. Various prediction methods have been developed. However, the accuracy of PM prediction is still not satisfactory even for a few days in the future. Therefore, new techniques or a combination of the existing methods need to be investigated for improving the accuracy of the predicted PM. There is a well-introduced method called Copula, and we want to combine it with singular spectrum analysis (SSA) method for PM prediction. In this study, first, we…

Earth satellite010504 meteorology & atmospheric scienceslcsh:GeodesyPolar motion010502 geochemistry & geophysics01 natural sciencesCopula (probability theory)Prediction methodsddc:550Applied mathematicsEOPSSASingular spectrum analysis0105 earth and related environmental sciencespolar motionData processinglcsh:QB275-343Full Paperlcsh:QE1-996.5lcsh:Geography. Anthropology. RecreationGeologyInternational Earth Rotation and Reference Systems ServiceMatemática Aplicadaprediction550 Geowissenschaftenlcsh:Geologylcsh:GCopulaSpace and Planetary SciencePolar motionPredictionHybrid modelEarth, Planets and Space
researchProduct