Search results for "Certified reference materials"

showing 10 items of 43 documents

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
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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
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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
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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
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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
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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
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Fractionation of mercury in sediments during draining of Augusta (Italy) coastal area by modified Tessier method

2013

Abstract A modified Tessier method was applied to sediments dredged from Augusta (Italy) coastal area with the purpose of establishing the amount and the forms in which mercury is present in the different sediment fractions. The mercury fractionation was made by measuring the concentration of the metal ion on the solutions and directly on the sediment fractions obtained by sequential extraction. The measurements on the solutions as well as that on the solid fractions were carried out by using a Direct Mercury Analyser, DMA 80. This new instrument does not require sample preparation, and gives results comparable to those obtained with CV-AAS and ICP-MS and few minutes are necessary for each …

Environmental remediationAugustaAnalyserRemediationSedimentchemistry.chemical_elementFractionationSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturaliAnalytical ChemistryMercury (element)SedimentsCertified reference materialschemistryMercury(II) ionEnvironmental chemistryEnvironmental scienceSettore CHIM/01 - Chimica AnaliticaSample preparationFractionationSpectroscopyMicrochemical Journal
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Direct and fast determination of polychlorinated biphenyls in contaminated soils and sediments by thermal desorption-gas chromatography-tandem mass s…

2019

Abstract A direct procedure based on thermal desorption-gas chromatography-tandem mass spectrometry (TD–GC–MS–MS) was developed for the fast extraction of seven polychlorinated biphenyls (PCBs) from sediments and soils. PCBs were directly extracted, from 20 to 75 mg of sample, without any chemical pre-treatment or use of organic solvents, after the addition of 10 µL internal standard (PCB 195) in acetone. Sample treatment was totally automated. PCBs were extracted at 250 °C for 20 min, using a helium flow and the PCBs were trapped in a cryogenic Tenax trap at −10 °C. After that, analytes were directly desorbed at 270 °C and introduced to the GC–MS–MS system. Recoveries were established usin…

Geologic SedimentsChromatographyGas Chromatography/Tandem Mass SpectrometrySoil testChemistryOrganic ChemistryExtraction (chemistry)TemperatureTenaxThermal desorptionReproducibility of ResultsGeneral MedicineReference StandardsMass spectrometryPolychlorinated BiphenylsBiochemistryGas Chromatography-Mass SpectrometryAnalytical ChemistrySoilCertified reference materialsTandem Mass SpectrometrySoil waterSolventsHumansSoil PollutantsJournal of Chromatography A
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Speciation of methylmercury in market seafood by thermal degradation, amalgamation and atomic absorption spectroscopy

2014

Sample thermal decomposition followed by mercury amalgamation and atomic absorption has been employed for the determination of methylmercury (MeHg) in fish. The method involves HBr leaching of MeHg, extraction into toluene, and back-extraction into an aqueous l-cysteine solution. Preliminary studies were focused on the extraction efficiency, losses, contaminations, and species interconversion prevention. The limit of detection was 0.018µgg(-1) (dry weight). The intraday precision for three replicate analysis at a concentration of 4.2µgg(-1) (dry weight) was 3.5 percent, similar to the interday precision according to analysis of variance (ANOVA). The accuracy was guaranteed by the use of for…

Health Toxicology and Mutagenesischemistry.chemical_elementlaw.inventionchemistry.chemical_compoundDry weightlawAnimalsCysteineMethylmercuryDetection limitChemistrySpectrophotometry AtomicFishesPublic Health Environmental and Occupational HealthGreen Chemistry TechnologyMercuryGeneral MedicineReplicateMethylmercury CompoundsPollutionMercury (element)Certified reference materialsSeafoodEnvironmental chemistryLeaching (metallurgy)Atomic absorption spectroscopyEnvironmental MonitoringEcotoxicology and Environmental Safety
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Cold vapour atomic fluorescence determination of mercury in milk by slurry sampling using multicommutation

2004

Abstract A highly sensitive mechanized method has been developed for the determination of mercury in milk by atomic fluorescence spectrometry (AFS). Samples were sonicated for 10 min in an ultrasound water bath in the presence of 8% (v/v) aqua regia, 2% (v/v) antifoam A and 1% (m/v) hydroxilamine hydrochloride, and after that, they were treated with 8 mmol l −1 KBr and 1.6 mmol l −1 KBrO 3 in an hydrochloric medium. Atomic fluorescence measurements were made by multicommutation, which provides a fast alternative in quality control analysis, due to the easy treatment of a large number of samples (approximately 70 h −1 ), and is an environmentally friendly procedure, which involves a waste ge…

MERCUREDetection limitHydrochlorideAnalytical chemistrychemistry.chemical_elementBiochemistryAnalytical ChemistryMercury (element)Waste treatmentchemistry.chemical_compoundCertified reference materialschemistrySlurryEnvironmental ChemistryAqua regiaSpectroscopyAnalytica Chimica Acta
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