Search results for "absorptio"

showing 10 items of 2815 documents

Atomic-absorption spectrometric determination of calcium, magnesium and potassium in leaf samples after decomposition with molten sodium hydroxide

1991

Abstract The decomposition of standard leaf samples of varied origin and nature by fusion with sodium hydroxide in an open system has been studied. The use of sodium nitrate as an auxiliary agent facilitated the mineralization of most of the samples. The solutions obtained were analysed for calcium, magnesium and potassium by flame atomic-absorption spectrometry. The method is fast and quite precise, with absolute standard deviations of 0.04–0.13, 0.002-0.03 and 0.04–0.12% for calcium, magnesium and potassium contents of O.8-5.0, 0.13–0.48 and 0.36–2.2% respectively. The limits of detection (μg/ml) in the determination step were 0.10 for calcium, 0.011 for magnesium, and 0.09 for potassium.

Detection limitMagnesiumSodiumPotassiumAnalytical chemistrychemistry.chemical_elementCalciumAnalytical Chemistrylaw.inventionchemistry.chemical_compoundchemistrylawSodium hydroxideSodium nitrateAtomic absorption spectroscopyNuclear chemistryTalanta
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GFAAS determination of selenium in infant formulas using a microwave digestion method.

1994

A method for determining the selenium content of infant formulas is proposed. It includes wet digestion with nitric acid and hydrogen peroxide in medium pressure teflon bombs in a microwave oven and determination by graphite furnace atomic absorption spectrometry (GFAAS). The absence of interferences is checked. Values obtained for the limit of detection (19.4 ng/g), precision (RSD = 2.2%) and accuracy by analysis of a reference material show that the method is reliable.

Detection limitMicrowave ovenSpectrophotometry AtomicAnalytical chemistrychemistry.chemical_elementInfantHydrogen PeroxideNitric Acidlaw.inventionchemistry.chemical_compoundSeleniumchemistrylawNitric acidHumansSample preparationInfant FoodMagnesiumMicrowave digestionGraphite furnace atomic absorptionAtomic absorption spectroscopyMicrowavesSeleniumPalladiumFood ScienceDie Nahrung
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Indirect Determination of Cyanide by Atomic Absorption Spectrometry

1995

Abstract Two methods for determination of cyanide by atomic absorption spectrometry (AAS) are developed. Both methods are based on the formation of an ion association compound between a metal complex, (Ag(CN)2 − or Cu(CN)3 2-), and a quaternary ammonium ion (benzyldimethylhexadecylammonium ion). The ion association compound is extracted into isomethylbutylketone (IBMK) and the metal is determined by AAS directly in extract. The method based on the formation of silver cyanide complex provides a reproducibility of 2.5%, a recovery of 99% and a detection limit of 1.7 μg/L while the method based on the formation of copper complex gives a reproducibility of 6%, a recovery of 93% and a detection …

Detection limitSilver cyanideCyanideBiochemistry (medical)Clinical BiochemistryAnalytical chemistryIon-associationBiochemistryAnalytical ChemistryIonlaw.inventionMetalchemistry.chemical_compoundchemistryLiquid–liquid extractionlawvisual_artElectrochemistryvisual_art.visual_art_mediumAtomic absorption spectroscopySpectroscopyNuclear chemistryAnalytical Letters
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Some observations on the sensitivity of flow-injection techniques for atomic absorption spectrophotometry

1989

Abstract Different strategies for coupling flow-injection manifolds to atomic absorption spectrometers in order to obtain better sensitivity are compared. Using a T-connector interface, different carriers and flow compensation solvents have been assayed in an attempt to improve the sensitivity of flow-injection analysis. Manganese and copper determinations in sewage sludge have been used as a test system and the analytical parameters of both batch and flow-injection methods are compared.

Detection limitSpectrometerAnalytical chemistrychemistry.chemical_elementManganeseCopperAnalytical ChemistryVolumetric flow ratelaw.inventionchemistrylawSensitivity (control systems)Atomic absorption spectroscopySpectroscopySludgeMicrochemical Journal
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Vapor-phase introduction of alkyltin compounds in atomic absorption spectrophotometry

1990

Abstract Different systems for the introduction of alkyltin compounds in atomic absorption spectrophotometry using the vapor-phase introduction approach have been compared. Samples and standards were introduced in both quartz cell and flame atomizer using a vertical and a horizontal reactor. The better sensitivity was obtained with the quartz cell and the horizontal reactor.

Detection limitVolatilisationlawChemistryVapor phaseAnalytical chemistryTrace analysisAtomic absorption spectroscopyQuartzSpectroscopyAnalytical Chemistrylaw.inventionMicrochemical Journal
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Resolution of overlapped non-absorbing and absorbing solutes using either an absorption null-balance detection window or multivariate deconvolution a…

2004

Abstract Non-absorbing alkyl ether sulfates (AES) can be separated using anthraquinone-2-carboxylic acid (AQCA) as a probe; however, absorbing alkyl benzene sulfonates (ABS), if present, interfere indirect detection of most AES oligomers. Overcoming of this interference, as well as the simultaneous characterisation and evaluation of AES, fatty acids and ABS, was accomplished by using a diode-array detector and the procedures here discussed. First, it was shown that ABS can be made undetectable by using a 9 nm wide and 227 nm centred charge-absorptivity null-balance detection window (NBDW), where its contribution to the absorbance cancels the dilution effects that its presence induces on the…

Detection limitchemistry.chemical_classificationAnionsChromatographyResolution (mass spectrometry)ChemistryOrganic ChemistryAnalytical chemistryElectrophoresis CapillaryGeneral MedicineChromophoreBiochemistryAnalytical ChemistryDilutionAbsorbanceSurface-Active AgentsCapillary electrophoresisMultivariate AnalysisSpectrophotometry UltravioletAbsorption (electromagnetic radiation)AlkylJournal of chromatography. A
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Methylmercury and inorganic mercury determination in fish by cold vapour generation atomic absorption spectrometry

2000

Abstract Given that organic mercury is more dangerous than the inorganic form and that it is converted into methylmercury by biological methylation, we have studied and optimized a simple method for measuring both organic and inorganic mercury contents in fish, using a spectroscopic vapour generation technique, with a sequential reduction of the digested sample with stannous chloride and sodium tetrahydroborate. Prior to applying the method the sample was subjected to alkaline wet digestion. Due to the matrix interferences calibration curves with matrix addition were needed for mercury determinations. The analytical parameters of the method were: linearity from 10 to 200 ng of Hg in the red…

Detection limitchemistry.chemical_classificationChromatographyChemistryCalibration curveSodiumchemistry.chemical_elementGeneral MedicineChlorideAnalytical ChemistryMercury (element)law.inventionchemistry.chemical_compoundlawEnvironmental chemistrymedicineAtomic absorption spectroscopyInorganic compoundMethylmercuryFood Sciencemedicine.drugFood Chemistry
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Arsenic content of Spanish cows' milk determined by dry ashing hydride generation atomic absorption spectrometry.

1994

SummaryThe arsenic content of cows' milk consumed in Spain was determined. A procedure using dry ashing hydride generation atomic absorption spectrometry was developed for the purpose. Experimental conditions for the destruction of organic matter were established and an interference study was carried out. The method developed has a detection limit of 0·1 ng/g, a relative SD of 5%, and a recovery (mean ± CSI) of 100 ± 4%. The accuracy of the method was checked by analysis of a certified sample of IAEA milk powder (mean ± CSI: certified, 4·85 ± 0·32 ng/g; found, 5·04 ± 0·81 ng/g). The proposed procedure was used to analyse cows' milk samples. The extremely low arsenic levels found do not pres…

Detection limitchemistry.chemical_classificationHydrideSpectrophotometry AtomicRadiochemistryAnalytical chemistrychemistry.chemical_elementGeneral MedicineSensitivity and Specificitylaw.inventionArsenicCow milkMilkAshingchemistrylawSpainAnimalsAnimal Science and ZoologyOrganic matterCattleAtomic absorption spectroscopyArsenicFood ScienceThe Journal of dairy research
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Active alkaline traps to determine acidic-gas ratios in volcanic plumes: Sampling techniques and analytical methods

2014

In situ measurements have been the basis for monitoring volcanic gas emissions for many years and—being complemented by remote sensing techniques—still play an important role to date. Con- cerning in situ techniques for sampling a dilute plume, an increase in accuracy and a reduction of detection limits are still necessary for most gases (e.g., CO2, SO2, HCl, HF, HBr, HI). In this work, the Raschig-Tube tech- nique (RT) is modified and utilized for application on volcanic plumes. The theoretical and experimental absorption properties of the RT and the Drechsel bottle (DB) setups are characterized and both are applied simultaneously to the well-established Filter packs technique (FP) in the …

Detection limitgeographyAnalytegeography.geographical_feature_categoryalkaline traps plume sampling sulfur and halogen Etna volcanoDifferential optical absorption spectroscopyIon chromatographyMineralogySettore GEO/08 - Geochimica E VulcanologiaPlumeGeophysicsVolcanoGeochemistry and PetrologyAbsorption (electromagnetic radiation)Inductively coupled plasma mass spectrometryGeologyGeochemistry, Geophysics, Geosystems
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On-line bi-directional electrostacking for As speciation/preconcentration using electrothermal atomic absorption spectrometry.

2006

A method using bi-directional electrostacking (BDES) in a flow system is presented for As preconcentration and speciation analysis. Some parameters such as electrostacking time and applied voltage, support buffers and their concentrations were investigated. Boric acid plus sodium hydroxide at 0.1mol/l concentration was selected as support buffer to improve the pre-concentration factor (PF) for As(V). An analytical range from 2.0 to 50.0mugl(-1), and 0.35mugl(-1) as limit of detection, when applied 750V for 20min, were achieved. Under these conditions, a pre-concentration factor of 4.8 was obtained. The proposed method was applied to determine As(V) in mineral water and natural water samples…

Detection limitmedia_common.quotation_subjectAnalytical chemistrychemistry.chemical_elementAnalytical Chemistrylaw.inventionBoric acidchemistry.chemical_compoundSpeciationPotassium permanganateMineral waterchemistrySodium hydroxidelawAtomic absorption spectroscopyArsenicmedia_commonTalanta
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