Search results for "Libration"

showing 10 items of 901 documents

Determination of aluminum at the parts per billion level by solvent extraction and flame atomic emission spectrometry

1991

A new method for the determination of aluminum at the parts per billion level, by N 2 O/ C 2 H 2 flame emission spectrometry with prior solvent extraction with acetylacetone or 8-hydroxyquinoline in 4-methylpentan-2-one, has been performed. The influence of extraction conditions and instrumental parameters on the sensitivity, precision, and dynamic range of the emission calibration curves have been studied. The limit of detection is between 5 and 10 ppb for both ligands, the variation coefficient being 0.2 and 3% at levels of 75 and 25 ppb, respectively. The method has been applied to the determination of Al in water and the results obtained are compared with those found by the standard add…

Detection limitCalibration curveAcetylacetoneExtraction (chemistry)Parts-per notationAnalytical chemistrychemistry.chemical_elementAnalytical Chemistrychemistry.chemical_compoundchemistryAluminiumLiquid–liquid extractionStandard additionSpectroscopyMicrochemical Journal
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Development and characterization of a thermal inkjet-based aerosol generator for micro-volume sample introduction in analytical atomic spectrometry

2011

A novel system for the introduction of liquid samples into analytical plasmas for atomic spectrometric analysis is presented in this manuscript for the first time. The proposed “drop-on-demand” (DOD) aerosol generator is based on the use of a modified thermal inkjet cartridge. This system employs a lab-built microcontroller, which allows accessing all parameters important for driving the dosing cartridge for the generation of pL-droplets from sample volumes in the μL range. The droplet generation frequency, thus the resulting liquid flow rate, is variable over a wide range from the generation of isolated droplets up to a theoretical flow rate of approximately 2 mL min−1, with parallel opera…

Detection limitCartridgeNebulizerChemistryAnalytical chemistryCalibrationFigure of meritAtomic spectroscopyStandard solutionSpectroscopyAnalytical ChemistryVolumetric flow rateJournal of Analytical Atomic Spectrometry
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Determination of chromium(III) and chromium(VI) in mineral water by bidirectional electrostacking and electrothermal atomic absorption spectrometry

2001

Abstract A feasibility investigation was carried out on the use of bidirectional electrostacking for simultaneous separation and pre-concentration of Cr(III) and Cr(VI) and their electrothermal atomic absorption spectrometry (ETAAS) determination. The bidirectional electrostacking manifold was improved, and the effects of sample tube cross-section and electrostacking time on the pre-concentration factor were investigated. Results indicate that the sample tube cross-section and electrostacking time are the main influence factors on the electrostacking pre-concentration, as well as the electric field strength and ionic mobility. The method developed was suitable for the simultaneous separatio…

Detection limitChemistryAnalytical chemistrychemistry.chemical_elementConductivityBiochemistryAnalytical Chemistrylaw.inventionChromiumCertified reference materialslawStandard additionCalibrationEnvironmental ChemistryAtomic absorption spectroscopyQuantitative analysis (chemistry)SpectroscopyAnalytica Chimica Acta
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2,4,6-Triphenylpyrylium Ion Encapsulated into Zeolite Y as a Selective Electrode for the Electrochemical Determination of Dopamine in the Presence of…

2002

2,4,6-Triphenylpyrylium ion immobilized inside the supercages of zeolite Y enhances by 1-2 orders of magnitude the response of electrochemical oxidation of dopamine in neutral aqueous media accompanied by a remarkable inhibition of post-electron-transfer reactions. The negative charge of the zeolite framework in which the 2,4,6-triphenylpyrylium ion is incorporated blocks the electrochemical oxidation of the negative ascorbate ion, enabling the determination of micromolar concentrations of dopamine in the presence of a large excess (10(3)-10(4) times) of ascorbate in phosphate buffer (pH 7.4). Under optimized conditions, linear calibration plots were obtained for a differential pulse detect…

Detection limitChemistryDopamineInorganic chemistryAscorbic AcidElectrochemistryAscorbic acidSensitivity and SpecificityOrders of magnitude (mass)Analytical ChemistryIonDopamineCalibrationElectrodeElectrochemistryZeolitesmedicineZeoliteElectrodesOxidation-ReductionPyransmedicine.drugAnalytical Chemistry
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Determination of edible oil parameters by near infrared spectrometry

2006

Abstract A chemometric method has been developed for the determination of acidity and peroxide index in edible oils of different types and origins by using near infrared spectroscopy (NIR) measurements. Different methods for selecting the calibration set, after an hierarchical cluster analysis, were applied. After discrimination of olive oils from maize, seed and sunflower, the prediction capabilities of partial least squares (PLS) multivariate calibration of NIR data were evaluated. Several preprocessing alternatives (first derivative, multiplicative scatter correction, vector normalization, constant offset elimination, mean centering and standard normal variate) were investigated by using…

Detection limitChromatographyAnalytical chemistryNear-Infrared SpectrometryBiochemistryPeroxideSunflowerAnalytical ChemistryChemometricschemistry.chemical_compoundchemistryPartial least squares regressionCalibrationEnvironmental ChemistryPeroxide valueSpectroscopyAnalytica Chimica Acta
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Quantification of nortriptyline in plasma by HPLC and fluorescence detection

2009

Abstract A simple, sensitive and specific high-performance liquid chromatography method has been developed for the determination of nortriptyline (NT) in plasma samples. The assay involved derivatization with 9H-fluoren-9-ylmethyl chloroformate (Fmoc-Cl) and isocratic reversed-phase (C 18 ) chromatography with fluorescence detection. The developed method required only 100 μl of plasma sample, deproteinized and derivatized in one step. Calibration curves were lineal over the concentration range of 5–5000 ng/ml. The derivatization reaction was performed at room temperature in 20 min and the obtained NT derivative was stable for at least 48 h at room temperature. The within-day and between-day…

Detection limitChromatographyCalibration curveClinical BiochemistryNortriptylineCell BiologyGeneral MedicineDerivativeChloroformateBiochemistryHigh-performance liquid chromatographyFluorescenceAntidepressive AgentsRatsAnalytical Chemistrychemistry.chemical_compoundchemistryLimit of DetectionmedicineAnimalsHumansNortriptylineDerivatizationChromatography High Pressure Liquidmedicine.drugJournal of Chromatography B
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Determination of Paint Solvents by Vapour Phase Fourier Transform Infrared Spectrometry.

1997

Abstract A fast procedure has been developed for the direct determination of paint solvents. The method is based on the injection of small volumes of untreated solvent mixtures into a heated Pyrex glass reactor in which the sample is volatilized and introduced by means of a flow of nitrogen into an IR multiple pass gas cell and the spectrum in the mid-IR region is registered as a function of time. Data found for samples are interpolated in calibration graphs obtained by injecting different volumes of pure compounds which constitute the solvent mixture. A methylisobutylketone (MIBK) toluene mixture was used as test system to develop the proposed procedure. The method provides a limit of dete…

Detection limitChromatographyChemistryAnalytical chemistryInfrared spectroscopychemistry.chemical_elementPaint thinnerNitrogenTolueneAtomic and Molecular Physics and OpticsAnalytical ChemistrySolventchemistry.chemical_compoundPhase (matter)CalibrationSpectroscopySpectroscopy Letters
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A Fully Automated Assembly Using Solenoid Valves for the Photodegradation and Chemiluminometric Determination of the Herbicide Chlorsulfuron

2005

Abstract This paper presents a new photochemiluminescent system for the determination of chlorsulfuron in water samples. The light from a low‐pressure mercury lamp is used as a clean, reproducible, and inexpensive “reagent” for the derivation of the pesticide, performed in glycine buffer at pH 9.5. Then, the photo‐products from irradiation are oxidized by permanganate in sulfuric acid solution. The oxidation reaction was favored by using high temperatures. A comparative study and discussion about the use of polyphosphoric acid instead of sulfuric acid in the oxidation reaction is also presented. The use of solenoid valves allows for the easy, complete automation of the process with low samp…

Detection limitChromatographyChemistryCalibration curveBiochemistry (medical)Clinical BiochemistryPermanganateAnalytical chemistrySulfuric acidBiochemistryRedoxAnalytical Chemistrylaw.inventionMercury-vapor lampchemistry.chemical_compoundlawReagentElectrochemistryPhotodegradationSpectroscopyAnalytical Letters
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FI-on line photochemical reaction for direct chemiluminescence determination of photodegradated chloramphenicol.

2002

Abstract A new, simple, clean and selective flow injection strategy based on the tandem photochemical reaction-chemiluminescence detection was applied to the determination of chloramphenicol. The determination is based on the on-line photodegradation of the drug in a glycine buffer at pH 8.8 by using a photoreactor consisting of 697 cm×0.5 mm PTFE tubing helically coiled around an 8 W low-pressure mercury lamp. Photodegradated chloramphenicol is detected by direct chemiluminescence of resulting photo-fragments and their subsequent reaction with potassium permanganate in sulfuric acid medium as oxidant. The method allows the chemiluminescence determination of compounds which do not exhibit n…

Detection limitChromatographyChemistryCalibration curvePhotochemistryDosage formAnalytical Chemistrylaw.inventionPotassium permanganatechemistry.chemical_compoundlawPhotodegradationQuantitative analysis (chemistry)Antibacterial agentChemiluminescenceTalanta
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Solid-Phase Microextraction Liquid Chromatography/Tandem Mass Spectrometry To Determine Postharvest Fungicides in Fruits

2003

A method to determine five postharvest fungicides (dichloran, flutriafol, o-phenylphenol, prochloraz, tolclofos methyl) in fruits (cherries, lemons, oranges, peaches) has been developed using solid-phase microextraction (SPME) coupled to liquid chromatography (LC) with photodiode array (DAD), mass spectrometry (MS), or tandem mass spectrometry (MS/MS) with ion trap detection. Extraction involved sample homogenization with an acetone/water solution (5:1), filtration, and acetone evaporation prior to fiber extraction. The pesticides were isolated with a fused-silica fiber coated with 50-microm Carbowax/template resin. The effects of pH, ion strength, sample volume, and extraction time were in…

Detection limitChromatographyChemistryPesticide ResiduesReference StandardsSolid-phase microextractionMass spectrometryTandem mass spectrometryMass SpectrometryFungicides IndustrialAnalytical ChemistryLiquid chromatography–mass spectrometryFruitDesorptionCalibrationIndicators and ReagentsSpectrophotometry UltravioletSample preparationIon trapChromatography LiquidAnalytical Chemistry
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