Search results for "STANDARD"

showing 10 items of 3299 documents

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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Multicommutation Fourier transform infrared determination of benzene in gasoline

2004

A fully mechanized method to determine benzene in motor gasolines has been developed based on the use of Fourier transform infrared spectroscopy (FT-IR) and multicommutation. The flow network comprised a set of three-way solenoid valves and was controlled by means of a microcomputer furnished with an electronic interface and running by a software written in QUICK BASIC 4.5. The flow network and control software were designed to implement the multicommutation approach providing facilities to handle sample and reagent solutions, so that, sample dilution, external calibration and standard addition could be easily performed on-line. The method permits the direct determination of benzene without…

Detection limitChemistryDirect methodAnalytical chemistryInfrared spectroscopyBiochemistryFourier transform spectroscopyAnalytical Chemistrysymbols.namesakeFourier transformStandard additionsymbolsEnvironmental ChemistryGasolineFourier transform infrared spectroscopySpectroscopyAnalytica Chimica Acta
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Chemiluminescent method for detection of eutrophication sources by estimation of organic amino nitrogen and ammonium in water.

2006

An automatic method has been developed for the estimation of organic amino nitrogen (CH2-NH) and ammonium in water samples. We propose a continuous flow system in which nitrogen compounds react with hypochlorite reagent to produce chloramines. Subsequently, the mixture is mixed with luminol, generating a chemiluminescence signal. The signal emission at 425 nm, registered as a function of time, decreases as nitrogen concentration increases, due to the decrease on hypochlorite concentration. A large number of nitrogen compounds have been assayed and their sensitivities compared, in milligrams per liter nitrogen. The ammonium calibration graph, expressed as N, can be used for most of the assay…

Detection limitChloramineChromatographyMineralogychemistry.chemical_elementHypochloriteNitrogenAnalytical Chemistrylaw.inventionLuminolStandard curvechemistry.chemical_compoundchemistrylawAmmoniumChemiluminescenceAnalytical chemistry
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Fishing for a drug: solid-phase microextraction for the assay of clozapine in human plasma

1999

Solid-phase microextraction (SPME) was investigated as a sample preparation method for assaying the neuroleptic drug clozapine in human plasma. A mixture of human plasma, water, loxapine (as internal standard) and aqueous NaOH was extracted with a 100-micron polydimethylsiloxane (PDMS) fiber (Supelco). Desorption of the fiber was performed in the injection port of a gas chromatograph at 260 degrees C (HP 5890; 30 m x 0.53 mm I.D., 1 micron film capillary; nitrogen-phosphorous selective detection). Fibers were used repeatedly in up to about 75 analyses. The recovery was found to be 3% for clozapine from plasma after 30 min of extraction. However, in spite of the low recovery, the analyte was…

Detection limitChromatography GasChromatographymedicine.diagnostic_testChemistryReproducibility of ResultsLoxapineGeneral ChemistryReference StandardsSolid-phase microextractionSensitivity and SpecificityHigh-performance liquid chromatographyMatrix (chemical analysis)Therapeutic drug monitoringmedicineHumansSample preparationSolid phase extractionGas chromatographyClozapineJournal of Chromatography B: Biomedical Sciences and Applications
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Direct determination of benzene in gasoline by flow-injection Fourier transform infrared spectrometry

1993

Abstract A Fourier transform infrared spectrometric procedure for the automated determination of benzene in gasoline was developed, based on the use of flow-injection analysis. The method permits the direct determination of benzene without any pretreatment of samples, with a limit of detection of 0.02% (v/v) and a relative standard deviation of ca. 1% [for five independent analyses of a diluted sample containing a 0.4% (v/v) of benzene]. Results found by direct analysis agreed with those obtained by off-line and on-line standard addition methods. A rapid quality control procedure was developed, based on the on-line injection of gasoline samples (diluted 1 + 9 in hexane) into a carrier strea…

Detection limitChromatographyAnalytical chemistryInfrared spectroscopyBiochemistryAnalytical ChemistryHexanechemistry.chemical_compoundsymbols.namesakeFourier transformchemistryStandard additionsymbolsEnvironmental ChemistryGas chromatographyGasolineBenzeneSpectroscopyAnalytica Chimica Acta
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Determination of water-soluble UV-filters in sunscreen sprays by liquid chromatography.

2002

Abstract Liquid chromatography was used for the determination of the three most used water-soluble UV filters, benzophenone-4 (BZ4), terephthalylidene dicamphor sulfonic acid (TDS), and phenylbenzimidazole sulphonic acid (PBS), in aqueous sunscreen sprays. A C 18 stationary phase and an isocratic mobile phase of EtOH–20 m M sodium acetate buffer of pH 4.6 (30:70, v/v) were used at a flow-rate of 0.5 ml min −1 . Mobile phase was also used as solvent for samples and standards. UV detection was at 313 nm. The analytical run took 5.5 min. The limits of detection were 0.5, 0.9 and 2 μg ml −1 for BZ4, TDS and PBS, respectively. The proposed method does not involve highly toxic solvents.

Detection limitChromatographyAqueous solutionChemistryUltraviolet RaysOrganic ChemistryGeneral MedicineReversed-phase chromatographySulisobenzoneReference StandardsBiochemistryHigh-performance liquid chromatographySensitivity and SpecificityAnalytical ChemistrySolventchemistry.chemical_compoundPhase (matter)Spectrophotometry UltravioletSodium acetateSunscreening AgentsChromatography LiquidJournal of chromatography. A
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Determination of atranol and chloroatranol in perfumes using simultaneous derivatization and dispersive liquid-liquid microextraction followed by gas…

2013

Abstract A new analytical method based on simultaneous derivatization and dispersive liquid–liquid microextraction (DLLME) followed by gas chromatography–mass spectrometry (GC–MS), for the determination of the allergenic compounds atranol and chloroatranol in perfumes, is presented. Derivatization of the target analytes by means of acetylation with anhydride acetic in carbonate buffer was carried out. Thereby volatility and detectability were increased for improved GC–MS sensitivity. In addition, extractability by DLLME was also enhanced due to a less polar character of the solutes. A liquid–liquid extraction was performed before DLLME to clean up the sample and to obtain an aqueous sample …

Detection limitChromatographyAqueous solutionTime FactorsMolecular StructureLiquid Phase MicroextractionOsmolar ConcentrationHydrogen-Ion ConcentrationBiochemistryGas Chromatography-Mass SpectrometryAnalytical ChemistryPerfumeSolventMatrix (chemical analysis)chemistry.chemical_compoundchemistryReagentStandard additionBenzaldehydesSolventsEnvironmental ChemistryGas chromatography–mass spectrometryDerivatizationSpectroscopyAnalytica chimica acta
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Evaluation of C18 adsorbent cartridges for sampling and derivatization of primary amines in air

2004

Abstract The sampling efficiency of C18 solid-phase extraction cartridges was investigated for methylamine, ethylamine, propylamine, butylamine and pentylamine, in air. Determination of these analytes was based on derivatization with o-phthaldialdehyde–N-acetylcysteine (OPA–NAC) on the solid support and fluorescence detection at λexcitation=330 nm and λemission=440 nm of the eluted derivatives. The calibration model derived from aqueous standards was statistically comparable with the calibration model for air standards. Aqueous amines can be used as standards. The method was useful for calculating short-term exposure limits (STEL). A sampling time of 15 min at 30 ml min−1 was employed. Good…

Detection limitChromatographyButylamineFluorescence spectrometryAnalytical chemistryPropylamineBiochemistryAnalytical ChemistryStandard curvechemistry.chemical_compoundchemistryEnvironmental ChemistrySolid phase extractionPentylamineDerivatizationSpectroscopyAnalytica Chimica Acta
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Sensitive determination of free benzophenone-3 in human urine samples based on an ionic liquid as extractant phase in single-drop microextraction pri…

2007

Abstract Benzophenone-3 (BZ3), one of the compounds most commonly used as UV filter in cosmetic products, can be absorbed through the skin into the human body, since it can be found at trace levels in urine from users of cosmetic products that contain BZ3. Moreover, different undesirable effects have been attributed to this compound. Thus, sensitive analytical methods to monitor urinary excretion of this compound should be developed. This paper presents a selective and sensitive methodology for BZ3 determination at ultratrace levels in human urine samples. The methodology is based on a novel microextraction technique, known as single-drop microextraction (SDME). An ionic liquid (IL) has bee…

Detection limitChromatographyCentral composite designOrganic ChemistryAnalytical chemistryTemperatureIonic LiquidsGeneral MedicineBiochemistryHigh-performance liquid chromatographyChemistry Techniques AnalyticalAnalytical Chemistrychemistry.chemical_compoundBenzophenoneschemistryIonic strengthLiquid–liquid extractionStandard additionIonic liquidHumansSample preparationChromatography LiquidJournal of chromatography. A
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Analysis of Chlorpyrifos in Water, Fruit Juice, and Honeybee Extract by Chemiluminescent Elisa

2008

Abstract The suitability of competitive enzyme-linked immunosorbent assays (ELISAs) with chemiluminescent detection-based immobilized antigen (indirect assay) for rapid and accurate determination of chlorpyrifos in various food matrices was tested. The limit of detection (LOD) values were 1–1.75 ng mL−1, the standard curve midpoint (IC50) was 3.5 ng mL−1, and the assay duration was 1.5 h. Assay application to the analysis of honeybee extract resulted in chlorpyrifos recoveries varying between 62 and 83% in 5–15 ng mL−1 herbicide concentration range.

Detection limitChromatographyChemistryBiochemistry (medical)Clinical BiochemistryFOOD/FRUIT JUICESBiochemistryCHEMILUMINESCENCECHLORPYRIFOSAnalytical Chemistrylaw.inventionStandard curveHONEYBEEchemistry.chemical_compoundlawChlorpyrifosElectrochemistryELISAFruit juiceIC50SpectroscopyChemiluminescenceAnalytical Letters
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