Search results for "Chemical analysis."

showing 10 items of 308 documents

Spectrophotometric determination of phenols in water samples by the GHPSAM method

2001

Abstract The generalized H-point standard-additions method (GHPSAM) is proposed in order to obtain the phenol concentration in water samples when the matrix is completely unknown. The procedure involves solid-phase extraction in BondElut PPL cartridges and data handling of the UV-visible spectrophotometry measurements. The spectral regions where the unknown interferent behaviour can be considered as linear are found and the analyte concentration free from bias error is estimated. The percentages of recovery of phenols in spiked samples were similar to those obtained by HPLC. Cresols or chlorophenols can be also determined in real samples by this method. The concentration range tested was 0.…

Detection limitAnalyteChromatographymedicine.diagnostic_testChemistryHealth Toxicology and MutagenesisExtraction (chemistry)Public Health Environmental and Occupational HealthAnalytical chemistrySoil SciencePollutionHigh-performance liquid chromatographyAnalytical ChemistryMatrix (chemical analysis)chemistry.chemical_compoundSpectrophotometrymedicineEnvironmental ChemistryPhenolSolid phase extractionWaste Management and DisposalWater Science and Technology
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Atomic absorption spectrometric determination of molybdenum in lubricating oils with use of emulsions

1985

Abstract Samples (0.1 g) containing molybdenum disulphide are digested with aqua regia or with a (1 + 1) hydrofluoric/nitric acid mixture, without complete destruction of the matrix, and the molybdenum is determined in an air/acetylene flame, after emulsification with a non-ionic surfactant (Nemol K-39). The detection limit is ca. 30 μg Mo g−1, and the r.s.d. is 2.9% for 6 analyses of a sample containing 6.5 mg Mo g−1.

Detection limitChemistryInorganic chemistrychemistry.chemical_elementBiochemistryAnalytical Chemistrylaw.inventionMatrix (chemical analysis)chemistry.chemical_compoundAcetylenePulmonary surfactantNitric acidMolybdenumlawEnvironmental ChemistryAqua regiaAtomic absorption spectroscopySpectroscopyAnalytica Chimica Acta
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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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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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Determination of ruthenium in photographic emulsions - Development and comparison of different sample treatments and mass spectrometric methods

1999

Different sample treatment procedures were combined with inductively coupled plasma mass spectrometry (ICP-MS) and negative thermal ionisation mass spectrometry (NTI-MS) for the determination of ruthenium traces in photographic emulsions. Dissolution of the samples in concentrated ammonia solution was used in connection with ICP-MS by external calibration, which has the advantage of a simple sample preparation technique but introduces high amounts of the silver matrix into the mass spectrometer. On the other hand, isotope dilution mass spectrometry (IDMS) with an enriched 99Ru spike solution was applied for ICP-MS and NTI-MS measurements, respectively, in connection with a significant reduc…

Detection limitChromatographyChemistryAnalytical chemistrychemistry.chemical_elementIsotope dilutionMass spectrometryBiochemistryRuthenium/dk/atira/pure/sustainabledevelopmentgoals/clean_water_and_sanitationMatrix (chemical analysis)Sample preparationPhotographic emulsionSDG 6 - Clean Water and SanitationInductively coupled plasma mass spectrometry
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A solid-phase extraction and size-exclusion liquid chromatographic method for polyethylene glycol 25 p-aminobenzoic acid determination in urine: Vali…

2007

No previous publications about percutaneous absorption of polyethylene glycol 25 p-aminobenzoic acid (PEG-25 PABA) have been found in the literature and the expected levels to be found in human urine after sunscreens use are unknown. The method proposed here is suitable to determine PEG-25 PABA in the urine of sunscreens users in order to carry out studies on body accumulation/excretion. It is based on solid-phase extraction (SPE) with size-exclusion liquid chromatography determination. Solid-phase extraction allows the analyte to be retained and subsequently eluted for a clean-up, using a silica-based cartridge. The size-exclusion liquid chromatography of the eluted allows the rest of matr…

Detection limitChromatographyChemistryElutionExtraction (chemistry)Fluorescence spectrometryReproducibility of ResultsUrineBiochemistryPolyethylene GlycolsAnalytical ChemistryMatrix (chemical analysis)ExcretionSpectrometry FluorescenceChromatography GelHumansEnvironmental ChemistrySolid phase extraction4-Aminobenzoic AcidSunscreening AgentsSpectroscopyAnalytica Chimica Acta
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Electrochemical detection of uric acid and ascorbic acid using r-GO/NPs based sensors

2021

Abstract A sensitive and selective electrochemical sensor, based on reduced graphene oxide and gold nanoparticles obtained by simple co-electrodeposition, was developed for the detection of uric acid and ascorbic acid. Because of the electrochemical oxidation of both uric and ascorbic acid depending on the pH, the sensor performances were studied at different pH values. Excellent results were obtained for uric acid detection in a linear range from 10 to 500 µmol dm−3 with a sensitivity of 0.31 µA cm−2 µM−1. A limit of detection and quantification of 3.6 µM and 10.95 µmol dm−3, respectively, was calculated. Sensors showed good selectivity toward different interfering species present in the m…

Detection limitChromatographyGeneral Chemical Engineering02 engineering and technologyUrineUric acid Food010402 general chemistry021001 nanoscience & nanotechnologyAscorbic acid01 natural sciences0104 chemical sciencesElectrochemical gas sensorMatrix (chemical analysis)chemistry.chemical_compoundBody fluidsSettore ING-IND/23 - Chimica Fisica ApplicatachemistryLinear rangeElectrochemical sensorColloidal goldSettore ING-IND/17 - Impianti Industriali MeccaniciElectrochemistryUric acidAscorbic acid0210 nano-technology
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A cost-effective method for estimating di(2-ethylhexyl)phthalate in coastal sediments.

2013

This study describes the development of a new method for the analysis of di(2-ethylhexyl)phthalate (DEHP) using 0.1-0.3 g of sediment sample, based on matrix solid phase dispersion (MSPD) using C18 as dispersant phase (0.4 g) and acetonitrile-water as eluting solvent (3.4 mL 1:3.25, v/v). No evaporation step is required. 3 mL of extracts were processed on-line by in-tube solid phase microextraction (IT-SPME) coupled to capillary liquid chromatography (CapLC) and diode array detector (DAD). A short analytical column Zorbax SB C18 (35×0.5 mm, 5 μm) provided suitable results. FTIR-ATR was employed for characterizing sediment samples and MSPD procedure. The total analysis time was less than 20 …

Detection limitChromatographyOceans and SeasOrganic ChemistryAnalytical chemistryPhthalateEvaporationGeneral MedicineSolid-phase microextractionBiochemistryAnalytical ChemistryMatrix (chemical analysis)Solventchemistry.chemical_compoundchemistryChromatography detectorDiethylhexyl PhthalateSpectroscopy Fourier Transform InfraredSoil PollutantsLasers SemiconductorDispersion (chemistry)Solid Phase MicroextractionChromatography LiquidJournal of chromatography. A
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Rapid screening of organophosphorus pesticides in honey and bees by liquid chromatography—Mass spectrometry

2002

Twenty-two organophosphorus pesticide residues were simultaneously determined in honey and honeybee samples by extraction procedures based on solid-phase and liquid chromatography-atmospheric pressure chemical ionization-mass in positive and negative ionization modes. Pesticides in honeybee samples were extracted by matrix solid phase dispersion with C18 silica and subsequently eluted with a mixture of dichloromethane-methanol (85∶15, v/v). The average recoveries from spiked honeybees (0.5–10 μg g−1) ranged from 76% for coumaphos to 100% for omethoate, with relative standard deviations between 3 and 17%. Limits of detection were ≤0.13 μg g−1 and limits of quantification were ≤0.43 μg g−1. H…

Detection limitChromatographyOrganic ChemistryClinical BiochemistryExtraction (chemistry)Reversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryMatrix (chemical analysis)chemistry.chemical_compoundchemistryLiquid chromatography–mass spectrometryOmethoateSolid phase extractionChromatographia
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Improving detection limits for organotin compounds in several matrix water samples by derivatization-headspace-solid-phase microextraction and GC-MS.

2010

Triethyltin, tributyltin, diphenyltin and triphenyltin were selected as model compounds. The method is based on in situ ethylation and simultaneous headspace-solid-phase microextraction (HS-SPME) and gas chromatographic-mass spectrometry analysis (GC-MS). The extraction procedure was optimized studying some variables such as reaction time, salinity, sample volume and headspace volume. SPME-GC-MS and SPME-GC-FID techniques were compared; quality assurance parameters such as sensitivity, selectivity and precision were established. The proposed procedure showed limits of detection between 0.025 and 1 ng/L. The linearity was in the 0.025-5000 ng/L range. The precision expressed as relative stan…

Detection limitCromatografia de gasosChromatographyAnalytical chemistrySolid-phase microextractionAnalytical Chemistrylaw.inventionMatrix (chemical analysis)chemistry.chemical_compoundchemistrylawFlame ionization detectorSample preparationGas chromatographyCompostos organometàl·licsAigües residuals AnàlisiGas chromatography–mass spectrometryDerivatizationTalanta
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