Search results for "solution"

showing 10 items of 5638 documents

Simultaneous determination of oxybenzone and 2-ethylhexyl 4-methoxycinnamate in sunscreen formulations by flow injection-isodifferential derivative u…

2001

Abstract A flow injection procedure was developed for the simultaneous determination of two UV filters (oxybenzone and 2-ethylhexyl 4-methoxycinnamate) in sunscreen formulations, based on the isodifferential approach. The use of the second derivative spectra allowed a selective determination of the analytes free from matrix interferences and without pretreatment of samples. Standard solutions of the analytes were analyzed by the proposed procedure in order to select the appropriate wavelengths to solve the mixture. After this, the procedure was validated using commercial sunscreen formulations the concentrations of which were determined by an HPLC procedure. The two procedures gave comparab…

Detection limitAnalyteChromatographyInjection ProcedureAnalytical chemistryDerivativeStandard solutionBiochemistryAnalytical ChemistryMatrix (chemical analysis)chemistry.chemical_compoundchemistryEnvironmental ChemistryOxybenzoneSpectroscopySecond derivativeAnalytica Chimica Acta
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Automated high-performance liquid chromatographic determination of amphetamine in biological fluids using column-switching and on-column derivatizati…

1999

A rapid and simple liquid-chromatographic method has been developed for on-line quantification of amphetamine in biological fluids. Untreated samples (20 μL) are injected directly into the chromatographic system and purified on a 20 mm×2.1 mm i.d. pre-column packed with 30 μm Hypersil C18 stationary phase. After clean-up the analyte is transferred to the analytical column (125 mm×4 mm i.d., 5 μm LiChrospher 100 RP18) for derivatization and separation using a mixture of acetonitrile and the derivatization reagent (o-phthaldialdehyde andN-acetyl-L-cysteine) as the mobile phase. The experimental conditions for on-line derivatization and resolution of the amphetamine have been optimized, and th…

Detection limitAnalyteChromatographyResolution (mass spectrometry)Organic ChemistryClinical BiochemistryAnalytical chemistryBiochemistryHigh-performance liquid chromatographyFluorescence spectroscopyAnalytical Chemistrychemistry.chemical_compoundchemistryReagentDerivatizationQuantitative analysis (chemistry)Chromatographia
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Exploring hand-portable nano-liquid chromatography for in place water analysis: Determination of trimethylxanthines as a use case.

2020

Abstract Analytical performance and optimization of figures of merit of a portable nano liquid chromatograph (NanoLC) with UV detection at 255 nm have been established for in place analysis. Methylxanthines: caffeine, theophylline and theobromine were selected as target analytes. A fast lab method based on IT-SPME coupled on line with capillary liquid chromatograph (CapLC) with diode array detection (DAD) was employed for comparative studies. IT-SPME and solid phase extraction were coupled off-line to NanoLC for improving instrumental parameters, mainly detection capacity and selectivity. IT-SPME or SPE/portable NanoLC based methods were superior in terms of chromatographic resolution and o…

Detection limitAnalyteEnvironmental EngineeringChromatographyMaterials science010504 meteorology & atmospheric sciencesResolution (mass spectrometry)Capillary action010501 environmental sciences01 natural sciencesPollutionDiode arrayNano liquid chromatographyTheophyllineLimit of DetectionCaffeineEnvironmental ChemistryFigure of meritSolid phase extractionWaste Management and DisposalChromatography High Pressure LiquidSolid Phase MicroextractionWater Pollutants Chemical0105 earth and related environmental sciencesChromatography LiquidThe Science of the total environment
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Sensitive determination of parabens in human urine and serum using methacrylate monoliths and reversed-phase capillary liquid chromatography-mass spe…

2014

A method for the determination of parabens in human urine and serum by capillary liquid chromatography (cLC) with UV-Vis and mass spectrometry (MS) detection using methacrylate ester-based monolithic columns has been developed. The influence of composition of polymerization mixture was studied. The optimum monolith was obtained with butyl methacrylate monomer at 60/40% (wt/wt) butyl methacrylate/ethylene dimethacrylate ratio and 50wt% porogens (composed of 36wt% of 1,4-butanediol, 54wt% 1-propanol and 10wt% water). Baseline resolution of analytes was achieved through a mobile phase of acetonitrile/water in gradient elution mode. Additionally, dispersive liquid-liquid microextraction (DLLME)…

Detection limitAnalytegeographyChromatography Reverse-PhaseChromatographygeography.geographical_feature_categoryResolution (mass spectrometry)ChemistryOrganic ChemistryParabensGeneral MedicineUrineUrinalysisMethacrylateMass spectrometryBiochemistryMass SpectrometryAnalytical ChemistryLiquid chromatography–mass spectrometryLimit of DetectionHumansMethacrylatesMonolithBlood Chemical AnalysisJournal of chromatography. A
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Determination of carbonates in waters by on-line vapor generation FTIR

1998

Abstract An electrically heated gas-permeation unit (GPU) has been employed for the vapor-generation Fourier transform infrared (FTIR) determination of total carbonate in waters. The developed method is based on the simultaneous injection of 100 μ l sample and 100 μ l nitric acid in a two-channel manifold with a merging zone, which provides the generation of CO 2 through the GPU, heated at 90°C, from which CO 2 is swept by a stream of N 2 to a long-path infrared gas cell. Absorbance measurements were made in the range from 2500 to 2150 cm −1 and the corresponding flow injection recordings were obtained as a function of time. The areas of these peaks are interpolated in a calibration equatio…

Detection limitAqueous solutionChemistryInfraredAnalytical chemistryAbsorbancechemistry.chemical_compoundsymbols.namesakeFourier transformNitric acidCalibrationsymbolsFourier transform infrared spectroscopySpectroscopyVibrational Spectroscopy
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Gas-chromatographic elemental analysis via di(trifluorethyl)dithiocarbamato-chelates

1986

The capillary-gas-chromatographic conditions for the determination of trace metals after extraction from aqueous solution are optimized by coupling of capillaries and improvement of injection technique. Different detectors (FID and ECD) are tested. pH range and buffer systems for extraction of metal chelates are discussed.

Detection limitAqueous solutionChromatographyChemistryClinical BiochemistryExtraction (chemistry)General MedicineAnalytical ChemistryMetalElemental analysisvisual_artvisual_art.visual_art_mediumPh rangeGeneral Materials ScienceChelationTrace metalFresenius' Zeitschrift für analytische Chemie
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Fourier-transform infrared determination of nicotine in tobacco samples by transmittance measurements after leaching with CHCl3

1998

Abstract A new procedure is proposed for the FT-IR spectrometric determination of nicotine in tobacco. The method is based on the extraction of nicotine in CHCl 3 from tobacco samples, wetted with an aqueous solution of NH 3 (0.1 M), and the measurement of absorbance in the stopped-flow mode at 1316 cm −1 , using a spectral baseline correction established from 1334 to 1300 cm −1 . The procedure developed does not requires a complex sample preparation, and provides a limit of detection of 0.045 mg ml −1 nicotine, a sampling frequency of 3.3 h −1 and a coefficient of variation of 0.3% for five independent measurements of a tobacco sample with a nicotine content of 1.5% w/w. The accuracy of th…

Detection limitAqueous solutionChromatographyChemistryCoefficient of variationExtraction (chemistry)Analytical chemistryInfrared spectroscopyBiochemistryAnalytical ChemistryAbsorbanceNicotinemedicineEnvironmental ChemistrySample preparationSpectroscopymedicine.drugAnalytica Chimica Acta
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Development of a gas chromatography-mass spectrometry method for the determination of ultraviolet filters in beach sand samples

2014

An analytical method for the determination of eight fat-soluble ultraviolet (UV) filters in beach sand samples is presented for the first time. The method is based on a leaching process of the target compounds from sand samples using vortex mixer agitation and further centrifugation, followed by dispersive liquid–liquid microextraction (DLLME) of the supernatant and gas chromatography-mass spectrometry (GC-MS) analysis of the DLLME extract. The variables involved in the leaching and in the DLLME processes were studied to provide the best enrichment factors. In the first case, the leaching solvent type and volume, and the vortex mixer agitation time were studied. In the case of the DLLME, th…

Detection limitAqueous solutionChromatographyChemistryGeneral Chemical EngineeringGeneral EngineeringAnalytical chemistryVortex mixerDisperserRepeatabilityMass spectrometryAnalytical ChemistryLeaching (metallurgy)Gas chromatography–mass spectrometryAnal. Methods
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Ion mobility spectrometry as a fast analytical tool in benzalkonium chloride homologs determination.

2017

Abstract A novel procedure is proposed for the determination by ion mobility spectrometry (IMS) of C 12 , C 14 and C 16 benzalkonium chloride (BAC) homologs. The proposed method requires minimum sample treatment and the measurement was made in less than one minute. A high sensitivity was obtained for BAC determination by IMS with limit of detection values from 37 to 69 µg L −1 . Accuracy of the proposed methodology was evaluated through the analysis of aqueous and alcoholic samples spiked with BAC at concentration levels from 0.002% to 20% (w/v), providing recovery values from 91% to 104%. BAC was determined in sanitary alcohols, nasal sprays, postharvest products, algaecides, and treated s…

Detection limitAqueous solutionChromatographyChemistryIon-mobility spectrometry010401 analytical chemistryAnalytical chemistry010501 environmental sciences01 natural sciencesSwimming pool water0104 chemical sciencesAnalytical ChemistryBenzalkonium chloridemedicineBAC determination0105 earth and related environmental sciencesmedicine.drugTalanta
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Sequential injection analysis for benzophenone-4 and phenylbenzimidazole sulphonic acid in sunscreen sprays by solid-phase extraction coupled with ul…

2002

Abstract A sequential injection UV method was developed to determine benzophenone-4 (BZ4) and phenylbenzimidazole sulphonic acid (PBS) simultaneously, these being the most commonly used UV-filters in aqueous formulations used as sunscreen sprays. The selective elution of both was performed by on-line solid-phase extraction, by retention on a SAX microcolumn and separation by varying the pH of elution. The sensitivity obtained was 0.042±0.001 ml μg −1 for PBS and 0.0159±0.0003 ml μg −1 for BZ4. The limit of detection was 1.6 μg ml −1 for PBS and 0.6 μg ml −1 for BZ4. The R.S.D. of the results was 1–6% for PBS and 1–12% for BZ4. The method was validated using commercial sunscreen formulations…

Detection limitAqueous solutionChromatographyElutionExtraction (chemistry)Mass spectrometryBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryReagentBenzophenoneEnvironmental ChemistrySolid phase extractionSpectroscopyAnalytica Chimica Acta
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