Search results for "Spectrophotometry"

showing 10 items of 644 documents

Simultaneous Kinetic Determination of Carbamate Pesticides after Derivatization withp-Aminophenol by Using Partial Least Squares

1996

Abstract A method has been developed for the fast spectrophotometric determination of propoxur, carbaryl, and ethiofencarb in water samples using injection analysis in the stopped-flow mode. The method is based on the reaction between p -aminophenol and the phenolic compounds obtained from the pesticides, after a previous hydrolysis with 0.05 M NaOH at room temperature for 15 min. The partial least-squares treatment of the spectrophotometry kinetic data provides a simultaneous determination of the three carbamate pesticides assayed with a relative accuracy error lower than 5% in complex mixtures also containing formetanate, which is only partially hydrolyzed under the experimental condition…

Chromatographymedicine.diagnostic_testPropoxurAnalytical Chemistrychemistry.chemical_compoundHydrolysischemistryFormetanateEthiofencarbSpectrophotometryCarbarylPartial least squares regressionmedicineDerivatizationSpectroscopyMicrochemical Journal
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Comparison of spectrophotometric and HPLC methods for determining sialic acid in infant formulas

2011

Abstract Two methods for determining sialic acid in infant formulas – spectrophotometry and HPLC with fluorescence detection – have been optimised and validated, the first one allows to determine total sialic acid while the second allows to differentiate the two main forms of sialic acid (N-acetylneuraminic acid (Neu5Ac) and N-glycolylneuraminic acid (Neu5Gc)). A common sample preparation procedure (hydrolysis and purification) for both methods has been proposed. The linearity (from 6 to 150 μg of total sialic acid in the assay for spectrophotometry, and from 12.5 to 250 ng and 1 to 5 ng of Neu5Ac and Neu5Gc, respectively, for HPLC) is adequate. The detection and quantification limits (0.29…

Chromatographymedicine.diagnostic_testRelative standard deviationGeneral MedicineHigh-performance liquid chromatographyFluorescenceAnalytical ChemistrySialic acidHydrolysischemistry.chemical_compoundInfant formulachemistrySpectrophotometrymedicineSample preparationFood ScienceFood Chemistry
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Rapid and simultaneous high-performance liquid chromatography assay of polyamines and monoacetylpolyamines in biological specimens

2000

A rapid, resolutive and reproducible reversed-phase high-performance liquid chromatography (RP-HPLC) method was developed for polyamines and acetylpolyamines by adopting pre-column derivatization with benzoyl chloride. In a single run lasting less than 15 min ten polyamines were separated as well as traces of benzoic acid, methylbenzoate and benzoic anhydride. These contaminants, produced during the derivatization reaction, were almost all eliminated by washing steps envisaged in the same procedure. This simple and sensitive method can be applied to routine determination of polyamines in biological samples. A fine application of this procedure to the determination of endogenous content of p…

Chromatographymedicine.diagnostic_testorganic chemicalsBiogenic PolyaminesReproducibility of ResultsGeneral ChemistryReversed-phase chromatographyReference StandardsSensitivity and SpecificityHigh-performance liquid chromatographyBenzoic anhydridechemistry.chemical_compoundBenzoyl chloridechemistrySpectrophotometrymedicineSpectrophotometry UltravioletDerivatizationQuantitative analysis (chemistry)Chromatography High Pressure LiquidBenzoic acidJournal of Chromatography B: Biomedical Sciences and Applications
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A new selective fluorogenic probe for trivalent cations.

2012

[EN] A new selective chromo-fluorogenic probe for Fe 3+, Cr 3+ and Al 3+ is reported. Detection limits are in the ¿M range and the fluorogenic sensing ability could be observed by the naked eye when illuminated with UV-light. No response is observed with divalent cations. © 2012 The Royal Society of Chemistry.

ChromiumAcetonitrilesIronComplex formationInorganic chemistryLithiumPhotochemistryArticleCatalysisDivalentSynthesischemistry.chemical_compoundQUIMICA ORGANICAUltraviolet visible spectroscopyChemical structureNickelUltraviolet spectroscopyFerric ionMaterials ChemistryFerrous ionFluoresceinFluorescent Dyeschemistry.chemical_classificationDetection limitChemistryZinc ionFerric ionQUIMICA INORGANICACopper ionMetals and AlloysComplex formationCobaltMercuryGeneral ChemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIlluminationSpectrometry FluorescenceZinc ionCeramics and CompositesFluoresceinSpectrophotometry UltravioletNaked eyeCadmiumAluminumChemical communications (Cambridge, England)
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The use of direct determination of chromium in human urine by electrothermal atomic absorption spectrometry in diabetic patients.

1991

ChromiumChromatographySpectrophotometry AtomicClinical BiochemistryPharmaceutical Sciencechemistry.chemical_elementUrineBiological fluidAnalytical Chemistrylaw.inventionChromiumchemistrylawEnvironmental chemistryDrug DiscoveryDiabetes MellitusElectrochemistryHumansIndicators and ReagentsAtomic absorption spectroscopySpectroscopyJournal of pharmaceutical and biomedical analysis
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Distribution of Cr and Pb in artificial sea water and their sorption in marine sediments: an example from experimental mesocosms

2016

The uptake of two heavy metals (chromium and lead) in sediments in experimental mesocosms under exposure to different metal concentrations was evaluated by monitoring their concentrations over time both in seawater and in sediment. Two separate experiments under laboratory-controlled conditions were carried out for the two metals. Sediments were collected from a protected natural area characterized by low anthropic influence and were placed in mesocosms that were housed in aquaria each with seawater at a different metal concentration. At pre-established time intervals, seawater and sediment samples were collected from each mesocosm for chemical analyses. Quantification of chromium and lead …

ChromiumGeologic Sediments010504 meteorology & atmospheric sciencesHealth Toxicology and MutagenesisMetal ions in aqueous solutionchemistry.chemical_element010501 environmental sciencesGeologic Sediments01 natural scienceslaw.inventionMesocosmChromiumChromium; GF-AAS; Lead; Mesocosm; Seawater; Sediment; SorptionlawEnvironmental ChemistrySeawater0105 earth and related environmental sciencesGF-AASSpectrophotometry AtomicSedimentSorptionGeneral MedicineMesocosmPollutionKineticschemistryLeadEnvironmental chemistryEnvironmental scienceSorptionSeawaterSedimentAdsorptionAtomic absorption spectroscopyWater Pollutants ChemicalEnvironmental Monitoring
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Determination of chromium in treated crayfish,Procambarus clarkii, by Electrothermal AAS: Study of chromium accumulation in different tissues

1986

In the present study, the authors investigated the accumulation of chromium in muscle, hepatopancreas, antennal glands, and gills of Procambarus clarkii (Girard) from Lake Albufera following Cr(VI)-exposure. Determinations of chromium were made by using Electrothermal Atomic Absorption Spectroscopy and the standard additions method.

Chromiuminorganic chemicalsGillChromium CompoundsHealth Toxicology and Mutagenesischemistry.chemical_elementAstacoideaToxicologylaw.inventionChromiumlawAnimalsTissue DistributionProcambarus clarkiibiologySpectrophotometry AtomicGeneral Medicinebiology.organism_classificationCrayfishPollutionKineticschemistryEnvironmental chemistryStandard additionIndicators and ReagentsHepatopancreasAtomic absorption spectroscopyBulletin of Environmental Contamination and Toxicology
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Removal of trivalent chromium from tannery waste waters using bone charcoal

2002

International audience; The ability of bone charcoal to remove Cr(III) from aqueous solutions by adsorption has been investigated. The adsorbent used was first characterised and then the adsorption was studied as a function of time and amount of charcoal. Tests were carried out with synthetic solutions whose Cr concentrations (500 mg L-1) were similar to those found in some effluents of Moroccan tannery industries. Cr removal efficiencies higher than 90% were obtained at pH 3.5 using 3 g of bone charcoal and a stirring time of about 30 min. Results of Cr removal by all sieved fractions of bone charcoal had shown the same interesting capabilities for Cr(III) retention. The cross interference…

Chromiuminorganic chemicalschemistry.chemical_elementMineralogyIndustrial WasteHydrochloric acid02 engineering and technology010501 environmental sciences01 natural sciencesBiochemistryAnalytical Chemistrychemistry.chemical_compoundChromiumAdsorptionNitric acidSpecific surface areaCharcoal0105 earth and related environmental sciencesAqueous solutionSpectrophotometry Atomic[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyequipment and supplies6. Clean watercarbohydrates (lipids)MoroccochemistrySodium hydroxidevisual_artCharcoalvisual_art.visual_art_mediumMicroscopy Electron ScanningAdsorption0210 nano-technologyWater Pollutants ChemicalNuclear chemistry
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Cadmium and lead in infant cereals — electrothermal-atomic absorption spectroscopic determination

1999

Because infant cereals are an important component of the infant diet from the fourth month of life onwards and therefore contribute to the dietetic intake of metals by infants, cadmium and lead were measured in samples of cereals commercially available in Spain. For this purpose an electrothermal atomic absorption (ET-AAS) method for determining cadmium and lead in these products was studied. The ET-AAS instrumental conditions and temperature/time furnace program were selected. The analytical parameters of the method (linearity, detection and quantification limits and precision) show its usefulness in measuring cadmium and lead in infant cereal products. The method was applied to eight diff…

Chronic exposureEnvironmental Engineeringchemistry.chemical_elementFood Contaminationlaw.inventionlawInfant dietHumansEnvironmental ChemistryFood scienceLead (electronics)Waste Management and DisposalAnalysis methodCadmiumSpectrophotometry AtomicInfantfood and beveragesContaminationPollutionLeadchemistrySpainEnvironmental chemistryInfant FoodEdible GrainAtomic absorption spectroscopyCadmiumScience of The Total Environment
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Covalent DNA adducts formed by benzo[c]chrysene in mouse epidermis and by benzo[c]chrysene fjord-region diol epoxides reacted with DNA and polynucleo…

1997

The metabolic activation in mouse skin of benzo[c]chrysene (B[c]C), a weakly carcinogenic polycyclic aromatic hydrocarbon (PAH) present in coal tar and crude oil, was investigated. Male Parkes mice were treated topically with 0.5 mumol of B[c]C, and DNA was isolated from the treated areas of skin at various times after treatment and analyzed by 32P-postlabeling. Seven adduct spots were detected, at a maximum level of 0.89 fmol of adducts/microgram of DNA. Four B[c]C-DNA adducts persisted in skin for at least 3 weeks. Treatment of mice with 0.5 mumol of the optically pure putative proximate carcinogens (+)- and (-)-trans-benzo[c]chrysene-9,10-dihydrodiols [(+)- and (-)-B[c]C-diols] led to th…

ChryseneMaleStereochemistryPolynucleotidesToxicologyAdductchemistry.chemical_compoundDNA AdductsMiceAnimalsCarcinogenBiotransformationChromatography High Pressure LiquidSkinCarcinogenic Polycyclic Aromatic HydrocarbonSingle-Strand Specific DNA and RNA EndonucleasesAbsolute configurationGeneral MedicineDNAPhenanthreneschemistryCovalent bondPolynucleotideAutoradiographyEpoxy CompoundsSpectrophotometry UltravioletChromatography Thin LayerDNAChemical research in toxicology
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