Search results for "Chemical analysis."

showing 10 items of 308 documents

MICELLAR CHROMATOGRAPHIC PROCEDURE WITH DIRECT INJECTION FOR THE DETERMINATION OF SULFONAMIDES IN MILK AND HONEY SAMPLES

2001

The capability of liquid chromatography with micellar mobile phases of sodium dodecyl sulfate (SDS), of allowing the direct injection of biological fluids into reversed-phase columns, was applied to the determination of sulfonamides in milk and honey samples. The chromatographic behavior of a group of 15 sulfonamides was studied at pH 3.0 where the drugs showed a greater separation space. Acetonitrile was added to the mobile phase to decrease the retention of the most hydrophobic drugs and increase the efficiencies, which yielded a higher resolution. The samples were diluted with 0.10 M SDS to facilitate the solubilization of the matrix compounds and release the protein-bound drugs. The pro…

SulfamerazineChromatographyChemistryClinical BiochemistryPharmaceutical ScienceSulfadimethoxineSulfacetamideReversed-phase chromatographySulfapyridineBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryMatrix (chemical analysis)medicineSulfaguanidinemedicine.drugJournal of Liquid Chromatography & Related Technologies
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Polymer-matrix route to (Bi, Pb)2Sr2Ca2Cu3O10+δ: The role of Ca2CuO3☆

1993

Abstract The use of polyethylenimine as active matrix agent has provided a fast synthesis method for (Bi, Pb)2Sr2Ca2Cu3O10+δ, starting from aqueous acetic solutions combined with careful control of the procedural variables. The 110 K phase is obtained as the only superconducting phase after sintering in air during 42 h at 860°C. This technique yields homogeneously sized, large (ca. 20 μm) platelets of the superconducting material. The presence of an excess of calcium and copper over the stoichiometric requirements accelerates the formation of the superconducting phase. This excess, which appears in the resulting material as Ca2CuO3, influences the superconducting properties, other than Tc, …

SuperconductivityAqueous solutionChemistryInorganic chemistryAnalytical chemistrychemistry.chemical_elementSinteringGeneral ChemistryCondensed Matter PhysicsCopperMagnetic susceptibilityMatrix (chemical analysis)Phase (matter)General Materials ScienceStoichiometrySolid State Ionics
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Packing meterials with surface barriers, controlled distribution and topography of ligands for sample clean-up and analysis of biologically active so…

1991

Various types of, so-called, restricted access packings have been developed for sample clean-up and analysis of biologically active solutes by means of HPLC. The unique feature of these packings is that they prevent the access of matrix components such as protein whilst selectively retaining the drug components and their metabolites. This results from the fact that the particles of the packings possess a surface barrier for large solutes at the external or internal surface area and exhibit a controlled gradient in the chemical surface composition. They are grouped, according to their particle structures, into internal-surface reversed phases (ISRP), shielded hydrophobic phases (SHP), semi-p…

Surface (mathematics)Surface barrierChromatographyChemistryOrganic ChemistryClinical BiochemistryRestricted accessBiological activityBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryClean-upMatrix (chemical analysis)ParticleChromatographia
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The generalized H-point standard-additions method to determine analytes present in two different chemical forms in unknown matrix samples. Part I. Ge…

2000

This paper shows how the generalized H-point standard-additions method (GHPSAM) can be used to obtain the total concentration or concentrations of different chemical forms of an analyte when the matrix of the sample is completely unknown. The spectral regions where the interferent behaviour can be considered as linear are found and the analyte concentration free from bias error is estimated. This paper includes the already published features of the GHPSAM and a new modification of this method which allows the simultaneous determination of two chemical forms of an analyte in a sample.

Systematic errorAnalyteInternal standardChemistrySample (material)Analytical chemistryBiochemistryAnalytical ChemistryMatrix (chemical analysis)ChemometricsStandard additionElectrochemistryEnvironmental ChemistryPoint (geometry)SpectroscopyThe Analyst
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Gravimetric characterisation of the surface properties of a porous drug carrier

1995

The gas adsorption method is the most common means to characterise the topology of solid surfaces with regard to its use as an adsorbent. Adsorption isotherms are determined advanta-geously using a vacuum microbalance: Thermogravimetric techniques allow the observation of sample degassing and its optimization. The dry mass is determined in situ, the mass of gas adsorbed is measured directly and different gases can be used without calibration. From the isotherm the pore size distributions, specific surface area, fractal dimension and density can be derived. Commercially available gravimetric sorption apparata and vacuum balances as well as software for data evaluation are reviewed in tables.…

ThermogravimetryMatrix (chemical analysis)Thermogravimetric analysisMaterials scienceAdsorptionSpecific surface areaAnalytical chemistryGravimetric analysisSorptionPorosityJournal of Thermal Analysis
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Assessment of the antioxidant and antibacterial activities of different olive processing wastewaters.

2017

Olive processing wastewaters (OPW), namely olive mill wastewater (OMW) and table-olive wastewaters (TOW) were evaluated for their antibacterial activity against five Gram-positive and two Gram-negative bacteria using the standard disc diffusion and thin layer chromatography (TLC)-bioautography assays. Disc diffusion screening and bioautography of OMW were compared to the phenolic extracts of table-olive brines. Positive activity against S. aureus was demonstrated. The optimization of chromatographic separation revealed that hexane/acetone in the ratio of 4:6 was the most effective for phenolic compounds separation. A HPLC-MS analysis was performed showing that only two compounds, hydroxytyr…

Thin-Layer Chromatography0301 basic medicineDPPHStaphylococcuslcsh:MedicineWastewaterPathology and Laboratory MedicineBiochemistryAntioxidantsMass Spectrometrychemistry.chemical_compoundPlant ProductsMedicine and Health SciencesStaphylococcus Aureuslcsh:ScienceChromatography High Pressure LiquidMultidisciplinaryBioautographyAntimicrobialsChromatographic TechniquesOlivesDrugsAgriculture04 agricultural and veterinary sciencesPlants040401 food scienceThin-layer chromatographyBacterial PathogensAnti-Bacterial AgentsHexaneChemistryBioassays and Physiological AnalysisMedical MicrobiologyPhysical SciencesPathogensAntibacterial activityResearch ArticleMicrobial Sensitivity TestsResearch and Analysis MethodsMicrobiologyVegetable OilsFruitsInhibitory Concentration 5003 medical and health sciences0404 agricultural biotechnologyPhenolsPicratesMicrobial ControlOleaAcetonePhenolsMicrobial PathogensPharmacologyChromatographyBacteriaBiphenyl Compoundslcsh:RChemical CompoundsOrganismsBiology and Life SciencesAgronomyTyrosolPlanar Chromatography030104 developmental biologychemistryAntibacterialsHydroxytyrosollcsh:QChromatography Thin LayerBiochemical AnalysisCrop SciencePLoS ONE
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Batch experiments for the determination of the Ti(IV,III) couple in 1 moldm-3 HCl, 2 moldm-3 NaCl medium at 25°C

2009

The determination of the Ti(IV, III) redox couple formal potential in 1 M HCl 2 M NaCl medium at 25°C through batch experiments involving the preparation of Ti(IV) and Ti(III) mixtures via the reaction of Ti(IV) with Zinc amalgam, has been carried out with emf measurements in order to verify the correctness of the previous value that the authors obtained by a coulometric-potentiometric investigation in the same conditions. The results from the two independent methods are in good agreement: 9 ± 1 mV the first and 9 ± 2 the average batch result.

Ti(IVIII) coupleBatch experimentChemical analysis.Redox potentialZinc amalgamEmf measurement
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Optimization of a matrix solid-phase dispersion method for the analysis of pesticide residues in vegetables

1996

A multiresidue method based on matrix solid-phase dispersion (MSPD) is studied to determine chlorfenvinfos, chlorpyrifos, fenarimol, iprodione, procimydone, propiconazole, tetradifon, triadimefon and vinclozolin in artichokes, green beans, lettuces and tomatoes. Alumina, silica and Florisil were assessed as extracting phases, and the extracts from Florisil were the cleanest. To facilitate manual extraction, sand was added to the sample together with the dispersing phase. Three eluting systems were then studied, and dichloromethane proved to be the best. Further purification can be performed using solid-phase cleanup after diluting extracts with aqueous solutions. Octyl- and octadecyl-silica…

Time FactorsChromatographyChemistryOrganic ChemistryPesticide ResiduesReproducibility of ResultsGeneral MedicineBiochemistryGas Chromatography-Mass SpectrometryAnalytical ChemistryMatrix (chemical analysis)chemistry.chemical_compoundElectron capture detectorVegetablesSelected ion monitoringSample preparationGas chromatographyProcymidoneSolid phase extractionVinclozolinJournal of Chromatography A
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Do fluorescence and transient absorption probe the same intramolecular charge transfer state of 4-(dimethylamino)benzonitrile?

2009

International audience; We present here the results of time-resolved absorption and emission experiments for 4-(dimethylamino)benzonitrile in solution, which suggest that the fluorescent intramolecular charge transfer (ICT) state may differ from the twisted ICT (TICT) state observed in transient absorption.

Time Factorstime resolved spectraGeneral Physics and Astronomyvisible spectra010402 general chemistryPhotochemistry01 natural sciencesTime resolved spectraSpectral lineFluorescencechemistry.chemical_compoundspectrochemical analysisOrganic compoundsUltrafast laser spectroscopyNitrilesCharge exchangePhysical and Theoretical ChemistryVisible spectra:FÍSICA::Química física [UNESCO]Fluorescent DyesSpectrochemical analysis010405 organic chemistryChemistrycharge exchangeFluorescenceUNESCO::FÍSICA::Química física0104 chemical sciences3. Good health[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryBenzonitrileIntramolecular forceCharge exchange ; Fluorescence ; Organic compounds ; Spectrochemical analysis ; Time resolved spectra ; Visible spectraAbsorption (chemistry)Time-resolved spectroscopyLuminescenceorganic compoundsThe Journal of chemical physics
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Development of accurate mass spectrometric routine and reference methods for the determination of trace amounts of iridium and rhodium in photographi…

1999

For the determination of trace amounts of iridium and rhodium in photographic emulsions different sample treatment procedures were coupled with inductively coupled plasma mass spectrometry (ICP-MS) and, for iridium, also with negative thermal ionisation isotope dilution mass spectrometry (NTI-IDMS) and ICP-IDMS. IDMS determinations of iridium were carried out using an enriched 191Ir spike solution. Elimination of the silver matrix was established for both mass spectrometric methods, which prevents corresponding memory effects in the ICP-MS system and is essential for the formation of IrO2 - thermal ions, respectively. For NTI-MS measurements, the gelatine matrix of the emulsion must also be…

Trace AmountsAnalytical chemistrychemistry.chemical_elementIsotope dilutionMass spectrometry/dk/atira/pure/sustainabledevelopmentgoals/clean_water_and_sanitationAnalytical ChemistryMatrix (chemical analysis)chemistrySample preparationIridiumPhotographic emulsionSDG 6 - Clean Water and SanitationInductively coupled plasma mass spectrometrySpectroscopyJournal of Analytical Atomic Spectrometry
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