Search results for "Matrix"

showing 10 items of 3205 documents

Solid phase techniques in the extraction of pesticides and related compounds from foods and soils

1994

The application of SPE technology to the isolation of pesticides and related compounds from food and soils has grown enormously in the last decade. Much of this growth has been due to the relative ease of sample handling and the wide range of solid supports currently available for a variety of applications. The aim of this review is to present the methods for solid phase extraction (SPE) of pesticide residues from soils and foods. There are three main areas according to the type of approach used to handle the sample: solid phase extraction, solid phase clean-up (SPC), and matrix solid phase dispersion (MSPD). This review covers milk products, fatty foods, fruits, vegetables, and soils. Soli…

Matrix (chemical analysis)ChromatographyPesticide residueChemistryMechanical EngineeringEnvironmental chemistryPhase (matter)Extraction (chemistry)Filtration and SeparationGas chromatographySolid phase extractionPesticideDispersion (chemistry)Journal of Microcolumn Separations
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Comparative study of different approaches for the flow injection-fourier transform infrared determination of toluene in gasolines.

1994

Abstract A single channel flow injection manifold has been employed to carry out the direct determination of toluene in gasolines by FT—IR without any sample pretreatment and by using different strategies. Toluene can be directly determined by measuring the absorbance at 728 cm −1 , using a base line established between 835 and 575 cm −1 ; and in this case a limit of detection of 0.01% (v/v) can be obtained with a dynamic range up to 2% (v/v). In some cases it could be convenient to determine toluene by derivative flow-injection FT—IR in order to avoid matrix interferences in the analysis of some types of gasolines. Carrying out the first order derivative FI—FT—IR measurements on the 728 cm…

Matrix (chemical analysis)Detection limitAbsorbancechemistry.chemical_compoundChemistryAnalytical chemistryInfrared spectroscopyDerivativeGasolineBenzeneTolueneAnalytical ChemistryTalanta
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Sensitive sequential-injection system for the determination of 2-phenylbenzimidazole-5-sulphonic acid in human urine samples using on-line solid-phas…

2003

Abstract 2-Phenylbenzimidazole-5-sulphonic acid (PBS) is an UV-filter contained in many cosmetics as a sunscreen. A direct, selective and sensitive method to determine traces of PBS is presented. The on-line separation of this compound from urine matrix was directly coupled with fluorimetric detection in a sequential-injection system. The separation was performed using a SAX microcolumn in which the analyte was retained and eluted selectively. The determination is carried out without any derivatization reaction, by directly measuring the intrinsic fluorescence of the analyte. The wavelengths of excitation and emission were 301 and 681 nm, respectively. On-line standard addition calibration …

Matrix (chemical analysis)Detection limitAnalyteChromatographyChemistryElutionStandard additionFluorescence spectrometrySolid phase extractionStandard solutionAnalytical ChemistryTalanta
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Application of isotope-dilution laser ablation ICP-MS for direct determination of Pu concentrations in soils at pg g(-1) levels.

2003

The methods available for determination of environmental contamination by plutonium at ultra-trace levels require labor-consuming sample preparation including matrix removal and plutonium extraction in both nuclear spectroscopy and mass spectrometry. In this work, laser-ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) was applied for direct analysis of Pu in soil and sediment samples. Application of a LINA-Spark-Atomizer system (a modified laser ablation system providing high ablation rates) coupled with a sector-field ICP-MS resulted in detection limits as low as 3x10(-13) g g(-1) for Pu isotopes in soil samples containing uranium at a concentration of a few microg g(-1). …

Matrix (chemical analysis)Detection limitchemistryAnalytical chemistrychemistry.chemical_elementSample preparationIsotope dilutionUraniumMass spectrometryBiochemistryInductively coupled plasma mass spectrometryAnalytical ChemistryPlutoniumAnalytical and bioanalytical chemistry
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Multielemental determination of trace mineral elements in seawater by dynamic reaction cell inductively coupled plasma- mass spectrometry after Al(OH…

2020

Abstract A simple method has been developed for the simultaneous determination of 12 trace mineral elements in seawater using, in some cases, several target isotopes (51V, 52Cr, 55Mn, 58,60Ni, 59Co, 63,65Cu, 64,66,68Zn, 75As, 78Se, 111,113Cd, 206,207,208Pb y 238U) in seawater. The method combined a simple and fast Al(OH)3 co-precipitation method, to pre-concentrate mineral elements and to separate them from the seawater matrix, and inductively coupled plasma mass spectrometry using the dynamic reaction cell with NH3 gas to do quantitative determinations free from polyatomic interferences. The recoveries of trace elements after Al(OH)3 co-precipitation varies between 80% for 111Cd and 116% f…

Matrix (chemical analysis)IsotopeTrace mineralChemistryCoprecipitationPolyatomic ionAnalytical chemistrySeawaterInductively coupled plasma mass spectrometrySpectroscopyAnalytical ChemistryMicrochemical Journal
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Systematic procedure for the preparation of sets of calibration standards for x-ray fluorescence analysis of ceramic materials

1998

A systematic procedure for the preparation of optimized sets of calibration solid standards for the x-ray fluorescence analysis of ceramic materials is described. The matrix of the contents of the N analytes in the n standards (n ≥ N) is calculated from an n x N experimental design matrix, and from the upper and lower limits of the calibration range for each of the N analytes. Two procedures, which are useful for taking into account analyte interactions, are proposed for constructing the experimental design matrix, i.e. the scroll procedure and the procedure of the centers. A program developed to help the analyst in designing and preparing the set of standards following the proposed procedu…

Matrix (chemical analysis)Set (abstract data type)AnalyteCertified reference materialsChemistryCalibrationAnalytical chemistryDesign matrixX-ray fluorescenceSample preparationCeramic materialsSpectroscopyX-Ray Spectrometry
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FIA—FT—IR determination of ibuprofen in pharmaceuticals

1992

A method has been developed for the determination of Ibuprofen (2-[4-isobutylphenyl]-propionic acid) in pharmaceuticals by FT-IR, using the carbonyl band which this compound presents at 1710 cm(-1) in carbon tetrachloride solutions. Samples are dissolved in carbon tetrachloride. In this solvent the excipients are not soluble and so the drug can be directly determined without any additional treatment. The use of a simple FIA manifold permits one to carry out this analysis with a low consumption of reagent and the FT-IR provides a continuous monitoring of the spectral base-line which permits an accurate determination of the maximum in the absorbance band. Also, the FIA system permits easy and…

Matrix (chemical analysis)SolventAbsorbancechemistry.chemical_compoundChromatographychemistryReagentAnalytical chemistryCarbon tetrachlorideInfrared spectroscopySample preparationFourier transform infrared spectroscopyAnalytical ChemistryTalanta
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2,9-Dimethylpicene: Synthesis, Mutagenic Activity, and Identification in Natural Samples

1990

Abstract 2,9-Dimethylpicene (2,9-DMPic) has been conveniently synthesized via a new route involving oxidative photocyclization of suitable substituted diarylethylenes and has been characterized by high-resolution 400-MHz 1H-NMR spectroscopy. Furthermore, 2,9-DMPic exhibits a typical line narrowed emission spectrum in n-decane matrix frozen at 15 K (Shpol'skii effect). Its unambiguous identification in a natural sample has been performed by this technique, providing strong evidence for the formation of this compound through aromatization of triterpenoid natural precursors. The mutagenicity of this naturally occurring methylated polycyclic aromatic hydrocarbon (PAH) has been examined in six h…

Matrix (chemical analysis)chemistry.chemical_classificationTriterpenoidPolymers and PlasticsChemistryStereochemistryOrganic ChemistryMaterials ChemistryAromatizationPolycyclic aromatic hydrocarbonSpectroscopyCarcinogenPolycyclic Aromatic Compounds
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Determination of mycotoxins in multicereal flour by matrix solid phase dispersion and LC–MS/MS

2010

Matrix (chemical analysis)chemistry.chemical_compoundChromatographyChemistryPhase (matter)Lc ms msGeneral MedicineToxicologyDispersion (chemistry)MycotoxinToxicology Letters
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Application of matrix solid phase dispersion to the determination of imidacloprid, carbaryl, aldicarb, and their main metabolites in honeybees by liq…

2005

Abstract A method based on matrix solid phase dispersion (MSPD) using C18 as dispersant and dichloromethane–methanol as eluent and liquid chromatography–atmospheric pressure chemical ionization–mass spectrometry (LC–APCI–MS) has been developed for the simultaneous determination of imidacloprid, 6-chloronicotinic acid, carbaryl, aldicarb, aldicarb sulfoxide, and aldicarb sulfone in honeybees. The proposed method was compared with liquid–liquid extraction (LLE) combined with LC–APCI–MS analysis. Spiked blank samples were used as standards to counteract the matrix effect observed in the chromatographic determination. Recovery studies were performed at different fortification levels. Average re…

Matrix (chemical analysis)chemistry.chemical_compoundChromatographyColumn chromatographyAldicarbChemistryLiquid chromatography–mass spectrometryImidaclopridCarbarylExtraction (chemistry)Mass spectrometryAnalytical ChemistryTalanta
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