Search results for "Chemical analysis."

showing 10 items of 308 documents

Photochemical synthesis of pyrene perfluoroalkyl derivatives and their embedding in a polymethylmethacrylate matrix: a spectroscopic and structural s…

2014

A photochemical, alternative and eco-compatible approach to perfluoroalkyl derivatives of pyrene is presented. The perfluoroalkyl chain is regiospecifically introduced at the 1 position of pyrene. The synthesized products have been embedded in a polymethylmethacrylate matrix by photocuring at 365 nm. Both the photochemical reactions can be considered a “green tool” for the synthetic chemist in order to obtain materials with prospective optoelectronic applications. The so-obtained composites have been the object of a study by UV and fluorescence spectroscopy in order to explore their luminescence properties. The small angle X-ray scattering and the transmission electron microscopy techniques…

Materials scienceScatteringGeneral ChemistryMicrostructurePhotochemistryFluorescence spectroscopyPyrene PMMA Photochemical perfluoroalkylation OLEDMatrix (chemical analysis)chemistry.chemical_compoundchemistryTransmission electron microscopyMaterials ChemistryOLEDPyreneLuminescence
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Dynamics of the incorporation of Co into the wurtzite ZnO matrix and its magnetic properties

2015

Made available in DSpace on 2022-04-29T07:25:55Z (GMT). No. of bitstreams: 0 Previous issue date: 2015-07-25 Financiadora de Estudos e Projetos Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) Abstract Bulk Co-doped ZnO (Zn1-xCoxO) samples were prepared and studied with particular emphasis on their compositions, structures, and magnetic properties. A detailed microstructural analysis was conducted to investigate the nature of Co incorporation into the wurtzite ZnO matrix. The Zn1-xCoxO ceramic samples were prepared using the standard solid-state reaction method with different Co molar concentrations of u…

Materials scienceSpintronicsMechanical EngineeringMetals and AlloysAnalytical chemistryPhase diagramIonMatrix (chemical analysis)Condensed Matter::Materials ScienceParamagnetismNuclear magnetic resonanceSpintronicMechanics of MaterialsPhase (matter)visual_artMagnetic propertiesDilute magnetic oxideMaterials Chemistryvisual_art.visual_art_mediumZn1-xCoxOCeramicCo distributionPhase diagramWurtzite crystal structureJournal of Alloys and Compounds
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Extended gate electrode arrays for extracellular signal recordings

2000

Abstract We have fabricated arrays of planar gold electrodes arranged in a matrix of 8×8 with active areas ranging from 6 to 30 μm in diameter. An electronic amplification circuitry based on commercial junction field-effect transistors was used where the gold sensor fields act as extended gate electrodes (EGE) of the transistors, which leads to a new approach for long-term extracellular recording systems in vitro. The high input resistance of the amplification circuitry allows the use of small planar bare gold electrodes without further modification which therefore extends the frequency range of the measuring set-up down to the DC-level. The performance of our recording system has been test…

Materials sciencebusiness.industryTransistorMetals and AlloysAnalytical chemistryRangingCondensed Matter PhysicsCapacitanceSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionMatrix (chemical analysis)PlanarExtracellular signalSensor arraylawElectrodeMaterials ChemistryOptoelectronicsElectrical and Electronic EngineeringbusinessInstrumentationSensors and Actuators B: Chemical
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Application of the H-point standard additions method by using absorbance increment values as analytical signals

1991

Abstract This paper demonstrates how the absorbance increment (ΔA) between two wavelengths selected according to the fundamental criteria for application of the H-Point standard additions method (HPSAM) are only related to the analyte concentration. A procedure for calculation of the unknown analyte concentration with no bias error by applying HPSAM to ΔA values in much the same way as the method of standard additions (MOSA), is reported. The method was also applied to a calibration with a single standard. The results obtained on 6 samples with maximal separations between 65 and 0 nm are reported. Finally, the proposed method was applied to the resolution of different phenol-o-cresol mixtur…

Matrix (chemical analysis)AbsorbanceWavelengthAnalyteResolution (mass spectrometry)ChemistryStandard additionCalibrationAnalytical chemistryPoint (geometry)Analytical ChemistryTalanta
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Smart Sorption Materials in Green Analytical Chemistry

2019

The use of smart materials as alternative sorption materials for their use in greening sample preparation has been reviewed. It has been taking into consideration recent advances on the use of natural products, without any modification or purification, for making analyte extraction and pre-concentration and the use of specific materials in solid-phase extraction (SPE) and solid-phase microextraction (SPME) approaches. Inorganic materials, such as metal oxides, alumina-based, silica-based, and carbon-based materials together with biomimetic sorbents such as classical immunosorbents, aptamers, and molecularly imprinted polymers, have been reviewed as examples of these materials, stressing the…

Matrix (chemical analysis)AnalyteMaterials scienceAptamerMolecularly imprinted polymerNanotechnologySample preparationSorptionImmunosorbentsSmart material
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Analyte estimation using the generalized H-point standard additions method and a new methodology for locating linear spectral intervals for unknown i…

1998

An improvement in the way to locate linear spectral intervals for unknown interferents which overlap the analyte signal in UV–visible spectrophotometry is offered as an alternative to the method previously described by Campins-Falco et al. (Anal. Chim. Acta, 302, 323 (1995)). In that report, quotients of the second-derivative spectra of the sample and analyte were used. The new method improves on the old one by using first- instead of second-derivative data, thus eliminating the possible divisions by zero (inflection points for the analyte) obtained in the previous procedure. The linear intervals are now obtained by plotting for each wavelength the differences in first-derivative data betwe…

Matrix (chemical analysis)ChemometricsAbsorbanceAnalyteInternal standardChemistryApplied MathematicsStandard additionCalibrationAnalytical chemistryLinearityAnalytical ChemistryJournal of Chemometrics
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Evaluation of a Multidimensional Solid-Phase Extraction Platform for Highly Selective On-Line Cleanup and High-Throughput LC−MS Analysis of Triazines…

2001

A novel highly selective sample cleanup procedure based on the use of molecularly imprinted polymers (MIPs) as solid-phase extraction materials has been evaluated with respect to its applicability and routine use in environmental analysis. The method comprises the combination of a restricted access material (RAM) and a MIP allowing a selective sample preparation to be achieved in the online mode. This combination is called the size-selective sample separation and solvent switch (six-SPE). The RAM column combines size exclusion and adsorption chromatography, reducing the concentration of matrix molecules by a cutoff of 15 kDa. The MIP column selectively retains the triazine analytes whereas …

Matrix (chemical analysis)ChromatographyChemistryElutionSize-exclusion chromatographyExtraction (chemistry)Molecularly imprinted polymerAnalytical chemistrySample preparationSolid phase extractionHigh-performance liquid chromatographyAnalytical ChemistryAnalytical Chemistry
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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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