Search results for "Calibration"

showing 10 items of 890 documents

Double Laser LIBS and micro-XRF spectroscopy applied to characterize materials coming from the Greek-Roman theater of Taormina

2009

The laser-induced breakdown spectroscopy (LIBS) is an applied physical technique that has shown, in recent years, its great potential for rapid qualitative analysis of materials. The possibility to implement a portable instrument that perform LIBS analysis makes this technique particularly useful for in situ analysis in the field of cultural heritages. The aim of this work is to compare the results, obtained by LIBS measurements with X-Ray Fluorescence (XRF) ones, on calcareous and refractory materials coming from the Greek-Roman theater of Taormina. Calibration curves for LIBS and XRF were obtained by measuring certified reference materials and using them as standards. LIBS measurements we…

ChemistryCalibration curvebusiness.industryX-ray fluorescenceLaserCollimated lightSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)law.inventionCertified reference materialsOpticslawCalibrationLIBS micro-XRF calcareous material refractory material cultural heritagesLaser-induced breakdown spectroscopySpectroscopybusiness
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New Tools for Characterizing Metallic Nanoparticles: AgNPs, A Case Study.

2015

Currently, transmission electron microscopy (TEM) is the main technique for estimating the sizes of spherical nanoparticles (NPs) and through them, their concentrations. This paper demonstrates for the first time that C18 reversed-phase capillary liquid chromatography (Cap-LC) coupled to diode array detection (DAD) has the potential to estimate mean concentrations of silver nanoparticles (AgNPs) and thereby determine their average size. Direct injection of the sample without previous extraction or separation steps is carried out. Only a unique standard with a known AgNP size is needed for the calibration. In a first approach, the new method has been tested over silver nanoparticles, produce…

ChemistryCapillary action010401 analytical chemistryExtraction (chemistry)Analytical chemistryNanoparticle02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesDiode arraySilver nanoparticle0104 chemical sciencesAnalytical ChemistryTransmission electron microscopyCalibration0210 nano-technologyMetal nanoparticlesAnalytical chemistry
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Dating archeological lead artifacts from measurement of the corrosion content using the voltammetry of microparticles.

2011

A methodology for dating archeological lead artifacts based on the voltammetry of microparticles is described. This methodology is based on the comparison of the height of speci¿c voltammetric features from PbO2 and PbO corrosion products formed under long-term alteration conditions. Calibration of the method was performed with the help of a series of well-documented lead pieces from the funds of di¿erent museums of the Comunitat Valenciana (Spain) covering from the ¿fth century B.C. to present day. The variation of peak currents with the time of corrosion can be¿tted to the same potential rate law as that found by Reich (R = 0.070 ( 0.005), using measurements on the Meissner fraction in th…

ChemistryElectrodeOxideMineralogyPBO2ArchaeologyAnalytical ChemistryCorrosionSulfuric-acid-solutionBatteriesLead (geology)Electrochemical oxidationAge estimationForce microscopyPINTURACalibrationVoltammetryReductionAnalytical chemistry
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Direct determination of minerals in human diets by infrared spectroscopy and X-ray fluorescence

2014

The use of near and mid infrared spectroscopy and X-ray fluorescence (XRF) to determine the concentration of mineral elements in Spanish human diets was investigated. Thirty-five commercial baby foods, 6 children fast food menus and 13 university canteen menu samples were analysed by infrared and XRF spectroscopy and spectra evaluated by using reference data obtained by inductively coupled plasma optical emission spectroscopy (ICP-OES). Models for calcium, potassium, iron, magnesium, sodium and zinc determination were built and validated. Spectra were pre-treated by using different pre-processing algorithms (multiplicative scatter correction, standard normal variation, first derivate, ortho…

ChemistryInfraredPotassiumPartial least squares regressionCalibrationAnalytical chemistryInfrared spectroscopychemistry.chemical_elementX-ray fluorescenceInductively coupled plasmaSpectroscopySpectroscopyAnalytical ChemistryMicrochemical Journal
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Spray Atomization Models in Engine Applications, from Correlations to Direct Numerical Simulations

2011

Sprays are among the very main factors of mixture formation and combustion quality in almost every (IC) engine. They are of great importance in pollutant formation and energy efficiency although adequate modeling is still on development. For many applications, validation and calibration of models are still an open question. Therefore, we present an overview of existing models and propose some trends of improvement. Models are classified in zero dimensional and dimensional classes ranging from simple formulations aimed at close-to-real-time applications to complete detailed description of early atomization stages.

Chemistrybusiness.industryGeneral Chemical EngineeringMixture formationEnergy Engineering and Power TechnologyMechanical engineeringRangingCombustionFuel TechnologyCalibrationSpray atomizationProcess engineeringbusinessEfficient energy useOil & Gas Science and Technology – Revue d’IFP Energies nouvelles
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Chemometric extraction of analyte-specific chromatograms in on-line gradient LC-infrared spectrometry

2009

This work exploits the possibilities offered by the recently developed multivariate method named Science-Based Calibration (SBC), for the extraction of ‘analyte-specific’ chromatograms in on-line gradient reversed phase LC-infrared spectrometry (IR) in the presence of a high spectral and chromatographic overlapping between the analyte of interest, co-eluting sample matrix constituents and the mobile phase components. The SBC method uses an experimentally measured single response spectrum of the analyte of interest and representative noise to calculate an optimum regression vector (bopt(1)). Then, the bopt(1) vector is used to predict the concentration of the analyte of interest in the spect…

ChemometricsAnalyteChromatographyChemistryElutionExtraction (chemistry)CalibrationAnalytical chemistryFiltration and SeparationReversed-phase chromatographyStandard solutionMass spectrometryAnalytical ChemistryJournal of Separation Science
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Evaluation of infrared spectroscopy as a screening tool for serum analysis

2013

Abstract The application of attenuated total reflectance Fourier transform infrared (ATR-FT-IR) spectroscopy to the determination of clinical parameters in serum using partial least squares (PLS) has been evaluated as a point-of-care diagnostic tool. In this study the effect of using an increased size of the calibration set and the influence of the origin of samples and their interyear variation on the prediction capability of the method were considered. PLS-ATR-FT-IR provides a green, fast and cheap point-of-care tool for the determination of total protein. Albumin, glucose, urea, HDL, LDL and total cholesterol were predicted with relative errors between 15 and 32%. The analytical predicti…

ChemometricsAnalyteStandard errorChemistryCalibration (statistics)Attenuated total reflectionPrincipal component analysisPartial least squares regressionStatisticsSample (statistics)SpectroscopyAnalytical ChemistryMicrochemical Journal
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Quantitative determination of surface area of silica gel particles by near infrared spectroscopy and chemometrics

2008

Abstract Surface areas of silica gel particles have been quantitatively determined by using near infrared spectrometry and chemometrics. Surface areas of six silica gel samples with varying surface area (300–750 m2/g) have been determined by the common Brunauer–Emmett–Teller (BET) method and used in preparing mixtures of silica gel samples with varying surface area in the ranges 300–474 and 500–750 m2/g. The near infrared spectra of the mixtures were measured and the spectral profiles calibrated against the calculated surface area of the mixtures as dependent variable using partial least squares (PLS) technique. The models obtained from the calibrations were then used in predicting the surf…

Chemometricschemistry.chemical_compoundColloid and Surface ChemistryChemistrySilica gelNear-infrared spectroscopyPartial least squares regressionAnalytical chemistryCalibrationParticleInfrared spectroscopyBET theoryColloids and Surfaces A: Physicochemical and Engineering Aspects
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Analysis of trichothecenes in laboratory rat feed by gas chromatography-tandem mass spectrometry

2015

A method for the determination of seven trichothecenes, neosolaniol (NEO), diacetoxyscirpenol (DAS), deoxynivalenol (DON), nivalenol (NIV), fusarenon-X (FUS-X), 3-acetyldeoxynivalenol (3-ADON) and 15-acetyldeoxynivalenol (15-ADON), in laboratory rat feed by GC-MS/MS was developed. Sample extraction and purification was performed by an acidified mixture of acetonitrile/water (80-20% v/v). Limits of quantitation (LOQs) were between 1 and 10 μg kg(-1) for all studied trichothecenes. Eight concentration levels between the LOQ and 100 × LOQ were used for the calibration curves. Matrix-matched calibration was used for quantitation purposes to compensate the detector signal enhancement obtained fo…

Chromatography GasCalibration curveAnimal feedHealth Toxicology and MutagenesisTrichotheceneToxicologyTandem mass spectrometryDiacetoxyscirpenolchemistry.chemical_compoundTandem Mass SpectrometryAnimals LaboratoryAnimalsMycotoxinChromatographyGas Chromatography/Tandem Mass SpectrometryPublic Health Environmental and Occupational HealthGeneral ChemistryGeneral MedicineAnimal FeedRatschemistryGas chromatographyLaboratoriesTrichothecenesFood AnalysisFood ScienceFood Additives & Contaminants: Part A
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Quantification of poisons for Ziegler Natta catalysts and effects on the production of polypropylene by gas chromatographic with simultaneous detecti…

2020

[EN] This article describes a new simultaneous method for the analysis of sulfur-type poisons, hydrocarbons and permanent gases affecting the productivity of the Ziegler Natta catalyst during the synthesis of polypropylene on an industrial scale in a fluidized-bed reactor. The identification was achieved employing a configuration of the seven-valve chromatographic system, with events at different times, allowing distribution of the sample through multiple columns, and finally reaching the helium ionization detectors of pulsed discharge, flame ionization and mass spectrometry. The results obtained show a good precision of the method used because the variability was less than 1.02% in area an…

Chromatography GasCalibration curveHydrogen sulfidechemistry.chemical_element010402 general chemistryMass spectrometryPolypropylenes01 natural sciencesBiochemistryHeliumCatalysisMass SpectrometryPoisonsAnalytical Chemistrylaw.inventionchemistry.chemical_compoundGas chromatographiclawIonizationCIENCIA DE LOS MATERIALES E INGENIERIA METALURGICAFlame ionization detectorHydrogen SulfideZiegler–Natta catalystFlame IonizationChromatography010401 analytical chemistryOrganic ChemistryGeneral MedicineHydrocarbons0104 chemical sciences08.- Fomentar el crecimiento económico sostenido inclusivo y sostenible el empleo pleno y productivo y el trabajo decente para todoschemistryAcetyleneCalibrationPolypropyleneCarbonZiegler Natta catalysts
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