Search results for "Calibration"

showing 10 items of 890 documents

Spectral calibration and atmospheric correction of ultra-fine spectral and spatial resolution remote sensing data. Application to CASI-1500 data

2007

Imaging spectrometers operating in the solar spectrum measure the upwelling reflected solar radiation, and are an important tool in the bio/geochemical characterization of the Earth system. Surface reflectance is usually the starting point for the retrieval of biophysical parameters from remote measurements. Reliable radiometric and spectral calibrations and accurate atmospheric correction are mandatory in the interpretation of the surface reflectance. A complete surface reflectance retrieval scheme specifically designed for ultra-fine spectral resolution (bandwidth from 10 to 2 nm) and spatial resolution (pixel size less than 10 m) imaging spectrometers is presented in this work. The asses…

Spectrometerbusiness.industryAtmospheric correctionSoil Science550 - Earth sciencesGeologyImaging spectroscopyOpticsCalibrationRadiative transferRadiometryEnvironmental scienceComputers in Earth SciencesSpectral resolutionbusinessImage resolutionRemote sensingRemote Sensing of Environment
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Vicarious calibration of MERIS over dark waters in the near infrared

2005

Abstract We propose to evaluate the calibration of MERIS (MEdium Resolution Imaging Spectrometer) over dark waters in the near infrared. We work with 5 months of data, from July to November 2003, over five world sites: Venice and Lampedusa in Italy, El Arenosillo in Spain, MOBY/Lanai and CalCOFI/San Nicolas in the United States. The sites are all equipped with a CIMEL station that forms part of the AERONET network. The basic idea is to associate CIMEL sky radiance measurements with MERIS level-1b data in a twin geometry which corresponds to the same scattering angle. This vicarious calibration relies on an accurate description of the atmospheric scattering based on the CIMEL measurements. A…

Spectrometermedia_common.quotation_subjectNear-infrared spectroscopyImaging spectrometerDiffuse sky radiationSoil ScienceGeologyAERONET[SDE.MCG] Environmental Sciences/Global Changes[ SDE.MCG ] Environmental Sciences/Global Changes[SDU.STU.CL] Sciences of the Universe [physics]/Earth Sciences/ClimatologySkyCalibrationRadianceEnvironmental scienceComputers in Earth Sciences[ SDU.STU.CL ] Sciences of the Universe [physics]/Earth Sciences/ClimatologyRemote sensingmedia_common
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Liquid chromatography–electrospray quadrupole ion-trap mass spectrometry of nine pesticides in fruits

2004

A liquid chromatographic method, with electrospray ionization tandem mass spectrometry (LC-ESI-MS-MS), has been developed for determining acrinathrin, carbosulfan, cyproconazole, lambda-cyhalothrin, kresoxim methyl, pyrifenox, pyriproxyfen, propanil, and tebufenpyrad in fruits. The ions prominent in ESI spectra were [M + H]+ and [M + Na]+. In the mass analyzer, collision-induced dissociation fragmentation involved common pathways, for example, product ions of [M + H]+ resulted from the cleavage of the carbamic group or an oxygen bound. The utility of the method is demonstrated by the analysis of crude extracts obtained by matrix solid-phase dispersion (MSPD) using C18 as dispersant and dich…

Spectrometry Mass Electrospray IonizationElectrosprayChromatographyChemistryElectrospray ionizationOrganic ChemistryGeneral MedicineTandem mass spectrometryMass spectrometryBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryMatrix (chemical analysis)FruitCalibrationSolid phase extractionIon trapPesticidesChromatography LiquidJournal of Chromatography A
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New perspectives on diastereoselective determination of hexabromocyclododecane traces in fish by ultra high performance liquid chromatography-high re…

2014

a b s t r a c t A new analytical method is presented for diastereoisomer-specific identification and quantitation of hexabromocyclododecanes (HBCD) in fish samples. The method is based on extraction of the target analytes from samples with a mixture of organic solvents, with further three-stage clean-up includ- ing destructive removal of matrix components with sulphuric acid and acid-impregnated silica gel, and Florisil adsorption column chromatography. Ultra high performance liquid chromatography (UPLC) cou- pled with high resolution (HR) Orbitrap mass spectrometry featuring heated electrospray ionization (HESI-II) interface operated in negative ion mode was employed for the identification…

Spectrometry Mass Electrospray IonizationSalmo salarAnalytical chemistrySilica GelMass spectrometryOrbitrapBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrylaw.inventionMatrix (chemical analysis)chemistry.chemical_compoundColumn chromatographylawAnimalsChromatography High Pressure LiquidFlame RetardantsDetection limitHexabromocyclododecaneChromatographyChemistryOrganic ChemistryStereoisomerismGeneral MedicineRepeatabilityHydrocarbons BrominatedCalibrationWater Pollutants ChemicalJournal of chromatography. A
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Chemometric determination of arsenic and lead in untreated powdered red paprika by diffuse reflectance near-infrared spectroscopy.

2008

It has been evaluated the potential of near-infrared (NIR) diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) as a way for non-destructive measurement of trace elements at microg kg(-1) level in foods, with neither physical nor chemical pre-treatment. Predictive models were developed using partial least-square (PLS) multivariate approaches based on first-order derivative spectra. A critical comparison of two spectral pre-treatments, multiplicative signal correction (MSC) and standard normal variate (SNV) was also made. The PLS models built after using SNV provided the best prediction results for the determination of arsenic and lead in powdered red paprika samples. Relativ…

Spectroscopy Near-InfraredDiffuse reflectance infrared fourier transformChemistryNear-infrared spectroscopyAnalytical chemistryInfrared spectroscopychemistry.chemical_elementBiochemistryFourier transform spectroscopyAnalytical ChemistryArsenicChemometricsLeadPartial least squares regressionCalibrationEnvironmental ChemistrySpectroscopyCapsicumSpectroscopyArsenicAnalytica chimica acta
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Near Infrared Spectroscopy Detection and Quantification of Herbal Medicines Adulterated with Sibutramine.

2015

There is an increasing demand for herbal medicines in weight loss treatment. Some synthetic chemicals, such as sibutramine (SB), have been detected as adulterants in herbal formulations. In this study, two strategies using near infrared (NIR) spectroscopy have been developed to evaluate potential adulteration of herbal medicines with SB: a qualitative screening approach and a quantitative methodology based on multivariate calibration. Samples were composed by products commercialized as herbal medicines, as well as by laboratory adulterated samples. Spectra were obtained in the range of 14,000-4000 per cm. Using PLS-DA, a correct classification of 100% was achieved for the external validatio…

Spectroscopy Near-InfraredInjury controlTraditional medicinebusiness.industryQuantitative methodologyNear-infrared spectroscopyExternal validationPoison controlMultivariate calibrationDiscriminant AnalysisPathology and Forensic MedicinePartial least squares regressionAppetite DepressantsGeneticsmedicineLinear ModelsPlant PreparationsbusinessDrug ContaminationCyclobutanesSibutraminemedicine.drugJournal of forensic sciences
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Nondestructive Direct Determination of Heroin in Seized Illicit Street Drugs by Diffuse Reflectance near-Infrared Spectroscopy

2008

A new method has been developed for the fast and nondestructive direct determination of heroin in seized street illicit drugs using partial least-squares regression analysis of diffuse reflectance near-infrared spectra. Data were obtained from untreated samples placed in standard glass chromatography vials. A heterogeneous population of 31 samples, previously analyzed by a reference method, was employed to build the calibration model and to have a separated validation set. Based on the use of zero-order data for a calibration set of 21 samples, after standard normal variate and quadratic linear removed baseline correction (detrending), in the wavelength range from 1111 to 1647 nm, 8 PLS fac…

Spectroscopy Near-InfraredMean squared errorIllicit DrugsChemistryDirect methodStreet drugsNear-infrared spectroscopyAnalytical chemistryReproducibility of ResultsResidualAnalytical ChemistryHeroinHeterogeneous populationCalibrationCalibrationCluster AnalysisDiffuse reflectionLeast-Squares AnalysisAnalytical Chemistry
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The performance of the cryogenic buffer-gas stopping cell of SHIPTRAP

2018

Direct high-precision mass spectrometry of the heaviest elements with SHIPTRAP, at GSI in Darmstadt, Germany, requires high efficiency to deal with the low production rates of such exotic nuclides. A second-generation gas stopping cell, operating at cryogenic temperatures, was developed and recently integrated into the relocated system to boost the overall efficiency. Offline measurements using 223Ra and 225Ac recoil-ion sources placed inside the gas volume were performed to characterize the gas stopping cell with respect to purity and extraction efficiency. In addition, a first online test using the fusion-evaporation residue 254No was performed, resulting in a combined stopping and extrac…

Speichertechnik - Abteilung BlaumNuclear and High Energy PhysicsMaterials scienceDIRECT MASS MEASUREMENTSProtonBuffer gaschemistry.chemical_elementPenning trapsMass spectrometry7. Clean energy01 natural sciencesFusion-evaporation reaction productsNuclear physicsIonization0103 physical sciencesCalibrationStopping and extraction efficiencyNuclide010306 general physicsInstrumentationCALIBRATION[PHYS]Physics [physics]nobeliumSPECTROSCOPYMass spectrometry010308 nuclear & particles physicsTransfermium elementsCryogenic gas stopping cellExtraction timeHEAVIEST ELEMENTSchemistryIONIZATIONNobeliumOrder of magnitude
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Calibration of high voltages at the ppm level by the difference of $^{83\mathrm{m}}$Kr conversion electron lines at the KATRIN experiment

2018

The neutrino mass experiment KATRIN requires a stability of 3 ppm for the retarding potential at − 18.6 kV of the main spectrometer. To monitor the stability, two custom-made ultra-precise high-voltage dividers were developed and built in cooperation with the German national metrology institute Physikalisch-Technische Bundesanstalt (PTB). Until now, regular absolute calibration of the voltage dividers required bringing the equipment to the specialised metrology laboratory. Here we present a new method based on measuring the energy difference of two [superscript 83m]Kr conversion electron lines with the KATRIN setup, which was demonstrated during KATRIN’s commissioning measurements in July 2…

Speichertechnik - Abteilung BlaumPhysics - Instrumentation and DetectorsPhysics and Astronomy (miscellaneous)FOS: Physical sciences7. Clean energy01 natural sciencesNuclear physics0103 physical sciencesCalibrationddc:530[PHYS.PHYS.PHYS-INS-DET]Physics [physics]/Physics [physics]/Instrumentation and Detectors [physics.ins-det]010306 general physicsEngineering (miscellaneous)[ PHYS.PHYS.PHYS-INS-DET ] Physics [physics]/Physics [physics]/Instrumentation and Detectors [physics.ins-det]PhysicsTeoría de los quantaSpectrometer010308 nuclear & particles physicsPhysicsVoltage dividerInstrumentation and Detectors (physics.ins-det)MetrologyNeutrinoEnergy (signal processing)VoltageKATRIN
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Elimination of the unknown irrelevant matrix absorbance by using the H-Point Standard Additions Method (HPSAM)

1994

It is demonstrated how the H-Point Standard Additions Method (HPSAM) using DeltaA as analytical signal (from data at three previously selected wavelengths) is only related with analyte concentration when unknown irrelevant matrix absorbance is present. The method is compared with the most common previously reported methods, such as derivative spectroscopy or the compensation method. The obtained results show that the proposed HPSAM leads to the same found concentration of analyte as the other reported methods, except detection limits and standard deviation for six replicates which are lower, because of the use of absorbance data (instead of first derivative data as usual). In addition, the …

Standard curveDetection limitMatrix (chemical analysis)AbsorbanceAnalyteChemistryStandard additionAnalytical chemistryCalibrationStandard deviationAnalytical ChemistryTalanta
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