Search results for "Spectroscopy"

showing 10 items of 10293 documents

Some observations on the sensitivity of flow-injection techniques for atomic absorption spectrophotometry

1989

Abstract Different strategies for coupling flow-injection manifolds to atomic absorption spectrometers in order to obtain better sensitivity are compared. Using a T-connector interface, different carriers and flow compensation solvents have been assayed in an attempt to improve the sensitivity of flow-injection analysis. Manganese and copper determinations in sewage sludge have been used as a test system and the analytical parameters of both batch and flow-injection methods are compared.

Detection limitSpectrometerAnalytical chemistrychemistry.chemical_elementManganeseCopperAnalytical ChemistryVolumetric flow ratelaw.inventionchemistrylawSensitivity (control systems)Atomic absorption spectroscopySpectroscopySludgeMicrochemical Journal
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Application of stable isotopes and AF4/ICP-SFMS for simultaneous tracing and quantification of iron oxide nanoparticles in a sediment–slurry matrix

2016

One major challenge in nanomaterial analysis, especially in complex environmental matrices, is the unambiguous differentiation between natural and engineered nanomaterials (ENMs). Particularly with regard to the investigation of ENM's/engineered nanoparticle's (ENPs) fate, analytical methods are needed allowing for tracing and sensitive quantification. Several ENPs are metal-based and contain elements being omnipresent in environmental matrices (e.g., Al, Ti, Zn, Fe and non-metal Si) – hence, high background levels of these elements are expected, compromising sensitive detection. In this work we developed successfully a combined approach of stable isotope labeling (tracing) and reverse post…

Detection limitStable isotope ratioElution010401 analytical chemistryRadiochemistryAnalytical chemistry010501 environmental sciencesIsotope dilution01 natural sciencesSilver nanoparticle0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundColloidchemistryInductively coupled plasma mass spectrometrySpectroscopyIron oxide nanoparticles0105 earth and related environmental sciencesJournal of Analytical Atomic Spectrometry
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Fast, low-level detection of strontium-90 and strontium-89 in environmental samples by collinear resonance ionization spectroscopy

1993

Environmental assessment in the wake of a nuclear accident requires the rapid determination of the radiotoxic isotopes 89Sr and 90Sr. Useful measurements must be able to detect 108 atoms in the presence of about 1018 atoms of the stable, naturally occurring isotopes. This paper describes a new approach to this problem using resonance ionization spectroscopy in collinear geometry, combined with classical mass separation. After collection and chemical separation, the strontium from a sample is surface-ionized and the ions are accelerated to an energy of about 30 keV. Initially, a magnetic mass separator provides an isotopic selectivity of about 106. The ions are then neutralized by charge exc…

Detection limitStrontiumIsotopeAnalytical chemistrychemistry.chemical_elementAtomic and Molecular Physics and OpticsAnalytical ChemistryIonsymbols.namesakechemistryExcited stateRydberg atomPhysics::Atomic and Molecular ClustersRydberg formulasymbolsPhysics::Atomic PhysicsAtomic physicsSpectroscopyInstrumentationSpectroscopySpectrochimica Acta Part B: Atomic Spectroscopy
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Direct ATR-FTIR determination of sucrose in beet root.

2000

A simple and fast procedure has been developed for the direct determination of sucrose in beet root samples through attenuated total reflectance Fourier transform infrared absorbance measurements (ATR-FTIR) at 1056 cm(-1) with a baseline established between 1187 and 887 cm(-1). The method only requires a previous crushing or liquefaction of samples and it is free from matrix effects and from the interference of minoritary sugars and fermentation molecules. Aqueous solutions of sucrose can be used as standards and recovery values from 101 to 103% were found for spiked concentration levels from 3.5 to 10.5% (w/w). The limit of detection provided by this method corresponds to 0.15% (w/w) of su…

Detection limitSucroseAqueous solutionbiologyAnalytical chemistryInfrared spectroscopybiology.organism_classificationAnalytical ChemistryAbsorbancechemistry.chemical_compoundchemistryAttenuated total reflectionSugar beetFourier transform infrared spectroscopyTalanta
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PLS-NIR determination of total sugar, glucose, fructose and sucrose in aqueous solutions of fruit juices

1997

Abstract An analytical procedure has been developed for the direct determination of sugars in fruit juice samples. The method is based on the partial least-squares (PLS) treatment of first derivative near infrared (NIR) spectroscopic data obtained between 1200 and 2450 nm, using 1 mm pathlength cell and a multicomponent calibration set, including seven binary mixtures and 10 ternary mixtures of glucose, fructose and sucrose. The limit of detection values found are of the order of 0.2 g/100 ml for total sugar and 0.2, 0.4 and 0.5 g/100 ml for glucose, fructose and sucrose, respectively. Relative standard deviation values obtained vary from 0.4% to 2.3% for six independent measurements of ind…

Detection limitSucroseChromatographyAqueous solutionNear-infrared spectroscopyCalibration setFructoseBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryEnvironmental ChemistryFruit juiceSugarSpectroscopyAnalytica Chimica Acta
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Vapor-phase introduction of alkyltin compounds in atomic absorption spectrophotometry

1990

Abstract Different systems for the introduction of alkyltin compounds in atomic absorption spectrophotometry using the vapor-phase introduction approach have been compared. Samples and standards were introduced in both quartz cell and flame atomizer using a vertical and a horizontal reactor. The better sensitivity was obtained with the quartz cell and the horizontal reactor.

Detection limitVolatilisationlawChemistryVapor phaseAnalytical chemistryTrace analysisAtomic absorption spectroscopyQuartzSpectroscopyAnalytical Chemistrylaw.inventionMicrochemical Journal
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Derivative Fourier transform infrared spectrometric determination of ethanol in alcoholic beverages

1994

Abstract A derivative Fourier transform infrared (FT-TR) spectrometric procedure was developed for the direct determination of ethanol in alcoholic beverages, from beers to spirit samples. The method is based on first-order derivative FT-IR measurements between the peak at 1052 cm −1 and the valley at 1040 cm −1 , which are present in aqueous solutions and alcoholic beverages, by using a micro flow transmittance cell with ZnSe windows and a spacer of 0.029 mm. The method involves the accumulation of ten scans and provides accurate results in the determination of ethanol in alcoholic beverages without requiring any previous chemical treatment of the sample or a previous separation or extract…

Detection limitWineAqueous solutionChromatographyEthanolExtraction (chemistry)Analytical chemistryInfrared spectroscopyDerivativeBiochemistryAnalytical Chemistrysymbols.namesakechemistry.chemical_compoundFourier transformchemistrysymbolsEnvironmental ChemistrySpectroscopyAnalytica Chimica Acta
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Determination of glyphosate and aminomethylphosphonic acid in natural water using the capillary electrophoresis combined with enrichment step

2005

A previously elaborated capillary electrophoresis (CE) method used for the determination of glyphosate and aminomethylphosphonic acid (AMPA) was slightly modified in order to improve the sensitivity. However, detection limits attained (5 μg mL−1 for glyphosate and 4 μg mL−1 for AMPA) were still not satisfactory for analytical purposes, thus the addition of a preconcentration step before the CE analysis was proposed. AMBERLITE®IRA-900, a strong anion-exchange resin, was used to preconcentrate both analytes in environmental aqueous samples. The experimental conditions optimised in a previous work were readapted, by decreasing the eluent concentration due to CE limitations. Satisfactory result…

Detection limitaminomethylphosphonic acid (AMPA)Chromatographyanion-exchange resinsChemistrycapillary electrophoresisBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundColumn chromatographyCapillary electrophoresisglyphosateGlyphosateenvironmental analysisUltrapure waterEnvironmental ChemistryAminomethylphosphonic acidSample preparationHPLCSpectroscopyAnalytica Chimica Acta
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Fourier transform infrared spectrometric determination of Ziram.

2001

A procedure has been developed for vapour-phase Fourier transform infrared determination of Ziram, a dithiocarbamate pesticide. The method is based on the evolution of CS(2), after decomposition of the dithiocarbamate with diluted H(2)SO(4) at 50 degrees C. The CS(2) evolved was swept by a carrier flow of nitrogen to a laboratory-made infrared gas cell of 39 mm pathlength and 490 mul volume. The signals were registered as a function of time. The area of peaks obtained from absorbance measurement in the wavenumber range between 1600 and 1450 cm(-1) were interpolated in a calibration line established from Ziram standards treated in the same way as samples. The method provided an absolute limi…

Detection limitchemistry.chemical_classificationAnalyteZiramInfraredAnalytical chemistryInfrared spectroscopyAnalytical ChemistryAbsorbancesymbols.namesakechemistry.chemical_compoundFourier transformchemistrysymbolsDithiocarbamateTalanta
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Simultaneous determination of third-generation synthetic cannabinoids in oral fluids using cyclodextrin-silica porous sorbents

2022

Abstract A microporous material made of cyclodextrin units covalently immobilized into a silica network has found an innovative bioanalytical application in the sample clean-up and simultaneous isolation of three synthetic cannabinoids (ADB-CHMICA, MMB-CHMICA, and MDMB-CHMCZCA) from human oral fluid through solid-phase extraction. The subsequent quantitation is carried out using liquid chromatography coupled to fluorescence detection. The optimized experimental procedure gives recoveries ranging from 76% to 96% in oral fluid samples spiked with the studied cannabinoids at the µg L-1 level. High selectivity is obtained through the extraction procedure due to the presence of cyclodextrin in t…

Detection limitchemistry.chemical_classificationBioanalysisChromatographyCyclodextrinExtraction (chemistry)SorptionMicroporous materialAnalytical ChemistrychemistrySynthetic cannabinoidsmedicinePorous mediumSpectroscopymedicine.drugMicrochemical Journal
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