Search results for "Infrared"

showing 10 items of 2110 documents

Vibrational Spectrometry Strategies for Quality Control of Procymidone in Pesticide Formulations

2005

Abstract Two vibrational spectrometry–based methodologies were developed for procymidone determination in wettable powdered pesticide formulations. The Fourier‐transform infrared (FTIR) procedure was based on the selective extraction of procymidone by chloroform and determination by peak area measurement between 1451 and 1441 cm−1, using a baseline correction established between 1490 and 1410 cm−1, and a precision of 0.4% and a limit of detection of 0.01% w/w procymidone for a sample mass of 25 mg were obtained. For FT‐Raman determination, the selected conditions were peak area measurement between 1005 and 995 cm−1 Raman shift, with a baseline correction fixed between 1030 and 947 cm−1, and…

Detection limitChloroformChromatographyExtraction (chemistry)Analytical chemistryMass spectrometryAtomic and Molecular Physics and OpticsAnalytical Chemistrychemistry.chemical_compoundsymbols.namesakechemistryReagentsymbolsProcymidoneFourier transform infrared spectroscopyRaman spectroscopySpectroscopySpectroscopy Letters
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Direct determination of benzene in gasoline by flow-injection Fourier transform infrared spectrometry

1993

Abstract A Fourier transform infrared spectrometric procedure for the automated determination of benzene in gasoline was developed, based on the use of flow-injection analysis. The method permits the direct determination of benzene without any pretreatment of samples, with a limit of detection of 0.02% (v/v) and a relative standard deviation of ca. 1% [for five independent analyses of a diluted sample containing a 0.4% (v/v) of benzene]. Results found by direct analysis agreed with those obtained by off-line and on-line standard addition methods. A rapid quality control procedure was developed, based on the on-line injection of gasoline samples (diluted 1 + 9 in hexane) into a carrier strea…

Detection limitChromatographyAnalytical chemistryInfrared spectroscopyBiochemistryAnalytical ChemistryHexanechemistry.chemical_compoundsymbols.namesakeFourier transformchemistryStandard additionsymbolsEnvironmental ChemistryGas chromatographyGasolineBenzeneSpectroscopyAnalytica Chimica Acta
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Determination of edible oil parameters by near infrared spectrometry

2006

Abstract A chemometric method has been developed for the determination of acidity and peroxide index in edible oils of different types and origins by using near infrared spectroscopy (NIR) measurements. Different methods for selecting the calibration set, after an hierarchical cluster analysis, were applied. After discrimination of olive oils from maize, seed and sunflower, the prediction capabilities of partial least squares (PLS) multivariate calibration of NIR data were evaluated. Several preprocessing alternatives (first derivative, multiplicative scatter correction, vector normalization, constant offset elimination, mean centering and standard normal variate) were investigated by using…

Detection limitChromatographyAnalytical chemistryNear-Infrared SpectrometryBiochemistryPeroxideSunflowerAnalytical ChemistryChemometricschemistry.chemical_compoundchemistryPartial least squares regressionCalibrationEnvironmental ChemistryPeroxide valueSpectroscopyAnalytica Chimica Acta
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Quality control of Metamitron in agrochemicals using Fourier transform infrared spectroscopy in the middle and near range

2006

Abstract Two vibrational spectrometry-based methodologies were developed for Metamitron determination in pesticide formulations. Fourier transform-middle infrared (FT-MIR) procedure was based on the extraction of Metamitron by CHCl 3 and latter determination by peak area measurement between 1556 and 1533 cm −1 , corrected with a two points baseline established from 1572 to 1514 cm −1 . Fourier transform-near infrared (FT-NIR) determination was made after the extraction of Metamitron in acetonitrile and measuring the peak area between 6434 and 6394 cm −1 corrected using a two points baseline defined between 6555 and 6228 cm −1 . Repeatability, as relative standard deviation, of 5 independent…

Detection limitChromatographyChemistryAnalytical chemistryInfrared spectroscopyRepeatabilityMass spectrometryBiochemistryFourier transform spectroscopyAnalytical Chemistrysymbols.namesakeFourier transformsymbolsEnvironmental ChemistrySample preparationFourier transform infrared spectroscopySpectroscopyAnalytica Chimica Acta
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Determination of Paint Solvents by Vapour Phase Fourier Transform Infrared Spectrometry.

1997

Abstract A fast procedure has been developed for the direct determination of paint solvents. The method is based on the injection of small volumes of untreated solvent mixtures into a heated Pyrex glass reactor in which the sample is volatilized and introduced by means of a flow of nitrogen into an IR multiple pass gas cell and the spectrum in the mid-IR region is registered as a function of time. Data found for samples are interpolated in calibration graphs obtained by injecting different volumes of pure compounds which constitute the solvent mixture. A methylisobutylketone (MIBK) toluene mixture was used as test system to develop the proposed procedure. The method provides a limit of dete…

Detection limitChromatographyChemistryAnalytical chemistryInfrared spectroscopychemistry.chemical_elementPaint thinnerNitrogenTolueneAtomic and Molecular Physics and OpticsAnalytical ChemistrySolventchemistry.chemical_compoundPhase (matter)CalibrationSpectroscopySpectroscopy Letters
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Simultaneous determination of Folpet and Metalaxyl in pesticide formulations by flow injection Fourier transform infrared spectrometry

2003

Fourier transform infrared (FTIR) spectrometric methodology has been developed for the simultaneous determination of Folpet and Metalaxyl in pesticide formulations. The method involves the extraction of both active principles by sonication of the sample with CHCl3 and direct measurement of the absorbance using peak height values at 1798 cm −1 corrected with a baseline defined at 1810 cm −1 for Folpet, and peak area data established from 1677 to 1667 cm −1 corrected using a baseline from 1692 to 1628 cm −1 for Metalaxyl. Limits of detection (3 s) values of 17 and 16 gg −1 were found for Folpet and Metalaxyl, respectively, with results comparable with those found by liquid chromatography with…

Detection limitChromatographyChemistryExtraction (chemistry)Analytical chemistryInfrared spectroscopyBiochemistryFourier transform spectroscopyAnalytical ChemistryAbsorbancesymbols.namesakechemistry.chemical_compoundFourier transformsymbolsEnvironmental ChemistryFourier transform infrared spectroscopyMetalaxylSpectroscopyAnalytica Chimica Acta
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Near infrared determination of Diuron in pesticide formulations

2005

Abstract A simple, fast and environmentally friendly near infrared (NIR)-based methodology was developed for Diuron determination in pesticide formulations. This methodology was based on the pesticide extraction with acetonitrile and subsequent transmittance measurement determination by peak area measurement between 2021 and 2047 nm, corrected with a single point baseline established at 2071 nm. The repeatability, as relative standard deviation of five independent analysis of a 15.3 mg g −1 Diuron standard was 0.03% and the limit of detection 0.013 mg g −1 . The reagent consumption was clearly reduced in front of a chromatographic reference procedure from 39.1 ml acetonitrile per sample, re…

Detection limitChromatographyChemistryNear-infrared spectroscopyExtraction (chemistry)Analytical chemistryRepeatabilityBiochemistryFourier transform spectroscopyAnalytical Chemistrychemistry.chemical_compoundReagentEnvironmental ChemistrySample preparationAcetonitrileSpectroscopyAnalytica Chimica Acta
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Fourier transform infrared determination of Fluometuron in pesticide formulations

2003

Abstract A single method has been developed for Fourier transform infrared (FTIR) determination of Fluometuron in pesticide formulations. Samples were ultrasonically shaken with CHCl3 for 5 min and the FTIR spectra of sample extracts and standards were obtained at a nominal resolution of 4 cm−1 from 4000 to 900 cm−1 accumulating 25 scans. Fluometuron determination is based on the measure of peak area from 1342 to 1321 cm−1 corrected using a baseline defined from 1352 to 1294 cm−1. This procedure provided a limit of detection of 6.5 μg g−1, a sensitivity of 0.852 a.u. g mg−1 for a pathlength of 0.11 mm, a relative standard deviation of 1.6% for three analysis of a sample containing 50.4% (w/…

Detection limitChromatographyChloroformFluometuronResolution (mass spectrometry)Analytical chemistryHigh-performance liquid chromatographychemistry.chemical_compoundsymbols.namesakeFourier transformchemistryLinear regressionsymbolsFourier transform infrared spectroscopySpectroscopyVibrational Spectroscopy
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Improved detection limit for ammonium/ammonia achieved by Berthelot's reaction by use of solid-phase extraction coupled to diffuse reflectance spectr…

2005

Abstract The proposed procedure is based on the extraction of the indothylmol blue into C 18 solid-phase extraction (SPE) membranes and direct quantification on the membrane surface by diffuse reflectance spectroscopy. The analytical performance of the proposed method has been evaluated for standard solutions of ammonium using reflectance values, R , as well as the Kubelka–Munk function, F ( R ). The results have been compared with those obtained by the conventional method, which uses UV–vis absorption spectroscopy with a sensor-based method. The described methodology provided satisfactory linearity and reproducibility within the ammonium concentration intervals 25–250 μg L −1 and 25–500 μg…

Detection limitChromatographyDiffuse reflectance infrared fourier transformExtraction (chemistry)Analytical chemistryStandard solutionBiochemistryAnalytical ChemistryAmmoniachemistry.chemical_compoundchemistryEnvironmental ChemistrySample preparationAmmoniumSolid phase extractionSpectroscopyAnalytica Chimica Acta
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On-line solvent recycling: a tool for the development of clean analytical chemistry in flow injection Fourier transform infrared spectrometry. Determ…

1998

Abstract A flow injection strategy has been developed for the direct determination of ketoprofen in pharmaceuticals by Fourier transform infrared spectrometry also incorporating a distillation unit which allows the carbon tetrachloride employed to dissolve samples and standards and used as a carrier to be recovered on-line. The system developed permits a drastic reduction of reagent consumption and easy and fast sampling and cleaning of the measurement cell. For the quantification of ketoprofen in pharmaceuticals the carbonyl bands at 1712 and 1666 cm −1 were employed and the developed method provided a 3 σ limit of detection of 0.04 mg ml −1 , a dynamic range up to 10 mg ml −1 and typical …

Detection limitChromatographyDynamic rangeChemistryAnalytical chemistryInfrared spectroscopyBiochemistryAnalytical Chemistrylaw.inventionSolventsymbols.namesakeFourier transformlawReagentsymbolsEnvironmental ChemistryQuantitative analysis (chemistry)DistillationSpectroscopyAnalytica Chimica Acta
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