Search results for "Names"

showing 10 items of 6843 documents

Direct vapor generation Fourier transform infrared spectrometric determination of ethanol in blood

1996

Abstract A new procedure is proposed for a direct determination of ethanol in plasma and whole blood. The method is based on the injection of a discrete sample volume of 10 μl into an electrically heated Pyrex glass reactor in which, at a temperature of 90 °C, the ethanol is volatilized and introduced by means of a N 2 carrier flow inside a long-path infrared gas cell and the corresponding flow analysis recording registered as a function of time. The measurement of the area of the flow injection recording, obtained from the absorbance of the transient signal in the range 1150−950 cm −1 , allows the direct quantification of ethanol upto 2 g l −1 , with a limit of detection of 0.020 g l −1 an…

Detection limitChromatographyInfraredChemistryCoefficient of variationDrop (liquid)Analytical chemistryInfrared spectroscopyPlasmaBiochemistryAnalytical ChemistryAbsorbancesymbols.namesakeFourier transformsymbolsEnvironmental ChemistrySpectroscopyAnalytica Chimica Acta
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Mid- and near-infrared determination of metribuzin in agrochemicals

2008

Abstract Two infrared-based methodologies were developed for metribuzin determination in pesticide formulations after extraction with acetonitrile. Fourier transform mid infrared (MIR) procedure was based on peak area measurements between 1692 and 1670 cm −1 corrected with a baseline fixed at 1877 cm −1 . Fourier transform near infrared (NIR) determination was made by measuring the peak area between 6498 and 6332 cm −1 corrected using a two points baseline defined between 6570 and 6212 cm −1 . Repeatability, as relative standard deviation, of 5 independent measurements at mg g −1 concentration level was 0.3% and 0.03% for MIR and NIR, respectively, and limit of detection values of 9 and 17 …

Detection limitChromatographyInfraredChemistryNear-infrared spectroscopyExtraction (chemistry)Analytical chemistryRepeatabilitychemistry.chemical_compoundsymbols.namesakeFourier transformMetribuzinsymbolsAcetonitrileSpectroscopyVibrational Spectroscopy
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Novel approach for the determination of azithromycin in pharmaceutical formulations by Fourier transform infrared spectroscopy in film-through transm…

2013

Abstract This work reports the development of a new method for the determination of azithromycin in pharmaceutical formulations employing Fourier transform infrared (FTIR) technique. The measurements were performed using a novel approach based on a film-through transmission mode. Several variables that could influence the analytical performance of the method were evaluated (solvent, nominal resolution, number of scans, mode of measurement and spectral region selected for measurement). Acetonitrile was the best solvent for the determination of azithromycin, employing the absorption band of the C O group at 1729 cm− 1. The extraction of azithromycin from the formulations was made by mechanica…

Detection limitChromatographyInfraredChemistryResolution (electron density)Analytical chemistryAnalytical ChemistrySolventsymbols.namesakechemistry.chemical_compoundFourier transformAbsorption bandsymbolsFourier transform infrared spectroscopyAcetonitrileSpectroscopyMicrochemical Journal
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Fourier transform infrared determination of imidacloprid in pesticide formulations

2004

A simple method has been developed for Fourier Transform Infrared (FTIR) determination of Imidacloprid in pesticide formulations. Samples were diluted with CHCl3 and the FTIR spectra of samples and standards were obtained at a nominal resolution of 4 cm-1 from 4000 to 900 cm-1 accumulating 25 scans. Imidacloprid determination was based on the measure of either peak area from 1577 to 1567 cm-1 or peak height at 1572 cm-1, both corrected using a horizontal baseline defined at 1900 cm-1. The limits of detection achieved, of the order of 9 µg g-1, were appropriate for the determination of Imidacloprid in commercially available formulations. FTIR results were statistically comparable to those fo…

Detection limitChromatographyMaterials scienceHPLC-UVResolution (mass spectrometry)InfraredImidaclopridGeneral ChemistryHigh-performance liquid chromatographylcsh:Chemistrysymbols.namesakechemistry.chemical_compoundFourier transformchemistrylcsh:QD1-999FTIRImidaclopridsymbolsSample preparationFourier transform infrared spectroscopypesticide formulations
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Development of a simple and low cost device for vapour phase Fourier Transform Infrared spectrometry determination of ethanol in mouthwashes

2006

Abstract A new vapour phase manifold coupled with Fourier Transform Infrared (FTIR) spectroscopy was developed for ethanol determination in mouthwashes. Two microliters of samples were injected, without any previous pre-treatment into a reactor heated at 70 °C, and the vapour phase generated transported to the FTIR spectrometer using a carrier nitrogen flow of 6 ml min−1. FTIR spectra were continuously recorded, as a function of time, by accumulating two scans and employing 8 cm−1 nominal resolution. Analytical measurements for ethanol were made in the range from 1130 to 992 cm−1 with a baseline defined between 1158 and 957 cm−1. After ethanol measurement the carrier flow was increased to 3…

Detection limitChromatographyResolution (mass spectrometry)ChemistryAnalytical chemistryInfrared spectroscopyBiochemistryFourier transform spectroscopyAnalytical Chemistrysymbols.namesakeFourier transformPhase (matter)symbolsEnvironmental ChemistryGas chromatographyFourier transform infrared spectroscopySpectroscopyAnalytica Chimica Acta
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FT–Raman spectrometry determination of Malathion in pesticide formulations

2003

Abstract A fast and environmentally friendly method has been developed for Fourier transform–Raman (FT–Raman) spectrometry determination of Malathion in pesticide emulsifiable concentrate formulations. The method is based on the measurement of intensity peak height values at 1737 cm −1 Raman shift corrected using a baseline defined at 1900 cm −1 . Samples were diluted with CHCl 3 and the FT–Raman spectra collected in back-scattering mode over 3.3 min at a nominal resolution of 4 cm −1 accumulating 50 scans per spectra and using a laser power of 1250 mW. The developed procedure provided a limit of detection of 1.8% w/w in the original sample. Results found by FT–Raman spectrometry were stati…

Detection limitChromatographyResolution (mass spectrometry)ChemistryAnalytical chemistryInfrared spectroscopyMass spectrometryFourier transform spectroscopyAnalytical Chemistrysymbols.namesakeFourier transformsymbolsGas chromatographyRaman spectroscopyTalanta
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An Infrared Method, with Reduced Solvent Consumption, for the Determination of Chlorsulfuron in Pesticide Formulations

2003

A simple method has been developed for the determination of Chlorsulfuron in pesticide formulations by Fourier Transform Infrared (FTIR). Samples were diluted with CHCl3− , and the FTIR spectra of the samples and standards were obtained at a nominal resolution of 4 cm− 1 from 4000 to 900 cm− 1 with the accumulation of 25 scans. Chlorsulfuron determination was based on the measurement of peak area values from 1373 to 1363 cm− 1 which were corrected by use of a two points baseline defined from 1401 to 1302 cm− 1. The limit of detection achieved, which was of the order of 6 µg g− 1, was appropriate for the determination of Chlorsulfuron in commercially available formulations. FTIR results were…

Detection limitChromatographyResolution (mass spectrometry)ChemistryInfraredAnalytical chemistryPesticideHigh-performance liquid chromatographyAtomic and Molecular Physics and OpticsAnalytical ChemistrySolventsymbols.namesakeFourier transformsymbolsFourier transform infrared spectroscopySpectroscopySpectroscopy Letters
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DETECTION LIMITS FOR NATURAL CIRCULAR-DICHROISM OF CHIRAL COMPLEXES IN THE X-RAY RANGE

1993

Whereas both Magnetic Circular Dichroism and Faraday Rotation studies have been successfully carried out at the K-, L- and M-absorption edges of metal atoms in ferromagnetic systems, Natural optical activity of chiral complexes has not yet been detected quite unambiguously in the X-ray range. We review a number of theoretical arguments which confirm that the optical asymmetry factor gσ should be very small in the X-ray range for unoriented powdered samples, especially at the K-absorption edges. This stimulating challenge prompted us to start an intensive programme of measurements aimed at detecting natural circular dichroism in both the soft and “firm” X-ray ranges. Although some of our ex…

Detection limitCircular dichroismRange (particle radiation)Magnetic circular dichroismChemistrymedia_common.quotation_subjectXAFSSOFT-X-RAY SPECTROSCOPYGeneral EngineeringAnalytical chemistryX-rayGeneral Physics and AstronomyOPTICAL-ACTIVITYAsymmetryMolecular physicssymbols.namesakeROTATORY STRENGTHFerromagnetismNATURAL CDFaraday effectsymbolsABSORPTIONOPTICAL ASYMMETRYTRANSITION-METAL COMPLEXESmedia_commonJapanese journal of applied physics part 1-Regular papers short notes & review papers
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Flow injection Fourier transform infrared determination of caffeine in coffee

1999

Abstract A fully automatized procedure has been developed for the Fourier transform infrared (FT-IR) spectroscopic determination of caffeine in coffee samples. The method involves the on-line extraction of caffeine with CHCl3. Samples, weighed inside empty PTFE cartridges of 0.5 cm internal diameter (i.d.) and 1.5 ml volume, were humidified with four drops of 0.25 M NH3. The cartridge was installed in a flow manifold, in which samples were extracted in a closed-flow system with 1 ml CHCl3 during 6 min. Four hundred microliters of the extract were introduced in a microflow cell and absorbance measured as a function of time at 1659 cm−1, with a baseline established between 1900 and 830 cm−1, …

Detection limitFlow injection analysisChromatographyAnalytical chemistryStandard solutionAbsorbanceCartridgechemistry.chemical_compoundsymbols.namesakeFourier transformchemistrysymbolsSample preparationCaffeineSpectroscopyVibrational Spectroscopy
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Microwave-assisted vapour-generation Fourier transform infrared spectrometric determination of carbonate in waters

1998

Abstract A microwave-assisted vapour-generation Fourier transform infrared spectrometric procedure is proposed for the determination of total carbonate in waters. The method is based on the simultaneous injection of 100 μl of sample and 300 μl of 0.1 M nitric acid in a two-channel manifold with a merging zone; a coil located inside a microwave oven encourages the removal of CO 2 . The carbon dioxide is separated from the distilled water employed as carrier by means of gas–liquid separator and is introduced by a nitrogen carrier flow inside a long-path infrared absorption gas cell, from which the corresponding flow analysis recording is registered as a function of time in the wavenumber rang…

Detection limitMicrowave ovenAnalytical chemistryInfrared spectroscopyBiochemistryAnalytical Chemistrychemistry.chemical_compoundsymbols.namesakeFourier transformchemistryDistilled waterNitric acidsymbolsEnvironmental ChemistryCarbonateFourier transform infrared spectroscopySpectroscopyAnalytica Chimica Acta
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