Search results for "Spectroscopy"
showing 10 items of 10293 documents
Direct determination of lead in human milk by electrothermal atomic absorption spectrometry
1999
Abstract Infants are particularly sensitive to the toxic effects of lead. Since milk is their only or main food it is important to know the contribution of milk to lead intake. The purpose of this study was to develop a direct method for determining the lead content of human milk by electrothermal atomic absorption spectrometry when a deuterium lamp is the only background correction available. The optimum conditions for lead determination in breast milk: sample dilution in Triton ×-100, modifier (75 μg of palladium) and nitric acid contents (2%) and the graphite furnace program (mineralization: 1100°C; atomization: 2300°C) were selected. The analytical parameters are: linearity (20–300 ng m…
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…
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…
Solid-phase FT-Raman determination of caffeine in energy drinks
2005
Abstract A solid-phase vibrational spectrometry-based methodology (solid-phase Fourier transform-Raman spectrometry, SP-FT-Raman) has been developed for caffeine determination in commercial energy drink samples. The Raman spectra of caffeine, fixed on a C18 solid phase packed into a glass tube of 5 mm i.d., was obtained directly between 3500 and 70 cm −1 . In order to quantify caffeine, Raman intensity between 573 and 542 cm −1 corrected using a baseline defined between 580 and 540 cm −1 was used. A repeatability of 3%, as relative standard deviation of five analysis of a 200 mg l −1 concentration, and a limit of detection of 18 mg l −1 were obtained. The SP-FT-Raman procedure provides a sa…
Simultaneous determination of As, Cd, Cr and Pb in aqua regia digests of soils and sediments using electrothermal atomic absorption spectrometry and …
2002
A method was developed for the simultaneous multi-element determination of As, Cd, Cr and Pb in aqua regia digests of soils and sediments using an electrothermal atomic absorption spectrometer with a transversely heated graphite atomizer and longitudinal Zeeman-effect background correction. A fast furnace program with no pyrolysis stage or chemical modifier was used, and the total duration of the time-temperature program of the graphite furnace was 45 s. The method detection limits calculated from blank samples were 9.5 μg l−1, 0.18 μg l−1, 6.2 μg l−1 and 2.5 μg l−1 for As, Cd, Cr and Pb, respectively. Sample preparation procedures are briefly described. The accuracy of the method was confi…
Analysis of Chlorpyrifos in Water, Fruit Juice, and Honeybee Extract by Chemiluminescent Elisa
2008
Abstract The suitability of competitive enzyme-linked immunosorbent assays (ELISAs) with chemiluminescent detection-based immobilized antigen (indirect assay) for rapid and accurate determination of chlorpyrifos in various food matrices was tested. The limit of detection (LOD) values were 1–1.75 ng mL−1, the standard curve midpoint (IC50) was 3.5 ng mL−1, and the assay duration was 1.5 h. Assay application to the analysis of honeybee extract resulted in chlorpyrifos recoveries varying between 62 and 83% in 5–15 ng mL−1 herbicide concentration range.
Spectrofluorimetric Determination of Iproniazid and Isoniazid in a FIA System Provided with a Solid-Phase Reactor
1998
Abstract A FIA assembly is proposed for the fluorimetric determination of iproniazid and isoniazid. The oxidation of both drugs is carried out by H2O2. The excess of reagent is destroyed and removed from the flow-injection manifold by means of a metallic copper reactor which acts as catalyst in the decomposition of H2O2 and a home made debubbler. The calibration graphs were linear up to 14 μg ml−1 and 10 μg ml−1 (n=6) for iproniazid and isoniazid, respectively, with limits of detection of 0.008 μg ml−1 and 0.005 μg ml−1. The sample throughput was 24 h−1 for both drugs. The influence of foreign compounds was studied and the procedure was applied to determination of iproniazid and isoniazid i…
A Fully Automated Assembly Using Solenoid Valves for the Photodegradation and Chemiluminometric Determination of the Herbicide Chlorsulfuron
2005
Abstract This paper presents a new photochemiluminescent system for the determination of chlorsulfuron in water samples. The light from a low‐pressure mercury lamp is used as a clean, reproducible, and inexpensive “reagent” for the derivation of the pesticide, performed in glycine buffer at pH 9.5. Then, the photo‐products from irradiation are oxidized by permanganate in sulfuric acid solution. The oxidation reaction was favored by using high temperatures. A comparative study and discussion about the use of polyphosphoric acid instead of sulfuric acid in the oxidation reaction is also presented. The use of solenoid valves allows for the easy, complete automation of the process with low samp…
RAPID LIQUID CHROMATOGRAPHIC DETERMINATION OF TETRACYCLINES IN ANIMAL FEEDS USING A SURFACTANT SOLUTION AS MOBILE PHASE
2002
ABSTRACT A chromatographic procedure was developed for the determination of oxytetracycline (OTC), tetracycline (TC), chlortetracycline (CTC), doxycycline (DC) and minocycline (MINO) in animal feeds. Clear analyte-rich extracts were obtained using a 1 : 1 acetonitrile/water mixture buffered at pH 3. The extracts were injected into a conventional unprotected C18 chromatographic column and eluted with a mobile phase of 0.05 M sodium dodecyl sulfate/5% 1-butanol/0.01 M oxalic acid at pH 3. Good resolution was achieved for the five compounds, whereas OTC and TC coeluted with an optimized aqueous-organic mobile phase of methanol/acetonitrile/0.01 M oxalic acid at pH 3. Mean recoveries from spike…
A solid-phase extraction and size-exclusion liquid chromatographic method for polyethylene glycol 25 p-aminobenzoic acid determination in urine: Vali…
2007
No previous publications about percutaneous absorption of polyethylene glycol 25 p-aminobenzoic acid (PEG-25 PABA) have been found in the literature and the expected levels to be found in human urine after sunscreens use are unknown. The method proposed here is suitable to determine PEG-25 PABA in the urine of sunscreens users in order to carry out studies on body accumulation/excretion. It is based on solid-phase extraction (SPE) with size-exclusion liquid chromatography determination. Solid-phase extraction allows the analyte to be retained and subsequently eluted for a clean-up, using a silica-based cartridge. The size-exclusion liquid chromatography of the eluted allows the rest of matr…