Search results for "LIMIT"

showing 10 items of 2826 documents

A validated and fast procedure for FTIR determination of Cypermethrin and Chlorpyrifos.

2005

Abstract A FTIR methodology has been developed for the simultaneous determination of Cypermethrin and Chlorpyrifos in pesticide commercially available formulations. The method involves the extraction of both active principles with CHCl3 and direct measurement of the peak area values between 1747 and 1737 cm−1 corrected with a baseline defined at 2000 cm−1 for Cypermethrin and peak height values established at 1549 cm−1 corrected using a baseline situated at 1650 cm−1 for Chlorpyrifos. The limits of detection achieved were of the order of 0.7 and 0.4% (w/w), and the relative standard deviation 0.4 and 0.2% for Cypermethrin and Chlorpyrifos, respectively. The developed procedure provided stat…

Detection limitchemistry.chemical_compoundChromatographychemistryChlorpyrifosExtraction (chemistry)Analytical chemistrySample preparationHigh-performance liquid chromatographyFourier transform spectroscopyStandard deviationAnalytical ChemistryCypermethrinTalanta
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Direct determination of ethanol and methanol in liquid samples by means of vapor phase-Fourier transform infrared spectroscopy

1997

Abstract A FTIR procedure is proposed for the direct determination of methanol and ethanol in liquid samples, such as alcoholic beverages and eau-de-cologne, based on vapor generation from small injected volumes of untreated samples into a heated Pyrex glass reactor in which, at a temperature of 80°C, ethanol and methanol are volatilized and introduced into a long-path IR gas cell by means of a N2 carrier flow. The IR spectra obtained present two characteristic ethanol bands (1050 and 880 cm−1) and a single characteristic methanol band (1030 cm−1). The measurement of the area of the transient recording obtained for the wavenumber range between 1025–950 and 950–820 cm−1 allows us the determi…

Detection limitchemistry.chemical_compoundEthanolchemistryVapor phaseAcetoneEthyl acetateAnalytical chemistryInfrared spectroscopyMethanolFourier transform infrared spectroscopySpectroscopyVibrational Spectroscopy
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Immunoassays for pyraclostrobin analysis in processed food products using novel monoclonal antibodies and QuEChERS-based extracts

2013

Strobilurins are a family of synthetic natural-derived pesticides widely used for fungi control in many crops. As part of a larger research project, a collection of monoclonal antibodies to one of the most relevant strobilurins, i.e. pyraclostrobin, has been generated using functionalized haptens with the spacer arm located at different sites. The toxophore aliphatic moiety, as observed with other strobilurins, and the planar aromatic two-ring system characteristic of this molecule were revealed as the best tethering sites for high-affinity monoclonal antibody production. A central derivatization position did not generate a good immune response, but such derivatives were useful as heterolog…

Detection limitchemistry.chemical_compoundResidue (complex analysis)ChromatographychemistryPesticide residueStrobilurinQuechersDerivatizationHaptenStrobilurinsFood ScienceBiotechnology
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Spectrophotometric determination of carbaryl by on-line elution after its preconcentration onto polyurethane foam.

2000

Abstract An analytical methodology has been developed for the UV-spectrophotometric determination of carbaryl in waters after its preconcentration onto a polyether type polyurethane foam followed by on-line elution. The aforementioned strategy offers an easy way for in-field sampling and to improve the analytical sensitivity. Several chemical and flow variables (mass of sorbent, sample flow rate, sample volume and carrier flow rate) were studied to ensure the best performance of the system. Recovery studies, carried out on natural water samples spiked with known amounts of carbaryl at concentration levels between 250 and 500 μg l−1, provided recovery percentages between 94 and 105%. A detec…

Detection limitchemistry.chemical_compoundSorbentChromatographychemistryElutionCarbarylSorptionSolid phase extractionAnalytical ChemistryPolyurethaneVolumetric flow rateTalanta
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Spark source mass spectrometric assessment of boron and nitrogen concentrations in crystalline gallium arsenide

1999

The residual or doped element concentration [E] in GaAs measured by SSMS is only accurate with respect to the relative sensitivity coefficient RSCE. For a trace element concentration, the RSCE = [E]SSMS/[E]TRUE is set to unity, if no reference material or method is available to approximate the concentration to the true value. For boron a relative sensitivity coefficient of RSCB = 0.94 ± 0.08 was obtained using TI-IDMS as a reference method. RSCN = 1 is used for nitrogen determinations. A boron and nitrogen detection limit of 4.4 × 1013 cm–3 is achieved. SSMS was used as reference method to calibrate the FTIR factor fE = [E] / Iα due to the integrated local vibrational mode absorption Iα of …

Detection limitchemistry.chemical_compoundchemistryDopingAnalytical chemistrychemistry.chemical_elementInfrared spectroscopyMass spectrometryBoronBiochemistryNitrogenGallium arsenideBOROFresenius' Journal of Analytical Chemistry
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Determination of As, Sb, Se, Te and Bi in milk by slurry sampling hydride generation atomic fluorescence spectrometry

2003

A simple and fast analytical procedure has been developed for the determination of As, Sb, Se, Te and Bi in milk samples by hydride generation atomic fluorescence spectrometry (HG-AFS). Samples were treated with aqua regia for 10min in an ultrasound water bath and pre-reduced with KBr for total Se and Te determination or with KI and ascorbic acid for total As and Sb, the determination of Bi being possible in all with or without pre-reduction. Slurries of samples, in the presence of antifoam A, were treated with NaBH(4) in HCl medium to obtain the corresponding hydrides, and AFS measurements were processed in front of external calibrations prepared and measured in the same way as samples. Re…

Detection limitchemistry.chemical_compoundchemistryHydrideRelative standard deviationSlurryAnalytical chemistryAqua regiaChemical elementAscorbic acidAtomic fluorescence spectrometryAnalytical ChemistryTalanta
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Direct FIA—AS determination of potassium and magnesium in cement samples by use of the slurries approach

1992

A direct procedure has been developed for the flame atomic determination of potassium and magnesium in cement samples. A 50-mg sample is dispersed in 25 ml of 0.13M nitric acid; 100 mul of this slurry is injected in a double channel FIA manifold simultaneously with 100 mul of a 10% (w/v) lanthanum solution. This procedure allows the rapid extraction of potassium and magnesium by leaching of the sample; nitric acid is not necessary if only potassium must be determined and the sample can be diluted with only distilled water. Aqueous standards are used. The manifold employed includes a well-stirred mixing chamber, which provides an adequate on-line dilution of the sample, in order to obtain em…

Detection limitchemistry.chemical_compoundchemistryMagnesiumNitric acidPotassiumSlurryAnalytical chemistrychemistry.chemical_elementSample preparationAtomic spectroscopyAnalytical ChemistryDilutionTalanta
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Voltammetric behavior and assay of the contraceptive drug levonorgestrel in bulk, tablets, and human serum at a mercury electrode.

2004

The cyclic voltammograms of levonorgestrel (LNG) in Britton-Robinson buffers of pH 2-11 at the hanging mercury drop electrode showed a single two-electron irreversible cathodic peak over the whole pH range. This peak may be attributed to the reduction of the 3-keto-delta-4-group in the A-ring of the LNG molecule. The interfacial adsorptive character of levonorgestrel onto the surface of the hanging mercury drop electrode was identified by means of both cyclic voltammetry and chronocoulometry techniques. A simple, sensitive, and selective square-wave adsorptive cathodic stripping voltammetric procedure was developed for the quantitation of levonorgestrel. Under the optimized operational cond…

Detection limitendocrine systemChromatographyChemistrychemistry.chemical_elementPharmaceutical formulationDropping mercury electrodeAnalytical ChemistryMercury (element)Hanging mercury drop electrodeCathodic stripping voltammetrymedicineLevonorgestrelCyclic voltammetrymedicine.drugTalanta
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Estimation of the presence of unmetabolized dialkyl phthalates in untreated human urine by an on-line miniaturized reliable method

2015

Abstract At present, human exposure to dialkyl phthalates is assessed through urinary measurement of their metabolites due mainly to contamination in their analysis by their ubiquitous presence. An on-line miniaturized method and the processing of the untreated urine samples have been the key factors for minimizing contamination and achieving unbiased results. Di(2-ethylhexyl) (DEHP), diethyl (DEP), dibutyl (DBP) and mono-ethylhexyl (MEHP) phthalates in urine samples have been included in the study; MEHP as metabolite of the main dialkyl phthalate such as DEHP. On-line in-tube solid-phase microextraction (IT-SPME)-capillary liquid chromatography (CapLC) with diode array detection (DAD) is e…

Detection limitendocrine systemEnvironmental EngineeringChromatographyMetabolitePhthalic AcidsPhthalateEnvironmental ExposureUrineUrinalysisContaminationPollutionDiode arraychemistry.chemical_compoundKey factorschemistryHuman exposureHumansEnvironmental ChemistryEnvironmental PollutantsWaste Management and DisposalScience of The Total Environment
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On-line gel permeation chromatography–attenuated total reflectance–Fourier transform infrared determination of lecithin and soybean oil in dietary su…

2007

Gel permeation chromatography (GPC) with attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectrometry detection has been proposed for the simultaneous determination of lecithin and soybean oil in dietary supplements. The method involves the extraction of analytes with dichloromethane in an ultrasound water bath and the injection of 2 ml of centrifuged and filtered extracts into the system integrated by two Envirogel GPC columns (19 mm x150 mm, 19 mm x 300 mm) coupled on-line. Dichloromethane was used as mobile phase. A method has been developed to select the most appropriated wavenumber to be used for the determination of each considered compound from the calculation of a…

Detection limitfood.ingredientChromatographyFourier AnalysisChemistrySpectrum AnalysisOrganic ChemistryGeneral MedicineBiochemistryLecithinSoybean oilSoybean OilAnalytical ChemistryGel permeation chromatographyVegetable oilfoodLinear rangeAttenuated total reflectionDietary SupplementsLecithinsSpectroscopy Fourier Transform InfraredChromatography GelSoybeansFourier transform infrared spectroscopyJournal of Chromatography A
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