Search results for "Detection limit"

showing 10 items of 810 documents

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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Moiety and linker site heterologies for highly sensitive immunoanalysis of cyprodinil in fermented alcoholic drinks

2015

Cyprodinil is a new-generation anilinopyrimidine fungicide widely used in crop protection and frequently found in fruits. In this study, novel derivatives of cyprodinil with linker site heterologies were synthesized and employed in order to produce antibodies with enhanced affinity. Moreover, moiety-heterologous haptens were designed and prepared for assay sensitivity improvement. Two competitive enzyme-linked immunosorbent assays for the analysis of this active substance were developed using direct and indirect formats, achieving IC50 values around 0.15 μg/L. Analytical figures of merit and usability of the optimized assays were evaluated with wine and cider as model food processed matrice…

Detection limitWineHapten designChromatographyChemistryFood analysisFungicideWineAssay sensitivityHighly sensitiveCidersMoietyFermentationELISAHaptenLinkerFood ScienceBiotechnology
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Supercritical fluid extraction of resveratrol from grape skin of Vitis vinifera and determination by HPLC

2000

Supercritical fluid extraction of resveratrol from grape skin of Vitis vinifera was studied. Extraction variables such pressure, modifier concentration (ethanol), and extraction time were optimised. Final extraction conditions were: 40 degrees C, 150 bar, 7.5% ethanol and extraction time 15 min. Extraction recovery and precision (variation coefficient between 0.2 and 1.0%) were calculated. The resveratrol content in the ethanolic extract was determined by HPLC with UV detection at 306 nm. Acetic acid-methanol-water was used as the mobile phase, and C-18 and C-8 columns were tested, instrumental parameters were optimised, and analytical parameters were calculated (lineal interval 0-75 mg l(-…

Detection limitWinechemistry.chemical_compoundChromatographychemistryCoefficient of variationExtraction (chemistry)Supercritical fluid extractionResveratrolHigh-performance liquid chromatographyQuantitative analysis (chemistry)Analytical ChemistryTalanta
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Quantifying both ammonium and proline in wines and beer by using a PDMS composite for sensoring.

2019

Abstract Two of the reagents involved in the Berthelot's reaction, thymol and nitroprusside, were embedded in a PDMS composite in order to apply this assay to determine ammonium and proline, in wine and beers. Safety, portability, rapidity, cost-effectiveness and simplicity of the assay were improved. For the proline determination, a modified Berthelot's reaction, which included a ring cleavage of proline, was optimized. The accuracy of the assay was tested. The limits of detection for ammonium was 0.12 µg mL−1 and for proline was in the range from 0.7 to 4.1 µg mL−1, depending on the kind of wine (white, red, or sweet), for beer the LOD was 6 µg mL−1. The precision achieved was slower than…

Detection limitWinechemistry.chemical_compoundValidation studyChromatographychemistryReagentComposite numberfood and beveragesAmmoniumProlineThymolAnalytical ChemistryTalanta
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Analysis of insoluble silicate: Decomposition with molten sodium hydroxide and determination of Zr(IV) with chloranilic acid in medium-strong acid

1983

A rapid, accurate and precise method for the determination of zirconium in silicates is proposed. Insoluble or sparingly soluble samples are decomposed by means of molten sodium hydroxide. Chloranilic acid is employed as reagent for the spectrophotometric determination of Zr(IV). The limit of detection is 1.2×10−7 M and the relative standard deviation is 0.24%.

Detection limitZirconiumClinical BiochemistryRelative standard deviationInorganic chemistrychemistry.chemical_elementGeneral MedicineDecompositionSilicateAnalytical Chemistrychemistry.chemical_compoundchemistryChloranilic acidSodium hydroxideReagentGeneral Materials ScienceFresenius' Zeitschrift für analytische Chemie
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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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Major and Trace Element Geochemistry of the European Kupferschiefer – An Evaluation of Analytical Techniques

2018

Simple and rapid techniques are needed for routine quantitative chemical bulk-rock analyses of Kupferschiefer, a black shale containing variable amounts of silicates, base metal sulphides, carbonates and an organic content of up to 30 weight percent. In this study, WD-XRF, TXRF, and ICP-OES of acid- as well as peroxide-digested samples were tested as potential techniques based on their availability and adaptability to analyse major (Si, Ti, Al, Mg, Ca, Fe, K, but also Cu, Zn, Pb) and selected trace (Ag, As, Ba, Co, Mo, Ni, V) element concentrations. Because of the absence of a suitable reference material, a comparative study was undertaken using instrumental neutron activation analysis to a…

Detection limitblack shaleIsotopeChemistryTrace elementAnalytical chemistrysulphidescopper oresGeneral Chemistry010501 environmental sciences010502 geochemistry & geophysics01 natural scienceswhole-rock geochemistryDigestion (alchemy)Geochemistry and PetrologyWD-XRFICP-OESGeneral Earth and Planetary SciencesINAANeutron activation analysisOil shaleMass fractionBase metal0105 earth and related environmental sciencesGeneral Environmental Science
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Development of a sensitive and specific enzyme-linked immunosorbent assay for the determination of fludioxonil residues in fruit juices

2014

Fludioxonil is a fungicide with a singular mode of action that is widely employed in the treatment of fruit crops. A competitive enzyme-linked immunosorbent assay (cELISA) has been developed and validated for the determination of residues of this fungicide in fruit juices. A collection of monoclonal antibodies (mAbs) against the fungicide fludioxonil has been produced and characterized using direct and indirect cELISAs. The high affinity achieved (IC50lower than 0.5 μg L-1) considerably improved that obtained with previous polyclonal antibodies. The proposed cELISA was applied to the analysis of fludioxonil residues in apple juice and red grape must samples with a limit of quantification of…

Detection limitcELISAChromatographybiologymedicine.drug_classChemistryFungicideGeneral Chemical EngineeringGeneral EngineeringFludioxonilMonoclonal antibodyAnalytical ChemistryFungicidePolyclonal antibodiesbiology.proteinmedicineFruit juicesFudioxonilMode of actionSpecific enzymeAnal. Methods
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Determination of inorganic species of Sb and Te in cereals by hydride generation atomic fluorescence spectrometry

2011

A non-chromatographic fast, sensitive and easy method has been developed for the determination of Sb(III), Sb(V), Te(IV) and Te(VI) in cereal samples. The procedure is based on ultrasound assisted extraction and determination by hydride generation atomic fluorescence spectrometry (HG AFS). Preliminary studies were made in order to get the best extraction efficiency using 1 mol L-1 phosphoric acid, 1 mol L-1 nitric acid, aqua regia, 1 mol L-1 sulfuric acid and 6 mol L-1 hydrochloric acid. The extraction with aquaregia showed a clear interconversion of the species during the process, being H2SO4 the best extractant with efficiencies greater than 90% from the total content of Sb and Te quantif…

Detection limitcerealshydride generation atomic fluorescence spectrometryChemistryHydrideantimonyExtraction (chemistry)Hydrochloric acidSulfuric acidGeneral Chemistrychemistry.chemical_compoundspeciationNitric acidtelluriumAqua regiaPhosphoric acidNuclear chemistry
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Atomic fluorescence spectrometric determination of trace amounts of arsenic and antimony in drinking water by continuous hydride generation

1999

A highly sensitive and simple method has been developed for the determination of As(III), total As, Sb(III) and total Sb in drinking water samples by continuous hydride generation and atomic fluorescence spectrometry (HGAFS). For As determination, water samples aspirated in a carrier of 2 mol l(-1) HCl were merged with a reducing NaBH(4) 3%(m/v) solution, with sample and NaBH(4) flow rates of 12.5 and 1.5 ml min(-1) respectively. The hydride generated in a 170 cm reaction coil was transported to the detector with an Ar flow of 400 ml min(-1), and a limit of detection between 5 and 20 ng l(-1) was obtained. For Sb determination, 2.5 mol l(-1) HCl and 2%(m/v) NaBH(4) were employed, with respe…

Detection limitchemistryAntimonyTrace AmountsHydrideAnalytical chemistrychemistry.chemical_elementIodineAtomic fluorescence spectrometryArsenicAnalytical ChemistryVolumetric flow rateTalanta
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