Search results for "Reagent"

showing 10 items of 699 documents

Determination of phytic acid and its degradation products by ion-pair chromatography (IPC) coupled to inductively coupled plasma-sector field-mass sp…

2004

We developed a method for the determination of phytic acid (IP6) and its degradation products (IP1-IP5) by ion-pair chromatography coupled to a double focussing inductively coupled plasma-sector field-mass spectrometer (ICP-SF-MS). For the detection of the phosphorus species a mass resolution (m/Δm) of 4000 was needed in order to separate the 31P+ signal from the interfering clusterions. The separation of the six phosphorus species was enabled by a gradient elution using tetrabutylammonium hydroxide (TBA) as ion-pair reagent. Calibration data were reported and a detection limit of 230 ng g−1 for IP6 could be obtained. The method was firstly proved for a hydrolyzate of commercially available…

Detection limitPhytic acidChromatographyTetrabutylammonium hydroxidePhosphorusfood and beverageschemistry.chemical_elementMass spectrometryAnalytical Chemistrychemistry.chemical_compoundchemistryReagentInositolInductively coupled plasmaSpectroscopyJournal of Analytical Atomic Spectrometry
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Selective chlorine determination by gas diffusion in a tandem flow assembly and spectrophotometric detection with o-dianisidine

2001

Abstract A fast, selective, sensitive and automated method for determination of free chlorine in industrial formulations and water samples is proposed. The automation of the flow assembly is based on the “tandem flow” approach, which uses a set of solenoid valves acting as independent switches. The operating cycle for obtaining a typical analytical transient signal can easily be programmed by means of friendly software running in the Windows environment. The manifold is provided with a gas diffusion unit which permits the removal of interfering species as well as concentrating the chlorine. The determination of chlorine is performed on the basis of the oxidation of o-dianisidine as the colo…

Detection limitReproducibilityTandemChemistryAnalytical chemistrychemistry.chemical_elementSolenoidBiochemistryAnalytical ChemistryReagentpolycyclic compoundsChlorineEnvironmental ChemistryGaseous diffusionQuantitative analysis (chemistry)SpectroscopyAnalytica Chimica Acta
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Indirect spectrophotometric determination of p-aminobenzoic acid in sunscreen formulations by sequential injection analysis

2003

Abstract A simple indirect sequential injection spectrophotometric method for the determination of the UV-filter p -aminobenzoic acid (PABA) in sunscreen formulations is proposed. The determination is based on the reaction of PABA with hypochlorite in acidic medium and the subsequent measurement of the residual chlorine by using the well-known reaction with o -tolidine. The experimental variables involved in the sequential injection analysis (SIA) system (sandwich arrangement, volumes of sample and reagents, propulsion flow rate, reaction coil length) and adequate concentrations of reagents were studied. The SIA method has a linear range up to 20 μg ml −1 (3 s y / x / b detection limit) of …

Detection limitSequential injection analysisChromatographymedicine.diagnostic_testTolidineHypochloriteBiochemistryAnalytical Chemistrychemistry.chemical_compoundLinear rangechemistrySpectrophotometryReagentmedicineEnvironmental ChemistryAminobenzoic acidSpectroscopyAnalytica Chimica Acta
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Micropumping multicommutation turbidimetric analysis of waters

2007

Abstract A micropumping multicommutation manifold to perform turbidity determinations in waters is described. The procedure is based on the use of a combination of hydrazine sulfate and hexamethylenetetramine, to obtain an external standard of nephelometric turbidity units (NTU), which could compare the absorbance measurements at high wavelengths for samples with a calibration line obtained from a concentrated formazine standard diluted on-line. To minimize sample and reagent consumption and waste generation, the flow system was designed with two solenoid micro-pumps, one of them for the alternative introduction of the formazine standard and samples and the other one for the water carrier. …

Detection limitStandard curveAbsorbancechemistry.chemical_compoundChromatographyChemistryReagentCoefficient of variationAnalytical chemistryTurbidityFormazineAnalytical ChemistryDilutionTalanta
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Determination of sulphonamides in human urine by azo dye precolumn derivatization and micellar liquid chromatography

1995

Abstract A high-performance liquid chromatographic method for the determination of sulphonamides in urine is reported. The drugs (sulphadiazine, sulphaguanidine, sulphamethizole, sulphamethoxazole, and sulphathiazole) were diazotized with nitrite and coupled with N-(1-naphthyl)ethylenediamine dihydrochloride in a sodium dodecyl sulphate (SDS) micellar medium. Separation of the sulphonamide azo dyes was performed on a C18 column with a 0.05 M SDS-2.4% pentanol mobile phase, which permitted the direct injection of the urine samples. The limits of detection were in the 0.1–0.3 μg/ml range.

Detection limitSulfonamidesChromatographySodiumchemistry.chemical_elementGeneral ChemistryUrineHigh-performance liquid chromatographychemistry.chemical_compoundSpectrometry FluorescenceAnti-Infective AgentschemistryReference ValuesMicellar liquid chromatographyHumansIndicators and ReagentsSpectrophotometry UltravioletNitriteDerivatizationAzo CompoundsChromatography High Pressure LiquidMicellesAntibacterial agentJournal of Chromatography B: Biomedical Sciences and Applications
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Multicommutation as an environmentally friendly analytical tool in the hydride generation atomic fluorescence determination of tellurium in milk.

2003

The aim of this study is to show the advantages of the emerging multicommutation methodology based on the use of solenoid valves for Te determination in milk by hydride generation atomic fluorescence spectrometry (HG-AFS). The delivery of a series of alternating sequential insertions of small volumes of samples and reagents gives rise to new hydrodynamic processes and exciting analytical potentials by controlling the time of flow through the on/off-switched solenoid valves. This drastically reduces the reagent consumption by a factor of 4 and the generation of effluents (590 mL h(-1) instead of 750 mL h(-1) generated by the continuous-mode measurement) and also provides an improvement in th…

Detection limitTime FactorsHydrideSpectrophotometry AtomicAnalytical chemistrychemistry.chemical_elementSolenoidBiochemistryAtomic fluorescence spectrometryEnvironmentally friendlyAnalytical ChemistrySonicationMilkchemistryReagentCalibrationCalibrationAnimalsRegression AnalysisTelluriumTelluriumMicrowavesHydrogenAnalytical and bioanalytical chemistry
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Comparison of different sorbents for on-line liquid-solid extraction followed by high-performance liquid chromatographic determination of nitrogen-co…

1998

Abstract LiChrolut EN [poly(styrene-divinylbenzene), PSDVB], Carbograph (graphitized carbon black, GCB), Isolute CN (cyanopropylsilica), Isolute C 2 (ethylsilica), and LiChrospher RP18 (octadecylsilica) were studied for on-line solid-phase extraction of twelve nitrogen containing pesticides from water. Determination (UV 210 nm) was performed with a Spherisorb C 8 analytical column and an acetonitrile-water gradient. The mean recoveries from 50 ml ranged from 83% for RP18 to 44% for GCB, and decreased in the following order: RP18, CN, LiChrolut EN, C 2 , and GCB. GCB showed poor recoveries due to incomplete desorption with the acetonitrile-water gradient used, and memory effects were detecte…

Detection limitVinyl CompoundsChromatographyNitrogenChemistryElutionOrganic ChemistryExtraction (chemistry)General MedicineReversed-phase chromatographySilicon DioxideBiochemistryHigh-performance liquid chromatographyBackflush accountingCarbonAnalytical ChemistryPolystyrenesIndicators and ReagentsSpectrophotometry UltravioletSample preparationSolid phase extractionPesticidesChromatography High Pressure LiquidJournal of Chromatography A
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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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3,3?,5,5?-Tetramethylbenzidme for the colorimetric determination of manganese in water

1998

Manganese can be determined by colorimetry with previous oxidation of Mn(II) in a strong basic medium, using 3,3′,5,5′-tetramethylbenzidine as a chromogenic reagent. The molar absorptivity of the reaction product is 3.4 × 104 mol−1l cm−1l, the detection limit 3 ng/ml, the RSD (0.5 mg/l,n = 8) 0.9% and the calibration range (1-cm cells) 0.02–0.8 mg/1 V(V), Cr(VI) and Co(II) are the most significant interferences. The new method was compared with an AAS procedure (air-acetylene flame) with previous solvent extraction and also with a colorimetric method for the determination of manganese in sea and drinking water.

Detection limitchemistryStereochemistryChromogenicReagentchemistry.chemical_elementSeawaterManganeseMolar absorptivityColorimetryAnalytical ChemistryReaction productNuclear chemistryMikrochimica Acta
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