Search results for " solution"

showing 10 items of 3084 documents

Determination of aniline in vegetable oils by diazotization and coupling in a microemulsion medium

1990

Abstract A microemulsion containing sodium dodecyl sulphate and n -pentanol in a mass ratio of 1 : 4, water and a vegetable oil was investigated using pseudo-tenary phase diagrams. The medium can co-solve important amounts of vegetable oils and aqueous solutions over a wide range of ionic strengths. A procedure for the determination of 1.4–140 μg ml −1 of aniline in vegetable oils using ionic diazotization and coupling reactions was developed. The absorbance was measured in an optically clear microemulsion containing 4% or 20% of oil. The procedure is much simpler and rapid than the official chromatographic methods and gives almost the same limits of detection (ca. 05 μg ml −1 ) using no mo…

Detection limitChromatographyAqueous solutionmedicine.diagnostic_testChemistryBiochemistryAnalytical ChemistryAbsorbancechemistry.chemical_compoundVegetable oilAnilineSpectrophotometrymedicineEnvironmental ChemistryMicroemulsionTitrationSpectroscopyAnalytica Chimica Acta
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Micellar enhanced fluorimetric determination of carbendazim in natural waters

1994

Abstract A micellar enhanced flow-injection fluorimetric method was developed for the determination of carbendazim in natural water samples. The method is based on the direct injection of 500 μ1 of water into a three-channel flow manifold in which the samples are merged with a buffer solution and subsequently with a surfactant solution. Two alternative procedures were used: one based on the use of sodium dodecyl sulphate micelles in 0.1 M HCl, which permits a 2.6-fold enhancement of the sensitivity found in the absence of micelles to be obtained, and the other based on the use of cetyltrimethylammonium bromide in 0.1 M NaOH, which provides a 11.6-fold enhancement of sensitivity and a limit …

Detection limitChromatographyCarbendazimSodiumFluorescence spectrometrychemistry.chemical_elementBuffer solutionBiochemistryMicelleAnalytical Chemistrychemistry.chemical_compoundchemistryPulmonary surfactantBromideEnvironmental ChemistrySpectroscopyAnalytica Chimica Acta
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Development of a sensitive method for determining traces of prohibited acrylamide in cosmetic products based on dispersive liquid-liquid microextract…

2020

Abstract According to the European Regulation on cosmetic products, the presence of acrylamide in these consumer products is not allowed due to its mutagenic and potentially carcinogenic effects. Despite this ban, acrylamide might be present in those cosmetic products containing acrylamide-based polymers. However, there is no analytical method for its determination in this type of matrices. Based on this, the development of analytical methods for the determination of acrylamide in cosmetic products is required to guarantee consumer safety. In this work, an analytical method for determining traces of prohibited acrylamide in cosmetic products is presented for the first time. The method is ba…

Detection limitChromatographyChloroformAqueous solutionChemistry010401 analytical chemistryExtraction (chemistry)02 engineering and technology021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAnalytical ChemistrySolventchemistry.chemical_compoundAcrylamide0210 nano-technologyDerivatizationEnrichment factorSpectroscopyMicrochemical Journal
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Improved detection limit for ammonium/ammonia achieved by Berthelot's reaction by use of solid-phase extraction coupled to diffuse reflectance spectr…

2005

Abstract The proposed procedure is based on the extraction of the indothylmol blue into C 18 solid-phase extraction (SPE) membranes and direct quantification on the membrane surface by diffuse reflectance spectroscopy. The analytical performance of the proposed method has been evaluated for standard solutions of ammonium using reflectance values, R , as well as the Kubelka–Munk function, F ( R ). The results have been compared with those obtained by the conventional method, which uses UV–vis absorption spectroscopy with a sensor-based method. The described methodology provided satisfactory linearity and reproducibility within the ammonium concentration intervals 25–250 μg L −1 and 25–500 μg…

Detection limitChromatographyDiffuse reflectance infrared fourier transformExtraction (chemistry)Analytical chemistryStandard solutionBiochemistryAnalytical ChemistryAmmoniachemistry.chemical_compoundchemistryEnvironmental ChemistrySample preparationAmmoniumSolid phase extractionSpectroscopyAnalytica Chimica Acta
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Direct injection of edible oils as microemulsions in a micellar mobile phase applied to the liquid chromatographic determination of synthetic antioxi…

1999

Abstract A simple and quick procedure for analysis of hydrophobic samples by direct injection in a liquid chromatograph, without previous extraction, has been developed. The sample is solved in a water/sodium dodecyl sulphate/n-pentanol microemulsion without destroying the microemulsion structure, and injected. A micellar mobile phase containing 0.1 M SDS, 2.5% n-propanol and 10 mM phosphate of pH 3 is used. The procedure is applied to the determination of synthetic antioxidants (propyl gallate, tert-butylhydroquinone, 2,4,5-trihydroxybutyrophenone, nordihydroguaiaretic acid, octyl gallate, 3-tert-butyl-4-hydroxyanisole and dodecyl gallate) in sunflower, corn and olive oils. Linear calibrat…

Detection limitChromatographyExtraction (chemistry)Dodecyl gallateBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryMicellar liquid chromatographyMicellar solutionsEnvironmental ChemistryMicroemulsionOctyl gallateSpectroscopyPropyl gallateAnalytica Chimica Acta
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Uptake and translocation monitoring of imidacloprid to chili and tomato plants by molecularly imprinting extraction - ion mobility spectrometry

2019

Abstract The degradation of imidacloprid in soil and its uptake and translocation to chili and tomato plants was evaluated, as a proof of concept, of the possibilities of the combination of molecularly imprinted polymers (MIPs) and ion mobility spectrometry (IMS) for a fast and sensitive bioprocesses monitoring tool. To do it, a method based on the selective extraction of imidacloprid from soil and plant materials was developed. In the selected conditions, the MIP-IMS procedure provided a recovery of imidacloprid in soil and plant samples from 102 to 114%, for spiked concentration levels from 0.2 to 2.0 μg g−1. Precision of the methodology, expressed as the relative standard deviation (RSD)…

Detection limitChromatographyIon-mobility spectrometryChemistry010401 analytical chemistryRelative standard deviationMolecularly imprinted polymerChromosomal translocation02 engineering and technologyPesticideStandard solution021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundImidacloprid0210 nano-technologySpectroscopyMicrochemical Journal
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A rapid HPLC assay for zearalenone in laboratory cultures ofFusarium graminearum

1993

A high pressure liquid chromatographic (HPLC) method to determine zearalenone in corn contaminated withFusarium graminearum is described. After extraction with methanol-water and solvent partition, samples were cleaned up by applying the extract to a disposable silica cartridge and by eluting the toxin with a mixture of hexane/dry ethyl ether (5/5). Separation was achieved by a reverse phase μBondapak C18 column followed by fluorescence detection using an excitation wavelength at 274 nm and an emission wavelength at 440 nm. Detection limit was about 5 ng. Recoveries ranging from 85.37 to 100.97%, in standard solutions range 30–0.5 µg/ml, were found.

Detection limitChromatographyVeterinary (miscellaneous)Extraction (chemistry)EtherStandard solutionApplied Microbiology and BiotechnologyMicrobiologyHigh-performance liquid chromatographySolventHexanechemistry.chemical_compoundchemistryAgronomy and Crop ScienceZearalenoneMycopathologia
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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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Antibody-Capped Mesoporous Nanoscopic Materials: Design of a Probe for the Selective Chromo-Fluorogenic Detection of Finasteride

2012

[EN] The synthesis of capped mesoporous silica nanoparticles (MSN) conjugated with an antibody (AB) as a gatekeeper has been carried out in order to obtain a delivery system able to release an entrapped cargo (dye) in the presence of a target molecule (antigen) to which the conjugated antibody binds selectively. In particular, MSN loaded with rhodamine B and functionalized on the external surface with a suitable derivative of N-(t-butyl)- 3-oxo-(5a,17b)-4-aza-androst-1-ene-17-carboxamide (finasteride) have been prepared (S1). The addition of polyclonal antibodies against finasteride induced capping of the pores due to the interaction with the anchored hapten-like finasteride derivative to g…

Detection limitINGENIERIA DE LA CONSTRUCCIONAqueous solutionChromatographyQUIMICA INORGANICANanotechnologyGeneral ChemistryMesoporous silicaFull PapersMCM-41finasterideMatrix (chemical analysis)chemistry.chemical_compoundQUIMICA ORGANICAchemistryQUIMICA ANALITICAhybrid materialsFinasterideRhodamine BantibodiesSelectivityMesoporous materialmolecular gatesChemistryOpen
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Influence of water sample storage protocols in chemiluminescence detection of trace elements.

2002

This paper shows the influence of different sample storage protocols, on the chemiluminescence signal of some metal ions. The storage protocols studied were: acid addition (HCl or HNO(3)) and no reagent addition to filtered and refrigerated (T=4 degrees C) samples. Light emission was produced for the chemiluminescence reaction between luminol and hydrogen peroxide in buffer carbonate conditions (pH 10.8) catalysed by Cr(III), Co(II) and Cu(II). Batch and/or flow modes in different conditions were tested. Fe(II), Fe(III), Ni(II) and Mn(II) did not give chemiluminescence in the studied conditions. A parallel study of sensitivity and selectivity was performed. Then the presence or absence of t…

Detection limitMetal ions in aqueous solutionAnalytical chemistryAnalytical ChemistryLuminollaw.inventionchemistry.chemical_compoundchemistrylawReagentLight emissionHydrogen peroxideMasking agentChemiluminescenceTalanta
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