Search results for "Chloride"

showing 10 items of 1691 documents

Spectrofluorimetric determination of emetine by flow injection using barium peroxide and UV derivatization

1993

Abstract The flow-injection spectrofluorimetric determination of emetine was carried out by photoderivatization in the presence of barium peroxide, in a flow-injection assembly in which the PTFE tubing in the injection valve is helically coiled around the lamp. The sample solution merges with a barium peroxidephosphoric acid solution and then the resulting mixture is irradiated; pure distilled water is used as a carrier stream. The calibration graph is linear over the range 0.05–50 μ g ml −1 of emetine dihydrochloride. The influence of foreign compounds was studied and the method was applied to the determination of emetine in injection and human urine samples.

ChromatographyChemistryCalibration curveEmetine HydrochlorideFluorescence spectrometrychemistry.chemical_elementBariumBiochemistryAnalytical Chemistrychemistry.chemical_compoundDistilled waterBarium peroxideEnvironmental ChemistryDerivatizationQuantitative analysis (chemistry)SpectroscopyAnalytica Chimica Acta
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Supported liquid membrane extraction of glyphosate metabolites

2001

Use of the supported liquid membrane (SLM) technique for (aminomethyl)phosphonic acid (AMPA) extraction is presented. For the extraction of this analyte a suitable SLM system involves a liquid membrane containing Aliquat 336 – a cationic carrier that facilitates AMPA transport. The extraction of this compound, as in the case of glyphosate, is dependent on the donor phase pH and the concentration and type of counter-ion in the acceptor phase, although some differences are also observed. In both cases the transport mechanism is counter-coupled transport in which the driving force of mass transport over the membrane is created by the gradient of chloride anions from the acceptor to donor phase.

ChromatographyChemistryExtraction (chemistry)Filtration and SeparationAliquat 336ChlorideAcceptorAnalytical Chemistrychemistry.chemical_compoundMembraneLiquid–liquid extractionMass transferPhase (matter)medicinemedicine.drugJournal of Separation Science
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Development a mitigation strategy of enniatins in pasta under home-cooking conditions

2016

The effect of pasta cooking on the enniatins (ENs) contents was evaluated in white and whole-grain pasta. The cooking of pasta was performed for 10 min in boiling water. ENs were extracted from raw and cooked pasta by Solid-Liquid extraction with acetonitrile, and from cooking water by Dispersive Liquid–Liquid Micro-Extraction (DLLME) with a mixture of acetonitrile and carbone tetrachloride. Mycotoxin analysis was performed by Liquid Chromatography coupled to Tandem Mass Spectrometry. The effect of pasta cooking has a marked influence on the reduction of ENs levels. Reductions of 98–100% for ENA, 94–95% for ENA1, 14–49% for ENB and 53–65% for ENB1 were achieved after the process. ENs were d…

ChromatographyChemistryExtraction (chemistry)food and beverages04 agricultural and veterinary sciencesMass spectrometryTandem mass spectrometry040401 food sciencechemistry.chemical_compound0404 agricultural biotechnologyBoilingTetrachlorideMycotoxinVolume concentrationEnniatin AFood ScienceLWT - Food Science and Technology
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Isobaric vapor–liquid equilibria for 1-propanol+water+copper(II) chloride at 100kPa

2005

Abstract Isobaric vapor–liquid equilibria for the ternary system 1-propanol + water + copper(II) chloride has been measured at 100 kPa using a recirculating still. The addition of copper(II) chloride to the solvent mixture produced a salting-out effect of the alcohol, but the azeotrope did not tend to be eliminated when the salt content increased. The experimental data sets were fitted with the electrolyte NRTL model and the parameters of Mock's model were estimated. This model has proved to be suitable to represent experimental data in the entire range of compositions. The effect of copper(II) chloride on the vapor–liquid equilibrium of the 1-propanol + water system has been compared with …

ChromatographyChemistryGeneral Chemical EngineeringAnalytical chemistryGeneral Physics and AstronomyElectrolyteChloridePropanolchemistry.chemical_compoundAzeotropemedicineNon-random two-liquid modelCopper(II) chlorideIsobaric processPhysical and Theoretical ChemistryCopper chloridemedicine.drugFluid Phase Equilibria
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Gas phase chromatography of halides of elements 104 and 105

1992

On-line isothermal gas phase chromatography was used to study halides of261104 (T1/2=65 s) and262,263105 (T1/2=34 s and 27 s) produced an atom-at-a time via the reactions248Cm(18O, 5n) and249Bk(18O, 5n, 4n), respectively. Using HBr and HCl gas as halogenating agents, we were able to produce volatile bromides and chlorides of the above mentioned elements and study their behavior compared to their lighter homologs in Groups 4 or 5 of the periodic table. Element 104 formed more volatile bromide than its homolog Hf. In contrast, element 105 bromides were found to be less volatile than the bromides of the group 5 elements Nb and Ta. Both 104 and Hf chlorides were observed to be more volatile tha…

ChromatographyChemistryHealth Toxicology and MutagenesisPublic Health Environmental and Occupational HealthHalideHydrochloric acidPollutionChemical reactionChlorideIsothermal processAnalytical Chemistrychemistry.chemical_compoundNuclear Energy and EngineeringBromidemedicineHydrobromic acidRadiology Nuclear Medicine and imagingGas chromatographySpectroscopymedicine.drugJournal of Radioanalytical and Nuclear Chemistry Articles
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Gas-liquid chromatographic analyses of chlorination products of propionyl chloride

1981

Abstract Photochlorination of propionyl chloride with chlorine in the liquid phase at room temperature gives all eleven chloropropionyl chlorides from the mono-to the pentachloro isomer. The process was investigated every 2 h by gas-liquid chromatography, and the products were identified and estimated as their methyl esters by comparison with model compounds. The isomer distribution of the products was studied in detail. Because the process favours the 3-position, the main components were 3-chloropropionyl chloride up to 15 h, 3,3-dichloropropionyl chloride between 15 and 29 h, 3,3,3-trichloropropionyl chloride between 29 and 56 h and pentachloropropionyl chloride after 56 h of chlorination.

ChromatographyChemistryOrganic ChemistryLiquid phasechemistry.chemical_elementGeneral MedicineBiochemistryChlorideAnalytical ChemistryPropionyl chloridemedicineChlorineOrganic chemistryGas liquid chromatographicmedicine.drugJournal of Chromatography A
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Lipid hydroperoxides determination in milk‐based infant formulae by gas chromatography

2003

A simple gas chromatograph using a flame ionization detector and a polar capillary column method is proposed for determining hydroperoxides in the lipid fraction of milkbased infant formulas. Tricosanoic acid is used as internal standard. The method includes the following steps: a) the extraction of fat with chloroform/methanol (2:1, v/v), b) the reduction of hydroperoxide acids to hydroxide acids with hydrogen gas and palladium as a catalyst, c) the transmethylation to obtain the methyl esters with acetyl chloride and methanol/ hexane (4:1, v/v), and d) an acetylation with acetic anhydride/ pyridine (4:1, v/v) to obtain an acetoxy derivate of the hydroxide present. Two chromatography runs,…

ChromatographyChloroformChemistryGeneral ChemistryIndustrial and Manufacturing Engineeringlaw.inventionHexanechemistry.chemical_compoundAcetic anhydridelawAcetyl chlorideHydroxideFlame ionization detectorGas chromatographyMethanolFood ScienceBiotechnologyEuropean Journal of Lipid Science and Technology
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Determination of organic and inorganic anions in insect haemolymph and midgut contents by ion chromatography

1997

A simple and rapid ion-exchange chromatographic method with conductimetric detection for the determination of carboxylic acids (succinic, malic and citric) and inorganic anions (chloride, phosphate and sulphate) in haemolymph and midgut content of Lepidoptera larvae is provided. The mobile phase is 0.975 mM phthalic acid at pH 4.1. The procedure of sample extractions was simple. Comparison of the results with whose reported in the bibliography showed that the values were similar. The ion-exchange chromatographic–conductimetric detection method permits the analysis of various organic and inorganic anions in small biological samples.

ChromatographyConductometrybiologyfungiOrganic ChemistryIon chromatographyGeneral MedicinePhosphateBiochemistryChlorideAnalytical ChemistryPhthalic acidchemistry.chemical_compoundchemistrymedicinebiology.proteinCarboxylateQuantitative analysis (chemistry)medicine.drugOrganic anionJournal of Chromatography A
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Off-line dansylation of amines using C18 solid-phase packings: study of the fluorescence and chemiluminescence detection by post-column derivatizatio…

1999

Abstract Dansylation of amines (primaries and secondaries) using C18 solid-phase supports is described. The time of analysis and the handing sample have been markedly improved with respect to those required for solution dansylation. The dansylated amine derivates were injected onto the liquid chromatography system and fluorescence detected. The sensitivity and selectivity is better than the other dansylation procedures described in the literature and also better than other derivatization reagents such 1,2-napthoquinone 4-sulfonate (NQS) or 3,5-dinitrobenzoyl chloride (3,5-DNB). Dansyl compounds can also form chemiluminescent derivatives, therefore a post-column derivatization procedure with…

ChromatographyDansyl chlorideOxalic acidNQSBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistrypolycyclic compoundsEnvironmental ChemistryAmine gas treatingSolid phase extractionTCPODerivatizationSpectroscopyAnalytica Chimica Acta
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Determination of diphenhydramine hydrochloride by flow injection with Bromophenol Blue and turbidimetric measurement

1990

The study of a number of diphenhydramine-dye systems was carried out in order to determine the most suitable precipitate for the turbidimetric determination of diphenhydramine using flow injection (FI). The reagent selected was Bromophenol Blue. The chemical and FI variables were optimised. The calibration graph was linear over the concentration range 50-230 p.p.m. of diphenhydramine hydrochloride. A number of interfering substances were also investigated.

ChromatographyDiphenhydramine hydrochlorideCalibration curveDiphenhydramineBromophenol blueBiochemistryAnalytical Chemistrychemistry.chemical_compoundDiphenhydraminechemistryNephelometry and TurbidimetryReagentElectrochemistrymedicineEnvironmental ChemistryIndicators and ReagentsBromphenol BlueSpectroscopymedicine.drugThe Analyst
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