Search results for "Extraction"

showing 10 items of 2072 documents

Hard Cap Espresso Machine Extraction of Polyphenolic Compounds from Pulses

2018

A hard cap espresso machine was employed for the extraction of polyphenolic compounds from food samples as dry legumes and pulses. 100 mg of ground dry sample was mixed with a dispersing agent and placed in a refillable stainless steel capsule with a borosilicate filter. A complete polyphenol extraction was achieved by using 150 mL ethanol 50 % (v/v) in water and determined by Folin-Ciocalteu spectrophotometric method. The method provided a limit of detection of 0.4 mg g<sup>-1</sup>. The whole extraction procedure was achieved in less than one minute using the mild extraction conditions of 72°C and 19 bars given by the domestic machine. Fifteen varieties of food samples (3 lent…

Detection limitEspressoChromatographybiologyChemistryPolyphenolExtraction (chemistry)Extraction methodsGeneral ChemistrySorghumbiology.organism_classificationJournal of the Mexican Chemical Society
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Gas chromatographic behaviour of urea herbicides

2001

Gas chromatographic conditions for determining eight phenylurea (chlortoluron, diuron, fluometuron, isoproturon, linuron, metabenzthiazuron, metobromuron and monuron) and one sulfonylurea (chlorsulfuron) herbicides were assessed. Degradation products of the herbicides formed in the injector were used for identification. Most phenylureas formed their respective carbamic acid methyl esters, metabenzthiazuron formed an aminobenzothiazol and chlorsulfuron formed an aminotriazine plus a phenylsulfonamide. On-column injection of standards using a BP10 capillary column was evaluated to identify the chromatographic behaviour. Detection limits ranged from 0.05 ng for chlorsulfuron to 3 ng for monuro…

Detection limitFluometuronChromatographymedicine.drug_classOrganic ChemistryClinical BiochemistryBiochemistrySulfonylureaAnalytical Chemistrychemistry.chemical_compoundElectron capture detectorCarbamic acidchemistryChlortoluronmedicineGas chromatographySolid phase extraction
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Liquid chromatographic determination of trimethylamine in water.

2004

A method for the selective determination of trimethylamine (TMA) in aqueous matrices by liquid chromatography is reported. The proposed procedure is based on the derivatization of the analyte with 9-fluorenylmethyl chloroformate (FMOC) in a precolumn (Hypersil C18, 30 microm, 20 mm x 2.1 mm i.d.) connected on-line to the analytical column (LiChrosphere 100 RP18, 5 microm, 125 mm x 4 mm i.d.). Gradient elution was performed with a mixture of acetonitrile-water-0.05 M borate buffer (pH 9.0). The method has been applied to the direct determination of TMA in water within the 0.25-10.0 microg/ml concentration interval, and can also be adapted to the determination of TMA over the range 0.05-1.0 m…

Detection limitFluorenesChromatographyTertiary amineChemistryOrganic ChemistryWaterTrimethylamineGeneral MedicineReversed-phase chromatographyChloroformateSensitivity and SpecificityBiochemistryAnalytical ChemistryMethylamineschemistry.chemical_compoundSample preparationSolid phase extractionDerivatization
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Comparative assessment of three extraction procedures for determination of emerging Fusarium mycotoxins in pasta by LC–MS/MS

2013

Abstract A new rapid, sensitive, reproducible and reliable method was developed for the quantitative determination of enniatins A, A1, B and B1, beauvericin and fusaproliferin in dry and fresh pasta by liquid chromatography-triple quadrupole-tandem mass spectrometry. A comparative study of different rapid and economical extraction procedures was performed for the extraction of these mycotoxins in pasta. For this purpose, three different approaches were studied during the extraction step (Ultra-Turrax, ultrasonic bath and microwave). Optimal extraction conditions were reached using Ultra-Turrax with acetonitrile for 3 min without purification step. The chromatographic separation of the six m…

Detection limitFusariumChromatographybiologyChemistryExtraction (chemistry)food and beveragesMass spectrometrybiology.organism_classificationQuantitative determinationBeauvericinchemistry.chemical_compoundLc ms msMycotoxinFood ScienceBiotechnologyFood Control
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Comparison of different methods for extraction of polycyclic aromatic hydrocarbons (PAHs) from Sicilian (Italy) coastal area sediments.

2012

This paper describes a work aimed at improving the conditions of an extraction method, coupling GC-MS determination, for the analysis without cleanup phase, of polycyclic aromatic hydrocarbons (PAHs) from sediment samples. The automatic Soxhlet extraction in warm mode (using Extraction System B-811 Standard, Buchi) has demonstrated advantages for automation, reduced extraction time, and lower solvent use than for conventional Soxhlet extraction. Under these conditions, the recoveries are very good as they resulted greater than 85 % and, in most of the cases, near 100 %. The repeatability is also satisfactory (relative standard deviation less than 15 %). The detection limits are also accepta…

Detection limitGeologic SedimentsExtraction (chemistry)SedimentGeneral MedicineRepeatabilityChemical FractionationManagement Monitoring Policy and LawPollutionGas Chromatography-Mass SpectrometrySettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturaliMatrix (chemical analysis)Dry weightEnvironmental chemistryEnvironmental scienceEcotoxicologySeawaterSettore CHIM/01 - Chimica AnaliticaPolycyclic Aromatic HydrocarbonsGas chromatography–mass spectrometryAutomatic extraction .CRM . PAHs . Sediments . GC-MSSicilyWater Pollutants ChemicalEnvironmental MonitoringGeneral Environmental Science
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Improvement of the electrophoretic protein profiles of Leguminosae gums extracts using gamanase and application to the evaluation of carob–guar mixtu…

2004

Abstract A quantitative assay for guar gum in carob gum, based on the extraction of proteins in acetonitrile–water (7:3), separation by capillary electrophoresis and multiple linear regression (MLR) using the areas of nine selected peaks as predictors, was improved by performing the extraction in the presence of gamanase. In the absence of the enzyme, peak migration times and areas depended on the guar content, which complicated peak identification and evaluation. Manual correction of the migration times by comparison with standard electropherograms obtained with pure carob and carob–guar mixtures was required; however, when the proteins were extracted under sonication at 60 °C for 30 min i…

Detection limitGuar gumChromatographyChemistrySonicationExtraction (chemistry)GuarBiochemistryAnalytical ChemistryElectrophoresisCapillary electrophoresisEnvironmental ChemistrySample preparationSpectroscopyAnalytica Chimica Acta
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Development of a non-chromatographic method for the speciation analysis of inorganic antimony in mushroom samples by hydride generation atomic fluore…

2009

Abstract A simple and sensitive method has been developed for the direct determination of toxic species of antimony in mushroom samples by hydride generation atomic fluorescence spectrometry (HG AFS). The determination of Sb(III) and Sb(V) was based on the efficiency of hydride generation employing NaBH 4 , with and without a previous KI reduction, using proportional equations corresponding to the two different measurement conditions. The extraction efficiency of total antimony and the stability of Sb(III) and Sb(V) in different extraction media (nitric, sulfuric, hydrochloric, acetic acid, methanol and ethanol) were evaluated. Results demonstrated that, based on the extraction yield and th…

Detection limitHydrideExtraction (chemistry)Analytical chemistrychemistry.chemical_elementMass spectrometryAtomic and Molecular Physics and OpticsAnalytical Chemistrychemistry.chemical_compoundCertified reference materialschemistryAntimonyYield (chemistry)MethanolInstrumentationSpectroscopySpectrochimica Acta Part B: Atomic Spectroscopy
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Determination of organophosphorus pesticides in honeybees after solid-phase microextraction.

2001

A method based on solid-phase microextraction (SPME) followed by gas chromatography with nitrogen-phosphorus detection was developed for the purpose of determining 18 organophosphorus pesticide residues in honeybee samples (Apis mellifera). The extraction capacities of polyacrylate and poly(dimethylsiloxane) fibers were compared. The main factors affecting the SPME process, such as the absorption time profile, salt, and temperature, were optimized. The method involved honeybee sample homogenization, elution with an acetone:water solution (1:1) and dilution in water prior to fiber extraction. Moreover, the matrix effect on the extraction was evaluated. In samples spiked at the 0.2 mg kg(-1) …

Detection limitInsecticidesChromatographyChemistryElutionOrganic ChemistryExtraction (chemistry)Osmolar ConcentrationTemperatureGeneral MedicineBeesSolid-phase microextractionBiochemistrySensitivity and SpecificityAnalytical ChemistryDilutionOrganophosphorus CompoundsSolventsAnimalsSample preparationSaltsSolid phase extractionGas chromatographyJournal of chromatography. A
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Introducing a new and rapid microextraction approach based on magnetic ionic liquids: Stir bar dispersive liquid microextraction

2017

With the aim of contributing to the development and improvement of microextraction techniques, a novel approach combining the principles and advantages of stir bar sorptive extraction (SBSE) and dispersive liquid-liquid microextraction (DLLME) is presented. This new approach, termed stir bar dispersive liquid microextraction (SBDLME), involves the addition of a magnetic ionic liquid (MIL) and a neodymium-core magnetic stir bar into the sample allowing the MIL coat the stir bar due to physical forces (i.e., magnetism). As long as the stirring rate is maintained at low speed, the MIL resists rotational (centrifugal) forces and remains on the stir bar surface in a manner closely resembling SBS…

Detection limitMagnetic ionic liquidChromatographyChemistryMagnetism010401 analytical chemistryExtraction (chemistry)Analytical chemistryThermal desorption02 engineering and technologyRepeatability021001 nanoscience & nanotechnology01 natural sciencesBiochemistry0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundIonic liquidEnvironmental Chemistry0210 nano-technologySpectroscopyBar (unit)Analytica Chimica Acta
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Trace determination of volatile polycyclic aromatic hydrocarbons in natural waters by magnetic ionic liquid-based stir bar dispersive liquid microext…

2017

In this work, a novel hybrid approach called stir bar dispersive liquid microextraction (SBDLME) that combines the advantages of stir bar sorptive extraction (SBSE) and dispersive liquid-liquid microextraction (DLLME) has been employed for the accurate and sensitive determination of ten polycyclic aromatic hydrocarbons (PAHs) in natural water samples. The extraction is carried out using a neodymium stir bar magnetically coated with a magnetic ionic liquid (MIL) as extraction device, in such a way that the MIL is dispersed into the solution at high stirring rates. Once the stirring is ceased, the MIL is magnetically retrieved onto the stir bar, and subsequently subjected to thermal desorptio…

Detection limitMagnetic ionic liquidChromatographyTrace AmountsChemistry010401 analytical chemistryExtraction (chemistry)Analytical chemistryThermal desorption02 engineering and technology021001 nanoscience & nanotechnologyMass spectrometry01 natural sciences0104 chemical sciencesAnalytical ChemistryTap waterIonic strength0210 nano-technologyTalanta
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