Search results for "preparation"

showing 10 items of 939 documents

Automated on-line in-tube solid-phase microextraction-assisted derivatization coupled to liquid chromatography for quantifying residual dimethylamine…

2008

Abstract A method for the analysis of dimethylamine (DMA) by automated in-tube solid-phase microextraction (IT-SPME)-supported chemical derivatization coupled with high-performance liquid chromatography was developed. Extraction, derivatization and desorption were studied by using a capillary coated with 95% polydimethylsiloxane and 5% polydiphenylsiloxane. Solution derivatization and automated IT-SPME derivatization using 9-fluorenylmethyl chloroformate (FMOC) were compared. The proposed procedure provided adequate linearity, accuracy and precision in the 0.2–2.0 μg/mL concentration interval, and the limit of detection (LOD) was 50 ng/mL. The main advantages of the proposed procedure are: …

Detection limitChromatographyPolymersChemistryOrganic ChemistryGeneral MedicineChloroformateSolid-phase microextractionOnline SystemsBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundReagentSample preparationDerivatizationDimethylamineDimethylaminesSolid Phase MicroextractionChromatography Liquid
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Determination of hydroxylated benzophenone UV filters in sea water samples by dispersive liquid-liquid microextraction followed by gas chromatography…

2010

A new analytical method for the determination of four hydroxylated benzophenone UV filters (i.e. 2-hydroxy-4-methoxybenzophenone (HMB), 2,4-dihydroxybenzophenone (DHB), 2,2'-dihydroxy-4-methoxybenzophenone (DHMB) and 2,3,4-trihydroxybenzophenone (THB)) in sea water samples is presented. The method is based on dispersive liquid-liquid microextraction (DLLME) followed by gas chromatography-mass spectrometry (GC-MS) determination. The variables involved in the DLLME process were studied. Under optimized conditions, 1000 microL of acetone (disperser solvent) containing 60 microL of chloroform (extraction solvent) were injected into 5 mL of aqueous sample adjusted to pH 4 and containing 10% NaCl…

Detection limitChromatographySilylationOrganic ChemistryGeneral MedicineBSTFAChemical FractionationBiochemistryGas Chromatography-Mass SpectrometryAnalytical Chemistrychemistry.chemical_compoundBenzophenoneschemistryStandard additionSample preparationSeawaterGas chromatographyGas chromatography–mass spectrometryDerivatizationWater Pollutants ChemicalJournal of chromatography. A
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Determination of type A trichothecenes by high-performance liquid chromatography with coumarin-3-carbonyl chloride derivatisation and fluorescence de…

2000

A method for the analysis of type A trichothecenes T-2 toxin, HT-2 toxin, neosolaniol and diacetoxyscirpenol by high-performance liquid chromatography with fluorescence detection using coumarin-3-carbonyl chloride has been developed. Different parameters concerning the analytical procedure such as stability of both the reagent and derivatised analytes, time and temperature of the derivatisation reaction, were studied and optimised. Three different clean-up procedures (solid-phase extraction with silica gel or C-18 cartridges, and liquid-liquid partition between toluene and dihydrogen phosphate buffer) were tested in order to remove the excess reagent peaks. The last procedure gave the best …

Detection limitChromatographybiologyOrganic ChemistryTrichotheceneOryzaGeneral MedicineReversed-phase chromatographyHydrogen-Ion Concentrationbiology.organism_classificationBiochemistryHigh-performance liquid chromatographyFusarium sporotrichioidesZea maysDiacetoxyscirpenolAnalytical Chemistrychemistry.chemical_compoundSpectrometry FluorescencechemistryCoumarinsReagentSample preparationTrichothecenesChromatography High Pressure LiquidFluorescent DyesJournal of chromatography. A
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An environmentally friendly multicommutated alternative to the reference method for anionic surfactant determination in water

2004

Abstract It has been developed a fully mechanized procedure for the spectrophotometric determination of anionic surfactants in water expressed in terms of SDS concentration. The reference method, based on the reaction of SDS with methylene blue (MB) followed by extraction in chloroform, was mechanized in order to reduce the consumption of organic solvents. The system was based on the multicommutation approach and provided a 35 times reduction of the waste production without sacrificing the figures of merit of the method in terms of sensitivity and repeatability, for a dynamic linear range from 0.2 to 1.7 mg l−1. Results obtained for washing water samples were comparable with those obtained …

Detection limitChromatographymedicine.diagnostic_testChemistryExtraction (chemistry)Analytical chemistryRepeatabilityAnalytical ChemistrySolventPulmonary surfactantLinear rangeSpectrophotometrymedicineSample preparationTalanta
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Improving detection limits for organotin compounds in several matrix water samples by derivatization-headspace-solid-phase microextraction and GC-MS.

2010

Triethyltin, tributyltin, diphenyltin and triphenyltin were selected as model compounds. The method is based on in situ ethylation and simultaneous headspace-solid-phase microextraction (HS-SPME) and gas chromatographic-mass spectrometry analysis (GC-MS). The extraction procedure was optimized studying some variables such as reaction time, salinity, sample volume and headspace volume. SPME-GC-MS and SPME-GC-FID techniques were compared; quality assurance parameters such as sensitivity, selectivity and precision were established. The proposed procedure showed limits of detection between 0.025 and 1 ng/L. The linearity was in the 0.025-5000 ng/L range. The precision expressed as relative stan…

Detection limitCromatografia de gasosChromatographyAnalytical chemistrySolid-phase microextractionAnalytical Chemistrylaw.inventionMatrix (chemical analysis)chemistry.chemical_compoundchemistrylawFlame ionization detectorSample preparationGas chromatographyCompostos organometàl·licsAigües residuals AnàlisiGas chromatography–mass spectrometryDerivatizationTalanta
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Validation of Powder X-Ray Diffraction Following EN ISO/IEC 17025

2012

:  Powder X-ray diffraction (PXRD) is used widely in forensic science laboratories with the main focus of qualitative phase identification. Little is found in literature referring to the topic of validation of PXRD in the field of forensic sciences. According to EN ISO/IEC 17025, the method has to be tested for several parameters. Trueness, specificity, and selectivity of PXRD were tested using certified reference materials or a combination thereof. All three tested parameters showed the secure performance of the method. Sample preparation errors were simulated to evaluate the robustness of the method. These errors were either easily detected by the operator or nonsignificant for phase iden…

Detection limitEngineeringCertified reference materialsbusiness.industryX-ray crystallographyGeneticsAnalytical chemistrySample preparationProficiency testbusinessISO/IEC 17025Powder diffractionPathology and Forensic MedicineJournal of Forensic Sciences
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Minimizing the impact of sample preparation on analytical results: In-tube solid-phase microextraction coupled on-line to nano-liquid chromatography …

2020

The degradation kinetics and residual levels of the sulfonylurea herbicide tribenuron-methyl (TBM) in different environmental waters were studied using in tube-solid phase microextraction (IT-SPME) coupled on-line to nano-liquid chromatography (nanoLC) and UV diode array detection (DAD). This approach combines the high extraction efficiency of IT-SPME using polymeric coatings reinforced with metal oxide nanoparticles and the high sensitivity attainable by nanoLC, making possible the determination of TBM at low ppb levels (limit of detection, 0.25 ppb) without altering the sample matrix. The present study demonstrated that the preservation of the sample properties is essential to ensure accu…

Detection limitEnvironmental EngineeringChromatography010504 meteorology & atmospheric sciencesChemistryExtraction (chemistry)010501 environmental sciencesSolid-phase microextraction01 natural sciencesPollutionHydrolysisPhase (matter)Environmental ChemistryDegradation (geology)Tube (fluid conveyance)Sample preparationWaste Management and Disposal0105 earth and related environmental sciencesScience of The Total Environment
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Analysis of Polycyclic Aromatic Hydrocarbons and Their Oxygen-Containing Derivatives and Metabolites in Soils

2010

Although polycyclic aromatic hydrocarbons (PAHs) have been extensively studied, the knowledge of their oxygen-containing derivatives and metabolites (OPAHs) in soils is limited. We modified and tested an existing analytical protocol involving pressurized liquid extraction of soil followed by fractionation of target compounds into PAHs and OPAHs on a silica gel column and gas chromatography/ mass spectrometry-based separation and quantification. Polycyclic aromatic hydrocarbons and carbonyl-OPAHs were quantified directly after separation on silica gel columns, and hydroxyl/carboxyl-OPAHs were quantified after silylation with N,O-bis(trimethylsilyl)trifluoroacetamide. Recoveries between 78 an…

Detection limitEnvironmental EngineeringChromatographyOpahbiologySilylationChemistrySilica gelExtraction (chemistry)Industrial WasteFractionationManagement Monitoring Policy and Lawbiology.organism_classificationPollutionOxygenSoilchemistry.chemical_compoundEnvironmental chemistrySoil PollutantsSample preparationGas chromatographyPolycyclic Aromatic HydrocarbonsWaste Management and DisposalEnvironmental MonitoringWater Science and TechnologyJournal of Environmental Quality
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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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Zwitterionic Sulfonates as m/z Shift Reagents for 5-Methylcytosine Detection in Deoxyribonucleic Acids (DNA) Using Flow Injection Analysis and Electr…

2015

5-Methylcytosine (5-MC) is an important epigenetic modification of DNA. Abnormally high concentrations of this substance appear because of the hypermethylation of cytosine. Therefore, the measurement of the quantity of this compound in mammals is of great importance. Recently, we reported that several imidazolium-based zwitterionic sulfonates form complexes with 5-MC in solution, which can be studied by electrospray ionisation mass spectrometry (ESI-MS). It is shown in this paper that such an association can be utilised for the detection of 5-MC in a DNA sample using high-throughput a flow injection analysis ESI-MS method. A variety of the sulfonate zwitterions have been tested as m/ z shi…

Detection limitFlow injection analysisSpectrometry Mass Electrospray IonizationElectrosprayChromatographyChemistryElectrospray ionizationAnalytical chemistryReproducibility of ResultsDNAGeneral MedicineDNA MethylationTandem mass spectrometryMass spectrometryAtomic and Molecular Physics and OpticsSample preparation in mass spectrometryFlow Injection Analysis5-MethylcytosineAnimalsCattleA-DNASulfonic AcidsSpectroscopyEuropean Journal of Mass Spectrometry
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