Search results for "Extract"

showing 10 items of 2769 documents

Microwave-assisted extraction of OCPs, PCBs and PAHs concentrated by semi-permeable membrane devices (SPMDs)

2005

Abstract Microwave-assisted extraction (MAE) has been evaluated as an alternative to dialysis for extraction of some water-borne hydrophobic contaminants sampled by semi-permeable membrane devices (SPMDs). Seven organochlorine pesticides (OCPs), 11 polychlorinated biphenyls (PCBs) and 13 polycyclic aromatic hydrocarbons (PAHs) were accumulated in SPMDs at nanogram levels and extracted with three 3-min irradiation cycles with 33 mL of a solvent mixture hexane–water (10:1,v/v) in each cycle. The developed MAE method gave for all analytes investigated statistically comparable extraction yields with those found by dialysis carried out with a total volume of 250 mL hexane for 48 h at room temper…

chemistry.chemical_classificationChromatographyExtraction (chemistry)ContaminationBiochemistryAnalytical ChemistryHexaneSolventchemistry.chemical_compoundHydrocarbonchemistryEnvironmental chemistryEnvironmental ChemistrySample preparationSemipermeable membraneWater pollutionSpectroscopyAnalytica Chimica Acta
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Headspace-Liquid Phase Microextraction for Attenuated Total Reflection Infrared Determination of Volatile Organic Compounds at Trace Levels

2010

A combination of headspace (HS) sampling and liquid phase microextraction (LPME) has been successfully developed to solve sensitivity problems in attenuated total reflection (ATR) infrared determination of volatile organic compounds (VOCs). The HS sampling facilitates the selective extraction of the target volatile analytes from the sample matrix, while the liquid phase microextraction allows their preconcentration prior to infrared analysis. The direct determination of extracted analytes in the acceptor solvent provides high preconcentration factors of the order of 200 with a reduced consumption of organic solvents and a minimum generation of wastes, being thus the developed methodology a …

chemistry.chemical_classificationChromatographyExtraction (chemistry)XyleneAnalytical chemistryTolueneAnalytical ChemistrySolventchemistry.chemical_compoundchemistryAttenuated total reflectionVolatile organic compoundSample preparationBenzeneAnalytical Chemistry
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Selective extraction of small proteins from biological samples using a novel restricted access column with cation exchange properties

2000

The determination of proteins utilising a polymer-based restricted access suppor material with ion exchange properties (IERAM) is outlined. Solid phase extraction coupled on-line with a mincrobore reversed phase HPLC system for the quantitation of small marker proteins is demonstrated. The cation-exchange restricted access packings were characterised with respect to their adsorption and desorption kinetics. The IERAM material was also investigated by capacity, selectivity, and biocompatibility determinations when applied to the quantification of small molecular weight proteins such as cytochrome C, Lysozyme, Ribonuclease A, Myoglobin, Insulin, human serum albumin, and a Tryptic inhibitor.

chemistry.chemical_classificationChromatographyIon exchangebiologyChemistryOrganic ChemistryClinical BiochemistryExtraction (chemistry)PolymerReversed-phase chromatographyHuman serum albuminBiochemistryAnalytical ChemistryMatrix-assisted laser desorption/ionizationmedicinebiology.proteinPancreatic ribonucleaseSolid phase extractionmedicine.drug
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Continuous fractionation and solution properties of PIB. I. Search for the best mixed solvent and first results of the continuous polymer fractionati…

1987

To adopt a recently developed method for large scale fractionation (CPF = continuous polymer fractionation, a special kind of counter current extraction) to polyisobutylene (PIB), a systematic search for the best mixed solvent was performed. For this purpose, the essential parts of the phase diagrams solvent/nonsolvent/PIB were determined for 21 mixed solvents by cloud-point measurements; with eight systems of special interest, the molecular weight distributions of the polymers contained in the coexisting phases were also studied. On the basis of these experiments and of considerations concerning additional criteria for the performance of the continuous counter current extraction, the mixed…

chemistry.chemical_classificationChromatographyKetonePolymers and PlasticsExtraction (chemistry)Analytical chemistryGeneral ChemistryPolymerFractionationTolueneSurfaces Coatings and FilmsSolventchemistry.chemical_compoundchemistryMaterials ChemistryPolymer fractionationPhase diagramJournal of Applied Polymer Science
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Selective solid phase extraction of a drug lead compound using molecularly imprinted polymers prepared by the target analogue approach

2002

Molecularly imprinted polymers have been evaluated at the sample clean-up stage in the analysis of a drug lead compound. In order to circumvent quantification problems related to bleeding of the template, a structurally related analogue of the latter was used. This was selected based on criteria related to interaction site location, solubility, availability and stability of the analogue. Selection of suitable polymerisation conditions was then made using a small batch format (ca. 50 mg) and rapid assessment of binding in the equilibrium mode. It was found that the amount of template could be greatly reduced compared to the conventional protocol, requiring only 5 μmol of template per gram of…

chemistry.chemical_classificationChromatographyOrganic ChemistryClinical BiochemistryMolecularly imprinted polymerPolymerBiochemistryAnalytical Chemistrychemistry.chemical_compoundPhotopolymerchemistrySample preparationSolid phase extractionSolubilityMolecular imprintingLead compoundChromatographia
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CPF : Continuous polymer fractionation

1992

A method is presented by means of which it is possible to fractionate polymers according to their solubility on a technical scale. The CPF consists of a continuous counter-current extraction process in which a homogeneous mixture of a molecularly or/and chemically non-uniform high molecular weight product is divided into two portions of considerably lower non-uniformity. The principle of the CPF is described in general terms and examples are given for the fractionation of homopolymers.

chemistry.chemical_classificationChromatographyPolymers and PlasticsChemistryHomogeneousOrganic ChemistryExtraction (chemistry)Materials ChemistryFractionationPolymerSolubilityPolymer fractionationCondensed Matter PhysicsMakromolekulare Chemie. Macromolecular Symposia
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Characterisation of Diarylheptanoid- and Flavonoid-type Phenolics in Corylus avellana L. Leaves and Bark by HPLC/DAD-ESI/MS

2013

Introduction The leaves of Corylus avellana L. (common hazel, Betulaceae), a plant with a wide distribution in Europe, have been used in folk medicine for various diseases, but phytochemical exploration of C. avellana is still incomplete. To the best of our knowledge there is no previous report concerning diarylheptanoids in C. avellana, although these compounds show a frequent occurrence among Betulaceae plants. Objective To improve existing online chromatographic methods for the investigation of the phenolic compounds in C. avellana leaves and bark, focusing on diarylheptanoid-type molecules. Methods Dried and powdered leaves and bark of C. avellana were extracted with increasing polarity…

chemistry.chemical_classificationChromatographySoxhlet extractorFlavonoidDiarylheptanoidEthyl acetatePlant ScienceGeneral MedicineBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundComplementary and alternative medicinechemistryPhytochemicalvisual_artDrug Discoveryvisual_art.visual_art_mediumMolecular MedicineBarkDiarylheptanoidsFood SciencePhytochemical Analysis
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Continuous fractionation and solution properties of PIB. II. CPF optimization

1987

The quality of polymer fractionation depends on the choice of the mixed solvent as well as on the particular conditions of operating the continuous countercurrent extraction. With a polyisobutylene (PIB) sample of medium molecular weight Mw = 98,400 g/mol and U = (Mw/Mn) − 1 = 1.4 plus the mixed solvents toluene/2-butanone (TOL/MEK) and n-heptane/2-butanone (HEP/MEK) (both giving comparably good fractionation in equilibrium experiments), possible ways to optimize the CPF were tested. The mixed solvent HEP/MEK turns out to be superior to TOL/MEK for kinetic reasons. Due to the larger gap between its density and that of the pure polymer, the coexisting phases can still move through the column…

chemistry.chemical_classificationChromatographyTernary numeral systemPolymers and PlasticsExtraction (chemistry)Analytical chemistryGeneral ChemistryPolymerFractionationTolueneSurfaces Coatings and FilmsSolventchemistry.chemical_compoundchemistryMass transferMaterials ChemistryPolymer fractionationJournal of Applied Polymer Science
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Separation of isobutyl alcohol and isobutyl acetate by extractive distillation and pressure-swing distillation: Simulation and optimization

2006

Abstract We have studied, simulated and evaluated economically two separation alternatives of a mixture made up of 52 mole% of isobutyl alcohol and 48 mole% of isobutyl acetate by means of a practical case of a plant to treat 12,000 Tm/year of the original mixture. The simulation has been carried out satisfactorily by means of a package of commercial software (Aspen HYSYS ® ) using the thermodynamic model UNIQUAC with binary parameters obtained experimentally by us. The two processes evaluated (extractive distillation using n -butyl propionate as a solvent and pressure-swing distillation) have been optimized independently from each other and the best configurations have been evaluated econo…

chemistry.chemical_classificationChromatographyUNIQUACIsobutyl acetateChemistryFiltration and SeparationIsobutyl alcoholAnalytical Chemistrylaw.inventionSolventchemistry.chemical_compoundlawAzeotropic distillationPropionateOrganic chemistryExtractive distillationDistillationSeparation and Purification Technology
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Determination of polycyclic aromatic hydrocarbons in atmospheric particulate matter of Valencia city

1991

Polycyclic aromatic hydrocarbons (PAHs) were determined in atmospheric particulate matter in 11 sites of the Valencia area and at several times during the year. Sample analysis was carried out by ultrasonic acetonitrile extraction followed by reverse phase HPLC separation and fluorescence detection. The maximum concentration of total PAH developed in winter and spring. Mean values per sampling site varied from 0.193 to 1.668 μg/m3 of filtered air. Environmental noise and temperature were determined at those same 11 sites and correlated with PAH levels.

chemistry.chemical_classificationChromatographybiologyExtraction (chemistry)Polycyclic aromatic hydrocarbonReversed-phase chromatographyParticulatesbiology.organism_classificationBiochemistryHigh-performance liquid chromatographyHydrocarbonchemistryEnvironmental chemistryValenciaFresenius' Journal of Analytical Chemistry
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