Search results for "Solvent"

showing 10 items of 1395 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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Solvent quality as reflected in concentration- and temperature-dependent Flory-Huggins interaction parameters

2001

Flory-Huggins interaction parameters (χ) between poly(dimethylsiloxane) (weight-average molecular weight = 152 kg/mol) and various solvents (methyl ethyl ketone, toluene and n-octane) were determined as a function of composition and temperature with vapor-pressure measurements. These data, complemented by independent information for dilute and very concentrated solutions, serve as the basis for a discussion of solvent quality via different theoretical relations. Regardless of polymer concentration, the χ values fall from methyl ethyl ketone via toluene to n-octane, the ketone being the worst solvent and the hydrocarbon being the best solvent. The variation of χ with composition and temperat…

chemistry.chemical_classificationChromatographyKetonePolymers and PlasticsEnthalpyThermodynamicsConcentration effectPolymerFlory–Huggins solution theoryCondensed Matter PhysicsTolueneSolventchemistry.chemical_compoundHydrocarbonchemistryMaterials ChemistryPhysical and Theoretical ChemistryJournal of Polymer Science Part B: Polymer Physics
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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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Isobaric Vapor−Liquid Equilibria for Water + Acetic Acid + Sodium Acetate

2003

Isobaric vapor−liquid equilibria for the binary water + sodium acetate and acetic acid + sodium acetate systems and ternary mixtures of water, acetic acid, and sodium acetate have been measured at 100 kPa with a recirculating still. The addition of sodium acetate to water + acetic acid mixtures produced an appreciable rise in equilibrium temperature but a small effect on the relative volatility of water, which was augmented at higher water solvent concentrations and decreased at lower concentrations. These effects increased with higher salt concentrations. The experimental binary data sets have been correlated using a modified Mock's electrolyte NRTL model, which takes into account the asso…

chemistry.chemical_classificationChromatographyRelative volatilityGeneral Chemical EngineeringInorganic chemistrySalt (chemistry)General ChemistryElectrolyteSolventAcetic acidchemistry.chemical_compoundchemistryNon-random two-liquid modelIsobaric processSodium acetateJournal of Chemical & Engineering Data
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Determination of cationic surfactants by capillary zone electrophoresis and micellar electrokinetic chromatography with deoxycholate micelles in the …

2000

Mixtures of the cationic surfactants benzalkonium chloride (BKC) and cetylpyridinium chloride (CPC) were quickly resolved and reproducibly and reliably determined by using background electrolytes (BGEs) containing 80 mM borate, pH 8.5, bile salts and large concentrations of an organic solvent. When the bile salt is present, the separation mechanism changes from capillary zone electrophoresis (CZE) to a mixed micellar electrokinetic chromatography (MEKC)-CZE, with predominant MEKC interactions, which lead to an excellent resolution of all the solutes, including the C12-C18 homologues of BKC and CPC. A BGE containing 50 mM sodium deoxycholate and 30% ethanol for an extreme resolution, or 20% …

chemistry.chemical_classificationChromatographyResolution (mass spectrometry)Organic ChemistryCationic polymerizationSalt (chemistry)General MedicineCetylpyridinium chlorideBiochemistryMicelleMicellar electrokinetic chromatographyAnalytical Chemistrychemistry.chemical_compoundBenzalkonium chlorideSurface-Active AgentsCapillary electrophoresischemistryCationsmedicineSolventsMicellesmedicine.drugChromatography Micellar Electrokinetic CapillaryDeoxycholic AcidJournal of chromatography. A
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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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Method for Synthesis and Screening of Large Groups of Molecularly Imprinted Polymers

2011

A technique for the synthesis of molecularly imprinted polymers (MIPs) in small scale (∼55 mg) coupled with direct in situ processing and batch rebinding evaluation is reported. The primary assessment is based on quantification by HPLC or UV absorbance measurement of the amount of template released from the polymer in a given solvent. This method allows a rapid screening of the parameters of importance to reach a desired level of binding affinity capacity and selectivity for a given target molecule. This was demonstrated for the triazine herbicide terbutylazine, where an initial screening was performed for the type of functional monomer used in the MIP preparation. Thus among the six functi…

chemistry.chemical_classificationChromatographyTrifluoromethylMolecularly imprinted polymerPolymerAnalytical ChemistrySolventchemistry.chemical_compoundchemistryMethacrylic acidOrganic chemistryMethyl methacrylateSelectivityAcrylic acidAnalytical Chemistry
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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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Conformational characteristics of homo-oligopeptides of O-benzyl-L-tyrosine+

1983

Conformational studies of X[-L-Tyr(Bzl)-]n-series bound to polyethyleneglycol (X = H2, Nps; n = 3-8) in the solid state and in solvents of different polarities and capabilities of forming hydrogen bonds are reported. By using i.r. absorption, the occurrence of the beta-structure in the higher oligomers in the solid state was established. By means of i.r. absorption and CD the onset of that ordered conformation in solution was assessed as a function of chain length. The effects induced by the presence of the N-protecting group and added base, and by changing the nature of solvent on the conformational preferences of the [-L-Tyr(Bzl)-]n homo-peptides were also examined. The 2-nitrophenylsulph…

chemistry.chemical_classificationCircular dichroismChemical PhenomenaSpectrophotometry InfraredBase (chemistry)Protein ConformationStereochemistryHydrogen bondCircular DichroismInfrared spectroscopyBiochemistryPeptide ConformationSolutionsSolventChemistrychemistry.chemical_compoundchemistryTyrosineAbsorption (chemistry)OligopeptidesDerivative (chemistry)International Journal of Peptide and Protein Research
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