Search results for "Phase"

showing 10 items of 6344 documents

Phase Behavior of the System Linear Polyglycerol + Methanol + Carbon Dioxide

2011

To compare the phase behavior of linear and hyperbranched polymers, the phase envelopes of the ternary system linear polyglycerol + methanol + carbon dioxide were determined for polymers of varying molar mass. Phase changes were detected by a static synthetic method using the Cailletet setup for temperatures between 331 K and 421 K and pressures up to 13.1 MPa. Besides the vapor–liquid and liquid–liquid equilibria, also the vapor–liquid to vapor–liquid–liquid and vapor–liquid–liquid to liquid–liquid phase boundaries are reported. The experimental results are similar to systems with hyperbranched polymers (rather than linear polymers). For the systems with linear polymers, however, the bubbl…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesTernary numeral systemMolar massChemistryGeneral Chemical EngineeringBubbleGeneral ChemistryPolymerLower critical solution temperaturePhysics::Fluid DynamicsCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundChemical engineeringPhase (matter)Carbon dioxidePolymer chemistryMethanolJournal of Chemical & Engineering Data
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Spinodal demixing, percolation and gelation of biostructural polymers

1990

We present a variety of new experiments which concern the self-assembly of a polymeric network from homogeneous solutions of Agarose, a representative biostructural polysaccharide used for previous studies at our laboratories. They allow deriving a semi-quantitative phase diagram in the T, C plane. The diagram includes both the spinodal and gelation lines. Below a value of about 2% w/v, concentration is not sufficient for direct gelation; however, quenching of the sol from high temperatures to below the spinodal line initiates the spinodal demixing. The latter generates two sets of regions having respectively, higher- and lower-than-average polymer concentrations. In the higher-concentratio…

chemistry.chemical_classificationQuenchingSpinodalMaterials sciencePolymers and PlasticsPlane (geometry)Organic ChemistryDiagramKineticsPolymerCondensed Matter PhysicsCrystallographychemistryChemical physicsPercolationMaterials ChemistryPhase diagramMakromolekulare Chemie. Macromolecular Symposia
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Time-Resolved study of network self-organization from a biopolymeric solution

1991

Time-resolved studies of network self-organization from homogeneous solutions of the representative biostructural polymer agarose are presented. Solutions are temperature quenched and observed by several techniques. Consistent with previous suggestions by the authors, experiments at concentrations up to about 1.75% w/v provide direct kinetic evidence for the occurrence of at least two distinct processes, leading, in sequence, to self-assembly. These are as follows: (a) a liquid–liquid phase separation of the solution occurring via spinodal demixing and resulting in two sets of regions that have, respectively, higher and lower than average concentrations of random-coiled polymers; and (b) th…

chemistry.chemical_classificationQuenchingSpinodalOrganic ChemistryBiophysicsGeneral MedicinePolymerBranching (polymer chemistry)BiochemistryInstabilityBiomaterialschemistry.chemical_compoundchemistryChemical physicsHelixOrganic chemistryAgarosePhase diagramBiopolymers
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Physical and structural characterization of blends made with polyamide 6 and gamma-irradiated polyethylenes

1996

Abstract Morphological, calorimetric and rheological results of blends made with polyamide 6 and polyethylene gamma irradiated in air are presented. The polar oxidized groups grafted in the poliolefin chains through gamma-radiation induce “compatibilization” effects in the blends with a more uniform and finer distribution of the polyethylene “phase” in the polyamide matrix, with respect to blends made with the unirradiated polymer. This effect, observed with polyethylenes of different molecular structure, i.e. low density, linear low density and high density, was attributed to the presence of interactions among the functional oxidized groups of the polyethylene chains and the polyamide. Tes…

chemistry.chemical_classificationRadiationMaterials sciencePolymerCompatibilizationPolyethylenechemistry.chemical_compoundchemistryRheologyChemical engineeringPhase (matter)PolyamidePolymer chemistryMoleculeIrradiationRadiation Physics and Chemistry
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Interfacial properties of glassy polymer melts: A Monte Carlo study

1996

The properties of the interface between a polymer melt and a solid wall are studied over a wide range of temperatures by dynamic Monte Carlo simulations. It is shown that in the supercooled state near the glass transition of the melt an “interphase” forms, the structure of which is influenced by the wall. The thickness of this interphase is determined from the monomer density profile near the surface and is strongly temperature dependent. At low glass-like temperatures it is larger than the bulk radius of gyration of the chains.

chemistry.chemical_classificationRange (particle radiation)Materials sciencePolymers and PlasticsOrganic ChemistryMonte Carlo methodThermodynamicsPolymerCondensed Matter PhysicsCondensed Matter::Disordered Systems and Neural NetworksCondensed Matter::Soft Condensed MatterCrystallographychemistry.chemical_compoundMonomerchemistryMaterials ChemistryRadius of gyrationInterphaseSupercoolingGlass transitionMacromolecular Symposia
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Electrochemical monitoring of ROS generation by anticancer agents: the case of chartreusin

2017

Solution phase and solid-sate electrochemical techniques centered in the voltammetry of microparticles approach are applied for testing the cytotoxic activity of anticancer drugs. The possibility of electrochemical generation of reactive oxygen species (ROS) is exploited for evaluating their contribution to cellular damage. The described methodology is applied to the case of chartreusin (Ch) whose electrochemistry in non-aqueous solutions and in the solid state in contact with aqueous electrolytes is described in the absence (experimental data were confirmed by theoretical calculations) and in the presence of double-stranded DNA (dsDNA). In parallel, scanning electrochemical microscopy (SEC…

chemistry.chemical_classificationReactive oxygen speciesChartreusinGeneral Chemical EngineeringIntercalation (chemistry)Nanotechnology02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyElectrochemistry01 natural sciencesCombinatorial chemistrySolution phase0104 chemical scienceschemistry.chemical_compoundScanning electrochemical microscopychemistry0210 nano-technologyVoltammetryDNARSC Advances
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Polymer- and template-related factors influencing the efficiency in molecularly imprinted solid-phase extractions

1999

Abstract This review identifies the factors of importance in the development of molecularly imprinted polymers for use in solid-phase extractions and summarizes the results obtained to date in the area of bioanalysis, pharmaceutical analysis and environmental analysis.

chemistry.chemical_classificationRelated factorsBioanalysisChromatographychemistryEnvironmental analysisPhase (matter)Molecularly imprinted polymerSeparation methodPolymerSolid phase extractionSpectroscopyAnalytical ChemistryTrAC Trends in Analytical Chemistry
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Single-pump heart-cutting two-dimensional liquid chromatography applied to the determination of fatty alcohol ethoxylates.

2014

Abstract A setup for heart-cutting bi-dimensional liquid chromatography (LC–LC), constructed with a chromatograph provided with a single pump, an auxiliary 6-port 2-position valve (V 6/2 ) and a column selector valve (V CS ), is described. The possible ways of connecting the two valves for LC–LC, namely with V 6/2 first followed by V CS and vice versa, are compared. The possibility of using the setups for preconcentration followed by the backwards transfer of the preconcentrated solutes to the detector or to a second column is also shown. The V 6/2 -first configuration for LC–LC was applied to the characterization of industrial fatty alcohol ethoxylates (FAEs) using UV–vis detection. For th…

chemistry.chemical_classificationResponse factorChromatographySeries (mathematics)ElutionOrganic ChemistryAnalytical chemistryFatty alcoholWaterGeneral MedicineBiochemistryAnalytical Chemistrychemistry.chemical_compoundHydrocarbonchemistryDimension (vector space)Phase (matter)Gradient elutionFatty AlcoholsChromatography LiquidJournal of chromatography. A
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Use of reversed-phase C18 Sep-Pak cartridges for the purification and concentration of sepiapterin and other pteridines

1985

Abstract Several pteridines have been tested for their ability to bind to C 18 Sep-Pak. Riboflavin, sepiapterin, deoxysepiapterin, 6-acetyl-7,8-dihydropterin, 6-acetyldihydrohomopterin and 3′-hydroxysepiapterin were strongly retained and all but 6-acetyldihydrohomopterin quantitatively recovered upon elution with 2 ml of methanol. The effect of the concentration and volume of the sample, pH and salt concentration on the retention of sepiapterin have been studied. The procedure was very useful for the purification, desalting, solvent exchange and concentration of pteridines having high affinity for the cartridge. C 18 Sep-Pak has been applied succesfully to sample clean-up prior to high-perf…

chemistry.chemical_classificationSepiapterinChromatographyChemistryElutionDihydropterin oxidaseOrganic ChemistrySalt (chemistry)General MedicineBiochemistryAnalytical ChemistrySolventCartridgechemistry.chemical_compoundPhase (matter)MethanolJournal of Chromatography A
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O-Alkylation of a lignite humic acid by phase-transfer catalysis

2006

A mild phase-transfer catalytic reaction has been conducted to O-alkylate the acidic functions of a lignite humic acid (HA), using tetrabutylammonium hydroxide as the phase-transfer catalyst. The HA acidic functional groups were made to react, in tetrahydrofuran, by nucleophilic substitution with several alkyl halides-methyl iodide, and ethyl, propyl, and butyl, and benzyl bromide. The occurrence of the O-alkylation reaction was assessed by elemental analysis and 1H NMR, CPMAS 13C NMR, and FTIR spectroscopy. Bonding of alkyl groups increased the carbon and hydrogen content and the H/C ratios of all the humic reaction products. Increased nitrogen in the reaction products suggested incomplete…

chemistry.chemical_classificationSettore AGR/13 - Chimica AgrariaEtherAlkylationCarbon-13 NMRBiochemistryAnalytical ChemistryCatalysischemistry.chemical_compoundchemistryProton NMRNucleophilic substitutionHumic acidOrganic chemistrylipids (amino acids peptides and proteins)Humic substances O-Alkylation Phase-transfer catalysis Tetrabutylammonium hydroxide NMR FTIRAlkylAnalytical and Bioanalytical Chemistry
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