Search results for "Reduced viscosity"

showing 7 items of 7 documents

New biodegradable hydrogels based on an acryloylated polyaspartamide cross-linked by gamma irradiation

1999

Alpha, beta-poly(N-2-hydroxyethyl)-DL-aspartamide (PHEA), a synthetic biocompatible macromolecule, was functionalized with glycidyl methacrylate (GMA) in order to introduce in its side chains residues having double bonds and ester groups. The copolymer (PHG), obtained from PHEA and GMA, had a degree of derivatization of 29 mol%. PHG aqueous solutions are cross-linked by gamma radiation at 0 degrees C either in the presence or absence of N,N'-methylenebisacrylamide (BIS) giving rise to new hydrogel systems. In both cases gelation occurs at quite low doses (0.26 and 0.4 kGy, respectively). The obtained networks were characterized by FT-IR spectrophotometry which confirmed that the cross-linki…

Glycidyl methacrylateMagnetic Resonance SpectroscopyMaterials scienceBiomedical EngineeringBiophysicsBiocompatible MaterialsBioengineeringIn Vitro TechniquesBiomaterialsHydrolysischemistry.chemical_compoundEnzymatic hydrolysisMaterials TestingSpectroscopy Fourier Transform InfraredPolymer chemistryCopolymerReduced viscosityAqueous solutionHydrolysisHydrogelsBiodegradation EnvironmentalCross-Linking ReagentschemistryGamma RaysSelf-healing hydrogelsPeptidesMacromoleculeJournal of Biomaterials Science, Polymer Edition
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Liquid viscosity and flow rate effects on interfacial area in packed columns

1989

Abstract The influences of liquid kinematic viscosity and liquid flow rate on effective interfacial area for chemical absorption in a Raschig ring packed column were studied by absorbing carbon dioxide into potassium carbonate-bicarbonate-arsenite solutions. The viscosities of the absorbing liquid were varied by the addition of sugar. Analysis of the data shows that an increase in liquid flow rate increases the effective interfacial area over the whole viscosity range considered. The influence of liquid viscosity is more complex as the interfacial area increases with viscosity for low values, while decreasing at higher viscosities. Two correlations have been developed to express this behavi…

Packed bedViscosityRaschig ringTemperature dependence of liquid viscosityChemistryRelative viscosityIntrinsic viscosityGeneral EngineeringThermodynamicsViscosity indexReduced viscosityThe Chemical Engineering Journal
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On the factors governing the pressure dependence of the viscosity of moderately concentrated polymer solutions

1982

Viscosity measurements were carried out as a function of pressure and temperature with solutions of polystyrene in eight (endothermal) θ-solvents at the respective critical composition by means of a Searle-type apparatus. A rolling-ball viscometer was used for the investigation of the pure solvents. In all cases the viscosity coefficient increases in a more or less exponential manner when the pressure is raised. For θ-conditions, the volumes of activation of the solutions exceed that of the pure solvent by typically 10–15%. The exact amount of this extra efffect stemming from the presence of the polymer and its variation with temperature can be qualitatively correlated with the heats of mix…

Polymers and PlasticsChemistryRelative viscosityIntrinsic viscosityInherent viscosityViscometerThermodynamicsGeneral ChemistrySurfaces Coatings and FilmsSolventViscosityTemperature dependence of liquid viscosityMaterials ChemistryReduced viscosityJournal of Applied Polymer Science
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Rheological studies of moderately concentrated polystyrene solutions. I. A new method for the extrapolation of the zero-shear viscosity

1983

Measurements of the viscosity coefficient η of solutions of polystyrene (Mw = 6.0 × 105 and 1.77 × 106) in trans-decalin (TD, θ solvent) and toluene (TL, good solvent) as function of shear rate (11−104 s−1), concentration (4.24−11.21 wt %), and temperature (10–50°C) are reported. As a new theoretically grounded method for the determination of the zero-shear viscosity η0 it is proposed to plot η as a function of . The intercepts of the straight lines obtained by this procedure give η0 in good agreement with directly measured values.

Shear rateViscositychemistry.chemical_compoundChromatographyRheologyChemistryRelative viscosityGeneral EngineeringExtrapolationThermodynamicsPolystyreneReduced viscosityTolueneJournal of Polymer Science: Polymer Physics Edition
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1985

Viscosities were measured as a function of pressure and temperature with solutions of PVC 75 000 in cyclohexanone (CHO) and polymer contents ranging from 0,6 to 12 wt.-%, by means of a Searle-type (≥3 wt.-%) and a rolling-ball viscometer (<3 wt.-%). Furthermore, the influence of molecular weight was determined with solutions of 8 wt.-% of PVC 20 000, PVC 37 000 and PVC 100 000. (The numbers in the codes of the PVC specimens are their approximate molecular weights.) For all concentrations and molecular weights, the viscosity increases in a more or less exponential manner with increasing pressure. The ratio f1000 of the viscosity of the solution at 1 000 and 1 bar can be varied by the change …

Solventchemistry.chemical_classificationViscositychemistryIntrinsic viscosityPolymer chemistryViscometerActivation energyFractionationPolymerReduced viscosityDie Makromolekulare Chemie
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Solution properties of polyelectrolytes—V. Viscometric study of mixed polyanions in pure water

1990

Abstract A viscometric study of sodium polystyrene sulphonate (NaPSS) and sodium poly( l -glutamate) (NaPLG) in salt-free water has been carried out as a function of the total concentration, cm, and the concentration of one polyelectrolyte at fixed concentration of the other. The influences of the molecular weight and concentration are considered in order to establish the degree of compatibility. For the first time, an equation is proposed to define the reduced viscosity of the NaPSS + NaPLG mixture in water. The viscometric interaction parameter, Bm, taking into account the electrostatic and thermodynamic interactions between both polyions, is defined as a geometrical mean of the contribut…

Ternary numeral systemAqueous solutionPolymers and PlasticsChemistrySodiumOrganic ChemistryGeneral Physics and AstronomyThermodynamicsConcentration effectchemistry.chemical_elementCompatibility (geochemistry)Flory–Huggins solution theoryPolyelectrolytePolymer chemistryMaterials ChemistryReduced viscosityEuropean Polymer Journal
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Pressure influences on the viscosity of polymer solutions

1982

Of all physico-chemical quantities characterizing the behavior of liquids, the viscosity coefficient η is normally most sensitive to pressure. Early measurements of η(p) date back almost 100 years [1] but they were carried out with very different objectives [2]. Currently, one is particularly interested in polymer solutions, for instance because of the additives to motor oils and of oil recovery. The present paper reports on measurements with polystyrenes of high molecular uniformity in eight different solvents. It confines itself to zero-shear viscosities and discusses the possibilities of discovering the influence of pressure via the molecular structure of the solvent and via its thermody…

chemistry.chemical_classificationViscosityMaterials sciencechemistryTemperature dependence of liquid viscosityRelative viscosityIntrinsic viscosityInherent viscosityThermodynamicsViscosity indexPolymerReduced viscosity
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