Search results for "Relative viscosity"
showing 10 items of 14 documents
An expanded model and application of the combined effect of crystal-size distribution and crystal shape on the relative viscosity of magmas
2018
International audience; This study examines the combined effect of crystal-size distributions (CSD) and crystal shape on the rheology of vesicle free magmatic suspensions and provides the first practical application of an empirical model to estimate the relative effect of crystal content and CSD's on the viscosity of magma directly from textural image analysis of natural rock samples in the form of a user-friendly texture-rheology spreadsheet calculator. We extend and apply established relationships between the maximum packing fraction ϕm of a crystal bearing suspension and both its rheological properties and the polydispersity γ of a CSD. By using analogue rotational rheometric experiments…
Viscosity and density of binary mixtures of alcohols and polyols with three carbon atoms and water: equation for the correlation of viscosities of bi…
2009
Measurements have been made of the viscosity and density of binary mixtures of alcohols and polyols with three carbon atoms and water at 298.15 K and at atmospheric pressure, as a function of the mole fraction. Fits have been made of the experimental values corresponding to the excesses of molar volume (V E), the deviations of viscosity (Δη), and the excesses of Gibbs free energy of activation (G* E), by means of the Redlich–Kister equation. A new correlation equation is presented for studying the viscosity of such mixtures, and comparisons are made of the experimental values of viscosity versus the values obtained by means of the mentioned equation and the models of Heric and McAllister. L…
Thermodynamics of a polymer blend solution system studied by gel permeation chromatography and viscosity
1999
Binary and ternary interaction parameters and their derivatives have been calculated with the Flory-Huggins formalism developed for a ternary polymer system. The equilibrium compositions of the ternary system tetrahydrofuran/polybutadiene/polystyrene that forms two phases in equilibrium at 25°C have been used to solve the binodal equations. With this set of parameters, the viscosimetric interaction parameters have been computed. For the sake of comparison, the experimental viscosimetric parameter has been determined from intrinsic viscosity data of a polymer (3) in a "binary solvent" (solvent + polymer (2)). It has been clearly shown that composition-dependent parameters are necessary to re…
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…
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…
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.
Viscometric study of mixtures of neutral and charged polymers in aqueous solution
1997
The viscosity behaviour of aqueous mixtures formed by a polyelectrolyte (A) and a neutral polymer (B) such as polystyrene sulfonate (PSS)-polyvinylpyrrolidone (PVP) and polylysine (PLL)-PVP has been studied at 25°C. The intrinsic viscosity and viscosity interaction parameter of each polymer in water have been determined and have served us to estimate the compatibility of the different mixtures according to two different methodologies: (i) mixtures of two polymers in water as solvent and (ii) mixtures of either polymer A OFB in a solvent formed by either polymer B or A in water ("polymer solvent method"). By comparing the experimental and theoretical viscosity data it is clearly seen that: m…
Viscosity of Polymer Solutions over the Full Range of Composition: A Thermodynamically Inspired Two-Parameter Approach
2015
The approach yields the following relation for the relative viscosity η rel as a function of polymer concentration c (mass/volume): ln ηrel = c/(1 + pc + qc2). Reduced concentrations c (defined as c = c[η], where [η] is the intrinsic viscosity) are used instead of c to incorporate thermodynamic information. The parameters p and q account for changes in the free volume of the solvent caused by the polymer. The analysis of literature data for seven very dissimilar systems discloses the following common feature: p > 0 and q < 0. This means that the curves in the plots of ln ηrel as a function of c are normally located below the tangent at low c and above it at high c. The values of p and q cor…
Intrinsic viscosities of polyelectrolytes in the absence and in the presence of extra salt: Consequences of the stepwise conversion of dextran into a…
2011
Abstract Viscosities of dilute polymer solutions were measured in capillary viscometers for samples varying in their fraction f of charged units from 0.00 to 0.90. The dependence of the logarithm of the relative viscosity on polymer concentration c is in all cases reproduced quantitatively by three characteristic parameters: [ η ], the intrinsic viscosity; B , a viscometric interaction parameter (related to the Huggins constant); [ η ] , a parameter required only for polyelectrolytes at low concentrations of extra salt. In pure water [ η ] increases more than 80 times as the fraction f rises from zero to 0.90 and [ η ] starts from zero and goes up to ≈71 mL/g. Upon the addition of NaCl [ η …
Polyelectrolytes Revisited: Reliable Determination of Intrinsic Viscosities
2007
The linear extrapolation of (hh0)/(h0c) towards c !0 constitutes the basis of traditional methods to determine intrinsic viscosities (h), where h is the viscosity of polymer solutions of concentration c and h0 is the viscosity of the pure solvent. With uncharged macromolecules this procedure works well; for polyelectrolytes it fails because of the pronounced non-linearity of the above dependence at high dilution resulting from the increasing electrostatic inter- actions. This contribution presents a new method for the determination of (h). It rests upon the application of the laws of phenomenological thermodynamics to the viscosity of polymer solutions and introduces a generalized intrinsic…