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Viscosity extension

Extensional viscosity Extension cord External lubricant External plasticizers Exterol Exter press Exton... [Pg.388]

Gastonbonhomme Y, Petrino P, Chevalier JL (1994) UNIFAC visco group-contribution method for predicting kinematic viscosity - extension and temperature-dependence. Chem Eng Sci 49 1799-1806... [Pg.211]

To resolve this, in 1940 Dean, Bauer, and Berglund5 published low viscosity extensions for use between 2.0 and 4.2 cSt (at 98.9°C) for both the 0 and 100 VI curves together with a new set of constants for the intermediate range between 4.2 and 7.29 cSt. This meant that the VI tables constructed were broken into the following ranges (at 210°F) ... [Pg.49]

The equations for the low viscosity extension were, using kinematic viscosities at 100°F and 210°F,... [Pg.49]

The elongation viscosity defined by Equation (1.19) represents a uni-axial extension. Elongational flows based on biaxial extensions can also be considered. In an equi-biaxial extension the rate of deformation tensor is defined as... [Pg.10]

Revised material in Section 5 includes an extensive tabulation of binary and ternary azeotropes comprising approximately 850 entries. Over 975 compounds have values listed for viscosity, dielectric constant, dipole moment, and surface tension. Whenever possible, data for viscosity and dielectric constant are provided at two temperatures to permit interpolation for intermediate temperatures and also to permit limited extrapolation of the data. The dipole moments are often listed for different physical states. Values for surface tension can be calculated over a range of temperatures from two constants that can be fitted into a linear equation. Also extensively revised and expanded are the properties of combustible mixtures in air. A table of triple points has been added. [Pg.1287]

At first glance, the contents of Chap. 9 read like a catchall for unrelated topics. In it we examine the intrinsic viscosity of polymer solutions, the diffusion coefficient, the sedimentation coefficient, sedimentation equilibrium, and gel permeation chromatography. While all of these techniques can be related in one way or another to the molecular weight of the polymer, the more fundamental unifying principle which connects these topics is their common dependence on the spatial extension of the molecules. The radius of gyration is the parameter of interest in this context, and the intrinsic viscosity in particular can be interpreted to give a value for this important quantity. The experimental techniques discussed in Chap. 9 have been used extensively in the study of biopolymers. [Pg.496]

This chapter contains one of the more diverse assortments of topics of any chapter in the volume. In it we discuss the viscosity of polymer solutions, especially the intrinsic viscosity the diffusion and sedimentation behavior of polymers, including the equilibrium between the two and the analysis of polymers by gel permeation chromatography (GPC). At first glance these seem to be rather unrelated topics, but features they all share are a dependence on the spatial extension of the molecules in solution and applicability to molecular weight determination. [Pg.583]

Extensive tables and equations are given in ref. 1 for viscosity, surface tension, thermal conductivity, molar density, vapor pressure, and second virial coefficient as functions of temperature. [Pg.93]

Polymer solution viscosity is dependent on the concentration of the solvent, the molecular weight of the polymer, the polymer composition, the solvent composition, and the temperature. More extensive information on the properties of polymer solutions may be found ia refereaces 9 and 54—56. [Pg.164]

Although bulk polymerization of acrylonitrile seems adaptable, it is rarely used commercially because the autocatalytic nature of the reaction makes it difficult to control. This, combined with the fact that the rate of heat generated per unit volume is very high, makes large-scale commercial operations difficult to engineer. Lastiy, the viscosity of the medium becomes very high at conversion levels above 40 to 50%. Therefore commercial operation at low conversion requires an extensive monomer recovery operation. [Pg.278]

Tire Ya.rns, A method to iacrease the strength of viscose yam from the 0.2 N /tex (2.2 gf/den) standard to levels needed ia tires was first patented by Courtaulds ia 1935 (18). By raising the ziac concentration ia the spia bath to 4% the thread could be stretched more by immersing it ia a hot dilute acid bath duting extension. Filament strengths iacreased to about 0.3 N/tex (3.3 gf/den), and the cross section became rounder, with a thicker skin than regular viscose. Pairs of these yams were capable of beiag twisted iato tire cords which outperformed traditional cotton cords. [Pg.349]

Lubricants. Petroleum lubricants continue to be the mainstay for automotive, industrial, and process lubricants. Synthetic oils are used extensively in industry and for jet engines they, of course, are made from hydrocarbons. Since the viscosity index (a measure of the viscosity behavior of a lubricant with change in temperature) of lube oil fractions from different cmdes may vary from +140 to as low as —300, additional refining steps are needed. To improve the viscosity index (VI), lube oil fractions are subjected to solvent extraction, solvent dewaxing, solvent deasphalting, and hydrogenation. Furthermore, automotive lube oils typically contain about 12—14% additives. These additives maybe oxidation inhibitors to prevent formation of gum and varnish, corrosion inhibitors, or detergent dispersants, and viscosity index improvers. The United States consumption of lubricants is shown in Table 7. [Pg.367]

The WAG process has been used extensively in the field, particularly in supercritical CO2 injection, with considerable success (22,157,158). However, a method to further reduce the viscosity of injected gas or supercritical fluid is desired. One means of increasing the viscosity of CO2 is through the use of supercritical C02-soluble polymers and other additives (159). The use of surfactants to form low mobihty foams or supercritical CO2 dispersions within the formation has received more attention (160—162). Foam has also been used to reduce mobihty of hydrocarbon gases and nitrogen. The behavior of foam in porous media has been the subject of extensive study (4). X-ray computerized tomographic analysis of core floods indicate that addition of 500 ppm of an alcohol ethoxyglycerylsulfonate increased volumetric sweep efficiency substantially over that obtained in a WAG process (156). [Pg.193]


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See also in sourсe #XX -- [ Pg.225 ]




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