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Shear viscosity material

These essentially comprise a mixture of a skin-forming component, which comprises two distinct phases blended together, a high zero-shear viscosity material and a low zero-shear viscosity material, and a foam core-foaming component, which includes a blowing agent, physically dry blended together. The three materials are preferably selected from suitable homopolymers and copolymers of ethylene. CANADA... [Pg.65]

In addition to zero-shear viscosity, material elasticity plays an important role in determining coalescence behavior in the rotational molding process.For rotational molding grade material, this effect was first recognized from the experimental results obtained with impact modified polypropylenes and is illustrated in Fig. In this work, the relative elasticity of resins... [Pg.2680]

Inks. Basic raw materials for letterpress inks, such as mineral oils, soya bean oil, resins, and pigments, are essentiaHy the same as those used in web offset inks. Inks are tinctoriaHy weak, relatively fluid, and their low and high shear viscosities are low. [Pg.249]

A viscoelastic material also possesses a complex dynamic viscosity, rj = rj - - iv( and it can be shown that r = G jiuj-, rj = G juj and rj = G ju), where CO is the angular frequency. The parameter Tj is useful for many viscoelastic fluids in that a plot of its absolute value Tj vs angular frequency in radians/s is often numerically similar to a plot of shear viscosity Tj vs shear rate. This correspondence is known as the Cox-Merz empirical relationship. The parameter Tj is called the dynamic viscosity and is related to G the loss modulus the parameter Tj does not deal with viscosity, but is a measure of elasticity. [Pg.178]

The Rheometric Scientific RDA II dynamic analy2er is designed for characteri2ation of polymer melts and soHds in the form of rectangular bars. It makes computer-controUed measurements of dynamic shear viscosity, elastic modulus, loss modulus, tan 5, and linear thermal expansion coefficient over a temperature range of ambient to 600°C (—150°C optional) at frequencies 10 -500 rad/s. It is particularly useful for the characteri2ation of materials that experience considerable changes in properties because of thermal transitions or chemical reactions. [Pg.201]

Rheometric Scientific markets several devices designed for characterizing viscoelastic fluids. These instmments measure the response of a Hquid to sinusoidal oscillatory motion to determine dynamic viscosity as well as storage and loss moduH. The Rheometric Scientific line includes a fluids spectrometer (RFS-II), a dynamic spectrometer (RDS-7700 series II), and a mechanical spectrometer (RMS-800). The fluids spectrometer is designed for fairly low viscosity materials. The dynamic spectrometer can be used to test soHds, melts, and Hquids at frequencies from 10 to 500 rad/s and as a function of strain ampHtude and temperature. It is a stripped down version of the extremely versatile mechanical spectrometer, which is both a dynamic viscometer and a dynamic mechanical testing device. The RMS-800 can carry out measurements under rotational shear, oscillatory shear, torsional motion, and tension compression, as well as normal stress measurements. Step strain, creep, and creep recovery modes are also available. It is used on a wide range of materials, including adhesives, pastes, mbber, and plastics. [Pg.202]

Non-Newtonian fluids include those for which a finite stress 1,. is reqjiired before continuous deformation occurs these are c ailed yield-stress materials. The Bingbam plastic fluid is the simplest yield-stress material its rheogram has a constant slope [L, called the infinite shear viscosity. [Pg.630]

In a fluid under stress, the ratio of the shear stress, r. to the rate of strain, y, is called the shear viscosity, rj, and is analogous to the modulus of a solid. In an ideal (Newtonian) fluid the viscosity is a material constant. However, for plastics the viscosity varies depending on the stress, strain rate, temperature etc. A typical relationship between shear stress and shear rate for a plastic is shown in Fig. 5.1. [Pg.344]

Shear viscosities of the twin-screw blended materials were measured at 190°C and 290°C (Fig. 6), the same temperatures as the melt temperatures during processing 190°C for the composites and 290°C for the melt blends. [Pg.630]

The shear viscosity, especially as measured with capillary rheometers characterized by high shear rates, is hardly sensitive to material structure since the investigator usually has to deal with the substantially destroyed structure in the molten sample. Melt stretching experiments would normally provide much more information [33]. [Pg.5]

All sliding friction forces are dramatically affected by surface contamination. If the surface is covered with a material that prevents the adhesive forces from acting, the coefficient is reduced. If the material is a liquid which has low shear viscosity the condition exists of lubricated sliding where the characteristics of the liquid control the friction rather than the surface friction characteristics of the materials. It is possible by the addition of surface materials that have high adhesion to increase the coefficient of friction. [Pg.95]

While electrical conductivity, diffusion coefficients, and shear viscosity are determined by weak perturbations of the fundamental diffu-sional motions, thermal conductivity is dominated by the vibrational motions of ions. Heat can be transmitted through material substances without any bulk flow or long-range diffusion occurring, simply by the exchange of momentum via collisions of particles. It is for this reason that in liquids in which the rate constants for viscous flow and electrical conductivity are highly temperature dependent, the thermal conductivity remains essentially the same at lower as at much higher temperatures and more fluid conditions. [Pg.121]

Many materials are conveyed within a process facility by means of pumping and flow in a circular pipe. From a conceptual standpoint, such a flow offers an excellent opportunity for rheological measurement. In pipe flow, the velocity profile for a fluid that shows shear thinning behavior deviates dramatically from that found for a Newtonian fluid, which is characterized by a single shear viscosity. This is easily illustrated for a power-law fluid, which is a simple model for shear thinning [1]. The relationship between the shear stress, a, and the shear rate, y, of such a fluid is characterized by two parameters, a power-law exponent, n, and a constant, m, through... [Pg.384]

Fig. 4.2.2 Dimensionless shear rate and viscosity as a function of radius for a power-law fluid under the conditions shown in Figure 4.2.1. For a highly shear thinning material, the shear rate is large near the wall and close to zero near the center. The viscosity can vary by several orders of magnitude in the pipe. Fig. 4.2.2 Dimensionless shear rate and viscosity as a function of radius for a power-law fluid under the conditions shown in Figure 4.2.1. For a highly shear thinning material, the shear rate is large near the wall and close to zero near the center. The viscosity can vary by several orders of magnitude in the pipe.
Fig. 4.3.3 (a) Shear flow of a Newtonian fluid defined as the ratio of the shear stress and trapped between the two plates (each with a shear rate, (b) A polymeric material is being large area of A). The shear stress (a) is defined stretched at both ends at a speed of v. The as F/A, while the shear rate (y) is the velocity material has an initial length of L0 and an gradient, dvx/dy. The shear viscosity (r s) is (instantaneous) cross-sectional area of A. [Pg.407]

As a result, we find for sols that the divergence of the above zero shear viscosity rj0 and of two other linear viscoelastic material functions, first normal stress coefficient and equilibrium compliance 7°, depends on the divergence... [Pg.177]

Fig. 10. Experimental values of the gel stiffness S plotted against the relaxation exponent n for crosslinked polycaprolactone at different stoichiometric ratios [59]. The dashed line connects the equilibrium modulus of the fully crosslinked material (on left axis) and the zero shear viscosity of the precursor (on right axis)... Fig. 10. Experimental values of the gel stiffness S plotted against the relaxation exponent n for crosslinked polycaprolactone at different stoichiometric ratios [59]. The dashed line connects the equilibrium modulus of the fully crosslinked material (on left axis) and the zero shear viscosity of the precursor (on right axis)...
Oscillatory shear experiments are the preferred method to study the rheological behavior due to particle interactions because they directly probe these interactions without the influence of the external flow field as encountered in steady shear experiments. However, phenomena that arise due to the external flow, such as shear thickening, can only be investigated in steady shear experiments. Additionally, the analysis is complicated by the different response of the material to shear and extensional flow. For example, very strong deviations from Trouton s ratio (extensional viscosity is three times the shear viscosity) were found for suspensions [113]. [Pg.207]

With some concentrated suspensions of solid particles, particularly those in which the liquid has a relatively low viscosity, the suspension appears to slip at the pipe wall or at the solid surfaces of a viscometer. Slip occurs because the suspension is depleted of particles in the vicinity of the solid surface. In the case of concentrated suspensions, the main reason is probably that of physical exclusion if the suspension at the solid surface were to have the same spatial distribution of particles as that in the bulk, some particles would have to overlap the wall. As a result of the lower concentration of particles in the immediate vicinity of the wall, the effective viscosity of the suspension near the wall may be significantly lower than that of the bulk and consequently this wall layer may have an extremely high shear rate. If this happens, the bulk material appears to slip on this lubricating layer of low viscosity material. [Pg.125]

Kalyanasundaram, Kumar, and Kuloor (K2) found the influence of dispersed phase viscosity on drop formation to be quite appreciable at high rates of flow. The increase in pd results in an increase in drop volume. To account for this, the earlier model was modified by adding an extra resisting force due to the tensile viscosity of the dispersed phase. The tensile viscosity is taken as thrice the shear viscosity of the dispersed phase, in analogy with the extension of an elastic strip where the tensile elastic modulus is represented by thrice the shear elastic modulus for an incompressible material. The actual force resulting from the above is given by 3nRpd v. [Pg.339]

Here, v is the velocity vector field, p is the mass density of the fluid, D/Dt = S/Sf + V V is the material derivative, Vp is the gradient of the pressure, r[j is the shear viscosity, and F is the external force acting on the fluid volume. The right-hand side of Eq. (1) is a momentum balance between the internal pressure and viscous stress and the external forces on the fluid body. Any excess momentum contributes to the material acceleration of the fluid volume, on the left-hand side. [Pg.63]

Polymer rheology can respond nonllnearly to shear rates, as shown in Fig. 3.4. As discussed above, a Newtonian material has a linear relationship between shear stress and shear rate, and the slope of the response Is the shear viscosity. Many polymers at very low shear rates approach a Newtonian response. As the shear rate is increased most commercial polymers have a decrease in the rate of stress increase. That is, the extension of the shear stress function tends to have a lower local slope as the shear rate is increased. This Is an example of a pseudoplastic material, also known as a shear-thinning material. Pseudoplastic materials show a decrease in shear viscosity as the shear rate increases. Dilatant materials Increase in shear viscosity as the shear rate increases. Finally, a Bingham plastic requires an initial shear stress, to, before it will flow, and then it reacts to shear rate in the same manner as a Newtonian polymer. It thus appears as an elastic material until it begins to flow and then responds like a viscous fluid. All of these viscous responses may be observed when dealing with commercial and experimental polymers. [Pg.65]

Before the viscosity can be calculated from capillary data, as mentioned above, the apparent shear rate, 7 , must be corrected for the effect of the pseudoplastic nature of the polymer on the velocity profile. The calculation can be made only after a model has been adopted that relates shear stress and shear rate for this concept of a pseudoplastic shear-thinning material. The model choice is a philosophical question [11] after rheologlsts tried numerous models, there are in general two simple models that have withstood substantial testing when the predictions are compared with experimental data [1]. The first Is ... [Pg.83]


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