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Viscoelastic deformation, measurement

In this paper, we report some rheological results on the effect of addition of sodium bentonite, a commonly-used antisettling system, to a pesticide suspension concentrate. Steady state shear stress-shear rate measurements were carried out to obtain the yield value and viscosity as a function of shear rate. These e]q>eriments were supplemented by low deformation measurements to investigate the viscoelastic... [Pg.30]

One method that attempts to characterize the viscoelastic behavior is the force-deformation measurement. In this approach, a force point is applied... [Pg.113]

While the eventually pore liquid is reorganizing as a result of the external load (or deformation), the gel skeleton has to take over the external load thus deforming until an equilibrium state is reached. The deformation at given load is then a measure for the stiffness of the gel. As the term in the brackets of (21.46a) tends to 1 for large times the prefactor provides the Young s modulus of the gel in equilibrium if no additional viscoelastic deformation is contributing [95]. [Pg.491]

Creep is defined as a long-term property measured by deforming a sample at a constant stress and monitoring the flow (strain) over a period of time. Viscoelastic materials flow or deform if subjected to loading (stress). In a creep experiment, a constant stress is applied and the resulting deformation measured as a function of temperature and time. Just as stress relaxation is an important property to structural engineers and polymer scientists, so is creep behavior. [Pg.37]

Figures 16.1-3 show Ryshkewitch-Duckworth plots for dicalcium phosphate or lactose mixtures with sodium dodecyl sulfate as well as the Ryshkewitch-Duckworth plots for each of the pure components. As previously observed by Wu et al. [20] and Tye et al. [10] no dependence on dwell time was noted. We did note that tablets were not formed for some materials when short dwell times, comparable to production conditions, were used. Presumably, insufficient time is given for viscoelastic deformation of the materials that is, in part, responsible for adhesion. Viscoelestic recovery upon decompression may also contribute to lamination of tablets on decompression. Figures 16.1-3 and Figme 16.6 show the importance of tablet porosity to tablet tensile strength. Porosity should be considered a measure of the outcome of the tableting process. Figures 16.1-3 show Ryshkewitch-Duckworth plots for dicalcium phosphate or lactose mixtures with sodium dodecyl sulfate as well as the Ryshkewitch-Duckworth plots for each of the pure components. As previously observed by Wu et al. [20] and Tye et al. [10] no dependence on dwell time was noted. We did note that tablets were not formed for some materials when short dwell times, comparable to production conditions, were used. Presumably, insufficient time is given for viscoelastic deformation of the materials that is, in part, responsible for adhesion. Viscoelestic recovery upon decompression may also contribute to lamination of tablets on decompression. Figures 16.1-3 and Figme 16.6 show the importance of tablet porosity to tablet tensile strength. Porosity should be considered a measure of the outcome of the tableting process.
Fig. 25 Variation of the complex shear modulus of the PDMS/CNT suspension. Filled symbol viscoelastic behaviour measured just after the compressive deformation, the CNT s are supposed to be well dispersed in the PDMS matrix. Open symbols viscoelasticity beahaviour measured at the end the aggregation process under /o = 30 %... Fig. 25 Variation of the complex shear modulus of the PDMS/CNT suspension. Filled symbol viscoelastic behaviour measured just after the compressive deformation, the CNT s are supposed to be well dispersed in the PDMS matrix. Open symbols viscoelasticity beahaviour measured at the end the aggregation process under /o = 30 %...
The concept of distortional energy as a measure for the critical magnitude of the stress state a material can endure at a point in an elastic material (von Mises criterion) cannot be carried over directly to viscoelastic materials because viscoelastic deformation involves dissipative mechanisms. Thus, at any point in time the energy balance must be written as. [Pg.403]

In order to determine the viscoelastic properties of silicone gel materials, vibrational measurement techniques are used. The principle of vibrational measurement techniques involves determining die viscoelastic quantities by observing the responding mechanical behavior when cyclic deformation is applied repeatedly. Dynamic viscoelastic property measurements are performed with a dynamic mechanical spectrometer such as the RDA-II from Rheometrics. This instrument measures the complex modulus G and loss factor tan S from the torque measured by the transducer equipped at the upper portion of the sample chamber when shear deformation is applied to the sample at a specified shear strain and frequency from the actuator at the bottom of the sample chamber. [Pg.344]

From the previous discussions and Equation 7.5 it is evident that the measured value of adhesive fracture energy or fracture toughness typically reflects the extent of plastic and viscoelastic deformations in the region of the crack tip. In polymeric materials the extent of such deformations is highly dependent upon the test rate and temperature and, therefore, the measured values of Gc and Kc are often dependent upon these test parameters. [Pg.314]

Direct volumetric measurement of UHMWPE wear Wear estimates that rely on thickness (or surface scanning) measurements are plagued with creep and recovery errors associated with viscoelastic deformation and some shape memory properties in UHMWPE [33]. Where possible, such techniques should be avoided, in... [Pg.384]

Viscoelasticity studies provide valuable data that can be correlated with fat crystal network structure. Parameters derived from such studies include the storage (solidlike or elastic) modulus (G ) and the loss (liquidlike or viscous) modulus (G") (Davis, 1973). Small-deformation measurements take place below a critical value of deformation (yield point). In plastic fats, G is substantially higher than G" (Rousseau et al., 1996c Drake et al., 1994). [Pg.553]

Some of the papers referenced do this for rubber, nylon and tooth dentins. Peterlin, Zhurkov et al. and Becht have also made quantitative measures of bond rupture. In answer to your second question, our experimental evidence (J. Polym. Sci. A-1, 7, 2125 (1969) indicates only a small fraction of the total work of fracture can be attributed to primary bond rupture. The remainder may be attributed to secondary bond rupture, plastic and viscoelastic deformation somewhat analogous to work of plastic deformation at the tip of a crack in metals. [Pg.433]

The viscoelastic nature of polymers results in deformation behavior that is both time (frequency) and temperature dependent. It is valuable to assess the long-term behavior of polymers at a fixed temperature to predict lifetimes in various applications. It is possible to do using the WLF equation, which expresses the shift factor, ax, as a function of temperature. By this time-temi)erature superposition (TTS) approach, viscoelastic parameters measured at various temperatures are used to construct a master curve of sample deformation by means of a shift along the log time axis. Thus, stress relaxation and creep experiments enable effective predictions of long-term behavior over various temi)eratures that can be acquired in a short period of time. [Pg.1245]

Creep tests can be conducted in eitho- tensile or flexural modes. The time-dependent viscoelastic deformation of polymers and composites is compared and the differences in material compliance is analyzed. The constitutive relationship for creep compliance that takes into account the effect of di-latational stresses is determined. Estimation of lifetime under non-isothermal conditions is also ixe-sented. Not only are the thermal and mechanical loading of great importance to estimation of life expectancy, but also the influence of the chemical medium and immersion time. Two possible methods of obtaining this information are discussed (1) time-temperature extrapolation of the measured aging process, and (2) a functional estimation of time-temperature collectives, the latter being more precise. [Pg.2]

Different deformational measurements are used to obtain linear viscoelastic data. It may be in simple shear or in elongation. However, the behaviour of rubber during... [Pg.180]

The viscosity given by Eq. (3.98) not only follows from a different model than the Debye viscosity equation, but it also describes a totally different experimental situation. Viscoelastic studies are done on solid samples for which flow is not measurable. A viscous deformation is present, however, and this result shows that it is equivalent to what would be measured directly, if such a measurement were possible. [Pg.189]

Deformation is the relative displacement of points of a body. It can be divided into two types flow and elasticity. Flow is irreversible deformation when the stress is removed, the material does not revert to its original form. This means that work is converted to heat. Elasticity is reversible deformation the deformed body recovers its original shape, and the appHed work is largely recoverable. Viscoelastic materials show both flow and elasticity. A good example is SiEy Putty, which bounces like a mbber ball when dropped, but slowly flows when allowed to stand. Viscoelastic materials provide special challenges in terms of modeling behavior and devising measurement techniques. [Pg.166]


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Deformation measurement

Viscoelastic measurements

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