Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Small Deformation Theory

If an initially unloaded elastie body is subjeeted to surfaee or body forees, it will be deformed. If the forees are removed, the deformation will disappear, and the body will be returned to the same state it was in before the forees were applied. Certain materials are observed to behave elastieally for limited deformations, but, if those deformations are exeeeded, then the internal strueture of the material may be altered and inelastie deformation may oeeur. The stresses in the body may be different than those that the material would have experieneed if it had responded elastieally, i.e., the stresses may be affeeted by the change in material strueture. When the forees are removed, some residual deformation may remain. These qualitative observations suggest a set of constitutive assumptions whieh will be stated in mathematieal terms below. [Pg.121]

To provide an elementary treatment, in this seetion the theory is eon-strueted in terms of the elassieal small strain tensor s defined as the symmetrie [Pg.121]

Motivated by the qualitative observations made above, a set of internal state variables deseribing the internal strueture of the material will be intro-dueed ab initio, denoted eolleetively by k. Their physieal meaning or preeise properties need not be established at this point, and they may inelude sealar, veetor, or tensor quantities. The following eonstitutive assumptions are now made  [Pg.122]

The elastie limit funetion is assumed to be eontinuous and smooth, i.e., differentiable in e and k. At a fixed value of k, this equation defines a smooth elosed surfaee in strain spaee oriented in sueh a way that the outward normal [Pg.122]

Here c[-], which will be called the elastic modulus tensor, is a fourth-order linear mapping of its second-order tensor argument, while b[-], which will be called the inelastic modulus tensor, is a linear mapping of k whose form will depend on the specific properties assigned to k. They depend, in general, on and k. For example, if k consists of a single second-order tensor, then in component form [Pg.123]


Another generalization uses referential (material) symmetric Piola-Kirchhoff stress and Green strain tensors in place of the stress and strain tensors used in the small deformation theory. These tensors have components relative to a fixed reference configuration, and the theory of Section 5.2 carries over intact when small deformation quantities are replaced by their referential counterparts. The referential formulation has the advantage that tensor components do not change with relative rotation between the coordinate frame and the material, and it is relatively easy to construct specific constitutive functions for specific materials, even when they are anisotropic. [Pg.119]

As with any constitutive theory, the particular forms of the constitutive functions must be constructed, and their parameters (material properties) must be evaluated for the particular materials whose response is to be predicted. In principle, they are to be evaluated from experimental data. Even when experimental data are available, it is often difficult to determine the functional forms of the constitutive functions, because data may be sparse or unavailable in important portions of the parameter space of interest. Micromechanical models of material deformation may be helpful in suggesting functional forms. Internal state variables are particularly useful in this regard, since they may often be connected directly to averages of micromechanical quantities. Often, forms of the constitutive functions are chosen for their mathematical or computational simplicity. When deformations are large, extrapolation of functions borrowed from small deformation theories can produce surprising and sometimes unfortunate results, due to the strong nonlinearities inherent in the kinematics of large deformations. The construction of adequate constitutive functions and their evaluation for particular... [Pg.120]

Figure 9.9 Dimensionless critical droplet size for breakup (capillary number Ca<- = Crj a/r) as a function of viscosity ratio M of the dispersed to the continuous phase for two-dimensional flows in the four-roll mill. The data sets correspond from bottom to top to ff — 1.0(0), 0.8 (A), 0.6 (0), 0.4 (V), and 0.2 ( ), with a defined in Eq. (9-17). The fluids are those described in Fig. 9-7. The solid lines are the predictions of a small-deformation theory, while the dashed lines are for a large-deformation theory. The closed squares are from Rallison s (1981) numerical solutions (see also Rallison and Acrivos 1978). (From Bentley and Leal 1986, with permission from Cambridge University Press.)... Figure 9.9 Dimensionless critical droplet size for breakup (capillary number Ca<- = Crj a/r) as a function of viscosity ratio M of the dispersed to the continuous phase for two-dimensional flows in the four-roll mill. The data sets correspond from bottom to top to ff — 1.0(0), 0.8 (A), 0.6 (0), 0.4 (V), and 0.2 ( ), with a defined in Eq. (9-17). The fluids are those described in Fig. 9-7. The solid lines are the predictions of a small-deformation theory, while the dashed lines are for a large-deformation theory. The closed squares are from Rallison s (1981) numerical solutions (see also Rallison and Acrivos 1978). (From Bentley and Leal 1986, with permission from Cambridge University Press.)...
Delaby, I., Ernst, B., and Muller, R. (1995) Drop deformation during elongational flow in blends of viscoelastic fluids. Small deformation theory and comparison with experimental results. Rheol. Acta, 34 (6), 525-533. [Pg.104]

The theory is initially presented in the context of small deformations in Section 5.2. A set of internal state variables are introduced as primitive quantities, collectively represented by the symbol k. Qualitative concepts of inelastic deformation are rendered into precise mathematical statements regarding an elastic range bounded by an elastic limit surface, a stress-strain relation, and an evolution equation for the internal state variables. While these qualitative ideas lead in a natural way to the formulation of an elastic limit surface in strain space, an elastic limit surface in stress space arises as a consequence. An assumption that the external work done in small closed cycles of deformation should be nonnegative leads to the existence of an elastic potential and a normality condition. [Pg.118]

Specific applications of the theory are not considered in this chapter. Only one example, that of small deformation classical plasticity, is worked out in Section 5.3. The set of internal state variables k is taken to be comprised of... [Pg.118]

It is consistent with the approximations of small strain theory made in Section A.7 to neglect the higher-order terms, and to consider the elastic moduli to be constant. Stated in another way, it would be inconsistent with the use of the small deformation strain tensor to consider the stress relation to be nonlinear. The previous theory has included such nonlinearity because the theory will later be generalized to large deformations, where variable moduli are the rule. [Pg.144]

The entire theory of Section 5.2 may now be repeated, substituting S, E, and K for s, e, and k, respectively. Obviously, the results will parallel those of Section 5.2, with referential variables in place of the small deformation variables. Rather than repeat the development in Section 5.2, the results may be obtained by substituting majuscules for minuscules in the salient equations. The stress relation (5.3) becomes... [Pg.154]

There have been several theories proposed to explain the anomalous 3/4 power-law dependence of the contact radius on particle radius in what should be simple JKR systems. Maugis [60], proposed that the problem with using the JKR model, per se, is that the JKR model assumes small deformations in order to approximate the shape of the contact as a parabola. In his model, Maugis re-solved the JKR problem using the exact shape of the contact. According to his calculations, o should vary as / , where 2/3 < y < 1, depending on the ratio a/R. [Pg.155]

Small deformations of the polymers will not cause undue stretching of the randomly coiled chains between crosslinks. Therefore, the established theory of rubber elasticity [8, 23, 24, 25] is applicable if the strands are freely fluctuating. At temperatures well above their glass transition, the molecular strands are usually quite mobile. Under these premises the Young s modulus of the rubberlike polymer in thermal equilibrium is given by ... [Pg.321]

Ronca and Allegra (12) and Flory ( 1, 2) assume explicitly in their new rubber elasticity theory that trapped entanglements make no contribution to the equilibrium elastic modulus. It is proposed that chain entangling merely serves to suppress junction fluctuations at small deformations, thereby making the network deform affinely at small deformations. This means that the limiting value of the front factor is one for complete suppression of junction fluctuations. [Pg.440]

With mixed-valence compounds, charge transfer does not require creation of a polar state, and a criterion for localized versus itinerant electrons depends not on the intraatomic energy defined by U , but on the ability of the structure to trap a mobile charge carrier with a local lattice deformation. The two limiting descriptions for mobile charge carriers in mixed-valence compounds are therefore small-polaron theory and itinerant-electron theory. We shall find below that we must also distinguish mobile charge carriers of intennediate character. [Pg.6]

Equation 8.24 is valid when the overall dimensions of the laminate are small so that the deflections are small. For large laminates, however, the deflections may become too large to satisfy the assumptions of linear theory. In this case a large-deflection plate theory must be used [15]. For long, narrow strips, the small-deformation laminated plate theory can still be used with the modified condition k2 = 0 in place of M2 = 0. This results in a cylindrical curvature, kc, given by... [Pg.252]

In other statistical theories of rubber elasticity (see e.g. reviews 29,34)) the Gaussian statistics is not valid even at small deformations and the intramolecular energy component is dependent on deformation. [Pg.47]

Mathematical modelling of the compression of single particles 2.5.2.7 Hertz model. The mechanics of a sphere made of a linear elastic material compressed between two flat rigid surfaces have been modelled for the case of small deformations, normally less then 10% strain (Hertz, 1882). Hertz theory provides a relationship between the force F and displacement hp as follows ... [Pg.40]

Although a key characteristic of the mechanical behavior of rubber-like materials is their ability to undergo large elastic deformations, we will present here some important results from the theory of linear elasticity [1], which is valid only for small deformations. These serve our present purposes better than the nonlinear theory, because of their simpler character and physical transparency. [Pg.2]

Figure 4 allows several conclusions First of all, the prediction of the Reissner result matches the FEM result in the small deformation region well, which shows that the finite size of the contact area does not lead to strong deviations from the analytical theory based on point like contact. This justifies an application of this result to derive elastic constants of the shell material from the measurements at small deformations. [Pg.121]

For a plastic fat, the yield stress was defined as the stress at the limit of linearity in a small deformation rheological test. Agreement between theory and experiment was found to be good. [Pg.270]

The three elastic constants are the Frank elastic constants, called after Frank, who introduced them already in 1958. They originate from the deformation of the director field as shown in Fig. 15.52. A continuous small deformation of an oriented material can be distinguished into three basis distortions splay, twist and bend distortions They are required to describe the resistance offered by the nematic phase to orientational distortions. As an example, values for Miesowicz viscosities and Frank elastic constants are presented in Table 15.10. It should be mentioned that those material constants are not known for many LCs and LCPs. Nevertheless, they have to be substituted in specific rheological constitutive equations in order to describe the rheological peculiarities of LCPs. Accordingly, the viscosity and the dynamic moduli will be functions of the Miesowicz viscosities and/or the Frank elastic constants. Several theories have been presented that are more or less able to explain the rheological peculiarities. Well-known are the Leslie-Ericksen theory and the Larson-Doi theory. It is far beyond the scope of this book to go into detail of these theories. The reader is referred to, e.g. Aciemo and Collyer (General References, 1996). [Pg.587]

We now turn to the theory of rolling particles off surfaces. We use the treatment of Bhattacharya and Mittal to compute the radius of the smallest particle that can be moved due to the torque exerted on the particle by the wall shear. As the particles sit on the surface, there will be a very small deformation Xq caused by the adhesive force between the particle and the surface. This deformation is given by the following equation ... [Pg.79]

Since elastic oscillation theory confines itself, normally, to small deformations only, the last term in relation (13.7) can be neglected as a small quantity of the second order, compared to the first two terms. As a result, the matrix of the deformation tensor takes the form... [Pg.398]


See other pages where Small Deformation Theory is mentioned: [Pg.120]    [Pg.121]    [Pg.158]    [Pg.163]    [Pg.164]    [Pg.165]    [Pg.662]    [Pg.522]    [Pg.10]    [Pg.120]    [Pg.121]    [Pg.158]    [Pg.163]    [Pg.164]    [Pg.165]    [Pg.662]    [Pg.522]    [Pg.10]    [Pg.118]    [Pg.121]    [Pg.83]    [Pg.81]    [Pg.73]    [Pg.117]    [Pg.67]    [Pg.79]    [Pg.103]    [Pg.105]    [Pg.129]    [Pg.41]    [Pg.122]    [Pg.451]    [Pg.67]    [Pg.659]    [Pg.174]    [Pg.401]    [Pg.284]    [Pg.31]   


SEARCH



Deformation theory

Small theory

© 2024 chempedia.info