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Elasticity first-order

Since this agrees with the first Bom differential cross section for (in)elastic scattering, Femii s Rule 2 is therefore valid to first order in the interaction F. [Pg.2021]

Polyolefin melts have a high degree of viscoelastic memory or elasticity. First normal stress differences of polyolefins, a rheological measure of melt elasticity, are shown in Figure 9 (30). At a fixed molecular weight and shear rate, the first normal stress difference increases as MJM increases. The high shear rate obtained in fine capillaries, typically on the order of 10 , coupled with the viscoelastic memory, causes the filament to swell (die swell or... [Pg.317]

In this chapter the regimes of mechanical response nonlinear elastic compression stress tensors the Hugoniot elastic limit elastic-plastic deformation hydrodynamic flow phase transformation release waves other mechanical aspects of shock propagation first-order and second-order behaviors. [Pg.15]

Fig. 2.2. The characteristic stress pulses produced by shock loading differ considerably depending upon the stress range of the loading. The first-order features of the stress pulses can be anticipated from critical features of the stress-volume relation. In the figure, P is the applied pressure and HEL is the Hugoniot elastic limit. Characteristic regimes of materials response can be categorized as elastic, elastic-plastic, or strong shock. Fig. 2.2. The characteristic stress pulses produced by shock loading differ considerably depending upon the stress range of the loading. The first-order features of the stress pulses can be anticipated from critical features of the stress-volume relation. In the figure, P is the applied pressure and HEL is the Hugoniot elastic limit. Characteristic regimes of materials response can be categorized as elastic, elastic-plastic, or strong shock.
With nanosecond time resolution, sensitive, accurate detectors, studies of these release waves have proven to be particularly revealing. First-order descriptions of release properties were obtained with rudimentary instrumentation from the earliest studies [65A01] it has required the most sophisticated modern instrumentation to provide the necessary detail to obtain a clear picture of the events. Characteristically different profiles are encountered in the strong-shock, elastic, and elastic-plastic regimes. [Pg.41]

Release waves for the elastic-plastic regime are dominated by the strength effect and the viscoplastic deformations. Here again, quantitative study of the release waves requires the best of measurement capability. The work of Asay et al. on release of aluminum as well as reloading, shown in Fig. 2.11, demonstrates the power of the technique. Early work by Curran [63D03] shows that limited time-resolution detectors can give a first-order description of the existence of elastic-plastic behavior on release. [Pg.42]

In this chapter studies of physical effects within the elastic deformation range were extended into stress regions where there are substantial contributions to physical processes from both elastic and inelastic deformation. Those studies include the piezoelectric responses of the piezoelectric crystals, quartz and lithium niobate, similar work on the piezoelectric polymer PVDF, ferroelectric solids, and ferromagnetic alloys which exhibit second- and first-order phase transformations. The resistance of metals has been investigated along with the distinctive shock phenomenon, shock-induced polarization. [Pg.136]

Curve 1 represents the total energy of the hydrogen molecule-ion as calculated by the first-order perturbation theory curve 2, the naive potential function obtained on neglecting the resonance phenomenon curve 3, the potential function for the antisymmetric eigenfunction, leading to elastic collision. [Pg.43]

Figure 24. Shown is the derivative of the first-order spherical Bessel function determining the effective decrease in the elastic field gradient produced by a phonon of wavelength k (x = kR). Figure 24. Shown is the derivative of the first-order spherical Bessel function determining the effective decrease in the elastic field gradient produced by a phonon of wavelength k (x = kR).
In a first-order fluid (Newtonian) only significant dimensionless groups can be derived which include elastic behaviour [88]. [Pg.39]

Ed being the energy of the fast electron. To a good approximation, the effect of inelastically scattered electrons on the elastic electron wave field may be treated via a first order perturbation method. From Equation (4) we have... [Pg.162]

As explained above, the QM/MM-FE method requires the calculation of the MEP. The MEP for a potential energy surface is the steepest descent path that connects a first order saddle point (transition state) with two minima (reactant and product). Several methods have been recently adapted by our lab to calculate MEPs in enzymes. These methods include coordinate driving (CD) [13,19], nudged elastic band (NEB) [20-25], a second order parallel path optimizer method [25, 26], a procedure that combines these last two methods in order to improve computational efficiency [27],... [Pg.58]

Also known for some time is a phase transition at low temperature (111K), observed in studies with various methods (NQR, elasticity measurement by ultrasound, Raman spectrometry) 112 temperature-dependent neutron diffraction showed the phase transition to be caused by an antiphase rotation of adjacent anions around the threefold axis ([111] in the cubic cell) and to lower the symmetry from cubic to rhombohedral (Ric). As shown by inelastic neutron scattering, this phase transition is driven by a low-frequency rotatory soft mode (0.288 THz 9.61 cm / 298 K) 113 a more recent NQR study revealed a small hysteresis and hence first-order character of this transition.114 This rhombohedral structure is adopted by Rb2Hg(CN)4 already at room temperature (rav(Hg—C) 218.6, rav(C—N) 114.0 pm for two independent cyano groups), and the analogous phase transition to the cubic structure occurs at 398 K.115... [Pg.1261]

The first term in both Equations 17 and 18 is the constant surface-tension contribution and the second term gives the first-order contribution resulting from the presence of a soluble surfactant with finite sorption kinetics. A linear dependence on the surfactant elasticity number arises because only the first-order term in the regular perturbation expansion has been evaluated. The thin film thickness deviates negatively by only one percent from the constant-tension solution when E = 1, whereas the pressure drop across the bubble is significantly greater than the constant-tension value when E - 1. [Pg.493]

They developed a continuum elastic-free energy model that suggests these observations can be explained as a first-order mechanical phase transition. In other recent work on steroids, Terech and co-workers reported the formation of nanotubes in single-component solutions of the elementary bile steroid derivative lithocholic acid, at alkaline pH,164 although these tubules do not show any chiral markings indicating helical aggregation. [Pg.340]

An elastic continuum model, which takes into account the energy of bending, the dislocation energy, and the surface energy, was used as a first approximation to describe the mechanical properties of multilayer cage structures (94). A first-order phase transition from an evenly curved (quasi-spherical) structure into a... [Pg.304]

The absolute instability of the "metastable" states in the framework of classical elasticity manifests itself in dynamics as well. The associated elastodynamical problem reduces to a solution of the nonlinear wave equation = o (uJu . It is convenient to rewrite it as a mixed type first order system... [Pg.188]

We note here that gel is a coherent solid because its structure is characterized by a polymer network, and hence, the above theoretical considerations on crystalline alloys should be applicable to gels without essential alteration. It is expected that the curious features of the first-order transition of NIPA gels will be explained within the concept of the coherent phase equilibrium if the proper calculation of the coherent energy and the elastic energy of the gel network is made. This may be one of the most interesting unsolved problems related to the phase transitions of gels. [Pg.24]

Whereas the error in the calculated value of the elastic scattering phase shift is usually of second order in the error in H, the error in Zeff is of first order the values of Zeg therefore tend to be rather less accurate than the corresponding phase shifts. Consequently, the value obtained for Zeg provides a sensitive test of the accuracy of a wave function, although admittedly in a very restricted region of configuration space where the positron is close to one of the electrons. Drachman and Sucher (1979) developed an alternative method of calculating Zeg in which the delta function A(ri — rt) is replaced by a global operator but, because it is... [Pg.265]


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See also in sourсe #XX -- [ Pg.224 ]




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Elasticity order

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