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Deformed regions

In this case the shear stress (in the plastic deformation region) depends on how much plastic strain y that has accumulated and the current rate of deformation y. For example, in shock compression the shear stress t behind the shock front (where y is nominally zero) is a function of y only, as given by the implicit relationship... [Pg.221]

We first consider strain localization as discussed in Section 6.1. The material deformation action is assumed to be confined to planes that are thin in comparison to their spacing d. Let the thickness of the deformation region be given by h then the amount of local plastic shear strain in the deformation is approximately Ji djh)y, where y is the macroscale plastic shear strain in the shock process. In a planar shock wave in materials of low strength y e, where e = 1 — Po/P is the volumetric strain. On the micromechanical scale y, is accommodated by the motion of dislocations, or y, bN v(z). The average separation of mobile dislocations is simply L = Every time a disloca-... [Pg.245]

The three deformation regions are also apparent on the strength versus concentration relationships. The most dramatic drop of the yield point was observed at small filler concentrations (up to 0.15). On further filling the characteristic remained almost unchanged. [Pg.31]

Figure 12 shows the spectrum for the deformation region in an ethylene-helium stream and an ethylene-hydrogen stream. In the deformation region the two bands at 1451 and 1438 cm-1 due to ethylene alone appear to weaken and shift slightly and a new band (or perhaps two) appears at about 1415 cm-1. Figure 12 also shows that under reaction conditions the ZnH band is shifted from 1709 to 1655 cm 1 the corresponding shift in the OH band is from 3490 to 3510 cm-1. [Pg.24]

Figure 18 shows the spectrum of C3D6 in the CH deformation region. We would expect the normal isotope effect to shift C—D deformations about 400 cm-1, that is, completely out of this region. Thus, the observed bands are due to C—C vibrations. The band at 1473 cm-1 (with a shoulder at 1460 cm-1) can only correspond to the 1545 cm-1 band in C3H6. The... [Pg.31]

Stretching region C-H Stretching region C=C Deformation region C-H AdefC-H/AstrC-H ... [Pg.100]

We can begin to understand the contrast mechanism by considering the ciystal to be made up of three distinct regions, namely the perfect crystal above the defect, the perfect crystal below the defect, and the deformed region around the defect (Figure 8.15(a)). We set the hmit of the deformed region as that where the effective misorientation ( ) arotmd a defect exceeds the perfect crystal... [Pg.207]

Around defects, the scattering power differs from that in the perfect crystal because X-rays which do not satisly the Bragg condition in the perfect crystal may be diffracted in the deformed region arotmd the defect. Just as in the Lang projection topograph, these regions behave as small crystals which diffract kinematically and the net result is an increase in the intensity over that from the perfect crystal. [Pg.243]

The IR spectra of methyllithium exhibited two C—H bending vibrational modes at 1480 and 1427 cm . Their assignment was again substantiated by significant isotopic shifts to 1100 and 1043 cm in the deuterium compound (Table 1). Only one weak band was observed for ethyllithium in the C—H deformation region at 1450 cm . Moreover, a new sharp peak was detected at 1385 cm and ascribed to the C—H symmetrical bending mode of CH3. Its absence in the IR spectrum of methyllithium is a further indication that free methyl groups exist only in ethyllithium. [Pg.231]

The mid-infrared VCD of some members of this series has also been investigated (59, 60) with an aim, in part, to identify features diagnostic of conformation. In the methyl deformation region (1450 cm ), all members of the... [Pg.143]

At very small strains within the viscoelastic region (e<0.5%), deformation within the PP solid is confined to disordered amorphous regions [97,98) due to their inherently low stiffness at temperatures above their Tg (-10 °C). In this deformation region, spherulites undergo affine deformation on the whole. Inside the spherulites, rotation of lamellae occurs [101]. The resulting orientation of lamellae depends on their position within the spherulite in respect to the orientation of the external deformation [102-104],... [Pg.56]

EA resulting from the transformation of EDA (Table II) shows up by a weak band at approximately 1520 cm-1—i.e., at the frequency observed for 5B(NH3+). In the deformation region, the spectra observed during the transformation of the TEA Y-zeolite do not show any noticeable effect. [Pg.522]

The crack develops in the extreme deformation region and produces a circle under the indenter, entirely below the contact surface (broken-line circle). [Pg.102]

How does the elevation of the deforming region change with time ... [Pg.6]

Figure 11 FTIR spectra of the CH3-N+ and CH2 deformation region in mixed micelles of DTAC/SDS-d25. From top, XSDS = 0.86, 0.20, 0.0. The bottom spectrum is a difference spectrum with pure DTAC micelles subtracted from the XSDs = 0.20 sample (T = 23°C). Reprinted from ref. 47. Copyright 1990 American Chemical Society. Figure 11 FTIR spectra of the CH3-N+ and CH2 deformation region in mixed micelles of DTAC/SDS-d25. From top, XSDS = 0.86, 0.20, 0.0. The bottom spectrum is a difference spectrum with pure DTAC micelles subtracted from the XSDs = 0.20 sample (T = 23°C). Reprinted from ref. 47. Copyright 1990 American Chemical Society.

See other pages where Deformed regions is mentioned: [Pg.639]    [Pg.220]    [Pg.194]    [Pg.97]    [Pg.830]    [Pg.388]    [Pg.270]    [Pg.166]    [Pg.20]    [Pg.25]    [Pg.30]    [Pg.206]    [Pg.211]    [Pg.198]    [Pg.97]    [Pg.390]    [Pg.33]    [Pg.39]    [Pg.183]    [Pg.59]    [Pg.17]    [Pg.31]    [Pg.264]    [Pg.1213]    [Pg.127]    [Pg.5]    [Pg.6]    [Pg.16]    [Pg.195]    [Pg.328]    [Pg.335]    [Pg.428]    [Pg.212]    [Pg.13]    [Pg.100]    [Pg.222]   
See also in sourсe #XX -- [ Pg.294 ]




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