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Perfect solid strength

Fracture strength of a perfect solid containing a single crack Griffith s law... [Pg.82]

The above results are all for a perfect solid under stress, with a single microcrack inside. For randomly disordered solids, the appropriate modification of the above Mott formula has not been developed yet. However, some quantitative features of the fracture propagation process in extremely disordered solids, like the percolating solid near its percolation threshold, are quite obvious and interesting. Although the (equilibrium) strength erf of the solid vanishes near the percolation threshold Pc erf (Ap) ), the... [Pg.118]

Certain aspects of the photoacoustic effect suggest that this technique might be generally applicable to all chiral solids regardless of crystal class, size or perfection, or strength of absorption. Although subsequent theoretical developments and experimental results have caused us to limit considerably the predicted scope of this method, nevertheless, it is possible now to say clearly that the experiment does work and offers prospects for unique results. In this paper we review briefly the nature of the theory and practice of condensed phase photoacoustic spectroscopy and its extension to the measurement of natural circular dichroism, and present initial results for single crystals and powders. [Pg.376]

An estimate of the theoretical breaking strength of a perfect solid based on the creation of two new surfaces shows that the maximum breaking strength is equal to where E, y, and... [Pg.259]

In fig. 26 the Arrhenius plot ln[k(r)/coo] versus TojT = Pl2n is shown for V /(Oo = 3, co = 0.1, C = 0.0357. The disconnected points are the data from Hontscha et al. [1990]. The solid line was obtained with the two-dimensional instanton method. One sees that the agreement between the instanton result and the exact quantal calculations is perfect. The low-temperature limit found with the use of the periodic-orbit theory expression for kio (dashed line) also excellently agrees with the exact result. Figure 27 presents the dependence ln(/Cc/( o) on the coupling strength defined as C fQ. The dashed line corresponds to the exact result from Hontscha et al. [1990], and the disconnected points are obtained with the instanton method. For most practical purposes the instanton results may be considered exact. [Pg.66]

Brittle fracture may be considered, therefore, as two layers of atoms being pulled apart until the interatomic forces fall below their maximum (Fig. 8.82). Using this information it is possible to calculate the fracture strength of a perfect crystalline solid (a,h), e.g. [Pg.1353]

In a perfect crystal, all atoms would be on their correct lattice positions in the structure. This situation can only exist at the absolute zero of temperature, 0 K. Above 0 K, defects occur in the structure. These defects may be extended defects such as dislocations. The strength of a material depends very much on the presence (or absence) of extended defects, such as dislocations and grain boundaries, but the discussion of this type of phenomenon lies very much in the realm of materials science and will not be discussed in this book. Defects can also occur at isolated atomic positions these are known as point defects, and can be due to the presence of a foreign atom at a particular site or to a vacancy where normally one would expect an atom. Point defects can have significant effects on the chemical and physical properties of the solid. The beautiful colours of many gemstones are due to impurity atoms in the crystal structure. Ionic solids are able to conduct electricity by a mechanism which is due to the movement of fo/ 5 through vacant ion sites within the lattice. (This is in contrast to the electronic conductivity that we explored in the previous chapter, which depends on the movement of electrons.)... [Pg.201]

PLASTIC DEFORMATION. When a metal or other solid is plastically deformed it suffers a permanent change of shape. The theory of plastic deformation in crystalline solids such as metals is complicated but well advanced. Metals are unique among solids in their ability to undergo severe plastic deformation. The observed yield stresses of single crystals are often 10 4 times smaller than the theoretical strengths of perfect crystals. The fact that actual metal crystals are so easily deformed has been attributed to the presence of lattice defects inside the crystals. The most important type of defect is the dislocation. See also Creep (Metals) Crystal and Hot Working. [Pg.1315]

Since real surfaces are not smooth or perfectly flat and most epoxy adhesives are viscoelastic fluids, it is necessary to understand the effects of surface roughness on joint strength. A viscous liquid can appear to spread over a solid surface and yet leave many gas pockets or voids in small surface pores and crevices. Even if the liquid does spread spontaneously over the solid, there is no certainty that it will have sufficient time to fill in all the voids and displace the air. The gap-filling mechanism is generally competing with the setting mechanism of the liquid. [Pg.55]

By the first decade of this century it was established that material failures occur at such low stress levels, because real materials do not usually have a perfect crystalline structure and almost always some vacancies, interstitials, dislocations and different sizes of thin microcracks (having linear structure and sharp edges) are present within the sample. Since the local stress near a sharp notch may rise to a level several orders of magnitude higher than that of the applied stress, the thin cracks in solids reduce the theoretical strength of materials by similar orders, and cause the material to break at low stress levels. The failure of such (brittle or ductile) materials was first identified by Inglis (1913) to be the stress concentrations occurring near the tips of the microcracks present within the sample. [Pg.84]

The packing, or solid support in a packed column, serves to hold the liquid stationary phase in place so that as large a surface area as possible is exposed to the mobile phase. The ideal support consists of small, uniform, spherical particles with good mechanical strength and a specific surface area of at least 1 mVg. In addition, the material should be inert at elevated temperatures and be uniformly wetted by the liquid phase. No substance that meets all these criteria perfectly is yet available. [Pg.960]


See other pages where Perfect solid strength is mentioned: [Pg.99]    [Pg.271]    [Pg.368]    [Pg.36]    [Pg.123]    [Pg.74]    [Pg.245]    [Pg.179]    [Pg.11]    [Pg.31]    [Pg.300]    [Pg.681]    [Pg.662]    [Pg.170]    [Pg.873]    [Pg.876]    [Pg.348]    [Pg.1526]    [Pg.34]    [Pg.498]    [Pg.361]    [Pg.221]    [Pg.591]    [Pg.18]    [Pg.410]    [Pg.4728]    [Pg.617]    [Pg.619]    [Pg.622]    [Pg.589]    [Pg.2271]    [Pg.307]    [Pg.243]   
See also in sourсe #XX -- [ Pg.99 , Pg.100 ]




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