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Surface-melted phase

One particularly vivid example is the cluster of 55 atoms bound by Lennard-Jones forces, effectively Ar55 or by metallic binding forces. Besides its solid and liquid phases, this cluster (and others of similar size and constitution) can exhibit a surface-melted phase [15, 24, 25], Strictly, as animations show, the term surface melting is not really accurate. In the phase that shows a high mobility of the atoms in the surface layer, the actual motion of almost all of those atoms is a large-amplitude, very anharmonic vibration, while at least one atom is promoted to move rather freely around the shell as a floater the average is about one surface atom in 15 becomes a floater. The floater atom exchanges positions occasionally with an atom in the outer shell, so that, over time, all the surface atoms are, at some time, a floater. This process allows all the surface atoms to permute their positions and eventually to occupy all the surface sites - as one would expect of a liquid. [Pg.226]

T.L. Boggs et al, AIAA J 8 (2), 370-72 (1970) CA 72, 113371 (1970) Scanning electron microscopy is used to study the surface structure of solid proplnts, prepd from AP (1) and polyurethane or caiboxylated polybutadiene. Polyurethane proplnts are self-extinguish-ing at high pressure due to the flow of molten binder over I crystals. I crystals formed a thin surface melt with gas liberation in the molten phase... [Pg.947]

Sm specific surface are of the melt phase on bed volume basis (m 1) Sv volumetric specific surface area (m 1)... [Pg.275]

Fig. 23 The bonds that constitute crystalline domains must lie nearly parallel to the jy-axis with an angle 6 of less than 20°. Furthermore, the bonds must have at least three neighbors that satisfy 0.7a < Jr + r < 1.3a and ry < r0/2. Note that the crystalline stems deep inside the crystal (black spheres) have six neighbors, while those on the free sin-faces (hatched spheres) have four neighbors. The stems at the half-crystal site, or at the kink site, (white sphere) have three neighbors. Stems attached on the free surface, and those floating in the melt phase have less than three neighbors... Fig. 23 The bonds that constitute crystalline domains must lie nearly parallel to the jy-axis with an angle 6 of less than 20°. Furthermore, the bonds must have at least three neighbors that satisfy 0.7a < Jr + r < 1.3a and ry < r0/2. Note that the crystalline stems deep inside the crystal (black spheres) have six neighbors, while those on the free sin-faces (hatched spheres) have four neighbors. The stems at the half-crystal site, or at the kink site, (white sphere) have three neighbors. Stems attached on the free surface, and those floating in the melt phase have less than three neighbors...
The thickness of the QLLs is different on different faces, and becomes thinner as the temperature is decreased. Thus, the temperature at which a QLL disappears depends on the face. When the surface is covered by Q.LLs, crystal growth is regarded as a solution or melt phase growth, whereas on a naked surface it is due to vapor growth. Thus, the repeated Habitus change may be explained. The presence of QLLs was confirmed by ellipsometry. [Pg.76]

Thermal treatment. Heating of the material may cause desorption of weakly bound species from the surface and can therefore be used to clean surfaces. A positive side effect is that annealing reduces the number of surface defects since it increases the diffusion rates of surface and bulk atoms. There can also be some unwanted side effects surface melting and other types of phase transitions may occur well below the bulk melting point, leading to other than the desired surface structure. [Pg.151]

Heat is conducted from the outer surface through the melt to the free interface, where some of the heat is absorbed as heat of fusion, melting some more solid, and the rest is conducted into the solid phase. The densities of melt and solid are usually different. We denote the melt phase with subscript l and the solid with subscript s. The thickness of the molten layer increases because of melting, and there is also a slight increase due to a decrease in density as the solid melts. If there were no decrease in density, the thickness of the molten layer would remain Xs. Thus, the relationship between Xt and Xs is given by... [Pg.190]

Stabilization of the thickness pore size heat and gas barrier performance of the protecting surface layer, hindrance of the dipping of the melt phase... [Pg.330]

The situation is fully analogous to complete wetting at the surfaces of fluids or fluid mixtures [220], of course. Perhaps the closest analogy occurs between surface-induced lamellar ordering and the surface melting [220] of crystals - the distinction being, of course, that in the latter case it is the disordered rather than the ordered phase that is stabilized by the surface. [Pg.35]

The term melt fracture has been applied from the outset [9,13] to refer to various types of visible extrudate distortion. The origin of sharkskin (often called surface melt fracture ) has been shown in Sect. 10 to be related to a local interfacial instability in the die exit region. The alternating quasi-periodic, sometimes bamboo-like, extrudate distortion associated with the flow oscillation is a result of oscillation in extrudate swell under controlled piston speed due to unstable boundary condition, as discussed in Sect. 8. A third type, spiral like, distortion is associated with an entry flow instability. The latter two kinds have often been referred to as gross melt fracture. It is clearly misleading and inaccurate to call these three major types of extrudate distortion melt fracture since they do not arise from a true melt fracture or bulk failure. Unfortunately, for historical reasons, this terminology will stay with us and be used interchangeably with the phase extrudate distortion. ... [Pg.269]

S. M. Scala and G. W. Sutton, The Two-Phase Hypersonic Boundary Layer— A Study of Surface Melting, 1958 Heat Transfer and Fluid Mechanics Institute. Stanford Stanford University Press, 1958, 231-240. [Pg.517]

For the next two types of theoretical models, the elementary reaction cell consists of a spherical particle of one reactant surrounded by a melt of the other reactant. In the first case, the product layers (C) grow on the surface of the more refractory particles (B) due to diffusion of atoms from the melt phase (A) through the product layer (see Fig. 20b). At a given temperature, the concentrations at the interphase boundaries are determined from the phase diagram of the system. Numerical calculations by Nekrasov et al. (1981, 1993) have shown satisfactory agreement with experimental results for a variety of systems. [Pg.129]


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See also in sourсe #XX -- [ Pg.226 ]




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