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Wall-induced stabilization

Tweed twinning. When impurity concentrations are sufficiently large, twin walls are stabilized and thus twin wall densities can be extremely high. As a result, mean twin domain sizes can decrease dramatically for relatively small concentrations of solute. In some instances, the twin walls adopt a characteristic checkerboard-like microstructure known as a tweed pattern with orthogonal modulations of -100-200 A. The formation and energetics of tweed twins are discussed in Chapter 3 of this volume by Salje and also in Putnis and Salje (1994) and Salje (1999). Examples of compositionally induced tweed textures include the doped superconductor YBa2(Cui-jcM f)307.8 for M = Co and Fe (Van Tendeloo et al 1987, Schmahl et al 1989, Xu et al. 1989) as well as As-doped lead phosphate (Bismayer et al. 1995) and Sr-doped anorthite (Tribaudino et al. 1995). Diffraction patterns of twin tweeds exhibit characteristic cross-shaped intensities superimposed on the primary spots. [Pg.147]

At short interparticle distances, the van der Walls forces show that two metallic particles will be mutually attracted. In the absence of repulsive forces opposed to the van der Walls forces the colloidal metal particles will aggregate. Consequently, the use of a protective agent able to induce a repulsive force opposed to the van der Walls forces is necessary to provide stable nanoparticles in solution. The general stabihzation mechanisms of colloidal materials have been described in Derjaguin-Landau-Verway-Overbeck (DLVO) theory. [40,41] Stabilization of colloids is usually discussed... [Pg.263]

Much can be learned by analyzing the structure of a flame in more detail. Consider, for example, a flame anchored on top of a single Bunsen burner as shown in Fig. 4.3. Recall that the fuel gas entering the burner induces air into the tube from its surroundings. As the fuel and air flow up the tube, they mix and, before the top of the tube is reached, the mixture is completely homogeneous. The flow velocity in the tube is considered to be laminar and the velocity across the tube is parabolic in nature. Thus the flow velocity near the tube wall is very low. This low flow velocity is a major factor, together with heat losses to the burner rim, in stabilizing the flame at the top. [Pg.151]

The Presumed Probability Density Function method is developed and implemented to study turbulent flame stabilization and combustion control in subsonic combustors with flame holders. The method considers turbulence-chemistry interaction, multiple thermo-chemical variables, variable pressure, near-wall effects, and provides the efficient research tool for studying flame stabilization and blow-off in practical ramjet burners. Nonreflecting multidimensional boundary conditions at open boundaries are derived, and implemented into the current research. The boundary conditions provide transparency to acoustic waves generated in bluff-body stabilized combustion zones, thus avoiding numerically induced oscillations and instabilities. It is shown that predicted flow patterns in a combustor are essentially affected by the boundary conditions. The derived nonreflecting boundary conditions provide the solutions corresponding to experimental findings. [Pg.205]

MTS with different wall thicknesses were prepared according to Coustel et al. [7] who have shown that decreasing the alcalinity of the synthesis gel increased the wall thickness. Different MTS with wall thicknesses between 8.6 A and 14.5 A were synthesized, but no differences in stability were observed (Table 2). Wall thickness in this range of size does not seem to be a crucial parameter and does not explain the difference of stability between our synthesis and literature results. Probably the field of variation of porosity was to small ( 25%) (Table 2) to induce significant changes of stability. [Pg.671]

All our preliminary CVD experiments were carried out under an atmosphere of N2 gas in order to determine the intrinsic ability of the studied molecules to serve as precursors to ceramic materials. Further studies could be run under a reactive medium such as H2 in order to reduce the C and O content of the films. This was done in the case of compound 19. Cold-wall CVD experiments on this molecule were performed at 973 K and normal pressure under H2 carrier gas. These experiments resulted in the formation of highly pure VC films.38 XPS and EPMA-WDS analyses of these films showed both the free carbon and oxygen contents to be lower than the limits of detection of the techniques. Various factors can account for these results diminution of the C content induced by H2, stabilization of the Cp ligand in the gas phase due to the presence of f-butyl groups, and decomposition mechanism involving a methyl activation leading to the formation of V = CH2 species.38... [Pg.162]

Fig. 12. Schematic variation of the order parameter profile /(z) of a symmetric (f=l/2) diblock copolymer melt as a function of the distance z from a wall situated at z=0. It is assumed that the wall attracts preferentially species A. Case (a) refers to the case % %v where non-linear effects are still negligible, correlation length and wavelength X are then of the same order of magnitude, and it is also assumed that the surface "field" Hj is so weak that at the surface it only induces an order parameter 0.2 n if mb is the order parameter amplitude that appears for %=%t at the first-order transition in the bulk. Case (b) refers to a case where % is only slightly smaller than %t, such that an ordered "wetting layer" of thickness 1 [Eq. (76)] much larger than the interfacial thickness which is of the same order as [Eq. (74)] is stabilized by the wall, while the bulk is still disordered. The envelope (denoted as m(z) in the figure) of the order parameter profile is then essentially identical to an interfacial profile between the coexisting ordered phase at T=Tt for (zl). The quantitative form of this profile [234] is shown in Fig. 13. From Binder [6]... Fig. 12. Schematic variation of the order parameter profile /(z) of a symmetric (f=l/2) diblock copolymer melt as a function of the distance z from a wall situated at z=0. It is assumed that the wall attracts preferentially species A. Case (a) refers to the case % %v where non-linear effects are still negligible, correlation length and wavelength X are then of the same order of magnitude, and it is also assumed that the surface "field" Hj is so weak that at the surface it only induces an order parameter 0.2 n if mb is the order parameter amplitude that appears for %=%t at the first-order transition in the bulk. Case (b) refers to a case where % is only slightly smaller than %t, such that an ordered "wetting layer" of thickness 1 [Eq. (76)] much larger than the interfacial thickness which is of the same order as [Eq. (74)] is stabilized by the wall, while the bulk is still disordered. The envelope (denoted as m(z) in the figure) of the order parameter profile is then essentially identical to an interfacial profile between the coexisting ordered phase at T=Tt for (z<l) and the disordered phase (for z>l). The quantitative form of this profile [234] is shown in Fig. 13. From Binder [6]...

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Stability induced

Wall-stabilization

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