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Boundary cell

In most cases, and in all cases found in this book, the cells of the boundaries are themselves inert, and have no interactions with the grid ingredients other than to constrain their movements in certain directions. However, more generally the boundary cells can be constructed to have active properties just like any other ingredient, following rules (see below) that permit joining, breaking,... [Pg.13]

A series of rules describing the breaking, / B,and joining, J, probabilities must be selected to operate the cellular automata model. The study of Kier was driven by the rules shown in Table 6.6, where Si and S2 are the two solutes, B, the stationary cells, and W, the solvent (water). The boundary cells, E, of the grid are parameterized to be noninteractive with the water and solutes, i.e., / b(WE) = F b(SE) = 1.0 and J(WE) = J(SE) = 0. The information about the gravity parameters is found in Chapter 2. The characteristics of Si, S2, and B relative to each other and to water, W, can be interpreted from the entries in Table 6.6. [Pg.96]

The main disadvantage is the long period required to reach equilibrium, even if the time is shortened by use of short cells or a synthetic boundary cell to reduce the distance the various species must travel as equilibrium is established. [Pg.126]

Although the molecular weight of the polysaccharide was not determined, its rapid rate of diffusion on ultracentrifugation, and the fact that synthetic boundary-cells had to be used, indicated that the molecular weight was less than 10,000. The molecular weight of buckwheat-honey polysaccharide is 9,000. [Pg.307]

Sedimentation velocity experiments were performed using a 12-mm Kel-F double-sector capillary synthetic boundary cell. Each equilibrium experiment was performed with aid of two separate 12-mm, 4° singlesector aluminum cells, one containing solvent and the other solution. In all cases the schlieren angle was 65°. [Pg.233]

When the stack is modeled, boundary conditions are set only for the boundary cells in the case of the other cells, the nodes at the interconnections are linked together when two cells are connected in series. Figure 7.24 also shows the connections between the cells in a stack. [Pg.229]

Boundary Cells. A cell on the boundary has one wall in contact with the gutside world and hence the flux through that wall is K.M and not J. Generally we want to replace J1 with KM over that fraction of the cell surface in common with the outer boundary. One method for doing so is to replace J in (66) by (K in those parts of the d-dimensional sphere surrounding point r that stick outside the cell aggregate volume. Thus (67,68) take the same form for the boundary points except that F takes on the form, for d = 3,... [Pg.191]

Several designs have gained popularity, and they are named after their inventors Abramson (flat cell), Briggs, Briggs-Mattson, Hamilton-Stevens, Mattson [252,253], Riddick, and van Gils. A moving-boundary cell is shown and described in [7,47]. [Pg.43]

The ultracentrifugation experiment was performed using a Beckman Model E Instrument with a capillary synthetic boundary cell at 30°C. Toluene was used as the solvent and solution concentrations were 1% (w/v). [Pg.39]

Fig. 20 (78). Sedimentation diagram of bovine apoerythrocuprein. The protein concentration was 2.1 mg and 4.1 mg dissolved in 5 mM phosphate buffer, pH 7.2. Direction of sedimentation left to right, speed 60,000 rpm. Schlieren bar angle 50°, 12 mm Al-valve synthetic boundary cell. Photographs were taken at 16-min intervals after reaching full speed... Fig. 20 (78). Sedimentation diagram of bovine apoerythrocuprein. The protein concentration was 2.1 mg and 4.1 mg dissolved in 5 mM phosphate buffer, pH 7.2. Direction of sedimentation left to right, speed 60,000 rpm. Schlieren bar angle 50°, 12 mm Al-valve synthetic boundary cell. Photographs were taken at 16-min intervals after reaching full speed...
Figure 8. Ultracentrifugal patterns of Pseudomonas cellulases Pictures were taken at 45 minutes after rotation had reached a maximum speed of 55,430 r.p.m. at 17°C. Protein concentration was 0.45% (Cellulase A) and 0.7% (Cellulases B and C) in 1/15M phosphate buffer of pH 7.0. The synthetic boundary cell was employed for Cellulases B and C... Figure 8. Ultracentrifugal patterns of Pseudomonas cellulases Pictures were taken at 45 minutes after rotation had reached a maximum speed of 55,430 r.p.m. at 17°C. Protein concentration was 0.45% (Cellulase A) and 0.7% (Cellulases B and C) in 1/15M phosphate buffer of pH 7.0. The synthetic boundary cell was employed for Cellulases B and C...
Suzuki, N., Prosser, C.L., and Dahms, V., 1986. Boundary cells between longitudinal and circular layers Essential for electrical slow waves in cat intestine. Am. J. Physiol, 280 G287-G294. [Pg.105]

The particle positions and velocities from cells, which are situated on the boundaries between processor domains, are copied to the neighboring processor (see Figure 26.15). Thus the number of particles located in the boundary cells defines the communication overhead. [Pg.744]

Thermal fluctuations probably would have the same effect on real cells. As with the rigid boundary cell, we are using three volts but the weak anchoring reduces the critical voltage considerably. Notice that turn-on time is faster but turn-off is much slower than with the rigid-boundary cell because of the... [Pg.10]

Intuitively, a cellular collapse is a strong deformation retract that pushes the interior of a maximal cell in, using one of its free boundary cells as the starting point, much like compressing a body made of clay. The cellular collapses can be defined for arbitrary CW complexes. [Pg.189]

Available experimental data on thermal (R.Steinberger-WUkens et al., 2006) and current (Bujalski et al., 2007) cycling do not reveal the oscillations of stack voltage discussed above. However, the measurements cited were performed with short two-cell stacks in such stacks both cells are boundary cells and the cooling heat flux from the cell to the chamber walls could damp the disturbances. The model above is formulated for a stack element located far enough from the boundary cells. In other words, thermal waves are expected to develop in large stacks with several tens of cells, in which core elements in the middle of the stack are thermally well insulated from the chamber walls. [Pg.225]

The value of cq is obtained from a synthetic boundary cell run, which we describe later. The term Cp refers to the position at the plateau region. [Pg.252]

The value of cq is usually obtained from an independent synthetic boundary experiment that is relatively simple. A layer of pure solvent (e.g., 6.45 mL) is placed over a solution (e.g., 0.15 mL) of known concentration in a synthetic boundary cell, and a sedimentation velocity (8000 rpm) is run to obtain a graph ... [Pg.253]

Two ultracentrifuge sedimentation equilibrium experiments were carried out with ribonuclease in aqueous solution. The first was run in a conventional 12-mm cell and the second was performed in a synthetic boundary cell. The schematic diagrams of the ultracentrifuge patterns are shown in the following ... [Pg.264]

For free surfaces, the pressure and stress deviators in the cell adjacent to the boundary are set to the negative value of the state values in the boundary cell. For piston boundaries, the pressure in the adjacent cell is set equal to the piston pressure. For continuum boundaries the pressure and stress deviators in the adjacent cell are set equal to the values in the boundary cell. For axis boundaries the pressures and stress deviators in the adjacent cell across the axis are set equal to the values in axis cells adjacent to the axis. The coordinates of the cells adjacent to the boundary cells are calculated by linear extrapolation. [Pg.401]

The mechanical properties of a metal or alloy are determined by the microstructore of toe material. This is the so-called microstructure-prop-erties relationship. Microstructoral features that affect mechanical performance include grain size, sub-grain structure (low-angle boundaries, cells, etc.), the distribution of matrix and particle phases, the atomic structure of the matrix phase (e.g., single element or solid solution), disloca-... [Pg.70]

Optical Method. This is the most frequently used technique and utilizes either the strain imposed on the crystal by the domain boundaries or the differences of birefringence imposed by different orientations of the polar axis. The sign of polarity is observed by the application of small perturbing electric fields, which cause wall motion or enhanced wall contrast by small angular rotation of the polar direction away from an easy crystallographic direction. Most difficulties are usually experienced in the observation of 180° domains, for in this case the mechanical distortion of boundary cells is smallest and birefringence differences are zero because the angle between polar... [Pg.210]

One of the first approaches employed to impose a non-slip boundary condition at an external wall or at a moving object in a MFC solvent was to use ghost or wall particles [36,81]. In other mesoscale methods such as LB, no-slip conditions are modeled using the bounce-back rule the velocity of the particle is inverted from v to -V when it intersects a wall. For planar walls which coincide with the boundaries of the collision cells, the same procedure can be used in MFC. However, the walls will generally not coincide with, or even be parallel to, the cell walls. Furthermore, for small mean free paths, where a shift of the cell lattice is required to guarantee Galilean invariance, partially occupied boundary cells are unavoidable, even in the simplest flow geometries. [Pg.38]

Fig. 4.9 Schematic illustration of one solution to the firing squad synchronization problem, adapted from Fischer (1965). Signal A (solid line) travels at velocity 1, and signal B (dashed line) travels at velocity 1/3. General cells contain black dots and boundary cells are shaded. Fig. 4.9 Schematic illustration of one solution to the firing squad synchronization problem, adapted from Fischer (1965). Signal A (solid line) travels at velocity 1, and signal B (dashed line) travels at velocity 1/3. General cells contain black dots and boundary cells are shaded.

See other pages where Boundary cell is mentioned: [Pg.181]    [Pg.103]    [Pg.210]    [Pg.210]    [Pg.217]    [Pg.811]    [Pg.178]    [Pg.217]    [Pg.74]    [Pg.1117]    [Pg.745]    [Pg.346]    [Pg.349]    [Pg.262]    [Pg.242]    [Pg.547]    [Pg.678]    [Pg.68]    [Pg.212]    [Pg.69]    [Pg.113]    [Pg.113]   
See also in sourсe #XX -- [ Pg.210 ]




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Dislocation Cells and Grain Boundaries

Moving-boundary cell

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