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Percolation solids

In a disordered solid, as modelled by the percolation model (discussed in Section 1.2) with intact bond concentration p on a lattice, there occur various vacancy clusters (voids), or pre-existing cracks, of different sizes and shapes. The typical crack size in such a percolating solid being of the size of the correlation length (see Section 1.2.1) the application of the Griffith fracture criterion gives (Chakrabarti 1988, Ray and Chakrabarti 1985a,b) from equation (3.4)... [Pg.95]

We will give next two specific and limiting forms of this distribution, indicating their derivations for percolating solids. It should be noted, however, that these forms are not specific to percolation models only they can be applied to much wider classes of disorder. [Pg.108]

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]

It follows from (6.57, 58) that pmix — /iL can have one or two minima at 0 < x < 1, thus one or two (stable or stable + metastable) states of supercooled liquids can exist. At high temperatures, T > T, and at low temperatures, T < fm, only one equilibrium state exists. If two equilibrium states coexist, they differ by the degree of clusterization. If a clusterized fraction is large enough, the state must be treated as solid one. Indeed, in the system at x > xc 0.16 an infinite (percolated) solid cluster is formed and at (1 — x) > (1 — x)c 0.16 a percolated liquid cluster appears. So, at x > xg 0.84 the mixed state is really a solid with heterophase liquid fluctuations. The temperature at which the stable state with x > xg exists, is the thermodynamic glassing temperature, Tgh. [Pg.249]

The precursor should be either a liquid or a solid with sufficient vapor pressure and mass transport at the desired temperature, preferably below 200°C. Liquids are preferred to solids owing to the difficulty of maintaining a constant flux of source vapors over a non-equilibrium percolation (solid) process. Such nonbubbling processes are a function of surface area, a non-constant variable with respect to both time and particle size. The upper temperature limit is not dictated by chemical factors rather it is a limitation imposed by the stability of the mass flow controllers and pneumatic valves utilized in commercial deposition equipment. It must be stressed that while the achievement of an optimum vapor pres-... [Pg.30]

Whatever the mechanism and the method of operation, it is clear that the leaching process will be favored by increased surface per unit volume of sohds to be leached and by decreased radial distances that must be traversed within the solids, both of which are favored by decreased particle size. Fine solids, on the other hand, cause slow percolation rate, difficult solids separation, and possible poor quahty of sohd product. The basis for an optimum particle size is estabhshed by these characteristics. [Pg.1673]

It is classification by contacting method that provides the two principal categories into which leaching equipment is divided (I) that in which the leaching is accomphshed oy percolation and (2) that in which particulate solids are dispersed into a hquid and subsequently separated from it. Each includes batch and continuous units. Materials which disintegrate during leaching are treated in equipment of the second class. [Pg.1673]

Batch Percolators The batch tank is not unlike a big nutsche filter it is a large circiilar or rectangiilar tank with a false bottom. The solids to be leached are dumped into the tank to a uniform depth. They are sprayed with solvent until their solute content is reduced to an economic minimum and are then excavated. Countercurrent flow of the solvent through a series of tanks is common, with fresh solvent entering the tank containing most nearly exhausted material. In a typical ore-dressing operation the tanks are 53 by 20 by 5.5 m (175 by 67 by 18 ft) and extract about 8200 Mg (9000 U.S. tons) of ore on a 13-day cycle. Some tanks operate under pressure, to contain volatile solvents or increase the percolation rate. A series of pressure tanks operating with countercurrent solvent flow is called a diffusion battery. [Pg.1673]

Screw-Conveyor Extractors One type of continuous leaching equipment, employing the screw-conveyor principle, is strictly speaking neither a percolator nor a dispersed-solids extractor. Although it is often classed with percolators, there can be sufficient agitation of the solids during their conveyance by the screw that the action differs from an orthodox percolation. [Pg.1675]

Leaching Cycle and Contact Method As is true generally, the choice between continuous and intermittent operation is largely a matter of the size and nature of the process of which the extraction is a part. The choice of a percolation or solids-dispersion technique depends principally on the amenability of the extraction to effective, sufficiently rapid percolation. [Pg.1676]

Fig. 12. Tensile strength a, vs. number of backbone bonds per monomer 1 /a, reported for a range of polymers by Vincent [75]. The solid line is the theoretical line for vector percolation analysis of strength discussed herein. Fig. 12. Tensile strength a, vs. number of backbone bonds per monomer 1 /a, reported for a range of polymers by Vincent [75]. The solid line is the theoretical line for vector percolation analysis of strength discussed herein.
Often, the immobilized product has a structural strength sufficient to prevent fracturing over time. Solidification accomplishes the objective by changing a non-solid waste material into a solid, monolithic structure that ideally will not permit liquids to percolate into or leach materials out of the mass. Stabilization, on the other hand, binds the hazardous constituents into an insoluble matrix or changes the hazardous constituent to an insoluble form. Other objectives of solidiflcation/stabilization processes are to improve handling of the waste and pri uce a stable solid (no free liquid) for subsequent use as a construction material or for landfilling. [Pg.176]

It is also preferred where suspended solids create a high pressure drop, or dissolved gases create bubbles in the carbon bed. For a downflow or percolation system, an influent line should be installed at the top of the column, with an effluent at the bottom. To prevent the column from draining during operation, the effluent line from the last column should extend from the bottom of the column to above the top of the column. This will keep the column filled with liquid at all times during operation and prevent siphoning from occurring. [Pg.431]

The cluster properties of the reactants in the MM model at criticality have been studied by Ziff and Fichthorn [89]. Evidence is given that the cluster size distribution is a hyperbolic function which decays with exponent r = 2.05 0.02 and that the fractal dimension (Z)p) of the clusters is Dp = 1.90 0.03. This figure is similar to that of random percolation clusters in two dimensions [37], However, clusters of the reactants appear to be more solid and with fewer holes (at least on the small-scale length of the simulations, L = 1024 sites). [Pg.422]

Thienylacetarnidocephalosporanic acid (7.0 g) was suspended in water (60 ml) and stirred with pyridine (7 ml) until the acid dissolved. The resulting solution (pH 5.9) was kept at 35°C for 3 days, then filtered and extracted with methylene chloride (4 x 60 ml). The methylene chloride extract was back-axtracted with a little water and the total aqueous solutions were then percolated through a column of Dowex 1x8 resin, (100 to 200 mesh, 150 g) in the acetate form at pH 4.3. The column was washed with water until the optical rotation of the eluate fell to zero and the eluate (500 ml) was freeze-dried. The residual white solid was dissolved in the minimum volume of methanol and after a few minutes the pyridine derivative crystallized this is the cephaloridine product. [Pg.285]

A solution of the piperidino-diol (9 grams) in acetic anhydride (18 ml) was heated at 90°C for 1 hour, the solution cooled, excess acetic anhydride destroyed by the careful addition of water, and the resulting solution carefully made alkaline with 2N caustic soda solution to precipitate a solid product. The soiid was dried, extracted with n-hexane and the solution filtered free of insoluble material before percolation down a column (4x1" diameter) of alumina. Eiution with n-hexane gave a fraction (4.2 grams) which was crystallized twice from ether to give the diacetate, MP 176°-180°C. [Pg.1159]

The aqueous percolate is concentrated to dryness by lyophilization, and the solid product obtained is purified by taking up In boiling absolute ethanol, cooling and recovering the solid product paromomycin = -t64° (1% in water). 8y analysis it contains 45.17%... [Pg.1168]

During filtration the suspended solids are trapped between the grains of filter media. Because there must always be space remaining for the water to percolate, there is a limit to the total volume of solid sludge that can be tolerated before backwashing is required. Designers typically set this limit at 25% of the total void volume and, irrespective of the media grain size, the void volume is approximately 45% of the total media volume. [Pg.321]

The solid phase used in this extraction is a weak ion exchanger and the material is preconditioned with a wash of 0.5 ml of 0.5M phosphoric acid followed by 1 ml of deionized water. A volume of 0.5 ml of the serum containing the tricyclic antidepressant drug standards is mixed with 0.5 ml of deionized water and allowed to percolate slowly through the packing. [Pg.204]

Chromatography is a physical method of separation in which the components to be separated are distributed between two phases, one of which is stationary (the stationary phase), while the other (the mobile phase) moves in a definite direction. A mobile phase is described as a fluid which percolates through or along the stationary bed in a definite direction . It may be a liquid, a gas or a supercritical fluid, while the stationary phase may be a solid, a gel or a liquid. If a liquid, it may be distributed on a solid, which may or may not contribute to the separation process. ... [Pg.24]


See other pages where Percolation solids is mentioned: [Pg.4]    [Pg.84]    [Pg.96]    [Pg.114]    [Pg.4]    [Pg.84]    [Pg.96]    [Pg.114]    [Pg.368]    [Pg.87]    [Pg.1673]    [Pg.1673]    [Pg.1674]    [Pg.1675]    [Pg.2013]    [Pg.2138]    [Pg.65]    [Pg.301]    [Pg.366]    [Pg.368]    [Pg.368]    [Pg.394]    [Pg.397]    [Pg.386]    [Pg.413]    [Pg.80]    [Pg.139]    [Pg.216]    [Pg.122]    [Pg.415]    [Pg.75]    [Pg.150]    [Pg.151]    [Pg.555]   
See also in sourсe #XX -- [ Pg.3904 ]




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