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Uniform particles

Fluidized leaching and washing is a countercurrent operation with downflow of solids, called counter-down. The following equation for generalized fluidization [Pg.496]

Denote the superficial liquid-solids velocity ratio (.L/pfA)/(S/psA) by N, and let (S/psut) =At. which is the minimal cross-sectional area if the solids were to flow at their terminal velocity, up in the absence of fluid flow, and can, therefore, be called terminal cross-sectional area. Then Eq. (2) can be reduced to a dimensionless form in terms of a reduced area, A, defined as follows [Pg.496]

Equation (3) is plotted in the upper diagram of Fig. 2 as A versus with TV as a parameter. It shows that corresponding to any value of TV, there exists a minimum value of A at which the fluidized leacher/washer possesses the least cross-sectional area or the maximum throughput. This minimum A corresponds to theflooding point characteristic of all counter-down systems and can be calculated by setting the derivative d4 /d = 0, thus yielding [Pg.497]

These three parameters at maximum throughput are shown in Fig. 3 as functions of the liquid/solids ratio TV. [Pg.497]

If the leaching or washing of the solids needs an average residence time 6, the required height Z of the fluidized solids bed can be calculated  [Pg.497]


A Gaussian distribution of particle size is the result of copolymer manufactured by suspension polymerization. A jetting process produces beads with more uniform particle size. The uniformity coefficient is a numerical method of indicating closeness of all beads to the same size. [Pg.376]

The batch process is similar to the semibatch process except that most or all of the ingredients are added at the beginning of the reaction. Heat generation during a pure batch process makes reactor temperature control difficult, especially for high soHds latices. Seed, usually at 5—10% soHds, is routinely made via a batch process to produce a uniform particle-size distribution. Most kinetic studies and models are based on batch processes (69). [Pg.27]

Because of this interaction, PVP has found appHcation in surfactant formulations, where it functions as a steric stabilizer for example to generate uniform particle-size polystyrene emulsions (110—112). In a variety of formulations, a surfactant s abiHty to emulsify is augmented by PVP s abiHty to stabilize coUoids stericaHy and to control rheology. [Pg.532]

Example. The Pechini method for fuel cell electrode preparation. La, Ba, Mn niU ates - - CgHgO — citrate complex - - C2FI6O2 — gel. Metal nitrates are complexed with citric acid, and then heated with ethylene glycol to form a transparent gel. This is then heated to 600 K to decompose the organic content and then to temperatures between 1000 and 1300K to produce tire oxide powder. The oxide materials prepared from the liquid metal-organic procedures usually have a more uniform particle size, and under the best circumstances, this can be less than one micron. Hence these particles are much more easily sintered at lower temperatures than for the powders produced by tire other methods. [Pg.235]

Sephadex. Other carbohydrate matrices such as Sephadex (based on dextran) have more uniform particle sizes. Their advantages over the celluloses include faster and more reproducible flow rates and they can be used directly without removal of fines . Sephadex, which can also be obtained in a variety of ion-exchange forms (see Table 15) consists of beads of a cross-linked dextran gel which swells in water and aqueous salt solutions. The smaller the bead size, the higher the resolution that is possible but the slower the flow rate. Typical applications of Sephadex gels are the fractionation of mixtures of polypeptides, proteins, nucleic acids, polysaccharides and for desalting solutions. [Pg.23]

Diatomaceous media are available in various shapes. Their relatively uniform particle size establishes high efficiency in retaining solid particles of sizes less than 1/tm as well as certain types of bacteria. Media in the form of plates and cartridges are manufactured by sintering a mixture of diatomite with a binder. [Pg.136]

Okubo et al. [87] used AIBN and poly(acrylic acid) (Mw = 2 X 10 ) as the initiator and the stabilizer, respectively, for the dispersion polymerization of styrene conducted within the ethyl alcohol/water medium. The ethyl alcohol-water volumetric ratio (ml ml) was changed between (100 0) and (60 40). The uniform particles were obtained in the range of 100 0 and 70 30 while the polydisperse particles were produced with 35 65 and especially 60 40 ethyl alcohol-water ratios. The average particle size decreased form 3.8 to 1.9 /xm by the increasing water content of the dispersion medium. [Pg.207]

Uniform macroporous polymer particles have been prepared in the size range of 5-20 iitm by the multistage emulsion polymerization methods. Several methods are available in the literature describing the synthesis and the properties of macroporous uniform particles. The main steps of these methods may be summarized as follows. [Pg.220]

A typical scanning electron micrograph of the uniform macroporous polystyrene-divinylbenzene particles is given in Fig. 20. First studies on the synthesis of macroporous uniform particles were started by Ugelstad et al. [109]. They used a two-step activated swelling method to obtain macroporous uniform particles in the... [Pg.220]

The woven wire mesh type are formed to control the open space between the wires, thereby limiting the maximum size particle that can pass through. The cartridge is installed in cases or small vessels to facilitate quick replacement, or they can be arranged for backwash by use of proper piping connections. The wire wound units have consistent spaces for uniform particle size filtering. [Pg.279]

The effect on the process of a change in operation of the mixer system (impeller, baffles, etc.) is the final measurement of performance. Thus, operations such as blending, uniform particle suspension, reaction, gas absorption, etc., may be acceptable under one physical system and not so to the same degree under a slightly modified one. The ratio per unit volume on scale-up must be determined experimentally. [Pg.323]

Discussion. The turbidity of a dilute barium sulphate suspension is difficult to reproduce it is therefore essential to adhere rigidly to the experimental procedure detailed below. The velocity of the precipitation, as well as the concentration of the reactants, must be controlled by adding (after all the other components are present) pure solid barium chloride of definite grain size. The rate of solution of the barium chloride controls the velocity of the reaction. Sodium chloride and hydrochloric acid are added before the precipitation in order to inhibit the growth of microcrystals of barium sulphate the optimum pH is maintained and minimises the effect of variable amounts of other electrolytes present in the sample upon the size of the suspended barium sulphate particles. A glycerol-ethanol solution helps to stabilise the turbidity. The reaction vessel is shaken gently in order to obtain a uniform particle size each vessel should be shaken at the same rate and the same number of times. The unknown must be treated exactly like the standard solution. The interval between the time of precipitation and measurement must be kept constant. [Pg.729]

Considerable increases in the capacity density of the electrodes have been achieved through the use of high-density / -Ni(OH)2 with a uniform particle size, a narrow range of pore sizes, and a high tapping density (1.9-2.0gem"3) [15, 16]. [Pg.136]

Thru a combination of sedimentation and transmission measurements, a particle size distribution can be found. Tranquil settling of a dispersion of non-uniform particles will result in a separation of particles according to size so that transmission measurements at known distances below the surface at selected time intervals, will, with Stokes law, give the concn of particles of known diameter. Thus, a size frequency distribution can be obtained... [Pg.522]

Manufacture of highly water-absorbent polymers with uniform particle size and good flowability can be carried out by reverse phase suspension polymerization of (meth)acrylic acid monomers in a hydrocarbon solvent containing crosslinker and radical initiator. Phosphoric acid monoester or diester of alka-nole or ethoxylated alkanole is used as surfactant. A polymer with water-absorbent capacity of 78 g/g polymer can be obtained [240]. [Pg.605]

Han, S.C. and Han, M.H., Fracmre behavior of NR and SBR vulcanizates fibed with ground rubber having uniform particle size, J. Appl Polym. Sci., 85, 2491, 2002. [Pg.1064]

As an alternative approach towards the above requirement, Somorjai introduced the method of electron lithography [119] which represents an advanced HIGHTECH sample preparation technique. The method ensures uniform particle size and spacing e.g. Pt particles of 25 nm size could be placed with 50 nm separation. This array showed a uniform activity similar to those measured on single crystal in ethylene hydrogenation. The only difficulty with the method is that the particle size is so far not small enough. Comprehensive reviews have been lined up for the effect of dispersion and its role in heterogeneous catalysis [23,124,125]. [Pg.90]


See other pages where Uniform particles is mentioned: [Pg.707]    [Pg.27]    [Pg.33]    [Pg.11]    [Pg.10]    [Pg.17]    [Pg.45]    [Pg.501]    [Pg.311]    [Pg.389]    [Pg.1229]    [Pg.14]    [Pg.209]    [Pg.570]    [Pg.360]    [Pg.203]    [Pg.207]    [Pg.210]    [Pg.216]    [Pg.220]    [Pg.221]    [Pg.710]    [Pg.369]    [Pg.805]    [Pg.345]    [Pg.73]    [Pg.404]    [Pg.797]    [Pg.799]    [Pg.521]    [Pg.294]    [Pg.127]   


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