Particles inert” fine

Separatory operations may isolate the more hazardous components from tlie diluent or inert. Screening of solids, in effect, separates tlie more hazardous dusts (small particles and fines) from the less liazardous larger pieces of material. Centrifuges, like all liigh-speed equipment, must be securely positioned to provide protection to all persomiel working in the vicinity. 

Currently, hydrogen and methanol are the main fuels used in PEMFCs. The electrochemical oxidation of hydrogen on a wide range of metal surfaces is very facile, but in the acidic environment in which the catalyst must work only Pt and Pd show reasonable activity and stability. Many factors influence the activity and stability of a Pt/C catalyst, of which the dispersion of Pt particles seems to be particularly important. In general, to achieve the maximum number of active sites, Pt particles are finely dispersed on an inert support. The relationship between Pt particle size and surface area can be calculated by the following simple relationship (assuming spherical particles) [3] ... 

Sodium Dispersions. Sodium is easily dispersed in inert hydrocarbons (qv), eg, white oil or kerosene, by agitation, or using a homogenizing device. Addition of oleic acid and other long-chain fatty acids, higher alcohols and esters, and some finely divided soHds, eg, carbon or bentonite, accelerate dispersion and produce finer (1—20 -lm) particles. Above 98°C the sodium is present as Hquid spheres. On cooling to lower temperatures, soHd spheres of sodium remain dispersed in the hydrocarbon and present an extended surface for reaction. Dispersions may contain as much as 50 wt % sodium. Sodium in this form is easily handled and reacts rapidly. For some purposes the presence of the inert hydrocarbon is a disadvantage. 

Another method that has great potential for the preparation of advanced prepregs and has been explored extensively requites fine powders. The reinforcing fibers are coated with fine particles of the resin and, when heated, the resin flows over the fiber. This method requites finely divided particles either in aqueous solution, in an inert volatile solvent, or as high dielectric material that can be charged and coated by electrostatic attraction to the fiber. Synthetic methods that make fine particles, similar to that described for PEEK (23), are needed. 

Filter aids should have low bulk density to minimize settling and aid good distribution on a filter-medium surface that may not be horizontal. They should also be porous and capable of forming a porous cake to minimize flow resistance, and they must be chemically inert to the filtrate. These characteristics are all found in the two most popular commercial filter aids diatomaceous silica (also called diatomite, or diatomaceous earth), which is an almost pure silica prepared from deposits of diatom skeletons and expanded perhte, particles of puffed lava that are principally aluminum alkali siheate. Cellulosic fibers (ground wood pulp) are sometimes used when siliceous materials cannot be used but are much more compressible. The use of other less effective aids (e.g., carbon and gypsum) may be justified in special cases. Sometimes a combination or carbon and diatomaceous silica permits adsorption in addition to filter-aid performance. Various other materials, such as salt, fine sand, starch, and precipitated calcium carbonate, are employed in specific industries where they represent either waste material or inexpensive alternatives to conventional filter aids. 

Perlite and Solka-floc are finely divided powders manufactured from a volcanic mineral and from wood pulp respectively, which have filtration properties very similar to those of diatomite. Like diatomite, they are inert to a wide range of process liquids. Like diatomite, they are available in a range of particle-size distributions to give the desired clarity and flowrate in different applications. On a cost-of-use basis, they are as economical as, or more economical than, diatomite. 

Certain three-dimensional electrodes, also known as slurry or fluidized-bed electrodes, are sometimes used as well in order to have a strongly enhanced working surface area. Electrodes of this type consist of fine particles of the electrode material (metal, oxide, carbon, or other) kept in suspension in the electrolyte solution by intense mixing or gas bubbling. A certain potential difference is applied to the system between an inert feeder elecnode and an auxiliary electrode that are immersed into the suspension. By charge transfer, the particles of electrode material constantly hitting the feeder electrode acquire its potential (fully or at least in part), so that a desired electrochemical reaction may occur at their surface. In this reaction, the particles lose their charge but reacquire it in subsequent encounters with the feeder electrode. 

Fixed-bed reactors are used for testing commercial catalysts of larger particle sizes and to collect data for scale-up (validation of mathematical models, studying the influence of transport processes on overall reactor performance, etc.). Catalyst particles with a size ranging from 1 to 10 mm are tested using reactors of 20 to 100 mm ID. The reactor diameter can be decreased if the catalyst is diluted by fine inert particles the ratio of the reactor diameter to the size of catalyst particles then can be decreased to 3 1 (instead of the 10 to 20 recommended for fixed-bed catalytic reactors). This leads to a lower consumption of reactants. Very important for proper operation of fixed-bed reactors, both in cocurrent and countercurrent mode, is a uniform distribution of both phases over the entire cross-section of the reactor. If this is not the case, reactor performance will be significantly falsified by flow maldistribution. 

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