Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Surface area excess

Even when size and size distribution per se impose no restrictions on the process, the filtration, washing, or centrifugation steps which usually follow crystallization may call for special crystal characteristics. Since fine crystals have a large specific surface area, excessive loss of product during washing may be encountered. Time and cost of filtration or centrifugation are highly dependent on crystal size distribution. [Pg.32]

Stearic acid and metal stearates are widely used as dispersants, especially in cases where high filler loadings are required. Examples are polyolefins filled with aluminium hydroxide or magnesium hydroxide where 60 weight percent of filler or more may be needed to achieve sufficient flame retardancy [129, 130]. Of course the correct level of addition depends upon the amount of filler surface to be covered, and therefore upon the amount of filler, and its specific surface area. Excess additive is to be avoided as it can seriously destabilise some polymers and give yellowing problems [127]. [Pg.389]

The surface excess per square centimeter F is just n/E, where n is the moles adsorbed per gram and E is the specific surface area. By means of the Gibbs equation (111-80), one can write the relationship... [Pg.350]

Catalyst particles are usually cylindrical in shape because it is convenient and economical to fonii tliem by extmsion—like spaghetti. Otlier shapes may be dictated by tlie need to minimize tlie resistance to transport of reactants and products in tlie pores tlius, tlie goal may be to have a high ratio of external (peripheral) surface area to particle volume and to minimize the average distance from tlie outside surface to tlie particle centre, witliout having particles tliat are so small tliat tlie pressure drop of reactants flowing tlirough tlie reactor will be excessive. [Pg.2702]

Thus, the porosity of an aerogel is ia excess of 90% and can be as high as 99.9%. As a consequence of such a high porosity, aerogels have large internal surface area and pore volume. [Pg.6]

When a battery produces current, the sites of current production are not uniformly distributed on the electrodes (45). The nonuniform current distribution lowers the expected performance from a battery system, and causes excessive heat evolution and low utilization of active materials. Two types of current distribution, primary and secondary, can be distinguished. The primary distribution is related to the current production based on the geometric surface area of the battery constmction. Secondary current distribution is related to current production sites inside the porous electrode itself. Most practical battery constmctions have nonuniform current distribution across the surface of the electrodes. This primary current distribution is governed by geometric factors such as height (or length) of the electrodes, the distance between the electrodes, the resistance of the anode and cathode stmctures by the resistance of the electrolyte and by the polarization resistance or hinderance of the electrode reaction processes. [Pg.514]

Catalyst lifetimes are long in the absence of misoperation and are limited primarily by losses to fines, which are removed by periodic sieving. Excessive operating temperatures can cause degradation of the support and loss of surface area. Accumulation of refractory dusts and chemical poisons, such as compounds of lead and mercury, can result in catalyst deactivation. Usually, much of such contaminants are removed during sieving. The vanadium in these catalysts may be extracted and recycled when economic conditions permit. [Pg.203]

External Dilute-Phase Upflow Cooler. The external ddute-phase upflow design (68) offers some control in the range of heat removal duties but generates relatively low heat-transfer coefficients [60—170 W/(m K)]- This design substantially increases the surface area requirement and thereby reduces the ultimate duty that can be achieved from a single bundle. In addition, poor mechanical rehabdity has been continuously experienced because of excessive erosion at the lower tube sheets as a result of the high catalyst fluxes and gas velocities imposed. [Pg.219]

Rotary atomisation produces an excellent surface finish. The spray has low velocity, which allows the electrostatic forces attracting the paint particles to the ground workpiece to dominate, and results in transfer efficiencies of 85—99%. The pattern is very large and partially controlled and dkected by shaping ak jets. The spray when using a metallic cup has relatively poor penetration into recessed areas. Excessive material deposited on the edges of the workpiece can also be a problem. [Pg.331]

Resistance Heating of Contacts. The contact material, contact area, and heat dissipating abihty, as well as the heat dissipating abihty of the stmcture to which the material is attached, limit the amount of current that a contact can transport. Excessive current heats and softens the metal contact. This softening results in an increase in the surface area of the contact and a corresponding reduction in contact resistance. [Pg.30]

Automobile exhaust catalysts have been developed that maximize the catalyst surface area available to the flowing exhaust gas without incurring excessive pressure drop. Two types have been extensively studied the monolithic honeycomb type and the pellet type. [Pg.484]

Dry filters are usually deeper than viscous filters. The dry filter media use finer fibers and have much smaller pores than the viscous media and need not rely on an oil coating to retain collected dust. Because of their greater resistance to air flow, dry filters must use lower filtration velocities to avoid excessive pressure drops. Hence, dry media must have larger surface areas and are usually pleated or arranged in the form of pockets (Fig. 17-64), generally sheets of cellulose pulp, cotton, felt, or spun glass. [Pg.1608]

Another important parameter is the temperature difference between the evaporator outlet temperature on the steam side and on the exhaust gas side. This difference is known as the pinch point. Ideally, the lower the pinch point, the more heat recovered, but this calls for more surface area and, consequently, increases the back pressure and cost. Also, excessively low... [Pg.91]

If the system is still leaking excessively, the total surface area shall be tested. [Pg.790]

There are two possible causes. The first could be incorrect control of water treatment and blowdown. This can result in excessive levels of suspended solids in the boiler water, organic matter in the boiler water or high alkalinity. The second can be mechanical. If the boiler is operated below its designed working pressure it will increase the efflux velocity of the steam leaving the water surface area to a point where it may lift the water surface and drop the water level. It is important therefore to give due consideration to the steam load required from the boiler. [Pg.345]

Based on available results, it can be summarized that the particle size of tantalum powder increases (specific charge decreases) with the increase in temperature, K2TaF7 concentration and excess sodium. In addition, an increase in the specific surface area of the melt and Na/K ratio also leads to the formation of coarser tantalum powder. The most important conclusion is that for the production of finer tantalum powders with higher specific charges, the concentration of K2TaF7 in the melt must be relatively low. This effect is the opposite of that observed in the electrochemical reduction of melts. [Pg.336]

Thorium oxide on activated carbon was prepared by absorption of thorium nitrate from its solution in anhydrous acetone on the activated carbon Supersorbon. The excess solution was decanted, the catalyst was dried at 80 °C, and the adsorbed thorium oxide was decomposed by excess 5% ammonium hydroxide solution. After repeated washing and decanta-nation with distilled water and acetone, the catalyst was dried at 180°C. It was then stabilized by heating to 360°C for 5 hr in a stream of nitrogen. The content of thorium oxide was 2.9% (wt.). The BET surface area was 870 m2/g. Prior to kinetic measurements, the catalyst was modified by passing over acetic acid vapors (100 g acid/1 g catalyst). [Pg.27]


See other pages where Surface area excess is mentioned: [Pg.63]    [Pg.63]    [Pg.11]    [Pg.78]    [Pg.61]    [Pg.88]    [Pg.47]    [Pg.127]    [Pg.484]    [Pg.105]    [Pg.262]    [Pg.257]    [Pg.58]    [Pg.311]    [Pg.223]    [Pg.226]    [Pg.193]    [Pg.320]    [Pg.1686]    [Pg.98]    [Pg.1085]    [Pg.339]    [Pg.200]    [Pg.451]    [Pg.3]    [Pg.175]    [Pg.594]    [Pg.277]    [Pg.124]    [Pg.186]    [Pg.571]    [Pg.1170]    [Pg.541]    [Pg.277]   
See also in sourсe #XX -- [ Pg.341 ]




SEARCH



Surface excess

© 2024 chempedia.info