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Pore size factors affecting

The erosion of graphite in nozzle appHcations is a result of both chemical and mechanical factors. Changes in temperature, pressure, or fuel-oxidizing ratio markedly affect erosion rates. Graphite properties affecting its resistance to erosion include density, porosity, and pore size distribution... [Pg.513]

Inspection of Fig. 15.3 reveals that while for jo 0.1 nAcm , the effectiveness factor is expected to be close to 1, for a faster reaction with Jo 1 p,A cm , it will drop to about 0.2. This is the case of internal diffusion limitation, well known in heterogeneous catalysis, when the reagent concentration at the outer surface of the catalyst grains is equal to its volume concentration, but drops sharply inside the pores of the catalyst. In this context, it should be pointed out that when the pore size is decreased below about 50 nm, the predominant mechanism of mass transport is Knudsen diffusion [Malek and Coppens, 2003], with the diffusion coefficient being less than the Pick diffusion coefficient and dependent on the porosity and pore stmcture. Moreover, the discrete distribution of the catalytic particles in the CL may also affect the measured current owing to overlap of diffusion zones around closely positioned particles [Antoine et ah, 1998]. [Pg.523]

In the subsurface, kerosene volatilization is controlled by the physical and chemical properties of the solid phase and by the water content. Porosity is a major factor in defining the volatilization process. Galin et al. (1990) reported an experiment where neat kerosene at the saturation retention value was recovered from coarse, medium, and fine sands after 1, 5, and 14 days of incubation. The porosity of the sands decreased from coarse to fine. Figure 8.9 presents gas chromatographs obtained after kerosene volatilization. Note the loss of the more volatile hydrocarbons by evaporation in all sands 14 days after application and the lack of resemblance to the original kerosene. It is clear that the pore size of the sands affected the chemical composition of the remaining kerosene. For example, the fractions disap-... [Pg.160]

Experiments were designed to study the effects of porous media on spray combustion and resulting emissions. A number of factors could affect combustion performance with the presence of porous inserts, including the location, thickness, and pore size of the porous insert and operating conditions such as firing rate and fuel-air ratio. For different operating conditions, the baseline tests without porous inserts were completed. After the baseline tests, the same operating conditions were repeated with porous layers installed at various locations. More tests were then completed with different porous material properties. [Pg.457]

With the possible exception of pore size and distribution, these characteristics can affect both physical and chemical sorption mechanisms. In chemical sorption, the overriding factor is the surface groups on the sorbent. However, the sorbent substrate itself can affect the ability of the coated sorbent to collect a substance, especially if the desired reaction does not occur rapidly. [Pg.181]

A variety of factors affect the horizontal and vertical migration of PAHs, including contaminant volume and viscosity, temperature, land contour, plant cover, and soil composition (Morgan Watkinson, 1989)- Vertical movement occurs as a multiphase flow that will be controlled by soil chemistry and structure, pore size, and water content. For example, non-reactive small molecules (i.e., not PAHs) penetrate very rapidly through dry soils and migration is faster in clays than in loams due to the increased porosity of the clays. Once intercalated, however, sorbed PAHs are essentially immobilized. Mobility of oily hydrophobic substances can potentially be enhanced by the biosurfactant-production capability of bacteria (Zajic et al., 1974) but clear demonstrations of this effect are rare. This is discussed below in more detail (see Section 5 5). [Pg.132]

Factors that could potentially affect microbial retention include filter type, eg, structure, base polymer, surface modification chemistry, pore size distribution, and thickness fluid components, eg, formulation, surfactants, and additives sterilization conditions, eg, temperature, pressure, and time fluid properties, eg, pH, viscosity, osmolarity, and ionic strength and process conditions, eg, temperature, pressure differential, flow rate, and time. [Pg.140]

The use of membranes for separating particles of colloidal dimensions is termed dialysis. The most commonly used membranes are prepared from regenerated cellulose products such as collodion (a partially evaporated solution of cellulose nitrate in alcohol plus ether), Cellophane and Visking. Membranes with various, approximately known, pore sizes can be obtained commercially (usually in the form of sausage skins or thimbles ). However, particle size and pore size cannot be properly correlated, since the permeability of a membrane is also affected by factors such as electrical repulsion when. the membrane and particles are of like charge, and particle adsorption on the filter which can lead to a blocking of the pores. [Pg.18]

Based on Equation 10.3, chemical mobility differs from water mobility by a factor of 1 + (pb/x)Xd. This factor is also known as the retardation factor. The larger the retardation factor, the smaller is the velocity of the chemical species in relationship to the velocity of water. Note, however, that the retardation factor contains a reactivity factor (Kd) and two soil physical parameters, bulk density (pb) and porosity (t). The two parameters affect retardation by producing a wide range of total porosity in soils as well as various pore sizes. Pore size regulates the nature of solute flow. For example, in very small pores, solute movement is controlled by diffusion, while in large pores, solute flow is controlled by mass flow. [Pg.398]


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See also in sourсe #XX -- [ Pg.33 ]

See also in sourсe #XX -- [ Pg.604 ]




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