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Solids, specific surface area

The morphologic characterization of the immobilized enzyme is important to correlate the biocatalyst performance with porous structure parameters. BET analysis, which is usually based on N2 isothermal adsorption at 77 K, allows determining the solid-specific surface area, total pore volume, pore size distribution, and mean pore diameter. It is not recommended for solids with a low specific surface area (<5 m g ). Table 2 shows the specific smface area, mean pore diameter, and total pore volume determined by BET for the pure sol-gel silica matrix having TEOS as the precursor and the same matrix with the encapsulated CGTase. [Pg.321]

Here, Sy is the solid specific surface area (per unit solid volume). [Pg.299]

Pore volume (cm /g) and the total volume of the pores in the solid Specific surface area (m /g)... [Pg.361]

Dye adsorption from solution may be used to estimate the surface area of a powdered solid. Suppose that if 3.0 g of a bone charcoal is equilibrated with 100 ml of initially 10 Af methylene blue, the final dye concentration is 0.3 x 10 Af, while if 6.0 g of bone charcoal had been used, the final concentration would have been 0.1 x Qr M. Assuming that the dye adsorption obeys the Langmuir equation, calculate the specific surface area of the bone charcoal in square meters per gram. Assume that the molecular area of methylene blue is 197 A. ... [Pg.420]

While a thermodynamic treatment can be developed entirely in terms of f(P,T), to apply adsorption models, it is highly desirable to know on a per square centimeter basis rather than a per gram basis or, alternatively, to know B, the fraction of surface covered. In both the physical chemistry and the applied chemistry of the solid-gas interface, the specific surface area is thus of extreme importance. [Pg.571]

The specific surface area of a solid is one of the first things that must be determined if any detailed physical chemical interpretation of its behavior as an adsorbent is to be possible. Such a determination can be made through adsorption studies themselves, and this aspect is taken up in the next chapter there are a number of other methods, however, that are summarized in the following material. Space does not permit a full discussion, and, in particular, the methods that really amount to a particle or pore size determination, such as optical and electron microscopy, x-ray or neutron diffraction, and permeability studies are largely omitted. [Pg.572]

A variety of experimental data has been found to fit the Langmuir equation reasonably well. Data are generally plotted according to the linear form, Eq. XVn-9, to obtain the constants b and n from the best fitting straight line. The specific surface area, E, can then be obtained from Eq. XVII-10. A widely used practice is to take to be the molecular area of the adsorbate, estimated from liquid or solid adsorbate densities. On the other hand, the Langmuir model is cast around the concept of adsorption sites, whose spacing one would suppose to be characteristic of the adsorbent. See Section XVII-5B for an additional discussion of the problem. [Pg.615]

The surface area of a given mass of solid is inversely related to the size of the constituent particles. Thus, for the idealized case where these are equi-sized cubes of edge length /, the specific surface area A, being the surface area of I gram of solid, is given by (cf. p. 26)... [Pg.21]

An interesting example of a large specific surface which is wholly external in nature is provided by a dispersed aerosol composed of fine particles free of cracks and fissures. As soon as the aerosol settles out, of course, its particles come into contact with one another and form aggregates but if the particles are spherical, more particularly if the material is hard, the particle-to-particle contacts will be very small in area the interparticulate junctions will then be so weak that many of them will become broken apart during mechanical handling, or be prized open by the film of adsorbate during an adsorption experiment. In favourable cases the flocculated specimen may have so open a structure that it behaves, as far as its adsorptive properties are concerned, as a completely non-porous material. Solids of this kind are of importance because of their relevance to standard adsorption isotherms (cf. Section 2.12) which play a fundamental role in procedures for the evaluation of specific surface area and pore size distribution by adsorption methods. [Pg.24]

The physical adsorption of gases by non-porous solids, in the vast majority of cases, gives rise to a Type II isotherm. From the Type II isotherm of a given gas on a particular solid it is possible in principle to derive a value of the monolayer capacity of the solid, which in turn can be used to calculate the specific surface of the solid. The monolayer capacity is defined as the amount of adsorbate which can be accommodated in a completely filled, single molecular layer—a monolayer—on the surface of unit mass (1 g) of the solid. It is related to the specific surface area A, the surface area of 1 g of the solid, by the simple equation... [Pg.41]

The quantity of undrainable residual moisture caimot be predicted without the benefit of experimental data. Equation 17 (6) indicates the important parameters where the exponents were determined using limited experimentation. Introducing the approximation that is proportional to 1/d, where s is the specific surface area per weight of solid, the modified equation for undrainable liquid becomes... [Pg.400]

Characterization. When siHca gel is used as an adsorbent, the pore stmcture determines the gel adsorption capacity. Pores are characterized by specific surface area, specific pore volume (total volume of pores per gram of solid), average pore diameter, pore size distribution, and the degree to which entrance to larger pores is restricted by smaller pores. These parameters are derived from measuring vapor adsorption isotherms, mercury intmsion, low angle x-ray scattering, electron microscopy, gas permeabiHty, ion or molecule exclusion, or the volume of imbibed Hquid (1). [Pg.491]

The structure of the cake formed and, consequently, its resistance to liquid flow depends on the properties of the solid particles and the liquid phase suspension, as well as on the conditions of filtration. Cake structure is first established by hydrodynamic factors (cake porosity, mean particle size, size distribution, and particle specific surface area and sphericity). It is also strongly influenced by some factors that can conditionally be denoted as physicochemical. These factors are ... [Pg.76]

The significance of this novel attempt lies in the inclusion of both the additional particle co-ordinate and in a mechanism of particle disruption by primary particle attrition in the population balance. This formulation permits prediction of secondary particle characteristics, e.g. specific surface area expressed as surface area per unit volume or mass of crystal solid (i.e. m /m or m /kg). It can also account for the formation of bimodal particle size distributions, as are observed in many precipitation processes, for which special forms of size-dependent aggregation kernels have been proposed previously. [Pg.245]

Secondary minerals. As weathering of primary minerals proceeds, ions are released into solution, and new minerals are formed. These new minerals, called secondary minerals, include layer silicate clay minerals, carbonates, phosphates, sulfates and sulfides, different hydroxides and oxyhydroxides of Al, Fe, Mn, Ti, and Si, and non-crystalline minerals such as allophane and imogolite. Secondary minerals, such as the clay minerals, may have a specific surface area in the range of 20-800 m /g and up to 1000 m /g in the case of imogolite (Wada, 1985). Surface area is very important because most chemical reactions in soil are surface reactions occurring at the interface of solids and the soil solution. Layer-silicate clays, oxides, and carbonates are the most widespread secondary minerals. [Pg.166]

Main physico-chemical characteristics of the solids weight percents of metals and additives, specific surface area, metallic dispersion. [Pg.346]

Magnesium oxide is always blended with the zinc oxide prior to ignition. Magnesium oxide promotes densification of the zinc oxide, preserves its whiteness and renders the sintered powder easier to pulverize (Crowell, 1929). The sintered mixed oxide has been shown to contain zinc oxide and a solid solution of zinc oxide in magnesium oxide (Zhuravlev, Volfson Sheveleva, 1950). Specific surface area is reduced compared with that of pure zinc oxide and cements prepared from the mixed oxides are stronger (Crowell, 1929 Zhuravlev, Volfson Sheveleva, 1950). [Pg.206]

Nonmetal electrodes are most often fabricated by pressing or rolling of the solid in the form of fine powder. For mechanical integrity of the electrodes, binders are added to the active mass. For higher electronic conductivity of the electrode and a better current distribution, conducting fillers are added (carbon black, graphite, metal powders). Electrodes of this type are porous and have a relatively high specific surface area. The porosity facilitates access of dissolved reactants (H+ or OH ions and others) to the inner electrode layers. [Pg.441]

A commonly used method of determining the specific surface area of a solid is by the adsorption of a gas onto the solid and the determination of the monolayer capacity. Most methods make use of the Brunauer, Emmett, and Teller equation, commonly referred to as the BET equation, for calculating the surface area on the basis of monolayer adsorption. The BET equation can be written as... [Pg.129]

C. H. Giles, T. H. MacEwan, S. N. Natchwa and D. Smith, Studies in Adsorption, Part XI A System of Classification of Solution Adsorption Isotherms and its Use in Diagnosis of Adsorption Mechanism and its Measurement of Specific Surface Area of Solids, J. Chem. Soc., p. 3973,1960. [Pg.222]

The solid matrix has a high specific surface area. [Pg.833]


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See also in sourсe #XX -- [ Pg.611 ]




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