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Silica specific surface area

Besides specific surface area, silicas are also characterised by their porosity. Most of the silica s are made out of dense spherical amorphous particles linked together in a three dimensional network, this crosslinked network building up the porosity of the silica. Where the reactivity of diborane towards the silica surface has been profoundly investigated, little attention has been paid to the effect of those reactions on the pore structure. However different methods are developed to define the porosity and physisorption measurements to characterise the porosity parameters are well established. Adsorption isotherms give the specific surface area using the BET model, while the analysis desorption hysteresis yields the pore size distribution. [Pg.347]

The TiVOx Catalyst. Industrial waste gases frequently contain nitrous oxide emissions (N0X). This pollutant can be removed by co-proportionation with ammonia in the presence of a suitable catalyst. Vanadia (vanadium oxide) is an active material to this end and titania (titanium oxide) is often used as a support because it also has a promoting effect. To improve this catalyst, and to make it cheaper, titania and vanadia were deposited on a high-specific-surface—area silica. The most successful version was obtained by co-impregnation of the active compounds. [Pg.193]

Silica sols are often called colloidal silicas, although other amorphous forms also exhibit colloidal properties owing to high surface areas. Sols are stable dispersions of amorphous siUca particles in a Hquid, almost always water. Commercial products contain siUca particles having diameters of about 3—100 nm, specific surface areas of 50—270 m /g, and siUca contents of 15—50 wt %. These contain small (<1 wt%) amounts of stabilizers, most commonly sodium ions. The discrete particles are prevented from aggregating by mutually repulsive negative charges. [Pg.477]

In which the ratio m/n is close to 3. The silane was produced by free radical copolymerization of vinyltriethoxysilane with N-vinylpyrrolidone. Its number-average molecular weight evaluated by vapour-phase osmometry was 3500. Porous silica microballs with a mean pore diameter of 225 A, a specific surface area (Ssp) of 130 m2/g and a pore volume of 0.8 cm3/g were modified by the silane dissolved in dry toluene. After washings and drying, 0.55% by weight of nitrogen and 4.65% of carbon remained on the microballs. Chromatographic tests carried out with a series of proteins have proved the size-exclusion mechanism of their separation. [Pg.148]

After it is washed, dried, and granulated, this silica gel has a very high specific surface area (about 700 m2-g 1) and is useful as a drying agent, a support for catalysts, a packing for chromatography columns, and a thermal insulator. [Pg.732]

Separation methods, multichromato-graphic la 56 Serine la 246,356 lb 132 Serotonin la 70,76,239,240,262,355, 380 lb 37-39,231,243,348 Serotonin metabolites lb 327 Serum lipids la 89 Serum proteins la 74 Sesquiterpene derivatives lb 239,446 Sesquiterpene esters lb 239 Sesquiterpene glucosides la 327 Sesquiterpene lactones lb 448 Sevin lb 387-389 Si 50 000, specific surface area la 91 Silica gel, caffeine-impregnated la 85 -, surface modified la 3 Silica gel 60, specific surface area la 91... [Pg.494]

The second case study. This involves all silica micro- and mesoporous SBA-15 materials. SBA-15 materials are prepared using triblock copolymers as structure-directing templates. Typically, calcined SBA-15 displays pore sizes between 50 and 90 A and specific surface areas of 600-700 m g with pore volumes of 0.8-1.2cm g h Application of the Fenton concept to mesoporous materials looks simpler since mass transfer would be much less limited. However, it is not straightforward because hydrolysis can take place in the aqueous phase. [Pg.135]

The second preparation route uses flame hydrolysis, a versatile way to produce all kinds of oxides with high specific surface areas. The advantages of fumed silica over xerogels are the better mechanical properties and higher purity of the former. [Pg.190]

Catalyst material Pt/Sn on alumina/silica filament Specific surface area lOSm m ... [Pg.290]

Retention on silica or alumina adsorbents is a function of the specific surface area, the degree of surface continination (particularly that of water), the prior thermal conditioning of... [Pg.105]

We have recently tested the Tx model described above by obtaining T, measurements in powder samples with known S/V. Samples used were constructed from fumed silica (CAB-O-SIL M-5 and TS-500, Cabot Corp.), and were either hydrophilic (M-5) or treated by the manufacturer to be hydrophobic (TS-500). Powder of each type was pressed into a polycarbonate cylinder, with a degree of compression controlling the pore space volume of each sample. These materials have a very high specific surface area (200 m2 g 1 for M-5, 212 m2 g-1 for TS-500), which is not expected to change significantly even at the maximum compaction pressure used. [Pg.310]

Table 2. Characteristics of the silica templates and the corresponding carbon materials a unit cell parameter Sbet- specific surface area Vp total pore volume (at P/Po=0.95) Pore size determined according to the BJH method - Maximum value of the BJH pore size distribution peak calculated from the adsorption branch of the N2 isotherm. Table 2. Characteristics of the silica templates and the corresponding carbon materials a unit cell parameter Sbet- specific surface area Vp total pore volume (at P/Po=0.95) Pore size determined according to the BJH method - Maximum value of the BJH pore size distribution peak calculated from the adsorption branch of the N2 isotherm.

See other pages where Silica specific surface area is mentioned: [Pg.240]    [Pg.74]    [Pg.180]    [Pg.206]    [Pg.240]    [Pg.74]    [Pg.180]    [Pg.206]    [Pg.577]    [Pg.594]    [Pg.630]    [Pg.633]    [Pg.634]    [Pg.158]    [Pg.733]    [Pg.189]    [Pg.212]    [Pg.417]    [Pg.105]    [Pg.164]    [Pg.165]    [Pg.199]    [Pg.624]    [Pg.677]    [Pg.678]    [Pg.685]    [Pg.853]    [Pg.854]    [Pg.428]    [Pg.228]    [Pg.200]    [Pg.204]    [Pg.298]    [Pg.446]    [Pg.460]    [Pg.31]   
See also in sourсe #XX -- [ Pg.91 ]




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