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Solid silica

The viscosity of liquid silicates such as drose containing barium oxide and silica show a rapid fall between pure silica and 20 mole per cent of metal oxide of nearly an order of magnitude at 2000 K, followed by a slower decrease as more metal oxide is added. The viscosity then decreases by a factor of two between 20 and 40 mole per cent. The activation energy for viscous flow decreases from 560 kJ in pure silica to 160-180kJmol as the network is broken up by metal oxide addition. The introduction of CaFa into a silicate melt reduces the viscosity markedly, typically by about a factor of drree. There is a rapid increase in the thermal expansivity coefficient as the network is dispersed, from practically zero in solid silica to around 40 cm moP in a typical soda-lime glass. [Pg.309]

The production of copper from sulphide minerals is accomplished with a preliminary partial roast of die sulphides before reaction widr air in the liquid state, known as mattes, to form copper metal (conversion). The principal sources of copper are minerals such as chalcopyrite, CuFeSa and bornite CuaFeSa, and hence the conversion process must accomplish the preferential oxidation of non, in the form of FeO, before the copper metal appears. As mentioned before, tire FeO-SiOa liquid system is practically Raoultian, and so it is relatively easy to calculate the amount of iron oxidation which can be canned out to form this liquid slag as a function of the FeO/SiOa ratio before copper oxidation occurs. The liquid slag has a maximum mole fraction of FeO at the matte blowing temperatures of about 0.3, at solid silica saturation. [Pg.339]

Thin layer chromatography (TLC) Solid (silica gel) Liquid (solvent, often a mixture). Also called developer. [Pg.138]

Taking an entirely different tack on supported phase transfer catalysts, Sawicki, Chapter 12, initially used polyethers chemically bound to silica. But, he also demonstrated that solid silica or alumina alone may function as liquid-solid phase transfer catalysts, probably through mechanisms entirely different than the classical PTC sequence. [Pg.4]

Hydrophobic silica defoamers work on a basis which may not be chemical at all. They are basically finely divided solid silica particles dispersed in a hydrocarbon or silicone oil which serves as a spreading vehicle. Kulkarni [Ind. Eng. Chem. Fundam., 16, 472 (1977)] theorizes that this mixture defoams by the penetration of the silica particle into the bubble and the rupture of the wall. Table 14-31 lists major types of defoamers and typical applications. [Pg.129]

Solid silica spheres are prepared by the Stober8 method. This involves the condensation of TEOS in alcoholic solution of water and ammonia. The mechanism of this synthesis was elucidated by Van Blaaderen et al.20,21 The particle growth is rate-limited by the production of hydrolysed monomer molecules. It involves a surface condensation of monomers and oligomers, while aggregation of particles is only occurring in the early stages of the condensation. [Pg.22]

Fig. 8.1. Photograph of catalyst pieces, courtesy Haldor Topsoe A/S www.haldortopsoe.com Rings, daisy (star) rings and pellets are shown. The daisy rings maximize catalyst area and minimize resistance to gas flow. In operation (700-900 K), the catalyst consists of a molten vanadium-alkali metal sulfate/pyrosulfate layer on a porous solid silica substrate. The outside diameter of the largest piece (far left) is 20 mm. Fig. 8.1. Photograph of catalyst pieces, courtesy Haldor Topsoe A/S www.haldortopsoe.com Rings, daisy (star) rings and pellets are shown. The daisy rings maximize catalyst area and minimize resistance to gas flow. In operation (700-900 K), the catalyst consists of a molten vanadium-alkali metal sulfate/pyrosulfate layer on a porous solid silica substrate. The outside diameter of the largest piece (far left) is 20 mm.
Active S02 oxidation catalyst consists of molten vanadium-alkali metal pyrosulfate layer on porous solid silica substrate. Catalytic S02+ /202- S03 oxidation takes place with dissolved V S 0 ionic complexes by reactions like ... [Pg.90]

Silicon-organic interactions, where silicon is present as solid silica and as a dissolved species in aqueous solution, are examined using classical electrostatic and solvation theory, crystal chemistry, thermodynamics, and ab initio molecular orbital calculations. Specifically, I address why various silica polymorphs and other oxides interact... [Pg.171]

Cyclohexane was used as solvent k Two different types of acid catalysts were tested SA was a solid Silica-Alumina, a Lewis acid-type of catalyst used in petroleum cracking TFA was trifluoroactic acid, a proton acid. [Pg.21]

Gas phase adsorption on solids (silica gels, activated charcoal, synthetic zeolites, molecular sieves) is also practised industrially. It is more suitable for the purihcation of effluents that display some complexity of composition. Its effectiveness depends on many parameters, particularly the volatility and polarity of the feedstock components. [Pg.21]

The supramolecular binding motifs described here were also used to attach catalysts to solid (silica) supports (128). The active metal complex could be switched from palladium to rhodium by using a polar solvent that breaks up the binding of the supramolecular motif. Allylic alkylation and hydroformylation catalysis could be carried out by using the same support "receptor" material and different "guest" ligands for the two metals a... [Pg.113]

To understand elastic mechanical properties, the discussion of the storage of energy of deformation provides a powerful approach. Dynamic mechanical measurements at higher strain on filled silicone elastomers show that the energy of deformation may be related to an entropic and an enthalpic part. The entropic part is mainly due to the restriction of the conformational space of the polymer chain by the presence of the solid silica particles. Whereas the enthalpic part of the energy of deformation is related to... [Pg.774]

FIGURE 18.5 LPC distribution during handling of a 30 wt% solids silica abrasive slurry in a VPDS for slurry delivery (BOC Edwards P2200). [Pg.575]

When CMP was first emerging as an important process, microporous membranes were tested in a tangential flow filtration (TFF) mode. In typical CMP slurries, TFF was found to be unacceptable due to the high solids content. Also, there was insufficient control of the retentate build-up on the membrane face, called concentration polarization. TFF works best with applications that have lower solids and a greater spread between retained and passed species. The excessive polarization we observed with high solids silica slurries prevented useful fractionation. TFF may be useful for the newer slurries with low solids content. Three critical questions to any filter design in slurry applications are (i) how sharp can the filtration curve be to enable clean fractionation, (ii) how is retained material handled to control filter life, and (iii) how does media selection affect the above two points. [Pg.590]


See other pages where Solid silica is mentioned: [Pg.182]    [Pg.309]    [Pg.3]    [Pg.82]    [Pg.517]    [Pg.369]    [Pg.479]    [Pg.481]    [Pg.145]    [Pg.524]    [Pg.478]    [Pg.624]    [Pg.170]    [Pg.832]    [Pg.32]    [Pg.158]    [Pg.271]    [Pg.407]    [Pg.1377]    [Pg.337]    [Pg.553]    [Pg.623]    [Pg.85]    [Pg.163]    [Pg.242]    [Pg.242]    [Pg.175]    [Pg.273]    [Pg.106]   


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Amorphous solids silica

Extraction, solid phase using silica-based adsorbent

Silica gels adsorbant, solid phase extraction

Silica gels as solid supports

Silica solid adsorbent

Silica solid phase profile

Silica solid support

Solid silica mean pore diameter

Solid silica-alumina

Solid-liquid interface silica

Solid-phase extraction silica based

Solid-phase extractions with fluorous silica gel

Solid-supported reagents silica

Standard Test Method for Linear Thermal Expansion of Solid Materials with a Vitreous Silica Dilatometer, (Withdrawn)

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