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Silica high surface area

Small amounts of inorganic fillers such as fumed silica, high surface area alumina, bentonites, glass spheres and ceramics are mixed with polyols such as propylene glycol to increase viscosity for printed electrodes. Proposed printed electrodes are carbon black, graphite, metallic or plated metaUic particles. [Pg.232]

The physical properties of cured polysiloxane materials are dramatically influenced by fillers (1,2). So-called non-reinforcing (extenders) and reinforcing fillers are typically used the most common reinforcing filler is silica. High surface area silica, called fumed silica, is formed by burning the product mixture obtained from the trichlorosilane (TCS) reaction of equation 8. Only a small amount of untreated... [Pg.16]

Adsorption may in principle occur at all surfaces its magnitude is particularly noticeable when porous solids, which have a high surface area, such as silica gel or charcoal are contacted with gases or liquids. Adsorption processes may involve either simple uni-molecular adsorbate layers or multilayers the forces which bind the adsorbate to the surface may be physical or chemical in nature. [Pg.16]

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]

Figure 14.14 Schematic diagram of the SFC olefins analyser system Cl, high-surface-area silica column C2, silver-loaded silica column VI and V2, six-poit valves FID, flame-ionisation detector UV, ulcaviolet monitor detector. Figure 14.14 Schematic diagram of the SFC olefins analyser system Cl, high-surface-area silica column C2, silver-loaded silica column VI and V2, six-poit valves FID, flame-ionisation detector UV, ulcaviolet monitor detector.
Figure 15 High-surface area silica treated with aqueous solution of 1 wt% vinyltrimethoxy silane. A silica was polymerized with styrene and washed with CS2 three times. Polystyrene produced in experiment A was deposited with B silica and the silica washed with CS2 three times. (From Ref. 77.)... Figure 15 High-surface area silica treated with aqueous solution of 1 wt% vinyltrimethoxy silane. A silica was polymerized with styrene and washed with CS2 three times. Polystyrene produced in experiment A was deposited with B silica and the silica washed with CS2 three times. (From Ref. 77.)...
Liquid-solid chromatography (LSC). This process, often termed adsorption chromatography, is based on interactions between the solute and fixed active sites on a finely divided solid adsorbent used as the stationary phase. The adsorbent, which may be packed in a column or spread on a plate, is generally a high surface area, active solid such as alumina, charcoal or silica gel, the last... [Pg.216]

Highly dispersible, high-surface area silica offers nearly 40% reduction of RR and approximately 30% reduction of heat buildup. [Pg.922]

Figure 4.1. Supported catalyst, consisting of small particles on a high surface area carrier such as silica or alumina, along with two simplified model systems, which in general offer much better opportunities for characterization at the molecular level. Figure 4.1. Supported catalyst, consisting of small particles on a high surface area carrier such as silica or alumina, along with two simplified model systems, which in general offer much better opportunities for characterization at the molecular level.
Pt particles remain highly dispersed in the reaction mixture during mesostructure formation. All measurements including XRD, SAXS, and TEM indicate a well-ordered silica structure. N2 physisorption measurement indicated high surface areas (523-661 m g ) and meso-sized pores (112-113 A) for the silica supports produced in the presence of different Pt particles. [Pg.157]

Zeolites have ordered micropores smaller than 2nm in diameter and are widely used as catalysts and supports in many practical reactions. Some zeolites have solid acidity and show shape-selectivity, which gives crucial effects in the processes of oil refining and petrochemistry. Metal nanoclusters and complexes can be synthesized in zeolites by the ship-in-a-bottle technique (Figure 1) [1,2], and the composite materials have also been applied to catalytic reactions. However, the decline of catalytic activity was often observed due to the diffusion-limitation of substrates or products in the micropores of zeolites. To overcome this drawback, newly developed mesoporous silicas such as FSM-16 [3,4], MCM-41 [5], and SBA-15 [6] have been used as catalyst supports, because they have large pores (2-10 nm) and high surface area (500-1000 m g ) [7,8]. The internal surface of the channels accounts for more than 90% of the surface area of mesoporous silicas. With the help of the new incredible materials, template synthesis of metal nanoclusters inside mesoporous channels is achieved and the nanoclusters give stupendous performances in various applications [9]. In this chapter, nanoclusters include nanoparticles and nanowires, and we focus on the synthesis and catalytic application of noble-metal nanoclusters in mesoporous silicas. [Pg.383]

PT catalysts are often difficult to separate from the product, while it is also desirable that the catalyst should be reusable or recyclable. Distillation and extraction are the most common separation processes. The main disadvantage of lipophilic quats is their tendency to remain in the organic phase and consequently contaminate the product. Therefore, extraction in water often is not satisfactory. Furthermore, products in the fine chemicals industry often have high boiling points and/or are heat sensitive, which makes separation of the catalyst by distillation impossible. Often the only means to remove the catalyst in these cases is to adsorb it using a high surface area sorbent such as silica, Florisil or active carbon (Sasson, 1997). After filtration, the catalyst can then be recovered by elution. [Pg.121]


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