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Silica charging

Here the transfer-moulding process where by the epoxy-silica charge is transferred to the mould to encapsulate the integrated circuit is shown. Note that in this case the fragile integrated-circuit pattern is placed inside the heated mould (typically at about 170-180 °C)... [Pg.398]

The aluminium is highly susceptible to atmospheric oxidation, which would dull its reflective surface. To prevent this, a thin layer of silica is deposited on top, following the aluminizing. This is done by placing a silica charge in a molybdenum boat, also on the axial members of the carriage,... [Pg.207]

Relaxations in the double layers between two interacting particles can retard aggregation rates and cause them to be independent of particle size [101-103]. Discrepancies between theoretical predictions and experimental observations of heterocoagulation between polymer latices, silica particles, and ceria particles [104] have promptetl Mati-jevic and co-workers to propose that the charge on these particles may not be uniformly distributed over the surface [105, 106]. Similar behavior has been seen in the heterocoagulation of cationic and anionic polymer latices [107]. [Pg.192]

Assume is -25 mV for a certain silica surface in contact with O.OOlAf aqueous NaCl at 25°C. Calculate, assuming simple Gouy-Chapman theory (a) at 200 A from the surface, (b) the concentrations of Na and of Cr ions 10 A from the surface, and (c) the surface charge density in electronic charges per unit area. [Pg.215]

Ong S W, Zhao X L and Eisenthal K B 1992 Polarization of water-molecules at a charged interface second harmonic studies of the silica water interface Chem. Phys. Lett. 191 327-35... [Pg.1305]

Figure C2.12.2. Fonnation of Br0nsted acid sites in zeolites. Aqueous exchange of cation M witli an ammonium salt yields tlie ammonium fonn of tlie zeolite. Upon tliennal decomposition ammonia is released and tire proton remains as charge-balancing species. Direct ion-exchange of M witli acidic solutions is feasible for high-silica zeolites. Figure C2.12.2. Fonnation of Br0nsted acid sites in zeolites. Aqueous exchange of cation M witli an ammonium salt yields tlie ammonium fonn of tlie zeolite. Upon tliennal decomposition ammonia is released and tire proton remains as charge-balancing species. Direct ion-exchange of M witli acidic solutions is feasible for high-silica zeolites.
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]

We showed that these mesoporous silica materials, with variable pore sizes and susceptible surface areas for functionalization, can be utilized as good separation devices and immobilization for biomolecules, where the ones are sequestered and released depending on their size and charge, within the channels. Mesoporous silica with large-pore-size stmctures, are best suited for this purpose, since more molecules can be immobilized and the large porosity of the materials provide better access for the substrates to the immobilized molecules. The mechanism of bimolecular adsorption in the mesopore channels was suggested to be ionic interaction. On the first stage on the way of creation of chemical sensors on the basis of functionalized mesoporous silica materials for selective determination of herbicide in an environment was conducted research of sorption activity number of such materials in relation to 2,4-D. [Pg.311]

Coagulation involves the addition of chemicals to alter the physical state of dissolved and suspended solids. This facilitates their removal by sedimentation and filtration. The most common primary coagulants are alum ferric sulfate and ferric chloride. Additional chemicals that may be added to enhance coagulation include activate silica, a complex silicate made from sodium silicate, and charged organic molecules called polyelectrolytes, which include large-molecular-weight polyacrylamides, dimethyl-diallylammonium chloride, polyamines, and starch. [Pg.248]

The use of bonded, silica column supports has also become a useful way to characterize cationic, water-soluble polymers. CATSEC SEC columns from Micra Scientific contain a silica support with a polymerized polyamine-bonded phase. This imparts a cationic surface charge on the packing that can be... [Pg.573]

The mechanism by which analytes are transported in a non-discriminate manner (i.e. via bulk flow) in an electrophoresis capillary is termed electroosmosis. Eigure 9.1 depicts the inside of a fused silica capillary and illustrates the source that supports electroosmotic flow. Adjacent to the negatively charged capillary wall are specifically adsorbed counterions, which make up the fairly immobile Stern layer. The excess ions just outside the Stern layer form the diffuse layer, which is mobile under the influence of an electric field. The substantial frictional forces between molecules in solution allow for the movement of the diffuse layer to pull the bulk... [Pg.198]

Cs NMR results for Cs on the surfaces of illite, kaolinite, boehmite and silica gel (Figure 3) show that for this large, low charge cation the surface behavior is quite similar to the interlayer behavior. They also illustrate the capabilities of NMR methods to probe surface species and the effects of RH on the structural environments and dynamical behavior of the Cs. The samples were prepared by immersing 0.5 gm of powdered solid in 50 ml of O.IM CsCl solution at 2 5°C for 5 days. Final pHs were between 4.60 and 7.77, greater than the zero point of charge, except for boehmite, which has a ZPC... [Pg.161]

A chemical compound of lime and silica with fiber reinforcement for added strength. It is cast as a wet slurry into molds and charged into autoclaves, finally being machined to accurate size. [Pg.121]

Zeolites are crystalline alumina-silicates having a regular pore structure. Their basic building blocks are silica and alumina tetrahedra. Each tetrahedron consists of silicon or aluminum atoms at the center of the tetrahedron with oxygen atoms at the comers. Because silicon and aluminum are in a +4 and +3 oxidation state, respectively, a net charge of -1 must be balanced by a cation to maintain electrical neutrality. [Pg.130]

Some manufacturers use the principle of the adsorption of a gas by a porous material such as silica gel or charcoal. Since the adsorbent is a solid and cannot migrate from the phial, these valves cannot suffer reversal of charge. [Pg.100]


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See also in sourсe #XX -- [ Pg.6 ]




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Charge silica capillary wall

Charge-stabilized silica spheres

Negative charged silica

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