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Silanization calcium silicate

Oyane, A., Kawashita, M., Nakanishi, K, Kokubo,T., Minoda, M., Miyamoto, T. and Nakamura, T. (2003) Bonelike apatite formation on ethylene-vinyl alcohol copolymer modified with silane coupling agent and calcium silicate solutions. Biomaterials, 24, 1729-1735. [Pg.364]

The columns are usually made from glass which is silanized to remove polar silanol Si-OH groups from its surface that can contribute to the peak tailing of the peaks of polar analytes. These columns have internal diameters of 2-5 mm. The columns are packed with particles of a solid support which are coated with the liquid stationary phase. The most commonly used support is diatomaceous earth (mainly calcium silicate). This material is usually acid washed to remove mineral impurities and then silanized as shown in Figure 11.4 to remove the polar Si-OH groups on the surface of the support, which can lead to tailing of the analyte peak. [Pg.211]

FIGURE 14.1.21 Scanning electron micrograph of EVOH fibers constituting a fabric, which were treated with silane coupling agent and calcium silicate solution, and then soaked in SBF for 2 days. [Pg.405]

Calcium silicate microparticles increase the modulus more efficiently than the nanoparticles. In this case, a silane-treatment of the CaSiOj surface ensures good filler-matrix bonding and favors stress transfer via the interface. The flexural strength decreases slightly, but remains above that of the neat matrix. The fracture surfaces of these composites (EP/AljOj/CaSiOj) occur extensively rugged and... [Pg.50]

Talc is magnesium calcium silicate and may be in a rough spherical form, such as Nytal, or a platy configuration known as Mistron Vapor. The platy talc assists in calendering and extrusion operations and provides good reinforcement. Talc is inert, hence finds use in electrical resistant apphcations and where good water resistance is needed. Various particle size talcs are available and the platy talc may be untreated or contain a surface treatment, Mistron ZSC has zinc stearates, Mistron CB contains a mercapto silane for suUur cures, and Mistron PXL has a vinyl silane for peroxide cures. [Pg.66]

Initially, silanes were used in compounds based on EPM containing calcined clay and which were intended for electrically insulating applications. It was noticed that the insulating properties were improved and stabilised, especially in a moist environment mechanical properties were also improved. The same type of improvement was noted with hydrated alumina. The most suitable coupling agent, with peroxide crosslinking, is vinyl tri( 1-methoxy-ethoxy) silane with sulphur and accelerator crosslinking systems mercaptopropyl trimethoxy silane is recommended. Silanes have recently been made available as masterbatches and can be added directly to mineral fillers.The use of silanes has now extended to non-black compounds for applications other than cables when silicas and other types of filler (aluminium and calcium silicates) are used. [Pg.112]

Silica is reduced to silicon at 1300—1400°C by hydrogen, carbon, and a variety of metallic elements. Gaseous silicon monoxide is also formed. At pressures of >40 MPa (400 atm), in the presence of aluminum and aluminum halides, silica can be converted to silane in high yields by reaction with hydrogen (15). Silicon itself is not hydrogenated under these conditions. The formation of silicon by reduction of silica with carbon is important in the technical preparation of the element and its alloys and in the preparation of silicon carbide in the electric furnace. Reduction with lithium and sodium occurs at 200—250°C, with the formation of metal oxide and silicate. At 800—900°C, silica is reduced by calcium, magnesium, and aluminum. Other metals reported to reduce silica to the element include manganese, iron, niobium, uranium, lanthanum, cerium, and neodymium (16). [Pg.471]

It is well known that organosilicon compounds do not become equally well attached to all mineral substrates. While silicates always readily lend themselves to coating with silane and polysiloxane [19-21], the same cannot always be said of calcium carbonate [19, 20]. Calcium carbonate (calcite), a widely used filler, is generally considered difficult to cover with silanes. Given the proven, good attachment of silicone resin to calcium carbonate fillers in silicone resin emulsion paints [2, 22], the question arises as to whether only higher polymeric siloxanes are able to form hydrophobic protective coatings on calcium carbonate. [Pg.827]

The existence of a chemical reaction between filler and coupling agent depends not just on the nature of the coupling agent but also on the filler. Silanes react readily with glass beads, metal hydroxides, clay, silica, the silicates, wollastonite, mica and various oxides, but not with calcium carbonate, carbon black or barium sulphate. [Pg.48]

Non-black fillers may also be employed, but it is important to use neutral or medium high pH grades such as silane-treated calcined clay, synthetic sodium aluminum silicate, platy talc, neutral pH silicas, diatomaceous earth, hydrated aluminum silicate, calcium meta silicate, precipitated calcium carbonate, and so on. An indication of non-black filler requirements for one point of hardness increase is shown in Table 5.10. [Pg.171]


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Calcium silicate

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