Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Agglomerates 257-9 titanate

Spherical, Fine-Particle Titanium Dioxide. Spherical, fine-particle titanium dioxide that has no agglomeration and of mono-dispersion can be manufactured by carrying out a gas-phase reaction between a tetraalkyl titanate vapor and methanol vapor in a carrier gas to form an initial fine particle, which can then be hydrolyzed with water or steam (572). [Pg.164]

Some elucidation of the mechanism of elastomer reinforcement is being obtained by precipitating chemically-generated fillers into network structures rather than blending badly agglomerated filler particles into elastomers prior to their cross-linking. This has been done for a variety of fillers, for example, silica by hydrolysis of organosilicates, titania from titanates, alumina from aluminates, etc. [85-87], A typical, and important, reaction is the acid- or base-catalyzed hydrolysis of tetraethylorthosilicate ... [Pg.370]

The overall yield is essentially 100 by any of the preparation methods, but the physical characteristics of the ion exchangers are dependent on preparation conditions. For example, sodium titanate prepared by Eqs. la and lb with hydrolysis in one liter of water per mole of Ti(OC3H7)4 has a bulk density of 0.U5 g/cm3 and a specific surface area of lO-UO m /g. The same material prepared by Eqs. la and lb and hydrolyzed in a solution of 100 ml of water in 1000 ml of acetone for each mole of Ti(OC2H7)4 has a bulk density of 0.35 g/cm3 and a specific surface area of 200-UOO m /g. In all cases, the materials consist of agglomerates of 50-100 A particles with the degree of aggregation of the particles determining both the bulk density and surface area. [Pg.131]

It is also possible to retain the hydrothermally produced barium titanate particles in aqueous suspension to form the basis of a tape-casting slurry capable of producing < 3 /mi dielectric layers. This route avoids the risk of the formation of hard agglomerates on drying the precipitates. [Pg.101]

The barium bis-isopropoxide was prepared by the metal/alcohol reaction method. Appropriate amounts of these alkoxides were dissolved in a mutual solvent, such as isopropyl alcohol or benzene, for a barium and titanium molar ratio of 1 1. The solution was refluxed for 2 h with vigorous stirring before the hydrolysis reaction. Drops of deionized triply distilled water were slowly added to the solution, which was continuously stirred. The reaction was carried out in a C02-free atmosphere. The hydrated oxide was dried in vacuum or in a dry helium atmosphere at 50°C for 12 h. At this stage the oxide was a finely divided, stoichiometric titanate with 50-150 A (maximum agglomerate size <1 pm) particles and was more than 99.98% pure. TEM photomicrographs of the as-prepared and the calcined (700°C for 1 h) powders are shown in Fig. 8. The rectilinear symmetry of the particles is evident in the calcined powders. [Pg.90]

The information about nanocrystalline ferroic powders fabricated by various chemical synthesis technologies is reported in Table 5.2. Their possible applications are also listed. Powders of the same ferroics for two different applications might be obtained by different techniques since the requirements of size distribution, morphology, agglomeration and impurity composition are determined by different technological conditions. For example, barium titanate is a dielectric with high dielectric constant and it is widely used in multilayer ceramic capacitors, whereas semiconducting properties of rare-earth doped BaTiOs are important for thermistors. [Pg.301]

The maximum specific surface of barium titanate corresponds to the heating rates interval 35-60 °C/h. (Table 5.10). Slower or faster heating also yields fine oxide powders, but with coarser particles or stronger agglomerates than those in so called optimal regime. An optimal mode of thermally activated synthesis uses the optimality criterion such as minimum particle size of the final product. [Pg.339]

Figure 12.7 Fracture origins, (a) In a silicon nitride bending test specimen (b) In a barium titanate (PTC ceramic) bending test specimen (c) In an alumina bending test specimen. The origins are an agglomeration of coarse. Figure 12.7 Fracture origins, (a) In a silicon nitride bending test specimen (b) In a barium titanate (PTC ceramic) bending test specimen (c) In an alumina bending test specimen. The origins are an agglomeration of coarse.

See other pages where Agglomerates 257-9 titanate is mentioned: [Pg.632]    [Pg.302]    [Pg.640]    [Pg.96]    [Pg.103]    [Pg.56]    [Pg.175]    [Pg.85]    [Pg.364]    [Pg.288]    [Pg.307]    [Pg.632]    [Pg.310]    [Pg.238]    [Pg.770]    [Pg.498]    [Pg.95]    [Pg.99]    [Pg.266]    [Pg.117]    [Pg.23]    [Pg.76]    [Pg.811]    [Pg.195]    [Pg.55]    [Pg.364]    [Pg.159]    [Pg.1315]    [Pg.691]    [Pg.117]    [Pg.615]    [Pg.278]    [Pg.18]    [Pg.265]    [Pg.157]    [Pg.220]    [Pg.291]    [Pg.125]    [Pg.3]   
See also in sourсe #XX -- [ Pg.42 ]




SEARCH



Agglomerate Agglomeration

Agglomeration

Agglomerator

Agglomerization

Titan

Titanate

Titanates

Titanation

Titane

© 2024 chempedia.info