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Particles, preparation

Abrasive particle properties can be attributed to the method or process used to generate the particles. The surface properties can be altered or modified by varying the physical conditions (temperature, pressure, time) or chemical composition of the initial reactants. This section will survey the various preparation techniques for silica, alumina, and diamond. [Pg.230]

Alumina is traditionally formed via thermal dehydration of aluminum hydroxides [94,95]. The final size and crystallinity of the alumina abrasives largely depend on the temperature and time of the thermal treatment process. It has been reported that the total reaction conversion occurs at a temperature of 1500 K. Technical grades of calcined alumina are commonly used for smelting, ceramics, and abrasive particles. Other common forms of alumina produced are fused and white tabular alumina. Fused alumina is produced by melting calcined alumina at a high-temperature furnace for extended time periods. White tabular alumina is composed of large well-developed crystals of [Pg.230]

FIGURE 7.16 S5inthesis of fumed silica via vapor phase hydrolysis of silicon tetrachloride in an oxygen flame (from Ref. 83). [Pg.230]

Other than single crystalline and polycrystalline diamonds, cluster diamond (CD) [96] is another variety that contains a core and an overgrown region containing a plurality of diamond crystallites extending outward from the core. Some CD, which consists of ultrafine diamond particles with a mean particle size of 5 nm, shows excellent lubricating ability [97]. [Pg.231]


Brunauer and co-workers [129, 130] found values of of 1310, 1180, and 386 ergs/cm for CaO, Ca(OH)2 and tobermorite (a calcium silicate hydrate). Jura and Garland [131] reported a value of 1040 ergs/cm for magnesium oxide. Patterson and coworkers [132] used fractionated sodium chloride particles prepared by a volatilization method to find that the surface contribution to the low-temperature heat capacity varied approximately in proportion to the area determined by gas adsorption. Questions of equilibrium arise in these and adsorption studies on finely divided surfaces as discussed in Section X-3. [Pg.280]

V. BASIC FEATURES OF MONOSIZED POLYMERIC PARTICLES PREPARED BY ACTIVATED SWELLING AND POLYMERIZATION... [Pg.15]

The mitochondrial complex that carries out ATP synthesis is called ATP synthase or sometimes FjFo-ATPase (for the reverse reaction it catalyzes). ATP synthase was observed in early electron micrographs of submitochondrial particles (prepared by sonication of inner membrane preparations) as round, 8.5-nm-diameter projections or particles on the inner membrane (Figure 21.23). In micrographs of native mitochondria, the projections appear on the matrixfacing surface of the inner membrane. Mild agitation removes the particles from isolated membrane preparations, and the isolated spherical particles catalyze ATP hydrolysis, the reverse reaction of the ATP synthase. Stripped of these particles, the membranes can still carry out electron transfer but cannot synthesize ATP. In one of the first reconstitution experiments with membrane proteins, Efraim Racker showed that adding the particles back to stripped membranes restored electron transfer-dependent ATP synthesis. [Pg.694]

PS/PHEM A particles in micron-size range were also obtained by applying the single-stage soapless emulsion copolymerization method [124]. But, this method provided copolymer particles with an anomalous shape with an uneven surface. PS or PHEMA particles prepared by emulsifier-free emulsion polymerization were also used as seed particles with the respective comonomer to achieve uniform PS/PHEMA or PHEMA/PS composite particles. PS/PHEMA and PHEMA/PS particles in the form of excellent spheres were successfully produced 1 iLitm in size in the same study. [Pg.220]

The macroporous particles prepared by using only linear polystyrene as diluent yielded lower pore volume and specific surface area values. [Pg.221]

The interaction between particle and surface and the interaction among atoms in the particle are modeled by the Leimard-Jones potential [26]. The parameters of the Leimard-Jones potential are set as follows pp = 0.86 eV, o-pp =2.27 A, eps = 0.43 eV, o-ps=3.0 A. The Tersoff potential [27], a classical model capable of describing a wide range of silicon structure, is employed for the interaction between silicon atoms of the surface. The particle prepared by annealing simulation from 5,000 K to 50 K, is composed of 864 atoms with cohesive energy of 5.77 eV/atom and diameter of 24 A. The silicon surface consists of 45,760 silicon atoms. The crystal orientations of [ 100], [010], [001 ] are set asx,y,z coordinate axes, respectively. So there are 40 atom layers in the z direction with a thickness of 54.3 A. Before collision, the whole system undergoes a relaxation of 5,000 fsat300 K. [Pg.240]

Mono- and Multilayers of Spherical Polymer Particles Prepared by Langmuir-Blodgett and Self-Assembly Techniques... [Pg.213]

For the characterization of Langmuir films, Fulda and coworkers [75-77] used anionic and cationic core-shell particles prepared by emulsifier-free emulsion polymerization. These particles have several advantages over those used in early publications First, the particles do not contain any stabihzer or emulsifier, which is eventually desorbed upon spreading and disturbs the formation of a particle monolayer at the air-water interface. Second, the preparation is a one-step process leading directly to monodisperse particles 0.2-0.5 jim in diameter. Third, the nature of the shell can be easily varied by using different hydrophilic comonomers. In Table 1, the particles and their characteristic properties are hsted. Most of the studies were carried out using anionic particles with polystyrene as core material and polyacrylic acid in the shell. [Pg.218]

Fig. 1 shows the XRD patterns of the TiOa particles prepared using different concentration of nitric acid(a) and TENOHfb). These particles are only dried at 105°C without any calcination. [Pg.238]

The crystallite size of the particles prepared at different HNO3 and TENOH concentration can be determined by the Scheirers equation [5] and is listed in Table 1. The titania particles prepared using... [Pg.238]

In this work, flame spray pyrolysis was applied to the synthesis of titania particles to control the crystal structure and crystallite size and compared with the particle prepared by the conventional spray pyrolysis... [Pg.761]

Another distinguishing feature of titania prepared by flame spray pyrolysis is the draar e of anatase crystallite size with the increase of flame temperature. Generally, the increase of preparation temperature increases the crystallite size in other processes such as sol-gel method, hydrothermal method [2, 3], flame processing and conventional spray pyrolysis. The decrease of crystallite size was directly related to the decrease of particle size. Fig. 5 shows SEM and TEM images of titania particles prepared by flame spray pyrolysis. [Pg.763]

Fig. 5. SEM images of titania particles prepared by flame spray pyrol is with various flame ten jeratures (a) 900TC (b) llOOt (c) 1400r (d) 1600t (e) IQOOTC (f) TEM image of titania particles at 160013... Fig. 5. SEM images of titania particles prepared by flame spray pyrol is with various flame ten jeratures (a) 900TC (b) llOOt (c) 1400r (d) 1600t (e) IQOOTC (f) TEM image of titania particles at 160013...
Fig. 6. Comparison of initial rate with titama particles prepared by flame spray pyrolysis and spray pyrolysis. Fig. 6. Comparison of initial rate with titama particles prepared by flame spray pyrolysis and spray pyrolysis.
Before studying the reactivity of the nanoparticles, it is necessary to evaluate whether the synthetic method employed would lead to particles of clean unoxidized surface, able to react with incoming molecules. For this purpose we used, besides physical techniques (which are sometimes difficult to handle due to the high oxidability of particles prepared in this way), molecular methods, namely IR and NMR spectroscopy, as well as magnetic measurements which can give a precise description of the surface properties of the particles. [Pg.238]

This species has been used as precursor of nanogold particles by electrodeposition. When the electrodeposition is induced from the isotropic state at 117 °C, the nanoparticles obtained are nanodots aggregated in a spherical-like shape. In contrast, the morphology of the nano particles prepared from the SmA mesophase at 111 °C consist of leaf-like forms interlocked in rosettes. [Pg.388]

Sawadaishi, T. and Shimomura, M. (2005) Two-dimensional patterns of ultra-fine particles prepared by self-organization. Colloid. Surf. A, 257-258, 71-74. [Pg.200]

TEM imugv uf Pt particles prepared via polyol method (wilhoul sarfaclanl)... [Pg.31]

Bifunctional spacer molecules of different sizes have been used to construct nanoparticle networks formed via self-assembly of arrays of metal colloid particles prepared via reductive stabilization [88,309,310]. A combination of physical methods such as TEM, XAS, ASAXS, metastable impact electron spectroscopy (MIES), and ultraviolet photoelectron spectroscopy (UPS) has revealed that the particles are interlinked through rigid spacer molecules with proton-active functional groups to bind at the active aluminium-carbon sites in the metal-organic protecting shells [88]. [Pg.34]

Figure 20. A TEM snapshot of large polyhedral particles prepared by the inverse micelle system being broken by the ligand addition. The ligand featured here is decanethiol. (Reprinted with permission from Ref. [32], 2005, American Chemical Society.)... Figure 20. A TEM snapshot of large polyhedral particles prepared by the inverse micelle system being broken by the ligand addition. The ligand featured here is decanethiol. (Reprinted with permission from Ref. [32], 2005, American Chemical Society.)...
In the chemical preparation of unprotected metal colloids, the metal concentration usually has a significant influence on the particle size of obtained metal nanoclusters. For example, when increasing Pd concentration from 0.1 to 1.0 mM in the preparation of Pd metal colloids by the thermal decomposition of Pd acetate in methyl isobutyl ketone, the average Pd particle size increased from 8 to 140nm [6,7]. However, in the alkaline EG synthesis method, the size of metal nanoclusters was only slightly dependent on the metal concentration of the colloidal solution. The colloidal Pt particles prepared with a metal concentration of 3.7 g/1 had an average diameter of... [Pg.329]

Interestingly, it was found that gold particles were not produced with monodisperse amorphous Si02 particles prepared by the method of Stober et al. [26]. Flence, silica... [Pg.394]

Most striking is the increase in the fluorescence intensity of a CdS colloid as it undergoes photoanodic dissolution. As the colloidal particles become smaller they fluoresce with a greater quantum yield Very small CdS particles prepared by the methods described in section 5.1, fluoresce with a quantum yield of 3 %... [Pg.130]

Fig. 2.18 Vesicle structures with silica wall (A) mesostructured silica vesicle (B) hollow capsule composed of silica particles prepared by LbL assembly. Fig. 2.18 Vesicle structures with silica wall (A) mesostructured silica vesicle (B) hollow capsule composed of silica particles prepared by LbL assembly.

See other pages where Particles, preparation is mentioned: [Pg.142]    [Pg.166]    [Pg.105]    [Pg.221]    [Pg.473]    [Pg.70]    [Pg.74]    [Pg.93]    [Pg.215]    [Pg.237]    [Pg.439]    [Pg.490]    [Pg.512]    [Pg.237]    [Pg.239]    [Pg.240]    [Pg.240]    [Pg.761]    [Pg.763]    [Pg.165]    [Pg.240]    [Pg.243]    [Pg.40]    [Pg.90]    [Pg.329]    [Pg.702]   
See also in sourсe #XX -- [ Pg.91 ]

See also in sourсe #XX -- [ Pg.295 ]

See also in sourсe #XX -- [ Pg.373 ]




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