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Silicones conversion

The reactivity and product selectivity increase as dispersing agents were introduced. Simultaneously, a higher silicon conversion was also obtained. A higher silicon conversion will decrease the burden of waste disposal. Therefore, this study provides a convenient and economical way for the preparation of highly effective CuCl catalyst that can be used in practical production using the direct process. [Pg.328]

Highly active CuCl catalysts for the direct process of methylchlorosilane synthesis were prepared by reducing Cu with a sodium sulfite solution in the presence of dispersing agents. Several well-known dispersants, e.g. SDBS, were used in this study. When SDBS was used, a catalyst in the form of small flakes was obtained that gave the best performance in reactivity, product selectivity and silicon conversion. This provides a convenient way to prepare the CuCl catalyst for use in industrial production. [Pg.328]

Silicon conversion table. For conversion of substrate doping density to resistivity, and vice versa, and to determine carrier mobility, position a ruler vertically over the chart. For a certain doping density (ordinate) and applied bias (solid lines) the depletion region width (left abscissa) and capacitance (right abscissa) are given. The distance between two dopant atoms is shown (broken line, left abscissa) idealizing the positions of the dopants to be in an fee lattice. [Pg.273]

Under these reaction conditions, w-propyl chloride hardly decomposed to form propylene and hydrogen chloride with the amount of propylene being formed at a rate below 0.2 mmol/h. This probably accounts for the low silicon conversion, because hydrogen chloride is necessary for the formation of propyldichlorosilane. [Pg.152]

The rate of formation of ethyldichlorosilane was almost the same as those for dichlorovinylsilane and trichlorosilane. While the silicon conversion was 13% for 5 h, the overall selectivities for dichlorovinylsilane, dichloroethylsilane, and trichlorosilane were 39, 23, and 38%,... [Pg.174]

It is recognized that transmission IR only presents an integrated picture of the silicon conversion throughout the whole thickness of the resist. However, the bulk of the oxidation occurs at the surface, and the equivalent oxide thickness obtained from the calibration curve for thermally grown oxide films can be taken to represent the approximate thickness of the plasma-treated films. The thickness of the oxide film formed by the various pretreatments is summarized in Table II. [Pg.343]

Consider the combustion reaction between a solid reactant and a gas oxidizer present initially in the constant volume of a porous medium (see Section IV,D,1). In this case, thermodynamic calculations for the silicon-nitrogen system have been made for constant volumes (Skibska et al, 1993b). The calculations yield the adiabatic combustion temperature, as well as pressures and concentration, as functions of the silicon conversion. As shown in Fig. 34a, the reactant gas pressure (curve 3) increases even though conversion increases. This occurs because... [Pg.156]

The reaction shown is important in the industrial preparation of dichlorodimethylsilane for eventual conversion to silicone polymers... [Pg.102]

The equilibrium is more favorable to acetone at higher temperatures. At 325°C 97% conversion is theoretically possible. The kinetics of the reaction has been studied (23). A large number of catalysts have been investigated, including copper, silver, platinum, and palladium metals, as well as sulfides of transition metals of groups 4, 5, and 6 of the periodic table. These catalysts are made with inert supports and are used at 400—600°C (24). Lower temperature reactions (315—482°C) have been successhiUy conducted using 2inc oxide-zirconium oxide combinations (25), and combinations of copper-chromium oxide and of copper and silicon dioxide (26). [Pg.96]

Manufacture of P-Silicon Carbide. A commercially utilized appHcation of polysdanes is the conversion of some homopolymers and copolymers to siHcon carbide (130). For example, polydimethyl silane is converted to the ceramic in a series of thermal processing steps. SiHcon carbide fibers is commercialized by the Nippon Carbon Co. under the trade name Nicalon (see Refractory fibers). [Pg.263]

This reaction is carried out in tall fluidized beds of high L/dt ratio. Pressures up to 200 kPa are used at temperatures around 300°C. The copper catalyst is deposited onto the surface of the silicon metal particles. The product is a vapor-phase material and the particulate silicon is gradually consumed. As the particle diameter decreases the minimum fluidization velocity decreases also. While the linear velocity decreases, the mass velocity of the fluid increases with conversion. Therefore, the leftover small particles with the copper catalyst and some debris leave the reactor at the top exit. [Pg.183]

Energy Spectrometry (EDS) uses the photoelectric absorption of the X ray in a semiconductor crystal (silicon or germanium), with proportional conversion of the X-ray energy into charge through inelastic scattering of the photoelectron. The quantity of charge is measured by a sophisticated electronic circuit linked with a computer-based multichannel analyzer to collect the data. The EDS instrument is... [Pg.179]

When formulating a silicone adhesive, sealant, or coating, based on hydrosilylation addition cure, one must consider the following properties of the uncured product pot life, dispensing technique, rheology, extrusion rate, cure performance. These characteristics directly affect the processing properties of the polymer base or crosslinker parts. The degree of cure conversion at the temperature of interest is determined by properties such as tack free time, cure profile and cure time. Once... [Pg.703]

Fig. 7.8. High temperature conversion of a-silicon nitride with an MgO additive to the p-pha.se is thought to be a consequence of dissolution of the a phase in a magnesium silicate with subsequent recrystallization from the melt. Enhanced dissolution rate should then strongly influence a. p conversion [84B01]. Fig. 7.8. High temperature conversion of a-silicon nitride with an MgO additive to the p-pha.se is thought to be a consequence of dissolution of the a phase in a magnesium silicate with subsequent recrystallization from the melt. Enhanced dissolution rate should then strongly influence a. p conversion [84B01].
Fig. 7.9. Measurements of the degree of conversion of ct p silicon nitride at a fixed time and various temperatures are thought to show the strong influence of shock modification on the high temperature dissolution [84B01]. Fig. 7.9. Measurements of the degree of conversion of ct p silicon nitride at a fixed time and various temperatures are thought to show the strong influence of shock modification on the high temperature dissolution [84B01].
Amorphous silicon modules experience a conversion efficiency loss of about 10 percent when initially exposed to sunlight, but then stabilize at the reduced figure. The mechanism for this reduction is being actively investigated, but is still not well understood. Individual modules made with other PV materials do not exliibit such loss of conversion efficiency, but combinations of modules in arrays do exhibit systematic reductions in power output over their lifetimes. Estimated at about 1 percent per year on average, based on data to date, these reductions are most likely associated with deteriorating electrical connections and non-module electrical components. [Pg.1059]

Conventional electronic devices are made on silicon wafers. The fabrication of a silicon MISFET starts with the diffusion (or implantation) of the source and drain, followed by the growing of the insulating layer, usually thermally grown silicon oxide, and ends with the deposition of the metal electrodes. In TFTs, the semiconductor is not a bulk material, but a thin film, so that the device presents an inverted architecture. It is built on an appropriate substrate and the deposition of the semiconductor constitutes the last step of the process. TFT structures can be divided into two families (Fig. 14-12). In coplanar devices, all layers are on the same side of the semiconductor. Conversely, in staggered structures gate and source-drain stand on opposing sides of the semiconductor layer. [Pg.257]

Entries on new materials, including re-cyclate plastics, fullerenes, hard-surfaced polymers, dendrimers, transflective materials, rapid prototyping materials, silicone nitride, supercritical fluids, bulk molding compounds, conversion coatings, folic acid, replacements for chloro-fluorocarbons ... [Pg.602]


See other pages where Silicones conversion is mentioned: [Pg.67]    [Pg.57]    [Pg.1590]    [Pg.1590]    [Pg.1591]    [Pg.173]    [Pg.174]    [Pg.211]    [Pg.1590]    [Pg.1590]    [Pg.1591]    [Pg.69]    [Pg.67]    [Pg.57]    [Pg.1590]    [Pg.1590]    [Pg.1591]    [Pg.173]    [Pg.174]    [Pg.211]    [Pg.1590]    [Pg.1590]    [Pg.1591]    [Pg.69]    [Pg.1794]    [Pg.469]    [Pg.471]    [Pg.471]    [Pg.471]    [Pg.23]    [Pg.49]    [Pg.304]    [Pg.103]    [Pg.680]    [Pg.705]    [Pg.641]    [Pg.196]    [Pg.506]    [Pg.26]   
See also in sourсe #XX -- [ Pg.637 , Pg.638 ]

See also in sourсe #XX -- [ Pg.637 , Pg.638 ]




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