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Carbon dispersed mixture

When the recycle soot in the feedstock is too viscous to be pumped at temperatures below 93°C, the water—carbon slurry is first contacted with naphtha carbon—naphtha agglomerates are removed from the water slurry and mixed with additional naphtha. The resultant carbon—naphtha mixture is combined with the hot gasification feedstock which may be as viscous as deasphalter pitch. The feedstock carbon—naphtha mixture is heated and flashed, and then fed to a naphtha stripper where naphtha is recovered for recycle to the carbon—water separation step. The carbon remains dispersed in the hot feedstock leaving the bottom of the naphtha stripper column and is recycled to the gasification reactor. [Pg.423]

The mechanism of this carbothermal reduction has been intensively investigated [170, 171] and a scheme of consecutive partial reactions has been proposed revealing that the reaction rate is controlled by diffusion and gas phase processes. Therefore, it can be concluded that the reaction rate may become the higher the finer the distribution of the solid educts is. That is, if we are able to start from a colloidal dispersed mixture of sUica and carbon, it is to be expected that the reaction temperature will drop as well as that finer SiC particles can be obtained. [Pg.103]

FIGURE 5.2.5 Universal self-similarity in coalescing liquid-liquid dispersions (neutrally buoyant benzene-carbon tetrachloride mixture with water). Data of Wright and Ramkrishna (1994). (Reproduced with permission of the American Institute of Chemical Engineers. Copyright 1994 AIChE. All rights reserved.)... [Pg.212]

Figure 7.16 Resistivity of ternary polymer/ polymer/carbon black mixture as function of carbon black (CB) content and morphology. The percolation threshold is the highest for uniformly dispersed CB particles (open triangles), lower for the case of particles... Figure 7.16 Resistivity of ternary polymer/ polymer/carbon black mixture as function of carbon black (CB) content and morphology. The percolation threshold is the highest for uniformly dispersed CB particles (open triangles), lower for the case of particles...
In the depolymeri2ed scrap mbber (DSR) experimental process, ground scrap mbber tines produce a carbon black dispersion in ok (35). Initially, aromatic oks are blended with the tine cmmb, and the mixture is heated at 250—275°C in an autoclave for 12—24 h. The ok acts as a heat-transfer medium and swelling agent, and the heat and ok cause the mbber to depolymeri2e. As more DSR is produced and mbber is added, less aromatic ok is needed, and eventually virtually 100% of the ok is replaced by DSR. The DSR reduces thermal oxidation of polymers and increases the tack of uncured mbber (36,37). Depolymeri2ed scrap mbber has a heat value of 40 MJ/kg (17,200 Btu/lb) and is blended with No. 2 fuel ok as fuel extender (38). [Pg.15]

Pre-liming. Lime slurry, 0.25% lime on juice (0.250 g of CaO/100 g juice), is added to bring the pH of the mixture into the alkaline range. Insoluble calcium salts are precipitated as finely dispersed coUoids. Calcium carbonate in the form of recycled first carbonation sludge is added to provide coUoid absorption and stabilization. Temperature may be cool (50°C) or hot (80°C) depending on the temperature of the next step, or occasionally on the type of diffusion equipment. Retention time is 15 to 30 min. [Pg.26]

Gal-Or and Hoelscher (G5) have recently developed a fast and simple transient-response method for the measurement of concentration and volumetric mass-transfer coefficients in gas-liquid dispersions. The method involves the use of a transient response to a step change in the composition of the feed gas. The resulting change in the composition of the liquid phase of the dispersion is measured by means of a Clark electrode, which permits the rapid and accurate analysis of oxygen or carbon dioxide concentrations in a gas, in blood, or in any liquid mixture. [Pg.303]

The most popular bonded phases are, without doubt, the reverse phases which consist solely of aliphatic hydrocarbon chains bonded to the silica. Reverse phases interact dispersively with solvent and solute molecules and, as a consequence, are employed with very polar solvents or aqueous solvent mixtures such as methanol/water and acetonitrile/water mixtures. The most commonly used reverse phase appears to be the brush type phase with aliphatic chains having four, eight or eighteen carbon atom chains attached. These types of reverse phase have been termed C4, C8 and Cl8 phases respectively. The C8... [Pg.76]


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