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Pressurized coal carbonization system

C designates the non-reactive elemental carbon contained in the char product The chemical reaction is assumed to be the rate controlling step. This assumption is justified in the Discussion of Results. The reactions are considered to be first order with respect to fraction of carbon remaining in coal as well as converted to hydrocarbons and m 1 order with respect to H2 partial pressure. The details of the development of the model is reported elsewhere ( ). The experimental data correlated was obtained from dilute phase operation in an excess of hydrogen atmosphere, so the partial pressure of hydrogen was considered to be approximately equal to the total system pressure and was assumed constant along the length of the reactor. [Pg.203]

Pressure of Carbonization. The effect of a pressurized carbonization is to create a closed system preventing loss of volatile materials. Hence, carbon yields increase. Further, the material normally lost as volatiles in open systems is now retained and the effect of this, by reducing turbulence and bubble formation, is to enhance the size of resultant optical textures. Hiittinger and Rosenblatt (54) report such effects when gas pressures up to 15 MPa pressure (150 bar) were applied to the carbonization of a coal-tar pitch. If higher pressures are used, the pressure being applied hydraulically to the carbonization system, then the effect of pressures at, say, 300 MPa, is to enhance the viscosity of the total system and this prevents coalescence of the mesophase. The resultant appearance of the carbon has been described as botryoidal (55, 56) and an example is Figure 8. [Pg.22]

Figure 1, Flow diagram of pressurized coal-carbonization system... Figure 1, Flow diagram of pressurized coal-carbonization system...
The processes using physical absorption require a solvent circulation proportional to the quantity of process gas, inversely proportional to the pressure, and nearly independent of the carbon dioxide concentration. Therefore, high pressures could favor the use of these processes. The Recitsol process requires a refrigeration system and more equipment than the other processes. This process is primarily used in coal gasification for simultaneous removal of H2S, COS, and CO2. [Pg.22]

SNR s fluidized-bed cogeneiation system is an early example of the commercial development of AFBC technology. Foster Wheeler designed, fabricated, and erected the coal-fired AFBC/boHer, which generates 6.6 MWe and 37 MW thermal (also denoted as MWt) of heat energy. The thermal energy is transferred via medium-pressure hot water to satisfy the heat demand of the tank farm. The unit bums 6.4 t/h of coal and uses a calcium to sulfur mole ratio of 3 to set the limestone feed rate. The spent bed material may be reiajected iato the bed as needed to maintain or build bed iaventory. The fly ash, collected ia two multicyclone mechanical collectors, may also be transferred pneumatically back to the combustor to iacrease the carbon bumup efficiency from 93%, without fly ash reiajection, to 98%. [Pg.260]

Solvent-Refined Coal Process. In the 1920s the anthracene oil fraction recovered from pyrolysis, or coking, of coal was utilized to extract 35—40% of bituminous coals at low pressures for the purpose of manufacturing low cost newspaper inks (113). Tetralin was found to have higher solvent power for coals, and the I. G. Farben Pott-Broche process (114) was developed, wherein a mixture of cresol and tetralin was used to dissolve ca 75% of brown coals at 13.8 MPa (2000 psi) and 427°C. The extract was filtered, and the filtrate vacuum distilled. The overhead was distilled a second time at atmospheric pressure to separate solvent, which was recycled to extraction, and a heavier liquid, which was sent to hydrogenation. The bottoms product from vacuum distillation, or solvent-extracted coal, was carbonized to produce electrode carbon. Filter cake from the filters was coked in rotary kilns for tar and oil recovery. A variety of liquid products were obtained from the solvent extraction-hydrogenation system (113). A similar process was employed in Japan during Wodd War II to produce electrode coke, asphalt (qv), and carbonized fuel briquettes (115). [Pg.89]


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Carbon system

Carbonate systems

Carbonized coal

Coal carbon

Coal carbonates

Pressure systems

Pressurized coal carbonization

Pressurizing system

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