Carbon pilot plant

Table 19 Carbon Pilot Plant Results for Petrochemical and Refining Wastewaters...

The TOSCOAL Process. The Oil Shale Corp. (TOSCO) piloted the low temperature carbonization of Wyoming subbituminous coals over a two-year period in its 23 t/d pilot plant at Rocky Falls, Colorado (149). The principal objective was the upgrading of the heating value in order to reduce transportation costs on a heating value basis. Hence, the soHd char product from the process represented 50 wt % of the starting coal but had 80% of its heating value. 

Both the Toth and Alcoa processes provide aluminum chloride for subsequent reduction to aluminum. Pilot-plant tests of these processes have shown difficulties exist in producing aluminum chloride of the purity needed. In the Toth process for the production of aluminum chloride, kaolin [1332-58-7] clay is used as the source of alumina (5). The clay is mixed with sulfur and carbon, and the mixture is ground together, pelletized, and calcined at 700°C. The calcined mixture is chlorinated at 800°C and gaseous aluminum chloride is evolved. The clay used contains considerable amounts of silica, titania, and iron oxides, which chlorinate and must be separated. Silicon tetrachloride and titanium tetrachloride are separated by distillation. Resublimation of aluminum chloride is requited to reduce contamination from iron chloride. 

Australian Vanadium—Uranium Ore. A calcareous camotite ore at YeeHrrie, AustraHa, is iU-suited for salt roasting and acid leaching. Dissolution of vanadium and uranium by leaching in sodium carbonate solution at elevated temperature and pressure has been tested on a pilot-plant scale... 

Process development on fluidized-bed pyrolysis was also carried out by the ConsoHdation Coal Co., culminating in operation of a 32 t/d pilot plant (35). The CONSOL pyrolysis process incorporated a novel stirred carbonizer as the pyrolysis reactor, which made operation of the system feasible even using strongly agglomerating eastern U.S. biturninous coals. This allowed the process to bypass the normal pre-oxidation step that is often used with caking coals, and resulted in a nearly 50% increase in tar yield. Use of a sweep gas to rapidly remove volatiles from the pyrolysis reactor gave overall tar yields of nearly 25% for a coal that had Eischer assay tar yields of only 15%. 

Adsorption. Adsorption (qv) is an effective means of lowering the concentration of dissolved organics in effluent. Activated carbon is the most widely used and effective adsorbent for dyes (4) and, it has been extensively studied in the waste treatment of the different classes of dyes, ie, acid, direct, basic, reactive, disperse, etc (5—22). Commercial activated carbon can be prepared from lignite and bituminous coal, wood, pulp mill residue, coconut shell, and blood and have a surface area ranging from 500—1400 m /g (23). The feasibiUty of adsorption on carbon for the removal of dissolved organic pollutants has been demonstrated by adsorption isotherms (24) (see Carbon, activated carbon). Several pilot-plant and commercial-scale systems using activated carbon adsorption columns have been developed (25—27). 

Figure 14-12 illustrates the influence of system composition and degree of reaetant eonversion upon the numerical values of for the absorption of CO9 into sodium hydroxide solutions at constant conditions of temperature, pressure, and type of packing. An excellent experimental study of the influence of operating variables upon overall values is that of Field et al. (Pilot-Plant Studie.s of the Hot Carbonate Proce.s.s for Removing Carbon Dioxide and Hydrogen Sulfide, U.S. Bureau of Mines Bulletin 597, 1962). 

Many operating data for carbonate plants are cited by Kohl and Riesenfeld (Gn.s Purification, Gulf, 1985) but not including tower heights. Pilot plant tests, however, are reported on 0.10- and 0.15-m (4- and 6-in) columns packed to depths of 9.14 m (30 ft) of Raschig rings hy Benson et al. (Chem. Eng. Prog., 50, 356 [1954]). 

Four pilot plant experiments were conducted at 300 psig and up to 475°C maximum temperature in a 3.07-in. i.d. adiabatic hot gas recycle methanation reactor. Two catalysts were used parallel plates coated with Raney nickel and precipitated nickel pellets. Pressure drop across the parallel plates was about 1/15 that across the bed of pellets. Fresh feed gas containing 75% H2 and 24% CO was fed at up to 3000/hr space velocity. CO concentrations in the product gas ranged from less than 0.1% to 4%. Best performance was achieved with the Raney-nickel-coated plates which yielded 32 mscf CHh/lb Raney nickel during 2307 hrs of operation. Carbon and iron deposition and nickel carbide formation were suspected causes of catalyst deactivation. 

Feed gases to most, if not all, methanation systems for substitute natural gas (SNG) production are theoretically capable of forming carbon. This potential also exists for feed gases to all first-stage shift converters operating in ammonia plants and in hydrogen production plants. However, it has been demonstrated commercially over a period of many years that carbon formation at inlet temperatures in shift converters is a relatively slow reaction and that, once shifted, the gas loses its potential for carbon formation. Carbon formation has not been a common problem at the inlet to shift converters. It has been no problem at all in our bench-scale work, and it is not expected to be a problem in our pilot plant operations. 

There are several factors that may be invoked to explain the discrepancy between predicted and measured results, but the discrepancy highlights the necessity for good pilot plant scale data to properly design these types of reactors. Obviously, the reaction does not involve simple first-order kinetics or equimolal counterdiffusion. The fact that the catalyst activity varies significantly with time on-stream and some carbon deposition is observed indicates that perhaps the coke residues within the catalyst may have effects like those to be discussed in Section 12.3.3. Consult the original article for further discussion of the nonisothermal catalyst pellet problem. 

Centaur A process for reducing sulfur dioxide emissions from sulfuric acid plants. An activated caibon with both absorptive and catalytic properties is used. The technology uses fixed beds of Centaur carbon to oxidize sulfur dioxide to sulfuric acid in the pores of the carbon. The sulfuric acid is recovered as dilute sulfuric acid, which is used a make-up water in the sulfuric acid production process. Developed by Calgon Carbon Corporation in the 1990s. Calgon Carbon and Monsanto Enviro-Chem operated a Centaur pilot plant at an existing sulfuric acid facility in 1996. 

HIsmelt A direct iron smelting process in which noncoking coal, fine iron ore, and fluxes and gases, are injected into a molten iron bath the carbon monoxide produced is used to prereduce the ore in a fluidized bed. Under development by CRA, Australia, since the early 1980s, joined by Midrex Corporation in 1988. Their joint venture company, Hismelt Corporation, commissioned a pilot plant at Kwinana, near Perth, Australia, in 1993. 

Seacoke A process for making tar and coke by carbonizing mixtures of coal and petroleum residuum. The tar would be used in an oil refinery and the coke would be used for generating electricity. The process was sponsored by the U.S. Office of Coal Research 1964-1969 the work was carried out by EMC Corporation, Atlantic Richfield Company, and Blaw-Knox Company. Results from the pilot plant were encouraging but the project was abandoned because the benefits were judged insufficient to justify the complexity. 

In recent years, attempts have been made to make use of the advantages of the supercritical carbon dioxide in chemical reactions. The first technical examples concerning the use of carbon dioxide in a pilot-plant scale chemical reaction were heterogeneous catalyzed hydrogenation and radical polymerization [38-42]. Meanwhile, hydrogenation reactions have been scaled up in a 1000 t/a commercial multipurpose plant. 

In a pilot plant [2,13], superalloy scrap containing Mo, W, Cr, Fe, Co, and Ni is pretreated in a furnace with carbon to transfer refractory metals (Mo, W, etc.) into carbides. The melt is granulated and the resulting material is charged into titanium baskets. Diaphragm-type electrolytic cells are used for anodic dissolution of the granulated material. Fe, Co, Ni, and small amounts of Cr are dissolved into a calcium chloride solution by the current. The metal carbides are not dissolved and remain as an anodic residue in the baskets. 

Pilot plant tests were made in a cyclic fixed fluidized bed unit over a range of conditions. Catalyst-to-oil ratio was varied from 3 to 5 and WHSV was varied from 32 to 53, inversely. The reactor temperature was held at 975°F for the cracking and steam stripping cycles, and at 1200°F for the regeneration cycles. After regeneration, carbon on catalyst was effectively zero. 

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