Coal conversion process

Synthesis gas is obtained either from methane reforming or from coal gasification (see Coal conversion processes). Telescoping the methanol carbonylation into an esterification scheme furnishes methyl acetate directly. Thermal decomposition of methyl acetate yields carbon and acetic anhydride,... [Pg.68]

Produced from Co l. Estimates of the cost of producing methanol from coal have been made by the U.S. Department of Energy (DOE) (12,17) and they are more uncertain than those using natural gas. Experience in coal-to-methanol faciUties of the type and size that would offer the most competitive product is limited. The projected costs of coal-derived methanol are considerably higher than those of methanol produced from natural gas. The cost of the production faciUty accounts for most of the increase (11). Coal-derived methanol is not expected to compete with gasoline unless oil prices exceed 0.31/L ( 50/bbl). Successful development of lower cost entrained gasification technologies could reduce the cost so as to make coal-derived methanol competitive at oil prices as low as 0.25/L ( 40/bbl) (17) (see Coal conversion processes). [Pg.423]

A new countercurrent continuous centrifugal extractor developed in the former USSR (214) has the feature that mechanical seals are replaced by Hquid seals with the result that operation and maintenance are simplified the mechanical seals are an operating weak point in most centrifugal extractors. The operating units range between 400 and 1200 mm in diameter, and a capacity of 70 m /h has been reported in service. The extractors have been appHed in coke-oven refining (see Coal conversion processes), erythromycin production, lube oil refining, etc. [Pg.77]

Synthetic Fuel. Solvent extraction has many appHcations in synthetic fuel technology such as the extraction of the Athabasca tar sands (qv) and Irish peat using / -pentane [109-66-0] (238) and a process for treating coal (qv) using a solvent under hydrogen (qv) (239). In the latter case, coal reacts with a minimum amount of hydrogen so that the solvent extracts valuable feedstock components before the soHd residue is burned. Solvent extraction is used in coal Hquefaction processes (240) and synthetic fuel refining (see Coal conversion processes Fuels, synthetic). [Pg.79]

Coal is used ia industry both as a fuel and ia much lower volume as a source of chemicals. In this respect it is like petroleum and natural gas whose consumption also is heavily dominated by fuel use. Coal was once the principal feedstock for chemical production, but ia the 1950s it became more economical to obtain most industrial chemicals from petroleum and gas. Nevertheless, certain chemicals continue to be obtained from coal by traditional routes, and an interest in coal-based chemicals has been maintained in academic and industrial research laboratories. Much of the recent activity in coal conversion has been focused on production of synthetic fuels, but significant progress also has been made on use of coal as a chemical feedstock (see Coal CONVERSION processes). [Pg.161]

The term feedstock in this article refers not only to coal, but also to products and coproducts of coal conversion processes used to meet the raw material needs of the chemical industry. This definition distinguishes between use of coal-derived products for fuels and for chemicals, but this distinction is somewhat arbitrary because the products involved in fuel and chemical appHcations are often identical or related by simple transformations. For example, methanol has been widely promoted and used as a component of motor fuel, but it is also used heavily in the chemical industry. Frequendy, some or all of the chemical products of a coal conversion process are not isolated but used as process fuel. This practice is common in the many coke plants that are now burning coal tar and naphtha in the ovens. [Pg.161]

Whereas Geldart s classification relates fluidized-bed behavior to the average particle size in a bed, particle feed sizes maybe quite different. For example, in fluidized-bed coal (qv) combustion, large coal particles are fed to a bed made up mostly of smaller limestone particles (see Coal conversion processes). [Pg.73]

Coal can be converted to gas by several routes (2,6—11), but often a particular process is a combination of options chosen on the basis of the product desired, ie, low, medium, or high heat-value gas. In a very general sense, coal gas is the term appHed to the mixture of gaseous constituents that are produced during the thermal decomposition of coal at temperatures in excess of 500°C (>930°F), often in the absence of oxygen (air) (see Coal CONVERSION PROCESSES, gasification) (3). A soHd residue (coke, char), tars, and other Hquids are also produced in the process ... [Pg.62]

Process Pa.ra.meters, The most notable effects ia gasifiers are those of pressure (Fig. 1) and coal character. Some initial processiag of the coal feedstock maybe requited. The type and degree of pretreatment is a function of the process and/or the type of coal (see Coal conversion processes, CLEANING AND DESULFURIZATION). [Pg.65]

Occidental Petroleum Coal Conversion Process. Garrett R D Co. (now the Occidental Research Co.) developed the Oxy Coal Conversion process based on mathematical simulation for heating coal particles in the pyrolysis unit. It was estimated that coal particles of 100-mm diameter could be heated throughout their volumes to decomposition temperature (450—540°C) within 0.1 s. A large pilot faciUty was constmcted at LaVeme, California, in 1971. This unit was reported to operate successfully at feed rates up to 136 kg/h (3.2 t/d). [Pg.94]

Imperial Chemical Industries (ICI) operated a coal hydrogenation plant at a pressure of 20 MPa (2900 psi) and a temperature of 400—500°C to produce Hquid hydrocarbon fuel from 1935 to the outbreak of World War II. As many as 12 such plants operated in Germany during World War II to make the country less dependent on petroleum from natural sources but the process was discontinued when hostihties ceased (see Coal conversion PROCESSES,liquefaction). Currentiy the Fisher-Tropsch process is being used at the Sasol plants in South Africa to convert synthesis gas into largely ahphatic hydrocarbons at 10—20 MPa and about 400°C to supply 70% of the fuel needed for transportation. [Pg.76]

In this process, any sulfur present in the coal exits the gasifier as hydrogen sulfide which is removed by various processes such as a Hohnes-Stretford unit where the sulfide is absorbed and regenerated. The resulting sulfur is filtered out as a cake (39 wt %) which is sold as a valuable feedstock (see Coal CONVERSION PROCESSES, GASIFICATION SULFURREMOVAL AND RECOVERY). [Pg.454]

Gasification. Gasification converts soHd fuel, tars, and oils to gaseous products such as CO, H2, and CH that can be burned direcdy or used in synthesis gas (syngas) mixtures, ie, CO and mixtures for production of Hquid fuels and other chemicals (47,48) (see Coal conversion processes, gasification Euels, synthetic-gaseous fuel Hydrogen). [Pg.158]

The red tetrathiomolybdate ion appears to be a principal participant in the biological Cu—Mo antagonism and is reactive toward other transition-metal ions to produce a wide variety of heteronuclear transition-metal sulfide complexes and clusters (13,14). For example, tetrathiomolybdate serves as a bidentate ligand for Co, forming Co(MoSTetrathiomolybdates and their mixed metal complexes are of interest as catalyst precursors for the hydrotreating of petroleum (qv) (15) and the hydroHquefaction of coal (see Coal conversion processes) (16). The intermediate forms MoOS Mo02S 2> MoO S have also been prepared (17). [Pg.470]

C -Chemisty. A great deal of research has been undertaken on the development of PGM catalysts for the manufacture of chemicals and fuels from syngas, a mixture of CO and H2 obtained from coal gasification (see Coal conversion processes). [Pg.173]

Partial oxidation of heavy Hquid hydrocarbons requires somewhat simpler environmental controls. The principal source of particulates is carbon, or soot, formed by the high temperature of the oxidation step. The soot is scmbbed from the raw synthesis gas and either recycled back to the gasifier, or recovered as soHd peUitized fuel. Sulfur and condensate treatment is similar in principle to that required for coal gasification, although the amounts of potential poUutants generated is usually less (see Coal conversion processes, gasification). [Pg.353]

Sasol Fischer-Tropsch Process. 1-Propanol is one of the products from Sasol s Fischer-Tropsch process (7). Coal (qv) is gasified ia Lurgi reactors to produce synthesis gas (H2/CO). After separation from gas Hquids and purification, the synthesis gas is fed iato the Sasol Synthol plant where it is entrained with a powdered iron-based catalyst within the fluid-bed reactors. The exothermic Fischer-Tropsch reaction produces a mixture of hydrocarbons (qv) and oxygenates. The condensation products from the process consist of hydrocarbon Hquids and an aqueous stream that contains a mixture of ketones (qv) and alcohols. The ketones and alcohols are recovered and most of the alcohols are used for the blending of high octane gasoline. Some of the alcohol streams are further purified by distillation to yield pure 1-propanol and ethanol ia a multiunit plant, which has a total capacity of 25,000-30,000 t/yr (see Coal conversion processes, gasification). [Pg.119]

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