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Carbon sulfur burning

The impure iron is made into steel by burning out most of the carbon, sulfur, and phosphorus. Today there are three common furnace types for making steel—the open-hearth furnace (85% of U.S. production), the electric arc furnace (10%), and the Bessemer converter (5%). These furnaces differ in construction but the chemistry is basically similar. [Pg.404]

Sulfur is determined as the further loss of weight on extraction with carbon disulfide in a Wilcv extractor or other suitable apparatus. After the extraction, the crucible ought to be allowed to dry in the air away from flames until all the inflammable carbon disulfide has escaped. It is then dried in the oven to constancy of weight, and the residue is taken as charcoal. Ash is determined by igniting the residue in the crucible until all carbon has burned away. A high result for ash may indicate that the water extraction during the determination of potassium nitrate was not complete. The analytical results may be calculated on a moisture-free basis for a closer approximation to the formula by which the manufacturer prepared the powder. [Pg.48]

Table VI gives the distribution of carbon, sulfur, and nitrogen in the products for runs at 983°C and 1038°C. One-hundred fifteen percent of stoichiometric air was used in both runs. The feed gas was pure air. It is apparent that the carbon, nitrogen, and sulfur impurities were almost completely burned out, i.e., 89% or more burn-out was achieved. The effluent melt contained less than 3% of the carbon and sulfur in the feed melt and 11% or less of the nitrogen. Table VI gives the distribution of carbon, sulfur, and nitrogen in the products for runs at 983°C and 1038°C. One-hundred fifteen percent of stoichiometric air was used in both runs. The feed gas was pure air. It is apparent that the carbon, nitrogen, and sulfur impurities were almost completely burned out, i.e., 89% or more burn-out was achieved. The effluent melt contained less than 3% of the carbon and sulfur in the feed melt and 11% or less of the nitrogen.
Rain is naturally slightly acidic but is made more acid by burning fuels and can contain carbonic, sulfuric and nitric acids. Explain how they are formed. [Pg.148]

The oxidation of carbon, sulfur, and nitrogen, resulting mostly from fossil fuel burning, disturbs redox conditions in the atmosphere. [Pg.207]

The 25-year, effort to reduce the emissions from automobiles has greatly benefited the air quality over major cities. Even with this success, more needs to be done. None of the successful efforts has had a large impact on the emission of carbon dioxide. Many of the pollution control schemes used on automobiles actually slightly increase the emission of carbon dioxide. Burning natural gas verses coal reduces the sulfur emissions of power plants. It also slightly reduces the emission of carbon dioxide because natural gas has the least carbon and the most hydrogen of any of the fossil fuels. Unfortunately, increased use of natural gas will also increase the quantity that can escape into the atmosphere. Methane, the major component of natural gas is a potent green house gas. [Pg.17]

Sulfur particles are yellow sugar particles are sweet water is a fluid and consists of liquid particles ice particles are solid carbon particles burn in the barbecue, they smolder and turn to ash the smallest copper particles are the smallest possible copper portions . [Pg.76]

When any substance that contains sulfur burns completely, the sulfur forms sulfur dioxide. For example, when methanethiol, CFi3SFi, burns completely, it forms carbon dioxide, water, and sulfur dioxide. Small amounts of this strong-smelling substance are... [Pg.219]

Serious cadmium losses have been reported when organic samples were ignited and ashed by the dry-ash method (12), This was confirmed during work of the Project. A sample of spiked crude oil was ignited to a carbonaceous residue, and the carbon was burned off in a muffle furnace after the residue was wetted with a few drops of sulfuric acid. The inorganic ash was solubilized with dilute hydrochloric acid and then was analyzed by flame atomic absorption. Recovery of added cadmium averaged 78%. [Pg.91]

Because fossil fuels are the remains of once-living organisms, fuels like coal contain sulfur. In electrical power plants, sulfur burns along with the carbon in coal, forming sulfur dioxide (SO ). There also is some sulfur in gasoline, so motor vehicles are also a source of SO3 (not SO2 because catalytic converters convert SO into SO3). Sulfur dioxide and trioxide are both noxious gases (see the section in chapter 3 titled The NO Problem ) and two of the main components of so-called London smog. Oxides of sulfur cause respiratory disease and contribute to the formation of haze that reduces atmospheric visibility. [Pg.149]

Commercial sulfur is usually 99,9% or higher in purity. Dark" sulfur contains hydrocarbon impurities up to about 0,5% bright sulfur contains less than about 0.1% (measured as carbon). Dark sulfur causes difficulties in some types of sulfur-burning plants. However, methods for uar dark sulfur without difficulty have been developed. Another quality factor is the ash content, riiich should be quite low to avoid dust that will accumulate in the catalyst bed. Solid impurities can be removed from mdten sulfur by filtration 41. Alternatively, by using a hot gas filter, dust arising from ash in the sulfur can be removed from the hot gas leaving the sulfur burner. [Pg.296]

Nonmetals also undergo synthesis reactions with oxygen to form oxides. Sulfur, for example, reacts with oxygen to form sulfur dioxide. And when carbon is burned in air, carbon dioxide is produced. [Pg.263]

Carbon disulfide burns in oxygen to yield carbon dioxide and sulfur dioxide according to the following chemical equation. [Pg.302]

When coal—which is mostly carbon—bums, sulfur burns along with it to form sulfur dioxide (SO ). In the atmosphere, the reactions previously shown take place as winds blow SO, SO3, and H SO hundreds of miles from their sources. like H SO from natural sources, H SO from anthropogenic sources washes from the atmosphere in the next rain, sleet, or snowstorm. [Pg.296]

In addition to gas and acid systems, all sulfur burning acid plants have sulfur handling systems. Carbon steel is often used along with various grades of stainless steel and acid resistant brick where improved corrosion resistance is desired (Louie, 2008). [Pg.353]

Petroleum is a mixture of hydrocarbons— chemical combinations of hydrogen and carbon. When burned completely, the hydrocarbons should yield only water (H2O) and carbon dioxide (CO2). When the burning is incomplete, carbon monoxide (CO) and various oxygenated hydrocarbons are formed. Since most burning uses air, nitrogen compounds also exist. In addition, there are other elements associated with the hydrocarbons in petroleum such as sulfur, nickel, and vanadium, just to name a few. [Pg.480]

Precaution Combustible incompat. with oxidizers keep away from sources of ignition and heat forms very slippery films with water Hazardous Decomp. Prods. On burning, carbon, sulfur, and nitrogen oxides may evolve... [Pg.869]

Ash is the noncombustible residue remaining after the burning of any substance. Although quite variable in physical form and chemical composition, ash is typically composed of silicates, oxides, carbon, sulfur, and metals. Workers may be exposed to ash from coal and oil-fired power plants, ash from ineinerators, ash from wood and other plant materials, and volcanic ash. A significant portion of most airborne ash is in the respirable size range. Fisher et al. (58) and Hatch et al. (59) described coal and oil fly ash, Fruchter et al. (60) described volcanic ash from the 1980 Mount St. Helens eruption in the United States, and Alarie et al. (61) described ash from munieipal incinerators. [Pg.111]

Black Powder. Black powder is mainly used as an igniter for nitrocellulose gun propellant, and to some extent in safety blasting fuse, delay fuses, and in firecrackers. Potassium nitrate black powder (74 wt %, 15.6 wt % carbon, 10.4 wt % sulfur) is used for military appHcations. The slower-burning, less cosdy, and more hygroscopic sodium nitrate black powder (71.0 wt %, 16.5 wt % carbon, 12.5 wt % sulfur) is used industrially. The reaction products of black powder are complex (Table 12) and change with the conditions of initia tion, confinement, and density. The reported thermochemical and performance characteristics vary greatly and depend on the source of material, its physical form, and the method of determination. Typical values are Hsted in Table 13. [Pg.50]

Seaweeds. The eadiest successful manufacture of iodine started in 1817 using certain varieties of seaweeds. The seaweed was dried, burned, and the ash lixiviated to obtain iodine and potassium and sodium salts. The first process used was known as the kelp, or native, process. The name kelp, initially apphed to the ash of the seaweed, has been extended to include the seaweed itself. About 20 t of fresh seaweed was used to produce 5 t of air-dried product containing a mean of 0.38 wt % iodine in the form of iodides of alkah metals. The ash obtained after burning the dried seaweed contains about 1.5 wt % iodine. Chemical separation of the iodine was performed by lixiviation of the burned kelp, followed by soHd-Hquid separation and water evaporation. After separating sodium and potassium chloride, and sodium carbonate, the mother Hquor containing iodine as iodide was treated with sulfuric acid and manganese dioxide to oxidize the iodide to free iodine, which was sublimed and condensed in earthenware pipes (57). [Pg.361]

There are explosion hazards with phthahc anhydride, both as a dust or vapor in air and as a reactant. Table 11 presents explosion hazards resulting from phthahc anhydride dust or vapor (40,41). Preventative safeguards in handling sohd phthahc anhydride have been reported (15). Water, carbon dioxide, dry chemical, or foam may be used to extinguish the burning anhydride. Mixtures of phthahc anhydride with copper oxide, sodium nitrite, or nitric acid plus sulfuric acid above 80°C explode or react violently (39). [Pg.484]

Chemical recovery ia sodium-based sulfite pulpiag is more complicated, and a large number of processes have been proposed. The most common process iavolves liquor iaciaeration under reduciag conditions to give a smelt, which is dissolved to produce a kraft-type green liquor. Sulfide is stripped from the liquor as H2S after the pH is lowered by CO2. The H2S is oxidized to sulfur ia a separate stream by reaction with SO2, and the sulfur is subsequendy burned to reform SO2. Alternatively, ia a pyrolysis process such as SCA-Bidemd, the H2S gas is burned direcdy to SO2. A rather novel approach is the Sonoco process, ia which alumina is added to the spent liquors which are then burned ia a kiln to form sodium aluminate. In anther method, used particulady ia neutral sulfite semichemical processes, fluidized-bed combustion is employed to give a mixture of sodium carbonate and sodium sulfate, which can be sold to kraft mills as makeup chemical. [Pg.274]

Elemental sulfur in either its ore or its refined state can generaUy be recognized by its characteristic yeUow color or by the generation of sulfur dioxide when it is burned in air. Its presence in an elemental state or in a compound can be detected by heating the material with sodium carbonate and mbbing the fused product on a wet piece of silver metal. A black discoloration of the silver indicates the presence of sulfur. The test is quite sensitive. Several other methods for detecting smaU amounts of elemental sulfur have also been developed (34). [Pg.124]

The moisture content of cmde sulfur is determined by the differential weight of a known sample before and after drying at about 110°C. Acid content is determined by volumetric titration with a standard base. Nonvolatile impurities or ash are determined by burning the sulfur from a known sample and igniting the residue to remove the residual carbon and other volatiles. [Pg.124]


See other pages where Carbon sulfur burning is mentioned: [Pg.361]    [Pg.419]    [Pg.165]    [Pg.156]    [Pg.439]    [Pg.1177]    [Pg.358]    [Pg.409]    [Pg.30]    [Pg.418]    [Pg.1187]    [Pg.846]    [Pg.656]    [Pg.429]    [Pg.162]    [Pg.191]    [Pg.204]    [Pg.948]    [Pg.1000]    [Pg.623]    [Pg.453]    [Pg.212]    [Pg.3]    [Pg.351]    [Pg.332]   
See also in sourсe #XX -- [ Pg.20 ]




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