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Blast furnace, 5.19

Any lead(II) sulphate formed in this process is converted to lead(II) silicate by reaction with the quartz. The oxide produced is then mixed with limestone and coke and heated in a blast furnace. The following reactions occur ... [Pg.167]

The process of extraction requires first smelting (to obtain the crude metal) and then refining. In smelting, iron ore (usually an oxide) is mixed with coke and limestone and heated, and hot air (often enriched with oxygen) is blown in from beneath (in a blast furnace). At the lower, hotter part of the furnace, carbon monoxide is produced and this is the essential reducing agent. The reduction reactions occurring may be represented for simplicity as ... [Pg.391]

Oxygen enrichment of steel blast furnaces accounts for the greatest use of the gas. Large quantities are also used in making synthesis gas for ammonia and methanol, ethylene oxide, and for oxy-acetylene welding. [Pg.21]

In 1990, U.S. coke plants consumed 3.61 x 10 t of coal, or 4.4% of the total U.S. consumption of 8.12 x ICf t (6). Worldwide, roughly 400 coke oven batteries were in operation in 1988, consuming about 4.5 x 10 t of coal and producing 3.5 x 10 t metallurgical coke. Coke production is in a period of decline because of reduced demand for steel and increa sing use of technology for direct injection of coal into blast furnaces (7). The decline in coke production and trend away from recovery of coproducts is reflected in a 70—80% decline in volume of coal-tar chemicals since the 1970s. [Pg.162]

Calcium. Calcium is the fifth most abundant element in the earth s cmst. There is no foreseeable lack of this resource as it is virtually unlimited. Primary sources of calcium are lime materials and gypsum, generally classified as soil amendments (see Calcium compounds). Among the more important calcium amendments are blast furnace slag, calcitic limestone, gypsum, hydrated lime, and precipitated lime. Fertilizers that carry calcium are calcium cyanamide, calcium nitrate, phosphate rock, and superphosphates. In addition, there are several organic carriers of calcium. Calcium is widely distributed in nature as calcium carbonate, chalk, marble, gypsum, fluorspar, phosphate rock, and other rocks and minerals. [Pg.245]

The combustible components of the gas are carbon monoxide and hydrogen, but combustion (heat) value varies because of dilution with carbon dioxide and with nitrogen. The gas has a low flame temperature unless the combustion air is strongly preheated. Its use has been limited essentially to steel (qv) mills, where it is produced as a by-product of blast furnaces. A common choice of equipment for the smaller gas producers is the WeUman-Galusha unit because of its long history of successful operation (21). [Pg.63]

A furnace is a device (enclosure) for generating controlled heat with the objective of performing work. In fossil-fuel furnaces, the work appHcation may be direct (eg, rotary kilns) or indirect (eg, plants for electric power generation). The furnace chamber is either cooled (waterwaH enclosure) or not cooled (refractory lining). In this article, furnaces related to metallurgy such as blast furnaces ate excluded because they ate coveted under associated topics (see... [Pg.140]

Pure iron is a silvery white, relatively soft metal and is rarely used commercially. Typical properties are Hsted in Table 1. Electrolytic (99.9% pure) iron is used for magnetic cores (2) (see Magnetic materials, bulk). Native metallic iron is rarely found in nature because iron which commonly exhibits valences of +2 and +3 combines readily with oxygen and sulfur. Iron oxides are the most prevalent form of iron (see Iron compounds). Generally, these iron oxides (iron ores) are reduced to iron and melted in a blast furnace. The hot metal (pig iron) from the blast furnace is refined in steelmaking furnaces to make steel... [Pg.411]

The Stuckofen or old high bloomery appeared in Germany in ca 1300 AD. This type of furnace was 3—5 m high and enclosed a tapered vertical shaft that was 1—1.2 m in diameter. Small openings near the bottom were provided for no22les (tuyeres, pronounced tweers) that permitted air, suppHed by bellows, to be blown into the furnace. Modem blast furnaces have essentially the same fundamental design. [Pg.412]

In the United States, the first ironworks was built at Jamestown, Virginia, in 1619. The Hammersmith furnace in Saugus, Massachusetts, built in 1645, operated until 1675. This early American ironworks has been restored and is called the Saugus Iron Works. Iron blast furnaces appeared in many locahties where there were deposits of iron ore. Small bodies of iron ore in New Jersey, Connecticut, Massachusetts, Pennsylvania, and New York formed the basis of many small colonial furnaces. [Pg.412]

Ironmaking in the United States did not expand rapidly until after the Revolutionary War. Then, as the colonists moved westward, the need for iron prompted the estabUshment of ironworks near the new settiements. A blast furnace built by Jacob Anschut2 in 1796 was the beginning of the iron and steel center in Pittsburgh, Pennsylvania. [Pg.412]

In 1979, there were 168 blast furnaces in the United States, most located in Pittsburgh and Chicago, and these produced ca 8 x 10 t of pig iron. By 1992, most of the blast furnaces in the Pittsburgh area had disappeared. Only 44 blast furnaces were operating in the United States, producing ca 4.7 x lO t of pig iron. The drop in pig iron production can be attributed to decreased and more efficient use of steel products, competition from steel imports, and rapid growth of scrap-based steelmaking. [Pg.412]

The Utah deposit is located in southwestern Utah near Cedar City. The iron ore deposits are of contact metamorphic origin. The cmde ore contains 35 to 65% iron, primarily in the form of magnetite and goethite. Mining is done by the open pit method. The cmde ore is cmshed, screened at —75 mm (—200 mesh size) and shipped as lump ore containing 54% iron. The ore is rescreened at the steel mill to produce lump ore (10—64 mm) for the blast furnace and sinter feed (0—10 mm) for the sinter plant. [Pg.413]

Ironmaking refers to those processes which reduce iron oxides to iron. By the nature of the processes, the iron produced usually contains carbon and/or other impurities which are removed in downstream processing. There are three principal categories of ironmaking processes, in order of commercial importance blast furnace, direct reduction, and direct smelting. [Pg.414]

Blast Furnace. The blast furnace is the predominant method for making iron. Estabhshed for centuries as the premier ironmaking process, blast furnace ironmaking both enabled and profited from the Industrial Revolution. Although the fundamental principles of operation are unchanged, the blast furnace has evolved into a highly efficient and productive process. [Pg.414]

Thermochemistry. From an overall heat and mass balance point of view, the main chemical reactions of the blast furnace include oxidation of carbon in the zone in front of the tuyeres (raceway) to give CO plus heat. [Pg.415]

Mass and energy balances are used to evaluate blast furnace performance. Many companies now use sophisticated computeri2ed data acquisition and analysis systems to automatically gather the required data for daily calculation of the mass and heat balances. Typical mass and heat balances are shown in Figure 4 and Table 5, respectively. [Pg.417]

Fig. 5. Flow diagram depicting the principal units and auxiliaries in a modem blast furnace plant, and showing the steps in the manufacture of pig iron from... Fig. 5. Flow diagram depicting the principal units and auxiliaries in a modem blast furnace plant, and showing the steps in the manufacture of pig iron from...

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Blast Furnace Products

Blast furnace accretions

Blast furnace cement

Blast furnace cement composition

Blast furnace coke production

Blast furnace coke requirements

Blast furnace construction

Blast furnace dust

Blast furnace energy consumption

Blast furnace feeding

Blast furnace feeding practice

Blast furnace heat balance

Blast furnace injection

Blast furnace model

Blast furnace operation

Blast furnace oxygen enrichment

Blast furnace performance data

Blast furnace processes

Blast furnace reaction zones

Blast furnace slag

Blast furnace slag cement concrete

Blast furnace slag cements

Blast furnace slag composition

Blast furnace slags, thermal

Blast furnace stove

Blast furnace tapping requirements

Blast furnace walls

Blast furnace, alternative

Blast furnace, lead

Blast furnaces Germany

Blast furnaces Sweden

Blast furnaces, plastics waste used

Cold blast cupola furnace

Dicalcium silicate disintegration of air-cooled blast-furnace slag

Effect of air preheating on blast furnace efficiency

Furnace charcoal blast

Gas, blast furnace

Granulated blast furnace slag

Ground granulated blast furnace slag

Hearth of Blast Furnace

Hot blast cupola furnace

Iron blast furnace

Iron disintegration of air-cooled blast-furnace slag

Ironmaking blast furnace

Ironmaking blast-furnace process

Lead blast furnace slags

Lead blast furnace slags fuming

Lead, blast-furnace smelting

Lead, blast-furnace smelting slags

Modern blast furnace

Operational data of cold blast cupola furnaces with a bag filter for dust abatement

Packed blast furnace

Permeability blast furnace

Phosphoric Acid Production by the Blast-Furnace Process

Port Pirie blast furnace

Portland blast furnace cement

Portland blast furnace slag cement

Precipitator blast-furnace pipe

Preparation of Blast Furnace Feed

Production of Blast Furnace Coke

Production of Pig Iron in a Blast Furnace

Recycling steel blast furnaces

Regenerators blast-furnace stoves

Residence Time Distribution of a Blast Furnace

Schematic outline and miniature model of a (cold blast) cupola furnace

Steel Production Based on the Blast Furnace Route

The Blast Furnace

The Lead Blast Furnace

The ironmaking blast furnace

Use of Mixed Plastic Waste in Blast Furnaces

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