US2279399A - Blast furnace process - Google Patents
Blast furnace process Download PDFInfo
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- US2279399A US2279399A US297940A US29794039A US2279399A US 2279399 A US2279399 A US 2279399A US 297940 A US297940 A US 297940A US 29794039 A US29794039 A US 29794039A US 2279399 A US2279399 A US 2279399A
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- Prior art keywords
- furnace
- blast furnace
- slag
- preheated
- blast
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- 238000000034 method Methods 0.000 title description 13
- 230000008569 process Effects 0.000 title description 11
- 239000000463 material Substances 0.000 description 26
- 239000002893 slag Substances 0.000 description 17
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical group [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 14
- 235000019738 Limestone Nutrition 0.000 description 12
- 239000006028 limestone Substances 0.000 description 12
- 230000004927 fusion Effects 0.000 description 11
- 239000007789 gas Substances 0.000 description 10
- 230000004907 flux Effects 0.000 description 9
- 229910052742 iron Inorganic materials 0.000 description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 239000012535 impurity Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 4
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000000470 constituent Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 3
- 239000000292 calcium oxide Substances 0.000 description 3
- 239000000446 fuel Substances 0.000 description 3
- 239000012768 molten material Substances 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 2
- 229910000805 Pig iron Inorganic materials 0.000 description 2
- 235000011941 Tilia x europaea Nutrition 0.000 description 2
- 230000001174 ascending effect Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 239000000571 coke Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000001627 detrimental effect Effects 0.000 description 2
- 230000008030 elimination Effects 0.000 description 2
- 238000003379 elimination reaction Methods 0.000 description 2
- 239000004571 lime Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 238000013517 stratification Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000006477 desulfuration reaction Methods 0.000 description 1
- 230000023556 desulfurization Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- 235000013980 iron oxide Nutrition 0.000 description 1
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 238000005272 metallurgy Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21B—MANUFACTURE OF IRON OR STEEL
- C21B5/00—Making pig-iron in the blast furnace
- C21B5/02—Making special pig-iron, e.g. by applying additives, e.g. oxides of other metals
- C21B5/023—Injection of the additives into the melting part
Definitions
- the greater portion of the fluxing material, limestone or similar calcareous material which is added to the usual burden fed to. the blast furnace in admixture with the oreand coke, serves no useful purpose and is in fact deleterious to the desired ore reduction, until the said flux material reaches the lowest heat zone in the furnace, and that the same may be most advantageously omitted'in major part from the burden mixture and fed instead to the furnace at the said lowest heat zone, with marked advantage on the furnace efllciency and on the furnace capacity, as well as more effectiveLv performing its intended function of de-sulfurizing the pig iron product produced in the furnace.
- the solid constituents of the blast furnace charge consist of fuel (carbon), iron-bearing material (ore), and fluxing material (limestone). These are dropped into the top T of the furnace F in more or less admixture wherefrom they descend" is heated sufliciently to drive oif thecarbon dioxide from the calcium carbonate of the limestone. The carbon dioxide gas thus liberated unites with the ascending gas mixture and passes through the stock column-and out of the furnace.
- region X the constituents of the charge are predominantly in a solid state.
- region B the solid constituents of the charge become molten as they pass downward through the hotter zone and drop into the furnace hearth, where the slag layer S forms above the iron layer I.
- Region B is an important one for it is here where the gangue materials of the charge melt and unite to form slag.
- the ease of penetration and uniform distribution of gases passing through this region, the contact of the gases with the unreduced iron-oxides, and the rate of movement or material through the furnace, are greatly dependent upon the amount and physical characteristics of the slag formed.
- the production of slag although it be incidental to the production of metal, is important in that it sets alimit upon the chemical and thermal requirements of the process as a whole.
- the slag is formed by fusion of certain impurities in the materials charged into the fur-'- nace.
- the chemical balance of impurities in thecharged fuel and metalbearing materials is such that the fusion of those impurities alone results in the formation of a slag whose properties are conducive neither tosmooth and economic furnace operation nor to adequate desulfurization of the metal product.
- it is necessary to charge additional limestone material, known as flux in such proportion asto form a slag whose properties will permit smooth furnace operation and chemically inhibit the inclusion of certain undesirable constituents in the metal product.
- the common means of obtaining a properly fluxed slag is to charge the flu'xing material, usually in the form of limestone or a similar calcareous material, into the top of the furnace in admixture with the carbon and ore wherefrom it descends into the hotter zones of the furnace andin the descent is first calcined to calciumoxe d' n sm l fi- A; large proportion of the flux added at the p. of ihs ilrn q ildfid. geld: e i purwith the molten'oxides contained in the ironbearing and fuel materials.
- This condition does not exist excepting in the slag bath which is located below the tuyeres and in one of the lowest zones of the furnace. Indeed, the presence of this added flux material in furnace zones above that of the molten slag surface is essentially detrimental to the smooth and economic operation of the furnace for the following reasons:
- the preheated calcium oxide (calcined limestone) in finely divided form readily fuses and reacts with the impurities in the melting and melted charge to form a fluid slag overlying the molten metal Ion the hearth of the furnace F.
- the oxygen content of the preheated gases from the hot blast main augment the usual air blast supplied by tuyeres W and increase the sensible heat energy being supplied to the furnace F.
- Theapparatus used to practice the process of the invention comprises an insulated container A into which a powdered preheated calcined flux and adaptations of the same are contemplated as may fall within the scope of the accompanying, claims.
- the method of reducing iron ores in a blast furnace which includes charging into the upper part of the furnace iron ore admixed with carbon, preheating finely divided calcinated calcareous fiuxing agent, blowing by preheated air the preheated finely divided calcinated calcareous fluxing agent into the lower part of the furnace at a point below the normal fusion zone thereof but above the zone of molten material on the furnace hearth, regulating the introduction of the preheated air and the preheated finely divided calcinated calcareous iluxing agent to produce stratification of the said fiuxing agent in a layer immediately adjacent to and overlying the surface of the molten metal bath within the furnace hearth, and continuing the introduction of the the carbon burned.
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
Description
April 1942- c. a. HOGBERG ETAL 9,399
BLAST FURNACE PROCESS Filed 001;. 4, 1939 aw M 5 Rm 0 m e C m Patented 14, 1942 anus-r FURNACE rnocEss Carl G, Hogberg and George E. Steudel,
Application October 4, 19 9, Serial No. 297,94 2 Claims. -(CI. 75-41) invention relates to metallurgy, and more particularly to 'the manufacture of pig iron in a blast furnace, and one of the objects of the-present invention is to provide an improved blast furnace process. Another object is to introduce required flux materials within the blast furnace at the point the said materials are needed. Still another object is to increase the operating efiiciency of a blast furnace. Other objects and advantages will be apparent as the invention is more fully hereinafter described.
In accordance with the above objects we have discovered that the greater portion of the fluxing material, limestone or similar calcareous material, which is added to the usual burden fed to. the blast furnace in admixture with the oreand coke, serves no useful purpose and is in fact deleterious to the desired ore reduction, until the said flux material reaches the lowest heat zone in the furnace, and that the same may be most advantageously omitted'in major part from the burden mixture and fed instead to the furnace at the said lowest heat zone, with marked advantage on the furnace efllciency and on the furnace capacity, as well as more effectiveLv performing its intended function of de-sulfurizing the pig iron product produced in the furnace.
In the operation of the blast furnace process, the materials within the furnace undergo a series of transitions between the molten, solid, and gaseous states. These transitions are generally confined to various zones.- In order to more clearly describe these zones within the blast furnace. reference will be made to the attached drawing wherein is illustrated in vertical cross-section a typical blast furnace, together with the improved means of the present invention, the latter being shown partly. in elevation and partly in fra mentary section.
'In generalgthe usual blast furnace process is a countercurrent reaction of descending solid and' molten material with that of ascending gases.
The solid constituents of the blast furnace charge consist of fuel (carbon), iron-bearing material (ore), and fluxing material (limestone). These are dropped into the top T of the furnace F in more or less admixture wherefrom they descend" is heated sufliciently to drive oif thecarbon dioxide from the calcium carbonate of the limestone. The carbon dioxide gas thus liberated unites with the ascending gas mixture and passes through the stock column-and out of the furnace. In region X the constituents of the charge are predominantly in a solid state. In region B, however, the solid constituents of the charge become molten as they pass downward through the hotter zone and drop into the furnace hearth, where the slag layer S forms above the iron layer I.
Region B is an important one for it is here where the gangue materials of the charge melt and unite to form slag. The ease of penetration and uniform distribution of gases passing through this region, the contact of the gases with the unreduced iron-oxides, and the rate of movement or material through the furnace, are greatly dependent upon the amount and physical characteristics of the slag formed.
The production of slag, although it be incidental to the production of metal, is important in that it sets alimit upon the chemical and thermal requirements of the process as a whole. The slag is formed by fusion of certain impurities in the materials charged into the fur-'- nace. In practically all cases, the chemical balance of impurities in thecharged fuel and metalbearing materials is such that the fusion of those impurities alone results in the formation of a slag whose properties are conducive neither tosmooth and economic furnace operation nor to adequate desulfurization of the metal product. As a result, it is necessary to charge additional limestone material, known as flux, in such proportion asto form a slag whose properties will permit smooth furnace operation and chemically inhibit the inclusion of certain undesirable constituents in the metal product.
The common means of obtaining a properly fluxed slag is to charge the flu'xing material, usually in the form of limestone or a similar calcareous material, into the top of the furnace in admixture with the carbon and ore wherefrom it descends into the hotter zones of the furnace andin the descent is first calcined to calciumoxe d' n sm l fi- A; large proportion of the flux added at the p. of ihs ilrn q ildfid. geld: e i purwith the molten'oxides contained in the ironbearing and fuel materials. This condition does not exist excepting in the slag bath which is located below the tuyeres and in one of the lowest zones of the furnace. Indeed, the presence of this added flux material in furnace zones above that of the molten slag surface is essentially detrimental to the smooth and economic operation of the furnace for the following reasons:
1. The presence, in zones where it is not necessary to the successful operation of the process, of a large portion of calcareous fiuxing material, either in a molten or solid state, is detrimental to the process in that it (a) impairs the contact of the unreduced metal-bearing materials with that of the gases, thus delaying the reduction of that material and (b) decreases the reducing power of the furnace gases as a result of a liberation from the flux of inert carbon dioxide gas which-dilutes the gas mixture and makes less effective the strong reducing power of carbon monoxide.
2. The presenceof a high lime (CaO)' content flux in the 'higher fusion zones of the furnace results inthe production, in those zones, of a slag whose melting temperature is considerably in excess to that of a slag formed from the fusion of "the impurities of the charge other than thos introduced by the fiuxing material.
. 3. The smooth and economic operation of the furnace is'impaired by the higher viscosity. inherent with the higher lime content molten mixtures as exist before the fusion of the oxides material is charged at B. The fiux material flows by gravity down .the inclined bottom walls of the container A through outlet opening into an aspirating chamber G. Preheafed air obtained from a hot blast main by a pipe D is passed first through a compressorE which forces the air blast through the aspirator Q. The fiuxing material falling through openlngO is carried by the stream of the air blast into one or more pipes P leading to the interior of the furnace F at a point (or points) below the normal fusion tzone 13.
Thus introduced, the preheated calcium oxide (calcined limestone) in finely divided form readily fuses and reacts with the impurities in the melting and melted charge to form a fluid slag overlying the molten metal Ion the hearth of the furnace F. The oxygen content of the preheated gases from the hot blast main, augment the usual air blast supplied by tuyeres W and increase the sensible heat energy being supplied to the furnace F. v
Having hereinabove disclosed the present invention generically and given one specific embodiment of the same, it is believed apparent that the same may be widely varied without essential departure therefrom and all such modifications of that slag with the more siliceous and alumiv nous oxides of the coke ash.
4. Experience has proved that the rate of iron production decreases when the slag formed is excessively limy, that is, excessively high in calcium oxide;
For reasons outlined above, the present invention proposes to add either part or=all of the flux to the materials within the furnace in-a manner and at a point in the furnace that will result in the elimination, to a great degree, of the disadvantageous conditions as outlined above.
We propose to accomplish this result by adding .a calcined preheated fluxing material to the aggregate within the furnace F at a point below the normal fusion zone of the furnace by means of the apparatus illustrated in the drawing. We have determined that by adding the preheated calcium oxide to the charge in the furnace at a point below} the normal fusion zone of the fur-'- nace the disadvantageous aspects associated with the higher lime content slags in the slag fusion zone of the furnace (zone B) may be eliminated withbuhideleteriously affecting the elimination of sulfur in the blast furnace process, while at the same time increasing the reduction efliciency of the process and. the capacity of the furnace.
Theapparatus used to practice the process of the invention comprises an insulated container A into which a powdered preheated calcined flux and adaptations of the same are contemplated as may fall within the scope of the accompanying, claims.
What we claim is: i 1. The method of reducing iron ores in a blast furnace whichincludes charging into the upper part of the furnace iron ore admixed with carbon, preheating finely divided calcinated limestone, blowing by preheated air the preheated finelydivided calcinated limestone into the lower part of the furnace at a point below the normal fusion zone thereof but above the zone of molten material on the furnace hearth, regulating the introduction of the preheated air and the preheated finely divided calcinated limestone to produce stratification of the limestone in a layer immediately adjacent to and overlying the surface of the molten metal bath within the furnace hearth, and continuing the introduction of the preheated air blast and the preheated finely divided calcinated limestone until there has been introduced to the blast furnace a quantity of limestone approximately equivalent tothat required by the ash in the carbon burned.
2. The method of reducing iron ores in a blast furnace which includes charging into the upper part of the furnace iron ore admixed with carbon, preheating finely divided calcinated calcareous fiuxing agent, blowing by preheated air the preheated finely divided calcinated calcareous fluxing agent into the lower part of the furnace at a point below the normal fusion zone thereof but above the zone of molten material on the furnace hearth, regulating the introduction of the preheated air and the preheated finely divided calcinated calcareous iluxing agent to produce stratification of the said fiuxing agent in a layer immediately adjacent to and overlying the surface of the molten metal bath within the furnace hearth, and continuing the introduction of the the carbon burned. g CARL G. HOGBERG.
GEO. E. STEUDEL.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US297940A US2279399A (en) | 1939-10-04 | 1939-10-04 | Blast furnace process |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US297940A US2279399A (en) | 1939-10-04 | 1939-10-04 | Blast furnace process |
Publications (1)
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US2279399A true US2279399A (en) | 1942-04-14 |
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Family Applications (1)
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US297940A Expired - Lifetime US2279399A (en) | 1939-10-04 | 1939-10-04 | Blast furnace process |
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2918365A (en) * | 1953-08-10 | 1959-12-22 | Yawata Seitetsu K K | Method for controlling compositions of molten pig iron and slag in a blast furnace |
US3148973A (en) * | 1961-02-20 | 1964-09-15 | Inland Steel Co | Iron ore reduction process |
US3231367A (en) * | 1961-11-24 | 1966-01-25 | Nat Steel Corp | Iron producing blast furnace operations |
US3318686A (en) * | 1963-07-02 | 1967-05-09 | Koppers Co Inc | Method and apparatus for transporting particulate material to a metallurgical furnace |
US3377157A (en) * | 1965-04-26 | 1968-04-09 | United States Steel Corp | Method of operating a blast furnace to produce pig iron and cement slag |
EP0180712A1 (en) * | 1984-07-10 | 1986-05-14 | Dr. Küttner GmbH & Co. KG | Process and apparatus for introducing acid slag-forming elements into a cupola furnace |
-
1939
- 1939-10-04 US US297940A patent/US2279399A/en not_active Expired - Lifetime
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2918365A (en) * | 1953-08-10 | 1959-12-22 | Yawata Seitetsu K K | Method for controlling compositions of molten pig iron and slag in a blast furnace |
US3148973A (en) * | 1961-02-20 | 1964-09-15 | Inland Steel Co | Iron ore reduction process |
US3231367A (en) * | 1961-11-24 | 1966-01-25 | Nat Steel Corp | Iron producing blast furnace operations |
US3318686A (en) * | 1963-07-02 | 1967-05-09 | Koppers Co Inc | Method and apparatus for transporting particulate material to a metallurgical furnace |
US3377157A (en) * | 1965-04-26 | 1968-04-09 | United States Steel Corp | Method of operating a blast furnace to produce pig iron and cement slag |
EP0180712A1 (en) * | 1984-07-10 | 1986-05-14 | Dr. Küttner GmbH & Co. KG | Process and apparatus for introducing acid slag-forming elements into a cupola furnace |
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