WO2005118892A1 - Agglomeratstein zum einsatz in schacht-, corex- oder hochöfen, verfahren zur herstellung von agglomeratsteinen und verwendung von eisenerz-fein- und -feinststäuben - Google Patents
Agglomeratstein zum einsatz in schacht-, corex- oder hochöfen, verfahren zur herstellung von agglomeratsteinen und verwendung von eisenerz-fein- und -feinststäuben Download PDFInfo
- Publication number
- WO2005118892A1 WO2005118892A1 PCT/EP2005/005626 EP2005005626W WO2005118892A1 WO 2005118892 A1 WO2005118892 A1 WO 2005118892A1 EP 2005005626 W EP2005005626 W EP 2005005626W WO 2005118892 A1 WO2005118892 A1 WO 2005118892A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- agglomerate
- fine
- stones
- iron ore
- solidification
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B1/00—Preliminary treatment of ores or scrap
- C22B1/14—Agglomerating; Briquetting; Binding; Granulating
- C22B1/24—Binding; Briquetting ; Granulating
- C22B1/242—Binding; Briquetting ; Granulating with binders
- C22B1/243—Binding; Briquetting ; Granulating with binders inorganic
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B7/00—Working up raw materials other than ores, e.g. scrap, to produce non-ferrous metals and compounds thereof; Methods of a general interest or applied to the winning of more than two metals
- C22B7/02—Working-up flue dust
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F27—FURNACES; KILNS; OVENS; RETORTS
- F27D—DETAILS OR ACCESSORIES OF FURNACES, KILNS, OVENS, OR RETORTS, IN SO FAR AS THEY ARE OF KINDS OCCURRING IN MORE THAN ONE KIND OF FURNACE
- F27D1/00—Casings; Linings; Walls; Roofs
- F27D1/0003—Linings or walls
- F27D1/0006—Linings or walls formed from bricks or layers with a particular composition or specific characteristics
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F27—FURNACES; KILNS; OVENS; RETORTS
- F27D—DETAILS OR ACCESSORIES OF FURNACES, KILNS, OVENS, OR RETORTS, IN SO FAR AS THEY ARE OF KINDS OCCURRING IN MORE THAN ONE KIND OF FURNACE
- F27D1/00—Casings; Linings; Walls; Roofs
- F27D1/04—Casings; Linings; Walls; Roofs characterised by the form, e.g. shape of the bricks or blocks used
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B1/00—Preliminary treatment of ores or scrap
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
Definitions
- the invention relates to an agglomerate stone for use in shaft, Corex or blast furnaces, a method for producing such agglomerate stones and the use of fine or very fine iron ore dusts.
- iron-containing dusts with the finest and fine grain of up to 3 mm are obtained in large quantities. In order to be able to use these dusts for metal production, they have to be cut into pieces. Sintering and pelleting are common processes for making fine and fine ores used in smelting.
- sintering ore dust When sintering ore dust, a mixture of moistened fine ore together with coke breeze or another carbon carrier and aggregates of limestone, quicklime, olivine or dolomite is usually placed on a circumferential grate, the so-called “sintering belt” and ignited from above. The carbon contained in this mixture burns with the help of the air drawn through the sintering belt, causing the ore grains to cake. When the end of the sintering belt is reached in this way the layer on the belt is completely sintered. The solidified iron ore is broken, sieved while still glowing and fed to a cooler, in which it is cooled so gently that its strength is not impaired. The sinter obtained after further screening of the fine components of the cooled sinter mixture is suitable for direct use in the blast furnace due to its high gas permeability and good reducibility.
- the known sintering process can usually only economically bring ore dusts into a lumpy form that have grain sizes of 2 mm and more. Ore dust with a significantly lower grain size can be used for metal extraction by pelleting.
- pellets produced by pelleting can have a uniform grain compared to lump ores, a constant one Quality and good gas flow during the reduction can be guaranteed.
- pellets can therefore only be used to a limited extent.
- the blocks are then heated to a temperature above 1000 ° C when they sink from the high filling position towards the hot zone of the OxiCup furnace.
- the carbon carrier contained in the blocks is converted into CO gas, which causes a direct reduction in the iron oxide content of the blocks.
- the OxiCup process thus provides an economical method for reusing dusts from iron production.
- the invention proposes an agglomerate stone for use in shaft, Corex or blast furnaces, which (in% by weight) 6 - 15% of a cement binder, up to 20% of a carbon carrier, up to 20% of residual and recyclable materials, optionally up to 10% of a solidification and solidification accelerator, and the remainder of the iron ore present in stone format in the form of particles with a grain size of less than 3 mm and an early strength of at least after three days 5 N / mm 2 and after 28 days has a cold compressive strength of at least 20 N / mm 2 .
- iron ore fine and very fine dusts which are in stone format are used in accordance with the invention.
- Such iron ores contain essentially no metallic iron, but only pure iron oxide, which can be contaminated with little gait. Therefore, agglomerate stones according to the invention have fundamentally different properties than those in. State of the art so far from residual and circular waste stones.
- Ore stones of the type according to the invention have a significantly higher early and final strength than the known residual material stones. Due to the high compressive strength of at least 20 N / mm 2 present in the finished state in the case of agglomerate stones according to the invention, they can safely withstand the pressure of the pouring column in the blast furnace.
- agglomerate stones according to the invention regularly achieve a minimum hot compressive strength of 10 N / mm 2 .
- composition of the ore stones according to the invention is coordinated with one another in such a way that in blast furnace use, when the binding properties of the cement material collapse with increasing temperature and heating duration, the latter Temperature-forming sponge iron as a supporting structure, the gas permeability of the stone and of the entire furnace content can be maintained.
- the particular strength and shape retention of agglomerate stones according to the invention make these stones particularly suitable for use in shaft, Corex or blast furnaces.
- agglomerate stones according to the invention can contain up to 20% of residual and circular substances also contributes to the advantages of the invention with regard to the problem of disposal of residual and circular substances.
- residual and circular substances are mixtures of materials which, in addition to iron in metallic and oxidic form Contain impurities.
- Such residual and recycle materials occur, for example, in the production and processing of steel in the form of filter dusts, top dusts or mill scale.
- the final strength of the agglomerate stones according to the invention is in each case so high that they withstand the loads which occur when used in the respective furnace. Since agglomerate stones according to the invention can be significantly larger, they are suitable for use in large furnaces, such as shaft, Corex or blast furnaces, and there ensure the improved gasification during the reduction.
- the early strength of the agglomerate stones obtained according to the invention is sufficient for them to be able to be transported a short time after their manufacture. This makes it possible, for example, to stack the agglomerate stones according to the invention soon after they have been formed in a drying room, in which they can then be dried particularly effectively.
- Agglomerate stones according to the invention can be produced on stone-making machines known per se, such as are used for example for the production of paving stones.
- Such block making machines allow a particularly cost-effective production and contribute to the fact that agglomerated stones according to the invention can be produced at a particularly favorable • the economics of their use further enhancing price.
- agglomerate stones according to the invention enable the economical use of iron ore dusts over the entire width of the conceivable grain sizes up to 3 mm.
- dusts with a grain size of up to 1 mm can be processed and used just as easily as iron ore dust with a grain size of up to 500 ⁇ m that typically occurs in the area of certain deposits.
- Such ore dust which is obtained in the range from 5 to 30 ⁇ m when pelleting iron ores, so-called "pellet feed”, can also be used in that agglomerate stones according to the invention are produced from them.
- Studies show that even dusts collected in aqueous solution and produced in the production of ore concentrates with grain sizes of up to 7 ⁇ m can be used profitably for iron production if they are used to form agglomerate stones according to the invention.
- the iron ores contained in fine-grained agglomerate stones according to the invention are preferably in haematitic (Fe 2 0 3 ), magnetitic (Fe 3 0 4 ) and / or wustitic (FeO) modification, the grain diameter of which is also preferably less than 0.1 mm.
- the invention also makes it difficult to sinter or pelletize to supply ferrous materials for the production of pig iron. Accordingly, iron ore in the form of geothite (FeO (OH)) can be used for the production of agglomerate stones according to the invention. This applies even if the geothite has a grain size of up to 2 mm, whereby grain sizes that are significantly smaller than 2 mm can also be used.
- FeO geothite
- the content of iron should be at least 40% by weight in an agglomerate stone according to the invention.
- the invention makes use of the idea, already known per se, of coldly binding the iron dust to be used in stone form without special heat treatment with the aid of a cement.
- cement binding also enables slag guidance, in particular its proportions of MgO, CaO, SiO 2 , Al 2 O 3 , during the production of pig iron, via the respective cement portion of the agglomerate stone. to vary.
- Portland cement or metallurgical cement which is available at low cost, can be used as the cement binder.
- the binder in question is mixed with the iron ore dust as a hydraulic cement phase.
- the early strength determined after 3 days becomes at least 5 N / mm 2 and that which can be determined after 28 days
- Cold compressive strength of at least 20 N / mm 2 achieved in each case particularly reliably with agglomerate stones according to the invention.
- the special behavior of the agglomerate stones according to the invention when heated has turned out to be particularly advantageous for use in a furnace for producing pig iron.
- the embedding of the iron ore dust present in stone format in a cement binder at temperatures of up to 400 ° C. results in an increase in strength.
- the temperature range of more than 400 ° C to 800 ° C there is only a slow decrease in strength. Due to this behavior, the agglomerate stones keep their shape as long as they pass through the furnace, so that they are safely transported to the hot melting zone. Only at temperatures above 800 ° C to 1000 ° C does their strength drop faster.
- the iron sponge formed in this temperature range during the reduction ensures the shape retention of the agglomerate stone during further heating and maintains its gas permeability.
- the agglomerate stone according to the invention can, in addition to the cement binder, optionally also a setting and solidification accelerator, such as water glass, alumina cement, calcium chloride, an alkali salt, in particular a Na salt, or a Cellulose glue, such as paste, included.
- a setting and solidification accelerator such as water glass, alumina cement, calcium chloride, an alkali salt, in particular a Na salt, or a Cellulose glue, such as paste, included.
- the ore stones processed according to the invention in dust form can be used both directly-reducing with a reducing agent (carbon carrier) and without a reducing agent. If a reducing agent is present, the maximum content of the carbon carrier in the agglomerate stone should not be more than 20% by weight.
- an optimal adaptation of the proportion to the proportion by weight of iron is achieved if the agglomerate stone contains 8-15% by weight of the carbon carrier.
- the proportion of volatile components in an agglomerate stone according to the invention is high, the otherwise reduced reducibility can be compensated for by increased contents of the C-carrier component.
- the grain size of the carbon carrier is preferably up to 2 mm. C-beams with such a grain size are available at particularly low cost and are difficult to use when extracting iron.
- Agglomerate stones according to the invention should have a cylindrical, cuboid or polygonal shape, on the one hand to ensure sufficient stability and on the other hand after filling into the furnace to ensure that there are sufficient gaps between them for the through-gasing of the bed.
- the shaping surface is optimally used.
- the water content of the agglomerate stone according to the invention should be less than 25%. The production of earth-moist, crumbly green bodies is simplified compared to the processing of masses with a higher moisture content. In addition, by limiting the water content of the green bodies according to the invention, it is avoided that excess water in the oven has to be expelled with high energy expenditure.
- Agglomerate stones according to the invention are particularly easy to produce.
- stone-like iron ore in the form of fine or very fine dust with a maximum grain size of 3 mm with a binder present as a hydraulic cement phase as well as optionally with a carbon carrier, with residual and circulating materials and / or a solidification and solidification accelerator with the stipulations mixed that the proportion of cement binder in the mixture obtained (in wt .-%) 6 - 15%, the proportion of the carbon carrier up to 20%, the proportion of residual and circulating materials up to 20% and the proportion of solidification and solidification accelerators up to 10%.
- the mixture obtained is filled into molds. According to a first process variant, the mixture is then pressed before it is dried.
- Diag. 1 the strength of an agglomerate stone according to the invention plotted against the temperature
- Diag. 2 the strength of a conventional agglomerate stone plotted against temperature
- Diag. 3a the temperature of an agglomerate stone according to the invention plotted over the heating time
- Diag. 3b the stone height of an agglomerate stone according to the invention plotted over the heating-up time
- Diag. 3c shows the weight loss of an agglomerate stone according to the invention plotted over the heating-up time.
- the agglomerate stones examined were each subjected to the so-called "modified RuL test".
- the melting behavior of the agglomerate stones in the chimney shaft is simulated with a chimney gas atmosphere under static conditions. In this way, statements can be made as to whether the formation of sponge iron from the reduction of the iron carriers of the agglomerate stones is sufficient to counteract the breakdown of the cement bond that occurs with increasing warming, without the gasification of the chimney being negatively affected by softening or disintegration of the agglomerate stones is hindered.
- the simulation ends in the temperature range of 1000 - 1100 ° C.
- the grain size of the iron ore dust was between 5 and 30 ⁇ m.
- the iron ore dust was mixed with coke in the form of coke dust as a carbon carrier and a quick-setting, commercially available standard cement as a cement binder.
- the mixture obtained contained (in% by weight) 70 to 80% iron dust, 10 to 15% coke and 10 to 15% cement binder.
- the mixture composed in this way was shaken in a known stone molding machine and pressed to block-shaped agglomerate stones, which had a hexagonal base with an edge length of approx. 30 mm and a height of 110 mm. After drying, the agglomerate stones were subjected to the RuL test. This resulted in a degree of reduction
- Diag. 3b is the weight loss dG, which occurs in g as the heating time t h increases , of the agglomerate stones (line “KS”) produced using coal dust and tested in experiment I (line “KS”) and that produced using charcoal as a carbon carrier, but otherwise with those in the experiment I matching agglomerate stones (line “HK”) again applied over the heating time t h .
- KS agglomerate stones
- HK agglomerate stones
- the diagrams 3a - 3c show by the observed change in the increase in the stone temperature T s , the height H s and the weight loss dG of the agglomerate stones KS and HK, that metallization begins at temperatures above 800 ° C.
- This process can be observed independently with both investigated carbon carrier materials (coke dust, charcoal).
- the support structure that forms as a result of the metallization counteracts the drop in strength that occurs at high temperatures, so that up to the area of a blast furnace where the solid material becomes plastic on its way down due to the ever higher temperatures (“cohesive zone”) sufficient strength of the agglomerate stones is guaranteed for the gasification and locomotion.
- iron ore dust is initially from a concentrate that came from the Carol Lake, Canada deposit, with a grain size of up to 500 ⁇ m and a hematite / magnetite ratio of 1: 1 with coke dust as a carbon carrier and a quick-setting one , standard commercial cement has been mixed as a cement binder.
- the mixture obtained contained (in% by weight) 70 to 80% iron ore dust, 10 to 15% coke dust and 10 to 15% cement.
- Agglomerate stones were produced from the mixture composed in this way in the manner already explained for experiment I.
- the agglomerate stones obtained in this way were also subjected to the modified RuL test.
- the degree of reduction was 95.6% and the degree of decarburization was 85%.
- the trivalent iron level was completely reduced.
- iron dust consisting of magnetite and a grain size of up to 1 mm from a concentrate, which came from the Guelbs / Kedia deposit, Mauritania, was also mixed with coke dust and quick-setting, commercially available cement binder.
- the iron ore content of the mixture obtained was 75% by weight, its coke content 13% by weight and its cement content 12% by weight.
- the agglomerate stones also produced from this mixture in the manner already described in connection with experiment 1 have also been subjected to the RuL test. It gave a degree of reduction of 88.3% and a degree of decarburization of 83.2%.
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- Environmental & Geological Engineering (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Manufacturing & Machinery (AREA)
- General Engineering & Computer Science (AREA)
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- Geochemistry & Mineralogy (AREA)
- Manufacture And Refinement Of Metals (AREA)
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP05745341A EP1753884A1 (de) | 2004-06-03 | 2005-05-25 | Agglomeratstein zum einsatz in schacht-, corex- oder hochöfen, verfahren zur herstellung von agglomeratsteinen und verwendung von eisenerz-fein- und -feinststäuben |
BRPI0511806-9A BRPI0511806A (pt) | 2004-06-03 | 2005-05-25 | pedra de aglomerado para o emprego em fornos de cuba, fornos para processo corex ou alto-forno, processo para a produção de pedras de aglomerado e emprego de pó fino e finìssimo de minério de ferro |
AU2005250105A AU2005250105B2 (en) | 2004-06-03 | 2005-05-25 | Agglomerated stone for using in shaft furnaces, corex furnaces or blast furnaces, method for producing agglomerated stones, and use of fine and superfine iron ore dust |
US11/628,352 US8025727B2 (en) | 2004-06-03 | 2005-05-25 | Agglomerated stone for using in shaft, corex or blast furnaces, method for producing agglomerated stones and use of fine and superfine iron ore dust |
CA 2569247 CA2569247A1 (en) | 2004-06-03 | 2005-05-25 | Agglomerated stone for using in shaft, corex or blast furnaces, method for producing agglomerated stones and use of fine and superfine iron ore dust |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE200410027193 DE102004027193A1 (de) | 2004-06-03 | 2004-06-03 | Agglomeratstein zum Einsatz in Schacht-, Corex- oder Hochöfen, Verfahren zur Herstellung von Agglomeratsteinen und Verwendung von Eisenerz-Fein- und -Feinststäuben |
DE102004027193.3 | 2004-06-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2005118892A1 true WO2005118892A1 (de) | 2005-12-15 |
Family
ID=34968601
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2005/005626 WO2005118892A1 (de) | 2004-06-03 | 2005-05-25 | Agglomeratstein zum einsatz in schacht-, corex- oder hochöfen, verfahren zur herstellung von agglomeratsteinen und verwendung von eisenerz-fein- und -feinststäuben |
Country Status (10)
Country | Link |
---|---|
US (1) | US8025727B2 (de) |
EP (1) | EP1753884A1 (de) |
CN (1) | CN1961085A (de) |
AU (1) | AU2005250105B2 (de) |
BR (1) | BRPI0511806A (de) |
CA (1) | CA2569247A1 (de) |
DE (1) | DE102004027193A1 (de) |
RU (1) | RU2366735C2 (de) |
UA (1) | UA87686C2 (de) |
WO (1) | WO2005118892A1 (de) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102005062036A1 (de) * | 2005-12-22 | 2007-06-28 | Thyssenkrupp Steel Ag | Agglomeratstein zum Einsatz in Schacht-, Corex- oder Hochöfen |
WO2009068452A1 (de) * | 2007-11-30 | 2009-06-04 | Chemische Fabrik Budenheim Kg | Metallrückstände und kohlenstoffträger enthaltender formkörper |
EP2405025A1 (de) | 2010-07-08 | 2012-01-11 | MFG Metall- und Ferrolegierungsgesellschaft mbh Hafner, Blondin & Tidou | Verfahren zur Herstellung von Legierungsformlingen |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BR112012011771B1 (pt) | 2009-11-17 | 2019-10-08 | Vale S.A. | Aglomerado de finos de minério a ser usado em um processo de sinterização, e método para produção de aglomerado de finos de minério |
US10144981B2 (en) * | 2012-02-28 | 2018-12-04 | Kobe Steel, Ltd. | Process for manufacturing reduced iron agglomerates |
EP2662457A1 (de) * | 2012-05-07 | 2013-11-13 | Siemens VAI Metals Technologies GmbH | Verfahren und Vorrichtung zur Herstellung von Agglomeraten und Verwendung der Agglomerate in einem FINEX®-Verfahren |
BR102019023195B1 (pt) * | 2019-11-05 | 2021-01-19 | Vale S.A. | processo de produção de aglomerado de finos de minério de ferroe o produto aglomerado |
EP4342865A1 (de) | 2022-09-22 | 2024-03-27 | ThyssenKrupp Steel Europe AG | Agglomeratstein zum einsatz in einem elektroofen |
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US4846884A (en) * | 1981-09-24 | 1989-07-11 | Sumitomo Metal Industries, Ltd. | Process for producing cold-bonded iron ore for use in a blast furnace |
US20020152839A1 (en) * | 1999-11-01 | 2002-10-24 | Jay Aota | Cold bonded iron particulate pellets |
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2004
- 2004-06-03 DE DE200410027193 patent/DE102004027193A1/de not_active Withdrawn
-
2005
- 2005-05-25 CA CA 2569247 patent/CA2569247A1/en not_active Abandoned
- 2005-05-25 US US11/628,352 patent/US8025727B2/en not_active Expired - Fee Related
- 2005-05-25 BR BRPI0511806-9A patent/BRPI0511806A/pt not_active Application Discontinuation
- 2005-05-25 WO PCT/EP2005/005626 patent/WO2005118892A1/de active Application Filing
- 2005-05-25 EP EP05745341A patent/EP1753884A1/de not_active Withdrawn
- 2005-05-25 AU AU2005250105A patent/AU2005250105B2/en not_active Ceased
- 2005-05-25 UA UAA200612702A patent/UA87686C2/ru unknown
- 2005-05-25 CN CNA2005800178681A patent/CN1961085A/zh active Pending
- 2005-05-25 RU RU2006146980A patent/RU2366735C2/ru active
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JPS53142301A (en) * | 1977-05-18 | 1978-12-12 | Nippon Steel Corp | Treating method for finely powdered raw material |
US4846884A (en) * | 1981-09-24 | 1989-07-11 | Sumitomo Metal Industries, Ltd. | Process for producing cold-bonded iron ore for use in a blast furnace |
US20020152839A1 (en) * | 1999-11-01 | 2002-10-24 | Jay Aota | Cold bonded iron particulate pellets |
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DATABASE WPI Section Ch Week 197904, Derwent World Patents Index; Class M24, AN 1979-06671B * |
INAZUMI T ET AL: "RECYCLING OF LD CONVERTER SLUDGE AND IRON-BEARING FINES USING THE NCP COLD-BOND-PELLET PROCESS", CONSERVATION AND RECYCLING, PERGAMON PRESS. OXFORD, GB, vol. 6, no. 4, 1983, pages 167 - 179, XP002045280 * |
PATENT ABSTRACTS OF JAPAN vol. 003, no. 019 (C - 037) 17 February 1979 (1979-02-17) * |
See also references of EP1753884A1 * |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
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DE102005062036A1 (de) * | 2005-12-22 | 2007-06-28 | Thyssenkrupp Steel Ag | Agglomeratstein zum Einsatz in Schacht-, Corex- oder Hochöfen |
WO2009068452A1 (de) * | 2007-11-30 | 2009-06-04 | Chemische Fabrik Budenheim Kg | Metallrückstände und kohlenstoffträger enthaltender formkörper |
EP2405025A1 (de) | 2010-07-08 | 2012-01-11 | MFG Metall- und Ferrolegierungsgesellschaft mbh Hafner, Blondin & Tidou | Verfahren zur Herstellung von Legierungsformlingen |
DE102010031101A1 (de) * | 2010-07-08 | 2012-01-12 | Mfg Metall- Und Ferrolegierungsgesellschaft Mbh Hafner, Blondin & Tidou | Verfahren zur Herstellung von Legierungsformlingen |
Also Published As
Publication number | Publication date |
---|---|
EP1753884A1 (de) | 2007-02-21 |
DE102004027193A1 (de) | 2005-12-29 |
RU2366735C2 (ru) | 2009-09-10 |
UA87686C2 (ru) | 2009-08-10 |
BRPI0511806A (pt) | 2008-01-15 |
US20080250980A1 (en) | 2008-10-16 |
CA2569247A1 (en) | 2005-12-15 |
US8025727B2 (en) | 2011-09-27 |
AU2005250105B2 (en) | 2010-07-22 |
AU2005250105A1 (en) | 2005-12-15 |
CN1961085A (zh) | 2007-05-09 |
RU2006146980A (ru) | 2008-07-20 |
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