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EP0061011A1 - Procédé pour la fabrication d'agents de désulfuration de fonte ou d'acier fondus - Google Patents

Procédé pour la fabrication d'agents de désulfuration de fonte ou d'acier fondus Download PDF

Info

Publication number
EP0061011A1
EP0061011A1 EP82101427A EP82101427A EP0061011A1 EP 0061011 A1 EP0061011 A1 EP 0061011A1 EP 82101427 A EP82101427 A EP 82101427A EP 82101427 A EP82101427 A EP 82101427A EP 0061011 A1 EP0061011 A1 EP 0061011A1
Authority
EP
European Patent Office
Prior art keywords
mixture
weight
calcium oxide
calcium
content
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP82101427A
Other languages
German (de)
English (en)
Other versions
EP0061011B1 (fr
Inventor
Albert Braun
Willi Dr. Portz
Georg Dr. Strauss
Hans-Martin Dipl.-Ing. Delhey
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Krupp Stahl AG
Hoechst AG
Original Assignee
Krupp Stahl AG
Hoechst AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Krupp Stahl AG, Hoechst AG filed Critical Krupp Stahl AG
Priority to AT82101427T priority Critical patent/ATE9596T1/de
Publication of EP0061011A1 publication Critical patent/EP0061011A1/fr
Application granted granted Critical
Publication of EP0061011B1 publication Critical patent/EP0061011B1/fr
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21CPROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
    • C21C1/00Refining of pig-iron; Cast iron
    • C21C1/02Dephosphorising or desulfurising
    • C21C1/025Agents used for dephosphorising or desulfurising
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21CPROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
    • C21C7/00Treating molten ferrous alloys, e.g. steel, not covered by groups C21C1/00 - C21C5/00
    • C21C7/04Removing impurities by adding a treating agent
    • C21C7/064Dephosphorising; Desulfurising
    • C21C7/0645Agents used for dephosphorising or desulfurising

Definitions

  • the present invention relates to a process for the production of desulfurization agents with a content of 1-6% by weight of chemically bound water based on calcium oxide and carbon-containing calcium carbide for pig iron and steel melts.
  • the finely divided lime was preferably introduced into the jet of carbide tapped from the furnace. Although the amount of lime that can be introduced into the molten carbide is limited and working with liquid carbide is associated with dangers, it was previously believed in specialist circles that this method could not be dispensed with because it was believed that only a mixture of CaC produced in the melt 2 and Ca0 are best suited for the desulfurization of molten metals. Desulphurization agents based on calcium carbide, which contain substances that release water at the temperature of the molten metal, are already known from DE-AS 22 52 795.
  • These agents which are mixtures of commercially available carbide with, for example, Ca (OH) 2 as water-releasing substance and possibly carbon, have the disadvantage that they are mixtures produced by mechanical mixing, in which carbide particles are present separately from Ca (OH) 2 particles , which leads to a higher consumption, uneven and violent gas reactions and a large spread regarding the desulfurization effect when using these products, which makes a targeted use of these agents difficult.
  • the solidified block still has an average temperature of more than 400 ° C, preferably between 400 ° C and the solidification temperature of the melt, it is then broken down to grain sizes less than 150 mm and added to the comminuted and still at least 400 ° C hot mixture Calcium oxide in such an amount that the total Ca0 content in the resulting mixture corresponds to the CaO content desired in the end product. So much calcium oxide is preferably added that a total Ca0 content of over 45 to 90% by weight results in the mixture.
  • this mixture is then mixed intensively with free carbon and carbonate in the presence of air or nitrogen with a moisture content of 5 to 20 g / m 3 (at 1.013 bar and 273.15 K) at temperatures below 100 ° C., preferably at 10-50 ° C., to particle sizes less than 10 mm, preferably smaller than 0.1 mm, ground.
  • the end product contains 0.5 to 8% by weight of free carbon and 0.5 to 20% by weight of carbonates of calcium, magnesium or sodium.
  • a calcium carbide-calcium oxide starting melt mixture with a Ca0 content of 20 to 45% by weight is used, which was obtained in a known manner by thermal means from lime and coke.
  • a calcium carbide-calcium oxide starting melt mixture with a CaO content of over 45 to 80% by weight is first prepared by adding finely divided calcium oxide to an existing calcium carbide melt which has a calcium oxide content of up to 45% by weight enters a Ca0 content of at most 80% by weight and only then solidifies the whole into a block before breaking it at temperatures above 400 ° C.
  • the process according to the invention also has the further advantages, inter alia, that a certain Möller composition is not set in each case to produce the carbide melt and the lime is not finely ground beforehand to a specific grain size must, but that it can be assumed that a carbide block, the CaC 2: CaO weight ratio fluctuate within a very wide range, ie practically any can be, and the lime can also be used in coarse-grained form, for example in a grain size between 8 and 60 mm.
  • composition according to the invention is that present on the surface of each grain Ca (OH) 2 close to CaC 2, whereby the desulfurizing very early and is set uniformly in motion. With comparable desulfurization results, smaller amounts of the desulfurization agent are required and more targeted results are possible.
  • the block After the block had cooled to an average temperature of about 600 ° C, it was crushed to grain sizes smaller than 150 mm and the carbide, which was still 500 ° C, was covered with so much lime with a grain size of 8 to 60 mm that the resulting mixture contained a total Ca0 content of 50% by weight.
  • 850 kg of this mixture were mixed with 100 kg of limestone (grain size less than 1 mm) and 50 kg of coke breeze (grain size less than 3 mm) and with a passage of 1500 m 3 / h of air with a moisture content of 10 g / m 3 (at 15 ° C ) milled in a rotary mill with a throughput of 500 kg / h at 50 ° C to grain sizes between 0 and 0.1 mm.
  • the product obtained contained 2% by weight of chemically bound water.
  • Calcium carbide is produced thermally from lime and coke in a known manner, the lime-coke mixture in the entire Möller being adjusted to a weight ratio of approximately 110:40, which corresponds to a carbide with a CaO content of approximately 45% by weight.
  • Ca0 with a grain size of 3-8 mm is added to the tapping jet of this carbide in such an amount that an average content of approx. 80% by weight Ca0 results in the tapping crucible (about 1.2-1.3 t Ca0 per tonne of tapping jet).
  • the block is pre-crushed to a grain size of less than 150 mm and as much lime with a grain size of 8 to 60 mm is layered on the hot mixture. that the average Ca0 content is 90% by weight.
  • 875 kg of this mixture are mixed with 100 kg of limestone (grain size less than 1 mm) and 25 kg of coke breeze (grain size less than 3 mm) and with passage of 1500 m 3 / h of air with a moisture content of 10 g / m 3 (at 15 0 C ) in a rotary mill with a throughput of 500 kg / h at 50 ° C to a grain size smaller than 0.1 mm.
  • the product obtained contains 2.5% by weight of chemically bound water.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Refinement Of Pig-Iron, Manufacture Of Cast Iron, And Steel Manufacture Other Than In Revolving Furnaces (AREA)
  • Treatment Of Steel In Its Molten State (AREA)
  • Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
  • Manufacture And Refinement Of Metals (AREA)
EP82101427A 1981-03-24 1982-02-25 Procédé pour la fabrication d'agents de désulfuration de fonte ou d'acier fondus Expired EP0061011B1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT82101427T ATE9596T1 (de) 1981-03-24 1982-02-25 Verfahren zur herstellung von entschwefelungsmitteln fuer roheisen- oder stahlschmelzen.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE3111509 1981-03-24
DE19813111509 DE3111509A1 (de) 1981-03-24 1981-03-24 Verfahren zur herstellung von entschwefelungsmitteln fuer roheisen- oder stahlschmelzen

Publications (2)

Publication Number Publication Date
EP0061011A1 true EP0061011A1 (fr) 1982-09-29
EP0061011B1 EP0061011B1 (fr) 1984-09-26

Family

ID=6128139

Family Applications (1)

Application Number Title Priority Date Filing Date
EP82101427A Expired EP0061011B1 (fr) 1981-03-24 1982-02-25 Procédé pour la fabrication d'agents de désulfuration de fonte ou d'acier fondus

Country Status (10)

Country Link
US (1) US4400292A (fr)
EP (1) EP0061011B1 (fr)
JP (1) JPS57169010A (fr)
AT (1) ATE9596T1 (fr)
BR (1) BR8201618A (fr)
CA (1) CA1184384A (fr)
DD (1) DD202183A5 (fr)
DE (2) DE3111509A1 (fr)
ES (1) ES510769A0 (fr)
ZA (1) ZA821939B (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0220522A1 (fr) * 1985-10-03 1987-05-06 Hoechst Aktiengesellschaft Mélange désulfurant pour bains métalliques, son procédé de fabrication et son utilisation

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2326539A1 (de) * 1973-05-24 1974-12-12 Sueddeutsche Kalkstickstoff Verfahren zur herstellung wasserhaltiger gemische auf basis calciumcarbid fuer die entschwefelung von metallschmelzen
DE2236160C3 (de) * 1971-07-26 1975-10-09 Acieries Reunies De Burbach-Eichdudelange S.A. Arbed, Luxemburg Mittel zur Entschwefelung von flüssigem Roheisen und Verfahren zu seiner Herstellung
DE2252795B2 (de) * 1972-10-27 1977-02-03 Süddeutsche Kalkstickstoff-Werke AG, 8223 Trostberg Entschwefelungsmittel fuer metallschmelzen mit wasserabspaltendem zusatz
DE2741588A1 (de) * 1977-09-15 1979-03-29 Sueddeutsche Kalkstickstoff Mittel zum entschwefeln von eisenschmelzen
DE2037758C3 (de) * 1970-07-30 1979-08-02 Hoechst Ag, 6000 Frankfurt Verfahren zur Herstellung von CaIciumkarbid zur Entschwefelung von Metallschmelzen
EP0019086A2 (fr) * 1979-05-19 1980-11-26 Hoechst Aktiengesellschaft Procédé pour la fabrication d'agents de désulfurisation de fonte ou d'acier fondus
EP0031534A1 (fr) * 1979-12-29 1981-07-08 Hoechst Aktiengesellschaft Procédé pour la fabrication d'agents de désulfuration de fonte ou d'acier fondus
EP0031552A1 (fr) * 1979-12-29 1981-07-08 Hoechst Aktiengesellschaft Agent de désulfuration et procédé pour sa fabrication
EP0019087B1 (fr) * 1979-05-14 1983-07-20 Hoechst Aktiengesellschaft Matières de désulfuration pour bains de fonte et d'acier ainsi que procédé pour leur fabrication

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1408188A1 (de) * 1959-12-19 1968-10-17 Hoesch Ag Verfahren zur Entschwefelung von Roheisenbaedern
AT264560B (de) * 1966-08-25 1968-09-10 Gustav Dipl Ing Wolfram Basisches Stahlherstellungsverfahren
IT1047585B (it) * 1975-09-26 1980-10-20 Centro Speriment Metallurg Perfezionamento alla disossidazione e desolforazione dell acciaio

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2037758C3 (de) * 1970-07-30 1979-08-02 Hoechst Ag, 6000 Frankfurt Verfahren zur Herstellung von CaIciumkarbid zur Entschwefelung von Metallschmelzen
DE2236160C3 (de) * 1971-07-26 1975-10-09 Acieries Reunies De Burbach-Eichdudelange S.A. Arbed, Luxemburg Mittel zur Entschwefelung von flüssigem Roheisen und Verfahren zu seiner Herstellung
DE2252795B2 (de) * 1972-10-27 1977-02-03 Süddeutsche Kalkstickstoff-Werke AG, 8223 Trostberg Entschwefelungsmittel fuer metallschmelzen mit wasserabspaltendem zusatz
DE2326539A1 (de) * 1973-05-24 1974-12-12 Sueddeutsche Kalkstickstoff Verfahren zur herstellung wasserhaltiger gemische auf basis calciumcarbid fuer die entschwefelung von metallschmelzen
DE2741588A1 (de) * 1977-09-15 1979-03-29 Sueddeutsche Kalkstickstoff Mittel zum entschwefeln von eisenschmelzen
EP0019087B1 (fr) * 1979-05-14 1983-07-20 Hoechst Aktiengesellschaft Matières de désulfuration pour bains de fonte et d'acier ainsi que procédé pour leur fabrication
EP0019086A2 (fr) * 1979-05-19 1980-11-26 Hoechst Aktiengesellschaft Procédé pour la fabrication d'agents de désulfurisation de fonte ou d'acier fondus
EP0031534A1 (fr) * 1979-12-29 1981-07-08 Hoechst Aktiengesellschaft Procédé pour la fabrication d'agents de désulfuration de fonte ou d'acier fondus
EP0031552A1 (fr) * 1979-12-29 1981-07-08 Hoechst Aktiengesellschaft Agent de désulfuration et procédé pour sa fabrication

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0220522A1 (fr) * 1985-10-03 1987-05-06 Hoechst Aktiengesellschaft Mélange désulfurant pour bains métalliques, son procédé de fabrication et son utilisation

Also Published As

Publication number Publication date
ZA821939B (en) 1983-02-23
CA1184384A (fr) 1985-03-26
DD202183A5 (de) 1983-08-31
EP0061011B1 (fr) 1984-09-26
BR8201618A (pt) 1983-02-08
DE3260809D1 (en) 1984-10-31
JPH0135883B2 (fr) 1989-07-27
ES8302104A1 (es) 1983-02-01
US4400292A (en) 1983-08-23
DE3111509A1 (de) 1982-10-07
ATE9596T1 (de) 1984-10-15
ES510769A0 (es) 1983-02-01
JPS57169010A (en) 1982-10-18

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