EP0019086A2 - Process for producing desulfurizing agents for pig iron or steel melts - Google Patents

Process for producing desulfurizing agents for pig iron or steel melts Download PDF

Info

Publication number
EP0019086A2
EP0019086A2 EP80101984A EP80101984A EP0019086A2 EP 0019086 A2 EP0019086 A2 EP 0019086A2 EP 80101984 A EP80101984 A EP 80101984A EP 80101984 A EP80101984 A EP 80101984A EP 0019086 A2 EP0019086 A2 EP 0019086A2
Authority
EP
European Patent Office
Prior art keywords
mixture
calcium oxide
weight
cao content
calcium
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
EP80101984A
Other languages
German (de)
French (fr)
Other versions
EP0019086B1 (en
EP0019086A3 (en
Inventor
Albert Braun
Willi Dr. Portz
Georg Dr. Strauss
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.)
Hoechst AG
Original Assignee
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=6071196&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP0019086(A2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Hoechst AG filed Critical Hoechst AG
Priority to AT80101984T priority Critical patent/ATE2092T1/en
Publication of EP0019086A2 publication Critical patent/EP0019086A2/en
Publication of EP0019086A3 publication Critical patent/EP0019086A3/en
Application granted granted Critical
Publication of EP0019086B1 publication Critical patent/EP0019086B1/en
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 method for producing desulfurizing agents based on calcium oxide-containing calcium carbide for pig iron and steel melts.
  • lime calcium carbide
  • lime calcium oxide
  • 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 dangerous, it was previously thought 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 metal melts.
  • This mixture is then ground with vigorous mixing and with the exclusion of moisture at temperatures above 100 ° C. to particle sizes of less than 10 mm, preferably less than 10 ⁇ m, and the ground product is cooled, likewise with the exclusion of moisture.
  • a calcium carbide-calcium oxide starting melt mixture with a CaO content of 20 to 45% by weight which was obtained in a known manner from lime and coke in a thermal manner.
  • 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 to a CaO content of up to 80% by weight and only then allow the whole to solidify 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 that the lime does not have a specific grain size beforehand must be finely ground, but that it can be assumed that a carbide block whose CaC 2: CaO weight ratio fluctuates within a very wide range, ie can be practically arbitrary, and the lime also in coarse-grained form, for example in a grain size between 8 and 60 mm, can be used.
  • 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.
  • the mixture was then ground in the absence of moisture at a temperature of 100 ° C. to particle sizes between 0 and 100 ⁇ m and the ground product was cooled to room temperature with the exclusion of moisture.
  • 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 - 60 mm is layered on the hot mixture that the through Sectional CaO content is 90% by weight.
  • the mixture is then ground to a grain size of less than 100 ⁇ m with the exclusion of moisture at a temperature above 100 ° C. and the ground product is cooled to room temperature in the absence of moisture.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Treatment Of Steel In Its Molten State (AREA)
  • Refinement Of Pig-Iron, Manufacture Of Cast Iron, And Steel Manufacture Other Than In Revolving Furnaces (AREA)
  • Coating With Molten Metal (AREA)

Abstract

Die vorliegende Erfindung betrifft ein Verfahren zur Herstellung von Entschweflungsmitteln auf Basis von Calciumoxid enthaltendem Calciumcarbid für Roheisen- oder Stahlschmelzen, indem man zunächst aus Kalk und Koks ein Calciumcarbid-Calciumoxid-Schmelzgemisch mit einem CaO-Gehalt von 20 bis 80 Gew% erzeugt, welches man zu einem Block erstarren läßt. Während der erstarrte Block noch eine Durchschnittstemperatur von mehr als 400°C aufweist, bricht man diesen auf Korngrößen kleiner als 150 mm vor und gibt auf das zerkleinerte und noch mindestens 400°C heiße Gemisch Calciumoxid in einer solchen Menge auf, daß der sich in der Mischung ergebende Gesamtgehalt an Ca0 dem im Endprodukt gewünschten CaO-Gehalt entspricht. Anschließend wird die Mischung unter intensiver Vermengung und Feuchtigkeitsausschluß bei Temperaturen oberhalb 100°C auf Korngrößen kleiner als 10 mm gemahlen.The present invention relates to a process for the production of desulphurizing agents based on calcium oxide-containing calcium carbide for pig iron or steel melts, by first producing a calcium carbide-calcium oxide melt mixture with a CaO content of 20 to 80% by weight from lime and coke, which one freezes into a block. While the solidified block still has an average temperature of more than 400 ° C, it is broken down to grain sizes of less than 150 mm and is added to the crushed and still at least 400 ° C hot mixture of calcium oxide in such an amount that the The resulting total Ca0 content corresponds to the CaO content desired in the end product. The mixture is then ground with intensive mixing and exclusion of moisture at temperatures above 100 ° C. to particle sizes smaller than 10 mm.

Description

Die vorliegende Erfindung betrifft ein Verfahren zur Herstellung von Entschweflungsmitteln auf Basis von Calciumoxid enthaltendem Calciumcarbid für Roheisen-und Stahlschmelzen.The present invention relates to a method for producing desulfurizing agents based on calcium oxide-containing calcium carbide for pig iron and steel melts.

Es ist allgemein bekannt, Roheisen- und Stahlschmelzen mit Hilfe von Calciumoxid (nachfolgend kurz als Kalk bezeichnet) enthaltendem Calciumcarbid (nachfolgend Carbid genannt) zu entschwefeln (DE-PS 1 160 457, DE-PS 20 37 758).It is generally known to desulfurize pig iron and steel melts with the aid of calcium carbide (hereinafter referred to as lime) containing calcium oxide (hereinafter referred to as lime) (DE-PS 1 160 457, DE-PS 20 37 758).

Bei der Herstellung solcher Entschweflungsmittel ging man in der Regel bislang so vor, daß man in schmelzflüssiges Carbid die erforderliche Menge an feinteiligem Kalk eintrug, um in der Schmelze eine homogene Mischung zu erzeugen, die man anschließend abkühlen ließ und zerkleinerte.In the manufacture of such desulfurizing agents, the procedure up to now has generally been to add the required amount of finely divided lime to molten carbide in order to produce a homogeneous mixture in the melt, which was then allowed to cool and comminute.

Bevorzugt trug man dabei den feinteiligen Kalk in den Strahl des aus dem Ofen abgestochenen Carbides ein. Obwohl die in Carbidschmelze eintragbare Menge Kalk begrenzt und das Arbeiten mit flüssigem Carbid mit Gefahren verbunden ist, war man in Fachkreisen bisher der Auffassung, auf diese Methode nicht verzichten zu können, da man der Meinung war, nur eine in der Schmelze hergestellte Mischung von CaC2 und Ca0 sei für eine Entschweflung von Metallschmelzen am besten geeignet.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 dangerous, it was previously thought 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 metal melts.

Überraschenderweise wurde nun gefunden, daß man die Nachteile der bekannten Arbeitsweisen vermeiden und ein hochwirksames Entschweflungsmittel für Roheisen- und Stahlschmelzen erhalten kann, wenn man zunächst auf thermischem Wege aus Kalk und Koks ein Carbid-Calciumoxid-Ausgangsschmelzgemisch mit einem beliebigen CaO-Gehalt von 20 bis 30 % erzeugt, welches man durch Abkühlenlassen zu einem Block erstarren läßt. Während der erstarrte Block noch eine Durchschnittstemperatur von mehr als 400°C, vorzugsweise zwischen 400°C und der Erstarrungstemperatur der Schmelze aufweist, bricht man ihn dann auf Korngrößen kleiner als 150 mm vor und gibt auf das zerkleinerte und noch mindestens 4000C heiße Gemisch Calciumoxid in einer solchen Menge auf, daß der sich in der entstehenden Mischung ergebende Gesamtgehalt an Ca0 dem im Endprodukt gewünschten CaO-Gehalt entspricht. Vorzugsweise gibt man so viel Calciumoxid auf, daß sich in der Mischung ein Gesamtgehalt an CaO von über 45 bis 90 Gew% ergibt. Anschließend wird dann diese Mischung unter intensiver Vermengung und unter Feuchtigkeitsausschluß bei Temperaturen oberhalb 100°C auf Korngrößen kleiner als 10 mm, vorzugsweise kleiner als 10 µm, gemahlen und das gemahlene Produkt, ebenfalls unter Ausschluß von Feuchtigkeit, abgekühlt.Surprisingly, it has now been found that the disadvantages of the known procedures can be avoided and a highly effective desulfurizing agent for pig iron and steel melts can be obtained if a carbide-calcium oxide starting molten mixture with any CaO content of 20 to is first obtained thermally from lime and coke 30% generated, which is allowed to solidify into a block by allowing it to cool. While the solidified block still has an average temperature of more than 400 ° C, preferably between 400 ° C and the solidification temperature of the melt is then breaks it to particle sizes smaller than 150 mm and gives onto the crushed and still at least 400 0 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. It is preferable to add enough calcium oxide to give a total CaO content of over 45 to 90% by weight in the mixture. This mixture is then ground with vigorous mixing and with the exclusion of moisture at temperatures above 100 ° C. to particle sizes of less than 10 mm, preferably less than 10 μm, and the ground product is cooled, likewise with the exclusion of moisture.

Vorzugsweise setzt man ein Calciumcarbid-Calciumoxid-Ausgangsschmelzgemisch mit einem CaO-Gehalt von 20 bis 45 Gew% ein, das in bekannter Weise auf thermischem Wege aus Kalk und Koks gewonnen wurde. Man kann aber auch so verfahren, daß man zunächst ein Calciumcarbid-Calciumoxid-Ausgangsschmelzgemisch mit einem CaO-Gehalt von über 45 bis 80 Gew% herstellt, indem man in eine vorliegende Calciumcarbidschmelze, die einen Calciumoxidgehalt bis zu 45 Gew% aufweist, feinteiliges Calciumoxid bis zu einem CaO-Gehalt von maximal bis zu 80 Gew% einträgt und erst dann das Ganze zu einem Block erstarren läßt, bevor man diesen bei Temperaturen oberhalb 400°C vorbricht.It is preferable to use a calcium carbide-calcium oxide starting melt mixture with a CaO content of 20 to 45% by weight, which was obtained in a known manner from lime and coke in a thermal manner. However, one can also proceed in such a way that 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 to a CaO content of up to 80% by weight and only then allow the whole to solidify into a block before breaking it at temperatures above 400 ° C.

Außer daß das Vermischen des Kalkes mit einer Carbidschmelze und den damit verbundenen Schwierigkeiten vermieden werden kann, besitzt das erfindungsgemäße Verfahren u.a. auch die weiteren Vorteile, daß zur Erzeugung der Carbidschmelze nicht jeweils eine bestimmte Möllerzusammensetzung eingestellt, und daß der Kalk vorher nicht auf eine bestimmte Korngröße feingemahlen werden muß, sondern daß von einem Carbidblock ausgegangen werden kann, dessen CaC2 : CaO-Gewichtsverhältnis innerhalb eines sehr weiten Bereiches schwanken, d.h. praktisch beliebig sein kann und der Kalk auch in grobkörniger Form, beispielsweise in einer Korngröße zwischen 8 und 60 mm,eingesetzt werden kann.In addition to the fact that the mixing of the lime with a carbide melt and the difficulties associated with it can be avoided, 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 that the lime does not have a specific grain size beforehand must be finely ground, but that it can be assumed that a carbide block whose CaC 2: CaO weight ratio fluctuates within a very wide range, ie can be practically arbitrary, and the lime also in coarse-grained form, for example in a grain size between 8 and 60 mm, can be used.

Beispiel 1example 1

Aus einer für die Herstellung von technischem Carbid üblichen Schmelze mit einem CaC2-Gehalt von 80 Gew% und CaO-Gehalt von 20 Gew% wurde in einem Tiegel durch Abkühlenlassen dieser Schmelze in bekannter Weise ein Carbidblock entsprechender Zusammensetzung erzeugt.From a melt customary for the production of technical carbide with a CaC 2 content of 80% by weight and a CaO content of 20% by weight, a carbide block of the appropriate composition was produced in a crucible in a known manner by allowing this melt to cool.

Nachdem sich der Block auf eine Durchschnittstemperatur von etwa 600°C abgekühlt hatte, wurde er auf Korngrößen kleiner als 150 mm vorgebrochen und das noch 500°C heiße Carbid mit so viel Kalk einer Korngröße von 8 bis 60 mm überschichtet, daß die sich ergebende Mischung einen Ca0-Gehalt von insgesamt 50 Gew% enthielt.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.

Anschließend wurde die Mischung unter Ausschluß von Feuchtigkeit bei einer Temperatur von 100°C auf Korngrößen zwischen 0 und 100 µm gemahlen und das gemahlene Produkt unter Feuchtigkeitsausschluß auf Raumtemperatur abgekühlt.The mixture was then ground in the absence of moisture at a temperature of 100 ° C. to particle sizes between 0 and 100 μm and the ground product was cooled to room temperature with the exclusion of moisture.

Mit 1500 kg von diesem Produkt wurden 300 000 kg einer Roheisenschmelze, die 0,03 Gew% Schwefel enthielt, in bekannter Weise entschwefelt. Der S-Gehalt des behandelten Eisens betrug weniger als 0,005 Gew%.With 1500 kg of this product, 300,000 kg of a pig iron melt containing 0.03% by weight of sulfur were desulfurized in a known manner. The S content of the treated iron was less than 0.005% by weight.

Beispiel 2Example 2

In bekannter Weise wird aus Kalk und Koks Calciumcarbid thermisch hergestellt, wobei die Kalk-Koks-Mischung im gesamten Möller auf ein Gewichtsverhältnis von etwa 110 :

  • 40 eingestellt wird, was einem Carbid mit einem CaO-Gehalt von etwa 45 Gew% entspricht.
Calcium carbide is thermally produced in a known manner from lime and coke, the lime-coke mixture in the entire Möller to a weight ratio of about 110:
  • 40 is set, which corresponds to a carbide with a C aO content of about 45% by weight.

Dem Abstichstrahl dieses Carbides wird Ca0 der Körnung 3 - 8 mm in einer solchen Menge zudosiert, daß sich im Abstichtiegel ein Durchschnittsgehalt von ca. 80 Gew% Ca0 ergibt (auf 1 Tonne Abstichstrahl etwa 1,2-1,3t Ca0).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).

Nach dem Abkühlen des Tiegels auf eine Durchschnittstemperatur von nicht unter 600°C, was bereits nach 4 Stunden der Fall ist, wird der Block auf eine Korngröße kleiner als 150 mm vorgebrochen und auf das heiße Gemisch so viel Kalk der Körnung 8 - 60 mm geschichtet, daß der Durchschnitts-CaO-Gehalt 90 Gew% beträgt. Anschließend wird unter Ausschluß von Feuchtigkeit bei einer Temperatur oberhalb 100°C auf eine Korngröße kleiner als 100 µm gemahlen und das gemahlene Produkt unter Ausschluß von Feuchtigkeit auf Zimmertemperatur abgekühlt.After the crucible has cooled to an average temperature of not less than 600 ° C, which is already the case after 4 hours, the block is pre-crushed to a grain size of less than 150 mm and as much lime with a grain size of 8 - 60 mm is layered on the hot mixture that the through Sectional CaO content is 90% by weight. The mixture is then ground to a grain size of less than 100 μm with the exclusion of moisture at a temperature above 100 ° C. and the ground product is cooled to room temperature in the absence of moisture.

Mit diesem Gemisch werden, bezogen auf den Calciumcarbidgehalt, die gleichen Entschwefelungsergebnisse erzielt, wie im Beispiel 1 geschildert.With this mixture, based on the calcium carbide content, the same desulfurization results are achieved as described in Example 1.

Claims (6)

1. Verfahren zur Herstellung von Entschweflungsmitteln auf Basis von Calciumoxid enthaltendem Calciumcarbid für Roheisen- und Stahlschmelzen, dadurch gekennzeichnet, daß man zunächst aus Kalk und Koks ein Calciumcarbid-Calciumoxid-Schmelzgemisch mit einem CaO-Gehalt von 20 bis 80 Gew% erzeugt, welches man durch Abkühlenlassen zu einem Block erstarren läßt; daß man dann, während der erstarrte Block noch eine Durchschnittstemperatur von mehr als 400°C aufweist, diesen auf Korngrößen kleiner als 150 mm vorbricht und auf das zerkleinerte und noch mindestens 400°C heiße Gemisch Calciumoxid in einer solchen Menge aufgibt, daß der sich in der entstehenden Mischung ergebende Gesamt- gehalt an Ca0 dem im Endprodukt gewünschten CaO-Gehalt entspricht, anschließend die Mischung unter intensiver Vermengung und Feuchtigkeitsausschluß bei Temperaturen oberhalb 100°C auf Korngrößen kleiner als 10 mm mahlt und man das gemahlene Produkt, ebenfalls unter Ausschluß von Feuchtigkeit,abkühlen läßt.1. A process for the preparation of desulfurizing agents based on calcium oxide-containing calcium carbide for pig iron and steel melts, characterized in that a calcium carbide-calcium oxide melt mixture with a CaO content of 20 to 80% by weight is first produced from lime and coke, which one solidify by cooling to a block; that one then, while the solidified block still has an average temperature of more than 400 ° C, breaks it down to grain sizes smaller than 150 mm and gives up on the crushed and still at least 400 ° C hot mixture calcium oxide in such an amount that the the resulting total Ca0 content corresponds to the desired CaO content in the end product, then the mixture is milled to a particle size of less than 10 mm with intensive mixing and exclusion of moisture at temperatures above 100 ° C. and the ground product is allowed to cool, also in the absence of moisture. 2. Verfahren nach Anspruch 1, dadurch gekennzeichnet, daß man auf das vorgebrochene Gemisch grobkörniges Ca0 mit einer Korngröße von 8 bis 60 mm aufgibt.2. The method according to claim 1, characterized in that one gives up coarse-grained Ca0 with a grain size of 8 to 60 mm on the pre-broken mixture. 3. Verfahren nach Anspruch 1 oder 2, dadurch gekennzeichnet, daß man auf das vorgebrochene Gemisch so viel Ca0 aufgibt, daß die entstehende Mischung über 45 bis 90 Gew% Ca0 enthält.3. The method according to claim 1 or 2, characterized in that so much Ca0 is added to the pre-broken mixture that the resulting mixture contains over 45 to 90% by weight Ca0. 4. Verfahren nach einem der Ansprüche 1 bis 3, dadurch gekennzeichnet, daß man das Vorbrechen bei Temperaturen zwischen 400°C und der Erstarrungstemperatur vornimmt.4. The method according to any one of claims 1 to 3, characterized in that the preliminary breaking is carried out at temperatures between 400 ° C and the solidification temperature. 5. Verfahren nach einem der Ansprüche 1 bis 4, dadurch gekennzeichnet, daß man das Calciumcarbid-Calciumoxid-Ausgangsschmelzgemisch mit einem CaO-Gehalt von 20 - 45 Gewichts% in bekannter Weise aus Kalk und Koks auf thermischem Wege gewinnt.5. The method according to any one of claims 1 to 4, characterized in that the calcium carbide-calcium oxide starting melt mixture with a CaO content of 20-45% by weight is obtained in a known manner from lime and coke by thermal means. 6. Verfahren nach einem der Ansprüche 1 bis 4, dadurch gekennzeichnet, daß man das Calciumcarbid-Calciumoxid Ausgangsschmelzgemisch mit einem CaO-Gehalt von über 45 bis 80 Gewichts% herstellt, indem man in eine vorliegende Calciumcarbidschmelze, die einen Calciumoxidgehalt bis zu 45 Gewichts% aufweist, feinteiliges Calciumoxid bis zu einem CaO-Gehalt von maximal bis zu 80 Gewichts% einträgt und erst dann zu einem Block erstarren läßt.6. The method according to any one of claims 1 to 4, characterized in that one produces the calcium carbide-calcium oxide starting melt mixture with a CaO content of over 45 to 80% by weight by in a present calcium carbide melt having a calcium oxide content of up to 45% by weight has, finely divided calcium oxide up to a CaO content of up to 80% by weight and only then solidifies into a block.
EP80101984A 1979-05-19 1980-04-14 Process for producing desulfurizing agents for pig iron or steel melts Expired EP0019086B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT80101984T ATE2092T1 (en) 1979-05-19 1980-04-14 PROCESS FOR THE MANUFACTURE OF DESULPHURIZING AGENTS FOR MELTED PIG IRON OR STEEL.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19792920353 DE2920353A1 (en) 1979-05-19 1979-05-19 METHOD FOR THE PRODUCTION OF DEHANIZING AGENTS FOR CRUDE IRON OR STEEL MELT
DE2920353 1979-05-19

Publications (3)

Publication Number Publication Date
EP0019086A2 true EP0019086A2 (en) 1980-11-26
EP0019086A3 EP0019086A3 (en) 1981-04-01
EP0019086B1 EP0019086B1 (en) 1982-12-22

Family

ID=6071196

Family Applications (1)

Application Number Title Priority Date Filing Date
EP80101984A Expired EP0019086B1 (en) 1979-05-19 1980-04-14 Process for producing desulfurizing agents for pig iron or steel melts

Country Status (9)

Country Link
US (1) US4318822A (en)
EP (1) EP0019086B1 (en)
JP (1) JPS55154519A (en)
AT (1) ATE2092T1 (en)
CA (1) CA1141965A (en)
DE (2) DE2920353A1 (en)
ES (1) ES8101120A1 (en)
NO (1) NO151971C (en)
ZA (1) ZA802943B (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0061012A1 (en) * 1981-03-24 1982-09-29 Hoechst Aktiengesellschaft Process for producing desulfurizing agents for pig iron and steel melts
EP0061011A1 (en) * 1981-03-24 1982-09-29 Hoechst Aktiengesellschaft Process for producing desulfurizing agents for pig iron or steel melts
EP0031534B1 (en) * 1979-12-29 1984-08-22 Hoechst Aktiengesellschaft Process for producing desulfurizing agents for pig iron or steel melts
EP0220522A1 (en) * 1985-10-03 1987-05-06 Hoechst Aktiengesellschaft Mixture for desulfurizing metal melts, process for manufacturing it and its use

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5002733A (en) * 1989-07-26 1991-03-26 American Alloys, Inc. Silicon alloys containing calcium and method of making same
US5397379A (en) * 1993-09-22 1995-03-14 Oglebay Norton Company Process and additive for the ladle refining of steel
US6179895B1 (en) 1996-12-11 2001-01-30 Performix Technologies, Ltd. Basic tundish flux composition for steelmaking processes
CN107344188A (en) * 2017-07-28 2017-11-14 靖西天桂铝业有限公司 Bauxite washing tail mud dry treatment and comprehensive utilization new technology

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AT264560B (en) * 1966-08-25 1968-09-10 Gustav Dipl Ing Wolfram Basic steelmaking process
DE1919414B2 (en) * 1969-04-17 1977-07-14 Hoechst Ag, 6000 Frankfurt METHOD AND DEVICE FOR COOLING CALCIUM CARBIDE PICKED IN VESSELS
DE1935567B2 (en) * 1969-07-12 1971-05-13 Knapsack AG, 5033 Hurth Knapsack PROCESS FOR THE PRODUCTION OF CALCIUM CARBIDE OF CERTAIN QUALITY
DE2037758C3 (en) * 1970-07-30 1979-08-02 Hoechst Ag, 6000 Frankfurt Process for the production of calcium carbide for the desulfurization of metal melts
DE2326539C3 (en) * 1973-05-24 1975-11-13 Sueddeutsche Kalkstickstoff-Werke Ag, 8223 Trostberg Process for the production of a desulphurisation mixture for iron melts from calcium carbide and at least one water-containing substance
FR2290240A1 (en) * 1974-11-06 1976-06-04 Unibra Sa IMPROVEMENTS IN GAS DESULFURATION
DE2919324A1 (en) * 1979-05-14 1980-12-04 Hoechst Ag DEHANIZER FOR RAW IRON AND STEEL MELTING AND A METHOD FOR THE PRODUCTION THEREOF

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0031534B1 (en) * 1979-12-29 1984-08-22 Hoechst Aktiengesellschaft Process for producing desulfurizing agents for pig iron or steel melts
EP0061012A1 (en) * 1981-03-24 1982-09-29 Hoechst Aktiengesellschaft Process for producing desulfurizing agents for pig iron and steel melts
EP0061011A1 (en) * 1981-03-24 1982-09-29 Hoechst Aktiengesellschaft Process for producing desulfurizing agents for pig iron or steel melts
EP0220522A1 (en) * 1985-10-03 1987-05-06 Hoechst Aktiengesellschaft Mixture for desulfurizing metal melts, process for manufacturing it and its use

Also Published As

Publication number Publication date
EP0019086B1 (en) 1982-12-22
ATE2092T1 (en) 1983-01-15
NO151971C (en) 1985-07-10
DE3061404D1 (en) 1983-01-27
ES491355A0 (en) 1980-12-16
EP0019086A3 (en) 1981-04-01
JPS6353245B2 (en) 1988-10-21
JPS55154519A (en) 1980-12-02
US4318822A (en) 1982-03-09
CA1141965A (en) 1983-03-01
NO151971B (en) 1985-04-01
DE2920353A1 (en) 1980-11-27
ES8101120A1 (en) 1980-12-16
ZA802943B (en) 1981-06-24
NO801468L (en) 1980-11-20

Similar Documents

Publication Publication Date Title
EP0061012B1 (en) Process for producing desulfurizing agents for pig iron and steel melts
DD223468A5 (en) METHOD AND DEVICE FOR PRODUCING LIQUID RAW STEEL OR STEEL PREPARED PRODUCTS
EP0019086A2 (en) Process for producing desulfurizing agents for pig iron or steel melts
DE2037758C3 (en) Process for the production of calcium carbide for the desulfurization of metal melts
EP0031552B1 (en) Desulphurising composition and process for its production
EP0220522B1 (en) Mixture for desulfurizing metal melts, process for manufacturing it and its use
EP0031534B1 (en) Process for producing desulfurizing agents for pig iron or steel melts
EP0019087B1 (en) Desulphurising agents for pig iron and steel melts, and process for their manufacture
DE3739154A1 (en) LEADING ADDITIVE FOR STEEL MELTING
DE2708424C2 (en) Process for desulfurization of pig iron melts
DE2709062A1 (en) MEANS AND METHODS FOR DESULFURIZING METAL IRON
EP0061011B1 (en) Process for producing desulfurizing agents for pig iron or steel melts
DE2303668C3 (en) Preparations for treating molten steel
EP0582970A1 (en) Additive for desulfurization of liquid pig and cast iron and process for desulfurizing
DE2236160C3 (en) Means for desulphurizing liquid pig iron and process for its manufacture
DE724643C (en) Process for the production of Thomas slag with a high content of ammonium citrate-soluble phosphoric acid
DE835613C (en) Cleaning agent for iron and steel melts
DE2048203B2 (en) Casting aids for use in casting metal
DE3310329C2 (en)
DE2658315C2 (en) Reducing agents for steel production
DE2952761A1 (en) Desulphurising of molten metals, esp. crude iron or steel - using mixed crystals of calcium carbide and calcium oxide which is partly hydrated
DE3000927C2 (en) Desulfurization of ferrous metals
DE2507160A1 (en) METHOD FOR MANUFACTURING HIGH-DURABILITY CAST IRON AND REFINING AGENTS TO PERFORM THEREOF
DE1235966B (en) Process for the production of graphite steel
EP0884395A1 (en) Agent for fluoride-free treatment of steel melts in the casting ladle, process for its manufacture and its use

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Designated state(s): AT BE DE FR GB IT LU NL SE

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Designated state(s): AT BE DE FR GB IT LU NL SE

17P Request for examination filed

Effective date: 19810408

ITF It: translation for a ep patent filed
GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Designated state(s): AT BE DE FR GB IT LU NL SE

REF Corresponds to:

Ref document number: 2092

Country of ref document: AT

Date of ref document: 19830115

Kind code of ref document: T

REF Corresponds to:

Ref document number: 3061404

Country of ref document: DE

Date of ref document: 19830127

ET Fr: translation filed
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19830430

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

26 Opposition filed

Opponent name: SKW TROSTBERG AKTIENGESELLSCHAFT

Effective date: 19830921

PLBN Opposition rejected

Free format text: ORIGINAL CODE: 0009273

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: OPPOSITION REJECTED

27O Opposition rejected

Effective date: 19841108

NLR2 Nl: decision of opposition
PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 19900322

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: SE

Payment date: 19900326

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: LU

Payment date: 19900328

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: AT

Payment date: 19900329

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 19900331

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: BE

Payment date: 19900411

Year of fee payment: 11

ITTA It: last paid annual fee
PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 19900430

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 19900618

Year of fee payment: 11

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Effective date: 19910414

Ref country code: AT

Effective date: 19910414

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Effective date: 19910415

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Effective date: 19910430

BERE Be: lapsed

Owner name: HOECHST A.G.

Effective date: 19910430

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Effective date: 19911101

GBPC Gb: european patent ceased through non-payment of renewal fee
NLV4 Nl: lapsed or anulled due to non-payment of the annual fee
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Effective date: 19911230

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Effective date: 19920201

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

EUG Se: european patent has lapsed

Ref document number: 80101984.5

Effective date: 19911108