Title of Invention	METHOD FOR DECHROMING AND/OR DENICKELFYING LIQUID SLAGS.
Abstract	In a method for dechroming and/or denickelifying liquid slags or slag mixtures, in which the liquid slag is charged onto a metal bath, in particular an iron bath, and reduced by feeding carbon or carbon carriers, the carbon feed into the metal bath is effected until a decrease of the Cr and/or Ni oxide contents of the slag to a value of between 0.8 wt.-% and 0.2 wt.-%. As the pregiven Cr oxide content range of the slag is reached, reductants having higher reduction potentials such as, e.g. , Al, Ca, Si, Fe-Si or Ca-Si are added in order to lower the Cr and/or Ni oxide contents to below 0.15 wt.-%, preferably below 0.08 wt.-%.

Title of Invention

METHOD FOR DECHROMING AND/OR DENICKELFYING LIQUID SLAGS.

Abstract

In a method for dechroming and/or denickelifying liquid slags or slag mixtures, in which the liquid slag is charged onto a metal bath, in particular an iron bath, and reduced by feeding carbon or carbon carriers, the carbon feed into the metal bath is effected until a decrease of the Cr and/or Ni oxide contents of the slag to a value of between 0.8 wt.-% and 0.2 wt.-%. As the pregiven Cr oxide content range of the slag is reached, reductants having higher reduction potentials such as, e.g. , Al, Ca, Si, Fe-Si or Ca-Si are added in order to lower the Cr and/or Ni oxide contents to below 0.15 wt.-%, preferably below 0.08 wt.-%.

Full Text	- l - Method for Dechroming and/or Denickelifying Liquid Slags The invention relates to a method for dechroming and/or denickelifying liquid slags or slag mixtures and dusts, in which the liquid slag is charged onto a metal bath, in particular an iron bath, and reduced by feeding carbon or carbon carriers. Liquid steelworks slags derived from the production of special steels or ferrochromium, depending on their origin and, in particular, on the portion and composition of the scrap admixtures applied in the production of steel, above all contain relatively high amounts of chromium oxide. Also manganese oxides are found in relatively high amounts. In certain steel slags, even relatively high nickel and relatively high vanadium contents are observed. In the case of steel slags having relatively high vanadium contents, it has already been proposed in EP 770 149 to recover, after a first reduction process using carbon carriers, vanadium in a separate consecutively arranged reduction converter using reductants having higher reduction potentials. To this end, all of the chromium and manganese was, at first, reduced carbothermally, wherefor the slag was treated over an extended period of time above a metal bath into which carbon carriers such as, for instance, methane gas were injected. A quite considerable portion of the amount of carbon introduced was consumed in order to maintain the necessary temperatures because of the relatively long treatment time proposed. The use of a separate reduction reactor which, as a rule, also was to be heated separately, for the separation of vanadium naturally will be economically effective only if vanadium is present in accordingly high amounts with the economy resulting from the value of the recovered vanadium. If, in the first place, the dechroming of steel slags to as large an extent as possible is to be envisaged, this will involve relatively long - 2 - treatment times and hence relatively high thermal losses in the known mode of procedure. The invention aims to enhance a method of the initially defined kind to the extent that the safe dechroming under the simultaneous reduction of the overall treatment time will be feasible even if economic credits by the recovery of expensive metallic raw materials cannot be ensured. To solve this object, the method according to the invention essentially consists in that the carbon feed into the metal bath is effected until a decrease of the Cr and/or Ni oxide contents of the slag to a value of between 0.8 wt.-% and 0.2 wt.-% and that, upon attainment of the pregiven Cr oxide content range of the slag, reductants having higher reduction potentials such as, e.g., Al, Ca, Si, Fe-Si or Ca-Si are added in order to lower the Cr and/or Ni oxide contents to below 0.15 wt.-%, preferably below 0.08 wt.-%. The method according to the invention is, thus, carried out using but a single converter, wherein, due to the fact that the carbothermal reduction using carbon carriers such as, e.g., hydrocarbons is stopped already at a point of time at which the slag has still a relatively high chromium or Ni oxide content which, as a rule, is unacceptable to the effect that such slags cannot be directly used as cement grinding additives, the treatment time is substantially shortened until that point of time and, due to the fact that upon attainment of such predefined and relatively high chromium and/or Ni oxide contents reductants having higher reduction potentials are then immediately added in the same converter, it is feasible to complete the method within a relatively short period of time and bring the chromium and/or Ni oxide contents safely below the pregiven limit values. By such a stepwise reduction, it is, of course, feasible to lower the contents of also other special steel accompanying elements such as, e.g., molybdenum or vanadium in the slags to noncritical values. - 3 - In this respect, within the context of the method according to the invention, it is advantageously proceeded such that the addition of Fe-Si is effected in amounts ranging from 3 to 15 kg/ton slag, preferably 6 to 10 kg/ton slag. If other substances capable of being reduced by such reductants were contained in the slag, such as, for instance, vanadium oxide, manganese oxide, nickel oxide or molybdenum oxide, these are, of course, simultaneously reduced into the bath in this method step. The reduced slag formed as a result of the carbothermal reduction reacts relatively slowly with the subsequently introduced reductant, wherein the speed of the reaction and, in particular, the reduction kinetics may be substantially enhanced if, as in accordance with a preferred further development of the invention, the bath is flushed with an inert gas after the addition of the reductants having higher reduction potentials. Due to the stirring action exerted by the injected inert gas, which may be comprised of, for instance, nitrogen or argon, the reaction is substantially accelerated such that extremely short treatment times will do for obtaining the final chromium oxide contents sought. In the main, it is advantageously proceeded in a manner that the first carbothermal reduction is carried out over a period of 15 to 3 0 minutes and the second reduction is carried out over a period of 3 to 10 minutes. In the following, the invention will be explained in more detail by way of an exemplary embodiment. Exemplary embodiment In a converter, 3 tons of a slag having the directional analysis indicated below are charged in the liquid state onto 10 tons of pig iron: - 4 - The metal oxide contents by the simultaneous charging of carbon and oxygen were subsequently 1owered to the following contents: After this, the addition of 3 0 kg f errosilicone and the flushing of the bath with 55 Nm3 nitrogen were effected over a period of 5 minutes. The reduction effect of the silicone dissolved in the iron bath produced the following final slag composition: - 5 - It was feasible to perform the entire two-stage reduction process in one converter, whereby a chromium oxide content of 0.3 wt.-% was found after a treatment time of 2 0 minutes, departing from a chromium oxide content of 6 . 7 wt.-% at the end of the carbothermal reaction. In the subsequent silico-thermal reduction over a period of 5 minutes, the chromium oxide content could be lowered from 0.3 wt.-% to 0.07 wt.-%. On account of the relatively short treatment time, the thermal losses could be substantially lowered and the carbon carriers fed could be utilized for the reduction to a higher extent. Claims:- 1. A method for dechroming and/or denickelifying liquid slags or slag mixtures, in which the liquid slag is charged onto a metal bath, in particular an iron bath, and reduced by feeding carbon or carbon carriers, characterized in that the carbon feed into the metal bath is effected until a decrease of the Cr and/or Ni oxide contents of the slag to values of between 0.8 wt. -% and 0.2 wt. -% and that, upon attainment of the pregiven Cr oxide content range of the slag, reductants having higher reduction potentials such as, e.g., Al, Ca, Si, Fe-Si or Ca-Si are added in order to lower the Cr and/or Ni oxide contents to below 0.15 wt.-%, preferably below 0.08 wt.-%. 2. A method according to claim 1, characterized in that the addition of Fe-Si is effected in amounts ranging from 3 to 15 kg/ton slag, preferably 6 to 10 kg/ton slag. 3. A method according to claim 1 or 2, characterized in that the bath is flushed with an inert gas after the addition of the reductants having higher reduction potentials. 4. A method according to claim 1, 2 or 3, characterized in that the first carbothermal reduction is carried out over a period of 15 to 30 minutes and the Second reduction is carried out over a period of 3 to 10 minutes. In a method for dechroming and/or denickelifying liquid slags or slag mixtures, in which the liquid slag is charged onto a metal bath, in particular an iron bath, and reduced by feeding carbon or carbon carriers, the carbon feed into the metal bath is effected until a decrease of the Cr and/or Ni oxide contents of the slag to a value of between 0.8 wt.-% and 0.2 wt.-%. As the pregiven Cr oxide content range of the slag is reached, reductants having higher reduction potentials such as, e.g. , Al, Ca, Si, Fe-Si or Ca-Si are added in order to lower the Cr and/or Ni oxide contents to below 0.15 wt.-%, preferably below 0.08 wt.-%.

Full Text

- l -
Method for Dechroming and/or Denickelifying Liquid Slags
The invention relates to a method for dechroming and/or denickelifying liquid slags or slag mixtures and dusts, in which the liquid slag is charged onto a metal bath, in particular an iron bath, and reduced by feeding carbon or carbon carriers.
Liquid steelworks slags derived from the production of special steels or ferrochromium, depending on their origin and, in particular, on the portion and composition of the scrap admixtures applied in the production of steel, above all contain relatively high amounts of chromium oxide. Also manganese oxides are found in relatively high amounts. In certain steel slags, even relatively high nickel and relatively high vanadium contents are observed. In the case of steel slags having relatively high vanadium contents, it has already been proposed in EP 770 149 to recover, after a first reduction process using carbon carriers, vanadium in a separate consecutively arranged reduction converter using reductants having higher reduction potentials. To this end, all of the chromium and manganese was, at first, reduced carbothermally, wherefor the slag was treated over an extended period of time above a metal bath into which carbon carriers such as, for instance, methane gas were injected. A quite considerable portion of the amount of carbon introduced was consumed in order to maintain the necessary temperatures because of the relatively long treatment time proposed.
The use of a separate reduction reactor which, as a rule, also was to be heated separately, for the separation of vanadium naturally will be economically effective only if vanadium is present in accordingly high amounts with the economy resulting from the value of the recovered vanadium. If, in the first place, the dechroming of steel slags to as large an extent as possible is to be envisaged, this will involve relatively long

- 2 -
treatment times and hence relatively high thermal losses in the known mode of procedure.
The invention aims to enhance a method of the initially defined kind to the extent that the safe dechroming under the simultaneous reduction of the overall treatment time will be feasible even if economic credits by the recovery of expensive metallic raw materials cannot be ensured. To solve this object, the method according to the invention essentially consists in that the carbon feed into the metal bath is effected until a decrease of the Cr and/or Ni oxide contents of the slag to a value of between 0.8 wt.-% and 0.2 wt.-% and that, upon attainment of the pregiven Cr oxide content range of the slag, reductants having higher reduction potentials such as, e.g., Al, Ca, Si, Fe-Si or Ca-Si are added in order to lower the Cr and/or Ni oxide contents to below 0.15 wt.-%, preferably below 0.08 wt.-%. The method according to the invention is, thus, carried out using but a single converter, wherein, due to the fact that the carbothermal reduction using carbon carriers such as, e.g., hydrocarbons is stopped already at a point of time at which the slag has still a relatively high chromium or Ni oxide content which, as a rule, is unacceptable to the effect that such slags cannot be directly used as cement grinding additives, the treatment time is substantially shortened until that point of time and, due to the fact that upon attainment of such predefined and relatively high chromium and/or Ni oxide contents reductants having higher reduction potentials are then immediately added in the same converter, it is feasible to complete the method within a relatively short period of time and bring the chromium and/or Ni oxide contents safely below the pregiven limit values. By such a stepwise reduction, it is, of course, feasible to lower the contents of also other special steel accompanying elements such as, e.g., molybdenum or vanadium in the slags to noncritical values.

- 3 -
In this respect, within the context of the method according to the invention, it is advantageously proceeded such that the addition of Fe-Si is effected in amounts ranging from 3 to 15 kg/ton slag, preferably 6 to 10 kg/ton slag. If other substances capable of being reduced by such reductants were contained in the slag, such as, for instance, vanadium oxide, manganese oxide, nickel oxide or molybdenum oxide, these are, of course, simultaneously reduced into the bath in this method step.
The reduced slag formed as a result of the carbothermal reduction reacts relatively slowly with the subsequently introduced reductant, wherein the speed of the reaction and, in particular, the reduction kinetics may be substantially enhanced if, as in accordance with a preferred further development of the invention, the bath is flushed with an inert gas after the addition of the reductants having higher reduction potentials. Due to the stirring action exerted by the injected inert gas, which may be comprised of, for instance, nitrogen or argon, the reaction is substantially accelerated such that extremely short treatment times will do for obtaining the final chromium oxide contents sought.
In the main, it is advantageously proceeded in a manner that the first carbothermal reduction is carried out over a period
of 15 to 3 0 minutes and the second reduction is carried out
over a period of 3 to 10 minutes.
In the following, the invention will be explained in more detail by way of an exemplary embodiment.
Exemplary embodiment
In a converter, 3 tons of a slag having the directional analysis indicated below are charged in the liquid state onto 10 tons of pig iron:

- 4 -

The metal oxide contents by the simultaneous charging of carbon and oxygen were subsequently 1owered to the following contents:

After this, the addition of 3 0 kg f errosilicone and the flushing of the bath with 55 Nm3 nitrogen were effected over a period of 5 minutes. The reduction effect of the silicone dissolved in the iron bath produced the following final slag composition:

- 5 -

It was feasible to perform the entire two-stage reduction process in one converter, whereby a chromium oxide content of 0.3 wt.-% was found after a treatment time of 2 0 minutes, departing from a chromium oxide content of 6 . 7 wt.-% at the end of the carbothermal reaction. In the subsequent silico-thermal reduction over a period of 5 minutes, the chromium oxide content could be lowered from 0.3 wt.-% to 0.07 wt.-%. On account of the relatively short treatment time, the thermal losses could be substantially lowered and the carbon carriers fed could be utilized for the reduction to a higher extent.

Claims:-
1. A method for dechroming and/or denickelifying liquid slags or slag mixtures, in which the liquid slag is charged onto a metal bath, in particular an iron bath, and reduced by feeding carbon or carbon carriers, characterized in that the carbon feed into the metal bath is effected until a decrease of the Cr and/or Ni oxide contents of the slag to values of between 0.8 wt. -% and 0.2 wt. -% and that, upon attainment of the pregiven Cr oxide content range of the slag, reductants having higher reduction potentials such as, e.g., Al, Ca, Si, Fe-Si or Ca-Si are added in order to lower the Cr and/or Ni oxide contents to below 0.15 wt.-%, preferably below 0.08 wt.-%.
2. A method according to claim 1, characterized in that the addition of Fe-Si is effected in amounts ranging from 3 to 15 kg/ton slag, preferably 6 to 10 kg/ton slag.
3. A method according to claim 1 or 2, characterized in that
the bath is flushed with an inert gas after the addition of
the reductants having higher reduction potentials.
4. A method according to claim 1, 2 or 3, characterized in
that the first carbothermal reduction is carried out over a
period of 15 to 30 minutes and the Second reduction is carried
out over a period of 3 to 10 minutes.

In a method for dechroming and/or denickelifying liquid slags or slag mixtures, in which the liquid slag is charged onto a metal bath, in particular an iron bath, and reduced by feeding carbon or carbon carriers, the carbon feed into the metal bath is effected until a decrease of the Cr and/or Ni oxide contents of the slag to a value of between 0.8 wt.-% and 0.2 wt.-%. As the pregiven Cr oxide content range of the slag is reached, reductants having higher reduction potentials such as, e.g. , Al, Ca, Si, Fe-Si or Ca-Si are added in order to lower the Cr and/or Ni oxide contents to below 0.15 wt.-%, preferably below 0.08 wt.-%.

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Patent Number

206611

Indian Patent Application Number

IN/PCT/2002/00864/KOL

PG Journal Number

18/2007

Publication Date

04-May-2007

Grant Date

03-May-2007

Date of Filing

26-Jun-2002

Name of Patentee

HOLCIM LTD

Applicant Address

ZURCHERSTRASSE 156, CH 8645 JONA,

Inventors:

#	Inventor's Name	Inventor's Address
1	EDLINGER ALFRED	DALMAWEG 13, A-6780 BARTHOLOMABERG,

PCT International Classification Number

C22 B 7/04

PCT International Application Number

PCT/AT01/00012

PCT International Filing date

2001-01-18

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1	GM 63/2000	2000-01-28	Australia