US20160376672A1 - Mixture, use of this mixture and process for conditioning a slag located on a metal melt in a metallurgical vessel in iron and steel metallurgy - Google Patents
Mixture, use of this mixture and process for conditioning a slag located on a metal melt in a metallurgical vessel in iron and steel metallurgy Download PDFInfo
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- US20160376672A1 US20160376672A1 US15/038,735 US201415038735A US2016376672A1 US 20160376672 A1 US20160376672 A1 US 20160376672A1 US 201415038735 A US201415038735 A US 201415038735A US 2016376672 A1 US2016376672 A1 US 2016376672A1
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- mixture
- mass
- slag
- proportions
- iron
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- 239000002893 slag Substances 0.000 title claims abstract description 119
- 239000000203 mixture Substances 0.000 title claims abstract description 112
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 title claims abstract description 42
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 28
- 239000002184 metal Substances 0.000 title claims abstract description 28
- 229910052742 iron Inorganic materials 0.000 title claims abstract description 20
- 238000000034 method Methods 0.000 title claims abstract description 13
- 238000009865 steel metallurgy Methods 0.000 title claims abstract description 10
- 230000003750 conditioning effect Effects 0.000 title claims abstract description 6
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 37
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 31
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 25
- 239000004411 aluminium Substances 0.000 claims abstract description 24
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 24
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims abstract description 15
- 229910052749 magnesium Inorganic materials 0.000 claims abstract description 15
- 239000011777 magnesium Substances 0.000 claims abstract description 15
- 239000000395 magnesium oxide Substances 0.000 claims description 29
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 22
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims description 19
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 18
- 239000000292 calcium oxide Substances 0.000 claims description 17
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 claims description 16
- 229910052593 corundum Inorganic materials 0.000 claims description 13
- 239000008188 pellet Substances 0.000 claims description 13
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 12
- 229910001845 yogo sapphire Inorganic materials 0.000 claims description 12
- 239000000377 silicon dioxide Substances 0.000 claims description 11
- 229910052681 coesite Inorganic materials 0.000 claims description 9
- 229910052906 cristobalite Inorganic materials 0.000 claims description 9
- 229910052682 stishovite Inorganic materials 0.000 claims description 9
- 229910052905 tridymite Inorganic materials 0.000 claims description 9
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 claims description 5
- 239000001095 magnesium carbonate Substances 0.000 claims description 4
- 229910000021 magnesium carbonate Inorganic materials 0.000 claims description 4
- 235000012239 silicon dioxide Nutrition 0.000 claims description 2
- 238000010891 electric arc Methods 0.000 abstract description 9
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 50
- TWHBEKGYWPPYQL-UHFFFAOYSA-N aluminium carbide Chemical compound [C-4].[C-4].[C-4].[Al+3].[Al+3].[Al+3].[Al+3] TWHBEKGYWPPYQL-UHFFFAOYSA-N 0.000 description 14
- 239000001301 oxygen Substances 0.000 description 14
- 229910052760 oxygen Inorganic materials 0.000 description 14
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 13
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 12
- 238000005187 foaming Methods 0.000 description 12
- 235000013980 iron oxide Nutrition 0.000 description 10
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 8
- 239000002994 raw material Substances 0.000 description 8
- 229910002092 carbon dioxide Inorganic materials 0.000 description 7
- 239000010459 dolomite Substances 0.000 description 7
- 229910000514 dolomite Inorganic materials 0.000 description 7
- 239000000654 additive Substances 0.000 description 6
- 239000000155 melt Substances 0.000 description 6
- 239000001569 carbon dioxide Substances 0.000 description 5
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 5
- 239000000347 magnesium hydroxide Substances 0.000 description 5
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 5
- 238000010079 rubber tapping Methods 0.000 description 5
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 4
- 229910000805 Pig iron Inorganic materials 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 4
- 239000000470 constituent Substances 0.000 description 4
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 4
- 229910002091 carbon monoxide Inorganic materials 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 229910002804 graphite Inorganic materials 0.000 description 3
- 239000010439 graphite Substances 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 2
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 235000011941 Tilia x europaea Nutrition 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 230000002238 attenuated effect Effects 0.000 description 2
- 235000012255 calcium oxide Nutrition 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- SZVJSHCCFOBDDC-UHFFFAOYSA-N ferrosoferric oxide Chemical compound O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- 239000004571 lime Substances 0.000 description 2
- 238000010310 metallurgical process Methods 0.000 description 2
- 238000007670 refining Methods 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 229910001341 Crude steel Inorganic materials 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910002090 carbon oxide Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 239000010431 corundum Substances 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 238000007667 floating Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- -1 however Inorganic materials 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000010309 melting process Methods 0.000 description 1
- 238000005272 metallurgy Methods 0.000 description 1
- 150000002926 oxygen Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000011819 refractory material Substances 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 239000003923 scrap metal Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000161 steel melt Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
- C21C7/00—Treating molten ferrous alloys, e.g. steel, not covered by groups C21C1/00 - C21C5/00
- C21C7/0087—Treatment of slags covering the steel bath, e.g. for separating slag from the molten metal
Definitions
- the invention relates to a mixture comprising magnesium, carbon and aluminium to be introduced into the slag located on a metal melt in iron and steel metallurgy, the use of such a mixture, and a method for conditioning a slag located on a metal melt in a metallurgical vessel, for example in a converter, in an electric arc furnace, or in a ladle, in iron and steel metallurgy.
- oxygen is blown for this purpose by means of a lance onto the pig iron melt located in a converter lined with an alkaline refractory material.
- the process of this blowing of oxygen onto the pig iron melt is also referred to as refining.
- iron contaminants in particular iron contaminants in the form of carbon, manganese, silicon and phosphorous, are oxidised by the oxygen blown in and together with added burnt lime form a slag layer floating on the metal melt.
- the crude steel melt is produced by melting scrap metal, pig iron, liquid iron and/or direct reduced iron and further raw materials.
- the slag must be selectively influenced or conditioned with regard to chemical and physical properties.
- the basicity i.e. the mass or molar ratio of the alkaline components to the other components of the slag (which for example can be calculated in accordance with the following formula: [xCaO+MgO]/[xSiO 2 +Al 2 O 3 +further components]), of the initially acidic or non-alkaline slag must therefore be increased in order to reduce the corrosive attack of the slag on the alkaline lining of the metallurgical vessel in which the metal melt is located and thus attenuate the erosion of the lining and increase the service life thereof.
- slag conditioners have a component increasing the basicity of the slag, this component in particular being lime, dolomite lime, or dolomite.
- the viscosity of the slag may also be desirable to adjust the viscosity of the slag by the slag conditioner. It is often desirable for the viscosity of the slag during the refinement to be as low as possible such that the iron constituents oxidised by the applied oxygen can be incorporated well into the slag. Furthermore, it may be desirable when tapping or following tapping for the slag to have a high viscosity such that the slag remaining in the converter following the tapping can be better applied to the refractory lining of the converter. Due to this applied slag layer, a corrosive attack of a metal melt on the lining of the converter can be reduced. The process of applying the slag to the converter is also referred to as “maintaining” the converter.
- the known methods for maintaining the converter on the one hand include what is known as “slag washing”, in which the slag is distributed over the tapping and charging side by pivoting the converter.
- a further maintaining method is what is known as “slag splashing”, in which the slag is mechanically sprayed with the aid of a nitrogen gas flow of a lance.
- slag foaming slag is chemically foamed by adding a carbon carrier. The slag foamed in the case of slag foaming is also referred to as “foamed slag”.
- the foamed slag has insulating properties, such that the heat losses from the melt can be attenuated and energy can be saved. Furthermore, components of the metallurgical vessel in which the iron melt is located may be protected by the foamed slag against heat radiation.
- one object of the invention is to provide a slag conditioner by means of which the basicity and the MgO content of the slag can be quickly increased in order to be able to reduce the attack of the slag on the refractory lining of the metallurgical vessel in which the metal melt is located with the slag located thereon.
- a further object of the invention lies in providing a slag conditioner by means of which the viscosity of the slag can be selectively adjusted.
- a further object of the invention lies in providing a slag conditioner by means of which a foaming of the slag can be achieved.
- a further object of the invention lies in providing a slag conditioner by means of which an increase of the iron output of the primary metallurgical process can be achieved.
- a mixture or a slag conditioner to be introduced into the slag located on a metal melt in iron and steel metallurgy is provided in accordance with the invention, wherein the mixture comprises magnesium, carbon and aluminium in the following mass proportions:
- the mixture according to the invention or the slag conditioner according to the invention is suitable to be introduced into slags on metal melts in any metallurgical vessel, but in particular for slags in converters, electric arc furnaces and ladles.
- the proportions of magnesium and aluminium in the mixture according to the invention are specified as proportions of the oxides thereof Mgo and Al 2 O 3 in the mixture, as is usual in refractory technology.
- magnesium and in particular aluminium may also be present in the mixture according to the invention in a form other than the oxide form, for example in metallic form or, with regard to aluminium, in the form of carbide.
- the MgO saturation of the slag is achieved more quickly by the proportion of MgO in the mixture according to the invention, such that the corrosive attack of the slag on the refractory lining of the metallurgical vessel holding the metal melt is reduced. Furthermore, the viscosity of the slag increases with rising MgO content.
- Magnesium is present in the mixture according to the invention preferably as oxide, i.e. in the form of MgO.
- the proportions of magnesium in the mixture according to the invention are preferably present exclusively in the form of MgO, particularly preferably in the form of sintered or fused magnesia.
- MgO may be present in the mixture according to the invention in proportions of at least 45 mass %, i.e. for example also in proportions of at least 48, 50, 52, 54, 56, 57, 58, 59, 60 or 61 mass %. Furthermore, MgO may be present in the mixture in proportions of at most 90 mass %, i.e. for example also in proportions of at most 88, 86, 84, 82, 80, 78, 76, 74, 72, 70, 69, 68, 67, 66, 65, 64 or 63 mass %.
- the proportion of carbon in the mixture according to the invention when the mixture is added to the slag, reacts with oxygen located in the slag to form carbon oxides, in particular to form carbon monoxide CO and carbon dioxide CO 2 .
- the carbon in the mixture oxidises immediately and fiercely with oxygen proportions of the slag, such that the slag foams up spontaneously when the mixture is introduced.
- the slag thus rises in height, as with slag foaming, and covers the refractory lining of the metallurgical vessel.
- the radiation of the electric arcs is shielded partially or completely with respect to the furnace wall as a result of the increased volume of the foamed slag. Due to the increased content of MgO, the slag at the same time obtains the necessary viscosity in order to also remain adhered to the wall during and after the foaming.
- the carbon in the mixture may react directly with oxygen of the metal melt and may remove oxygen from the metal melt. This oxygen removed from the metal melt must not later be removed to a greater extent from the metal melt in additional steps by deoxidising agents, for example aluminium.
- At least some of the oxygen with which the carbon from the mixture according to the invention introduced into the slag reacts originates from iron oxides in the slag that are reduced by the carbon to form metallic iron.
- iron oxides are fluxing agents, which reduce the viscosity of the slag. Since the proportion of iron oxides in the slag is reduced by the edition of the mixture, the viscosity of the slag can thus be increased. The output of recovered iron in the overall process is also increased.
- a foaming of the slag can thus be achieved on the one hand.
- the viscosity of the slag can be increased.
- the extent of the foaming of the slag and also the viscosity thereof can thus be set selectively by the proportion of carbon in the mixture.
- the carbon may be present in the mixture substantially in pure form, for example in the form of graphite or coke, but for example also combined with further constituents, for example with aluminium proportions or magnesium proportions of the mixture.
- the proportions according to the invention of carbon in the mixture are present partially, largely, or also completely in the form of aluminium carbide (Al 4 C 3 ).
- Carbon is present in the mixture according to the invention in proportions of at least 5 mass %, i.e. for example also in proportions of at least 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22 or 23 mass %. Furthermore, carbon is present in the mixture according to the invention in proportions of at most 40 mass %, i.e. for example also in proportions of at most 38, 36, 34, 32, 31, 30, 29, 28, 27, 26 or 25 mass %.
- Aluminium calculated as Al 2 O 3
- aluminium may be present in the mixture in a proportion of at least 1 mass %, i.e. for example also in a proportion of at least 2, 3, 4 or 5 mass %.
- aluminium, calculated as Al 2 O 3 may be present in the mixture in proportions of at most 20 mass %, i.e. for example also in proportions of at most 18, 16, 14, 13, 12, 11, 10, 9, 8 or 7 mass %.
- the proportion of aluminium in the mixture according to the invention is calculated herein as Al 2 O 3 , wherein, however, the proportions according to the invention of aluminium in the mixture preferably are not present in oxide form as Al 2 O 3 , but are preferably present partially, largely, or also completely in metallic form and/or in the form of carbide, i.e. as Al 4 C 3 .
- this aluminium carbide at the same time forms a carrier both of the proportion of aluminium and of carbon in the mixture.
- the aluminium carbide component is particularly advantageous inasmuch as both the aluminium and the carbon of the aluminium carbide can react with oxygen proportions in the slag, and oxidic constituents of the slag, in particular iron oxides, can be reduced as a result. With corresponding reactions the aluminium proportion of the aluminium carbide oxidises into Al 2 O 3 and the carbon proportion of the aluminium carbide oxidises into CO 2 .
- slag conditioners comprise magnesium proportions, these are regularly present in the form of magnesium carbonate (MgCO 3 ), dolomite, or sometimes also in the form of magnesium hydroxide (Mg(OH) 2 ).
- MgCO 3 magnesium carbonate
- dolomite magnesium hydroxide
- Mg(OH) 2 magnesium hydroxide
- magnesium present in the form of magnesium carbonate, dolomite or magnesium hydroxide leads only to a delayed increase of the basicity and of the MgO content of the slag. Furthermore, it has been found in accordance with the invention that the basicity and the MgO content of the slag can be increased much more quickly and effectively by introducing magnesium in the form of magnesium oxide into the slag.
- the mixture according to the invention is produced, in contrast with the prior art, in such a way that the component comprising magnesium is provided in particular in the form of MgO and merely to increase the basicity and MgO content in the mixture, whereas the foaming of the slag is caused by other components in the mixture, in particular by the components comprising carbon and aluminium.
- the slag conditioner according to the invention no further carbonates have to be introduced either into the primary metallurgical process, the resource efficiency is higher, i.e. the specific consumption and the total weight of slag conditioner to be introduced into the slag and to be transported is lower than in the prior art.
- the emissions of carbon dioxide can be reduced by the slag conditioner according to the invention if carbonate-containing slag formers are replaced by the slag former according to the invention.
- the mixture may contain a proportion of magnesium carbonate less than 10 mass %, i.e. for example also a proportion less than 9, 8, 7, 6, 5, 4, 3, 2, 1 or 0.5 mass %.
- the mixture may contain a proportion of Mg(OH) 2 less than 10 mass %, i.e. for example also a proportion less than 9, 8, 7, 6, 5, 4, 3, 2, 1 or 0.5 mass %.
- the mixture may contain a proportion of dolomite, in particular of raw dolomite, less than 10 mass %, i.e. for example also a proportion less than 9, 8, 7, 6, 5, 4, 3, 2, 1 or 0.5 mass %.
- the mixture may contain a proportion of calcium carbonate or of limestone less than 10 mass %, i.e. for example also a proportion less than 9, 8, 7, 6, 5, 4, 3, 2, 1 or 0.5 mass %.
- the mixture is preferably present in a relatively low grain size, for example % in a grain size less than 0.5 mm to an extent of at least 70 mass %, 80 mass %, or at least 90 mass %, or also 100 mass.
- the grain size of the components of the mixture according to the invention below the grain sizes specified hereinafter may be present in the respective specified mass proportions, wherein the mixture according to the invention for example also may fulfil only one of the following conditions in respect of its grain size:
- the mixture according to the invention has this very small mean grain size, a particularly good and uniform distribution and particularly also a quick dissolution of the mixture in a slag can be achieved.
- the mixture may be provided in compacted or pressed form, for example in the form of pellets.
- a mixture according to the invention which in particular may have the previously described grain size distribution, can be pressed into pellets without addition of additives.
- these pellets may have an almond-shaped, rod-shaped or spherical form, for example with a maximum length of for example 50 mm, 40 mm, or 30 mm.
- the pellets may also have a minimum diameter for example of 5, 10, 15, 20, or 25 mm. Pellets with a corresponding size can be easily handled, but at the same time are still small enough that they quickly disintegrate in a slag following addition thereto, and the advantages of the small grain size distribution according to the invention can materialise there quickly.
- the mixture according to the invention contains a proportion of calcium oxide (CaO), since the basicity of the slag can be further increased thereby and the attack of the slag on the refractory lining of the metallurgical vessel can be lowered.
- the CaO of the mixture in particular then has an advantageous basicity-reducing effect when the ratio of CaO to SiO 2 in the mixture does not exceed a certain measure.
- the basicity of the slag can be increased in particular by the CaO when the ratio of mass proportions of CaO to SiO 2 in the mixture is not below 0.7.
- the ratio of the mass proportions of CaO to SiO 2 in the mixture according to the invention may not lie below 0.7.
- SiO 2 may enter the mixture according to the invention fundamentally via impurities of the raw materials of said mixture.
- the mixture may comprise calcium oxide and silicon dioxide in the following mass proportions:
- SiO 2 0 to 7 mass %.
- CaO may also be present in the mixture for example in proportions of at least 0.1 or 0.2 or 0.5 or 1 or 1.5 or 2 mass %, and for example in proportions of at most 10, 9, 8, 7, 6, 5, 4, 3 or 2.5 mass %.
- SiO 2 may be present in the mixture for example in proportions of at least 0.1 or 0.2 or 0.5 or 1 or 1.5 or 2 mass %, and for example in proportions of at most 7, 6, 5, 4, 3 or 2.5 mass %.
- the mixture may be provided in the form of pellets, wherein the mixture is pressed into pellets without the addition of additives. If, however, additives are used in order to press the mixture into pellets, CaO may be used as such a press additive.
- the mixture in contrast to the previously disclosed inventive concept, in accordance with which the mixture contains proportions of CaO of at most 10 mass %, the mixture may contain proportions of CaO of up to 40 mass %.
- the mixture preferably does not contain any additive for pressing, such that the proportion of CaO in the mixture, as described above, does not lie above 10 mass %.
- the mixture may comprise iron oxides in the following mass proportions:
- iron oxide stands for the sum of all iron oxides in the mixture, i.e. in particular FeO and Fe 2 O 3 , but for example also Fe 3 O 4 and Fe 2 O.
- Iron oxides may be present in the mixture for example also in proportions of at least 0.1 mass %, 0.2 mass %, 0.4 mass %, 0.6 mass %, or 0.8 mass %, and for example at most in proportions of 7 mass %, 6 mass %, 5 mass %, 4 mass %, 3 mass %, 2.8 mass %, 2.6 mass %, 2.4 mass %, 2.2 mass %, or 2 mass %.
- the mixture may also comprise only small proportions of further components, for example in proportions less than 5 mass %, 4 mass %, 3 mass %, 2.5 mass %, 2 mass %, 1.5 mass %, or also less than 1 mass %.
- the mixture may comprise proportions of the following components below the mass proportions specified hereinafter:
- magnesia-carbon products that have been used in the steel industry, in particular as inner linings of basic oxygen furnace converters, in electric arc furnaces or in ladles, are suitable in part as raw material for the mixture according to the invention.
- correspondingly recycled magnesia-carbon products can be used partially, largely or exclusively as raw material for the mixture according to the invention.
- the invention also relates to the use of recycled magnesia-carbon products as raw material for the mixture according to the invention and the use of such recycled magnesia-carbon products as slag conditioner according to the invention.
- magnesia in particular sintered magnesia
- carbon in particular graphite
- corundum in particular aluminium carbide
- the invention also relates to a method for conditioning a slag located on a metal melt in a metallurgical vessel in iron and steel metallurgy, said method comprising the following steps:
- the mixture can be provided in compacted or pressed form, for example in the form of pellets.
- the mixture provided is introduced onto the slag and sinks thereinto, such that it can develop its effect there.
- the mixture according to the invention is suitable in principle as a slag conditioner for slags on a metal melt in any metallurgical vessel, for example for metal melts in converters, electric arc furnaces, or ladles.
- the mixture according to the invention is particularly preferably used as a slag conditioner for slags on metal melts located in a metallurgical vessel with an alkaline lining, i.e. in particular with a lining based on at least one of the following materials: magnesia, magnesia-carbon, doloma or doloma-carbon.
- the invention also relates to the use of a mixture according to the invention described herein for conditioning a slag located on a metal melt in a metallurgical vessel in iron and steel metallurgy.
- the carbon was present in the mixture in the form of graphite and aluminium carbide.
- Aluminium was present in the mixture in the form of metallic aluminium and in the form of aluminium carbide.
- Recycled magnesia-carbon products were used exclusively as raw materials.
- the mixture was provided in the form of pressed, almond-shaped pellets without additional additives, with a thickness of approximately 15 mm and a length of approximately 30 mm.
- the grain size distribution of the mixture in the pellets is specified in Table 2.
- the mixture was used as a slag conditioner for a slag on a metal melt located in an oxygen converter.
- the mixture was placed on the slag located on the melt. Due to the placement of the mixture on the slag, the basicity of the slag could be increased. Furthermore, due to the proportions of carbon, aluminium and aluminium carbide in the mixture, it was possible to achieve a foaming of the slag. Lastly, the viscosity of the slag could be adjusted to the desired measure.
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- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Refinement Of Pig-Iron, Manufacture Of Cast Iron, And Steel Manufacture Other Than In Revolving Furnaces (AREA)
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Abstract
The invention relates to a mixture comprising magnesium, carbon and aluminium to be introduced into the slag located on a metal melt in iron and steel metallurgy, to the use of such a mixture and also to a process for conditioning a slag located on a metal melt in a metallurgical vessel, for example, in a converter, in an electric arc furnace or in a ladle, in iron and steel metallurgy.
Description
- The invention relates to a mixture comprising magnesium, carbon and aluminium to be introduced into the slag located on a metal melt in iron and steel metallurgy, the use of such a mixture, and a method for conditioning a slag located on a metal melt in a metallurgical vessel, for example in a converter, in an electric arc furnace, or in a ladle, in iron and steel metallurgy.
- In steel and iron metallurgy the pig iron melt is separated from undesired constituents before casting.
- If a converter is used then in the case of the LD method, which is currently the most widespread, oxygen is blown for this purpose by means of a lance onto the pig iron melt located in a converter lined with an alkaline refractory material. The process of this blowing of oxygen onto the pig iron melt is also referred to as refining. During refining, iron contaminants, in particular iron contaminants in the form of carbon, manganese, silicon and phosphorous, are oxidised by the oxygen blown in and together with added burnt lime form a slag layer floating on the metal melt.
- In an electric arc furnace the crude steel melt is produced by melting scrap metal, pig iron, liquid iron and/or direct reduced iron and further raw materials.
- Once the metal melt refined in the primary metallurgical apparatus has the desired properties, this is tapped through the tapping channel into the ladle for secondary metallurgical treatment.
- The slag must be selectively influenced or conditioned with regard to chemical and physical properties.
- In order to condition the slag it is known to provide the slag with what are known as slag conditioners in order to be able to change the properties of the slag.
- The basicity, i.e. the mass or molar ratio of the alkaline components to the other components of the slag (which for example can be calculated in accordance with the following formula: [xCaO+MgO]/[xSiO2+Al2O3+further components]), of the initially acidic or non-alkaline slag must therefore be increased in order to reduce the corrosive attack of the slag on the alkaline lining of the metallurgical vessel in which the metal melt is located and thus attenuate the erosion of the lining and increase the service life thereof. For this reason, slag conditioners have a component increasing the basicity of the slag, this component in particular being lime, dolomite lime, or dolomite.
- It is additionally expedient to adjust the content of MgO in the slag by addition of a slag conditioner, such that it lies in the range of saturation of MgO in the slag and a corrosive attack of the slag on the lining is thus attenuated.
- It may also be desirable to adjust the viscosity of the slag by the slag conditioner. It is often desirable for the viscosity of the slag during the refinement to be as low as possible such that the iron constituents oxidised by the applied oxygen can be incorporated well into the slag. Furthermore, it may be desirable when tapping or following tapping for the slag to have a high viscosity such that the slag remaining in the converter following the tapping can be better applied to the refractory lining of the converter. Due to this applied slag layer, a corrosive attack of a metal melt on the lining of the converter can be reduced. The process of applying the slag to the converter is also referred to as “maintaining” the converter. The known methods for maintaining the converter on the one hand include what is known as “slag washing”, in which the slag is distributed over the tapping and charging side by pivoting the converter. A further maintaining method is what is known as “slag splashing”, in which the slag is mechanically sprayed with the aid of a nitrogen gas flow of a lance. Lastly, in the case of what is known as “slag foaming”, slag is chemically foamed by adding a carbon carrier. The slag foamed in the case of slag foaming is also referred to as “foamed slag”.
- Besides the maintaining of the converter by means of the foamed slag, this also has further advantageous effects. The foamed slag has insulating properties, such that the heat losses from the melt can be attenuated and energy can be saved. Furthermore, components of the metallurgical vessel in which the iron melt is located may be protected by the foamed slag against heat radiation.
- In order to generate a foamed slag in an electric arc furnace, carbon blown into the slag is additionally burned by means of oxygen to form carbon monoxide, and the carbon monoxide gas necessary for foaming is provided in this way. In the case of the melting process in an electric arc furnace, a foaming of the slag layer is of importance, since this shields the light arc by means of a volume increase, attenuates radiation losses at the furnace wall, improves the energy transfer to the melt, and thus likewise saves energy.
- On this basis, one object of the invention is to provide a slag conditioner by means of which the basicity and the MgO content of the slag can be quickly increased in order to be able to reduce the attack of the slag on the refractory lining of the metallurgical vessel in which the metal melt is located with the slag located thereon.
- A further object of the invention lies in providing a slag conditioner by means of which the viscosity of the slag can be selectively adjusted.
- A further object of the invention lies in providing a slag conditioner by means of which a foaming of the slag can be achieved.
- Lastly, a further object of the invention lies in providing a slag conditioner by means of which an increase of the iron output of the primary metallurgical process can be achieved.
- In order to achieve these objects, a mixture or a slag conditioner to be introduced into the slag located on a metal melt in iron and steel metallurgy is provided in accordance with the invention, wherein the mixture comprises magnesium, carbon and aluminium in the following mass proportions:
- MgO: 45-90 mass %;
- C: 5-40 mass %; and
- Al2O3: 1-20 mass %.
- The mixture according to the invention or the slag conditioner according to the invention is suitable to be introduced into slags on metal melts in any metallurgical vessel, but in particular for slags in converters, electric arc furnaces and ladles.
- All of the values specified herein in % are values in mass %, in each case in relation to the total mass of the mixture according to the invention.
- The proportions of magnesium and aluminium in the mixture according to the invention are specified as proportions of the oxides thereof Mgo and Al2O3 in the mixture, as is usual in refractory technology. However, as described herein, magnesium and in particular aluminium may also be present in the mixture according to the invention in a form other than the oxide form, for example in metallic form or, with regard to aluminium, in the form of carbide.
- The MgO saturation of the slag is achieved more quickly by the proportion of MgO in the mixture according to the invention, such that the corrosive attack of the slag on the refractory lining of the metallurgical vessel holding the metal melt is reduced. Furthermore, the viscosity of the slag increases with rising MgO content.
- Magnesium is present in the mixture according to the invention preferably as oxide, i.e. in the form of MgO. The proportions of magnesium in the mixture according to the invention are preferably present exclusively in the form of MgO, particularly preferably in the form of sintered or fused magnesia.
- MgO may be present in the mixture according to the invention in proportions of at least 45 mass %, i.e. for example also in proportions of at least 48, 50, 52, 54, 56, 57, 58, 59, 60 or 61 mass %. Furthermore, MgO may be present in the mixture in proportions of at most 90 mass %, i.e. for example also in proportions of at most 88, 86, 84, 82, 80, 78, 76, 74, 72, 70, 69, 68, 67, 66, 65, 64 or 63 mass %.
- The proportion of carbon in the mixture according to the invention, when the mixture is added to the slag, reacts with oxygen located in the slag to form carbon oxides, in particular to form carbon monoxide CO and carbon dioxide CO2. When the mixture is introduced into the slag, the carbon in the mixture oxidises immediately and fiercely with oxygen proportions of the slag, such that the slag foams up spontaneously when the mixture is introduced. The slag thus rises in height, as with slag foaming, and covers the refractory lining of the metallurgical vessel. In an electric arc furnace the radiation of the electric arcs is shielded partially or completely with respect to the furnace wall as a result of the increased volume of the foamed slag. Due to the increased content of MgO, the slag at the same time obtains the necessary viscosity in order to also remain adhered to the wall during and after the foaming.
- If the mixture comes into direct contact with the metal melt, for example because it arrives through a rinser at an opening in the slag layer, the carbon in the mixture may react directly with oxygen of the metal melt and may remove oxygen from the metal melt. This oxygen removed from the metal melt must not later be removed to a greater extent from the metal melt in additional steps by deoxidising agents, for example aluminium.
- At least some of the oxygen with which the carbon from the mixture according to the invention introduced into the slag reacts originates from iron oxides in the slag that are reduced by the carbon to form metallic iron. In contrast to metallic iron, however, iron oxides are fluxing agents, which reduce the viscosity of the slag. Since the proportion of iron oxides in the slag is reduced by the edition of the mixture, the viscosity of the slag can thus be increased. The output of recovered iron in the overall process is also increased.
- Due to the proportion of carbon in the mixture, a foaming of the slag can thus be achieved on the one hand. In addition, the viscosity of the slag can be increased. The extent of the foaming of the slag and also the viscosity thereof can thus be set selectively by the proportion of carbon in the mixture.
- The carbon may be present in the mixture substantially in pure form, for example in the form of graphite or coke, but for example also combined with further constituents, for example with aluminium proportions or magnesium proportions of the mixture. In particular, it may be that the proportions according to the invention of carbon in the mixture are present partially, largely, or also completely in the form of aluminium carbide (Al4C3).
- Carbon is present in the mixture according to the invention in proportions of at least 5 mass %, i.e. for example also in proportions of at least 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22 or 23 mass %. Furthermore, carbon is present in the mixture according to the invention in proportions of at most 40 mass %, i.e. for example also in proportions of at most 38, 36, 34, 32, 31, 30, 29, 28, 27, 26 or 25 mass %.
- Aluminium, calculated as Al2O3, may be present in the mixture in a proportion of at least 1 mass %, i.e. for example also in a proportion of at least 2, 3, 4 or 5 mass %. Furthermore, aluminium, calculated as Al2O3, may be present in the mixture in proportions of at most 20 mass %, i.e. for example also in proportions of at most 18, 16, 14, 13, 12, 11, 10, 9, 8 or 7 mass %.
- The proportion of aluminium in the mixture according to the invention, as described before, is calculated herein as Al2O3, wherein, however, the proportions according to the invention of aluminium in the mixture preferably are not present in oxide form as Al2O3, but are preferably present partially, largely, or also completely in metallic form and/or in the form of carbide, i.e. as Al4C3.
- If aluminium is present in the mixture as carbide, this aluminium carbide at the same time forms a carrier both of the proportion of aluminium and of carbon in the mixture.
- If carbon and aluminium are present in the mixture in the form of aluminium carbide, the aluminium carbide component is particularly advantageous inasmuch as both the aluminium and the carbon of the aluminium carbide can react with oxygen proportions in the slag, and oxidic constituents of the slag, in particular iron oxides, can be reduced as a result. With corresponding reactions the aluminium proportion of the aluminium carbide oxidises into Al2O3 and the carbon proportion of the aluminium carbide oxidises into CO2.
- Insofar as slag conditioners according to the prior art comprise magnesium proportions, these are regularly present in the form of magnesium carbonate (MgCO3), dolomite, or sometimes also in the form of magnesium hydroxide (Mg(OH)2). In this respect it is considered advantageous in accordance with the prior art, in the event of contact of these components of the slag conditioners in question with the slag, for the magnesium carbonate to be cleaved into magnesium oxide and carbon dioxide, for the dolomite to be cleaved into magnesium oxide and calcium oxide and also carbon dioxide, and for the magnesium hydroxide to be cleaved into magnesium oxide and steam. Here, the carbon dioxide and the steam cause a foaming of the slag.
- It has been found, however, in accordance with the invention that magnesium present in the form of magnesium carbonate, dolomite or magnesium hydroxide leads only to a delayed increase of the basicity and of the MgO content of the slag. Furthermore, it has been found in accordance with the invention that the basicity and the MgO content of the slag can be increased much more quickly and effectively by introducing magnesium in the form of magnesium oxide into the slag. In this respect the mixture according to the invention is produced, in contrast with the prior art, in such a way that the component comprising magnesium is provided in particular in the form of MgO and merely to increase the basicity and MgO content in the mixture, whereas the foaming of the slag is caused by other components in the mixture, in particular by the components comprising carbon and aluminium. Since, due to the slag conditioner according to the invention, no further carbonates have to be introduced either into the primary metallurgical process, the resource efficiency is higher, i.e. the specific consumption and the total weight of slag conditioner to be introduced into the slag and to be transported is lower than in the prior art. In addition, the emissions of carbon dioxide can be reduced by the slag conditioner according to the invention if carbonate-containing slag formers are replaced by the slag former according to the invention.
- In accordance with the invention the mixture may contain a proportion of magnesium carbonate less than 10 mass %, i.e. for example also a proportion less than 9, 8, 7, 6, 5, 4, 3, 2, 1 or 0.5 mass %.
- Furthermore, the mixture may contain a proportion of Mg(OH)2 less than 10 mass %, i.e. for example also a proportion less than 9, 8, 7, 6, 5, 4, 3, 2, 1 or 0.5 mass %.
- Furthermore, the mixture may contain a proportion of dolomite, in particular of raw dolomite, less than 10 mass %, i.e. for example also a proportion less than 9, 8, 7, 6, 5, 4, 3, 2, 1 or 0.5 mass %.
- Furthermore, the mixture may contain a proportion of calcium carbonate or of limestone less than 10 mass %, i.e. for example also a proportion less than 9, 8, 7, 6, 5, 4, 3, 2, 1 or 0.5 mass %.
- The mixture is preferably present in a relatively low grain size, for example % in a grain size less than 0.5 mm to an extent of at least 70 mass %, 80 mass %, or at least 90 mass %, or also 100 mass.
- By way of example, the grain size of the components of the mixture according to the invention below the grain sizes specified hereinafter may be present in the respective specified mass proportions, wherein the mixture according to the invention for example also may fulfil only one of the following conditions in respect of its grain size:
- <1 mm: 100 mass %;
- <500 μm 100 mass %;
- <315 μm: at least 90 or 95 mass % and at most 100 mass %;
- <200 μm: at least 85 or 90 mass % and at most 95 or 100 mass %;
- <100 μm: at least 65 or 70 mass % and at most 75 or 80 mass %;
- <63 μm: at least 45 or 50 mass % and at most 65 or 70 mass %.
- Since the mixture according to the invention has this very small mean grain size, a particularly good and uniform distribution and particularly also a quick dissolution of the mixture in a slag can be achieved.
- In order to be able to achieve good handling of the mixture according to the invention in spite of this small grain size of the mixture, the mixture may be provided in compacted or pressed form, for example in the form of pellets. In order to provide the mixture in the form of pellets, a mixture according to the invention, which in particular may have the previously described grain size distribution, can be pressed into pellets without addition of additives. By way of example, these pellets may have an almond-shaped, rod-shaped or spherical form, for example with a maximum length of for example 50 mm, 40 mm, or 30 mm. The pellets may also have a minimum diameter for example of 5, 10, 15, 20, or 25 mm. Pellets with a corresponding size can be easily handled, but at the same time are still small enough that they quickly disintegrate in a slag following addition thereto, and the advantages of the small grain size distribution according to the invention can materialise there quickly.
- It may be that the mixture according to the invention contains a proportion of calcium oxide (CaO), since the basicity of the slag can be further increased thereby and the attack of the slag on the refractory lining of the metallurgical vessel can be lowered. The CaO of the mixture in particular then has an advantageous basicity-reducing effect when the ratio of CaO to SiO2 in the mixture does not exceed a certain measure.
- It has been found in accordance with the invention that the basicity of the slag can be increased in particular by the CaO when the ratio of mass proportions of CaO to SiO2 in the mixture is not below 0.7. Thus, the ratio of the mass proportions of CaO to SiO2 in the mixture according to the invention may not lie below 0.7.
- SiO2 may enter the mixture according to the invention fundamentally via impurities of the raw materials of said mixture.
- The mixture may comprise calcium oxide and silicon dioxide in the following mass proportions:
- CaO: 0 to 10 mass %,
- SiO2: 0 to 7 mass %.
- CaO may also be present in the mixture for example in proportions of at least 0.1 or 0.2 or 0.5 or 1 or 1.5 or 2 mass %, and for example in proportions of at most 10, 9, 8, 7, 6, 5, 4, 3 or 2.5 mass %.
- SiO2 may be present in the mixture for example in proportions of at least 0.1 or 0.2 or 0.5 or 1 or 1.5 or 2 mass %, and for example in proportions of at most 7, 6, 5, 4, 3 or 2.5 mass %.
- As already discussed, the mixture may be provided in the form of pellets, wherein the mixture is pressed into pellets without the addition of additives. If, however, additives are used in order to press the mixture into pellets, CaO may be used as such a press additive. In this case, in contrast to the previously disclosed inventive concept, in accordance with which the mixture contains proportions of CaO of at most 10 mass %, the mixture may contain proportions of CaO of up to 40 mass %. However, the mixture preferably does not contain any additive for pressing, such that the proportion of CaO in the mixture, as described above, does not lie above 10 mass %.
- The mixture may comprise iron oxides in the following mass proportions:
- iron oxide: 0 to 7 mass %
- Here, iron oxide stands for the sum of all iron oxides in the mixture, i.e. in particular FeO and Fe2O3, but for example also Fe3O4 and Fe2O.
- Iron oxides may be present in the mixture for example also in proportions of at least 0.1 mass %, 0.2 mass %, 0.4 mass %, 0.6 mass %, or 0.8 mass %, and for example at most in proportions of 7 mass %, 6 mass %, 5 mass %, 4 mass %, 3 mass %, 2.8 mass %, 2.6 mass %, 2.4 mass %, 2.2 mass %, or 2 mass %.
- It has been found in accordance with the invention that the advantageous effects described herein of the mixture according to the invention as slag conditioner may be adversely influenced by the presence of further components in the mixture.
- Thus, besides the aforementioned components, i.e. MgO, C, Al, Al4C3, CaO, SiO2, iron oxides and optionally Al2O3, the mixture may also comprise only small proportions of further components, for example in proportions less than 5 mass %, 4 mass %, 3 mass %, 2.5 mass %, 2 mass %, 1.5 mass %, or also less than 1 mass %.
- By way of example, the mixture may comprise proportions of the following components below the mass proportions specified hereinafter:
- Cr2O3: <0.2 mass %;
- P2O5: <0.2 mass %;
- TiO2: <0.2 mass %;
- K2O+Na2O <0.5 mass %;
- ZrO2 <0.2 mass %.
- It has been found surprisingly in accordance with the invention that magnesia-carbon products that have been used in the steel industry, in particular as inner linings of basic oxygen furnace converters, in electric arc furnaces or in ladles, are suitable in part as raw material for the mixture according to the invention. In this respect, correspondingly recycled magnesia-carbon products can be used partially, largely or exclusively as raw material for the mixture according to the invention. In this respect, the invention also relates to the use of recycled magnesia-carbon products as raw material for the mixture according to the invention and the use of such recycled magnesia-carbon products as slag conditioner according to the invention.
- By way of example, besides recycled magnesia-carbon products, at least one of the following further raw materials may also be selected as raw materials for the mixture according to the invention: magnesia (in particular sintered magnesia), carbon (in particular graphite), corundum, or aluminium carbide.
- The invention also relates to a method for conditioning a slag located on a metal melt in a metallurgical vessel in iron and steel metallurgy, said method comprising the following steps:
-
- providing a mixture according to the invention described herein;
- introducing the mixture into the slag located on the metal melt in the metallurgical vessel.
- As described herein, the mixture can be provided in compacted or pressed form, for example in the form of pellets.
- The mixture provided is introduced onto the slag and sinks thereinto, such that it can develop its effect there.
- The mixture according to the invention is suitable in principle as a slag conditioner for slags on a metal melt in any metallurgical vessel, for example for metal melts in converters, electric arc furnaces, or ladles. The mixture according to the invention is particularly preferably used as a slag conditioner for slags on metal melts located in a metallurgical vessel with an alkaline lining, i.e. in particular with a lining based on at least one of the following materials: magnesia, magnesia-carbon, doloma or doloma-carbon.
- The invention also relates to the use of a mixture according to the invention described herein for conditioning a slag located on a metal melt in a metallurgical vessel in iron and steel metallurgy.
- Here, the use may be implemented as disclosed herein.
- All of the features of the invention disclosed herein may be combined with one another arbitrarily, individually or in combination.
- The invention will be explained in greater detail on the basis of the following practical example.
- A mixture comprising magnesium, carbon and aluminium and also further components in the mass proportions according to Table 1 was first provided in the practical example.
-
TABLE 1 Mass proportions Component [%] MgO 62.6 C 24.6 Al2O3 6.4 CaO 2.4 SiO2 2.3 Fe2O3 1.3 Cr2O3 0.05 P2O5 0.08 TiO2 0.08 K2O 0.05 Na2O 0.08 ZrO2 0.06 - The carbon was present in the mixture in the form of graphite and aluminium carbide.
- Aluminium was present in the mixture in the form of metallic aluminium and in the form of aluminium carbide.
- Recycled magnesia-carbon products were used exclusively as raw materials.
- The mixture was provided in the form of pressed, almond-shaped pellets without additional additives, with a thickness of approximately 15 mm and a length of approximately 30 mm.
- The grain size distribution of the mixture in the pellets is specified in Table 2.
-
TABLE 2 Grain size Mass proportions [%] <63 μm 55 <100 μm 72 <200 μm 92 <250 μm 97 <500 μm 100 - The mixture was used as a slag conditioner for a slag on a metal melt located in an oxygen converter. Here, the mixture was placed on the slag located on the melt. Due to the placement of the mixture on the slag, the basicity of the slag could be increased. Furthermore, due to the proportions of carbon, aluminium and aluminium carbide in the mixture, it was possible to achieve a foaming of the slag. Lastly, the viscosity of the slag could be adjusted to the desired measure.
Claims (8)
1. A mixture for introducing into the slag located on a metal melt in iron and steel metallurgy, said mixture comprising magnesium, carbon and aluminium in the following mass proportions:
MgO: 45 to 90 mass %;
C: 12 to 40 mass %;
Al2O3: 1 to 20 mass %.
2. The mixture according to claim 1 , with a proportion of MgCO3 of less than 10 mass %.
3. The mixture according to claim 2 , being present in the form of pellets.
4. The mixture according to claim 3 , the granularity of which is present in a grain size less than 0.5 mm to an extent of at least 70 mass %.
5. The mixture according to claim 1 , comprising calcium oxide and silicon dioxide in the following mass proportions:
CaO: 0 to 10 mass %;
SiO2: 0 to 7 mass %.
6. The mixture according to claim 1 , comprising iron oxide in the following mass proportions:
iron oxide: 0 to 7 mass %.
7. A method for conditioning a slag located on a metal melt in a metallurgical vessel in iron and steel metallurgy, said method comprising the following steps:
providing a mixture, said mixture comprising magnesium, carbon and aluminium in the following mass proportions:
MgO: 45 to 90 mass %;
C: 12 to 40 mass %;
Al2O3: 1 to 20 mass %; and
introducing the mixture into the slag located on the metal melt in the metallurgical vessel.
8. (canceled)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP13195334.1A EP2878685B9 (en) | 2013-12-02 | 2013-12-02 | Method for conditioning a slag on molten metal from the processing of iron and steel in a metallurgical vessel |
| EP13195334.1 | 2013-12-02 | ||
| PCT/EP2014/071022 WO2015082093A1 (en) | 2013-12-02 | 2014-10-01 | Mixture, use of this mixture and process for conditioning a slag located on a metal melt in a metallurgical vessel in iron and steel metallurgy |
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| US20160376672A1 true US20160376672A1 (en) | 2016-12-29 |
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| US (1) | US20160376672A1 (en) |
| EP (1) | EP2878685B9 (en) |
| CN (1) | CN105705662A (en) |
| ES (1) | ES2559024T3 (en) |
| HR (1) | HRP20151446T1 (en) |
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| WO (1) | WO2015082093A1 (en) |
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| GB9005431D0 (en) * | 1990-03-10 | 1990-05-09 | Foseco Int | Metallurgical flux compositions |
| GB9108889D0 (en) * | 1991-04-25 | 1991-06-12 | Foseco Int | Metallurgical fluxes |
| US5946339A (en) * | 1997-07-22 | 1999-08-31 | Itz A Gaz, Inc. | Steelmaking process using direct reduction iron |
| CN101302577B (en) * | 2008-06-16 | 2010-09-01 | 东北大学 | Self-propagating MgO-based desulfurizer and preparation method thereof |
| CN102660662A (en) * | 2012-05-11 | 2012-09-12 | 西峡县兴宝冶金保温耐材有限公司 | Method for producing deoxidized furnace protecting agent by utilizing waste magnesia carbon brick and gangue |
| CN103537635B (en) * | 2012-07-11 | 2015-10-21 | 攀钢集团研究院有限公司 | A kind of semi-steel heat-preservation agent and application thereof |
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2013
- 2013-12-02 RS RS20150849A patent/RS54471B1/en unknown
- 2013-12-02 SI SI201330101T patent/SI2878685T1/en unknown
- 2013-12-02 PL PL13195334T patent/PL2878685T3/en unknown
- 2013-12-02 PT PT131953341T patent/PT2878685E/en unknown
- 2013-12-02 EP EP13195334.1A patent/EP2878685B9/en active Active
- 2013-12-02 ES ES13195334.1T patent/ES2559024T3/en active Active
- 2013-12-02 HU HUE13195334A patent/HUE026614T2/en unknown
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2014
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- 2014-10-01 MX MX2016005055A patent/MX2016005055A/en unknown
- 2014-10-01 WO PCT/EP2014/071022 patent/WO2015082093A1/en not_active Ceased
- 2014-10-01 CN CN201480062204.6A patent/CN105705662A/en active Pending
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